ZMP
si:dkey-121a11.3
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:A5PME5]
Human Orthologue:
KIAA1614
Human Description:
KIAA1614 [Source:HGNC Symbol;Acc:29327]
Mouse Orthologue:
BC034090
Mouse Description:
cDNA sequence BC034090 Gene [Source:MGI Symbol;Acc:MGI:2672904]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa24132 | Nonsense | Available for shipment | Available now |
| sa37481 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa24133 | Essential Splice Site, Missense | Available for shipment | Available now |
| sa10557 | Nonsense | Available for shipment | Available now |
| sa24134 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24132
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 |
|---|---|---|---|---|---|
| ENSDART00000105667 | Nonsense | 114 | 1060 | 1 | 9 |
| ENSDART00000136458 | Nonsense | 114 | 130 | 2 | 2 |
| ENSDART00000142454 | None | None | 747 | None | 7 |
Genomic Location (Zv9):
Chromosome 22 (position 16676222)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 16427980 |
| GRCz11 | 22 | 16454250 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTTGGGGCTCCAGCAGCAGCGATGAAGACGGTGAACCTCGCAAACCCT[T/A]GATGTTCCTCACCCGAGACTCCAATCCAGAACTTGAATATGATCCCATCT
Long Flanking Sequence:
TATCCAAAAAGTTGTAGCTCTCAGAAAATTCTCACATTGCAAGCATTCGAACATATGTTCATATGAATAATCCCAGTAATTAGTCAATGATTGTCTCTTAATGGAGTCTCTATCCCTCCCCTCAGCCACCATAATGTTCAACTGACTCCCTGATTCAACCATGGAGGACGCAGTGCCCTCTGAGGATGCTGAACCTCTGACTGCATCCTCCAAAAACACAGACATCCATGATGCGGAGCCAGAGGATGGGCGTCCTTCCAGCACTAGCCCGGAGCCTGGCTCCACATCCTTTCCCTCTAATCAGCAAACTCATGGCTCTGCCGTATCAGCCCTGCAGTCCAAAGTCAAGGCCCTCTCAGAGCGCAAAGTTGTCTGGAAAGAACCTGGAAGCAAGAACCAGGACAAGTGGGTGGTTCCTGGGACCTTCAGGCTGGGATACGCCCTCACAGATGCTTGGGGCTCCAGCAGCAGCGATGAAGACGGTGAACCTCGCAAACCCT[T/A]GATGTTCCTCACCCGAGACTCCAATCCAGAACTTGAATATGATCCCATCTCTTCTGAAGCCTTCCTGGCAGTTCCCCGTGGCCTTGGAGAAGGAGCGAGTCTGGAGAACCTCTCGAATGATGCTTGCGGAGCACAAGATGACTCTTCAACATCCCATAAACCTTGGATGCCACCAAAGTATTTCTGGAGGTCCATTAGACAAGAGAAGTCGGTTCCAAATGGAGATGTTCCGGTGGGGAAAGATGGAGGAAGCTTACCTTGGGCTGGTGGAGCCAAAATGCAAAAGTTTCCAAGGGAACTTCAAAGGTCTGACAGTCTGGAGAGTCACCTGCGCAAGTACAATCATGGTGAGGTGGGACAGAGTGGACTGTGGAGAGCCGACAGCTTGGAGAGCATGTGCAGCAATGGAAGCTCCCTGTCTCTGGCCGAGAGAGTCGAGATGAACCGTGGACTTCTTAAACAGATGCTGCAGAAAGCCCAGAACAAAGATCACATACCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37481
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 |
|---|---|---|---|---|---|
| ENSDART00000105667 | Nonsense | 590 | 1060 | 4 | 9 |
| ENSDART00000136458 | None | None | 130 | None | 2 |
| ENSDART00000142454 | Nonsense | 293 | 747 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 22 (position 16686192)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 16437950 |
| GRCz11 | 22 | 16464220 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAACATTTCAGAAGCTAAAGAAGAAGGTTCGAAAATTTGACAGCAAGCGG[G/T]AATCTTTGTATGTAAATGGCCTCAGGACTCCATCACCTCTGGACTGCAAC
Long Flanking Sequence:
AGGATGCAGAGGTGCGCTACCTAGAGAGGCTACGCCAAAGACGCAGGGCTGGAGAAAGAGCGCAGGGCTTGTTGGTATCAAAACCCACCTTGTCTTCTTACATCAATGGAAAGGCAGAGACTGGACATGGGTCACATGAGTCAATATTTTGGAAGACAAAAGCCAAGAAGAGTTTGTTAAATGGCAAAAGTCCTGAGGCACTAAACAGGTCATGCAACTCTTGTGGGATCTTTTTAAATGAACCTCAAGGACCTAGCTTGAACTCAAATACTCTGTCCTTACCTAATGGGGAAGTTGAAGGGAAGAAGATACCATGTTGGGTTGCTCCCACCCTTCCCAACCGGCTTGTCCGGATTGAACAGATTAAGGAAACATACATTGGGACAAGTCCCGCTATTGTGCACAGCGATGGAACACACTGCAGCCCTTCGGATAACAGTAATGGTAGAGGAACATTTCAGAAGCTAAAGAAGAAGGTTCGAAAATTTGACAGCAAGCGG[G/T]AATCTTTGTATGTAAATGGCCTCAGGACTCCATCACCTCTGGACTGCAACAAACTTGCAACACCCAACGGAACTCAAATGTATCTCTTGAATGGAGTAGCATTGCCACTCAATCCCTATGCCCCAGATACACTTGGACAGAGAATCCCGGCCACATCCAGCAAAGGTCCCGTGGCACCTCCATTACCCCCCAAAGCAGAGCCACCCAGTTCTCAGCCAGCCCAGCCAACCCCTCCACCTCTACAACCCAAAAAATCAGCCCTGAAATCCAGCTCCAAGAATCGCACTAATGATCCGCGGACTGTCACAATTATGCCTTCGTCAGAGTACCACATGGTTCATCTGGACTCCACAGACGCTGGGGGCACTGTGGACAATTGTCCTCAGGAGCAGACTCCCCCTGTTTTGGGTTACTGGGAGGACAGATCTGTAATGGTCACCCCTGGAGCCTTACTCAGGACGAGCCCAGTTCTGTGTGCTCGAAATTTTCCTGTACAAGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24133
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:
Essential Splice Site, Missense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000105667 | Essential Splice Site | 897 | 1060 | 6 | 9 |
| ENSDART00000136458 | None | None | 130 | None | 2 |
| ENSDART00000142454 | Missense | 601 | 747 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 22 (position 16690264)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 16442022 |
| GRCz11 | 22 | 16468292 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACACCACCACCAGCTGAAGAAAGCCCCGTCACTGCAGACGATACGACTG[G/T]TTAGCATCTGCCTTAAAATTGGATATGTCTGTTTACATGCTACTAATGAA
Long Flanking Sequence:
TGCATGTCGCTGCATCCCAAATTTCAAGCTTGCTAAACTCTGACCTGTGAATTCACGTCACGTGAATGTGTGAGACCAATCGAGGATCAAAACCTGACCACTCAAAGCAAAATACTCAAACTCTAGTGTGACCGCAGCTTTAATCGTGTCAGAGAACTAAAAACTGTCATCAATGTACTGAATGGACTGAATGTGAAAAGAAAAGTAAGCACACTGAAATGACCTGTTATGGCTTTTCCAGAGCGGTAACAGATGCTGATCAACGGGAAGGTCGACCCAAGCTCTCCCTGCGGAGGTTTTTCTCTGCCATGGGGCTGAACAGTGTGGGGTTGCTGGGAAAGGGTCGATCCAGCAGCATGGATCAGCTTAGCCTGCACCCCAAACCCAACTCAAACCTAAACCAAAACTCCAGGCCCACGTCGCCCTCGCCCTCCCCCAGCCCCACACACAGACACCACCACCAGCTGAAGAAAGCCCCGTCACTGCAGACGATACGACTG[G/T]TTAGCATCTGCCTTAAAATTGGATATGTCTGTTTACATGCTACTAATGAACTGTTGGTAGATCATGATGATAGTATGTGAGCTGAACTGACAGTATCATTTCTTATCACTAGGGGTCTCCATTTCTCCAGCTGAGGAGATCTTCCTCTGCTCAAAACCTCCAAATCCCTAGGAAAAAAACGGATCGCTCTTCTGCATACACTCCAGGAGAACAACCTTGTAGTCCTGTATTAACCAGGTACATATTTTATACATTATATAAATTATTAACACTTTGATTTGGTTCATCACTTTTATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATGGGTGACATGGTGGTTAGCACTGTCGCATCACAGCTGGTACAAGTCCCCGCTGGGTCAGTTGGTATTTCTGTGTGGAGTTTGCATGTTCTCCTCGTGTTCCAGTGGGTTTCCTCTGGGTGCTCCGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10557
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 |
|---|---|---|---|---|---|
| ENSDART00000105667 | None | None | 1060 | None | 9 |
| ENSDART00000136458 | None | None | 130 | None | 2 |
| ENSDART00000142454 | Nonsense | 609 | 747 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 22 (position 16690290)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 16442048 |
| GRCz11 | 22 | 16468318 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCGTCACTGCAGACGATACGACTGGTTAGCATCTGCCTTAAAATTGKATA[T/A]GTCTGTTTACATGCWACTAATGAACTGTTGGTAGATCATGATGATARTAT
Long Flanking Sequence:
AGCTTGCTAAACTCTGACCTGTGAATTCACGTCACGTGAATGTGTGAGACCAATCGAGGATCAAAACCTGACCACTCAAAGCAAAATACTCAAACTCTAGTGTGACCGCAGCTTTAATCGTGTCAGAGAACTAAAAACTGTCATCAATGTACTGAATGGACTGAATGTGAAAAGAAAAGTAAGCACACTGAAATGACCTGTTATGGCTTTTCCAGAGCGGTAACAGATGCTGATCAACGGGAAGGTCGACCCAAGCTCTCCCTGCGGAGGTTTTTCTCTGCCATGGGGCTGAACAGTGTGGGGTTGCTGGGAAAGGGTCGATCCAGCAGCATGGATCAGCTTAGCCTGCACCCCAAACCCAACTCAAACCTAAACCAAAACTCCAGGCCCACGTCGCCCTCGCCCTCCCCCAGCCCCACACACAGACACCACCACCAGCTGAAGAAAGCCCCGTCACTGCAGACGATACGACTGGTTAGCATCTGCCTTAAAATTGGATA[T/A]GTCTGTTTACATGCTACTAATGAACTGTTGGTAGATCATGATGATAGTATGTGAGCTGAACTGACAGTATCATTTCTTATCACTAGGGGTCTCCATTTCTCCAGCTGAGGAGATCTTCCTCTGCTCAAAACCTCCAAATCCCTAGGAAAAAAACGGATCGCTCTTCTGCATACACTCCAGGAGAACAACCTTGTAGTCCTGTATTAACCAGGTACATATTTTATACATTATATAAATTATTAACACTTTGATTTGGTTCATCACTTTTATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATGGGTGACATGGTGGTTAGCACTGTCGCATCACAGCTGGTACAAGTCCCCGCTGGGTCAGTTGGTATTTCTGTGTGGAGTTTGCATGTTCTCCTCGTGTTCCAGTGGGTTTCCTCTGGGTGCTCCGGTTTCCCCCACAATCCAAAGACATGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24134
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 |
|---|---|---|---|---|---|
| ENSDART00000105667 | Essential Splice Site | 939 | 1060 | 7 | 9 |
| ENSDART00000136458 | None | None | 130 | None | 2 |
| ENSDART00000142454 | None | None | 747 | None | 7 |
Genomic Location (Zv9):
Chromosome 22 (position 16690502)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 16442260 |
| GRCz11 | 22 | 16468530 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTCTGCATACACTCCAGGAGAACAACCTTGTAGTCCTGTATTAACCAG[G/A]TACATATTTTATACATTATATAAATTATTAACACTTTGATTTGGTTCATC
Long Flanking Sequence:
CAGAGCGGTAACAGATGCTGATCAACGGGAAGGTCGACCCAAGCTCTCCCTGCGGAGGTTTTTCTCTGCCATGGGGCTGAACAGTGTGGGGTTGCTGGGAAAGGGTCGATCCAGCAGCATGGATCAGCTTAGCCTGCACCCCAAACCCAACTCAAACCTAAACCAAAACTCCAGGCCCACGTCGCCCTCGCCCTCCCCCAGCCCCACACACAGACACCACCACCAGCTGAAGAAAGCCCCGTCACTGCAGACGATACGACTGGTTAGCATCTGCCTTAAAATTGGATATGTCTGTTTACATGCTACTAATGAACTGTTGGTAGATCATGATGATAGTATGTGAGCTGAACTGACAGTATCATTTCTTATCACTAGGGGTCTCCATTTCTCCAGCTGAGGAGATCTTCCTCTGCTCAAAACCTCCAAATCCCTAGGAAAAAAACGGATCGCTCTTCTGCATACACTCCAGGAGAACAACCTTGTAGTCCTGTATTAACCAG[G/A]TACATATTTTATACATTATATAAATTATTAACACTTTGATTTGGTTCATCACTTTTATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATGGGTGACATGGTGGTTAGCACTGTCGCATCACAGCTGGTACAAGTCCCCGCTGGGTCAGTTGGTATTTCTGTGTGGAGTTTGCATGTTCTCCTCGTGTTCCAGTGGGTTTCCTCTGGGTGCTCCGGTTTCCCCCACAATCCAAAGACATGTGGTACAGGTAAATTGAATAAAACTAAATTGGCCGTAGTGTCTATGTTAATGAGTGTGTATGTATGATTCCCAGTAATGGGTTGCCGCTGGAAGGGTATCTGCTGTGTAAAACATATGCTGAATGAGTTGGCGGTTCATTCCGCTGAATAAAGGGATTAAACTGAATGAAAATTAATAATATAATATAATATAATATAATATAACATTTTGCCA
Associated Phenotype:
Not determined