ZMP
Q32PT0_DANRE
Ensembl ID:
Description:
LOC566456 protein [Source:UniProtKB/TrEMBL;Acc:Q32PT0]
Human Orthologue:
UNC13C
Human Description:
unc-13 homolog C (C. elegans) [Source:HGNC Symbol;Acc:23149]
Mouse Orthologue:
Unc13c
Mouse Description:
unc-13 homolog C (C. elegans) Gene [Source:MGI Symbol;Acc:MGI:2149021]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa44379 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa30353 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa30352 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24749 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa30351 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa30350 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa30349 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39504 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa44379
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 |
---|---|---|---|---|---|
ENSDART00000075229 | Nonsense | 90 | 414 | 2 | 2 |
ENSDART00000124494 | Nonsense | 90 | 1393 | 1 | 8 |
Genomic Location (Zv9):
Chromosome Zv9_scaffold3505 (position 94838)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 3726760 |
GRCz11 | 18 | 3804264 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAATATATCTCTTGAAGAGGATGACGGCAAAACCGACTGTTCTTCTCTCT[C/A]GCCAACATTCAGTTACCGCGTAGCAATTGCCAACGGACTGCCCAAAAATG
Long Flanking Sequence:
GAGGCCTCTTCTGAAGAACAGCCTTGAATATTTCCCTCACTGAGGATGTGCGATGATTTCGACTCTGCACAACCGCTTCTGAGGTCACTTCTTCTCTAGACGCTTTTATACCTCAGGGTTGACTATCAAAACTCATAAGTGTCTGTGTGCTTCCCTGTCGAGCACTGCTGGATTCGAGACCAGTTTTGCTTCGCTGCATCCGGAGTGCAAAACTGCTGAACCATCGCCCTCCATGGTTTCTGCCCATTTCAAAAAGCTATCGTCTTACATTGTAAAGATTTGCAAAGGAATGTTTACAAAGAAACTGGCAACTACCACCAAGAAGAAAGAGAGCAGCGAAAACAAAAAAGAACCCAAATCGACGTCCCCTGAATTGCACGCTCGCAACCCGACGTTCTCCACCACACTAAAAAGCACAGTTAAAAAAATCTCCAAATGCTCATCCACACGCAATATATCTCTTGAAGAGGATGACGGCAAAACCGACTGTTCTTCTCTCT[C/A]GCCAACATTCAGTTACCGCGTAGCAATTGCCAACGGACTGCCCAAAAATGCCCTGTTTCTGAACAATGAATTTCATGAGGTCTTGTCAATTGATAGCGATTACTCTGACTCTCTGAACGAGGCAAAACTTGTCCATAGATTCGATGAACAAAAAGCTTACACGATGCCAGTAAGAAGGAATCGGAAGAGTTTGATTAGTTTGGCGCCCTCCGATGGCAGCTCGGAGGGGGAACGTGGAGAGCGCAGCAGTCTCCACACCCTCCGATTGGGCGCCTTGAAAAAGCTAAGGAAATGGAAGAAGAGCCAAGAATGCGTGTCCTCAGACTCGGAGGCCAGCAATTGGAGAAAAACTCTTGGCATTCGAAGCAAATCTTTGGACAGGGCCGGCCGACACCAGAAAACCACTACCCTGGAGCCAGGATCTAGCTCCACGGGATGCATCAGTCAGACTCAGGATGTGATGGAGATGATTTTCAAGGAGCTTCAGGGAATCAGTCAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30353
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 |
---|---|---|---|---|---|
ENSDART00000075229 | Nonsense | 300 | 414 | 2 | 2 |
ENSDART00000124494 | Nonsense | 300 | 1393 | 1 | 8 |
Genomic Location (Zv9):
Chromosome Zv9_scaffold3505 (position 94209)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 3726131 |
GRCz11 | 18 | 3804893 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTGGTGCAGAGTGAAATCGAGCAGCTCCGTTCAGGTTTCGTGCAGTCC[A/T]GACGCGAGACTCGAGACATTCATGATTACATCCGACAGATCAGCCAACAG
Long Flanking Sequence:
TTGTCCATAGATTCGATGAACAAAAAGCTTACACGATGCCAGTAAGAAGGAATCGGAAGAGTTTGATTAGTTTGGCGCCCTCCGATGGCAGCTCGGAGGGGGAACGTGGAGAGCGCAGCAGTCTCCACACCCTCCGATTGGGCGCCTTGAAAAAGCTAAGGAAATGGAAGAAGAGCCAAGAATGCGTGTCCTCAGACTCGGAGGCCAGCAATTGGAGAAAAACTCTTGGCATTCGAAGCAAATCTTTGGACAGGGCCGGCCGACACCAGAAAACCACTACCCTGGAGCCAGGATCTAGCTCCACGGGATGCATCAGTCAGACTCAGGATGTGATGGAGATGATTTTCAAGGAGCTTCAGGGAATCAGTCAGATCGAGTCCGAGCTCTCAGAACTGCGAGGGCATGTAAACGCCCTCAAAAGCTCCATCGATGAGATCTCCAGCAGTGTGGAGGTGGTGCAGAGTGAAATCGAGCAGCTCCGTTCAGGTTTCGTGCAGTCC[A/T]GACGCGAGACTCGAGACATTCATGATTACATCCGACAGATCAGCCAACAGAGCAACAAAGCTACTCTGAGATTTCTAAATGTGCCTGAGGAGAAGTACGAAAAAACCGAAGAACTTATCTATCAGATCCTAAAAGAGAAAATGGGTTTCATTGATGCACGTAAGGCATTTAAAATTGAACTAGCCCATCGGCTGGGGCAACAAAGAGAATGTTACAATGCTAAACCACGACCAATTATAGTTATATTTGCAAGCCCGCAAGACAGAGATTTAGTTTTGAAAAAATGTTATAAGCTTAAAGGGACTGGAATATCCATCTCCACTGACAGTCTAGCACACGACTCGAAAGAAAAGAGAGAAAAGCCGATAGCTTCATCTCAGACATACGAAAGCATGGACATCAAGGTCTCGGCTAAAGACAAGGCTGAAAGTGATGACTGGGACTCCATGGAAAGCGACAAAGAGCTTGATGAGTTAAACAAGAACAAATATGCAATTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30352
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 |
---|---|---|---|---|---|
ENSDART00000075229 | None | None | 414 | None | 2 |
ENSDART00000124494 | Nonsense | 814 | 1393 | 1 | 8 |
Genomic Location (Zv9):
Chromosome Zv9_scaffold3505 (position 92667)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 3724589 |
GRCz11 | 18 | 3806435 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAGAAGCCTAAAACCAAGAAGATCCAAGCTAAACCTGAATCAGCTCCA[C/T]AAACTTTGCAGCGACAAGATGTGAACCACCACCTCCAGCAGAACCAGAAA
Long Flanking Sequence:
ACCTTGAACAAGGTGCTGATTCAGGTTTGGATGCCTCAACTGAACAGAACATAATCTCTGAAATCAGTAGCCCATTTGACCCAGCAGCTAACCCTGGTTTCCCTGAAAAAATTATTAAGTGTCTTGAGGTTGATTTGCAATTTGAAGGTGAGACGTTCTTGACACTAGATAGCACTCCTGAGACAGGAGACCAAGATATAGACATGGAGCCTGAGTTTTTAGAACCTGAGTTAGAACCTGAAGTTGAGGCTGTGATTGAACCAATGATTAAACAAGAACGAGAACCAATGCCACAGCCAGAACCTGAACTAGAACCTGAACTAGAACCTGAACCAGAACCTGAACCAGAACCTGAACAAGAACCAGAACCAGAACCAGAACCAGTGATTGAACCCATTCCAAAACCAGTACCAGTATCAGTATCTAAACCTGTGGTTGAACAGCAAACCGAAAAGAAGCCTAAAACCAAGAAGATCCAAGCTAAACCTGAATCAGCTCCA[C/T]AAACTTTGCAGCGACAAGATGTGAACCACCACCTCCAGCAGAACCAGAAATCCTCAGCTATGTACCGGAGCCAGAGTGAGATTAGAAATGAGAAGGTTGAGGATGTCCCCAAATCCTGGAGTAGCAGGCTCAGCATCGACCTCAGCGAGAAAACCTTCGGCTTTGGGGGATTTGGATCCACCCTGCAAAGAGCAAAGTCAGCTTTGGATTTTGTGTGGAATAAAGGTTCCCAGAGTACTAGCGCACCGGTTGAAGAAACCAGCAACACCTCGTTCATGGGCCGGTTCAGAACCACATCCACAGCCAATAGCTCCAGTACAACCATTGATTCTGACGTCTACACAGAACCTTTCTATTACAAGGCAGAAGAAGAGGAACAACAACAGCAACAACCTGCTGAGCAACCTGTGGACAATGAAACGCATTATGTTGAGGTGATGGAACAAGTGCTAGCCAATCTGGAAAACAGAACAAACGCAAACGAACCCGAGGAACAGTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24749
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 |
---|---|---|---|---|---|
ENSDART00000075229 | None | None | 414 | None | 2 |
ENSDART00000124494 | Nonsense | 872 | 1393 | 1 | 8 |
Genomic Location (Zv9):
Chromosome Zv9_scaffold3505 (position 92493)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 3724415 |
GRCz11 | 18 | 3806609 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGGCTCAGCATCGACCTCAGCGAGAAAACCTTCGGCTTTGGGGGATTT[G/T]GATCCACCCTGCAAAGAGCAAAGTCAGCTTTGGATTTTGTGTGGAATAAA
Long Flanking Sequence:
CTCCTGAGACAGGAGACCAAGATATAGACATGGAGCCTGAGTTTTTAGAACCTGAGTTAGAACCTGAAGTTGAGGCTGTGATTGAACCAATGATTAAACAAGAACGAGAACCAATGCCACAGCCAGAACCTGAACTAGAACCTGAACTAGAACCTGAACCAGAACCTGAACCAGAACCTGAACAAGAACCAGAACCAGAACCAGAACCAGTGATTGAACCCATTCCAAAACCAGTACCAGTATCAGTATCTAAACCTGTGGTTGAACAGCAAACCGAAAAGAAGCCTAAAACCAAGAAGATCCAAGCTAAACCTGAATCAGCTCCACAAACTTTGCAGCGACAAGATGTGAACCACCACCTCCAGCAGAACCAGAAATCCTCAGCTATGTACCGGAGCCAGAGTGAGATTAGAAATGAGAAGGTTGAGGATGTCCCCAAATCCTGGAGTAGCAGGCTCAGCATCGACCTCAGCGAGAAAACCTTCGGCTTTGGGGGATTT[G/T]GATCCACCCTGCAAAGAGCAAAGTCAGCTTTGGATTTTGTGTGGAATAAAGGTTCCCAGAGTACTAGCGCACCGGTTGAAGAAACCAGCAACACCTCGTTCATGGGCCGGTTCAGAACCACATCCACAGCCAATAGCTCCAGTACAACCATTGATTCTGACGTCTACACAGAACCTTTCTATTACAAGGCAGAAGAAGAGGAACAACAACAGCAACAACCTGCTGAGCAACCTGTGGACAATGAAACGCATTATGTTGAGGTGATGGAACAAGTGCTAGCCAATCTGGAAAACAGAACAAACGCAAACGAACCCGAGGAACAGTACCAAGAAGAGGAATACAATGTCTCACAGGAGTATGATCTCTCTCAAGACGCCAACCTTGTACTGGAATATGATTGCAGCCTCGATGAACAGTATGATGAGGAATACAGTGAGGACTACGATGACAATCCTATGACTGAAGACACAGCAGAATATGAGGTTAGTTTAGTGGATTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30351
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 |
---|---|---|---|---|---|
ENSDART00000075229 | None | None | 414 | None | 2 |
ENSDART00000124494 | Nonsense | 977 | 1393 | 1 | 8 |
Genomic Location (Zv9):
Chromosome Zv9_scaffold3505 (position 92178)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 3724100 |
GRCz11 | 18 | 3806924 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAACAAGTGCTAGCCAATCTGGAAAACAGAACAAACGCAAACGAACCC[G/T]AGGAACAGTACCAAGAAGAGGAATACAATGTCTCACAGGAGTATGATCTC
Long Flanking Sequence:
AATCAGCTCCACAAACTTTGCAGCGACAAGATGTGAACCACCACCTCCAGCAGAACCAGAAATCCTCAGCTATGTACCGGAGCCAGAGTGAGATTAGAAATGAGAAGGTTGAGGATGTCCCCAAATCCTGGAGTAGCAGGCTCAGCATCGACCTCAGCGAGAAAACCTTCGGCTTTGGGGGATTTGGATCCACCCTGCAAAGAGCAAAGTCAGCTTTGGATTTTGTGTGGAATAAAGGTTCCCAGAGTACTAGCGCACCGGTTGAAGAAACCAGCAACACCTCGTTCATGGGCCGGTTCAGAACCACATCCACAGCCAATAGCTCCAGTACAACCATTGATTCTGACGTCTACACAGAACCTTTCTATTACAAGGCAGAAGAAGAGGAACAACAACAGCAACAACCTGCTGAGCAACCTGTGGACAATGAAACGCATTATGTTGAGGTGATGGAACAAGTGCTAGCCAATCTGGAAAACAGAACAAACGCAAACGAACCC[G/T]AGGAACAGTACCAAGAAGAGGAATACAATGTCTCACAGGAGTATGATCTCTCTCAAGACGCCAACCTTGTACTGGAATATGATTGCAGCCTCGATGAACAGTATGATGAGGAATACAGTGAGGACTACGATGACAATCCTATGACTGAAGACACAGCAGAATATGAGGTTAGTTTAGTGGATTATGTTGAAGAAACCGAGGAACCGGAAGCAGAGACAGAGGAACAGGAGGAGGTCAAAGAGGAGGTGCGGGAGGTTCAGGAAACATCTGAAATTAAAGGAGAAGATGTGGTAAAAGAGACCGTAGAGCAAGAGGATGAGAATAAAAATGTTACAGAGGTTCCTGTGCAAGAAGCACCACCCAAAAAAAGGATACGTCCCACATTCAAAGAGGCAGCACTGAGAGCTTACAGGAAGCAGATGGCGGAGCTGGAGCAGCAGATCCTGGCAGGAGGTACGAACCAACTAGTTATGTGTAGTGACATGTTTACTGCTTACATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30350
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 |
---|---|---|---|---|---|
ENSDART00000075229 | None | None | 414 | None | 2 |
ENSDART00000124494 | Nonsense | 1019 | 1393 | 1 | 8 |
Genomic Location (Zv9):
Chromosome Zv9_scaffold3505 (position 92050)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 3723972 |
GRCz11 | 18 | 3807052 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATGATTGCAGCCTCGATGAACAGTATGATGAGGAATACAGTGAGGACTA[C/A]GATGACAATCCTATGACTGAAGACACAGCAGAATATGAGGTTAGTTTAGT
Long Flanking Sequence:
TGGAGTAGCAGGCTCAGCATCGACCTCAGCGAGAAAACCTTCGGCTTTGGGGGATTTGGATCCACCCTGCAAAGAGCAAAGTCAGCTTTGGATTTTGTGTGGAATAAAGGTTCCCAGAGTACTAGCGCACCGGTTGAAGAAACCAGCAACACCTCGTTCATGGGCCGGTTCAGAACCACATCCACAGCCAATAGCTCCAGTACAACCATTGATTCTGACGTCTACACAGAACCTTTCTATTACAAGGCAGAAGAAGAGGAACAACAACAGCAACAACCTGCTGAGCAACCTGTGGACAATGAAACGCATTATGTTGAGGTGATGGAACAAGTGCTAGCCAATCTGGAAAACAGAACAAACGCAAACGAACCCGAGGAACAGTACCAAGAAGAGGAATACAATGTCTCACAGGAGTATGATCTCTCTCAAGACGCCAACCTTGTACTGGAATATGATTGCAGCCTCGATGAACAGTATGATGAGGAATACAGTGAGGACTA[C/A]GATGACAATCCTATGACTGAAGACACAGCAGAATATGAGGTTAGTTTAGTGGATTATGTTGAAGAAACCGAGGAACCGGAAGCAGAGACAGAGGAACAGGAGGAGGTCAAAGAGGAGGTGCGGGAGGTTCAGGAAACATCTGAAATTAAAGGAGAAGATGTGGTAAAAGAGACCGTAGAGCAAGAGGATGAGAATAAAAATGTTACAGAGGTTCCTGTGCAAGAAGCACCACCCAAAAAAAGGATACGTCCCACATTCAAAGAGGCAGCACTGAGAGCTTACAGGAAGCAGATGGCGGAGCTGGAGCAGCAGATCCTGGCAGGAGGTACGAACCAACTAGTTATGTGTAGTGACATGTTTACTGCTTACATTATAAGTGTTCATACTTGCGGGTAGAAAAAAACAATGCTGCATTTAGTCCAATCATTAAACTTATAAAATATGAACAATTTTTAAAACGGATTTGATTAGAGATACATTTAGTAAGTAAGGCACATTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30349
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 |
---|---|---|---|---|---|
ENSDART00000075229 | None | None | 414 | None | 2 |
ENSDART00000124494 | Nonsense | 1076 | 1393 | 1 | 8 |
Genomic Location (Zv9):
Chromosome Zv9_scaffold3505 (position 91881)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 3723803 |
GRCz11 | 18 | 3807221 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCGGGAGGTTCAGGAAACATCTGAAATTAAAGGAGAAGATGTGGTAAAA[G/T]AGACCGTAGAGCAAGAGGATGAGAATAAAAATGTTACAGAGGTTCCTGTG
Long Flanking Sequence:
TCAGAACCACATCCACAGCCAATAGCTCCAGTACAACCATTGATTCTGACGTCTACACAGAACCTTTCTATTACAAGGCAGAAGAAGAGGAACAACAACAGCAACAACCTGCTGAGCAACCTGTGGACAATGAAACGCATTATGTTGAGGTGATGGAACAAGTGCTAGCCAATCTGGAAAACAGAACAAACGCAAACGAACCCGAGGAACAGTACCAAGAAGAGGAATACAATGTCTCACAGGAGTATGATCTCTCTCAAGACGCCAACCTTGTACTGGAATATGATTGCAGCCTCGATGAACAGTATGATGAGGAATACAGTGAGGACTACGATGACAATCCTATGACTGAAGACACAGCAGAATATGAGGTTAGTTTAGTGGATTATGTTGAAGAAACCGAGGAACCGGAAGCAGAGACAGAGGAACAGGAGGAGGTCAAAGAGGAGGTGCGGGAGGTTCAGGAAACATCTGAAATTAAAGGAGAAGATGTGGTAAAA[G/T]AGACCGTAGAGCAAGAGGATGAGAATAAAAATGTTACAGAGGTTCCTGTGCAAGAAGCACCACCCAAAAAAAGGATACGTCCCACATTCAAAGAGGCAGCACTGAGAGCTTACAGGAAGCAGATGGCGGAGCTGGAGCAGCAGATCCTGGCAGGAGGTACGAACCAACTAGTTATGTGTAGTGACATGTTTACTGCTTACATTATAAGTGTTCATACTTGCGGGTAGAAAAAAACAATGCTGCATTTAGTCCAATCATTAAACTTATAAAATATGAACAATTTTTAAAACGGATTTGATTAGAGATACATTTAGTAAGTAAGGCACATTTATATAACACATTTGCCGTAAACCCAAAGAGCTTTACAATTGTATGAGGGAGTCCTTTCACCCCACCACCATTTACTCATTTAGAAGACACTTGTGAGGATTAGAGAAGCACTTGCAATTATCAGAGAGTTGCAGTGTGGTTATGCAACATATGCTCGTTCTGAAAACGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39504
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 |
---|---|---|---|---|---|
ENSDART00000075229 | None | None | 414 | None | 2 |
ENSDART00000124494 | Nonsense | 1281 | 1393 | 7 | 8 |
Genomic Location (Zv9):
Chromosome Zv9_scaffold3505 (position 29807)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 3661729 |
GRCz11 | 18 | 3869295 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCATCATCCTCTACAGGTGCAGTAGAGAAGAGCTCGAAACACGGAGCC[G/T]AGGACAAAACCCAGAACATCATCATGGCCATGAAGGAGCGCATGAAGATC
Long Flanking Sequence:
TGGACAACAGTATTAGTTCAAAGCGGGTAAAAGCAGGTAAAATAGATTAAAACTATCGTTTCAAAGCTGTCCAAATGTGACTGTTTACACACATCAGCTGTCGACGGAAGTTCTTCGCATTCTCCTTGCGCATACACGCAAAGCATAATGGGTAATTTTGTGTTCCAAGAAAAAGGTCTATAGGGACTGATGGTATAGACGGTGAGCATGGACACAGAACTAGCACTAGTTGTAAGCCCCTTTCACACAGTGATACTGGTAAATATATGGAAAATTTAAGGAACGACTTTATCGGTAAATTTAAAAAAGCGCTGTTCACGCAGGCGATGACGTTTCGGAATTTTTCCAGAAAAGATCGTTCACACATCCATTCCAAAATAGCGGTAAATTCTGACATCATTAACCAGAAATGACCTTTAAACGGCTGCGCTTGTATTTGTAAATCACACTGTGCATCATCCTCTACAGGTGCAGTAGAGAAGAGCTCGAAACACGGAGCC[G/T]AGGACAAAACCCAGAACATCATCATGGCCATGAAGGAGCGCATGAAGATCAGGGAGAAGAACCGGCCCGAAGTGTTCGAGGTCATTCAGGAGATGTTCCAGCTCTCGAAAGAGGACTTTATCACTCATCTGAAGACCGCCAAACAGGCTGTGCTGGAGGGAACGTCCAAGTGGTCCGCCAAAATCACCATCACAGGTCAGCAAAAAAGAAACCTTTTCACAGTTCCTCTAGTTTTTTGTCATAGTTAGTAGCGCAGTGAATGGAAGAGGGTCTTTATTTTTAATAGGTAAATTTGTCCAAGGCTTGTTTTTGACAAGACTTATAATACAATTATATATTATATTATGTTATATTAGGTTAGATTAGATTAAATTGTTATAATGTATTATATTTAGTGCTGTCAAAATTAGTGCCTTAGCGCATGCGATTAATTTGAAAAATTTAACGCATAAAAAAAAAATTAACACAATTGCAGGGTTTTTTTTTTACTTGCTGTTGTG
Associated Phenotype:
Not determined