ZMP
si:dkey-231l1.6
Ensembl ID:
ZFIN ID:
Description:
Ankyrin repeat and IBR domain-containing protein 1 [Source:UniProtKB/Swiss-Prot;Acc:Q1L8G6]
Human Orthologue:
ANKIB1
Human Description:
ankyrin repeat and IBR domain containing 1 [Source:HGNC Symbol;Acc:22215]
Mouse Orthologue:
Ankib1
Mouse Description:
ankyrin repeat and IBR domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:1918047]
Alleles
There are 8 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa5929 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa36917 | Nonsense | Available for shipment | Available now |
| sa23595 | Nonsense | Available for shipment | Available now |
| sa23596 | Essential Splice Site | Available for shipment | Available now |
| sa6124 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa17107 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa5929
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 |
|---|---|---|---|---|---|
| ENSDART00000085980 | Nonsense | 436 | 1053 | 8 | 20 |
| ENSDART00000133628 | Nonsense | 436 | 1060 | 9 | 20 |
Genomic Location (Zv9):
Chromosome 19 (position 45444431)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 44342653 |
| GRCz11 | 19 | 43938226 |
KASP Assay ID:
554-3931.1 (used for ordering genotyping assays)
KASP Sequence:
CAATCCACTGGTGCCCTGTAGCCAGATGTGAAAGAGCCGTTCGTCTGACT[C/T]GACCAGGCCCTGGAGCTTCTGACCCGCTGAGCTTCCCGTTGCTGAAAGCC
Long Flanking Sequence:
TCCAAGAAGGGGAGGCTCATAACATCTTCTGCCCTGCTTACGACTGCTTCCAGCTGGTTCCAGTGGAGGTCATTGAAAGCGTCGTCTCCAGAGAAATGGATAAGCGCTACCTGCAGTTTGACATTAAGGTACAATCGAGGCTCACAAAGTGGTAGAAAGCGTTTCAGACCTGCCATTTCTTCAGTCTTATCTCACACCGTCTGATGCCGGCTGTGAATCAAAATGCTGAGCTCATGCTAGTGTTTGTTTAAGGGGGAAAAAACAGCTTTTGTAAACAAGCTCAGGAGTCAAACATTGGCTAAATATCACGCCGATTTGGATTTAGATGATGTATAGACTGAAATTGGTTTTGGAGATTTTGGTTTTTGTTTAATTTACGTCATCAGATACAAAGAGGGGGTTTTAACAGGTTTCTTTTTCATCTGCAGGCGTTTGTGGATAATAATCCTGCAATCCACTGGTGCCCTGTAGCCAGATGTGAAAGAGCCGTTCGTCTGACT[C/T]GACCAGGCCCTGGAGCTTCTGACCCGCTGAGCTTCCCGTTGCTGAAAGCCCCTGCTGTAGACTGTGGAAAAGGACATCTCTTCTGCTGGTGTGTTTCCTTTTGTCTGTGCATTATTCATTCGTATCTTTCCCACATTGCTCTTAAAATAAATAAAAGCGTGTTTTCCACTATGGTGCCTAATGGTTCTGAGAACAGTTAGGTATGCTTCTAGTTGTGGATGCATTTGGCCAAAAAACAAGACGTTTTAAGCTAAGCTTCAGTTATATTGGTGTTAAAGCAATTTAATAAAATAACCACATTTTATTGTTGTTAATTTTATTATTAGTGAATTTGCGAGAGCCGGCGAAGCAGTGGCGCAGTAGGTAGTGCTGTTGCTTCACAGCAAGAAGGTCACTGGGTCGCTGGTTCGATCCTTGGCTCAGTTGTCGTTTCTGTGTGTAGTTTGCATGTTCTCCGTGCATTCGCGTGGGTTTCCTCCGGGTGCTCCGGTTTCCCCCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36917
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000085980 | Nonsense | 477 | 1053 | 9 | 20 |
| ENSDART00000133628 | Nonsense | 477 | 1060 | 10 | 20 |
Genomic Location (Zv9):
Chromosome 19 (position 45448806)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 44347028 |
| GRCz11 | 19 | 43942601 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCTGTCTCTCAGGGAGTGTCTTGGGGATGCTCATGAACCCTGTGACTG[T/A]GAAACATGGAAGATGTGGCTGCAGAAAGTGTCTGAGATGAAGCCTGAAGA
Long Flanking Sequence:
CTAAAAAAAGTAACACATAGGGGCAAACACGTCTTGCGCCTTATTAAACCGGGTGTACGATAGGGCCCTTAATATGAATTTGGTTGTAGTTTTGTTTTATGTTTGTTTAAATTACAGCTACGAAAAGAAAGAAATTACATTTGTAAACTTTAAAAATAAATGACAAAATGCAGTAAAATAATATTTTTTTCATTTGTAAATTATAAATGTAAACTTTAAATGTAAAACTTATATACATGATCAAAATAAACATATAACATAATGAAAAATACATGTGTTTTATTAAAAAGAATGTGTTTTTATAGTAACAAGATCTTATGTGCTCTTAAAATGTGAGATTTTCTTTCAAATATGATCTGTTTATAAAGATAGGACTGGTTTTCTGAGATTCACGAGATGTTAATGTGTTTCCTGCAACATGTCATCACCGTTCATTTTATCTCTTGCTTTTTCCTGTCTCTCAGGGAGTGTCTTGGGGATGCTCATGAACCCTGTGACTG[T/A]GAAACATGGAAGATGTGGCTGCAGAAAGTGTCTGAGATGAAGCCTGAAGAACGTAGGAGCTCTGCTGCACTGTTATTTATGTTGTAGTTCAAGTTTGATTGTTTTCATCCAGTACATGATAATATAATACACCTATTGCATTACATTGTGTTACCTGAAAAGAGATCAGGGGTGGCACGGTGGCTTACATTCACCTAACAGCAAGAAGGTCGCTGGTTTGAGTTCCGGCTGTGCCAGTTGGCATTTTAGTTTTGCATGTTCTCCTCGTGTTGGTGTGGGTTTGCTCCGGTTTCCCCCACAGTCCAAACACATGCGCTATAGATGAATTGAATAAACTAAATTGGTCGTAGTCTATGAGTGTGAGTGTGTGACTGCGAGAGTGTTTCAGGACTTGGTTGGAGCTGGAAGGGCATCCTTTGTGTAAAACATATGCTGGAATAGTTGGCGGTTCATTGCACTGTGGCGACCACTGATGAATAAGGCTGAAATGAAAATAAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23595
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000085980 | Nonsense | 500 | 1053 | 10 | 20 |
| ENSDART00000133628 | Nonsense | 500 | 1060 | 11 | 20 |
Genomic Location (Zv9):
Chromosome 19 (position 45449425)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 44347647 |
| GRCz11 | 19 | 43943220 |
KASP Assay ID:
2261-3699.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGATCATAAGACTTCATCTGCATCTCTCTGAACAGTGGCTGGTGTGAGC[G/T]AAGCTTATGAAGATGCTGCCAACTGCCTGTGGTTACTCTCCAACTCCAAA
Long Flanking Sequence:
ATAATATAATACACCTATTGCATTACATTGTGTTACCTGAAAAGAGATCAGGGGTGGCACGGTGGCTTACATTCACCTAACAGCAAGAAGGTCGCTGGTTTGAGTTCCGGCTGTGCCAGTTGGCATTTTAGTTTTGCATGTTCTCCTCGTGTTGGTGTGGGTTTGCTCCGGTTTCCCCCACAGTCCAAACACATGCGCTATAGATGAATTGAATAAACTAAATTGGTCGTAGTCTATGAGTGTGAGTGTGTGACTGCGAGAGTGTTTCAGGACTTGGTTGGAGCTGGAAGGGCATCCTTTGTGTAAAACATATGCTGGAATAGTTGGCGGTTCATTGCACTGTGGCGACCACTGATGAATAAGGCTGAAATGAAAATAAAATTAGGACTGGGCCTTGATCAAATCACTCCACCTTGTATTATTGTTTGAAATAGCCCCTTTGTTTAAGGGATGATCATAAGACTTCATCTGCATCTCTCTGAACAGTGGCTGGTGTGAGC[G/T]AAGCTTATGAAGATGCTGCCAACTGCCTGTGGTTACTCTCCAACTCCAAACCCTGTGCCAACTGCAAATCCCCCATCCAGAAAAACGAAGGCTGTAATCACATGCAGTGTGCAAAGGTCAGTCCAGCGCAGCTTTCCCCCCCCCTCTTTTCTTGCTAGTCCTGCAACATGGCTTTGTTCACTCAGTAGTATTTGTGCATTAAACGGAGCGCTCCCTTAAAAATGATGCAGAGTCTGATGACATATGAACACAGACGGTCACACGGGACACATTTGATAAATTAAAACCTCAAGGGAATGGTAGTGCATCTTGATAAACACATTTGCGAATGAATTGTTTGAGAATTGTCTTCTTAGTCATACATGATGGACTAATAAGGTCATAATTAATAAGGTGCTATTGGGACACTGTTGCTCTTCCTTCACAGCATGCTTATCCACATGCATTTGCATTCTTTTTGCCCCTTTAACATGCAATTGTCATTATGAAATCTCTTATGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23596
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 |
|---|---|---|---|---|---|
| ENSDART00000085980 | Essential Splice Site | 743 | 1053 | 16 | 20 |
| ENSDART00000133628 | Essential Splice Site | 743 | 1060 | 17 | 20 |
Genomic Location (Zv9):
Chromosome 19 (position 45458121)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 44356343 |
| GRCz11 | 19 | 43951916 |
KASP Assay ID:
2261-3700.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTATTTCTAAAGATCATCTGTGTTATCATAATTTTCCCCTCTTTTTCA[G/A]TTTTGCTGGCGGGACGTGGGACTGGGAGTATCTGGGATTTGCTTCTCCTG
Long Flanking Sequence:
TATATTAATATTTAAATATATATTAATATTTAAATAAATATATTAAAAATATAGAATTATATAAATAAAAATAAACATAAGTATATAAAAAAATATATTATAAATAAATTTTTATTATATATATATTTTTTTGAATATATTTATATATTTATTTAAATATTTATTTATATTTTTAAATTATGTATTATGTATTTATATTTTATTCATATTATGTATTTAGTATATATATGTGTGTGTGTGTGTGTGTGTGTATTATATATTTTTTATATATTTAAATATTTATTGAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTTATATACATATATATCTAATCTAATCTTCTCTAATTTCACAAATACAGTAGATCTTTCATCTGAGGGCTCTTTCAGTTTAAATGCAGAACTATTTCTAAAGATCATCTGTGTTATCATAATTTTCCCCTCTTTTTCA[G/A]TTTTGCTGGCGGGACGTGGGACTGGGAGTATCTGGGATTTGCTTCTCCTGAGGTATGATGGCATCACCACCTCTGTGTTTGACCTGTTTCTGTTTTTGACTAACCTCTGCTATTGCTAAACTCACGCAGCCTGTCGGAGCTGTAGCTTCACTAGACTGTTAACAATTAAGAGAGTTGTGTGTTGCTGTAAAATACTAGCAGTCATTGAATCTCATTCTGTGTCCAAAGATGGTGAGGAATCACCCAGTACGGGGATCAAATGCACAGCGCGAGAGCAATTACAATGCAGGAGGCCAGCCGCAGGTACTGATGAACGAAGATGAAAAGCTCAATTTGGTCCAGTATTAATTTGCATGTGCTGTATATGACATCTAAACCTCATCCTTGCCGTTAGCCTTAATGTAATCTGGTGTTTTAGATGTTAAGGCTGGTCATATCCTGGAATATTCCAGATAAACGACTATGCCACTATTTGATTTAAAGCAGAATTCCTGTCCTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6124
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000085980 | None | None | 1053 | None | 20 |
| ENSDART00000133628 | Essential Splice Site | 824 | 1060 | 18 | 20 |
Genomic Location (Zv9):
Chromosome 19 (position 45461351)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 44359573 |
| GRCz11 | 19 | 43955146 |
KASP Assay ID:
554-3823.1 (used for ordering genotyping assays)
KASP Sequence:
AACACATGAACGAGCCACTGAACGACACTCATACTCACTCTGAAATATGT[G/A]TGTGTTTGTGTTTATAGAAACACATGAGGGAGGCACTTCACAACGGCATG
Long Flanking Sequence:
ATAGCTTCCTATTAAAAATATGAATTTAAAAGAGAGATTTGTGAGGGGTGTACTTGCATATTTAAATGCAGAGACATTCATTTTTATTTGTGACTTATTTGTGCATGTATGATGTGCTTTATTTTAATCCGTAGATCATAATTAGGCATATGGCACTTTACTCTTTATAAAAACATTAAGATTGGATCTCTTTAATGCACCAGTGAGAGATGCCCATCAGTATTGTTGTTTATATTTTGAAGGCCGTATGCATTTCTCCCCTTGTTATTGCTCTGTGTAGTCAAATGATGTTCCTGCTGCTGTTGCAGGAGTACTCTGAGTTCCAGTACAGACGGAGACACCGGCAGCGGCGACGAGGAGACCTGCTCCGACTGCACAGCCTGCGCAGCAACACTCCTGAACCACATGACTCCAGCGACGCCACCGCAGGTACAGCACTGCCTGAAACACAACACATGAACGAGCCACTGAACGACACTCATACTCACTCTGAAATATGT[G/A]TGTGTTTGTGTTTATAGAAACACATGAGGGAGGCACTTCACAACGGCATGGCATCTCTACGGTAAATAATCTGTTTATACAAATGTTAGTTATATTGGTCACACACAGAGTCATACACGGTATGTTATGCAGTGAAATGCTTAAGCTGGATTTAAACTTTCGCCTGGCACCTCAAGAAACAGACAAGGCTTTTATACTTGCCGCGTTCACCGTTGTGATATTCTGCAAAGGGCACATAGTTTACCCATTTTCTATGATTTAATATTAACATTATGGTTGTTCTGAGTGCGCCAGTTTAGGTTCAGTTCAACACTCAGATGTTTTTGTTATAATGTGTTCAAAAGTGTCATGTTGTGGGCGTGTACAAAGCTCGCTGTTTTAGGGGCGTGTTGCTTCACATGAAAATTAGTTTCCCGCCCAACGTAACAAGGGGGCGGAGCCAAGAGCTCCCACGCTCTGTGTTTGCAATAGATAGGCAGACAGAGAAGTTAAGATCAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17107
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 |
|---|---|---|---|---|---|
| ENSDART00000085980 | None | None | 1053 | None | 20 |
| ENSDART00000133628 | Nonsense | 1050 | 1060 | 20 | 20 |
Genomic Location (Zv9):
Chromosome 19 (position 45466618)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 44364840 |
| GRCz11 | 19 | 43960413 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACATAAAATCAGTTCTGGTGGCCTTAGACGAAATGTGTTTTCTTTGGGT[C/T]GAAGATGGAAGGGGTTTTCATGCAKTACAAAATAAGGGCGYAATACAGCT
Long Flanking Sequence:
AAGCCGAGCAGACTGAAGCGGAGAGTGCTGAGATGGAGAGTAAAGAGGGGGAGGTTTCGGAGTGTGTTGAAGATGCTAAAACGGAGGCTTCAGATCTCACTGTTTGTCCTGAAAGCAGCGCCGATCCGCAGGTAAACAGTCTATCTTTGGAGTGGGAGGAGGAAGTGCATCTAGTTTGAGGAGCGAGTGTCATTACGTTTACCAACTGAGTGCTCTTATTGTGCCAAAACACTACACGATGGAAGCGGAAGTGCTCGTGCTGTGATCTGAGACAGGCGTTGATTGTGTTGCACAGCGCTTTGGAAGAAAAGCGATCAGGTTTGTGCTCGTGGAAGTTCATGATTGGATCATTCACTAATCATATTTGTGTGTTTGTTTTTGCACATTCATCTGTAAGTTTGGTTCTTCTCTGCATTTAGCATCAAATTGTGGAAAAACTAACGTTGCGCGGACATAAAATCAGTTCTGGTGGCCTTAGACGAAATGTGTTTTCTTTGGGT[C/T]GAAGATGGAAGGGGTTTTCATGCATTACAAAATAAGGGCGTAATACAGCTTTACCTTCTCTGAGCAAAAAAAAAGAAAAAGAAAGACGACTACCCATGCATTACCACCATCATCTACAGAAGACGTTTAATAGTGTGATCATCGTTTATATACTGAGCTATTTTAAAGAACAGGTATCATTTGACGACATGTATTAAAGACTTTTATTTTCATTATAATACTCAACACAGTACTCATAAATGCTCCTTCAGGTTTAGCCAATGTCTGGTTTTGAGTTTTTAATTATTCAAAATATAATATTTAGGTGACATGGTGGTTCAGTGGTTAGCACTATCGCCTTACAGCAAAAAGGTCGCTGGTTCAAGTCTCAGCTGGGTCAGTTGGCATTTCTGTGTGGAGTTTGCATGCTCTCTCTGTATTGGTGTGGGTTTCCTTCAGGTGCTCCGGTTTCCCCCACAGTCCAAACACATGCTTTGTAAGTGAATTGAATACACTAAATT
Associated Phenotype:
Not determined