ZMP
anks1b
Ensembl ID:
ZFIN ID:
Description:
Ankyrin repeat and sterile alpha motif domain-containing protein 1B [Source:UniProtKB/Swiss-Prot;Acc
Human Orthologue:
ANKS1B
Human Description:
ankyrin repeat and sterile alpha motif domain containing 1B [Source:HGNC Symbol;Acc:24600]
Mouse Orthologue:
Anks1b
Mouse Description:
ankyrin repeat and sterile alpha motif domain containing 1B Gene [Source:MGI Symbol;Acc:MGI:1924781]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa40270 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa20254 | Essential Splice Site | Available for shipment | Available now |
sa2161 | Essential Splice Site | F2 line generated | Not yet available |
sa16530 | Nonsense | Available for shipment | Available now |
sa15624 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa40270
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 |
---|---|---|---|---|---|
ENSDART00000024367 | Nonsense | 275 | 1281 | 6 | 26 |
ENSDART00000133509 | Nonsense | 275 | 1280 | 6 | 26 |
The following transcripts of ENSDARG00000003512 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 17176788)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 18119628 |
GRCz11 | 4 | 18108604 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGAACTGCACTAGATATACTTAGAGAACATCCGTCTCAGAAATCACAA[C/T]AAATTGCTTCTCTCATACACGGTAAAGTGTTTCACAGATTTCTATACGCA
Long Flanking Sequence:
TCATTGATTACTTAATCTTTCTTCAATTTTTTTTTTTTTTTTGGGATTCAACAGAAGAAACTCAAACAGGTTTGGGAAAAGTAAAGGACGAGTTAAATAAACCCTTTTGGGTGAACTCTCCCTTTAAATAGTCTTGTTAAATAAATATTCCAAGCTTTGCTTTAGATTTTGTTTGCCATCTTTTGTAAAATAGGACCACAATAATTAGACAAAGACTGCAAATCGCATCTACCTAGTTAGCTTTTTGTATTTTAAGTGTTTCAGTATCATCATAGGCTGATGGAACAGTTGTGTGGTGTTGCTTTAACTGGTAATAAATCCAGTTATCTTAGAAAACTGTAATAAATGTACAAATTAAAAACTTTGACAAAACACTAAACATAAAGAATCCAAATTAATATGTTTTTCTCTTTTTATCAGGGATTGATGCCAACATCAGAGATTGCCAAGGAAGAACTGCACTAGATATACTTAGAGAACATCCGTCTCAGAAATCACAA[C/T]AAATTGCTTCTCTCATACACGGTAAAGTGTTTCACAGATTTCTATACGCACACACTGAAACTTTTTTTTATGGGAAATACACCCCTTAAAACACACACAAGCACACTCTCACACACGTGCACAATTTGACAAGGGAGTGCGTTCTTGGTGGAGATCAGAAAGCGGATGCTTGCAGATTGATAAAATTCATTCCAGGAAGTTTGTGTTAGATTGAGAACAATGGTTGTTTAATGCGTTAGAAATCCCTGTTCCCTGACATACTTTGGACAAAAAACAATATCAAACGCTTTCAATGATGTGTCTTCAGTCTTGTTAATTAGCTGTTCATGAGATTACATGTTTATTACTTTGTTACCACATTCAGCGTTTTTTACTGCTGTTGAATTTTGTTCAGCCTGTTTTCAACTTTCTTGTACAATTTCAACTAAACTCATTCTTTCCAGCAGAGTTAATCATACAAAACAAAAGACACTGGGTTATTTGAACCCAACGTTCCACTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20254
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024367 | Essential Splice Site | 282 | 1281 | 7 | 26 |
ENSDART00000133509 | Essential Splice Site | 282 | 1280 | 7 | 26 |
The following transcripts of ENSDARG00000003512 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 17175615)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 18118455 |
GRCz11 | 4 | 18107431 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTTTATGTTTGTCTGTTTATTGTATGTTAATAAATTGTTTTTCCCTCT[A/G]GATTATATGATGTCAGATTGTGACAGAGGGAATTTTCACGAAGACTTAGC
Long Flanking Sequence:
CTAAATCACCCGTCATCCTACAGAACAGAGGCGAAATTAAAGTTTTCCTCCCTGCCTCTGTGTGGGCAGTGAAGCAGAATCCTTAGCGTGAAGGAATCTCAAAATCACACTTGCTGTGGTTTTAAAATCTACAGTCTTTGACGGGATGCTGAAACTATTGTTGTTTTCATGGTCACCGTGTGGCTTGTGCAACCTATAGTTGTTTGGAGCTACAATTACAACCACCTCATTTTGGTTTTCACCAACCTAAAATGCCTTTTTTCTTTTCTTTTTTTTAAAGAGAGAGATTGAAAAAAGGGGGAGTAAATAAGACAAAATGGAATGTATATACATAGTTACTTGCTTTCTTTCAGGTCCTGTATAGAAATCACACTGTAAGGCTTTAGTTATCCTCAACTATAACTTAACAATCGTATCCTAACCTTGCTGGCTCATGTCAAATGTGTTTTTGTGTTTATGTTTGTCTGTTTATTGTATGTTAATAAATTGTTTTTCCCTCT[A/G]GATTATATGATGTCAGATTGTGACAGAGGGAATTTTCACGAAGACTTAGCACGACATCGGCCAATACCTACACCACGCACTTCAATACCGTCTCCTGTGCCCTCACCGTCTCTACGGCATAAAAGTATGTTTATTTTATTGCTTTAAAACAGTACTTTTAATAATAACAGTGACTAATCATGCTTGTATTTACATAATATATTTGTGTATGTGTGTGTGTTCACACACACACACACACACACACACACACACATGGTCAAGACGATCTGCTGCAGTTCAAACCGAGCATCAGAATGGGGGTAGAAACATGATTTAAGTGATTTTGAACATTGAATGGTTGGGAGTATTTCAGAAATTGCTAATCTACTGGGATTTTAATGCACAACCATCTCTAGGGTTTACCGAAAATGGTCTGAAAAATAGAAAAAATCCAGTGAGCCGCAGAGCTGTGGGTGCAAATGCCTTGTTAATGCCAGAGGTCAGAGGAGAATGGCCAGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2161
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024367 | Essential Splice Site | 423 | 1281 | 10 | 26 |
ENSDART00000133509 | Essential Splice Site | 423 | 1280 | 10 | 26 |
The following transcripts of ENSDARG00000003512 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 17153738)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 18096578 |
GRCz11 | 4 | 18085554 |
KASP Assay ID:
554-2938.1 (used for ordering genotyping assays)
KASP Sequence:
CTATATATTTATCTGTTATGACTCTATTTTCTGTCATSTTGTCTGTTTGC[A/T]GGACAAGCGATGTGTTGAAATTGCCCATTCTCCATCACTGGATGTGTTTT
Long Flanking Sequence:
GTCTTTCTTTCAATCCCATGTGACGAATGGCCTTGCCCTTGTGCTCGGTACATGATGAATGTGTCTAAAGCCTTCTGTGTGATGCAGGATTTGGGACTGACGGCTAGAGTAATAGTCGTCTGAGGAAAAAATCGATGGGGTTCATGGGAAATAAGTGCGATGACAATGAGGGCAGCTTGGCCTGCGCTGTGTTTACTTTGAGAAATGGTTGCCCTCACACACCTGCCGCGTCGCACCCATAAAGACAAACAGGCAGCGGGAGGTGATGGCAATGTTTCACTGAAGATGATGGAGAAGGATGTCATGGGTGGATGTTTATCCTTGTCATTCTGCCTCTGAGATGAAATAGTTTGTCTAGGTGGGGAGGAACTCTCAGTTGGATACCGATTGTTTTTTCCCCACTCTTTTTATTGCGTGTATCGCCTTTTATGTGATGTGTTTATGTGTTACCTATATATTTATCTGTTATGACTCTATTTTCTGTCATCTTGTCTGTTTGC[A/T]GGACAAGCGATGTGTTGAAATTGCCCATTCTCCATCACTGGATGTGTTTTTACCAGAGGATGAGGACAACCCTTACGAGTCAGTGGCTACAGCTGTCACACGCAAGCCCTGCTCTCTAGACATCAACCTTCACAACGCCTGTCCTCGCAACGGTTAGTAACTGCAAATCGATGGAGGAAAAAAATCAATCAGCAGGTGGCTGATGTAAATAATCTGCTCTCTAACTCATGGTTTGCACGTATTGGAGAAAACTCACTGTTTACACTACATGAAGTCATGAAACCGAAAATCAATTTTCCAATTCCTCAATTTACTTTCAAACAAGCAATTCATTTAGTTTAAAAGAGCAGGATTTTTGATTATAATGTGAAATGTTCATAAACATATAATGAATATAATATAATAATAATTTAATAATTATATAAAACATATTATAAATATTTAAGACACAGTACACTCTATGCACAATGGATTAAATCAATAGATAAGTATAGTATTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16530
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 |
---|---|---|---|---|---|
ENSDART00000024367 | Nonsense | 725 | 1281 | 13 | 26 |
ENSDART00000133509 | Nonsense | 725 | 1280 | 13 | 26 |
The following transcripts of ENSDARG00000003512 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 17067417)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 18010257 |
GRCz11 | 4 | 17999233 |
KASP Assay ID:
2259-4806.1 (used for ordering genotyping assays)
KASP Sequence:
GGAGCAACTGCACAGGTGGCTCYAKTCCAGCAAACAGYAATACAGGCTAC[G/T]AAGAAAGAGCCTGCACTCTTGGGAGGATGAGGTCTATGCCAAAAAACGTT
Long Flanking Sequence:
GCAGAAAGAAAGAATGAAGCCTTGGAAATCTGATTTGAATGATTCCTTCTCTTTTTTTCCCCCTTACAGATGAAGCAACGTACCAGAAGGAGTGCATAGAGCGAGACGACCGGAGAAACAGCCACGTTCCTGAGCAGTTCGCTGGCCTTCTTCATGGTTCATCTCCTGCCTGCGAATCTCCTGACAACCCTTACCAACTTTACGGAAAAGTGCGAAAGTTCAGTGTTCCTGAGCCTCCGCTCAGGCACGGGAATTTCCTCCGAGCACCAGAGTACTCTCCTCCCTTCCCTCGCACTGGCAGCGAGGCGTCTGCTCTTAAAACTCAAAGAGAAGTCAAACCGCAGGTAGTCTACAGGACGATTTTTCACACCAGGGTCAACCAGGGTCCAGTAACGTTTGGCGAACAAGTGGACAAGACCACAGGGGTGCATGCAAGGAACGGGGAGGCCCGGAGCAACTGCACAGGTGGCTCTAGTCCAGCAAACAGCAATACAGGCTAC[G/T]AAGAAAGAGCCTGCACTCTTGGGAGGATGAGGTCTATGCCAAAAAACGTTTTGGACCTTCAGCTGTCCCGAAACTTCTCTAAATCAGACTCTAACCTGGTGGCTGTGTCTCCCATTGAAGAGGAGCAGTGGGGTTCCAGAGGGCAGAGCAGCCCTGGTAAAAGCAGCCCCAGCAGACTAGAGCGAACCCCCTCCTTTACCGCAGAGTGGGAAGAGGTAATAACGTTTTAATTACCAGCTAATTGTGGAATCATTTCCACTTAATTAATTCACTTAGCTTGAAGTAACCAAGCTGACTGGCTTGAAAGGTTTTCTTTGGATGCTCGGCGTATGGTTTTGATGTGTGATGCAAAATCCTGCCCTTTCGCCAGAATTTATTCAACAGCGTTGTCATGACAGCAAAATGATTTTTAATGCGTTTCTTTAATATTGTGAATATGCATAATGATAGGCCCGGGACATGGTTTGTGTGTCTGTTTTGCACTGATGGTGATCTGTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15624
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 |
---|---|---|---|---|---|
ENSDART00000024367 | Nonsense | 877 | 1281 | 16 | 26 |
ENSDART00000133509 | Nonsense | 877 | 1280 | 16 | 26 |
The following transcripts of ENSDARG00000003512 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 17045893)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 17988733 |
GRCz11 | 4 | 17977709 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGTGGAGGACCAGGACCTGCTGGAGATTGGGATTTTAAACTCTGCCCAC[A/T]GACARCGACTTCTTCAGGCTATTCGCCTTTTGCCCAGGGTGAGTAGAGAC
Long Flanking Sequence:
GTATTAATTGTCATTATTACTGTCATCATCATAATTATGATCACTTGTTCATTTGTTGCTACTGTTGAAGGCTGTTGTTCCTGAGGACTGTTTTTGTAATATGACAAATTTTGTTTTTATATTATTTTGCTGTAGTGCAGTGATGTTGTGGAACAGTAATTTTTTTTTGTATTATTTATTATTTAATTTTGTTAATTTTTTATTTAATTTTATTATTATGTTTTGTTATCACTTTGGCACATTGGTGTACATTATAGATTTATATAATTAATAGATGTAATAAATGTCAAACTGATAAAATTATATTTGCATACTGCAGGGCATTCATTTGTGTAGCTCATTATTATAACATCTGCTTTCATCTTCAGCATAATGTAGCAATGAATTTAATAAATAATATGTATTTCATTTTACAATTGTATGCCCTTTTTTCCCTGCAGGGCAGTAATGTTGTGGAGGACCAGGACCTGCTGGAGATTGGGATTTTAAACTCTGCCCAC[A/T]GACAGCGACTTCTTCAGGCTATTCGCCTTTTGCCCAGGGTGAGTAGAGACATCAGGGACGTCCTACAGCTCACAAGAGACTGCTGCCAGCTCCAAAAATACCTGCTAACAATGCATTTAGAAGCAGGCTTATTCTTAAAGCATAATAAGAAACGGTCCATCACACCTTATAAACATGTACATGTTTTCCTTTGCAAAAAATCCAATGAATAATTTAAACCTGATCATTTCAGATTATTTAAAATATTTGTCAAAATTCATTAACTCAAAACAAAATGAGTATTTCTTTTGACTCAACGCAATTTCTCACAATGTTGGTTACAATTTAATCATAAAATCAAATAAACTCAGTTGTGCATTAAAAAAAAAATCTAAACAAAGTGTTAGTCAGAAGCAGCATTTGTTAATAGACTGGTTTATGAACTTACGTGGTTATGCACTTATTTCACCTACACTATAGAGCAGAGATGCCCAAACTAGGGCCCAAAGGCCAAAATTGGC
Associated Phenotype:
Not determined