ZMP
si:dkey-251e24.6
Ensembl ID:
ZFIN ID:
Human Orthologue:
WDR19
Human Description:
WD repeat domain 19 [Source:HGNC Symbol;Acc:18340]
Mouse Orthologue:
Wdr19
Mouse Description:
WD repeat domain 19 Gene [Source:MGI Symbol;Acc:MGI:2443231]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32654 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17659 | Essential Splice Site | Available for shipment | Available now |
sa15311 | Nonsense | Available for shipment | Available now |
sa19481 | Nonsense | Available for shipment | Available now |
sa19480 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32654
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 |
---|---|---|---|---|---|
ENSDART00000034477 | Nonsense | 363 | 1345 | 11 | 36 |
ENSDART00000131257 | Nonsense | 363 | 1345 | 11 | 37 |
ENSDART00000135905 | Nonsense | 57 | 241 | 2 | 7 |
The following transcripts of ENSDARG00000037406 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 20312053)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 20836464 |
GRCz11 | 1 | 21529401 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCACCAAGCTGCCTATACTGGGAGACAGCAGTGGCACTAGAATTGCCTA[T/A]CTTACATCCCTGCTGGAGGTTACAGTCGCTAATCCAGTGGAAGGGGTAAG
Long Flanking Sequence:
TAAAAATGAAATAAATTGAATCGATGATTGAATACCCTGGCAGTGTATTTTTGGCTATTGTACAACTATTGTGGTTTAGGGTAACATATTGTATACTCTTAAAGTTACATCATCCTCAGGCCTGCCTATTTCAGACCAACGCTCCACTGCTTTCCAATTCATTTATGACAGTTTCATTCACCACCGTAAAAACATATGTTTGGAGATAACACTGTTGTGTTTGTCTGTCAGTATCAAGATACATGACCTGACTGATCTGAAGGAGATGTATGCTATAGTCACTCTGGATGAGGAGACCAAAGGTATTAAATCATTTTGGTGCGTGTTAGTGCACTGTAAATAGCAATTCTTAGTTCTCTGGTGTCTTTCTCAGGCCTTGATCAGATGTGTTGGACTGATGACGGGCAGCTGTTAGCCGTGTCGTCTCAGCAGGGCACTTTGCATGTCTTTCTCACCAAGCTGCCTATACTGGGAGACAGCAGTGGCACTAGAATTGCCTA[T/A]CTTACATCCCTGCTGGAGGTTACAGTCGCTAATCCAGTGGAAGGGGTAAGAGGATGACACAGATTTGTATGCTTCAGTAAAAATTAAATAATCTTAGTTTAAAGAATAAAAATCATTGCTTTCTCACAGTGATGATGGCAAATTACACTTATATGACTTATATGACTTTCAAATTACAGATGTGACTGTTTATTTTTTTCTGTATTGTGACGCAGTTCCTAGAGAAACAGAATATTAAATGAGAAAACAGTGGGTGTGGCTTGTTTTTTTTTTTTACTGTGAGCTGATTGGATATAATGGAGTAGGCATTTCATTCAGAAAGGTCGAGAAAAGGGTGTTAGGAGAGTTACTACCCCTAACACACACCTCCTCCTCCTCCTCACTATTTCTGTTTGTTGTCACGGGGCTGTCAAAACTGACAGTTGGAGGGGTGTGGTTAAGTATGTTAACCACGCCCAATGCCTCAGACAGACATAATCTGTGAAAGGTCAAACTAATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17659
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000034477 | Essential Splice Site | 593 | 1345 | 16 | 36 |
ENSDART00000131257 | Essential Splice Site | 593 | 1345 | 16 | 37 |
ENSDART00000135905 | None | None | 241 | None | 7 |
The following transcripts of ENSDARG00000037406 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 20308445)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 20832856 |
GRCz11 | 1 | 21525793 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAGAAGACAAAGTCTATACRTATGCYTTCCACAAAGACACYATACAAGG[T/C]AAAAATATATGAGTAAATGTTTTATTATAAATAAGTAMTAAAATTAGWGT
Long Flanking Sequence:
AACCTGGCCTCTCTTGTACCAGATCACTTAAATGTATCATTCTTTGGTTCTACAGACCGGGTTGATTCAGTGTTTCTATTTCGAAGATTGGCAGAGTGTGACTGAGTATCGACACACAGTGGGTGTACGCAAAGTCTTTCCAGACCCCAATGGAACACGTCTTGTTTTTATCGATGAAAAAAGTGACGGCTTCCTATACTGCCCGGTAAACACAAACAAACTAAATTTCCACTCTTACAAGAAACATTGTTTACCTGTCATCATGTCATGTAAGATGTGCATGACCTAATTTGGTATGTAGAATTTAAAAAAAAGAGGATGTGACATGAATTAATTTTTTTTTCCTTATAGGTGAATGACTCAGTGTTTGAGATCCCAGACTTTTCTCCTGCTATTAAAGGGGTGTTGTGGGAAAACTGGATCAGCAGTAAGGGTGTGTTTGTAGCCTATGAAGAAGACAAAGTCTATACGTATGCCTTCCACAAAGACACTATACAAGG[T/C]AAAAATATATGAGTAAATGTTTTATTATAAATAAGTAATAAAATTAGTGTCGGGTGGCTCATTGGTTAAGCACTGTCGCTTCACAGCAAGAAGGTCGCTGGTTCGAGTCTCGGCTGGGCCGGTTGGCATTTCTGTGTGGAGTTTGCATGTTCTCCGGGTGCTCAGGTTTCCCCCACAATCCAAACACATGTGCTATACTGTGGATGAATTGGATGAACTAAATTGGCCATAGTGGATAAGTGTGTGTGGGTGAATGCGAGAGTGTATTTCCCAGTACTGGGATGCGGCTGGAAGGGCATCCGGTGCGTAAAACGTATGCTTGAATAGTTGGTGGTTCCATCCACTGTGGTGGAATAAAGGACTAAGGACCTAATGAATAAGGACTAAGCTCAAGGAAAATGAATAAATAAATAAATGAATGAGTTATCTTTTTAATCATCTACAATATTATCAAAGTAGTTTTGAAACTATGCAAGCTGCCATTATTAAGTTTGCTACTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15311
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 |
---|---|---|---|---|---|
ENSDART00000034477 | Nonsense | 736 | 1345 | 19 | 36 |
ENSDART00000131257 | Nonsense | 736 | 1345 | 19 | 37 |
ENSDART00000135905 | Nonsense | 93 | 241 | 3 | 7 |
The following transcripts of ENSDARG00000037406 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 20301399)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 20825810 |
GRCz11 | 1 | 21518747 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCAAAATTTGCTGGCGGGTCATTTGGCCAWGTTCTGCAATGACTACAAC[C/T]GAGCCCAGGACCTCWATCTAAYATCTTCATATCCTATGGCGGCCCTAGAG
Long Flanking Sequence:
ATCCATAATGCAAAAAATTATGTTGTAATAGAAACCCAAGGTGCTTGACAGAGCAGTCAATTTTTTGATTATAAAAAAAATTTCAAATAACATAATTTAAAAATAATGAAAAAACTTTTTATATTTAAGAAAAAGGTATTAATACAAACTTTATCTGTGTGTATTTATGATAATTTAAATCAATGTCAGGGTTGCCTTTCGCTTAAGGAACAGCTTTGTTAAGAGTGAAAAGGAAGGGCATCAGCTGTGTAAAACATATGCAGGAATAGTTGGTGGTTCATTCCACTGAGGTGACCCCTCATAAATAAGGGACTAAGCTGAAGGAAAATGAATGAATGAAGATATAATGTGTGTAAATCCAACTTAGGAAACAACAAAATTGTACAGCAATTGACAGAACTCTTTATGCTCTTAACTGTTTGTCTCAACTGTGTCTGTAGGGAATAGAGGATCAAAATTTGCTGGCGGGTCATTTGGCCATGTTCTGCAATGACTACAAC[C/T]GAGCCCAGGACCTCTATCTAACATCTTCATATCCTATGGCGGCCCTAGAGGTAAATTAGGCATGCAAACACACACATACATGAGTGTTTAAAAGTTTGCAGCTACGCATATGAATGAGTTCAAACTTTCCAAGTCACTTTGACTACTGCTGCTGCTGTTGTGTTTGTAGATGAGAAGGGATCTGCAGCATTGGGACAGTGCATTGCAGCTGGCTAAAAGACTGGACCCAGATGAGATCCCATTCATTTCTAAAGAATATGCAATACAACTGGAGTTTGTGTAAGTCAGCTAATTTCATTTACTAAATTATAATAATCTGTACAAATACTTTATTATAAGTGATGCTGTATGTTTTTTTGTGCTAGATGATGGCGTATGAAAGCACATACAGTTTTATAGAGTGCTGCAGCATACTGTAAATGAGAAAAATAGGATTTTTATTTTGTATTATAACAGATAATAAGCTATGTGACCAAGATAATTCTCATCTCATAGTTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19481
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 |
---|---|---|---|---|---|
ENSDART00000034477 | Nonsense | 746 | 1345 | 19 | 36 |
ENSDART00000131257 | Nonsense | 746 | 1345 | 19 | 37 |
ENSDART00000135905 | Nonsense | 103 | 241 | 3 | 7 |
The following transcripts of ENSDARG00000037406 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 20301367)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 20825778 |
GRCz11 | 1 | 21518715 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTGCAATGACTACAACCGAGCCCAGGACCTCTATCTAACATCTTCATA[T/A]CCTATGGCGGCCCTAGAGGTAAATTAGGCATGCAAACACACACATACATG
Long Flanking Sequence:
AACCCAAGGTGCTTGACAGAGCAGTCAATTTTTTGATTATAAAAAAAATTTCAAATAACATAATTTAAAAATAATGAAAAAACTTTTTATATTTAAGAAAAAGGTATTAATACAAACTTTATCTGTGTGTATTTATGATAATTTAAATCAATGTCAGGGTTGCCTTTCGCTTAAGGAACAGCTTTGTTAAGAGTGAAAAGGAAGGGCATCAGCTGTGTAAAACATATGCAGGAATAGTTGGTGGTTCATTCCACTGAGGTGACCCCTCATAAATAAGGGACTAAGCTGAAGGAAAATGAATGAATGAAGATATAATGTGTGTAAATCCAACTTAGGAAACAACAAAATTGTACAGCAATTGACAGAACTCTTTATGCTCTTAACTGTTTGTCTCAACTGTGTCTGTAGGGAATAGAGGATCAAAATTTGCTGGCGGGTCATTTGGCCATGTTCTGCAATGACTACAACCGAGCCCAGGACCTCTATCTAACATCTTCATA[T/A]CCTATGGCGGCCCTAGAGGTAAATTAGGCATGCAAACACACACATACATGAGTGTTTAAAAGTTTGCAGCTACGCATATGAATGAGTTCAAACTTTCCAAGTCACTTTGACTACTGCTGCTGCTGTTGTGTTTGTAGATGAGAAGGGATCTGCAGCATTGGGACAGTGCATTGCAGCTGGCTAAAAGACTGGACCCAGATGAGATCCCATTCATTTCTAAAGAATATGCAATACAACTGGAGTTTGTGTAAGTCAGCTAATTTCATTTACTAAATTATAATAATCTGTACAAATACTTTATTATAAGTGATGCTGTATGTTTTTTTGTGCTAGATGATGGCGTATGAAAGCACATACAGTTTTATAGAGTGCTGCAGCATACTGTAAATGAGAAAAATAGGATTTTTATTTTGTATTATAACAGATAATAAGCTATGTGACCAAGATAATTCTCATCTCATAGTTAAAAAAATCTTCAGTTTTGAAGGCCAAAATAACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19480
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000034477 | Nonsense | 879 | 1345 | 23 | 36 |
ENSDART00000131257 | Nonsense | 879 | 1345 | 23 | 37 |
ENSDART00000135905 | Nonsense | 236 | 241 | 7 | 7 |
The following transcripts of ENSDARG00000037406 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 20298707)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 20823118 |
GRCz11 | 1 | 21516055 |
KASP Assay ID:
554-6256.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCAGCTGTATGAGAAAGGCCAGTACTATGACAAAGCTGCCTCTGTCTA[C/A]ATACGCTGTAAAAACTGGTAAAACAACATTATAGTAACAGTGACAATTGT
Long Flanking Sequence:
ATGACAAATAATAATAATAATGCAAGCAAAAATAAATGATGTACAGTATTCTTATTATTATGCTATTATGACTGATTAGTGAGAAATTAGACAAAACAGGTCCTCTGACATGATATGGAAATCTTGAACCATGATCATAAATAGCAGATTTTGATCATATGAGTGTTTGTAGTTTCAGGATCATGATGAGAGCTGTCTGGCAGGAGTGGCTCGTATGTCTATTCGAATGGGTGACATTCGTAGAGGAGCAAACCAGGCCATCAAACACCCCAGTAAAGCTCTGAAAAAAGACTGCGGAGCCATCCTGGAGAGCATGAAGGTGTGTGTGCGTGTGTGTGTGTGTGTGTGTGTTCATTAACAAACAAACTACTTCTATTTGCTCTGTTAAAGAGCTCCAAGCTTGTTTCAAAGTTGGGTAAATGTGTTTGTGTGCAGCAATACTCAGAAGCAGCTCAGCTGTATGAGAAAGGCCAGTACTATGACAAAGCTGCCTCTGTCTA[C/A]ATACGCTGTAAAAACTGGTAAAACAACATTATAGTAACAGTGACAATTGTGTATATTTTACATACAAACAAGCTTGTAAATAACAGTAATTTTGTAAATTATAAGGATTAACCCTTTCATCTTCAGGGCAAAGGTGGGAGAGCTCTTGCCCCATGTGACTTCCCCAAAGATTCACCTTCAGTACGCTAAGGCAAAAGAAGCTGATGGAAAGTATGTAGCAAATATGTTTCAAAAACTTAGAAGTCACTTCATAATATTTCAGTAATATTTTTAGCTAAAAAAGTTTTCCAGTATTTTCCATATTTTTAACAATGTATCCATGTTTCATGTTGCACATGACCATTTTAAGTCACCTAGTTTTGCTATGGAACTGCACAAATGAAGATTGTGTTAAAACTACTTAATAAAGGACAAAAGTAAAATAACAGAAGCAAAATATCAAGTTGCAAGCAGCAATGATGGGCCCTGGTGGCTTCATAAAAGCAATACACCATGGGCAC
Associated Phenotype:
Not determined