ZMP
im:7156990
Ensembl ID:
ZFIN ID:
Human Orthologue:
ANKRD5
Human Description:
ankyrin repeat domain 5 [Source:HGNC Symbol;Acc:15803]
Mouse Orthologue:
Ankrd5
Mouse Description:
ankyrin repeat domain 5 Gene [Source:MGI Symbol;Acc:MGI:2441685]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42881 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32132 | Nonsense | Available for shipment | Available now |
sa36348 | Essential Splice Site | Available for shipment | Available now |
sa39151 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32131 | Nonsense | Available for shipment | Available now |
sa36347 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42881
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084606 | Nonsense | 46 | 663 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 17 (position 12270344)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 12252866 |
GRCz11 | 17 | 12406932 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAGATAGTCTGTACAGGTGTATTCAACCTGATAAACCTGACTGAACCC[A/T]AACATGGACTCGGTGCACTGTATCAGGCAACTGTGGATAAAGATGAAGAG
Long Flanking Sequence:
GATTCATGATTGGGGGAGCGAGACAGATTTGCATGGATGTAACAATTATATATTTTTATTTGTTAGACCCTCACCATAGAAAATATGATAGAAAACTACTTTAAGTTACATATTATTTATAGAAACTTCTTGGTTTTATTGGGGGCCCCTGATTTCCTGATGCCCTAAATGGCTGCTTACCTTGCCTATTGGTTAAATCCGGCCCTATATATGTTTATCTCTCATCAAGGCACAACAAGCTTTGGCAATACTAAAAAATTGAATGTACACATGATATGATATTCTATTTTAATGTTAATGCTATTTATCATTTCTTAAAACAGACCATGAATGAAGAAACAGAGATGACTTCAGAAAGTGGTGTTTCGAGGATGGCAAAGAGTAACGTGGAGATCCTACAGATCTACAAACTCCTGCAACATGTACGGGAAAAGAACAAACCACAGATAAAAAAGATAGTCTGTACAGGTGTATTCAACCTGATAAACCTGACTGAACCC[A/T]AACATGGACTCGGTGCACTGTATCAGGCAACTGTGGATAAAGATGAAGAGCTAGTACAGTTCCTTCTGTCTCTGAGAGCCCATCCCGACACACAGGATAAGAAGGGCTGCACACCGCTCATGCTGGCTGCACAGTTGGGCTACTACAATATTGTGCATATTTTGATCAAAGGTTATGCAGATGTGAATTGTACAGATAAAGAGGGCAAAGGTGAGAACATATATTTAGAAATGTATGGTACTCTATAGTTATAGAATTTATCTTGTTATTTAAGATAGTAAAAGGTGACAAAATATTGACAGAATTTACTTTTTTGGTTGAACTATCACTTTATTACATTAGATATCACTTCATTCAACATGTTAATTTCATTCTTTCTTCAGATAGAAAGAATTAAGGTTTTTGAAAAAAACATTTGCAAAGGGGGGGGGGGGTATATCCTCTGATTTTCTTTTATTAATATACGCTTAAAGGGTATTTAGAGCATGTGTTTAGAATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32132
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084606 | Nonsense | 207 | 663 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 17 (position 12269381)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 12251903 |
GRCz11 | 17 | 12405969 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAGGCATCTAAAGCTGGTGCATTAAAGCTTGTAAGAGCCATTTCAAAA[A/T]AAGGAGGGAATCCTAACTTAGTTGATGTAGAAGGACGGTGTGCTGCCCAC
Long Flanking Sequence:
TACGCTTAAAGGGTATTTAGAGCATGTGTTTAGAATATATTCTAAACTTCTATTGTTTTATTTGCAGGGGTGCTGTTTTACTGTATCTCTCCATCCAAAGAACACGCTCTCTGCCTGCAGATGGCGCTCGCCAGCAAGGCAAATTTCAACAACGTTTCTAATTCAGGAAAGCCCCTTCTTGTGTTTGCCTGTGAGAAAGCAAAGGACTGTGAAGACCTGTGCATAAACATTCTGGAGAAAGGAGCTGATCCCGATGCAGTTGATCAGGTTTCAAATATAAGCTTCCTCTTATTTTGATTCAATAAAAAAAGCAATCAATCATTATACAAGGGTTTCTTAGACAGACACAATTTTACAGCATTTTAATAGACAAATGTGAAATCTGATAAAGTGGAATTATTATAGTTTGTCCTGTTGGTTCCCCATAGGTGACACGATGTTCTGCGCTCATGGAGGCATCTAAAGCTGGTGCATTAAAGCTTGTAAGAGCCATTTCAAAA[A/T]AAGGAGGGAATCCTAACTTAGTTGATGTAGAAGGACGGTGTGCTGCCCACTTTGCTGCAGAAGGAGGTTTTCTTGAGGTTATTTAAATGCATTGTTAAGAGCACAAAATGTGGCATTGTTTCACTTCGGAGAGTATGACTGTCTTTGTTTTGTTTTAGGTTTTACAGGTGCTGTCAGCATACTCGGCAGACTTTTGTGTAAGCACAACAAATGGCAACACACCACTGCACTTTGCTGCTGCCGGTGGGTTCAATGAGTGCTGTAGATTCCTGTCTCAGAGAGGTATGATCTAAAGGTTTTCTATTATTTCCAAAAATGGAGAATAAGAGCCAGTAAAGTACCATGAACTCAAAACTAACCATATTGAGAACAATTCATCTATGCATGTCATTAAGAAAAAAAGCTTTCCCTTGTATTATAAAATTAAAATCTGACAACCCTGCTTATTTTAAGTTAAATTCTTAGATTACATTTGTCTGAGGTATTGGGCGTGGCTAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36348
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084606 | Essential Splice Site | 232 | 663 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 17 (position 12269302)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 12251824 |
GRCz11 | 17 | 12405890 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAGGACGGTGTGCTGCCCACTTTGCTGCAGAAGGAGGTTTTCTTGAGG[T/G]TATTTAAATGCATTGTTAAGAGCACAAAATGTGGCATTGTTTCACTTCGG
Long Flanking Sequence:
ACTGTATCTCTCCATCCAAAGAACACGCTCTCTGCCTGCAGATGGCGCTCGCCAGCAAGGCAAATTTCAACAACGTTTCTAATTCAGGAAAGCCCCTTCTTGTGTTTGCCTGTGAGAAAGCAAAGGACTGTGAAGACCTGTGCATAAACATTCTGGAGAAAGGAGCTGATCCCGATGCAGTTGATCAGGTTTCAAATATAAGCTTCCTCTTATTTTGATTCAATAAAAAAAGCAATCAATCATTATACAAGGGTTTCTTAGACAGACACAATTTTACAGCATTTTAATAGACAAATGTGAAATCTGATAAAGTGGAATTATTATAGTTTGTCCTGTTGGTTCCCCATAGGTGACACGATGTTCTGCGCTCATGGAGGCATCTAAAGCTGGTGCATTAAAGCTTGTAAGAGCCATTTCAAAAAAAGGAGGGAATCCTAACTTAGTTGATGTAGAAGGACGGTGTGCTGCCCACTTTGCTGCAGAAGGAGGTTTTCTTGAGG[T/G]TATTTAAATGCATTGTTAAGAGCACAAAATGTGGCATTGTTTCACTTCGGAGAGTATGACTGTCTTTGTTTTGTTTTAGGTTTTACAGGTGCTGTCAGCATACTCGGCAGACTTTTGTGTAAGCACAACAAATGGCAACACACCACTGCACTTTGCTGCTGCCGGTGGGTTCAATGAGTGCTGTAGATTCCTGTCTCAGAGAGGTATGATCTAAAGGTTTTCTATTATTTCCAAAAATGGAGAATAAGAGCCAGTAAAGTACCATGAACTCAAAACTAACCATATTGAGAACAATTCATCTATGCATGTCATTAAGAAAAAAAGCTTTCCCTTGTATTATAAAATTAAAATCTGACAACCCTGCTTATTTTAAGTTAAATTCTTAGATTACATTTGTCTGAGGTATTGGGCGTGGCTAACATATTTAACCACGCCCCTCTAACTGCCAGTTTTGTCAACTCTGTGACAACAAACAGAAATGGTAAGGAGCAGGGGCTGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39151
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084606 | Nonsense | 275 | 663 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 17 (position 12265989)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 12248511 |
GRCz11 | 17 | 12402577 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTATTACATGAAGTAATATTTTTGATTTTTCTATATCTAAAATAGGATG[T/A]AATCCCAAACTGAGGAATCTGGAAGGTCAACTTCCAAGCCAAGTCGCCAA
Long Flanking Sequence:
GACGTGTCACAAGGAGCTGGATGCTTGTAGAAGTTGTGAAATGAAGGCCACTTAACTGTTCAGGTCTGGTATGCAGAGAAGGGTTGCAGAAAGAGGAAGTATGTTTGGGTACAAGAGCCAAAGGACTGCAGAATGACTGATGATTTACGATACACCAAAACTCCACCTGTTATATCAGTTGTGTATATATGCTGGAGTCAGGGAAATGTTAGTTAGCTGAGAACCTCCTGAATGTAATTCTTGTATTGCATTGGGGTAACGTAACCCAGCTCTGCCCTCGATTTATTCATTTGTTTCTAATAAATGACTAATATTTTTGACATTGAAGAAAACCCTTTCCTGACCTTTTTTATTGAAAACACATGGAATTGGCAAGATATTCCAACAACAACGCATGCAAAACATTTTTAAAGAAGTAATATTTCACAGGCTTTATTTTGACGTTAGCTGTTTATTACATGAAGTAATATTTTTGATTTTTCTATATCTAAAATAGGATG[T/A]AATCCCAAACTGAGGAATCTGGAAGGTCAACTTCCAAGCCAAGTCGCCAAAAGCAACGGCCACAAAGCTGCATTGAAGGAGCTTAAGAAAGCAGAGAAAAGGCATGTGAAGTTTTCTGCACCTGATGCCATAAACCCCAATGAACCCTGGGCTATCACGCTTCACGACTGGTCCTGTGAACATGAGGCAGCCTTGCGCAGATCCTTTGAATCCGCTGTAGAGCTGAATAAACCTGTTCAAACAGTTTCTCTGGAGACATTCATGTCTTTGCTGTCCACGAATCAAGCACCAGTGAGTAATGAGAACCTGCAGAGGATAATCAAGCAGCATGACAAAAACCATAAAAATGTCATCAATCTAAATGAGTTTTTCAAAGGCCTCAAATACCTCCAAAAGCCCTTTGTCATTTCATCCTATGCTCCAAAGCCGGCTAAAAAAGAAAAGGGCCCCAAGGAAAAGAAGAGAAATAAATGTACCTCATTATTGCCCATATGTATGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32131
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 |
---|---|---|---|---|---|
ENSDART00000084606 | Nonsense | 542 | 663 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 17 (position 12265190)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 12247712 |
GRCz11 | 17 | 12401778 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCAGTTCTATAAGACTCCACTTTTGACAGCGTGCAGCTGTGGAAACTAC[C/T]AAGTCGCCGAATTCCTCATTTCACTGGGGTAAGTTTACTAGTTACTTAAT
Long Flanking Sequence:
ATGAGAACCTGCAGAGGATAATCAAGCAGCATGACAAAAACCATAAAAATGTCATCAATCTAAATGAGTTTTTCAAAGGCCTCAAATACCTCCAAAAGCCCTTTGTCATTTCATCCTATGCTCCAAAGCCGGCTAAAAAAGAAAAGGGCCCCAAGGAAAAGAAGAGAAATAAATGTACCTCATTATTGCCCATATGTATGATGCCACCTGAGCTTATCTGCAAAAGAGAAGACAGTGGGCTACCGTACTACATGATAGAGATCTGCCAGCTGTATACTCACACCAAACCCTTCAACCGAGACCAACCTTCAATCCACCACATTGAGAACGATTCGGCTTGGTATATCGAGCCGGAAAAGATCTATAGCAACATCAATTACTGTGTGAGGAGTGGAGATCTAGAATCTCTAAGATTGGCGTTTGCCCAACAAGTGCCTGTTGATATCAAAGATCAGTTCTATAAGACTCCACTTTTGACAGCGTGCAGCTGTGGAAACTAC[C/T]AAGTCGCCGAATTCCTCATTTCACTGGGGTAAGTTTACTAGTTACTTAATACTACTAGGGATGCAAGGATTAACTGATTTCACTATTAACTGCGTTTTAATTCATCACGGTTAATTAATTGCACGGAACAAAACTGCTGCAACTAAACAAAGTTTTGCCAACTGTGTGCTAGTTTAAAATTCCTAGCTCATACACTGAGGCTAATACGCATGTACACTGGATTAACCATGGCTAAGTCCATAAACTAAGGGCCGTTCACATAACGCATCTTTTGCGTGCACAAGTTAGTTTTTTTCAATGGAAGTGCGCGCATATTGGGTGCAACGCACTTGTGCTTTCCAGGCACCCCTAGTTGAAAATGTGTTGCAAGCGCACAGCGAGTTAAGTAACAAGGACTGACTGATCAGCTTCATACTTTGTACGGAGTATACACATTTCTACTCAAAACAAACTCAACTCAAAAACTCACATTTCTACTCAAAAAAAAATTATTATAAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36347
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 |
---|---|---|---|---|---|
ENSDART00000084606 | Nonsense | 628 | 663 | 7 | 7 |
Genomic Location (Zv9):
Chromosome 17 (position 12262006)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 12244528 |
GRCz11 | 17 | 12398594 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAATTTTCTTTTTAAGTAAATAGTCAACACAATGTTTGTTTTCCCAGGG[C/T]AAAATTGCTTGGACATTGCTATGATTTATGGCAATGCTAGAATTGTTCAA
Long Flanking Sequence:
TTGTTTTGGGAAATTATGTATAAATCTAATTTTCCAAAAATTGACCTTCATGATGGATTTTGCAGTCTTGGGCTGAGTATATTTAAAATCCAAAGCGACTTACAATTGAGGAGGTATTCAGCGATTAATCAAGACAATAAACAAAAGAAGTGCTAATTATACCAAGGGAACCGTTAGTGCTCATATAATTAAGTGCTAGGGTAAGATGAGGAGAGTGTTTCTTTTATAGTGAGAAGAGTGTTTCTAAAGGTGGTTTGTCAAGCCCTCTCACCTGTGTGTGAAGCACACTTCATAAATGCACCACAACGTCATTCCTTCCAAATAGCAGACATTAATTCAACCAAACAAATATACAGTTAATATGAAATGACATGTATATCATTGATGGTAAACAATTTTACTCAGCCCAAACATTTGGACATTTAGTGAATGTGTATATGTATTTTTTGTTTAATTTTCTTTTTAAGTAAATAGTCAACACAATGTTTGTTTTCCCAGGG[C/T]AAAATTGCTTGGACATTGCTATGATTTATGGCAATGCTAGAATTGTTCAATTGATTACATCCAAAGTTAAAAATCTTCCAAAAAATAAAAACAACGGGAAGGGAAAATAAAGACCACCTGCTTCAATGCCAGCTTCTTCTGTATAAAAAAGGTAAATGGAACAATACCAAAACAATGTCATGGTTAAGTATTGTTGGAGTTTTTCTATAACCTGTGCATGTCTTCTGTGTGTGAATGTTCCTTCTCCTGCCCAATTGAATTTTTCAAACTGTTTTCCATTGAATTCCATTGTGTTTTTTCCTACTATGGATATCTGTGGCTAGTGGTTTACAATATACAGAAAGACAAGCATAGATAGATGCACTGTAAAAAAAAAAAAAAGTAGAGTTAACTTAAAATTTTAAAGCAACCGGCTGCAAAGCAATTTTGAGGTTAGTCAACTTCAGTGTTTAAAGTGGTGCTAAATATTTTTTTTAAGTTGAGTTAACTCAGGGCGACGC
Associated Phenotype:
Not determined