GNB1L Products

Description

The GNB1L gene codes a guanine nucleotide-binding protein subunit beta-like protein 1 that is a member of the WD repeat protein family. Isoform 1 is 327 amino acids long with a mass of around 35 kDA while isoform 2 exists at 212 amino acids long and nearly 23 kDA. Members of the WD repeat protein family are known for their involvement in many cellular responses such as: cycle progression, signal transduction, apoptosis, and gene regulation. The GNB1L gene can be found on chromosome 22q11, and if deleted, will cause DiGeorge syndrome. The GNB1L gene has been researched regarding its role in schizophrenia, spinal cord disease, carcinoma, cat eye syndrome, hypopharynx cancer, and visceral leishmaniasis. GNB1L gene interacts with genes KLHL12 and UBC in pathways such as the beta-agonist/beta blocker.

Bioinformatics

Entrez	54584 Human
Uniprot	NP_443730 Human NP_443730.1 Human Q9BYB4 Human
Product By Gene ID	54584
Alternate Names	DGCRK3 G-protein beta subunit-like protein guanine nucleotide binding protein (G protein), beta polypeptide 1-like guanine nucleotide binding protein beta-subunit-like polypeptide guanine nucleotide-binding protein subunit beta-like protein 1 GY2WD40 repeat-containing protein deleted in VCFS KIAA1645 WD repeat-containing protein 14 WDR14G protein subunit beta-like protein 1 WDVCF

Research Areas for GNB1L

Find related products by research area and learn more about each of the different research areas below.

Signal Transduction