ZMP
si:dkey-70o15.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens WDFY3, WD repeat and FYVE domain containing 3 (WDFY3) [Source:Uni
Human Orthologue:
WDFY4
Human Description:
WDFY family member 4 [Source:HGNC Symbol;Acc:29323]
Mouse Orthologue:
Wdfy4
Mouse Description:
WD repeat and FYVE domain containing 4 Gene [Source:MGI Symbol;Acc:MGI:3584510]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22333 | Essential Splice Site | Available for shipment | Available now |
sa11120 | Essential Splice Site | Available for shipment | Available now |
sa22332 | Nonsense | Available for shipment | Available now |
sa13732 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22333
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 |
---|---|---|---|---|---|
ENSDART00000112653 | Essential Splice Site | 978 | 3182 | 15 | 62 |
ENSDART00000137709 | None | None | 132 | None | 3 |
ENSDART00000139394 | None | None | 674 | None | 17 |
ENSDART00000145287 | None | None | 157 | None | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 31266708)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 30912656 |
GRCz11 | 13 | 31043106 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTGGAGAAAATCAGCCTTCTGTCACCTTAGAAGAGGCCAGCTGCACAA[G/A]TACAGTTCCTCCCAGTCCTCTCACACTTCCTTTTTGGATTACTGCCTGTT
Long Flanking Sequence:
ATTTATTTTTTTTTTATAAATGTTCCTTCTGCCACTTTTAATCAATTTGATGCATTCTTACAGCAACTACAATAATTCTAGCCATTTTTTTCTGTAGTTGTCAGAGGAGCTGCAGCTGGCTGTGGCTCATCATGTCCAGACTCTGGTGAAGTCCGAGAGAAACAGGCAGATCATGTGTGAATTTGGTCTGTTGTCTACACTGTTGACTCACTGCAAAGACATCCTCATCGACAATTCCCATTCGCTACACTTGCCCATTGTCCGGATTCTCGAGAAACTTGCCTCTCAGTCCATGGATCAGAAGTGCCTGAGGTCAGCATGCATTTGCTGTTAACATCCTCACAAAAAAATGCAATATGATAAATAGATGATTATATGATTGTATGCTGTTAAATAGTGTGCTTTGCTTTATATTAGGCACTTCCTGTGTCTTGGGGATCCACTGATGTGTTGTGGAGAAAATCAGCCTTCTGTCACCTTAGAAGAGGCCAGCTGCACAA[G/A]TACAGTTCCTCCCAGTCCTCTCACACTTCCTTTTTGGATTACTGCCTGTTTCGTGAAAAACATTTGATCTTATTGTTACATCCATTTGGATTTCAATACAATAATGATGGTTTTATATTGTTTTTGGTTTTTACTTTCACAGATCAGACCAAAGACTCTGAGGAGAACAACAAGAAGTCATTGAAAAGGGCAATGAAAAGAAGTTTTAGTTTACTGAAAACACCTTTAGACAGTGGGATGGTAGTTCCTCTTCACAGAATCATAAGTCTTGTCTCCATCACGTCACCACGGAACTTTCAGCCACACAAAGTCTCCATTTCCCCTTCCTTTGTGGAGTTTGACATGACCGACAGTGGCTATGGGTAAGTGTTTAATAAACAATTAATATGGACCCTTTCACAAGGCGCGTTTAATGGTCATCAGCATCTTAAATCCTTGAAAATTTTTATATTTTAAAACATATGCCAATGTATTATATACATTTATTAAAATGTATTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11120
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 |
---|---|---|---|---|---|
ENSDART00000112653 | Essential Splice Site | 1375 | 3182 | 22 | 62 |
ENSDART00000137709 | None | None | 132 | None | 3 |
ENSDART00000139394 | None | None | 674 | None | 17 |
ENSDART00000145287 | None | None | 157 | None | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 31261888)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 30907836 |
GRCz11 | 13 | 31038286 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTCAGCGGAACATCCCGGACRATTGGGGCAGCCCTTGTTGGTTGTTTTG[G/A]TAAAATGCAGATNNCCTCTGYTAGGGCTRCACAATATATCRTTTTAGCATTG
Long Flanking Sequence:
GGAAGTGTTAAGTGCTGATCAGGTGGAGACTATTTATGGACAAGGCACCAAATACATCGGCAACTACCTCGCTCTTAATGTTCAAGGTGAAAAATGTTCCGTCTTAGTTTTCAATTTTATGAAAATCTTTATTCATTCAAGTGTTTGTTTAGGATGCAAGACAGATGGTACGATGTCCCATACAAAGATGGTCTCTCCAGAGAGGATTTCCTTTGCCATAAACCCAGCGGTATCCACTATCACTACTGTAGTAGATATTAGAGATACGTATAATGAAGTGGATTGTCGCCTTATAGCCAAAGAGGTGATTTTATTTCTCTTCCATTCACAAAATCAACCATTTTGATCATTCTGTCACAATTAGTGCACATATTATTTTTAATTGCAGATGGGGATTACGTCACGTGATAATTGCACTCCTGTCTTCCTGGCTCATAATATCAGTCAGCACCTCAGCGGAACATCCCGGACGATTGGGGCAGCCCTTGTTGGTTGTTTTG[G/A]TAAAATGCAGATCCTCTGTTAGGGCTGCACAATATATCATTTTAGCATTGAAATTGCGGTGTGAAGTGCAATGTTGAATCTGGATTGTAATTTATCATTTGTATATGTTTTTGAGGCCTGTGATCTTATGAGGATTTTAAAAACTTTTAGGCATAATAAATTGTACTGTATGTAAATTTAATAGCTATTCTACATGATTCTATTGACTACACAGTATTATTTTACATATAGTTATTAAATTACCAGATCTGAATACTGTTTCACTTCTCAGGAAAACGATTAAAACACTGTTTATTTAATTAATAGTTTTTCTTTATTGTATTTATCTATGCTTGTAGATTGTTTAGTATATTTCGTGCAGATGCACTCTCATACAGAACCATTCCAATCAATTTCTAAATATAGATATTCAAGTGACCTGGTGAAATGTCAGTTTGTTTTCAATTTCATGCAGCACTATCCTCTACAGTAAAACAAGACTTTGCAGCATTTGTTTTGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22332
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112653 | Nonsense | 1416 | 3182 | 23 | 62 |
ENSDART00000137709 | None | None | 132 | None | 3 |
ENSDART00000139394 | None | None | 674 | None | 17 |
ENSDART00000145287 | None | None | 157 | None | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 31261225)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 30907173 |
GRCz11 | 13 | 31037623 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGTTTGGTGGCGATGGCTTCAGACGACAGCTCTTTATATGCCTCTATC[A/T]AAGTTCTGCTCTCAGTTTTGGAGACTAATCCTGCGATGGAGCAGGAAATG
Long Flanking Sequence:
GTACTGTATGTAAATTTAATAGCTATTCTACATGATTCTATTGACTACACAGTATTATTTTACATATAGTTATTAAATTACCAGATCTGAATACTGTTTCACTTCTCAGGAAAACGATTAAAACACTGTTTATTTAATTAATAGTTTTTCTTTATTGTATTTATCTATGCTTGTAGATTGTTTAGTATATTTCGTGCAGATGCACTCTCATACAGAACCATTCCAATCAATTTCTAAATATAGATATTCAAGTGACCTGGTGAAATGTCAGTTTGTTTTCAATTTCATGCAGCACTATCCTCTACAGTAAAACAAGACTTTGCAGCATTTGTTTTGAAAGCAAACTTTTGAATTTGTATTATTTTTTACCTTGCTTTCCAGGTGTAAGGACCTTCAAATCGTACAGTGCTTCTAGTAGCTTCCAGTATATTGGTGGTCCTGCTGCTATTCTGAGTTTGGTGGCGATGGCTTCAGACGACAGCTCTTTATATGCCTCTATC[A/T]AAGTTCTGCTCTCAGTTTTGGAGACTAATCCTGCGATGGAGCAGGAAATGAAACGGACCAACGGGTATAAGGTAGTGCTGTCAATTAAAGTATGATTAGAGATGTACTGTAACAAATCCAAGATAGAGATTAAATTGTTTTTGCTTTGTTTGTTGGCAGCTCTTATCATTCTTGCTGAAGATGAAGGTTCAGTTGATCAGCAACAGGATTTTCCAGCTCATTCTGGCCATCGTGGGTACAATGGAGCTGGGCATTGTACCGGTTTGCATCCCAAATGTCTGTGCCTTTCAGGATGTTCTATGCGACTTTGAGGTGAGTTTTAGATTAGGGAGCTGTAGTGTTTTACTTCATAGCTACAATGTTATTTGCTTTGTGACTAGCATTATAAATGCTTTTAAACAAAGTCCCTTTAAAGCAAGTCATTTCACTCGACGGCCATCCTTGAAACGCCTCTCGGGCAGTATGCTCGGGCATTCGGTTTGAATGGGGAAACATCAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13732
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112653 | Nonsense | 2514 | 3182 | 46 | 62 |
ENSDART00000137709 | None | None | 132 | None | 3 |
ENSDART00000139394 | Nonsense | 57 | 674 | 2 | 17 |
ENSDART00000145287 | None | None | 157 | None | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 31231567)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 30877515 |
GRCz11 | 13 | 31007965 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAACTTCAGTGTTCCTAGTTTTCTTCAAYAATGACCACKTCAAKGCATAT[A/T]AAAGGTGAAATGAGAGTCCTTGTGATTTAAGTGGGTAAAGAACTGTTTGT
Long Flanking Sequence:
AACTAAATATGTAAGTGCATTTATATAAGTTTTAACCAAAAGATGAATTACTCTTTTACTGCATAGTGGTTACATCAATTAAGATGAATTTATTTCTGTGCATACAGTAGGTACAACAACAGATAACATCTTAAATGTTCTATCTTTATCATAGTGTGAGGGACTCGTATATTTGCAGCATGATGAATAAAGAGAAAAACTCAGTGACCCCGAGCTGCAAGCGCTGGTCATATGATGACATCAAAGAGGCCAATTTCATGCGCTTTCTGCTTGAGGTGAGATTCACAGAGCACATATTCATTTCATCAGTTCAAATAATTATTACGCAATGCAAATCGTGATTTTCCTTTTGATGCTTGACAAACACGCATGTCTACATTAATATATCTGCTTAACTAATTAATTTCTTAAATCTTTAGGACAATGCTCTGGAAATATTCTTAAAGAACGGAACTTCAGTGTTCCTAGTTTTCTTCAACAATGACCACGTCAATGCATAT[A/T]AAAGGTGAAATGAGAGTCCTTGTGATTTAAGTGGGTAAAGAACTGTTTGTAAGGTAGCACAGGCTAAATTGATTTATCTTTCTCTCTCTCTTTCTCTCTCTCTCTCTTTCTTTGTCCTGTTTCCAGGTTGTGCTCTGTGGTCTCCTCATTAAAGGGAAGGGGAGAGACTGTGCTTAATGTGAGGTGAGTGTCAAAAGCATTTCGCAGACAGCTGCCACTTCAGTCAGAGAGTCTGTGATGCTTTTCTTTTGAAACAGACCAGAGTTTTGTGGTTTCAAAGTTTCTAGAAAACACATTCTCGTACGTGTGCGGTTAAATATTGACAGTAAGACTCTCAATCCCCTAAACAATATCCCGGCATTACAGTGAAACTACAATTACTGCATCTTCAGCATTTCCCACCAATTAAAACAGCTTCAGTAACTTTTCAAAGTCATGAACAGCCGATACAACCCTGAATGTTATAGTTGCTAATTATCTGCGAGGGTGCAATAAGCTTT
Associated Phenotype:
Not determined