Gene Gene information from NCBI Gene database.
Entrez ID 79041
Gene name Transmembrane protein 38A
Gene symbol TMEM38A
Synonyms (NCBI Gene)
TRIC-ATRICA
Chromosome 19
Chromosome location 19p13.11
miRNA miRNA information provided by mirtarbase database.
223
miRTarBase ID miRNA Experiments Reference
MIRT519551 hsa-miR-106a-5p PAR-CLIP 23446348
MIRT519550 hsa-miR-106b-5p PAR-CLIP 23446348
MIRT519549 hsa-miR-17-5p PAR-CLIP 23446348
MIRT519548 hsa-miR-20a-5p PAR-CLIP 23446348
MIRT519547 hsa-miR-20b-5p PAR-CLIP 23446348
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
26
GO ID Ontology Definition Evidence Reference
GO:0005267 Function Potassium channel activity IEA
GO:0005267 Function Potassium channel activity ISS
GO:0005267 Function Potassium channel activity TAS 19095005
GO:0005634 Component Nucleus IEA
GO:0006811 Process Monoatomic ion transport IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
611235 28462 ENSG00000072954
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9H6F2
Protein name Trimeric intracellular cation channel type A (TRIC-A) (TRICA) (Transmembrane protein 38A)
Protein function Intracellular monovalent cation channel required for maintenance of rapid intracellular calcium release. Acts as a potassium counter-ion channel that functions in synchronization with calcium release from intracellular stores (By similarity). Op
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF05197 TRIC 40 231 TRIC channel Family
Sequence
Sequence length 299
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
AUTISM SPECTRUM DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Essential Hypertension Hypertension BEFREE 21803293
★☆☆☆☆
Found in Text Mining only
Hypertensive disease Hypertension BEFREE 21803293
★☆☆☆☆
Found in Text Mining only