ZMP
KIF21A (2 of 2)
Ensembl ID:
Description:
kinesin family member 21A [Source:HGNC Symbol;Acc:19349]
Human Orthologue:
KIF21A
Human Description:
kinesin family member 21A [Source:HGNC Symbol;Acc:19349]
Mouse Orthologue:
Kif21a
Mouse Description:
kinesin family member 21A Gene [Source:MGI Symbol;Acc:MGI:109188]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24729 | Nonsense | Available for shipment | Available now |
sa30310 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa39494 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa1024 | Nonsense | Available for shipment | Available now |
sa44352 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa14802 | Essential Splice Site | Available for shipment | Available now |
sa44353 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa44354 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa24729
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 |
---|---|---|---|---|---|
ENSDART00000004087 | Nonsense | 66 | 1647 | 1 | 39 |
Genomic Location (Zv9):
Chromosome 25 (position 36796530)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 35204146 |
GRCz11 | 25 | 35709085 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTACTCCAACTGCACCGAGAAGCTGATCGAGGGCTGTTTTGAGGGATA[C/A]AACGCCACCATATTTGCATACGGACAGGTTTGTGTGGGATTTGTACTTTA
Long Flanking Sequence:
GATTCCTACTTGTCTTCCTCGTGATGAAGAGTAGGCAAAATCTAAGTGCGGACGGGCTCCTGGGCCTGTGCCCATAATGCCCACTGGTTAATCTGGCCCTGATTACACCCATACTTTAGATGCTCGCTAGGCATTCAATGTTGGTCATCTGACGCCACAACCTAAATCTATATATTTAATCCAAGGTAATCATACAGTCAGAATCTTTTACCGGCTCATACCTATTTTCAACACATCAGGAGCCTCTGGTTGTGAATTCATCATACCTTCATGTTTAATCATATTCTCTCATCTCTGTGTTTCAGGATTCGTCCTCAGCTGGCGAAGGAGAAGATCGAGGGATGCCACATCTGCACGTTTGTGATGCCCGACGAACCGCAGGTGGTTCTGGGAAAAGATAAAGCCTTCACGTATGATTATGTGTTCGATATGGACTCCACGCAGGACAACATCTACTCCAACTGCACCGAGAAGCTGATCGAGGGCTGTTTTGAGGGATA[C/A]AACGCCACCATATTTGCATACGGACAGGTTTGTGTGGGATTTGTACTTTAAAGGAGACATTTAAAAGAGATTATTTATGCTGAGCACTGTGTGTATGTATGTATGTATGTATGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTTTTTTTTTTTTATTTATTTATGTGTATGTGTGTGAATATATATATATATCTGCTGTTTATGTATTGTCCTAAATGTGAGGGGTATTGATATATCCAGGGATTTCTGATGGCAGGTTGCAGGTTTGGATTGGGCCTGGTTTATTTCTGCATGTGTGTTTCATGTCGTCTCTCGGATCTGTGACCAGTGCAGCATCTGACCTGCATTTCATGGCTGATTTCCTCCGAACAGCAGCTCTGATGTGTGGGTTAATCCCGATTTATCAACATTCCCGCTCGTCTGCCAGACACGCACTGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30310
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000004087 | Essential Splice Site | 326 | 1647 | 6 | 39 |
Genomic Location (Zv9):
Chromosome 25 (position 36804669)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 35212285 |
GRCz11 | 25 | 35717224 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGACTCCAAACTCACCCGCCTCCTGCAGGACTCACTGGGCGGAAACAGG[T/A]CTGTGTCTCAATACCTGCTGGATTCTCTCATTGCTTTCATTACCGCCATT
Long Flanking Sequence:
ACACCACAGGGGCTTCTCCAAACACACTTACCAACATTTCTCTGTCTGATATTTGCTCCAGTTAATCAGGAAGGGACCATTCTGTTCTCTCTTGCTCATCGGATGGAGATGCTACTTTTATTGGCAAATCTTGTATGCAATATTCCAGTTGTGTGCATGAATTGAATTCACATCTTTGAATAGATACACAGCTCATGATGAAAACATATCTCACGCAGGAAAATCACCGATTATGTCGAGCACGCACCATATGTCAGTCTTCATCATTTGTTTTGCACTCGTCACTTTAGGGCTTCTGTGCTATGGAAAAATGTTCTTTGGGATAAATAAAGATTCTTCTTGTCTTACTGTGCGGTGAATATAAGTGTTTGTGTGTGCTGTAGTTGGCGTTGGGGAACGTGATCAGTGCTCTAGGGGACAGAAGCAAGCGCTCGACGCATGTGCCTTACCGAGACTCCAAACTCACCCGCCTCCTGCAGGACTCACTGGGCGGAAACAGG[T/A]CTGTGTCTCAATACCTGCTGGATTCTCTCATTGCTTTCATTACCGCCATTTTCTTCCCAATCACACACAGCTTGAGCTTGTTTTTCACAACTGCATCATTGTTCGATGTGATGCATGCATGACTGTTGTGTTCTGTTGTATCCCTGCTGAAAAAACAGCTTAAACCAGCTTAGGCGAGCACTTCTTGTGTTATCCGTAAGTAGATCCCGGAGAGCCTCTTTTAACTCTGCTTTTTACAAGACCTTTATAAGATGTCACACAGGCAGAGCAGACGTGTCCCACATGTTTTGGTCGTGCCCCAAGCGTACTCCTTACTGGTCAACCATATTCAATACATTGTCTAAAGTGTGTGAAGTACAGCTAATGCCTAGTTCAGACTGCGTGATTTTAGCCCCGGTTTTGGCTCGCCGACAGGTTTTGAGAAATCGCCGACAAATGCCTGAAATCACAGGCAAATCGCTGCTCGTGCATGCGAGTGACAATCACACAGTATGAACGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39494
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000004087 | Essential Splice Site | 556 | 1647 | 12 | 39 |
Genomic Location (Zv9):
Chromosome 25 (position 36815251)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 35222867 |
GRCz11 | 25 | 35727806 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATATTTAAAACAGAGATTTTTGAACACTACACACAATAGATTTTTGATTT[A/T]GCATTATTCTCTTGCAGTGCCAACAAAGACGAAACGCAAGAAGATGGAGA
Long Flanking Sequence:
CCACCAAACTGTCGTAAAAGCACACGTCTAGTCTGAGCTCCTCCCCAGGAGAATTGTCAGTCTATAGCGATCGCTGATTGGCACCTGTACTAGAAGGCGGGGCTTCATTCGACATATTTACTAGTGACACGTCTAGTGTATTCTATAGGCTTTGGTTCACTGTAGTTAATACAGTATACTGGGGCATTCATTAATAAAGAGTTGTCCATACTATAATACATACAGTACAGTACAGTTAGTATGGTACAAATACACTAGTGTTTACAATATAATAGTACAGTATTTTTGTTCAATTGGGCAGATCATGATCTAATCTAAAGCACAGTATTAAAAATTGCAAGATATTTCAATAAATAGATGTCAGTTAAAAAAAGTCCAGTGGTTCATCATATCTGTCATAACATCATCTTTCCTTCATAATTTTCTTTTTTTTCTGATAATCCATGCTGCATATTTAAAACAGAGATTTTTGAACACTACACACAATAGATTTTTGATTT[A/T]GCATTATTCTCTTGCAGTGCCAACAAAGACGAAACGCAAGAAGATGGAGAGCAGAAGACTGAGAAAGAGCAGTCAGAATCGACCAATCAGGAGCCAGAGATGGTATGACTGACAGCCGGCTCACTCAATCAGAACACAGCTTGATGGATCTGTCTTTGATGTGTGACATTTTTTGCTCAGGAGGCCAGTGATCGTGAGGAAGGCGATGGAGAAGAAGATGAGGAAGATGTGGAGGAAGAGGAGATGGAGGCTGAGGAGAGCTCTGAAGAGACGGACTCTGAGCTCGATGAGAAGGGTAATAATGCAAAACCAGCACTCTAACTTAAGAGGATTCATTAAATGACTGACCGATGTTGAAAATGAACCTTTAAGCTACATAGTAAACGTGCTAAACATTCTTTCAAAGCACTATATATGAAATATTAGATAATATAATTACTATAATTAGAAATATAATGCAAAAATCACATTTTTAAGGGCTCTTTAAAACATTAAATCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1024
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 |
---|---|---|---|---|---|
ENSDART00000004087 | Nonsense | 802 | 1647 | 17 | 39 |
Genomic Location (Zv9):
Chromosome 25 (position 36818316)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 35225932 |
GRCz11 | 25 | 35730871 |
KASP Assay ID:
554-0928.1 (used for ordering genotyping assays)
KASP Sequence:
TGTGTGTWTGTTTTCCGTGTGTGCAGCATCAGCTCAAACTGCTGGAGGCA[C/T]AGAAGAGACAACAGGAGCTCATCCTGCGCAGGAAAACCGAGGAGGTCTAT
Long Flanking Sequence:
AGTCACAGTATGAGAAACAGCTGAAGAAACTACAGCTTGACCTGACAGAGATGAAGAAGACCAAAGTAAGAGACCGAGCACCACTCTACACACACTCTCCATTACAGCAGATGGTCAACAGCACCACCCGGTGGTCAAAACACACATACAAACACACACATGCACAGCTCTGCAAACATAAAAAAGATCTGAAACCAGAGTTTGTGTGTGCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTGTGTTCATGACTGTGTGTTAATGTGTGTGTGTTCAGGTGCGTCTCATGAAGCAGATGAAGGAGCAGCAGGAGAAGAGCAGAATGGCTGAATCCCGCAGAAACAGAGAGATCGCCACGCTCAAGAAGGACCAGCGCAAACAAGAGGTGCATGATGGGAAACAGCAGTGATGCGTGTCTGTGTGTGTGTTTTATGTGTGCGTGACGGTGTGTGTTTGTTTTCCGTGTGTGCAGCATCAGCTCAAACTGCTGGAGGCA[C/T]AGAAGAGACAACAGGAGCTCATCCTGCGCAGGAAAACCGAGGAGGTCTATTATCACACACACTTTTACTGATTTTACTACACTGTATAGACAAACACACTCATTCATTCACTATATAGACAAACACACTCATTCATTCACTATATAGATAAACATTCATTCACTTTATAGATAAACACACTAATTCATACACTATATAGACAAACACACTCATTTCTTAACTACACTATATAAATATATAATATTTATAAACACACTCATACATTCACTATATAAACACACTCATTTAGTCACTATATAGACAAACACACTCATTTATTCACTATATAGACAAACACACTCATTCATGCACTATATAGACAAACACACTCATTTATTCACTATATTGACAAACATACTCGTTTATTCACTATATAGATAGACTCACTCATTCATACACTATATAGATAAACACACTCATACATTCACTATATAAACACACTTTTTCATTTACTACATGGA
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa44352
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 |
---|---|---|---|---|---|
ENSDART00000004087 | Essential Splice Site | 1031 | 1647 | 22 | 39 |
Genomic Location (Zv9):
Chromosome 25 (position 36826100)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 35233716 |
GRCz11 | 25 | 35738655 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGAAGCTCGATTCCTTCTGGACCATTTCATGTCGATGGCCCTCAATAAG[G/A]TCTCCAGCTGACAGTCTCATTATTAATAACGAGCTATGATGTTACCGATA
Long Flanking Sequence:
GCATATTTATCTGACGTTTTCCCAGCTTGTAGTAGTCGATCAAAAAGCGATTTAGTTTCTTATGACTTTACACTAGCAGTGGAATTTACTGTGATGTGACGGGGCTTGATCATAATCCAGGGGCTTGATCAAAAGTCTCTTTCAACAAAAAAATGATCAGAGTCACAGCCAGCATCCCACAAAAAGCACTTCCAGCCTCATTTTGTGCATTTCAAATCGCAAAATCCAAAAAGCCGCACACCGTATATTTTTGACTGCTTTGAATGGAGACATTTTTCCATATTAAAATATTATGGCGGGTCTTGAGATTGAATTACTTACCTGTGTGGGTCCCGGAATAAAAAAACGTTTGGGAATCCCTGATCTATCAGACTTTACTGTTTGTTTTTCTCCTGTAGGAGGAGGGCGATGCTGTCGATGTCTCGGCTGTGATCAGCTCCTGCACTCTGGCCGAAGCTCGATTCCTTCTGGACCATTTCATGTCGATGGCCCTCAATAAG[G/A]TCTCCAGCTGACAGTCTCATTATTAATAACGAGCTATGATGTTACCGATAATCACCGACTTTTAAAGCTATAGCACGTGTGGTGTTCATCCTTCAGGGTCTTCAGGCAGCTCAGAAGGAGTCTCAGATAAAGGTAATGGAGGGACGGCTGAAGCAAACCGAGATCAACAGTGCAACCCAAAACCAGCTGCTCTTCCACATGCTGAAGGAGAAGGCAGAGTTTAACCCGGAGCTGGATGCGTTATTGGGGAACGCTCTTCAAGGTAGGAATACTCCTCCTAGGACGCATGCATTAGATCTTTGATTTGCTCCTGAAACTTAAACAGAGACGCCATCAGTTAGGACTGGGCGATTAATTGAAGAGGACATGAACAATAACTTATGTGTTGCATGTTATCCTCCGAATAGTGCTGTCTTGGATCACACTTATCTTCTAAATTAATTTCCTACTTATTTCTCAAAGAAAATCTTCTCTCAGAATAACGGCGGCCTCTTTGTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14802
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000004087 | Essential Splice Site | 1087 | 1647 | 23 | 39 |
Genomic Location (Zv9):
Chromosome 25 (position 36826364)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 35233980 |
GRCz11 | 25 | 35738919 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCAGAGTTTAACCCGGAGCTGGATGCGTTATTGGGGAACGCTCTTCAAGG[T/C]AGGAATACTCCTYCTAGGACGCATGCATTAGAYCTTTGATTTGCTCCTGA
Long Flanking Sequence:
TGGAGACATTTTTCCATATTAAAATATTATGGCGGGTCTTGAGATTGAATTACTTACCTGTGTGGGTCCCGGAATAAAAAAACGTTTGGGAATCCCTGATCTATCAGACTTTACTGTTTGTTTTTCTCCTGTAGGAGGAGGGCGATGCTGTCGATGTCTCGGCTGTGATCAGCTCCTGCACTCTGGCCGAAGCTCGATTCCTTCTGGACCATTTCATGTCGATGGCCCTCAATAAGGTCTCCAGCTGACAGTCTCATTATTAATAACGAGCTATGATGTTACCGATAATCACCGACTTTTAAAGCTATAGCACGTGTGGTGTTCATCCTTCAGGGTCTTCAGGCAGCTCAGAAGGAGTCTCAGATAAAGGTAATGGAGGGACGGCTGAAGCAAACCGAGATCAACAGTGCAACCCAAAACCAGCTGCTCTTCCACATGCTGAAGGAGAAGGCAGAGTTTAACCCGGAGCTGGATGCGTTATTGGGGAACGCTCTTCAAGG[T/C]AGGAATACTCCTCCTAGGACGCATGCATTAGATCTTTGATTTGCTCCTGAAACTTAAACAGAGACGCCATCAGTTAGGACTGGGCGATTAATTGAAGAGGACATGAACAATAACTTATGTGTTGCATGTTATCCTCCGAATAGTGCTGTCTTGGATCACACTTATCTTCTAAATTAATTTCCTACTTATTTCTCAAAGAAAATCTTCTCTCAGAATAACGGCGGCCTCTTTGTTTACAAGTTTCTGGGTGTCCACGTGGTTTCCATCATGTGATTTGATGTTGTTTGAATGGCGGAGGCAGGAATTCATTTAAATTAGTGATTTCAGATGGGACGGGCTGCACCTCACGTTCATTCAATACCGATTACAAAACCAGAGAACATTTGTTTCGTTTAAAAGTAGAGACTTCAAGCTTTATGTTGATATATTTCTCGTCTGTGAGGCAAGTATTCGCTGAGATTCCAGCACGTTTACTGACTCTAGAGGGTCATAAAGCCTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44353
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000004087 | Essential Splice Site | 1282 | 1647 | 32 | 39 |
Genomic Location (Zv9):
Chromosome 25 (position 36835021)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 35242637 |
GRCz11 | 25 | 35747576 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATATCTGAACCACATTCATTGGCTTGCGTGCCTGAGATTGTTTGTTTTA[T/A]GAAGTATTTTGGGTGAACTACAGTGCCATAAAAAAGTATTTGCTTTTATT
Long Flanking Sequence:
CATCTTGAACTCGGCGCTTTTATTTTCTCCAGCGCTTGTATAAAACAAAGAGGTTAAGAGATGTTTTCGCCTTACAGACGCTGACTACTTATGATTATTTGCACCTGAAGTGATGTTGGTTATTTAAGTTGAACTCTAATGTTATTTTTCAAGTACATATTTCTCTGTGTGTGAATATGTACGGTAGGTGTGCATGCATTCAAAGTTCAGTTCATCTTTTTAAGTTTGTGTTTCAAGCATTTAAACATTTTGTTAAACACTACAGAAAATAAGGGGATGATGGCAGATTCTGTAATATTATATGCAGTTTGTACAGTCTTAGAGAACACAGGGATGTGGCTATGATTGAGAGCATTTGGGTTTTTTGTTTGTCTTTTCTCACACACAAATGATTTCACAAGTCTCTTCACTTCCCTTTTCTGTTTATTTTGTGTTATTTGCATGTGGATGAATATCTGAACCACATTCATTGGCTTGCGTGCCTGAGATTGTTTGTTTTA[T/A]GAAGTATTTTGGGTGAACTACAGTGCCATAAAAAAGTATTTGCTTTTATTTCATGATATTCTTTTTTTTTAGTCGTTATTTATAAAATTATAAATAATAAACTGGGTTCACTATGGCAAAATTAAACAAAAAAAGTCAAATCTTAAAACTTAATAAAATATCATATACCAAATAAAATCTCAAATAATGAAAAAATAAACAACAGAAATGAATAAAAGTGCTAAAACTTTTAATAGAGCTCAAATGAAAACAAGCTCCAAAAATAAAAGTTAATAATACTGATAAAATGCTTTCTGTTGTCGTATTCAGTTATGATTGAATGAAGATGAAATCAGTTTAGTAAAAAAGTAAGAAAAATATAAATGGATGGATGGATAAATGGATGGATAAAATGATGGCTAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44354
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000004087 | Nonsense | 1345 | 1647 | 34 | 39 |
Genomic Location (Zv9):
Chromosome 25 (position 36842870)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 35250486 |
GRCz11 | 25 | 35755425 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCAGTTAACTATATTAACCTGGGTTTTTCCTTTTTTCAGATCGTACCTG[T/A]AAAGTTTGGAATTTAGTGACGGGACAGGAGATCATGTCTCTGGGCGGCCA
Long Flanking Sequence:
GCCATTTCCAGGCTGCTTTCCAGCCTGTTCTTAGCTGGTCAGGCTGGAAAATGACCAGCTAAATCCAGCTAAAACCAGCTTGATCAGCCTGGTTTAAGCTGGACATAGCTGGTTTTGGCTGGGCTCCCATCCTGGCTAGGCTGGTCAAGCTGGTTTTAGCTGGTCATCTCCCAGCCTGACCAGCTAAGACCAGGCTGGAAATGGCTGGAAACCAGCCTGGAAATGGCCAAAACCCCTCTAAAACCAGCCTGGTCGACCAGCTAAAACCAGCCACCCAACCTAGGCTGGTTTAAGCTTTTTTTTCAGTAGGGATAGCCAATCAAAACTGGGCTATTTTCAATTATACCTCAGATTCAGATCAGTCTAAAGATGCTCCCATAGAATCACCAAGCATCTGACTCTCATCTCCGGGAACTGGGTCATAAATATAACCCTAAGACATTGAATGGTTTCAGTTAACTATATTAACCTGGGTTTTTCCTTTTTTCAGATCGTACCTG[T/A]AAAGTTTGGAATTTAGTGACGGGACAGGAGATCATGTCTCTGGGCGGCCACCCTAACAACGTAGTGTCAGTGCGCTACAGCTCTAGTCTGGTCTTTACCGTCTCCACCTCCTACATCAAAGTCTGGGACATCCGAGACTCTGCCAAATGCATCCGGACACTCACGTGCGTCCTAAACAACTCATGATTATCAGATATGCAATATTTGAGATGAAATCAGAGAGCTCCCTTATCCTCCGTAGACATCAAGGTGTAATTAGGGGAAAATAAGTCAGTAGTTGATAGTGGGAATTGGTACTTAAACTGAAGTGTTACCATAATTTGTGTTCTGGTATTGAAATCTTCTCCTTTGTTTTTTCATTTAGCTCGTCAGGTCTGGTGAACACTGGTGATATGTGTGCCGCTAGCACCAATCGCACCGTGACCATACCGGCTGGAGAAAATCAGATTAACCAAATCTACCTGAACCCGTCCGGCACCGTTCTCTATGCTGCCGCCGGA
Associated Phenotype:
Not determined