ZMP
capn2b
Ensembl ID:
ZFIN ID:
Description:
calpain 2, (m/II) large subunit b [Source:RefSeq peptide;Acc:NP_001018177]
Human Orthologue:
CAPN2
Human Description:
calpain 2, (m/II) large subunit [Source:HGNC Symbol;Acc:1479]
Mouse Orthologue:
Capn2
Mouse Description:
calpain 2 Gene [Source:MGI Symbol;Acc:MGI:88264]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24190 | Nonsense | Available for shipment | Available now |
sa19299 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9474 | Nonsense | Available for shipment | Available now |
sa37530 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24190
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 |
---|---|---|---|---|---|
ENSDART00000077958 | Nonsense | 290 | 696 | 7 | 21 |
ENSDART00000105101 | Nonsense | 290 | 695 | 7 | 20 |
ENSDART00000130493 | Nonsense | 7 | 413 | 8 | 22 |
Genomic Location (Zv9):
Chromosome 22 (position 26932867)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 26321647 |
GRCz11 | 22 | 26341544 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTATCGTGGTCGCAAGGAAAAGCTGGTTCGTATGCGCAACCCTTGGGGA[C/T]AGGTGGAGTGGACCGGAGCCTGGAGCGACAAGTAAGGTTTCATTACTGCA
Long Flanking Sequence:
ATCAGAAAAGCACCGACCAATTTGTTTCAGATCATCCAGAAAGCCCTGGAGGCTGGAGCTTTGCTGGGCTGCTCCATCGACGTGAGATTTCTATATTTATGACATCCACAAATTACTAGACTGCATGTTTGTAGAATGTTTGGATGCAAAACGAATAGCTGTTTATGGAACAATTATCAATAGAAAAACGACTGAATTTTTTTTATAATATTTGAAATTTTGTTGAAGTAGTTTCTGCCCAATCAGATGTAATTTTGAGTCATAAGCCCCACCCACTCTATTTTTATCTGTAGATCACAAGTGCTGCTGATTCAGAAGCCATCACTCGTCAGAAGCTGGTCAAAGGCCACGCCTACTCACTCACAGGGGCAACAGAGGTATGATTATTATTATTATTTTAAATAACATAATTAAAATATTTAGTTTTTAAAGCTTTTTTGTCTCAGGTGAACTATCGTGGTCGCAAGGAAAAGCTGGTTCGTATGCGCAACCCTTGGGGA[C/T]AGGTGGAGTGGACCGGAGCCTGGAGCGACAAGTAAGGTTTCATTACTGCAATATATGTGTTACATGCAGTCATGGAATTTCTGGAGTATCATGGAAATTTAAAGGGTCTGTTCCAGACATTTAAAGTTAGGGAAATTAATATATTTTTTATCCAATTGAATATCAAGGACTGTTTTGTTGCTTTAATTTTTTGTTTCTAATGAATTATAGATTTTGTTGATGTCTGACAATATGAAGTCATTCCAAAACGTGGGCTACATATTGTTTGTAAAAACATGCTAAGTAGGTAAATGCAGATTTAAAAATGCAGTCCCCATCAAGCCAAAATATGTAGGCCTACATATTTTACATGATTATTCTCTCGTTCAATCATACTATAACATAAAGCCATTTGTTAATTCATTGTTTTTAATGAAAATGTTTTTCATGTATTGCCGGTCGTTATGGTTAGGCTATTTTTATAGCCATTTTATTTCTTGCCCCCTTGGCAACTGGTTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19299
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077958 | Nonsense | 395 | 696 | 10 | 21 |
ENSDART00000105101 | Nonsense | 395 | 695 | 10 | 20 |
ENSDART00000130493 | Nonsense | 112 | 413 | 11 | 22 |
ENSDART00000077958 | Nonsense | 395 | 696 | 10 | 21 |
ENSDART00000105101 | Nonsense | 395 | 695 | 10 | 20 |
ENSDART00000130493 | Nonsense | 112 | 413 | 11 | 22 |
Genomic Location (Zv9):
Chromosome 22 (position 26928440)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 26317314 |
GRCz11 | 22 | 26337211 |
KASP Assay ID:
2261-6935.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTTTGGATGAATCCACAATTTGTGGTGAAACTGGATGAAGAAAATGTC[G/T]AAGATAAGGAGAAGGGCTGCAGTTTTGTAGTGGGTCTGATTCAGAAGAAC
Long Flanking Sequence:
AATCTTAACCAATGTACATAGTCTGAGCCGATAGGAGCCATGATAAATAGTTCACCTGTCGAGTCTTTTGGTTCTTGAGTCGTTCGTTCATCACATGACAGAATGACTCAAACCCGAGGACTCGAGAGATGAACGGATCAATTCTTTTTCTGGCTCTAAACGCATATGATTGGCCCGTGAGGAACGAATGACTCAAACCCGATAGAGGACTCGAGAGATGAACGGATCAATTCTTTTTCCGGCTCTAAACGCAGAGGATTAGCTTCTGCCTTTCCGCTAACGACTCAAAAGACTTGAAATGAATGATACCATAATTAACACTTCTTGTATGTACTGCCTCTTATTGAATCGCCACTTAAATTTTAGTCGCTTTGGACAAAAGCGTCTGCTAAATGATTGAATGTAAATGTAAAAATTTTGCTGACCGGTTCATTTAATGCTCTACAGACACATTTTGGATGAATCCACAATTTGTGGTGAAACTGGATGAAGAAAATGTC[G/T]AAGATAAGGAGAAGGGCTGCAGTTTTGTAGTGGGTCTGATTCAGAAGAACCGCCGGCGCCTGAGGAAAACTGGAGAGGATATGAACACTATTGGCTTTGCTATTTATGAGGTGGGTGGAGACATCTAAAAGAGGTTGACGACGAAGAAATAAACATAATTACTTCTAAAGAATTACAAAATTACATTAGAATAACCCCAAATATAATGTTTTTTTTTTTCTTTTTACATCCACAGCTCCCCCAGGAGGTAAGATTAAACTACTTACAACTTTCTCTTGGCTAACATTTCACCTTTTTTCCTACACATCATGACGCTTTGTGTGAATCCATGTAGACAGTTAGTAAAACATTCACCTCGGTCACATCTACCACACAAGCTCACATGAAATGAATTCAAGAAAAAAATTAGCATGAGGTAAAAAACGTCCCACAATTAAGTGTTTCAGTTTTGGTGTGAACCCAGCATTACACTGAAACCTGCTCAGCTAATGTTTTCGTCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9474
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077958 | Nonsense | 395 | 696 | 10 | 21 |
ENSDART00000105101 | Nonsense | 395 | 695 | 10 | 20 |
ENSDART00000130493 | Nonsense | 112 | 413 | 11 | 22 |
ENSDART00000077958 | Nonsense | 395 | 696 | 10 | 21 |
ENSDART00000105101 | Nonsense | 395 | 695 | 10 | 20 |
ENSDART00000130493 | Nonsense | 112 | 413 | 11 | 22 |
Genomic Location (Zv9):
Chromosome 22 (position 26928440)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 26317314 |
GRCz11 | 22 | 26337211 |
KASP Assay ID:
2261-6935.1 (used for ordering genotyping assays)
KASP Sequence:
CATTTTGGATGAATCCACAATTTGTGGTGAAACTGGATGAAGAAAATGTY[G/T]AAGATAAGGAGAAGGGCTGCAGTTTTGTAGTGGGTCTGATTCAGAAGAAC
Long Flanking Sequence:
AATCTTAACCAATGTACATAGTCTGAGCCGATAGGAGCCATGATAAATAGTTCACCTGTCGAGTCTTTTGGTTCTTGAGTCGTTCGTTCATCACATGACAGAATGACTCAAACCCGAGGACTCGAGAGATGAACGGATCAATTCTTTTTCTGGCTCTAAACGCATATGATTGGCCCGTGAGGAACGAATGACTCAAACCCGATAGAGGACTCGAGAGATGAACGGATCAATTCTTTTTCCGGCTCTAAACGCAGAGGATTAGCTTCTGCCTTTCCGCTAACGACTCAAAAGACTTGAAATGAATGATACCATAATTAACACTTCTTGTATGTACTGCCTCTTATTGAATCGCCACTTAAATTTTAGTCGCTTTGGACAAAAGCGTCTGCTAAATGATTGAATGTAAATGTAAAAATTTTGCTGACCGGTTCATTTAATGCTCTACAGACACATTTTGGATGAATCCACAATTTGTGGTGAAACTGGATGAAGAAAATGTC[G/T]AAGATAAGGAGAAGGGCTGCAGTTTTGTAGTGGGTCTGATTCAGAAGAACCGCCGGCGCCTGAGGAAAACTGGAGAGGATATGAACACTATTGGCTTTGCTATTTATGAGGTGGGTGGAGACATCTAAAAGAGGTTGACGACGAAGAAATAAACATAATTACTTCTAAAGAATTACAAAATTACATTAGAATAACCCCAAATATAATGTTTTTTTTTTTCTTTTTACATCCACAGCTCCCCCAGGAGGTAAGATTAAACTACTTACAACTTTCTCTTGGCTAACATTTCACCTTTTTTCCTACACATCATGACGCTTTGTGTGAATCCATGTAGACAGTTAGTAAAACATTCACCTCGGTCACATCTACCACACAAGCTCACATGAAATGAATTCAAGAAAAAAATTAGCATGAGGTAAAAAACGTCCCACAATTAAGTGTTTCAGTTTTGGTGTGAACCCAGCATTACACTGAAACCTGCTCAGCTAATGTTTTCGTCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37530
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 |
---|---|---|---|---|---|
ENSDART00000077958 | Nonsense | 525 | 696 | 14 | 21 |
ENSDART00000105101 | Nonsense | 524 | 695 | 13 | 20 |
ENSDART00000130493 | Nonsense | 242 | 413 | 15 | 22 |
Genomic Location (Zv9):
Chromosome 22 (position 26924426)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 26313300 |
GRCz11 | 22 | 26333197 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCCACATACTGTGCCTATTTTTGTTTTCAGGAGACTGTCTCAGATGAT[C/T]AAGTTGATTCAAAGTTTAGGGGGATGTTCGTAAAACTTGCCGGACCTGTA
Long Flanking Sequence:
AGTTTGCATGTTCCCCCAGTGTTTGCGTCAGTTTCCTCTGGGTGCGCCGATTTCCCCCACAGTCCAAAGACATGTGGTATAGGTAAATTGGGTAAGCTAAAATGTCCGTAGTGTATGTGTGTGTGAATGGGGGTGTATGGATGTTTCCTAGTGATGGTTTGCAGCTGGAAGAGCATCCGCTATGTATAATATATGCTGGATTAGTTGGTGGTTCATTCCGCTGTGGCAACCCCGAATTAATAAAGGGACTAAGCCAAAAATAAATGAATGAATTAATTGGTGGTTTGTTCTGCTGTGGCAACCCCTAATAAATAAGGGACTAAGCTGAAGAAAAAAATGAATGAATGAATGATTCAGTTGCCTCTTATTACACAAAAAGCAGCAATAATAATAAAAATATATCATAGGTGGTAATAAAACTTTACCACAAATAAGTCGATAAACAGTCCATTCCCACATACTGTGCCTATTTTTGTTTTCAGGAGACTGTCTCAGATGAT[C/T]AAGTTGATTCAAAGTTTAGGGGGATGTTCGTAAAACTTGCCGGACCTGTAAGTGAAGACCATTTATACCGCAGTACAAATGTATATTTTCTGAAAGCAGATCAAAAGCATACTGTACCTCTCTCTCTAGGACATGGAAATCTCACCCCTGGAGCTCATGACCATCTTTAACAAAGTCATTGCAAAACGTAAGTTCTCATGCATCATTTAGTTCTCACTCAAGATCTGATGGATCTGTCCGAGGAACTATTTTGTGTGTTGTTCAACAGGCACTGACATTAAGTCGAGCACCTTCACTTTGGATACGTGTCGTGTCATGGTGAACCTCATGGACGTATCCTTCCAGCTGCAGCTGAATTTATTGTGTTTGCATTAACTTGACGTAAGCACTCAAGTCAGGAATTGCGAGTATTTGATGTGTTGTTGTATTGTCAGCTTCTCTTAACTGATCTCAGGACAGTGGAAATGGAAAACTAGGGCTGGGAGAGTTTGCTACTCTGT
Associated Phenotype:
Not determined