TMEM38B
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Official Full Name
transmembrane protein 38B -
Synonyms
TMEM38B;transmembrane protein 38B;C9orf87, chromosome 9 open reading frame 87;trimeric intracellular cation channel type B;bA219P18.1;D4Ertd89e;FLJ10493;TRIC B;C9orf87;OTTHUMP00000021849;OTTHUMP00000063855;RP11-219P18.1;TM38B_HUMAN;TRIC-B;TRICB
Recombinant Proteins
- Human
- Zebrafish
- Mouse
- Rhesus macaque
- Rat
- Bovine
- zebrafish
- Xenopus tropicalis (Western clawed frog) (Silurana tropicalis)
- Mus musculus
- E.coli
- Mammalian Cells
- HEK293
- GST
- His
- Non
- His&Fc&Avi
- Myc&DDK
Involved Pathway
TMEM38B involved in several pathways and played different roles in them. We selected most pathways TMEM38B participated on our site, such as , which may be useful for your reference. Also, other proteins which involved in the same pathway with TMEM38B were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.
| Pathway Name | Pathway Related Protein |
|---|
Protein Function
TMEM38B has several biochemical functions, for example, potassium channel activity. Some of the functions are cooperated with other proteins, some of the functions could acted by TMEM38B itself. We selected most functions TMEM38B had, and list some proteins which have the same functions with TMEM38B. You can find most of the proteins on our site.
| Function | Related Protein |
|---|---|
| potassium channel activity | KCNK5A,KCNK5,KCNQ2A,KCNV2,KCNJ11L,AQP1,KCNF1A,KCNA1,KCNQ3,KCNK7 |
Interacting Protein
TMEM38B has direct interactions with proteins and molecules. Those interactions were detected by several methods such as yeast two hybrid, co-IP, pull-down and so on. We selected proteins and molecules interacted with TMEM38B here. Most of them are supplied by our site. Hope this information will be useful for your research of TMEM38B.
env;7242199;env
Resources
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References
- Marini, JC; Blissett, AR; et al. New Genes in Bone Development: What's New in Osteogenesis Imperfecta. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM 98:3095-3103(2013).
- Rubinato, E; Morgan, A; et al. A novel deletion mutation involving TMEM38B in a patient with autosomal recessive osteogenesis imperfecta. GENE 545:290-292(2014).
