ZMP
si:dkey-159f12.3
Ensembl ID:
ZFIN ID:
Description:
Kazrin-A [Source:UniProtKB/Swiss-Prot;Acc:A9C3W3]
Human Orthologue:
RP1-21O18.1
Human Description:
Kazrin [Source:UniProtKB/Swiss-Prot;Acc:Q674X7]
Mouse Orthologue:
9030409G11Rik
Mouse Description:
RIKEN cDNA 9030409G11 gene Gene [Source:MGI Symbol;Acc:MGI:1918779]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16379 | Nonsense | Available for shipment | Available now |
sa21311 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16379
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110432 | Nonsense | 58 | 814 | 1 | 16 |
ENSDART00000139787 | Nonsense | 58 | 786 | 1 | 15 |
The following transcripts of ENSDARG00000076923 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 27645400)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 26773318 |
GRCz11 | 8 | 26792457 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCGAGCTGGAAGAACCGGGAGAACCGCAGGAACATCAGCAGCAGCAGCAA[C/T]AACAGAACCACCAGGGTAAGAAKCTGCACCTGTGACCGCTTATGTCACTT
Long Flanking Sequence:
GTTTAAAGAGCCGCTCAGAGTCTCTCGTGCGTTCAACTCTCTCTACGAGCGCGCGCGGCGGCAGGAGTCGTTTAGTGAAGCACGCTGTTTTATTCTCTCCCGAGTGTCTGTGTCTCTCTGTTTATCTTTCTCCCTGACAGCCACATCTACACATTAGACAGCATGACACTTTAAAAATCCGCCCTCAGCTTGTGGATTCTGGGGGATTTCTGCGCTTATAAAAGAGAGGACACAGTCAGAATGGGATTTTTGTAAGCTTATGATGCAGCAGGCGATATGACTCGCTCCGTGGGTTCCGTGGATTCTTCCCGCAGGCGAAGATCCGGAGAATGATGGAGGAGAATAAGCAGCTCGCTCAGCGGATCGATGGCGCGATCCAGTGCGCGAAGCAGGATGTGGCGAACCTGCGCGCGGAGCTCACAGCCACCGGCCACAGACTGGCAGAACTCGGCGAGCTGGAAGAACCGGGAGAACCGCAGGAACATCAGCAGCAGCAGCAA[C/T]AACAGAACCACCAGGGTAAGAATCTGCACCTGTGACCGCTTATGTCACTTACCTGTGTGACCTTCGAGTGACTGACAGAAAGTCTCTTTCTCTCTGATTTAGTGTAATGAGACTCTGTTTTCACTTCCATCATTAACAAATAGAGTTCTTCAGGACACTTTTGAGAGAATAAGTGTTTTAGTAAAATGATTGTTCACTGAAAAATGAAAAAAATACTGTCAGTTTGCTCAGCCTCTGGCTACTTCAAGATGTAGGTGACATTTTTGTTGAGGAAAACCTTTTTTTTTAAAAGAAGATTTTTATTTTCTCACTTAAACCATGTTCCTTGGTGGTTTTGGTACACATTTAGAATATAAAAAAACACATACAGTTAAAATATAATTAATACTCAAAGATTCCTGATGATACATTGAGCTGTTATCAAGATTGTGGTAAAGTTGGTTTTTATATTCACACATTTAGACTTTCTCCTTACTAATATAATTTCAGAAATGTATTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21311
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110432 | Essential Splice Site | 515 | 814 | None | 16 |
ENSDART00000139787 | Essential Splice Site | 487 | 786 | None | 15 |
The following transcripts of ENSDARG00000076923 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 27575855)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 26703773 |
GRCz11 | 8 | 26722912 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATGCCGATGTACATGCGCGCCTGTGCCGACAACGTCAAAAGCGGGAAGG[T/G]AAATGACAACCTGTCATTTTATTACTTAAACAGTTGTCTACGTCATTATT
Long Flanking Sequence:
TTTTGTGGAGAAGAAAGTCAAACAGGTTTAGAACAGGTAAAGAGCAGATTTAATTTTCACTTTTGAGTGAATTCTATTTACATTACTATCCCTGTAATGTAAATAGAAGAAAACAACGTTTCCTCTTCGATATTTCTCCTATTAGTATCTCAGAATGAATACATAGCTTACATTACTTTAACAGGACCGCATTGTTGTGATGCCTGGGAAGAGGGAAGCGAGCGAGGTGAATATGCTCATGTAAATTTACCTCTCGTTAAGCTCCGCCCCTCTCTCCTAATCCACCAATCTAGACTCCGACAGTTTGTCAAGCCCCGCCCGCCTCAGCGTGAGCCTATCAGAATGCGAGGAGCAGCTGGATCGTCTTCAGCAGGTGGAGCTCGCGCGCTCGGCGCCCATGTGTCGTTGGAGGGCAGGAACCGTGCAGGCGTGGCTGGAAGTGATTATGGCCATGCCGATGTACATGCGCGCCTGTGCCGACAACGTCAAAAGCGGGAAGG[T/G]AAATGACAACCTGTCATTTTATTACTTAAACAGTTGTCTACGTCATTATTCTCTAATCTATTGCGCACTGCTGATCATATCAGCTTTTAATGCTGTAGGGTGTTTCAACAAGCAGTGTTTGGCATGAATGTTCAATCTGTGTCTTTATTAGGTCTTGTTAGTTCTTACGGATGAGGATCTGGGAAATGTTTTGGGAATCAGTAACTCAATGCATCGCAGGAAACTCCGTCTGGCCATTGAAGATTACAGGGATGCTGAAGCAGGACATGGGTGAGACATGCCATAAGACAACAACAAAAACATAACAGAAAATTCACTCATAGAGGAAACCCCTACAGTCCTCATTACTGACACAGTCAAGGTCAATTTAAAAACATCTTATTATTCGATGTTTGTAATGACAAGGCATGTTAATAGTTCAAAAAAGTAATTTAAACACTTTTATGTCACAATCAAACTAAAAATTATGCCAGAAAAGAAATCTGCCATCATTTACTTGC
Associated Phenotype:
Not determined