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    ALG9 ALG9 alpha-1,2-mannosyltransferase [ Homo sapiens (human) ]

    Gene ID: 79796, updated on 3-Nov-2024

    Summary

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    Official Symbol
    ALG9provided by HGNC
    Official Full Name
    ALG9 alpha-1,2-mannosyltransferaseprovided by HGNC
    Primary source
    HGNC:HGNC:15672
    See related
    Ensembl:ENSG00000086848 MIM:606941; AllianceGenome:HGNC:15672
    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
    CDG1L; DIBD1; GIKANIS; LOH11CR1J
    Summary
    This gene encodes an alpha-1,2-mannosyltransferase enzyme that functions in lipid-linked oligosaccharide assembly. Mutations in this gene result in congenital disorder of glycosylation type Il. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]
    Expression
    Ubiquitous expression in testis (RPKM 3.4), thyroid (RPKM 3.0) and 25 other tissues See more
    Orthologs
    mouse all
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    Genomic context

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    See ALG9 in Genome Data Viewer
    Location:
    11q23.1
    Exon count:
    27
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (111768025..111871581, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (111778034..111881824, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (111652919..111742305, complement)

    Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene salt inducible kinase 2 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:111563346-111563859 Neighboring gene RN7SK pseudogene 273 Neighboring gene protein phosphatase 2 scaffold subunit Abeta Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:111594031-111594566 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:111603371-111604187 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:111605768-111606404 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr11:111636139-111637042 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 5519 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 3900 Neighboring gene uncharacterized LOC124902756 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 3901 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr11:111685391-111686590 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 5520 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 5521 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:111709725-111710226 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 3902 Neighboring gene H3K27ac hESC enhancer GRCh37_chr11:111749557-111750176 Neighboring gene G protein subunit gamma 5 pseudogene 3 Neighboring gene ferredoxin-fold anticodon binding domain containing 1 Neighboring gene cilia and flagella associated protein 68

    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 novel phenotype in N-glycosylation disorders: Gillessen-Kaesbach-Nishimura skeletal dysplasia due to pathogenic variants in ALG9. Tham E, et al. Eur J Hum Genet, 2016 Feb. PMID 25966638, Free PMC Article
    2. Heterozygosity of ALG9 in Association with Autosomal Dominant Polycystic Liver Disease. Boerrigter MM, et al. Genes (Basel), 2023 Sep 2. PMID 37761895, Free PMC Article
    3. Quality control of glycoproteins bearing truncated glycans in an ALG9-defective (CDG-IL) patient. Vleugels W, et al. Glycobiology, 2009 Aug. PMID 19451548
    4. Missense variant c.1460 T > C (p.L487P) enhances protein degradation of ER mannosyltransferase ALG9 in two new ALG9-CDG patients presenting with West syndrome and review of the literature. Himmelreich N, et al. Mol Genet Metab, 2022 Aug. PMID 35839600
    5. Common variations in ALG9 are not associated with bipolar I disorder: a family-based study. Baysal BE, et al. Behav Brain Funct, 2006 Jul 21. PMID 16859551, Free PMC Article

    See all (47) citations in PubMed

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?
    1. Heterozygosity of ALG9 in Association with Autosomal Dominant Polycystic Liver Disease.
      Title: Heterozygosity of ALG9 in Association with Autosomal Dominant Polycystic Liver Disease.
    2. Missense variant c.1460 T > C (p.L487P) enhances protein degradation of ER mannosyltransferase ALG9 in two new ALG9-CDG patients presenting with West syndrome and review of the literature.
      Title: Missense variant c.1460 T > C (p.L487P) enhances protein degradation of ER mannosyltransferase ALG9 in two new ALG9-CDG patients presenting with West syndrome and review of the literature.
    3. LncRNA MEG3 contributes to drug resistance in acute myeloid leukemia by positively regulating ALG9 through sponging miR-155.
      Title: LncRNA MEG3 contributes to drug resistance in acute myeloid leukemia by positively regulating ALG9 through sponging miR-155.
    4. ALG9 is a novel disease gene in the genetically heterogeneous autosomal dominant polycystic kidney disease (ADPKD) spectrum.
      Title: ALG9 Mutation Carriers Develop Kidney and Liver Cysts.
    5. ALG9 is upregulated in peripheral blood mononuclear cells of galactosaemia patients.
      Title: Classical galactosaemia: novel insights in IgG N-glycosylation and N-glycan biosynthesis.
    6. Our study shows that some pathogenic variants in ALG9 can present as a lethal skeletal dysplasia with visceral malformations as the most severe phenotype
      Title: A novel phenotype in N-glycosylation disorders: Gillessen-Kaesbach-Nishimura skeletal dysplasia due to pathogenic variants in ALG9.
    7. Due to the ALG9 deficiency, cells accumulated the lipid-linked oligosaccharides Man(6)GlcNAc(2)-PP-dolichol and Man(8)GlcNAc(2)-PP-dolichol.
      Title: Quality control of glycoproteins bearing truncated glycans in an ALG9-defective (CDG-IL) patient.
    8. Observational study of gene-disease association. (HuGE Navigator)
      Title: Common variations in ALG9 are not associated with bipolar I disorder: a family-based study.
    Submit: New GeneRIF Correction

    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
    ALG9 congenital disorder of glycosylation
    MedGen: C2931006 OMIM: 608776 GeneReviews: Congenital Disorders of N-Linked Glycosylation and Multiple Pathway Overview
    		not available
    Gillessen-Kaesbach-Nishimura syndrome
    MedGen: C1849762 OMIM: 263210 GeneReviews: Not available
    		not available

    Variation

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    See variants in ClinVar

    See studies and variants in dbVar

    See Variation Viewer (GRCh37.p13)

    See Variation Viewer (GRCh38)

    Genotypes

    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

    • FLJ21845, DKFZp586M2420

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables alpha-1,2-mannosyltransferase activity IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    enables alpha-1,2-mannosyltransferase activity TAS
    Traceable Author Statement
    more info
    		  
    enables dol-P-Man:Man(6)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase activity IGI
    Inferred from Genetic Interaction
    more info
    		 PubMed 
    enables dol-P-Man:Man(8)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase activity IGI
    Inferred from Genetic Interaction
    more info
    		 PubMed 
    Process Evidence Code Pubs
    involved_in dolichol-linked oligosaccharide biosynthetic process IGI
    Inferred from Genetic Interaction
    more info
    		 PubMed 
    involved_in dolichol-linked oligosaccharide biosynthetic process TAS
    Traceable Author Statement
    more info
    		  
    involved_in protein N-linked glycosylation IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    involved_in protein N-linked glycosylation IMP
    Inferred from Mutant Phenotype
    more info
    		 PubMed 
    Component Evidence Code Pubs
    is_active_in endoplasmic reticulum membrane IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    located_in endoplasmic reticulum membrane TAS
    Traceable Author Statement
    more info
    		  
    is_active_in lumenal side of endoplasmic reticulum membrane IC
    Inferred by Curator
    more info
    		 PubMed 
    located_in membrane HDA PubMed 

    General protein information

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    Preferred Names
    alpha-1,2-mannosyltransferase ALG9
    Names
    asparagine-linked glycosylation 9 alpha-12-mannosyltransferase-like protein
    asparagine-linked glycosylation 9 homolog (S. cerevisiae, alpha- 1,2-mannosyltransferase)
    asparagine-linked glycosylation 9 homolog (yeast, alpha- 1,2-mannosyltransferase)
    asparagine-linked glycosylation 9, alpha-1,2-mannosyltransferase homolog
    asparagine-linked glycosylation protein 9 homolog
    disrupted in bipolar affective disorder 1
    disrupted in bipolar disorder protein 1
    dol-P-Man dependent alpha-1,2-mannosyltransferase
    dol-P-Man:Man(6)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase
    dol-P-Man:Man(8)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase
    dolichyl-P-Man:Man(6)GlcNAc(2)-PP-dolichol alpha-1,2-mannosyltransferase
    dolichyl-P-Man:Man(8)GlcNAc(2)-PP-dolichol alpha-1,2-mannosyltransferase
    loss of heterozygosity, 11, chromosomal region 1 gene J product
    NP_001071158.1
    NP_001071159.1
    NP_001071160.1
    NP_001339338.1
    NP_001339339.1
    NP_001339340.1
    NP_001339341.1
    NP_001339342.1
    NP_001339343.1
    NP_001339344.1
    NP_001339345.1
    NP_001339346.1
    NP_001339347.1
    NP_001339348.1
    NP_001339349.1
    NP_001339350.1
    NP_001339351.1
    NP_001339352.1
    NP_079016.2
    XP_005277780.1
    XP_006718976.1
    XP_016873803.1
    XP_024304463.1
    XP_047283565.1
    XP_054225956.1
    XP_054225957.1
    XP_054225958.1
    XP_054225959.1
    XP_054225960.1

    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_009210.2 RefSeqGene

      Range
      5000..94386
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. NM_001077690.1 → NP_001071158.1  alpha-1,2-mannosyltransferase ALG9 isoform b

      See identical proteins and their annotated locations for NP_001071158.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (2) uses an alternate in-frame splice site in the central coding region, compared to variant 1. The resulting isoform (b) lacks a 7-aa internal segment, compared to isoform a.
      Source sequence(s)
      AK025498, AL136927, AP001781
      Consensus CDS
      CCDS73379.1
      UniProtKB/Swiss-Prot
      Q6ZMD5, Q7Z4R4, Q96GS7, Q96PB9, Q9H068, Q9H6U8
      Related
      ENSP00000484200.1, ENST00000614444.4
      Conserved Domains (1) summary
      pfam03901
      Location:60 → 482
      Glyco_transf_22; Alg9-like mannosyltransferase family

    2. NM_001077691.2 → NP_001071159.1  alpha-1,2-mannosyltransferase ALG9 isoform c

      See identical proteins and their annotated locations for NP_001071159.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (3) contains a distinct 5' UTR and lacks an in-frame portion of the 5' coding region, compared to variant 1. The resulting isoform (c) has a shorter N-terminus compared to isoform a. Variants 3, 9, and 10 all encode the same isoform (c).
      Source sequence(s)
      AK025498, AP001781, BC009255, DA257621, FP884232
      Consensus CDS
      CCDS41714.1
      UniProtKB/TrEMBL
      B4DQI3
      Related
      ENSP00000435517.1, ENST00000531154.5
      Conserved Domains (1) summary
      cl21590
      Location:1 → 318
      PMT_2; Dolichyl-phosphate-mannose-protein mannosyltransferase

    3. NM_001077692.2 → NP_001071160.1  alpha-1,2-mannosyltransferase ALG9 isoform d

      See identical proteins and their annotated locations for NP_001071160.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (4) contains a distinct 5' UTR, lacks an in-frame portion of the 5' coding region, and uses an alternate in-frame splice site in the central coding region, compared to variant 1. The resulting isoform (d) has a shorter N-terminus and lacks a 7-aa internal segment, compared to isoform a. Variants 4-8 all encode the same isoform (d).
      Source sequence(s)
      AK025498, AL136927, AP001781, DA257621, FP884232
      Consensus CDS
      CCDS53709.1
      UniProtKB/TrEMBL
      B4DQI3
      Related
      ENSP00000381090.2, ENST00000398006.6
      Conserved Domains (1) summary
      cl21590
      Location:1 → 311
      PMT_2; Dolichyl-phosphate-mannose-protein mannosyltransferase

    4. NM_001352409.1 → NP_001339338.1  alpha-1,2-mannosyltransferase ALG9 isoform d

      Status: REVIEWED

      Description
      Transcript Variant: This variant (5), as well as variants 4 and 6-8, encodes isoform d.
      Source sequence(s)
      AP001781, FP884232
      Consensus CDS
      CCDS53709.1
      UniProtKB/TrEMBL
      B4DQI3
      Conserved Domains (1) summary
      cl21590
      Location:1 → 311
      PMT_2; Dolichyl-phosphate-mannose-protein mannosyltransferase

    5. NM_001352410.1 → NP_001339339.1  alpha-1,2-mannosyltransferase ALG9 isoform d

      Status: REVIEWED

      Description
      Transcript Variant: This variant (6), as well as variants 4, 5, 7, and 8, encodes isoform d.
      Source sequence(s)
      AP001781, FP884232
      Consensus CDS
      CCDS53709.1
      UniProtKB/TrEMBL
      B4DQI3
      Conserved Domains (1) summary
      cl21590
      Location:1 → 311
      PMT_2; Dolichyl-phosphate-mannose-protein mannosyltransferase

    6. NM_001352411.2 → NP_001339340.1  alpha-1,2-mannosyltransferase ALG9 isoform d

      Status: REVIEWED

      Description
      Transcript Variant: This variant (7), as well as variants 4-6 and 8, encodes isoform d.
      Source sequence(s)
      AP001781, FP884232
      Consensus CDS
      CCDS53709.1
      UniProtKB/TrEMBL
      B4DQI3
      Conserved Domains (1) summary
      cl21590
      Location:1 → 311
      PMT_2; Dolichyl-phosphate-mannose-protein mannosyltransferase

    7. NM_001352412.2 → NP_001339341.1  alpha-1,2-mannosyltransferase ALG9 isoform d

      Status: REVIEWED

      Description
      Transcript Variant: This variant (8), as well as variants 4-7, encodes isoform d.
      Source sequence(s)
      AP001781, FP884232
      Consensus CDS
      CCDS53709.1
      UniProtKB/TrEMBL
      B4DQI3
      Conserved Domains (1) summary
      cl21590
      Location:1 → 311
      PMT_2; Dolichyl-phosphate-mannose-protein mannosyltransferase

    8. NM_001352413.1 → NP_001339342.1  alpha-1,2-mannosyltransferase ALG9 isoform c

      Status: REVIEWED

      Description
      Transcript Variant: This variant (9), as well as variants 3 and 10, encodes isoform c.
      Source sequence(s)
      AP001781, FP884232
      Consensus CDS
      CCDS41714.1
      UniProtKB/TrEMBL
      B4DQI3
      Conserved Domains (1) summary
      cl21590
      Location:1 → 318
      PMT_2; Dolichyl-phosphate-mannose-protein mannosyltransferase

    9. NM_001352414.2 → NP_001339343.1  alpha-1,2-mannosyltransferase ALG9 isoform c

      Status: REVIEWED

      Description
      Transcript Variant: This variant (10), as well as variants 3 and 9, encodes isoform c.
      Source sequence(s)
      AP001781, FP884232
      Consensus CDS
      CCDS41714.1
      UniProtKB/TrEMBL
      B4DQI3
      Conserved Domains (1) summary
      cl21590
      Location:1 → 318
      PMT_2; Dolichyl-phosphate-mannose-protein mannosyltransferase

    10. NM_001352415.1 → NP_001339344.1  alpha-1,2-mannosyltransferase ALG9 isoform e

      Status: REVIEWED

      Description
      Transcript Variant: This variant (11), as well as variant 12, encodes isoform e.
      Source sequence(s)
      AP001781, FP884232
      UniProtKB/TrEMBL
      B4DQI3
      Conserved Domains (1) summary
      cl21590
      Location:1 → 311
      PMT_2; Dolichyl-phosphate-mannose-protein mannosyltransferase

    11. NM_001352416.1 → NP_001339345.1  alpha-1,2-mannosyltransferase ALG9 isoform e

      Status: REVIEWED

      Description
      Transcript Variant: This variant (12), as well as variant 11, encodes isoform e.
      Source sequence(s)
      AP001781, FP884232
      UniProtKB/TrEMBL
      B4DQI3
      Conserved Domains (1) summary
      cl21590
      Location:1 → 311
      PMT_2; Dolichyl-phosphate-mannose-protein mannosyltransferase

    12. NM_001352417.1 → NP_001339346.1  alpha-1,2-mannosyltransferase ALG9 isoform f

      Status: REVIEWED

      Description
      Transcript Variant: This variant (13) encodes the longest isoform (f).
      Source sequence(s)
      AP001781, FP884232
      Conserved Domains (1) summary
      pfam03901
      Location:60 → 482
      Glyco_transf_22; Alg9-like mannosyltransferase family

    13. NM_001352418.1 → NP_001339347.1  alpha-1,2-mannosyltransferase ALG9 isoform g

      Status: REVIEWED

      Source sequence(s)
      AP001781, FP884232
      Conserved Domains (1) summary
      pfam03901
      Location:60 → 441
      Glyco_transf_22; Alg9-like mannosyltransferase family

    14. NM_001352419.1 → NP_001339348.1  alpha-1,2-mannosyltransferase ALG9 isoform h

      Status: REVIEWED

      Source sequence(s)
      AP001781, FP884232
      UniProtKB/TrEMBL
      B4DQI3
      Conserved Domains (1) summary
      cl21590
      Location:1 → 318
      PMT_2; Dolichyl-phosphate-mannose-protein mannosyltransferase

    15. NM_001352420.2 → NP_001339349.1  alpha-1,2-mannosyltransferase ALG9 isoform i

      Status: REVIEWED

      Source sequence(s)
      AP001781, FP884232
      UniProtKB/TrEMBL
      B4DQI3
      Conserved Domains (1) summary
      cl21590
      Location:1 → 311
      PMT_2; Dolichyl-phosphate-mannose-protein mannosyltransferase

    16. NM_001352421.2 → NP_001339350.1  alpha-1,2-mannosyltransferase ALG9 isoform j

      Status: REVIEWED

      Source sequence(s)
      AP001781, FP884232
      UniProtKB/TrEMBL
      B4DQI3
      Conserved Domains (1) summary
      cl21590
      Location:1 → 311
      PMT_2; Dolichyl-phosphate-mannose-protein mannosyltransferase

    17. NM_001352422.2 → NP_001339351.1  alpha-1,2-mannosyltransferase ALG9 isoform k

      Status: REVIEWED

      Source sequence(s)
      AP001781, FP884232
      UniProtKB/TrEMBL
      B4DQI3
      Conserved Domains (1) summary
      cl21590
      Location:1 → 286
      PMT_2; Dolichyl-phosphate-mannose-protein mannosyltransferase

    18. NM_001352423.2 → NP_001339352.1  alpha-1,2-mannosyltransferase ALG9 isoform l

      Status: REVIEWED

      Source sequence(s)
      AP001781, FP884232
      UniProtKB/TrEMBL
      B4DQI3
      Conserved Domains (1) summary
      cl21590
      Location:1 → 270
      PMT_2; Dolichyl-phosphate-mannose-protein mannosyltransferase

    19. NM_024740.2 → NP_079016.2  alpha-1,2-mannosyltransferase ALG9 isoform a

      See identical proteins and their annotated locations for NP_079016.2

      Status: REVIEWED

      Description
      Transcript Variant: This variant (1) encodes isoform a.
      Source sequence(s)
      AK025498, AP001781, BC009255
      Consensus CDS
      CCDS73380.1
      UniProtKB/Swiss-Prot
      Q9H6U8
      Related
      ENSP00000482437.1, ENST00000616540.5
      Conserved Domains (1) summary
      pfam03901
      Location:60 → 489
      Glyco_transf_22; Alg9-like mannosyltransferase family

    RNA

    1. NR_147984.2 RNA Sequence

      Status: REVIEWED

      Source sequence(s)
      AP001781, FP884232

    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_000011.10 Reference GRCh38.p14 Primary Assembly

      Range
      111768025..111871581 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_017018314.3 → XP_016873803.1  alpha-1,2-mannosyltransferase ALG9 isoform X4

    2. XM_024448695.2 → XP_024304463.1  alpha-1,2-mannosyltransferase ALG9 isoform X3

      Conserved Domains (1) summary
      pfam03901
      Location:60 → 482
      Glyco_transf_22; Alg9-like mannosyltransferase family

    3. XM_005277723.6 → XP_005277780.1  alpha-1,2-mannosyltransferase ALG9 isoform X1

      See identical proteins and their annotated locations for XP_005277780.1

      Conserved Domains (1) summary
      pfam03901
      Location:60 → 489
      Glyco_transf_22; Alg9-like mannosyltransferase family

    4. XM_006718913.4 → XP_006718976.1  alpha-1,2-mannosyltransferase ALG9 isoform X2

      Conserved Domains (1) summary
      pfam03901
      Location:60 → 489
      Glyco_transf_22; Alg9-like mannosyltransferase family

    5. XM_047427609.1 → XP_047283565.1  alpha-1,2-mannosyltransferase ALG9 isoform X5

    RNA

    1. XR_001747968.3 RNA Sequence

    2. XR_001747967.3 RNA Sequence

    3. XR_007062503.1 RNA Sequence

    4. XR_001747977.2 RNA Sequence

    5. XR_007062504.1 RNA Sequence

    6. XR_001747974.2 RNA Sequence

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060935.1 Alternate T2T-CHM13v2.0

      Range
      111778034..111881824 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054369984.1 → XP_054225959.1  alpha-1,2-mannosyltransferase ALG9 isoform X4

    2. XM_054369983.1 → XP_054225958.1  alpha-1,2-mannosyltransferase ALG9 isoform X3

    3. XM_054369981.1 → XP_054225956.1  alpha-1,2-mannosyltransferase ALG9 isoform X1

    4. XM_054369982.1 → XP_054225957.1  alpha-1,2-mannosyltransferase ALG9 isoform X2

    5. XM_054369985.1 → XP_054225960.1  alpha-1,2-mannosyltransferase ALG9 isoform X5

    RNA

    1. XR_008488452.1 RNA Sequence

    2. XR_008488451.1 RNA Sequence

    3. XR_008488453.1 RNA Sequence

    4. XR_008488456.1 RNA Sequence

    5. XR_008488454.1 RNA Sequence

    6. XR_008488455.1 RNA Sequence

    Nucleotide Protein
    Heading Accession and Version
    Protein Accession Links
    GenPept Link UniProtKB Link
    Q9H6U8.2 GenPept UniProtKB/Swiss-Prot:Q9H6U8

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