Gene Gene information from NCBI Gene database.
Entrez ID 5119
Gene name Charged multivesicular body protein 1A
Gene symbol CHMP1A
Synonyms (NCBI Gene)
CHMP1PCH8PCOLN3PRSM1VPS46-1VPS46A
Chromosome 16
Chromosome location 16q24.3
Summary This gene encodes a member of the CHMP/Chmp family of proteins which are involved in multivesicular body sorting of proteins to the interiors of lysosomes. The initial prediction of the protein sequence encoded by this gene suggested that the encoded prot
SNPs SNP information provided by dbSNP.
7
SNP ID Visualize variation Clinical significance Consequence
rs114931496 G>A Benign, conflicting-interpretations-of-pathogenicity Non coding transcript variant, synonymous variant, coding sequence variant, missense variant
rs200606123 G>A,T Conflicting-interpretations-of-pathogenicity Non coding transcript variant, stop gained, coding sequence variant, synonymous variant
rs201479143 C>T Likely-benign, conflicting-interpretations-of-pathogenicity Non coding transcript variant, missense variant, coding sequence variant, synonymous variant
rs397515426 G>A Pathogenic Non coding transcript variant, coding sequence variant, stop gained, missense variant
rs398122918 C>A,T Pathogenic Intron variant
miRNA miRNA information provided by mirtarbase database.
430
miRTarBase ID miRNA Experiments Reference
MIRT890440 hsa-miR-103a CLIP-seq
MIRT890441 hsa-miR-107 CLIP-seq
MIRT890442 hsa-miR-1179 CLIP-seq
MIRT890443 hsa-miR-1200 CLIP-seq
MIRT890444 hsa-miR-1207-5p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
79
GO ID Ontology Definition Evidence Reference
GO:0000421 Component Autophagosome membrane IDA 17984323
GO:0000776 Component Kinetochore IDA 26040712
GO:0000776 Component Kinetochore IEA
GO:0000794 Component Condensed nuclear chromosome IDA 11559747
GO:0000815 Component ESCRT III complex IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
164010 8740 ENSG00000131165
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9HD42
Protein name Charged multivesicular body protein 1a (Chromatin-modifying protein 1a) (CHMP1a) (Vacuolar protein sorting-associated protein 46-1) (Vps46-1) (hVps46-1)
Protein function Probable peripherally associated component of the endosomal sorting required for transport complex III (ESCRT-III) which is involved in multivesicular bodies (MVBs) formation and sorting of endosomal cargo proteins into MVBs. MVBs contain intral
PDB 2JQ9 , 2YMB , 4A5X
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03357 Snf7 4 174 Snf7 Family
Tissue specificity TISSUE SPECIFICITY: Expressed in placenta, cultured skin fibroblasts and in osteoblast cell line MG-63. {ECO:0000269|PubMed:8863740}.
Sequence
Sequence length 196
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Virion - Hepatitis viruses
Endocytosis
Necroptosis
  HCMV Late Events
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
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Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Pontocerebellar hypoplasia type 8 Likely pathogenic rs2543458244, rs398122918 RCV003148450
RCV000033060
Pontoneocerebellar hypoplasia Likely pathogenic rs2151511838 RCV003226733
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
CHMP1A-related disorder Likely benign; Conflicting classifications of pathogenicity; Benign rs200605916, rs187184327, rs753406733, rs201479143, rs114931496, rs367970292, rs116776046, rs61730918, rs61747591, rs397515426, rs200710259, rs546864527 RCV003953653
RCV003952567
RCV003970894
RCV003947515
RCV003927774
RCV003946554
RCV003916844
RCV003912696
RCV003972623
RCV004757955
RCV003953045
RCV004731055
Clear cell carcinoma of kidney Benign; Likely benign rs61747591, rs200710259 RCV005896657
RCV005898919
Familial cancer of breast Likely benign rs139678649 RCV005919169
Gastric cancer Likely benign rs758430703 RCV005928400
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Cytomegalovirus Infections Associate 19640981
Infections Associate 19640981
Pancreatic Neoplasms Associate 19216755
Parkinson Disease Associate 34148545
Squamous Cell Carcinoma of Head and Neck Associate 30259648