ZMP
si:ch211-127h20.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate Rap guanine nucleotide exchange factor (GEF) 1 (RAPGEF1) [Source
Human Orthologue:
RAPGEF1
Human Description:
Rap guanine nucleotide exchange factor (GEF) 1 [Source:HGNC Symbol;Acc:4568]
Mouse Orthologue:
Rapgef1
Mouse Description:
Rap guanine nucleotide exchange factor (GEF) 1 Gene [Source:MGI Symbol;Acc:MGI:104580]
Alleles
There are 9 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa14124 | Nonsense | Available for shipment | Available now |
| sa41138 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa17359 | Essential Splice Site | Available for shipment | Available now |
| sa10846 | Nonsense | Available for shipment | Available now |
| sa18908 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa34334 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa27140 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa14124
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 |
|---|---|---|---|---|---|
| ENSDART00000064017 | Nonsense | 249 | 1085 | 6 | 25 |
| ENSDART00000139947 | Nonsense | 241 | 1077 | 5 | 24 |
Genomic Location (Zv9):
Chromosome 8 (position 12348729)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 11793492 |
| GRCz11 | 8 | 11831197 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGAGGAAGTAGCCCCTCCGAAACCCCCTCTACCTGGACTCAAAGTGCCT[G/T]AACAACACTGGTACKTAAGCTTTACTTGRCTTTCACCACAATAACATTTT
Long Flanking Sequence:
GTTTACTCACACTTCACTTGTTCCAAACCTGTTTGACTTTCTGTCTTCCATTAAACACAAAAGAAGATACTTTGAAGATTGTTGGAAACCTGTAACCATTGACTGCCATCATATTTGTTTTATACTATGGAATTTAATGGATTCAGGTTTTCATTTTTCTTAATAATATATTTAATAAAGAAATAAAATAATAAAGGTTTGGAACAAGTGATGAGTAAATTACATAATGTTAATTTTTTTGGTGAACTTTCTTTTTAAATACAAATAATATGGATAAAATCCACCTGTACATGCTGTGTATTGTGATGTGTCAGCACTAATACTGTTATTCATTTTTACCACATTATTATGGCAGTGTCCCTGAGCCCCCTGTCATTGAGACGAAGGAACCCATCTTGAATGACAGCCCTGCCCCAGCTGAGAACATTGAGACCCCAAATGATGTACCTGAGGAGGAAGTAGCCCCTCCGAAACCCCCTCTACCTGGACTCAAAGTGCCT[G/T]AACAACACTGGTACGTAAGCTTTACTTGACTTTCACCACAATAACATTTTCAAAAACAATAAGTGATTTCATTTTTTTTCCTCTTTCAAATATTTTCCAAATTATGTTTCGCAGAGGCAGGATTTTTTCACAGTATTTCCAGTAATATTTTTTCTTCTGGAGAAAGTCTTATGGTTTATTTTCGCCACATAAACAGAGTTTTAACATTTTTTCAACCCCATTTTAAGGTCAGTATTATTAGCGTTTTAAGCAAAGGTTTTTTTCTACAGAACAAACCATCGTTATGCAATGACTTGCCAGCTTATCCTGACTTGCCTAATTAACCTAGTTAAGACTTTAAATGGCACTTTTAGCTAGTATCTTGAAAAACATCTAGTAAAATATTATGTACTGCAGGGATGCTCATAATAACCGATTAACCGTTAACCAAAAGGGTGCTTTTCTAACCAATTTATGGTATCAGTTAAACAATTAAAAATATCATTAGTATTTTATTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41138
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 |
|---|---|---|---|---|---|
| ENSDART00000064017 | Nonsense | 250 | 1085 | 6 | 25 |
| ENSDART00000139947 | Nonsense | 242 | 1077 | 5 | 24 |
Genomic Location (Zv9):
Chromosome 8 (position 12348726)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 11793489 |
| GRCz11 | 8 | 11831194 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAAGTAGCCCCTCCGAAACCCCCTCTACCTGGACTCAAAGTGCCTGAA[C/T]AACACTGGTACGTAAGCTTTACTTGACTTTCACCACAATAACATTTTCAA
Long Flanking Sequence:
TACTCACACTTCACTTGTTCCAAACCTGTTTGACTTTCTGTCTTCCATTAAACACAAAAGAAGATACTTTGAAGATTGTTGGAAACCTGTAACCATTGACTGCCATCATATTTGTTTTATACTATGGAATTTAATGGATTCAGGTTTTCATTTTTCTTAATAATATATTTAATAAAGAAATAAAATAATAAAGGTTTGGAACAAGTGATGAGTAAATTACATAATGTTAATTTTTTTGGTGAACTTTCTTTTTAAATACAAATAATATGGATAAAATCCACCTGTACATGCTGTGTATTGTGATGTGTCAGCACTAATACTGTTATTCATTTTTACCACATTATTATGGCAGTGTCCCTGAGCCCCCTGTCATTGAGACGAAGGAACCCATCTTGAATGACAGCCCTGCCCCAGCTGAGAACATTGAGACCCCAAATGATGTACCTGAGGAGGAAGTAGCCCCTCCGAAACCCCCTCTACCTGGACTCAAAGTGCCTGAA[C/T]AACACTGGTACGTAAGCTTTACTTGACTTTCACCACAATAACATTTTCAAAAACAATAAGTGATTTCATTTTTTTTCCTCTTTCAAATATTTTCCAAATTATGTTTCGCAGAGGCAGGATTTTTTCACAGTATTTCCAGTAATATTTTTTCTTCTGGAGAAAGTCTTATGGTTTATTTTCGCCACATAAACAGAGTTTTAACATTTTTTCAACCCCATTTTAAGGTCAGTATTATTAGCGTTTTAAGCAAAGGTTTTTTTCTACAGAACAAACCATCGTTATGCAATGACTTGCCAGCTTATCCTGACTTGCCTAATTAACCTAGTTAAGACTTTAAATGGCACTTTTAGCTAGTATCTTGAAAAACATCTAGTAAAATATTATGTACTGCAGGGATGCTCATAATAACCGATTAACCGTTAACCAAAAGGGTGCTTTTCTAACCAATTTATGGTATCAGTTAAACAATTAAAAATATCATTAGTATTTTATTTTTTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17359
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000064017 | Essential Splice Site | 480 | 1085 | 9 | 25 |
| ENSDART00000139947 | Essential Splice Site | 472 | 1077 | 8 | 24 |
Genomic Location (Zv9):
Chromosome 8 (position 12335117)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 11779880 |
| GRCz11 | 8 | 11817585 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
RCAGATCCCCCAGAGCCCCCCACCCCTGCCGGAGAAGAAGAGTCGCCAKA[G/T]TGAGTATAAAGAATTCAGAWGGGTTGTTTAGAGGAYTGCAAATCACTGGG
Long Flanking Sequence:
TCATGAAGTTGTGAATAAAGTGAGAAATGTGATATGAATGGGTACATTTCTGAGTATCTACTTTCAAAAAAATGAATGATTTTTATCTTCTCTCTCTTTTTTCCTGGCTTATTCAGACACAGCAGAGAGCTACGACCCTGACTATGACTTCTTGCATCAAGACCTGTCCAGCACTGAGCAGATCCCTCACACACACACAGGGGGTTGTCTGAGCCCCCTCCCCGAATCTCTCCACGAATCTTCCTCATTTCCAGTCCAGCACCAGTCGATGCCTCCTGCCCTCCCGAAGAAGGAACGGCGGCCACCTCTGCCTCCAGTGGAACGACTCTACTCTCAATATGACAACGTTCCAGATGAGGACATGCACACTCCACCCTTCCCTCTCTTCGGTGCAATCCCCCCCTCAAACCCTGGAGTATTTATGGGGAACTTCGGTCCCAGTGAGAACACACAGATCCCCCAGAGCCCCCCACCCCTGCCGGAGAAGAAGAGTCGCCATA[G/T]TGAGTATAAAGAATTCAGATGGGTTGTTTAGAGGATTGCAAATCACTGGGTTACAGAGACCTGTCTAGTTGGAAGTACAGCAGTTTTGGTGAAAGTCTTCAATTTTGGTTCTTTCCCTTTTATTTCCCTTTTAGTTTACTGTAATGACAATTTTCAGTTCCGTTTTTTGGCAATAAATGCAAATAAGGCCAAAAATGTAGAGTTGCAGAAAAAAAGAAGTCATGAATAATTTAAACTGAAAAAACTAGGGATGCACCGGTACCAATTTTTTTAGAACTGATCTGATCCCGATAACAAAGTTCTGAGTATCGACCGATACAGATTTGATCCCGATACTGTGCCGTTTTTTTTTAAAGCATAATACAGTTTCTATAGTTCTAGTGTGAATGCAGCTTCATCCAGGGTCATCCAGGTACTCCGGTTTCCTCCACAGTCCAAAGACATGTTTTACAGGTGAATTGAATAAGCTACATTAGCTGTAGTTTTTATGTGTGTGGGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10846
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 |
|---|---|---|---|---|---|
| ENSDART00000064017 | Nonsense | 603 | 1085 | 12 | 25 |
| ENSDART00000139947 | Nonsense | 595 | 1077 | 11 | 24 |
| ENSDART00000064017 | Nonsense | 603 | 1085 | 12 | 25 |
| ENSDART00000139947 | Nonsense | 595 | 1077 | 11 | 24 |
Genomic Location (Zv9):
Chromosome 8 (position 12317643)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 11762406 |
| GRCz11 | 8 | 11800111 |
KASP Assay ID:
2260-0229.1 (used for ordering genotyping assays)
KASP Sequence:
TGACGCCTGCCTGTGCTTKTGCTGTCCTCCCTCTTGTTTTYCTGTAGAGC[G/T]AAAGTGCTAATGATGAAGGTGGGGAGGGTGAATACGTCAATCTGTATTCA
Long Flanking Sequence:
CCCGCTCAGTCTGACGTCAGTCCACTTGTAATGTAGCCGACTGCTTTTATTATAATTGAGTAATATAGTTTTATTGCATAATAAATGTTGCTTCCAGTTTAGACACTTTGTTAGGCTAATAACAGATATCATCTGCTGGAAGAATTGTTTAATGTAATAGCCCTAAACAAATGTGATTATTTATTGTGATGTTATTGTTCATCCTATTTCTTTTGCTGCAGTCGAGGCACTCTCAAGGCCATGGATTTGCAACAATTAAGTGTGTTTCTGGCAGACTACTCAACATGTGTAGTAGACTCACTATAACGCTCTTCTTCTTGCCAGGTTTCCAGGCGCCAGTAATGCAGGATCTTGCTTTGCAAAAAAGTGTCTTTTAATTTCAACCCCGCCAAAAAAGCAACAGTGTATTTGAGCTGTTTTTCAGCTCCCTTTTGGCCATCAGCTTTACTCTGACGCCTGCCTGTGCTTGTGCTGTCCTCCCTCTTGTTTTTCTGTAGAGC[G/T]AAAGTGCTAATGATGAAGGTGGGGAGGGTGAATACGTCAATCTGTATTCATCCAACCAGGCCAATGGAGATGTGACTCTCTCCAATGGAGTAAGTAACAGCATGTCAGCTGTCGGTGGCCTCACATGCTGCGTTCTGTGCTGTTTGTGACTGTAATGCTTGGCTTTGCTTCATGCAAACTGGATAATTGCTATTTTACTTAACGCTTGCCGCCAAGGTGCACTCTGCGAGTGCTAAGAATCAACAAACAAGAAATATCTTGCATGTTAATCTGAGCCTGTCCTAACTAACAGCGTCTGGCAATATTGTTGCGCAAGACAATATTGTTTTATGCTTGGTGGCTTCGTCTTGTGAAATGTCATTGGTTCAAAATCCTGCTTTAAATGTTGGATATTAAGTGTCTAGTAGGGCTGAACGATAAATCGAATGTGATTTTTGTGCCCATTTGTTTATAAAGCCGTCTCTTTTAATCAGTTGTGAATCTCCATTAGTGTGTTCTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18908
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 |
|---|---|---|---|---|---|
| ENSDART00000064017 | Nonsense | 603 | 1085 | 12 | 25 |
| ENSDART00000139947 | Nonsense | 595 | 1077 | 11 | 24 |
| ENSDART00000064017 | Nonsense | 603 | 1085 | 12 | 25 |
| ENSDART00000139947 | Nonsense | 595 | 1077 | 11 | 24 |
Genomic Location (Zv9):
Chromosome 8 (position 12317643)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 11762406 |
| GRCz11 | 8 | 11800111 |
KASP Assay ID:
2260-0229.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACGCCTGCCTGTGCTTGTGCTGTCCTCCCTCTTGTTTTTCTGTAGAGC[G/T]AAAGTGCTAATGATGAAGGTGGGGAGGGTGAATACGTCAATCTGTATTCA
Long Flanking Sequence:
CCCGCTCAGTCTGACGTCAGTCCACTTGTAATGTAGCCGACTGCTTTTATTATAATTGAGTAATATAGTTTTATTGCATAATAAATGTTGCTTCCAGTTTAGACACTTTGTTAGGCTAATAACAGATATCATCTGCTGGAAGAATTGTTTAATGTAATAGCCCTAAACAAATGTGATTATTTATTGTGATGTTATTGTTCATCCTATTTCTTTTGCTGCAGTCGAGGCACTCTCAAGGCCATGGATTTGCAACAATTAAGTGTGTTTCTGGCAGACTACTCAACATGTGTAGTAGACTCACTATAACGCTCTTCTTCTTGCCAGGTTTCCAGGCGCCAGTAATGCAGGATCTTGCTTTGCAAAAAAGTGTCTTTTAATTTCAACCCCGCCAAAAAAGCAACAGTGTATTTGAGCTGTTTTTCAGCTCCCTTTTGGCCATCAGCTTTACTCTGACGCCTGCCTGTGCTTGTGCTGTCCTCCCTCTTGTTTTTCTGTAGAGC[G/T]AAAGTGCTAATGATGAAGGTGGGGAGGGTGAATACGTCAATCTGTATTCATCCAACCAGGCCAATGGAGATGTGACTCTCTCCAATGGAGTAAGTAACAGCATGTCAGCTGTCGGTGGCCTCACATGCTGCGTTCTGTGCTGTTTGTGACTGTAATGCTTGGCTTTGCTTCATGCAAACTGGATAATTGCTATTTTACTTAACGCTTGCCGCCAAGGTGCACTCTGCGAGTGCTAAGAATCAACAAACAAGAAATATCTTGCATGTTAATCTGAGCCTGTCCTAACTAACAGCGTCTGGCAATATTGTTGCGCAAGACAATATTGTTTTATGCTTGGTGGCTTCGTCTTGTGAAATGTCATTGGTTCAAAATCCTGCTTTAAATGTTGGATATTAAGTGTCTAGTAGGGCTGAACGATAAATCGAATGTGATTTTTGTGCCCATTTGTTTATAAAGCCGTCTCTTTTAATCAGTTGTGAATCTCCATTAGTGTGTTCTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34334
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 |
|---|---|---|---|---|---|
| ENSDART00000064017 | Nonsense | 693 | 1085 | 14 | 25 |
| ENSDART00000139947 | Nonsense | 685 | 1077 | 13 | 24 |
Genomic Location (Zv9):
Chromosome 8 (position 12310120)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 11754883 |
| GRCz11 | 8 | 11792588 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGTTTGATTGACCACGATGAGATCATGTCTCGCATAACACTAAAGCAA[G/T]AGGTAAACTTTTGCGTTCGTTATTGCATACAGTATGCACATATACAGTTT
Long Flanking Sequence:
AAAAAAGACTTTGTATTGGTAATCCTTACTCAATGTCTTTCCATTTGCTTCTACAGTACATCTGAAGTGGCGGTCTTTCTCTGTTGATGTCAACTTGTGGACTTCCATAGCAACTACATTGCAATATTCTTAACCACACCCTTCATACCAGTAGTTTACTATGAGGGAATGATGTGCAAAAGAAAGCCTCGCCCCTACTCAATATCCCATTTTAAATATTGAGTGATTGGAAATGCATCAACACACTGAAATAAAAGACTTAGCAACTTCTAGTTCAAACATATTATGGTATTTACTATGATTTAGAGTCAAATACTTACATACTGCACCTTTAAAACTATTTCAGAGATTAAAATCTGATTAAAAAGATTTGTATCACCTGTACTTTGATTTGCAGCTGGAAGCAGAAGTGTGTGGACTCAGATTTGACCTCAGAAGAGGTGGATGAGCTCTGTTTGATTGACCACGATGAGATCATGTCTCGCATAACACTAAAGCAA[G/T]AGGTAAACTTTTGCGTTCGTTATTGCATACAGTATGCACATATACAGTTTTGCTTTTTGAAATGCATAGGTTGTGATGATAGTGAAAGCATTAGTTTTTACTCTGCTGCCATCTGCCTGTGACTTAACGCTATTTCAGTGATGAATTGAAGCGCATATAAAACTCCAATGTCAGGAGAATTAAAAATAGACAAGACCGTTAATAAGTAGACCACTCTACAATAAGACAATATGCGACCCTGGAACACAAAACCAGTCATAAGTGTCAATGTTTGGAGATCAGGTTTTGTACATTATCTAAAAGCTGAATAAAGGAGCTTTCCATTAAAATATGTTTTTTTAGATAGGATATATGGTCAAAATGCAGAATTTTGAAAATCTGGAATATGATGATGCAAATAGATCAAAATGTTGAGAAATTTGCCTTTAAAATTGTCTATTTAAAGTGTTTGGCAATGCATATTACTAATACAAAATTGAGTTGTCATAAAATTACAGTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27140
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000064017 | Essential Splice Site | 993 | 1085 | 24 | 25 |
| ENSDART00000139947 | Essential Splice Site | 985 | 1077 | 23 | 24 |
Genomic Location (Zv9):
Chromosome 8 (position 12299057)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 11743820 |
| GRCz11 | 8 | 11781525 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTAGCTGTCATGTTCTGTGTGTAATGTTCCTATGTTTCCACAAAATGC[A/T]GAGGTCTCATCCTCCAGGACTTAACGTTTGTGCATCTTGGGAATCCTGAC
Long Flanking Sequence:
TTCAAGTTTATTTGTATAGCTCTTTTCACAGTAATTATAGTTTCAAAAGCAGCTTTACAAAACATGCACATTAATGCATTAAAATCAAATTTGGAAAAATTTGTGTTATTAGATACTATAATTTCGTTAGTTAGTAATAACTTTAACTAATTAACTTGTAACTAATAGCTTTAAACAGTTAATGTTGTTGTATATAAGCATAGTTAACGTGCAGTTATATAGCATACAGGTGATGTCTCATCTATGCATCACTGACCCTTGTTTCTCAGATGATGGTCACTGTAACTGATGTTGTCTTCACAGGGTTTGGAGGAATATTGCACTTTAATTGACAGTTCGTCCTCTTTCCGGGCGTACAGAGCAGCTTTGGCAGACGTGGAGCCTCCATGTATACCGTACCTGTAAGTACAGATGTCAGTCGTTTAAGAAAAATACACACTTTAAGTTGTAATCTAGCTGTCATGTTCTGTGTGTAATGTTCCTATGTTTCCACAAAATGC[A/T]GAGGTCTCATCCTCCAGGACTTAACGTTTGTGCATCTTGGGAATCCTGACCACATTGAAGGAAAGATCAACTTTTCCAAACGCTGGCAGCAGTTTAATATTTTAGACACTATGAGGCGTTTCCAGCAAGTGTGAGTACTCGGACCAACATAAAAAATATCATTTATAATATTTATGATAATAATTTAGCTTTTATATTCAGTAAGTAATTAATTTGGATTGTGAAAATTTGTTTTTGATTTTATTAGAGATAGAGCCCTGTGACAAGAGTTTTATCTTTTCCTTTTTTTCATTAATTATTTTTTTGAATGGATTTTATGGTTAAAGAAAATGTTTGTCACTTTGAAATTTGTTCACTTTATAAAATCCATTTTAGGGTTCTATGAAATCCGAAAGTTTTATCCAATTTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTATATATATATATATATATATATATATATATATATATTC
Associated Phenotype:
Not determined