ZMP
si:ch211-152c12.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate mouse mitogen-activated protein kinase binding protein 1-like (M
Human Orthologue:
WDR62
Human Description:
WD repeat domain 62 [Source:HGNC Symbol;Acc:24502]
Mouse Orthologue:
Wdr62
Mouse Description:
WD repeat domain 62 Gene [Source:MGI Symbol;Acc:MGI:1923696]
Alleles
There are 8 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa11070 | Nonsense | Available for shipment | Available now |
| sa16137 | Nonsense | Available for shipment | Available now |
| sa22583 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11070
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000084850 | Nonsense | 164 | 1478 | 5 | 31 |
| ENSDART00000099509 | Nonsense | 175 | 1519 | 5 | 32 |
| ENSDART00000114410 | Nonsense | 125 | 1439 | 4 | 30 |
| ENSDART00000143726 | None | None | 252 | None | 6 |
Genomic Location (Zv9):
Chromosome 15 (position 5483202)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 5626929 |
| GRCz11 | 15 | 5614780 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGCTATATAGTGTCTGTGGGATACCAACACGACAGGACTGTCAGCGTCT[G/A]GGAGTGGAAGGTGGGTTTTATCTGCCCRACTRCTATGAAGAGCTGYGTTT
Long Flanking Sequence:
CAATAAGTAAACAGTTCAATGTGGTGCAGTGAATGTGCAAATTTTAAACGTGCAAAGGTTAAACAGTGCAGTTATTGCGAGGAGTTTAAGTTAGAGGAGAGTGGGGGGTGTATTGGGGGGGGGGGGGGGGGGGGCAAAAGAGTCAGTGGGGGGCAGAGTTCAGGAGGGAGACAGCTCTGGGGAAAAAGCTATGTATTTATGTATTCACTTGTTTGTTGTTTTTAATTGTTTATTTATCATAGAAATGTTTTTGCCAAAAATAGCCTTGGTTGCTGACATGGCATTAAATAAAAAATTCATTACATGCTCCTTGTCTCTATTTTCTTCTGTTGCTGGACAGAGTGGGCACATGCCCTGTGTGCGGGTGTGGGATGTGGCAGAGCGGACGCAGGTGGCAGAGGTCCAGTGTCATAAGTATGGGGTGTCATGTGTGGCATTCTCCCCCAACGGGAGCTATATAGTGTCTGTGGGATACCAACACGACAGGACTGTCAGCGTCT[G/A]GGAGTGGAAGGTGGGTTTTATCTGCCCGACTACTATGAAGAGCTGTGTTTAATCCTTGAAAAATGCTAAACCCTTCATGTATTTGGAGGAATAATGTACATGACCGAAGTGTTTTGAGAGCCTGGAAAATTCAATCAGGGTTAAAAGTTTTTTTTTCCTTCTAGCATACAAAAATGTGATTTTGTGAAAATGGTGAAATACTGACCTGGCATTAAAGGGATAGTTCATCCAAAAATGTGAATTTTCTTAATTTATTCACCCTTTACTTGTTGTAAACCTGTTGGATTTTTATTTTTTTTTTTTCTGTTAAACACAAAAGACATTTTGACAAAAGCTGTAAACCTGTAACCAATGGCTGTTTCTCAATTCCAAGAACGCAGAGAACGGACTTGCGTTCCTGTGAAGAGCGGTCTTGCCGGGTGTCCTCGGAAGAACGAACTCTAAAGACTGCGAGGGTAGAGAACGTGTCCTGTGAGAAGTGAGATGCTGCGTTCTTCATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16137
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 |
|---|---|---|---|---|---|
| ENSDART00000084850 | Nonsense | 335 | 1478 | 9 | 31 |
| ENSDART00000099509 | Nonsense | 350 | 1519 | 9 | 32 |
| ENSDART00000114410 | Nonsense | 296 | 1439 | 8 | 30 |
| ENSDART00000143726 | None | None | 252 | None | 6 |
Genomic Location (Zv9):
Chromosome 15 (position 5494605)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 5615526 |
| GRCz11 | 15 | 5603377 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAMKTCTACTTTTCTAGGCATTTGTTCAGTGCAAATCCAGAAGCACARTA[T/A]CCAGATACCTTGGCTTTAACYTTTGACCCCGTGACCAAGCACTTGACGTG
Long Flanking Sequence:
CAGGCGACGATGTCACCAATCAAAATTAAGGCGCCGCTTTCCGCTTATGTCTTATTGCCCATCACCATAAATTAAAATAAGGATGCATGACAGCTGAGCGGGACTCTGCAAATTAAACCATGAAGCTCTGACCAACGTGAGGAGAGTTTACTCACACATGTCTTGTTTTGGCTCTTTTGGTCTGTGTAAAAACTTTGCCGTGTGAAAGCGAACCGCACCAACAACAAAAATAACATTGTAACATTTTTAATCCCTGTTTCGGAATAAATGAATCGATTTACAGGTGTGAAAGCACCGTAACTAGCTATAATGAATATCTAAATCGTACCACTGTTACATCAGTGATTCTACAGTAACACTGGTGTAAGTAAACCCTTCAGCTGAGTATCTGTAGTTCTCAATATCATCTGTATGTTTATTTATTTCACTTTTGTATGAACATTTTTCTTTGAATTCTACTTTTCTAGGCATTTGTTCAGTGCAAATCCAGAAGCACAGTA[T/A]CCAGATACCTTGGCTTTAACCTTTGACCCCGTGACCAAGCACTTGACGTGCGTGTATAATGACCACAGCGTGTACGTTTGGGATGTGCGGGACATCAGGAACGTAGGAAAGGTCTATTCAGCCCTGTACCACAGCGGATGTGTGTGGAGTGTGGAGGTGGGTTAGTGACAGACCGTTCATGTTGATGTCAATGATTACATGCTACACCCATGCAATAATGTATGAATATTCACTGCAGACCTATCCAGAGCTTGAAGATCCATCGGCGGCCTGTTTGTCACCGGGGTCTTTCCTCACTTGCTCATCTGATAACACCATCCGCTTGTGGAGAAGCGAGTCCCCACAGAGTCACAGCGCTGCACTCGGCCTTCGACACAACCTTTATAGCCAGGTACAGACAACTGCAAGAAATCATAAATGTAGATGTCTAAATAAAGTGTGATTTCATTTTTTATAATCTCTTAATTATAAAGATGTTAATCTTTATAATCTCTTAGTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22583
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 |
|---|---|---|---|---|---|
| ENSDART00000084850 | Essential Splice Site | 1360 | 1478 | 29 | 31 |
| ENSDART00000099509 | Essential Splice Site | 1401 | 1519 | 30 | 32 |
| ENSDART00000114410 | Essential Splice Site | 1321 | 1439 | 28 | 30 |
| ENSDART00000143726 | None | None | 252 | None | 6 |
Genomic Location (Zv9):
Chromosome 15 (position 5527717)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 5582414 |
| GRCz11 | 15 | 5570265 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGGACAATCAAGATTCTGCAGATAACAACAGCATTCCAGAGGAAACGG[G/A]TAGGTTAAATACACACAAATGCCTCACTTTGTTTGAAACAGAGTTTGTCT
Long Flanking Sequence:
ACTAAACGCCTTACCAAATGTCGAGCACAGCAAAGAGAACATGATCCCACCATCCTCTCCTGTGGTTTCGTCTGCACCGCTTCATCAGTCTCCTGTCCTGGGAAACCACAGTGCCCGGGCATCTCTTCGACTGGACCTCATTGGCCACAATCGTGCCAGTTTGTCACCTGTGTCACTGAAGAGCCGCCGAGGGAAGGTCGAACATCACGATTCTCCACGGCGCCAGGCTTTAGTGACGCCCACCGAGATGAGGTCACTGGGGAAAGAGAGTCGCAAGCAAATCTCAAACATTGAGCAGAGTTTGGCCCCTTCAGACAGGCTCTCTACAGGGGCCGGGATGTTTAGCAGGAGCCCCATGGTCAGGCAAACCAGTGATACTGTGTTTGAAGACCTGCAGTCAGTGAGATCTGACCAGACGTCTGTGAGTTCTCCAATGACCAACGCAGTATCTCAGGACAATCAAGATTCTGCAGATAACAACAGCATTCCAGAGGAAACGG[G/A]TAGGTTAAATACACACAAATGCCTCACTTTGTTTGAAACAGAGTTTGTCTTGGGTGTACAGAGTAAATTACATAAGGGATACTGTACATTCAGGTGAATTTTATTGCAGATTAAAGCCCAACAGGCTTATTAGCAGCCTGACACAAAGTGGCTGTTGTATGACTTAAAGGGGAAATGAAGCACTCAGTCAAGTTTACATTATTTTGTAAATGGATTTCCACTTTAATGTAAAATATTACAAACTCGATTAATGTAAGCATTTACCAGAAGACAGCATGTTTTACTATAAATTTTCGACATAGAGCGCAGCCATTTTTCAATATCGCTGTGTCTGACATCACAGGGTTGGTTCCGTTCCCTCAGCTGAACAGATACAGTGGAAGTAAAGCACTGAACACGGAGACTGAACAGCCTAATTTAACCCAATGCGTGGAGTTGTGGACGTGGAGCTGCTGCAAATACAAGCATCAGATGTGTGTCTAACATAAAAACATATATTT
Associated Phenotype:
Not determined