ZMP
LOC566115
Ensembl ID:
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.
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.
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
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.
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 |
---|---|---|---|---|---|
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.
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.
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 |
---|---|---|---|---|---|
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.
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.
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