Busch Lab

ZMP

capn9

Ensembl ID:
ENSDARG00000012341
ZFIN ID:
ZDB-GENE-010724-2
Description:
calpain-9 [Source:RefSeq peptide;Acc:NP_001003501]
Human Orthologue:
CAPN9
Human Description:
calpain 9 [Source:HGNC Symbol;Acc:1486]
Mouse Orthologue:
Capn9
Mouse Description:
calpain 9 Gene [Source:MGI Symbol;Acc:MGI:1920897]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa25682 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa39702 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa25682
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000007732 Essential Splice Site 505 688 13 20
Genomic Location (Zv9):
Chromosome 1 (position 54457788)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 53231291
GRCz11 1 53891034
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAACTGCTCCTAAAGTTACCTGTATGTATGTTTGTGTCTACTTTTTGAA[G/A]CCACCGAAACCAAACCCACCTGAAGAGGAGACTGATGAGGAGAAAGGCCT
Long Flanking Sequence:
TTGTGCATCCCTATTGTAATTATACTATATTAATTATACTTTATGTTGTGAGTATATTTTTTGTGATGCACAGGGATAAATCCGATTTTGGAATATCTTTGGTTCGTTAATTTTTTATTAGAATTTGTTTAGCTAGCTTCATGCATCAAGCCACCAGTCATTATACACAAATTTATAAATGCATTTATGAATTAATTTCCTTACTCAATTGCTTGTACCCCATTATATATCTATAGTGAACTACAAAATAAAATTTCCATTAGATTTTATTTGCTTTGAACAACTGAACCCAATCATGAACTGATTCTTCATTGCTATGTTTTTCAGTGAGGTGGGAAACAAAATTGAAGCTGATCTGCCAGAGGTGAGTCAAATATAATCACTGGATAATTTTATTATATCCCTAGGAAGGACATATCAAAGTCAAAAGCAGATTGCTCTTAAATAGGTAAAACTGCTCCTAAAGTTACCTGTATGTATGTTTGTGTCTACTTTTTGAA[G/A]CCACCGAAACCAAACCCACCTGAAGAGGAGACTGATGAGGAGAAAGGCCTGAGGAAACTCTTTGAACAGGTCGCTGGACCGGTAAGAAAACTACAGTCTACTGTCTAAAGGGAATAGGGTATATGCCGAGCTAGTGCAGTTCCCATGCTGATACACTTCCGGTGACCTGTTATTGTGAACTTTTTACCATTTTTACGGTTCATTATACAGCATCGATGTTGTAATGTCATTAAAATACATTCAGTTAAATAAACTTAAGCATTTATTTTTATTTGCTCAAGCGTAAAACAAGACAAAAAGCTGTTTACTCGCACACGCTTGTCAGAATCGGCAGGCTAACACAGAAGCTCCATTGAATATACTGGGGTAAAATAAATGCTCATATTATAAAGATATGGCGGGGGAAATGTAATTTAATGCAGTGCTTCTTGTACAATCTGAGACCCACTTTAAATCGGATTTCACTCAGCTAGTGGAGATCGCTGATTTTTAAAGAAAAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39702
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000007732 Nonsense 583 688 16 20
Genomic Location (Zv9):
Chromosome 1 (position 54454471)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 53227974
GRCz11 1 53887717
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTCCTGAACTGAGTATAGGTGGATGGATCAGGAATGATGGAATTTTCC[G/T]AGTTCAAAGTCTTCTGGGATAAACTCAAGAAGTGGATCGTAAGTTACAGG
Long Flanking Sequence:
TATTTTCTCTTTTTCGGACCATTCTCTGTAAACCCTAGAGATGGCTGTGCATGAAAATCCCAGTAGATCAGCAGATTTTGAAATACTAACACCAACAACCGTGCCACATTCAAAGTCACTTCAATCACCTTTCTTCCCCATTCTGATGCTTGGTTTAAACTACAGCAGATCATCTTGACCGTGTCTACATGCCTAAATGCATTGAGCTGCTGTCATGCGATTGGCTAATCAGAAATTTGCTTTAACGAGCAGTTGGACAAGTGTACCTAATAAAGTGGCCGGTAAGTTTGATTACAAATGACATGTTTTCATGTTGACTATTGATAGGTATAAATGCAGAAAACTTGAGTTATTAGTTCTTGCAAATAAAATCTTCAGATAAACTTATCTTATAGGCTACATGCTATTCTACAAGTGATAGCTCTGAATATATTCTGTAATGTGGCCGAGTTTTCCTGAACTGAGTATAGGTGGATGGATCAGGAATGATGGAATTTTCC[G/T]AGTTCAAAGTCTTCTGGGATAAACTCAAGAAGTGGATCGTAAGTTACAGGATCATATATTTACTTGTCAGTTGTCGGTTTACAATGAATAACCTGCATCGTTACACAAATCAACGTTGTTTTTTGTTGCAGATGCTGTTTCTGTCTTATGATGTGGATCGTTCTGGAACCATGTCTTCCTATGAGCTCCGCAGCGCTCTTAATGCTGCAGGTAAACACACTTATAATGGATTATAAGCATATATAAATATTTATTAACAGTATTTTATCTAATCAAATCTTGAGTGGTCACTTAAAAAGTGATTATTTACTTATTACACAATTAAAATTGTATTCAAATTACTTTTTTAAATGATTTCTAAATAAGGATTTTAATGAATTAACCCAATACTAACTTAAATCCATGTAAATGTCAATGCATAGACAGTTCCAATTAAACTCTTTTAATACTTTAAATTTAAATGCCCTTAGCTTTATTAAAAATGTAATAGTTAAGAAAAG
Associated Phenotype:
Not determined