ZMP
si:ch211-72g23.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens WDR17, WD repeat domain 17 (WDR17) [Source:UniProtKB/TrEMBL;Acc:B
Human Orthologue:
WDR17
Human Description:
WD repeat domain 17 [Source:HGNC Symbol;Acc:16661]
Mouse Orthologue:
Wdr17
Mouse Description:
WD repeat domain 17 Gene [Source:MGI Symbol;Acc:MGI:1924662]
Alleles
There are 9 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa32719 | Nonsense | Available for shipment | Available now |
| sa32720 | Essential Splice Site | Available for shipment | Available now |
| sa38280 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa30584 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa31216 | Nonsense | Available for shipment | Available now |
| sa19535 | Nonsense | Available for shipment | Available now |
| sa39649 | Essential Splice Site, Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32719
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 |
|---|---|---|---|---|---|
| ENSDART00000110824 | Nonsense | 92 | 1292 | 2 | 29 |
| ENSDART00000136300 | Nonsense | 92 | 1283 | 2 | 28 |
Genomic Location (Zv9):
Chromosome 1 (position 39132744)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 38060006 |
| GRCz11 | 1 | 38778310 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCCAGTGCCAGCGCTGATAACCTGCTCATCATCTGGAATGTGGCTGAG[C/T]AGAAGGCTGTCGCAAGGCTAGATAACACCAAAGGTATAATCCCTACAGCA
Long Flanking Sequence:
AAACCCCGGTAAATCTTGAAACCGGTTATTGTTCCATGCCTAGTCAATATTATTAGCTCCCTTTTCTGCTTGTTTGTATCTTGCAAAACAACTAGTAAATAAATTATAAACTCATCATGGCAAAAGAAATTGAAGCTATTAGTTTTTTTTTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGCGTGCGTGCGTGCGTGCGTGTGTGTGTGTGTGTTGAAAAAAGTATATTTACTCCAATAAACAGCACTTTGGAAATATTTACTACTCTGATAAAACTAGTCACCCTATTTTTCTTCTTGATTACCACTGACTGAAATCTGTTCTTCTAGCTTGATCACAGATATAACGAGTTTAAGCTGCGAGCGATCATGTCCGAACACAAGAAGACAATCACAGCTATATCGTGGTGTCCACACAACCCTGAGGTGTTTGCCAGTGCCAGCGCTGATAACCTGCTCATCATCTGGAATGTGGCTGAG[C/T]AGAAGGCTGTCGCAAGGCTAGATAACACCAAAGGTATAATCCCTACAGCAGAATAAAGTGCATTTATTTATTCCATATATATGTATATATATATATATATATATATATATATATATATATATATATATATATATATAAATTACTCCACCTGATGTCATATTCATCAACGTAACATATTCTCAGACTAAAGATGTCTCTTTTAATTAACAATAATTTAATAGTTTTAATTCAGCTGTTTGAGGTGAAGTCTTAACTAAAGGAATTAACTAAATGAATGTTTCTCAGGTATCCCAGCATCTCTAAGCTGGTGCTGGAACGCAGGCGACAGTGTTGCGTTCGTATCCCACCGGGGTCCTCTCTATATTTGGACAGTCTCGGGGCCAGACTCAGGAGTCACAGTGCACAAGGAGGCTCACAGTTTCCTCTCAGACATCTGCCTTTTCCGCTGGCATCCACTGAAGAAGGGGAAAGTAGTGTTTGGACACACTGATGGCAGTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32720
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 |
|---|---|---|---|---|---|
| ENSDART00000110824 | Essential Splice Site | 303 | 1292 | 5 | 29 |
| ENSDART00000136300 | Essential Splice Site | 305 | 1283 | 5 | 28 |
Genomic Location (Zv9):
Chromosome 1 (position 39135784)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 38063046 |
| GRCz11 | 1 | 38781350 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGGCTTCCACGCACTTCATGTTTTAAACTCCCCACCAGCAAAGAAATG[T/A]ATGTGTGTATATTTTTACCATATAGTGCATATCATAAATGAGCACATGCT
Long Flanking Sequence:
CAGAGGAATGCTTTCTGAAGTATGTTAGAAACCGGAAGTCATTAACTTCATCCATTGTCATCCATTGTAACTTTTCATACTCTCAACATCATTGGCTATGAGTTTTCAACATTCTTCAAAATCTTTCTGTTTTGTGTTCAACAGAATAAAGAAACTCTTAAAGGTTTGGAACCACTTGACAATGAGTAAATGGTACATTTTCAGTTTTACTATCCCTTTATTGGGCTAACTTTGGATCTGATATTTAGAATTATCAACATGTGTTAAATACATTTACATTTAAATGTTAAACAGCAGTGAACCACCTTAGTTTAAAATTTACACTCAATCATATATTTACAAGTTTTAAAAAAATGTATTATTTTGAATTCCTAAGATTCTCAAGTTGGTGTGCTGAGAATATGGAACGTATCACGAGCGACTCCTCTGGATAACTTCAAACTGAAGAAAACTGGCTTCCACGCACTTCATGTTTTAAACTCCCCACCAGCAAAGAAATG[T/A]ATGTGTGTATATTTTTACCATATAGTGCATATCATAAATGAGCACATGCTTACAAAAATTCATATTTTTTATCAATGTCTCAGTTAATATTAACAATATATATTGCTTATACATAAGAAGTGTAGTCAACATCTTACAGGCATCGTAACCACCTGGTCGACCTTTTATTTATTATCATTATCATTATTTTATTTAATTTCTTATTACCATTTATCAGAGTTGTGTCAGTATATCCTCCAAGGCAAGCGAGGGCCTAAATAATATTTTCAAGCAGTGCACCTTAGAGGGTTAAGCAAATAAAACAAATACATTTACAGCCGAGAAAAAATATTGAACACGTCACCTTTTTTCTTAAAAAGCATATTTCTAAAGGTGCTGTTGACTTGAAATTTTCCCAGCATGTTGGTAACAACCAAATAAATCTATAAAGGCAAAGAAAACAAATCGAATTAGTTTACAAATTAAGTTTCACATAATAAAATCAAATGATGCAGAGAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38280
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000110824 | Nonsense | 571 | 1292 | 12 | 29 |
| ENSDART00000136300 | Nonsense | 573 | 1283 | 12 | 28 |
Genomic Location (Zv9):
Chromosome 1 (position 39141434)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 38068696 |
| GRCz11 | 1 | 38787000 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACATGAATATGTGTTTATGTTGACCAGGACTGTCCGTATCTGGGATTA[T/A]ACCCAAGACGCTTGCATTAACGTGCTAAGTGGTCACACCGCTCCAGTGCG
Long Flanking Sequence:
CTCGGTCCTGAAGGGCTGGTGTCCCGCAAAGTTTAGCTACAACTTCCTTCAATACACCTGCCTGGAATTTTCAAAAAGAGCTTGATTAGCTGGTTTAGGTGTGTCTGATTGGGGTTGGAACTAAACTGTGCAGGACACTGGCCCTCCAAGACTGAGTTTGGGCACCCCTGTTTTAAAACATCAGCTGCACAGTCTACAATTCTAGTTATTAGAAACACATGCCTCATAACATGCACAAAACTACTTCCATGTTTTTAATATGACTTCCATGTTTTTGTGTGTAAGTTACATTTTTCTCAAGATTTTATTTCACTAATAAACTGTAAAAGCCATTGTAAAATCTTGGGGGAGAACAGAGTGGATCATTCCAAGTTTTGACACCACTCTAGGGCATTTATAGAGTAGCGCTGATCAAATGGTTGTGTGGAATTGTGTGATGCTACATTCACAACACATGAATATGTGTTTATGTTGACCAGGACTGTCCGTATCTGGGATTA[T/A]ACCCAAGACGCTTGCATTAACGTGCTAAGTGGTCACACCGCTCCAGTGCGGGGTCTTATGTGGAACACAGAGGTGCCGTATCTTTTGACCTCAGGGAGCTGGGACTACACCATTCGTGTCTGGGACACCAGAGACGGCACCTGTCTAGACACTGTTTATGACCATGGAGCTGACGTCTACGGTAGTGTATGAAATTCATAATTATATACTGTAGATGGATTTCTGTGGAAGAATGACAATTCTAGTTTTTGCCTAAATTTGTTAAGACATGCTTTATCACCCTCCAGAAGTATATACTTTTTCAATAACAATCAGCTTGATTTAGGTGTCAGATACCACATGACTAAGTAACTGGATGTAAAATATTTATTTGAATTGAAATATTTAATTACAAATGATTGCTCCGATAAATCATCTCAAATAAAACGATTGCTAGCAAGGGGAGAATTGAAACTAGGCAAACATTAACAAAAGTTGCATTTATCACATCACATTTAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30584
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 |
|---|---|---|---|---|---|
| ENSDART00000110824 | Nonsense | 674 | 1292 | 13 | 29 |
| ENSDART00000136300 | Nonsense | 676 | 1283 | 13 | 28 |
Genomic Location (Zv9):
Chromosome 1 (position 39145775)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 38073037 |
| GRCz11 | 1 | 38791341 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACTCCTCTAATCGCTCCCTTAGTAGTCAACATCCTCACTGACCACAGCT[G/A]GGACGACATTATTGGCAACACAGGTTAAAACATATGAGCGTATTAAATTC
Long Flanking Sequence:
ATAGTTTGCAACCACTTACCTTTAAAAAAAAAATTAGTAAATCCAATTAACAATTTTTTTCAGTGTATTAGAATTTTAAATAGTACATGTTATTATTGCTACTTCTAAGATTGGTATAAAAAAGAACCACTAAACTACTGGTATCAGATATCACTCTGAATAATTGCCTGCAGTTAAATTTGTATTAGCTAAAATTTTAATATCAGTACATCTCTAGTTCAAAGACCTTAATAGATAATAGGGTAACAGTATTTTTTAAAGGATGCTTTATTTCCTTTATTCAGAAAATGCATGCAGTAGCATCATTGTATGTCATTTCAAGGCAATTAATACATAATTTAAACAGCTTTATGACACCATGTGATATCCCCCAGGTCTGACATGTCACCCCAGTCGTCCATTCACCATGGCTTCCTGCTCCAGAGACTCCACGGTCAGACTTTGGTCACTCACTCCTCTAATCGCTCCCTTAGTAGTCAACATCCTCACTGACCACAGCT[G/A]GGACGACATTATTGGCAACACAGGTTAAAACATATGAGCGTATTAAATTCACTCTGCATACATTGCTTTTGTAAAGGCATTAAAGCCTTTTTAATTTTTACAAATCTAGATCGTGCTATGGTTCCCGGGGCTCCTCCTTTGTTGTGTGGAAAGGTTTCCCGAGATATCAAACAGGAACTAGATAAACTCTCAAGTGACGTGCGCATGAAGAAGCTGCGGTGGTTCTCCGAGTGTTTCTCCGTGAGTCAATCTCAACACAGAACTCTCACTGGACTTTATGTAGACATCTATATAAAGGGTTATTTGCTTTCTCTGTGCAGCCACCAGGAGGGAGTCATAACCTGTGGGATCTGGTTGCTGTAATCAACGGACAGGATGATAGTCTTCTTCCGCAGTACTATGGGCAGGGCATCATGCATATGAAACACTTGGTCCGCTTTAAAACTGTGAGTGTCTAAACAGAGATGGAACTTTCTAATAATGCCACAATTGAAATGGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31216
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 |
|---|---|---|---|---|---|
| ENSDART00000110824 | Nonsense | 705 | 1292 | 14 | 29 |
| ENSDART00000136300 | Nonsense | 705 | 1283 | 14 | 28 |
Genomic Location (Zv9):
Chromosome 1 (position 39145947)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 38073209 |
| GRCz11 | 1 | 38791513 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCCGGGGCTCCTCCTTTGTTGTGTGGAAAGGTTTCCCGAGATATCAAA[C/T]AGGAACTAGATAAACTCTCAAGTGACGTGCGCATGAAGAAGCTGCGGTGG
Long Flanking Sequence:
GTTAAATTTGTATTAGCTAAAATTTTAATATCAGTACATCTCTAGTTCAAAGACCTTAATAGATAATAGGGTAACAGTATTTTTTAAAGGATGCTTTATTTCCTTTATTCAGAAAATGCATGCAGTAGCATCATTGTATGTCATTTCAAGGCAATTAATACATAATTTAAACAGCTTTATGACACCATGTGATATCCCCCAGGTCTGACATGTCACCCCAGTCGTCCATTCACCATGGCTTCCTGCTCCAGAGACTCCACGGTCAGACTTTGGTCACTCACTCCTCTAATCGCTCCCTTAGTAGTCAACATCCTCACTGACCACAGCTGGGACGACATTATTGGCAACACAGGTTAAAACATATGAGCGTATTAAATTCACTCTGCATACATTGCTTTTGTAAAGGCATTAAAGCCTTTTTAATTTTTACAAATCTAGATCGTGCTATGGTTCCCGGGGCTCCTCCTTTGTTGTGTGGAAAGGTTTCCCGAGATATCAAA[C/T]AGGAACTAGATAAACTCTCAAGTGACGTGCGCATGAAGAAGCTGCGGTGGTTCTCCGAGTGTTTCTCCGTGAGTCAATCTCAACACAGAACTCTCACTGGACTTTATGTAGACATCTATATAAAGGGTTATTTGCTTTCTCTGTGCAGCCACCAGGAGGGAGTCATAACCTGTGGGATCTGGTTGCTGTAATCAACGGACAGGATGATAGTCTTCTTCCGCAGTACTATGGGCAGGGCATCATGCATATGAAACACTTGGTCCGCTTTAAAACTGTGAGTGTCTAAACAGAGATGGAACTTTCTAATAATGCCACAATTGAAATGGAAAAGCTTTCTGGATGTGAAGCTTTCTGATGAATATTGTGCTTTTAGTATTTCTAATGTAGTTTACTCTGTCTTTCATGTAGTCTGAAGCACAAGAGCTGACCATTGTAAAGATGTCAAAGTTCGGGGGAGGTATTGGAGCACCGAGTAAAGAGGAAAGGCTCAAGAATGCAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19535
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 |
|---|---|---|---|---|---|
| ENSDART00000110824 | Nonsense | 808 | 1292 | 16 | 29 |
| ENSDART00000136300 | Nonsense | 808 | 1283 | 16 | 28 |
Genomic Location (Zv9):
Chromosome 1 (position 39146470)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 38073732 |
| GRCz11 | 1 | 38792036 |
KASP Assay ID:
2259-0838.2 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTAAAGAGGAAAGGCTCAAGAATGCAGCTGAAATCCATATCAGACTGGGT[C/T]AAATCCAGAGATACTGTGAGCTCATGGTGGAACTGGGAGAGGTAAAATCT
Long Flanking Sequence:
TGACGTGCGCATGAAGAAGCTGCGGTGGTTCTCCGAGTGTTTCTCCGTGAGTCAATCTCAACACAGAACTCTCACTGGACTTTATGTAGACATCTATATAAAGGGTTATTTGCTTTCTCTGTGCAGCCACCAGGAGGGAGTCATAACCTGTGGGATCTGGTTGCTGTAATCAACGGACAGGATGATAGTCTTCTTCCGCAGTACTATGGGCAGGGCATCATGCATATGAAACACTTGGTCCGCTTTAAAACTGTGAGTGTCTAAACAGAGATGGAACTTTCTAATAATGCCACAATTGAAATGGAAAAGCTTTCTGGATGTGAAGCTTTCTGATGAATATTGTGCTTTTAGTATTTCTAATGTAGTTTACTCTGTCTTTCATGTAGTCTGAAGCACAAGAGCTGACCATTGTAAAGATGTCAAAGTTCGGGGGAGGTATTGGAGCACCGAGTAAAGAGGAAAGGCTCAAGAATGCAGCTGAAATCCATATCAGACTGGGT[C/T]AAATCCAGAGATACTGTGAGCTCATGGTGGAACTGGGAGAGGTAAAATCTTAAAAATGCTGATGCTTATTTTCTGATGATTATTTTCTTATTTTCTGATGCTTGTTTTCTTATGATGATTACTATTTTCTGTGAAAAGTTCTACTTAAGTGTTTTAAGTGTTTAAAACAAGTTATTTCTGTTAAAGAAATAAATAGGGCGTATTATGCAAAAATCACTTTTATAAGGGGTTTAAACACAGTTATGTGGCAATAGTGTGTAAATATAATCAGCTTCTAATGGTAAAAATGAACTAATACTGTTTTTTAATAATCACCCTTTATAAAAACAGTCTGCAGAAACACTCTGACATTCTCCCTTTGTACATGTCATAAGAGGGGGAAAGCCCCGCCCATTAGTAATGATCTTTCTCTCTCTAGCACAGACAGCCCTGAGTGAGAAGCAGCCATCTGCCATTAAAGTTTACCTGCCAAAGATAATATCAGTGACTCAGGGGAATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39649
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, Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000110824 | Essential Splice Site | 1190 | 1292 | 28 | 29 |
| ENSDART00000136300 | Splice Site | None | 1283 | None | 28 |
Genomic Location (Zv9):
Chromosome 1 (position 39156463)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 38083725 |
| GRCz11 | 1 | 38802029 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAGTAAAGAATATATTTAAATATGTTCTTTGTTTTCATTTTTTTTACAC[A/T]TACATAGAGTGGCAGATGACAGTTTGTATACTTCACCATCTGAGGCCCAG
Long Flanking Sequence:
GGTCTCCTGAGTCTGGCGGGAGCACATTTCGCTTAGCTTAGCTGAGCATAAATGACTGAATCGGATTAGATTATTAGAATTTCTGAAAAAAAATTACCAAAAAATTTTGACAATTGTCCGATTTAAAACTTGACTCTTCTGTAGTTACTCTGTGTACTAAGAAGGATGGTAAATTAAAAAGTTGCTGTTTTCTAGGCCGATAATGATAGGGACTATACTCTCATTATGGCATATAATGATGCCAAGTTATTATGTAGTGCCAGAAAATAGTGCCCAGATAGATAACGTGACCTCTTGCTTGCACAGGGAGCATATTCCGGTCACAGTGCATAATATCACTGCATCTGCTGCTACATCAAGTTCCTTAATTATTATACTGGACTGATAGTACTATATAGTTCCTCTCCATATCAGCCTACAAATCAAGAACTTTTCATTTTTTGATTGGTCTTAGTAAAGAATATATTTAAATATGTTCTTTGTTTTCATTTTTTTTACAC[A/T]TACATAGAGTGGCAGATGACAGTTTGTATACTTCACCATCTGAGGCCCAGAAGACAGAGTATAGCCAAATATTGAGTCGAATAAGAGAAGAGCCCATCAAGGGTCTTGAGGGTCCAGACTATGTGACTGGCTCCAACTTACCCAGTCATTCTGATGTCCAGATTTCCTGCTTCACTGGCCTCAGGATACAGGTAGTTTTCTTGTGAGCAGCCTTGTATTTTACTACCTCAAATGTCACTGAACTTATATCTGCCTCTTTGTTTTGTCTGGAAGGGACCAGCGTTCTTCCTGGAAGACGGCAAATCTGCTATTTCACTCAACGATGCCTTGATGTGGGCAAAAGTGAACCCTTTCTCTCCACTGGGGACGGGCGTACGCCTCAACCCCTTCTGAGCACAAATACAACAAATGTGAGCAGTATTTTTGGTGGCTTTGGCTCATGAAAATCAGCGTCTTAAAAGAAAACAACATTCCTGTTTTCTTCCCGAAATCTTGATGTA
Associated Phenotype:
Not determined