Transmembrane protein 151b
Lua error in Module:Infobox_gene at line 53: attempt to index field 'wikibase' (a nil value). Transmembrane protein 151B is a protein that in humans is encoded by the TMEM151B gene.[1]
Nomenclature
[edit | edit source]The Transmembrane protein 151B gene is also known as TMEM151B, C6orf137, and bA444E17.5.[2]
Gene
[edit | edit source]The gene is located on the positive strand of chromosome 6 at the location 6p21.1 from the chromosome position 44270450 to 44279444, for a total length of 8,995 base pairs.[3] It is a complex locus that contains both TMEM151B and SPATS1.[4] TMEM151B has one paralog: TMEM151A.[5]
Transcript
[edit | edit source]The mRNA contains 3 exons, with a transcribed mRNA length of 4911bp, and the coding region containing 1701bp.[3]
Protein
[edit | edit source]The protein has a length of 566 amino acids and contains two transmembrane domains.[2] According to Compute pI/Mw, molecular weight of approximately 61 kDa, which matches the weight listed on NCBI, and a theoretical isoelectric point of 6.72.[7][2] The human TMEM151B protein composition is poor in lysine and arginine, lysine comprising 1.4% of the amino acids and arginine making up 0.8% of the total protein. The mouse ortholog is also arginine poor.[8]
Expression
[edit | edit source]RNA-seq gene expression profiling shows high expression in the brain, and notable expression in the testes.[10] NCBI geo profiles similarly show localization to the brain tissues.[11] Within the mouse brain, TMEM151B has high expression particularly within the cerebellum, medulla, and olfactory bulb according to the Allen Brain Atlas.[9]
Protein interactions
[edit | edit source]The TMEM151B protein interacts with one other protein according to BioGRID.[12]
- SREBF2- a transcription factor precursor which is imbedded in the endoplasmic reticulum membrane; activates genes involved with cholesterol biosynthesis.[13]
Homology and evolution
[edit | edit source]The TMEM151B gene is conserved within most vertebrates, and appears to be conserved within some invertebrates. Its paralog, TMEM151A, has a 47.7% sequence identity with TMEM151B.[5][14] The evolution rate is relatively slow: between the rate of change in fibrinogen alpha and cytochrome c.[5][15]
Research
[edit | edit source]Alternative splicing of TMEM151B along with 4 other genes were linked to colorectal cancer.[16] It was also found to be up-regulated in post-menopausal breast cancer.[17][18] A SNP found within TMEM151B is associated with the development of lean muscle.[19]
References
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Further reading
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