Busch Lab

ZMP

CIT

Ensembl ID:
ENSDARG00000089856
Description:
citron (rho-interacting, serine/threonine kinase 21) [Source:HGNC Symbol;Acc:1985]
Human Orthologue:
CIT
Human Description:
citron (rho-interacting, serine/threonine kinase 21) [Source:HGNC Symbol;Acc:1985]
Mouse Orthologue:
Cit
Mouse Description:
citron Gene [Source:MGI Symbol;Acc:MGI:105313]

Alleles

There are 9 alleles of this gene:

Allele Name Consequence Status Availability
sa26387 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa12291 Nonsense Available for shipment Available now
sa33521 Nonsense Mutation detected in F1 DNA Not yet available
sa26386 Nonsense Mutation detected in F1 DNA Not yet available
sa38447 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa26385 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa12822 Nonsense Available for shipment Available now
sa10643 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa26387
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
ENSDART00000122274 Essential Splice Site 81 1989 2 46
Genomic Location (Zv9):
Chromosome 5 (position 2746755)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 2362898
GRCz11 5 2633108
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACCAGAGCTCATGAAGATCAAACATGTGGCCAACTTTGTTAATAAATG[T/C]AAGTCACACATTCCACAGTTGTGGACACATTTCAACTATTTTCCATTCAT
Long Flanking Sequence:
TATATATATATATATATATATATATATATATATATATATATATTTTTTTTTTTTTAATTTTTTAATTTTTTTTTAATTTGATAATCTACAGAACAAACCAACGTTATACAATAACATTCCTAATTACCCTAACCTGCCTAGTTAACCTAATTACCCTAGTTAAGCCTTTAAATGTCACTTTAAGCTGTTTAGAAGTGCTGTATAGTACTGTTGTTTGTGTAGTAACTGCATTTTATGGAGTGATTATTGCGTTGCTGTAACCTGTAGTCTGATTGCATTTGTTCCATGTATTCATTAATGTGGATAAAGTGAATGTTTGCAGTGATTTTCACTTTTTTGTATTTTGTGTTTCACCAGGGGAAGTGCAGTATGTCTGGTTTTACAGGAGTGAATGCACTGAGCAGAGAGGGACTGATTGATGCTCTGCTGCTGCTCTTTCAAGAGTGTTCAACACCAGAGCTCATGAAGATCAAACATGTGGCCAACTTTGTTAATAAATG[T/C]AAGTCACACATTCCACAGTTGTGGACACATTTCAACTATTTTCCATTCATTTTACATAAACAGGAATGATATACATAACAGATGTGTAAAATACAGTCAAATCAATTCAATATTACTGTAAAAAGACATTTAAAACGCTTAAATATGACAGGGAGCATTGATTCTGTTACTTATTGCTGACTTTTATGTTTAACAGAGCAAGAAAATTTTCACAGTATGTCTGATAATATTTTTTCTTCTGGAGAAAGTCTTTTTTGTTTTATTTCTACTAGAATAAAAGCAGTTTTAAAATTTTTAAACACCATTTTTGTGTGTGTGTCAGATTCTGAAGTGGTGGCTGAAGTTCAGGAGCTTCTCCCTGGAAAGAAGGATTTTGAGGTGAGGGGAATTGTGGGAAGAGGACAGTTCTCCGAGGTGCAGGTGGTGAAGGAGAGAGCCACAGGAGACGTGTACGCCATGAAGATCATGGACAAAAACAGCCTGCGCTCTCACCACAATGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12291
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
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Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000122274 Nonsense 423 1989 9 46
Genomic Location (Zv9):
Chromosome 5 (position 2684944)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 2301087
GRCz11 5 2571297
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGCACCCTCGCTCAGGCTTCCACGGCCGAGACCTGCCCTTTGTAGGGYG[G/A]TGCTTCAGTCGGGCCCTCACAGCACTGGCCAAGTCTGAGTGAGTACACAC
Long Flanking Sequence:
TGCCNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTAGCTCTCCCTTAAAAAATCTCTCTCTCTCTCCTTTAATATTCAAAATTCTCTCTCTCTCTTTCTTCCTCATTCTCTCTCCCTCTATCTTTCTCCCACAATATCTCTCTCTCTCCCTCATTCTCTCTCTCTTTCTCCTCTAGTCTGTTTTCCTCTGCGAGCCGCTCACACGTTGTTTTCTCCTGTGGTCTCCTCCAGCGCTCCCTCCGTTTGTTCCGTCTCTGCGTTCTGAAGATGACGCCTGTAATTTCGAGGCTCCGGAGCGACCCCCCCGCCCCGCCACCGCCGCTGCCCAGCCAGAGCACCCTCGCTCAGGCTTCCACGGCCGAGACCTGCCCTTTGTAGGGTG[G/A]TGCTTCAGTCGGGCCCTCACAGCACTGGCCAAGTCTGAGTGAGTACACACACGCACACACACACACACACACACACATACACACACACGCATGCTTGTTTTACTAGTCTAGTCACAGGTGGTCCATTGGTGCGGAGACGGCCGCATCACCACGGCGACTGTCACCAGGCAACATTGTGGCTGAATGCGAGGTATTGCTGCGGTTCTCTTGTGCGCATCGTTTCACGTGCCTTTAAGATGAATGAGTATGTGTGTGTGTGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGCGTGTGCGGATGTTTTTATCTCCGGAGACTCGCGAATCGCACAATATCTCACTGATGTGTTGTCATGTGCATGCAGGAGGAACGGGAAACCCTCGTCTGGCGTGTGTGTGTGTGAGCACAATGAGATCCTCTTCATGTAAACAGTGTGATGTGTTTGCTGAGATGCGGTCTGCGTTTAGAGATTGTTGTTGGTGTTTATTGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33521
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
ENSDART00000122274 Nonsense 731 1989 17 46
Genomic Location (Zv9):
Chromosome 5 (position 2609192)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 2225335
GRCz11 5 2495545
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTGGAGCGGCGAGAGAATAAACTGAAGGACGACATCCAGACCAAATCC[C/T]AGCAGATCCAACAGATGGCTGAAAAGATACTGGTGAGAGAGAGAGACGGA
Long Flanking Sequence:
TTCAGCAATATTAGTATTGGATTGTCTCCAGAACAAACCACTGTTATACAATGACTTGCCTAATCACCCTAACTGTACCCTAATTACCCTAGTGAAGCCTTTAAATGTCACTTTAAGCTGAATACTAGTGTCTTGAAGAATATCTAGTCTAATATTATGTGCTGTCAACATGGCAAAGAGAAAGAAATCAGTTACTAGAAATGACTAGAAACTAGTGTGACTAGAAATGTGTCTCTGTTAAACAGAAATTGTGGGAGAAATACACAGGGAGGCTAATAATTAAATTAAAGACTTAATTTACCACACTTGTGAATTGCAGAAGATTACTGAAAATGCAGCTGTATTTAACTTTGACCCCTGTGGTAAACACTGGTATTTTAGCTCTTAAATATGTTTCTGATGTCCAGGATGGCAGAAAGACTCTGGAAAACCAGGTGAAGCGTCTGGAGATGGTGGAGCGGCGAGAGAATAAACTGAAGGACGACATCCAGACCAAATCC[C/T]AGCAGATCCAACAGATGGCTGAAAAGATACTGGTGAGAGAGAGAGACGGATCAGACTAGCAAAGATTAAACCACTAACACGCCTCCTTAACCAGCTGACCTACAACACACACACACACACACACACACACACACACACACACTCCTAAGTCTGTGTTTGCACTGTCATCTCAGTTTCTTGCAGATTAGCATATGACAACACACACACACACACACACATGTCCCATCTGCTGCCACACACACCGCTTCATGCAGTCTCCTTAAGCAGCTCTCAGCTTCTCAAAGCATTTATACTGTGTGTATTGCTGGTGTGTGTGTGTGTATGCCTGCATGGTGTGTTTAGGAGCTGGAGGAAAACTTACGTGAGACTCAGGCTACAGCGCAGAGGATGGAAGCACATCTAGTCCAGAAAGAGCGACTCTATGAGGACAAAATCAAGGTAGAGTTCAGAATAGTGTGTAAATCAGTCCATTAGATGACACTTTTGATGAGGTATTGCTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa26386
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
ENSDART00000122274 Nonsense 892 1989 21 46
Genomic Location (Zv9):
Chromosome 5 (position 2593913)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 2210056
GRCz11 5 2480266
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCAGAACGCCAAACTGGAGGAGCATCTGGAGAAGATGAGCCAGCAGGAG[C/T]AAACCAGAAAGAGCCGCATCATGGAGCTGGAGACCCGGCTCAGAGAGGTC
Long Flanking Sequence:
CTGTAAACTAAACACCCCCGGGTTGCCAACTTTAGTTCAGTACCCGATCAAATCGGCCGCCCAAAACCTACTGCATCCTGTTCTCAACCTCACCCCCGAACACCCTCTCCCCCTGGTCTCCCGGGTTTTCAGAAACGTCGGCAGGTTAGATGATCTCTCTCTCTATTGTAAGTTGTAGTGCTGTATTTATACCGATTTGCTCGCATATCAGGAATGTGTGTTGTGTTGGCAGATTGAAAGAAGCAAAGTCTGCATGTCTTTAGCGTTTTCCCTTATCGCAAACACAACAGCAGTCTGGTAACGTTAGTGGATTCGTTGTAATTTTGGGGTTAATTATTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGTGTCAGGAAAGCTCAGGAGGAGATGATCTCAGAGCTTCGGCAGCAGAAGTTTTATCTGGAGTCGCAGGCGGGTAAACTAGAAGCGCAGAACGCCAAACTGGAGGAGCATCTGGAGAAGATGAGCCAGCAGGAG[C/T]AAACCAGAAAGAGCCGCATCATGGAGCTGGAGACCCGGCTCAGAGAGGTCAGAGACGCGGCGTTTCTCCTTCATTTACAATTAAGCTTAAGCGAGTGTTTAATTCAGGATCCTGATCTTTTAGTGATTACAATTGTGCAGCTTTACACTGTGAATGAATGCAGGCTAAACAAGCAGATGTGACAGAAAACTTGTTTAATAACCTTGGAGAGACATGCATTTAGGTGCCACCACAATTTGTTTTGTGATTGTTATGTTACAGGGAGGCTGAAATGCTCCATACATGTGATTTTGAATAAATCGGGAGGTTTTCCCTGTTCTTCTGTTCCTCTACTAGTGGTTCTGACTGGTTGTGCACCATTCATGTGAACACTACTTCCCTGTAATTAATTACTTAAAACAGGATTGTCTTTTTCACTGCAATAGTTATTACTAATTTAGGATTAATATACAAGTTTAAAAACATGGTTGATGAATACAAGTAGAGCAACATGATTCCTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38447
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000122274 Essential Splice Site 1058 1989 25 46
Genomic Location (Zv9):
Chromosome 5 (position 2578535)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 2194678
GRCz11 5 2464888
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCGTGTGCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCA[G/T]AACATCGAGACCCTGAAGACCACCTGCAGCATGCTGGAGGAGCAGGTGGT
Long Flanking Sequence:
CCTGGGATTTTTAATAACCACAGAGAGTCGGAACCTCGGTTTAACATCTCATCTGAACGACGGCGCTCAGTGAGCAGTATAGAGTCCCCATCACTATACTGGGGCATTAGGACCCACACAGACTACATGTCAAGTTCTGGAGCTCATTAAATATGTAATACTGAAATGGGTAAGGCGTTTTAGAATGACCAAAACAACAGTTCAGATGTTTTACAGTGTTCAGCCTGCTGGTTTGACCATTCACACAGATCACATGATCTCTAATAAGTTTCTCCTACTCGGTTATACGCATCTGTTTTTTATGCGCATCTTGGCATTTCCATCAACAGGTTTTTATATGCATATCCAAACTGCACAGAAAAATAGTTGGATGGAAACTTAGCTTGTGTGTGTGTGTGTGTGCGTGTGCGTGTGCGTGTGCGTGCGCGTGCGTGTGCGTGCGCGTGCGTGTGCGTGTGCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCA[G/T]AACATCGAGACCCTGAAGACCACCTGCAGCATGCTGGAGGAGCAGGTGGTGGAGCTGGAGAGTCTGAACGATGAGCTGCTGGAGAAGGAGAGGCAGTGGGAGAACTGGAGATCTGCTCTGGAGGACGAGAAGAGCCAGGCGGAGCGCAGAACCAGAGACATGCAGAGACTGCTGGACAATGAGAAGCAGAACCGGTAACTCGTATATCCATCATTCACACAATGAGAAGCAGAACCGGTAACTCGTATATCCATCATTCACACAATGAGAAGCAGAACCGGTAACTCGTATATCCATCATTCACACAATGAGAAGTAGAATGGTTACTTGTGCAGTTGAAGTCAAAATTATTCGCCCCCCCTTTGATTTTTTTTTTTTATATTTACCAAATGATGTTTAACAGATTGAGGAAATGTTCACAGTATGTCTGATAATATTTTTTCTTCTGGAGAAAGTCTTATTTGTTTTATTCCGGCTAAAATAAAAGCAGTTTTTAATTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa26385
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
ENSDART00000122274 Essential Splice Site 1122 1989 25 46
Genomic Location (Zv9):
Chromosome 5 (position 2578339)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 2194482
GRCz11 5 2464692
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGAACCAGAGACATGCAGAGACTGCTGGACAATGAGAAGCAGAACCGG[T/C]AACTCGTATATCCATCATTCACACAATGAGAAGCAGAACCGGTAACTCGT
Long Flanking Sequence:
ACAGTTCAGATGTTTTACAGTGTTCAGCCTGCTGGTTTGACCATTCACACAGATCACATGATCTCTAATAAGTTTCTCCTACTCGGTTATACGCATCTGTTTTTTATGCGCATCTTGGCATTTCCATCAACAGGTTTTTATATGCATATCCAAACTGCACAGAAAAATAGTTGGATGGAAACTTAGCTTGTGTGTGTGTGTGTGTGCGTGTGCGTGTGCGTGTGCGTGCGCGTGCGTGTGCGTGCGCGTGCGTGTGCGTGTGCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCAGAACATCGAGACCCTGAAGACCACCTGCAGCATGCTGGAGGAGCAGGTGGTGGAGCTGGAGAGTCTGAACGATGAGCTGCTGGAGAAGGAGAGGCAGTGGGAGAACTGGAGATCTGCTCTGGAGGACGAGAAGAGCCAGGCGGAGCGCAGAACCAGAGACATGCAGAGACTGCTGGACAATGAGAAGCAGAACCGG[T/C]AACTCGTATATCCATCATTCACACAATGAGAAGCAGAACCGGTAACTCGTATATCCATCATTCACACAATGAGAAGCAGAACCGGTAACTCGTATATCCATCATTCACACAATGAGAAGTAGAATGGTTACTTGTGCAGTTGAAGTCAAAATTATTCGCCCCCCCTTTGATTTTTTTTTTTTATATTTACCAAATGATGTTTAACAGATTGAGGAAATGTTCACAGTATGTCTGATAATATTTTTTCTTCTGGAGAAAGTCTTATTTGTTTTATTCCGGCTAAAATAAAAGCAGTTTTTAATTTTTTAAAAGCCATTTTAAGGTCAATATTATTAGCCCTTCAAGCTATTTTTTTTTGATAGTCTCCAGAACAAACCATCATTATACAATAACTTGCCTAATTACTCTAACTTTACCCTAATTACCCTAGTGAAGCCTTTAAATGTCACTTTAAGCTGTATAGAAGTGTCTTGAAGAATATCTAGTCTAATATTATTTAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12822
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
ENSDART00000122274 Nonsense 1152 1989 26 46
ENSDART00000122274 Nonsense 1152 1989 26 46
Genomic Location (Zv9):
Chromosome 5 (position 2577247)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 2193390
GRCz11 5 2463600
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGGTTGAGCTGGCGGTTCGGGAACACAAAGCTGAGATCGTGGCTTTGCAG[C/T]AGGCCCTGAAAGAGCAGAGACTGAAGGCAGAGAGTCTGTCTGACACTGTG
Long Flanking Sequence:
TGTTAAACAGAAATTGGGGGAAAAATAAACAGGGAGGCTAATAATTCAGGGGGGCTAATAATTCTGACTTCAACTGTATATCCATCATTCACACAACGAGAAGCAGAGCCGGTAACACCATATCCATCATTCACACCACAGTGTCACTAGACAAGTTCAAGTTTATTTTGTTGTCAATCTGCCACATGTGTAAACATACAGTGGAAATTAAATGTGATGTCTCGCAAATCCTCGGCGCTACATAAATACTGCGATATTGATGCTTAAATGATATATTGTTCAGCCCTAAAGCAAACTAAAACCAAACTGAGATTTAGAGGAAATTTGTGAATTGTTAGCTATTAATAAATCTGGAATAACCTTGTGACCAACCTCCAAAATAGTATATTTGCTGTAATTGTGTCTTGTTCAGGTTGCGAGCAGACCAGCGCAGCACTGAGTCTCGGCAGGCGGTTGAGCTGGCGGTTCGGGAACACAAAGCTGAGATCGTGGCTTTGCAG[C/T]AGGCCCTGAAAGAGCAGAGACTGAAGGCAGAGAGTCTGTCTGACACTGTGAGTTACACACACACACACACACACACACACACACACACACACACACACACACCACAACTGCACGTTCACTCCACCTCCCCATATTTATATTCCTGCTCTAATTATGAATAAGCAGAACTGTTATACACAGTTGAAGTCAAATGTTTACGATTTTTTCTTCTTGTAATATTTCCCAAACGTTGTTGAATATCATCAGGAATTGTTCACAGTGTTTCCTCTAATGTTTTTCCCTGTGGAGAAAGCCTTATTTGTTTTATTTTGACTAAAATGAAAGCAGTTTTACATTGGATTAAACCCATTTTAAGCTCAATATTATTAGCCCCCTTTAGCAATATTAGTTTTCGATAATCTCCAGAACAAACCACTGTTATAGAATGACTTACCTATTACCCTAACTTTACCCTAATTACCCTAGTGAAGCCTTTAAATGTCACTTTAAGCTGAATACTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10643
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
ENSDART00000122274 Nonsense 1152 1989 26 46
ENSDART00000122274 Nonsense 1152 1989 26 46
Genomic Location (Zv9):
Chromosome 5 (position 2577247)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 2193390
GRCz11 5 2463600
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGGTTGAGCTGGCGGTTCGGGAACACAAAGCTGAGATCGTGGCTTTGCAG[C/T]AGGCCCTGAAAGAGCAGAGACTGAAGGCAGAGAGTCTGTCTGACACTGTG
Long Flanking Sequence:
TGTTAAACAGAAATTGGGGGAAAAATAAACAGGGAGGCTAATAATTCAGGGGGGCTAATAATTCTGACTTCAACTGTATATCCATCATTCACACAACGAGAAGCAGAGCCGGTAACACCATATCCATCATTCACACCACAGTGTCACTAGACAAGTTCAAGTTTATTTTGTTGTCAATCTGCCACATGTGTAAACATACAGTGGAAATTAAATGTGATGTCTCGCAAATCCTCGGCGCTACATAAATACTGCGATATTGATGCTTAAATGATATATTGTTCAGCCCTAAAGCAAACTAAAACCAAACTGAGATTTAGAGGAAATTTGTGAATTGTTAGCTATTAATAAATCTGGAATAACCTTGTGACCAACCTCCAAAATAGTATATTTGCTGTAATTGTGTCTTGTTCAGGTTGCGAGCAGACCAGCGCAGCACTGAGTCTCGGCAGGCGGTTGAGCTGGCGGTTCGGGAACACAAAGCTGAGATCGTGGCTTTGCAG[C/T]AGGCCCTGAAAGAGCAGAGACTGAAGGCAGAGAGTCTGTCTGACACTGTGAGTTACACACACACACACACACACACACACACACACACACACACACACACACCACAACTGCACGTTCACTCCACCTCCCCATATTTATATTCCTGCTCTAATTATGAATAAGCAGAACTGTTATACACAGTTGAAGTCAAATGTTTACGATTTTTTCTTCTTGTAATATTTCCCAAACGTTGTTGAATATCATCAGGAATTGTTCACAGTGTTTCCTCTAATGTTTTTCCCTGTGGAGAAAGCCTTATTTGTTTTATTTTGACTAAAATGAAAGCAGTTTTACATTGGATTAAACCCATTTTAAGCTCAATATTATTAGCCCCCTTTAGCAATATTAGTTTTCGATAATCTCCAGAACAAACCACTGTTATAGAATGACTTACCTATTACCCTAACTTTACCCTAATTACCCTAGTGAAGCCTTTAAATGTCACTTTAAGCTGAATACTA
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa5276
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000122274 Nonsense 1791 1989 41 46
Genomic Location (Zv9):
Chromosome 5 (position 2533817)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 2149960
GRCz11 5 2420170
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTTAATGTGTGTGTGTGTGTGTGTGTGTGTGCAGGAGATCGAGACGTCT[G/T]AACCCTGCAGCTGYATTCACTTCACCGGATACAGTATCATCATCGGCACC
Long Flanking Sequence:
AAATATTGCTATTAACTAATTTCTTAAGTTAAGAAATATTCTGCAAAATGTATTTGTGTAACAAAAATAAATACAATTCCTCTGCTTCTCTACATTTATTCATACACAACTGTTGAATTTATTTGCAGCATTTAAGGCAAAGTCATTAATAAGCAACTAATTCAACTGCCTAAAAAAGAACAGTAATGGAAGTGATTTAACTACTGTAACTACCTGTAAATAAATACACCCAACAATGATCATGACATCACTGTAGAGGATCATAAAGCTGTTGTTTAACTGAATGAAGTGTGTGTTTCAGATCGACACAGGCATGTGTATCTGTGCTGCGATGCCCAATAAAATCACCATCCTGCGCTTCAATGACACACTCAACAAGTTCTGCATCAGAAAGGTGAAGTACAGTATAAAACACCTCTTCCTGCACGCCAGAGATTAGTGATTATCATCTGTTAATGTGTGTGTGTGTGTGTGTGTGTGTGCAGGAGATCGAGACGTCT[G/T]AACCCTGCAGCTGCATTCACTTCACCGGATACAGTATCATCATCGGCACCAACAAGTTCTATGAGATCGAGATGAAGCAGTACGTGCTGGAAGGTGAGAGGATCCATACTGGTGCTGGAGTGCTAGAAACACTGTTTCTGACATCATAAGAGTGCATTAAACCGCAGACGGCGCTCTAGGCGGGTGTTAACAGTAGATGGCGCTCTATGCTAGTGTATAACAGTAGATGGCGCTCTAGGCTAGTGTATAATAGTAGTTGGCGCTCTATGCTAGTGTATAACAGTAGATGGCGCTCTAGGCTAGTTTATAACAGTAGATGGCGCTCTAGGCTAGTTTATAACAATAGATGGCGCTCTAGGCTAGTTTATAACAGTAGATGGCGCTCTAGGCTAGTTTATAACAGTAGATGGCGCTCTAGGCTAGTTTATAACAGTAGATGGCGCTCTAGGCTTGTTTATGACAGTAGATGGCGCTCTAGGCTAGTTTATAACAGTAGATGG
Associated Phenotype:
Not determined