Description

retinitis pigmentosa 2 homolog (human) [Source:MGI Symbol;Acc:MGI:1277953]

Location

Chromosome X: 20,364,481-20,405,653 forward strand.

GRCm38:CM001013.2

About this gene

This gene has 5 transcripts (splice variants), 63 orthologues, 1 paralogue and is a member of 1 Ensembl protein family.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
Rp2h-002ENSMUST000001153874498310aaENSMUSP00000111045
 
Protein coding
CCDS72346Q9EPK2 NM_001290644
NP_001277573
TSL:1GENCODE basicAPPRIS ALT2
Rp2h-001ENSMUST000000333724417347aaENSMUSP00000033372
 
Protein coding
CCDS30041Q9EPK2 NM_133669
NP_598430
TSL:1GENCODE basicAPPRIS P3
Rp2h-003ENSMUST000001153911398347aaENSMUSP00000111049
 
Protein coding
CCDS30041Q9EPK2 NM_001290643
NP_001277572
TSL:1GENCODE basicAPPRIS P3
Rp2h-004ENSMUST000001336191615322aaENSMUSP00000138724
 
Nonsense mediated decay
-Q9EPK2 -TSL:1
Rp2h-005ENSMUST000001343491545369aaENSMUSP00000138352
 
Nonsense mediated decay
-Q9EPK2 -TSL:1

Gene-based displays