Busch Lab

ZMP

LOC566115

Ensembl ID:
ENSDARG00000076213
Human Orthologue:
DOCK4
Human Description:
dedicator of cytokinesis 4 [Source:HGNC Symbol;Acc:19192]
Mouse Orthologue:
Dock4
Mouse Description:
dedicator of cytokinesis 4 Gene [Source:MGI Symbol;Acc:MGI:1918006]

Alleles

There are 9 alleles of this gene:

Allele Name Consequence Status Availability
sa38073 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa38072 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa15407 Nonsense Available for shipment Available now
sa38071 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa9878 Nonsense Available for shipment Available now
sa44301 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa32532 Nonsense Available for shipment Available now
sa44300 Nonsense Mutation detected in F1 DNA Not yet available
sa38070 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa38073
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
ENSDART00000087817 Essential Splice Site 6 1945 1 55
Genomic Location (Zv9):
Chromosome 25 (position 22337462)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 21569338
GRCz11 25 21666886
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAATAGAAGTAATTATTGAATGTATTTTTGGTATATTTTCACCCACTGGG[G/A]TAAACGTTTCCATCTCGTCCACATGCAGTTACGCAAACAAAGATCGCTCA
Long Flanking Sequence:
TGGTAGGCTAGAGAAGCGTAGGTGGGAAGATGTTTATTGTTTCCTTTTAAAGTAACATTACCTACTTTTATATTACATTTTTTATTATTATTTTTATTTATGTTACAAAAAACAATAAATAAAATAGTTGAGAGTTCTTCTCTGTTCTAAATTGACAACTAAGCAACATAATATAATTTGCTAGTGTAAAGTCATTTTCTAACAAATGCCTCAGTTCTCACAATTTTTAATAAAGTAATTCAAATTTGAAACGTTATGCCCTTAAAAACAGTTTTGTGTGTGTTTTTCTTTCTTTGTTTTTTTTTTTAAGATCAGATGCAGTCTATACCAAGACATGACCGGGAGCTATACAAAATGGATTTGACCTTGAGACTTTGAGCAGTACAATTTGAATAGTTGCCATTTAAGAATAAGATTGCTGTGTTAGTAGTGTTTTTACATTTAATTTTGAAATAGAAGTAATTATTGAATGTATTTTTGGTATATTTTCACCCACTGGG[G/A]TAAACGTTTCCATCTCGTCCACATGCAGTTACGCAAACAAAGATCGCTCAGTCTTCGGATTTGTTTCAAGTTGATTTACTTAATGTTTTCTCCTTTTGTTTGTTTCCTTTTCTTTAGTGCTGGCAAACTTTCGAGGAATGGTTCAGCATGGACTCCCACTGGAGATCGGTGACACGGTGCAGATTTTGGAAAAATGTGAAGGTAATCGCTGTTTTATTGTGTAGATGACAATCAGCCACTTCAAAACTGTATGTTCTTCGATTAAGAGACAAAAGTATACTTAAAAATTCATGAGTCTGATGTCAGACCTGCTTTGAGATTTGTGCTTTAATGAGAAATGGTGAATGGGATGAATGTACAAACAATAAATTGTATTAAATGAATCCATTAGTATATGATACTGTAGAAATAACTACCATTTTGAGAACTGACATGTAGAATTGGAGGACTTACACTCTCATATTTATTGAAAGGGGGGGAGAAACCTATTTTTGACCCTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38072
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087817 Essential Splice Site 54 1945 3 55
Genomic Location (Zv9):
Chromosome 25 (position 22332247)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 21564123
GRCz11 25 21661671
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCGTAGGATGGTACAGAGGATTTATCACAAAGAATCCAAATGTAAAGG[T/G]AAGCCTGTGCATAATTTATATAATCCCTTTATTTCTCTCTTGATCTGTTT
Long Flanking Sequence:
ATAAAACTCGTCTAGATTGGTGCCATATTCTGAAAGATGCTTTAACAATTGGATCCGGAGAATACCTTAATACTGGGTCAGAAAGAGGAATCTTAGAGCATAGCAAAGCAGATGATGCACAGTACTTTTAACTATTAGCTGTGGAATTAACCCATTAGCATTACCATTTCACCATTATTTCCACAACAGAAAGTTATTAAATATGAAATTACAGTGTTTTGGTTCAGAGCAGTAATGATTAAGAGTAATTACAGTATTTAAAGGATTCTACTTGGATATGTCTTTTATTAGTATATTTTCTTCAGGTCATTATTGTAGAAACACCCTTAATGAACTTGTTGATAATTTGTGCATTAAATAATTGAACAAATACTTTTATTAATAATTTAAAGCCTTCTGCATGTTTAATATTGATGTTTGCATTATACATATGACATATTATAAATGTAATTCCGTAGGATGGTACAGAGGATTTATCACAAAGAATCCAAATGTAAAGG[T/G]AAGCCTGTGCATAATTTATATAATCCCTTTATTTCTCTCTTGATCTGTTTTATTTTTCCTGTATCTGTTTCCTCTGCTTTGACTCTCAGTCCATTTATATACAGATGGTTTGTTTTCTCTTGTGTGCTTTACAGCAGTAATTGGCTCATTAAATAATTTCTGTGCTCTCTCCTCAGGGAATATTCCCAAGCTCCTACATTCACCTCAAGAATGCCCACGTCAAAAACAAAGGGTGAGAGTCAGTCAATTCTAGATATAAATATACAGATCTTACTGCATGTAATGAGCTGAATTGATTTATACATTTGCACTAATTGGTGGATGGATAGAAAGCCACATATATGACAGGAAAAATCAAAGCAAGCCGTTGTAAATCTGTGATGCATATCTTCGGTTTGGAGGTTTACATTTGAGGGAATAAAACAAGCACTGATAAATAAAACAACCTTTGCCATTTGTAAAGGTTGCCAGTACCAGATTAAACAGTACTCTCCAAATAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15407
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087817 Nonsense 225 1945 8 55
Genomic Location (Zv9):
Chromosome 25 (position 22310281)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 21542157
GRCz11 25 21639705
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGATGAGCTCCAGCCTCGGGGAGGAGCTGGAGRTCWTCTTCTCTGTCTA[C/A]GACAGCAGGGAAATGCGACCAATCAGGTGCYGTTTCTGACTCTARACACA
Long Flanking Sequence:
GTTTTTTAGTCTACTTTGCTTAGCAATGCTGCATTTACTTGATCCAAAGTAGAGCAAAAACAGTACAAATTGTAAATATTTTGACTATTTAAAAGAACTGTTTTAAATTTGAAAATTAAGTTTCTTCGAAGCTTAATTTTTAGCTTCATTATTCCAGTCAAATGATTCTTCAGAATCATTCTAATATTCTAATAGACAAAGTAGACAATAAAATATAAATATAAAACATATCTATATTTTATGTACAGTATACAGCTAACACATAGATCCAGCCATGGTGTAGTTGGTTGAACCGATTACCATTAGATATGTTGAGTGATCATGTTGTTATAAATGTCATTGTCATTGGAATGATGTATAATTGTTTTTAAATAGATGGAGAGACGTCACCGCAGACGTGAGGCTCCTCCGCAGGCCAGCCTGCACCACCTGTTCCTTCAGATGAAGAGCATGATGAGCTCCAGCCTCGGGGAGGAGCTGGAGGTCTTCTTCTCTGTCTA[C/A]GACAGCAGGGAAATGCGACCAATCAGGTGCCGTTTCTGACTCTAGACACACAGCTGCAAGTCTATGATTGACTAAAACAGGATTTATACAACTTAAATTGAATATGCTGTCATTATTTAAAGGGATAGTACACACAAAAAATTAAAATGTACAGTAATCACTATTTACTCACCCTCTTTTATTTTCGAGTTTTATTTTCTGTTGAACGCAAAAGAAGAAAGCTGGAAATCTGTAACCGTTGACATCCATAGTAGAAAAAACAAATACTATGAAAGTCAATGGTTACAGCAGGTTTTCATCATTCTTAAAAATATCTTCTTTTGTTTTTAACAGATAAATGAAGCCCATTAACAAGTAACAAGAAACAAGTGATTAGATGATGACAGCATTTTCATTTTTAGTTGAAACATACCCGCGGCGTTTAAACCAACAAAATAGCAAAAGATTTAATTTTTAGTGTCTTTGAGTAATTATTCACATCTTCTGATCCTTTTATTAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38071
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087817 Essential Splice Site 760 1945 22 55
Genomic Location (Zv9):
Chromosome 25 (position 22257453)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 21489329
GRCz11 25 21586877
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTCCTGTCCCATGAAAGTAAAGGCATCAGCCCCATCACACACACACAGG[T/C]GAGACAGATAGTGTTGTACGATACACTGGTACTACGATACCATCGCAATA
Long Flanking Sequence:
TGGGAAATATTTAAAGAAGAAAAAAAATCAAAGGTGGACTAATAATTCTGACTCAACTGTATGTATAATTATATATATAATATTTATTTTTCTAGCCGAAATATATATATTATATATAAATTATATATATATATATATATATATATATAAATTGGAAATACTGAATAAGACAAATAAATTGGTAATAATTTTGACTTCAACTCTATATATCTGTATATTTATTATATTTATATGTATATTAATATATAATATGTGTGTTTTAGTAAAAGTTGTCAAAATTTGTCAGGCTGTGTATGCAACAGCTGATTGGTTGTCATGTGTCCCACAGGCGTCAGAGTACTTGTTTAAGTACATTGTTCAGTCTCGGCGTCTGTATGCGGCAGCTACTGGAGGACAGAATGAAGAGGAGTTTCGCTGCTCTGTTCATGAACTCTTCAAATCCATCCACCTGTTCCTGTCCCATGAAAGTAAAGGCATCAGCCCCATCACACACACACAGG[T/C]GAGACAGATAGTGTTGTACGATACACTGGTACTACGATACCATCGCAATACCGTGGCTTTCAGAACAAAACCGTTGCTCTTTTTACTAACAGTTGTTCTTTGGCTGACAGCTGTAGTTCCAAATGCTTGACAATAGGGGGCAGTGTGGGGGGCAGCACACTGCTTCTACAACACATTGGGCTCTATTTTGACGGTCCATGCGCAAAGTGCAAAGCGCAGGGCGCAATCGCATTCAGGGCATGTCAGGATCCACTTTTGCTAATATAAGGACGGAAAAATCCGCTTTGCGCTATGGTGTATGGTCTAAAAGGGTTGAGCTTATTCTCCTAATTTGTTATAGGTGTGTTTTGAGAATAAATCAATTAGAGTCTCATCTCCTATTCCCTTCAAAAGTCTGTTGCATCGCGCCATCGTGCATTTGCTATTTACATGACGTAAAGTAAGTGTAAGTGGAAAAACTGAGCATTTCACAAACAAGAAAACAGTTAAACAGAGCATCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9878
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087817 Nonsense 1047 1945 31 55
Genomic Location (Zv9):
Chromosome 25 (position 22239090)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 21470966
GRCz11 25 21568514
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTATTTTTGTGTTGTTTAAGGTATGGTGACATGAGAGTGATGATTGGTTG[T/A]GAGATTTTCAGCATGTGGCAGCATTTGGGTAAGTTGATGTGTTTAGGATG
Long Flanking Sequence:
CCTATTTTTATCTCTGCATAATATTCATCAACCAGCCTTGCCTCCAACTGGAAATGTTTCCACCATCTAAGAGGAAAAAAGTTCTGGAGAAGTGAGACATTTTCTTCTTTTTCCTTTTTATAACATCAGACTCCTACTGAGATTGAGATTTGAGGAAGTTATAGAGTGAAACGAAACACTTTGTGTAATGAGACAAGTTATTTAGCAGCAGGTTTGAGGATTTATTGTATTTGGATAACTGGTGGTTTTATACGGTGAGCATTTTGCATTTTGCATTCTGCGCCTTGTCCTCATTTGTAAGTCGCTTTGGATAAAAGCGTCTGCTAAATGACTAAATGTAAATGTAAAATGTATAAAAAGGAAGACCTGTATAAAATGATTAATTCATTATTTTAGGATCATTTATTTTCCTTATAGTTAGATTTTGTTGATTTGATTTTAGTTGATTGATTATTTTTGTGTTGTTTAAGGTATGGTGACATGAGAGTGATGATTGGTTG[T/A]GAGATTTTCAGCATGTGGCAGCATTTGGGTAAGTTGATGTGTTTAGGATGACAAATTGATAAAGTGACTTTTCTTTCTTCAGTAGAACATAAAGTCAGCAGCTATAACACTTTGAAAGTTAAAAAAACTGAAATGTATACAGTACAGGCAAAACAAAATTAGCCTCATGGCTTGCTGAGGCTGTGGATTAAAGGCAATAATGTTGTAAACAATGTTCTCTTCATAAGACCTCCATATATCAGGAATATCTATTCATTATGATTTGCCTATATCTATGTGTGTGTTGTTGTTTTTTTTACTCTAAAAGTGCAGGTAACCATTAACTTGCAATAAATGAATCACCAAATATCACCCTTTCAGCAAAAACTTCTTTAAATTCACACACAATACAGATAATTTCATTTTTAGAACTGGATTTCACTTTTCTGTCCAAAGGGACAGAGCTTAAGGTTTGCAATACTATAATTCACCTCATACTTGGTTTATGTCTTACAGTGCAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44301
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087817 Essential Splice Site 1174 1945 38 55
Genomic Location (Zv9):
Chromosome 25 (position 22231749)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 21463625
GRCz11 25 21561173
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTGTATTTGTCTCTGTGCGTGTGGACCTCAGTGTGTGTTATATTGTTC[A/C]TCTCTTCACAGGGACTGCATGAAGATCGGGGAGGTTGATGGGAAAACGAT
Long Flanking Sequence:
CACACACACACACACCTTTAAACACATACAAACACCCATACATGCATATACACACATACAAGCATACACACACACACAAAGGCACAGAAGAACAAACACACACACACACACACACAAACACACCTGTTGTATGCATGCATAAATACGCACAGGCACAAAACACACACACACACCCATACAAGCACAAACACACACATGCAGTACATACAGGACGCAAATGCATAAACATTCACACAAACATACTCAGTCATGAACACACATATACACACCTTTACATCCATAAACTCACACAGTCACAAACATACACACATCTTTAAACACATACATACTGTACATGCATACATACATATATACACAAACAGAGACACTCATTTACACAAACAAGGACCTGCGCACACTTAGATGCACACACAACACACACACTTACTCGTACAAACACTCACATACATACAGTGTATTTGTCTCTGTGCGTGTGGACCTCAGTGTGTGTTATATTGTTC[A/C]TCTCTTCACAGGGACTGCATGAAGATCGGGGAGGTTGATGGGAAAACGATGGGATGTACAGTCAACCTTCTGGTTAGTTCTATTACTGATCATGACAACAAGTGCACTATTGTTCATGTATTTCCATTTATCCACATTGTAAACATCACACACTGGCTTTTTATTGTTGTTTTTGATGAACAAATGTAACTTTTCTGCTGATGTTGTTCTGTTTCTTTCAGAACTTCTACAAAACTGAGCTGAATAAAGAAGAAATGTACATCCGTTATATTCACAAGCTCTATGAGCTGCACCTGAAGGCACAAAATTACACCGGTAATATTCACTCCACATAATTGGCTTGATTGGTAGCTAAATTAAGTCATTTTATTTATTTTTAAGAATAAGAGAAACAATAAAAGGAAGCTCTGACAAAGTCCCATACATCAATAGTCTTTTCTGATCCATCCTTTTACAAATGGCAGACAAATCCCCTGCTGTAAGCATGTAGATTGCTGAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32532
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087817 Nonsense 1206 1945 39 55
Genomic Location (Zv9):
Chromosome 25 (position 22231503)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 21463379
GRCz11 25 21560927
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTGATGTTGTTCTGTTTCTTTCAGAACTTCTACAAAACTGAGCTGAAT[A/T]AAGAAGAAATGTACATCCGTTATATTCACAAGCTCTATGAGCTGCACCTG
Long Flanking Sequence:
GTCATGAACACACATATACACACCTTTACATCCATAAACTCACACAGTCACAAACATACACACATCTTTAAACACATACATACTGTACATGCATACATACATATATACACAAACAGAGACACTCATTTACACAAACAAGGACCTGCGCACACTTAGATGCACACACAACACACACACTTACTCGTACAAACACTCACATACATACAGTGTATTTGTCTCTGTGCGTGTGGACCTCAGTGTGTGTTATATTGTTCATCTCTTCACAGGGACTGCATGAAGATCGGGGAGGTTGATGGGAAAACGATGGGATGTACAGTCAACCTTCTGGTTAGTTCTATTACTGATCATGACAACAAGTGCACTATTGTTCATGTATTTCCATTTATCCACATTGTAAACATCACACACTGGCTTTTTATTGTTGTTTTTGATGAACAAATGTAACTTTTCTGCTGATGTTGTTCTGTTTCTTTCAGAACTTCTACAAAACTGAGCTGAAT[A/T]AAGAAGAAATGTACATCCGTTATATTCACAAGCTCTATGAGCTGCACCTGAAGGCACAAAATTACACCGGTAATATTCACTCCACATAATTGGCTTGATTGGTAGCTAAATTAAGTCATTTTATTTATTTTTAAGAATAAGAGAAACAATAAAAGGAAGCTCTGACAAAGTCCCATACATCAATAGTCTTTTCTGATCCATCCTTTTACAAATGGCAGACAAATCCCCTGCTGTAAGCATGTAGATTGCTGAAGCACTCGTCAGAAAAATGATGGGGACACAGCACAAGGCTGGGGCTATATTGCTGAACTTTAACCACTGACTCTTCACAGCCTCATGTTTGGGTAGAAAAAAATAACACTAACTTTTCCTCACACTTCAGAGCACAGCGCCTTCGCGATATCATTTAACCGGGGTCTGTTACAGTGGGTGGATTTCAAGTTTCCTGGGTCTGTGCAATCAACAAATAGGCGGGGCTTCAGTTTCGTATCGACGTCACC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44300
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
ENSDART00000087817 Nonsense 1694 1945 51 55
Genomic Location (Zv9):
Chromosome 25 (position 22204303)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 21436179
GRCz11 25 21533727
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTACATGTTATGTTTTTTTCAGCCCAGTCCATCTACCTCAAGTCTGAGCT[C/A]AAATCACTCCGGCTCCCACAATGTGAACAGCTCTGCTCCCTCCAGCAACA
Long Flanking Sequence:
TACTTTTCAAGACACTTCTATACAGCTTAAAGTGAAATTTAAAGGCCTAACTATGGTAATTAGGTTAACTAGGCAGGTTAGGGTAATTAGGCAAGTTATTGTAAAATGATGGTTTGTTCTGTTGACTACTGAAAAAAATTAGCTTAAAGGGACTAATAATGTTGTCCTTAAAATGGATTTAAAAAAATTAAGAACTGCTTTTATTCTAGCTAAAATAAAACAAATAAGACTTACTCCGGGAGAAAAAAATATTATCAGACATACTGTGAAAATTTCCTTGCTCTAAACATCATTTTGGAAATATTTGAAAAAGACAAAGAAATTCAAAGATGGTTATTAATTCTGATTTCAATTGTAGATATGTGAGTGTATATATTTGTGTGTGTGTACACATTTTTATATATAAATAAACTATATTTATATCAGCTCATTTACTACTTATCACATTATGTACATGTTATGTTTTTTTCAGCCCAGTCCATCTACCTCAAGTCTGAGCT[C/A]AAATCACTCCGGCTCCCACAATGTGAACAGCTCTGCTCCCTCCAGCAACAGAGGTGATTCAGTTCAACAGAGCAGAAGCAAACCGTTCTCACAGCGGCTGCAGCACAGTTACCAGCATTTTACAGCACTGCCTCATTTACTCTGTTATCTTTCTTTCTTTTCATCAGCTTCTCCACTGCCGTCTGACAAGCACAAACACACCAGAGATAATGCCTGCCTTTCTCCACGGGACAGACTCTGCAGCGGCATTTTCCCAAACCCACTGGATCCCTCACAGGTCAGGACAACTGCAAAAAAAAAAAAACACAATACGAAAGAAACAATGGAAATATGCTCGTTTTACAAGTCACCTAAATTTGAATAGCTGAGTTTTACCATTTTTTTTTATCCAATCTGCCGATATCTGGCTAGAGCACTTTTAGCTTAACATAAATCATTGAATCCGATTAGTCCATTGAGATTTCGGTGTACATGTATTGAGCATATCTAAATTCACGTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38070
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
ENSDART00000087817 Nonsense 1888 1945 55 55
Genomic Location (Zv9):
Chromosome 25 (position 22199365)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 21431241
GRCz11 25 21528789
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCCCACAGATATGCCGATTCGCAGGGGCAGCAAGACTCCTCCACCCTA[C/A]AGTGTGTACGAGCGGAACAACCCTCGGCGGGCGACGCCACTGCCTCACAG
Long Flanking Sequence:
AAGTTAAATAAAAATACAAATGTATTTAAACTTTTATTTGACAAAATCAAGTTGGATCAACTCAACTGCATTTAATTGTCTAAATAGTTTTTTTCTTGTTGTTGTTGGTTCTACACAAATTAATTGGATGGAAATCCTGCCCTCAATTAAATTGAGTTCCTCCTATAAGTTATTTTATAGAGTGCATGCAGTCCTACTGTGTATGAACAGCTAGCATGAAAACTTACTAATTCTTAATAACTGTTTGTCCTTGATTATTTTGCTCCTCAGTCAATGGTGCCACCCCTGACACCCTCCCCGACCGATGGCTTGCCGATGGGGAGTCTGGCGTCTCATTCACCTGCCCGCTCCGGCAGTTACAGCAGTGGCATCTCATCCCTCAGCCGATGCAGTGTCTCTGAAACATGCGGCATTGACCTGCCACCAGCCGACCCTCCTCTACCACCCGCCATGCCCACAGATATGCCGATTCGCAGGGGCAGCAAGACTCCTCCACCCTA[C/A]AGTGTGTACGAGCGGAACAACCCTCGGCGGGCGACGCCACTGCCTCACAGTCTGTCAGTGCCACCGAGTACCGAAAACCCCAGCCTGAGTGCCAAACCCCAGCTGAACCGTACACAGAGGATTAATTCTGAGCCACGGCACCGGCCCACACCCAGAAAGGTTTCACAGCTGTAGTGTGGCAATGGTAACTAAACGGACTATTTTTTGCAATCCTCGACTGTAAAATTACTGTAGGTTATGTATCATAATTGCGAATGTTTTCAATTGCAGGGAGGCGGATTTATTTAGAGGGCTGAGAGTTGTGGATTAATAGGTAAATCTCATTAATAGAGAAACCATGAAATGTCATAGAAATGATAAATTATTCATTCATTCATTCATTCATTTATAAGTCCCTTATTTATCAGGAGTCACCACAGCAGAATGAACCACCAATTATTGAATTACTTTTAAATTGCACTTCAAATTGAGTACTATTATGCTGCAAAATATATAGTAAA
Associated Phenotype:
Not determined