ZMP
si:dkey-114g7.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate chaperone, ABC1 activity of bc1 complex like (S. pombe) (CABC1)
Human Orthologue:
ADCK4
Human Description:
aarF domain containing kinase 4 [Source:HGNC Symbol;Acc:19041]
Mouse Orthologue:
Adck4
Mouse Description:
aarF domain containing kinase 4 Gene [Source:MGI Symbol;Acc:MGI:1924139]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24977 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa35821 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa32019 | Nonsense | Available for shipment | Available now |
sa6367 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa24977
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000006829 | Essential Splice Site | 1 | 624 | None | 15 |
ENSDART00000140621 | Essential Splice Site | 1 | 623 | None | 15 |
ENSDART00000006829 | Essential Splice Site | 1 | 624 | None | 15 |
ENSDART00000140621 | Essential Splice Site | 1 | 623 | None | 15 |
Genomic Location (Zv9):
Chromosome 15 (position 13608057)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 14653654 |
GRCz11 | 15 | 14589611 |
KASP Assay ID:
554-7318.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGGACACTTCATAGAGACGCTGAGGAGACTCTAAACTCTCAATACGAG[T/A]AAGTAACGATAACATTACTGGTAGGAAACTACACTGCTGTGATAATTTAT
Long Flanking Sequence:
AGGGCTCCCAAATCACCAAATCTGCCCCAACTAATGAATAACTACTCGTATCCATTTAAAATGATTTACTATTATGGTGGTACGTTTTTTAAAAGTTTTTTTTGTTTTTAGAGCCTTTTAGTTATGTGACAATTGGATTAATAAAAGGTGTTGTTTAAATCCGTTCATAAAAACCCCAAACATAGGTCTGGAGTTAGAAAATTTTGACTTATGAATGTGAAATTTAGCAAGCAGTTCATCACATAACACTTTTTAATTTTGGGTTTTTATTTTTGGTGCTCATACGCAGTAAAGCCCAACACTACATTCATTATATATAAACCGGCTTGCCATATATCGGTTAAAACCCACCCTCCTTTGACGTTTCAAATCCTGATTGGTTATGTCGGCTGTCAATCATCAGGGCCTTTCCGTGTCCGGTAGTGTTGCAAAACAGAGGTTTGTGGAGTGAAAGGACACTTCATAGAGACGCTGAGGAGACTCTAAACTCTCAATACGAG[T/A]AAGTAACGATAACATTACTGGTAGGAAACTACACTGCTGTGATAATTTATGAAGACTATGAAAGCAACAGTGTAGTTTGACGTGCACGTGAGTAAAAAATGCAATGTTATTCAAAACTTGTGTGTTGATACATATTGGATACATGGCCTGAATGGATTTATTTTAATAATGCAATATTTTTACACTATCATAAACACATATGACAATGTATGGATTGGGTAAATAATCTGTAAAGCGTGTTAACTTTACATCAAACGTAAACTTAGTTTTATCCAATGCTTCTCAACTCAGTCCTTGATAAGGGTGAAAAAATATTCAGATTGACAGAGGTAGAGTGAGTGAAGCTAATACGTTTCTGACTAAAAACATTCCTGAGTAAAAGTAAAAATAAGGACAAACCTCGACTTGTTTGTTTAAAAAAGCAGCCTTACAAATATGAAACAGTGAAAGGTCATAGTAACTTATAGAAATAATATTGTCATAAGTATTCGTTTTCTGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35821
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000006829 | Essential Splice Site | 1 | 624 | None | 15 |
ENSDART00000140621 | Essential Splice Site | 1 | 623 | None | 15 |
ENSDART00000006829 | Essential Splice Site | 1 | 624 | None | 15 |
ENSDART00000140621 | Essential Splice Site | 1 | 623 | None | 15 |
Genomic Location (Zv9):
Chromosome 15 (position 13608057)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 14653654 |
GRCz11 | 15 | 14589611 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGGACACTTCATAGAGACGCTGAGGAGACTCTAAACTCTCAATACGAG[T/A]AAGTAACGATAACATTACTGGTAGGAAACTACACTGCTGTGATAATTTAT
Long Flanking Sequence:
AGGGCTCCCAAATCACCAAATCTGCCCCAACTAATGAATAACTACTCGTATCCATTTAAAATGATTTACTATTATGGTGGTACGTTTTTTAAAAGTTTTTTTTGTTTTTAGAGCCTTTTAGTTATGTGACAATTGGATTAATAAAAGGTGTTGTTTAAATCCGTTCATAAAAACCCCAAACATAGGTCTGGAGTTAGAAAATTTTGACTTATGAATGTGAAATTTAGCAAGCAGTTCATCACATAACACTTTTTAATTTTGGGTTTTTATTTTTGGTGCTCATACGCAGTAAAGCCCAACACTACATTCATTATATATAAACCGGCTTGCCATATATCGGTTAAAACCCACCCTCCTTTGACGTTTCAAATCCTGATTGGTTATGTCGGCTGTCAATCATCAGGGCCTTTCCGTGTCCGGTAGTGTTGCAAAACAGAGGTTTGTGGAGTGAAAGGACACTTCATAGAGACGCTGAGGAGACTCTAAACTCTCAATACGAG[T/A]AAGTAACGATAACATTACTGGTAGGAAACTACACTGCTGTGATAATTTATGAAGACTATGAAAGCAACAGTGTAGTTTGACGTGCACGTGAGTAAAAAATGCAATGTTATTCAAAACTTGTGTGTTGATACATATTGGATACATGGCCTGAATGGATTTATTTTAATAATGCAATATTTTTACACTATCATAAACACATATGACAATGTATGGATTGGGTAAATAATCTGTAAAGCGTGTTAACTTTACATCAAACGTAAACTTAGTTTTATCCAATGCTTCTCAACTCAGTCCTTGATAAGGGTGAAAAAATATTCAGATTGACAGAGGTAGAGTGAGTGAAGCTAATACGTTTCTGACTAAAAACATTCCTGAGTAAAAGTAAAAATAAGGACAAACCTCGACTTGTTTGTTTAAAAAAGCAGCCTTACAAATATGAAACAGTGAAAGGTCATAGTAACTTATAGAAATAATATTGTCATAAGTATTCGTTTTCTGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32019
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000006829 | Nonsense | 85 | 624 | 3 | 15 |
ENSDART00000140621 | Nonsense | 85 | 623 | 3 | 15 |
Genomic Location (Zv9):
Chromosome 15 (position 13626520)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 14635191 |
GRCz11 | 15 | 14571148 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGGAATTGAGAAGTGGGAGGAGATGGACCTGGATGAAGCTGCAAAGTG[G/A]TCGGTCGCCTCAGAAATGCCACCAGACTTTTCCAGTAAAGACGGAAGGGG
Long Flanking Sequence:
TCCTTTATTATTACACAAGAGTATAGCTCCTAACCATATTGACCTAGAAAAGAAGCAACATTTAATTTTCCATTGCTTTTAGTACATGATGAAATTACGGAAGTGTCAAGCTTTAAATGGGAAAACTATTAAATCTATTTTGGATTTTTTTTTTTTGTGAGATGCTTATGGTCTAATCCGATTCAATGATTTATGCTAAGCTAAAAGTCCTGGAGTATGACTTAATCGATGTAAAAATAGTAAAACTTAACTGTATAACTCTAGGGGACTTTAAAAGTAGCCTAATTTCAAAAACCGTGGAGTGTTTCTTTAACAATTTATTGGACGTTACTATCATAATTCGCAAAGAGCAAAACGGGGGAAGATATAAATAGACAGAAATAGAGACCACTTTGCTGATTATATCTTATTTTAAATGAACATTTTCAGACTTCTAAGACTGATGAGTTTGCTGGAATTGAGAAGTGGGAGGAGATGGACCTGGATGAAGCTGCAAAGTG[G/A]TCGGTCGCCTCAGAAATGCCACCAGACTTTTCCAGTAAAGACGGAAGGGGTGAAACATCAGAGACACCTGTTGGTGCTGCTACTGGCACCATTAAAGGAGCCGGCTGGCCTGCTCAAAACACTCGATTCTTGCATGTTTCAGCATCTCAACACCATTTTAGGTTTGTCCATGACTCTATAGTGGCCAGGTTGAGTCCTGAAGACATTCAAAGGGCAAGGGAGGCAAAACAGAACATTGCCAGGCCTGTTAGACAAAAGGTGAGGACATCTGAATTTTTTTTTTTTTTTGTCAAACATTACAAGGACATTTTAGCCAATAATGAAAAATGAACTCATCCTCAAGTGGATCCAAACATTAAATGCAAAAGATGACATTTTGAAAAAGTTTAAAATGTCCGTCCTTTGACTGCCCTAGTTGGGAAAACAAATATTGAAAACAAATATTATTGTCAAGTCATGGTTACAGTTCTCCAACTTTCTTTAAAATATCTTCTTTGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6367
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000006829 | Nonsense | 316 | 624 | 8 | 15 |
ENSDART00000140621 | Nonsense | 316 | 623 | 8 | 15 |
Genomic Location (Zv9):
Chromosome 15 (position 13633410)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 14628301 |
GRCz11 | 15 | 14564258 |
KASP Assay ID:
554-5016.1 (used for ordering genotyping assays)
KASP Sequence:
AGAAACTCTCATCAWTTGAGGAAAAGCCTTTTGCTGCTGCCTCCATTGGA[C/T]AAGTTCATCATGGAGTTTTGCCTGRTGGGAAGGAAATCGCTATGAAGATA
Long Flanking Sequence:
TCAATCCAATAGAGCACTTTTGGGATGTGGTGGAAAAAGAGATTTGTGTCATGAATGCGCAGTCGACAAATCTGCAGCAACTGCGTGACGCTATCATGTCAATATGGAGCAAAATCTCTGAGGAATATTTCTAGTAATTGTTGAATCTATGCCACGCAGGATTAAGGCAGTTCTGAAGGCAAAAGGTGATCCAACCTGGTACTAGCAAGGTGTATCTAATAAAGTGGCTGGTACTGGTACTGTATTTGCATATATTACCAGTTCAGAAGCCAAAAAATATGATTTTGGTAAACTAATACAATACAAGATGACGGTGTTGAGTAACGCAGCATGAAAAAGTGAACACGGTTTTTATCAGAACTGCCATTTCAGACGTTTAGTTGTTGTTTGCTGATATTAACTGATTTCTGCAGAAAGTGCTTGAGGAGGAGTTAGGCTCTGGATGGAGGGAGAAACTCTCATCAATTGAGGAAAAGCCTTTTGCTGCTGCCTCCATTGGA[C/T]AAGTTCATCATGGAGTTTTGCCTGGTGGGAAGGAAATCGCTATGAAGATACAGGTCATAGACTCGATTTTTTTCTAGATTAAGAATATGTATCGATATGACACAGCTAAACAATACTTTTTTGTTTGTTTGTTTATACAGTACCCTGGTGTTGCTGAAAGCATTCATAGTGACATCAACAATCTGATGTCTGTTCTGAAGATGAGTGTTGTTCTGCCTGATGGTGAGCACTGGCTAATGCTTTCACTTTTGAGTTTCAGCAAGATGAAGTGTGCATGTCGTAAACCTTAACATGAGAGGTAAGTTCTGGTGATTAATTTCTGCAGGTCTGTTTGCTGACAGTAGCCTTGAGGTCCTTCAGAGAGAGCTGGCATGGGAATGTGACTATGAAAGAGAGGCGAAGTGTGCCAAGCGCTTCAGGTATACTTGACTATAATAAATATCTATGATATCATATCTATGTGGGCAACTTGGTGGCTCAGAGCAAGAAGGTCACTGGTT
Associated Phenotype:
Not determined