ZMP
NP_571093.1
Ensembl ID:
Description:
huntingtin [Source:RefSeq peptide;Acc:NP_571093]
Human Orthologue:
HTT
Human Description:
huntingtin [Source:HGNC Symbol;Acc:4851]
Mouse Orthologue:
Htt
Mouse Description:
huntingtin Gene [Source:MGI Symbol;Acc:MGI:96067]
Alleles
There are 11 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa15014 | Essential Splice Site | Available for shipment | Available now |
| sa39659 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa19545 | Nonsense | Available for shipment | Available now |
| sa39658 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa38282 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa45079 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa19544 | Nonsense | Available for shipment | Available now |
| sa39657 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa12352 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15014
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 |
|---|---|---|---|---|---|
| ENSDART00000074777 | Essential Splice Site | 385 | 3121 | 11 | 67 |
Genomic Location (Zv9):
Chromosome 1 (position 41740855)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 40657096 |
| GRCz11 | 1 | 41359883 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGKAGAAAMATGGTGTTGTAACAATATGCMTTGTATGTTATGCTTTTATT[A/T]GGCAAACTGTTGTCAGGTGAAGAAGARGGTTTGGARGAWGATCCTGAGAG
Long Flanking Sequence:
TTTCCTTTATTGGTTTAAATGGCTTTTGTGCTGATCAAGTTCTTTATAACTCACCAATAACAGGCTGTCTTTAAATTCAGCTACTAATATTTCCTTCACTGCTTCTTGGCATTTTATATTCTCCTTGTTAGCCGATTACAAATCGGTGCCTTCAAAATTCCCTGCAAACCAATTTTCTAGATCTCACCAAGCATGTGCTCCTAATCCTGTGCTTCTTTCTTCCTCTAACCCTCAAACTGAATTGCTGGGCTTTTTCTTCTCTTCCTGTTTCCTGCATACAGCCGGCGGGTCAACATGCAGTCCTCTCCTTCTCAGGAAGCAGAAAGGTGACTTCTTGTCTGCCCTTCTTTTGCATCTAACCTACTGACACGTTTCTGGCCATCACACAGTTTGCTAATAAATGTGTGGTTGTAGTTTTAGACTATTAAAAGCTGTTGAGATGTTGTTTATAGTAGAAAAATGGTGTTGTAACAATATGCATTGTATGTTATGCTTTTATT[A/T]GGCAAACTGTTGTCAGGTGAAGAAGAGGGTTTGGAGGATGATCCTGAGAGGGCAGAGGTTACCACAGGATCCTTCACTGGTAAGTTGAGGAGAGCTGTGCTGTTACGCTTCACTCCTGAGAGTTTCCTCTAGAACAGGGCTCGGGAACCTTTTTTCAGCAAAGGAAAAAAAAAAGAAATGCCATTTTAGATTTTTTTTGGCAAATGCATTTTTTTAAAGAGCCATTGGGGTATGTTTATATTTTTATTTATGTATATGTACACTACCAGTCAATAGTTTGAGGCTGTTTTTAAGAAAAGAAAGAAAGTTATTCTGTTCATCAAGGCAGCATTATTTATTAAATAATAATTTATCCAGGGTGTCTGTGGGGTCTTAAAAAGTAATTAAAGTTGATAAATCAATTATGAGCATATTAAGTACCTTAAAAGGTATTAAAAAGTCTTTTTATGAGATGTAAAATTTTGTTTAAGCGTTGTCCAAAGTGTCTGACTCCAAAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39659
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 |
|---|---|---|---|---|---|
| ENSDART00000074777 | Nonsense | 472 | 3121 | 12 | 67 |
Genomic Location (Zv9):
Chromosome 1 (position 41736149)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 40652390 |
| GRCz11 | 1 | 41355177 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGTGCATCAGAGCAGGGAGTCGGGCCTGATACTCCAGATGAGGAAGAC[G/T]AGGAAGACATGCTAAGCCGTAGCTCAAGCGGAGGCGCCGGGCTTGTCAGC
Long Flanking Sequence:
TTGTTTTATTGAGAATAGTGAGACTAAAGGCTGCTGAAAATTCAGCTTAGCCATCACAGGAATAATTTAGTTTTTGCAAAAAAAAAAAAAAATAATAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAACAGCTTATTCTAATAGTGTTTTATAATATTTTGATGATGATGATAAAGAGATTTAATTAAAAAAAAGTATAATTCATTTTCTTATTTTACTTTGTTGTTGAGGCTTGTATTTGAGAATAATGTGTTGTTTCCCTCTGTCATGTTTCTTCAAGCCTCTGTCGGTGGTGACAGCTCCAGTGAAGCTCCCTCCTCATCAGGTGTTTCGTCTCTCGGCACGTCTGACATCATCACTGAGCAGCCACGCTCCTCCCAGCATGCCTTGCAGCCTGGTGACTCGGTGGACCTGAGTGCATCAGAGCAGGGAGTCGGGCCTGATACTCCAGATGAGGAAGAC[G/T]AGGAAGACATGCTAAGCCGTAGCTCAAGCGGAGGCGCCGGGCTTGTCAGCACATCCGGCGACCTGGTAACCGATGCCAACCAGATGTCAGCCGGAGCCGTGTCTTCATCTCCCCCTAGCGAGAGTTCTCAGACGACTACGGAGGGGCCGGACTCCGCCGTGACGCCTTCTGACTGCGCAGAGCTCGTAAGTGTCACCAGCACCAGCAGACGCTATCGGAAATATTCACCACCTTCCCCAACTCTAACAGAAGGGCCGGACACGCAATCGGAAAGCGGCTCATCCGTCTACAGGCCGTCCTCTTCTTCCACCTCCTCTACCTCGTCTTCTTCCTCCACCTTTTCTGCCATCTCTTCCTCTAGCAGTAGTGACCAGGTCAGCAGAGGACGGGGGGTGAGGCTATTGTTGCTCTTCCCCGCCCGGTATAACCCCGCCCATCATAGAGCTCTGCCCTTTATTTGTCCCACCCCCACAAATGCACGACCTCTATCCTGAGGCGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19545
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 |
|---|---|---|---|---|---|
| ENSDART00000074777 | Nonsense | 546 | 3121 | 13 | 67 |
Genomic Location (Zv9):
Chromosome 1 (position 41733641)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 40649882 |
| GRCz11 | 1 | 41352669 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCTGATGTGTAGGTGCTGGATGGCAGTGAGAGTCAGTACTCAGGGATG[C/T]AGATCGGCACACTGCAGGATGAGGAGGAGGAGGGCTCGGCTCCACCACCT
Long Flanking Sequence:
TTAATCATTTGGTAAATTGACACTTTAGGAATTACAATCACTTTAAGAATAATAATAAAATATAGCTAAAGGGTGCCCATTACAACTAGGTAATTAATGACTTAAAATGAAACCAAAAAATATTTTTAAAATAAAAATAAAAATTATAATAGCTTCGAATTTGATCCCCCTTCAGCCAAACTACAAAACAACAACTTACAATTGCATAAATCAGCAGCAATTTTTTGTTAATGCAAGTGACATTAGAGCAACAGCCTACATTTGGTTTTTGTGAGGCCCAAAATTGTCATGACATGCATACAGCTTCTTTTCCAAAGACAGCGTTTTTATGCATTCCTTAAAGTGAAAGCGCATGTTGACTGTGATTTGTTCTTTGTGGCCATGTGCATGAATGAGCTGCTGTGAATGTTTGCGAGTTCGGTTCATTGGGATGGTTTTGAACTGTAAATATGTCTGATGTGTAGGTGCTGGATGGCAGTGAGAGTCAGTACTCAGGGATG[C/T]AGATCGGCACACTGCAGGATGAGGAGGAGGAGGGCTCGGCTCCACCACCTGACAAGCCTCCAGAACCTTTCTCTCAGTCAGCACTGGGTACACACTCATTCCGTTTTTCACACTTATTCATTTATTTAAAAATATTAATATTTTGATAAATATCGATGTTGACAATTTTTCACACTTTCGTTTAGGCCGGTTAATGGCTGTGGTTTTACAGGCATCACAGTCTAATCACTTCACTTTGTTCATTTGATCTATTCTAGAGTATACAGTTACTCATTAAATAGTTGATGCTGAAAATCGAGGTTGTTTTAGTAAATGAAATCTAAAGCTAAGAATAAAAGCTAATTGTGGAATTTATTATAATGCTACATGGCATCGTTTATTAGAAAGTTAGATGGCAGGAACCACTGCTACTTCATAAACGTCACTTTAGAGCTAGTGTTTGAATGATTCTCTAGTTTAATGTCTAAACTGATGACAAAACAGGTGATTTAGTTGACATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39658
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 |
|---|---|---|---|---|---|
| ENSDART00000074777 | Essential Splice Site | 1074 | 3121 | 26 | 67 |
Genomic Location (Zv9):
Chromosome 1 (position 41721538)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 40637779 |
| GRCz11 | 1 | 41340566 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTACTGTTCTTTGTTTGTATTTAACGTGTTTTTGCACCTGCTTTTGTA[G/A]CTGTTGCACCCAAGTGCATGAAGAGTCCATGGGCAGGTGAGGAGGAGTCT
Long Flanking Sequence:
GTAATTTATTACTTTTACTCAACACTGAATATGTTTAAGAAATTATCATTACAATATATTTAAATCTTTTTTTATGTATAATTCCCAAATTATGTTTAACAGAGCAAGGACATTTTCACAGTATGTCTGATCATTTTTTTTCTTCTGTAAAAAGTTTTATTTGTTTTATTTTGGCTTGAATAAAAGCACTTTGGCTAATAATTCAAGAGGGCTTATAATTCTGACTTCAACTGTGTGTGTGTGCGTGCGTGTGTGCGTGCGCATGCGTATGGGTTATTTCTGTCTGTGTTCATCATTATAGTGGGTAGATTTTGTTTGTTGTTCTGCAATATGGGTCTTTTTCATTCAATTCCTTGTATTTATCAAATTTAATCTGTCAATAGTGACCGAACAGCCTAAGGTAAAGTGTTTATTTTCATGACAAAAGCAGTGTGTAGAGTCATTTCAGTCTTTTACTGTTCTTTGTTTGTATTTAACGTGTTTTTGCACCTGCTTTTGTA[G/A]CTGTTGCACCCAAGTGCATGAAGAGTCCATGGGCAGGTGAGGAGGAGTCTAGCCCCGCCTCCTCAAAGGTGGAGGAGCCGTGGCCTGCTCTCAACGACCGCTCTCTGGTTGTTATGGTGGAGCAGCTGTTCTCACATCTGCTGAAGATCCTCAACATCTGCGCTCATGTGCTTGACGACACTCCACCCGGTCCTGCGGTCAAGGTGAAGGAATCCCTCAAAAGATACTGATTACAAAAAAAATGTTTAAGTATTATATATTTACCCTATCTATTGAAAACATCTGTATTTCTGATTTCTGTTAACATTTGTTTTTTCAGGCTTCTTTACCTTCATTGGCCAACACTCCATCTCTCAGTCCAATCAGACGGAAGGGTAAGGAGAAGGACATGATGGAGGCAGGCACCACCCCTATGAGCCCAAAGAAAGGCGGAGAGAGCAACACAGGTGCAGTCACAGCTACAGTGCCACCTGTAAAGATCAATAATACTTTTTTGAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38282
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000074777 | Essential Splice Site | 2188 | 3121 | 49 | 67 |
Genomic Location (Zv9):
Chromosome 1 (position 41697217)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 40613458 |
| GRCz11 | 1 | 41316245 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAATATAGATACTCTGATTGCATATGTTTGTGTGTGTGTGTGTGTGTTGC[A/G]GGTGAGCCTGGGTTTTATCAGACTGTGTTGAGTCTGTGTGGCGTGTTGAG
Long Flanking Sequence:
TGTTAGCAACATTAAAATGTTAGCAAAAAGTTCAAATGTTAAATGCTAGCAATGTGCTAAAGATCCTTGCAAAGTTATGTCATGTTACCAATGTGTTAAAATGTGAGCAATGAGTTAAAACCATTAGCCATGTGCTTATTTTACACTTCAAGTTAAAATACTAAAAACATCACAGTGAAATGTTGAATTCTTGAGTGTTTGAACATTTTAAAGTTATTGTGTTTAGCGTTTATTTTGTCTACTGCTTAAATGCAGGTTACAAGTTAATGAAATTGTGTAAATGTGTAAGTAAAGTTACCTTAGCACATATTGTGCAACCAAATGCACAGACAAGGATTGAGTTCACCTTGTTTATTGTGAAATGAACCAGAAAACAGACCCTGAAAACACTGGATCGTTAGCTGCTTCTGCTATTCTAAATAAACAGAGCTGCAAATTATTGTAAGGAGATAATATAGATACTCTGATTGCATATGTTTGTGTGTGTGTGTGTGTGTTGC[A/G]GGTGAGCCTGGGTTTTATCAGACTGTGTTGAGTCTGTGTGGCGTGTTGAGTCAGTACCTGCTGTCTCTGTCCAAACTGCCATCCTCAATGCACATTCCCAAAGACAGAGAGACACTCATTACCACCTTCAGCACCCTCGCTATAGAGGTAAGACATCCTGTTCAAATAAGATGATTTTATATATATATAGCTAGCTGACATTATCGAGTATGTCATAAATATATGACTTCAGAGTCCAAAGCATTCACTGCATTAAGAAGCCTATTACAACACAGGCAAAAGCCCTCAAATTAAATTTATGAAAACAAAATAATTATTTATAAGTTCTTTTTTTAAATATAATAAAAATAGTATTTAATATAACTGAAAAGGTGCATCTGGAAAGTATTCATTGCACTTGACTTTTTCCACATTTTTTTAATGTTACAGCTATTTTTTATTTTTATTTTTGCTCAACTTTGGCTGATATATAGACAGTACAGGTATTTATCATATTGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45079
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 |
|---|---|---|---|---|---|
| ENSDART00000074777 | Nonsense | 2330 | 3121 | 52 | 67 |
Genomic Location (Zv9):
Chromosome 1 (position 41693844)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 40610085 |
| GRCz11 | 1 | 41312872 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAACATGAGTTGCTATGTCTGTGATTTTTAGACCAGCGTGAATGGCATTG[T/A]TGTGAGATCATGGCTGAGCTGGTTGAAGGTCTGCAGACTGTCCTGACTCT
Long Flanking Sequence:
GTAAAACAATTAATTGCAAACTGAAATAAATATAATTTGATTATATGGTTTGGAATTTGATGTTTAAGTGATCATTTGCATTTTGTTGCGGTTATTTTGCGTTTATTTATTTTGCAGGGTCGCTATAATATATTGTGAATTTTTGCTGATTTTGCGTTGGATTCAGCTATCGCGGAAACGCAAAAAAACTAGGGGGTCTGAATAGTATTAACAGTATATTTAATTCATATTTTCTTTTTTTAGACTGTCTTAACCCGCCACAGCTGAAATCTACCTGCATTTGGCTGGTTGGTGGGTGTTATATAAATGGATTATGGGTTATATAAAATCACAAACTTCACGTGTACAACTTAATTTTTTTTTTATATATATCCACATTGGCTATTGGCCAAAATTATTTGAGAAAATTGACTTATCTGATCTAGTCAAACTTCCAGTATCGTGTGTCTCTAACATGAGTTGCTATGTCTGTGATTTTTAGACCAGCGTGAATGGCATTG[T/A]TGTGAGATCATGGCTGAGCTGGTTGAAGGTCTGCAGACTGTCCTGACTCTAGGTCACCACAAAAACAAGAACATCCCAGCGTTTCTTACACCCACCCTACGAAACGTCATCATTAGTCTGGCCAGGCTGCCCCTTGTGAACAGCTACACCCGAATCCCACCACTGGTGAGAGAGTGAAGTATTTATATATGTGTGTGTGTGTATGTATTATGTGCTTAGAACTGTATTAAAGTGTTCTTATGTTTGGTTTTCCAGGTCTGGAAGCTGGGCTGGTCCCCCAAGCTGAGTGGAGAATTTGGCACAGCTTTGCCAGAGATCCCGGTAGAGTTCCTGCAGGAGAAGGATGTGTTCAGAGAGTTCCTCTACCGCATTAACACTCTGGGTACGAGACTAATTTCAGACCGGTCTGTTGCTTTAAAATAAGTTCAGAAAATGCATTTGAAGTTATATTTTAGTGTCTGCATTAAATAGAATTTACAGAAGGGATTTTATATACATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19544
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 |
|---|---|---|---|---|---|
| ENSDART00000074777 | Nonsense | 2714 | 3121 | 60 | 67 |
Genomic Location (Zv9):
Chromosome 1 (position 41686043)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 40602284 |
| GRCz11 | 1 | 41305071 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGAACTGCAGAAGGTGCATCCACCAGAAGATGAGATCCTCAACCAATA[C/A]CTTGTTCCAGCAATCTGTAAAGCAGCAGCAGTGCTTGGCATGGTGAGTGT
Long Flanking Sequence:
TTCTTCCAGGAATACCCACTTCACAGTATAAAAAATGTAAATAATTCCTGCCCAAGGCATGCTCAGGGGTGTGATGCCTGGTTCAAAGCTGTTAGTAGTGTATTGACGACACTTCTGAATGAACTGCCAACTTATCCAGCATATGTTTTACGCAGCAGATGCCCTTCCAGCAGCAACCCATCACTGGGAAACCCGTCTCCAAAACTAGCACTTAATTCTCTGAGCACAAACAGTTGTATATTTAGTATTGCCTCTTGCTGTTGAATCTCTGAATGCCTCCTTAATTGTAAGTCACTTTAAACAAAAGCATCTGCTAAATGACAATGTAAATGTTCTAAACTACACTTCCGTTGCAGTTCACTCACCTCTTCTATCTCTCTCTTTTAGCTGCTGGCAGTGTCTGATCTCTTCACCGAGAGGAATCAGTTTGATATGATGTTCTCCACACTGACTGAACTGCAGAAGGTGCATCCACCAGAAGATGAGATCCTCAACCAATA[C/A]CTTGTTCCAGCAATCTGTAAAGCAGCAGCAGTGCTTGGCATGGTGAGTGTTTACATGCACTTTTGACTCTTTATATGTGACTGATGTTAACAATGTGGACTGATGTACCTGTATCAGGATAAAGCCATTGCAGAGCCTGTTTGCCGTCTGCTGGAGAGCACGTTACGCAGCACTCATCTGCCCAGTCGAATCGGGGCTCTTCATGGAGTTCTGTATGTGCTGGAGTGTGACCTACTGGACGATACAGCGCGACAGCTTATACCGACTGTCAGTGAATACCTGCTGTCTAACCTTAAAGCTTTAGCACAGTGAGTAATGCTTAAAACTGAACGCACACAAACACACCTAACACACATTATTTACTGTCTGTCTAAACTTTAGCTTTCACACATACAGCTTGTTTACATAATGTAACTATTTAATTTCTTAATTTTCTACTGTTAATTAAAGGCATATTTAATCCTAATATGAAAATTCTGTCATTAACTTACACTTTATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39657
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 |
|---|---|---|---|---|---|
| ENSDART00000074777 | Nonsense | 2951 | 3121 | 65 | 67 |
Genomic Location (Zv9):
Chromosome 1 (position 41679313)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 40595554 |
| GRCz11 | 1 | 41298341 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTAATCTGTGGCAATTTCTTGCGCCAGGATTCGCAAAGGTTTTCCGAGT[G/T]AGGCACGTGTTGTGGCCAGGATCCTTCCTCAGTTCCTGGATGACTTTTTC
Long Flanking Sequence:
ACTGCAATTTGCAAATTGAAACCACCGAAAACCGCTAAAGTCGACTATATGGTGAATGATGCTCTATGTTTTCCTCAAAAACCATAAATCATTTTCAAGGACTAAATTGAATTCATTTTGGATGTCAAGTGGGTAGTAAATCATCAGGACATTTTCATTCTGGTAGTGAACTAATCACTTACGCATATTAATGTTCTTATTATTTTGTAAAAAAACTGAGATTTTTCTTATTTGGAATGTAAAGAAACCAAACTGTTCCTCTTAATGATGGCCCTCATTTTACACTACAGGAAAGGAGAAGGGAAGTCCTGGACGTCCTGCTGATGCAGACCCCACAGCTCCTGACAGCGAGTCAGTCATCGTCGCAATGGAGCGTGTATCTGTTCTGTTTGACAGGTATGTATGTTTAACCATATATTTTTGTTCCAGTGATTCATCACAATATATCTGCCTAATCTGTGGCAATTTCTTGCGCCAGGATTCGCAAAGGTTTTCCGAGT[G/T]AGGCACGTGTTGTGGCCAGGATCCTTCCTCAGTTCCTGGATGACTTTTTCCCACTGCAGGATGTTATGAACAAAGTCATTGGGGAGTTCCTGTCCAATCAGCAGCCTTACCCACAGTTCATGGCTACAGTGGTCTACAAGGCAAGTGCCATATTTTAGGCACTGATGTCTTTTGTAATGCTTTATGCACTCTGTGATCTTAAATGAATTTGTTTGTAAAGGTTTGGTCATATTAGCAAAATATCAGGGAAATCTATAAAAAGGTCAGTTCAGTTGTCTGTTATCATAGTGTAGTGATATATGAAGCACTGCTTACACAGATATTTTTACATTTATATGTGTGCATTTTCTATCCAAAACAACACTGTATACAAGTTACATATTTTTTTTGATTCTGATTTTTGATTTAGGCACAAATTACACATTTGATCAGTTCCCTGGGAATCAAACTGTGACTAGTTGAGCTACAAGAAGTCAGTGTAGCCAAAGTTAATGCTTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12352
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 |
|---|---|---|---|---|---|
| ENSDART00000074777 | Nonsense | 3081 | 3121 | 67 | 67 |
Genomic Location (Zv9):
Chromosome 1 (position 41676475)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 40592716 |
| GRCz11 | 1 | 41295503 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGGTGGACATTAGCCTCTTTTGCTTGRTCGCTATGGACTTCTACCGACAT[C/T]AGATCGATGAGGAGTTAGACCGCAGGGCCTTCCAGTCTGTCTTTGAGATG
Long Flanking Sequence:
TGGTGTATGTTTGTGGGTGTCACCGTTCCAAATTAAACCGCAGCTTTTTGCTTATAATGTCTTATTGTTTATTGTCACAGATTAAATAAGGACGCATGACAGCTAAGTGAGAGAGTTTACTTGCACGTGACTTGCTATTTTGGTCCTTTTAGAAACTTTGCAGAGTGAAAGCGAACCATACCATGAACAAAGTGCAACATTGTAACAATTTTATTCTCTGTTTCGGAACAAAACCGTCAATCTACAGGTGTGAAATAGCATTAAACATGCATATGATACCCAAAAAGCCTGCACCAAAAATGTATGAATTAATCTACTGTTACACCCCTACCTTGCACTGGTAACAGCACACTTCATGCTTTTCCATTTCCTCTTCCTCCACGTTTTCCTTAACTTGTTTCTTCCGCTGTAGCCTGCCTCATGTCATCAGCCGCATGGGGAAATCTGACACGGTGGACATTAGCCTCTTTTGCTTGGTCGCTATGGACTTCTACCGACAT[C/T]AGATCGATGAGGAGTTAGACCGCAGGGCCTTCCAGTCTGTCTTTGAGATGGTGGCTTCCCCTGGTAGTCCGTATTACCAACTACTGTGCTGTTTGCAGAGCATTCACCAAGACACGTCTCTATAGAACAGACCAAAAAAAAAAAAAAAGATCAGTAGGATCACCATGGCAAATTAAGCATCAAAATGAAGGTAATATAACACCCAAGCAGAAGACATACACTCACCAGGATGCATGACAGACTTTGGATTGGATTTACAGAGTGGAATCGGTTGCTATGATACTCTCCGAGATTGCTCCAAATAGTTCATAGTTATTAGAGACAGTGGGACCAATCCAAGCAAAACTGCACTTTCACTAGTCTGTGGCCACAACGCACCAATGAACATCATTTATCTGTAATTAAAAATATAAGAAAAGCAGCACTACATTCAGAATATTCAACTGCTATCACAGTATGTGCACCTGGCCACTGAAGCGTTTTTCCTGAGCTGAGTTAAG
Associated Phenotype:
Not determined