ZMP

rp2

Ensembl ID:

ENSDARG00000044339

ZFIN ID:

ZDB-GENE-040426-2795

Description:

protein XRP2 [Source:RefSeq peptide;Acc:NP_998611]

Human Orthologue:

RP2

Human Description:

retinitis pigmentosa 2 (X-linked recessive) [Source:HGNC Symbol;Acc:10274]

Mouse Orthologue:

Rp2h

Mouse Description:

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

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa17284	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa17284

Status:

Available for shipment
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Availability:

Order Allele From ZIRC
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Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000065117	Nonsense	76	311	2	6
ENSDART00000136920	Nonsense	141	376	2	6

Genomic Location (Zv9):

Chromosome 6 (position 37470185)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	37543943
GRCz11	6	37521837

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GTGTGTTCTTCAGAGATTGTAAAGACATCAAATGCGTGGTGGCCTGTCAG[C/T]AGTTCCGCACGAGAGACTGCAAGAAAATGGACGTCTTTTTGTGCTGYGCC

Long Flanking Sequence:

ATTGTGCAACCCTACCTGGTGGTAGAGAGATTCTTTAAATTAATTGAAAAGGACTTTTGCTAAACAGGATAATCATTCATCTGTATTATGTCAAGCCCCACTTACTAAAACAAGGTATTTTAGTAGTTTATACTAAGTATAACGGAACAATAAGTTAATAGGAAGCCAGAGAGCAAAGATCGGCAATCATGTTTTTTTTTTTACAGCTTTTTAAGTTCTGCTTTTAGCAACACTAACATGTGTGTTTTTACTTGCAGGTCGACCCCAAAGACTTTATGCTGACAGGCCTCAAGAATGAGACCGTGGGCAGGTTACCAGGCAAGCTCAACGGTCAGCAGTTTGTCATTCAGGACTGCGAAAACTGTAACATATTTGTGTTGGACCATTCGGCAACTATTACCATCGATGACTGTGTGAACTGCCGCATTGTGTTAGGTCCGGTCAAAGGCAGTGTGTTCTTCAGAGATTGTAAAGACATCAAATGCGTGGTGGCCTGTCAG[C/T]AGTTCCGCACGAGAGACTGCAAGAAAATGGACGTCTTTTTGTGCTGCGCCACCCAGCCCATAATCGAGTCTTCTACAGGCATGAAGTTTGGCTGCTTCCAGTATTACTACCCTGAGCTGGCTTTCCACTTTAAAGATGCAGGTCTCAGCATTTTTAACAACAACTGGAGCAATATTCATGACTTCACACCTGTCTCTGGAGAAACTAACTGGAGTCTCCTGCCAGAGGATGCTGTTGTCCTGGACCATGTGCCTCTTCCAGATCCTGAGTCAGAGTTCAAGTCTGTGAGAATTGCTACTGAAGCAGGTCGGAGTATAGTGCCTCTGACTAAAGGGAGCCGGCGAACAGAGAGCGAAGAGTCTTGTCTGTTTGTGTTCTTCGCTGGAGACTACACCACTGCTAATGCCCGCAAGCTCATCGATGAGGTTAGAACTTATTTGTGACGCTGCAATACCAAACCATGATGTGGACAATCCAACATCAAACTAAAAATTACTTTA

Associated Phenotype:

Not determined