ZMP
si:ch211-195h23.3
Ensembl ID:
ZFIN ID:
Description:
si:ch211-195h23.3 [Source:RefSeq peptide;Acc:NP_001123874]
Human Orthologue:
CARD8
Human Description:
caspase recruitment domain family, member 8 [Source:HGNC Symbol;Acc:17057]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31297 | Essential Splice Site | Available for shipment | Available now |
sa38353 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19856 | Nonsense | Available for shipment | Available now |
sa19857 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31297
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108591 | Essential Splice Site | 83 | 478 | 5 | 13 |
ENSDART00000123673 | Essential Splice Site | 83 | 478 | 5 | 13 |
Genomic Location (Zv9):
Chromosome 2 (position 44006429)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 44091930 |
GRCz11 | 2 | 43944928 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGGTTACAGGCTTCCAAAAAAACTGAAACTGTTTTGGAGCATGTGGATG[G/A]TGAGTAAACATGGTATAATTTTTATTTTAAATGTAATAATAAATGTAATA
Long Flanking Sequence:
TTAATAAAACTATTATGATTAGAAATGTGTCAAAAAAAAAAAAATCTTCTTTCCGTTAAATAAAAACTGGGGGGAAAAAAAATAGGTCAGGGGGCTAATAATTCTGACTTTAACTGTGTGTGTATATATATACTCCTATGTTTCAGACTAGAATCTGTCATTTTATTCATAGTTACGAAAATTCAACTTAAGTCAAATATCCTTGTCATGTAGCTGGTTATGCTGTAGCATGACATTTGTCACTTTGATACTTTTTCTCAGGGATGCGTATATCATTATCAGATTCAGATGACGAGTCCACTTCGAAACGACGTTTTAGGCACCCAAGAAGCTTAAGCATGGGTATGTACTCTCAGATTTTATAAACAAATATAAATACAAATTTAATTATAGTTTATAAACATGTTTTACAGGCACAAGATCGAGGACAGTTAAACGCCATAGATTTCACAGGTTACAGGCTTCCAAAAAAACTGAAACTGTTTTGGAGCATGTGGATG[G/A]TGAGTAAACATGGTATAATTTTTATTTTAAATGTAATAATAAATGTAATAAATTTAAATAATCTCATTACTGCGATCAGGTGCACATTGAGAATCACACTCATAACTTTATCATTGTGAGTGCAAAAATGACCATACAATACAAAATGATGTAAACGTAGATATTAAGCTTTCGTATCTCAGGTGACCGATGGTGTTCTGTGCTTTGCATTAAAAAAATTTTAGCTTTCTGTCTGTTTTGTTATCCTTGCTTTTTTATTTACCAAAGCCAGTTTTTAATCTTCATTTGATTACTGGCAATCATTCATTTTTTTCAGCAACAGAAGTCTGAATATAACTTTTTAAGCAAAAAAAACAACAACAAAAAAACAAACAAACTATAAATTATAAACTGTTATTCTGTTTATGACTATATACTCTGTAGTTCAGTGGTGTTATGAGGTCATATTTGAGATCTAGTTTCTTGTACTGTTAATGCATGTCACTTATGAATTTGTTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38353
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:
C > A
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108591 | Splice Site, Nonsense | 117 | 478 | 7 | 13 |
ENSDART00000123673 | Splice Site, Nonsense | 117 | 478 | 7 | 13 |
Genomic Location (Zv9):
Chromosome 2 (position 44007118)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 44092619 |
GRCz11 | 2 | 43945617 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACCTGAACTTATTCAAGAAGATGACAAGTACAAAGACAAGAATACATA[C/A]AGGTATTGAACAGTTGTGTTCTTTGGAATCTGTAAAAAGATAATGTGTTG
Long Flanking Sequence:
GATGGTGTTCTGTGCTTTGCATTAAAAAAATTTTAGCTTTCTGTCTGTTTTGTTATCCTTGCTTTTTTATTTACCAAAGCCAGTTTTTAATCTTCATTTGATTACTGGCAATCATTCATTTTTTTCAGCAACAGAAGTCTGAATATAACTTTTTAAGCAAAAAAAACAACAACAAAAAAACAAACAAACTATAAATTATAAACTGTTATTCTGTTTATGACTATATACTCTGTAGTTCAGTGGTGTTATGAGGTCATATTTGAGATCTAGTTTCTTGTACTGTTAATGCATGTCACTTATGAATTTGTTTCTTACTTTTTCCCTAGGTGCAGAATCATCTTCAGGACAAACAGTGAGTAGCAACTGTCATGTGTTCTGGCTTTCATAAAATCAAAAAGAGAAAGATCATTCTTTCCTTTGTTTCAGCCCTCAGATGATGCAGAAATATTCACACCTGAACTTATTCAAGAAGATGACAAGTACAAAGACAAGAATACATA[C/A]AGGTATTGAACAGTTGTGTTCTTTGGAATCTGTAAAAAGATAATGTGTTGAATTGCTTACCTTTAAATGTAAACCTTCAATGACTCATGTCTATATATAGGACACTTTTTTAAACACAACCTGACAAAAGTCTTGTCGCCTATCCACGTTTTAGGAACAACAAATAATAACTTCTAGTTGATCATTTGGTATCAGAAGTGGCTTATATAAAAGGCAAAGACCTCTAGATTACGCTTATTTTACCAAAATAAAATATGATCATGCCTTGATTTTTAATTATTTTAATTAGGACAGTAAAGTCTGCTTAGACAAAAGTCTTGTCACTTAACAAAAATAATGTACAGTATAGAATATAAGTCATGGTGCAGTGGAAAAAGAATGAATATTGTGTCTGACTCTCATTAGCCTGGAGGACTGCATCCATACATCTCTGCAATGACTCAAATAACTGATTAATAAAGTCATCTGGAATGGCAAAGAAAGCGTTCTTGCAGGACTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19856
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 |
---|---|---|---|---|---|
ENSDART00000108591 | Nonsense | 365 | 478 | 11 | 13 |
ENSDART00000123673 | Nonsense | 365 | 478 | 11 | 13 |
Genomic Location (Zv9):
Chromosome 2 (position 44013454)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 44098955 |
GRCz11 | 2 | 43951953 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACTATTTTAGACAAAGCTGAAGATTGTAAGGAAGTGTGGAGCCGACCA[C/T]GAGTATCACTTAAAGGTAAAAAACATTTGGTTGTTCAAACTTTGTGTAGG
Long Flanking Sequence:
AAATACACTTCATTATTTTGTTAAAATCTATTATTTCTCATAATATTTAATCAAATAGTATAACCTTACCTCACCTTTGAAAGTACTTTTCTTCAGCTCTGATTACATGAAATGGCCTTAGATGGGATCCATTTGTCTATAGCCAGGGTGTTCATGAATTTGTCAATCTTCCTCTATTTTGCTAGCAACGCCTTCCATCAATCCAGTTGGTTCCCAAACATAAAAATCATGCACCACCCTACATTTTTTCTATTTTTAGGACCGTTTCAAACAAATGTACATCACGATATGGAAATAAAATGACAATTTTAACTTCAGTTTCATGCCGACTTGATGCTGCTATTGATGTTGTTTTTTTTCAGAGCGAGATCTTTGAGCATAATAATTTTGGTCCAAACTTCCATCCCTCATTTCAAGTGTTTTTGAGTGTTGACGTTAAAAAGGTTGGATTGACTATTTTAGACAAAGCTGAAGATTGTAAGGAAGTGTGGAGCCGACCA[C/T]GAGTATCACTTAAAGGTAAAAAACATTTGGTTGTTCAAACTTTGTGTAGGGGTGATTTTTTTATATGTTTGATGAATAATTTAAGTTTGTCTGTGGAGGCATTCATCTGTGTTGGGGAAGTTTGTCATAATTTTACGCAATTGAACAACAATTAAGCTGTTTTCTAATCTAAAACATAACTACACGGGCTATTAATGTGAAGGCTTTATTATTAAGGGAAAACAAAATACAAACCTACATAGCCCTGTGTGAAAATAGAGTTCAAGTTCTGTAGCCACACCCAAATCTGATTACTGCTACAGCTGTTTATAATCAAGAAATCACTTAAATAGGAGCTGCCTGACAAAGTGAAGTAGACCAAAAGATCCTCAAAATCGAGACCCAATCCAAATTCAAAAACAAATGAGAAAGAAAATAACTAAGATCTGTCAGGCTTGTTAACCTTTCCAGACATTTCTAAAGCATTGAGCCTGCAGTGAACCAAAGCGAGATCCATTATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19857
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108591 | Nonsense | 436 | 478 | 13 | 13 |
ENSDART00000123673 | Nonsense | 436 | 478 | 13 | 13 |
Genomic Location (Zv9):
Chromosome 2 (position 44016483)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 44101984 |
GRCz11 | 2 | 43954982 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTATACAGCGAACTTCATAATGCCGATACAAATCAGAGGAAAATGAGATG[C/A]CTGTTTATGGCTCTGGACTCTGGAGGAGCTTCTGTGAAAGCAGAGTTTTA
Long Flanking Sequence:
CAAGTCAAGGAGTAGAACCTCCAGAGCACAGAATGATTTCAGGTTTTACTTTAATATTTCAATATAATGTCAAATGAATATTTTTTCTTATCATTGTTTCTTGCACATACTCTACACCACAGGTGTCAAGTCCAGTTCCTGGAGGGCCACAGCTCTTCACTAAATTCGCTTCAACACACTCACCTGTGGGTTTAAAACAAGCCTGAAGGACTCAATTAGTTTGATCAGATGTTTAATTAGAGTTAAAGCTAAACTGTGCAGAGCTGCGGCCCTCCAGGAACTGTATTTGACACTTGTGCTCTACACATTCTTTTAATGAGTAACATCAATATTTGGTTTCAATCAGGAAGTGAATTTGTGGATGCCCTCAGAGGTAAACTCATTCAGAGAGTTTCATCAGTGATGGCGATTGCTGACAGCCTGAGGAGCAAACACATGATTACAGATGAATTATACAGCGAACTTCATAATGCCGATACAAATCAGAGGAAAATGAGATG[C/A]CTGTTTATGGCTCTGGACTCTGGAGGAGCTTCTGTGAAAGCAGAGTTTTACCGTCTGCTAAAGAAGAACGAACCTCATCTAGTAGAGGAACTGGAGTCTGGACACAGCAAATCCTTCAGACGTCAGTAATGCTGAGAGTAAGGGTGCTTTCACACCTGTGAATCGATTCAGTTGTTCCGAAACAGAGATTACAATTGTTACATTGTTGCTCTTTACTCTTGGAGCGGTTCGCTTTCACACTGCAAAGTTTCTAATCGGACCAAAAGAGCTAAAACAAGTCACGTGCGAGTAAACTCTCCTTACATTGGTCAGAGTGTCAGGGTTTATTTTGCAGCGTCTCGCTAAACTGTCAGGACAGGTGGTGGTTTGGTGGTGATTGACAGGGTGCGCGCGTGTGACGTGTCTGAGGAGAGATGCGGTGGGGAGGGGTGAGAAGGGTGCGCGACGATGCCTATTTGAGGACCGGGAGGGAGATGCGAGATTACCGGGAGATCATCACT
Associated Phenotype:
Not determined