ZMP
si:dkey-108d22.4
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate piccolo (Presynaptic cytomatrix protein) (PCLO) [Source:UniProtK
Human Orthologue:
BSN
Human Description:
bassoon (presynaptic cytomatrix protein) [Source:HGNC Symbol;Acc:1117]
Mouse Orthologue:
Bsn
Mouse Description:
bassoon Gene [Source:MGI Symbol;Acc:MGI:1277955]
Alleles
There are 19 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa26245 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa26246 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9380 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa1417 | Nonsense | Available for shipment | Available now |
sa33409 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33410 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33411 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33412 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40241 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17573 | Nonsense | Available for shipment | Available now |
sa33413 | Essential Splice Site | Available for shipment | Available now |
sa20227 | Nonsense | Available for shipment | Available now |
sa11716 | Nonsense | Available for shipment | Available now |
sa20228 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa26245
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092381 | Nonsense | 24 | 4152 | 1 | 32 |
ENSDART00000136117 | None | None | 3096 | None | 15 |
ENSDART00000143963 | None | None | 3298 | None | 20 |
Genomic Location (Zv9):
Chromosome 4 (position 10451602)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 11388229 |
GRCz11 | 4 | 11387078 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGAAAGGGTCCTCCTCAAGGGAGTAAGCCACCTCAGCAGGGTCCCCCT[A/T]AAGGGCAGGGACCTCTTCAGCAAGGGCCCAAACCTGGTGGACCAGGACCC
Long Flanking Sequence:
AACAGCTTTTAAATAAATACAGCACATTTTCATCAATCACCTATTTTGGAAAGATTTATGTTGACCTGAGAGTAATATGAAGTTAACCTTATGTTTGTTCACTTCACAGGCCACCAGAGACTCAAGCTGGGGGTACCAAAGTCCCAGTCGGTCTCAGTAAGAGTCGAACAGTAGATGCTTTTGGAGAGGGGCCGCCTCCCAAGCCAAAGCCTGGACGCAGCCCCTCCTCCCTCAGCCTCCTTGAGTCACGTTTCCGGCAGGAGCCCAAAGACCCAGAACAACCAAGAACTGGCATGTTCTCATCTGGCTTCCTGAGTGGGGCCAACCCTTTGAGTGCGGTTTCTTCTGCTGTCTCCTCTGCCAGCATCCCAAAGTTTAGTTTGTTTGGTGATGATGAAGAGGAGGAGTCTGCAAAGCAGGAAGGAAAGCCTCCTGGTCCACAGAGCGGAGTGGGAAAGGGTCCTCCTCAAGGGAGTAAGCCACCTCAGCAGGGTCCCCCT[A/T]AAGGGCAGGGACCTCTTCAGCAAGGGCCCAAACCTGGTGGACCAGGACCCCAGCAAGGACCCAAACCTGGTGGACCAGAAGCTCAACATCAGGCACCTAAACCTGGAGCACCAGGACCTCAACAGGGACCTAAACCTGGTGGACCTGGACCTCAGCAACAAGGACCTAAACCTGGTGGACCGGGAATTCAGCAGCAAGGACCTAAACCCAGTGGACCTGGGCCTCAGCAGCAAGGACCTAGACCTGGTGGACCTGGACCTCAGCAGCAAGGACCTAAACCTGGTGGACCTGGACCTCAGCAGCAAGGATCTAAACCTGGTGGACCTGGACCTCAACAGCAAGGACCCAAACCTGGAGGACCAGGGCCCCAGCAACAAGGGCCTGGAAAACCTGGCCCAGGGGTTGCAGGAAAACCTAGTGGACCTCAACAGCAGGGTAAACCTGGGCCAGGTGCTCTATCAGAAGGGCCTGGTAAAGCTGCACCAGCTCCAGGAAAAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26246
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 |
---|---|---|---|---|---|
ENSDART00000092381 | Nonsense | 335 | 4152 | 2 | 32 |
ENSDART00000136117 | None | None | 3096 | None | 15 |
ENSDART00000143963 | None | None | 3298 | None | 20 |
Genomic Location (Zv9):
Chromosome 4 (position 10453284)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 11389911 |
GRCz11 | 4 | 11388760 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGACCACAGCAGGGACCTCAGCCTGGACAACTAGGGGCAAAACGTGGA[C/T]AGCCTCCACCACTTCAGAAACCTTCACAGAGCCCAAAAGGTAGTCCCCAA
Long Flanking Sequence:
GCTTTTAATAACAGCAAGTTCACTACAAATTACCATGCTATATACTGGATGTTTTGTTCTGCTCAGCATAAATAAATAATGTTCTGCAAGGCCTTTTTAATGCACACAGCTTGAAGTAATTTAAATGCAGATGGCTATTCTTACAAAAATGATATTGTGCTGCATTTGTGCTCATATACCTTGACATTATCTTCTTGTTTTCACAGAGTAAGGAATGGCTGTGTCTGAACTGTCAGATGCAGCGGGCGATGGGTGGCATGGAGCCTCCTGGACCTCCAATGATGAAGCAGCCACCCAAGCAGGGCTCAGCACCTCCCTCCCCACAAAGGAAAGAACCACCGCCTGGATCTCCCTCCAAGGTTGAGCCTGGTAAAAAGCCCCCAATGCTGACCAAACAACAGAGTATTGCTGATACAGGCAAGGGAAGTACACCTCCAACAACACCAAAATCTGGACCACAGCAGGGACCTCAGCCTGGACAACTAGGGGCAAAACGTGGA[C/T]AGCCTCCACCACTTCAGAAACCTTCACAGAGCCCAAAAGGTAGTCCCCAACCATCTCCAGCCAAAACAACCCCGAAGCAGGACGGAGGGGGCTTTTTTGGAGGATTTGGTCTTGGAGGTTTGACAGAGGTAACAAAACCCTCTCCAGCTGCCCAAGCTACAGAGTCCGTCACAGGAAAACTCTTCAGTGGTTTTGGTGGGGGGTCCAAACCTCAGGGTGGCTCTGCAGCTCCAGCAAGTGAGTCCGTCACAGGAAAACTTTTCAGTGGCTTCAGTGGCCTCACAGAGACGACAAAACCTTTACCAGCACAATCTCAGTCCACTGAGAGCGTTTCTGGAAAGATGTTTGGTTTTGGATCATCCTTCCTGAGCTCTGCCACCAATCTCATCTCTGGGGAGGAATCAAAGTCTCCCCCTGATTCTCCCGCAGGATCACCCCCTGATTCCCCCATTGGGTCAGATGCAGACTCCCCTGCTGGATCCCCCCCAGACTCTGGCTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9380
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092381 | Nonsense | 1261 | 4152 | 10 | 32 |
ENSDART00000136117 | Nonsense | 409 | 3096 | 1 | 15 |
ENSDART00000143963 | Nonsense | 409 | 3298 | 1 | 20 |
Genomic Location (Zv9):
Chromosome 4 (position 10480040)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 11416667 |
GRCz11 | 4 | 11415516 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAGARCTAAGACAGGARGCAGAAATGGAGGAAATCCGCAGGTCTTCCTG[C/A]TCAGACCTCTCCCCAAGCATRGATTCAGAACCAGAGAGTTTTGAGMTWCT
Long Flanking Sequence:
GAGCTTAACAGTACAGCAACTGTACGCCAGACATCAGATGACGGTGAGCCAGAGAGCCTTACAGACTCTCCTGATGACAGATCAAGAGGCGAAGGCTCTTCCAGTTTGCATGCATCCAGTTTTACCCCTGGAACGTCTCCAACATCTTTGTCTTCTCTTGATGAAGACAGTGACAGCAGCAGCCCAAGTCATGTTCGATCCAGTGGTGAGGGCAAACAGCAGAGGAAAGCAAAACACCGGCAGCCAGGTCAGATGCTTCCTACCATTGAGGATTCATCAGAGGAAGAGGAGTTGCGAGAAGAAGAGGAGCTTCTGAGAGAACAGGAGAAGCAAAAGGGCTCAGGAAAAAAGTCAAAGAAAGACAAAGAAGAGATAAGGGCACAGAGAAGGAGAGAAAGGCCTAAAACTCCTCCAAGTAATCTCTCACCAATTGAGGATGCATCTCCCACAGAAGAGCTAAGACAGGAGGCAGAAATGGAGGAAATCCGCAGGTCTTCCTG[C/A]TCAGACCTCTCCCCAAGCATAGATTCAGAACCAGAGAGTTTTGAGATACTCCCCGAGAAAATTGTTGCTGTCCAAAAAGTTTATCAGCTACCAACATCAGTCTCGCTGTATTCTCCCACAGATGAGCAACATGCTGATAATCAGTCCAAAGAAAAGGGAAAGCAATCATTAAAAACGGCAGAAGAGGCATATGAAGAGATTATGCTTAAAGCCAAATCTCCTACTAATGAGGGAAAGGAATCTCCACCTGGTAAAGTATCTCTGTATGGGGGCATGCTAATAGAAGATTATGCCTATGAGTCTCTTGTTGATGATGCATCCTGTGAGCAGGAGCCAGAAAAGCTTAATGTGTCAGAGAAACCAAAAAAACCTCTAAGATCTCCTGATGAGGTTTATGAGGATATGATGCAAAGAAAAGAGATTATGATTAAGAAACATGAGCTAAAGCATGATAAGCCAATGGAAGATGTACCTAAACCTGAAACCGAGTTGGTCAATAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1417
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 |
---|---|---|---|---|---|
ENSDART00000092381 | Nonsense | 1878 | 4152 | 10 | 32 |
ENSDART00000136117 | Nonsense | 1026 | 3096 | 1 | 15 |
ENSDART00000143963 | Nonsense | 1026 | 3298 | 1 | 20 |
Genomic Location (Zv9):
Chromosome 4 (position 10481889)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 11418516 |
GRCz11 | 4 | 11417365 |
KASP Assay ID:
554-1338.1 (used for ordering genotyping assays)
KASP Sequence:
CTCAGCAGTCACAAACAACTAGAGTACCACTGGCATTCACACGGATAACT[G/T]AATCTATTGAAAGTCAAGAAATTTGTGGTCCAGAGAAAGTAGTTTCTAGC
Long Flanking Sequence:
GAGACAGTGTACCAATAAAACAGCCTCTAGGTCAAGGCTACAAGCCCCATGTTCCCCCTCCTGTACCACCAAAGCCGTCCTCTATCCCTGCAGGCCTAAACTTCAGTCACAAGCAAGGGGAAAGTTTTAAACCTCCCATAGCTCCCAAGCCCATGGCCGGTGCTCAGCCATCCTTAACAGCCCACACTCCCACAAGACCTACAATACTTACTACAAGCAGTGCAGACAACGTCCTTAACTTGAGTCCTTCTGCTGAGAGTAGGACAGGAACCACATCTCCCCTTAAGTCTCCTACATCACCCAGGTTTGGCAAAGTTTTGCGTGACACATATGTTGTTATTACTTTGCCATCTCAGCCCAGTTCACCTACAGAAGGTATCACAACCCAAGCATCAATAAGTCCTAGCCAAGAATCACATCAAAAACTGCCTCCTTCACCACCTCAACCAACTCAGCAGTCACAAACAACTAGAGTACCACTGGCATTCACACGGATAACT[G/T]AATCTATTGAAAGTCAAGAAATTTGTGGTCCAGAGAAAGTAGTTTCTAGCATGAGTCATGTCTATGAGGCTATTTCAGCCTCAACACAGCCTCAAACGGTTATTCCAAATGTTGGTGTTCAGGTAGTTACCACCGAAGTCCAAAGAACCACAGTCTCTGTTGTTCATGAAAGAACACCACCTCCACATCCCATGCCAAGAGCCACTGGCATTTCTGTTGTTCAAGAAACTACTAAACCTGAAGCAGTTCAAATACAGAATGGTCATGCCTATCATCCTGGTGAAGTAGTGGATCTCCGAACCCCAAAAATAGATGCAGTAACATCCATGAAAGGTATAGATCTGTCTTCCTCTGAATCAAGGCGACAGTCTCTTGCTGTTGATAGTGGTGGACGTCAACAAAGTGCTGTGCAGTCATCAGTAGTGAACCTAAGTACTGACACTTCTTCAGTTTCAGTGGTTACCGACAACATAACAATCCTCACGTGCACAGCCACTGTA
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:
sa33409
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 |
---|---|---|---|---|---|
ENSDART00000092381 | Nonsense | 1968 | 4152 | 10 | 32 |
ENSDART00000136117 | Nonsense | 1116 | 3096 | 1 | 15 |
ENSDART00000143963 | Nonsense | 1116 | 3298 | 1 | 20 |
Genomic Location (Zv9):
Chromosome 4 (position 10482161)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 11418788 |
GRCz11 | 4 | 11417637 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAGAAACTACTAAACCTGAAGCAGTTCAAATACAGAATGGTCATGCCTA[T/A]CATCCTGGTGAAGTAGTGGATCTCCGAACCCCAAAAATAGATGCAGTAAC
Long Flanking Sequence:
ACATCTCCCCTTAAGTCTCCTACATCACCCAGGTTTGGCAAAGTTTTGCGTGACACATATGTTGTTATTACTTTGCCATCTCAGCCCAGTTCACCTACAGAAGGTATCACAACCCAAGCATCAATAAGTCCTAGCCAAGAATCACATCAAAAACTGCCTCCTTCACCACCTCAACCAACTCAGCAGTCACAAACAACTAGAGTACCACTGGCATTCACACGGATAACTGAATCTATTGAAAGTCAAGAAATTTGTGGTCCAGAGAAAGTAGTTTCTAGCATGAGTCATGTCTATGAGGCTATTTCAGCCTCAACACAGCCTCAAACGGTTATTCCAAATGTTGGTGTTCAGGTAGTTACCACCGAAGTCCAAAGAACCACAGTCTCTGTTGTTCATGAAAGAACACCACCTCCACATCCCATGCCAAGAGCCACTGGCATTTCTGTTGTTCAAGAAACTACTAAACCTGAAGCAGTTCAAATACAGAATGGTCATGCCTA[T/A]CATCCTGGTGAAGTAGTGGATCTCCGAACCCCAAAAATAGATGCAGTAACATCCATGAAAGGTATAGATCTGTCTTCCTCTGAATCAAGGCGACAGTCTCTTGCTGTTGATAGTGGTGGACGTCAACAAAGTGCTGTGCAGTCATCAGTAGTGAACCTAAGTACTGACACTTCTTCAGTTTCAGTGGTTACCGACAACATAACAATCCTCACGTGCACAGCCACTGTAGCTTACGGTAGTGATGCATCTCTGGCTACATCAGTGCCTCTCCAACTTACAACAGCGAAATCGTTTGAGCCTGTGTCTCAAATTATTTACAGACCTGTGGATTGTCAACCAGAGAAACCCATAAATCTCTCTACAACCATGGGTAAAACTCACTCTCTTCCTGTAACAATAGCTCCTACAATGGCAAACAATGGCATTAGTGCAGCTTTACCTCCTAACCTAGAAACAGGCTTATCAGGTGCAGTTGACCTTACCACAGTGAAACCTGCACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33410
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 |
---|---|---|---|---|---|
ENSDART00000092381 | Nonsense | 1996 | 4152 | 10 | 32 |
ENSDART00000136117 | Nonsense | 1144 | 3096 | 1 | 15 |
ENSDART00000143963 | Nonsense | 1144 | 3298 | 1 | 20 |
Genomic Location (Zv9):
Chromosome 4 (position 10482243)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 11418870 |
GRCz11 | 4 | 11417719 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAAAATAGATGCAGTAACATCCATGAAAGGTATAGATCTGTCTTCCTCT[G/T]AATCAAGGCGACAGTCTCTTGCTGTTGATAGTGGTGGACGTCAACAAAGT
Long Flanking Sequence:
AGCCCAGTTCACCTACAGAAGGTATCACAACCCAAGCATCAATAAGTCCTAGCCAAGAATCACATCAAAAACTGCCTCCTTCACCACCTCAACCAACTCAGCAGTCACAAACAACTAGAGTACCACTGGCATTCACACGGATAACTGAATCTATTGAAAGTCAAGAAATTTGTGGTCCAGAGAAAGTAGTTTCTAGCATGAGTCATGTCTATGAGGCTATTTCAGCCTCAACACAGCCTCAAACGGTTATTCCAAATGTTGGTGTTCAGGTAGTTACCACCGAAGTCCAAAGAACCACAGTCTCTGTTGTTCATGAAAGAACACCACCTCCACATCCCATGCCAAGAGCCACTGGCATTTCTGTTGTTCAAGAAACTACTAAACCTGAAGCAGTTCAAATACAGAATGGTCATGCCTATCATCCTGGTGAAGTAGTGGATCTCCGAACCCCAAAAATAGATGCAGTAACATCCATGAAAGGTATAGATCTGTCTTCCTCT[G/T]AATCAAGGCGACAGTCTCTTGCTGTTGATAGTGGTGGACGTCAACAAAGTGCTGTGCAGTCATCAGTAGTGAACCTAAGTACTGACACTTCTTCAGTTTCAGTGGTTACCGACAACATAACAATCCTCACGTGCACAGCCACTGTAGCTTACGGTAGTGATGCATCTCTGGCTACATCAGTGCCTCTCCAACTTACAACAGCGAAATCGTTTGAGCCTGTGTCTCAAATTATTTACAGACCTGTGGATTGTCAACCAGAGAAACCCATAAATCTCTCTACAACCATGGGTAAAACTCACTCTCTTCCTGTAACAATAGCTCCTACAATGGCAAACAATGGCATTAGTGCAGCTTTACCTCCTAACCTAGAAACAGGCTTATCAGGTGCAGTTGACCTTACCACAGTGAAACCTGCACAGACCATGGTTGCAATGAATGGGTCCACTGCAGCAGTGGTCACTGCTGTAATTGCAGAGGATGATGGAAAACCTGTTGATCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33411
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 |
---|---|---|---|---|---|
ENSDART00000092381 | Nonsense | 2465 | 4152 | 11 | 32 |
ENSDART00000136117 | Nonsense | 1613 | 3096 | 2 | 15 |
ENSDART00000143963 | Nonsense | 1613 | 3298 | 2 | 20 |
Genomic Location (Zv9):
Chromosome 4 (position 10483917)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 11420544 |
GRCz11 | 4 | 11419393 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGAGAAAATAAAGCAGCAGCGCTTAGCTGAAGAGCTTGAGTGGGAGAGG[C/T]AGGAGATACAGCGTTTCCGTGAGCAGGAGCAACTTCTTGTGCAGAAGGAG
Long Flanking Sequence:
GGGTGTCTAGTGTCCTGAGATCTTCCAATGGTATTGTTTATTCTTCTGTAGCAGCACCAGTACCTTCTACCTATGCCATAACTACCCAGCCTGGATCTATTTTCAGCACATCCTATAATACTCTATCAGGCATGCATACAAGTGACACTATGCCTTCATTGTCAAATCTGCAAAATCAGCCTCTCACTAGATCCCATAGTTTTCTTTCAACTATTGCTTTAACCACAGCAGAAGGGCAAATTGACCTACCCTTAAATCTGGAGACTAGTGCTTCAAGGGCTGGCCTGTCCTCAACTCTCTCTGGTGAGGTTTCTACAGTCACCACAGTGACAGGACTAGATACATACACAAATGCTTCACTTGATGCAATTGCAGCATCTTTAGAAGCTCTGTCTTCACCCATGGTTCCAGGAGATGGACAGTACCAAATGGAGCGTGAGTTTCTTGAGCTTGAGAAAATAAAGCAGCAGCGCTTAGCTGAAGAGCTTGAGTGGGAGAGG[C/T]AGGAGATACAGCGTTTCCGTGAGCAGGAGCAACTTCTTGTGCAGAAGGAGCTGGAAGAACTTCAGGCCATGAAACAGCAAATATTGTGTCAGCAAGAAGAAGAGAGACAAGCCCACCTAATGATGCAAAAGGAAACTTATGCGCAGCAACAGGAACAGTTAGAGCAGATCCAAAGACTTCAGGAACAGCTGAGGCAACAGTTGGAGGAACAGAAGTTCAGGCAAATGTATCCAGGTGAAGTCTTGCCAGAGGCTCTTGTTGTCACAGGAGAAAGAAAGATGGACAGTGGCTGCCAGACTGATGAAGAGGATAATACCGAAAAGGCCTACACTGCAGGTAGAAAGAAGAAAACCACAAAGAAAAGTGTTGATAGCTGTGTACAGACAGATGATGAAGACCAGGATGAGTGGGAAGTTCCTGCTCGAGGCAGGCGCAGTAGACCACGTGGTGGTAAAAATGGCATGGCTGAGAGAGGTGCTGTTTCAGTTCAAGCCCTAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33412
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 |
---|---|---|---|---|---|
ENSDART00000092381 | Nonsense | 2514 | 4152 | 11 | 32 |
ENSDART00000136117 | Nonsense | 1662 | 3096 | 2 | 15 |
ENSDART00000143963 | Nonsense | 1662 | 3298 | 2 | 20 |
Genomic Location (Zv9):
Chromosome 4 (position 10484064)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 11420691 |
GRCz11 | 4 | 11419540 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAAGAGAGACAAGCCCACCTAATGATGCAAAAGGAAACTTATGCGCAG[C/T]AACAGGAACAGTTAGAGCAGATCCAAAGACTTCAGGAACAGCTGAGGCAA
Long Flanking Sequence:
CTATGCCTTCATTGTCAAATCTGCAAAATCAGCCTCTCACTAGATCCCATAGTTTTCTTTCAACTATTGCTTTAACCACAGCAGAAGGGCAAATTGACCTACCCTTAAATCTGGAGACTAGTGCTTCAAGGGCTGGCCTGTCCTCAACTCTCTCTGGTGAGGTTTCTACAGTCACCACAGTGACAGGACTAGATACATACACAAATGCTTCACTTGATGCAATTGCAGCATCTTTAGAAGCTCTGTCTTCACCCATGGTTCCAGGAGATGGACAGTACCAAATGGAGCGTGAGTTTCTTGAGCTTGAGAAAATAAAGCAGCAGCGCTTAGCTGAAGAGCTTGAGTGGGAGAGGCAGGAGATACAGCGTTTCCGTGAGCAGGAGCAACTTCTTGTGCAGAAGGAGCTGGAAGAACTTCAGGCCATGAAACAGCAAATATTGTGTCAGCAAGAAGAAGAGAGACAAGCCCACCTAATGATGCAAAAGGAAACTTATGCGCAG[C/T]AACAGGAACAGTTAGAGCAGATCCAAAGACTTCAGGAACAGCTGAGGCAACAGTTGGAGGAACAGAAGTTCAGGCAAATGTATCCAGGTGAAGTCTTGCCAGAGGCTCTTGTTGTCACAGGAGAAAGAAAGATGGACAGTGGCTGCCAGACTGATGAAGAGGATAATACCGAAAAGGCCTACACTGCAGGTAGAAAGAAGAAAACCACAAAGAAAAGTGTTGATAGCTGTGTACAGACAGATGATGAAGACCAGGATGAGTGGGAAGTTCCTGCTCGAGGCAGGCGCAGTAGACCACGTGGTGGTAAAAATGGCATGGCTGAGAGAGGTGCTGTTTCAGTTCAAGCCCTAACTGAGATATCTGTACAAACAGACTCTGGAACACTAAGGGGGCACTCTGTGCAGGTAGATGCCAGAGTAGATTATCCTGACTCTGACAGAACATCATCTCCAAAGAGACGCCCCATTCCACTTGATATTGGCCAATCCCCTCTCCTCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40241
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 |
---|---|---|---|---|---|
ENSDART00000092381 | Nonsense | 3009 | 4152 | 12 | 32 |
ENSDART00000136117 | Nonsense | 2157 | 3096 | 3 | 15 |
ENSDART00000143963 | Nonsense | 2157 | 3298 | 3 | 20 |
Genomic Location (Zv9):
Chromosome 4 (position 10486088)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 11422715 |
GRCz11 | 4 | 11421564 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACAACAGAGCTACCACCAAATGCTCTTGCTCCAGCAGAAAGCCAGACAA[C/T]AAGCTGCTCTCCTCTCTGAATTAGATTCTACAAAAATTGCATCTAGCTAT
Long Flanking Sequence:
GTGAGCTAGATCTGGTTGAAAGGGAGTCTTCCAAACTGCGTAAAAAGCAAGCTGAACTGGATGAGGAAGAAAAGGAGATTGATGCCAAGCTGCGATACCTGGAGATGGGCATTAACCGACGAAAGGATGCATTGCTCAAAGAAAGGGAGAAAAGGGAAAGGGCCTATCTGCAGAGTGTTGCAGAAGACCGTGACTACATGTCTGACAGTGAGGTGAGTAACATTCGTGAGACTAGAGGTGGAGAGGATATCGGTGGACATGGGCTTGAGAGACCACGAACTGCACCCCAGTCAGAACTTGATGAGTTTGTTCCTCCACAGACCAAGCATGACCAGTATGGAAAATATTCCCAGTACCAGTACTCTCAGTACCAGCAGTCCCTGTACCAGCCTCAGTCACCATACCAATCCCAGTCTATCTACTCTTCTGTTCCGTCTCTGACTGCCTCACAACAACAGAGCTACCACCAAATGCTCTTGCTCCAGCAGAAAGCCAGACAA[C/T]AAGCTGCTCTCCTCTCTGAATTAGATTCTACAAAAATTGCATCTAGCTATGACACCTCATCTTACTTGGGAGGAAAATACAGCAACCACCTTGACTTGCATAGCTTAGAAGACCGTGCTGGCAGCATGGCAGTCAGTCCAATGTCCAATGTATCTGCTGACTCCTTCTATTCAGACCTAGATCAACATCAAACACCAAGAAGCTACATGCTTTTAGAAGATGCAGCAGAACTTGCCAAAAGCACTGGTAGCCTTTCATCCACCAGCTATGGCATTGCTGAAAGGGAACTGGCCAAAGCAGAGCGTCTTCTGAGACATGCTGCTGCAGATGTCAGTTCAGACTACCTGGGCAGCTCTTCCAGGCTCCATTCCTATGGTAAGGCCCAAGATGAAGAGGACCCAATGGAAGAGCCATTTGAACTGAAGCTTTTAAAACAGCAACTGAAACAGGAGTTCAGGAGAAGCACAGGGGGCACTGAAAGCTTAGAGCAGCTTGCTGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17573
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 |
---|---|---|---|---|---|
ENSDART00000092381 | Nonsense | 3358 | 4152 | 13 | 32 |
ENSDART00000136117 | Nonsense | 2514 | 3096 | 3 | 15 |
ENSDART00000143963 | Nonsense | 2514 | 3298 | 3 | 20 |
Genomic Location (Zv9):
Chromosome 4 (position 10487160)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 11423787 |
GRCz11 | 4 | 11422636 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAAAGCAGAAGGTGAAGCCTCTTCTGAGACCTCAGCATTCCAGACTCCCT[C/A]GGGCAGGTCAAAACCTACAAGCCTCCCYATTGTACAAAGTGGGCGTGGAC
Long Flanking Sequence:
GTATAGTATTAGTAGACTGACCTTAGAGAAGCAGGCTGCCAAGCAACTCCCAACATCTATGCTTTACCAGAAACACAAAAACACCAGCAACATTGGCAAGTACTCCTCAATGCAGGATAGCAGGGGTCTAGAAACAGACTATAGTAGTTATCTTGGGTCCAGTAGCTCTTCTCCCAGGTCAAGCAGACTTATGCAGGATGAGATCACCTTTGGGTTACGGAAAAATATTGCCGAACAACAGAAATACCTGGGTTCCACACTTGGGGCCAATTTGGCAGGTTCACTCAATCTGGGTCAAAGCCTGAATCTGAGCCCAGGAATGAGGTCATCTTTAGGAGAAGACTCTTCTTATCCTAGTGGAAGCAGGTCTCGTCCTTCTTCTAGACCCTCATCCGTATATGGGCTTGACTTGTCCATTAAACGAGACCTCTCAAGTTCCTCTCTAAGGCTCAAAGCAGAAGGTGAAGCCTCTTCTGAGACCTCAGCATTCCAGACTCCCT[C/A]GGGCAGGTCAAAACCTACAAGCCTCCCTATTGTACAAAGTGGGCGTGGACGTATTCCTATCGTGGCACAGAATTCAGAGGAAGAGAGCCCACTGAGTCCAGTTGGTCAGCCAATGGGTATGGCACGGGCATCTGCAGGTCCACTCCCACCCATATCTGCAGACTCTCGTGATCAGTTTGGATCATGCATGTCTCTACAAGAATCTCAACAGCAACATCTCAGAGAAGATCCTTCAAGAGGACGTGGCTATGTGCTAATGGATGATCTGCAGGGCACCATGTCTGATAGTGAAGGTAATTTGTTTGTCCACAAACTGTCCTCTTGGAGAGATTCTACATACACAGTCTCAGTTTTTTACTTATCTGTGTTTCATCTTGCAAGTGCTTCTTCTAGTCTATATGAAGGCATTGGTTTTCTGAATACATTTGCTTTCTGTCTTGTCTGAGCTTGCTTATTCTTTGCTTAAAAATGGAAGCAATCACAATGTCACAGTTGTCTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33413
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092381 | Essential Splice Site | 3508 | 4152 | 15 | 32 |
ENSDART00000136117 | Essential Splice Site | 2642 | 3096 | 5 | 15 |
ENSDART00000143963 | Essential Splice Site | 2642 | 3298 | 5 | 20 |
Genomic Location (Zv9):
Chromosome 4 (position 10490468)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 11427095 |
GRCz11 | 4 | 11425944 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTACAAAGATTGTAAAGAAATATTTGTCTGAATGTGCTTATGCATCTTT[A/G]GGGAAAGTTTCACTACCCGTTTCCTCATGCAAGAATAAAACTACTGAGGG
Long Flanking Sequence:
GATTGTATGGGCCAAAGCTGGGCCAGAGAAATTTTGTATAAGATCAAATTGTTTTAGTTTTTTTTTTTTTTTTTTTTGTAAAAAAAAAATAAAGAATTGAGTCCTCAGGGTTTTTTAAGGTTTGCATGTGAGAATAACTGCTCCACTTTGTATAACCATTTCCTTTTCTGTCCCAGATGGCTCTGTATTGTTTGAATATAAGACATACGTACCTTAGCTGTTTCTAGTACCTGATATTACCAGAGGGCCCTTAGGGGTTTGTTTTCACAGACTGGCAAGCAAGACTTTAACGTTTTAATTTCCATCTGTTTTTCTGAAGCGTACCACCTGCGTCGAGAAGAAACCGACTGGTTTGATAAACCGAGAGACGGACGCGCTGAAAACGGACAAGGGATGGAGAGAAGACAGGTATTTGAAATAAAAATCAGCAAAATGCTATTGCAAAAGCATATTACAAAGATTGTAAAGAAATATTTGTCTGAATGTGCTTATGCATCTTT[A/G]GGGAAAGTTTCACTACCCGTTTCCTCATGCAAGAATAAAACTACTGAGGGATCCCAAAGATCGTAGTGTATCAGGTAAGACATGCAACTTGTCAAATACTCTATGCTACTTGGCATTCTGACACGCTCCAACAATGCAGACAGCTGCCCATGGTAAAAGAGGATCTGTTCGCCTACCAGGCAAGCATGGAGAAATGCCCGAGGCTTATGTCTATGCAAACATTAGTTTCGCCATGCTGAGATTGCATTGGCACAGTTTTATTTTAGGCCTACTACTAAACAACACATTATCCCTTCTCCAATTCCCCTTTAGCGTCCTCTTGTGGCGCTTCATTTTGCCAGATCATTGCACACGAAATGTCAACAGACACAAACCCGCTGAGCAAACAGCACATCAGCGGTCTTGCCCCCCTTCTTATGCTTTGGTATGTCACGTAGGTGGGGCTGATTCCCTTCTGTCTGTTGTGTCACTGTTCCTTTAAGCATTAGAACAGGGCAGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20227
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 |
---|---|---|---|---|---|
ENSDART00000092381 | Nonsense | 3566 | 4152 | 16 | 32 |
ENSDART00000136117 | Nonsense | 2700 | 3096 | 6 | 15 |
ENSDART00000143963 | Nonsense | 2700 | 3298 | 6 | 20 |
Genomic Location (Zv9):
Chromosome 4 (position 10492398)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 11429025 |
GRCz11 | 4 | 11427874 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGAGACATCGGTGCATATGTGGCCAAAGTATTACCTGGAGGAGCAGCA[G/T]AACAGACGGGGAAGATTGTGGAAGGTAGGCACCTCAATGAAAGGCGGTTA
Long Flanking Sequence:
GGAGCGTTCTGGTGCCAGGCTCAGACTCTATCTTTCTCAATCCTGATAAGGAGAATAACACAAGTTCTTTTCCATGCTCAGAGCCTTCTCCCCAAACAGCACACCTAACACGCATATTCTATTCAGTCAAATATCTGTGTGTGTGTGAACTCGTGAAAATTTATTGGTACAAAAATGTTAAGTACTTAAGCTGGTTAAAACATCAATTGTTGAAATCACTGATGGTTAGAGTAATTGAACCCTTTAATCCAAAATCTTTCAGTTATTGTGTTTGACAATTAAAGGAAATTTACAGATCAAACAAATATAGCAAATTGAACTAAATAATTCCACTTTTCATGCTTGTTCACCCTCTGTGCAGGTATTTGACCTCCTTATTTTAATACAATTTCTCCACAGGAAATGGACTGGGAATTAGAGTGGTTGGAGGGAAAGAGGTCCCGGGAAGCAATGGAGACATCGGTGCATATGTGGCCAAAGTATTACCTGGAGGAGCAGCA[G/T]AACAGACGGGGAAGATTGTGGAAGGTAGGCACCTCAATGAAAGGCGGTTACACTTTAAAAGACATGTTCCTGTGTGGGTTCACTGACTGGGTTAAGCTGAAGCGGTGTATCGATGCTCACTGTCTTTTAAGGCAGAGAGAGAATCGCATGAGTTAACGTTAAAGGGCACAAAGTGACGTGATATTTCAGGGCAGGAGACAGAAAAAAAACAAATGATGTTAATTTGCGTGATTCTTCACCTCCGGGCTTGCAGAATGACTCATTCTTGATGTGAGAGATAAAGATAGAGAAGGAGAAAATGAAGTTGAAGCTTCAGGTTCATGACTGTGTTTCCTCTGCAGTGTATACTGTCGGTGTAGGTGTTGCACAGATCAGTGTTAAATTTATATCGAAACTTTGACTGAGATGTCTCTAGGGTGTTCAGTTCAAAAGAGTTTGAGGTTTTACTGCTTTACCACGGTCTTCTTTACCATGCAGTTATGTAAATGTGCACTTTGCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11716
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 |
---|---|---|---|---|---|
ENSDART00000092381 | Nonsense | 3580 | 4152 | 17 | 32 |
ENSDART00000136117 | Nonsense | 2714 | 3096 | 7 | 15 |
ENSDART00000143963 | Nonsense | 2714 | 3298 | 7 | 20 |
Genomic Location (Zv9):
Chromosome 4 (position 10496209)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 11432836 |
GRCz11 | 4 | 11431685 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATTTTATATTTGTATGTGTGTRTTTGCATAGGAATGCAAGTCCTGGAGT[G/A]GAACAACATTTCMTTGAGTGGTAARACGTAMGAGGAGGTGCAAGGGCTGG
Long Flanking Sequence:
TGTGATTATGTATGGGGTTGTCATGGCTACAACAGTCATGTGACTGACGTATATTTTCAAGCTCAGTGTAACAGGCTGGTGTTAAGCTGTGGAGTAATGTGAGCCGGCTGTTTAGTCTCTCACATTAAACAGTAAAATCTTTAAGCGTGTAAATGACCCGAGTACACATTCACCCCCAGGGATCCCAAGCATCCAACGTAACGTAGGAGGTTCGAAACGCCCAAAGAGGGCATACCTGGCCTACCTGAAGACACGCTTTCATCTGTGTAAGTGCGCTAAGAGGTTTTGGTTTGCTGTGACTTGGCGTGAAATCTGTTGCACGTGTTTCCTCTCCTTTCTCACAGGATTTCTTCAGCACAGCTTGTTTAATCGAACTTGATGCTTGATGTTGCAGTGCTTATTACAGTATATTTGATCAAATGTAAATAAAATTCATTGTATAAAGCGGCTGATTTTATATTTGTATGTGTGTGTTTGCATAGGAATGCAAGTCCTGGAGT[G/A]GAACAACATTTCCTTGAGTGGTAAGACGTACGAGGAGGTGCAAGGGCTGGTTGGTCACCAGGTTGGAGAGGCCGAATTATGTATCAGACTGTGAGTGTCAGATTTGCTTAATTAATAGTTATGTGCTACTTTTTATTTCTGTTTTCTATCTAGCTCTGAATGAAACATGATATTTAAAGCCCCAATGTACAAATGCGGATTTACAATTTATTTACCAAATATTCAGACTCAATACTTTGAATATGTTTTAACAAATCTAAATATTAAGAAAATTGCTATTTAAGTTGGGCAAATTAAGTGTTTAGCAAAGCATTTTCCTAATGAATAATTAAGATTTGATACATTTAGGGTACAAAGTATCTGACATATCTTAATGGAACATGATCTGTAAACAATATTCTAATGATTTTTGCCTTAAAAGAAACTATTACCAAAAATAAACCTATGCAACTTGAGACTTTTGTGGTCCAGGGTCACATATTGATTTCCTGCTTGCTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20228
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 |
---|---|---|---|---|---|
ENSDART00000092381 | Essential Splice Site | 3696 | 4152 | 20 | 32 |
ENSDART00000136117 | Essential Splice Site | 2830 | 3096 | 10 | 15 |
ENSDART00000143963 | Essential Splice Site | 2830 | 3298 | 10 | 20 |
Genomic Location (Zv9):
Chromosome 4 (position 10497178)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 11433805 |
GRCz11 | 4 | 11432654 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCAAACAAAAAAACACGTCTTTCCTTACTGCTGATGTTTTTTGTTTCTT[A/T]GAACTCTGAGGGTACAAAAACTCAGTCCCACCCAGTTTCAGGAGAAATCC
Long Flanking Sequence:
CAGGGTCACATATTGATTTCCTGCTTGCTTTACTAAACTCCTCAATTTCTTTTTATCTCCAGTGACATAAATATGCTGTCTGATTCTGATAGCTCCCATCTAGACCTGCATGACCAGGTTAAAGGTGAGAACCTCGAGTCATTGAAAAAGACAATCAAATGAAATTGTCTTAATTAACCACAGTGACTACTAACACCTGACTTCTAAATATACAGGGGACAGACCTCCACGGTCACCAGGTGTGGACCCCAAGCAGCTGGCTGCCGAGCTGCAGAAAGTGTCCCAGCAGCAGGTGCCGTCCTCCTCTGCGTCAGCACTGGATAAACCCTCAGCGTCTGCAGGCTCCAGTGCAGTTCCCAGTCCTGGCCAGCCTGGTTCACCCTCTGTCAGCAAGAAACGCCACAGCAAGGTATGCATATCCCATGTGCACAATTATTTTGGATACAGAAAGTCAAACAAAAAAACACGTCTTTCCTTACTGCTGATGTTTTTTGTTTCTT[A/T]GAACTCTGAGGGTACAAAAACTCAGTCCCACCCAGTTTCAGGAGAAATCCAGGTAGATTTGAGCTCTCATCATCTCAGCTACATCTGTAGCTCATTAAGCAAACCTCCAAGTGGAATTTTAAAACTGTAATTTAGAGACCTGTAAAAGTGGAAATTTCAATATGAAACTATCTACGACTAGAAATTAGCTGCTTATGAATGAACACTCTATGAAATCACTCATATTTAATTTCACACTTAATTCATTGATTAAAAGAGTGTATTTATGTAATAGTCATTTGCCTTTTCAACAGAAGAAAGACATTTTTACTTTCTTCTATGTTGCAGCTTCAAATAAATTATGACAAACAGCTGGGAAATCTCATCGTCCATGTTCTCCAAGCACGGAATCTGGCGCCTCGGGACAATAATGGCTACTCTGATCCATTCGTTAAAGTTTACTTGCTGCCAGGTAGAGGGTAAGTACTTTCTGCAAATCTCAACTTACTGGAATTGAGTCT
Associated Phenotype:
Not determined