Gene Gene information from NCBI Gene database.
Entrez ID 81853
Gene name Transmembrane protein 14B
Gene symbol TMEM14B
Synonyms (NCBI Gene)
-
Chromosome 6
Chromosome location 6p24.2
miRNA miRNA information provided by mirtarbase database.
104
miRTarBase ID miRNA Experiments Reference
MIRT1431381 hsa-miR-1245b-3p CLIP-seq
MIRT1431382 hsa-miR-1470 CLIP-seq
MIRT1431383 hsa-miR-3143 CLIP-seq
MIRT1431384 hsa-miR-3145-3p CLIP-seq
MIRT1431385 hsa-miR-331-5p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
9
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 29033352, 32296183, 36217029
GO:0006783 Process Heme biosynthetic process IBA
GO:0007399 Process Nervous system development IEA
GO:0016020 Component Membrane IEA
GO:0021987 Process Cerebral cortex development IMP 29033352
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
619865 21384 ENSG00000137210
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9NUH8
Protein name Transmembrane protein 14B
Protein function Primate-specific protein involved in cortical expansion and folding in the developing neocortex. May drive neural progenitor proliferation through nuclear translocation of IQGAP1, which in turn promotes G1/S cell cycle transitions. {ECO:0000269|
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03647 Tmemb_14 13 105 Transmembrane proteins 14C Family
Tissue specificity TISSUE SPECIFICITY: Mainly expressed in the outer subventricular zone (OSVZ) of the fetal brains. {ECO:0000269|PubMed:29033352}.
Sequence
Sequence length 114
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
6
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
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
HYPERPARATHYROIDISM GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
MAJOR DEPRESSIVE DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
OTOSCLEROSIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Carcinoma Hepatocellular Associate 37380717
★☆☆☆☆
Found in Text Mining only
Neuroblastoma Associate 36037157
★☆☆☆☆
Found in Text Mining only