ZMP
ankhd1
Ensembl ID:
ZFIN ID:
Human Orthologues:
ANKHD1, ANKHD1-EIF4EBP3, ANKRD17
Human Descriptions:
ANKHD1-EIF4EBP3 readthrough [Source:HGNC Symbol;Acc:33530]
ankyrin repeat and KH domain containing 1 [Source:HGNC Symbol;Acc:24714]
ankyrin repeat domain 17 [Source:HGNC Symbol;Acc:23575]
ankyrin repeat and KH domain containing 1 [Source:HGNC Symbol;Acc:24714]
ankyrin repeat domain 17 [Source:HGNC Symbol;Acc:23575]
Mouse Orthologues:
Ankhd1, Ankrd17
Mouse Descriptions:
ankyrin repeat and KH domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:1921733]
ankyrin repeat domain 17 Gene [Source:MGI Symbol;Acc:MGI:1932101]
ankyrin repeat domain 17 Gene [Source:MGI Symbol;Acc:MGI:1932101]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10239 | Nonsense | Available for shipment | Available now |
sa37325 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa23949 | Essential Splice Site | Available for shipment | Available now |
sa37324 | Nonsense | Available for shipment | Available now |
sa23948 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10239
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 |
---|---|---|---|---|---|
ENSDART00000112410 | Nonsense | 883 | 2602 | 15 | 34 |
ENSDART00000147947 | Nonsense | 888 | 2607 | 15 | 34 |
Genomic Location (Zv9):
Chromosome 21 (position 25819392)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 26389210 |
GRCz11 | 21 | 26425905 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGCGGCAGGGGTGGAGATGCCCGGCACCCCCCTGCCCTTGCAGGCCACA[C/T]AGCTGGGCTCTGACAACGAGTGTGAGGGGATTCACGAAAAGGAGGACCAC
Long Flanking Sequence:
CACAGAACTTATGATGCTTGTCCGATGTCAGCTTTTTGGGTTTAAGCATTAGTCTTGTTTCCCTTCTAGGTGCGTCCAAGCAGAGACTAAGCTCCCTTCAGAGCAACTCTGTGGCCTCGGGTGGCCTAGACGCCGACCTACTGCCGCCCTTCCACCCCTATCAGCCTCTGGAGTGCATTGTTGAGGAGACAGAGGGCAAGCTGAACGAGCTGGGCCAGCGCATCAGTGCCATCGAGAAGGCCCAGCTCCAATCGCTCGAGCTCATCCAGGGTGAGCCGCTCACCAAAGACAAGATCGAGGAGCTGAAGAAGAGTCGCGAAGAGCAGGTGCAGAAGAAGAAGAAGATCTTGAAGGAGCTGCAGAAGGTGGAGCGGCAGTTGCAGCTGAAGACGCAGCAGCAGTTCACCAAAGAATACATGGAGACCAAGGGGCTCAAGGAGGAGCTGGGCCAGGCGGCAGGGGTGGAGATGCCCGGCACCCCCCTGCCCTTGCAGGCCACA[C/T]AGCTGGGCTCTGACAACGAGTGTGAGGGGATTCACGAAAAGGAGGACCACAGGCCCACCCCCACCAATGAGGAGGATGAAGACGAGGAGGAAGATGAAGACGACATCGACTGTGCCAAGCTGCCACAGGTGAACACCATTCTGCAGCCACCGCCGCCTCCTCCGCCTCAGAACCAGGTCCTCCAGAGCCCCCCTCTGCAGACCAGCTTCGTCCCCATCCAGCCTCTGACCCCACAGCTGTCCACAGATTTCAGTAGCGCCGAGTACCCGGGGAGCAGCAGCCCAGACCTGCAGAGGGTGTTGCTGGGCCAGCCACTCACCGGCTTGGGCCCGGGGCTTCTTGCACAGGCATCTGACGGACTCATGGTCGCCACACCTGCACAGACGCTCACAGATACGCTCGATGACATCATGGCGGGTGAGCTCACTGCTACTGTGGCTTCCTTTCAGGATGTCGACCAGTGATAAGAAATGCAATAACTGTTTTAGCGTTGGGAATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37325
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112410 | Essential Splice Site | 1200 | 2602 | 19 | 34 |
ENSDART00000147947 | Essential Splice Site | 1205 | 2607 | 19 | 34 |
Genomic Location (Zv9):
Chromosome 21 (position 25813700)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 26383518 |
GRCz11 | 21 | 26420213 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAACATCATCAAAATCCTTCTGAATGCTGGTGCTGAGATCAACTCTAGG[T/C]CAGAACATCTGTGCCCATTGGTTTAATCAGTTGTCTTAAGATTCATATTA
Long Flanking Sequence:
AGAGTCAGGACCTCAGTTTAACAACTCATCCGAAAGACAGAACTCACTGACAGTATAGTGTCCCCTTTACATTACTGGGGCATTATGCCCCCTGCTGGCCTCACTAACACCACTTCCAACAGCAACCTAGTTTTCCCATGTAGTCAGTACTGACCAGGCTCAGCCCTGCTTAGCTTCAGTGAGTAACCCGTCTTGGGCTGCTGGGTGATATGGCTGTGGTTTGATACTCTCAGCCACTTTTTTACATTATGCCGCTTATTTAATTTTTATGACTAGTCTCTGTTATTCTGTCTGCATTTTCCCCATTATGGAAGCTGTAGGATGTTATACATTACCATTAATATCAATCTTTCCAGGTGGTGGAGCTGCTGTTGCTTCGTGGGGCTAACAAGGAGCACCGTAATGTTTCTGACTACACTCCGCTCAGTCTCGCGGCCTCAGGTGGCTACGTCAACATCATCAAAATCCTTCTGAATGCTGGTGCTGAGATCAACTCTAGG[T/C]CAGAACATCTGTGCCCATTGGTTTAATCAGTTGTCTTAAGATTCATATTAGGAAATATCAAGATACTGACTGTGTAAACTCTTGTTTCAGGACTGGCAGTAAGCTGGGCATTTCACCACTGATGTTGGCAGCCATGAATGGGCACGTGCCTGCAGTGAAGCTGCTGTTGGACATGGGCTCTGACATCAATGCACAGATCGAGACCAATCGTAACACAGCACTGACCCTGGCCTGCTTTCAGGGTCGAGCAGAGGTTGTCAGCCTGCTCCTGGACAGGAAGGCCAATGTGGAACACCGTGCCAAGGTCTGTAATTACATGTTACTTGGGCAAAAAGGAAAACATGAAATTTGAACTTCTTATATAGTAAAAGACTCTGACTGTTTGTGTGTAGTTAAAGAAAACCGTCGTTTGAGCAGTCGAAACATTCAAGATTATTTTATTTTAAAGATGTTGTAATATAAAACTAAATGGTCTTTCCACTAGACTGGTCTCACCCCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23949
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 |
---|---|---|---|---|---|
ENSDART00000112410 | Essential Splice Site | 1455 | 2602 | 24 | 34 |
ENSDART00000147947 | Essential Splice Site | 1460 | 2607 | 24 | 34 |
Genomic Location (Zv9):
Chromosome 21 (position 25812356)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 26382174 |
GRCz11 | 21 | 26418869 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCAAACAAGAACGCCAGCATTCTGCTCAAGGAGCTTGATCTGGAAAAG[G/A]TTTGTCTCTTCTGATAACCAGTTAGATTAGCTAACTATCTTGTTGAGGAG
Long Flanking Sequence:
GCTGGGGCTGACGTGGATGCAGCTGATAACCGCAAGATAACCCCCCTCATGGCAGCATTTCGCAAAGTGAGTGTAGTTGATAGGAATAAGTGGACATCTTGCAGTAAACCAATTTTTGTTTTTAGAGTAGCACCAGTGATGCTTAATAAATAAAATGCCATAATCACTGAAATGTGTTTTTTTTTTTTAGGGCCATGTAAAAGTGGTGCAGTATCTGGTGAAGGAAGTTAACCAGTTTCCATCTGATATTGAGTGCATGAGATACATTGCAACTATTGCAGATAAGGTATGAAGGATCTTCTAGTGATGCAGAGCATATTCATAGAAAACTGTTTTAATCATTTGGCATGCCTTTAATGGCTGTTTATATTTACACTCTTTAGGAGCTGCTCAAGAAGTGTCATCAGTGCATGGAAACCATTGTCAAAGCCAAAGATCAGCAGGCAGCTGAAGCAAACAAGAACGCCAGCATTCTGCTCAAGGAGCTTGATCTGGAAAAG[G/A]TTTGTCTCTTCTGATAACCAGTTAGATTAGCTAACTATCTTGTTGAGGAGTTTTATAGTAGTCAACCTTTTTTGACAACGTATCATGGTTTTTAATTTGTAACAGTCTCGTGAGGAAAGCAAAAAGCAGGCTCTGGCTGCAAAGCGTGAGAAGAGAAAGGAGAAGCGCAAGAAAAAGAAGGAAGAGCAGAAGAGGAAGCTGGAGGAAGAGGAGGCAAAAGTGAAAGAGGTGTCGTTTGAGATGCTGGATCAGAAGGAGGACTCTGCAGAAGGTCAGGAAAACTTTAGGTCTAGATATCATGAAAACAAATTAAAGTTAATGCCCGAAATAAATAAATAATTAAAATCCGAGTGCATTTAAAGAATAATCTGTACAAATTCTTAAACCCAAAGTCAATCTATTAATCTGTCTTCTGTTGATGCATGAAAAAACTAACATTATTTTAATTGAACCTCCTATTCATTTAATATCAAGCGTCACTTTTCAGTTTTATCATGAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37324
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 |
---|---|---|---|---|---|
ENSDART00000112410 | Nonsense | 2188 | 2602 | 29 | 34 |
ENSDART00000147947 | Nonsense | 2193 | 2607 | 29 | 34 |
Genomic Location (Zv9):
Chromosome 21 (position 25809006)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 26378824 |
GRCz11 | 21 | 26415519 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCACCAACACCCTACTACCCCATGGCTCCAGGGGCCCTGCAGGAGCAG[C/T]AGTCTGTGTTTGTGCCTCCAGGAGCCACACAGGAGACCCTTAAACAACAG
Long Flanking Sequence:
CACAGATTGCACCTTCTCCCATCAGTTGCGCTCCTACAACACCTACGACCCCTCCACCTTCATCTGCAGCCACTGCTGCAACTCCACAGCATCCTCCAAAGCCAGAGCCGGCCAGCCTTAGCACCCCAGCTAAAGAAAAGCCTGTCACAGAGATTGCAGCACCCACTGCAGGAGCGCCATCTGACGGGCCCAGCGCCTCTGCTCCCCTGCACTTCACCTCATCTCCTTCAGGCCCCTCGATGCTGCCCCCACAGCCCGAGAGCCGGCAGACGCTTCCATCACACTTTCCCCCCAGCACAGAATCCAGTTCCTCTTCCTCATCTCAGCCAGGCTCATCTCACCCTGTCACACGCCTGCCACCTCCAACCTCCAGCAACACCATCACTAATACCAGCAGCACCTTACCTCATTACGGCTCCCCCACAGCGCCCGGTGTGTCCCCGCGCATGCAACCACCAACACCCTACTACCCCATGGCTCCAGGGGCCCTGCAGGAGCAG[C/T]AGTCTGTGTTTGTGCCTCCAGGAGCCACACAGGAGACCCTTAAACAACAGCCGCCGCCTCAGCCCACCCTTGCTCCAGCAGGCATGCCTCCTCCCTCTCTTCCAATGTCCTCCACTATGGGCATGATAAATGGCTCTCAAATGCACCTGCACAGTGGAAAAGCGCAACTGCCCCCCAACTTTGGCCCTGCTGCTCTTTTTAATCACTTCAGCAGCATCTTTGACAACAACCAGGTGGGCAACAACCAGGTTTGGGGTGCCTGCCATCTGCCTGCTCGTACCCCACCAGAGCAGCCCTACAGTGGCACAACAAATGCCTACATAGGGGGAATGGGGCAAATGGAAAGTGTCATGCCTCCTCCTGATGGCTCAAAAGCGCCAGGGTATCGCTGCTCCACACAGCGGATGGTCTCCAGTCCCATTGGTGAGTGAAGCAGTTTATATCAAATGTCGAGTCTTGCTCCCAACTTTCTATCCCATCTTTTATGTTTTGCTTCAGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23948
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 |
---|---|---|---|---|---|
ENSDART00000112410 | Nonsense | 2390 | 2602 | 31 | 34 |
ENSDART00000147947 | Nonsense | 2395 | 2607 | 31 | 34 |
Genomic Location (Zv9):
Chromosome 21 (position 25804779)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 26374597 |
GRCz11 | 21 | 26411292 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGATGCTCTTTTCATTCCTCATCGATTATAGGCGAGTCTCCAGTGCCCT[C/A]GGTGTCCTCTGGGGCATCGTCACCTCTTTGCACATCTACGGTGACTCCTG
Long Flanking Sequence:
AGGTACCAAAGGGTACCACACCCCTAATGATTTGGTTCAAGAGTTTAATTTGATTTGGAGCTAAACTTGCTTGAAAAGTGGCTGTCCAAGAAAAGCATTATACACCCTGCCTTAAGTGAATTATAGCTGAAGAACCCGCTGCTTGTTTATTTGTGCAATTGGGGTCAAATTCTTTTAGTAACACTCTTGTATTCACTCTCTACAACAGGAATACACCCCATGGATGGCTCAATGTCCTCATCCACTGCACTCACCAGCTTTACCACAAGCATATCTGCAAGTCCTGTTTTCCTGCCGGGTCCTGCTCCAGTGGGTACACCCTCCTTCAGCCGCCAGCACTTCTCTCCCCATCCCTGGAGTGCCTCCACCTCTTGTACGTCAACAAATATGTCCTTTGAATTTAGATGGACCACAATTATTGACAACTATTATCTGACCAATTTGATTTTACTGATGCTCTTTTCATTCCTCATCGATTATAGGCGAGTCTCCAGTGCCCT[C/A]GGTGTCCTCTGGGGCATCGTCACCTCTTTGCACATCTACGGTGACTCCTGCTCTGATCCAGGCAAAACCTAGTAGCTCCAACCAGCAGGACCGCAAAGTGCCCCCACCCATCGGAACAGAGCGCTTGGCCCGAATCCGGCAAACTGGCTCAGTCAACCACACCATGCTACCCACCAGCTACACCCCACCAGTTGGACAGGGTGGCATCTGGTCTTTTGGAGTGGGCAGTGCCTCCGGTGAGCATGACTTAGATGTAGTTGACATTTACAAATGGTTTTACAAAGGAAATTATTTACTTATGTAGTACCAATCATTGGGCATTAAACTTGAAGTTAATATAGAACTGACAGATGATGCAGACAAAAAAAGTACTTTCTTCCGATCTATATGTATGTATGTATGTATGTATGTATGTATATGTATTTATACTGCAAACAATCGGATAATAAATTGCAAGAGATCAACCCAAGCATATATCTGATACAATTTTTACATTTAAT
Associated Phenotype:
Not determined