ZMP
bx248082.1
Ensembl ID:
ZFIN ID:
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 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa2840 | Nonsense | F2 line generated | Not yet available |
sa6417 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa11390 | Nonsense | Available for shipment | Available now |
sa22790 | Nonsense | Available for shipment | Available now |
sa39085 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22789 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa2840
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000112288 | Nonsense | 337 | 1074 | 6 | 19 |
ENSDART00000131227 | Nonsense | 337 | 1074 | 7 | 20 |
Genomic Location (Zv9):
Chromosome 16 (position 18135258)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 16176495 |
GRCz11 | 16 | 16084472 |
KASP Assay ID:
554-2580.1 (used for ordering genotyping assays)
KASP Sequence:
CATATTCACACTCAAGTTGCTGTATTTTTCCCTTTTCAGTGCGGTATTTG[T/A]ATGTGCGCTGCTTCCATGTTTGAAGAGCCTGTTGAWATTCCTTGTGGTCA
Long Flanking Sequence:
TAGATGTTGGGTTGAATTTGGATTTTTGTTACTTTCTAACAACCTAAAATCAACCAAATATCAACATCATTTGACGTCATTACTGGACATCAAAATAACATTGTCCTTCGACGCTGGCTAGACGTTGAATTTTGGTCACCTGACATCACAACCTTAATTGAACATAATATTAACGCCATATGACGTTATGTGCCTGCTGGACAACTAGATGCACTACAGAATGTTATGTTTACACACATCCACAAATTGCATGGAAATGCATCAGTTTTTAACGGCATAATACTCACTACTCTTGAGTACTTTTGAAAGGGCTACTTTTTACTTATACTTTGAGTAATATTTGCAACAGATACTTTTACTCTACTTGCACTACATTTTAGCGAAGTAATTGTACTTTTACTTGATTATGATTTTTCAGTACTCTTTCCACCACTGGGTATATAAACCTGACATATTCACACTCAAGTTGCTGTATTTTTCCCTTTTCAGTGCGGTATTTG[T/A]ATGTGCGCTGCTTCCATGTTTGAAGAGCCTGTTGATATTCCTTGTGGTCATGAGTTCTGCAGGGGATGCTGGGAAAGGTGAGCTTTTATTTCTTTTTTTTTATTCAGTATTTTAGTCACACTGTGAGTTCTCTCTACTGCTGTAACATCATATAACATTCATGTGTGTTTTTTTTCCCTCCCTTTGGAAAGTTTCTTGAATTTGAAGATTCAGGAGGGGGAGGCCCATAATATCTTTTGCCCTGCCTATGACTGCTTCCAGCTGGTTCCTGTCGAGGTCATTGAGAGCATCGTGTCTAAAGAGATGGACAAACGTTATCTTCAGTTTGACATCAAGGTATAATTACATGATCGGTTACATATTAGTTTCAATTGTGTGCATAGTTGTATTACAAATATTTTCTGATATGGACTTTTAGAATAAAATTTCACTTCATAGAAGTCAAGTCAGCATTAAGCTGCAGTTTTTATTCCGACTTCATTAATAGCTTTCCAATCACA
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa6417
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 |
---|---|---|---|---|---|
ENSDART00000112288 | Essential Splice Site | 363 | 1074 | 6 | 19 |
ENSDART00000131227 | Essential Splice Site | 363 | 1074 | 7 | 20 |
Genomic Location (Zv9):
Chromosome 16 (position 18135179)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 16176416 |
GRCz11 | 16 | 16084393 |
KASP Assay ID:
554-4786.1 (used for ordering genotyping assays)
KASP Sequence:
CTGTTGAWATTCCTTGTGGTCATGAGTTCTGCAGGGGATGCTGGGAAAGG[T/A]GAGCTTTTATTTCTTTTTTTTTATTCAGTATTTTAGTCACACTGWGAGTT
Long Flanking Sequence:
TTACTGGACATCAAAATAACATTGTCCTTCGACGCTGGCTAGACGTTGAATTTTGGTCACCTGACATCACAACCTTAATTGAACATAATATTAACGCCATATGACGTTATGTGCCTGCTGGACAACTAGATGCACTACAGAATGTTATGTTTACACACATCCACAAATTGCATGGAAATGCATCAGTTTTTAACGGCATAATACTCACTACTCTTGAGTACTTTTGAAAGGGCTACTTTTTACTTATACTTTGAGTAATATTTGCAACAGATACTTTTACTCTACTTGCACTACATTTTAGCGAAGTAATTGTACTTTTACTTGATTATGATTTTTCAGTACTCTTTCCACCACTGGGTATATAAACCTGACATATTCACACTCAAGTTGCTGTATTTTTCCCTTTTCAGTGCGGTATTTGTATGTGCGCTGCTTCCATGTTTGAAGAGCCTGTTGATATTCCTTGTGGTCATGAGTTCTGCAGGGGATGCTGGGAAAGG[T/A]GAGCTTTTATTTCTTTTTTTTTATTCAGTATTTTAGTCACACTGTGAGTTCTCTCTACTGCTGTAACATCATATAACATTCATGTGTGTTTTTTTTCCCTCCCTTTGGAAAGTTTCTTGAATTTGAAGATTCAGGAGGGGGAGGCCCATAATATCTTTTGCCCTGCCTATGACTGCTTCCAGCTGGTTCCTGTCGAGGTCATTGAGAGCATCGTGTCTAAAGAGATGGACAAACGTTATCTTCAGTTTGACATCAAGGTATAATTACATGATCGGTTACATATTAGTTTCAATTGTGTGCATAGTTGTATTACAAATATTTTCTGATATGGACTTTTAGAATAAAATTTCACTTCATAGAAGTCAAGTCAGCATTAAGCTGCAGTTTTTATTCCGACTTCATTAATAGCTTTCCAATCACACTGATCAGTCCTCTTGCTGGAGTTTGTTGTGTTTAGTGGCATTGTGTAGTCAGTCTTGAATAGAGAACTACTGAAATGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11390
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 |
---|---|---|---|---|---|
ENSDART00000112288 | Nonsense | 537 | 1074 | 10 | 19 |
ENSDART00000131227 | Nonsense | 537 | 1074 | 11 | 20 |
Genomic Location (Zv9):
Chromosome 16 (position 18129495)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 16170732 |
GRCz11 | 16 | 16078709 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGCCAACTGCAAATCTCCCATTCAGAAGAATGAGGGATGTAACCACATG[C/T]AATGTGCCAAGGTTATTTGCGTAATAACAATAATAGATCTATTTATAGAC
Long Flanking Sequence:
CACAAATCTTTTACAAAACAACAAAGTAATATGTTATTAGGTTAATCTTTGACCTTGTTTGACCCACACTGATAAATCTCCCAAAAACATTCAAACTATTGCATAGAACAGCCATAATATATTTAGTAGAAATGTAATTTTCCTCCATGCTAACGATTGACATGACATGGATGTTTCTCCTCGCAGGGAATGTCAAGGAGAGGCCCATGAACCATGTGACTGCCAAACATGGAAGATGTGGCTCCAGAAAGTTACTGATATGAAACCAGAAGAACGTGAGCATGTCTTGCTGTACACTTGTACTCCATAAATTTCCTGAAGTACCTGAAGTAAGTGCTTTTGGACCTCAAGCATATTTATTTCTGTCTTTTTCCATTTCAGTGGCAGGTGTAAGTGAGGCGTATGAAGATGCTGCCAACTGCCTGTGGTTACTCACCAACTCCAAATCCTGTGCCAACTGCAAATCTCCCATTCAGAAGAATGAGGGATGTAACCACATG[C/T]AATGTGCCAAGGTTATTTGCGTAATAACAATAATAGATCTATTTATAGACTGGGCTAAGAAAAGGTTGGACACTTGGGGGTTTTAAGTGCTGTAAAATTACGTGTACAGTTCATGTAAACAGAGCATCTAGGAAGTTTGACAAAAGCTTCAAATTCAGTACAGAAAGCCTTCTTAGCTTTAGGCTTGGGTGGTAATGTGGTAATATGGTATACTGCGGGATCTAAAAATAGCACGGTATCAGTTTCAATACCGTTAAACCATCATAAAAAACAATGCAATTACATAGGCGAAGAGGATTAAATATTATGATTGTGGTTAAATATAAAATATTTAATGCCTGAAAATGCAAATGCGTGATTGTCATCACGGGACTGTGTGGAGGAGAAAGAGAGAGGTGAGGAAAGATGACAAGTCGCGCACCAAGTAACCTGGTCTCGAAAAAGAACAACCTCTGAAGTTTTTCAGTATTCCGGGGTAAATGTGAACAAGGCAATTTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22790
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 |
---|---|---|---|---|---|
ENSDART00000112288 | Nonsense | 568 | 1074 | 11 | 19 |
ENSDART00000131227 | Nonsense | 568 | 1074 | 12 | 20 |
Genomic Location (Zv9):
Chromosome 16 (position 18126242)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 16167479 |
GRCz11 | 16 | 16075456 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAGTGGAAAAAACACAGTTCCTCTACTGGAGGGTACTACCGCTGCACA[C/T]GATATGAGGTCATTCAGCAAGTGGAGGAGCAGTCTAAAGAGATGACTGTT
Long Flanking Sequence:
GCATCACTGTTTATTATTATGGGCTTGACGATCATAATTAAACGTTAAGCTTAAAATGTGTTTTTAAAAGTGCTTCCTTTGCTACAGCAGGCTTATGGAAATCAGGAGAAATTTCTCTAATTACTGAACAAGAAATGTGTGTGTGCCTTAGAAAGGAATGTATTGATCTTAATTCAATCTTGATAATCCAGCAACAAGGTTACTAAACAGGGAAATACATTGCAAATGCTGGCACTCCAAAAATAAAAAAGGTTGAGAGATAGTTTCCTAGCAACACACATAATCCCTGCTGTCAGAATTCCATAACTCCCAGTGTGCTGCCTGCTAGACTTATATATGCGTTTGTGACATACAAAGTAGGTTAGTAGTTTGTCTTGGTAGAGGGGCGGTTAATCAAGAATGTCTTTGTGTCTGTACAGTGCAAGTATGATTTTTGCTGGATCTGTCTGGAAGAGTGGAAAAAACACAGTTCCTCTACTGGAGGGTACTACCGCTGCACA[C/T]GATATGAGGTCATTCAGCAAGTGGAGGAGCAGTCTAAAGAGATGACTGTTGAGGTACACATTCTTGCTTACATGCTAAAAAAAACATGTATTTTATTTCTGTACACAGAAAAGTATTTCCACAAATACTTACATTTTTACAACTGTAAACGGAAGTTTTTAAAGCATTAGTAAATTTTAGATCTCACTATTCTGTTCAATTCGTCTTTATTTCTATAGTGCTTTTACAATGTAGATCGTGTCAAAGCAGCTTGACAAAGAAGAGGATCTAGTCAAAAGTTTTAAATTAAAACTCCCCTAAAACACTAATGAGTGTCTGTGTGTTTGCATAAACATATTACACATGTGTTGTTCTTTTGTTTTTGCAGGCTGAGAAGAAACACAAGAACTTCCAGGAATTAGATCGCTTCATGCATTATTACACACGTTTTAAGAACCACGAACACAGTTACCAGGTAAAAAAAAATCATTAATAATTCTAACTTGTTCTATAAAGCCTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39085
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112288 | Nonsense | 610 | 1074 | 12 | 19 |
ENSDART00000131227 | Nonsense | 610 | 1074 | 13 | 20 |
Genomic Location (Zv9):
Chromosome 16 (position 18125802)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 16167039 |
GRCz11 | 16 | 16075016 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCAGGAATTAGATCGCTTCATGCATTATTACACACGTTTTAAGAACCAC[G/T]AACACAGTTACCAGGTAAAAAAAAATCATTAATAATTCTAACTTGTTCTA
Long Flanking Sequence:
ATCTGTCTGGAAGAGTGGAAAAAACACAGTTCCTCTACTGGAGGGTACTACCGCTGCACACGATATGAGGTCATTCAGCAAGTGGAGGAGCAGTCTAAAGAGATGACTGTTGAGGTACACATTCTTGCTTACATGCTAAAAAAAACATGTATTTTATTTCTGTACACAGAAAAGTATTTCCACAAATACTTACATTTTTACAACTGTAAACGGAAGTTTTTAAAGCATTAGTAAATTTTAGATCTCACTATTCTGTTCAATTCGTCTTTATTTCTATAGTGCTTTTACAATGTAGATCGTGTCAAAGCAGCTTGACAAAGAAGAGGATCTAGTCAAAAGTTTTAAATTAAAACTCCCCTAAAACACTAATGAGTGTCTGTGTGTTTGCATAAACATATTACACATGTGTTGTTCTTTTGTTTTTGCAGGCTGAGAAGAAACACAAGAACTTCCAGGAATTAGATCGCTTCATGCATTATTACACACGTTTTAAGAACCAC[G/T]AACACAGTTACCAGGTAAAAAAAAATCATTAATAATTCTAACTTGTTCTATAAAGCCTGAATGTAAAATGTTTATAAGGTTATTCTTAAAATATTTTCTTAATGCAATCACTTATGAAGAACTACTTTTAACTTTTTATTAAGGGTAACATTCAGTAACCTCTTTGTGATAGTTGTTTAAAACAACAATTGTCGCTTTGCCTAAACACAGCTCATAAATATTATGTGTAACACTTAAATGAACTCATATTGCAATGCTTTCTTATAGGTAGAACTGTAGATATACATTAATGTTAGACTAATGTAAACCTTAAATTGTTTAATCCAGCACACTTTATTGTGCACTTACAACAGCCAAGCAGAATAGAGCTTGGAAGATCAGATAGACTAAAACTTTCCAGTTTTGTGTGCAGTATTTTGTCATATGGTCAGTGAACATACGTTTCTAAGTCTATAGACTGATTTAGACGTTGCATGTTTGAGAATATTGCAGTTTTTGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22789
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 |
---|---|---|---|---|---|
ENSDART00000112288 | Essential Splice Site | 762 | 1074 | 16 | 19 |
ENSDART00000131227 | Essential Splice Site | 762 | 1074 | 17 | 20 |
Genomic Location (Zv9):
Chromosome 16 (position 18102875)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 16144112 |
GRCz11 | 16 | 16052089 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCTGGTGGAACATGGGACTGGGAGTATTTGGGTTTCGCCTCTCCTGAG[G/A]TAACATTTTTTAAGCCTGTTTTACAAACTTTGTGTTATTTGTGTCTTAAA
Long Flanking Sequence:
TTATTTATGTACTCCTGGATTTTGTATAAGTGTAGTGGAGTTTGTAGTATCTGTTTTTTATATTATTGTTTCAATGGAAAAGGCAGTGATAATCAAGCAGTACAACCAACACACACAAAAAGCTAATGCTACAATGTAGTTTTAAAATATACAAAATGTTTTTTTTATGACCGTAATACGCAATATATTTATAGAAATAAAATGTTTATAAATCATTATGATTGAAGTTAAGAGTGTTCAATTCAGAGTACTTTTTTAAGAACTTAACCATGTGTGTTGTAAACTACAATTTTTACATACACTAAAGTAAAGGGGGTCCATTGTGACTAAACACTGTATGTTCAGAACTTCCTAACTGTTGCTTATTGTTTGTGACAAATGTACCTGCAGCCTCTCAATGTAAAGAAGCCCATAAAACCTAACACTTCTATTATTTCCTCTATTACAGTTTTGCTGGTGGAACATGGGACTGGGAGTATTTGGGTTTCGCCTCTCCTGAG[G/A]TAACATTTTTTAAGCCTGTTTTACAAACTTTGTGTTATTTGTGTCTTAAAAGAATGTGTTAAATTTGTATTTTTGGCCAATGTAGTGGTGGTTTTGGCTGTGCAAACCGGTCTGTAGAAGAAGATGTGAATGTGTGAGACCTGTGATGTGCAGTTAAACCGTGTACCGCTATTGTGTTCTAAAGATCCAGAGGAATCATGCCTTTCTCGGGGGAATTGATCCGAGAGAGCACTGTCAATATACAGGAAGCCATCCACAGGTATTGAAGAATCCTCATCTCAGGAACGGCTGAACGAAACGTGGAATGGCACCTGTCATGTATACTCCATCTGTCATGTCCACTTTCTCCTCTTTTATTTTTTTGGTCGCATGTTGACTTTTTCTTTATACTCTATTGACGCTATTCATATATTCAGACCTTCTAGATTAGGAATTGACCCACTGGTAAGCCCCCGCCACCCCCTTAGTTACTGTTGCTAACTCGGACAACAAACAGAGTC
Associated Phenotype:
Not determined