ZMP
zgc:101809
Ensembl ID:
ZFIN ID:
Description:
lymphocyte cytosolic protein 2 [Source:RefSeq peptide;Acc:NP_999882]
Human Orthologue:
LCP2
Human Description:
lymphocyte cytosolic protein 2 (SH2 domain containing leukocyte protein of 76kDa) [Source:HGNC Symbo
Mouse Orthologue:
Lcp2
Mouse Description:
lymphocyte cytosolic protein 2 Gene [Source:MGI Symbol;Acc:MGI:1321402]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa43670 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa37342 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa43671 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa31060 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa1278 | Essential Splice Site | Available for shipment | Available now |
| sa29621 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa23970 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa43670
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 |
|---|---|---|---|---|---|
| ENSDART00000059420 | Essential Splice Site | 48 | 501 | 3 | 21 |
| ENSDART00000145050 | Essential Splice Site | 48 | 500 | 3 | 19 |
Genomic Location (Zv9):
Chromosome 21 (position 29056640)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 30275884 |
| GRCz11 | 21 | 30312579 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCACCGTATATATGCAATCTTATGATGATAAAATACGTTTTTTTCCTC[A/T]GAATATGTCTGAAAATGACCTTCGAAGGTTTCCACAGCTTCATGCACCGT
Long Flanking Sequence:
TTAGAAACCCTAGTGACCAAGAAATGTTCAACTCCGAAACAGTCACATACAGTGCTCTGCAAGTACACCCCTCTCAAATCTATCTTTTAAATATTTTGAATAGGAAGCTATACAATATTATATTTGTGCATATACTTTAGATTAGTCAGTACTGAAGCCAAATCTGGAGCTTATCTAACAAAATAACTTGCAATAATGGTCCTGAAACTAGTACACCCAAATTTATTTGTTATAGAAAAATATTAAATACAAAAAAAGGAAAAATCCTCTTCTGAATTTAAATGTATTATCTTTCAATTTCTAAATATGTTTGTAACTAAAATATTATTTTAATAAATATATCTGTTTAATAAATCTGTTTTGTTTAAATGCACCAAAATAAATTGCCTATATTCACTGAGAATTTGATAAAAATATTAATTTTCAAAATGGAGTGTACTCAATTATGTTGAGCACCGTATATATGCAATCTTATGATGATAAAATACGTTTTTTTCCTC[A/T]GAATATGTCTGAAAATGACCTTCGAAGGTTTCCACAGCTTCATGCACCGTAAGTACTGATTATAGTTTTATTTTGTACTCATGTATTCATTTTTCTAGTTTTATTTTCTCAGTTTATTTTGTGTTGCTTAAGTATTACGTTACAGCACAGAACTTGTTCATTTTGTTTGCCATTGATTTTACAATAGTTACTCCATTCAGAGACACACTTTAAGACAGAAATCCCCAAAAAATAAGCCATTTTTCGCAATGTAACTTGACAAATCGACAATTTGATGACAAATCAAGAATATACAGTTGAAGTCAGAATTATTAGCCCTCTTTTGATTTTATTTTATTTTTTTTAAATATTTCCCAAATTATTTTTAACAGAGCAAGGAAATTTTCACAGTATGTCTGATAATCTTTTTTCTTCTGGAGAAGGTCTTATTTGTTTTATTTCCGCTAGAATAAAAGCAGTTATTAATTTTTTTTAAACATTTTTGGGACAAAATTATTAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37342
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 |
|---|---|---|---|---|---|
| ENSDART00000059420 | Essential Splice Site | 171 | 501 | 7 | 21 |
| ENSDART00000145050 | Essential Splice Site | 171 | 500 | 7 | 19 |
Genomic Location (Zv9):
Chromosome 21 (position 29072287)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 30291531 |
| GRCz11 | 21 | 30328226 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGGCCCAGATCTGTCCTGCTAAACCCATGGACAACTGTGATTACATTGG[T/C]ACACACAAATGAACAGTTTTCAGTCTTGTGGTCATTGGAGTCTATTGGAA
Long Flanking Sequence:
TTGTACACATATTGGGCCTTCTGTATTGTCGAACCTGGCTTTTAAGAAAACTACAATTTAAAAAAGATTTTCAACCAGCCAAACAACCAAAGTGGCTAGTGGGAGCAACTGTCTAACCCGCCACAGCTGAAATCTACCCACATTTGGCGAGCTAGCAGGTGTTAATGTCAAGCCCTGAATATACTTATTGCAATAAACAGAGGTTTAGCAATAAATTTAATACTCAGTATCGGCTTCAAAAATCTTGATCGGAGCATCCCTATTTTAAAATAATCAGCATCACATGTAGCTAACATGACATTCCTCAATAAGACTAGTGATGAAGATGACTATGAGAATCCAGACTCAAATAATGATGATGATGCAAGCGGTGGAGATTATGAGTCGCCGGCGGAGGGTTCAGACAGTGATAACAGCTATGAGCCGCCACCGAGTGAGCCATCCGAAGACAAGGCCCAGATCTGTCCTGCTAAACCCATGGACAACTGTGATTACATTGG[T/C]ACACACAAATGAACAGTTTTCAGTCTTGTGGTCATTGGAGTCTATTGGAAAAGTCATGATGGGATTCCTTTGTTACCAGATAATAACCGAACACGTGTAGTGAACCGAAGTCAACCTCCTGTCCCTCCAGAGCGACCAGGCCCTGGACCCTCAGTGCCCCCTGTAGACCGGCCAAGTGTGAGTCCTTCATATTTCCAAACAGTATGTGGCCGTCTTTGCCTCTAATCTAATTTTTGGATTGTTCTCTGAAATAATCTCTATTTTACACTCTTTAGGTTGGAATGCATGAGAGAATGAGAGAAGAGAGGCCCCAGACCCCGAAAAGACCAGCAGGTAAGACTCTATAACCATAACCATGACCTAGCAGATTGTTTTGATGATCATATGATGATCTTTTTTATTTATTTACTGTGGATTCTTGCTGGTCTTCTTATTGCATTTAATCATATTTTAGCAATTTTCTTGAATTGAAATGATTTGCATAGTTTTGGCTCCGTCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43671
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 |
|---|---|---|---|---|---|
| ENSDART00000059420 | Essential Splice Site | 203 | 501 | 8 | 21 |
| ENSDART00000145050 | Essential Splice Site | 203 | 500 | 8 | 19 |
| ENSDART00000059420 | Essential Splice Site | 203 | 501 | 8 | 21 |
| ENSDART00000145050 | Essential Splice Site | 203 | 500 | 8 | 19 |
Genomic Location (Zv9):
Chromosome 21 (position 29072466)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 30291710 |
| GRCz11 | 21 | 30328405 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGCGACCAGGCCCTGGACCCTCAGTGCCCCCTGTAGACCGGCCAAGTG[T/C]GAGTCCTTCATATTTCCAAACAGTATGTGGCCGTCTTTGCCTCTAATCTA
Long Flanking Sequence:
TATACTTATTGCAATAAACAGAGGTTTAGCAATAAATTTAATACTCAGTATCGGCTTCAAAAATCTTGATCGGAGCATCCCTATTTTAAAATAATCAGCATCACATGTAGCTAACATGACATTCCTCAATAAGACTAGTGATGAAGATGACTATGAGAATCCAGACTCAAATAATGATGATGATGCAAGCGGTGGAGATTATGAGTCGCCGGCGGAGGGTTCAGACAGTGATAACAGCTATGAGCCGCCACCGAGTGAGCCATCCGAAGACAAGGCCCAGATCTGTCCTGCTAAACCCATGGACAACTGTGATTACATTGGTACACACAAATGAACAGTTTTCAGTCTTGTGGTCATTGGAGTCTATTGGAAAAGTCATGATGGGATTCCTTTGTTACCAGATAATAACCGAACACGTGTAGTGAACCGAAGTCAACCTCCTGTCCCTCCAGAGCGACCAGGCCCTGGACCCTCAGTGCCCCCTGTAGACCGGCCAAGTG[T/C]GAGTCCTTCATATTTCCAAACAGTATGTGGCCGTCTTTGCCTCTAATCTAATTTTTGGATTGTTCTCTGAAATAATCTCTATTTTACACTCTTTAGGTTGGAATGCATGAGAGAATGAGAGAAGAGAGGCCCCAGACCCCGAAAAGACCAGCAGGTAAGACTCTATAACCATAACCATGACCTAGCAGATTGTTTTGATGATCATATGATGATCTTTTTTATTTATTTACTGTGGATTCTTGCTGGTCTTCTTATTGCATTTAATCATATTTTAGCAATTTTCTTGAATTGAAATGATTTGCATAGTTTTGGCTCCGTCAACACAGAATTGGATTTAGGTCAAGTTGCAAAATCTTCAGTGGAAACAATGACGTCAGTGTAGCATTTAACCAGAAGAAGGGGAAAGAACTTGCGCACGTAACAATCAGTGACAACAACAATGGCAGATTCCAGAGCTGTGTTCGCTCTGTAGGCGCTGATAAGTTTATTAGCATTATTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31060
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 |
|---|---|---|---|---|---|
| ENSDART00000059420 | Essential Splice Site | 203 | 501 | 8 | 21 |
| ENSDART00000145050 | Essential Splice Site | 203 | 500 | 8 | 19 |
| ENSDART00000059420 | Essential Splice Site | 203 | 501 | 8 | 21 |
| ENSDART00000145050 | Essential Splice Site | 203 | 500 | 8 | 19 |
Genomic Location (Zv9):
Chromosome 21 (position 29072466)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 30291710 |
| GRCz11 | 21 | 30328405 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGCGACCAGGCCCTGGACCCTCAGTGCCCCCTGTAGACCGGCCAAGTG[T/C]GAGTCCTTCATATTTCCAAACAGTATGTGGCCGTCTTTGCCTCTAATCTA
Long Flanking Sequence:
TATACTTATTGCAATAAACAGAGGTTTAGCAATAAATTTAATACTCAGTATCGGCTTCAAAAATCTTGATCGGAGCATCCCTATTTTAAAATAATCAGCATCACATGTAGCTAACATGACATTCCTCAATAAGACTAGTGATGAAGATGACTATGAGAATCCAGACTCAAATAATGATGATGATGCAAGCGGTGGAGATTATGAGTCGCCGGCGGAGGGTTCAGACAGTGATAACAGCTATGAGCCGCCACCGAGTGAGCCATCCGAAGACAAGGCCCAGATCTGTCCTGCTAAACCCATGGACAACTGTGATTACATTGGTACACACAAATGAACAGTTTTCAGTCTTGTGGTCATTGGAGTCTATTGGAAAAGTCATGATGGGATTCCTTTGTTACCAGATAATAACCGAACACGTGTAGTGAACCGAAGTCAACCTCCTGTCCCTCCAGAGCGACCAGGCCCTGGACCCTCAGTGCCCCCTGTAGACCGGCCAAGTG[T/C]GAGTCCTTCATATTTCCAAACAGTATGTGGCCGTCTTTGCCTCTAATCTAATTTTTGGATTGTTCTCTGAAATAATCTCTATTTTACACTCTTTAGGTTGGAATGCATGAGAGAATGAGAGAAGAGAGGCCCCAGACCCCGAAAAGACCAGCAGGTAAGACTCTATAACCATAACCATGACCTAGCAGATTGTTTTGATGATCATATGATGATCTTTTTTATTTATTTACTGTGGATTCTTGCTGGTCTTCTTATTGCATTTAATCATATTTTAGCAATTTTCTTGAATTGAAATGATTTGCATAGTTTTGGCTCCGTCAACACAGAATTGGATTTAGGTCAAGTTGCAAAATCTTCAGTGGAAACAATGACGTCAGTGTAGCATTTAACCAGAAGAAGGGGAAAGAACTTGCGCACGTAACAATCAGTGACAACAACAATGGCAGATTCCAGAGCTGTGTTCGCTCTGTAGGCGCTGATAAGTTTATTAGCATTATTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1278
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 > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000059420 | Essential Splice Site | 223 | 501 | 10 | 21 |
| ENSDART00000145050 | Essential Splice Site | 223 | 500 | 10 | 19 |
Genomic Location (Zv9):
Chromosome 21 (position 29077223)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 30296467 |
| GRCz11 | 21 | 30333162 |
KASP Assay ID:
554-1193.1 (used for ordering genotyping assays)
KASP Sequence:
TAGAAATGTTGTTGTTGAAGTTACCCAGTAAACAATGYTGTTTTTACTCC[A/T]GCACCAGCTGTGGACCGCAGTAAAAAACCAGGAACTTTGGATAGAATTCA
Long Flanking Sequence:
CCTTTTGAGTTCAGAATTTTTACATTTTCATGTCTCTGTTCCAAAACAAGTTTAGCAGGAATTAAACGTTAAAAGATTTAAATAGATTGAAGGAAACAAAATAATTAGGATGAAGAACAGTACAACAACTGCATTTCTGCAGTCAGTTTCATGAGACCTAATAATAATAAAATAACCTAATAATGAGACCTAAGCATCGTGCTGGATTTTGAACACGTTTTAGTGCACTTATTTTTTATTGCTTAGATTATAGTTTAAAGTAAGTACACTTGGGTGCTGGGCATTGATTATATTGGTCATCTTAATGTCATGTGGACATTGCACATGGTTAAGCGCTGAGGCAGGCCAGACTAAACACTTTTAAAACCTTTAGTCATTCTGAGAACATACAAAGGCTCTCATTTTTGATGAAACATTCAAATCTATGATCGTTTTCAGCTAAAGATGAATTAGAAATGTTGTTGTTGAAGTTACCCAGTAAACAATGTTGTTTTTACTCC[A/T]GCACCAGCTGTGGACCGCAGTAAAAAACCAGGAACTTTGGATAGAATTCACCCTCCAGCTGTAGCAGGTCTGTTTGTAATAATTAAAAATTATGATAAATAAATAATAACTATAATAACAGTCATGATACAAATCAGATGCCATTTATTTGACCTGGTGTCAAAGCCACCATTAAAGATAATACAGGCTTTGTCTAAAGGAAAAGATTTACCAATTTTAACAGTCTTTATCAAACTTTAAACTGACTGTCTTCACAGGAGGAAGAGGAACTAGCTCACTTGATAGAGTAAGTTTGGTTTGTTCTGTCTTTATTTCACACAAATTGTTCTGAATAACAAATGTTTTCATTGAAAAAGTAGATTATTTCTGTTACGAAGCAGACGCCGGCAAAAAAAACTTGCAGATCCAGATGCAGTTTATTAAAGGCGAGGTCGTACAGGCAAAACGGGAGTAAAACAACAGCATAAGGGTTGTCCAATAAACATGATCAAAACACAGGC
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:
sa29621
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 |
|---|---|---|---|---|---|
| ENSDART00000059420 | Essential Splice Site | 254 | 501 | 11 | 21 |
| ENSDART00000145050 | Essential Splice Site | 254 | 500 | 11 | 19 |
Genomic Location (Zv9):
Chromosome 21 (position 29077510)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 30296754 |
| GRCz11 | 21 | 30333449 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAAACTGACTGTCTTCACAGGAGGAAGAGGAACTAGCTCACTTGATAGA[G/A]TAAGTTTGGTTTGTTCTGTCTTTATTTCACACAAATTGTTCTGAATAACA
Long Flanking Sequence:
TTATATTGGTCATCTTAATGTCATGTGGACATTGCACATGGTTAAGCGCTGAGGCAGGCCAGACTAAACACTTTTAAAACCTTTAGTCATTCTGAGAACATACAAAGGCTCTCATTTTTGATGAAACATTCAAATCTATGATCGTTTTCAGCTAAAGATGAATTAGAAATGTTGTTGTTGAAGTTACCCAGTAAACAATGTTGTTTTTACTCCAGCACCAGCTGTGGACCGCAGTAAAAAACCAGGAACTTTGGATAGAATTCACCCTCCAGCTGTAGCAGGTCTGTTTGTAATAATTAAAAATTATGATAAATAAATAATAACTATAATAACAGTCATGATACAAATCAGATGCCATTTATTTGACCTGGTGTCAAAGCCACCATTAAAGATAATACAGGCTTTGTCTAAAGGAAAAGATTTACCAATTTTAACAGTCTTTATCAAACTTTAAACTGACTGTCTTCACAGGAGGAAGAGGAACTAGCTCACTTGATAGA[G/A]TAAGTTTGGTTTGTTCTGTCTTTATTTCACACAAATTGTTCTGAATAACAAATGTTTTCATTGAAAAAGTAGATTATTTCTGTTACGAAGCAGACGCCGGCAAAAAAAACTTGCAGATCCAGATGCAGTTTATTAAAGGCGAGGTCGTACAGGCAAAACGGGAGTAAAACAACAGCATAAGGGTTGTCCAATAAACATGATCAAAACACAGGCAAGAGGTCAGGCTAGGTAGCAACAAATCAAAACGAGGAACAAGGCAAGAGTCAAAATACAGGAAAACAAACAAGAAGAAATGCTTTGTAATGTTTGTGATAGAAACAAGACTCAAAATGTGAGTGAAAGAAGATTATTTCAATGTGGTGATGTCATTGGCCCCTGAACATTTTCTGCTTGTTGTCAAACTATTTCATATTACTGTAACACAAGGCAATTCAATGATAACTTATTTTTAAAACAGCTAACATAGCATTATTCTTCAATATGTGGAGCTTTTTGGATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23970
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 |
|---|---|---|---|---|---|
| ENSDART00000059420 | Essential Splice Site | 363 | 501 | 17 | 21 |
| ENSDART00000145050 | Essential Splice Site | 362 | 500 | 15 | 19 |
Genomic Location (Zv9):
Chromosome 21 (position 29083879)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 30303123 |
| GRCz11 | 21 | 30339818 |
KASP Assay ID:
2261-5779.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTACGCAGCGTTAATCCCAGTCGATCACTACCGGCTAAACTGCAGGAGG[G/A]TAAGCTAAGCACACATTACACTAGTTTGATGAAATCTTCATTCAGTCAGA
Long Flanking Sequence:
GCTGGTGCAACACCATAGGTTCTTATGGGAAACAAAAATGGTTCTTCAATGGCATTGATGCAAAAATACAATTTCAGAAGCATATTTATTTAAGATTGTTGACATAAATATAGCACTCACTTCTTTCAACCGTTGTTTTTTCTTTTTTCTTTTAGTTTCATGATGACAGTAAGTAACCGAATCATATATTGTATTTGCATATCTTGATGAGAGAGTTAGCTTTGTTATCACAAACTAATGAGAAAGTGTTTTAATGCTCTGCGATTGTTCCAGCTGCCAGGCAAACCTCCAACACATTTCCACTGCATGCCAGGAATCCGTCACCGAGACCGCCAGGAACACACGGACAGTCTTTTCAAACCGACAGGCATGTGTCAAATGCTGAATGAATGATAAAAATACAAGTCAAGTTACAGATCCTCTGTTATTTTTGACTGTTCTCTGCTTTATTTTACGCAGCGTTAATCCCAGTCGATCACTACCGGCTAAACTGCAGGAGG[G/A]TAAGCTAAGCACACATTACACTAGTTTGATGAAATCTTCATTCAGTCAGAATACCTGTTAAATATTTGATGTTGTTAAATTGAAGCAATGACTGATCACCGGAGAAGTGCAAGAGCTTCACCACCACAAACAGACATGGGCGGCAGACAGGTACAGTAGAAATGCTTACAGTAATACTTTCACCTTAAAAAGATTATCTGCTATTCATTTACTCCCCCACATACTATCCAAGATGTTAGTGACACTTCTGTTAAGTGAAAACATTTTTAGACGAAACTGTGGAAATTGGTGATATCATAAAAAAGCAACACTCTGAGAGTTCAAGGCATGATATATAAGATTTTTTTCATTAAAGTATGCAATAACTATTAGAACGGTGTTCTATATTTTGCTGACTTGTGTACTCGCATTATGCCAAATGTTACGAGTAATGTTCAAATCCAGAGAAATAAGCTATTTTAACTAGTGACCTGTGTGTTTATGCTGATTACCAGTGTTGG
Associated Phenotype:
Not determined