Busch Lab

ZMP

NEK10

Ensembl ID:
ENSDARG00000025335
Description:
NIMA (never in mitosis gene a)- related kinase 10 [Source:HGNC Symbol;Acc:18592]
Human Orthologue:
NEK10
Human Description:
NIMA (never in mitosis gene a)- related kinase 10 [Source:HGNC Symbol;Acc:18592]
Mouse Orthologue:
Nek10
Mouse Description:
NIMA (never in mitosis gene a)- related kinase 10 Gene [Source:MGI Symbol;Acc:MGI:2685128]

Alleles

There are 11 alleles of this gene:

Allele Name Consequence Status Availability
sa42826 Nonsense Mutation detected in F1 DNA Not yet available
sa11151 Nonsense Available for shipment Available now
sa22955 Essential Splice Site Available for shipment Available now
sa12878 Nonsense Available for shipment Available now
sa42825 Nonsense Mutation detected in F1 DNA Not yet available
sa18477 Essential Splice Site Available for shipment Available now
sa6449 Nonsense Mutation detected in F1 DNA Not yet available
sa36262 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa42826
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
ENSDART00000029001 Nonsense 86 1099 5 40
ENSDART00000123061 Nonsense 86 1150 5 41
Genomic Location (Zv9):
Chromosome 16 (position 53676915)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 49946576
GRCz11 16 50150896
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTCCATTTCCTTGTCTAACTAGTGTTTGTTTTGATAACAGCGTGACATA[C/A]AGAAAGCAGAGATATTTCAATGACCAGCCACATCACAGATTATTCCTGGA
Long Flanking Sequence:
AGTTTTTCCTTAGCAAGTAAAATTATCTGTCATTGGGTAAATGAAATAATGTTTTTTTTCCATTTGAAATCTAAGTAAGAAAGTTTTTTTTTGCATAAATCATAAACATTACATAAAATTGCAGTAATTAAATAGAATTCTGCAGCTCCTGGTTAGCTATAATTCAGACTTAACATATCTTTGCGATGTGACTACACATATTGCCATTTTGAAGCTGAAACAATATACTGTATTGTGCAGCCCTAAAATAGTACATTTTAATTTTGAATTTGTACGTTTAATTTGTATTCACCTCTTCCCAACTTTAGGCTTCATCTCTGAGTCAATCAAAAGGACACAAGTCTCAAACTTCCACAAATGTTCCTGAGCACCGGAAAAATGCCACTGAAGCGTCTGAGCTGGAAAACTTTAGGTGCTCAGTCGCTCATGTTATCTGTTCAATTTGCTCTTGTTCCATTTCCTTGTCTAACTAGTGTTTGTTTTGATAACAGCGTGACATA[C/A]AGAAAGCAGAGATATTTCAATGACCAGCCACATCACAGATTATTCCTGGACATCTTCACTGCCTTGATCAATAACAGGCTTGGTTGTAGGTCTGTATTTATGTGTATATGTGTTATGCTAATAATTAGGGCTGTGTGGTATTGAAGAAAAAAAATGTAATGCTAGAAATGTGATATTTGCTATATGCAATGCAATAATTGCCAGTTCATTTCGCTGTGGCTACCCCTCCCCTAATAAATAAAGGGCTAGGTCGAAGGAAAATAAATGAATGATACAATAATTTTAAGAAAAGATATTAGTTATAGTTTCACATTATTTTTGGGAAAAGAAAACATCACTACAACTTCTAAAAATGGATAAAACAATTCAAATATTTTGACTAACAAAAACAAACAAATAAAAATAAATAAATATCACCACCACTTTGTATAGTTTTTGTATATCATTCACATTAAAATTTTAACAGATTTTTGGAAAAGCAAACCAGCATGTGCACTCTG
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa3955
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000029001 None None 1099 None 40
ENSDART00000123061 Essential Splice Site 145 1150 7 41
Genomic Location (Zv9):
Chromosome 16 (position 53675061)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 49944722
GRCz11 16 50149042
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTAATTGGATCTTAAYGCAAAGCATCACCTACATTGCTGTTCCTCCAACA[G/T]AAAGCCTTCTTTGAGCTCCAAGGAGYCAGTCAACTCGTGAAGGTAAAGGA
Long Flanking Sequence:
CAATAATAACAATAAACCTATTAATAATATTAATAATAATATTAATTATTATTATTATTATTATTATTATTATTATACCTATTAGAGATAAATAGATAAATTAATTAAATAATAATAGATAAATCTAATTGTATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATATACCTATTAGAGGATTATAATTTTCAAATAATATTTAAAATTATTTATTTATAAACATTTTTATTTATTAATTTATTTGTTTATTGTTATTATTATTATTATTATTATTATTATTATTATTATTATTTTATCAATCTAAGCTGACATGAACAAACAATGAATGCGTCAAATTTATGGAATATGTATCTTAATAAACAAAGATGTTAGCATTATTTTGCCAAAGATTAATAAACAATGTGAAAACTGTTGTTTATTGTTGACCAATAAGAGCTAATTGGATCTTAATGCAAAGCATCACCTACATTGCTGTTCCTCCAACA[G/T]AAAGCCTTCTTTGAGCTCCAAGGAGCCAGTCAACTCGTGAAGGTAAAGGATTTCACAGTCTTCAAATACTGTAGATGGACAGTCACATGTGGAAATTCACTGTGCTTTATCGAATGTTTTTCAGCACATGGAGTCGGTTGCATCTGTGTATCTCGAATGCGGAGAACAGACGCTGGAAATCGAGCAGCTGGTAGCAATGACATGTGAGAAAAGCAATATGTTATATAGCATGTACAGCATAGGAATGTGCACAATGAAGAATAATGTGGTGCTCTGCTTGTTCCCCACATCATTTGCTCTCCAGATATCTTTCAGAAGTTGTCTACTGTTGAGGAGCAAAGACAGTGGATTATTAATTGTGAAGCACATAAGGTATGTGTTGGAAAACGAAGATTATACACTACCTGACAAAAGTCTTGTCGTTAATCCCAGTTGTAAGAGCACAAATAATAACTTGACTTCTAGTTGATCCTTTGGAGAAGTGACAGAAGTTTGATTTC
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa28748
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000029001 Nonsense 185 1099 10 40
ENSDART00000123061 Nonsense 185 1150 9 41
Genomic Location (Zv9):
Chromosome 16 (position 53674755)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 49944416
GRCz11 16 50148736
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGAATAATGTGGTGCTCTGCTTGTTCCCCACATCATTTGCTCTCCAGA[T/A]ATCTTTCAGAAGTTGTCTACTGTTGAGGAGCAAAGACAGTGGATTATTAA
Long Flanking Sequence:
TTTATCAATCTAAGCTGACATGAACAAACAATGAATGCGTCAAATTTATGGAATATGTATCTTAATAAACAAAGATGTTAGCATTATTTTGCCAAAGATTAATAAACAATGTGAAAACTGTTGTTTATTGTTGACCAATAAGAGCTAATTGGATCTTAATGCAAAGCATCACCTACATTGCTGTTCCTCCAACAGAAAGCCTTCTTTGAGCTCCAAGGAGCCAGTCAACTCGTGAAGGTAAAGGATTTCACAGTCTTCAAATACTGTAGATGGACAGTCACATGTGGAAATTCACTGTGCTTTATCGAATGTTTTTCAGCACATGGAGTCGGTTGCATCTGTGTATCTCGAATGCGGAGAACAGACGCTGGAAATCGAGCAGCTGGTAGCAATGACATGTGAGAAAAGCAATATGTTATATAGCATGTACAGCATAGGAATGTGCACAATGAAGAATAATGTGGTGCTCTGCTTGTTCCCCACATCATTTGCTCTCCAGA[T/A]ATCTTTCAGAAGTTGTCTACTGTTGAGGAGCAAAGACAGTGGATTATTAATTGTGAAGCACATAAGGTATGTGTTGGAAAACGAAGATTATACACTACCTGACAAAAGTCTTGTCGTTAATCCCAGTTGTAAGAGCACAAATAATAACTTGACTTCTAGTTGATCCTTTGGAGAAGTGACAGAAGTTTGATTTCTCTGATGAATCATCTGTTGAACTGCATCCCAATTATCACAAATACTGCAGAAGACCTACTGGAACCCGCATGCGCCTAAGATTCATAATTAAAGAATTAAAAAAATTAAGGCATGCTGTTTCGAGGGGTCTGAGGCTGTGTTAGATTCCATGTGCAGAAGTTTATTAAAGGGGTTAGGCAGAGACATAACGAATAAACAGGCAGAGAGTCCAATAACAAACACGGGCAAATCCAGACAACCTAGTGAGAGCGAAGGCAGAGGTTCAGTATAACAACAATCAGTCCAAAACAGAGCAAAATACACAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11151
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
ENSDART00000029001 Nonsense 340 1099 14 40
ENSDART00000123061 Nonsense 340 1150 13 41
Genomic Location (Zv9):
Chromosome 16 (position 53669356)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 49939017
GRCz11 16 50143337
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCTTWAAATTGTACTTTAAATTTTGGCAAACTGYTTTTTTTCCAGAGAA[C/T]GAGTGTATGTGTCCGATCGCTCCACCATTGATTCAATTTCCAGCGCCAAT
Long Flanking Sequence:
TTGCTTTGCTCGGTGCAGTGTGTGCGGGATCAGCTGCGTCAGTGTGATGGTGTGCCGGTTCTGCTCAGTCTCCTGCACTCAGAGCACATCAAGCTGCTGTGGAGCACTGTTTGGGTTCTCGTTCAGCTCTGTCAGGATCCCGACACCAGCGCTGAGGTCCGGGCCTGGGGCGGCGTGCAGCAACTACTGCGCATCTTACATGGGTGGGTCATGCTAATTTTGATATTACATGTTCTTTTTCACTTTTAGCATCTTTTGCTGCATAATAGGGGTTTAGGGGCAGTTCTAGGGGCAGTGGAAGTCTATGGGGCAAAAAGTGCAGTGCGACCGCAGAGGTTTTAAAAAAACTATTTGCTACAATCTATTTTTTCCTACACACATATAAATATTATATTGCATCATTTTGATTAACATTTTAATACTATTTTAATGTTTAAACAGCATTTTAGGTCCTTTAAATTGTACTTTAAATTTTGGCAAACTGTTTTTTTTCCAGAGAA[C/T]GAGTGTATGTGTCCGATCGCTCCACCATTGATTCAATTTCCAGCGCCAATGCAGCAGGCAGAATCCACAGTCAGCAGGTGTCAGCAGTGGTGTGCGCTCATGAAACAGCGGAGAACACCATCAGTCTGCAGTCAGGTGAGGAGACTCAGAAAATGTAGGAATTATGAACCTAAAGCCTGTTTTACACTGCAAGTGTGAGCAGAGCGTGAGCAGCGCGTGTTTTTCGCCGTCCATGTTAACAGATTAGAGCTTTCATACTGCATGCAGAAGCAGCATGTCAGCACGAGAAGTAGTTTGGGCAATGGGTCTATTTTGGCCACGTTGCTCACACTCAATTAAAGTGACAGTGCATTGATATGGACCAAAACACATTGAATGACAAAAAAAGTATTTAAAAAGACAATTAAAAAGTAGAGATTTTACCCTATAAATGCATCAATAAGATCCACAGATTTTTATATATTCAATCAAATGAACTTAAACGATTAAAATAAAATATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22955
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000029001 Essential Splice Site 385 1099 14 40
ENSDART00000123061 Essential Splice Site 385 1150 13 41
Genomic Location (Zv9):
Chromosome 16 (position 53669219)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 49938880
GRCz11 16 50143200
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGGTGTGCGCTCATGAAACAGCGGAGAACACCATCAGTCTGCAGTCAGG[T/C]GAGGAGACTCAGAAAATGTAGGAATTATGAACCTAAAGCCTGTTTTACAC
Long Flanking Sequence:
TCCCGACACCAGCGCTGAGGTCCGGGCCTGGGGCGGCGTGCAGCAACTACTGCGCATCTTACATGGGTGGGTCATGCTAATTTTGATATTACATGTTCTTTTTCACTTTTAGCATCTTTTGCTGCATAATAGGGGTTTAGGGGCAGTTCTAGGGGCAGTGGAAGTCTATGGGGCAAAAAGTGCAGTGCGACCGCAGAGGTTTTAAAAAAACTATTTGCTACAATCTATTTTTTCCTACACACATATAAATATTATATTGCATCATTTTGATTAACATTTTAATACTATTTTAATGTTTAAACAGCATTTTAGGTCCTTTAAATTGTACTTTAAATTTTGGCAAACTGTTTTTTTTCCAGAGAACGAGTGTATGTGTCCGATCGCTCCACCATTGATTCAATTTCCAGCGCCAATGCAGCAGGCAGAATCCACAGTCAGCAGGTGTCAGCAGTGGTGTGCGCTCATGAAACAGCGGAGAACACCATCAGTCTGCAGTCAGG[T/C]GAGGAGACTCAGAAAATGTAGGAATTATGAACCTAAAGCCTGTTTTACACTGCAAGTGTGAGCAGAGCGTGAGCAGCGCGTGTTTTTCGCCGTCCATGTTAACAGATTAGAGCTTTCATACTGCATGCAGAAGCAGCATGTCAGCACGAGAAGTAGTTTGGGCAATGGGTCTATTTTGGCCACGTTGCTCACACTCAATTAAAGTGACAGTGCATTGATATGGACCAAAACACATTGAATGACAAAAAAAGTATTTAAAAAGACAATTAAAAAGTAGAGATTTTACCCTATAAATGCATCAATAAGATCCACAGATTTTTATATATTCAATCAAATGAACTTAAACGATTAAAATAAAATATTAAAATTAAAATTGATTAAAATTAAATATTTATTTGGACCCGAACTACAAAACCAAATTTAACACAATTAGTATTAGTTTTGCTTAAGTTGCACACTAGTTTGATCATGTTTAAATATCATTATAACTATATTGTTGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12878
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
ENSDART00000029001 Nonsense 516 1099 19 40
ENSDART00000123061 Nonsense 516 1150 18 41
Genomic Location (Zv9):
Chromosome 16 (position 53665809)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 49935470
GRCz11 16 50139790
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTAAACCAGAACCGTCCTCCTATAAGAGTGGTCAATGGTTATGCGGTTT[T/A]GGAGCATCTAGGMAGCGGAGCTTTTGGCAGCGTCTTTAAGGTCAAGATGA
Long Flanking Sequence:
TATTATTTCTATATTTAATTAAAATATTTTTACTTTTTTGTTTCTTTAATTTTATTTAAAGATAATATATGAATTTTATTTCTTTTTTAAGATTTCTTTTTTTTTGCTTTTTTTCTGCATGATATAGTTGTTGTTTTTTTATTTTTTTATTCATCGATATCGTTACTTTTATGAAACCATTTTTTAACATTTATTGGTTCTAAATGGTTTGTTTGTTTCCAGGCTGTTTTCTCCAGATTTGTTTGAGATGTTTATCGATGTCGGTCACTACGTTCGAGACATTACTGCATATGAACCGCTGCAACAGAAAATCATGCTTTTATCTGTAAGATCCTGAAGTTATTACACTCATAAAATACACTGGAATATTTTCTCTCTTGCATATTTACATTATGACTGTGTTTATCTGCAGCCAGAAGAGTTGGATATTCTTAGGGAAAGCATCGAGACAGTAAACCAGAACCGTCCTCCTATAAGAGTGGTCAATGGTTATGCGGTTT[T/A]GGAGCATCTAGGAAGCGGAGCTTTTGGCAGCGTCTTTAAGGTCAAGATGACCTGTGCTGGTTATTGTTGGTTAATAGTTAAATCAAGCCATTCACGGTTGTTTTTTGCGCCCACTCATAGGTTCGTAAGCAGAACGGACAGAACATTCTGGCACTTAAAGAGGTCAACTTTCACAATCCGGCCTTTGGCAAAGATAAGCGATCCAGAGACAGCAGTGTTGAGAAGATTGTGTCTGAAATGACCATCATTAAAGAACAGGTTAATCTCATTCATAAACAGCTCCAACATTTCATTCCACTTCATTTAGGTCAGACGTCCACCTAGTGCTCTATTTTAACGATCTAAGCACAGAGTCTAAAGCTCATGGTGCAATTGCACCAAGATTCTGTCTGAGTCCACTTTTGCTATTTTAAGGTCGGGAAAAACATCTGTTCACAAGGCGCATGGTCTAAAAAGGTTTATCTTTATTCTCTTTTGGCATAACCTGCATTAAACTGTAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42825
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
ENSDART00000029001 Nonsense 576 1099 21 40
ENSDART00000123061 Nonsense 576 1150 20 41
Genomic Location (Zv9):
Chromosome 16 (position 53663826)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 49933487
GRCz11 16 50137807
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAACCTCCATCTCTGTCCACACAATCTTCAAAAAATATGTCTTTTTTTT[C/T]AGATGTCTCATCCGAACATTGTAAAATACTTCAAAACATTTTTAGAAGGT
Long Flanking Sequence:
TAATCCCCAAGGATTTCTGTCATTTTGTCAGGTTAGCCTGAACAAGCGCAAGGAATATCTGGTGCATTAGTACATGTAATTTGGAGTTTAAACTGTACCTGTCCATTCTCTCGTTGTGTCTATATGTAAAAATGCTGTAATTGCTTTAAATTGAATATGGATGTGTAAAACGGAATGAGATTATGTACTTTACTCTTGCCTTTCTGTCTCGAAGCTTCTCATAAATAGAAGATGAGTAAGTTTAATCATGTATGTGCGGTGGCTTACTAATTTGCCTTTTATAATTTGGCTAAATTTAATTTGTTAATTTTTATTTTTTCCCCTTTATGTTAAATTGTTGCGTGTTTCCCTGGCCCTAGATAGGGGAGGCACGTAACAATTGGGGGCTCGTCCGGGATTTAAAGGGACTTGCCAATAGCCTTTCAAAAGATCTAGCTTGGTGACAAACCTTGAACCTCCATCTCTGTCCACACAATCTTCAAAAAATATGTCTTTTTTTT[C/T]AGATGTCTCATCCGAACATTGTAAAATACTTCAAAACATTTTTAGAAGGTAAATACTATTTTGATTTTTTTTTTTTCATACACACATACATACTCATACTGTTGCATGTACAGTGAAGTTCAATGATTGTCAGAATGTTGAATGTTGAAGTCAGAATTATTAGCCCCCCTGGTTTATTAGAACCCCCCCTTCCCCCCAGGATAGTTTTTCCCCCAATTTCTGTTTAAGGGAGAGTAGCTCTTTTCAACACATTTCTAAACATAATAGTTTTAATAGCTCATTTCTAATAACTTATTTATTTTATCTTTGTCATGATGACAGTAAATAATATTTGACTAGATAAAGGGGCTAATAATATTAAAGGGGCTAATAATATTGACCTTAAAAAAATTTAAAACTGCTTTTATTCTAGCCGAAATAAAACAAATAAGACTTTCTCCAGAAGAAATAAATATTATCAGACATACTTTGAAAATTTCCTTGCTCTGTTAAACATCATT
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa28747
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000029001 Nonsense 751 1099 26 40
ENSDART00000123061 Nonsense 751 1150 25 41
Genomic Location (Zv9):
Chromosome 16 (position 53652901)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 49922562
GRCz11 16 50126882
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTAGATTGTGGAAGCTGTTTATGAGCCACTAGAAGACAAAACCTTCTCC[G/T]AAAGAGTAACCGACATGATTAAATGGTAGGATTCCCTGAAAACTGCTTTC
Long Flanking Sequence:
CAATTCTCACTTAAAAAAATACATTTTCTCAGTTTTAATATGAAATGTTGCATGTATTGAAAAACAATAACACAAATAAATACATAAATAAATAAATAAATAAATATGTGAATGTAAAAAATAGCTTAAATTTTTTTAGCATAGTATCAATAATATTTCTATATCAAATAAAACTATATATATATATATAGTTTTTTCAATTTTTTTCAATCATTTTTATATATATATATATATATATATATAAATCAAAATTATGATTGAAAAAAATTATTTTAGATTTAAAAAAATAACATTTCAAGGCTTCTTTCATTTTTTTTACGTTAAATAAGCCAAGTGAGACCCCTTTCTTTAAATGATGCTTTTTAATTACATTTTTACCAGACATTTTTACTCACATGTTTCAAATGTTTGTCAGATTTGATTATTCTGAATTTTAATGTCGTTCATGTGTTTAGATTGTGGAAGCTGTTTATGAGCCACTAGAAGACAAAACCTTCTCC[G/T]AAAGAGTAACCGACATGATTAAATGGTAGGATTCCCTGAAAACTGCTTTCTGCTTTCAGATATAAACACATGCAGCCTGGATACAGATATGAGATTGTTGTAGAAATGTAAAATCTTGAAAATGACACACAATTTCATATGTTTTTTTTATTTATTTTATTTTAATTAAATGAAGAGAAATTATGATCTGAAAGTGATGCAACAGATGTATTATTTTACCAGCATTGTTATTATTATTCTTATTATAAGAAAAGCCTTTGTGTTATAAATTATATTTAAAGAAAAATGTGTATCAAATGTCCTTTGTGCTGCCAGCCATTGGAATTTAAATACTGAGTTTTAAGTATGAATAGGGTTTAATTAAGTTTTTGATTTATGTGATAACATTGAATGTATTTGTGTTGCCTGTTTTCTGTGAAATGTGTGATGTGAACGCTGCTGTGGTTGTGTGGTGAAGCCAAAAATAAATTTAAAGTAAAGTAAAAAATATTTATAATTCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18477
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000029001 Essential Splice Site 759 1099 26 40
ENSDART00000123061 Essential Splice Site 759 1150 25 41
Genomic Location (Zv9):
Chromosome 16 (position 53652874)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 49922535
GRCz11 16 50126855
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACTAGAAGACAAAACCTTCKCCGAAAGAGTAACCGACATGATTAAATGG[T/A]AGGATTCCCTGAAAACTGCTTTCNNNNNNNAGATATAAACACATGCAGCC
Long Flanking Sequence:
CTCAGTTTTAATATGAAATGTTGCATGTATTGAAAAACAATAACACAAATAAATACATAAATAAATAAATAAATAAATATGTGAATGTAAAAAATAGCTTAAATTTTTTTAGCATAGTATCAATAATATTTCTATATCAAATAAAACTATATATATATATATAGTTTTTTCAATTTTTTTCAATCATTTTTATATATATATATATATATATATATAAATCAAAATTATGATTGAAAAAAATTATTTTAGATTTAAAAAAATAACATTTCAAGGCTTCTTTCATTTTTTTTACGTTAAATAAGCCAAGTGAGACCCCTTTCTTTAAATGATGCTTTTTAATTACATTTTTACCAGACATTTTTACTCACATGTTTCAAATGTTTGTCAGATTTGATTATTCTGAATTTTAATGTCGTTCATGTGTTTAGATTGTGGAAGCTGTTTATGAGCCACTAGAAGACAAAACCTTCTCCGAAAGAGTAACCGACATGATTAAATGG[T/A]AGGATTCCCTGAAAACTGCTTTCTGCTTTCAGATATAAACACATGCAGCCTGGATACAGATATGAGATTGTTGTAGAAATGTAAAATCTTGAAAATGACACACAATTTCATATGTTTTTTTTATTTATTTTATTTTAATTAAATGAAGAGAAATTATGATCTGAAAGTGATGCAACAGATGTATTATTTTACCAGCATTGTTATTATTATTCTTATTATAAGAAAAGCCTTTGTGTTATAAATTATATTTAAAGAAAAATGTGTATCAAATGTCCTTTGTGCTGCCAGCCATTGGAATTTAAATACTGAGTTTTAAGTATGAATAGGGTTTAATTAAGTTTTTGATTTATGTGATAACATTGAATGTATTTGTGTTGCCTGTTTTCTGTGAAATGTGTGATGTGAACGCTGCTGTGGTTGTGTGGTGAAGCCAAAAATAAATTTAAAGTAAAGTAAAAAATATTTATAATTCTATTCTTCATCCCAAGTACAACTAATGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6449
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
ENSDART00000029001 None None 1099 None 40
ENSDART00000123061 Nonsense 825 1150 26 41
Genomic Location (Zv9):
Chromosome 16 (position 53650751)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 49920412
GRCz11 16 50124732
KASP Assay ID:
554-4639.1 (used for ordering genotyping assays)
KASP Sequence:
AGAAGTACTTYCTGGAGAGCAACAGGACTAGAATGTGTGGCCCGATACAA[C/T]AGGTTTGAAAATTCTCKACTTCTGAATGAAGCARAAAKGATTTATTAAAA
Long Flanking Sequence:
CAGAACAAACCACTGTTATACAGTGACTTGCCTAATTACCCTAGTTCAGCCTTTAAATGTCACTTTAAGCTGAATATTAATGTCTTCAAAAACATCCAGTCAAATATTTTGTGCTGTCATCATAGCAAAGAGAAAAGAAATCAGTTATTAGAAATGAGTTATTAAAACTATTATGTTTAGAAATGTGTCGAAAAAATCAGCTCTCCATTAAACACACATTAGGGAAGGAACATACTGGGGCGCTAATAATTCTGACTTCAACTCTACGTATATATGCTTTATATGTTGTCTTTTTTTTGTTCAGGTGTTTGACTCCAAATGCAGACGTCCGTCCAGACATCATCGAGGTCAGTTCCAGAATCTCTGATATCATGATGAGGTTTGTGGATAGTCTCTGTGTATCCCATAATGCACTGGAGAGAAGGGCGGAGCGAGACAGGAAGAGAGCGCAGAAGTACTTTCTGGAGAGCAACAGGACTAGAATGTGTGGCCCGATACAA[C/T]AGGTTTGAAAATTCTCTACTTCTGAATGAAGCAGAAATGATTTATTAAAACTATAATGTTTAAAAATGTGTTGAAAAAAATATTATCTCCATTAAACAGCACTTGCAAAATATATATATATATAAAATAATAGTAACATATTACTTATTCAATCCCAGAAAATATCTTACATTAACATTTACAGTTACATTTTCTGATACTTGCTCATACCTATCGTAGTTCTTGCTTAAATATGAACATGTTTACTCATCTCATTCATTCATTGATTTTCCTGCGGCTTAGTCTCTGATTTATTAGGGGTCACCACAGCGGAATGAACCGCCAACTATTCCAGCATATGTTTGACACATCGGATGCTCTTCCAGCCACAGCCCAGTATTGGGAAACACGTATACACTCTCGCATTCACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36262
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
ENSDART00000029001 Essential Splice Site 855 1099 29 40
ENSDART00000123061 Essential Splice Site 928 1150 30 41
Genomic Location (Zv9):
Chromosome 16 (position 53648439)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 49918100
GRCz11 16 50122420
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACGTCCACATCAGTTTTAGTAGTTGGAGGAGAACAAAAGCAGAGTCAAG[G/A]TAACAACTTACACCTGATACATGCAATCTTAATAAATCACAATCTAAACA
Long Flanking Sequence:
TGTAAATAGGCATTACTTTCCTTTAAAAAGTACCATTTTTAGTTTATTTTTATTAAGAAGTAAAACATATGCTAGAAGAGTTGGTGGTTCAATCTGCTGTGGCGACCCCGGAAAAATAAGGGACTAAGCTGAAGGAGAATTAATGAATGAATGAGAAAAAAAAACTATAAGAGTACAGTTAAAGTACTGAACCGATAAGTGGTATCGATAAAAGTTTTAATACTGTTAAAACCTTAATGACACCCATCCCTAGAAGTAACACAAGATTTAATATATTACTTTTAAAAGTAACTTTTCCCAACACTGATTCAGTGTACCTGTTTATTCTTTGAGAAATAAACCTGTTTGCTACAAAATGATTCTGTCTGGACATTCATGTGTGTGTATTGTTTTTTTGATTCAGGGATTAAGCTTGAAAAATCAAGATGAATCACAGTCTGAGAGCTTTGAAACGTCCACATCAGTTTTAGTAGTTGGAGGAGAACAAAAGCAGAGTCAAG[G/A]TAACAACTTACACCTGATACATGCAATCTTAATAAATCACAATCTAAACATTTACTTTAACAGTGAATAGAGGCATCAAAGTACAGTTGAAGTCAGGATTATTAGCCCCCCTGTTTTTCCCCCCAATTTCTGTTTAACGGAGAGATTTTTTTCAACACATTTCTAAACATATTAGTTTTAAAAACTCATTTCTAATAACTGATTTATTTTATCTTTGCCATGATGACAGCACATTATATTTGACTAGATATTCTTCAAGACACTTCTATACAGCTTAAAGTCACATTTAAAGGCTTAACTAGGTTAAGTTAACTAGGCAGGTTAGTGTAATTAGGCAAGTTATTGTACATTGATGATTTGATCTGTAGACTATTAAAAAAAAACATATAGCTTATAGGGGCTAATAATATTGACCTTAAAATGGTTTTTAAAAAATTAAAAACTGCTTTTATTCCAGCTGAAATAAAACAAATAAGACTTTCTCCAAAGCAAAAAAATAA
Associated Phenotype:
Not determined