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MAX MYC associated factor X [ Homo sapiens (human) ]

Gene ID: 4149, updated on 14-Nov-2024

Summary

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Official Symbol
MAXprovided by HGNC
Official Full Name
MYC associated factor Xprovided by HGNC
Primary source
HGNC:HGNC:6913
See related
Ensembl:ENSG00000125952 MIM:154950; AllianceGenome:HGNC:6913
Gene type
protein coding
RefSeq status
REVIEWED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
PDMCS; bHLHd4
Summary
The protein encoded by this gene is a member of the basic helix-loop-helix leucine zipper (bHLHZ) family of transcription factors. It is able to form homodimers and heterodimers with other family members, which include Mad, Mxi1 and Myc. Myc is an oncoprotein implicated in cell proliferation, differentiation and apoptosis. The homodimers and heterodimers compete for a common DNA target site (the E box) and rearrangement among these dimer forms provides a complex system of transcriptional regulation. Mutations of this gene have been reported to be associated with hereditary pheochromocytoma. A pseudogene of this gene is located on the long arm of chromosome 7. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]
Expression
Ubiquitous expression in spleen (RPKM 18.6), lymph node (RPKM 17.0) and 25 other tissues See more
Orthologs
mouse all
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Genomic context

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See MAX in Genome Data Viewer
Location:
14q23.3
Exon count:
10
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 14 NC_000014.9 (65006101..65102695, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 14 NC_060938.1 (59210965..59307534, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 14 NC_000014.8 (65472819..65569413, complement)

Chromosome 14 - NC_000014.9Genomic Context describing neighboring genes Neighboring gene CHURC1-FNTB readthrough Neighboring gene H3K4me1 hESC enhancer GRCh37_chr14:65421611-65422488 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:65426829-65427347 Neighboring gene RAB15, member RAS oncogene family Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 5845 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:65441391-65442168 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr14:65448241-65448742 Neighboring gene uncharacterized LOC107984655 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 8540 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr14:65471811-65473010 Neighboring gene farnesyltransferase, CAAX box, subunit beta Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 5846 Neighboring gene microRNA 4706 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:65544121-65545096 Neighboring gene uncharacterized LOC100506321 Neighboring gene H3K27ac hESC enhancer GRCh37_chr14:65568306-65568806 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 5847 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 8541 Neighboring gene RNA, U2 small nuclear 14, pseudogene Neighboring gene uncharacterized LOC124903329

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Expression

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  • Project title: HPA RNA-seq normal tissues HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?
  1. Genotype and clinical phenotype characteristics of MAX germline mutation-associated pheochromocytoma/paraganglioma syndrome.
    Title: Genotype and clinical phenotype characteristics of MAX germline mutation-associated pheochromocytoma/paraganglioma syndrome.
  2. NMR-identification of the interaction between BRCA1 and the intrinsically disordered monomer of the Myc-associated factor X.
    Title: NMR-identification of the interaction between BRCA1 and the intrinsically disordered monomer of the Myc-associated factor X.
  3. A recurrent de novo MAX p.Arg60Gln variant causes a syndromic overgrowth disorder through differential expression of c-Myc target genes.
    Title: A recurrent de novo MAX p.Arg60Gln variant causes a syndromic overgrowth disorder through differential expression of c-Myc target genes.
  4. Validation of Myc-Associated Protein X (MAX) regulation in growth hormone secreting and nonfunctional pituitary adenoma.
    Title: Validation of Myc-Associated Protein X (MAX) regulation in growth hormone secreting and nonfunctional pituitary adenoma.
  5. MORC2 and MAX contributes to the expression of glycolytic enzymes, breast cancer cell proliferation and migration.
    Title: MORC2 and MAX contributes to the expression of glycolytic enzymes, breast cancer cell proliferation and migration.
  6. Integrated analysis of mRNA-seq and miRNA-seq reveals the potential roles of Egr1, Rxra and Max in kidney stone disease.
    Title: Integrated analysis of mRNA-seq and miRNA-seq reveals the potential roles of Egr1, Rxra and Max in kidney stone disease.
  7. Succinate dehydrogenase and MYC-associated factor X mutations in pituitary neuroendocrine tumours.
    Title: Succinate dehydrogenase and MYC-associated factor X mutations in pituitary neuroendocrine tumours.
  8. miR-22 Suppresses EMT by Mediating Metabolic Reprogramming in Colorectal Cancer through Targeting MYC-Associated Factor X.
    Title: miR-22 Suppresses EMT by Mediating Metabolic Reprogramming in Colorectal Cancer through Targeting MYC-Associated Factor X.
  9. MAX deficiency impairs human endometrial decidualization through down-regulating OSR2 in women with recurrent spontaneous abortion.
    Title: MAX deficiency impairs human endometrial decidualization through down-regulating OSR2 in women with recurrent spontaneous abortion.
  10. Case Report: Pheochromocytoma and Synchronous Neuroblastoma in a Family With Hereditary Pheochromocytoma Associated With a MAX Deleterious Variant.
    Title: Case Report: Pheochromocytoma and Synchronous Neuroblastoma in a Family With Hereditary Pheochromocytoma Associated With a MAX Deleterious Variant.
Submit: New GeneRIF Correction See all GeneRIFs (64)

Phenotypes

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Find tests for this gene in the NIH Genetic Testing Registry (GTR)

Review eQTL and phenotype association data in this region using PheGenI

Copy number response

Description
Copy number response
Triplosensitivity

No evidence available (Last evaluated 2021-07-20)

ClinGen Genome Curation Page
Haploinsufficency

Sufficient evidence for dosage pathogenicity (Last evaluated 2021-07-20)

ClinGen Genome Curation PagePubMed

EBI GWAS Catalog

Description
Genome-wide association study identifies loci affecting blood copper, selenium and zinc.
EBI GWAS Catalog
Genome-wide association study of anthropometric traits in Korcula Island, Croatia.
EBI GWAS Catalog
Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.
EBI GWAS Catalog
Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.
EBI GWAS Catalog
Seventy-five genetic loci influencing the human red blood cell.
EBI GWAS Catalog

Variation

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See variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

HIV-1 interactions

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Protein interactions

Protein Gene Interaction Pubs
Envelope surface glycoprotein gp120 env HIV-1 gp120 downregulates expression of c-Myc, Max, and 14-3-3epsilon proteins, and decreases phosphorylation of ATP-dependent tyrosine kinases (Akt) at Ser-473 in human mesangial cells (HMC) PubMed

Go to the HIV-1, Human Interaction Database

Pathways from PubChem

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Interactions

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Products Interactant Other Gene Complex Source Pubs Description

General gene information

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Markers

Homology

Clone Names

  • MGC10775, MGC11225, MGC18164, MGC34679, MGC36767

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables DNA binding IDA
Inferred from Direct Assay
more info
 PubMed 
enables DNA-binding transcription factor activity IBA
Inferred from Biological aspect of Ancestor
more info
  
enables DNA-binding transcription factor activity, RNA polymerase II-specific IDA
Inferred from Direct Assay
more info
 PubMed 
enables DNA-binding transcription factor activity, RNA polymerase II-specific ISA
Inferred from Sequence Alignment
more info
  
enables DNA-binding transcription factor binding IPI
Inferred from Physical Interaction
more info
 PubMed 
contributes_to DNA-binding transcription repressor activity, RNA polymerase II-specific IDA
Inferred from Direct Assay
more info
 PubMed 
enables DNA-binding transcription repressor activity, RNA polymerase II-specific IDA
Inferred from Direct Assay
more info
 PubMed 
enables E-box binding IMP
Inferred from Mutant Phenotype
more info
 PubMed 
contributes_to RNA polymerase II transcription regulatory region sequence-specific DNA binding IDA
Inferred from Direct Assay
more info
 PubMed 
enables identical protein binding IPI
Inferred from Physical Interaction
more info
 PubMed 
enables protein binding IPI
Inferred from Physical Interaction
more info
 PubMed 
enables protein dimerization activity IEA
Inferred from Electronic Annotation
more info
  
enables protein-containing complex binding IEA
Inferred from Electronic Annotation
more info
  
enables sequence-specific double-stranded DNA binding IDA
Inferred from Direct Assay
more info
 PubMed 
Process Evidence Code Pubs
involved_in cellular response to peptide hormone stimulus IEA
Inferred from Electronic Annotation
more info
  
involved_in cellular response to starvation IEA
Inferred from Electronic Annotation
more info
  
involved_in negative regulation of gene expression IEA
Inferred from Electronic Annotation
more info
  
involved_in negative regulation of transcription by RNA polymerase II IDA
Inferred from Direct Assay
more info
 PubMed 
involved_in neuron apoptotic process IEA
Inferred from Electronic Annotation
more info
  
involved_in positive regulation of DNA-templated transcription IDA
Inferred from Direct Assay
more info
 PubMed 
involved_in positive regulation of transcription by RNA polymerase II IBA
Inferred from Biological aspect of Ancestor
more info
  
involved_in protein-containing complex assembly IEA
Inferred from Electronic Annotation
more info
  
involved_in regulation of transcription by RNA polymerase II IDA
Inferred from Direct Assay
more info
 PubMed 
involved_in response to axon injury IEA
Inferred from Electronic Annotation
more info
  
involved_in response to insulin IEA
Inferred from Electronic Annotation
more info
  
involved_in retina development in camera-type eye IEA
Inferred from Electronic Annotation
more info
  
Component Evidence Code Pubs
part_of MLL1 complex IDA
Inferred from Direct Assay
more info
 PubMed 
part_of Mad-Max complex IPI
Inferred from Physical Interaction
more info
 PubMed 
part_of Myc-Max complex IPI
Inferred from Physical Interaction
more info
 PubMed 
located_in PML body IEA
Inferred from Electronic Annotation
more info
  
part_of RNA polymerase II transcription regulator complex IBA
Inferred from Biological aspect of Ancestor
more info
  
part_of RNA polymerase II transcription regulator complex IDA
Inferred from Direct Assay
more info
 PubMed 
located_in chromatin IDA
Inferred from Direct Assay
more info
 PubMed 
located_in chromatin ISA
Inferred from Sequence Alignment
more info
  
located_in dendrite IEA
Inferred from Electronic Annotation
more info
  
located_in nucleoplasm TAS
Traceable Author Statement
more info
  
located_in nucleus IDA
Inferred from Direct Assay
more info
 PubMed 
located_in nucleus NAS
Non-traceable Author Statement
more info
 PubMed 
part_of protein-DNA complex IDA
Inferred from Direct Assay
more info
 PubMed 
part_of protein-DNA complex IMP
Inferred from Mutant Phenotype
more info
 PubMed 

General protein information

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Preferred Names
protein max
Names
class D basic helix-loop-helix protein 4

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

Genomic

  1. NG_029830.1 RefSeqGene

    Range
    4815..101409
    Download
    GenBank, FASTA, Sequence Viewer (Graphics), LRG_530

mRNA and Protein(s)

  1. NM_001271068.2 → NP_001257997.1  protein max isoform g

    See identical proteins and their annotated locations for NP_001257997.1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (7) lacks two alternate in-frame exons in the coding region and includes an alternate 3' terminal exon compared to variant 1. It encodes isoform g which is shorter and has a distinct C-terminus, compared to isoform a.
    Source sequence(s)
    AI769390, AL833643, BC013669, HY018878
    UniProtKB/Swiss-Prot
    P61244
    Conserved Domains (1) summary
    pfam00010
    Location:15 → 49
    HLH; Helix-loop-helix DNA-binding domain

  2. NM_001271069.2 → NP_001257998.1  protein max isoform h

    See identical proteins and their annotated locations for NP_001257998.1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (8) lacks two alternate in-frame exons in the coding region and includes an alternate 3' terminal exon, compared to variant 1. It encodes isoform h which is shorter and has a distinct C-terminus, compared to isoform a.
    Source sequence(s)
    AL139022, AL833643, DB482510
    Conserved Domains (1) summary
    cl00081
    Location:15 → 48
    bHLH_SF; basic Helix Loop Helix (bHLH) domain superfamily

  3. NM_001320415.2 → NP_001307344.1  protein max isoform i

    Status: REVIEWED

    Description
    Transcript Variant: This variant (11) contains an alternate internal exon in its 5' coding region resulting in a frameshift compared to variant 1. The encoded isoform (i) has a shorter and distinct N-terminus compared to isoform a.
    Source sequence(s)
    AL833643, BC025685
    Consensus CDS
    CCDS81813.1
    UniProtKB/TrEMBL
    G3V302

  4. NM_001407094.1 → NP_001394023.1  protein max isoform a

    Status: REVIEWED

    Source sequence(s)
    AL139022
    UniProtKB/Swiss-Prot
    A6NH73, A8K265, A8K4G4, A8K824, P25912, P52163, P61244, Q14803, Q96CY8

  5. NM_001407095.1 → NP_001394024.1  protein max isoform b

    Status: REVIEWED

    Source sequence(s)
    AL139022

  6. NM_001407096.1 → NP_001394025.1  protein max isoform j

    Status: REVIEWED

    Source sequence(s)
    AL139022

  7. NM_001407097.1 → NP_001394026.1  protein max isoform j

    Status: REVIEWED

    Source sequence(s)
    AL139022

  8. NM_001407098.1 → NP_001394027.1  protein max isoform k

    Status: REVIEWED

    Source sequence(s)
    AL139022
    UniProtKB/TrEMBL
    G3V5L1
    Related
    ENSP00000452405.1, ENST00000555419.5

  9. NM_001407099.1 → NP_001394028.1  protein max isoform l

    Status: REVIEWED

    Source sequence(s)
    AL139022
    UniProtKB/TrEMBL
    G3V563
    Related
    ENSP00000452197.1, ENST00000557746.5

  10. NM_001407100.1 → NP_001394029.1  protein max isoform l

    Status: REVIEWED

    Source sequence(s)
    AL139022
    UniProtKB/TrEMBL
    G3V563

  11. NM_001407101.1 → NP_001394030.1  protein max isoform l

    Status: REVIEWED

    Source sequence(s)
    AL139022
    UniProtKB/TrEMBL
    G3V563

  12. NM_001407102.1 → NP_001394031.1  protein max isoform l

    Status: REVIEWED

    Source sequence(s)
    AL139022
    UniProtKB/TrEMBL
    G3V563

  13. NM_001407103.1 → NP_001394032.1  protein max isoform c

    Status: REVIEWED

    Source sequence(s)
    AL139022

  14. NM_001407104.1 → NP_001394033.1  protein max isoform c

    Status: REVIEWED

    Source sequence(s)
    AL139022

  15. NM_001407105.1 → NP_001394034.1  protein max isoform i

    Status: REVIEWED

    Source sequence(s)
    AL139022
    UniProtKB/TrEMBL
    G3V302

  16. NM_001407106.1 → NP_001394035.1  protein max isoform i

    Status: REVIEWED

    Source sequence(s)
    AL139022
    UniProtKB/TrEMBL
    G3V302
    Related
    ENSP00000450955.1, ENST00000557277.5

  17. NM_001407107.1 → NP_001394036.1  protein max isoform i

    Status: REVIEWED

    Source sequence(s)
    AL139022
    UniProtKB/TrEMBL
    G3V302

  18. NM_001407108.1 → NP_001394037.1  protein max isoform m

    Status: REVIEWED

    Source sequence(s)
    AL139022
    UniProtKB/TrEMBL
    Q6V3B1

  19. NM_001407109.1 → NP_001394038.1  protein max isoform m

    Status: REVIEWED

    Source sequence(s)
    AL139022
    UniProtKB/TrEMBL
    Q6V3B1
    Related
    ENSP00000452286.1, ENST00000555667.5

  20. NM_001407110.1 → NP_001394039.1  protein max isoform m

    Status: REVIEWED

    Source sequence(s)
    AL139022
    UniProtKB/TrEMBL
    Q6V3B1

  21. NM_001407111.1 → NP_001394040.1  protein max isoform n

    Status: REVIEWED

    Source sequence(s)
    AL139022

  22. NM_001407112.1 → NP_001394041.1  protein max isoform n

    Status: REVIEWED

    Source sequence(s)
    AL139022

  23. NM_001407113.1 → NP_001394042.1  protein max isoform g

    Status: REVIEWED

    Source sequence(s)
    AL139022

  24. NM_001407114.1 → NP_001394043.1  protein max isoform o

    Status: REVIEWED

    Source sequence(s)
    AL139022

  25. NM_002382.5 → NP_002373.3  protein max isoform a

    See identical proteins and their annotated locations for NP_002373.3

    Status: REVIEWED

    Description
    Transcript Variant: This variant (1) encodes the longest isoform (a) which is also known as the long form.
    Source sequence(s)
    AL833643, BC004516, BC025685
    Consensus CDS
    CCDS9771.1
    UniProtKB/Swiss-Prot
    A6NH73, A8K265, A8K4G4, A8K824, P25912, P52163, P61244, Q14803, Q96CY8
    UniProtKB/TrEMBL
    Q8TAX8
    Related
    ENSP00000351490.4, ENST00000358664.9
    Conserved Domains (1) summary
    cd11406
    Location:24 → 92
    bHLHzip_Max; basic Helix-Loop-Helix-zipper (bHLHzip) domain found in protein Max and similar proteins

  26. NM_145112.3 → NP_660087.1  protein max isoform b

    See identical proteins and their annotated locations for NP_660087.1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (2) lacks an alternate in-frame exon in the coding region compared to variant 1. It encodes isoform b (also known as the short form) which is shorter than isoform a.
    Source sequence(s)
    BC025685, BC027924, BF038005
    Consensus CDS
    CCDS9772.1
    UniProtKB/TrEMBL
    Q8TAX8
    Related
    ENSP00000351175.4, ENST00000358402.8
    Conserved Domains (1) summary
    cd11406
    Location:15 → 83
    bHLHzip_Max; basic Helix-Loop-Helix-zipper (bHLHzip) domain found in protein Max and similar proteins

  27. NM_145113.3 → NP_660088.1  protein max isoform c

    See identical proteins and their annotated locations for NP_660088.1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (3) uses an alternate in-frame exon in the 3' coding region compared to variant 1. The resulting protein (isoform c) has a distinct C-terminus and is shorter than isoform a.
    Source sequence(s)
    AK290929, AL833643, BC025685, BC027924, X60287
    Consensus CDS
    CCDS41965.1
    Related
    ENSP00000451907.1, ENST00000553928.5
    Conserved Domains (1) summary
    cd11406
    Location:24 → 92
    bHLHzip_Max; basic Helix-Loop-Helix-zipper (bHLHzip) domain found in protein Max and similar proteins

  28. NM_145114.3 → NP_660089.1  protein max isoform d

    See identical proteins and their annotated locations for NP_660089.1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (4) lacks one alternate in-frame exon in the coding region and includes an alternate 3' terminal exon compared to variant 1. It encodes isoform d which is shorter and has a distinct C-terminus, compared to isoform a.
    Source sequence(s)
    BC013669, BF038005, HY018878
    Consensus CDS
    CCDS9774.1
    UniProtKB/Swiss-Prot
    P61244
    Related
    ENSP00000246163.2, ENST00000246163.2
    Conserved Domains (1) summary
    pfam00010
    Location:24 → 58
    HLH; Helix-loop-helix DNA-binding domain

  29. NM_197957.4 → NP_932061.1  protein max isoform f

    See identical proteins and their annotated locations for NP_932061.1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (6) lacks an alternate in-frame exon in the coding region and includes an alternate 3' terminal exon, compared to variant 1. It encodes isoform f which is shorter and has a distinct C-terminus, compared to isoform a.
    Source sequence(s)
    AI917842, AL139022, BC013669, BF038005
    Consensus CDS
    CCDS9770.1
    UniProtKB/Swiss-Prot
    P61244
    Related
    ENSP00000342482.2, ENST00000341653.6
    Conserved Domains (1) summary
    cl00081
    Location:24 → 57
    bHLH_SF; basic Helix Loop Helix (bHLH) domain superfamily

RNA

  1. NR_073137.2 RNA Sequence

    Status: REVIEWED

    Description
    Transcript Variant: This variant (9) contains an alternate 5' exon and lacks an alternate internal exon compared to variant 1. This variant is represented as non-coding because it lacks a large portion of the coding region, including the translational start codon, found in variant 1.
    Source sequence(s)
    AL139022

  2. NR_073138.2 RNA Sequence

    Status: REVIEWED

    Description
    Transcript Variant: This variant (10) contains an alternate 5' exon, lacks an alternate internal exon and includes an alternate 3' terminal exon compared to variant 1. This variant is represented as non-coding because it lacks an in-frame ORF compared to variant 1.
    Source sequence(s)
    AL139022

  3. NR_176275.1 RNA Sequence

    Status: REVIEWED

    Source sequence(s)
    AL139022

  4. NR_176276.1 RNA Sequence

    Status: REVIEWED

    Source sequence(s)
    AL139022

  5. NR_176277.1 RNA Sequence

    Status: REVIEWED

    Source sequence(s)
    AL139022

  6. NR_176278.1 RNA Sequence

    Status: REVIEWED

    Source sequence(s)
    AL139022

  7. NR_176279.1 RNA Sequence

    Status: REVIEWED

    Source sequence(s)
    AL139022

  8. NR_176280.1 RNA Sequence

    Status: REVIEWED

    Source sequence(s)
    AL139022

  9. NR_176281.1 RNA Sequence

    Status: REVIEWED

    Source sequence(s)
    AL139022

  10. NR_176282.1 RNA Sequence

    Status: REVIEWED

    Source sequence(s)
    AL139022

  11. NR_176283.1 RNA Sequence

    Status: REVIEWED

    Source sequence(s)
    AL139022

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000014.9 Reference GRCh38.p14 Primary Assembly

    Range
    65006101..65102695 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_011536773.4 → XP_011535075.1  protein max isoform X1

    Conserved Domains (1) summary
    pfam00010
    Location:24 → 75
    HLH; Helix-loop-helix DNA-binding domain

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060938.1 Alternate T2T-CHM13v2.0

    Range
    59210965..59307534 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_054376084.1 → XP_054232059.1  protein max isoform X1

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_145116.1: Suppressed sequence

    Description
    NM_145116.1: This RefSeq was permanently suppressed because currently there is insufficient support for the transcript and the protein.
Nucleotide Protein
Heading Accession and Version
Protein Accession Links
GenPept Link UniProtKB Link
P61244.1 GenPept UniProtKB/Swiss-Prot:P61244

Gene LinkOut

The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.

Chemical Information
Molecular Biology Databases
Research Materials
Tools
Miscellaneous