ZMP
si:ch211-160d20.1
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC799247 [Source:RefSeq peptide;Acc:NP_001076532]
Human Orthologues:
CAPN5, CAPN6
Human Descriptions:
calpain 5 [Source:HGNC Symbol;Acc:1482]
calpain 6 [Source:HGNC Symbol;Acc:1483]
calpain 6 [Source:HGNC Symbol;Acc:1483]
Mouse Orthologues:
Capn5, Capn6
Mouse Descriptions:
calpain 5 Gene [Source:MGI Symbol;Acc:MGI:1100859]
calpain 6 Gene [Source:MGI Symbol;Acc:MGI:1100850]
calpain 6 Gene [Source:MGI Symbol;Acc:MGI:1100850]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43148 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11881 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa43148
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 |
---|---|---|---|---|---|
ENSDART00000098972 | Nonsense | 158 | 685 | 4 | 21 |
ENSDART00000128707 | Nonsense | 158 | 717 | 4 | 21 |
Genomic Location (Zv9):
Chromosome 18 (position 35022925)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 36702081 |
GRCz11 | 18 | 36683089 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCCTGTGAGAGAGGGCCGTCTGCTTTTCAGCTACTCTCGCACCAGCAAC[G/T]AGTTCTGGAGCGCCCTGGTGGAGAAAGCTTATGCCAAGTCAGTTCCAGCA
Long Flanking Sequence:
GCAGAATGAACTGACAACAGATGTTTTAAATAAATGCTATTATTTAAACTTTGCATTCATATAAGAATCATGGAAGCAAATGTATGCAAGCATTTCCAAAGTATTCATCAGGTCATGTTTTCATCAATCAATCAATCAATCAATCAATCAATCAATCAATCAATCAATCAATCAATCAATCAATCAATCAATCAATCAATCAATCAATCAATCAATCAATCAATCAATCAATCAATCAATCAATCAGCATATTACAATGATAATAAAGGATCAAGTGACTGAAGAATGGAGTAAAAATTATGTAGGGGCAAAATAATAATTTAAGATATAAAACTGTTATTTCATGTTGTGAAATGTGACCTCTCTCTCTCTCTCTCTCTCTCTCTGTCTCTCTTTCTGTGTAGTTCTGGCAGTATGGTGAGTGGGTGGAGGTGGTAGTGGATGACAGGCTGCCTGTGAGAGAGGGCCGTCTGCTTTTCAGCTACTCTCGCACCAGCAAC[G/T]AGTTCTGGAGCGCCCTGGTGGAGAAAGCTTATGCCAAGTCAGTTCCAGCATATGTGTCCTTGACTGTGTGGATGTGTGAATGTTCATTAGCAGCCATTGTTCCTCTCTGTTTTATTTTTAGAAAAACATCCAGTTGTAAAACAAACCTTTTCAAATGCAGCTCATGGATGTCGAGCAATTCATTTAGAAACAATCCAAGCAGTGGAAGCCAATTAGCAGAATTCAGATGAGTGTGTGTGTGTCTGTTCTTAAAAGTGAAATTGAGTGTGAGAGGGGGGTGGGTGAAAGAGGGAAGGTGGGATTTTATTTACTAACAATATGCATGTTTTAATGTGTAGTAGCTGAAACTGTTTGTCTATGGAATTCAATCCTTAACCCAGAGACATTCCAACTTCATATGAAAACTTCATTCATTCATTCATTCATTCATTTTCTTTTCGGCTTAGTCTTTTTATTAATCTGGGGTGGCCACAGTGGAATGAACCACCAACTTATCCAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11881
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098972 | Essential Splice Site | 498 | 685 | 12 | 21 |
ENSDART00000128707 | Essential Splice Site | 530 | 717 | 12 | 21 |
Genomic Location (Zv9):
Chromosome 18 (position 35042089)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 36721245 |
GRCz11 | 18 | 36702253 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGGGGAGTTTTTCCTCCGCATTTACACCAAAACTGGCAACWTACAAGGG[T/C]ATGCAGAATCACAAACAAACATCAGCTCTRAGTTTTGATTGCAGCTTAAT
Long Flanking Sequence:
TTAATCATTTACATGTGTAGTTGCTTGCTTGCTTGCTTATTTATTTGAAAACTCAGACCCTTTCTGTCAATTATTTGCATATTTAAATTCCTACTAATTTGCAGTTCAATGTTCAGCAAATGTATCTTTTGTATTTCCTGCTTGTCTCACCTCTTCATTTTGTCTTTCAGGTTCCCCCTGAGGTAAGCAGTATGTCATCTAGCAGCATAAAAATACACATACAAAACACTTTTTTATACGGATAAACAAACAAACACATTCACACAATTTACCATCTTGTCCGTCTTCAGCTGAAGGACAGCCCTGGATCTCTGGATCAGCAGTTCTTCTCCAGCAACCGTGCGATTTCTCGCTCCGGCAAGTACCGCAGCATCAGGAGCGTCTGGAGGAAAGTTCACCTGGAGCCCGGCAGTTACGTCATCCTGGCCTCCACTTACAGACCCAACCAGCAGGGGGAGTTTTTCCTCCGCATTTACACCAAAACTGGCAACATACAAGGG[T/C]ATGCAGAATCACAAACAAACATCAGCTCTGAGTTTTGATTGCAGCTTAATGCTGTTCAGCGGTTAACTATGTGAAACTTTCAAATCTGCTTCACAGCTTTCAGGATTTCCCCTGCACCAACAACTACTCTGCGGTAAGACTTCTGCCGACAGAAAAGAGATAAAAGAGGCGATTCTATAGTTGAAGTAACATTTTTAACATTTAATGTTTTTATTTCTTATTTAAAAAAGATGTTTATAGTCATATGAATCACAATATCACACAGGCCATAAAGATATAGCAATTTTTGGATTAAATAATTTTGTGTTGCTCAATTTAGTCCTAATTAGTCGTTTGCATAATTTTCCTATAATGTATTACTGTGTAATCAAAATATCAAAATATTGTTTTTAAATTAACTTTTAGTATTGTTTTGCTCTGAATAATCATCCTTTATAATTCTTACATAAACTTATTTATCATTTGTGTTTTAAAATATGTTTATGTATTTATAGATAGAT
Associated Phenotype:
Not determined