ZMP
si:ch211-69m14.1
Ensembl ID:
ZFIN ID:
Description:
Novel FERM domain containing protein [Source:UniProtKB/TrEMBL;Acc:A8DZC9]
Human Orthologue:
FRMD5
Human Description:
FERM domain containing 5 [Source:HGNC Symbol;Acc:28214]
Mouse Orthologue:
Frmd5
Mouse Description:
FERM domain containing 5 Gene [Source:MGI Symbol;Acc:MGI:2442557]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23313 | Nonsense | Available for shipment | Available now |
sa19205 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10808 | Nonsense | Available for shipment | Available now |
sa13053 | Essential Splice Site | Available for shipment | Available now |
sa36659 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa7447 | Missense | Mutation detected in F1 DNA | Not yet available |
sa23312 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23313
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 |
---|---|---|---|---|---|
ENSDART00000113280 | Nonsense | 79 | 540 | 4 | 14 |
ENSDART00000135133 | Nonsense | 77 | 179 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 18 (position 26437262)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 26510517 |
GRCz11 | 18 | 26492895 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATATGTTTACTCTGCTTTATGTTTTGCCTTTGTGTGCTGTTTTCAGGTA[T/A]CTCGTCTTCCTGCAGATTAAGAGAGATTTGTATCATGGTCGTCTCCTTTG
Long Flanking Sequence:
CTTAAGTAAGATTTATCAAATATATTTGTTATAAAACCTTTTTTGATTTGTGTTATTTTTGTGTTTATGTCTGTCTTAAAGATGACAGAACAAATGCTACATGTAATCCAACCAGGACTATTGTAAATATATAATTTACTTTTGTGGTCATGACCAAACAAAACAAGAAAATCTAGTTAAAGTATAAAGTGTTTTTAACCACTACTGTCTTTTTCTCTCTTTTTTTAGCTTAATAGCTTTTGACACAGCAGTGCAATTCTCAAATCATTCTTTAATTCGAAAATAAAAATCTAATTTTAACCAAATCAACGAGAAATATTGAGCATTTTACATCTGTACTAATTCAGATCAATTCCTTTTACTTTTTGTCCTTCTTTACCAGACTTCCCTACTCAAAAATAGACTTTCAGTAATACTTTTATAGTTCAACAGAAATGTGGAGGATTATTATATATGTTTACTCTGCTTTATGTTTTGCCTTTGTGTGCTGTTTTCAGGTA[T/A]CTCGTCTTCCTGCAGATTAAGAGAGATTTGTATCATGGTCGTCTCCTTTGCAAAACATCTGACGCGGCCATGTTGGCAGCTTACATCTTACAAGGTAAAGTAGAAGAAAATTTGACTAACCTATTGTAAACCTAGTCCTCGATATCAGGGGTCACCAATCTCATTTCTGGAGGTCCGGGGCCCTGCAGGGTTTAGCTCCAACTTGCCTCAACACACCTGCCTAGGTGTTTCAAGTAGTGAGACCTTGATTAGAGACCTAGTGAGACCTTGATTAGCTTGTTCAGGTGTGTTTGATTAGGGTTGGAGCTAAATTCTACTGGACAATTGACCTCCAGGAACAAGTTTGGTGATCCCTGCTGTATAGCATAGCACAGGCAAAATAAAGTTTTTAAGTTCCATTTTGAGTACATCCATTGTCTGCCATTTATCTAGGGCCAGGGCAGCAGTCTCAGTTGACGATCAGGGTTTGATGAGGCAAATGCTTTTTCCAAACCTATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19205
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 |
---|---|---|---|---|---|
ENSDART00000113280 | Nonsense | 164 | 540 | 6 | 14 |
ENSDART00000135133 | Nonsense | 162 | 179 | 6 | 6 |
ENSDART00000113280 | Nonsense | 164 | 540 | 6 | 14 |
ENSDART00000135133 | Nonsense | 162 | 179 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 18 (position 26426794)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 26500049 |
GRCz11 | 18 | 26482427 |
KASP Assay ID:
2261-2262.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTAATGTTTTGCAGAGGTCAAACCCCAGAGACTTCTGAGCTGAAGTTCT[T/A]GCAGAAAGCACAAATGCTTGAAACATACGGTGTGGATCCTCATCCGTGCA
Long Flanking Sequence:
CAGCCTCTCTGTCAAAAAAAGAAATAGCAACTTTTCATTTTCCGTCAGTTTTAGTACAAGATGGAACTACATAAGAGTCAATAGATCATAGTAAATAGGAAATCATAGTAAATAGAAAACTCTTTTTGTGAAATTTTACAGTGAGATGCTTGTGGTCTAATGCAATTCAATGATTTATGCTAAGCTTAGCTAAAAGTCTCCCGTCATACCTGAAGATTATAGCTGAATGGATTAAAAAATGGTAAAACTCAACTGTTTAACTTTAGGGAGTTGTAAAATGAATTTCCCAAAAAATGGAGTGTTACTTTAAGTTGTGGCGATTAAAAAAAAATAATAAAAAGGATAAAACCACTACCAATGTGGATTTGGTTTAACAACAGTGACATCAGTCCTGAAATGTAATTGGTTGCTGTGCTGATGTTGTGTTTTTTCCACCAGTGATGATGTTTTCTTAATGTTTTGCAGAGGTCAAACCCCAGAGACTTCTGAGCTGAAGTTCT[T/A]GCAGAAAGCACAAATGCTTGAAACATACGGTGTGGATCCTCATCCGTGCAAGGTTAGTTGGCTCTACCTTACACTTAAAAAAAAAACCTGGTTCCAGAATGAATTTTGAGTTTCTTAAACTTCTTTTTTGTTGTTGTACAGAGCAGCCTTTCATTATATTATGTTAATGAAACACAGGAAAGATAGTTATTCAGACAGTTTGATTCCATCTTAACACACCCAAAACAATGCAGTGGCAGGCAGCGTGTTTTTTTTTTGCTACTTTCAACCTGGCACAGTTACCATTTTCACATCATGCACCACCACATTGTTTAAACAGCAAATGCATTTGCACCTATTTGTGTGTTCATGCACTGTAAAAATAGCTATTAATTAACAGTTTCTGTATTTTGTGTTTTCCATTTATTTATGGTAATGAATTCNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNN
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10808
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 |
---|---|---|---|---|---|
ENSDART00000113280 | Nonsense | 164 | 540 | 6 | 14 |
ENSDART00000135133 | Nonsense | 162 | 179 | 6 | 6 |
ENSDART00000113280 | Nonsense | 164 | 540 | 6 | 14 |
ENSDART00000135133 | Nonsense | 162 | 179 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 18 (position 26426794)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 26500049 |
GRCz11 | 18 | 26482427 |
KASP Assay ID:
2261-2262.1 (used for ordering genotyping assays)
KASP Sequence:
CTTAMTGTTTTGCAGAGGTCAAACCCCAGAGACTTCTGAGCTGAAGTTCT[T/A]GCAGAAAGCACAAATGCTTGAAACATACGGTGTGGATCCTCATCCGTGCA
Long Flanking Sequence:
CAGCCTCTCTGTCAAAAAAAGAAATAGCAACTTTTCATTTTCCGTCAGTTTTAGTACAAGATGGAACTACATAAGAGTCAATAGATCATAGTAAATAGGAAATCATAGTAAATAGAAAACTCTTTTTGTGAAATTTTACAGTGAGATGCTTGTGGTCTAATGCAATTCAATGATTTATGCTAAGCTTAGCTAAAAGTCTCCCGTCATACCTGAAGATTATAGCTGAATGGATTAAAAAATGGTAAAACTCAACTGTTTAACTTTAGGGAGTTGTAAAATGAATTTCCCAAAAAATGGAGTGTTACTTTAAGTTGTGGCGATTAAAAAAAAATAATAAAAAGGATAAAACCACTACCAATGTGGATTTGGTTTAACAACAGTGACATCAGTCCTGAAATGTAATTGGTTGCTGTGCTGATGTTGTGTTTTTTCCACCAGTGATGATGTTTTCTTAATGTTTTGCAGAGGTCAAACCCCAGAGACTTCTGAGCTGAAGTTCT[T/A]GCAGAAAGCACAAATGCTTGAAACATACGGTGTGGATCCTCATCCGTGCAAGGTTAGTTGGCTCTACCTTACACTTAAAAAAAAAACCTGGTTCCAGAATGAATTTTGAGTTTCTTAAACTTCTTTTTTGTTGTTGTACAGAGCAGCCTTTCATTATATTATGTTAATGAAACACAGGAAAGATAGTTATTCAGACAGTTTGATTCCATCTTAACACACCCAAAACAATGCAGTGGCAGGCAGCGTGTTTTTTTTTTGCTACTTTCAACCTGGCACAGTTACCATTTTCACATCATGCACCACCACATTGTTTAAACAGCAAATGCATTTGCACCTATTTGTGTGTTCATGCACTGTAAAAATAGCTATTAATTAACAGTTTCTGTATTTTGTGTTTTCCATTTATTTATGGTAATGAATTCNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNN
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13053
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113280 | Essential Splice Site | 233 | 540 | 9 | 14 |
ENSDART00000135133 | None | None | 179 | None | 6 |
Genomic Location (Zv9):
Chromosome 18 (position 26421903)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 26495249 |
GRCz11 | 18 | 26478897 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAATGACARWSCTGTATCAGTGCACCTTTAATAATSGTTTRTTATGCAC[A/C]GGACAAAAAGATCATCTTGACATACTTTGCACCCACCCCAGAGGCCTGCA
Long Flanking Sequence:
AGATAGATAGAGAGATAGATAGAGAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAAATACACAGTCGGACGGACAGACAGACAGACAGATTAATCCTACAACCTATATGCCTTCCTGCAATCAGCTGCGACAAACTTTATTTTTTCCATCCTCTCGAACAGGAACGAAGTGACCAAACTGAAGTTTGAGGGAAAGACCTTCCATATATATGCAAATCAGAAAGAGGTGAGAGCATTAACCATCCCAACAGTCGCATATTCAAAGATAATTTGAATAAACTACCTTATGACAATGACACAATCTCTGACACTTTAATAATTCTTTTCAATGACAGTCCTGTATCAGTGCACCTTTAATAATCGTTTATTATGCAC[A/C]GGACAAAAAGATCATCTTGACATACTTTGCACCCACCCCAGAGGCCTGCAAGCACCTTTGGAAATGCGGTGTTGAAAATCAAGCCTTCTACAAGTGAGTTTCTTTGCACTTCTCCTTTCGGCGAGACACACTTGTTTGGTTAAACAGGTGAAATGCTTCTGAAAAGGGCAACTGTGAGATAAACAAATCCCGGAAATAATTTGTCCTTTTTTGGCTATTCCAAATTGCGCACACTGTCATTTCCTTTTCCTAGTGCATGATATTTAAGAGCGGTAAATAAGCTGACTAATAACTAATAATGCAAGACAGTTCGTCTGGACACCTGCGTCACTGTTTTTGACCTCACGGGGGTCATCAAATGGAACAGCCACGTGTCGCGAATGACCTTTACTGCACAGGGGATGAGAGATGTGATCTGCTAGCTCCTCCAGAGGGATGTCTGTGCCCATTTCAGTCACGGCTGATTGTACGTGTCCTTGCCCACGCCATGGGAAAGTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36659
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113280 | Essential Splice Site | 343 | 540 | 13 | 14 |
ENSDART00000135133 | None | None | 179 | None | 6 |
Genomic Location (Zv9):
Chromosome 18 (position 26416331)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 26489677 |
GRCz11 | 18 | 26474157 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTGTCCCTCGCACCCGCCGGAGAGCGGTACACATCTCCATCATGGAAG[G/A]TGAGAGTCCAGTTTTAAGCACGAGTTCAGCTGGAAGCATAGGCACAGAGC
Long Flanking Sequence:
AAGTTTACTTTTGGGCTGAAGTGTGAATGCAAACAGAACTAGTTTTGTTTGTGTCTGTACGAAGCGGTCTTTCAGTTAGATTTACATTTACTTTCATTAGTGAAAATGATGGCAAAATATTTCACTCTAGCAGGGGTGAAGCTTTTATAACTAGTTTTTGTTTAATTTCAGTGGAAGAGTAGCCAAAGAGGTAATGGAGCAGAGTGCAAAAATTAAAAGGGAGCCTCCAGAAATACACAGGTATGCATGAGTGCTAAACGTATATATTTACGTTTATTCAGTGTGTGTTTGGTCCACATGCATGATAGAGCGACTGCTGTCTGTCATTAGGAGATGTACTGTAATGTGATAAATGTGTGTGTGGATCCAGTACTGTATGTGTATGTGTCACAGGGCTGGCCTGGTGCCTAGCAGGAGCTGTCCATCTATCACTCACGGGCCGCGACTAAGCAGTGTCCCTCGCACCCGCCGGAGAGCGGTACACATCTCCATCATGGAAG[G/A]TGAGAGTCCAGTTTTAAGCACGAGTTCAGCTGGAAGCATAGGCACAGAGCTAAATGTCACAGTACTGAATGTTTTGAAATATGATCAAAATGCTGTGGAAAATAGCAAAGCTAAAGTTTGGGAACACATGATTTAATGGGAATTCATGCCATAAAGATATAAAGGAGAGGTCAAGAAGATATTAGGATGGCAACAGTGTCTGTGCAGTTTTAACATATATTTTACATATTTAAAAATTATATTAATTTGTTTATTTTATTTTATTTTACATTTCTATCCAATGTGTATTTGTGTCTATAAAAGTGGATATACATTTGAAGTCAGAATTATTAGCCCTGTTTATTCCCCCCCCCCCCCCCCCCCAATTTCTGTTTAATGGAGAGATGCGTTTTTTGATGCATTTCTAAACATAATAGTTTTAATAACTCATTTCTAATGATTTTTTTGAAGACACTTCTATACAGCTTAAAGTGACATTTAAAGGCTTTACTAGGTTAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7447
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:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113280 | Missense | 501 | 540 | 14 | 14 |
ENSDART00000135133 | None | None | 179 | None | 6 |
Genomic Location (Zv9):
Chromosome 18 (position 26402733)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 26476079 |
GRCz11 | 18 | 26460566 |
KASP Assay ID:
554-4329.1 (used for ordering genotyping assays)
KASP Sequence:
TCTTGCTCCTCCTCCTCATCGTYCTCACCGAGTCCGATCTTGACATTGCA[T/A]TTTTACGTGATATCCGCCAGACCCCCGAGTTTGAGCAGTTCCATTACGAA
Long Flanking Sequence:
CTCTCATATCTTCCCCTTCCTTTTGTCCAGGACTGGAATCCTTGCGGGACAGTGCCCACTCCACTCCAGTGCGCTCCGTGTCCCATGGCGACTCCTTTATGCCACGTTCGCGAAGCCAGATGACGGACTCCGGTGACAGGACAGCGATAATCTCTGATGAGAGCTACAGTCCCTCCGACAGCGTTCTGCCCACACCAGTAGCAGAGCACAGCCTGGAGCTGGCAGTCTCACGCCAGATCAACGGCGCCCCCTGCAGCATAGAGGAGGAGAAGGAGTCGGAGGCGGGTACGCCCTCCGTGGGCGATGTGGCTGAATTTGGCGCAGACAGTAGGGCGGCGGGCCCCATGCAGATCGCTGGCAGGGAGGCCCCGCTCAGTGAAGCTGAACAGGTGAATAAGTTTGTTTTAAGTGTACTCCGTCTGCTCCTTGTGACCATTGGACTCCTCTTTGTCTTGCTCCTCCTCCTCATCGTCCTCACCGAGTCCGATCTTGACATTGCA[T/A]TTTTACGTGATATCCGCCAGACCCCCGAGTTTGAGCAGTTCCATTACGAATACTTTTGTCCCCTCAGACGGTGGTTTGCCTGCAAGCTCCGCTGGGTGGGCGGGCTGCTCATTAACAAGTGAAATTGAGGCACTAAAGCGCATAAAGCCTCCCTTGTTGGGGTCGAGAAGATGCTAAACACGTGGAGAGAACGAGAGAGACAGAAGGAGGGCATCGACCTGTCCCATGAGCCCAGCTTCTTTCATGACACTCCTGCTGACACGTGGTGGTGGACTACCAGGCCCACAGCTCCTCTTCTCTTCCACTTTAAGTTCTTTCTCCCCCTCCATTTTTAATTTTTTTCGTCTTTTTTTTTGTCATTTTTATTTTGCTTTTGATTTCCACTTTTTGGATTTCAGGTCATTTCAGGTATTTTATTTTTACAAAAAAAGAAAAAAAGAAAGAAAAAAATTCAAAGACTTGAGAAGATTTTATCGTTCCTTAAATAGGAAATATGAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23312
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113280 | Nonsense | 525 | 540 | 14 | 14 |
ENSDART00000135133 | None | None | 179 | None | 6 |
Genomic Location (Zv9):
Chromosome 18 (position 26402659)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 26476005 |
GRCz11 | 18 | 26460492 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCGAGTTTGAGCAGTTCCATTACGAATACTTTTGTCCCCTCAGACGGTG[G/A]TTTGCCTGCAAGCTCCGCTGGGTGGGCGGGCTGCTCATTAACAAGTGAAA
Long Flanking Sequence:
TCCGTGTCCCATGGCGACTCCTTTATGCCACGTTCGCGAAGCCAGATGACGGACTCCGGTGACAGGACAGCGATAATCTCTGATGAGAGCTACAGTCCCTCCGACAGCGTTCTGCCCACACCAGTAGCAGAGCACAGCCTGGAGCTGGCAGTCTCACGCCAGATCAACGGCGCCCCCTGCAGCATAGAGGAGGAGAAGGAGTCGGAGGCGGGTACGCCCTCCGTGGGCGATGTGGCTGAATTTGGCGCAGACAGTAGGGCGGCGGGCCCCATGCAGATCGCTGGCAGGGAGGCCCCGCTCAGTGAAGCTGAACAGGTGAATAAGTTTGTTTTAAGTGTACTCCGTCTGCTCCTTGTGACCATTGGACTCCTCTTTGTCTTGCTCCTCCTCCTCATCGTCCTCACCGAGTCCGATCTTGACATTGCATTTTTACGTGATATCCGCCAGACCCCCGAGTTTGAGCAGTTCCATTACGAATACTTTTGTCCCCTCAGACGGTG[G/A]TTTGCCTGCAAGCTCCGCTGGGTGGGCGGGCTGCTCATTAACAAGTGAAATTGAGGCACTAAAGCGCATAAAGCCTCCCTTGTTGGGGTCGAGAAGATGCTAAACACGTGGAGAGAACGAGAGAGACAGAAGGAGGGCATCGACCTGTCCCATGAGCCCAGCTTCTTTCATGACACTCCTGCTGACACGTGGTGGTGGACTACCAGGCCCACAGCTCCTCTTCTCTTCCACTTTAAGTTCTTTCTCCCCCTCCATTTTTAATTTTTTTCGTCTTTTTTTTTGTCATTTTTATTTTGCTTTTGATTTCCACTTTTTGGATTTCAGGTCATTTCAGGTATTTTATTTTTACAAAAAAAGAAAAAAAGAAAGAAAAAAATTCAAAGACTTGAGAAGATTTTATCGTTCCTTAAATAGGAAATATGAAATATTTTGTTGCAACGAGAACGTTGCCTTCATTTATATTTATTTTACAATAATACTTGTTAAAGTCTTATTAAATG
Associated Phenotype:
Not determined