ZMP
vtg3
Ensembl ID:
ZFIN IDs:
Description:
Vtg3 protein [Source:UniProtKB/TrEMBL;Acc:Q0P421]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41779 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa14938 | Nonsense | Available for shipment | Available now |
sa21846 | Nonsense | Available for shipment | Available now |
sa44735 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa35022 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa9585 | Nonsense | Available for shipment | Available now |
sa31815 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa41779
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 |
---|---|---|---|---|---|
ENSDART00000014979 | Essential Splice Site | 18 | 1251 | 2 | 28 |
ENSDART00000103418 | Essential Splice Site | 25 | 538 | 2 | 15 |
Genomic Location (Zv9):
Chromosome 11 (position 7524547)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 7368650 |
GRCz11 | 11 | 7378489 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTAATGTTTTTTCTTTTTCTCCCATTAGCCAGCGAGATGGCAAATTATG[G/A]TATGTAAATGCAATATATATCAATCTCATTACTTATTACTTACCTGTGCT
Long Flanking Sequence:
CAGCTGTGACAGAGAAATTTTGCTATGTGGGTATTTACACAGCAGAGGTACAGTGCATGCATGTAGAGTTGTGACTGGAAGTGTAGCTTTCTGGTGAAGTGGAGCCGATCAACAAATCACAGCACATTATGTTAGCTGACCAATCAGAGCCTCTTGAGGGTTGGCCTTTAGAGGAACTAGGAAATATGTCAGCCATTTTCATGTTAACAGAGTAGCTGTATATAATCAAAGTAAAATATTTATAAAAAATCATGTGATTGTTTACAAATGAAGTATGAACACACATTGCTTTGCATTTTATTAACACAAACAAGCCTTAATAAGACACTTTGGACCACCCCTTTAAATTGTATTCTATGCATTGAGATTTTTGTGTGTTTTTATTATTTAGTCAAGTAATTCAATTACTTATTGTTTACCCAAATATGCTTGTTTACATGAAATAAGAACAGTAATGTTTTTTCTTTTTCTCCCATTAGCCAGCGAGATGGCAAATTATG[G/A]TATGTAAATGCAATATATATCAATCTCATTACTTATTACTTACCTGTGCTTTCACACTAGCACTTTTGGTCCACACCTGGGTTCGTTTGACGTCAGAGTATGGTACGTTTAGCTAGTGTGAATGCTGCCTTCTGAACTCGGGTGCGCACCTAAGTCTGCCTGAAAGAGGTGGCCTGGAGTACGGTTCGCTCGAACTCTGGTGCAGTTCACATCTGGTATGAATGCAATCGTACCAAATAACGGAAGTGATCCGCTAACAGTACAACAAACTTTAGTTTTCATAACGTTCATTCATGCGTGTGTGTCTGTGTATCATCTACCTTGGTGACAAGCGGGACTGACCCAGTGCAAACAGTAATAATGTCTGCTTGTCTCCACCAGAAAAAAACTTCTGCAGACTTAATGTTCTGATTTTTTAATATTTTTTGCTGCAGATAGATGCAAGTTGCTCCCTATATTTTGCTTTTGATAACAAAGGCAACATTTTCTGTAAAAGCAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14938
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 |
---|---|---|---|---|---|
ENSDART00000014979 | Nonsense | 321 | 1251 | 8 | 28 |
ENSDART00000103418 | Nonsense | 328 | 538 | 8 | 15 |
Genomic Location (Zv9):
Chromosome 11 (position 7520109)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 7364212 |
GRCz11 | 11 | 7374051 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCCAACAGATTTTAGATTTAATCAAGCGCCTCGCACAGGCTAATWTATA[T/A]CATGTGGACAGTGARACCAGCACAGAAATTCTGGACCTAATTCAGTTGAT
Long Flanking Sequence:
AGCGTTGTTTCCACTGTGAAACACACCTACACAGTGAAGTCCACAGCAGACGGTGGTCAGATTACTAAAGCATTTGCTCAGGAGCGCCAATATTTCTCTCCGTTCAATGTAAAGGGAGGAAACTTCCGAATGTTGGCATTGTAAGTGCTTCTAACTGTTATCAACTTTCAAGTGGTTGCACTCCTGATTAATCAATGATGTTGTGCTTCCTTTTACCAGGCGGGACATTGAACTTCTTAAAGTTTCAGACACAACTGACAAAGTAGTGACTGGACAGGTGCAGAGCAGAGGCAACCTGATGTATAAGACAAATAAGGACCTCAAACCAATACCTGTTGTGATGCTTAACCTGAACGACCCAGTGCCCAAGGCAAACTTCAAAGATTATATAAACATTTAAGCATATACAGACATGAGAATTAACTCATTAATCGTTTAAATCATACTTTACTCCAACAGATTTTAGATTTAATCAAGCGCCTCGCACAGGCTAATATATA[T/A]CATGTGGACAGTGAAACCAGCACAGAAATTCTGGACCTAATTCAGTTGATGCGGGTAACAACACTTGATAATCTAGAGCATTTATGGAAGCAGGTCTCAGGAAATGATGAGCACAGGTATGTTCACCCTTCTCTAAATACTATACAATCTAATATTCAAGATGATCAATTTCCCCTGTTGACTTTCTTTTTTTTTTGGTCAGGCGGTGGTTCTTGGACTTGGTTGTGGAGGTAACAGATGAAAGAATTCTCAAATTCCTTGAGGCCAGATACAAAGCAGGAGACATCACAGCGAATGAGGCAGGACAAGCACTGGTAGTGGCATTTAACCACTTGTCCGCTGAGCCTGTGTCGGTGGCATTAGCTCAGGTGAGACAGTGACCAAGTTAAATGTATGTTAGAATCCTTTTTTATCTGCCGTCTGATACGCTCTTCCGCTCTCCAGGAGTTCCTGACCATTCCTTTCAGTAAATCCCATCCTCTCCTGTGGAACACTGTAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21846
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 |
---|---|---|---|---|---|
ENSDART00000014979 | Nonsense | 601 | 1251 | 12 | 28 |
ENSDART00000103418 | None | None | 538 | None | 15 |
Genomic Location (Zv9):
Chromosome 11 (position 7516366)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 7360469 |
GRCz11 | 11 | 7370308 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCCTACTCTCTGCTCAAAGGCTTTGCCAAGTCCCGTACCCCTGATAAT[C/T]AACATCTGTAAGCATGGTGCAAACTACAATGTGCTCTTCTCCTCTCTGTT
Long Flanking Sequence:
TTGTAGAACATTGTTGACCAATGTGGACCTGTTACTGTAGGTACTTTTTGAAAAGTTGCTTCCTGCGGGCTTTGTAACTTAATTTCTGAGAGTGTAATCATGGTTGGTTAATATGATAAAATTGCCATTTACATTTGGAACATTTCCACAAATTTTCACCATGACTGTTGCTAACAGGAGTAATTTAAGGATCAAGAAGCTACTTTTCCACTAGCAAAGACCTCTTTCTTCAGACGCTGACCATAACTCTATATCTACTCTAACTCTGTATCTATCTTTTATATTTGCAGGTACAGGATATTGTCTTAAACCTCTTCGTACAGAAACATTTACCAGCTGAAATCCGCATGCTGGCCTGCATAGTTCTTCTAGAGACCAAGCCGTCCACAGCTCTGATTTCAGTAGTAAGTGAGGTCCTTCTAGAAGAGGCTGATCTGCAGGTTGCCAGTTTCTCCTACTCTCTGCTCAAAGGCTTTGCCAAGTCCCGTACCCCTGATAAT[C/T]AACATCTGTAAGCATGGTGCAAACTACAATGTGCTCTTCTCCTCTCTGTTTATGAATTGCACTGATTTCTCTTTCCTTCTCCTAAATAGATCTATTGCCTGTAATATTGCCATGAAGATTCTAACCCGTAAACTTGGCCACTTGAGTTACCGCTACAGCAAGAACCTGCACTTTGACTGGTTCCATGGTGGGTTCTTGTTAAAAAGACAATGCTAGCTATGTTATAAAGCCTTTAAGTAAACCGGGAATGGTCTGATGTTGCTTCTTATTTCTTCAGATGACTTTTTATTTGGGACATCTGCTGATGTTTATATGCTTCAGAATGAAAGTCCCATCCCCACAAAACTTATGCTTAAGGGAAAATTTCATTTCATTGGGAGAATACTGCAATTTCTTGAGGTAAACAAATCAAAGCAGAATTTACTGTAATTTTATGTATACCCTGTTTTATAAATAATGTCATTTATATTTCCAGTTTGGTATCCGTGCAGATGGACTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44735
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 |
---|---|---|---|---|---|
ENSDART00000014979 | Essential Splice Site | 710 | 1251 | 15 | 28 |
ENSDART00000103418 | None | None | 538 | None | 15 |
Genomic Location (Zv9):
Chromosome 11 (position 7515788)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 7359891 |
GRCz11 | 11 | 7369730 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTCACGAAAGATTTAGGAATCAGCGATTTGGCTTCCATATTGAAAATT[G/A]TGAGCATCTCTGTTTCAGATTTTATTTATGTTTCTTGTCAATCATTATTT
Long Flanking Sequence:
TCTCCTAAATAGATCTATTGCCTGTAATATTGCCATGAAGATTCTAACCCGTAAACTTGGCCACTTGAGTTACCGCTACAGCAAGAACCTGCACTTTGACTGGTTCCATGGTGGGTTCTTGTTAAAAAGACAATGCTAGCTATGTTATAAAGCCTTTAAGTAAACCGGGAATGGTCTGATGTTGCTTCTTATTTCTTCAGATGACTTTTTATTTGGGACATCTGCTGATGTTTATATGCTTCAGAATGAAAGTCCCATCCCCACAAAACTTATGCTTAAGGGAAAATTTCATTTCATTGGGAGAATACTGCAATTTCTTGAGGTAAACAAATCAAAGCAGAATTTACTGTAATTTTATGTATACCCTGTTTTATAAATAATGTCATTTATATTTCCAGTTTGGTATCCGTGCAGATGGACTCAAAGATCTGTTTGCTGGAAAAATCCCAGAACTCACGAAAGATTTAGGAATCAGCGATTTGGCTTCCATATTGAAAATT[G/A]TGAGCATCTCTGTTTCAGATTTTATTTATGTTTCTTGTCAATCATTATTTTAATTTCTGATCTATGCCAATCTTTTAAAGCTCTCTAACTGGCAGAGCCTACCAAAAGACAAGCCTCTTTTGACAGCTTATGCAAGAGTTTTTGGACAGGAAGCCTTTTTAATGGATGTAAGCAGAGACTCAGTTCAAAGCATCATAAAGGTATTTCATTGTGTTATTTTAACAAGATAAAAAAAAATATTGGATTGATTTTTTTGTTTTTGTAGATTAAAATAAACCTTTTCCATTGTTTTCTGCTGTTTAGTCTTTCAGTCCTTCTGCAGGAAAGGAGAGTAAAGTTTGGGAAAGGATTCAAGATGTTCAGAAAGGGACTTCATGGCACTGGACTAAGCCGCATCTTGTGTATGAGGCTCGGTTCATACAGCCGACATGTCTGGGTCTCCCAGTTGAAATCAGCAAATATTATTCCGTAGTAAATGCTGTTACAATGAAAGGTGATGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35022
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014979 | Essential Splice Site | 1039 | 1251 | 23 | 28 |
ENSDART00000103418 | None | None | 538 | None | 15 |
Genomic Location (Zv9):
Chromosome 11 (position 7508979)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 7353082 |
GRCz11 | 11 | 7362921 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGTAAAGTGTTACCCATTTTGTTATGTTTTATGTCTCCTTCTTTGTAT[A/T]GGAGACAAGAGATGAGAACACCTCCTGTGAGGAACGCAAAACATCCAGTT
Long Flanking Sequence:
AGCCTCAGGTAGAATAAGACCAGAGGAGCCAGCCAGGAGAGATATGGGAGAGAGAGGGGAAAAAAGTGCAACCGCCTTCGCCGAGAGCCAAGGAAGAAAATCTTTAAACAATTCTTAACTACTCATGTCCTCTTTATGCATGTCCTTCTAGTGCGTTTACAATGAATGACAATAGAAAAGTGTCAAAATCAACAGTTTACACACAGGAGTTTATGAGTAGTTAATCATAATCTGCCCCTCCAAGTAAAGTCACGACATAATTGTACATTAACAGCTCATGCGTTTATGTTGGTTACATTTAGCTTAAACTTAGTTGTTAATTAATACATTATTTAATAACACAACATGTTTTAACAAGTCATTAAGGTAGCCAATCATACATGAACTCTTGTGACTCATGTTGTAATTAAAGTTAATTAATGATTAGTGCATCATTATTCATGTACTGTGATTGTAAAGTGTTACCCATTTTGTTATGTTTTATGTCTCCTTCTTTGTAT[A/T]GGAGACAAGAGATGAGAACACCTCCTGTGAGGAACGCAAAACATCCAGTTCACTCCCAGTAACTCAGGTGACACTCAAATATTTGAAATTGAAATCTAAAGTATATATTTTTTTATTATTTAAGGTATAAACTTTTCAATCTCTCTGTGATGTAGGATCTAGATGTCACTCCAGACCCGGTAGTCACAGTAAAAGCACTTAGTTTAAGTCCACAAGCAAAACCCCTTGGCTATGAAGGCGTAGCCTTTTATCTGCCAACTGCCCAAAAAGACGACATTGAAATGATCGTCTCTGAAGTTGGTGAAGAAGCAAACTGGAAAATGTGTGCCAATGCACATTTTGATAAGACTCATACATCAGCAAAGGTAAATGTTTTAAAGTTTTCTTATTCTCATAAATTTCCATATTGCCCCATTGATTTTTGTTTTATTAGTCTCTACATATTAAACTTTAGTGTGAGCCAAAGTCTAGGTGGTAGGCCGGATTGAACGTTAGGCCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9585
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 |
---|---|---|---|---|---|
ENSDART00000014979 | Nonsense | 1139 | 1251 | 25 | 28 |
ENSDART00000103418 | None | None | 538 | None | 15 |
Genomic Location (Zv9):
Chromosome 11 (position 7507899)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 7352002 |
GRCz11 | 11 | 7361841 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTAGTTGATTTTTGTCTTTTCAGGCTCATCTCAGATGGGGTGCAGAGTG[T/A]CAAACATATGAKGTTTCTATGAGAGTGTCCGCAGCGTGCCAACCAGAGTC
Long Flanking Sequence:
ACTCATAGACATTATAAAGTTTCTAGATTGATATCTTTTTCCTGCACTGTCGAAGAGACATTATAGGGTTGATTTCTATCATTCATATCGGCAAGATGCTTTAATGAATCATCACTCTAAGCTGTCAATCAACTCTATACAACAAAACTTACCTAGCAACCATTTAACAACAGCGATTTCTCAGCATTAGAACATTGTAGGGACCTGTGGATGGGCTCATTTGACTCATGCTAGCCAATGCACTTCCTGTATGCTACACATGCAAGCAGAGATTGTTTACATGATAATATTGATTAGCTAAGTGCTATAACATACTAGAAAAAGTATTAAGATTCGGTCTAACACATAAATGAGGGCTAACAACTGCCAGGCAACCACCTAACAACGCCTTAGCACTAACACTGTTGGCTTTCTCAAGCCAGTACCAAAGTTTGTCAATGAACTTTAGCTTCTAGTTGATTTTTGTCTTTTCAGGCTCATCTCAGATGGGGTGCAGAGTG[T/A]CAAACATATGATGTTTCTATGAGAGTGTCCGCAGCGTGCCAACCAGAGTCCAAACCATCTATAAGCACAAAGATTAACTGGGGGACTCTGCCCTCAGTATTCACAACAGTTGGTCAAATGTAAATTCATTATCAATTTGAATTTTTTGAAATATCAAAGTACAGCTAGGAATATTATTCATTATACCGACTTTCTACTGAATCCTTTTTTCTCAGAGTTCAAGAGTATGTACCTGGCGTGTCTTACATTATGGGTTTCTACCAGAAAAAGGAGGAAAACCCAGAACGGCAGGCATCTGTCATCGTTGTAGCATCCTCACCAGAGACCTTTGACCTGAAAGTGAAAATTCCAGAGGTTATTGTCAAATTATCACATGCTGTTATATATTTTTCAATTTTAATCTTCTAAAAGGAAAATTCTTCCTTTTTTAAAAATATTGGCTCATATTACAACTTTCCTAGAGTTAAACAGTTCAGTGTTTTATTTTTGAAGCCATTAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31815
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014979 | Essential Splice Site | None | 1251 | 27 | 28 |
ENSDART00000103418 | Essential Splice Site | None | 538 | 14 | 15 |
Genomic Location (Zv9):
Chromosome 11 (position 7506032)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 7350135 |
GRCz11 | 11 | 7359974 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAACTTTTGGGGATCGAAGCTGCAAATCTCACCATGTCAACTTAACAGG[T/C]TAATTTATGAACTATGGGTTACAAAACTGGTTGTTCCTGTGTACCGACAT
Long Flanking Sequence:
TTACTAGCTGGCCTCTAATAACCTCACCCCTCTAAACCTCACTTCCATTTGGGCCGCGGCACCAATGTAATCTCTTACACCACCCAACCCGCTCCGAGCTGGGATTGAACTGGAGACTCTCCGCATGCAAGTCAGTTGCTCTAACAAGGAGGCTAAAGACCAAGGCCTCTAGCTTCTGTCGCTAGAGAAATTGTTTAGGGTTCAGAAGAGTGAGGATTACCAGCACTGGACTTTACTTTCTGGCATCTGTTACACTTTTGGTCCAATCTGATTCAGTGATTTATGTTAAGCTAAGCTAAAAGTGTTCTTTCCAGACCCAGAGACTGGCTGAATGAATTAAAAAATGGTCAATCCAATAATGAGTTCCTGAATATGTTAGCTGAAACATTAACATTACTTTATACGTCCTTTCTAGCGAACTATCTACAAAAAGAAAATTCCCTCACCAATTGAACTTTTGGGGATCGAAGCTGCAAATCTCACCATGTCAACTTAACAGG[T/C]TAATTTATGAACTATGGGTTACAAAACTGGTTGTTCCTGTGTACCGACATAAATTCAATGTTACTCTTTGTCCCTTACAGGCTGATGTCATAGAACATTTCTGGAGGACTAAACTGACAACGTGAAATGAATGAATCATCAAATGTTGTGAATTGTTTGTACATTCCGGACATTTGATTAATTATTGATTTGGATACTAAATATGTGCTTAAAAGCAACATATGTTAAGTACTCCAACAAATAAAACATGCATGAAGAGATCATCTGTGGGATTAATTTATTTTATGATAGTTCATCATAATCCAGCCTAGATAGATTTACTTGTAGAGTCTCAACAACATTAATCTTTATGTTCAGAATGTTAATGAGATGGCACAGACTAGCAACACCTGAAAAACAAATTATGAGTGTACAGCCTAGCTTCATGGGCTGCTTCCAGTGGAACCAATTGGAAATAAATATCTTTAGTTTTGTGAAATGTTGCTATGAAAGTTATTCAA
Associated Phenotype:
Not determined