Probable G-protein coupled receptor 22 is a protein that in humans is encoded by the GPR22 gene.
Integral membrane protein GPR155, also known as G protein-coupled receptor 155, is a protein that in humans is encoded by the GPR155 gene. Mutations in this gene may be associated with autism.
Mesoderm-specific transcript homolog protein is a protein that in humans is encoded by the MEST gene.
Neuronal cell adhesion molecule is a protein that in humans is encoded by the NRCAM gene.
Homeobox A4, also known as HOXA4, is a protein which in humans is encoded by the HOXA4 gene.
Olfactory receptor 2F1 is a protein that in humans is encoded by the OR2F1 gene.
Ubiquitin-conjugating enzyme E2 H is a protein that in humans is encoded by the UBE2H gene.
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 5 is an enzyme that in humans is encoded by the NDUFA5 gene. The NDUFA5 protein is a subunit of NADH dehydrogenase (ubiquinone), which is located in the mitochondrial inner membrane and is the largest of the five complexes of the electron transport chain.
Zinc finger protein 655 is a protein that in humans is encoded by the ZNF655 gene.
Carboxypeptidase A1 is an enzyme that in humans is encoded by the CPA1 gene.
Zinc finger protein 277 is a protein that in humans is encoded by the ZNF277 gene.
Uncharacterized methyltransferase WBSCR22 is an enzyme that in humans is encoded by the WBSCR22 gene.
Homeobox protein DLX-6 is a protein that in humans is encoded by the DLX6 gene.
Zinc finger protein with KRAB and SCAN domains 5 is a protein that in humans is encoded by the ZKSCAN5 gene. The protein contains a SCAN box and a KRAB A domain.
Carboxypeptidase A4 is an enzyme that in humans is encoded by the CPA4 gene.
Putative methyltransferase NSUN5 is an enzyme that in humans is encoded by the NSUN5 gene.
Polypeptide N-acetylgalactosaminyltransferase 11 is an enzyme that in humans is encoded by the GALNT11 gene.
Kelch-like protein 7 is a protein that in humans is encoded by the KLHL7 gene.
Homeobox protein Hox-A2 is a protein that in humans is encoded by the HOXA2 gene.
In molecular biology, MEST intronic transcript 1, antisense RNA, also known as MESTIT1 or PEG1-AS is a long non-coding RNA. It is an imprinted gene, which is paternally expressed. In humans, it is found on chromosome 7q32, imprinted genes on chromosome 7 are believed to be involved in Russell-Silver syndrome (RSS). However, it is believed that MESTIT1 is unlikely to cause Russell-Silver syndrome as there is a lack of mutations in this gene in Russell-Silver syndrome patients. MESTIT1 may regulate the expression of the MEST gene.
