Busch Lab

ZMP

chd7

Ensembl ID:
ENSDARG00000075211
ZFIN ID:
ZDB-GENE-070912-179
Description:
LOC569471 protein [Source:UniProtKB/TrEMBL;Acc:A7E291]
Human Orthologue:
CHD7
Human Description:
chromodomain helicase DNA binding protein 7 [Source:HGNC Symbol;Acc:20626]
Mouse Orthologue:
Chd7
Mouse Description:
chromodomain helicase DNA binding protein 7 Gene [Source:MGI Symbol;Acc:MGI:2444748]

Alleles

There are 10 alleles of this gene:

Allele Name Consequence Status Availability
sa32899 Nonsense Mutation detected in F1 DNA Not yet available
sa596 Nonsense F2 line generated Not yet available
sa19733 Nonsense Available for shipment Available now
sa44530 Nonsense Mutation detected in F1 DNA Not yet available
sa6835 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa32898 Nonsense Mutation detected in F1 DNA Not yet available
sa44529 Nonsense Mutation detected in F1 DNA Not yet available
sa39811 Nonsense Mutation detected in F1 DNA Not yet available
sa19732 Nonsense Available for shipment Available now
sa11593 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa32899
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000016208 Nonsense 39 3140 1 37
ENSDART00000114089 Nonsense 39 653 2 3
ENSDART00000121586 Nonsense 39 62 2 2
ENSDART00000135230 Nonsense 39 3140 2 38

The following transcripts of ENSDARG00000075211 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 21604321)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 22149736
GRCz11 2 21807798
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGGCCTAGGGGACTGTGGCTACCCTCAAGGTCAGACAAATCCTATGAGT[C/T]AACAGATGCCCCATGAGCACCAAGGCTATGGGCAGCTTCCTCCTTCTCTT
Long Flanking Sequence:
TCAAAGGTTGGCAAAGAGTCAGTTACAACTGATTTAACTGCAAAAAAGCCCCAGTCTCACCACCCTTCAACTGCTCTTATATCTCAAAAGTTCTGACTCACTTGCTAAAAATTTAATAAAGCATGCTTAAAGTGAACAAAATGCAAAAAGCTTGCTCTCACCTAGCGATATTTGTTAATTCTCTCTCTCTCTCTCTCTCCCCCTTTACAGGTCCTGTAACCTGACTTCGCCTGACGCTGCGTTCTCTGAGAGAATTAAGGAAATATGGAGTGACATGTTGCAGATTAGTTAGCGGATTAGCGGATTTGAGGACATCCACCTCTGTGTGAGCACACATTCCCTGTCCTGCTTCTGAAGCTTGGCTGCACAGCAGGAGCACTGCAGCCATGGCTGACCCAGGCATGATGAGCCTCTTCGGAGATGATGGGAATCTGTTCTCTGATGAGTTGGAGGGCCTAGGGGACTGTGGCTACCCTCAAGGTCAGACAAATCCTATGAGT[C/T]AACAGATGCCCCATGAGCACCAAGGCTATGGGCAGCTTCCTCCTTCTCTTCACCTCTCCTCACCTGCAGTCCCTGGACAGGCTAAGCTTGGCCACCATTTTGACCCCTTTAATCAGTACGAGCAACCCAAGATGCATCCAATGGACCAGCAAGGGGGTCGGATGATGGGGAATGGACCAGTGAATGGCATGTCCTCCCCACATTCCCGATATCATGGTGCTCAGGCAGGTGCTGGAGGTGCTGCAGGGCATCATGTTTACCCAGGTGCGCAAGGAGATGGACGGAGCCAATCTTTCCCAGACAGCGGAAATACATGGGGTGCTCAACCAATGCAGGTGCCTGAACAAACTAGACCCCCCTTTCAGCAGCAACCCCCTCAAGCCTCGTCTCATCAGCATGGCCCTGCTGGACCACAAGGACATGCCCACCAAATGGGCCCTTTTATTGGCCGTGGTGACTATGCCATACAGGGCCACAACCAGACCCAAACACCTCCCAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa596
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000016208 Nonsense 40 3140 1 37
ENSDART00000114089 Nonsense 40 653 2 3
ENSDART00000121586 Nonsense 40 62 2 2
ENSDART00000135230 Nonsense 40 3140 2 38

The following transcripts of ENSDARG00000075211 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 21604318)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 22149733
GRCz11 2 21807795
KASP Assay ID:
554-0506.1 (used for ordering genotyping assays)
KASP Sequence:
GCCTAGGGGACTGTGGCTACCCTCAAGGTCAGACAAATCCTATGAGTCAA[C/T]AGATGCCCCATGAGCACCAAGGCTATGGGCAGCTTCCTCCTTCTCTTCAC
Long Flanking Sequence:
AAGGTTGGCAAAGAGTCAGTTACAACTGATTTAACTGCAAAAAAGCCCCAGTCTCACCACCCTTCAACTGCTCTTATATCTCAAAAGTTCTGACTCACTTGCTAAAAATTTAATAAAGCATGCTTAAAGTGAACAAAATGCAAAAAGCTTGCTCTCACCTAGCGATATTTGTTAATTCTCTCTCTCTCTCTCTCTCCCCCTTTACAGGTCCTGTAACCTGACTTCGCCTGACGCTGCGTTCTCTGAGAGAATTAAGGAAATATGGAGTGACATGTTGCAGATTAGTTAGCGGATTAGCGGATTTGAGGACATCCACCTCTGTGTGAGCACACATTCCCTGTCCTGCTTCTGAAGCTTGGCTGCACAGCAGGAGCACTGCAGCCATGGCTGACCCAGGCATGATGAGCCTCTTCGGAGATGATGGGAATCTGTTCTCTGATGAGTTGGAGGGCCTAGGGGACTGTGGCTACCCTCAAGGTCAGACAAATCCTATGAGTCAA[C/T]AGATGCCCCATGAGCACCAAGGCTATGGGCAGCTTCCTCCTTCTCTTCACCTCTCCTCACCTGCAGTCCCTGGACAGGCTAAGCTTGGCCACCATTTTGACCCCTTTAATCAGTACGAGCAACCCAAGATGCATCCAATGGACCAGCAAGGGGGTCGGATGATGGGGAATGGACCAGTGAATGGCATGTCCTCCCCACATTCCCGATATCATGGTGCTCAGGCAGGTGCTGGAGGTGCTGCAGGGCATCATGTTTACCCAGGTGCGCAAGGAGATGGACGGAGCCAATCTTTCCCAGACAGCGGAAATACATGGGGTGCTCAACCAATGCAGGTGCCTGAACAAACTAGACCCCCCTTTCAGCAGCAACCCCCTCAAGCCTCGTCTCATCAGCATGGCCCTGCTGGACCACAAGGACATGCCCACCAAATGGGCCCTTTTATTGGCCGTGGTGACTATGCCATACAGGGCCACAACCAGACCCAAACACCTCCCAGAATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19733
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000016208 Nonsense 377 3140 1 37
ENSDART00000114089 Nonsense 377 653 2 3
ENSDART00000121586 None None 62 None 2
ENSDART00000135230 Nonsense 377 3140 2 38

The following transcripts of ENSDARG00000075211 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 21603307)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 22148722
GRCz11 2 21806784
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTACCCTGCTCCGGCAGGGCCTCAGCGCTACCCTACACCTGGGGGTCAA[C/T]AGGGACCATTGCACCAGCAGCCCATTCATGTGAACCAAATCAATACCCAG
Long Flanking Sequence:
CACAAGGCCTCCCTCAGGAAGCCAATCATTTTTTGGGTCACGTGGGTATGACTCAGAATCCTGGCATGTCGGGACCCCCCATACGTCACCTAGCACAACCTTCTCAGCAGCATCAGCAGCCCAATCAGCAGTTTCTCCACAGGCCTGGCCAGGGTCCGGTTCATCCAGATTCTGTTGCGAGCCACAACCCCCAGTTCCCACAAAGCCCTTCACGACAGCAACAGCAGCAGCAGCAAGTGATGGGTGGAAGACCCCACCAAAACATGGGATTTAACATGCACAACCAGCAAGTTCCTTCCAACACCGTAAACAGCTCAGGGCAGTACCCTCCCTATTCTTCATATGGCAACCTTAATCAGGGATTAGCCAACACATCAGGGATGAGTCCCAACTTGAGCCTTACCACCAGCAGTAACAGCAACCCTAATGCTCCTGTGACCCAGGTGCAGCGCTACCCTGCTCCGGCAGGGCCTCAGCGCTACCCTACACCTGGGGGTCAA[C/T]AGGGACCATTGCACCAGCAGCCCATTCATGTGAACCAAATCAATACCCAGCCTATGCATCCAGCTCAGAACCAGGCTACAGCCCAGCCGAAGCTGCAGCAACATCTACCACCTCCACCTCAGGGATCATACTCCTCCCCTCCTTCCATGTCGCCCATGAGGAATTTAGCCACCCCTGCAGGCACTCCACCTCCCCAGCAGGTACGCCCTCCCAGTGCAGGTTTGGCTACCGATGTGGGTGGTTACCCCGGAGTACCACATCAGTCTCAAGGCCCAATGGCTCATGCCCAGAGGGGAGCTGGCCCAATGAACGCAGCACAGCCACTTCCCCACCAGCAGCTGCCATCACATTCTACACACCCTCATCCTCCAACAACCCAGATGTACGCTGCTTTGTCACCCAATCACAGAGCTACAGCTGCACAAGGAAGATCTTCAACAACACCGGGTGGAAACCACACAGAACCACCAGGCCCACAGGACCAGAGGCTACATGCCCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44530
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000016208 Nonsense 853 3140 5 37
ENSDART00000114089 None None 653 None 3
ENSDART00000121586 None None 62 None 2
ENSDART00000135230 Nonsense 853 3140 6 38

The following transcripts of ENSDARG00000075211 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 21581940)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 22127355
GRCz11 2 21785417
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAGTTGCCGGATGCGGAAGGTCCTGTGGTGGAGAAGATCATGGGGATG[C/T]GAATGGGAAAGAAAGAGGTGAGCTGAGCCGCTGAAAGCCTCTCACACCAG
Long Flanking Sequence:
GTTAGTTGTGCATACTGTTCAAAAATATCGTCATTGCCATTTTTTATCTTTCTCTAAAGTAATTGCCTTGTAAGACCTCAATGAATATACTTTTGCATTTTTGCCATTGTGTAATTTGGGTGTATGTGTGTGTGCTTGACTACAGAAGAGACGATCTAGTCGGCAGGTGAAGAGGAAGCGATATACTGAAGATCTTGAATTTAGAATTTCAGATGACGACGATGGAGATGATTCTGCAGGACCAAAGTCTCCAACTACATCTGAGCAGCAGGTCAATATCACGAGGACTTATGGTTGTGTGTGTGTGTGTAAAATTGTTTATAATTGTGCTGATAGCTGATTAACAGTCCCCACAGTAGAGCTGGAAAACTGCTGATGTAACCTGCTGTTTGTTATGCATGATGGATGTTCTCACACTGACTCTGTGTCCTTCATTCCCCTGTGTGCTGTAGGAGTTGCCGGATGCGGAAGGTCCTGTGGTGGAGAAGATCATGGGGATG[C/T]GAATGGGAAAGAAAGAGGTGAGCTGAGCCGCTGAAAGCCTCTCACACCAGTTTAAACCGCTGCTGTCTGCTGGATCAAGGCAGATTACACCTAACAGCTGTCTCAAATCCTGCCCCAGACCCTGTGATTGCCAGGACGATGCCTGAGTGGGCTGATATTGTCTTCAGCATGACAGTGGTAGTATTAATCCAGGAAAGGCCATGGCCAGTTCAGAGTAAAGCCGTTGCAAGGTCTTGAGATGAAGCCGTGTAAGAATAAACTGTCTCTCAGCGTGATAAATCTCAGATCCTTAGTTGCAGGCCGTGGCAGCGCACAATGTTACTCCTTTGAAACCGCTCCACAAAACAAAGCCTGGCCAAAAATAATACGCCGTGCATGGCTCTTAGTAGCACAGCTGCAAATGGGCTCCCGCCCGAGGAAATGGTAGGTTTGGCGTCTGCCGTAGCGCTGTGGTTTTGGCAGGAAGCCAGGCCCTGGGTCAGCTCCCTGTGAATGGGGCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6835
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000016208 Essential Splice Site 859 3140 6 37
ENSDART00000114089 None None 653 None 3
ENSDART00000121586 None None 62 None 2
ENSDART00000135230 Essential Splice Site 859 3140 7 38

The following transcripts of ENSDARG00000075211 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 21581122)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 22126537
GRCz11 2 21784599
KASP Assay ID:
554-4054.1 (used for ordering genotyping assays)
KASP Sequence:
ATAAATGCACCCTTTTCAAACAACTAATTAATGTTTCTGCTTATTTTACA[G/A]TTGGCGTCTGGTGAAGAGATAGAAGTCGAAGAGTTTTACGTCAAATTCAA
Long Flanking Sequence:
GTTACTCCTTTGAAACCGCTCCACAAAACAAAGCCTGGCCAAAAATAATACGCCGTGCATGGCTCTTAGTAGCACAGCTGCAAATGGGCTCCCGCCCGAGGAAATGGTAGGTTTGGCGTCTGCCGTAGCGCTGTGGTTTTGGCAGGAAGCCAGGCCCTGGGTCAGCTCCCTGTGAATGGGGCTGTGTGTGGTAGAAGAGCTGAAGTGATTCATGACTCAGCCGCACAGCGTACTACTAGCTGGAGAAAGAGAATAGGAGGAGGATTGCTCTTGCTTTTTTTTTTTTTCATCCCCACCCAGTCTGTCTTGTCATTGCTTTTGTCCTGGGGCATTAAATTTCAGAGCAATGCCAAAATGCAGAGTTGTTTTTCACAGGAAATGGTTTACGCTTCTGATGTTGTGATGGATCAAAATTACGCTAACTAGTTATTTGAACGCTCCAAGCATGGTATAAATGCACCCTTTTCAAACAACTAATTAATGTTTCTGCTTATTTTACA[G/A]TTGGCGTCTGGTGAAGAGATAGAAGTCGAAGAGTTTTACGTCAAATTCAAGGGCTTGTGAGTATTGCATTAAAACTATTGTCTAATCTGACTGTGTAGCATGCAAATAGAAAACAATTGTTGATCTCATTTGTCAGTTTTTGCAAACTAAGCTAAAGGTCATTGGGTTTTCTCATCATGTCAAATAGACATGCTTTAATCCAAAGCATAGATTAAACTTGCTTAAACATGCTTAGTCTTGTTTATCTGACATAAGCAACTTATTTAATGTTATTTTTTCTAAGTTCATTCAATAAGTAAATTTAATTGTCTTGTTTTTTTTTTCAGCTCTTACTTGCATTGTCGCTGGGCAGACATTGAAGAGCTGGAGAAGGATAAGAGAATCCAGCAGAAGATCAAGAGGTTCAGGGCTAAACAGGCCCTTAGTACCTTCGTAACTGAGGTTAGAATTGACCCTCCATTTTCTTTGTCATCCACCATTTTGTCTTTTTTTATTATTCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32898
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000016208 Nonsense 962 3140 9 37
ENSDART00000114089 None None 653 None 3
ENSDART00000121586 None None 62 None 2
ENSDART00000135230 Nonsense 962 3140 10 38

The following transcripts of ENSDARG00000075211 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 21579824)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 22125239
GRCz11 2 21783301
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACTTTGTACCTGGTAAAGTGGTGCTCCTTGCCTTATGAGGACAGCACGT[G/A]GGAGTTAAAAGCTGACATAGACCAAGTGAAGATTGAGGAGTTTGAGAGAG
Long Flanking Sequence:
GGTGGGGTTTTCCCAGAGAGGTATATGCCACCCACATCATAAAAGCTCTGAAAATATTCCACCTGGTAGATTCTCATTTAGAGGCTTGTAGTAGTTGCGGCTCAAGCACCAGTGTAATTGGCATTCTGCAGTGCTCCATCTAACCAATCAATCACACTCTTATTGACAGATGGATGATGAGCCCTTCAACCCAGATTATGTGGAGGTGGACAGGGTTCTGGATGTGTCTGAAAGCACAGATGAAAATGGAGAGGTATGACTTCTCTCTATCATCAATCCACTTCAATCGTTCTCAAACCATCTGTCTCTCAAAACAACATGGGTTACCTTGATTGAAGCTCTTACTCTGTTGCAGCTATGAAGATGTCAGTCACACCGCCCCCAGAAAATTTAGAAAAAATTTGAGAACCATCGTTTAGATAAGTTGTGTTGTGTGTTCCTACAGCTTGTGACTTTGTACCTGGTAAAGTGGTGCTCCTTGCCTTATGAGGACAGCACGT[G/A]GGAGTTAAAAGCTGACATAGACCAAGTGAAGATTGAGGAGTTTGAGAGAGTGATGGCGCGTGAGCCGCAGCTGAAGCGCGTGGTAAGAGCTGGCACTCTTCTAGCCTTCTCTTTATTTTCTCTTTGGAGTGCTGAGCTAGTGAGGGGAGAGGGCCACGTTCTTGCGGTTGCACAGAAACCACTAACGGGAATTGTTTTATTTGAAACAGGAGCGACCTCCCACCAGCGACTGGCAGAAATCCGAGAGTTCCAGAGAATATAAAAACGCCAATGCGCTCAGGGAATACCAGCTGGAGGGAGTCAACTGGCTGCTCTTCAACTGGTACAACACGTATGTATGCAATTACCCAGCTGTCCAGCCGCACCGCTTGCACATATGTGTGCTAAACCATGGTTTTTGATACTATTTAAGTGTTAAGATGCTTTGAATTTGAGTTGTTGTTTTTTTTTTTTTTTTTTTTTCCTCAGACGAAACTGCATTTTAGCTGATGAAATGGGAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44529
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000016208 Nonsense 1033 3140 11 37
ENSDART00000114089 None None 653 None 3
ENSDART00000121586 None None 62 None 2
ENSDART00000135230 Nonsense 1033 3140 12 38

The following transcripts of ENSDARG00000075211 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 21579346)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 22124761
GRCz11 2 21782823
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATTTGAGTTGTTGTTTTTTTTTTTTTTTTTTTTTCCTCAGACGAAACTG[C/A]ATTTTAGCTGATGAAATGGGACTTGGTAAAACAATCCAATCCATCACATT
Long Flanking Sequence:
TTGCCTTATGAGGACAGCACGTGGGAGTTAAAAGCTGACATAGACCAAGTGAAGATTGAGGAGTTTGAGAGAGTGATGGCGCGTGAGCCGCAGCTGAAGCGCGTGGTAAGAGCTGGCACTCTTCTAGCCTTCTCTTTATTTTCTCTTTGGAGTGCTGAGCTAGTGAGGGGAGAGGGCCACGTTCTTGCGGTTGCACAGAAACCACTAACGGGAATTGTTTTATTTGAAACAGGAGCGACCTCCCACCAGCGACTGGCAGAAATCCGAGAGTTCCAGAGAATATAAAAACGCCAATGCGCTCAGGGAATACCAGCTGGAGGGAGTCAACTGGCTGCTCTTCAACTGGTACAACACGTATGTATGCAATTACCCAGCTGTCCAGCCGCACCGCTTGCACATATGTGTGCTAAACCATGGTTTTTGATACTATTTAAGTGTTAAGATGCTTTGAATTTGAGTTGTTGTTTTTTTTTTTTTTTTTTTTTCCTCAGACGAAACTG[C/A]ATTTTAGCTGATGAAATGGGACTTGGTAAAACAATCCAATCCATCACATTCCTCTATGAGATATACCTGAAGGGAATCCACGGTCCTTTTCTTGTGATTGCTCCTCTTTCCACTATTCCCAACTGGGAGAGGGAGTTCAGGACATGGACGGAGCTAAACGTAGTGGTCTATCATGGTAGCCAGGCCAGCCGAAAGACCATTCAGGCCTACGAGATGTACTACAGGGACACACAGGTAAATAATTCCTTTGTCATTTTATATGCATTGATTTATTTTCTCATTTGAGTTGTAGAAGATAATGTTTCACAATATTTCTGCTGGACTATATTCGTAGGGTTGTTTATCATAAGAAATTTCTCTCTTCCTGCAGGGACGTATAATAAAGGGAGCCTACAAATTCCATGCCGTCATCACCACATTTGAGATGATCCTGACAGACTGCCCTGAGCTACGAAATGTGCCATGGCGCTGCGTGATTATTGATGAGGCTCATAGGCTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39811
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000016208 Nonsense 1433 3140 16 37
ENSDART00000114089 None None 653 None 3
ENSDART00000121586 None None 62 None 2
ENSDART00000135230 Nonsense 1433 3140 17 38

The following transcripts of ENSDARG00000075211 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 21577302)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 22122717
GRCz11 2 21780779
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCACAAGGGCTGGTGGCTTGGGTATTAACCTAACTGCAGCTGATACATG[T/A]ATTATATTTGATTCTGACTGGAACCCTCAAAATGACCTGCAGGTAAGCAT
Long Flanking Sequence:
CGACAAGCTGCTCCCCAAACTGAAGGCTGGGGGTCACCGTGTGCTCATCTTTTCCCAGATGGTGCGCTGTCTGGACATCCTGGAGGACTACCTCATCCAGAGACGGTAGGATCCTTACAGCACTAGCTAATTTAGATAAATACTTTTAATAATAAGCCGTAGTTTAACATATACTTAATAAGAACAAGTGTTGTTGTTTTTTCATGGGTTTTTATTTATTTTTTAACATTTGTATTACTGCAAATCAATGTTTGCCATGAAGAAAGACTTGGACCTGACTATCATTGTAAAGGATATTAGCAAATAGATGTTTATAGTTAACCTACGGCCTATTTCCTTCATTGTAGGTATCCATATGAGCGTATAGATGGCAGAGTTCGAGGGAATCTCCGCCAGGCAGCTATTGACCGCTTCTCTCGACCAGACTCTGACCGCTTTGTATTCCTGCTGTGCACAAGGGCTGGTGGCTTGGGTATTAACCTAACTGCAGCTGATACATG[T/A]ATTATATTTGATTCTGACTGGAACCCTCAAAATGACCTGCAGGTAAGCATGCTAGTTTCATGATCACATTATTGCAGTTGGAAGTAAAATTGTGCTGGACTTTCAGTGGAACTTTTTTTTTTTTTTTTTTAAATGTTCTTTTTTTTATAATCTTATGACTGCATTTCAGCTAGATTCAATTGAAAATACTCTATCACATTGTGCAACCTTAGTGCTTTATAGTGTTTGAGTCCTCAAAGGCGGTGTATGTGACCGGTTTGTGCTGTTGCCTCCAGGCACAAGCTCGATGCCACAGGATAGGACAGAGCAAGTCTGTGAAGATTTACCGCCTGATCACCAGAAACTCCTACGAAAGAGAGATGTTTGACAAGGCCAGCTTGAAGTTAGGACTGGACAAGGCTGTGCTTCAGTCCATGAGCGGCAGGGAGAATGCTGCCAATGGGGTATGAACTGCACACAGCGCCACCATTTTGTGGTGTTTCACTGAAACCGTATTCCAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19732
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000016208 Nonsense 1449 3140 17 37
ENSDART00000114089 None None 653 None 3
ENSDART00000121586 None None 62 None 2
ENSDART00000135230 Nonsense 1449 3140 18 38

The following transcripts of ENSDARG00000075211 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 21577023)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 22122438
GRCz11 2 21780500
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTCCTCAAAGGCGGTGTATGTGACCGGTTTGTGCTGTTGCCTCCAGGCA[C/T]AAGCTCGATGCCACAGGATAGGACAGAGCAAGTCTGTGAAGATTTACCGC
Long Flanking Sequence:
TATCATTGTAAAGGATATTAGCAAATAGATGTTTATAGTTAACCTACGGCCTATTTCCTTCATTGTAGGTATCCATATGAGCGTATAGATGGCAGAGTTCGAGGGAATCTCCGCCAGGCAGCTATTGACCGCTTCTCTCGACCAGACTCTGACCGCTTTGTATTCCTGCTGTGCACAAGGGCTGGTGGCTTGGGTATTAACCTAACTGCAGCTGATACATGTATTATATTTGATTCTGACTGGAACCCTCAAAATGACCTGCAGGTAAGCATGCTAGTTTCATGATCACATTATTGCAGTTGGAAGTAAAATTGTGCTGGACTTTCAGTGGAACTTTTTTTTTTTTTTTTTTAAATGTTCTTTTTTTTATAATCTTATGACTGCATTTCAGCTAGATTCAATTGAAAATACTCTATCACATTGTGCAACCTTAGTGCTTTATAGTGTTTGAGTCCTCAAAGGCGGTGTATGTGACCGGTTTGTGCTGTTGCCTCCAGGCA[C/T]AAGCTCGATGCCACAGGATAGGACAGAGCAAGTCTGTGAAGATTTACCGCCTGATCACCAGAAACTCCTACGAAAGAGAGATGTTTGACAAGGCCAGCTTGAAGTTAGGACTGGACAAGGCTGTGCTTCAGTCCATGAGCGGCAGGGAGAATGCTGCCAATGGGGTATGAACTGCACACAGCGCCACCATTTTGTGGTGTTTCACTGAAACCGTATTCCAGATGGTTCATTAATCAAACATACTTTGCACATGTTGGCAGTCAGTGGAAAGACCTCTAATTCCTGTGCCCTGAGACTTATTTTCCTTTTTACCATGTGCCTAAATTTGTCCACCCTGTAAAATACCCAAGATGAAAAAGTCAAATTTATTGAGATTTGTATTTTGTGAAATGAATACATTCCTCTCTCTTTATTTTAGGTTCAGCAGCTCTCTAAAAAGGAGATTGAGGATCTCCTGCGTAAAGGAGCATATGGAGCTCTAATGGAAGAGGAGGATGAGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11593
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000016208 Nonsense 1541 3140 18 37
ENSDART00000114089 None None 653 None 3
ENSDART00000121586 None None 62 None 2
ENSDART00000135230 Nonsense 1541 3140 19 38

The following transcripts of ENSDARG00000075211 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 21576493)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 22121908
GRCz11 2 21779970
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAATGGAAGAGGAGGATGAGGGATCCAAGTTCTGTGAAGAAGACATTGAT[C/T]AGATTTTGCAGAGAMGTACACAGACCAKTACAATTGAATCAGAAGGCAAA
Long Flanking Sequence:
AAGTCTGTGAAGATTTACCGCCTGATCACCAGAAACTCCTACGAAAGAGAGATGTTTGACAAGGCCAGCTTGAAGTTAGGACTGGACAAGGCTGTGCTTCAGTCCATGAGCGGCAGGGAGAATGCTGCCAATGGGGTATGAACTGCACACAGCGCCACCATTTTGTGGTGTTTCACTGAAACCGTATTCCAGATGGTTCATTAATCAAACATACTTTGCACATGTTGGCAGTCAGTGGAAAGACCTCTAATTCCTGTGCCCTGAGACTTATTTTCCTTTTTACCATGTGCCTAAATTTGTCCACCCTGTAAAATACCCAAGATGAAAAAGTCAAATTTATTGAGATTTGTATTTTGTGAAATGAATACATTCCTCTCTCTTTATTTTAGGTTCAGCAGCTCTCTAAAAAGGAGATTGAGGATCTCCTGCGTAAAGGAGCATATGGAGCTCTAATGGAAGAGGAGGATGAGGGATCCAAGTTCTGTGAAGAAGACATTGAT[C/T]AGATTTTGCAGAGACGTACACAGACCATTACAATTGAATCAGAAGGCAAAGGCTCAACATTTGCTAAGGTGAAGACATCACCCTCCCCCTTGGCTGTTGTATTAATGATTTTAACCCAAAAAATTGACCCATTCATCAATGTTATTGCATAATTGGCTTTATAGAAGCATACTCCCCATTTAATCTTGCTCCTAAAATAGAGCAACCTAAAGGGTAAGTGTCTCTGATCTGACCATTTATATAATTTTTTTCCCTTACCAGGCAAGTTTTGTGTCCGCTGGGAACAGAACCGACATTTCTCTGGAGGACCCAGATTTCTGGCAGAAATGGGCAAAAAAAGCAGAGCTGGACCTGGATGCGATCAATGGCAGGGTAAGCTGTGACTTAACAGAGAAAAAGGAGCTCTCTTGTGCCGTGTCTCGCAGGAGATGCTGCATGAATTGAGGCACTAATCTATAGCACTTCTCTCTTGTGTAATTGTGCAGAGCACTTACGGCTGA
Associated Phenotype:
Not determined