Busch Lab

ZMP

DOCK2

Ensembl ID:
ENSDARG00000076562
Description:
dedicator of cytokinesis 2 [Source:HGNC Symbol;Acc:2988]
Human Orthologue:
DOCK2
Human Description:
dedicator of cytokinesis 2 [Source:HGNC Symbol;Acc:2988]
Mouse Orthologue:
Dock2
Mouse Description:
dedicator of cyto-kinesis 2 Gene [Source:MGI Symbol;Acc:MGI:2149010]

Alleles

There are 14 alleles of this gene:

Allele Name Consequence Status Availability
sa18092 Essential Splice Site Available for shipment Available now
sa42326 Nonsense Mutation detected in F1 DNA Not yet available
sa35622 Nonsense Mutation detected in F1 DNA Not yet available
sa7387 Missense Mutation detected in F1 DNA Not yet available
sa22408 Nonsense Available for shipment Available now
sa42325 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa14649 Nonsense Available for shipment Available now
sa35621 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa22407 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa18092
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000115295 Essential Splice Site 327 1739 10 73
Genomic Location (Zv9):
Chromosome 14 (position 1564982)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 1623118
GRCz11 14 1649353
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAATAAYAAGAAATGCACGATGGGTCTGCGGAGGCCRTTCGGCGTCGCTG[G/A]TAAATACCATAAAAATATACACTCCTCAGCCACTTTATTAGGTACWCCTT
Long Flanking Sequence:
GTGTTGGATTGTCTCCAGAACAAACCACTGTTATACAATGACTTGCCTAATTACCCTAACTTTACCCTAATTACCCTAGTGAAGCCTTTAAATGTCACTTTAAGCTGAATACTAGTGTCTTGAAGAATATCTAGTCTAATAGTATGTGCTGTCATCATGGCAAAGAGAAAATAAATCAGTTATTAAAACTATTATGTTTAGAAATGTGTTGAGAAAATCTTCTCTCAGATAAATATAAAAGAGTTTACATTTAAAAGAAGGGTGAATAATTGACTCCAACTGTACATAGCTATTCATGTAAGGTATAGCGCTAAAAACAGACTCATATTTAGTGATGTGCTGAGGATTAAACCTCTCTCTGCAGGATCTGGGGAACAAAGACCTGAACCGAGAGAAGATTTACCTGATCTGTCAGATTGTGCGCGTGGGCCGAATGGAGCTGAAAGATAACAATAACAAGAAATGCACGATGGGTCTGCGGAGGCCGTTCGGCGTCGCTG[G/A]TAAATACCATAAAAATATACACTCCTCAGCCACTTTATTAGGTACTCCTTACTAGTACCAGGTAGGACCCCCTTTTGCCTTCAGAACTGCCTTAATCCTTGGTGGCATAGATTTAACAAGGTACTGGAAATATTCCTCAGAGATCTTGCTCCACATTGACATGATAGCATCACGCAGTTGCTGCAGATTTGTCGGCTGCACATCCAGTATGTGAATCTACCTTTCCATTACATTCCAGAGGTGCTCTGTTGGGTTGAGATCTGGTGACTGTTGAGGCCATTTGAGTACAGAGCACTCATTGTCATGTTCAAGAAACCAGTCTGAGATGATTGAGCTTTATGACATGCTGCGTTATCCTGCTGGAAGTAGCCATCAGAAGATGGAGACACTGTGCTCATAAAGGGATGGACATGGTCAGCAGCAATACTCAGGTAGGCTGTGGTGTTGACTCCATGCTCAATTTGTACTAATGGATCCAAAGTGTGCCAAGAAAATCTCCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42326
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000115295 Nonsense 376 1739 12 73
Genomic Location (Zv9):
Chromosome 14 (position 1562860)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 1620996
GRCz11 14 1647231
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTTCTTACACACTCTGCTGAATAAAGTGACGACGACGCGTGGTGACAGT[G/T]GAGGACAAGGTACGACTTGCTGCTCTGATCTCTGAGAAAATGATGGAACA
Long Flanking Sequence:
TCCCTTTGTACGTGTCATCAGAGGGGGAAAGCCCCGCCCACTGGTGACAATCTCTCCCTCATTAGCATAGAATATTAGTTTTGTTTTTGATTCTATTCTGACACAGACATTTGTAGCCCCGCCCTCTTTTGAAAAGAGCACAGTCTCATTTGCATTTAAAGAGACAGTCACCAAAACACCACAATCAGGATTAAAGCCTATAAGGGTCAGTTTCAGAGAGTTATAAACATTATTTGTGTGCTATTTTGAGCTGAAACATCACCCACACACACACTAGGGACACCACAGACTTATTGTACATCTTTGTTTTTGCATAATAGGTCCCTTTTAAAATATGAACACAGTTATATAGTTTATACAGTATGTGTTCATGTTATAGATTTTTTTTAATTTTTCTTCTTTTAATATGTGTGTTTGTGTGTGTGTGTTTTAGGGTCATCGCTGAGAACGACTTCTTACACACTCTGCTGAATAAAGTGACGACGACGCGTGGTGACAGT[G/T]GAGGACAAGGTACGACTTGCTGCTCTGATCTCTGAGAAAATGATGGAACAGCAGCAGTGATCAGACTCTCTGCTGACGCTTTAATACTCACTAAAGCCGTAATCCTGTCTGCACACACACACACATTCTCAAAGAGAGAGAGAGAGCAACCTAGCTTTCCCATGTGGTCTCCCATCCAGGTACTGACCGGGCGCAGCCCTGCTTAGCTTCAGTGGGCGACCATGTGAAAGTTGCAGAGAGCTAGCTGCCGGCTAACACACAACACACATTTAACATTACATTTACAGTTCTACATTTAACATTATCAGCAACAGTAGTGGTAACAGTGACTTTTACACACTACTGAATATTTTAACTATTTTTTTTATTCAGCTGATTATTTCTTCATTTTATTTTTTATTAAATTACAGGCTATAAGTTATGTTTGTTAAAACCAAACATGTCTTGGAGCACTGTTTTTGTAATAAATAGAAAGCAAATTACATTAGTCTCCTCCAATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35622
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
ENSDART00000115295 Nonsense 619 1739 18 73
Genomic Location (Zv9):
Chromosome 14 (position 1552983)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 1611119
GRCz11 14 1637354
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCTACATTAATAAAATAATGCATCTGTCTGTGTGTCTGTCAGTGGGTT[T/A]GTTGGGTCTGCTGAAGTGGAGAACTCGTCCTGAGATGCTGAAGAAGAACC
Long Flanking Sequence:
GTGAAACTGTCACACAGGGTTATGGGGTTTAAACACAGTTGTGTGTCAGCAGTGTGTGAATATAAGCAGCATCTAATGGTAAACATCTATTATTTGTATTGTTTATAATCAGACTGGATAAAGGAAACACTTTGATTGACATTCTCTCTTTGTACGTGTCATCAGAGGGGGAAAGCCCCGCCCACTGGTGACCATCTCTCGCTCATTAGCATGGGACGTTAGTCTTGTTATTGAATCTGCCACTATGCTGACACACAAGCATTTGTAGCTCCGCCCTCTTCTGAAAAGAGGACAATCTCATTTGAATTTAAAGAGACAGTCACCAAAACACCACAATTAGGACTAAAGACTAAAAGGGTAGGTTTCAGAGAGTTATAAACATTATTTGTGTGCTGTTTTAACTTCTTTTAACTTCACACACACACACTCTAGGGACATCCTAGGGATTTATTTCTACATTAATAAAATAATGCATCTGTCTGTGTGTCTGTCAGTGGGTT[T/A]GTTGGGTCTGCTGAAGTGGAGAACTCGTCCTGAGATGCTGAAGAAGAACCTGCAGGAGCTCAAACTCATCGACGGAGAAGAAGTTGTGAAGGTGTGTGGCACTGAAACTATTAATGAACTGCACTAGAAACTTACTTTAGCATGCGTGTTTGTTAATGCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTAGTTTCTGCAGGACACTCTGGATGCTCTGTTCAACATCATGATGGAACATTCTCAGACTGACGACTATGATATTTTGGTGTTTGACGCTCTGGTAAGCAGCATCCAAACACACACACAGTCAAAGTCAGAATTATTAGCCCTCCTGTATATTTTTTTTTTCCCAATTTTTGTTTGAAGATAATAAGATTTTTTTTCATTTCTAAACATAATAGTTTTAATAACTATTAATAGTTTTAATCTTTGCCATGATGACAGCACATAATATTAGACTAGATATTCTTCAAGACACTAGGATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7387
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:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000115295 Missense 721 1739 21 73
Genomic Location (Zv9):
Chromosome 14 (position 1550108)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 1608244
GRCz11 14 1634479
KASP Assay ID:
554-4227.1 (used for ordering genotyping assays)
KASP Sequence:
TAAATTWAATGTGTGCTTTAGGAAGCTGATGTCGGTGTTGAAGACTTATC[T/A]GGATGTGTCGAGTCGCGGCGAGGCCTGTGAACCCATCCTGAGGACACTTA
Long Flanking Sequence:
ACACAAGAGGGCAGTGTGTGTGTGTGTGTGTTTCATGTCAATTATGTGCAAAATGTCAATTACAGAATTGAAAATAATCCAGGTCAAGTCAGAGTGAAGAAATTTGGCATATCAATATTATTAATCTTTATTATGTTTTCATTTTAATGTGTATATTAACATATATGCATATGCAAAATAATTGTTAAGTAGCAGTTTTTAATTATTTCTTTAGATTTGGCTTAAAATAGGACGTTCGGTTTATATAAATAATTAATTTGGCTATACATTTATTAATATAACCTCTTAACTGTCAGCCCATTTTTTGAGTTTACACATGAAATGCATATTATATTATTATATTATATTATATTATATTATATTATATTATATTATATCATATTATAATGTCAAGATTTTTATGTATTTAATATGTACTAAAAACAAAATATCAATTTCAATAGTGCAAAGTAAATTTAATGTGTGCTTTAGGAAGCTGATGTCGGTGTTGAAGACTTATC[T/A]GGATGTGTCGAGTCGCGGCGAGGCCTGTGAACCCATCCTGAGGACACTTAAAGCTCTGGAGTACATCTTCAAATTCATCGTCCGCTCTAGAATGCTCTATTCACAGTAAGTCTGAGTGGGGGATTGATTCTGAAAGACTCAAATGATGAAAGACCAAACAAGACACGCACACACACACACACACACACACACACACACACACACACACACACGCACACGCACACAAACACACACACACAATTTTAAAAAGCCACACAATTTTAGCAATTTAGATGTAACAACTTGAAATGTATTTTATTTTATATTTTATTTTATTTCATAAAATTATTTAATAATTAATTAATTAGTTTGTTTTTGTGTTAGTTTTTTATTTTTTTTACTAAAGTATTTTTATTTTATCTTATTATTTTTTCAAATATAATTTATTTTAATTAATAATTAATTAATTTGTTTGTTTTTATGTTTGTTTTTATTTGTTTTTTGATTTTATTTGATTTATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22408
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
ENSDART00000115295 Nonsense 849 1739 27 73
Genomic Location (Zv9):
Chromosome 14 (position 1537075)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 1595211
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAAAGTGAGCTCCATGACTGAGATAGTGGGCAGCAGACTCTTCCATAGA[C/T]AAGGTGAAACACACACACACACACACACACACACACACACACACACACAC
Long Flanking Sequence:
TTTTAGTTAAGTTGAAATGAACATATGGAGGCACAGTGGCTCAATGGTTAGCACTAGAGCCTCACAGCAAGAAGGTGTCTGGTTCGAGTCCGAGTTGTGTGTTTCCTTTGGGTGCTCTGGTTTCCCCCACAGTCCAAACACATGCACTATATTGATGAACTAAACTGGCTGTAGTGTATGAGTGTGTGTGTGTGTGTGGGTGTTTCCCAGTACTGGGTTGCAGCTAGAAGGGCATCCGCTGCGTAAAACATAGGCTGGAATAGTTGGCGGTTCATTCCACAGTGTTAACCCCTGAGATAGAGACTAAGACTAAGGAAAATGAATGAATGATAACTGACTCTTGTGTCATGTGTGACCTCTCTCTCTCTCTGTGTGTGTGTGTGTGTGTGTGTTTCAGTAAGCTGTTGTATGATTTCTACACCTGTATCCCTCCGGATAAACTACAGAAACACAAAGTGAGCTCCATGACTGAGATAGTGGGCAGCAGACTCTTCCATAGA[C/T]AAGGTGAAACACACACACACACACACACACACACACACACACACACACACACACACATTCACATGCAGACATACAGAGACACACACACTTACACAGATATACACACACACACAAGCTCACATAGATACATATACACACACAAGCACAAAAACACACTTCATTCACACACAGACACACTCATTCATACACACACACACACACACACATGCATACAGAGAACAGATACACACACACAGATACACACAGACACACACATAATAACCACAAGCTCACAGAGATACACATGCACAAACGTGCATACACACACTGAACATGCACACATTAAACACACGAAAAACGCACATACAAGCTCACACAGATACATATACACATACAAGCTCACACNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNCACACACACACACATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42325
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
ENSDART00000115295 Essential Splice Site 989 1739 36 73
Genomic Location (Zv9):
Chromosome 14 (position 1497772)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 1555908
GRCz11 14 1582828
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCAGGCAGGCGCTGCTGTTTTCTACACAAATGCAAATCCAGTTATTTCC[G/A]TATTGCATTTGAACGTCGACAGTTTCTGCCGGCTGTAAATCTGTTTTTCA
Long Flanking Sequence:
ACTAGATGGCGCCAAACAGACAAAAACGAAAATAGCTGATGGAGTATACACTAACCTGTGCATTATTTAGACACAAGATGGCGCCAAACTGACAAAAAAATTGCTATAGTGACAGAAACTAAATCAGCTGATGGAATATACACTAACCTGCGCATTATTCAGTGACAAGATGTCGCCAAACAGTCAAAAACGAAAACAGCTGATGAAGTATACACTAACCTGCACATTATTCAGACACAAGATGGCACCAAACAGTCAAAAACACAACGCTAACAGAAACGAAACTGACCGACTGGCTGAATGACCAATCAGAATCGAGTATTCGAGACAGCCGTGTAATAAACACAAATATTGACCTCTTAAAATTGCTTCATTTATCTGTTAATAAACAGTCTCACAATATTTTAAGCATAAAATCTAAACCACAAACTTTCCTTTCTCCACCAGGAATGCAGGCAGGCGCTGCTGTTTTCTACACAAATGCAAATCCAGTTATTTCC[G/A]TATTGCATTTGAACGTCGACAGTTTCTGCCGGCTGTAAATCTGTTTTTCAGTGTTGCTGTCATTTTCAGAGCGCGTCATTTGTCACTGGAAATTGCTAGGTGATGTCTCGCATTTGCATATCCAGATGACAAATTTGCATGTATGTGATCCGTGCAACATGCAAATTCCTCTCCGCAGAGTTTTTTCCGTTAGCAAGGCAATTGATTATACCTTTTTGGTCACAGTTGCTCAGACTTTGTGTTTGTGGTTTAAGGAGACTTTTAACCCTCAATATTAAGCTTTGTCACACTGTGTTTTGTGCATGAATGATTCATGGAGAGGATCTGGCGCCCATTGGACTCGCTGAGCAACCACCTGAGGTTGGCACGGGCAAAGAAAACGTTTGACTTCACAAAGAGCGCACATTTCTGTATTTTAGGAAGCACTATAACCGAGCAATCTCAACTTTCCTCATCCCCCAGAGGACGGAGGCATGAAGACAGAGAGCAAAGGGAAGAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14649
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
ENSDART00000115295 Nonsense 1314 1739 61 73
Genomic Location (Zv9):
Chromosome 14 (position 1453476)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 1496344
GRCz11 14 1538532
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACYCTGTGTAAGGAGTTGRCAGATCAGTTTGAGATGGAGGTCTTCGACTA[C/A]GAGCTCCTCGGACAGAAACTGGTAACACACACAYACANNACACACACCTTCW
Long Flanking Sequence:
CTTGCCTAAATCAGTTATTAGAAATGAGTTATTAAAGTATTAGGATTAGAAATGTGTTGAAGAAAATCGGCTCTCCGTTAAACAGAAATCAGGAAGGCTGATAATTCTGACTTCTCAGACAATGTACAATATAATATGATGAATAATTGTTTTGTGGTGAATGTGCATGTTGTGTGTGAATATTTCAGTGGTCAGAGGAGCAGTGTCTGCCTCAGCTGGACTATCAGACGCCTCAGTCTCAGAGACAACTCAAAGAGTCACTCTACGACAACATCATCAGCTACTTCGACAAGGGCAAGGTCTGCTCACACACACACACACACACACACACACACACAGAGCTACTGTCGAACAGGATGTTGATGATGTTTACAAGTGTTGTTTTGTGTGTAAAGTGTTGTTGTTGTTTGTTTTTCTGTGTGTGTGTGTCAGATGTGGGAGGAGGCCATTACTCTGTGTAAGGAGTTGGCAGATCAGTTTGAGATGGAGGTCTTCGACTA[C/A]GAGCTCCTCGGACAGAAACTGGTAACACACACACACAACACACACCTTCATCTTTCGTAGTAATTAAAAACACAAATTGTCAATTTTGGTTTCAAGCGGACTTTAATCAATTATAATAAACTGAAGTGTGTTTTATTGCTGTGAACTTTCCCCATCACAGAATCAACAGGCCAAGTTCTACGAGAACATCATGAAGATCCTGCGGCCCAAGCCAGACTACTTTGCGGTGGGATATTACGGCTGCGGCTTCCCTCCATTCCTCAGGGTCAGTGTGTATATGATGATATGTGAGTGTGTGTGTGTGTGTATGTAAGTGTGTATGCATGTTTGGACTGTAATATAGTGTTGTGTTCGTCCAGAATAAAGTGTTCATCCACCGGGGGAAAGAGTACGAGCGCAGGGAGGATTTCCAGAGTCAGCTGATGAGTCAGTTTCCCAGCGCTGTCAGACTCAACATCACCACCATGCCTGGAGACGACATCAAAAACTCCAACATGCAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35621
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
ENSDART00000115295 Essential Splice Site 1404 1739 63 73
Genomic Location (Zv9):
Chromosome 14 (position 1452973)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 1495841
GRCz11 14 1538029
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACATCACCACCATGCCTGGAGACGACATCAAAAACTCCAACATGCAGTG[T/C]ATCCTGCAGTATAATATTTATAATACTTTTTTGTTGCCATTCTTGTATAT
Long Flanking Sequence:
GCTCCTCGGACAGAAACTGGTAACACACACACACAACACACACCTTCATCTTTCGTAGTAATTAAAAACACAAATTGTCAATTTTGGTTTCAAGCGGACTTTAATCAATTATAATAAACTGAAGTGTGTTTTATTGCTGTGAACTTTCCCCATCACAGAATCAACAGGCCAAGTTCTACGAGAACATCATGAAGATCCTGCGGCCCAAGCCAGACTACTTTGCGGTGGGATATTACGGCTGCGGCTTCCCTCCATTCCTCAGGGTCAGTGTGTATATGATGATATGTGAGTGTGTGTGTGTGTGTATGTAAGTGTGTATGCATGTTTGGACTGTAATATAGTGTTGTGTTCGTCCAGAATAAAGTGTTCATCCACCGGGGGAAAGAGTACGAGCGCAGGGAGGATTTCCAGAGTCAGCTGATGAGTCAGTTTCCCAGCGCTGTCAGACTCAACATCACCACCATGCCTGGAGACGACATCAAAAACTCCAACATGCAGTG[T/C]ATCCTGCAGTATAATATTTATAATACTTTTTTGTTGCCATTCTTGTATATATTGCATTACATTATATTGATTTAATTAATTCAGACGCATATACTTTTTTGCACTCTCATACTGTATGTTATATTATTTGCATTATGCTTAAAATAATATGAATAATAATAAAGAATAATAGAATAACACCACCTTGCACTAATAGATGATTTAAGACTTTAGTAAAGGAACATGTTAATATAAATATATTATATATATTTAGACTAATGCTTTTTATATTGAAACATCTATTCTGTGAAATTAAGTAAAAAAAATAAATTAAAATAAATCTGTTTACAAAATATTTAGTGTTGAGCACCTGGATGTGAATTGCGCATGCATGGTCAGGTTTGTTGTTCTTATGCGTTCTGCATCAGATATCCAGTGTTTTACAGTGCAGCCAGTTCTAGAGATCCCACCGCGTCTGAAGAACAAACCAGTGCCGGATCAGATCATCAAGTGAGTCTCAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22407
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000115295 Essential Splice Site 1489 1739 67 73
Genomic Location (Zv9):
Chromosome 14 (position 1449930)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 1492798
GRCz11 14 1534986
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACATCATTATTTGGAAGAATAAGGTCAATGAGTATCGTTATTTTTTCCA[C/A]CAGACCACGATCAGTCCTCTGGAGAATGCCATTGAGACGATGGGACAGAC
Long Flanking Sequence:
TTTCACACAAGTCTTCGTACATGAGGCCCCTGATGTTTTCTGCACTTCTTTTGCAGTTTCTACAAGTCCAACTACGTGCAGCGATTCCAGTATTCCAGACCCGTCAGGAAAGGAAAAGTAGATCCTGACAATGAGTTTGCTGTGAGTCACACACAAATACTTTTTGTCTCTTTCATACACACACACACACACACACACACACACTGATATAATGATGTGAGTTGACTCTTGTCTTGTGTCTTCAGTCGATGTGGATTGAGCGCACCACATTCATCACCGCATACAAACTGCCGGGAATCCTGCGCTGGTTTGAGGCCATCAACATCACACACGTGAGTCTCACAGCTGTACTCTGCGCAGTGTGTGCGGCATGACTTTACACTGTTGCATGACTACATTCTGCATTGTCAGTTCTATTTAATGCACTAATGTTCAGCGTTACCTGAGGAATACATCATTATTTGGAAGAATAAGGTCAATGAGTATCGTTATTTTTTCCA[C/A]CAGACCACGATCAGTCCTCTGGAGAATGCCATTGAGACGATGGGACAGACCAATGAGAAGATCCTCACCATGATCAACCAGTACCAGTGTGATGAGACGTTACCCATAAACCCCCTGTCCATGCTGCTCAACGGCATCGTGGATCCTGCCGTCATGGGAGGATTTGCCAAATACGAGAAGGTCAGGCTCAGAGGAGTGTGTGTGCGTGTGTGTGTGAGTGAGAGTGTTTTTTTTGTTTGTGTGTGTTTCTGTGTGTGTGTGTGTGTGTGCATGTTTGTGTGAGAGTTTGTATGTGTTACACATGTGCCTGTGTGTATGTTTGAGAATGTGTGTGTTTGTGCATTTTTCTGGGGTTTTGTGTGTGTGTAAAGGACTGAGTGAGTGAGTGACTGAGTGTGTGTGTGTGTGCACATGTGCCTGTGTGTAAGTGAGAGTTTGTAAAAATGCATGCAAATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGCATG
Associated Phenotype:
Not determined