ZMP
col4a4
Ensembl ID:
ZFIN ID:
Description:
Type IV collagen alpha 4 chain [Source:UniProtKB/TrEMBL;Acc:Q4TZW9]
Human Orthologue:
COL4A4
Human Description:
collagen, type IV, alpha 4 [Source:HGNC Symbol;Acc:2206]
Mouse Orthologue:
Col4a4
Mouse Description:
collagen, type IV, alpha 4 Gene [Source:MGI Symbol;Acc:MGI:104687]
Alleles
There are 10 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa35965 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa32056 | Nonsense | Available for shipment | Available now |
| sa22697 | Essential Splice Site | Available for shipment | Available now |
| sa42601 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa2802 | Nonsense | F2 line generated | Not yet available |
| sa6390 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa22696 | Nonsense | Available for shipment | Available now |
| sa18383 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa35965
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 |
|---|---|---|---|---|---|
| ENSDART00000061186 | Essential Splice Site | 546 | 1670 | 23 | 47 |
Genomic Location (Zv9):
Chromosome 15 (position 35256973)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 36131164 |
| GRCz11 | 15 | 35989133 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAGGAGTGAAAGGAAAGAAAGGAGAGGTTATGACGTTAAGCATAAAAG[G/T]TGAAGTGTTTTAAATATTTTAAGACTAACCACAAATTGTGTAAAAACCAA
Long Flanking Sequence:
CACTTGCTTCTACAATTTATTTTATTATGTAAATATGAGCATCTTGAGTGTAGCTGTCCATGGTGCTGAGTATTTTTGCTGTGATTTGTGTGCCCGTTAGGGGGCAGCAAAGTATCTTTTTTTAACTAATATGAACACACCTGCTTATTTCACATTCTTTTATAGGTCCTGATGGAGGATGTGCATGTGATCCTCCTGGTGATCTTCCTGGGGATCCAGGCCCTCCAGGCCCTCCGGGTGAACCTGGTGATCCCGGGCAGAAAGGTTTCAGAGGCCCCCTTGGTGAAATTGGACTCAGTGGAGACAATGGTGTGAATGGGATAACTGTATGTAAACCTGCTCGAGATTCATGTGAGAAAATGTGAAAATGCATTGTGTTTGCATGTGTAAAGGTGTCCGGTTTTGTGTGTCTGTTGTGAATTCTTAGGGTTCCAGAGGCTTAACAGGTCCCAGAGGAGTGAAAGGAAAGAAAGGAGAGGTTATGACGTTAAGCATAAAAG[G/T]TGAAGTGTTTTAAATATTTTAAGACTAACCACAAATTGTGTAAAAACCAATTGTGTTTTCGTGTTATTATTCTGCATAAACAGGGTGTGAATTACAGCTGGATTTGATTAAACTAATTTACTCGTGATCCCCATGAAGGACATCAAAACAAAATGTGTGTGTGTGGAGGGTCTGCTTTTTATTTATTTATTTATGTATTTATTTATTTATTTATTGATCACTTTATTGTTTTTTAAACATTCAAACACATTGACTTTCACATTTGGTCTAACAAACATTTACACAGCATTTAACAATAAGAGATGCAATATAAAAACAATGCATATGAAAGTATTCAAAAAACAGCCATGAAAATTATAGGAATAAAACAATACAAACCCATACAGACTCCATATGAACAGGCGGTCATGAGAAGAGCCAGAAATATTAGTGCTGATTTCAAACATCCTCTTTTCAGTGAATATCAGCTGTTGCCATAAGGAAAAAGACTGTGAATGCCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32056
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000061186 | Nonsense | 881 | 1670 | 30 | 47 |
Genomic Location (Zv9):
Chromosome 15 (position 35244385)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 36118576 |
| GRCz11 | 15 | 35976545 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCCTTCAGGGACCCGCAGGAGTCAACGGTGACGGTGGAAATCCTGGATA[T/A]CCTGGACCAAAGGGTAAAGAGTCTTTCGAAGAGAGCTTAATGTGTTTTAG
Long Flanking Sequence:
ATATTTTGGGTGTTTTGGCGTTTTTGGACAGCTTTTGGGCTGGAAAAGTCAGCTATATCTGGCAACAATGCTAATAATATCGTCAATATTGTTTTGTTTTTTTTTTCTACAGGTATGTCTGGTGTTCCAGGGTATCCTGGTAGAAAAGGGGAAAGGGGGAAGGATGGTGCACCAGGACCACCTGGACGCCCAGGTAAGAGTCCAGAGCAGTGCGATAAAGGAGATGAGGGTCTGCCTGGCAAGAAAGGAGAACAAGGCTTAATTGGACATAGAGGTAAGTAGAGTTCACTGCATTAGCATACATTTGTTAAGACTGTTGGCTAACAATGTGACTTTTCTATGTTAGGCTACCCTGGAGAGAAGGGGTCACTTGGGGAGCTGGGATGTCCTGGCATTGGAGCCAAAGGAGCCCGGGGTAAACCTGGTACTCCTGGACCCCAAGGATGCATAGGCCTTCAGGGACCCGCAGGAGTCAACGGTGACGGTGGAAATCCTGGATA[T/A]CCTGGACCAAAGGGTAAAGAGTCTTTCGAAGAGAGCTTAATGTGTTTTAGGAAGTTAATTTTAATGTTAAATGTAACTCAATTACAACAAATGCCTTTAACTGCCATCTGTAACAATACATTTGGCTTGGATTTGTATGGAAGTTAGATAGATGTGGTCATCAAGGCTTATTTTAAATACACAATAGATTTACACCGCTAAGAGATTTTGTCTTGTTTCTAGTCCAAATATCTAAACAATCTTAAATCAACAAGCATATTCTAGACATGTAAAAATGTTGCTTTATTTTTAGAAATAATGAGTCAAAATTAAGTGAGATTTTTCCTAAAACAAGCACAATAATCAATTTGTGGGGCAAGTAAAATAATATTGTTTTCAGTTTGAACTTTGAAATAAGATTATTTTAATTTCATATTTTTAATGTTGACATATTATTCTGAAACCAAAACATACATTTTTTTTACTTAAATGCTTCATGGTTTAAAATGTTGAAAAACTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22697
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 |
|---|---|---|---|---|---|
| ENSDART00000061186 | Essential Splice Site | 886 | 1670 | 30 | 47 |
Genomic Location (Zv9):
Chromosome 15 (position 35244370)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 36118561 |
| GRCz11 | 15 | 35976530 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGGAGTCAACGGTGACGGTGGAAATCCTGGATATCCTGGACCAAAGGG[T/C]AAAGAGTCTTTCGAAGAGAGCTTAATGTGTTTTAGGAAGTTAATTTTAAT
Long Flanking Sequence:
TGGCGTTTTTGGACAGCTTTTGGGCTGGAAAAGTCAGCTATATCTGGCAACAATGCTAATAATATCGTCAATATTGTTTTGTTTTTTTTTTCTACAGGTATGTCTGGTGTTCCAGGGTATCCTGGTAGAAAAGGGGAAAGGGGGAAGGATGGTGCACCAGGACCACCTGGACGCCCAGGTAAGAGTCCAGAGCAGTGCGATAAAGGAGATGAGGGTCTGCCTGGCAAGAAAGGAGAACAAGGCTTAATTGGACATAGAGGTAAGTAGAGTTCACTGCATTAGCATACATTTGTTAAGACTGTTGGCTAACAATGTGACTTTTCTATGTTAGGCTACCCTGGAGAGAAGGGGTCACTTGGGGAGCTGGGATGTCCTGGCATTGGAGCCAAAGGAGCCCGGGGTAAACCTGGTACTCCTGGACCCCAAGGATGCATAGGCCTTCAGGGACCCGCAGGAGTCAACGGTGACGGTGGAAATCCTGGATATCCTGGACCAAAGGG[T/C]AAAGAGTCTTTCGAAGAGAGCTTAATGTGTTTTAGGAAGTTAATTTTAATGTTAAATGTAACTCAATTACAACAAATGCCTTTAACTGCCATCTGTAACAATACATTTGGCTTGGATTTGTATGGAAGTTAGATAGATGTGGTCATCAAGGCTTATTTTAAATACACAATAGATTTACACCGCTAAGAGATTTTGTCTTGTTTCTAGTCCAAATATCTAAACAATCTTAAATCAACAAGCATATTCTAGACATGTAAAAATGTTGCTTTATTTTTAGAAATAATGAGTCAAAATTAAGTGAGATTTTTCCTAAAACAAGCACAATAATCAATTTGTGGGGCAAGTAAAATAATATTGTTTTCAGTTTGAACTTTGAAATAAGATTATTTTAATTTCATATTTTTAATGTTGACATATTATTCTGAAACCAAAACATACATTTTTTTTACTTAAATGCTTCATGGTTTAAAATGTTGAAAAACTGAAATAAAAATAAAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42601
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 |
|---|---|---|---|---|---|
| ENSDART00000061186 | Nonsense | 1063 | 1670 | 35 | 47 |
Genomic Location (Zv9):
Chromosome 15 (position 35238780)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 36112971 |
| GRCz11 | 15 | 35970940 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATGCTGTCTTGTATAGGCGACAGTGGTGAATCTATTTGTACGCCAGGG[C/T]GAACAGGTGAGAGAGGGCCATGTGGAGACAATGGTGTGCCAGGTAGGACT
Long Flanking Sequence:
GGCAGAGGATCGTGAGTTTAGAAATGCATTTTTATCGAATAGAAGAAGCACTCGTATTTTTACCGTGGGTTTGAACACAATATGTGATCAGCCGCATAAGGATTAAACCTGAGAGATACAGTACAAGCACTGATCTATAATAGGCAAGTTATTACAAGCTGCACAGAGCGATTACAACTTATTACACACAATTAAACACATAATAATATAAACTACATATATGAACTACAGAAAACAAGGCAACAAGTCTAATCACACTTGCATGTTATGATCTGTTGGAGGATGAAACTGGTCCATATAAACTTTAATGGTTGCTGACAAAGTCCCTGTCATAGTCTGATAGGGGCTCTTTAATTAAACTGTCGACTTTTACCAATACAAGTAAATCAAACTATCATTTTAAATTTAGTTATATGTCATTATATATGAGATTTATTACAAAATGTCTTTTCATGCTGTCTTGTATAGGCGACAGTGGTGAATCTATTTGTACGCCAGGG[C/T]GAACAGGTGAGAGAGGGCCATGTGGAGACAATGGTGTGCCAGGTAGGACTTTCTTAGCTTTTATTTGATTTTGTTCACCCTATTGTTTTGGTACTTTAAAACAAGAAAAAAAAAACAGATCTACAGAAGATCTAAAATCTCTGTTTTACACAAAAGGTCCCTGTGGGGAGAGAGGAGACAATGGTGACATTGGACCAGCAGGTCCAGATGGAAACTGTGGCCCTCCTGGGCCACCCGGGATCAATGGTCATATTGGACCTCCAGGTAAAATACAGATTATGAATTTTAAAAAATATATATAAAATATGTATATACAGTTAAAGTCGGAATAATTATTATTAATTAATTTTTAGTATTATTATTATTAATTATTATTATTATTATGATAACGCTCATTCAATCATGTGATAACATTTGAATCGGCTGGGATTTATGTGCAATATGTAGATTTTTTGACTGTTTTAATTGTATTGATAAGATCTAAAAAATATGTATTTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2802
Status:
F2 line generated
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 |
|---|---|---|---|---|---|
| ENSDART00000061186 | Nonsense | 1433 | 1670 | 45 | 47 |
Genomic Location (Zv9):
Chromosome 15 (position 35228084)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 36102275 |
| GRCz11 | 15 | 35960244 |
KASP Assay ID:
554-2947.1 (used for ordering genotyping assays)
KASP Sequence:
ATACCATCTTATCSTTTTCTATACCAGGACCTCCGGGACCAGATGGTGAT[C/T]GAGGTCCCCCTGGAAGAAATGAGACACTTTCTACAGGCTTTCTTYTAGTG
Long Flanking Sequence:
AATGACCAAAGCAATATTTCAGATGTTTTACAATGTGGACCGTCCACTGGTTGGTCCATTAATACCATCTCATTGTGCCAATTTTTGCTATCACATGTTAAAACAAAATCACATGATTTTTTTTTTTTTTTTGTGAATGCTGGAAGGTAATCTGTAAATGTGTTTGATTTGTAGTTTATGCACGATTATTCTTATTGGATAGAACATTTATCCTACTTCTATCTGTTTTTTATGCATATTTAAAAAAATTTTTTGCACATCTTGGCATGTCAATAAAGCATTCTTAATGATATTCCTAAATTCTCATAAAAATAATTGGATGGAAACATAGCTACTGTTTTATCTTTTTGCTCTTGCCATCCAATCATTCAATCACTTCATTCTTTTTCATTTCTTTAGCATTTATCAAGAGCAACTCACATCCAGCCATTTGTGCATCATCTTATTGACATACCATCTTATCCTTTTCTATACCAGGACCTCCGGGACCAGATGGTGAT[C/T]GAGGTCCCCCTGGAAGAAATGAGACACTTTCTACAGGCTTTCTTCTAGTGATGCACAGCCAGTCCCGCTATGTGCCGACTTGTCCTGCAGGCCTTACACAGTTGTGGAACGGCTACAGTCTGCTTTACCTGGAGGGTCAGGAGAGAGCACACACACAAGATCTGGGTATGTGGCTAAAGCTCATATTGACATTTAAAAGTGACTATGATTACTGTCTAGGTTTCTGTAAGAACCGTATTATGTAACAACAAATGCTATTAGACACATATATATTTTATCTGACATTTTTATGTTAACACTTGTAGTTCTGGTCTTGTGCTCCATTTGGTCCAGACTTAAAAAGGATTTAATTTGATTAGTCATGGTTCTGGCTTGGTGTTTGGTGATTTTAAATAAATTTCATTCTATATTAATTTATTAATGAATTTTAATTTATATTGGCAAAAAAAAAACTCATATTATATAATTTGACGATGCAGGCTTTTTAAAAAATTTATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6390
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 |
|---|---|---|---|---|---|
| ENSDART00000061186 | Essential Splice Site | 1488 | 1670 | 45 | 47 |
Genomic Location (Zv9):
Chromosome 15 (position 35227917)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 36102108 |
| GRCz11 | 15 | 35960077 |
KASP Assay ID:
554-5283.1 (used for ordering genotyping assays)
KASP Sequence:
AGTCTGCTTTACCTGGAGGGTCAGGAGAGAGCACACACACAAGATCTGGG[T/A]ATGTGGCTAAAGCTCATAYTGACATTTAAAAGTGACTATGATTACTGTCT
Long Flanking Sequence:
TTTGTAGTTTATGCACGATTATTCTTATTGGATAGAACATTTATCCTACTTCTATCTGTTTTTTATGCATATTTAAAAAAATTTTTTGCACATCTTGGCATGTCAATAAAGCATTCTTAATGATATTCCTAAATTCTCATAAAAATAATTGGATGGAAACATAGCTACTGTTTTATCTTTTTGCTCTTGCCATCCAATCATTCAATCACTTCATTCTTTTTCATTTCTTTAGCATTTATCAAGAGCAACTCACATCCAGCCATTTGTGCATCATCTTATTGACATACCATCTTATCCTTTTCTATACCAGGACCTCCGGGACCAGATGGTGATCGAGGTCCCCCTGGAAGAAATGAGACACTTTCTACAGGCTTTCTTCTAGTGATGCACAGCCAGTCCCGCTATGTGCCGACTTGTCCTGCAGGCCTTACACAGTTGTGGAACGGCTACAGTCTGCTTTACCTGGAGGGTCAGGAGAGAGCACACACACAAGATCTGGG[T/A]ATGTGGCTAAAGCTCATATTGACATTTAAAAGTGACTATGATTACTGTCTAGGTTTCTGTAAGAACCGTATTATGTAACAACAAATGCTATTAGACACATATATATTTTATCTGACATTTTTATGTTAACACTTGTAGTTCTGGTCTTGTGCTCCATTTGGTCCAGACTTAAAAAGGATTTAATTTGATTAGTCATGGTTCTGGCTTGGTGTTTGGTGATTTTAAATAAATTTCATTCTATATTAATTTATTAATGAATTTTAATTTATATTGGCAAAAAAAAAACTCATATTATATAATTTGACGATGCAGGCTTTTTAAAAAATTTATAAAAACGTGCATCATTTGCAGTTATTATCAGAATTGTTTGTTTAGAATACATACATGTGTGTAATTTTTAACACACTTATCAATTTAATACAAAAAGTCAAATTTTTAAGAGAAAATAAATAAATCTGCTATTTAAACAAAGATTTAGGCTTAATTTATTTAACTTATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22696
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000061186 | Nonsense | 1577 | 1670 | 46 | 47 |
Genomic Location (Zv9):
Chromosome 15 (position 35226407)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 36100598 |
| GRCz11 | 15 | 35958567 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGACCGTCTTGACCCAGTGTGTCCACCCAAATGGAGGAGCCTCTGGACC[G/T]GATTTTCATTCATGATGGTAAGGAAAAAGCTCAGCTCCGTTTAAAATCAA
Long Flanking Sequence:
TTGGATATGTGGGGGAAACTGGAGCACCCGGAGGAAATCCATGTGAACATGGGGAGAACATGTAAACTGAACGCAGAATTGCCAACTGATCCAGCTGGGGCTCTAACCAGCGACTGTCTTGCTGTGAGGCGATTGTGCTACCCACTGCGCCACCATTCTGCCTGCAGGGCATGTTATAAACTAAAACACAAGACATTTTCAAACTGTTTTCTGTGTGCGTGTGTGTTTTACCAGGCCAGGCAGGTTCGTGTTTGCCAGTGTTCAGCACGATGCCGTTCTCCTGTTGTAATATGGACACTTGTGATTACGCCAGCCGCAATGACAAATCCTATTGGCTGTCTACAAATGCCCCCATTCCTAATAAGCCTCTGAAAGGGCAGGATATCGAGGAACACATCAGCAGGTGTGTGGTGTGTGAAGCTCCAACACCAACCATTGCAATACACAGTCAAGACCGTCTTGACCCAGTGTGTCCACCCAAATGGAGGAGCCTCTGGACC[G/T]GATTTTCATTCATGATGGTAAGGAAAAAGCTCAGCTCCGTTTAAAATCAATCAATCAACATCTGTCTGTCTGTCTATCTATTGTAAGGTAAGACTATCTGTCCGTCCGTCCATCCGTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTAGCTATCTATCTATCTATCTATCTATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCTATCCCTACAGTATCTATCTATCCATCCATCCATTCATCCATCCATCCATCCATCCCTACAGTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCCCTACAGTATCTATCTATCCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18383
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000061186 | Nonsense | 1583 | 1670 | 47 | 47 |
Genomic Location (Zv9):
Chromosome 15 (position 35224946)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 36099137 |
| GRCz11 | 15 | 35957106 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGAATTTTGATATTAAGCANACTTTAAATMACCTGTCTGTGTTCCAGTA[T/A]ACGGGGTCAGGGGATGAAGGCGGTGGACAGTCTCTGACATCAACAGGAAG
Long Flanking Sequence:
TCCATCCATCCCTACAGTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCCATCCAGCTAGAGTCAATATCATTACTAATACAAAAGATATCAATATTGATTAATATCAATTAATCAATATTTAGTTTCAGTTTGGCAATTTGATTCTTATCGATATGATTTTGATTCTATTCAATATCAATTAGTTATTAGTATTGTAATTAAGTCAACTGAAGGACCACCACTCCAAATGTGGAAGCAAATGGTCAGACTTTAATTGATAATTACCAAAACAAACACATTTTTTCAGTGGATTAACTTGCACAGATTCATTATTCACCCTAAGAATAACAATGTGAGCTAGCCGAATAAGCAATTCAGTGAATTTTGATATTAAGCAGACTTTAAATCACCTGTCTGTGTTCCAGTA[T/A]ACGGGGTCAGGGGATGAAGGCGGTGGACAGTCTCTGACATCAACAGGAAGCTGTTTGCAAGACTTCCGCAGTCAGCCATTTGTGGAGTGCCAAGGTCCCCGTGGCACATGCAGTTATTTCGCCAGCATCTACAGTTTCTGGATGACTATAGACATGGAGCACAATGACTCCAGTCCTCACGGTCCTGTGATCACAGAGGAAAGGCAGCAGCGCGACAGCACCAGCAGATGCAGCATCTGCATGATGAATGACCCCAACCAATGATACAAGCCAATGGTATTTTCTAAACTGCACTGAGAATGCACATCAACACATCACTTGTTGTTTGAGTGATTGAGATGCTTTTTGGTCACTTTGTTTTTGGAGAGGACAAGAATGAACATTATTTGTGACCATTGAACTACACAGCTGTGAACTTTTTACTTCATGGGATTTGTTCCAACATAACCTCTTTACACAGCACGCATCTTTGCTTCTTGTCTTTGATTTCATTTTGGTGC
Associated Phenotype:
Not determined