ZMP
wdr33
Ensembl ID:
ZFIN ID:
Description:
WD repeat domain 33 (wdr33), transcript variant 2, mRNA [Source:RefSeq DNA;Acc:NM_001024221]
Human Orthologue:
WDR33
Human Description:
WD repeat domain 33 [Source:HGNC Symbol;Acc:25651]
Mouse Orthologue:
Wdr33
Mouse Description:
WD repeat domain 33 Gene [Source:MGI Symbol;Acc:MGI:1921570]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13555 | Nonsense | Available for shipment | Available now |
sa15874 | Nonsense | Available for shipment | Available now |
sa31252 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13555
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 |
---|---|---|---|---|---|
ENSDART00000025131 | Nonsense | 27 | 1164 | 1 | 25 |
ENSDART00000124113 | Nonsense | 27 | 557 | 2 | 15 |
ENSDART00000138885 | Nonsense | 14 | 992 | 2 | 19 |
ENSDART00000025131 | Nonsense | 27 | 1164 | 1 | 25 |
ENSDART00000124113 | Nonsense | 27 | 557 | 2 | 15 |
ENSDART00000138885 | Nonsense | 14 | 992 | 2 | 19 |
The following transcripts of ENSDARG00000018272 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 5080241)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 5525969 |
GRCz11 | 2 | 5437851 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTTCCAYATGCCTCGCTTCCAGCACCAGGCTCYCCGWCAGCTGTTCTA[C/A]AAGAGGCCCGACTTCGCCCAGCAGCAGGCCATGCAGCAGCTCACCTTCGA
Long Flanking Sequence:
TTGGTTTATTCCTGCAAAAAAAAGTCCTGGAAAGCTATTTTGATCCATTGCAGTTCAACTGAAAGAACATATTAGCATAACCTGTGTAACACTTACTTGGTTACTTGCATAATAAAATGAGAAAAATGGTTCTTATTTAAAGATGGTGGTTTAAGTTGTCGATAACCTTGTGTATTGATTTGTAGTATTGTACTTACCCCCCGCCCCCCAAAGAGTGTTGTTGTCTATGCCCAAATTTTTCAATCACACAATCACATACATTTCTAAAATGAATCCGTGTCATTAACCATGGTTTTTTTTGCCTATGTGTTGTTGTTTTGCATTGATCTGTGCATTTAGTTGCTGATGTTCTCTTGAATTTAGCCAGCGGAAAGAACCCTTAATTTCTCTCCATATCCTCAGGTGTACTAAACCGTGACCATGGCGACTGACATCGGCTCCCCTCCGCGGTTCTTCCATATGCCTCGCTTCCAGCACCAGGCTCCCCGTCAGCTGTTCTA[C/A]AAGAGGCCCGACTTCGCCCAGCAGCAGGCCATGCAGCAGCTCACCTTCGACGGCAAGCGCATGAGAAAAGCCGTCAACCGCAAAACCATCGATTACAATCCATCCGTCATCAGACATCTAGAGGTATTAGCCTAGCAGAAATACAACTCTCTTTTTTATTGTATGTATTTATTTGGTATAGTTCTGCTTTCACCTCACCCTACAGTTTTTTTTCCTGTAACTTGTTAAGTTTGATTTGTATTGTAAGAATATATTTACTTTCCCAGTACTGGGTTGCAGCTGGAAGGGCATCCGCTGCATAAAACATTCTGGATAAGTTGGCGGTTCATTCTGCTGTAGCGACCCCTTATTAATAAAGGGACTAAGCAAATAAGAAAATGAATGAATATATTTACATGTTTGCACTGAGTAAGATGCACTTAGTCTTGTCGCACATGTATATAATGTACCATCTATATCTGTACAGTTACAATAAAAGCCATTCTATTAGGTTAGTGCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15874
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 |
---|---|---|---|---|---|
ENSDART00000025131 | Nonsense | 27 | 1164 | 1 | 25 |
ENSDART00000124113 | Nonsense | 27 | 557 | 2 | 15 |
ENSDART00000138885 | Nonsense | 14 | 992 | 2 | 19 |
ENSDART00000025131 | Nonsense | 27 | 1164 | 1 | 25 |
ENSDART00000124113 | Nonsense | 27 | 557 | 2 | 15 |
ENSDART00000138885 | Nonsense | 14 | 992 | 2 | 19 |
The following transcripts of ENSDARG00000018272 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 5080241)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 5525969 |
GRCz11 | 2 | 5437851 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTTCCAYATGCCTCGCTTCCAGCACCAGGCTCYCCGWCAGCTGTTCTA[C/A]AAGAGGCCCGACTTCGCCCAGCAGCAGGCCATGCAGCAGCTCACCTTYGA
Long Flanking Sequence:
TTGGTTTATTCCTGCAAAAAAAAGTCCTGGAAAGCTATTTTGATCCATTGCAGTTCAACTGAAAGAACATATTAGCATAACCTGTGTAACACTTACTTGGTTACTTGCATAATAAAATGAGAAAAATGGTTCTTATTTAAAGATGGTGGTTTAAGTTGTCGATAACCTTGTGTATTGATTTGTAGTATTGTACTTACCCCCCGCCCCCCAAAGAGTGTTGTTGTCTATGCCCAAATTTTTCAATCACACAATCACATACATTTCTAAAATGAATCCGTGTCATTAACCATGGTTTTTTTTGCCTATGTGTTGTTGTTTTGCATTGATCTGTGCATTTAGTTGCTGATGTTCTCTTGAATTTAGCCAGCGGAAAGAACCCTTAATTTCTCTCCATATCCTCAGGTGTACTAAACCGTGACCATGGCGACTGACATCGGCTCCCCTCCGCGGTTCTTCCATATGCCTCGCTTCCAGCACCAGGCTCCCCGTCAGCTGTTCTA[C/A]AAGAGGCCCGACTTCGCCCAGCAGCAGGCCATGCAGCAGCTCACCTTCGACGGCAAGCGCATGAGAAAAGCCGTCAACCGCAAAACCATCGATTACAATCCATCCGTCATCAGACATCTAGAGGTATTAGCCTAGCAGAAATACAACTCTCTTTTTTATTGTATGTATTTATTTGGTATAGTTCTGCTTTCACCTCACCCTACAGTTTTTTTTCCTGTAACTTGTTAAGTTTGATTTGTATTGTAAGAATATATTTACTTTCCCAGTACTGGGTTGCAGCTGGAAGGGCATCCGCTGCATAAAACATTCTGGATAAGTTGGCGGTTCATTCTGCTGTAGCGACCCCTTATTAATAAAGGGACTAAGCAAATAAGAAAATGAATGAATATATTTACATGTTTGCACTGAGTAAGATGCACTTAGTCTTGTCGCACATGTATATAATGTACCATCTATATCTGTACAGTTACAATAAAAGCCATTCTATTAGGTTAGTGCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31252
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 |
---|---|---|---|---|---|
ENSDART00000025131 | Nonsense | 708 | 1164 | 15 | 25 |
ENSDART00000124113 | None | None | 557 | None | 15 |
ENSDART00000138885 | Nonsense | 695 | 992 | 16 | 19 |
The following transcripts of ENSDARG00000018272 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 5064442)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 5510170 |
GRCz11 | 2 | 5422052 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGCTCTGGTGGACCTCCAGGCAGTATTATGGGACCACCGCCACGAGGA[C/T]AGGGTCCTCCACAAGGAAATATGATGCATCAGGACATGAGGGGGCCTGTG
Long Flanking Sequence:
TCACTGTATTGTGAATATGAACAATAAGAAAATTCTTTGTTTGTCAACAGCAACTGAAGATTGAGCGAATGGCACAGTTGCAGGAGCAGGGACTTCCTCCCCCTACTGGACAGCAGTCAGGACCAGTTCCGTCCTTTCCAGGGCAAGGTGGTCCAATGCCTCCTCCAGCACAAGGCTTCCCTCAGTCCATGCCTCCACAGCAAACACCACACAACATGCCTCCTGTTGGACCAGGGGGGATGCCTGGTCCATTCATACCTTCAGGCCAAATGGGCCCACCGGGACCTCCCATGCACCAGGGTCCGCCTCCACAGGGCATGATGGGACCTCCAGACATGCATGGACCTCCACGTCATCCCGGCCCTCACAGGAACATTGGACCCCAGGGTCCTCCTGGCATGCCGCCAGGCCCCAGAGGCATGCAAGGACCTCCCCCAGGAGGGATGCACCCTGGCTCTGGTGGACCTCCAGGCAGTATTATGGGACCACCGCCACGAGGA[C/T]AGGGTCCTCCACAAGGAAATATGATGCATCAGGACATGAGGGGGCCTGTGCCCCATGGAAACATGATGGGCCCTCAGGGACCCATGCAAGGGGGTATGATGGGCCCTCCGCTCAGGACTCATGGCATGGGAAATATGCATGGGATGGGACCTCCTCCTGGGGGTATGCATGGACCACCAAACAACATGCAAGGGCCACCAGGAAATATACAAGGACCTCAAAGCAGCATGCAGGGCCCCCCACCATATATGCAGGGCAAACCCCCACACATGGGTGATGGAAATCGAGGACAGTTCAGCCAGGTGATTATTCCTTACACCCATGAATGTTAAAAGGGTCACGAAACACCAAAACACATTTTTTGAGCTGTTGACAGTCGTATATGTGTCCCATTCTGCTAAAAACACTATTAGGACACCTATATTTCACTAAAAAGTGTAAATTGGTTGTTTTTGCGTTATTTCAAGCAAATTCGTACTTCCTGTTTGAAACGAATTTTT
Associated Phenotype:
Not determined