ZMP
arhgap29b
Ensembl ID:
ZFIN ID:
Description:
Rho GTPase-activating protein 29 [Source:UniProtKB/Swiss-Prot;Acc:Q6PCS4]
Human Orthologue:
ARHGAP29
Human Description:
Rho GTPase activating protein 29 [Source:HGNC Symbol;Acc:30207]
Mouse Orthologue:
Arhgap29
Mouse Description:
Rho GTPase activating protein 29 Gene [Source:MGI Symbol;Acc:MGI:2443818]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18561 | Essential Splice Site | Available for shipment | Available now |
sa9978 | Nonsense | Available for shipment | Available now |
sa39792 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa6007 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39793 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18723 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9335 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa18561
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 |
---|---|---|---|---|---|
ENSDART00000016071 | Essential Splice Site | 325 | 1337 | 10 | 24 |
ENSDART00000141921 | Essential Splice Site | 325 | 1337 | 10 | 23 |
Genomic Location (Zv9):
Chromosome 2 (position 14991766)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 15502593 |
GRCz11 | 2 | 15171183 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCAACAARTCAATTCCTTAAATTCCACACATTTTCCCCTTATTCCAACA[G/A]CCACTGCTGGCCCGCAAGAATGACCTGGACAAGCAGAGGAAAGAGATTAA
Long Flanking Sequence:
ATCTTTAATTAAATACCATAACCTACCCTCCTCCCTCGAATGCCTAAAGGAGTTACAGGAATTAATGACCTTAAATTACTATTTTAAAGTACAATAAAGGTCATTTCAGATTTTAATATGAGTTTGTAATCTTGTATATCACAAATTACAAGATTACATATTACATGTTTAGACATATAAAATCTTTTTTCACACTATTTATATTTTTATTGTGTTTTGAACCCTTTCTAAAATATTTTTAATAGTCAATTTCAGTGATAAAGTGACAGTATTTTAAAATTTTCTGTTTTTATCTTAAGGATTTCATGCCTTTCCGGGATATCTATGTCTCTGCCTTTAAAAATGAAATCGAGTACAATCATGTACTGCTCCAAACGGCTGCAGCTCTTCAGACCAACAAATTCACACAGGTAACCTCTATTGATTCCTCCGAACGCTTTTAGCCAACTATTCAACAAATCAATTCCTTAAATTCCACACATTTTCCCCTTATTCCAACA[G/A]CCACTGCTGGCCCGCAAGAATGACCTGGACAAGCAGAGGAAAGAGATTAAAGAACAATGGCAAAGAGAGCTGAAGAAAATGGTACTAATGCCTATTTGAATTGGAATTTCATCACTAACTCAACATTTCTTCAAAATGATAGCACATAACCTACGTGTGTTTTCAGAACGAGTCAGAAAGTGCTTTAAAGAAGGCTCGGCTGTTGAAAATGCAGAAGAGGGAGGAATACGAGAAGGCCCGGAGCTCGACCAGCCGTACCGAGGAGGAGCAGCCAGCAGCTGGAGGCAGGACACTGGAGAAGAAACGCAGAGTTGAGGAAGAGGCCCTACAGAAGGTACTGTAGAAATTACACTATAAAAACTTTTAAAGCTTTTAATTCAACACACACACACAGACACACCCTTGAGTTTATTGTCCGCGTTTACTATGCATCAAAGCAGCAATAAGAAACACAGAGCTTGTGAGACTTTCCTTAACAACGATGTTATGTGTAAAAATAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9978
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 |
---|---|---|---|---|---|
ENSDART00000016071 | Nonsense | 343 | 1337 | 10 | 24 |
ENSDART00000141921 | Nonsense | 343 | 1337 | 10 | 23 |
Genomic Location (Zv9):
Chromosome 2 (position 14991821)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 15502648 |
GRCz11 | 2 | 15171238 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCTGGCCCGCAAGAATGACCTGGACAAGCAGAGGAAAGAGATTAAAGAA[C/T]AATGGCAAAGAGAGCTGAAGAAAATGGTACTAATGCCTATTTGAATTGGA
Long Flanking Sequence:
CAGGAATTAATGACCTTAAATTACTATTTTAAAGTACAATAAAGGTCATTTCAGATTTTAATATGAGTTTGTAATCTTGTATATCACAAATTACAAGATTACATATTACATGTTTAGACATATAAAATCTTTTTTCACACTATTTATATTTTTATTGTGTTTTGAACCCTTTCTAAAATATTTTTAATAGTCAATTTCAGTGATAAAGTGACAGTATTTTAAAATTTTCTGTTTTTATCTTAAGGATTTCATGCCTTTCCGGGATATCTATGTCTCTGCCTTTAAAAATGAAATCGAGTACAATCATGTACTGCTCCAAACGGCTGCAGCTCTTCAGACCAACAAATTCACACAGGTAACCTCTATTGATTCCTCCGAACGCTTTTAGCCAACTATTCAACAAATCAATTCCTTAAATTCCACACATTTTCCCCTTATTCCAACAGCCACTGCTGGCCCGCAAGAATGACCTGGACAAGCAGAGGAAAGAGATTAAAGAA[C/T]AATGGCAAAGAGAGCTGAAGAAAATGGTACTAATGCCTATTTGAATTGGAATTTCATCACTAACTCAACATTTCTTCAAAATGATAGCACATAACCTACGTGTGTTTTCAGAACGAGTCAGAAAGTGCTTTAAAGAAGGCTCGGCTGTTGAAAATGCAGAAGAGGGAGGAATACGAGAAGGCCCGGAGCTCGACCAGCCGTACCGAGGAGGAGCAGCCAGCAGCTGGAGGCAGGACACTGGAGAAGAAACGCAGAGTTGAGGAAGAGGCCCTACAGAAGGTACTGTAGAAATTACACTATAAAAACTTTTAAAGCTTTTAATTCAACACACACACACAGACACACCCTTGAGTTTATTGTCCGCGTTTACTATGCATCAAAGCAGCAATAAGAAACACAGAGCTTGTGAGACTTTCCTTAACAACGATGTTATGTGTAAAAATACGAGTGCTAGAAAACCTAGCAAATGCTTGAATGTTGTTCTAGTGTTTTGCTCACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39792
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 |
---|---|---|---|---|---|
ENSDART00000016071 | Nonsense | 406 | 1337 | 11 | 24 |
ENSDART00000141921 | Nonsense | 406 | 1337 | 11 | 23 |
Genomic Location (Zv9):
Chromosome 2 (position 14992095)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 15502922 |
GRCz11 | 2 | 15171512 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGAGGCAGGACACTGGAGAAGAAACGCAGAGTTGAGGAAGAGGCCCTA[C/T]AGAAGGTACTGTAGAAATTACACTATAAAAACTTTTAAAGCTTTTAATTC
Long Flanking Sequence:
TCTGCCTTTAAAAATGAAATCGAGTACAATCATGTACTGCTCCAAACGGCTGCAGCTCTTCAGACCAACAAATTCACACAGGTAACCTCTATTGATTCCTCCGAACGCTTTTAGCCAACTATTCAACAAATCAATTCCTTAAATTCCACACATTTTCCCCTTATTCCAACAGCCACTGCTGGCCCGCAAGAATGACCTGGACAAGCAGAGGAAAGAGATTAAAGAACAATGGCAAAGAGAGCTGAAGAAAATGGTACTAATGCCTATTTGAATTGGAATTTCATCACTAACTCAACATTTCTTCAAAATGATAGCACATAACCTACGTGTGTTTTCAGAACGAGTCAGAAAGTGCTTTAAAGAAGGCTCGGCTGTTGAAAATGCAGAAGAGGGAGGAATACGAGAAGGCCCGGAGCTCGACCAGCCGTACCGAGGAGGAGCAGCCAGCAGCTGGAGGCAGGACACTGGAGAAGAAACGCAGAGTTGAGGAAGAGGCCCTA[C/T]AGAAGGTACTGTAGAAATTACACTATAAAAACTTTTAAAGCTTTTAATTCAACACACACACACAGACACACCCTTGAGTTTATTGTCCGCGTTTACTATGCATCAAAGCAGCAATAAGAAACACAGAGCTTGTGAGACTTTCCTTAACAACGATGTTATGTGTAAAAATACGAGTGCTAGAAAACCTAGCAAATGCTTGAATGTTGTTCTAGTGTTTTGCTCACACTTGAACAGTTGAACATCTACTAATACATGATTAAAATTCATGGTTTTAATATTAGTTAATGCTTTGATGGTTAACTTAAATTAACAGCGAAGAGGTTTAATGGTAACACTTTAAAATAATGGTCCATTATGTGTTTACTAACATGAACACACTATTAGTAATACATTTATTACTCTATTCATTCATCGTTGTTCAAGCTAGTTATATTACTTAAGTTAAATAACATTAGTTCATGTTAACTGACTGTGCATTAACTAATGTTAACAAGCACAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6007
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 |
---|---|---|---|---|---|
ENSDART00000016071 | Nonsense | 414 | 1337 | 12 | 24 |
ENSDART00000141921 | Nonsense | 414 | 1337 | 12 | 23 |
Genomic Location (Zv9):
Chromosome 2 (position 14994766)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 15505593 |
GRCz11 | 2 | 15174183 |
KASP Assay ID:
554-3734.1 (used for ordering genotyping assays)
KASP Sequence:
TGGCTGATGGTCTGTTTTTGTGGTAACTCCAGGCAGAGGAAGCGCAGGAG[C/T]AGTATAAAGCCTGTGTGGCYGATCTGGAGGCCAAGAAGGTCAGCCTGTCA
Long Flanking Sequence:
GCGTTATATAAATACACATTACATTACATGACAACAGCCATTCTTCTCCTTGGGCAGTTTTGAAAAAAAATATTTGATTCACTTCGAATGTTCATTGCTGTTAATAAAATTATTAGAAATAGCATCTGATATAGTGTGTTGAAGTAGGTATATAAAATTTGCAATTTGCCCAACTTGTATAGTGCTGGAAAAGTTTGACCTTAAAAGTGTTTGAAAAGCGCTTAAATTTGATGTTGGGAAAGGTGTATAAACCCTGATGGACATTAAACTATACATTATTGTTGCTGTATCATTCTGTAAACCTCTAACAACTAAAAGAAATTACCTCACATACCATTTGAAAAAAAACAAATGAGCAGGATTTTTCTTTCTAAAATGTATTTTGAATGGCTTGATGGCACAGAAATGACATAAAACAGGCTAGTAAAATGACTGTACTCGTGTTTTGCTTGGCTGATGGTCTGTTTTTGTGGTAACTCCAGGCAGAGGAAGCGCAGGAG[C/T]AGTATAAAGCCTGTGTGGCCGATCTGGAGGCCAAGAAGGTCAGCCTGTCAAACGCTAAGAGTGAGATCCTCGCACAGATTCGGAAGCTGGTCTTCCAATGTGACCTGACCCTCAAAGCGGTCTGTATCCCTGTCACAACACTATTACACACTACTGTTGAAAAATGCGCAGCGGTTTTCTTCTTCTTCTTCTTTGTTTAATTCTTCTTCATTTAATTCTTATATAAGAAGCTTCGGTTTTTAATAATAATTTTATATGTACAGTTGAAGTCAGAATTATTAGCCTTTTTTTTTTTTTTTTCAAACGACGTTAAACAGCAAGGAGTTTTTCCACAGTATTTCCTATAAAAAAAAATTCTTCTGGAGAAAGTCTTATTTGATTTATTTTGGCTAGAATAAACACAATTTAAATGTTTTGAAACCCTTTTTTAATCAATATTATTAAATCCCTAAAGCAATATTTTTTTTAATTGTCTACAGAACAAATTTAACAATTTAACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39793
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000016071 | Nonsense | 1012 | 1337 | 22 | 24 |
ENSDART00000141921 | Nonsense | 1012 | 1337 | 22 | 23 |
Genomic Location (Zv9):
Chromosome 2 (position 15013431)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 15524258 |
GRCz11 | 2 | 15192848 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTCTACAAGAGACACTCGTCTGTGATCATCCCAGCTCAGCTCATGGAG[G/T]AAGGGAAGGAAATGAAGACTGGAGACCACAGAGTACAAACATCTGGTTAG
Long Flanking Sequence:
GTGAAATATAACCCAGCACTTAATCACATTTTTGTTAATTGTTCTGCAGAGTTTCAGAGCAAGCTGAGGAGAACAAGATGACCGCTAGTAACCTGGGCATCATCTTTGGCCCCACGCTCATTAAGCCCAGACATTTGGAGGCAGAAGTGTCGCTTTCCTCCCTGGTTGACTATCCTCACCAGGCCCGCATGGTGGAGCTGCTCATCAAACACCATCAGATGATCTTTGACGTGCCCCTCAGCCCCATGTCTCCAACCAGTCCAACTGTATCACAGGCTTCCTTTGGGTCCAGCATCCAGGACAAAGAGTCCAAACTCAGCCGTCACTCTAGATCCCTGATGGACATCAAAGAGGTAGGATGGCCTAGAGAATAGAAACCAGACTCGGTAGGATTAATTTAAGGAGATATTAAAGTTTTTGATTTGTTTTTTCTCCTCATTCAGAGTGCAAAACTCTACAAGAGACACTCGTCTGTGATCATCCCAGCTCAGCTCATGGAG[G/T]AAGGGAAGGAAATGAAGACTGGAGACCACAGAGTACAAACATCTGGTTAGTATGAGACTACATTTACACTAATCCAGATAAATCTGAAAATGACTCTTTGGTCTAATAGCAGTCTGCATGTACACAATCATTCTTTTCCACTAAAATTGGTCACCCACACACTGAAATGACAGAAAATGCTTTTGTCCTTGCTTTCGTTTTTGAAGTGACCAAAAGTAGCCAAGCTCAAAGAGTTTTAGATACTGATTGTACCACGATTATAATAGTTTTTTTTTAATTAGTTTTAGTTGTTATTTTGTTTTGAGTTTTTGTTTTCAAATCCAGTTAGTTCTAATTAGTTTTTAGGGGCAGATTTACAAATTTTTATTAGTTTCTATATTTTGAAATCGCTTGGTTTTAGTTTAGTTTTGATTAGTTTCAGTATTAGTTTTATAAATTAGAGTATTTGTTAGGTGCAAGATACAAAATCATCAGAATATACTATAATAACTCAACCAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18723
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 |
---|---|---|---|---|---|
ENSDART00000016071 | Nonsense | 1037 | 1337 | 23 | 24 |
ENSDART00000141921 | Nonsense | 1037 | 1337 | 23 | 23 |
ENSDART00000016071 | Nonsense | 1037 | 1337 | 23 | 24 |
ENSDART00000141921 | Nonsense | 1037 | 1337 | 23 | 23 |
Genomic Location (Zv9):
Chromosome 2 (position 15015301)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 15526128 |
GRCz11 | 2 | 15194718 |
KASP Assay ID:
2259-1746.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTATTTTTTTTCTCAAGCAGGTGAGGGCTCAGATGTCAACGGGGTTGGTT[T/A]GACTTCTGTTGACTCCACATCTGTGTTCAACCGGCCTGGTGCCAGCAGCC
Long Flanking Sequence:
TAAAACTGGCATTGTGGAGTTAATAGATTTCCTTCTAAAAGGCTTATATATTAAATACATTTACAAAGGCAAAAAAGAAGGACGTTTTTGCTATAATTTTAGTTAGTTTCAGTTAGTTTTGTATGTACACAATACATTTTCAGTTATTTCTAGTTTTTTTTTATTTTTAAAAACTCTTTTTTTTATTTTTATTTCAGTTAACGAAAAGGATTTTTCAATTCTAGTTTTGTTTTTTCGTTAATTTTCGTTAACAATAATAACCTTGAACAGAACCTGTATTTGTCAATTTAAAGGGATAGTTCACTTTATAATGAAAACTGCTGCCCCTTAAGTAGGCTAAAATTTTAAAGATCGACAATCTTGAGCACCTAAGGTTTAAAAAAAAGTGTAATATAACATTTTAACTCTATTCAGATGTTTGTTTTGATGTGTATGTAATTGTATAAAAAAGTATTTTTTTTCTCAAGCAGGTGAGGGCTCAGATGTCAACGGGGTTGGTT[T/A]GACTTCTGTTGACTCCACATCTGTGTTCAACCGGCCTGGTGCCAGCAGCCGAATGGTGCAGCTGAGACCTCAGCGTGCCAAGCCGGTGTCTCGACCAATCAGCATGCCCATAGACCGCCTACTCAACGAACGCAACAGCCGCAACACAGTGGAGCATGATCACTCACCCGCCGCCATTGAGGAGACCACTGAACCAGAGAAACCGACAACACCACGGCACACCAACTTTTACAGGAACCCCTTCATTGACACTCAGACGCTGAGGAGGACCTGGGACAGGCAGTACAGACATTATGACGTCACGCCCAGGACTGCAATGATAGTGGCCAACCTGCCACCTTCCGGTGTGCAGAAACAGCCTGAAATTAGTATGGGATCCCAAAGCAGCACCTCTAGAAAAGATGGTACAAGCCAGTCTGGTGTGGCTCCAATATCGTTCAGAGCAGCACGGACACTAAAACCCTCTTCTCCTGGAACGTTCTATAGACCTCCCTCTGGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9335
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 |
---|---|---|---|---|---|
ENSDART00000016071 | Nonsense | 1037 | 1337 | 23 | 24 |
ENSDART00000141921 | Nonsense | 1037 | 1337 | 23 | 23 |
ENSDART00000016071 | Nonsense | 1037 | 1337 | 23 | 24 |
ENSDART00000141921 | Nonsense | 1037 | 1337 | 23 | 23 |
Genomic Location (Zv9):
Chromosome 2 (position 15015301)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 15526128 |
GRCz11 | 2 | 15194718 |
KASP Assay ID:
2259-1746.1 (used for ordering genotyping assays)
KASP Sequence:
GTATTTTTTYTCTCAARCAGGTGAGGGCTCAGATGTCAACGGGGTTGGTT[T/A]GACTTCTGTTGACTCCACATCTGTGTTCAAYCGGCCTGGTGCCAGCAGCC
Long Flanking Sequence:
TAAAACTGGCATTGTGGAGTTAATAGATTTCCTTCTAAAAGGCTTATATATTAAATACATTTACAAAGGCAAAAAAGAAGGACGTTTTTGCTATAATTTTAGTTAGTTTCAGTTAGTTTTGTATGTACACAATACATTTTCAGTTATTTCTAGTTTTTTTTTATTTTTAAAAACTCTTTTTTTTATTTTTATTTCAGTTAACGAAAAGGATTTTTCAATTCTAGTTTTGTTTTTTCGTTAATTTTCGTTAACAATAATAACCTTGAACAGAACCTGTATTTGTCAATTTAAAGGGATAGTTCACTTTATAATGAAAACTGCTGCCCCTTAAGTAGGCTAAAATTTTAAAGATCGACAATCTTGAGCACCTAAGGTTTAAAAAAAAGTGTAATATAACATTTTAACTCTATTCAGATGTTTGTTTTGATGTGTATGTAATTGTATAAAAAAGTATTTTTTTTCTCAAGCAGGTGAGGGCTCAGATGTCAACGGGGTTGGTT[T/A]GACTTCTGTTGACTCCACATCTGTGTTCAACCGGCCTGGTGCCAGCAGCCGAATGGTGCAGCTGAGACCTCAGCGTGCCAAGCCGGTGTCTCGACCAATCAGCATGCCCATAGACCGCCTACTCAACGAACGCAACAGCCGCAACACAGTGGAGCATGATCACTCACCCGCCGCCATTGAGGAGACCACTGAACCAGAGAAACCGACAACACCACGGCACACCAACTTTTACAGGAACCCCTTCATTGACACTCAGACGCTGAGGAGGACCTGGGACAGGCAGTACAGACATTATGACGTCACGCCCAGGACTGCAATGATAGTGGCCAACCTGCCACCTTCCGGTGTGCAGAAACAGCCTGAAATTAGTATGGGATCCCAAAGCAGCACCTCTAGAAAAGATGGTACAAGCCAGTCTGGTGTGGCTCCAATATCGTTCAGAGCAGCACGGACACTAAAACCCTCTTCTCCTGGAACGTTCTATAGACCTCCCTCTGGAG
Associated Phenotype:
Not determined