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    KANSL1 KAT8 regulatory NSL complex subunit 1 [ Homo sapiens (human) ]

    Gene ID: 284058, updated on 2-Nov-2024

    Summary

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    Official Symbol
    KANSL1provided by HGNC
    Official Full Name
    KAT8 regulatory NSL complex subunit 1provided by HGNC
    Primary source
    HGNC:HGNC:24565
    See related
    Ensembl:ENSG00000120071 MIM:612452; AllianceGenome:HGNC:24565
    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
    KDVS; NSL1; MSL1v1; CENP-36; hMSL1v1; KIAA1267; DEL17Q21.31; C17DELq21.31
    Summary
    This gene encodes a nuclear protein that is a subunit of two protein complexes involved with histone acetylation, the MLL1 complex and the NSL1 complex. The encoded protein has been implicated in a variety of cellular processes including enhancer regulation, cell proliferation, and mitosis. Mutations in this gene are associated with Koolen-de Vries Syndrome. [provided by RefSeq, May 2022]
    Annotation information
    Note: This gene has been reviewed for its involvement in coronavirus biology, and is locus in the vicinity of disease-associated variant(s).
    Expression
    Ubiquitous expression in testis (RPKM 12.3), ovary (RPKM 9.4) and 25 other tissues See more
    Orthologs
    mouse all
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    Genomic context

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    See KANSL1 in Genome Data Viewer
    Location:
    17q21.31
    Exon count:
    22
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 17 NC_000017.11 (46029916..46225367, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 17 NC_060941.1 (46891535..47087028, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (44107282..44302733, complement)

    Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105371800 Neighboring gene OCT4-H3K4me1 hESC enhancer GRCh37_chr17:44019777-44020277 Neighboring gene microtubule associated protein tau Neighboring gene ReSE screen-validated silencer GRCh37_chr17:44066175-44066366 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr17:44070003-44070564 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr17:44086993-44087496 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr17:44100868-44101486 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr17:44102104-44102721 Neighboring gene saitohin Neighboring gene MPRA-validated peak2868 silencer Neighboring gene H3K4me1 hESC enhancer GRCh37_chr17:44225973-44226474 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr17:44226475-44226974 Neighboring gene uncharacterized LOC107985027 Neighboring gene KANSL1 antisense RNA 1 Neighboring gene mitogen-activated protein kinase 8 interacting protein 1 pseudogene 1 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr17:44337043-44337589 Neighboring gene leucine rich repeat containing 37A Neighboring gene DND microRNA-mediated repression inhibitor 1 pseudogene 2

    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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    Related articles in PubMed

    1. A new blood DNA methylation signature for Koolen-de Vries syndrome: Classification of missense KANSL1 variants and comparison to fibroblast cells. Awamleh Z, et al. Eur J Hum Genet, 2024 Mar. PMID 38282074, Free PMC Article
    2. KANSL1 gene disruption associated with the full clinical spectrum of 17q21.31 microdeletion syndrome. Moreno-Igoa M, et al. BMC Med Genet, 2015 Aug 22. PMID 26293599, Free PMC Article
    3. Intragenic KANSL1 mutations and chromosome 17q21.31 deletions: broadening the clinical spectrum and genotype-phenotype correlations in a large cohort of patients. Zollino M, et al. J Med Genet, 2015 Dec. PMID 26424144
    4. 10-year-old female with intragenic KANSL1 mutation, no KANSL1-related intellectual disability, and preserved verbal intelligence. Keen C, et al. Am J Med Genet A, 2017 Mar. PMID 28211987
    5. Partial microduplication in the histone acetyltransferase complex member KANSL1 is associated with congenital heart defects in 22q11.2 microdeletion syndrome patients. León LE, et al. Sci Rep, 2017 May 11. PMID 28496102, Free PMC Article

    See all (81) citations in PubMed

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?
    1. A new blood DNA methylation signature for Koolen-de Vries syndrome: Classification of missense KANSL1 variants and comparison to fibroblast cells.
      Title: A new blood DNA methylation signature for Koolen-de Vries syndrome: Classification of missense KANSL1 variants and comparison to fibroblast cells.
    2. Recurrent KAT6B/A::KANSL1 Fusions Characterize a Potentially Aggressive Uterine Sarcoma Morphologically Overlapping With Low-grade Endometrial Stromal Sarcoma.
      Title: Recurrent KAT6B/A::KANSL1 Fusions Characterize a Potentially Aggressive Uterine Sarcoma Morphologically Overlapping With Low-grade Endometrial Stromal Sarcoma.
    3. Adult phenotype in Koolen-de Vries/KANSL1 haploinsufficiency syndrome.
      Title: Adult phenotype in Koolen-de Vries/KANSL1 haploinsufficiency syndrome.
    4. Analysis in epithelial ovarian cancer identifies KANSL1 as a biomarker and target gene for immune response and HDAC inhibition.
      Title: Analysis in epithelial ovarian cancer identifies KANSL1 as a biomarker and target gene for immune response and HDAC inhibition.
    5. These results show that a KANSL1 microduplication, in combination with the 22q11.2 deletion, is associated with increased risk of CHD in these patients, suggesting that KANSL1 plays a role as a modifier gene in 22q11.2DS patients.
      Title: Partial microduplication in the histone acetyltransferase complex member KANSL1 is associated with congenital heart defects in 22q11.2 microdeletion syndrome patients.
    6. One variant, p.Lys104Thr, was predicted damaging and appeared overrepresented in our 90-patient cohort compared to Genome Aggregation Database allele frequency (0.217 to 0.116). However, there was no difference in p.Lys104Thr allele frequency in the follow-up childhood epilepsy with centrotemporal spikes (CECTS) and atypical childhood epilepsy with centrotemporal spikes (ACECTS) cohort and controls.
      Title: KANSL1 variation is not a major contributing factor in self-limited focal epilepsy syndromes of childhood.
    7. This case expands the mild end of the neurodevelopmental spectrum seen in children with de novo KANSL1 mutation and KdVS.
      Title: 10-year-old female with intragenic KANSL1 mutation, no KANSL1-related intellectual disability, and preserved verbal intelligence.
    8. In KANSL1 haploinsufficiency syndrome, chromosome deletions are greatly prevalent compared with KANSL1 mutations.
      Title: Intragenic KANSL1 mutations and chromosome 17q21.31 deletions: broadening the clinical spectrum and genotype-phenotype correlations in a large cohort of patients.
    9. essential for mitotic spindle assembly and chromosome segregation
      Title: An epigenetic regulator emerges as microtubule minus-end binding and stabilizing factor in mitosis.
    10. KANSL1 gene haploinsufficiency is necessary and sufficient to cause the full spectrum of the 17q21.31 microdeletion syndrome.
      Title: KANSL1 gene disruption associated with the full clinical spectrum of 17q21.31 microdeletion syndrome.
    Submit: New GeneRIF Correction See all GeneRIFs (12)

    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

    Associated conditions

    Description Tests
    Koolen-de Vries syndrome
    MedGen: C1864871 OMIM: 610443 GeneReviews: Koolen-de Vries Syndrome
    		Compare labs

    Copy number response

    Description
    Copy number response
    Triplosensitivity

    No evidence available (Last evaluated 2013-04-11)

    ClinGen Genome Curation Page
    Haploinsufficency

    Sufficient evidence for dosage pathogenicity (Last evaluated 2013-04-11)

    ClinGen Genome Curation PagePubMed

    EBI GWAS Catalog

    Description
    Common variants at 6q22 and 17q21 are associated with intracranial volume.
    EBI GWAS Catalog
    Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study.
    EBI GWAS Catalog
    Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes.
    EBI GWAS Catalog

    Variation

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    See Variation Viewer (GRCh37.p13)

    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

    • KIAA1267, MGC102843, DKFZp727C091, DKFZp686P06109

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables histone acetyltransferase binding IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    		 PubMed 
    Process Evidence Code Pubs
    involved_in chromatin organization IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in positive regulation of DNA-templated transcription NAS
    Non-traceable Author Statement
    more info
    		 PubMed 
    involved_in regulation of mitochondrial transcription IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    Component Evidence Code Pubs
    part_of MLL1 complex IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    part_of NSL complex IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    part_of NSL complex IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    part_of histone acetyltransferase complex IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    located_in kinetochore IEA
    Inferred from Electronic Annotation
    more info
    		  
    located_in mitochondrion IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    located_in nucleoplasm IDA
    Inferred from Direct Assay
    more info
    		  
    located_in nucleoplasm TAS
    Traceable Author Statement
    more info
    		  
    located_in nucleus IDA
    Inferred from Direct Assay
    more info
    		  

    General protein information

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    Preferred Names
    KAT8 regulatory NSL complex subunit 1
    Names
    MLL1/MLL complex subunit KANSL1
    MSL1 homolog 1
    NSL complex protein NSL1
    centromere protein 36
    male-specific lethal 1 homolog
    non-specific lethal 1 homolog

    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_032784.1 RefSeqGene

      Range
      36946..200459
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. NM_001193465.2 → NP_001180394.1  KAT8 regulatory NSL complex subunit 1 isoform 2

      See identical proteins and their annotated locations for NP_001180394.1

      Status: REVIEWED

      Source sequence(s)
      AC217773, CR936218, KF495991
      Consensus CDS
      CCDS74084.1
      UniProtKB/TrEMBL
      A0A0G2JQF4, A0A9S7M8F4
      Related
      ENSP00000461812.2, ENST00000574590.6
      Conserved Domains (1) summary
      pfam15275
      Location:885 → 997
      PEHE; PEHE domain

    2. NM_001193466.2 → NP_001180395.1  KAT8 regulatory NSL complex subunit 1 isoform 1

      See identical proteins and their annotated locations for NP_001180395.1

      Status: REVIEWED

      Source sequence(s)
      AL137317, BC098376, BX538006
      Consensus CDS
      CCDS11503.2
      UniProtKB/Swiss-Prot
      A8K5E4, B3KT49, I3L4J3, Q6AW85, Q7Z3B3, Q8IYH1, Q9BRH0, Q9NTE7, Q9UFT0, Q9ULF3
      UniProtKB/TrEMBL
      A0A0G2JQF4
      Related
      ENSP00000262419.6, ENST00000262419.10
      Conserved Domains (1) summary
      pfam15275
      Location:885 → 1003
      PEHE; PEHE domain

    3. NM_001379198.1 → NP_001366127.1  KAT8 regulatory NSL complex subunit 1 isoform 1

      Status: REVIEWED

      Source sequence(s)
      AC217773, CR936218, KF495991
      Consensus CDS
      CCDS11503.2
      UniProtKB/Swiss-Prot
      A8K5E4, B3KT49, I3L4J3, Q6AW85, Q7Z3B3, Q8IYH1, Q9BRH0, Q9NTE7, Q9UFT0, Q9ULF3
      UniProtKB/TrEMBL
      A0A0G2JQF4
      Related
      ENSP00000461484.1, ENST00000572904.6
      Conserved Domains (1) summary
      pfam15275
      Location:885 → 1003
      PEHE; PEHE domain

    4. NM_001405854.1 → NP_001392783.1  KAT8 regulatory NSL complex subunit 1 isoform 1

      Status: REVIEWED

      Source sequence(s)
      AC217773, CR936218, KF495991
      Consensus CDS
      CCDS11503.2
      UniProtKB/Swiss-Prot
      A8K5E4, B3KT49, I3L4J3, Q6AW85, Q7Z3B3, Q8IYH1, Q9BRH0, Q9NTE7, Q9UFT0, Q9ULF3

    5. NM_001405855.1 → NP_001392784.1  KAT8 regulatory NSL complex subunit 1 isoform 1

      Status: REVIEWED

      Source sequence(s)
      AC217773, CR936218, KF495991
      UniProtKB/Swiss-Prot
      A8K5E4, B3KT49, I3L4J3, Q6AW85, Q7Z3B3, Q8IYH1, Q9BRH0, Q9NTE7, Q9UFT0, Q9ULF3

    6. NM_001405856.1 → NP_001392785.1  KAT8 regulatory NSL complex subunit 1 isoform 2

      Status: REVIEWED

      Source sequence(s)
      AC217773, CR936218, KF495991
      Consensus CDS
      CCDS74084.1
      UniProtKB/TrEMBL
      A0A9S7M8F4

    7. NM_001405857.1 → NP_001392786.1  KAT8 regulatory NSL complex subunit 1 isoform 2

      Status: REVIEWED

      Source sequence(s)
      AC217773, CR936218, KF495991
      UniProtKB/TrEMBL
      A0A9S7M8F4

    8. NM_001405858.1 → NP_001392787.1  KAT8 regulatory NSL complex subunit 1 isoform 2

      Status: REVIEWED

      Source sequence(s)
      AC217773, CR936218, KF495991
      UniProtKB/TrEMBL
      A0A9S7M8F4

    9. NM_001405859.1 → NP_001392788.1  KAT8 regulatory NSL complex subunit 1 isoform 3

      Status: REVIEWED

      Source sequence(s)
      AC217773, CR936218, KF495991

    10. NM_001405860.1 → NP_001392789.1  KAT8 regulatory NSL complex subunit 1 isoform 3

      Status: REVIEWED

      Source sequence(s)
      AC217773, CR936218, KF495991

    11. NM_001405861.1 → NP_001392790.1  KAT8 regulatory NSL complex subunit 1 isoform 4

      Status: REVIEWED

      Source sequence(s)
      AC217773, CR936218, KF495991

    12. NM_001405872.1 → NP_001392801.1  KAT8 regulatory NSL complex subunit 1 isoform 5

      Status: REVIEWED

      Source sequence(s)
      AC217773, CR936218, KF495991
      UniProtKB/TrEMBL
      A0A3B3IT55
      Related
      ENSP00000497628.1, ENST00000648792.1

    13. NM_001405873.1 → NP_001392802.1  KAT8 regulatory NSL complex subunit 1 isoform 5

      Status: REVIEWED

      Source sequence(s)
      AC217773, CR936218, KF495991
      UniProtKB/TrEMBL
      A0A3B3IT55

    14. NM_001405874.1 → NP_001392803.1  KAT8 regulatory NSL complex subunit 1 isoform 5

      Status: REVIEWED

      Source sequence(s)
      AC217773, CR936218, KF495991
      UniProtKB/TrEMBL
      A0A3B3IT55

    15. NM_001405875.1 → NP_001392804.1  KAT8 regulatory NSL complex subunit 1 isoform 6

      Status: REVIEWED

      Source sequence(s)
      AC217773, CR936218, KF495991

    16. NM_001405876.1 → NP_001392805.1  KAT8 regulatory NSL complex subunit 1 isoform 6

      Status: REVIEWED

      Source sequence(s)
      AC217773, CR936218, KF495991

    17. NM_001405877.1 → NP_001392806.1  KAT8 regulatory NSL complex subunit 1 isoform 6

      Status: REVIEWED

      Source sequence(s)
      AC217773, CR936218, KF495991

    18. NM_001405878.1 → NP_001392807.1  KAT8 regulatory NSL complex subunit 1 isoform 6

      Status: REVIEWED

      Source sequence(s)
      AC217773, CR936218, KF495991
      Related
      ENSP00000491765.1, ENST00000639531.1

    19. NM_001405879.1 → NP_001392808.1  KAT8 regulatory NSL complex subunit 1 isoform 7

      Status: REVIEWED

      Source sequence(s)
      AC217773, CR936218, KF495991
      Consensus CDS
      CCDS92348.1
      UniProtKB/TrEMBL
      A0A1W2PRB5
      Related
      ENSP00000461299.1, ENST00000575318.6

    20. NM_001405880.1 → NP_001392809.1  KAT8 regulatory NSL complex subunit 1 isoform 7

      Status: REVIEWED

      Source sequence(s)
      AC217773, CR936218, KF495991
      UniProtKB/TrEMBL
      A0A1W2PRB5
      Related
      ENSP00000492576.1, ENST00000638275.1

    21. NM_001405881.1 → NP_001392810.1  KAT8 regulatory NSL complex subunit 1 isoform 8

      Status: REVIEWED

      Source sequence(s)
      AC217773, CR936218, KF495991

    22. NM_001405882.1 → NP_001392811.1  KAT8 regulatory NSL complex subunit 1 isoform 9

      Status: REVIEWED

      Source sequence(s)
      AC217773, CR936218, KF495991

    23. NM_001405883.1 → NP_001392812.1  KAT8 regulatory NSL complex subunit 1 isoform 10

      Status: REVIEWED

      Source sequence(s)
      AC217773, CR936218, KF495991

    24. NM_001405884.1 → NP_001392813.1  KAT8 regulatory NSL complex subunit 1 isoform 11

      Status: REVIEWED

      Source sequence(s)
      AC217773, CR936218, KF495991

    25. NM_001405885.1 → NP_001392814.1  KAT8 regulatory NSL complex subunit 1 isoform 12

      Status: REVIEWED

      Source sequence(s)
      AC217773, CR936218, KF495991

    26. NM_015443.4 → NP_056258.1  KAT8 regulatory NSL complex subunit 1 isoform 1

      See identical proteins and their annotated locations for NP_056258.1

      Status: REVIEWED

      Source sequence(s)
      AC217773, AI253068, BC098376
      Consensus CDS
      CCDS11503.2
      UniProtKB/Swiss-Prot
      A8K5E4, B3KT49, I3L4J3, Q6AW85, Q7Z3B3, Q8IYH1, Q9BRH0, Q9NTE7, Q9UFT0, Q9ULF3
      UniProtKB/TrEMBL
      A0A0G2JQF4
      Related
      ENSP00000387393.3, ENST00000432791.7
      Conserved Domains (1) summary
      pfam15275
      Location:885 → 1003
      PEHE; PEHE domain

    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_000017.11 Reference GRCh38.p14 Primary Assembly

      Range
      46029916..46225367 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_047435800.1 → XP_047291756.1  KAT8 regulatory NSL complex subunit 1 isoform X3

    2. XM_047435801.1 → XP_047291757.1  KAT8 regulatory NSL complex subunit 1 isoform X4

    3. XM_011524628.4 → XP_011522930.1  KAT8 regulatory NSL complex subunit 1 isoform X2

      See identical proteins and their annotated locations for XP_011522930.1

      UniProtKB/TrEMBL
      A0A0G2JQF4, A0A9S7M8F4
      Conserved Domains (1) summary
      pfam15275
      Location:885 → 997
      PEHE; PEHE domain

    4. XM_047435794.1 → XP_047291750.1  KAT8 regulatory NSL complex subunit 1 isoform X1

      UniProtKB/Swiss-Prot
      A8K5E4, B3KT49, I3L4J3, Q6AW85, Q7Z3B3, Q8IYH1, Q9BRH0, Q9NTE7, Q9UFT0, Q9ULF3

    Reference GRCh38.p14 ALT_REF_LOCI_1

    Genomic

    1. NT_167251.2 Reference GRCh38.p14 ALT_REF_LOCI_1

      Range
      561512..758707
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054328563.1 → XP_054184538.1  KAT8 regulatory NSL complex subunit 1 isoform X4

    2. XM_054328562.1 → XP_054184537.1  KAT8 regulatory NSL complex subunit 1 isoform X3

    3. XM_054328560.1 → XP_054184535.1  KAT8 regulatory NSL complex subunit 1 isoform X2

    4. XM_054328561.1 → XP_054184536.1  KAT8 regulatory NSL complex subunit 1 isoform X5

    Reference GRCh38.p14 ALT_REF_LOCI_2

    Genomic

    1. NT_187663.1 Reference GRCh38.p14 ALT_REF_LOCI_2

      Range
      732028..927537 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054330103.1 → XP_054186078.1  KAT8 regulatory NSL complex subunit 1 isoform X3

    2. XM_054330104.1 → XP_054186079.1  KAT8 regulatory NSL complex subunit 1 isoform X4

    3. XM_054330101.1 → XP_054186076.1  KAT8 regulatory NSL complex subunit 1 isoform X1

      UniProtKB/TrEMBL
      A0A0G2JNT7

    4. XM_054330102.1 → XP_054186077.1  KAT8 regulatory NSL complex subunit 1 isoform X6

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060941.1 Alternate T2T-CHM13v2.0

      Range
      46891535..47087028 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054315778.1 → XP_054171753.1  KAT8 regulatory NSL complex subunit 1 isoform X3

    2. XM_054315779.1 → XP_054171754.1  KAT8 regulatory NSL complex subunit 1 isoform X4

    3. XM_054315777.1 → XP_054171752.1  KAT8 regulatory NSL complex subunit 1 isoform X5

    4. XM_054315775.1 → XP_054171750.1  KAT8 regulatory NSL complex subunit 1 isoform X2

      UniProtKB/TrEMBL
      A0A0G2JNB1

    5. XM_054315774.1 → XP_054171749.1  KAT8 regulatory NSL complex subunit 1 isoform X1

      UniProtKB/TrEMBL
      A0A0G2JNT7

    6. XM_054315776.1 → XP_054171751.1  KAT8 regulatory NSL complex subunit 1 isoform X6

    Nucleotide Protein
    Heading Accession and Version
    Protein Accession Links
    GenPept Link UniProtKB Link
    Q7Z3B3.3 GenPept UniProtKB/Swiss-Prot:Q7Z3B3

    Gene LinkOut

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

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