ZMP
zgc:153917
Ensembl ID:
ZFIN ID:
Description:
centaurin beta 1-like [Source:RefSeq peptide;Acc:NP_001074048]
Human Orthologue:
ACAP1
Human Description:
ArfGAP with coiled-coil, ankyrin repeat and PH domains 1 [Source:HGNC Symbol;Acc:16467]
Mouse Orthologue:
Acap1
Mouse Description:
ArfGAP with coiled-coil, ankyrin repeat and PH domains 1 Gene [Source:MGI Symbol;Acc:MGI:2388270]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa30628 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa9629 | Nonsense | Available for shipment | Available now |
| sa26928 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa30628
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000052902 | Essential Splice Site | 95 | 757 | 5 | 24 |
| ENSDART00000121993 | Essential Splice Site | 95 | 772 | 4 | 24 |
| ENSDART00000142891 | Essential Splice Site | 96 | 115 | 6 | 7 |
Genomic Location (Zv9):
Chromosome 7 (position 21247440)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 19837876 |
| GRCz11 | 7 | 20089844 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTAGAAAAGTTTTCTAAAAAGCTGTCAGCCATTGTTAGTGCTCAAGAGG[T/G]GAGTTGAGTTCTTCCTTTCTTTTTACTGTCACTGTTACTATAGTAACCCA
Long Flanking Sequence:
GTTCATGACATTTTGAGGTTTACCTTAGTTTGGAAAGAAATATTTGCCCAAATTAGTAAAGCTAATGTTAATGTGTGCCTAGACATTGTAAAAGATGAAAAGATAGAATAGACTTTAATGTTTTATAAAAAAAAAAAAAAAAAAAATTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTCATGTTATTTGCAATATTTAATAATATTGCTCTGCACCTAGATATACATATATTAATATGTAATATGTGCATATATTAAAATGTTGAAATTCTGTCTGACCCCAAATCTTTCAGCAAAAAAACATTTCCTTGATTGAAAGTAAAATTGGAAAAGAAAACATCCTGAAACCATTGAAAATGATTGAGAGTTAATAAACATCTAATTGAAGCTGCTTCTCTTTATTTCAGGACTGTTTAGAAAAGTTTTCTAAAAAGCTGTCAGCCATTGTTAGTGCTCAAGAGG[T/G]GAGTTGAGTTCTTCCTTTCTTTTTACTGTCACTGTTACTATAGTAACCCACTGTAAGTGCCAACAATCTGTTATGGGGATGTATTCCTGTTTTCCCTTTGCTTTTGGCCTGTCTCCCATTCCATGAATTGTGTTTCTCCAAACAGGAGTTGATCGAAACCACGCAGAAGGATGTGAAGTTGAAGCTACAGAATTTTGTTAAAGAGTAAGGCTTTTTTTACTCTTTCCTAAAGGCATTTTAGTTTTCAGTTACATGGCATTCAGGAAAAATTATTATCAATTATGGAATCATTTAATTGCACAAAAAATTCTTTATGGTGGTTAAAGGTTCTTGAGATGATTAAAATGTTCTTCACACTTGGTTAAAACAATCAACCAAGGCTCATTGGAAATATGTAATTAGGGCTACATTTTTGTGAACCGTGAAATATGTTGCTTCTGCGATGCTTCTTTGCAGCTTGTGTTGACATCAAAAAACCCCATATTAATTACTAGAGAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9629
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 |
|---|---|---|---|---|---|
| ENSDART00000052902 | Nonsense | 478 | 757 | 17 | 24 |
| ENSDART00000121993 | Nonsense | 478 | 772 | 16 | 24 |
| ENSDART00000142891 | None | None | 115 | None | 7 |
Genomic Location (Zv9):
Chromosome 7 (position 21230748)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 19821184 |
| GRCz11 | 7 | 20073152 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTCTTCAGCTCATGTGTGAATTAGGAAACACAGCRATTAACAAGATCTA[T/A]GAGGCGCGTATTGAAGAGATCACAATCAAGAAGCCTCAYCCCTCTAGTCC
Long Flanking Sequence:
ATGCTTAATTAAAAGAGCGTTTTACTTACACTTGAACCACATCTGACATGAGGCATAACGGCTTTAAAACCTTTCTTTTTTTTTTTTTAATTAAAGTTTAAGTCGACATCCAGTTGAGAAACGCTGCTCTCGCTGATGACAGTTTTTAACAGAAGTTCTAAGCAGCCTACCGGAAGGCTCTGGTCACTATGGCGCCCTCCATGCACTAATGAAGAAAAAGGTCTATACATCTAAAATTGATCTCTTTTGACTTGATGAAACCTGCAGAAACCTGAAGTCAATGGTTCCAGGTTTTCAGTTTTCATCAAAAGATCTTATAGTGATCTTCTTATAGTGTAGAAACTCATTAAGGTTTGAAACCACTTAAATGTTGTAAACAGTGTGTAAATTTTCATCTGTTTTTGTTTACTTGTCATATTTTTCTCCTTCCCTGACAATGTTTCTCATCACTTTCTTCAGCTCATGTGTGAATTAGGAAACACAGCAATTAACAAGATCTA[T/A]GAGGCGCGTATTGAAGAGATCACAATCAAGAAGCCTCACCCCTCTAGTCCCAGGTATAGTAGGTGCAGTGAGGCTTTTAATTAGCAGACTTACTTTGAATCAATGAAACTCTTTAATAATGGGATCTCTCTCTATGACTGATGTTTTCTCAGGCAAGATAAGGAGTCGTGGATTCGCTCTAAATATGTAGAGAAAAAATTCATCCACAAGCTCCCAGAGACTGGTCGAGGGCAGATTCTGCGGCGCTCCAGTGCCCGACGAAACCGATCCACCACAGAGGACAAACCCTGCACACGTCCTGCCCTTAAACCCAAACCCGGCAGGGTCACACTGCCACGACTCACCGGTACACACGAACACTGTTTGATTTCAAAGATTTCATAAACTGAAATGAAATAGTTATTGTAAAATACAAAACTGAATGTAACTACATTAAAATAGTAAAATATTAACTGAACATTGGGTAATCTGACCTGTGTGGAGGCAGACGTCCCACATGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26928
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 |
|---|---|---|---|---|---|
| ENSDART00000052902 | Essential Splice Site | 560 | 757 | 18 | 24 |
| ENSDART00000121993 | Essential Splice Site | 560 | 772 | 17 | 24 |
| ENSDART00000142891 | None | None | 115 | None | 7 |
Genomic Location (Zv9):
Chromosome 7 (position 21230401)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 19820837 |
| GRCz11 | 7 | 20072805 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTGCCCTTAAACCCAAACCCGGCAGGGTCACACTGCCACGACTCACCG[G/A]TACACACGAACACTGTTTGATTTCAAAGATTTCATAAACTGAAATGAAAT
Long Flanking Sequence:
TAAGGTTTGAAACCACTTAAATGTTGTAAACAGTGTGTAAATTTTCATCTGTTTTTGTTTACTTGTCATATTTTTCTCCTTCCCTGACAATGTTTCTCATCACTTTCTTCAGCTCATGTGTGAATTAGGAAACACAGCAATTAACAAGATCTATGAGGCGCGTATTGAAGAGATCACAATCAAGAAGCCTCACCCCTCTAGTCCCAGGTATAGTAGGTGCAGTGAGGCTTTTAATTAGCAGACTTACTTTGAATCAATGAAACTCTTTAATAATGGGATCTCTCTCTATGACTGATGTTTTCTCAGGCAAGATAAGGAGTCGTGGATTCGCTCTAAATATGTAGAGAAAAAATTCATCCACAAGCTCCCAGAGACTGGTCGAGGGCAGATTCTGCGGCGCTCCAGTGCCCGACGAAACCGATCCACCACAGAGGACAAACCCTGCACACGTCCTGCCCTTAAACCCAAACCCGGCAGGGTCACACTGCCACGACTCACCG[G/A]TACACACGAACACTGTTTGATTTCAAAGATTTCATAAACTGAAATGAAATAGTTATTGTAAAATACAAAACTGAATGTAACTACATTAAAATAGTAAAATATTAACTGAACATTGGGTAATCTGACCTGTGTGGAGGCAGACGTCCCACATGCAGATGGCAAAGACATGCCAGTAAAGTTACTGATAAAAAAAAGATGGACGGGTATTAATTAAACCCAAGACATCTCAGACAACACAAACACAAACATGCATACAGCTTGCTAACATTTGTTCCATGCATTTAATATATTGCCAAAAATGGACAAGATCATAATCAATTATACAAACACAGATATATTCTATATATTATTTTGTTTTCATTATTAATTAATGTAGTTAAATACAATTTCATGTAATACAATAAAATGTCATAAAATTCCAATTTCTACAAGCAAAATATAGTGGAAAAATAATTCATTTTAATTAATTGTTGGAACCAATACAGCAGCACTACTCTGTG
Associated Phenotype:
Not determined