Human (GRCh37.p13)
Description

retinal degeneration 3 [Source:HGNC Symbol;Acc:19689]

Gene Synonyms

C1orf36, LCA12

Location

Chromosome 1: 211,649,864-211,666,259 reverse strand.

GRCh37:CM000663.1

About this gene

This gene has 2 transcripts (splice variants), 1 paralogue and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000367002.4RD3-0014266195aaENSP00000355969.4
 
Protein coding
CCDS1498Q7Z3Z2 NM_183059.2GENCODE basic
ENST00000484910.1RD3-0023070No protein-
 
Processed transcript
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