XB-FEAT-5751696: Difference between revisions
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2018.11.13 | 2018.11.13 | ||
This gene was renamed to -like and its symbol appended with an "l" | This gene was renamed to guca1a-like, and its gene symbol appended with an "l". | ||
A true syntenic 'guca1a' was discovered, and an accompanying genepage created (XB-GENEPAGE-22061923). | |||
This genepage should be linked to human guca1a unless further evidence links it to another/different family member. However, its symbol and name should never be changed back to guca1a per KAB/Xenbase curatorial team. | |||
=Also known as= | =Also known as= | ||
Revision as of 11:13, 15 May 2019
guca1al
This is the community wiki page for the gene guca1al please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase.
nomenclature changes
01/12/2016 Human name has changed for Entrez Gene: 2978. From guanylate cyclase activator 1A (retina) to guanylate cyclase activator 1A
07.09.2018
Human symbol has changed for genepage ID: 5751696 From guca1al to guca1a
Human name has changed for Entrez Gene: 2978. guanylate cyclase activator 1A like to guanylate cyclase activator 1A
2018.11.13 This gene was renamed to guca1a-like, and its gene symbol appended with an "l".
A true syntenic 'guca1a' was discovered, and an accompanying genepage created (XB-GENEPAGE-22061923).
This genepage should be linked to human guca1a unless further evidence links it to another/different family member. However, its symbol and name should never be changed back to guca1a per KAB/Xenbase curatorial team.
Also known as
COD3; GCAP; GUCA; GCAP1; GUCA1; CORD14; C6orf131
Summary from NCBI
This gene encodes an enzyme that plays a role in the recovery of retinal photoreceptors from photobleaching. This enzyme promotes the activity of retinal guanylyl cyclase-1 (GC1) at low calcium concentrations and inhibits GC1 at high calcium concentrations. Mutations in this gene can cause cone dystrophy 3 and code-rod dystrophy 14. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]