Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Molecular function
- GO: Biological process
- GO: Cellular component
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: RP2 ENSGALG00000016728

Description

retinitis pigmentosa 2 (X-linked recessive) [Source:NCBI gene (formerly Entrezgene);Acc:418675]

Location

GRCg6a:CM000093.5

About this gene

This gene has 3 transcripts (splice variants).

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	Flags
ENSGALT00000129383.1	RP2-203	4477	391aa	ENSGALP00000090930.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-
ENSGALT00000126514.1	RP2-202	4419	352aa	ENSGALP00000078043.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-
ENSGALT00000026993.7	RP2-201	4232	324aa	ENSGALP00000026942.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-

Breeds

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.