GPRASP2 gene

G protein-coupled receptor associated sorting protein 2

The information on this page was automatically extracted from online scientific databases.

From NCBI Gene:

The protein encoded by this gene is a member of a family that regulates the activity of G protein-coupled receptors (GPCRs). The encoded protein has been shown to be capable of interacting with several GPCRs, including the M1 muscarinic acetylcholine receptor and the calcitonin receptor. Several transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, May 2010]

From UniProt:

May play a role in regulation of a variety of G-protein coupled receptors.

From NCBI Gene:

  • DEAFNESS, X-LINKED 7

From UniProt:

Deafness, X-linked, 7 (DFNX7): A congenital form of bilateral mixed or conductive hearing loss, which is progressive in some patients. Additional clinical features include ear anomalies and facial dysmorphism with bilateral ptosis. [MIM:301018]

Cytogenetic Location: Xq22.1, which is the long (q) arm of the X chromosome at position 22.1

Molecular Location: base pairs 102,712,176 to 102,717,733 on the X chromosome (Homo sapiens Annotation Release 109, GRCh38.p12) (NCBI)

Cytogenetic Location: Xq22.1, which is the long (q) arm of the X chromosome at position 22.1
  • DFNX7
  • GASP2