ZMP
wdr75
Ensembl ID:
ZFIN ID:
Description:
WD repeat-containing protein 75 [Source:UniProtKB/Swiss-Prot;Acc:Q7ZVR1]
Human Orthologue:
WDR75
Human Description:
WD repeat domain 75 [Source:HGNC Symbol;Acc:25725]
Mouse Orthologue:
Wdr75
Mouse Description:
WD repeat domain 75 Gene [Source:MGI Symbol;Acc:MGI:1920924]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21553 | Essential Splice Site | Available for shipment | Available now |
sa21552 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21553
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000059667 | Essential Splice Site | 481 | 832 | 14 | 21 |
The following transcripts of ENSDARG00000040730 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 42206241)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 41331411 |
GRCz11 | 9 | 41133198 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTGAGTTCAGACACACCCGTCTCACCGCACCCCTTTTCATTTGTGTTTC[A/T]GAGGCCCAGAACTACTGGTCATGTGATTTCGTTGGCAGTTATCATAACCT
Long Flanking Sequence:
CCGAAAACAATTGTACTGCTAAAAGATATGTTAAACTATGATAATCAATTTTTATTTTTTTTTTTTTTTTTTTATAGAGAAAGTTCGATGAACAGCATATGATTAAAAAAAAAAATCTTCTGTACCCTTAAAATCCTCTTCATCTTTTGGTTAAGTTTAATTTGTTCTTTCCAAATAAAAGTATGACGCTTTAAGCAGTATTTTACAAATTTTTCACAATTTTTATGCGCTCTGTGCTGTTAGCTTTGTCCTGAATACCACCGTCACTGAGGCCCACAGCGAGCGGATTACATCCATGTGCTTCAGCTCTTCAGAGGAGACCACCATGCTGGTGACCACAGCCCTGGACGGCCAGTTCAAAGCCTGGTGTCAGACTGCAGACGCTCAACGTGAGTCAAATCCTCCAGAACCTTCCAAAGGTGTTAATGTTGGATGAAGAAAAGCTCAAGTCTTGAGTTCAGACACACCCGTCTCACCGCACCCCTTTTCATTTGTGTTTC[A/T]GAGGCCCAGAACTACTGGTCATGTGATTTCGTTGGCAGTTATCATAACCTGAAGCCAAAGAACTGCTGTTTCTCAGCTGATGGCTCCATCCTGGCTGTGAGTTTTCAAGAAGTCCTAACATTATGGAGCCCGGAGACCTGGGAGCTGCTCACCACACTCTGCCAACCACCTGGAGAAATAAGGTGATTCGCTGACTGCAGATCAGCTTGACCAGACTCTTTCTGCTGTGTTTGTTTTAATAGGGGTACATTGTGCTTTAAAATTAGAGTATCATAGCTTATATTGATTAATACAATTGTGCAGGCTGAGGTTTAATCTAATTAAATGCTATGTATGCAACACAAGCTTCAGTAAAAACTATTACAAATTGCCTGCATGGAAACGAAAACAAACTATACACTGAAGATTTGGCAACCCAAAATACTATGAATGGTTGGAATTTATTTTATTAAATGAAGAAAATTTCTGTATTTTTGTGACCCACAATATTAGCATAACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21552
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 |
---|---|---|---|---|---|
ENSDART00000059667 | Nonsense | 629 | 832 | 17 | 21 |
The following transcripts of ENSDARG00000040730 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 42198368)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 41323538 |
GRCz11 | 9 | 41125325 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCCACGGCCTTTGTTCAGCCAGAGATACGTGTGTCTAGAAAGGGTGGAT[C/T]GAGCCGTGTTTGTTCCTCGAGAAGAGCCGTTCAACAGTTGTGATGAAAGC
Long Flanking Sequence:
GTAAGTGTTTAAAGGTCATCACCTACATCTCTTTAGTGTTTGGTTAGAAGTAATGTGTGTTTTTTTTTTTTTTATTGGTGCTCTTTTGGAAATCTCTTTTTGTCACTTTATAATTCAGTAAAAATAAAATATAAAATCAATAATGTGTTGTACAATTAGCTAAAATTTAAATGAACAATGTTGTGTCATAACCTTCAAAATATAGATGATGAAACTGCAAACCTTTAATAAAATGTATTGTAATAATTTAGGATACAAAAATACAGACACAATTTGATAAAGTGTGACAAATGAAACGCATTAAAGTGCATTATGGATGTTTTCTTTGCATTAGACTGAAAATGGCAGAAATCTGAAAATTGACAAGAGCATAAACGCCTTTAATTGATCACAAGCTGCTGTTTAATGTCTTCTCTGGTGTGTGTTCAGTGTTTGTGTTCAAGCCCAGCGAGCCACGGCCTTTGTTCAGCCAGAGATACGTGTGTCTAGAAAGGGTGGAT[C/T]GAGCCGTGTTTGTTCCTCGAGAAGAGCCGTTCAACAGTTGTGATGAAAGCTGTCAGTGGCTCAACAGATCTCAGCTCTACTTCCTCACACACAACATGGTACTTCAGTCATACCTAGAGTCAAAACATGTCCTTTTTTTTTATTATTAAGCTGATACTTGGATAACAATAAGTGCATGGCGTAAAATATATAGTATAATCTGCTGGTTTTAAACATACAGTATAATAATGGAATACAGATATTTAAGCAGCTATAACATTACAATTATCCCAACAAACAAAAAATATGCTAATTAATAATAGAAGAATATAAATAAAAAATAGGGGGGTTTCATTTACAAAGAAGGTAAGAAGGGGTCTCGACATTAAAAAACACAGGGTTGCACATTTTATAAAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGCATGTATATGTATATAAATTATGAGTTCAGATGCAAAACCCTCTAAATCCATTAGACCTTTTTTCTTGTAAA
Associated Phenotype:
Not determined