ZMP
ENSDARG00000012982
Ensembl ID:
Human Orthologues:
AL929601.1, NF1, NF1P4, NF1P5
Human Descriptions:
Uncharacterized protein [Source:UniProtKB/TrEMBL;Acc:C9IYV8]
neurofibromin 1 [Source:HGNC Symbol;Acc:7765]
neurofibromin 1 pseudogene 4 [Source:HGNC Symbol;Acc:7769]
neurofibromin 1 pseudogene 5 [Source:HGNC Symbol;Acc:7770]
neurofibromin 1 [Source:HGNC Symbol;Acc:7765]
neurofibromin 1 pseudogene 4 [Source:HGNC Symbol;Acc:7769]
neurofibromin 1 pseudogene 5 [Source:HGNC Symbol;Acc:7770]
Mouse Orthologue:
Nf1
Mouse Description:
neurofibromatosis 1 Gene [Source:MGI Symbol;Acc:MGI:97306]
Alleles
There are 12 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22673 | Nonsense | Available for shipment | Available now |
sa848 | Nonsense | Available for shipment | Available now |
sa10931 | Nonsense | Available for shipment | Available now |
sa22672 | Nonsense | Available for shipment | Available now |
sa32043 | Nonsense | Available for shipment | Available now |
sa35918 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39057 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22671 | Nonsense | Available for shipment | Available now |
sa35917 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa39056 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa22673
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 |
---|---|---|---|---|---|
ENSDART00000080328 | Nonsense | 147 | 2805 | 4 | 58 |
Genomic Location (Zv9):
Chromosome 15 (position 30264972)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 31086679 |
GRCz11 | 15 | 30967420 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCACTCAGCTGCGCAGCTCCGCCTCTGCTGTGCTTTTCTCTCTCAGCTG[C/A]AACAACTTTAATGCCGTCTTCAGTCGTATCTCCACCAGGTACCTCTCTAA
Long Flanking Sequence:
GATCCACTAATGTGTTTGCTGGGTGGTCTGTCATTGGATTTCATTACTGTTTGCTTCCCCCTTTCCTGCTTTCTACTAATTCAGACGCTTTTTCTACTCAGTGAAGTACATTTAAGTCAGGTTACTTGATACGTTTACAGGTCAGTTTTACTATTCTGACAAATGTTATCCACTTAGAGCTAGAGCTTCTTATTTTTATGCTTCTTTTACAAATGCATGGCAGATCCCTCAACAGTAAACTAAATTACACAATAAGGATAAGCTTTTACAATCCAATGGTTGAATAAGTTGGATAATACACTGTCAAAAAGAGAATATAAAATATGCTGTGTTTATGTGCATCATCAGCAACCTAAGGATTGCCTGAGGCTGGATGAGGCTATGTTGGTAAAACAGTTGCTGCCTGAAATCTGTCACTTCCTGCACTCGTACCGTGAGGGCCAGCAACACGCCACTCAGCTGCGCAGCTCCGCCTCTGCTGTGCTTTTCTCTCTCAGCTG[C/A]AACAACTTTAATGCCGTCTTCAGTCGTATCTCCACCAGGTACCTCTCTAACACAATGGGGGTTCCACAAGGCTTTGTTCTAGGACCTTTCTTATTGTGTAGAAATAGCTAATTTTAAATAAACTAAATATAAAGTCTATTGTACAAAGCTATTGTGGTTTGTTGTCTACTAAAAGAACCATTAAATATTATCAAATCATTGATGTTAATCTACCATTGTCTTGTTATAGGTTGCAAGAGCTCACAGTTTGTACAGAGGACACAGTGGATGTCCATGACATTGAGCTCATTCAGTATATCAATGTAGATTGCTCCAAGTTAAAGAGACTCCTACAAGGTAATGCATTCTCTAGTTTTTTTTTTTACCTTCGTGATCCACATATGTGTTGGTATAATGCATTTAGAGTAATCTTAAGTAATGTAAATCTAAAAAAATATGTAATACACTAGAACTAACTAGAAGGCAGTCATTTTGATAGATTTGTTTTTTATTAACTTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa848
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080328 | Nonsense | 316 | 2805 | 9 | 58 |
Genomic Location (Zv9):
Chromosome 15 (position 30260710)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 31082417 |
GRCz11 | 15 | 30963158 |
KASP Assay ID:
554-0751.1 (used for ordering genotyping assays)
KASP Sequence:
CATTTGTAGACAGTTTACGAAAGGCTCTTGGCCAACACAGCGGCAGCAAA[C/T]AATTGACGGAAAGTGCAGCTGTTGCATGCGTCAAACTCTGCAAAGCCTGC
Long Flanking Sequence:
TTATACAACTCAGAATTATTATCTCGCTGTATATTTTTTCCCCATTTCTGTTTAACGGAAATAATACTTTTTCAACACATTTCTAAACATAAGTTTTAATAACTCATTTATTTGGCAGCACATAATATTTTACTAGATATATTTCAGGAAACTAGGCCAGAAAAAAGTCATTGTAGCGGTTTGTTCAGTAGACAATCGACAAATATATATATTTATATAGTAATATTGACCTTAAAATGGTTTTAAAAAATTTTAAAACTGCTTTTATTCTAGCCAAAATATAATGCATAAGACTTTCTCCAGAGAAAAAATGTTGTCAGACATACTGTGAAATTTTTTTTTTGCTCCATTAAATATCACTTGAGAAATATTTGAAAAATAAAAAATATTTCACAGGATATTGCATTGATGACAAATCTTATTTGTTTGTTTTTTTTCATCAACAGAAGTCATTTGTAGACAGTTTACGAAAGGCTCTTGGCCAACACAGCGGCAGCAAA[C/T]AATTGACGGAAAGTGCAGCTGTTGCATGCGTCAAACTCTGCAAAGCCTGCACATATATCAACTGGGAGGATAATTCTGTCATCTTTCTCCTGGTTCAGTCCATCGTCATGGACCTTAAGGCAAGGATGTACATTGTAAATTAATAAATATGGTGTCCATAGAGAAAAGGAAGTATGAATTGAACAAGAGGTGTTTAAATTCTCTCTCTCTTTTGTCTTTCAGGGTCTCCTGTTTAACCCCACCAAACCTTTCTCAAGAGGTACGGGCTGCCAGAGCGCCGATGTAGATTTGATGATCGACTGCTTTGTGTCATGTTATCGCATCAATCCTCGCAACAACCAGCATTTTAAGGTAAGTTTGGTCACTAAATCTTAGGGAAATTTCTTAGGAATTCAGTATCCAATATCTTAAAGACATTTTTATATTATTACTATCAAAACATACTACGATAAAGGGAAGCTGTTTTCACATATTTTTAATTAGAGAGATATGTAAAAATA
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:
sa10931
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 |
---|---|---|---|---|---|
ENSDART00000080328 | Nonsense | 479 | 2805 | 13 | 58 |
Genomic Location (Zv9):
Chromosome 15 (position 30258273)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 31079980 |
GRCz11 | 15 | 30960721 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTTTATTACTTGCAGAGTTTGACATTCAAAGAGAAAATGACAACAAGTT[T/A]GAAGTTCAAGGAAAAGTCCACAGATCTTGATTCGCGTTCTTTGCTGCTGG
Long Flanking Sequence:
TTTGTATACAGACACTAAATTAACTACCAATAAAATATTTCTACCAATAAAATTATTACAATTATGATTATAATTTCTATTATGACTGTTTACTGTAATGTTAAAAATTCCATCAGCCTTCAAGTGACTGTATTAAAAATCACTGAATTTACAACATCTTAAGTTTATGGTCTGCACTGTACCTTTGCCAGTTGTTGCTTATTAATGTCTCGCGCTCATGTTTCTAGTCTCACCTGGACTGGTGGCCGAAGATTGACGCCATCTACTGCTACTCAGGAGAACTACGCACCATGTTTGCAGACACACTGGGTCGAGTGATTCAGAGTCTCAGTGCACATCCGCCTCTGAGGATGACATCAGTGAGACATGCTTAAATACTACACATTAAAATGCATACAGTCTATTACGTATAGAAAAACAAACACTGGACTTTGCATTGGTCAAAGTGGCATTTTATTACTTGCAGAGTTTGACATTCAAAGAGAAAATGACAACAAGTT[T/A]GAAGTTCAAGGAAAAGTCCACAGATCTTGATTCGCGTTCTTTGCTGCTGGCACTGGTCAAACTTATCCACGCTGACCCCAAACTAATGCTGCACGTGAGTATATAAGCCTGCTATATGGATTAAAGAGTTTTTAAATGTAATCTAAATAATCAATAATGATCAATGGTTAATAATCAAAATAGGTCAAATCTCTATGCTTTCAAGTTAAAAGGTAGATTTTTGTAGAAATGAGACGGTTAAACTACTTGTTTTTTGGGTCAAGAATATGAACATTTCGCAAATGTGTGGTATAATGTAAATGTAATTATTACTAGTTATCAAATTTGTATTGAGTAACATCTTTTAGCAGCTATTTTCCTTCACAAAATATTTTTATTTTTATTTTATTCACATAATTTTAAATGATGGAGCAGGTCTTGTTCCCTGACTGGGGAAAACAATGACATAATTAAAACTCTTTAAATGTGATTATGAATGTTACAATTTCAAATAAATCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22672
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 |
---|---|---|---|---|---|
ENSDART00000080328 | Nonsense | 700 | 2805 | 20 | 58 |
Genomic Location (Zv9):
Chromosome 15 (position 30252855)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 31074562 |
GRCz11 | 15 | 30955303 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAGGTGTGTCTGTACACGTTCCTGTGGAGTCCTGATGCAGAGGCTGTTT[T/A]GGTGGCCATGTCCTGTTTCAGGCATCTCTGTGAGGAGGCCGATATTCGCT
Long Flanking Sequence:
TTTACGTATACATTTTTTTAGTACCCAGTTGAAATTAATGTGCATGCGTTTGCTAAATTATTTTGTAAGATAAATTTTAGGCAATCATATTTAGTTTTGTAATTTAAATCATTAAAATTATAAATTTAAAATATATTTCTGAAAATGTCTCTTAAATGTTGAACATCCAGATATAAAATGTGTGGTTCAAATAGTTTTTCATTTAAAAAAAAATCACCTTATTGTAGGATCAGACTTTTACAATGATATTCTCAAATCAAATTGTTATGCATAATTATTTATAAATTAACCATATGCCTGTATCAGTTCTTTTTAAAATCATAATTCAAAATAGAAGTCTGAACAAAATAACAATTGCCCGTCCAGATAAAACAAGCTCATTTCCTCCACACAGGAGTGTGCTACACAGGGCAGTCTGATCCCCATCAGCAGACAGGCTCAGACCAAGCTGGAGGTGTGTCTGTACACGTTCCTGTGGAGTCCTGATGCAGAGGCTGTTT[T/A]GGTGGCCATGTCCTGTTTCAGGCATCTCTGTGAGGAGGCCGATATTCGCTGCAGTGTCGATGAGCTGCCTGTTCACACAGTCCTACCCAATTACAACACCTTCATTGAGCTTGCATCCGTCAGCAATATGATGGCCACAGGTCAGTGAATGCTGGATTTATTATTGCCAGACACTGTCATTTTTATTTATTTTTTGGAAATAAATATGGAACGATCAGTGATCTGAGGTTTTGTAAGGCTGCATTTACACTGCAGATCTTGTTGGTCAATTCCGATTTTGTGACTGCATCCGATTTTTTTGATGGTCAGATTTTTCCGATCTACTTGCTTACACTGCAGACATGAGGGCACAGATCTGATTCATATCGGATAAATTGCCACATATGAACAAGGCCTGAATCTGAATTGATTAAATCGTAATCCATGTGATTTGTTCCTGCTTACACATACATGGGCCACATCCGATCTGTGCCACATGGGAGAAAAAAAATCAGAATTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32043
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 |
---|---|---|---|---|---|
ENSDART00000080328 | Nonsense | 1244 | 2805 | 29 | 58 |
Genomic Location (Zv9):
Chromosome 15 (position 30240799)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 31062506 |
GRCz11 | 15 | 30943247 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCTGGCCAGAGTGTTAGTGACTCTCTTCGACTCTCGCCATCTGCTGTA[T/A]CAGCTGTTGTGGAATATGTTCTCCAAAGAGGTGGAGCTGGCAGACTCAAT
Long Flanking Sequence:
CATTATTTTTGTCTGTGCACTAATAATAAGCATATTTAGAAAAAAAACATCTCTTTCCCTGAAAACGTTTGCCAAAGAGATCTAATAGTGATTGGTTTTTGGTACCTTCAAAATGTGTTTTATTTGTTTCACAGAAAGCAAGGAAGTCATATTGGTTTTTGAAAGAATAGTTCAACCAAAAGTGAAATTCCTGTCATTTACTCGTGCTAAAGTTGTTCAGAATATGTATTAATTTCTTTATTTTGCAGTGTTTTTGTTCTTGTCTATAGAAGTCTGTGGGTACCTTAAACTATATATAATATATCAGTCTTACATGTTTGTAACAGCTTAATGGCAAATAAATGCTGACAGATTTCTTTTTTTATATCTCATGTTTAGCTCACAATGCATGGTAAGTATTGTTGGTCATCGGAGTGCTGTTGTGCTTAATGTTGTGCTGGTTTTCAGGATGAGCTGGCCAGAGTGTTAGTGACTCTCTTCGACTCTCGCCATCTGCTGTA[T/A]CAGCTGTTGTGGAATATGTTCTCCAAAGAGGTGGAGCTGGCAGACTCAATGCAGACGCTCTTTAGAGGAAATAGCCTAGCCAGCAAGATTATGACCTTCTGCTTCAAGGTGACGTGAAGCGGTGACAGTCATTCCATGAGTTCAGCCTTCATTGTTTTGCATGAGTTACCGCACTCCAATGCAAATTCCCTTCAAATCTGGCACTGTGTTCGCAGGTGTACGGAGCTGCGTATCTACAGAAGCTTCTGGAGCCGCTGTTGAGAGGAATCATCACTACACCAGAGTGGCAGCAGATCAGTTTTGAAGTGGACCCTACTAGGCACGTTTACCTACTTAAAGGAATATTTCACCCCTAAAATTAAAATTTGATATTAATTTATTACCACTCAGGCCATTTAAGACTTGTCTGTCTGTCTGTCTATTGTTCTATCTTTCTGTCTGTTTGCCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35918
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 |
---|---|---|---|---|---|
ENSDART00000080328 | Nonsense | 2090 | 2805 | 42 | 58 |
Genomic Location (Zv9):
Chromosome 15 (position 30191800)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 31013507 |
GRCz11 | 15 | 30894248 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCACGTCGTCACCCTGCTGGTGGCCACGGGCCCTCTCTCGCTGCGTGCAT[C/A]AACACACGGCCTGGTCATCAACATCATTCACTCGCTCTGCACATGCTCAC
Long Flanking Sequence:
GTTCCTGTCACAGTGCCTGACTTTAATGGTATTTGTTTACCTGCAACTGACTACCAGTACCCTATTACTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTCATCAAAGAAAAGTCCCTAAAAGGTTTGGATCCACTTGAGGATGAGTTGATGATGAAAAAGTGGTGGTTGATGCCTTTTAACTGCATATTCGTCTCATTGAAGCTAAAATGTCAAGTAAAGTCAGAGTGTTTAATGTAACAGTACTTGCTTTGCTAAATTTGTGTCTCAGGTGATTGGCCGAATGTGTAAGATCATCGACAAGACGTGTCTGTCTCCCACTCCGACCCTTGAGCAGCACCTCATGTGGGACGACATCGCCATCCTGGCCCGGTACATGCTCATGCTGTCCTTCAACAACTCTCTGGACGTGGCCGCTCATCTGCCATACCTGTTCCACGTCGTCACCCTGCTGGTGGCCACGGGCCCTCTCTCGCTGCGTGCAT[C/A]AACACACGGCCTGGTCATCAACATCATTCACTCGCTCTGCACATGCTCACAACTCAACTTCAGTGGTAAGGAGCCACAAAAAAAAGCATTATTTAAAGAAATAGATCAAAATTAAAACGGTCTCATATTTGGAATAGTTAAAGGGTTAGTTCACTCAAAGATGAAATATAATAGTTTTTCTTCTGTTAAACAAAAATAAGGTATTTTGAAGATTTTTTTTTATTTTGTTCTTACAATCAATGTCAATGACTGCTGGTTTCCAACATTCTTCAGGATATCTTTCTTTGTATTATATTGAAGAAAGAACTTCATACATGTTTATAACCACTTGAATGTGATTGTGTTCATTGTGATTCAATTTGATTCTGATTGCATCACTTGGTAAATGGTAAGTCTTTTACAGCGATCGAGAGTTTATACTTTTGATTAAAACATCAGCATAATATTGTAATGTGTATTTATATAGAGCATGTAACGTGTATAGCCATACACCCTAAGCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39057
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 |
---|---|---|---|---|---|
ENSDART00000080328 | Nonsense | 2232 | 2805 | 45 | 58 |
Genomic Location (Zv9):
Chromosome 15 (position 30186893)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 31008600 |
GRCz11 | 15 | 30889341 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCGGGCGCTGGTGGTGTTCGGCTGCATCAGTAAACGAGTGACTCACGGA[C/T]AGCTAAAGCAGATCATTCGTATTCTCAGTAAAGCCAGTCCTCTACTCAGC
Long Flanking Sequence:
CCTTCTTGCTATGAGACGACAGCACTACCTACTGCACCACTTCGTCGCCCATTTAAAGACATATTTTACCTAAAACAGTCATGCACAGGATAGTATAACAATTGATTTGTTAAATATTTCAAGCTGAAATTACACAGGCCTTTTCTTGGACACTTCAGACTTGGAGGACACGTATTGTAAAATGGAATAATAGGATCCTCTTTAAGTCTAATGTACACTTTATTAAATTTACAACTTATTTAATGTATTTATTTTTACTCAGGCCTGCATGAGGGACATTCCTGGATGCAAATGGCTAGATCAGTGGACTGAATTGGCGCAAAAGTGAGTTGAAAACATTTTATGAGTGTTTTGTGAAACTGTAAACCACATTTCAATCATATTTAAATAACTAACTGTCATCTCCACTGTTGGATAGGTTTGCGTTCCAGTATAACCCCTCTCTTCAGCCTCGGGCGCTGGTGGTGTTCGGCTGCATCAGTAAACGAGTGACTCACGGA[C/T]AGCTAAAGCAGATCATTCGTATTCTCAGTAAAGCCAGTCCTCTACTCAGCATTGATCGGGTAAGCTCTGTCTCAGATTCTCTCTCTTAGACTGCCTCATTTTAGATTTGATTCTAGTTTGGTGGCATTGATCGTTTTTGGAAAATGACTCAACTGATATTTATGTTGTAATGTGGTCTGCTGACTTTTACTTCATTGATAATGCTTTTAAATACCATATCTTTGCACTACTCAGAACTTAAGATTCCAGTTAATAGACTTTCATAGCCATTAGCATTACAGTCTTAGCATTAAAGGGATAGTTCATCCAAAAATGAAAATTTATTCACTATTTACTCATACTCTGTTGCAAATCTTTATAAGTTTCATTCTCTTGTTGAACACTAAAGAAGATATTTTGAAGAAAGCTGAAAGTATGTAAGCAGTGACTTCCATAGTAAGAAAAACAAATACTATGAAAGTAAATAGTTAGATTTTCAACATTTTTCAAAACATCTTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22671
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080328 | Nonsense | 2482 | 2805 | 51 | 58 |
Genomic Location (Zv9):
Chromosome 15 (position 30177928)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 30999635 |
GRCz11 | 15 | 30880376 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCGAAAGTGTCAGAGCGCAGTCTTGCACCTCCGTACTCCACAATAGGG[C/T]AGACCAGCCTTCGTCCACGCAAATCCATGAGTGTAGACATGGGCCAGCCG
Long Flanking Sequence:
AAAACCAAACCCATCTTCTACTTTACTAATTATTATTATAGAGCTAATTGGTAGTTTATTAGGCTAGTAGTGTTTGTTAATAGTTAATGTTTTGAATTGTGACCTAAAATAGTGTGTTATCTTTCATTTTCATTGCAAAATCTAAAGAACGTTTCTGTTACAGCTTTGCTCACAGTGTCAGAGGAAGTTAGGAGCCGCTGCAGTTTAAAGCACAGGAAATCATTGCTGCTTTCAGAAGTTACAATGGAGAACTTCCCCATGGACACATACACCGTTTACGACACTGAACCCGGGTGCAGGTATGAAGTTTTTCCACTTTATTTTTTTCTCCATTCACTTGTATTTCCAACTATATCCTATTGTTTATTTGAATGGCTTTTTTGTTTTTGTTGATTATCACACTTATTTTTTAATGTGTCAGGCTACTGCGTGAAAACCAGCCTTGGGCTTCTCCGAAAGTGTCAGAGCGCAGTCTTGCACCTCCGTACTCCACAATAGGG[C/T]AGACCAGCCTTCGTCCACGCAAATCCATGAGTGTAGACATGGGCCAGCCGTCTCAGGCCAATGCGAAGAAACTACTGGGTATTAGCGGTCTGATGACTTTGTTCTCTAAAAGTGGATATTTTAAAATGCTGTAGCTTTAATTTGGCTTCGTACTTATGATTTGTTTTGGGGATTTTTGTCTTTATTCTAGGCACTAGAAAGAGTTTCGATCACTTAATATCAGAATCCAAAGCCCCAAAAAGACCAGACATGGAGTCGGGCATCACCACACCTCCAAAGATGAGGCGGGTTTCTGAAAATGACTATGAGATCGGTGAGTACTTATTGATTAGATGTGTGGTGCAACATTCCAGTGCTGAGGTTGGGTTTTAGAAGTAAACACACCTTCATTTTCTCCATAAAGAAATAGTTTATTTTAATTAATACATTTTTAAAGAAAAACCTGTTGTGAACTTTGAGGTTGTTAATTAGTTTGTTGAACGCACTTTTAAAACACGTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35917
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080328 | Essential Splice Site | 2548 | 2805 | 52 | 58 |
Genomic Location (Zv9):
Chromosome 15 (position 30177614)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 30999321 |
GRCz11 | 15 | 30880062 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACCACACCTCCAAAGATGAGGCGGGTTTCTGAAAATGACTATGAGATCG[G/T]TGAGTACTTATTGATTAGATGTGTGGTGCAACATTCCAGTGCTGAGGTTG
Long Flanking Sequence:
ACTTTATTTTTTTCTCCATTCACTTGTATTTCCAACTATATCCTATTGTTTATTTGAATGGCTTTTTTGTTTTTGTTGATTATCACACTTATTTTTTAATGTGTCAGGCTACTGCGTGAAAACCAGCCTTGGGCTTCTCCGAAAGTGTCAGAGCGCAGTCTTGCACCTCCGTACTCCACAATAGGGCAGACCAGCCTTCGTCCACGCAAATCCATGAGTGTAGACATGGGCCAGCCGTCTCAGGCCAATGCGAAGAAACTACTGGGTATTAGCGGTCTGATGACTTTGTTCTCTAAAAGTGGATATTTTAAAATGCTGTAGCTTTAATTTGGCTTCGTACTTATGATTTGTTTTGGGGATTTTTGTCTTTATTCTAGGCACTAGAAAGAGTTTCGATCACTTAATATCAGAATCCAAAGCCCCAAAAAGACCAGACATGGAGTCGGGCATCACCACACCTCCAAAGATGAGGCGGGTTTCTGAAAATGACTATGAGATCG[G/T]TGAGTACTTATTGATTAGATGTGTGGTGCAACATTCCAGTGCTGAGGTTGGGTTTTAGAAGTAAACACACCTTCATTTTCTCCATAAAGAAATAGTTTATTTTAATTAATACATTTTTAAAGAAAAACCTGTTGTGAACTTTGAGGTTGTTAATTAGTTTGTTGAACGCACTTTTAAAACACGTGAGTTTAATAAATTTGAATTCATGCCTTAAAGGGGACCTATCATGCCTCTTTTTAGAAGATGTAAAATAAATCTGTAATGTCTCTTAAGTGTATGTGAAGTTTCAGCCCAAAATACCACACGCATACTGTTTTTATAACTCATTGAAGCTGCCCCCTTTGATGCTTTGGTCAAAATTTTACTGTTTTGGTTACTGTCGCTTTAAATTTAAATGAGATTGTAGCAGGGTGGAGCTACAAACTTGTATGCATCAGCATAGCAGCAGATTATCATGTTATCTCTGTGTAAGACTGAACATGTCAAAAGAAGCTGCAGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39056
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 |
---|---|---|---|---|---|
ENSDART00000080328 | Nonsense | 2638 | 2805 | 55 | 58 |
Genomic Location (Zv9):
Chromosome 15 (position 30175165)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 30996872 |
GRCz11 | 15 | 30877613 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAGGCACAACCTGCTGGACTCCAAGTTAAGCACCGTCCTTTCCATGTGC[C/T]AGGACCCGAACCTTCTGAACCCCGTCCATGGCATCATTCAGAACGTGGTC
Long Flanking Sequence:
ACCCCAAGATCCAGACGTTGCTCCTCACTGTACTGGTTTGTAACATACTTGTGCTTTAAATCCCCCTGCGCATGACCTTTTAGTCTATATTGAATAAACTGTATATTACATGTTTAATGTAGAGCTGAAAAAATTGAGAGATCATTTAGTTTCTTCTACAATGCCAATTTTATACTGTATGTACTGTTATATTACAAACTATTGTTTTTAATTGCAGGCAACACTGGTGAAGTACACTACAGACGAGTTTCATCAGCGGATCTTGTATGAGTATTTGGCTGAGGCCAGTGTGGTCTTCCCCAAGGTCTTTCCAGTTGTGTGAGTGTCTGCCATATTATAGATACCAACACCTTATTCTGTTGAGAACCATTAAACTTTCATAGGTTTCCTTCCTAAAAACATGTATTAGGCCTGTAGTTTGACATTCTTTCTGCCTGTGTCATTTTTATCTTAGGCACAACCTGCTGGACTCCAAGTTAAGCACCGTCCTTTCCATGTGC[C/T]AGGACCCGAACCTTCTGAACCCCGTCCATGGCATCATTCAGAACGTGGTCTATCATGAGGAGTCTCCCCCTCAGTACCAGCCGTCCTGCTTGCAGAGTAAAGCCGATCTCTCCTGTTACTTATTAACTTTAACATTTATAAGCAGAAACTTCCTTAAAGCTGCAGTTTGTAAAAGAAAATGATCCAAAATCTATGTTTGAGCACGTACACAACCAGCAGCCAGTGTTTAATACTACTGTACCTTAGCCTGAGTCACAACAGTAAACTTGTAATGATGTTGTTTGTTTCACTTGTAGGTTTTGACAGGAAATATCAGCTAGCCATAATTAGTTCATGTGTTGTTACTTTAAGTCTGTATACATAAAAAAAGACTCTAGTAGGCTATATCACATGCAGAGCTGCCAGGTTGCAGATCATTTATAGCCATGACGGTGTTTGATGGTAATGAAATGCATGTTAGTTATTTATTATTGGGTCAAAACTGTTGATTAGATTAGGAT
Associated Phenotype:
Not determined