Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
5119
Gene name Gene Name - the full gene name approved by the HGNC.
Charged multivesicular body protein 1A
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CHMP1A
Synonyms (NCBI Gene) Gene synonyms aliases
CHMP1, PCH8, PCOLN3, PRSM1, VPS46-1, VPS46A
Disease Acronyms (UniProt) Disease acronyms from UniProt database
PCH8
Chromosome Chromosome number
16
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
16q24.3
Summary Summary of gene provided in NCBI Entrez Gene.
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.
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.
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 information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000794 Component Condensed nuclear chromosome IDA 11559747
GO:0000815 Component ESCRT III complex IBA 21873635
GO:0005515 Function Protein binding IPI 11559748, 12445808, 14505570, 14519844, 16730941, 17711858, 19129479, 19129480, 19302785, 21988832, 23045692, 28514442, 32296183, 32814053
GO:0005769 Component Early endosome IDA 11559748
GO:0005771 Component Multivesicular body IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
164010 8740 ENSG00000131165
Protein
UniProt ID 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 information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Developmental delay Global developmental delay rs28941770, rs199469464, rs281865469, rs143747297, rs398123009, rs587777428, rs786205133, rs606231459, rs797044854, rs797045027, rs864309504, rs878853160, rs886039902, rs886042046, rs886041291
View all (32 more)
Mental retardation Intellectual Disability rs5742905, rs267607136, rs267607137, rs2131714307, rs267607038, rs267607042, rs80338685, rs137853127, rs80338815, rs28940893, rs387906309, rs121908096, rs121908099, rs587784365, rs121918315
View all (1024 more)
Multiple congenital anomalies Multiple congenital anomalies rs1057517732 23023333, 11559747, 11559748
Myopia Myopia rs387907109, rs146936371, rs587776903, rs786205127, rs398122836, rs199624584, rs587777625, rs786205216, rs758872875, rs764211125, rs1135402746, rs765658563, rs1555941129, rs1555941116, rs199923805
View all (6 more)
Unknown
Disease term Disease name Evidence References Source
Carcinoma Carcinoma GWAS
Schizophrenia Schizophrenia GWAS
Associations from Text Mining
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