ZMP
A8WFV8_DANRE
Ensembl ID:
Description:
LOC798746 protein [Source:UniProtKB/TrEMBL;Acc:A8WFV8]
Human Orthologue:
VPS13C
Human Description:
vacuolar protein sorting 13 homolog C (S. cerevisiae) [Source:HGNC Symbol;Acc:23594]
Mouse Orthologue:
Vps13c
Mouse Description:
vacuolar protein sorting 13C (yeast) Gene [Source:MGI Symbol;Acc:MGI:2444207]
Alleles
There are 16 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa34089 | Nonsense | Available for shipment | Available now |
| sa10606 | Nonsense | Available for shipment | Available now |
| sa20968 | Essential Splice Site | Available for shipment | Available now |
| sa20967 | Nonsense | Available for shipment | Available now |
| sa17562 | Nonsense | Available for shipment | Available now |
| sa20966 | Nonsense | Available for shipment | Available now |
| sa20965 | Nonsense | Available for shipment | Available now |
| sa12529 | Essential Splice Site | Available for shipment | Available now |
| sa20964 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa34089
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 |
|---|---|---|---|---|---|
| ENSDART00000110333 | None | None | 443 | None | 15 |
| ENSDART00000112651 | Nonsense | 529 | 3753 | 19 | 84 |
Genomic Location (Zv9):
Chromosome 7 (position 31027940)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 29420282 |
| GRCz11 | 7 | 29691432 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAGCCTGGACTGAACACTCAAATATATGAATGTACATTTATGTGCAGTA[T/A]GTAGCTGTGATTGTCAACTTTAAACTGCTGAGCACTTCGGTAACGTTCAG
Long Flanking Sequence:
AAGTGGTGCAAAAAATGTTTCAAAGCACATTTTGAAGATGTGTGTTTGCAATTGAATGTGCAGCACAGTTATTTAAGTAAACTAAAACTAAGACTAAAACTATTGCTCAACTATTTCTTAACTGCAATAAAATAAAAAATAAATTGTTTACCTCTGTTAAATTAAAATGACTAAACCAAAAACTGAAACTAAATATATGATAGCTAAATAGAAAATTGTTCACAAAACAAAAACTAAACTAAAACTAACAAAACCATTAATAAAATTAACTAAAACAAAACTGGAATTAACTTTTTTTAAAGTATCCACATAAAAACTAATTTAAAAGTGCTAAACTATAAAAAAAAAAAAAAAAAAATTTGCAAATTGTTTAAAGTATGTTTTATCAAACACATTGCACCTTAACAAAACTAAAGATGTGTAAAATATCAAATTTCTTACATATTTTTTTTAGCCTGGACTGAACACTCAAATATATGAATGTACATTTATGTGCAGTA[T/A]GTAGCTGTGATTGTCAACTTTAAACTGCTGAGCACTTCGGTAACGTTCAGAGAGGAGCCTGGAGTTCCAGAGATCCTCAAAGTGCAAATGATTGACCTCAGTACGTCCATCTCACAGAGACCAGGAGCACAGGCCATAAGGTACGCATCATGTATACCTTAACAGCAGCCAACAAACACACCTGTCATACACTTGATAGTGTATATACATATATAGGGCAAAATATAAAGTATACAGTGGGATTCAGTTTGATCTGATGTAGTAAATGCTGTGTGCTTCACACCTGTGACGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTGTTTATGTTGTATGTGTGTGTTTATATGGTTCACGAGGACACAAAATTGTTTATTGACATGGGTATGGCCTAGTTGTAGTCTATTAAGGTGTTTTACGAGGACATGTCTTGTGTCCTCATAATTCAAAACACTTAAAAGTCATACTTGACGGGTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10606
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 |
|---|---|---|---|---|---|
| ENSDART00000110333 | None | None | 443 | None | 15 |
| ENSDART00000112651 | Nonsense | 752 | 3753 | 23 | 84 |
Genomic Location (Zv9):
Chromosome 7 (position 31024975)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 29417317 |
| GRCz11 | 7 | 29688467 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGTTTCTGCCAGTTTYTCATCTYTAGARGAAATCATGGACAGAGCGTAT[G/T]AAAGATATTCACTGGAGYTGCGCAGTGTCCAGATACTCTACAGCAGATCA
Long Flanking Sequence:
TAGCCTACCAAACAAACCATCGTTATACAATAACTTGCCTAATTACCCTAACCTGCCTAGTTAACCTAATTAACCTAGTTAAGCCTTTAAATGTCACTTTAAGCTCTATAGAAGTGTCTTAAAAAATGTCTAGTAAAATATTATTTACTGTCATCAGGACAAAGATAAAATAAATCAGTTATTAGAAATAAGTTATTAAAACGAATATATTTAGTAATGTTTTAAAAAAAACTTCTCTCCGTGAAACAGAAATTGGGGAAAAAAATAAATAGGGGAGCGAATAACTCGGACTGTAACTGTAGCTTTTAGTGAATGTTTTACTCTAATCACCTGCCACATCTTAAGATGGAACTCTGCTTTTTTTTTAGTAATGTCTGACTAATAAAAATGTGTGTTTTGTTTTGTAAATGTGTGTGTAGTTAAACAGTGTAGATCAGGGTGGCCATCAGCAGGTTTCTGCCAGTTTCTCATCTTTAGAGGAAATCATGGACAGAGCGTAT[G/T]AAAGATATTCACTGGAGCTGCGCAGTGTCCAGATACTCTACAGCAGATCAGGTAAAAACAAGTCCTCACAGCGTGAAAAGGAACTGCCTACATTAACTGCTGCTTTAATTGCTTTCTCTTTTTGAAGGAGAGAAATGGAAAAGTGCTTGTCATGAAGGCCTTTCCCATCAACACATCCTGCAGCCAATGGACTTCACACTCCAACTGGCCAAATGTATGGTGGACAAGGATGCACGAATGCCCAGGTTAGTGCTCCATCTCTATTTTACAATAAAGAGAGTTAAATTGTTAGAGTTAGAATAAAAAAATAATAATAATAAAAAAAATTAACATCCCATTTCGAAAGTGCATATTTTTATGTGGGTCATATATTTTTGGTGCAGCTATGTTTATTAAAATAATATTTTAGTCAGCAAACATCTTTAGAAATAAAAAGATTTAAATTCATATTTAAGTTTGAAATAGTTTTATATTTTCTAAAAGTTCACATATTTTTTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20968
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000110333 | None | None | 443 | None | 15 |
| ENSDART00000112651 | Essential Splice Site | 885 | 3753 | 26 | 84 |
Genomic Location (Zv9):
Chromosome 7 (position 31021546)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 29413888 |
| GRCz11 | 7 | 29685038 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACCCCACAGTTCTGTCCTATGCTGTTGAGTCAGGTCAGAGAGAAAGAG[T/A]AGAAAAATCTTACAATAATAACCACATACTATAAATTTGTTGTTGAATTG
Long Flanking Sequence:
AACATGCAAACATAGACACTAGACTTTTAAATATCAGCATAAATGGTATTTTTTTTTATATAATGAATCCTTTCAAAAAATGGCAAAATGTTTTTTTTTTCATGTGTGCTGTTTAAAATGCAGCCAGTAATAAATAGTTGTATCCAATGAGAGTGTAGAATAGCCAACTCTATTTATAATTTTTACATTAAATGGGCAGGTTTTACTGTAAAATCGCCACAAACAACAAGCTTTCTGCACACCTACCAGATTGAGAATATATGAAAAAAACATTCTGTAGAAAATGTTGTATTTTATACTGAAATATTTCAGCCGTAAAAATTAGCTGGAAAATGATTTTGCTTTTTGCTAATACAGTATATTTTAGCGGTTGAAAAATGTTGATGCTGATGTTTTTCAGAAGGTGTTGGGGATGCCGCTGTCTAATACCAGGCCAAAGGTCTTGGCTTTAGACCCCACAGTTCTGTCCTATGCTGTTGAGTCAGGTCAGAGAGAAAGAG[T/A]AGAAAAATCTTACAATAATAACCACATACTATAAATTTGTTGTTGAATTGACTTTATTCACCGGTAATGCATACAGTATTTGACTGTATTTATGCATTCAGAGTCTGATGAAGACACTAGTGAGAAGTCTGTGGATGAAGAATCTCTCAGATCAACCTTGGAGGAACTGACTGAAGTGCAGTTTCAGTTTGAAGTCAAAGCGGTACGCTCATCCTTATCACTTTGTTTAAACCAGGGTTTCTCAAAGTCTGGACTCCACTCCGGATCCAGACCCACCTCCATTTTTAGGTTAAAGAGCACTAATTTTGTGTAAGGGATTAAAAATGTGGAAATTACTCCTTTCATAAACATATGTTACATTTGTAATCTTGTTTGTTTGGGATGGTCTAAAATTAAATGTAGGCGATAGTTTTTCTGTGTGATGTTATTTTAAAATATGACGTTTGCCACAACACTTCCAGAAAATAAAAGTTGACTAAGTAAATCGAGTTTTCAAAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20967
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 |
|---|---|---|---|---|---|
| ENSDART00000110333 | None | None | 443 | None | 15 |
| ENSDART00000112651 | Nonsense | 1175 | 3753 | 34 | 84 |
Genomic Location (Zv9):
Chromosome 7 (position 31017602)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 29409944 |
| GRCz11 | 7 | 29681094 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCAGCTTTAAGATGACCCTATACCCTGGGGCCACTGAGGGGGATGGCTA[C/A]ACTGACACCTCCAAAGTGGATGGCAAAGTTATCATGAGACTTGGCTGTAT
Long Flanking Sequence:
CATTTCTCACTGAAATAATGTCAATAATTATATTTTTATATTTATGTATTTATCTATTTTAAATAACATGTATTTGTTATATTTAAAGTAACATTTTTGAGGGCTGGCTTTACTTAACTATTACACATCTGTTCTTCAATATCAACATATCCAGCATTATACAGAGTCATCTGTTTTCCATGAGACCATATTATGCAAGTTAACCAAACATCTTGCTTTCATTTATGTCAGGCATTGATGCGTCTGTGATGGTTCAGGCAAAGGAAACAGATGTTTTTGCCCGTCTGCGTGACATTGTGGTTCTGGATGTGGACCCTAAGACCATCCACAAGAAGGTGAACTTTCAGCCATTTTGATTTCAGCACATTTGAAAATGGTACATTAGGTTCTGTTTTCCAGTCATGCTTGTGTTAATACTCCCAGGCGGTGTCCATCGTTGGAGAGGAAGTGTTCAGCTTTAAGATGACCCTATACCCTGGGGCCACTGAGGGGGATGGCTA[C/A]ACTGACACCTCCAAAGTGGATGGCAAAGTTATCATGAGACTTGGCTGTATCCAGATCGTCTACCTGCACAAATTCCTCATGTCTTTATTGGTGAGAATTTAAGTGAATGCACTTTTCAAATATATGTTGTCGTCTATATAACCCAGCCGTCTTATCTCTTATTGCAAAGTTTTGAAATCAGTATTTCTCTGTGCCTTTTTATATGTTGTATGGACATTTTCTTCTTGTCTCTTCCTTTGGTTTTGTTTTTGGCTCTGACTCCTTTTCCCCCCTCATAGTTTCCGTTAACTGTGTCTTCCTCTTTTCAGGACTCTTTTAGCTATCAGTACCCCTCTGCTGATGAGGTACAGGCTTGGGCATGATGCATTAAAGTCCTTCGCTTTGCAGCTTAACTTTAAATGCACCTTTGCACACACTGAAATTTATTTTTTCCTTTCTAAAATGTAATACTGCTGGATTTATCATACATGCATTTAAACCTTTCATTTTCAAGCAAGACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17562
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 |
|---|---|---|---|---|---|
| ENSDART00000110333 | None | None | 443 | None | 15 |
| ENSDART00000112651 | Nonsense | 2227 | 3753 | 54 | 84 |
Genomic Location (Zv9):
Chromosome 7 (position 30997803)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 29390145 |
| GRCz11 | 7 | 29661295 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAACCATCACAGCAGCCATGGCACCCAAACCCAAAGAAGAGCTGTCACAG[C/T]AGAAGTCTGGTGACCAGAACAGCCTCTGGTCTTTRATGAGCGTCGCTAAT
Long Flanking Sequence:
GGCTGGTGTCCTGCAGATTTTAGCTCCAGCTTGCCTCAACATACCTGCAAGGATGTTTCTAGAAAGCCTAGTAAGAGCTTGATTAACTAGCCCAGGTGTGTCTGATTGGGGTTGGAACTAAACTTTGCAGGACACTGGCCTTCCAGGACTGAGTTTGGACACCCCTGTGTTAGAGTAAAACTATTTTATCTCATTTTAAATCTGAAAAAAATAAAAATCTGAAACGTTTATATAATAAAAAATTGTATTATTTGTACTGTTAGTACTTTAAAAACATTCGTTAAACCTCCAGAAAGGGAAAATTTGAAGCAGTCTCTTTATTTTATTCATAGGTCTATATAGCATTGTATTATTTAAAATCTTTTGTTTTCATCATACTCATAATCAAGCAAAAATGCTTTTTCCCTATCTTGCTATATCAGATTTCTCCCATCATTCTCAACACCGTCATAACCATCACAGCAGCCATGGCACCCAAACCCAAAGAAGAGCTGTCACAG[C/T]AGAAGTCTGGTGACCAGAACAGCCTCTGGTCTTTGATGAGCGTCGCTAATGCGAACTACTGGTTCCTCGGAGTGGACACAGCTTCTGAGGTCACCGAGAGCTTCACAGATGTGGACAGCAGTAAAGATGGAGAGACCTTCGGATTAACGGTGAAGGTGGTGCAGGTTACGCTTGAGTCCGGTTTGGGCCATCGGACTGTTCCTCTGCTGCTTGCAGAGTCGTCCTTCAGCGTTACGGCTCAGAACTGGTCATCATTGCTCAGTGTTTCTGCAGATATGACACTAGAGGTCAATTACTTCAATGAGACTCATGCAGTATGGGAGCCACTGCTGGAGAGGGTGGACAATGGGAAACGCAGGTGGAACCTCAAATTGGATGTGAGAACCACATTTTGAATATAAATTTGCATTCCCTCCACATTAATCTAAACACTCAGGTTTTAAAAGTAATTTCTCCCCTACATAGGTGAAGTGCAGTAACTACGCAAACACTAAAACTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20966
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 |
|---|---|---|---|---|---|
| ENSDART00000110333 | None | None | 443 | None | 15 |
| ENSDART00000112651 | Nonsense | 2941 | 3753 | 63 | 84 |
Genomic Location (Zv9):
Chromosome 7 (position 30989961)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 29382303 |
| GRCz11 | 7 | 29653453 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCGAGCTCCAAATCATTCTTCTTTAACAAGCAGGACAGCGGGACTCTGT[T/A]GCGCATGGATCAGGTGATCATGCTTTGGCTGTGAATGTGATGCCTAATGT
Long Flanking Sequence:
AGGTGTTACTCTGCATGTGAAGTTTGACATCTCAACATTCTACTATAGAGTCCAAAAATGTTATTAATTTTAGGATTTGATTTTACAGCTTTCTATTAAAGAACAACATGTTTCTTGTTTGATGTTTTAGGTTGGGGTCAGTATCCAAATGAGCAGCTTTAATCTGACGCGGATTGTTACCATGAGCCCCTTCTACACACTCGTCAACAAGTCCTTGTTTGAGCTGGAGGTTGGAGAGGTGCAAAACAACAATGGCTCCAGCAACAAGTGGCACTACATTTCCTCCACTGAGGTCAGAGCTGAATTCATCTTTTATCGAAGGCAGCAGTATTCATGTTGTGTGTGTGTGTGTGTGTGTGTGTTGACTTTGATAATGTGTGTGTTACAGTGTTTGCCTTTCTGGCCTGAATCCAGCACAGAGAAGCTGTGTGTGCGGGTCGTGGGATGTGAATCGAGCTCCAAATCATTCTTCTTTAACAAGCAGGACAGCGGGACTCTGT[T/A]GCGCATGGATCAGGTGATCATGCTTTGGCTGTGAATGTGATGCCTAATGTACTGTATTAAAGGAATAGTTTACCTGAAATTTAAAATTCTGTCATCATTAACTCACCTTTCACTTGTTCCAAACTAGTTTGAGTTCATTTTTGTTCTGAAAAGAAAAGGATGCTATAAACCTGTAACCATTAACTTCCATAGTAGAAAAAACAAATACTATGGAAGTCACTTGTTTCCGACATTCTTCAAAATATCTTCTTTTTTGCTCAACAGAACAAATAAGCTCAAAAAGGTTTGCAACAAGTAAAGGGCGGGTAAATGATGACAGAAATGTCATCTCTTTAAATCATGTTAATAGCTCTATTAAATCTAATCATTGTTTTCATCAGTATGGTGGCGTGATAGTGGATGTGAATATCTCAGACCACTCCACTGTCATCAGCTTCACTGATTACTATGATGGAGCGGCACCTGCTTTAGTTGTGAATCACACACCCTCAGCCACGGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20965
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 |
|---|---|---|---|---|---|
| ENSDART00000110333 | None | None | 443 | None | 15 |
| ENSDART00000112651 | Nonsense | 3412 | 3753 | 75 | 84 |
Genomic Location (Zv9):
Chromosome 7 (position 30981257)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 29373599 |
| GRCz11 | 7 | 29644749 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGGAAATTCAGATTCTTTTCTCTCCTCATAGTTTCTGACACAGATGTA[T/A]GTGCTGGTTTTGGGTCTGGATGTTCTTGGAAATCCATTCGGGCTGATCCG
Long Flanking Sequence:
TTAATGTCTGCTCTGTTTGTGTGTGTTTTTGAATAGCTGCATTTGAGTCTGTCTTTGGGCTCCAGTGGAGATGAGTCTGAGCAGGGTGATATGGTCGCCATCCAGTCTGTCAACCTGCTGCTCAAAAGCATCGGTGCCACACTTACTGATGTGGATGATTTGATTTTCAAGTAAGTCAGACATGCACATTCTCAAATACTGGTTCATATGCTTATATGAAAACAAGTTTCACACGGTCACCTATTGACATTTTCCTTTCTCTTTTTTCAGACTGGCTTACTTTGAGGTGAAATATCAGTTCTACCGGCGAGATAAACTGATGTGGGCAGTAATCAGACACTACACTGAACAAGTGAGTGATCCAAGTACAAAATAATACAAAGTCAGAATTGGTTATATGTGCAAACGCTCTTCAACATCCTCATATTTTCATATTATGTCATTGTATGTGATGGAAATTCAGATTCTTTTCTCTCCTCATAGTTTCTGACACAGATGTA[T/A]GTGCTGGTTTTGGGTCTGGATGTTCTTGGAAATCCATTCGGGCTGATCCGGGGCTTATCAGAAGGAGTGGAAGCTTTCTTCTATGAGCCCATTCAGGTCTGAAACGTTCGGTTCATTTATCTCTCCATTCAGACCCCATCGTTTAATTCACTATGGATGTGAGAGTGTTATCACTCACAAAAAAAAAATTAATTCAGACAAGCACATTCACATAAAATGTGCATATCAAATATTATTACATTATTAGGTCAACTTCAGTCACCATTGTATGTATATCAATTTCATATATGCTTGTAAACTAAAATTCAGAATTACACACACATAATCACATTATTACATGTTACTGTTCCAAATGGGTTTGTACTCGTAAAACATTTGTATTTGTAAGTAGATTATGTAACATTTACATAACATAAAAAGCTCTTTATTACAGTTTTTACAGTTTCACAGGGCAATATTTTCATTTTATAAAAACTATCAGTAATAAAATCAATAATGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12529
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000110333 | None | None | 443 | None | 15 |
| ENSDART00000112651 | Essential Splice Site | 3444 | 3753 | 75 | 84 |
Genomic Location (Zv9):
Chromosome 7 (position 30981159)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 29373501 |
| GRCz11 | 7 | 29644651 |
KASP Assay ID:
2259-8943.1 (used for ordering genotyping assays)
KASP Sequence:
CCGGGGCTTATCAGAAGGAGTGGAAGCTTTCTTCTATGAGCCCATTCAGG[T/G]CTGAAACGTTCRGTTCATTTATCTCTCCATTCAGRCCCCATCGTTTAATT
Long Flanking Sequence:
CATCCAGTCTGTCAACCTGCTGCTCAAAAGCATCGGTGCCACACTTACTGATGTGGATGATTTGATTTTCAAGTAAGTCAGACATGCACATTCTCAAATACTGGTTCATATGCTTATATGAAAACAAGTTTCACACGGTCACCTATTGACATTTTCCTTTCTCTTTTTTCAGACTGGCTTACTTTGAGGTGAAATATCAGTTCTACCGGCGAGATAAACTGATGTGGGCAGTAATCAGACACTACACTGAACAAGTGAGTGATCCAAGTACAAAATAATACAAAGTCAGAATTGGTTATATGTGCAAACGCTCTTCAACATCCTCATATTTTCATATTATGTCATTGTATGTGATGGAAATTCAGATTCTTTTCTCTCCTCATAGTTTCTGACACAGATGTATGTGCTGGTTTTGGGTCTGGATGTTCTTGGAAATCCATTCGGGCTGATCCGGGGCTTATCAGAAGGAGTGGAAGCTTTCTTCTATGAGCCCATTCAGG[T/G]CTGAAACGTTCGGTTCATTTATCTCTCCATTCAGACCCCATCGTTTAATTCACTATGGATGTGAGAGTGTTATCACTCACAAAAAAAAAATTAATTCAGACAAGCACATTCACATAAAATGTGCATATCAAATATTATTACATTATTAGGTCAACTTCAGTCACCATTGTATGTATATCAATTTCATATATGCTTGTAAACTAAAATTCAGAATTACACACACATAATCACATTATTACATGTTACTGTTCCAAATGGGTTTGTACTCGTAAAACATTTGTATTTGTAAGTAGATTATGTAACATTTACATAACATAAAAAGCTCTTTATTACAGTTTTTACAGTTTCACAGGGCAATATTTTCATTTTATAAAAACTATCAGTAATAAAATCAATAATGCTGTGTGCCATATTATACATATATAAGTTGAAGTCAGAATTATTATCTACCCTTTCTCTCTTTTAAATATGATGTTTAACAGAGCAAGTAAATTTTAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20964
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 |
|---|---|---|---|---|---|
| ENSDART00000110333 | None | None | 443 | None | 15 |
| ENSDART00000112651 | Nonsense | 3670 | 3753 | 82 | 84 |
Genomic Location (Zv9):
Chromosome 7 (position 30969160)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 29361502 |
| GRCz11 | 7 | 29632652 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGATGTGTGTGAAGGAGATCGATGTGATCGGACATTTCAATAAAGAATG[G/A]GAATGTCAGTTTGAGAGTTTCCAGAGACCTCCATGCACAGAAGGAGGAGA
Long Flanking Sequence:
GGAATTAATGTCTGATGTATTTTCCTATATACTTTATATATTGCATTAATTGTCATGTAATCATTTGTTTTAATGTGTTGTAATTGAATTATTAACCCAAGAGCTTGTCAGAGTCCTGTGATTGACCATAATAATCATGTGGAATAAATCAATACTCCTCTTTAACACGATCATGATCATTTCTATGCTTTGCAGCTGATCGGTTCATACAAAAAAAGCCTATACTGGTGTGTTGTGGTGTACAAGTTTGTGTGTTTTTCAGAGATCTGAGATTAAACAGTTGGACGGGGAAATCTTCAGAGAACACTACATGTACCCAGGACACAGAAAAACAAACATCATGATCACCAACAGGTATTTCAACAACAGAACGAATGATTGAACTCTGGCATTTCCCACTTTTTCCATATGTTCTTGCTGTATGTGTTGGTTTATTTATCGTGCAGGAGAGTGATGTGTGTGAAGGAGATCGATGTGATCGGACATTTCAATAAAGAATG[G/A]GAATGTCAGTTTGAGAGTTTCCAGAGACCTCCATGCACAGAAGGAGGAGATCTGAAGATATATTACCGGGTACATGCTATAAATACTGCCAGTGTTAGCATTAAAACATAAACAATAGTATGCTGTTTTTCTAGGGCTGCACAATATATTGTTTCAGCATTGATATAGCAATGTGCAAATTCGGAATAGTCGCAGGATGTCCAGTTGGGATTATAGTTGATCACATGCTACAGTTCAGACCATAGTGCCCAGCAAGCATTTTTGTTTTTAAAAGATGTCTAATAGATGTCTAAACATAGTTGTATAGGCTAAAACAAGGCTAAATTTGGGCTTAGATTAGTCATCAAATAAACAAAAAATGAATGACTACGCATATAAAGTCTGTCTAATCTGTCTATTTCTTTAGGGCTATTCTTAGATGTCTATTAGAATTTGATTATTAAACACAAAATTGTTTGCTAGGTTGAGTCATTCAACGTGAGTGTTTATGATTTTACTGT
Associated Phenotype:
Not determined