ZMP
CHD6
Ensembl ID:
Description:
chromodomain helicase DNA binding protein 6 [Source:HGNC Symbol;Acc:19057]
Human Orthologue:
CHD6
Human Description:
chromodomain helicase DNA binding protein 6 [Source:HGNC Symbol;Acc:19057]
Mouse Orthologue:
Chd6
Mouse Description:
chromodomain helicase DNA binding protein 6 Gene [Source:MGI Symbol;Acc:MGI:1918639]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33968 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa10755 | Nonsense | Available for shipment | Available now |
sa44646 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17547 | Essential Splice Site | Available for shipment | Available now |
sa2320 | Essential Splice Site | F2 line generated | Not yet available |
sa20819 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa33968
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028607 | Essential Splice Site | 145 | 1642 | 3 | 33 |
Genomic Location (Zv9):
Chromosome 6 (position 51589040)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 51638222 |
GRCz11 | 6 | 51638221 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAGAGGTCAAAAAGGTCAAAAAAGGTCAAGATGTGAAGGTGAAAACGC[T/C]GGCTAAAAACCAGTGTGCGACACATACGCCCTCCAAGAGAGGGAGGAAGC
Long Flanking Sequence:
ACTCTAAACAAACTCTGTCGTTTTTTTTTTTTTTCAGATGTCTGCATCCTATGTACTAAAGCACACTCCATCCGCTGCTGCCTCGAATGCCTCTGACCAAAACGCACAAACTACATTTCCCATCGGCCACTTGGGCAAGGAACAACTACGAATCATCGGCGGGCCGCCCAATCACTGCATGGCTCACCCAAAGCACTCTGGGCCTGCAGTCAGCAGCCACAGTCTCCGGCCTTCAATGATAAACAACGAGGAGGATGATGGAGGGGGCGGGACCAAGGTGAAGAAGAAACGGAGGAAAAAAGACAAGAAAGAGTCGGAGTGGCACGAAGATGGACAGAGCAACGCTAAACCAAAGAGAAGGGAGCAAAAGGAAGGGAAAGAGATTCTTCCCAGAAAGACGAAGACAGCAAAGGAACAAAAGGATCATAAGAAGAGGGACGCAAAAGCCCAAAAAGAGGTCAAAAAGGTCAAAAAAGGTCAAGATGTGAAGGTGAAAACGC[T/C]GGCTAAAAACCAGTGTGCGACACATACGCCCTCCAAGAGAGGGAGGAAGCCAAAGTAAGTTGCGCATAAGAGGATTTTTGAGTTGCATATCAGTGAAATTTTATTACAATTTAAAACAACTGTATTCTGTTTTAATACCCTATAAATATATTCTAAAGCACAAATTAGAGATCTGCGCGGGACAAAATTTTGAATCCCGCTCCCGCCAGGTTTTAGCCTGAACCCGACCCGCTCCTGCCCCATTTTCTACCCGCCGCGCCCGATCCCGATTTGGGAGAACAAAACAGAAAACCACCCAGCTATACAGAGTCCAGAAAGCCTATAATATGCTGTCTGCATAAACACTTACAAACACACAGATAAGCACCAAGCACACACACACACAGACAAAGCTCTCTCTGTCAAACACACACACACACACACACACACACACCTCTTATTCGCTTGCACGTGCACAAACACATACATACACACAGACACACACAGCAACAAACAAGCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10755
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 |
---|---|---|---|---|---|
ENSDART00000028607 | Nonsense | 244 | 1642 | 7 | 33 |
Genomic Location (Zv9):
Chromosome 6 (position 51581941)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 51631123 |
GRCz11 | 6 | 51631122 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTGTTGTGCAGAAGAGGCGATCAGGGCGTCAAGTGAAGCGGCGGAAGTA[T/A]AACGAAGATCTTGATTTCAAGGTKRYGGATGATGACGGGGAGACCATCGC
Long Flanking Sequence:
TCCACATCAAGAGAAGTCAGCTGAGGTCGCTCGGGCATCTGTTTCGGATGCATCCTCGATGCCTACCTAGGGAGATGTTTGGGAGGAACACTCGGGGAAGACCCAGGACATGCTGGAGAGACTATGTCTCTCGGCTGGCCTGGGAATGCCTCGGGATCCCCCCAGAGGAAGAGGGGAGAGGGATATCTGAGGTTATCTTGCTGCCTTTGCGACCTGGCCCTGGAAAAACTGATGAAAATGAATGAATGAATAGTGTATATTTTCAAGTTCAGATTTCTGATTATTGTATATATTTTCGATATCATCTTAACTTGCCATCATTTAATAAATTAGAGAAAAAAATTCATTAAGTTTAATCAGAAGTGAAAGTACACACTTTCTGTCTTAGGGAGTGTATTTTTTAAATGTTTATGCTAACAACTTTGAAAAATGACTTTTTCTCATTTCTTTATTGTTGTGCAGAAGAGGCGATCAGGGCGTCAAGTGAAGCGGCGGAAGTA[T/A]AACGAAGATCTTGATTTCAAGGTTGTGGATGATGACGGGGAGACCATCGCTGTGTTGGGCTCGGGCCGAATCGCCGCCATGTCTTCCTCCACCCTCGCTTGGCAGGCTGAGGTAACCGTGGCAACATCTGTTTTTATGCCACACCACAGACCTGCCCTACTTCTGTAGGGGCGGAGATAACACTCTGGAATGATCCCCATCTGCTTTTTTTTTCTCCCCAGGAACCCCCTGAAGACGAGGCTAATATCATTGAGAAAATCCTCTCAGTGCGAACGGTCAACAAAGAGGTAAATGGTTCAGATTACACATATAAAAACTGCAGTAAAAGAGCTCATGAACTCTGAGGTCCATTGTCAAGGTTTTTACATTAAAAAAAGTAATGGGAGCAATTCCAGCATTATGGATGTGACATTTGAAGTAAAAACATAAACCTAAATTCACAGAGAAAGTATATTTAACATAATATTGAAACATCTGTTTATTTTTTCAAAACTACCAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44646
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 |
---|---|---|---|---|---|
ENSDART00000028607 | Nonsense | 432 | 1642 | 12 | 33 |
Genomic Location (Zv9):
Chromosome 6 (position 51576106)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 51625288 |
GRCz11 | 6 | 51625287 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTCGACCCTGTAAAAATCAAAGAGTTCGAAGAGCTCAAGAAAGTTCCT[G/T]AAATGAAGCATGTGGTAAGTCCTTGACTTCAAATAGAGCTGGTGTTTCCT
Long Flanking Sequence:
TATTTAATAATATGTTATTTGAGGACCTTTTCAGTTTTAATATAAATAAAAAACGCATTTTTCCTTCTGTTAAAATGGTATCTGGGTCAATTTTGGCCCGTACGTCAACAAATGGCTTTGTCTTAGACCACTTTCATTACTGAATATGCACCTTATCATTTGCCTAAATCTACTTGTGTTGTTTTGTTTTCTCCTCAGCCGGATGAAGACCTTTTCAATCCAGATTATATTGAGGTTGATCGGGTTTTAGAGATTGCTATCACCACAGATACAGAAACAGGAGAGGTGAGGCGCTCCTCAAATCGTCACTTGAAAACAAACCTATAATAAATACTTGTGGCGCCAGTCTTTTAATGTTGGCTTTGTTTGCATTTTAACAGGAAGTTACACACTACCTGGTGAAATGGTGCTCTTTGTCATATGAAGAGAGCACTTGGGAGCTTCAGGAAGATGTCGACCCTGTAAAAATCAAAGAGTTCGAAGAGCTCAAGAAAGTTCCT[G/T]AAATGAAGCATGTGGTAAGTCCTTGACTTCAAATAGAGCTGGTGTTTCCTCGTAACACGATTTATTGGTCAATTATACAGTGTGCATGTTTGCATTATGATCACGTGGTTCAACGTGGTTTAAGAACATGTTTATTTTTCTGTACAGCATGCATTTTGAAGGAAATGACTGTTGTCTTGTATTTGTTTTTATAATACAGGAAAGGCCTTTGCCAGAACAGTGGCAGAAACTGGAAAAATCCAGAGACTACAGGAATGGGAATCAGCTCCGAGAATACCAGCTAGAGGGAATGAACTGGCTGCTTTTCAACTGGTACAACAGGTAAAAAAGAAGATATTAGGGTTCACATTAATGTTTGAGTCTATTTAAAGGTATATTGTCACTAATTTAGGAATAATCTAAAGCTAATAAAAAAAAAGATTTACAAAATAAAACACCAATAAATTAGCATTTTAATCTGTTTTTTTTTTATTATTCATCTCAGTTGTTTATTTAGCTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17547
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028607 | Essential Splice Site | 477 | 1642 | 13 | 33 |
Genomic Location (Zv9):
Chromosome 6 (position 51575784)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 51624966 |
GRCz11 | 6 | 51624965 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAATACCAGYTAGAGGGAAYGAACTGGCTGCTTTTCAACTGGTACAACAG[G/T]TAAAAAAGAAGATATTAGGGYTCACATTAATGTTTGAGYCTATTTAAAGG
Long Flanking Sequence:
TATAATAAATACTTGTGGCGCCAGTCTTTTAATGTTGGCTTTGTTTGCATTTTAACAGGAAGTTACACACTACCTGGTGAAATGGTGCTCTTTGTCATATGAAGAGAGCACTTGGGAGCTTCAGGAAGATGTCGACCCTGTAAAAATCAAAGAGTTCGAAGAGCTCAAGAAAGTTCCTGAAATGAAGCATGTGGTAAGTCCTTGACTTCAAATAGAGCTGGTGTTTCCTCGTAACACGATTTATTGGTCAATTATACAGTGTGCATGTTTGCATTATGATCACGTGGTTCAACGTGGTTTAAGAACATGTTTATTTTTCTGTACAGCATGCATTTTGAAGGAAATGACTGTTGTCTTGTATTTGTTTTTATAATACAGGAAAGGCCTTTGCCAGAACAGTGGCAGAAACTGGAAAAATCCAGAGACTACAGGAATGGGAATCAGCTCCGAGAATACCAGCTAGAGGGAATGAACTGGCTGCTTTTCAACTGGTACAACAG[G/T]TAAAAAAGAAGATATTAGGGTTCACATTAATGTTTGAGTCTATTTAAAGGTATATTGTCACTAATTTAGGAATAATCTAAAGCTAATAAAAAAAAAGATTTACAAAATAAAACACCAATAAATTAGCATTTTAATCTGTTTTTTTTTTATTATTCATCTCAGTTGTTTATTTAGCTGCATTTAGGTTTATCAACGCTTATTAAAAAAAGCATTCAATCATTCATTTGTTCATTCATTCATTCATTCATTTTCCTTTGGCTAAGTCCCTTTATTCATCAGGGATCACCACATTGGAATAAATTACCAACTTTTGTTGGCTCCAGCATATGTTTTACACAGCTTATGCCCTTTCAGCTGCAACCCAGTACTGGGAAACATACACACTCATCCACACACATACACTACAGCCAATTTAGTTTATTCAATTCGCATGTCTTTGGACTGTGGGGAAAACAGAGCACCTGGAGGAAACCCATGCCAGCATGGGGAGAACATGCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2320
Status:
F2 line generated
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028607 | Essential Splice Site | 1452 | 1642 | 32 | 33 |
Genomic Location (Zv9):
Chromosome 6 (position 51547177)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 51596359 |
GRCz11 | 6 | 51596358 |
KASP Assay ID:
554-3298.1 (used for ordering genotyping assays)
KASP Sequence:
GAGGCATATTTAGGAWTTGTTTTACTGTAATCACATATCTTCTTTAAAAC[A/T]GGTGGACACGTCGTGAGCAGGCTGACTTCTAYCGTACAGTGTCCTCATTT
Long Flanking Sequence:
CAAGTAAAACGAAACACAACGTCACATCATTTGTTTCGGAAAATGAATAAGCAGTGTCTCAACATCCATATGAAAGCATCTGGCTGTCAGTCTTTGCTCCGCAGCACCCCCACACCTTGATGCTCATGACAAGAACAGCATGTGTAGTTGTCTTTTTTTTTCATGCACATGCATGAGTGAATGATATTTTTGCACTTTTACACAAAATAATTCATGATCAGATTACACAATACTGAAACCGCACGTCAAAATAACACATTGTCAGTATTTTTTGAGACCCCCCAAAATTTCACAAATCATGTTTTCAGGGGAGCCCATGCCTTATTTGGGGGAGCCGTGCTCCCCCTAGCTTCCCCTTAGCCCTTAGTTTGCATCCTGATTGGTAAATTGTTAGGGGTCACAGGTATGAGGTTAATAGTATGTGCAAAAAAATCTGGTAATTCAGTGTTTGAGGCATATTTAGGATTTGTTTTACTGTAATCACATATCTTCTTTAAAAC[A/T]GGTGGACACGTCGTGAGCAGGCTGACTTCTACCGTACAGTGTCCTCATTTGGAGTAGTGTATGACCCAGAGAAGAAGAACTTTGACTGGAGCCAGTTTCGTGCTCTTGCTCGATTGGAGAGAAAAACAGATGAAAGCTTAGAGAGATATTTCCACAGCTTTGTTTCAATGTGTCGCACTGCATGTAGACTGCCACCAAGAAAAGATGAAGGTAAGATGGATCTTATTTCATAGTTAGTAGAATTAATAGAAGCTCATTTTCTTGTAACATATACACAACTTTTTTATCTCAAATAGGCAATGTTGATCCTTCATTATTTGTGGACCCTATTACAGAAGAGCGAGCTGCCCGAACATTATATCGTATTGAGCTTTTGAGAAAGGTCCGCGAGCAAGTATTGCGCCACCCTCTTCTGGGAGCACGACTGCAGCTTTGTCGCCCTAGTCTGTACTTGCCGGTCTGGTGGGAATGTGGTAAACATGACCGTGATCTTCTCATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20819
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028607 | Nonsense | 1625 | 1642 | 33 | 33 |
Genomic Location (Zv9):
Chromosome 6 (position 51546572)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 51595754 |
GRCz11 | 6 | 51595753 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTATCCTTCCTGGAGGCCCACCGGAACTATGTTCATAAAGAAAACCAC[A/T]GATATCCAGTCCCAGGATTGCCCCACCATCATTGCTGCTTATATGATGCC
Long Flanking Sequence:
CTTGCTCGATTGGAGAGAAAAACAGATGAAAGCTTAGAGAGATATTTCCACAGCTTTGTTTCAATGTGTCGCACTGCATGTAGACTGCCACCAAGAAAAGATGAAGGTAAGATGGATCTTATTTCATAGTTAGTAGAATTAATAGAAGCTCATTTTCTTGTAACATATACACAACTTTTTTATCTCAAATAGGCAATGTTGATCCTTCATTATTTGTGGACCCTATTACAGAAGAGCGAGCTGCCCGAACATTATATCGTATTGAGCTTTTGAGAAAGGTCCGCGAGCAAGTATTGCGCCACCCTCTTCTGGGAGCACGACTGCAGCTTTGTCGCCCTAGTCTGTACTTGCCGGTCTGGTGGGAATGTGGTAAACATGACCGTGATCTTCTCATTGGTGTTGCTAAGCATGGCTTGAGTCGAACTGACTTCTACATCCTCAATGACCCCCAACTATCCTTCCTGGAGGCCCACCGGAACTATGTTCATAAAGAAAACCAC[A/T]GATATCCAGTCCCAGGATTGCCCCACCATCATTGCTGCTTATATGATGCCAACATTGGACATTGTCAGTCCCCACAACCTCCGGAGTATCACCCCACACCTGCACACCACACGCCAACACAGCTTGTCCATACTCATGGGCATCACCAGTCCAGTGAAGCATCAGAACCTGGAAGTTCCTTGGGTATAGGTTCAGGAAACAGGGAAGGATTTTTGGACTGCCCTCCATTGGATGACTCTCTGGAGTTGGGCTCTTTACAACATGAAGGCTTGACTTCCGATACACTACATGGCAAATCTGGTAAAGAGGCCTTCAATGGATTCCCATTCAATTCTGCAACTGGTGGGCAAAATATGCTAAATTCATATGGTGTGCAAGGGGAGCTAAATGGGACTCAGGGAGACATGGCAGACTCCATAGCTGGGAAACTTCGCAGTGATGTTTTGGTGGGAGAACAAGGATCCTCAGAGGAGACTGGGTTAATGGCTCCTTCAGTGGAA
Associated Phenotype:
Not determined