Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
441151
Gene name Gene Name - the full gene name approved by the HGNC.
Transmembrane protein 151B
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TMEM151B
Synonyms (NCBI Gene) Gene synonyms aliases
C6orf137, TMEM193, bA444E17.5
Chromosome Chromosome number
6
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6p21.1
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT720963 hsa-miR-6865-3p HITS-CLIP 19536157
MIRT720962 hsa-miR-2276-5p HITS-CLIP 19536157
MIRT720961 hsa-miR-301a-5p HITS-CLIP 19536157
MIRT720960 hsa-miR-301b-5p HITS-CLIP 19536157
MIRT720959 hsa-miR-6730-3p HITS-CLIP 19536157
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0016021 Component Integral component of membrane IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein
UniProt ID Q8IW70
Protein name Transmembrane protein 151B (Transmembrane protein 193)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF14857 TMEM151 46 492 TMEM151 family Family
Sequence
Sequence length 566
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Combined oxidative phosphorylation deficiency COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 8 rs587776508, rs576462794, rs118203917, rs387906327, rs139430866, rs387906962, rs138119149, rs387907061, rs1562800908, rs397515421, rs397514598, rs397514610, rs397514611, rs397514612, rs201431517
View all (155 more)
25058219, 29440775, 22277967, 21549344, 25705216, 27839525
Hydrops fetalis Hydrops Fetalis, Non-Immune rs28935477, rs1131691986
Leukoencephalopathy, with ovarian failure LEUKOENCEPHALOPATHY, PROGRESSIVE, WITH OVARIAN FAILURE rs138119149, rs587777590, rs587777591, rs200105202, rs1554148927
Multiple congenital anomalies Multiple congenital anomalies rs1057517732 22277967, 25058219, 24808023, 21549344
Unknown
Disease term Disease name Evidence References Source
Pulmonary hypoplasia Congenital hypoplasia of lung ClinVar
Rheumatoid arthritis Rheumatoid arthritis GWAS
Inflammatory Bowel Disease Inflammatory Bowel Disease GWAS
Crohn Disease Crohn Disease GWAS