ZMP
zgc:175192
Ensembl ID:
ZFIN ID:
Description:
breast cancer anti-estrogen resistance 1 [Source:RefSeq peptide;Acc:NP_001128605]
Human Orthologue:
BCAR1
Human Description:
breast cancer anti-estrogen resistance 1 [Source:HGNC Symbol;Acc:971]
Mouse Orthologue:
Bcar1
Mouse Description:
breast cancer anti-estrogen resistance 1 Gene [Source:MGI Symbol;Acc:MGI:108091]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36652 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11775 | Nonsense | Available for shipment | Available now |
sa9019 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39201 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa391 | Nonsense | Available for shipment | Available now |
sa1865 | Nonsense | F2 line generated | Not yet available |
sa11159 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa36652
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 |
---|---|---|---|---|---|
ENSDART00000058772 | Nonsense | 70 | 919 | 2 | 7 |
ENSDART00000126899 | Nonsense | 70 | 919 | 2 | 7 |
ENSDART00000128965 | Nonsense | 70 | 919 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 18 (position 22411516)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 22641739 |
GRCz11 | 18 | 22630805 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAATTGTTCCTGGCAACCGGCTGAAGATTCTCGTTGGCATGTATGATAAG[C/T]AGCAACAGCAGCAGCTACAGCAGTTAGCGAACCAACCCAGCCCAACCCAG
Long Flanking Sequence:
GGTCACCACAGAGGATGCTCTTTCAGCTGCAACCCAGTACTGGGAAAAATCTTTACACACTCATACATCATATGCTCATACATTATGGCCAATTTAGTTTATTCAATTCACCTACCGACACGAATATAGAGAGAACAAGCAAACTCCACACAGAAATGCTAACTGACTAAGCTAGGCCTTGAACTAGCAACCTTCTTGCTATGAGGCGATTATGCTACCCACTTTGCCACCGTGTCGCCCTCTATTTTGAGTTACACTCTTCATTTTATAACATAAACTTAACCTTTCTCTCTTCTCTCTTGCAGAATGTGTTGGCAAAAGCCCTGTATGACAATGTGGCGGAGTCTCCAGACGAGTTGTCCTTTCGGAAGGGCGACATCATGACCGTGCTGGAGCGGGACACGCAGGGCTTGGAAGGCTGGTGGCTCTGTTCGCTGCATGGCCGGCAAGGAATTGTTCCTGGCAACCGGCTGAAGATTCTCGTTGGCATGTATGATAAG[C/T]AGCAACAGCAGCAGCTACAGCAGTTAGCGAACCAACCCAGCCCAACCCAGAGCCTCATCAACCTGCCTCAGAGTGCCTACAACAAGATACCCCCTGCAGCCCAGTACACGGCCATGCACCCCGCCTTCACCCCCTCTGGCTCTGCCAACTCCACCAACCCAGACGGCGTTTACATGCTGCCCCCCAGCCATGGCTCTAGCCTCTACCAGGTGCCCTCCGGCCCCCCGACTCCACAGCCCCAACCCAAGGCCCCCGCTTTAGCAAAGAAGCAAACTCATGTGCAGTACCCTCCCACTACACAGGATGTCTACCAGGTGCCCCCCTCCATTAACGCACCAGGCCAGGACATCTACCAGGTGCCACCCGCTGCAGGAGGGCAGTGTCCCGGGCAGGACGTGTACCAGGTGCCACCCTCTGTGAACCAGACACAGGATGTTTACCAGATTCCCCCATCTTTAGACAGGAGCTGGGACTCTCCCAAACCCATGGGGAAGGTAGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11775
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 |
---|---|---|---|---|---|
ENSDART00000058772 | Nonsense | 72 | 919 | 2 | 7 |
ENSDART00000126899 | Nonsense | 72 | 919 | 2 | 7 |
ENSDART00000128965 | Nonsense | 72 | 919 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 18 (position 22411522)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 22641745 |
GRCz11 | 18 | 22630811 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCCTGGCAACCGGCTGAARATTCTCGTTGGCAWGTATGATAAGCAGCAA[C/T]AGCAGCAGCTACAGCAGTTAGCGAACCAAMCCAGCCCAACCCAGAGCCTC
Long Flanking Sequence:
CACAGAGGATGCTCTTTCAGCTGCAACCCAGTACTGGGAAAAATCTTTACACACTCATACATCATATGCTCATACATTATGGCCAATTTAGTTTATTCAATTCACCTACCGACACGAATATAGAGAGAACAAGCAAACTCCACACAGAAATGCTAACTGACTAAGCTAGGCCTTGAACTAGCAACCTTCTTGCTATGAGGCGATTATGCTACCCACTTTGCCACCGTGTCGCCCTCTATTTTGAGTTACACTCTTCATTTTATAACATAAACTTAACCTTTCTCTCTTCTCTCTTGCAGAATGTGTTGGCAAAAGCCCTGTATGACAATGTGGCGGAGTCTCCAGACGAGTTGTCCTTTCGGAAGGGCGACATCATGACCGTGCTGGAGCGGGACACGCAGGGCTTGGAAGGCTGGTGGCTCTGTTCGCTGCATGGCCGGCAAGGAATTGTTCCTGGCAACCGGCTGAAGATTCTCGTTGGCATGTATGATAAGCAGCAA[C/T]AGCAGCAGCTACAGCAGTTAGCGAACCAACCCAGCCCAACCCAGAGCCTCATCAACCTGCCTCAGAGTGCCTACAACAAGATACCCCCTGCAGCCCAGTACACGGCCATGCACCCCGCCTTCACCCCCTCTGGCTCTGCCAACTCCACCAACCCAGACGGCGTTTACATGCTGCCCCCCAGCCATGGCTCTAGCCTCTACCAGGTGCCCTCCGGCCCCCCGACTCCACAGCCCCAACCCAAGGCCCCCGCTTTAGCAAAGAAGCAAACTCATGTGCAGTACCCTCCCACTACACAGGATGTCTACCAGGTGCCCCCCTCCATTAACGCACCAGGCCAGGACATCTACCAGGTGCCACCCGCTGCAGGAGGGCAGTGTCCCGGGCAGGACGTGTACCAGGTGCCACCCTCTGTGAACCAGACACAGGATGTTTACCAGATTCCCCCATCTTTAGACAGGAGCTGGGACTCTCCCAAACCCATGGGGAAGGTAGGGAAAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9019
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 |
---|---|---|---|---|---|
ENSDART00000058772 | Nonsense | 276 | 919 | 3 | 7 |
ENSDART00000126899 | Nonsense | 276 | 919 | 3 | 7 |
ENSDART00000128965 | Nonsense | 276 | 919 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 18 (position 22450513)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 22680736 |
GRCz11 | 18 | 22669802 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCCGAGAYACCTTCCACCCAGCCAGGACATCTATGACGTGCCACCCACC[C/T]GAACCCAGTACATCCAAMAGGTAAAGAGTTCAGCAGAAAGAGCGACTGTG
Long Flanking Sequence:
AAACTGCAGCCAACAGTAAATTAGAGACAAAATGGAAAATCTAACAATGCATCAAAGCCGATTTTGTTACTAATCGTTCACATGTCCAAAACTGTGATAAAAGGTTAAAAAACTCCAGTCCACAATTAAGTTTTATATTAAAAATACATAATTTTGTGTTTTTTTTTCACCAAATCAGTGATATCATTTGTGAACTTGGCAATTAAAGAGGTAAAATCCTGTAATTTTGAGGTTGAGGTTGATTAACAGATAAAAACCTTGACCAAATCGATCATAAATAAAGTGCATCAGTTATCAACATTATTATCAGAATTATCAACAATCAATCACCAGTTAATTGTTTGCATCTCATGCAGTTGTTTTTCTGTCTTTCTCAGGTTGTTGTTCCCACACGGGTTGGTCAAGTCTATGTGTATGACACGGGAAAAAATGAACAGGACGAATATGATGTCCCGAGACACCTTCCACCCAGCCAGGACATCTATGACGTGCCACCCACC[C/T]GAACCCAGTACATCCAACAGGTAAAGAGTTCAGCAGAAAGAGCGACTGTGTCACTGCCTTGAGTTACAGATGTGCTTTAATGTCCATGTGAAGATCATTACACTGTAGGTTATTTGATAGCTTGTAATTTGTGCCTGAGCCAGTTGAAAATCGTTATTGATGATAATAGTCTTTAAGTGAATCGCAGACATCTGTAATGTGTGTGTGAGTGTGTGTGTAATAGATGATCGTCACACACTCTGGCAGACTCTAGAGAAGAGCCTTCACACTCATTAATAATACAAGCAATGAGAATATAAAATCCTTCCTTCATTTTCTTGCTTTCCTACAAGAATTTCCATTAATTGTTTGAAGATTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCGATTTTCTTTTTCTTTCTTTCTTTTTTTTCTTTCTCCTGATTTTGAAGATTTTTCTCATTCATTCTTTCTTTCATTCTTTTGAAAGATTTTCTTTCTTTCATTCTTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39201
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 |
---|---|---|---|---|---|
ENSDART00000058772 | Essential Splice Site | 317 | 919 | 4 | 7 |
ENSDART00000126899 | Essential Splice Site | 317 | 919 | 4 | 7 |
ENSDART00000128965 | Essential Splice Site | 317 | 919 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 18 (position 22458093)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 22688316 |
GRCz11 | 18 | 22677382 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGACACTCCACCTAGTGTGGATAAGAGCCAGCTGCACTACCAACAAACGG[T/C]ACCCATCCATCTTTTTCATATTTATCTTATTTGCATATTTGATCTGCACA
Long Flanking Sequence:
GAAAGAGAGCGATTGTAGGTGAAGGTGGAGGTCAGCGTCTCTGCAGAACTGCTGATTTCCTCCAGCTGTTGCTGTCTGAGGTCGTGCTCCTGTAATCTCTCCACATCAGTGTGAATGTGTCCCCTATTGAGTGTACCTGTGCTCCTTTTGACCCCCATTCATCCAAGTGCCTCGATTCCAAATCTGCTCTAACATGCACAAAAAAATAAGGGAAGTAAAAAATGGTTCAAAGTTTCTATGAGGTAGAGAAAAACCAAGGGCTCTGAAAAACAAATCAATAAAATGGGCAGAAACATAATTCAATTCAAGCCGGATCTACTTCTTGTCATGTATTTATGTCTTAAATTTAAATATGTGTGTCTTTTTTTGACCCTGTACTCTCTCTGTGCCACAGGTTTATGATACTCCTCCTATGGCAATGAAAGGCCCACCCAGTGGTCAGGAAATCTACGACACTCCACCTAGTGTGGATAAGAGCCAGCTGCACTACCAACAAACGG[T/C]ACCCATCCATCTTTTTCATATTTATCTTATTTGCATATTTGATCTGCACATTAATGGGTGCTTAAGAGATCTGAATTGCCTGAAACAAAATGCCACAAGTCTCTAATACATGCAGAAAGGATTGTGTAAGTGATTGCTACTTTTAGCCAGACTTGGCAACTGTATTACTGTTGACCGCCAGCTTCAAACACATGCTGCCCCTCCTAAACTCTACCCACTAATGACATCTCAGCCAATCTGACGACAGCAAATCATACAGCGTTAAATGATTCACAAGCAGAAATATTTTCTGATTGGCTAGTCAGTCAAACACAACACCTGTTTCATTTATATCTAGGAAGAATAATGTCAGCCCCCTCCCCCAACACAGCATCCAAAAGAAACAACAACCTTGCAGCACTATCAAATAGTGTTTAATTTTTTTAACAGTTCTAGACTGAACAAAATGATGTGAAACAAATTTCACTCATAAATTGCTAGTGTGTTTTACATCAAGTAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa391
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 |
---|---|---|---|---|---|
ENSDART00000058772 | Nonsense | 319 | 919 | 5 | 7 |
ENSDART00000126899 | Nonsense | 319 | 919 | 5 | 7 |
ENSDART00000128965 | Nonsense | 319 | 919 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 18 (position 22459837)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 22690060 |
GRCz11 | 18 | 22679126 |
KASP Assay ID:
554-0253.1 (used for ordering genotyping assays)
KASP Sequence:
ATTATAGGAGGCTTGTTTTGGTAAACACATTATTTCTTTTTACAGGTATA[T/A]GACATTCCTCCATCTGTCAGCAAAGACGTTCCAGATGGTCCAATCAGGGA
Long Flanking Sequence:
AAGATTTATGTACATTTGGCAAGCTGAACGCATTCTTTACTGTACAGGAGACACGGCATGGAGAAGATTGATTGACAATGGTCTAAATACATCTGTCATAGGGTGCAGAACACAATGCACCAATCAGGACGCAGAACACACTGAAAACATCAGTGAAACTACAAGGCTGCGAAAATGTGAACCGCATCATAGCGAGGGACCACTGTATTTTTACATTAATTAATGCTTGCTAACATCTAATGCTTGAAATAATATTTAACTGTTGCATAATTGAAGTTTTAAAGATCAACTCTTTGGCAAATCTCAAATGCAATCCGTTTGTTCATTTATATATGTTTTTATATTATAAGGGTGTAACACCTAAATTCCCTTGAAACCTTTAAAATGGCTTACACTCAACTTATATGAACCAAAAATGTAACAATCAGATCACTAATGACTTCAGTTATGATTATAGGAGGCTTGTTTTGGTAAACACATTATTTCTTTTTACAGGTATA[T/A]GACATTCCTCCATCTGTCAGCAAAGACGTTCCAGATGGTCCAATCAGGGAGGAAACGTACGACGTTCCTCCTCATTTTGCCAAGATGAAGAGCCTGGAGAATCAGAACCAAGCCTATCTGTCTCAGATCCCTGGCGGTCCCGAGCCTCCCATACCAGAGGATGTCTATGATGTTCCTCCTCCTCAGCTAATAGGAAAACGACAGCCTGAGGGCCAGGAGATCTACGACATCCCTGCCAGCCTGCGAAAAGGTGGCCCACAGGACCACCACCCCACAGATGTGTACGACTTCCCTCGTGAGCGCCCAGCAGGCGAAGATTCAGGCGATTACGTGTATGATGTGCCTCCACAGGTGGTCCGTGATGCAGCGGCCACCGAGGAGCTCACGGTCAGCTTCAAACGGCTGTCAGCGTCCAGCACTGGAAGCACTCGCAGTAATCTCTCCACGTCCTCTTTAGACATGGTGCCAGTGCGGGAATCTTCTGGGCCAGGTCGCTTGCT
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:
sa1865
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 |
---|---|---|---|---|---|
ENSDART00000058772 | Nonsense | 502 | 919 | 5 | 7 |
ENSDART00000126899 | Nonsense | 502 | 919 | 5 | 7 |
ENSDART00000128965 | Nonsense | 502 | 919 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 18 (position 22460384)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 22690607 |
GRCz11 | 18 | 22679673 |
KASP Assay ID:
554-1856.1 (used for ordering genotyping assays)
KASP Sequence:
TGCTGCTCCTGGATCTGGACCAGGCTATGGAGCGKCTGTCCCGTCATCAA[C/T]AGGCTGTGGARAGCTCYGTTTCWCTCCTCATGTCGTTCATCAGTGGAAAC
Long Flanking Sequence:
GGGAGGAAACGTACGACGTTCCTCCTCATTTTGCCAAGATGAAGAGCCTGGAGAATCAGAACCAAGCCTATCTGTCTCAGATCCCTGGCGGTCCCGAGCCTCCCATACCAGAGGATGTCTATGATGTTCCTCCTCCTCAGCTAATAGGAAAACGACAGCCTGAGGGCCAGGAGATCTACGACATCCCTGCCAGCCTGCGAAAAGGTGGCCCACAGGACCACCACCCCACAGATGTGTACGACTTCCCTCGTGAGCGCCCAGCAGGCGAAGATTCAGGCGATTACGTGTATGATGTGCCTCCACAGGTGGTCCGTGATGCAGCGGCCACCGAGGAGCTCACGGTCAGCTTCAAACGGCTGTCAGCGTCCAGCACTGGAAGCACTCGCAGTAATCTCTCCACGTCCTCTTTAGACATGGTGCCAGTGCGGGAATCTTCTGGGCCAGGTCGCTTGCTGCTCCTGGATCTGGACCAGGCTATGGAGCGTCTGTCCCGTCATCAA[C/T]AGGCTGTGGAGAGCTCCGTTTCTCTCCTCATGTCGTTCATCAGTGGAAACTGGCGCAGCTCCACTCAGATGGAGTCCAACCTCCCTGCCATCCGACAGGCCGTGGACCGCATCCGTGTGGCAGTCAGGGACCTGCTGGAATTCGCTAGAGGTGCTGTAGCCAATGCCACCCAGGCCACCGACCGCACACTGCAGACCAAGCTTGGCAAGCAGGTGCAGAAGATGGAGGAGGCCTTCCAAGGTCTGGTGAGGTACAGTCAGGCACTGGACACTTTGGGCTGGTCCCCTGCAGCCCTGATGACATCTCAGCCAGGCACAGGTGGGGATGACCTGGACCGGCTGATCATGTGTGCACGTGGTGTACCTGATGACACCAAGCAGTTAGCATCGTTTCTCCATGGCAATGCCTCTTTGCTCTTCAAACGGACAAACAAGCAGCAGCAGCTTCCTTTGCCACCTGTTCCTCATACCGGTGACTCGCTGACCAATAATAACAACATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11159
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 |
---|---|---|---|---|---|
ENSDART00000058772 | Essential Splice Site | 750 | 919 | 7 | 7 |
ENSDART00000126899 | Essential Splice Site | 750 | 919 | 7 | 7 |
ENSDART00000128965 | Essential Splice Site | 750 | 919 | 7 | 7 |
Genomic Location (Zv9):
Chromosome 18 (position 22465905)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 22696128 |
GRCz11 | 18 | 22685194 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACAAATACATKTATSAAATWTTACTCACTMGTGTCTCTAATCTTTAACA[G/A]CTGAAGCAGTTTGAACGACTAGAGCAGGAGGTCTCTMGACCAATCAACAA
Long Flanking Sequence:
GCGGTTTGGACTGTTCACACTGTCATTACCTCAGTCACATGAGGGGGAAAAAATTCGATTCGGGCTACATTTGCCTGCAGTGTGAACATAGCCTTATTGATCTGCGATCAATAAATGTAGTTTGTGTGGATGCTACTGCGCTACTTGACTAAAAAAATAGCTTTGCTAGTGAAAAGCTATTTGATTTAGAAAGTAGCGACACTACCTCCACACTACTGAGAAATGTAGTTAAGCTAGAAGCATCACTACTTGTAGCGACGCTACTGCCCAACACTGTTCATTAATATGTTTTAAATATCCTGCAAAAAAGTTGAAAGTCCCATGTTGTATTGCAAACCAACCATATTAATCTTTTAACTAACAAGTATACATTTTAAGTACATATAGATTTCATCATTTATAAAAAAATATACAAGGTGTATTAAGTAAAATATGAAAAATAACATTCTTTACAAATACATTTATGAAATATTACTCACTAGTGTCTCTAATCTTTAACA[G/A]CTGAAGCAGTTTGAACGACTAGAGCAGGAGGTCTCTCGACCAATCAACAATGACATTTCGGGTTGGACTCCGCCCTCTCACTACCCCCAGACGCAGCGCAGTAAACTGTGCATGGGCGACCGGCAGCTACTGCTTTTTTACATGGAGCAATGTGAAGCCAACATCACCACGCTCACCAACGCCATAGACGCGTTCTACTCCTCCATTAACAACAACCAGCCGCCCAAAATCTTCGTCGCCCACAGCAAGTTCGTCATCCTCAGTGCCCACAAGCTGGTCTTCATCGGAGACACGCTCTCTAGGCAAGCCAAGTCTCCAGAGGTTCGCACCAGAGTGGCACAGCACAGCAACACACTCTGCGACAAACTCAAAGACATTGTGGTCAGCACCAAAACAGCAGCCCTGCAGTACCCCTCGCCAGGATCCACCAGAGACATGACAGAGAGGGTGCGGGAGCTGGCGGGATGCACCCAACAGTTTCGCATGGCACTCAATCAGCT
Associated Phenotype:
Not determined