ZMP
cacna1c
Ensembl ID:
ZFIN ID:
Description:
voltage-dependent L-type calcium channel subunit alpha-1C [Source:RefSeq peptide;Acc:NP_571975]
Human Orthologue:
CACNA1C
Human Description:
calcium channel, voltage-dependent, L type, alpha 1C subunit [Source:HGNC Symbol;Acc:1390]
Mouse Orthologue:
Cacna1c
Mouse Description:
calcium channel, voltage-dependent, L type, alpha 1C subunit Gene [Source:MGI Symbol;Acc:MGI:103013]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa10930 | Nonsense | Available for shipment | Available now |
| sa6050 | Essential Splice Site | Confirmed mutation in F2 line | Not yet available |
| sa6943 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa44588 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa40287 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa38439 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa15296 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10930
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 |
|---|---|---|---|---|---|
| ENSDART00000016938 | Nonsense | 291 | 2195 | 7 | 49 |
| ENSDART00000028856 | Nonsense | 292 | 2168 | 6 | 47 |
| ENSDART00000132909 | Nonsense | 292 | 2196 | 6 | 48 |
Genomic Location (Zv9):
Chromosome 4 (position 19371735)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 20715070 |
| GRCz11 | 4 | 20436045 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTCCCCTCCTTCACATCGCTCTGCTCRTTCTGTTCGTCATCATCATTTA[T/A]GCCATCRTCGGCCTCGAGCTCTTCATGGGCAAGATGCATAGAACCTGTTT
Long Flanking Sequence:
ATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAACCTCTAAGTGGCATCTAGAATAAGCATTTTTCTTTGCCTGTCATGTTTATTTTATGTTAAAATCAATGAAAATAACCTATTCTTTGCCATAAAAAAGTAAAATTACTGAATCAAGACATAGGAGCCTGAGAAAAAAGCAAATGTTTTTGCATCTGAACTCTTCATATATGTTTTCTTATATATTAAAGGTCAACAATTAGCAGAACAGTTTTTTGCAGATTTTTGCGAGTGGGCCTGCTGATAATATACAATATGTTAATAATAAATCCTTCATTCCCAAAATCCCCAGAGAGAAATCCTTCTCTTCTGTGTTTTTAGCTTTGTTTCCTGTCTGCTTGCAGGTTTACAGGTGGTGCTGAACTCCATCATTAAAGCCATGGTTCCCCTCCTTCACATCGCTCTGCTCGTTCTGTTCGTCATCATCATTTA[T/A]GCCATCATCGGCCTCGAGCTCTTCATGGGCAAGATGCATAGAACCTGTTTCTTCTATAAAGATGGACACAAAGGTCAGGACTTCAGCTTTTGCTTCTCCCTTGAACTAGTCATTGACCCTGGTGTTTACCCAGATCAACTGTTTACTTTTAGGTCATATAGCTGAAGAGAAGCCGGCCCCCTGCGCTCCAAGCTCCGCCCATGGAAGACACTGCTCTCCGCCCAACATAACGCAGTGCATGATGGGATGGGAGGGCCCAAATGATGGAATCACGAACTTTGATAACTTTGCATTTGCCATGCTGACTGTGTTTCAGTGCATCACGATGGAGGGCTGGACTGATGTCCTGTACTGGGTGAGTCTGCTCCAGTATCGGCACACTACACAGTCCAGTATAGAGAGGCTCGAACATCTACTTTACTGAGACATATGTATAAGACAGAATTATCAATAAATCACACTCCTTAGTTTATATCCTAAAGGACACCTACTGGTCTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6050
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000016938 | Essential Splice Site | 316 | 2195 | 7 | 49 |
| ENSDART00000028856 | Essential Splice Site | 317 | 2168 | 6 | 47 |
| ENSDART00000132909 | Essential Splice Site | 317 | 2196 | 6 | 48 |
Genomic Location (Zv9):
Chromosome 4 (position 19371810)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 20715145 |
| GRCz11 | 4 | 20436120 |
KASP Assay ID:
554-3675.1 (used for ordering genotyping assays)
KASP Sequence:
ATGGGCAAGATGCATAGAACCTGTTTCTTCTATAAAGATGGACACAAAGG[T/G]CAGGACTTCAKCTTTTGCTTCTCCCTTGAACTAGTCATTGACCCTGKTGT
Long Flanking Sequence:
TAAGTGGCATCTAGAATAAGCATTTTTCTTTGCCTGTCATGTTTATTTTATGTTAAAATCAATGAAAATAACCTATTCTTTGCCATAAAAAAGTAAAATTACTGAATCAAGACATAGGAGCCTGAGAAAAAAGCAAATGTTTTTGCATCTGAACTCTTCATATATGTTTTCTTATATATTAAAGGTCAACAATTAGCAGAACAGTTTTTTGCAGATTTTTGCGAGTGGGCCTGCTGATAATATACAATATGTTAATAATAAATCCTTCATTCCCAAAATCCCCAGAGAGAAATCCTTCTCTTCTGTGTTTTTAGCTTTGTTTCCTGTCTGCTTGCAGGTTTACAGGTGGTGCTGAACTCCATCATTAAAGCCATGGTTCCCCTCCTTCACATCGCTCTGCTCGTTCTGTTCGTCATCATCATTTATGCCATCATCGGCCTCGAGCTCTTCATGGGCAAGATGCATAGAACCTGTTTCTTCTATAAAGATGGACACAAAGG[T/G]CAGGACTTCAGCTTTTGCTTCTCCCTTGAACTAGTCATTGACCCTGGTGTTTACCCAGATCAACTGTTTACTTTTAGGTCATATAGCTGAAGAGAAGCCGGCCCCCTGCGCTCCAAGCTCCGCCCATGGAAGACACTGCTCTCCGCCCAACATAACGCAGTGCATGATGGGATGGGAGGGCCCAAATGATGGAATCACGAACTTTGATAACTTTGCATTTGCCATGCTGACTGTGTTTCAGTGCATCACGATGGAGGGCTGGACTGATGTCCTGTACTGGGTGAGTCTGCTCCAGTATCGGCACACTACACAGTCCAGTATAGAGAGGCTCGAACATCTACTTTACTGAGACATATGTATAAGACAGAATTATCAATAAATCACACTCCTTAGTTTATATCCTAAAGGACACCTACTGGTCTTTCCCAGTTAGGGAGAAAGGTAGCACTTCGTTTTTGATGGTCCCTTTTAGACATTTGGTTTAATATAATATATAGTAA
Associated Phenotype:
This allele has been associated with this phenotype by genetic linkage analysis and may not be causal.
See FAQs for more info.
See FAQs for more info.
| Stage | Entity | Entity | Quality | Tag |
|---|---|---|---|---|
| Larval:Day 4 ZFS:0000036 |
eye ZFA:0000107 |
decreased size PATO:0000587 |
abnormal PATO:0000460 |
|
| Larval:Day 4 ZFS:0000036 |
gut ZFA:0000112 |
edematous PATO:0001450 |
abnormal PATO:0000460 |
|
| Larval:Day 4 ZFS:0000036 |
head ZFA:0001114 |
decreased size PATO:0000587 |
abnormal PATO:0000460 |
|
| Larval:Day 4 ZFS:0000036 |
locomotory behavior GO:0007626 |
quality PATO:0000001 |
abnormal PATO:0000460 |
|
| Larval:Day 4 ZFS:0000036 |
pericardium ZFA:0000054 |
edematous PATO:0001450 |
abnormal PATO:0000460 |
|
| Larval:Day 4 ZFS:0000036 |
sensory perception of sound GO:0007605 |
absent PATO:0000462 |
abnormal PATO:0000460 |
|
| Larval:Day 4 ZFS:0000036 |
skeletal muscle ZFA:0005277 |
degenerate PATO:0000639 |
abnormal PATO:0000460 |
|
| Larval:Day 4 ZFS:0000036 |
whole organism ZFA:0001094 |
anterior/posterior axis BSPO:0000013 |
decreased length PATO:0000574 |
abnormal PATO:0000460 |
| Larval:Day 4 ZFS:0000036 |
yolk ZFA:0000084 |
necrotic PATO:0000647 |
abnormal PATO:0000460 |
Mutation Details
Allele Name:
sa6943
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 |
|---|---|---|---|---|---|
| ENSDART00000016938 | Essential Splice Site | 569 | 2195 | 13 | 49 |
| ENSDART00000028856 | Essential Splice Site | 570 | 2168 | 12 | 47 |
| ENSDART00000132909 | Essential Splice Site | 570 | 2196 | 12 | 48 |
Genomic Location (Zv9):
Chromosome 4 (position 19382628)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 20725963 |
| GRCz11 | 4 | 20446938 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTGCCTCAGAGCATCACCAGCAGCCGGAGTGGCTCACCAATGTACAAGG[T/C]AMTCTACATTACAARGCTGTACATWTATCAMCATACTAATACTGACACTT
Long Flanking Sequence:
GTGTGTTTGTTGTGTTTTGATGCCAGTGTTGTGTTTTGATCATCACGGTGGCCCTCGAATCAGTGGCTAGATATCCATTAACGAGTTCAGACTGCCAGCGTTATTCAGATCAGATTTGTTTGCTATTTACCAAAAGAATCAAGAGCAGCAGTATTTACAGTCACTGCTAGCTGAAACACACATACAGTAGTTTTTATATTTCCAGAGAGTGCATTTAGTGAATACTGCATTCAGTAGGAATTGTGTCAGGATGCACAGATTTAAAACTTTGAACTTTTCATACAATTTTCCATCCTCCCTCTTTCTCTGTTTCTCTCTCTATCTCTTTGTATTTACAGTCGATATTCACGCCGGTGGAATCGGTTATGTCGGCGTAAGTGCCGTGCAGCAGTGAAATCAAACGTCTTCTACTGGCTGGTGATTTTTCTGGTATTTTTGAACACACTTACTATTGCCTCAGAGCATCACCAGCAGCCGGAGTGGCTCACCAATGTACAAGG[T/C]AATCTACATTACAAAGCTGTACATATATCACCATACTAATACTGACACTTCAAGAAATAGCTCCGCTCTCAACCCCTAGCCATATGCCATAGCATTTTTATTACCATTTAAAATAAGAGATTTAACATATTTTATTGAGAAATTTATTGTAAATGTGTATGTAGATGTGAGTTTTCAGCTATTCTTTGGTCCTTCATAAATTCATAAATGAACATTGAAAAATTACAAATGTCTGTCACTTAACGGCCACCTTTGATTGATACATCTTTTCTAAATAAAATTTTTCATTTAAAATAATAAGAACAAGACTGTATTTCATAATGATTGTTATTTTAGGTGTTATTATTGTGGTTTATGAATCTCACACTGAATAAATGTGTTGTTTATGTACTTACAGATATAGCCAATAAGGTGCTGCTGGCTCTCTTTACGGGTGAGATGCTGTTAAAGATGTACAGTCTGGGCCTACAGGCCTATTTTGTCTCCCTTTTCAACCGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44588
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 |
|---|---|---|---|---|---|
| ENSDART00000016938 | Nonsense | 595 | 2195 | 14 | 49 |
| ENSDART00000028856 | Nonsense | 596 | 2168 | 13 | 47 |
| ENSDART00000132909 | Nonsense | 596 | 2196 | 13 | 48 |
Genomic Location (Zv9):
Chromosome 4 (position 19383105)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 20726440 |
| GRCz11 | 4 | 20447415 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTACGGGTGAGATGCTGTTAAAGATGTACAGTCTGGGCCTACAGGCCTA[T/A]TTTGTCTCCCTTTTCAACCGATTTGACAGCTTTGTGGTGTGCGGTGGGAT
Long Flanking Sequence:
GAGTGGCTCACCAATGTACAAGGTAATCTACATTACAAAGCTGTACATATATCACCATACTAATACTGACACTTCAAGAAATAGCTCCGCTCTCAACCCCTAGCCATATGCCATAGCATTTTTATTACCATTTAAAATAAGAGATTTAACATATTTTATTGAGAAATTTATTGTAAATGTGTATGTAGATGTGAGTTTTCAGCTATTCTTTGGTCCTTCATAAATTCATAAATGAACATTGAAAAATTACAAATGTCTGTCACTTAACGGCCACCTTTGATTGATACATCTTTTCTAAATAAAATTTTTCATTTAAAATAATAAGAACAAGACTGTATTTCATAATGATTGTTATTTTAGGTGTTATTATTGTGGTTTATGAATCTCACACTGAATAAATGTGTTGTTTATGTACTTACAGATATAGCCAATAAGGTGCTGCTGGCTCTCTTTACGGGTGAGATGCTGTTAAAGATGTACAGTCTGGGCCTACAGGCCTA[T/A]TTTGTCTCCCTTTTCAACCGATTTGACAGCTTTGTGGTGTGCGGTGGGATTCTGGAAACCATCCTGGTGGAGACCAAAATAATGTCACCCCTGGGCATCTCTGTGTTGCGCTGCGTACGTCTGCTTCGCATCTTCAAGATCACCAGGTGTGTGTTAAAGATGTGTGTGTACTGTATGTTTAGGTCTTTTATTTTATGTTTATACTAATGAATACTGTCTACTTTCAGATACTGGAACTCTCTGAGTAATCTAGTGGCGTCTCTGTTGAACTCTGTGCGTTCGATCGCATCCCTGTTACTGCTGCTCTTCCTCTTCATTATCATCTTCAGTCTGCTCGGAATGCAGCTCTTTGGTGGAAAGTTCAACTTTGATGAGACTCGACGCAGCACATTTGATAATTTCCCTCAGTCTCTCCTCACCGTCTTTCAGGTTCTGCCACAGTCACACTCACAGCACACACTTGCAATATGGCTTTAAACAGGACTCGTGTTTGATTTGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40287
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000016938 | Nonsense | 718 | 2195 | 16 | 49 |
| ENSDART00000028856 | Nonsense | 719 | 2168 | 15 | 47 |
| ENSDART00000132909 | Nonsense | 719 | 2196 | 15 | 48 |
Genomic Location (Zv9):
Chromosome 4 (position 19383643)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 20726978 |
| GRCz11 | 4 | 20447953 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTGATTTGAATAATGTTTGTTGTCACAGATTTTGACCGGAGAGGACT[G/A]GAACTCTGTAATGTACGATGGCATCATGGCGTATGGAGGGCCGTCCTTTC
Long Flanking Sequence:
TGTGCGGTGGGATTCTGGAAACCATCCTGGTGGAGACCAAAATAATGTCACCCCTGGGCATCTCTGTGTTGCGCTGCGTACGTCTGCTTCGCATCTTCAAGATCACCAGGTGTGTGTTAAAGATGTGTGTGTACTGTATGTTTAGGTCTTTTATTTTATGTTTATACTAATGAATACTGTCTACTTTCAGATACTGGAACTCTCTGAGTAATCTAGTGGCGTCTCTGTTGAACTCTGTGCGTTCGATCGCATCCCTGTTACTGCTGCTCTTCCTCTTCATTATCATCTTCAGTCTGCTCGGAATGCAGCTCTTTGGTGGAAAGTTCAACTTTGATGAGACTCGACGCAGCACATTTGATAATTTCCCTCAGTCTCTCCTCACCGTCTTTCAGGTTCTGCCACAGTCACACTCACAGCACACACTTGCAATATGGCTTTAAACAGGACTCGTGTTTGATTTGAATAATGTTTGTTGTCACAGATTTTGACCGGAGAGGACT[G/A]GAACTCTGTAATGTACGATGGCATCATGGCGTATGGAGGGCCGTCCTTTCCTGGCATGCTTGTCTGCATTTACTTCATCATCCTCTTCATCTGTGGAAACTGTATCCTTAAAGCACCAGTTTGATGTGACACAAAAAAAGAAACAATCTGATTATAAAACTGATAGTTCTGTTCCTGAACTCTAAACAGACATCCTCCTGAATGTCTTCTTGGCCATTGCTGTGGACAACCTCGCAGACGCAGAGAGTCTAACATCAGCGCAGAAAGAGGAAGAGGAGGAGAAAGAGAGAAAGAAGCTGGCCAGGTTTAGTGACTCAGAGTTCACTTGAGTGCAGTGTTTTGAGATGGTCTGAGGGCCCATAAAACCTTCCTATGAGGATTTCCTGTCTCCTGCCTAATGAGCTCATTTAGACTGGATCAGTTATGACTTCATTAATTTAACATTGAGGAAATTAAGTATCATTTTACAGAAGTGTTTTTGCCCCTCTGAAGAGCTGTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38439
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 |
|---|---|---|---|---|---|
| ENSDART00000016938 | Essential Splice Site | 1081 | 2195 | 26 | 49 |
| ENSDART00000028856 | Essential Splice Site | 1082 | 2168 | 25 | 47 |
| ENSDART00000132909 | Essential Splice Site | 1082 | 2196 | 25 | 48 |
Genomic Location (Zv9):
Chromosome 4 (position 19387702)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 20731037 |
| GRCz11 | 4 | 20452012 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATTCTTCTACTGCACAGACACTTCTAAACAGACGCAGGCTGAGTGCAGG[T/C]GAAATCTCTTTGTCTTTGCCTATTAAGTTCAATATTTACAGTAAATAAAA
Long Flanking Sequence:
AGGGTGTTGAGGCCCCTGAGAGCAATCAACAGAGCCAAGGGCCTCAAAGTGAGTCTTTCTGTCTCATTCATAAAAATTGCACACATCTCTGTTCAGAGGCTGGCCTACAGTTTTCATACAATATAATGGATGTGCTGAGCATTTATTTTAATTGAGAGCCTTGTTTGCATTCACAGCATGTGGTTCAGTGTGTGTTTGTTGCCATCCGCACCATCGGGAATATCGTCATCGTCACCTCTTTGCTGCAGTTCATGTTTGCCTGTATTGGTGTTCAACTCTTTAAGGTAAGTTCTGCTGTTTCACTCTTTATAGATAATTGATAAAAATATATTTGTCTACAGAGAAAATTCTAAGTTTTTTCCTGGAACCCAGCTGTGTGTTGTTTGCACTTATTACAGTATTATTTAGTGTTAAATGCATGTAAACTGATGTTTTTTTTTATCTAGGGCAAATTCTTCTACTGCACAGACACTTCTAAACAGACGCAGGCTGAGTGCAGG[T/C]GAAATCTCTTTGTCTTTGCCTATTAAGTTCAATATTTACAGTAAATAAAAAAAGGTCATTAATATGTATATATGTGTGTGTGTTTTCTTTTTAACAGAGGGGCCTATATACTGTACAAGGATGGGAATGTTGGAAAGCCAGAGAAAGCTCAACGCTCCTGGGAGAACAGTGACTTCAACTTTGATGATGTCCTACAGGGCATGATGGCTCTGTTTGCTGTGTCCACTTTTGAGGGTTGGCCAGGGTGCGAGACACAAACAATCACATACACTACTTTTTAATATTCATTTGAAAATGTAATTAATACTTTTTGGTATCTGTTTTAATCTGTTTTAATTATCTGTTTTTGACCATCAATTGTATATACCTTACCAATAACTTTTAACTGTAAGAATACAAGGTGTGCCGTGTGAGCAGGTTCATATGCATGTCTCATGCTAAAATGTGTAAGACTTGAAAGCCCCCTTTTAAATATACATAGTCTAATTTAACCTAATCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15296
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 |
|---|---|---|---|---|---|
| ENSDART00000016938 | Essential Splice Site | 1510 | 2195 | 37 | 49 |
| ENSDART00000028856 | Essential Splice Site | 1483 | 2168 | 35 | 47 |
| ENSDART00000132909 | Essential Splice Site | 1511 | 2196 | 36 | 48 |
Genomic Location (Zv9):
Chromosome 4 (position 19400632)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 20743967 |
| GRCz11 | 4 | 20464942 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTTGCCATCTTCTACTTTGTTAGCTTTTATATGCTTTGCGCCTTYCTGG[T/C]GAGYTGACATCGATATRTCTTTCCAGTAAGCAACTTTGTTATTGTATATC
Long Flanking Sequence:
CATTGCTGATCGTAATGCTGTTCTTCATTTATGCCGTCATTGGGATGCAGGTCAGATGCAGCTTTATTTGCTCTTCCAAACTTCCTCCTCCTCTTTCCCCAAAGAGGTGCATTGATGTCTGTTACAGCTCCTGTACTTGTGCACAATTCATGATGTATTTTTGACTCCACAGATGTTTGGCAAAATCGCCCTGAGGGACAACAGTCAGATCAACCGAAACAACAACTTTCAGACATTTCCTCAGGCTGTTCTGCTTCTCTTCAGGTCAGTTTCCATCTAGCTCTCTCTCTCCATCACTCATTTGGTGTCTCTTTCTCACTCTGAGCTTGTGTATTTGTGTAGGTGTGCGACAGGAGAGGCGTGGCAGGAAATCATGCTGGCCTGTTCTCCAAACCGCCCTTGTGAGAAGGGGTCAGAGATCAACCATTCCAGCGAAGACTGTGGCAGTCACTTTGCCATCTTCTACTTTGTTAGCTTTTATATGCTTTGCGCCTTCCTGG[T/C]GAGTTGACATCGATATATCTTTCCAGTAAGCAACTTTGTTATTGTATATCAGCTGTGAATGTTGCTGTCAAATCTTCTCTCCCAGCATGACATCTTTTACCCCCTCCGTACAGTGTTTATCGTATCCATAATAATAGAAGCAGCGGGTGTGATTCAGGGGTTTGTGAGCCACTGTGATTTAGATTCTTCCTCTCCCGCAGATCATTAACCTTTTTGTGGCTGTCATCATGGACAACTTTGACTATTTAACACGGGATTGGTCGATACTGGGACCGCATCATCTAGATGAGTTCAAAAGAATATGGGCAGAATATGATCCTGAGGCTAAGTCAGTCACTCCTGTTTTGCCAACTTTCTCACTTGCACTTTCTCTAATCATCAATGTTTTTTAAAGAGATATACTTATACTTAGATTATTCAAATTAATATTATCATGCAGGGGTCGGATAAAGCATCTGGATGTAGTCACGTTACTGCGCAGAATTCAGCCACCTCTTGGA
Associated Phenotype:
Not determined