Busch Lab

ZMP

capn1a

Ensembl ID:
ENSDARG00000052702
ZFIN ID:
ZDB-GENE-040426-1263
Description:
calpain 1, (mu/I) large subunit a [Source:RefSeq peptide;Acc:NP_956739]
Human Orthologue:
CAPN1
Human Description:
calpain 1, (mu/I) large subunit [Source:HGNC Symbol;Acc:1476]
Mouse Orthologue:
Capn1
Mouse Description:
calpain 1 Gene [Source:MGI Symbol;Acc:MGI:88263]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa2687 Nonsense F2 line generated Not yet available
sa42288 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa2687
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000046066 Nonsense 229 704 6 22
Genomic Location (Zv9):
Chromosome 13 (position 43355779)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 42576738
GRCz11 13 42702798
KASP Assay ID:
554-2682.1 (used for ordering genotyping assays)
KASP Sequence:
GAGGCGTTTCAGARATGTACGAGCTCCGGAAAGCTCCMAGAGACTTGTAC[C/T]GAATCATCAGCAAAGCCCTGGACAGAGGCTCMCTGCTGGGCTGCTCTATT
Long Flanking Sequence:
CGGCTCCCGGTCAAAGACGGAGAGCTCATGTTTGTCCATTCAGCAGAGGGAAATGAGTTCTGGAGTGCCTTGGTGGAAAAAGCCTATGCTAAGTACGTCCTGATAGACATTTTGGTAAAGGCCAGCAACATTTGTGCTTGCTAAATCATTTACAAAATCGGTTTTGTCCCAGTCTTATTAAAGAGTTTACCGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGCGTGCGTGCGCGCGCGCGCGCGTGCGTGCGTGCGTGCGTGTGTGTGTGTGTGTGTGTGTGTGTCGGTTTGTTTGTTTGTTTTGTGGCAGGCTAAATGGCTCTTATGAAGCTCTTTCTGGAGGCTCTACCACTGAGGGTTTTGAGGATTTTACTGGAGGCGTTTCAGAAATGTACGAGCTCCGGAAAGCTCCAAGAGACTTGTAC[C/T]GAATCATCAGCAAAGCCCTGGACAGAGGCTCCCTGCTGGGCTGCTCTATTGATGTGAGAACCTCATTAGTTTAAGAGATGCTTCATGAAAACTGTTACCTACTTGAACTAATTTTTTACTTTTAGTTAAGTAGATGTCCAATCTTCTGTTTTCTTAGACTGTTTCCTTTAACTTTAATTTAAACCCGCAGAAATAAAAAAAATATATAACTTTAACTTAGGGTGCTTTCACACCTACACTTTTGTTTCGGAACGTATCTCGTTTGCCCAGTTAGCGCGGTTCGATTGGCCTATGTGAACAGGGCAATCGCGCTCTGTTCCGCGCCAAAGTAATCGCTCCGAGATCGCTTGAATGAGGTGGTCTCGGCTCGATTGAAACGAACCCTGGAGCGGTTCGATTGTAGTGAGAAAGCGATCCGATCCGAGCGCGGTTGTATCACTGTGTTTTATGGATATGTAATAGGCATATACGGCTATATGAAGAGAGAATTATGATTGGGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42288
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
ENSDART00000046066 Nonsense 390 704 11 22
Genomic Location (Zv9):
Chromosome 13 (position 43346042)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 42567001
GRCz11 13 42693061
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGTGTTCCTGTGCTGTTTTTCAGACACGTTCTGGATCAATCCACAGTA[T/G]AAGATCACACTGCTGGAGGAAGATGATGATCCGGAGGATGAAGAAGTGGC
Long Flanking Sequence:
GGAAAAAAAAATGTCATCTGGTGTTTACAGAAGAAAACAAAGATTATGTTTTATTTAAACACATTACAATTAAATAATGTAAATCCAAAAAAAAATCATCATTTTCAAGTAATCTCTTGTGTTTTTATAGTTAATAAAGTCATTAAACATTTTTTTTTATTATGATGTATATTTCACATCTAAATTTAATAGCTTTATATGTTCTTATGTGTTCAACAAAATATATTTACAATAATTCAAGCATTCAATATTACATTATACATGTTTTTGCTAATTAGGAAATATTAACTTATTATTATCAATGTTGAAAACCATATTATTTTATTAATACCGTGATGCATTAATTGTAGGATTCTTTGAATTTTAGGATGTTCAGAAAAACAGCATTTATTTAAAATGACATATCTTTACCGCCACCAGTTTCACCTAAGATTTAAAACAAATGGCTGCTCTGTGTTCCTGTGCTGTTTTTCAGACACGTTCTGGATCAATCCACAGTA[T/G]AAGATCACACTGCTGGAGGAAGATGATGATCCGGAGGATGAAGAAGTGGCCTGCAGCTTCCTGGTGGCTTTAATGCAGAAAGACCGCAGACGGTACCGCCGCCACGGACAAGATATGCACACTATCGGTTTTGCAATTTATGAGGTCAGGAGCCAATGGGTTCAGCTAGATTAGTACGCATATGATACAATAATCATATTCAGATGCACACTTAAAAATAATGATAAACCACCAAGACAACAGTAAAGAAATAGAAATAATTACATTATAAATAACTATTACATTATATTATATTATCTCCTACATTTTATAATGTAATTATTCATTTGATAAAGTAGATCATACAATTTTTATAAAGGAAAATTGTCTAATTGGTTTCTTTCTTCCGTTCTTTTCTCTGTAGGTTCCTGAAGAGGTATGAATCTTCTTCTTTTTTTTTTTTTTTTTGTCAAATAGGTTTGCTTATATAATTGTTTTGCCAACAAAACAGAAACCTGTTA
Associated Phenotype:
Not determined