ZMP
si:ch211-10e2.6
Ensembl ID:
ZFIN ID:
Description:
Chromodomain-helicase-DNA-binding protein 8 [Source:UniProtKB/Swiss-Prot;Acc:B0R0I6]
Human Orthologue:
CHD8
Human Description:
chromodomain helicase DNA binding protein 8 [Source:HGNC Symbol;Acc:20153]
Mouse Orthologue:
Chd8
Mouse Description:
chromodomain helicase DNA binding protein 8 Gene [Source:MGI Symbol;Acc:MGI:1915022]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa19827 | Nonsense | Available for shipment | Available now |
sa19826 | Nonsense | Available for shipment | Available now |
sa31293 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa19827
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 |
---|---|---|---|---|---|
ENSDART00000009942 | None | None | 2221 | None | 39 |
ENSDART00000013676 | Nonsense | 223 | 2160 | 1 | 35 |
ENSDART00000131837 | None | None | 2231 | None | 36 |
Genomic Location (Zv9):
Chromosome 2 (position 37817825)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 38132739 |
GRCz11 | 2 | 38115067 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAATGCGACATCTCCTGCGCAGGGGCAGGTCAAAGTTGGCACTGGAGTA[C/T]AAAGGCTGGTTCAAACTGCAAATGGCCCAATGAAACAGGTGTTACTGACC
Long Flanking Sequence:
TTCCTATTCTGAGTGACGTGGTCACAGATCCAGCTCTAATCCCAACTCCTGTCTCTGTTCCACTGCAAAACCTTCAAACTCAGCAGCTCAGCCAGATCCCCCATGAGGTCTCTGTTGCCTCTGCTCCCATTTCCATTCAGCCCTCCCTCTCGGTGGCCAGTAACAGCAGTGGTGCTGCAACAGTCTTGCTGAGCTCTTCTCTTGGTGTACCTGTGTCAGGGGCTCAAGTCACCCCTCAGCAGCAGACTCAGCAAATCACTGCTGTTACGCAACAGGCAGCGGGACAGCACGCCCCAAAAATTGTCATTCTGAAAGGCCCGCAGGGTCAGACTCAAGTGCTGCAGGGTGTCACAGGAGCCACGGGCTCTCCAGGGAAAGTCACCCTCGCTAGAGTTCTGACAGGGACCCCTCTTAGGCCCGGCATGGCAGTTGTTTCTGGAGGGACGGTATTAAATGCGACATCTCCTGCGCAGGGGCAGGTCAAAGTTGGCACTGGAGTA[C/T]AAAGGCTGGTTCAAACTGCAAATGGCCCAATGAAACAGGTGTTACTGACCTCAGTGCCCCAGACGCAATCGCAGGTGCAGACACAGCCTGTCCAGGTGCAAATACCTGTGCAGACACAGCTGCAGTCACCATCGCAGCCGCAACAGCTTCAGGCGCAGATCCAGGCTCAGACACAGGTGGCATTACAAACACAAGCCCAAACGCAGACTCCTACTTCTCCGGCAGCAGCAGGCATCCGACCTCAAAGTGTCACACTTTCTGCAGTACCACAGCAGGTCAGATTTTAACTTGAATTATCATCATACAGACTAAAACCTGAATAAACCACTCTAATAAATGATGTAAACAACTTTTAAAACCACTTTAATAAATTATAGGGAAAATCTGATATTTGACATCTGATATCTGACACTTACATTTTTGCTTTAACTATTCAATCTAAGTATTCAATCTAAAGTAAAGTGCAAAAATAAAGGTGCATGAAAAGCTACATAGACATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19826
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 |
---|---|---|---|---|---|
ENSDART00000009942 | Nonsense | 1559 | 2221 | 28 | 39 |
ENSDART00000013676 | Nonsense | 1589 | 2160 | 28 | 35 |
ENSDART00000131837 | Nonsense | 1350 | 2231 | 24 | 36 |
Genomic Location (Zv9):
Chromosome 2 (position 37804136)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 38119050 |
GRCz11 | 2 | 38101378 |
KASP Assay ID:
2259-2391.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCTTTTTCTGTCTTTTAGGGTTTTGCTGAGAGTACGTATGCTTTATTA[T/A]CTGAAGCAGGAGGTCATTGGAGAACATGCTGATTCTGTATTGAGTGGAGC
Long Flanking Sequence:
GCCTTGGGTGTTATTCTATCATGTATTCAGTAAGATCTACACTTACGTTTAATCTTCTTTTCTTATTCCACTGCTTTCATTGTGTATGTAGGATTGTTGCTTTTCAACTTTCATGTCAATTAATACATTTCAAGCCTGTGTAGGGTTTGAAACAGCATTTGTTTAATGTCAAGTAGACGGAGAGCTTTTATAGAGGCATGTAATGGCTTTCTCCTTTCCTTTAGGTCTGTCCATCCCTGTTCCTCGCGGCCGAAAGGGAAAGAGAGTGAAGGCTCAGAGCTCTTTTGACGTGCAGAAGGTTGAGTGGATCCGCAAATACAATCCTGACAGTCTGCTGCTGGATGACAGTTACAGAAAACACCTCAAACACCAGTGCAACAAGTACGTAAGATCCATCTAGGGCACTGTTTCATCATTTAATTGGCCTTGAGTGTCTTAATTTGGCTCTTTCTCCTTTTTCTGTCTTTTAGGGTTTTGCTGAGAGTACGTATGCTTTATTA[T/A]CTGAAGCAGGAGGTCATTGGAGAACATGCTGATTCTGTATTGAGTGGAGCTGATGCAAGGTATACATCGCCTCATGTTGTTGCTTTAGAGCAGTAATTGTCAATAGCATGTGCTAAATACACAATTGATAAATGCGTCAGGCAGAAATGCCTTGCAGGTTGTTCTACCTGTGCTTACATCTTTTGGTCAACTGGTCACATAGTTATAAACAAATATAATTGATACCTCTAATTAAAGTTATTTATTTGTTTGGTTAAAGAACTACTTTTCAGGATTGCAGTTTTATGAATTAATGTTCTTGAATTTTATTCTTAAACAATATTACATGACTCAAGAATTTGCACTTCTTTCTTCCTGCAAGAGGAAATGTAGTGTCTGACACAGCAAAAAAAATGCATGTTCATTCTAAAAATACCTGTGGATTAATTGTTTTTCAGCCTACATGTGAGGTTTTGTAATTAATCACAGTTTTCTTTTTTTTCTTTTTTTTTGGAAACCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31293
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000009942 | Nonsense | 1756 | 2221 | 32 | 39 |
ENSDART00000013676 | Nonsense | 1786 | 2160 | 32 | 35 |
ENSDART00000131837 | Nonsense | 1547 | 2231 | 28 | 36 |
Genomic Location (Zv9):
Chromosome 2 (position 37801447)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 38116361 |
GRCz11 | 2 | 38098689 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTTAAGATCGAGGCAGCAGAGAAGGGGGACCGTAGGCGAAGACGCTGC[G/T]AACAAGCTACCAAACTCAAAGAGATAGCCAGACAAGAGCGACAGCAACGG
Long Flanking Sequence:
AATGGAGCTGATCTCCTAGATTCTAATACTGCAGCTCATGTGATTAACTGAAATATTTAACCATAAATTTTACAAATGTTTATTGTTGCCTCATATATACTTTTTGTGTCTTAGAGGGGACTACGACAAGTACTCTGAAGATCCAGAGTTCAAACCCGCAACGAGACATGCCAAGGAGATGTATGAGGAGGTAAATGCTTTTTTTATTTATTATTTCTCTCTCTAATGGAAATAGGAACTTAAATGAAATTGTGTTTTTATGCTTTGCTCCTCAGGGTGATTCGGTGAATGCAGATGGTGAGATTTGTGTGGAGGATCGATCTGCCCCTATGCAAGTTGAAGGACCGTCTTCGGGATCATCTGATTTGTGTTACTGGCCCACCAGCTCATCGCTCACAGCCCGACTGCGACGTCTTATCACAGCTTACCAGCGCAGTTACAGACGAGAGCAGCTTAAGATCGAGGCAGCAGAGAAGGGGGACCGTAGGCGAAGACGCTGC[G/T]AACAAGCTACCAAACTCAAAGAGATAGCCAGACAAGAGCGACAGCAACGGTATGTTCGTTAATAAAACCTGAAGCATAATCTTCAGTCTCACTTTCCCAGAATTCTCACAAGCTTCTCTATTTCAGGTGGACTCGTAGAGAAGAGTGCGACTTTTACAGGGTGGTATCGACATTTGGGGTGGAAAGGATAAAGAAAGAAACAGATGCTCCAGAAGGGGACGAGCATCACATGGACTGGAATCGTTTCCGTTCTTTTGCTCGACTCGATAAGAAAACCGATGAGAGCTTGACACGTTACTTTAAGTGCTTCATGTCCATGTGTCGGAAAGTGTGTCACATTCGGCCAGGACGTGGAGACGGTATGTTATTGTTTTTTTTTTCTTATACACAAAACATAAAATGTGTAAACCAGGGGTCACCAACATGGTGCCCACGGGCACCAGGTAGCCCGCGAGGATCACATGTGTTGCCCACAGGCCTGTTCTAAAAAATAGCTTACC
Associated Phenotype:
Not determined