ZMP
zgc:175136
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC100136863 [Source:RefSeq peptide;Acc:NP_001108053]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36860 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18165 | Nonsense | Available for shipment | Available now |
sa8695 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23546 | Nonsense | Available for shipment | Available now |
sa9270 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa3009 | Nonsense | F2 line generated | Not yet available |
sa29226 | Missense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa36860
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 |
---|---|---|---|---|---|
ENSDART00000109429 | Nonsense | 20 | 599 | 3 | 5 |
ENSDART00000132237 | Nonsense | 47 | 626 | 3 | 5 |
The following transcripts of ENSDARG00000079916 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 30560885)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 14247511 |
GRCz11 | 19 | 14109706 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGTGATGTTCAAAGATTTTTAACACCTACCTTACCAGTGATTGGTTCT[G/T]AGGTGAAACAAAAGGCAATTTGGAATGAACTTTCCTATGGTTCTGTTCGT
Long Flanking Sequence:
AAAACATTTTTTACTACTCCAAAACAGGTTTGACTATTTAGTAAAGGGAAAATTGGCAACAGCTGCAGCTAGCAGGTATCCTGCTTTCTGATTGGTCAAAGGTGAAGACTAAAGTCTATAAGAGACTTCCACTGAGGAATGAGCTGAAAGCTGAAGTGAGGGCATCATAAAAGAAGCTGCTGCTCACTTGGTTTTTGTGGGTGTCTTAACAATGGGTTCTGGATTCTGTTCAATGTAAGCATTTGTCTGTCTGCAGCGGACTTGAATTGTACATTGGTCAACACAATGTTTGAAACTTTGTTTGCTTTCAGATTTCTTTTTGCCTTGTTTCCTGCTTATGTAACCTGTTGGGGGAATTATGAAGGTAAGACCAACACACTGCTATTGTTTCTCCTGAACATTGCTACCTTATACTGTATGTGTCTATTGTTTTTACAGGAAGCATGCCAGATGGTGATGTTCAAAGATTTTTAACACCTACCTTACCAGTGATTGGTTCT[G/T]AGGTGAAACAAAAGGCAATTTGGAATGAACTTTCCTATGGTTCTGTTCGTCAGCCATATTATCGAGGCACCCATGAAAGTTATGATGCCAAAGGAAGTTTGTTTGTGGGCTCAAATGCTAAATCATACACAAAAGACTGTCAGGCTCCAGCTAAAAGTGGCAATCGAGAAAATATGATGAATTTTAATTCTAATTCACTATCAAAATATGGTGGCTCAAGTTGTGGTCAACCCTCTACTCAATATGAGTCTCGTACAGATACTAATTCCCTCAAAAATGTCCAGGTTGGTAGCCGACTTGCTTCAGCCTTGTCTCAAAGTGGGCCCACATTGAGAAAAACCTTGAAAGTACCTGAATTGAGTAGTTTAAAAATCTCTAGAGGTGAATCTAGTTATGGGGCAGGTCAGAGTATTAACAATGTCCAGATAGCCAGTAACAGTTTTGGCCCACTGCTGAAAGGATCGCCTGTGCAATCAAATATAAATCCAGGAAAACTCTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18165
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109429 | Nonsense | 131 | 599 | 3 | 5 |
ENSDART00000132237 | Nonsense | 158 | 626 | 3 | 5 |
The following transcripts of ENSDARG00000079916 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 30561218)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 14247844 |
GRCz11 | 19 | 14110039 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGTTGGTAGCCGACTTGCTTCAGCCTTGTCTCAAAGTGGGCCCACATTG[A/T]GAAAAACCTWRAAAGTACCTGAATTGAGTAGTTTAAAAATMTCTAGAGGT
Long Flanking Sequence:
GCTTATGTAACCTGTTGGGGGAATTATGAAGGTAAGACCAACACACTGCTATTGTTTCTCCTGAACATTGCTACCTTATACTGTATGTGTCTATTGTTTTTACAGGAAGCATGCCAGATGGTGATGTTCAAAGATTTTTAACACCTACCTTACCAGTGATTGGTTCTGAGGTGAAACAAAAGGCAATTTGGAATGAACTTTCCTATGGTTCTGTTCGTCAGCCATATTATCGAGGCACCCATGAAAGTTATGATGCCAAAGGAAGTTTGTTTGTGGGCTCAAATGCTAAATCATACACAAAAGACTGTCAGGCTCCAGCTAAAAGTGGCAATCGAGAAAATATGATGAATTTTAATTCTAATTCACTATCAAAATATGGTGGCTCAAGTTGTGGTCAACCCTCTACTCAATATGAGTCTCGTACAGATACTAATTCCCTCAAAAATGTCCAGGTTGGTAGCCGACTTGCTTCAGCCTTGTCTCAAAGTGGGCCCACATTG[A/T]GAAAAACCTTGAAAGTACCTGAATTGAGTAGTTTAAAAATCTCTAGAGGTGAATCTAGTTATGGGGCAGGTCAGAGTATTAACAATGTCCAGATAGCCAGTAACAGTTTTGGCCCACTGCTGAAAGGATCGCCTGTGCAATCAAATATAAATCCAGGAAAACTCTCTCAGGGTGGACCTTCAGTTGTTAGTTCGGGACCAGTCTTTGTAGTTCAAGATAAAGAGAGTGCCCAAGGTCAAAATGGCTTTCCAGATTATGGAAAACCGCCTGTTCATAGACTCATTAAACCCTACAAGGGCAGTCAGACCTCTAGAGATGGTAGCTTGTCTGCTAGCAGTCTGGGAAAGGCATGGAAAAAGACACTTCAATACTCCAAGAGTGGAACTCAATACAATCTCGACACAGAGTTAAGAAAACCTTCCAAAAATGATTGCAAAGACAATCCTGCTGAGTCAATTGCCAGCTCTGGTGAGGTTCTTCGAAAGACCCAAGAAAGTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8695
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 |
---|---|---|---|---|---|
ENSDART00000109429 | Nonsense | 134 | 599 | 3 | 5 |
ENSDART00000132237 | Nonsense | 161 | 626 | 3 | 5 |
The following transcripts of ENSDARG00000079916 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 30561228)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 14247854 |
GRCz11 | 19 | 14110049 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCGACTTGCTTCAGCCTTGTCTCAAAGTGGGCCCACATTGAGAAAAACCT[T/A]RAAAGTACCTGAATTGAGTAGTTTAAAAATMTCTAGAGGTGAATCTAGTT
Long Flanking Sequence:
CCTGTTGGGGGAATTATGAAGGTAAGACCAACACACTGCTATTGTTTCTCCTGAACATTGCTACCTTATACTGTATGTGTCTATTGTTTTTACAGGAAGCATGCCAGATGGTGATGTTCAAAGATTTTTAACACCTACCTTACCAGTGATTGGTTCTGAGGTGAAACAAAAGGCAATTTGGAATGAACTTTCCTATGGTTCTGTTCGTCAGCCATATTATCGAGGCACCCATGAAAGTTATGATGCCAAAGGAAGTTTGTTTGTGGGCTCAAATGCTAAATCATACACAAAAGACTGTCAGGCTCCAGCTAAAAGTGGCAATCGAGAAAATATGATGAATTTTAATTCTAATTCACTATCAAAATATGGTGGCTCAAGTTGTGGTCAACCCTCTACTCAATATGAGTCTCGTACAGATACTAATTCCCTCAAAAATGTCCAGGTTGGTAGCCGACTTGCTTCAGCCTTGTCTCAAAGTGGGCCCACATTGAGAAAAACCT[T/A]GAAAGTACCTGAATTGAGTAGTTTAAAAATCTCTAGAGGTGAATCTAGTTATGGGGCAGGTCAGAGTATTAACAATGTCCAGATAGCCAGTAACAGTTTTGGCCCACTGCTGAAAGGATCGCCTGTGCAATCAAATATAAATCCAGGAAAACTCTCTCAGGGTGGACCTTCAGTTGTTAGTTCGGGACCAGTCTTTGTAGTTCAAGATAAAGAGAGTGCCCAAGGTCAAAATGGCTTTCCAGATTATGGAAAACCGCCTGTTCATAGACTCATTAAACCCTACAAGGGCAGTCAGACCTCTAGAGATGGTAGCTTGTCTGCTAGCAGTCTGGGAAAGGCATGGAAAAAGACACTTCAATACTCCAAGAGTGGAACTCAATACAATCTCGACACAGAGTTAAGAAAACCTTCCAAAAATGATTGCAAAGACAATCCTGCTGAGTCAATTGCCAGCTCTGGTGAGGTTCTTCGAAAGACCCAAGAAAGTGCACTGAGAAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23546
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109429 | Nonsense | 228 | 599 | 3 | 5 |
ENSDART00000132237 | Nonsense | 255 | 626 | 3 | 5 |
The following transcripts of ENSDARG00000079916 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 30561511)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 14248137 |
GRCz11 | 19 | 14110332 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCTTTCCAGATTATGGAAAACCGCCTGTTCATAGACTCATTAAACCCTA[C/A]AAGGGCAGTCAGACCTCTAGAGATGGTAGCTTGTCTGCTAGCAGTCTGGG
Long Flanking Sequence:
TACACAAAAGACTGTCAGGCTCCAGCTAAAAGTGGCAATCGAGAAAATATGATGAATTTTAATTCTAATTCACTATCAAAATATGGTGGCTCAAGTTGTGGTCAACCCTCTACTCAATATGAGTCTCGTACAGATACTAATTCCCTCAAAAATGTCCAGGTTGGTAGCCGACTTGCTTCAGCCTTGTCTCAAAGTGGGCCCACATTGAGAAAAACCTTGAAAGTACCTGAATTGAGTAGTTTAAAAATCTCTAGAGGTGAATCTAGTTATGGGGCAGGTCAGAGTATTAACAATGTCCAGATAGCCAGTAACAGTTTTGGCCCACTGCTGAAAGGATCGCCTGTGCAATCAAATATAAATCCAGGAAAACTCTCTCAGGGTGGACCTTCAGTTGTTAGTTCGGGACCAGTCTTTGTAGTTCAAGATAAAGAGAGTGCCCAAGGTCAAAATGGCTTTCCAGATTATGGAAAACCGCCTGTTCATAGACTCATTAAACCCTA[C/A]AAGGGCAGTCAGACCTCTAGAGATGGTAGCTTGTCTGCTAGCAGTCTGGGAAAGGCATGGAAAAAGACACTTCAATACTCCAAGAGTGGAACTCAATACAATCTCGACACAGAGTTAAGAAAACCTTCCAAAAATGATTGCAAAGACAATCCTGCTGAGTCAATTGCCAGCTCTGGTGAGGTTCTTCGAAAGACCCAAGAAAGTGCACTGAGAAACATGTTGCCGCCTCGTTATGAAGCAACTATTCCCAAATTTCAGCAAGTTCACAACAGTCGTGGACAATCAAATCAAATGTTTAAACCCATGTACCCCCCTCAAAATGGGGCTCAACAGAATGTTGGTAGAAAGTCCACAACTGCCAGTTCTGGGTTGATCCTGGTTCAGCAGGCTCCTACAGATGCTCTGAGTGGGAAAGAATCCAATAATCGTAATGTGTATCCTAGTTTTTCAGAGCGTGAAGTAGCATTTGCCTCTGGCCAGACTTCTCATCAATACCAACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9270
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 |
---|---|---|---|---|---|
ENSDART00000109429 | Nonsense | 239 | 599 | 3 | 5 |
ENSDART00000132237 | Nonsense | 266 | 626 | 3 | 5 |
The following transcripts of ENSDARG00000079916 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 30561543)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 14248169 |
GRCz11 | 19 | 14110364 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAGACTCATTAAACCCTACAAGGGCAGTCAGACCTCTAGAGATGGTAGCT[T/A]GTCTGCTAGCAGTCTGGGAAAGGCATGGAAAAAGACACTTCAATACTCCA
Long Flanking Sequence:
TGGCAATCGAGAAAATATGATGAATTTTAATTCTAATTCACTATCAAAATATGGTGGCTCAAGTTGTGGTCAACCCTCTACTCAATATGAGTCTCGTACAGATACTAATTCCCTCAAAAATGTCCAGGTTGGTAGCCGACTTGCTTCAGCCTTGTCTCAAAGTGGGCCCACATTGAGAAAAACCTTGAAAGTACCTGAATTGAGTAGTTTAAAAATCTCTAGAGGTGAATCTAGTTATGGGGCAGGTCAGAGTATTAACAATGTCCAGATAGCCAGTAACAGTTTTGGCCCACTGCTGAAAGGATCGCCTGTGCAATCAAATATAAATCCAGGAAAACTCTCTCAGGGTGGACCTTCAGTTGTTAGTTCGGGACCAGTCTTTGTAGTTCAAGATAAAGAGAGTGCCCAAGGTCAAAATGGCTTTCCAGATTATGGAAAACCGCCTGTTCATAGACTCATTAAACCCTACAAGGGCAGTCAGACCTCTAGAGATGGTAGCT[T/A]GTCTGCTAGCAGTCTGGGAAAGGCATGGAAAAAGACACTTCAATACTCCAAGAGTGGAACTCAATACAATCTCGACACAGAGTTAAGAAAACCTTCCAAAAATGATTGCAAAGACAATCCTGCTGAGTCAATTGCCAGCTCTGGTGAGGTTCTTCGAAAGACCCAAGAAAGTGCACTGAGAAACATGTTGCCGCCTCGTTATGAAGCAACTATTCCCAAATTTCAGCAAGTTCACAACAGTCGTGGACAATCAAATCAAATGTTTAAACCCATGTACCCCCCTCAAAATGGGGCTCAACAGAATGTTGGTAGAAAGTCCACAACTGCCAGTTCTGGGTTGATCCTGGTTCAGCAGGCTCCTACAGATGCTCTGAGTGGGAAAGAATCCAATAATCGTAATGTGTATCCTAGTTTTTCAGAGCGTGAAGTAGCATTTGCCTCTGGCCAGACTTCTCATCAATACCAACCTTTCAAAGTGACCCAGAATTCCAGAAATGCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3009
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 |
---|---|---|---|---|---|
ENSDART00000109429 | Nonsense | 322 | 599 | 3 | 5 |
ENSDART00000132237 | Nonsense | 349 | 626 | 3 | 5 |
The following transcripts of ENSDARG00000079916 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 30561791)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 14248417 |
GRCz11 | 19 | 14110612 |
KASP Assay ID:
554-2644.1 (used for ordering genotyping assays)
KASP Sequence:
GTTATGAAGCAACTATTCCCAAATTTCAGCAAGTTCACAACAGTCGTGGA[C/T]AATCAAATCAAATGTTTAAACCCATGTACCCCCCTCAAAATGGGGCTCAA
Long Flanking Sequence:
AGAGTATTAACAATGTCCAGATAGCCAGTAACAGTTTTGGCCCACTGCTGAAAGGATCGCCTGTGCAATCAAATATAAATCCAGGAAAACTCTCTCAGGGTGGACCTTCAGTTGTTAGTTCGGGACCAGTCTTTGTAGTTCAAGATAAAGAGAGTGCCCAAGGTCAAAATGGCTTTCCAGATTATGGAAAACCGCCTGTTCATAGACTCATTAAACCCTACAAGGGCAGTCAGACCTCTAGAGATGGTAGCTTGTCTGCTAGCAGTCTGGGAAAGGCATGGAAAAAGACACTTCAATACTCCAAGAGTGGAACTCAATACAATCTCGACACAGAGTTAAGAAAACCTTCCAAAAATGATTGCAAAGACAATCCTGCTGAGTCAATTGCCAGCTCTGGTGAGGTTCTTCGAAAGACCCAAGAAAGTGCACTGAGAAACATGTTGCCGCCTCGTTATGAAGCAACTATTCCCAAATTTCAGCAAGTTCACAACAGTCGTGGA[C/T]AATCAAATCAAATGTTTAAACCCATGTACCCCCCTCAAAATGGGGCTCAACAGAATGTTGGTAGAAAGTCCACAACTGCCAGTTCTGGGTTGATCCTGGTTCAGCAGGCTCCTACAGATGCTCTGAGTGGGAAAGAATCCAATAATCGTAATGTGTATCCTAGTTTTTCAGAGCGTGAAGTAGCATTTGCCTCTGGCCAGACTTCTCATCAATACCAACCTTTCAAAGTGACCCAGAATTCCAGAAATGCCCAGCCAGCCACTGACTCTTATGGTAGCTCTTCTAAGACTGGATATCAGACCTTCTCTTCTTTAAAGGGAACTTCATACAAACCAAGTTCAGGCTCCTCAAAGTCCTCTACAAGTGTGTTCAGTGCCACCAACCCCAATTTTGCTGAACCTAATGAGATTAACACGGTCCATGTAAGGCCTAACAAACCATTTGCAAGCAGCTTTGGTCAAGTACAGAGCCAAAGGGCTTCTGGTGACATTAGCAGAGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29226
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:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109429 | Missense | 488 | 599 | 3 | 5 |
ENSDART00000132237 | Missense | 515 | 626 | 3 | 5 |
The following transcripts of ENSDARG00000079916 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 30562290)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 14248916 |
GRCz11 | 19 | 14111111 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCTTTGGTCAAGTACAGAGCCAAAGGGCTTCTGGTGACATTAGCAGAG[G/A]TGCTTATCAAAGTTCCTTACCTTCCAGTTACATGGGTCTAATGCCTAGTA
Long Flanking Sequence:
ACAATCAAATCAAATGTTTAAACCCATGTACCCCCCTCAAAATGGGGCTCAACAGAATGTTGGTAGAAAGTCCACAACTGCCAGTTCTGGGTTGATCCTGGTTCAGCAGGCTCCTACAGATGCTCTGAGTGGGAAAGAATCCAATAATCGTAATGTGTATCCTAGTTTTTCAGAGCGTGAAGTAGCATTTGCCTCTGGCCAGACTTCTCATCAATACCAACCTTTCAAAGTGACCCAGAATTCCAGAAATGCCCAGCCAGCCACTGACTCTTATGGTAGCTCTTCTAAGACTGGATATCAGACCTTCTCTTCTTTAAAGGGAACTTCATACAAACCAAGTTCAGGCTCCTCAAAGTCCTCTACAAGTGTGTTCAGTGCCACCAACCCCAATTTTGCTGAACCTAATGAGATTAACACGGTCCATGTAAGGCCTAACAAACCATTTGCAAGCAGCTTTGGTCAAGTACAGAGCCAAAGGGCTTCTGGTGACATTAGCAGAG[G/A]TGCTTATCAAAGTTCCTTACCTTCCAGTTACATGGGTCTAATGCCTAGTAAGGAGGTACAAATATCTGCTAGTTCCTCAGCTCAATTTTATGGTTCTAGAAACCAGAACCAACTTGTTGAAACTCAAGAAGACACAGATGATATCAGATGCATTACAACCATTCCAAGTGAATTTGGCCAAGGTGCCATTCGAAGACTTTCTCCTAAGCTTTCCAGCAAATACAGACGAGGTTTGCTTCAAAGTGCACCATCATTACAAGATCATTGTATGTTTGAAATGTGATTGTTATAACATACTCTTCTTTCTTCCTGCCACAGTTAAACAAAATGGACAAGAAAGACTGGATTTTGTAGCCCCAAAATGTTATTCTAGTCTTGGTCAAAAGGGCTCAGTCAATTTCCAGGAAGTGAACCGGTCTGTCTAAAAGCACTTCAACGTCTGCCATAATGTAAGTACAGTTGCTTTACCTAGAGTTTAAACTTGTATATTTGGATGAGCA
Associated Phenotype:
Not determined