ZMP
si:dkey-163f12.6
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:Q5RIY9]
Human Orthologue:
FHAD1
Human Description:
forkhead-associated (FHA) phosphopeptide binding domain 1 [Source:HGNC Symbol;Acc:29408]
Mouse Orthologue:
Fhad1
Mouse Description:
forkhead-associated (FHA) phosphopeptide binding domain 1 Gene [Source:MGI Symbol;Acc:MGI:1920323]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa27183 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa15842 | Essential Splice Site | Available for shipment | Available now |
| sa31651 | Nonsense | Available for shipment | Available now |
| sa27184 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa15135 | Essential Splice Site | Available for shipment | Available now |
| sa41187 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa27183
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000061500 | Nonsense | 35 | 961 | 1 | 22 |
| ENSDART00000135766 | None | None | 322 | None | 7 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 21930516)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 21360413 |
| GRCz11 | 8 | 21392498 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGAGATCAGAAGATCAGCGCTTTATTAGAACAGATGGATAAACTCAGG[A/T]GACAAAATTCTTCCTCTACAGGTATGAGGATGCTATTAAGTGGATGACAT
Long Flanking Sequence:
GACAAGATTTTGTCAGGTAGTGTACAGCCATTATCTTAAACACTGCATAAACATTAATTTAATGTTTCACAGAACTTTGAAAGGTTGACGTAAAACATGCATCTTTCACATTATTTATATACTTTTATCAAAATGCCCCAAATCCTTTGCATTAAAATCCATCAACAAATATTGAAAGATCATGGCCACTGAAGTCTGCTATACCAGGAAAAGGCAAAAACACTCATTACAGATAGTAATTATTCAAGTTTCTTTATATTTAAGGTTTAATTTAAGCAATGCTTGCATTTTGGTGAAGCTATTTCTCCACTTTCCAAATTCATCGAAAATCTTTCAAGGGCTAATTAATAATTAACTGCTGCGCCTCATTTCAAGCTTGATCTGTTTAATGGATGCAGATGCTGGAGCTTCAGAGATGTTCTGGAGAGATGCTTGAACAGACTGTGACTGAGAGAGATCAGAAGATCAGCGCTTTATTAGAACAGATGGATAAACTCAGG[A/T]GACAAAATTCTTCCTCTACAGGTATGAGGATGCTATTAAGTGGATGACATGTATAGGTCATTTACATTCCTGTAATGTGGAAAAAAATATATAAATACTTTATCACAGAAAACCATATTTCACACAGGGTTAAACTTAATTTATGTACATTTAAATGTCTAAAAATACACTTTATACTCCATTTATAGTTCATTTATATTCATACTAAACTTCAGTTTGAAGATATTACTACTATTAAACTGTATTTTCTGTATTTTATTTCGTACTTTCTATTCATCCATTTAAATTGTATTTTATATTGTACTTTCTATTGTTTGAGTCATGATTTCAACAAAACAGCAAAATGGTTTATAATAAAAGTTTTTGTGATTAAATTTTGAGTAATATGGATGGAAATACACTGTTTTGTAGTGAAATTACAAATAAATTATTGCATAAATAAAAATATTTTGACATTTTTGTGGCATGTCTGTATAGTGAGTAAGATAACTTGTTGGAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15842
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000061500 | Essential Splice Site | 145 | 961 | 4 | 22 |
| ENSDART00000135766 | None | None | 322 | None | 7 |
Genomic Location (Zv9):
Chromosome 8 (position 21933572)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 21363469 |
| GRCz11 | 8 | 21395554 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCAGCGAGAACAGAGAGTTCAAGAARGGCTTCAATGTACTAAATCAARGG[T/A]GAGCAAGCTTAAGAYWGGGGAAAAAGTCAGGTAAAATAACTCCTGTATCT
Long Flanking Sequence:
CATTTGCATATATTGACATATGTCAGATTTCTATGGGGTCTTTCCTTCTCTGCTACAGCAAAGCATCTGTTGCATCTGTATGTGCTTAAATTAATTCCTGTCACACATCACACTGCACTCTTCAGTAAACTGACAGAGAGCAGGTTAATACGTTTACAAGCTGGGTGAAAACAGGTTAATGTGTTTACATGATCACATGCATTGTCGGTTTATTAAATGCAATCGGGTGAAGAAGTGCATGTAAACATACTCTTATCCATTACTTACCTCCACACAGCTTCCCACAATACCCAGCTCCGGAGGCTGATGCCTTGTCCATTAGGCCACTGGGCCAGATAGTATTCATTTATGAAATTAGACGTCATGTATCTGTTAATTATGTGTGCTGTAGGAACGAGCTTCTCTGCTGACAGAGCTGGAGAAACTGAAGCAGCTTCATGAGCAAACGCAGCAGCGAGAACAGAGAGTTCAAGAAAGGCTTCAATGTACTAAATCAAGGG[T/A]GAGCAAGCTTAAGACAGGGGAAAAAGTCAGGTAAAATAACTCCTGTATCTATTTTGATAACCTATATGAAATTTCTTTAAAGTTTGACAGTTTTCGCGAGCAGATTGTCAGGATTGCACACGTTTCTGACAAGCAACCAGACCAAGAGGTATAAGAAAACATTTCAGTTTATTCTAAAGACAAGTTTACATGAAATGATTTGAAAATTGCTGAAACATTTAAAAAAAAGTTATCTCTAAATATTTGTTAATGTCATTTTAAATGTATTTTTTTCTTTTAAATAAATTCTATGGTATTATTTTAAATGTCACAGAAATTTGATTTTGATACACTTTTGTTGAAAAAAGGCTCCAATCAAACAATCAAATAATTGTGGTGCCACATTACACATGACATATACACAAAAATACATTTAACTTGCATCCATATATTGTTTTAAACTGTTTTATTTGGGAAAATAGGAATAATGGGTCAAAATAGATAACAATATAGATTATGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31651
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 |
|---|---|---|---|---|---|
| ENSDART00000061500 | Nonsense | 504 | 961 | 12 | 22 |
| ENSDART00000135766 | None | None | 322 | None | 7 |
Genomic Location (Zv9):
Chromosome 8 (position 21939062)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 21368959 |
| GRCz11 | 8 | 21401044 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAGACTGGAGGGCTTTGAAAGCAAAAGCGCATCACACACATCAGAGAAA[C/T]AACCGGAATTGGATCAAACCGTAACATCCCTCCGGTATAACACAACAGAG
Long Flanking Sequence:
AGATGGAAAAAGCAAAGATTCAAGAGGCAGAGTTAAAAAAAATGCTGCGTGAATTACATCTCAAAGAGGAGGAGCAGACGAAAAAGATAAAGCAGTGTGAGGAAAGAGAAGCAATGGCTGAAGAAGAGCAACGACAGCACCGGGTCGAGGTGGAGGAGTACAGAGAGCAGGTGCGACAGCATGCGTTCACCATTGTGGCCATGGAAAATCAAATAAACAAAGCCAAGTGGAGTGAAGAAAGATGGAGAGAGATGGAAGACCAAAGAGACTTGCTGAAGGAGCAACTCAAAGGTGAGACACAGTTTCATTTTTCACCAAGAGAGGGCGCCTTCCCAGCAGCCCTATAGGTTCCCAATTAAAGCAAATTTGTGCAACAGATTTTATGTGTCCTACATACATGTTCTGTCTTCATTATCATGTTTACATTTCTTTTTACCACAGAAGCGCTTGATAGACTGGAGGGCTTTGAAAGCAAAAGCGCATCACACACATCAGAGAAA[C/T]AACCGGAATTGGATCAAACCGTAACATCCCTCCGGTATAACACAACAGAGCACTCATGAATATTAACCACAGAAATCAATATTACCTACATATAGTATATACCTGTACTGCCTAGAGTATCGCCTGAAATCTGCACACTGTTATTCTAAACATTTGACCAATTTAGCCACTAGTTGTGATTGTAACGTAGTTTTGAAGCATTACTGTGTAAAACACTGTCTTTACTGTGAGTTGAATATTATCCATAGTGTGAGCTCTCGTTAATGCATTATGTATGATGTTCGTTATTTATTCATGCATTATTTATGAAACTGTTGCTTAATAAGTAATTACACAGTCCATGCCTCTCTCTTTAAATCATCTGATATATCAGGCACTGCTGGAATGGAGCCACAGATACATCTTTTTTTCTATCTCAATTCATTTTTACTGCTTCTGTCAAAAGCCTAAATAGTTTATACATTGTAAATACAAGCATTATCAACACATTAGGGTTATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27184
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000061500 | Essential Splice Site | 515 | 961 | 13 | 22 |
| ENSDART00000135766 | None | None | 322 | None | 7 |
Genomic Location (Zv9):
Chromosome 8 (position 21941173)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 21371070 |
| GRCz11 | 8 | 21403155 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATTGTTATTGCTGTTATAAATCAGTCATGTGGTTTCTGATGGTTCCCTC[A/T]GGGCATCTCTGGCCTTATCTGAACAGGAAGTGGTCAGTCAGAGCGAGATC
Long Flanking Sequence:
TTTATTTATATTTTTGTTAAATATTTTTACATACACAAATATATTACACTTACATTTAGATTTATGTTTAGTTACAATTCATTTTAAAATATTCAATTATATTATATGAATTATTATATTATGCATATTATTTAAATTTTCATAATTTTGGCAGCTAGCTGAAATCAAATATTACCTATTGTTATTGTTTAATTAATATATTACTTCTTGTTATACTTCTTATTATTACAAATTAAAATTATTGCTAACATTTACTAATCCATTATTGTGTCTTTGTATTTGTTAACATTAGTTAGTGCACTGTCAAGTAATATTAACATATAAATGCTGTGAAATATACTGCATTTTACTTATTAATAGTTCGGGTTAGCTAATGCACAAATTTACACAACTGTTAAGTGTTTTTTTAATGGTGAGAAGTGATTATTTTGATAAGGAACGTCTATTCAGAATTGTTATTGCTGTTATAAATCAGTCATGTGGTTTCTGATGGTTCCCTC[A/T]GGGCATCTCTGGCCTTATCTGAACAGGAAGTGGTCAGTCAGAGCGAGATCATCAATGCACTGAGTCGTGATCTGGCTTTGGCTCACGCTCGGCTCTCTGATATGACAGGTGCCACACAATCAATACAACATGACAAACAACCGCGTTCTGTGTTCTCGTTTCACAACATGCATCTCTCTGCAGGAGAACTGAGTGAACAGCAGAAGCTGGAACTGGAGAGCCATAAAGCTTTAGTGATCGATCAAAGGATTCAACTGAGCACGCTCACAAACAAGCTGAGCATGATGTCACAACTAGTCCAACAGAAAGATGAAGAAACAAAGACACTGGGAGTAAAGCTTAGGTACAGTTAAAATCCTGAAAGACCCAGTGGACATAAACACACATAAATATCAAACCCAGTGGCGTGTTGTCTTTTTTTAAAAAAAGAGCAGAAACACAACAAATGAATGAGCTTCTGAAAAGGTACTGTTCTGTTTTTGATAGACAAACTGAAGAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15135
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 |
|---|---|---|---|---|---|
| ENSDART00000061500 | Essential Splice Site | 902 | 961 | 21 | 22 |
| ENSDART00000135766 | Essential Splice Site | 263 | 322 | 6 | 7 |
| ENSDART00000061500 | Essential Splice Site | 902 | 961 | 21 | 22 |
| ENSDART00000135766 | Essential Splice Site | 263 | 322 | 6 | 7 |
Genomic Location (Zv9):
Chromosome 8 (position 21951608)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 21381505 |
| GRCz11 | 8 | 21413590 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAGAAGAGTGGGCCATCATAACTGTATACCAAATGACAGCTWYGAAAAG[G/A]TAAGCTCGATGGCAGCAGTGGATTGGTTTTGAATCAKCGTTCTGCATGTG
Long Flanking Sequence:
CGGGAGATGGAGAATCTTCAGCAAGCTTTACAAGACAGCGTCATCCAGCTGCAACGAAACAAGCAGGAACGCGATGTTACCAACAGAAATAATAGGGTATCACACATACAGGCTCACACAGAAAGTGAGAAAGACTGACTGACACTTACTCTGTGATAGGAAAAAAAAAAAAAAAGGAAACATCAAAAAGGTGACTCGTTTCTAGATCAAACTTCCATTTGACTTTCTGTTGATTACCTGAGAAAACTATTTTGACTTGTTTTACCACTGTGATGGTATTACTTTTACTTTATGGAATGACAGATAACGCATCATTTTGAACATTTTCAGACACCATTTCTCACTGTCTGTCTATAGAAAGCCATCTTTAAGTGTCTTCATAGCTCCCCAAAGTGCTGTCTATAATAAAAGTGCTTTCTCAACAGAGCCTTAATACAGAGAAAATGGACAAAAGAAGAGTGGGCCATCATAACTGTATACCAAATGACAGCTATGAAAAG[G/A]TAAGCTCGATGGCAGCAGTGGATTGGTTTTGAATCAGCGTTCTGCATGTGTTTGATCGCCTGAACATATGTAAGGTCTAAATCCATGCTGTCTGGCGCAGGCTGCCTGGGGTTTTACGGAGAAACTCCACACTGTGCAGTTAATAGATTTTTCAGCAGCACCAAACAAATTTGCTCTTTCCTGAGCTCATAATCTCACAGCTATAAATGGAGCATGAATCTGTTCCAGTTTGCTTGATGTTAGACCTAATAAAAATAGCACAGGCAAGAATACAAGAATGCATCTATTTCATGCTTTTGGCTGCCATGATAATGTACCCATTTTTATGATATTTACATACTAAATAACTAAATCCTTAAATGAATACACACAGTATGTGCAATGGTACACAGAAATGACAGAATATACCTCATGAGTTATTATGATGATAGATTTATTCAATCATACGCATTAAATAATAACCCAAATTCCAGAAAAGTTCCAAAAATCAAGAATTTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41187
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000061500 | Essential Splice Site | 902 | 961 | 21 | 22 |
| ENSDART00000135766 | Essential Splice Site | 263 | 322 | 6 | 7 |
| ENSDART00000061500 | Essential Splice Site | 902 | 961 | 21 | 22 |
| ENSDART00000135766 | Essential Splice Site | 263 | 322 | 6 | 7 |
Genomic Location (Zv9):
Chromosome 8 (position 21951608)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 21381505 |
| GRCz11 | 8 | 21413590 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGAAGAGTGGGCCATCATAACTGTATACCAAATGACAGCTATGAAAAG[G/T]TAAGCTCGATGGCAGCAGTGGATTGGTTTTGAATCAGCGTTCTGCATGTG
Long Flanking Sequence:
CGGGAGATGGAGAATCTTCAGCAAGCTTTACAAGACAGCGTCATCCAGCTGCAACGAAACAAGCAGGAACGCGATGTTACCAACAGAAATAATAGGGTATCACACATACAGGCTCACACAGAAAGTGAGAAAGACTGACTGACACTTACTCTGTGATAGGAAAAAAAAAAAAAAAGGAAACATCAAAAAGGTGACTCGTTTCTAGATCAAACTTCCATTTGACTTTCTGTTGATTACCTGAGAAAACTATTTTGACTTGTTTTACCACTGTGATGGTATTACTTTTACTTTATGGAATGACAGATAACGCATCATTTTGAACATTTTCAGACACCATTTCTCACTGTCTGTCTATAGAAAGCCATCTTTAAGTGTCTTCATAGCTCCCCAAAGTGCTGTCTATAATAAAAGTGCTTTCTCAACAGAGCCTTAATACAGAGAAAATGGACAAAAGAAGAGTGGGCCATCATAACTGTATACCAAATGACAGCTATGAAAAG[G/T]TAAGCTCGATGGCAGCAGTGGATTGGTTTTGAATCAGCGTTCTGCATGTGTTTGATCGCCTGAACATATGTAAGGTCTAAATCCATGCTGTCTGGCGCAGGCTGCCTGGGGTTTTACGGAGAAACTCCACACTGTGCAGTTAATAGATTTTTCAGCAGCACCAAACAAATTTGCTCTTTCCTGAGCTCATAATCTCACAGCTATAAATGGAGCATGAATCTGTTCCAGTTTGCTTGATGTTAGACCTAATAAAAATAGCACAGGCAAGAATACAAGAATGCATCTATTTCATGCTTTTGGCTGCCATGATAATGTACCCATTTTTATGATATTTACATACTAAATAACTAAATCCTTAAATGAATACACACAGTATGTGCAATGGTACACAGAAATGACAGAATATACCTCATGAGTTATTATGATGATAGATTTATTCAATCATACGCATTAAATAATAACCCAAATTCCAGAAAAGTTCCAAAAATCAAGAATTTTTC
Associated Phenotype:
Not determined