Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
140738
Gene name Gene Name - the full gene name approved by the HGNC.
Transmembrane protein 37
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TMEM37
Synonyms (NCBI Gene) Gene synonyms aliases
PR, PR1
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2q14.2
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT459460 hsa-miR-552-3p PAR-CLIP 23592263
MIRT459459 hsa-miR-4272 PAR-CLIP 23592263
MIRT459458 hsa-miR-4709-5p PAR-CLIP 23592263
MIRT459457 hsa-miR-125a-3p PAR-CLIP 23592263
MIRT459456 hsa-miR-3126-5p PAR-CLIP 23592263
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005244 Function Voltage-gated monoatomic ion channel activity IEA
GO:0005262 Function Calcium channel activity IEA
GO:0006811 Process Monoatomic ion transport IEA
GO:0006816 Process Calcium ion transport IEA
GO:0016020 Component Membrane IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
618831 18216 ENSG00000171227
Protein
UniProt ID Q8WXS4
Protein name Voltage-dependent calcium channel gamma-like subunit (Neuronal voltage-gated calcium channel gamma-like subunit) (Transmembrane protein 37)
Protein function Thought to stabilize the calcium channel in an inactivated (closed) state. Modulates calcium current when coexpressed with CACNA1G (By similarity).
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15108 TMEM37 7 187 Voltage-dependent calcium channel gamma-like subunit protein family Family
Sequence
Sequence length 190
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Dementia Dementia N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Adenocarcinoma Associate 8421689
Breast Neoplasms Associate 23105141, 28468826
Diabetes Mellitus Type 2 Associate 29185012, 32705173
Graft vs Host Disease Stimulate 12829610
Graves Ophthalmopathy Associate 37900130
Hematologic Neoplasms Associate 28468826
Leukemia Associate 17412886, 22495388, 9326217
Leukemia Myelogenous Chronic BCR ABL Positive Associate 12393722, 12829610, 17412886, 9326217
Leukemia Myeloid Associate 23105141
Leukemia Myeloid Chronic Phase Associate 18548092