Busch Lab

ZMP

casp6l1

Ensembl ID:
ENSDARG00000025608
ZFIN ID:
ZDB-GENE-041010-48
Description:
caspase 6, apoptosis-related cysteine peptidase, like 1 [Source:RefSeq peptide;Acc:NP_001005973]
Human Orthologue:
CASP6
Human Description:
caspase 6, apoptosis-related cysteine peptidase [Source:HGNC Symbol;Acc:1507]
Mouse Orthologue:
Casp6
Mouse Description:
caspase 6 Gene [Source:MGI Symbol;Acc:MGI:1312921]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa1603 Essential Splice Site Available for shipment Available now
sa10094 Nonsense Available for shipment Available now
sa40102 Nonsense Mutation detected in F1 DNA Not yet available
sa38400 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa1603
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000041414 None None 242 None 6
ENSDART00000125012 Essential Splice Site 11 569 1 15
ENSDART00000136919 None None 249 None 6
ENSDART00000146586 None None 169 None 6
ENSDART00000147374 None None 253 None 7

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 3 (position 33102708)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 32834018
GRCz11 3 32965732
KASP Assay ID:
554-1544.1 (used for ordering genotyping assays)
KASP Sequence:
RCATTCACATAAATAACGATGGCAAGTCACACTAAGAGCGACGGATCCGG[T/A]AAGGGATTAGTTTAGTTTCTCTGTATGGAGATAAATAACTTGAATGTGTG
Long Flanking Sequence:
GTTTGCAGCTGTAAGGTCATCCACTGTGTAAAATCATATGCTGAATAAGTTGGTGGTTCATTTCACTGTGGCGACTCCTGATCAAATAAAGAGACTAAGCCGAATGAATGAATAAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAATTCAATGCGGAAGTAACCAACTGAGTTCCACCAAAGGTTTGCAGAGTTGTGATTGGGTAACGTTGTAGTGTCCTGTGATTGGTTAAAGATTTAGTGACCCACGATAGGTTTACTGTTGCACTTGGTGACTGGTCTGTGTTTGCTGAAGTTGGTTTGTCTCTACATTTCTTCTCAATTTCGCCTACATTCACATAAATAACGATGGCAAGTCACACTAAGAGCGACGGATCCGG[T/A]AAGGGATTAGTTTAGTTTCTCTGTATGGAGATAAATAACTTGAATGTGTGTAGCTACACTGTGAATGCTGTTCATGTGAGACCGCGAGTTTCATTTCCTTATTTTAGCACCTGATAAAGGTAGAAGGTATTTGTTCACAAATAACACCTTTTCGCGTTAAAACACATAAAATGTCAACTACAATGTTTGACTAAATGAGTTCATACTTACTGTAACTTGAGTCACAGCGCTTATAAAAAGAGTGTATTTTTTGTTTTAGCAGCTGTGGAGAAGGACAGCGCTTCAGCAGGACAGACAGGTAAAACTGAATCCACTTTATTGTCGTGTTTGTTCCAAGTATCAGAATGAGTGGAAATAGTTTGTATGGAGTGTAAATATAGCATTATTAGCCTATGTCTACTCTGCTTTGCTAGACAGCCTGTTTGCAAAGCCATTGAAATCCAGCTTGACCAGGTGCTCAATAAACAATACAGGCTTGACCTCAGTATATGTTCAGTGAA
Associated Phenotype:
Normal
Stage Entity Quality Tag
Larval:Day 5
ZFS:0000037
whole organism
ZFA:0001094
quality
PATO:0000001
normal
PATO:0000461

Mutation Details

Allele Name:
sa10094
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000041414 None None 242 None 6
ENSDART00000125012 Nonsense 66 569 4 15
ENSDART00000136919 None None 249 None 6
ENSDART00000146586 None None 169 None 6
ENSDART00000147374 None None 253 None 7

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 3 (position 33101569)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 32832879
GRCz11 3 32964593
KASP Assay ID:
2259-3702.1 (used for ordering genotyping assays)
KASP Sequence:
CCACAAGAGACGGGGAATGGCTCTCATATTTAATCATGAAAATTTCTTTT[G/A]GAAACTGGGATTGGGCTACCGTTCTGGAACRAATGCAGACAAGGAGAACC
Long Flanking Sequence:
GCTACAAAAGCTGTCACTGTGGAGGTACCCTTTCAAAAAGGGATACATTTTTACCTAAAGGGTCTATATATTGATACCTTAGTACAATAGTATCTTTTGAAAATTAAAGTACTAATGATATTACCTCTAACATAAGTAATATGTAAAAAAAAAAAAAAAAAAAAAAAAAACTAATATGTATCTTTTAGGTGCATACATGTACCTTCTGCAAGGGTACCACCCCATTGACAGCTCTGTACCTTTAATGTCTAGAGTGTGTGCAAGCCAAATGTTTGATGGTGTTTTCTTTTTTCAGTTGAAGAGAACCTGACAGAGACTGATAGCTTTAATCAAAGGTATTTTGCCAAAGATTGTAATCATATTAGTAATGGGGAATGTACTATACTTATGTATAAATAAATTGTTTGACAGTATATTTAGTATGGATCCTAATCAGGAGTATGATATGAACCACAAGAGACGGGGAATGGCTCTCATATTTAATCATGAAAATTTCTTTT[G/A]GAAACTGGGATTGGGCTACCGTTCTGGAACAAATGCAGACAAGGAGAACCTTATTAGAAGGTATTTAACCAAGCAAACAAAAAGTCCTATTAGTTGTGCATGCTAATATTGTACTGTTTTCTGGTCTTGGATTAAAGTTACTTTTGTTAATTTTTCTCTATAACTGTTGGTAGATTTCGAGAGCTGAATTTTGAAGTTAAAGCTTTTGATGATTACAAACGACATGAAGTTTTGTCCAAAATCACAGAGGGTATGTGTTGCTTGTATCTTTCATATATTCTCTTTAAGGCTAATTTTTTCATAATTTGCAAGCGTGCTAATTGAGCATGCTGAAATGACAAATGTTATTTGTTAAATTTAAAAACATTAATTATCCATATTTTTTCTACTAATTCTACTGATATGTAGCTGTTAAAATAATATTATATTTGTTATGTAAATCCAATTAACCTGTTTAATTGTATTTGATTTAGGTCTAAGAATATATCGGTGTAAAATAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40102
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000041414 None None 242 None 6
ENSDART00000125012 Nonsense 100 569 5 15
ENSDART00000136919 None None 249 None 6
ENSDART00000146586 None None 169 None 6
ENSDART00000147374 None None 253 None 7

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 3 (position 33101353)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 32832663
GRCz11 3 32964377
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTGGTAGATTTCGAGAGCTGAATTTTGAAGTTAAAGCTTTTGATGATTA[C/A]AAACGACATGAAGTTTTGTCCAAAATCACAGAGGGTATGTGTTGCTTGTA
Long Flanking Sequence:
CCACCCCATTGACAGCTCTGTACCTTTAATGTCTAGAGTGTGTGCAAGCCAAATGTTTGATGGTGTTTTCTTTTTTCAGTTGAAGAGAACCTGACAGAGACTGATAGCTTTAATCAAAGGTATTTTGCCAAAGATTGTAATCATATTAGTAATGGGGAATGTACTATACTTATGTATAAATAAATTGTTTGACAGTATATTTAGTATGGATCCTAATCAGGAGTATGATATGAACCACAAGAGACGGGGAATGGCTCTCATATTTAATCATGAAAATTTCTTTTGGAAACTGGGATTGGGCTACCGTTCTGGAACAAATGCAGACAAGGAGAACCTTATTAGAAGGTATTTAACCAAGCAAACAAAAAGTCCTATTAGTTGTGCATGCTAATATTGTACTGTTTTCTGGTCTTGGATTAAAGTTACTTTTGTTAATTTTTCTCTATAACTGTTGGTAGATTTCGAGAGCTGAATTTTGAAGTTAAAGCTTTTGATGATTA[C/A]AAACGACATGAAGTTTTGTCCAAAATCACAGAGGGTATGTGTTGCTTGTATCTTTCATATATTCTCTTTAAGGCTAATTTTTTCATAATTTGCAAGCGTGCTAATTGAGCATGCTGAAATGACAAATGTTATTTGTTAAATTTAAAAACATTAATTATCCATATTTTTTCTACTAATTCTACTGATATGTAGCTGTTAAAATAATATTATATTTGTTATGTAAATCCAATTAACCTGTTTAATTGTATTTGATTTAGGTCTAAGAATATATCGGTGTAAAATAACCAATTGCCAAAACTGTATTTACATTTAATGGACTTTCAACTCAATCAGAATTAAAATCATTTTGTTTAATAAAAATAAAAATATATTTTATATATGAGCAGTTCCAGCGTTATGGATGTGACATTTATAGAAAAATCTCAAAACATAAGTTGATGGAGGAAGTCTATGTTAACATTATATTGAAACATCCTTTTATATTTTTCTAAACAAATAGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38400
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000041414 Essential Splice Site 162 242 None 6
ENSDART00000125012 Essential Splice Site 489 569 None 15
ENSDART00000136919 Essential Splice Site 169 249 None 6
ENSDART00000146586 None 169 169 6 6
ENSDART00000147374 Essential Splice Site 199 253 None 7
Genomic Location (Zv9):
Chromosome 3 (position 33091850)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 32823160
GRCz11 3 32954874
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCCTTCCAGCAGGAGCAGATTTCATTATGTGTTACTCAACAGCTGAAGG[T/G]CAGTGTTTATATCTTTGTTTCGTTTTACTGAGATTTTATTATTGTTTTTC
Long Flanking Sequence:
CTTTAGAGATAGTGATATATATTTTTTATTATTGTATCGACACATGGTTTTCTAAATGAATTTTGGTTCTGTTTAATCCACAATATTCTTTTGGTTTCAGCCTCTGCTGCTGATCATGTAGATGCAGACTGTTTCGTCTGCATCTTTTTAAGTCATGGGGAAGATGGCCATGTTTATGCCAATGATAAGAAGATCGAAATACCTGAAATTACTGATTTGTTCAAGGGGGATAAATGTCGTAGTCTTGTGGGTAAACCCAAGATCTTCATCTGGCAGGTAATTGTGTTCTTCACAAAATGTCATCCACAAATCGGCATGTGAATTTAGATCTCATTTAAATCTGTGGTTTCTTTGAAAAAACAGGCTTGCCGTGGTGACAAACTGGATGATGCTGTGACTGAAATGAGTGTGGAGGATGTTGAAATGGCTGTAGATGCAGGAGTGCTTTACACCCTTCCAGCAGGAGCAGATTTCATTATGTGTTACTCAACAGCTGAAGG[T/G]CAGTGTTTATATCTTTGTTTCGTTTTACTGAGATTTTATTATTGTTTTTCTTTTAACAACTTGGATGCAATGTACCTCCATTACTGTAATGTCAGACTTTTAAAAATTGATTGCATTGTTTATTTTCTTTTAAAGGATTTTGCTCTTTTCGTGAGCCCTTGAATGGCTCATGGTACATTCAGGATCTGTGTGAAATCTTGGGGCGTTATCATTCAGAGCTACAGTTCACTGACATCCTGACGCTTGTTAACATGAAAGTTTCATTGCGCTCTGTACCAAACTGCAGGAATCGCGCTGCTATTGGCAAAAAACAGATGCCTTGCTTTGCGTCCATGCTCACAAAGAGGCTGTTTTTCAGAGACAATACTCAGATCCAATAGTGTTTTTTACTCCATGGCAATTTCAAATTCAGGGATTTTTTCATTTTCTTTTGGTGGGTTTGATTTTGCCAATTAAGATGTGATCCTGGAACGTCATTTCTGTTTTAAAATCTTATCCTT
Associated Phenotype:
Not determined