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Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: RD3 ENSG00000198570

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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.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000367002.4	RD3-001	4266	195aa	ENSP00000355969.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS1498	Q7Z3Z2	NM_183059.2	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000484910.1	RD3-002	3070	No protein	-	Gene/transcript that doesn't contain an open reading frame (ORF).Processed transcript		-	-	-

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Summary

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