ZMP
wu:fd12d03
Ensembl ID:
ZFIN IDs:
Description:
Wu:fd12d03 protein [Source:UniProtKB/TrEMBL;Acc:A9JRU7]
Human Orthologue:
CHD4
Human Description:
chromodomain helicase DNA binding protein 4 [Source:HGNC Symbol;Acc:1919]
Mouse Orthologue:
Chd4
Mouse Description:
chromodomain helicase DNA binding protein 4 Gene [Source:MGI Symbol;Acc:MGI:1344380]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13914 | Nonsense | Available for shipment | Available now |
sa16797 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13914
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 |
---|---|---|---|---|---|
ENSDART00000042209 | Nonsense | 267 | 1074 | 6 | 21 |
ENSDART00000092902 | Nonsense | 267 | 1953 | 5 | 39 |
Genomic Location (Zv9):
Chromosome 16 (position 34005910)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 31828394 |
GRCz11 | 16 | 31783982 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCCCGCCCACGACAACAGCAGCTCCTGTCGCTGCMCCACCCCCACCCCAG[C/T]AGCCCCCAGCAGTCCCACTGCGGAAAGCCAAGAYCAAAGAGGGCAAAGGT
Long Flanking Sequence:
CCAAATCTTCCTCTCAGCTATTAGCAGACTGGGGAATGAAAGACATCGACTACACCTTTACCCAGGAGGACTACAACTCTCTCACCAATTACAAAGCTTTCAGTCAGTTTGTCAGGTAGAGCAGTGCCTCTTCCACATCTCATGTTTTATTTTGTCCCATTTCAATTATCGCCTCATCCATCCTATATGCTATGTAGTGACTGATCTAAGATGTCTTATTTTTTCCACTCATGTTTAGGCCTCTAATTGCTGCTAAGAACCCTAAGATCGCTGTGTCAAAGATGATGATGGTTTTGGGAGCTAAGTGGCGGGAGTTCAGCACTAATAATCCAATGCGAGGCTCAGCGAGTGCCAATGCAGCCCTGGCAGCTGCCAATGTAGCTGCTGCAGTGGAAAGTATGGTGACCAAGGTGGATGCAGGAGGAGGAGGAGGACCGGCATTAGCCACAGCCCCGCCCACGACAACAGCAGCTCCTGTCGCTGCCCCACCCCCACCCCAG[C/T]AGCCCCCAGCAGTCCCACTGCGGAAAGCCAAGACCAAAGAGGGCAAAGGTCAGAGGAGAAGAGCAGAGAATGTGGATAAATGATGAACAGAGCACAGAATAATTTTTGAGGCCAAAAGTGTGATTATGTTATTTTTTACTTTGTGTTTGCTCCAGGCCCAAATGCACGTAGAAAGACCAAGCCTACCCCAAAGCCCCAGGACAAAAAGTCTAAAGCAAAGAAAGTGGCACCCCTCAAGATTAAACTGGGCAATTTTAAGAGAAAGCGTTCATCTGTATGTATATTTTCTCTGTATATTCTTTTGTTACTGCAACATAATTAGCACTATTGCTGAGTTAAACAGTATCATCAAAGTTTAAAAAAAGTATTATATGATATAAATGTTATATAATTATTATTTATATAATAAAATATTATTGTATAAACTATTTAGTATGTTATATTGGTATATTTTTAATTCAATTCATGTTCATTTCTATAGCAATTTTACAATGTAGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16797
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000042209 | Nonsense | 397 | 1074 | 9 | 21 |
ENSDART00000092902 | Nonsense | 397 | 1953 | 8 | 39 |
Genomic Location (Zv9):
Chromosome 16 (position 34004649)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 31827133 |
GRCz11 | 16 | 31782721 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCCAGCAGGGYGGWGAGATCATTCTGTGTGACACCTGTCCCAGAGCCTA[T/G]CACATGGTCTGTCTGGATCCTGACATGGAGAGGGCACYAGAGGGTACCTG
Long Flanking Sequence:
TCAAGGGAACGTATTTCAAATAACATTTGATAGATATTGTTATACATTTTGCATAGTTATTAATGGTAAATTCTGCTGAAGGGCAGTTAACATGTATTAAATCATGCATTTGTTTCTTCTCTCTATGGCTAACATTTTTTGTACCACTTACCCATGGTTTCTTCATTTAGAGCGGTGAGGAGGATGATGGCGAGAGCGATTTTGACAGTTTTTCTGTAAGCGATGGATCCAACAGTCGAAGCAGCCGCTCCAAGAATAAGAAGGCCAAGAGCTCCAAAAAGAAGAAGAAAAGTAAGTCAAAACACAGATTTCACACACTATAATAAACTACTATACTAGATTGATAACTTTACAGCCGTATATATTGATTGATATAATTCGTCTTTCTCTCTCACAGTGGATGAGGATGCTGACGGCTATGAAACAGATCATCAGGATTACTGTGAGGTTTGCCAGCAGGGCGGTGAGATCATTCTGTGTGACACCTGTCCCAGAGCCTA[T/G]CACATGGTCTGTCTGGATCCTGACATGGAGAGGGCACCAGAGGGTACCTGGAGCTGCCCCCACTGCGTATGTTCATGCAAATATGTCTTTTCCTTCAGCTGCTTTAGGGTCATCGAGTAAAATCTGTATTCTTTGCATGCGCACTATATTTCTACATTCCATTGTTATTTAATGACTAAAGTTTCTGTTGATGATGCATTATTTATGTCTCTCTCTCAGGAGAAGGAGGGCATTCAATGGGAGGCCCGCGAGGAGAGTTCTGAGGGCGAGGAGGAGAACGATGATGGAAGGAGGGATGATGGAGATGTGGAGGAGGAGGACGATCACCATATGGAGTTTTGCCGTGTGTGCAAGGATGGAGGAGAGCTGCTTTGCTGTGACACATGTCCCTCGTCCTACCACTTGCACTGTCTCAATCCGCCCCTGCCAGACATCCCCAATGGAGAGTGGATTTGCCCACGCTGCCTGGTGAGAGAGTTTTTGAATTTAGATTTTTTTTT
Associated Phenotype:
Not determined