Gene: RTL10

Alternate names for this Gene: BOP|C22orf29

Gene Summary:

Gene is located in Chromosome: 22

Location in Chromosome : 22q11.21

Description of this Gene: retrotransposon Gag like 10

Type of Gene: protein-coding

Gene: GNB1L

Alternate names for this Gene: DGCRK3|FKSG1|GY2|WDR14|WDVCF

Gene Summary: This gene encodes a G-protein beta-subunit-like polypeptide which is a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This protein contains 6 WD repeats and is highly expressed in the heart. The gene maps to the region on chromosome 22q11, which is deleted in DiGeorge syndrome, trisomic in derivative 22 syndrome and tetrasomic in cat-eye syndrome. Therefore, this gene may contribute to the etiology of those disorders. Transcripts from this gene share exons with some transcripts from the C22orf29 gene.

Gene is located in Chromosome: 22

Location in Chromosome : 22q11.21

Description of this Gene: G protein subunit beta 1 like

Type of Gene: protein-coding

rs17534001 in RTL10;GNB1L gene and Tonometry PMID 29785010 2018 Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma.