ZMP
si:ch211-51m24.3
Ensembl ID:
ZFIN ID:
Description:
chromodomain helicase DNA binding protein 4 [Source:RefSeq peptide;Acc:NP_001038323]
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 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23422 | Essential Splice Site | Available for shipment | Available now |
sa23421 | Nonsense | Available for shipment | Available now |
sa23420 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23422
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000005453 | Essential Splice Site | 475 | 1930 | 9 | 40 |
ENSDART00000092923 | Essential Splice Site | 476 | 1929 | 10 | 40 |
ENSDART00000130062 | Essential Splice Site | 476 | 1929 | 10 | 41 |
Genomic Location (Zv9):
Chromosome 19 (position 5663238)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 5122549 |
GRCz11 | 19 | 5039035 |
KASP Assay ID:
2261-2843.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCGCTGCCCGAGATCCCCAACGGAGAGTGGATCTGCCCTCGCTGCACTG[T/C]GAGTCAAACATGCTAGAGCTTAAAGGTCTGAGGTCAGACTGTTTTCAAGA
Long Flanking Sequence:
GAGACAGATCATCAGGATTACTGTGAGGTCTGCCAGCAGGGAGGTGAGATCATTCTCTGTGACACCTGTCCACGGGCCTATCACATGGTCTGCTTGGACCCCGACATGGAGAAGGCCCCTGAGGGTACCTGGAGCTGCCCACACTGCGTGAGTGAACCGGATGAATCTCAGATTGCACCGTTTGCCCTTTTGTTTTTGTCCAGCAAGCTTAATTAACATAGATGCCAGTAAAATTTAAGTGTTAAACCATCCCCTGCTTCTCCAGGAGAAGATGGGCATCCAGTGGGAGGCTCGTGAAGACGCGTCTGAGGGCGAGGAGGATAATGAGGCAGGAGGAGAGGCCGAAGAAGACGACCATCACATGGAGTTCTGCAGAGTCTGTAAGGATGGCGGAGAGCTGCTGTGCTGCGACTCATGCCCTTCGTCATACCACATCCACTGCCTGAACCCACCGCTGCCCGAGATCCCCAACGGAGAGTGGATCTGCCCTCGCTGCACTG[T/C]GAGTCAAACATGCTAGAGCTTAAAGGTCTGAGGTCAGACTGTTTTCAAGACGTTGATTTTATGACTTCGTAAATAGTTTGTAATAAATGTTAATATGAGAAATTATGTACATATATAAAATTTTGTTAATATGCATTTTTTTTTCAAATCTTAAAACTATAAATCTGATTGGGACTCAACATGCGTTGGTGTTAGGGATTTTAAATTAAGGACATGTATAATTGTTCTCTATCCTTTATATTTCCTTTATAAACTCCTGTATAACAGGCATGTCATTGGTAAATTGCACAGTAATTGTTGCATCTAATTGATTGTAAAAATATACATTTATAACAGATATGCAGTCTCATGTATGTATGTATATATGGACTATTCTTTTAAAATATATTCATTTAAATGGAACTTATATTTTTATATATTACTATGACATAAACATTATGTATAAACATTTTTTATTAATATAATTTATTATTTATATAAACATTCATTTTTATTATTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23421
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000005453 | Nonsense | 632 | 1930 | 12 | 40 |
ENSDART00000092923 | Nonsense | 633 | 1929 | 13 | 40 |
ENSDART00000130062 | Nonsense | 633 | 1929 | 13 | 41 |
Genomic Location (Zv9):
Chromosome 19 (position 5659159)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 5118470 |
GRCz11 | 19 | 5034956 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATAAGAAGAACAACTGTCACTACCTCATCAAATGGAGGGACTTAACATA[T/A]GATCAAGCCACATGGGAGTTGGAGGATATGGATTTACCAGACTATGACAC
Long Flanking Sequence:
ATGTTTGCCTTAGAAGAGTCAAAAACTTACATACAGCACCTTTAATTAGATTAAGATTTAATCTACTATGTGCATCCAGAGAATTGTTAATTACTATTTGTCATTTTGGCAGAATTTGCACCTAGTTTGAGTTTTTACTTCTCTTGCTGTTTCCAGCTGGAGATTCACTGTCAGGTGATGTTCAGAAACTACCAGCGCAAGAACGACATGGACGAACCTCCCCCCATAGACTTCGGAGGTGAAGGAGAAGAGGAGAAGAGCGACAAGAGAAAGAAAAAAGACCCCACATACGCACGGATGGAGGAGAAGTACTACCGCTTCGGCATCAAGATGGAGTGGATGGTCATTCATCGAATCCTGAACCACAGGTCAGTTGAACTCCACATCTCTGGACTCATTTTCGATCAGTTACATGGATTTACGTGTGCCGTTTACTTTCTTTTTAGTGTGGATAAGAAGAACAACTGTCACTACCTCATCAAATGGAGGGACTTAACATA[T/A]GATCAAGCCACATGGGAGTTGGAGGATATGGATTTACCAGACTATGACACGTATAAACTGCAGTACTGGAACCACAGGTATATACATGTACATAGACATTAATATTGACAACACAAACAGAATGATTCAAGTAACTATCATCATCATCATCATCATTGTTATTATCTTGGTGGATAATGTAATTGTTTGTTTTAGTATTCGTTTTATTACTATTAAATTTATCTGTTATTGTTGAAATATTTAGAATTTGTCTTTTTTTTTCTCTGTTAGTTAAAGTTGTAGTTTTGTATAAGTAGTTTTTTTTTTCCATTTGTCTTTATTTTACTGCCGTTCACGTTTACTTTATTTTAGATTTTGTTTATTCACTGCTCTAGTTTTTATTCATACTTTATTTTTGCTTATAATATAATTTTTTTTAATTTTATTATTTTGTAATATTACATTTAGAAAAGCTTAAATGGTACTATTTGATTTCTATTTGTTTCTGTTTTAGTATATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23420
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 |
---|---|---|---|---|---|
ENSDART00000005453 | Nonsense | 683 | 1930 | 13 | 40 |
ENSDART00000092923 | Nonsense | 684 | 1929 | 14 | 40 |
ENSDART00000130062 | Nonsense | 684 | 1929 | 14 | 41 |
Genomic Location (Zv9):
Chromosome 19 (position 5657328)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 5116639 |
GRCz11 | 19 | 5033125 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTAAACCAGGAAAGAAGATCAAGATCAAAGGGAAGATGCGCAAACTGGAC[C/T]GACCTCCAGAGAATCCTGTCGTGGATGTAAGCAAGCATTTTTCATTATGC
Long Flanking Sequence:
GTGCAACTAGATAACTAGAGTTGCGTAATATTTGTGTTCCTGCTGCAGCCATGGTACAGCAACAAAGTTCCTTGATTATTACGCATGAATAGAAGTATAGTTCCTAGCCATATCAACATGGCAACTTTTTATTTTCCATCGCTCTGGGTACACGATGTAACTTCAGAAGAGTCCAGCTTTAAATAGGAAAATTGTCTGATTGCTTTTATTAATTTAAGATGCCAATGGTCTAATCCGATTTAATGATCTATGCTAAGCTAAGGTAAAGGTGCTTACACTAGACCTGGAGATTGTCTCAATGGATTCAAATCCAATGAAATGTTAAAACTCAACTCAAACTTAACTCTAGGGGAATTGTGAAATGATACTTGGTGTTCCTTCAAGTGTGAGAAAATGCACATACATCTTCTGTTTCTCTTTCTTAAAGGGAGCTGATGATGGGTGATGAAGGTAAACCAGGAAAGAAGATCAAGATCAAAGGGAAGATGCGCAAACTGGAC[C/T]GACCTCCAGAGAATCCTGTCGTGGATGTAAGCAAGCATTTTTCATTATGCCATACACTATAATGACAACACATTCAACTCTTGTGTATTGTTCAGATTGACTACCCTTTCATTATGTTCGGGGTTGTATTTTACCCATTGACCTCCATTATAACCATGTTTTTGATTGCAAAGCCATGACACAGCCATGTATTAATATAATCATGAGTTCTTGATTGTTGGTGGTTTTCCTTGTTGGGAAGAGGTGGAATTTGTCAGTTTTACGGTTGATCATCAGTTGGGACCATTAACCCTTTAGATAGACCTGTGCAAATACGTTTCTGGCTATTCTGTGGGGTAAAAAATGTAGATTATAGTGTGTATTCATATATACACTTACTATGTTTACTATGATCTGAGAGCTGAGCTGCTTTTTTATTTTCTCAAACATATCAAGGTAATTGTGCAAAGTCTCTTACACGCGCACAGTATACTCCATATACAAGCCAGAAACTAAGCTTT
Associated Phenotype:
Not determined