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TMEM151B (transmembrane protein 151B)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
441151
Gene nameGene Name - the full gene name approved by the HGNC.
Transmembrane protein 151B
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
TMEM151B
SynonymsGene synonyms aliases
C6orf137, TMEM193, bA444E17.5
ChromosomeChromosome number
6
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6p21.1
miRNAmiRNA 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 IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
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
Causal
Disease name Disease term 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, rs397514613, rs397514614, rs200286768, rs397515463, rs397515464, rs397515465, rs397515466, rs587777218, rs587777244, rs587777417, rs587777418, rs587777419, rs587777583, rs587777584, rs587777585, rs587777589, rs587777591, rs587777593, rs587777594, rs115079861, rs587777788, rs144972972, rs606231472, rs869320746, rs886037734, rs730880255, rs886037735, rs886037736, rs730882154, rs730882155, rs794726869, rs114638163, rs143712760, rs780383722, rs200105202, rs1554169353, rs751459058, rs775690041, rs863224897, rs863225449, rs869025313, rs869025314, rs869025315, rs781798317, rs754022333, rs869320703, rs869320704, rs771894262, rs764427452, rs879255657, rs778100619, rs759477396, rs1057518742, rs1057518743, rs1057517685, rs1057519299, rs1057523346, rs1057524183, rs1060502161, rs184469579, rs1064794140, rs755122704, rs1064797230, rs202183509, rs1131691396, rs1131692037, rs1161932777, rs144042123, rs777725264, rs563189672, rs763672163, rs746538436, rs1554042187, rs767427194, rs1555532483, rs1394499137, rs1555532484, rs763658299, rs763770476, rs199863563, rs148620369, rs1554147776, rs761385155, rs1555575927, rs1555576642, rs1554169280, rs1407198979, rs1274363168, rs1555726849, rs770871640, rs1555404423, rs924099073, rs775439829, rs1554268077, rs1308121771, rs1047420796, rs1322974029, rs751069628, rs368934219, rs761709212, rs1555342802, rs761334309, rs1554116357, rs536000212, rs565910322, rs376766195, rs1562168768, rs763443331, rs1370579526, rs755068980, rs1567773277, rs761097220, rs780533096, rs746356243, rs1559114055, rs752550279, rs1559094461, rs146988468, rs1561990552, rs1298860043, rs746746116, rs1568293849, rs1559359546, rs1561938413, rs565224393, rs1565216037, rs1035101172, rs1565235204, rs763770414, rs764714439, rs777185638, rs1169927428, rs1229314240, rs1429774361, rs374954001, rs1599560256, rs1582724664, rs1574663066, rs778120270, rs1574675683, rs1365308037, rs1582970514, rs777028011, rs1582957532, rs1170907347, rs773688171, rs1777047446, rs947204455, rs1049082567, rs754537066, rs758094541, rs1689552727, rs2077262520, rs748779965, rs1785349774 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 name Disease term dbSNP ID References
Pulmonary hypoplasia Congenital hypoplasia of lung rs1569032634
Dysmorphic features Dysmorphic features 24808023, 21549344, 25058219, 22277967
Sclerocystic ovaries Sclerocystic Ovaries 21411543
Pericardial effusion Pericardial effusion

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