ZMP
LOC798445
Ensembl ID:
Human Orthologues:
CASP3, CASP6, CASP7
Human Descriptions:
caspase 3, apoptosis-related cysteine peptidase [Source:HGNC Symbol;Acc:1504]
caspase 6, apoptosis-related cysteine peptidase [Source:HGNC Symbol;Acc:1507]
caspase 7, apoptosis-related cysteine peptidase [Source:HGNC Symbol;Acc:1508]
caspase 6, apoptosis-related cysteine peptidase [Source:HGNC Symbol;Acc:1507]
caspase 7, apoptosis-related cysteine peptidase [Source:HGNC Symbol;Acc:1508]
Mouse Orthologues:
Casp3, Casp6, Casp7
Mouse Descriptions:
caspase 3 Gene [Source:MGI Symbol;Acc:MGI:107739]
caspase 6 Gene [Source:MGI Symbol;Acc:MGI:1312921]
caspase 7 Gene [Source:MGI Symbol;Acc:MGI:109383]
caspase 6 Gene [Source:MGI Symbol;Acc:MGI:1312921]
caspase 7 Gene [Source:MGI Symbol;Acc:MGI:109383]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41733 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa30654 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41733
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000076712 | Nonsense | 15 | 232 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 10 (position 43522750)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 42329245 |
GRCz11 | 10 | 42157625 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAACAGGGCGCTGATCGTCTCTGTGGAAAACTTTTATCCTGGGGCCTA[T/A]TTGTGCAGGAGAATCGGTGTGAAGAGAGACAGTCGAAGGCTTTACAAGAT
Long Flanking Sequence:
AGTGATGCATGAAAAAAGAAAGACTTGTTATAAGGAAAAAAGAACCGCTACAATGATTTCCATCAAGGGTTGCATGCTTAATATGCTGTTATAGCCAGGAAAGCAACTGTAGTCAGGCCTTCGGGAAAGTCGCTTTGTTACTTTTGTCCATGCTCTCCCTTATTGAAATGCTTCTGTCTGCTTCCTCACAATCTGGACAAGAGCAAACACCTTATAAAGCCCCTGCAGGGATCTGTTGGTCCTGTTTAGGCATGCAGAGTTATGTGCAAAATTGAAGAACTTGTGCAACATCGGTGGTAATGAAACAAGCGGTTTGCCCAACAGATGAGATTACAATGTGCAAAATTGGGCAGGACTCACATGGAGACTCGTGCAACTTATTCTGAGACGAAATTTGCCAGATCAAACATCATGTCTTGCAGATCTCCTCTCACTGCTGGTAAGAGTGTGAAGAACAGGGCGCTGATCGTCTCTGTGGAAAACTTTTATCCTGGGGCCTA[T/A]TTGTGCAGGAGAATCGGTGTGAAGAGAGACAGTCGAAGGCTTTACAAGATCCTCAGCGAACTGGGCTTTTCTGTGGACATCAGACTGGACATCGAGGCGGAGGAGATTTATCAAGCATTTAAAGCTGGTGAGACTTCCAATTTCATATCTGCATCCACAGTTGAAGTCAGAATTATTAGCCCCCCTGATTATTTTTTCTATGTTTAATGCAGAGGATTTTTTCAACATTTCAGCACGTAATAGTTTTAATAACTCATTTCTAATAACTGATTTCTTTTATTTTTGCCATGATGACAGCACACAACATCTGACTAAGATACTAGTATTCAGCTTAAAGTGACATTTAACGGCTTAACAAGGTTAAGGTTAAAGTTAATTAGTCAAGTTTTTGTATAACAGTGGTTTATTCTGGTGACAACCCAAAACAAAATATTGCTTAAGGGGGCTAATAATAAAATGGTTAAAAAAATTAAAACTGCTTTTATTTTAGCAGAAATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30654
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000076712 | Nonsense | 19 | 232 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 10 (position 43522760)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 42329255 |
GRCz11 | 10 | 42157635 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCTGATCGTCTCTGTGGAAAACTTTTATCCTGGGGCCTATTTGTGCAGG[A/T]GAATCGGTGTGAAGAGAGACAGTCGAAGGCTTTACAAGATCCTCAGCGAA
Long Flanking Sequence:
GAAAAAAGAAAGACTTGTTATAAGGAAAAAAGAACCGCTACAATGATTTCCATCAAGGGTTGCATGCTTAATATGCTGTTATAGCCAGGAAAGCAACTGTAGTCAGGCCTTCGGGAAAGTCGCTTTGTTACTTTTGTCCATGCTCTCCCTTATTGAAATGCTTCTGTCTGCTTCCTCACAATCTGGACAAGAGCAAACACCTTATAAAGCCCCTGCAGGGATCTGTTGGTCCTGTTTAGGCATGCAGAGTTATGTGCAAAATTGAAGAACTTGTGCAACATCGGTGGTAATGAAACAAGCGGTTTGCCCAACAGATGAGATTACAATGTGCAAAATTGGGCAGGACTCACATGGAGACTCGTGCAACTTATTCTGAGACGAAATTTGCCAGATCAAACATCATGTCTTGCAGATCTCCTCTCACTGCTGGTAAGAGTGTGAAGAACAGGGCGCTGATCGTCTCTGTGGAAAACTTTTATCCTGGGGCCTATTTGTGCAGG[A/T]GAATCGGTGTGAAGAGAGACAGTCGAAGGCTTTACAAGATCCTCAGCGAACTGGGCTTTTCTGTGGACATCAGACTGGACATCGAGGCGGAGGAGATTTATCAAGCATTTAAAGCTGGTGAGACTTCCAATTTCATATCTGCATCCACAGTTGAAGTCAGAATTATTAGCCCCCCTGATTATTTTTTCTATGTTTAATGCAGAGGATTTTTTCAACATTTCAGCACGTAATAGTTTTAATAACTCATTTCTAATAACTGATTTCTTTTATTTTTGCCATGATGACAGCACACAACATCTGACTAAGATACTAGTATTCAGCTTAAAGTGACATTTAACGGCTTAACAAGGTTAAGGTTAAAGTTAATTAGTCAAGTTTTTGTATAACAGTGGTTTATTCTGGTGACAACCCAAAACAAAATATTGCTTAAGGGGGCTAATAATAAAATGGTTAAAAAAATTAAAACTGCTTTTATTTTAGCAGAAATAAAACAAATGAGA
Associated Phenotype:
Not determined