Version 5.4
| Mus musculus Gene: Gnb1l | |||||||
|---|---|---|---|---|---|---|---|
| Summary | |||||||
| InnateDB Gene | IDBG-141813.6 | ||||||
| Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||
| Gene Symbol | Gnb1l | ||||||
| Gene Name | guanine nucleotide binding protein (G protein), beta polypeptide 1-like | ||||||
| Synonyms | ESTM55; Gm16314; Me49f07; OTTMUSG00000033458; Wdr14; Wdvcf | ||||||
| Species | Mus musculus | ||||||
| Ensembl Gene | ENSMUSG00000000884 | ||||||
| Encoded Proteins |
guanine nucleotide binding protein (G protein), beta polypeptide 1-like
guanine nucleotide binding protein (G protein), beta polypeptide 1-like
guanine nucleotide binding protein (G protein), beta polypeptide 1-like
guanine nucleotide binding protein (G protein), beta polypeptide 1-like
guanine nucleotide binding protein (G protein), beta polypeptide 1-like
guanine nucleotide binding protein (G protein), beta polypeptide 1-like
guanine nucleotide binding protein (G protein), beta polypeptide 1-like
guanine nucleotide binding protein (G protein), beta polypeptide 1-like
|
||||||
| Protein Structure | |||||||
| Useful resources | Stemformatics EHFPI ImmGen | ||||||
| Entrez Gene | |||||||
| Summary |
This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000185838:
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. [provided by RefSeq, Jul 2008] |
||||||
| Gene Information | |||||||
| Type | Protein coding | ||||||
| Genomic Location | Chromosome 16:18498768-18566679 | ||||||
| Strand | Forward strand | ||||||
| Band | A3 | ||||||
| Transcripts | |||||||
| Interactions | |||||||
| Number of Interactions |
This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 2 interaction(s) predicted by orthology.
|
||||||
| Gene Ontology | |||||||
Molecular Function |
|
||||||
| Biological Process |
|
||||||
| Cellular Component |
|
||||||
| Orthologs | |||||||
|
Species
Homo sapiens
Bos taurus
|
Gene ID
Gene Order
Not yet available
|
||||||
| Cross-References | |||||||
| SwissProt | |||||||
| TrEMBL | |||||||
| UniProt Splice Variant | |||||||
| Entrez Gene | |||||||
| UniGene | Mm.236139 | ||||||
| RefSeq | NM_001081682 NM_001285491 NM_001285493 NM_001285494 NM_023120 XM_006521789 XM_006521792 XM_006523146 | ||||||
| OMIM | |||||||
| CCDS | CCDS28022 CCDS70695 | ||||||
| HPRD | |||||||
| IMGT | |||||||
| MGI ID | |||||||
| MGI Symbol | |||||||
| EMBL | |||||||
| GenPept | |||||||
| RNA Seq Atlas | |||||||