ZMP
zgc:112032
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens WD repeat domain 13 (WDR13, zgc:112032) [Source:UniProtKB/TrEMBL;
Human Orthologue:
WDR13
Human Description:
WD repeat domain 13 [Source:HGNC Symbol;Acc:14352]
Mouse Orthologue:
Wdr13
Mouse Description:
WD repeat domain 13 Gene [Source:MGI Symbol;Acc:MGI:1914661]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41115 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa845 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa41115
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000033294 | Nonsense | 40 | 482 | 3 | 10 |
ENSDART00000139545 | None | None | 100 | None | 5 |
The following transcripts of ENSDARG00000022974 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 7508920)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 6895723 |
GRCz11 | 8 | 6939271 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCCCCAGTTCCGCACGCAGTACATCCGCCGGCGCAGCCAGCTGCTCCGC[G/T]AGAATGCCAAGTGTGGCTTTGAGCCGGGGCTGCGCAGGCAGTATCTGCGT
Long Flanking Sequence:
TGGCATGATAATCGTAACCGAACCGAACCTTGAGACTAGTGTAGGTTCACAGCTCTAATTAATTAGGTTATCAATATTTATTGCTTTATGTTTTAGGCTTATTTAGTTTTTATGTAATCTATGTAATGATATATATATATATATATATATATATATATATATATATATATATATTTTTTTTTTTTTTTTTTTTTTTTCTAATGACATATACAACTTTTATTTATTTATTATTTTTTTTTTTGTGTTTTCCTGTAGCCCTTGTGTTTCCTGCATCTCTCTGTGTTTGTGGATCTCATGGCTGCTGTTTGGCAGCAGGTGCTGGCAGTGGACGCAAGGTATGTGCAACGTCTCCCTGAAGTCTTTCATTGCATACATTTTTTACATCTGTAGTGTCTAATTATGTGTCTCTGCCTTTTTCCCTCAGGTACAATGCTTACCGCACACCTACGTTCCCCCAGTTCCGCACGCAGTACATCCGCCGGCGCAGCCAGCTGCTCCGC[G/T]AGAATGCCAAGTGTGGCTTTGAGCCGGGGCTGCGCAGGCAGTATCTGCGTCTGCGCAGTCAGTTGCTCGCCCTGCGTTACGGGCCTCTGTCAGAGCAGAGCAGCTTCAGAGCCAGCAGTGTGCGCAGTTCCCGCACCACACTGGATCGCATGGAGGTTAGGTGCATTCAGAAAAAAAAAAGGGGGTTGAGAAACAAAAATTAGGAGTTCCGGGCTGTATTAAGCCCCTACAAAAATACAGCCAGAGGGAAAGATTAAAATATCTTTATAGTCCCAGATATAAATAGCAATCCAGATCCAGGTCATTGTGTCGTGTGAGAGCTGCAGTGCATGTAGATTGCGAGCTCTATTATGCATGACGGGCTTTATGTTGCTGTTGTAGTGCTAAACTCAAAAATCACCCTTAAAACCTCCCTTGCCTTGGTTTCCTCCTTTCTTGGTCTTTTTTTATTCTTTTTTTCCGTGTTTCTGTAGGACTTTGAGGAGGATCCCAGGGCTCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa845
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000033294 | Nonsense | 222 | 482 | 6 | 10 |
ENSDART00000139545 | None | None | 100 | None | 5 |
The following transcripts of ENSDARG00000022974 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 7503431)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 6890234 |
GRCz11 | 8 | 6933782 |
KASP Assay ID:
554-0748.1 (used for ordering genotyping assays)
KASP Sequence:
GTAAAGGTGACTCTGAAGGGCCACGCTGGGCCTGTGACCGACTTCGCTTG[G/A]TCGCTGAGCAATGATATCATTGTGTCCACTTCAAAAGATGGCACTCTGCG
Long Flanking Sequence:
CTCTACAGCATATGTAAAAAAAAGCTCCTTAAAATAAAATGCTGCCTGAAATAGTCTATAACAGCATTATCAGAATTTAGCGATCATGATTAGCATTTTTCTATCAGATTTTTATAATCTATTTCTAAGAGGATACGGTTAAGGATTGCATATGCAAAAACAATAATTGTGATATGCTATAATTGAAGACATGGATTTTTGTAACATGCTGTTTTAGTTTAGGGAAAGAAGTCATCCTAATTTTGTGAGTGTTTCTACAGGTGGTTTGTCAAACCCACTAACCTGTAGAAATGCAGCAATCTCTTGTTAAATTTGATCATTAACATTTTTGACTTATTCATCTCCTCAGTTCCCCGTTTGCAGTTTGCTAATGACGATAAACACCTCCTCGCCTGCTGCTCATTGGATGGGACGTTGTCAATCATGACTCTGTCTCCGCCTCCTCCAACTGTAAAGGTGACTCTGAAGGGCCACGCTGGGCCTGTGACCGACTTCGCTTG[G/A]TCGCTGAGCAATGATATCATTGTGTCCACTTCAAAAGATGGCACTCTGCGAATCTGGAACACCGAAGATGGACGCTGCATCCGGGAGGTGGTCGACCCTGAGGGCAGTGAGCTGCTGTGCTGCACTTTTCAGCCCATGAACAACAACCTGACTGTGGTGAGTCCACATGAAACACTGCGGTAACAAATACCATCAGTCTTTTCAGTAATCCTATTAGAGTGTGAAATTAGCTCATGCTGCAAGCCAAAAAAAGTGTACTTTGAATGGAGAAATGAGTAATGCTGCTTATCTGCCAGCCTCACAACGGCGGTGAGCCACCTGTGAATGCATATCTGAATGACATTTGATATGAAACGTTACAGCAAAATATGCATACACAAAAAAATGTATTCGATGATAACATTTCTACTTTATTCACCTTTTCTGGTTTGCTTATAATGTGCATTCTAGATTAACTTTCATTTCTAGCAATTTGTCATTGCATATATTTGTATCCGCCT
Associated Phenotype:
Not determined