ZMP

prph2a

Ensembl ID:

ENSDARG00000038018

ZFIN ID:

ZDB-GENE-000616-8

Description:

peripherin 2a (retinal degeneration, slow) [Source:RefSeq peptide;Acc:NP_571641]

Human Orthologue:

PRPH2

Human Description:

peripherin 2 (retinal degeneration, slow) [Source:HGNC Symbol;Acc:9942]

Mouse Orthologue:

Prph2

Mouse Description:

peripherin 2 Gene [Source:MGI Symbol;Acc:MGI:102791]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa18634	Nonsense	Available for shipment	Available now
sa35349	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa18634

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC
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Mutation:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000055415	Nonsense	85	345	1	3

Genomic Location (Zv9):

Chromosome 12 (position 36425972)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	34796453
GRCz11	12	34897516

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

ACTTTTGGCWTRTTGTCTAAATGCCTTTGGTGGCAAAGTCTGCTACGACT[C/A]GCTCGACTCCTCCAARTATGCRAAATGGAAGTCTATTATGACGCCCTTTC

Long Flanking Sequence:

TTTTAATCGCTGTAGATGAAAATCCATTTTTAAGATAATGTTTCACACTGGCGTTCACCTTTAGAAGAATCTACTATGGATGAGATCATGAATGTTGCCAACAAGTTCTTGATTTACTGGAATGGATTACAAATTGAGCCTTGAACGTGCTTTCAGTCTTCGATTTTCGTAAGCCAACTCTGTGGAATTCATCAACCTCTGAAAAGACTTGTTTCTTCTTTCTTTGGACTTTAACCAGTTGTTCAACATGGCTCTCATGAAGGTAAAGTTTGACCTGAAGAAAAGGGTAAAGCTTGCCCAGATGCTATGGCTCATGTACTGGTTTTCCGTAATGGCAGGAGTGCTGGTCTTCAGCATGGGCCTTTTCTTTAAAATCGAACTCCGCAAAAGAAGTGAACTTATGGACAACAACGAAAGCCATTTTGTACCCAACATTCTAATCGGTGTGGGACTTTTGGCATGTTGTCTAAATGCCTTTGGTGGCAAAGTCTGCTACGACT[C/A]GCTCGACTCCTCCAAGTATGCGAAATGGAAGTCTATTATGACGCCCTTTCTCATTTGTTGTTTGGTCTTCAACTTCCTCCTTATTGTCACCGCGGCTATGTGTTTCGCCATGCGCATTCCTCTAGAGTTTACACTTGCGGAGGGCCTGAAAAATGGGATGAAGTACTACAAGGACACCGATACACCCGGGCGCTGCTACATGAAGAGGACTCTGGATCTCATGCAGATGGAGTTCCGATGCTGTGGCAACAACAATTACAAAGACTGGTTCGAGATCCAGTGGGTGAGCAACCGTTACCTGGACTTCAGCGCCAAAGAAGTCAAAGAGTGAGTGTCTTTTTGTTTCTTAATGTTCCGAAATAGTTTGGTCATATAGATAACCAAAGATTTGAGGCTCTTTTATTGCACCAAAACAGTTTCTTGTGATATAATTAAAAGAATAAAAAATAAATAAAGAATCTTTATTGGCATCAATGATTTCAGTAAGAACCATAAACGGT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa35349

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

T > G

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000055415	Nonsense	236	345	2	3

Genomic Location (Zv9):

Chromosome 12 (position 36424693)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	34797732
GRCz11	12	34898795

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CGACCCTGCATCCAACAGCAAATAACCAACAACTCAGCTCACTATAGCTA[T/G]GACCACTACACCGAAGACCTAAACATCTGGAAACGAGGCTGTCGGGACGC

Long Flanking Sequence:

CTGGTAGATTGGCTTGGAATAGGTGTTGAAGTTTTTAGCCTTAAAGAGGTAGTTTACTAAAAAATAGAAAATTTAATCGTCAGTTACTCACCCTTCAATGATTCCAAACCATTGTAAGCTTTTCTGTTGAACACACAAGTAAATGTTTTGAACAATGTAGGTAACTGGTAGCCGCTGATTTACAATGTAGAAACAATTATACAAGTCAATGGCTACCAGTTTAAAGCATTCTTCAAAATGTATTCATAATAGTTTTATGAAAATTAATAGTTTTATGAAAATTTCATATCATTCTAAACGAAATTGAAAATACAGTTTTTTTTAAAGAGTCTGCTGGTGTCATAAACATAAACAACTTTTTTTTTTATCCTCAGCCGAATCAGCAGCAATGTGGATGGCAAATACCTAATGGATGGCGTTCCCTTCAGCTGCTGCAATCCTAGCTCACCACGACCCTGCATCCAACAGCAAATAACCAACAACTCAGCTCACTATAGCTA[T/G]GACCACTACACCGAAGACCTAAACATCTGGAAACGAGGCTGTCGGGACGCTCTCGTCTCCTACTATGGTGGAATGATGAACACTATTGGGGTGCTTGTGCTGTTGGTCACCCTCCTGCAAGTAAGATGTTTAGCTTTGGCATATCTTAATGTGCTGATCCAGGATCAGACCTTAATTACTTACATTATGTTCCTCTAATCTTAATGGATTGTGCTATAAAGGTCAAACAGGTCTGTGATCAGTACTTAAGGTACATTTTGTCCAGTCCAGATAGATAATCTTGTAAACCGCCATTACAAGGTGTTTTTGTTGTCTTCCTCCTATTAAGGTAAATTCTAACTACTCATAGTGGGAGATTCGAGAGATCTTTTCTTAAAGAAATAATCCTTTTTTCGAAATAATCCTGTATCAGTGAGAGCTTAGTTGGAAAAGTAATATGTAGTCTTTGCATGACATTATACAATGTTCTCTGATGAGACCCCCGTTTTCATTAGTCATGT

Associated Phenotype:

Not determined