ZMP
prph2a
Ensembl ID:
ZFIN ID:
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 is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18634 | Nonsense | Available for shipment | Available now |
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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