ZMP
ankrd1b
Ensembl ID:
ZFIN ID:
Description:
ankyrin repeat domain-containing protein 1 [Source:RefSeq peptide;Acc:NP_001095858]
Human Orthologue:
ANKRD23
Human Description:
ankyrin repeat domain 23 [Source:HGNC Symbol;Acc:24470]
Mouse Orthologue:
Ankrd23
Mouse Description:
ankyrin repeat domain 23 Gene [Source:MGI Symbol;Acc:MGI:1925571]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa9471 | Essential Splice Site | Available for shipment | Available now |
| sa19034 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa35242 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa9471
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 |
|---|---|---|---|---|---|
| ENSDART00000113810 | Essential Splice Site | 124 | 283 | 5 | 9 |
| ENSDART00000113810 | Essential Splice Site | 124 | 283 | 5 | 9 |
Genomic Location (Zv9):
Chromosome 12 (position 17514003)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 16393713 |
| GRCz11 | 12 | 16442523 |
KASP Assay ID:
2260-5185.1 (used for ordering genotyping assays)
KASP Sequence:
AAATTCCCCTGACAGCACWTACATCTAAAGAACTAAAYGTGTTTCCTTTA[G/A]TTCAATCGTACAGCTCTACACAGAGCTTGCTCACAAGGAAACGTGGAAAT
Long Flanking Sequence:
CTGAAACCCTACAACAACCTTCAGTGTGAGGGTGAAGTCATTCTCAGCGGCCTTGATGTAAGATTTAAGCATGAATTAGCATTTTTCACAGAGCATAACATGATTAATAGTGTATTTAGAAATGTCTGATTTTGCAGACTGACAACAGCACTAATGACCTCCAGGTTGTGAAAAACAGTGTGCAGACAGAAGTCTACAAAAAACAGCCCAAACAAGAGCTAGTGGTAAACATCAATCATTGAGTTTCAGAATAATCGGTATTAATCAGATTTCTCAACAAACCCCTTAAGTAATCATATCTCATTACCCCGCAGAATGATTTTGTGGATGAAGATGACTTCCTGAAGGCAGCGCTGGATAATAAATTGCCAATGATCAAAAGTTACCTCGCCAGAGGTGCAGACCCAAATGCATGTGATAATGTGAGTGTTTTACCAAACACACCTAATGAAATTCCCCTGACAGCACTTACATCTAAAGAACTAAACGTGTTTCCTTTA[G/A]TTCAATCGTACAGCTCTACACAGAGCTTGCTCACAAGGAAACGTGGAAATTGTGAACGCACTTCTGGAAGCTGGTGCTTCAATAGGAAATAAAGACAAGGTATTGTAAAATGTTTACATTTTACTTCATTATGTTTGTGAATTAAGTTTTTTCTGATAGATATATTTATTAATGCTACTTTAAATGTCAGTGCAAATATTAATAAGAGTATTTTTTTTTTTTTTTGTAAAGGCAAGTCTGAAATATACTCTTTACTATTTTAAAGAAAGGTGTCAATATAATTGAAAACCACAATTTAGGGATTGTGGGTGGCACAGTGGGTAGCACTGTCACCTCACATCTAGAAAGTCGCTGGTTCGAGCCTCAACTGGGTCAGTCAATAATATCTGGATGCAGCCTTTATGATGCAAGCTGACATTGCATAACTCAACAATGCAATGCCAGACACAATGCACACAAATCGAGTGAGTGACGACACTGTGAGGGGTAGGGTTAGGGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19034
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 |
|---|---|---|---|---|---|
| ENSDART00000113810 | Essential Splice Site | 124 | 283 | 5 | 9 |
| ENSDART00000113810 | Essential Splice Site | 124 | 283 | 5 | 9 |
Genomic Location (Zv9):
Chromosome 12 (position 17514003)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 16393713 |
| GRCz11 | 12 | 16442523 |
KASP Assay ID:
2260-5185.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAATTCCCCTGACAGCACTTACATCTAAAGAACTAAACGTGTTTCCTTTA[G/A]TTCAATCGTACAGCTCTACACAGAGCTTGCTCACAAGGAAACGTGGAAAT
Long Flanking Sequence:
CTGAAACCCTACAACAACCTTCAGTGTGAGGGTGAAGTCATTCTCAGCGGCCTTGATGTAAGATTTAAGCATGAATTAGCATTTTTCACAGAGCATAACATGATTAATAGTGTATTTAGAAATGTCTGATTTTGCAGACTGACAACAGCACTAATGACCTCCAGGTTGTGAAAAACAGTGTGCAGACAGAAGTCTACAAAAAACAGCCCAAACAAGAGCTAGTGGTAAACATCAATCATTGAGTTTCAGAATAATCGGTATTAATCAGATTTCTCAACAAACCCCTTAAGTAATCATATCTCATTACCCCGCAGAATGATTTTGTGGATGAAGATGACTTCCTGAAGGCAGCGCTGGATAATAAATTGCCAATGATCAAAAGTTACCTCGCCAGAGGTGCAGACCCAAATGCATGTGATAATGTGAGTGTTTTACCAAACACACCTAATGAAATTCCCCTGACAGCACTTACATCTAAAGAACTAAACGTGTTTCCTTTA[G/A]TTCAATCGTACAGCTCTACACAGAGCTTGCTCACAAGGAAACGTGGAAATTGTGAACGCACTTCTGGAAGCTGGTGCTTCAATAGGAAATAAAGACAAGGTATTGTAAAATGTTTACATTTTACTTCATTATGTTTGTGAATTAAGTTTTTTCTGATAGATATATTTATTAATGCTACTTTAAATGTCAGTGCAAATATTAATAAGAGTATTTTTTTTTTTTTTTGTAAAGGCAAGTCTGAAATATACTCTTTACTATTTTAAAGAAAGGTGTCAATATAATTGAAAACCACAATTTAGGGATTGTGGGTGGCACAGTGGGTAGCACTGTCACCTCACATCTAGAAAGTCGCTGGTTCGAGCCTCAACTGGGTCAGTCAATAATATCTGGATGCAGCCTTTATGATGCAAGCTGACATTGCATAACTCAACAATGCAATGCCAGACACAATGCACACAAATCGAGTGAGTGACGACACTGTGAGGGGTAGGGTTAGGGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35242
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000113810 | Nonsense | 267 | 283 | 9 | 9 |
Genomic Location (Zv9):
Chromosome 12 (position 17517377)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 16397087 |
| GRCz11 | 12 | 16445897 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTGTATTCTGCAGGAGGGAAAGTCACCTATGGACAAGGTGTGTGAGTG[G/A]CAGAATGGAGCAAAATCAATCTTTGACAACTTTCAAGACAATAAAAAATA
Long Flanking Sequence:
TTATTAAACATAATTTTGTGCTTAACCAAAAACATAATAAACTGGAACAAAAGTAATTGATACATAAAACCAAACACTGTTAAACACCTAAAATGATTTCAAAGTCAGGGTAAATGTCAGATAGACTAGCCGAGGAAAGCCTGCTTCACCGTAAAATAGTTAATTCTTCAAGATTATCCAGTGAAATCACAGTAATGTACTTTACTATCTACTGTGAAGTTACAATATATGGCTTTAATTTCACAGTAATTTAATGTTACAAAAAACGAAAGTTAATTACTGTGAACAACTTCAACGGAATTTGTTGTGAATTTACATAGAGTATTTTACTGTGAAAGTAATGCAAATTTTAAAAAAGAAATTTACTGCGAATTTAAGGTCAAATTTTTCAAAATGCAAAAAAAGTAATTTTAGCAAAGGTTCAGGACTATTGCTTGCTCACGCTTATTATTTTGTATTCTGCAGGAGGGAAAGTCACCTATGGACAAGGTGTGTGAGTG[G/A]CAGAATGGAGCAAAATCAATCTTTGACAACTTTCAAGACAATAAAAAATAAATGCATCACATGACCACCTGGACAACTCTGGGCTTAATATCATCCAAATAAACTATTATGAGATATTATGAGCCTGCATATTAAAATCTAATATGTGAAGAAGATATATTATTGAGTTATAAGAATGTTTTGAGAGTTTTGGCAAAGCACTTCAACTTTTTTATTATTAAATTATAGAGAAAACAGAAAGGAATGCGAAGCCTAAATAAATATCGTCTTCTTTTGTTGACATGGGAATACAAATGAAACTGCTGAAATTAAATCATGAATGATAGGTGTGATTTGATATTCCAAAACTTTATTACAGAATGTGCTTTTTGTGCATGACGTCTGTACAGAATATGACATAAGAATTTTTGTACTATTATATGTAAATTTTGCTTGCAATTCCATTAAACCTTAACTAATAAAATACATTTTTAACACATCTGCGTCATCTTTCATTTTTT
Associated Phenotype:
Not determined