ZMP
epha4a
Ensembl ID:
ZFIN ID:
Description:
Ephrin type-A receptor 4a [Source:UniProtKB/Swiss-Prot;Acc:O13148]
Human Orthologue:
EPHA4
Human Description:
EPH receptor A4 [Source:HGNC Symbol;Acc:3388]
Mouse Orthologue:
Epha4
Mouse Description:
Eph receptor A4 Gene [Source:MGI Symbol;Acc:MGI:98277]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa25876 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa208 | Nonsense | Confirmed mutation in F2 line | Not yet available |
sa9644 | Nonsense | Available for shipment | Available now |
sa9998 | Essential Splice Site | Available for shipment | Available now |
sa17262 | Nonsense | Available for shipment | Available now |
sa15903 | Essential Splice Site | Available for shipment | Available now |
sa39898 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31294 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa25876
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 |
---|---|---|---|---|---|
ENSDART00000098632 | Essential Splice Site | 31 | 986 | 1 | 18 |
Genomic Location (Zv9):
Chromosome 2 (position 39840046)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 40170211 |
GRCz11 | 2 | 40135850 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGATACCGACTTTCGCATTAACCGCACGGGTCTACCCTCCTAATGAAGG[T/A]AAGGATTTACCAAAACCCAAGGAAATTTCAACAAGAGTTATGTTTTGTTG
Long Flanking Sequence:
GGTATTACCCATATATTATGAACTATGATCGGCTGGTAAAAGCAGCCCCTTTCTCTTCCTTTATGTATTTTCTGGCGCGTTCTCCTTAACGCGCGCACGCTCTGCATTCTCACACACAGGCGAGCTGAGTTGTTTTATGATTGCGCAATAGATTGAAAGAAGGACTTTTTATTTTTATACAATTCTTTCAATTATCATATACCTGAAAAATGGGCTGGCTATTTACCCGAATGGATGGACTGTTGACTTTTGGTGTCTCGCTGTGACAGGCACGTCAGGCAGTAAAGATCCGCCCCTCGGCGGTGTTCAGCAGCGCTGCGTGCATCACTCTCAAACGCTAATTCCACCGGGACAGACGCAACTTCGGTCCGCGCGCGGAGCGGAGGAGACGCACACGAAATGACACCAATGGCTGCGCTTGTGTTCACAGCGACTTTTGCGCTAATAATCTGGATACCGACTTTCGCATTAACCGCACGGGTCTACCCTCCTAATGAAGG[T/A]AAGGATTTACCAAAACCCAAGGAAATTTCAACAAGAGTTATGTTTTGTTGTTGTTTGGTATGCCACTTGGGACCGAGAGTGGCACAGCGCTATGACTGCCATTTGTTTTATTCATTTCGACACTTTATCTCACCAGCGAAAAGGAATTATATAACGTTTTTTTTCTCCGAAAGTCCCTTTGGGTATCTCCAAGTGTCTGCGGTTCCCAAAACCCGCAGATCAAATGGAAAGCTGAGCCGTTTCTTCTTCTTCTTCTACTTCTTCTTCTTCTTCAAAAGAAGTTTAAACTCGGACACTAATTGGGAGTAAACACTGCTTGTGCTTCGACCGATTTCCAATTTTGTTGGAAGTTTCTTTTTATTTATTTATTAATTTATTTTTGTTTCGTGATATATGCAGGGATTACCAGAATTGAAAATAGTCCACAATTCTCCTGTCAATTATTACATTTATTTACATTAAATGCGCGAATCTACAAAAAACGCGGACGGACAAATGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa208
Status:
Confirmed mutation in F2 line
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 |
---|---|---|---|---|---|
ENSDART00000098632 | Nonsense | 260 | 986 | 3 | 18 |
Genomic Location (Zv9):
Chromosome 2 (position 39836017)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 40166182 |
GRCz11 | 2 | 40131821 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAATGTACTGCGGAGCAGATGGAGAATGGCTGGTGCCTATTGGAAACTG[T/A]TTGTGTAACCCTGGCTATGAAGAACATGAAGGGACATGTCAAGGTAAGAC
Long Flanking Sequence:
GCTCAGCGGGTCTACATCGAGATCAAATTCACCCTGCGTGACTGCAACAGCCTGCCAGGAGTCATGGGAACCTGCAAGGAGACCTTTAATCTTTACTATTATGAGTCCAACAATGACAAAGAGCGATACATCCGAGAAAACCAGTTCACCAAAATCGACACCATTGCGGCTGATGAAAGCTTCACGCAGGTGGACATAGGAGACCGCATCATGAAGCTGAACACGGAGGTGAGGGATGTGGGGATTTTGACAAGGAAGGGCTTCTACCTGGCCTTCCAGGACGTTGGGGCTTGCATTGCCTTGGTATCAGTACGGATCTTCTACAAGAAATGCCCGCTTACTGTACGCAACCTGGCCCAATTTCCAGACACCACCACCGGCGCAGACACCTCATCGCTAGTGGAGGTACGCGGATCCTGTGTGGACAATTCGGAGGAACGTGAGGTCCCTAAAATGTACTGCGGAGCAGATGGAGAATGGCTGGTGCCTATTGGAAACTG[T/A]TTGTGTAACCCTGGCTATGAAGAACATGAAGGGACATGTCAAGGTAAGACCTCGGATACCTCCTTTGCTCAAGTTTTTCCTCACCAGGTTCTGTTATGATTTGAGACTTATCCACCTCTCAAACAAAAAGCAAAAAAAAAAGCCCCTATACAGCCCAGCAGCGCTATATTCTAGAATTTAAGATGAGATCATTGTAAGTGAAGCTGACCTGGATGCCCTTTCCCACTTTAGGGATGTGAGAGTTTACTCAGATGTAGACAGCTGGGTACTCGACGGATCACTGTGGATTAAGAGAGTGTTGCTATTCGAGTGGTCTGGTTATGATTATGAATTGCCCTGTTTGATATTAAAACACCTCCCTGCGGGTTTGTGCATGAGAAACGTTGGTGCTAATTATTTTGTTGGAGCAACAGCCGTGTGGTTTATGTGCAGAATCCGCTTAATTAGATCATGGGCGAAGGCCCGCATAGCCTTTTCACTCTCGTTCTTCTTTGCTATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9644
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098632 | Nonsense | 292 | 986 | 4 | 18 |
Genomic Location (Zv9):
Chromosome 2 (position 39804440)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 40134605 |
GRCz11 | 2 | 40100244 |
KASP Assay ID:
2259-2440.1 (used for ordering genotyping assays)
KASP Sequence:
CCTGTAAGATCGGYAACTACAGAGCTCTAGCCACAGACGGCAGCTGCTCT[A/T]AGTGTCCCCTGCACAGCTACTCTGTGAGAGAGGGATCTACTTCCTGTGCC
Long Flanking Sequence:
ACTTGCATTATTAGGCTGTTATAAAATCATTATATAATCAGTGGCATAAAAATATCTTAAAAGGCCTCATTTTATTTTATTTTTTTTACTGTGGATGTCAATGGCTACCGATTCCCAGCATGTTTCAAATTATCTCCTTTTGGGTTCAACAAAAAAGAGACTCATAAAGGTTTGAAAGAACCTGAGGATGAGTAAATTGGGTGAACAATTCCTGTAATGTTAATTTATAAAAACACTAATCATTTAATAGCACCGTTAAATGCAACCATTAGCAGATTTCAAAATGTTATTTGCACAGTGTTTCACATGAACATTCACAAACTGAGTGTCTTATGTTCGCTGGACTTGAACGACGAAAACTTTTATCTCCAGGTCATAATATATTTTAGCAGTATACTATGTTTCATGATCTGTAACGTCTCCACTTTCTCTGTTTCTTTCTCTGTGCAGCCTGTAAGATCGGCAACTACAGAGCTCTAGCCACAGACGGCAGCTGCTCT[A/T]AGTGTCCCCTGCACAGCTACTCTGTGAGAGAGGGATCTACTTCCTGTGCCTGTGATAAAGGCTTCTTCAGGTCTGAGACGGACCCTGCATCTATGCCCTGCACACGTAAGTGGATTTCACAGTATCTTCATGGATTAGAATACACTTTGTGCATCACATAACCTTTTTTTTGTATCAGGAGTTGGCATGGGCTGGTATAAGATACTGACGGTATGATAACCTTGGATATAATTATCACTGTGTTGTGATTACTGCTCTAAAAAATGTTTTTTTGTATATATATCAGGGTAAAAAAACACCTTTTCCCCCCATTGAACACCAATATTTTATTTTAAGAAACATTTGAAAGATTTTTTAAATTGTAAACATCTCAGGCTAATTTATAAAAAACAAATCATTGACTTTTTCTCTCTTTATTAGTTTTAAAAACACAGATTTCTTGACAACTTGAAAAGGCATCTTTGGTTATATAGGAAGCCACTGCCCTGTTCAGGTCCAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9998
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098632 | Essential Splice Site | 327 | 986 | 5 | 18 |
Genomic Location (Zv9):
Chromosome 2 (position 39798689)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 40128854 |
GRCz11 | 2 | 40094493 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGCTTAGTTTCTCTGACAGWGTGCATTTTTTNNCCAAAATTGTCTTTTCGY[A/T]GAGCCCCCATCTGCTCCTCAGCACCTCATTTCCAATGTGAACGAGACTTC
Long Flanking Sequence:
TTATGAGATCCCTATCAGCAAGTTGCTCAATTATGGAGATGTAATCATTCTCTCTCTCTTTCTTTCTCTCTCTCTCTCTCTCTTTCCCTCTCTGAGTGTATTTCCTTTTTGCACAGCTAGCACTGCGTCGCCTGTGGTGCTGGTTTGTCATAAATGTAATTATCTTTAAATTCAGCAGCGCCTGGTTAACGAATACACCGCAGAGAAAAACAACGCAAATATACACAAATACACAAAAGCACACAAACAGACTCCTATCTGTCATAGCCTGTAACATCATCTGCCTGCAGTGGCAATAAAAGGGGTGTGTATTTGTTTGCCATTGAAGATTCCCTTGCCAAGGGTGTATTTTGAGATCAATCTCTGCCACAGTCATAATCCTGTTTTGTTTGTTCCAGAACTTTCAGACATCACTGTAACGGAAATGAAGCATAAATCATGCGCTTATTTTGGCTTAGTTTCTCTGACAGTGTGCATTTTTTCCAAAATTGTCTTTTCGT[A/T]GAGCCCCCATCTGCTCCTCAGCACCTCATTTCCAATGTGAACGAGACTTCGGTGAATCTGGAGTGGACGGCTCCAGCATCCTCTGGTGGCAGACAGGACCTTGCCTATAACGTTATATGCAAGCGGTGCAGCTCGGACGGTCAACGCTGTCAGCCCTGTGGCAATGGCATCCATTTTTCCCCTCAGCAGCTGGGCCTACGCACTACCCGGGTGTCCATAAATGACCTGCAGGCTCACACCAACTACACCTTCGAGATCTGGGCAGTCAACGGGGTCTCCAAACAGAGTCCTGGACCCGAACAAGCAGTCTCTGTGACTGTTACCACCAACCAAGCGGGTAAGTGTGTGGCTTATGTTCACAAATTATTGTTGAACATGATATTTCCTCTGTCATGACTTCATTAAATACCAGAGTAATATCATCATGTGATCTGGTCGTAGGGTGGTGATGTGTTGAATTTCTCACCACACTCCGATCCCGAACATAGTCATCAACTCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17262
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098632 | Nonsense | 478 | 986 | 6 | 18 |
Genomic Location (Zv9):
Chromosome 2 (position 39794638)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 40124803 |
GRCz11 | 2 | 40090442 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CARCCCGAGAGACCCAATGGAGTCATTCTTGAGTACGAGGTCAAATACTA[T/G]GAGAAGGTGAGATGATTCRTGGGAAAGAAGTGTGCAAAACTTCTGCKTTG
Long Flanking Sequence:
ATTACAGATAAGCATGTGCACCCTAGATGACTGCATCAATGGACCTTCTGTAGTAGCAAAGTGGAATTATGAGAGGAGGGAAAGAATCAGAAGCTTTTGTCTGATTCTTATAGTGGATGATATAATATGTGCACTTTGACGATTCTGCTTTTTTTCTGGAAGTTATAAAACTGTAGTTACTATATTTTCAGACGTGCATTGCTTCCAGCGTTTTGTAGTAGTTGTTGTTGTTTTAAGTTTTCTCAGTTTGACAACATATATATCTCATACCTCATCATTGCTTTATTGCAATAGCATATTTGTGTTTCTCTGAAACAGCTGGTGGTTGATGTTCTCTTAGCAACACTAAGAGTTTTCTCTTTGTGTTTTTCTCCGGTTCCAGCTCCCTCTCCAGTTACCACCATCCAGGCCAAGGACATCACAAGACATGCTGTGTCTTTGGCATGGCAACAGCCCGAGAGACCCAATGGAGTCATTCTTGAGTACGAGGTCAAATACTA[T/G]GAGAAGGTGAGATGATTCATGGGAAAGAAGTGTGCAAAACTTCTGCTTTGAGGAATAGGCCGGCATATGTTGTGTCTTTGATGTTGGCCTAAAGCCCCATGAGGCTTCTTAACCAGAAACGTGGTCAACCATCTTCACCAGAAAGATTGTGATACTTGAGCTATTTAGTTAGGCAATCTGTCCTGTTTAAGAACTCTTTTAGACAGGTTCCTCATTCTCACAGCCTGAGGATAAGGATTTACTTTTGGTTAATGTAATTCAGACATAGTGACATGACTTTTTTTGTCAGGCCTAAGAAATGGGAGAGATATTCTTTGAACATTTTAAGTTGTTGCAATCAACGTAAAGCCTTCACTTAAGTCCTTAACATGGGCTGTATGATGTCAGGCACATCAAAACCAGAGAACTGCATTTTAGTTCATAGGCAGACCAGACTCACTCACACTCGCAGTAGGAGTCTGGTGAACTGGCGGGTCAGAACAGCATGGGGTGGATGGACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15903
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 |
---|---|---|---|---|---|
ENSDART00000098632 | Essential Splice Site | 534 | 986 | 7 | 18 |
Genomic Location (Zv9):
Chromosome 2 (position 39793412)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 40123577 |
GRCz11 | 2 | 40089216 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTGGCTACGGAGAATTCAGTGCCCCTTTTGAGTTCATGACCAACTCAGG[T/C]AGGTTTCCTTGTGCGTGTTACAGAACCAACAATGGCARGKCTTTGTTCCC
Long Flanking Sequence:
TAGGGGATATCGAAAAAACAATTAAACTTTCGTTCCTTTGCTTGTTTTGGTTCAAACTCAACATCATTTAAGTGGTTTGGATGTAGTGATGAAACGGGAATTTTGAACAAGCAAATTCAGGTTACACTCTAGGGAGCAAGTGAAAACAAAGATGGCATACTTGTTTTTGTACAACAAGGCTGCGGTTTTCCCTACAAAAGCCTGGCTGAGTTTTCAGTGTCAGATGCTAAACAAATTCTTTTGCCTTTTATTTTATGAGAGGTTGTTTCCAAATAAAACAATCCTAATAACAAATCTAACACACTGGTTCAACATTTCCTGTTTTGCTTATCCAATCAGGATCAAAACGAGCGCAGTTATCGCATAATGAAGACTTCGTCCCGAAGCGCTGAGATCAAAGGCCTGAGCCCACTCACCTCCTACGTGTTTCATGTGCGTGCCCGCACCGCTGCTGGCTACGGAGAATTCAGTGCCCCTTTTGAGTTCATGACCAACTCAGG[T/C]AGGTTTCCTTGTGCGTGTTACAGAACCAACAATGGCAAGTCTTTGTTCCCACAATTAGAGACCTGTGTTGAGTTTTAGGGTGGATCACCCATTCATCCGGAAACTATTTCTCTAAAGTAACATAATTATAGCTTTTGTGTATGTTTTCTTTTTCTTTACGATAGTTTCTTTGTTTGCTCACTACAAAGTCGCTGGTATTTTTAAAAAGCAGTTTAAAGCAAACTCTGTAAAGAGTGGAATGTTTTAGAGCTTTGATTCTAAGTTGGTTCAGAACCTTGAAAGAAACAGAATTTGTTCCTGACTGATGAAGCTAAGCTCTTCAATAAGAATTTAAAATGGCTGACAAGTTTGATCTGACACTTTACATGAAAATTATACATTTGATCTGAACTTTAATGTTGTTTTTTCTCTCAGTTCCTTCTCCCATCATCGGGGACGGAGCTAACTCCACCGTGCTCTTGGTGTCTGTGATCGGCAGTGTGATTTTGTTGCTCATCTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39898
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 |
---|---|---|---|---|---|
ENSDART00000098632 | Nonsense | 727 | 986 | 13 | 18 |
Genomic Location (Zv9):
Chromosome 2 (position 39779111)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 40109276 |
GRCz11 | 2 | 40074915 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACAGAAGAATGATGGACGGTTTACAGTGATTCAGCTGGTGGGCATCCTG[C/T]GAGGCATTGCTTCAGGAATGAAATATCTCTCCGATATGAGCTATGTCCAT
Long Flanking Sequence:
TTGGTAACATATTGGAGACTGTAAGGGGCTGTGAGTGTTCATATATGTTGCATTTATTTATTTATTTATTTTATTTTATTGCAGACATTACAGTAAGCTTTACTTTGACATTTCCTCAAGCGAGAATGACATTGACTGAAACTTTCTGTCATAAACCACGCCCACCAAAAGAGTACCATTGGTACCCTTTTAGCAGTGGAAACGCAAGCCTAATAAAGGTGACCTGTATCGTACCGTACTGTATACCACTCAGTGGAAATGGGCCATTATTCAAGCATTTTGAAGCAATAACAGCAAAAGCCCATTACTATGAATACTATAAATCCACTATCAACTTGTGAACAGATCTGCAACAAACACACATCTTAATACCAATTTTAAATGAGGCCTTTGGTACTCTCTTGTACTGTATTAACTTAATTCATTATATTAAATGTCTTTTAACCTCTCCACAGAAGAATGATGGACGGTTTACAGTGATTCAGCTGGTGGGCATCCTG[C/T]GAGGCATTGCTTCAGGAATGAAATATCTCTCCGATATGAGCTATGTCCATCGTGACTTGGCGGCTCGCAACATTCTGGTCAACAGCAACCTGGTGTGCAAAGTGTCCGACTTTGGCATGTCTCGAGTTTTGGAGGAAGACCCAGATGCTGCTTATACCACCAGAGTAAGTTTGACGCTTTGTACTTGTGTTTGCAACCATAACACAAGCTCTCTAACCCAATCATTCCCAGCATTTAACCCGCATGTGCTTATGAAACTGCCAGTATCTTTTCCAATTAGAATCAAAATTTTTCAATCAAACTAACTCCCAGTATGGAACGCTGAGTGTGCGTTTGCGAGTGTGTGCATGCGTGTGTGTGATTAACCCCCATGCATGTGTTTGCTATCTCTTTTGAAAGGAAATAACAGGAACCTATCAATCACAGGGAGGCAAGATACCCATTCGCTGGACGGCTCCTGAAGCCATTACTTACAGGAAGTTCACCTCTGCATCTGACGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31294
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098632 | Essential Splice Site | 831 | 986 | 14 | 18 |
Genomic Location (Zv9):
Chromosome 2 (position 39778534)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 40108699 |
GRCz11 | 2 | 40074338 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGTGATGTCATATGGAGAGCGGCCATATTGGGACATGAGCAACCAGGAT[G/A]TAAGTGTTTTTTAAGGAACAGACAAGGTTGATTTGTGTTTAAAGTGTTGT
Long Flanking Sequence:
GGTCAACAGCAACCTGGTGTGCAAAGTGTCCGACTTTGGCATGTCTCGAGTTTTGGAGGAAGACCCAGATGCTGCTTATACCACCAGAGTAAGTTTGACGCTTTGTACTTGTGTTTGCAACCATAACACAAGCTCTCTAACCCAATCATTCCCAGCATTTAACCCGCATGTGCTTATGAAACTGCCAGTATCTTTTCCAATTAGAATCAAAATTTTTCAATCAAACTAACTCCCAGTATGGAACGCTGAGTGTGCGTTTGCGAGTGTGTGCATGCGTGTGTGTGATTAACCCCCATGCATGTGTTTGCTATCTCTTTTGAAAGGAAATAACAGGAACCTATCAATCACAGGGAGGCAAGATACCCATTCGCTGGACGGCTCCTGAAGCCATTACTTACAGGAAGTTCACCTCTGCATCTGACGTCTGGAGCTATGGCATCGTCATGTGGGAAGTGATGTCATATGGAGAGCGGCCATATTGGGACATGAGCAACCAGGAT[G/A]TAAGTGTTTTTTAAGGAACAGACAAGGTTGATTTGTGTTTAAAGTGTTGTGTTAAATGTTTTGGTTTGGTTGTTTCTCTGTTTTAGGTGATAAAGGCCATTGAGGAAGGCTACAGGCTGCCTCCTCCCATGGACTGTCCAGTTTCTTTGCACCAGTTGATGTTGGATTGCTGGCAGAAAGAGCGCGCAGAAAGGCCAAAGTTCAGTCAAATTGTCAACATGCTGGACAAACTCATCCGCAACCCTAACAGCCTGAAAAGGACAGGAGGAGAAATAGCCAGGTAATAAATTCAATCTCAAGTTCAAGTTGCTTTATTAGTATGATATTTAGGACAGTATTGCCAAAGCATTTCAGATATGTATTAAATATGTAATATCAACATCATCAAATGAGTAAAATATACAGCAAATGAGAAATAAATGACAACAAAATTAATAAAGCAGACAATATCTCTAAAATGCATATTTATGAATAATTAGAATAAAAAGTGTATATTATAT
Associated Phenotype:
Not determined