Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
9725
Gene name Gene Name - the full gene name approved by the HGNC.
Transmembrane protein 63A
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TMEM63A
Synonyms (NCBI Gene) Gene synonyms aliases
HLD19, KIAA0792, hTMEM63A
Disease Acronyms (UniProt) Disease acronyms from UniProt database
HLD19
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1q42.12
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs1576074651 C>T Pathogenic Coding sequence variant, missense variant, non coding transcript variant
rs1576080546 A>T Pathogenic Coding sequence variant, intron variant, non coding transcript variant, missense variant
rs1576101665 C>T Pathogenic Coding sequence variant, missense variant, synonymous variant, non coding transcript variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT550853 hsa-miR-4418 PAR-CLIP 21572407
MIRT550852 hsa-miR-509-3-5p PAR-CLIP 21572407
MIRT550851 hsa-miR-509-5p PAR-CLIP 21572407
MIRT550850 hsa-miR-217 PAR-CLIP 21572407
MIRT550848 hsa-miR-6807-3p PAR-CLIP 21572407
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003676 Function Nucleic acid binding IEA
GO:0005227 Function Calcium activated cation channel activity IBA 21873635
GO:0005515 Function Protein binding IPI 28870237
GO:0005765 Component Lysosomal membrane HDA 17897319
GO:0005765 Component Lysosomal membrane IDA 20957757
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
618685 29118 ENSG00000196187
Protein
UniProt ID O94886
Protein name Mechanosensitive cation channel TMEM63A (Transmembrane protein 63A) (hTMEM63A)
Protein function Mechanosensitive cation channel with low conductance and high activation threshold (PubMed:30382938, PubMed:31587869, PubMed:37543036). In contrast to TMEM63B, does not show phospholipid scramblase activity (PubMed:39716028). Acts as a regulator
PDB 8EHW , 8GRS , 8WUA
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13967 RSN1_TM 50 214 Late exocytosis, associated with Golgi transport Family
PF14703 PHM7_cyt 227 410 Cytosolic domain of 10TM putative phosphate transporter Domain
PF02714 RSN1_7TM 421 693 Calcium-dependent channel, 7TM region, putative phosphate Family
Sequence
MMDSPFLELWQSKAVSIREQLGLGDRPNDSYCYNSAKNSTVLQGVTFGGIPTVLLIDVSC
FLFLILVFSIIRRRFWDYGRIALVSEADSESRFQRLSSTSSSGQQDFENELGCCPWLTAI
FRLHDDQILEWCGEDAIHYLSFQRHIIFLLVVVSFLSLCVILPVNLSGDLLDKDPYSFGR
TTIANLQTDNDLLWLHTIFAVIYLFLTVGFMRHH
TQSIKYKEENLVRRTLFITGLPRDAR
KETVESHFRDAYPTCEVVDVQLCYNVAKLIYLCKEKKKTEKSLTYYTNLQVKTGQRTLIN
PKPCGQFCCCEVLGCEWEDAISYYTRMKDRLLERITEEERHVQDQPLGMAFVTFQEKSMA
TYILKDFNACKCQSLQCKGEPQPSSHSRELYTSKWTVTFAADPEDICWKN
LSIQGLRWWL
QWLGINFTLFLGLFFLTTPSIILSTMDKFNVTKPIHALNNPIISQFFPTLLLWSFSALLP
SIVYYSTLLESHWTKSGENQIMMTKVYIFLIFMVLILPSLGLTSLDFFFRWLFDKTSSEA
SIRLECVFLPDQGAFFVNYVIASAFIGNGMELLRLPGLILYTFRMIMAKTAADRRNVKQN
QAFQYEFGAMYAWMLCVFTVIVAYSITCPIIAPFGLIYILLKHMVDRHNLYFVYLPAKLE
KGIHFAAVNQALAAPILCLFWLYFFSFLRLGMK
APATLFTFLVLLLTILVCLAHTCFGCF
KHLSPLNYKTEEPASDKGSEAEAHMPPPFTPYVPRILNGLASERTALSPQQQQQQTYGAI
HNISGTIPGQCLAQSATGSVAAAPQEA
Sequence length 807
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Neutrophil degranulation
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Gastric cancer Hereditary Diffuse Gastric Cancer rs137854571, rs63751108, rs34612342, rs121908383, rs121909144, rs121909775, rs121909219, rs121909223, rs63750871, rs80359530, rs121964873, rs121913530, rs606231203, rs121918505, rs587776802
View all (244 more)
21364753
Unknown
Disease term Disease name Evidence References Source
Leukodystrophy leukodystrophy, hypomyelinating, 19, transient infantile GenCC
Associations from Text Mining
Disease Name Relationship Type References
Demyelinating Diseases Associate 31587869
Leukodystrophy Hypomyelinating 2 Associate 31587869
Neoplasm Metastasis Associate 35920704
Pelizaeus Merzbacher like disease autosomal recessive 2 Associate 31587869, 33597727
Pulmonary Disease Chronic Obstructive Associate 19111454
Pulmonary Disease Chronic Obstructive Severe Early Onset Associate 19111454
Triple Negative Breast Neoplasms Associate 35920704