Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
81853
Gene name Gene Name - the full gene name approved by the HGNC.
Transmembrane protein 14B
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TMEM14B
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
6
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6p24.2
miRNA miRNA information provided by mirtarbase database.
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 information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 29033352, 32296183
GO:0005743 Component Mitochondrial inner membrane IBA 21873635
GO:0006839 Process Mitochondrial transport IBA 21873635
GO:0016021 Component Integral component of membrane IEA
GO:0021987 Process Cerebral cortex development IMP 29033352
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
619865 21384 ENSG00000137210
Protein
UniProt ID 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 information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Retinitis pigmentosa Retinitis Pigmentosa, RETINITIS PIGMENTOSA 62 rs267606794, rs200691042, rs397704718, rs202193201, rs267606793, rs2147483647, rs779886453, rs267606691, rs794728002, rs878853253, rs137853189, rs137853190, rs137853112, rs137853113, rs137853114
View all (1830 more)
Unknown
Disease term Disease name Evidence References Source
Alzheimer disease Alzheimer disease GWAS
Otosclerosis Otosclerosis GWAS
Associations from Text Mining
Disease Name Relationship Type References
Carcinoma Hepatocellular Associate 37380717
Neuroblastoma Associate 36037157