OSTM1
| Osteopetrosis-associated transmembrane protein 1 precursor | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Identifiers | |||||||||
| Symbol | OSTMP1 | ||||||||
| Pfam | PF09777 | ||||||||
| InterPro | IPR019172 | ||||||||
| |||||||||
Osteopetrosis-associated transmembrane protein 1 is a protein that in humans is encoded by the OSTM1 gene.[1][2][3] It is required for osteoclast and melanocyte maturation and function.[1]
Interactions
OSTM1 has been shown to interact with RGS19.[4]
References
- ^ a b Chalhoub N, Benachenhou N, Rajapurohitam V, Pata M, Ferron M, Frattini A, Villa A, Vacher J (Apr 2003). "Grey-lethal mutation induces severe malignant autosomal recessive osteopetrosis in mouse and human". Nat Med. 9 (4): 399–406. doi:10.1038/nm842. PMID 12627228.
{{cite journal}}: CS1 maint: multiple names: authors list (link) Cite error: The named reference "pmid12627228" was defined multiple times with different content (see the help page). - ^ Abrahams BS, Mak GM, Berry ML, Palmquist DL, Saionz JR, Tay A, Tan YH, Brenner S, Simpson EM, Venkatesh B (Jun 2002). "Novel vertebrate genes and putative regulatory elements identified at kidney disease and NR2E1/fierce loci". Genomics. 80 (1): 45–53. doi:10.1006/geno.2002.6795. PMID 12079282.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - ^ "Entrez Gene: OSTM1 osteopetrosis associated transmembrane protein 1".
- ^ Fischer, Thierry (Jul 2003). "Promotion of Gαi3 subunit down-regulation by GIPN, a putative E3 ubiquitin ligase that interacts with RGS-GAIP". Proc. Natl. Acad. Sci. U.S.A. 100 (14). United States: 8270–5. doi:10.1073/pnas.1432965100. ISSN 0027-8424. PMC 166218. PMID 12826607.
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Further reading
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