Description

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

Location
INSDC coordinates

chromosome:GRCm38:CM001013.2:20364481:20405653:1

Transcripts

This gene has 5 transcripts (splice variants) Show transcript tableHide transcript table

NameTranscript IDLengthProteinBiotypeCCDSUniProtRefSeqFlags
Rp2h-002ENSMUST000001153874498 bp310 aa (view)
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS72346Q9EPK2 NM_001290644
NP_001277573
GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).
Rp2h-001ENSMUST000000333724417 bp347 aa (view)
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS30041Q9EPK2 NM_133669
NP_598430
GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).
Rp2h-003ENSMUST000001153911398 bp347 aa (view)
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS30041Q9EPK2 NM_001290643
NP_001277572
GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).
Rp2h-004ENSMUST000001336191615 bp322 aa (view)
 
Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins.
-Q9EPK2 -
Rp2h-005ENSMUST000001343491545 bp369 aa (view)
 
Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins.
-Q9EPK2 -

Gene-based displays