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