ZMP
zgc:194983
Ensembl ID:
ZFIN ID:
Description:
WD and tetratricopeptide repeats protein 1 [Source:RefSeq peptide;Acc:NP_001124078]
Human Orthologue:
WDTC1
Human Description:
WD and tetratricopeptide repeats 1 [Source:HGNC Symbol;Acc:29175]
Mouse Orthologue:
Wdtc1
Mouse Description:
WD and tetratricopeptide repeats 1 Gene [Source:MGI Symbol;Acc:MGI:2685541]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16269 | Essential Splice Site | Available for shipment | Available now |
sa36280 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa45587 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa22967 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16269
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113358 | Essential Splice Site | 66 | 674 | 4 | 16 |
Genomic Location (Zv9):
Chromosome 16 (position 58490383)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 55258239 |
GRCz11 | 16 | 54966264 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGGTCACTCAGGCTKTGTCAACTGTCTGGAGTGGAATGAGAAAGGAGAG[T/G]AAGTTGTGTTCAGTCTAGAGCTGTGCAAWACGAYAAACACTCMCCGGSCA
Long Flanking Sequence:
GAAATAGCTATTAACTTTTTAGTTTTTTTGGTGGGGCCAGTGAAAATTTTGGCAGGGCAAGTAAAAATCTCAACCAATGGCCCGATCGGACCCATATAAAAAATCCTTAGCGTTGAACCCTGCACATGTCTTTGGACTTGTGGGGGAAACCAGAGCACCCGGAGGAAACCCACGCCAATACGGGGAAAACATGCAAACTCCACACAGCAACTGACCCAGCTGAGGCTTAAACCAGCGACCTTTTTGCTGTGAGACGAATCAGTGTGCAACTGCGTCGCCAAAAAAAGCATCAACTAATAAAATAAACAGATTGTTATCCTGTGGTGGTTGGGCAGAAATATGTCTATCATTATATTAATATTTATAGTTATCATCCTAAGTGTGAATAACTATTGGATTTGTGCTTCCTGCTCTAATATTAACGTATTGTTTGTTAATTGTGTATTTTTCAGGGTCACTCAGGCTGTGTCAACTGTCTGGAGTGGAATGAGAAAGGAGAG[T/G]AAGTTGTGTTCAGTCTAGAGCTGTGCAATACGATAAACACTCACCGGCCACTTTATTAGGTACACCTGTCCTACTGCTCGTTAATGCATATTTGTAATCAGCTAATCACATGGCAGCAGCTCAATGCATTTACACATGGTCAATAGGATCTGCTGCAGTTCAAAGCGAGCATCAGAATGGGAAAGAAAGGGGATTTAAGAGACTTTGAACGTGGCATGGTTGTTGCTGCCAGACGCACTGCTCTGAGTATTTCAGAAACTGCTGATCTACTGGGATTTTCATGCACAACCATCTCTAGGGTTTACAGAGAATGCTCCGACAAAGAGGAAATATCCAGTGAGCGGCAGTTCTGTGGGCGCAAATGCCTTGTTGATTAGGCCAGAGGTCAGAGGAGAATGGCCAGACTGGTTCCAGCTGATAGAAAGGCAACAGTAACTCAAATAAGCAGAAGAGCATCTCTGAACACACAACACGTCCAACATTGAGGCGGATGGGCTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36280
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113358 | Essential Splice Site | 297 | 674 | 9 | 16 |
Genomic Location (Zv9):
Chromosome 16 (position 58483990)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 55251846 |
GRCz11 | 16 | 54959871 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTTCAGTCCTGACGGCACCGAGCTGCTGGTCAACATGGGTGGAGAACAA[G/A]TAAAGAAACCGGTCCTGCTGTCTTTCTGCTGATGTTTTTAAGCAGAACTG
Long Flanking Sequence:
GCGGGGTTTTATTTTGGAGCCCCGCCTCTCGTCTTTTGCTTGCAGCAAACTAACGGTCATAGGGGAGTGGCTAAGCATATTTCAGCCAATCAGAATCATCAGAAAAGGAGAAGCAGATGAGCAGATTTTGGTTAAAAATTAGCAGAACGTTCTGTTGTATCAGTGGATTCACTTGTTGTTTTTATTATTATTATTATTGATTAATTGTCTTCCAGGAAGTCTCTGAGTCAGAGTTCGTCAGCAGGCGTTCACACGTTTTGCGATAAGCGAAAGTCAATACCGGATGGCGCTGGACAGTATTATGTTGCAGGTTTGTTGTTAGCGTTGTTTCGATGCTCATGAATGGAGTTTTAAGATTTTACTGAAGTGTGTCTCTGTTTGCAGGTCATTTACCTGTGAAGCTTCCGGACTATAATAACAGGTTGCGAGTTCTAGTGGCGACTTACGTTACGTTCAGTCCTGACGGCACCGAGCTGCTGGTCAACATGGGTGGAGAACAA[G/A]TAAAGAAACCGGTCCTGCTGTCTTTCTGCTGATGTTTTTAAGCAGAACTGAAGATGTTTTATTCGCTGCTTTGTGTTTGCAGGTGTATTTATTCGACCTGACGTTTAAGCAGAGGCCGTACACTTTTCTGCTGCCCAAAAAGTGCCATTCGTCAACAGGTAAGCTGTGAATGCAGTCATATTTATATTTATTTATTTAAATATATATATATATATATTTATATATATTGCAATTAAATTTTTTTTAGTATTTAATAAAATCTTATGTGATATTTATTAATATAATTTTATTATTTTATTATTTAATCCATATTGATATAATATTTCTGTAATAATTTTTAAATGTGTATTTTGTGATAGTTTATTATCATTCATTCATTAATTTTCTTTTCGACATAGTTCCTTTATTAATCTGGGGTTGCCACAGCGGAACGAACCGCCAAATTATTCAGAATATGTTTTACACAGCGGATGCCCTTCCAGCTGCAACCCATCACTGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45587
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113358 | Essential Splice Site | 297 | 674 | 9 | 16 |
Genomic Location (Zv9):
Chromosome 16 (position 58483989)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 55251845 |
GRCz11 | 16 | 54959870 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTCAGTCCTGACGGCACCGAGCTGCTGGTCAACATGGGTGGAGAACAAG[T/C]AAAGAAACCGGTCCTGCTGTCTTTCTGCTGATGTTTTTAAGCAGAACTGA
Long Flanking Sequence:
CGGGGTTTTATTTTGGAGCCCCGCCTCTCGTCTTTTGCTTGCAGCAAACTAACGGTCATAGGGGAGTGGCTAAGCATATTTCAGCCAATCAGAATCATCAGAAAAGGAGAAGCAGATGAGCAGATTTTGGTTAAAAATTAGCAGAACGTTCTGTTGTATCAGTGGATTCACTTGTTGTTTTTATTATTATTATTATTGATTAATTGTCTTCCAGGAAGTCTCTGAGTCAGAGTTCGTCAGCAGGCGTTCACACGTTTTGCGATAAGCGAAAGTCAATACCGGATGGCGCTGGACAGTATTATGTTGCAGGTTTGTTGTTAGCGTTGTTTCGATGCTCATGAATGGAGTTTTAAGATTTTACTGAAGTGTGTCTCTGTTTGCAGGTCATTTACCTGTGAAGCTTCCGGACTATAATAACAGGTTGCGAGTTCTAGTGGCGACTTACGTTACGTTCAGTCCTGACGGCACCGAGCTGCTGGTCAACATGGGTGGAGAACAAG[T/C]AAAGAAACCGGTCCTGCTGTCTTTCTGCTGATGTTTTTAAGCAGAACTGAAGATGTTTTATTCGCTGCTTTGTGTTTGCAGGTGTATTTATTCGACCTGACGTTTAAGCAGAGGCCGTACACTTTTCTGCTGCCCAAAAAGTGCCATTCGTCAACAGGTAAGCTGTGAATGCAGTCATATTTATATTTATTTATTTAAATATATATATATATATATTTATATATATTGCAATTAAATTTTTTTTAGTATTTAATAAAATCTTATGTGATATTTATTAATATAATTTTATTATTTTATTATTTAATCCATATTGATATAATATTTCTGTAATAATTTTTAAATGTGTATTTTGTGATAGTTTATTATCATTCATTCATTAATTTTCTTTTCGACATAGTTCCTTTATTAATCTGGGGTTGCCACAGCGGAACGAACCGCCAAATTATTCAGAATATGTTTTACACAGCGGATGCCCTTCCAGCTGCAACCCATCACTGAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22967
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 |
---|---|---|---|---|---|
ENSDART00000113358 | Essential Splice Site | 410 | 674 | 12 | 16 |
Genomic Location (Zv9):
Chromosome 16 (position 58481341)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 55249197 |
GRCz11 | 16 | 54957222 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACGCCATGCTGTACGGAAACCGTGCTGCTGCATACATGAAGCGCAAGTG[G/A]TGAGACCAGACATTTTTTGATGATCCGCTTACATCAGCTTGTAAAGGGAC
Long Flanking Sequence:
ACGACTCTTAATTTGAAAATCTGGAATCTGAGGGGTTCAAAATGTAAATATAAAGTTAATAAAATAATCTTCTTATTAATTTGATATAATTAATCTCACCGGCAGAATATTTTGCTTGCTTTAAGGAAAAAATTATTAACTTAAAAAAAATAAAACCATTTTGCCTTTCCAGAAAATGCTTACTGTTAAAATTTGTAAATATTTGGACTAGAGATGACAAACCTAAGAAAGAAATGCATTTTTTCATTGTGGCTACGCATGTTTGTATGTATATATGATATATTTACAAAATAATTAATTCATATAATTGTGTGTGCATTCAGCAGTGGCTCTGGTGATCTCCCTCTTCATCTGGAGAGGATAAAGCAGCGAGCGAACGATGCGTTTGCACGTCAGCAGTGGACTCAAGCCATTCAGCTCTACAGTCTGGGCATCCATGAGGCCGGACCCAACGCCATGCTGTACGGAAACCGTGCTGCTGCATACATGAAGCGCAAGTG[G/A]TGAGACCAGACATTTTTTGATGATCCGCTTACATCAGCTTGTAAAGGGACTTGTGTCTGATGTCTGCATTTACACTGTACATGCAAGCAAGTTTGGGCGCTGTCTTCCACTAATGTGCACTTTCACTTTAGACTCAGACTTAACTGGCTGTCTGTGTTACATGTATTCAGCCTATGTTGCAGCGCAATAACATGTATATAAACAAAATCAGCAATAGCAATCGTTTTTATAACCATCCCATCCCTTAAAAATACACAGTTCCCTGTGCATGATTACTTTAAACACACTTGAAATACTCAGTGACAGGCACATCAAATGATCAACTTTGCTTTAATTTAGCTGTAATGTGTTTTCAAGTAAACATTAATGTGTGTGTGTGTGTGTGTCTGGCAGGGATGGAGATCACTACGATGCGCTGCGGGACTGTCTGAAGGCCTTGTCTCTAAACCCGGGCCACCTGAAGGCTCATTTCCGTTTAGCGCGCTGCCTCTTTGAGCTGA
Associated Phenotype:
Not determined