Busch Lab

ZMP

vtg7

Ensembl ID:
ENSDARG00000092419
ZFIN ID:
ZDB-GENE-001201-6
Description:
vitellogenin 7 [Source:RefSeq peptide;Acc:NP_001096141]

Alleles

There are 7 alleles of this gene:

Allele Name Consequence Status Availability
sa37524 Nonsense Mutation detected in F1 DNA Not yet available
sa29795 Nonsense Mutation detected in F1 DNA Not yet available
sa24183 Nonsense Available for shipment Available now
sa39376 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa9666 Nonsense Available for shipment Available now
sa24182 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa37524
Status:
Mutation detected in F1 DNA
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
ENSDART00000078216 Nonsense 49 1358 3 28
ENSDART00000137998 None None 213 None 7
ENSDART00000138378 Nonsense 49 1343 3 27

The following transcripts of ENSDARG00000092419 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 22 (position 25330101)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 24830007
GRCz11 22 24857631
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAAGTATGAGGCTCTGCTCCTGGGTGGTCTTCCTCAAGAAGGTCTGGCC[A/T]GAGCAGGTATCAAAGTCAGCAGCAAGGTTCTCCTCAGTGCCATGACAGAG
Long Flanking Sequence:
CACATCAGTTAAAAATTCACTTACAAAGTGACACTCGTGTCAGCAAGAAATCACTATAAAAGGTCTGATGCTTTGAAGAGTTCTTCACAAACCACCAGCCATGAGAGCTGTTGTGCTTGCCCTGACTGTAGCCCTCGTGGGTAAGTTCAATTTTTCTAAATTCTACATTTTTATAAATTTTCCTAAAATATTTCTCATGGTAAAGTAATATTAAAACCTCTTAAAACAACATTAAACACTTCTAAACCTCATCTTAAAGTGATTTTAAAGGGGTATTCTTTTGTTTCTTTTAGCGAGTCAACAGATGAACCTTGGTAAGTAAAACAATTTGGTTATTTTGAAAATAGTACATATTACAAAATTGTACAAATGTACATCTATTGAGTTGTTTCTGACAAAATGAAAAACTCATTCCAGTTCCCGAGTTTGCCCATGATAAGACCTATGTGTACAAGTATGAGGCTCTGCTCCTGGGTGGTCTTCCTCAAGAAGGTCTGGCC[A/T]GAGCAGGTATCAAAGTCAGCAGCAAGGTTCTCCTCAGTGCCATGACAGAGAACACCTACCTGATGAAGGTAATGACTTTTATAAACTGAGGAAACTGTAGGTCTTCAAAATTGAAAGAAAAAAAAATAGGTGTTTAAAAGCATTGGCTGTTATAAGCAATGATATATTCCACTACAGCTTATGGATCCTCTACTCTACGAGTATGCTGGCACTTGGCCCAAGGATCCATTTGTTCCTGCTACTAAGCTCACCTCAGCACTGGCTGCTCAGCTTCAGATCCCCATCAAGTTTGAGTATGCTAATGGTGTGGTTGGCAAGGTTTTCGCCCCAGCAGGAGTCTCTCCTACAGTCATGAACTTGTACAGAGGTATCCTCAACATCCTTCAGCTCAACCTCAAGAAGACCCAGAACATCTACGAGCTGCAAGAGGTGAACTAAATCTCCTTAGAACATTTATGAAGTATTTTGAGTTCTACAATCTTATCATTTGACTTATTCCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa29795
Status:
Mutation detected in F1 DNA
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
ENSDART00000078216 Nonsense 245 1358 6 28
ENSDART00000137998 Nonsense 41 213 4 7
ENSDART00000138378 Nonsense 245 1343 6 27

The following transcripts of ENSDARG00000092419 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 22 (position 25329235)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 24829141
GRCz11 22 24856765
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAATGGTGCACTGATCGCTGAGGCAACAGTTGAGGAAGTGTATCAGTTCT[C/A]ACCCTTCAATGAGATCCATGGTGCTGCAATGATGGAAGCAAAGTATGATT
Long Flanking Sequence:
AGGTATCCTCAACATCCTTCAGCTCAACCTCAAGAAGACCCAGAACATCTACGAGCTGCAAGAGGTGAACTAAATCTCCTTAGAACATTTATGAAGTATTTTGAGTTCTACAATCTTATCATTTGACTTATTCCTCAAGGCTGGAGCTCAGGGAGTGTGCAGGACCCACTATGTCATCAATGAGGATCCAAAAACCAACCACATTATTGTCACCAAGTCTAAAGATTTGAGCCACTGCCAGGAGAGAATCATGAAGGATGTTGGCTTGGCATACACTGAGAGTTGTCCTGAATGCACAGAGGTAGTGAAGACTGGATAGAAGTCACTTGATAGAATTCAGAAATTTACCTACTTTAAATGTCAAGACTCAAATAACGTACCTTTCTCTCAACAGAGGGTCAAGAGTCTGATTGAAACTGCAACTTATAACTACATCATGAAACCAGCTGACAATGGTGCACTGATCGCTGAGGCAACAGTTGAGGAAGTGTATCAGTTCT[C/A]ACCCTTCAATGAGATCCATGGTGCTGCAATGATGGAAGCAAAGTATGATTGACCTACTATTGAGATCTCATTCAAAACTGCAAAGTAACAATATTATAGACACATTTCATTAACTAGAACTTTAAGTCAAAGTTTCTGAAATAATAATTTGTTTCAGACAAACCTTGGCTTTTGTTGAGATTGAGAAGACCCCTGTCGTTCCAATTAAAGCTGATTACATGCCTCGTGGATCCTTGCAGTATGAGTTTGCAACTGAGATTCTTCAGACCCCCATTCAACTTATGAAGATCAGTGATGCAACAGCTCAGGTATAATTTATTCTATAAAACCTTAAATTTCTGAGTCAAATCATTTGATACATGGAAAACAGACACCTGAACATTTCCCTTAATCTTCCTAGATTGTTGAGGTCCTGACGCACTTGGTTGCAAACAATAAAGACATGGTTCATGATGATGCTCCCCTTAAGTTTGTTCAGCTCGTCCAGCTCTTGCGTCTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa24183
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000078216 Nonsense 783 1358 17 28
ENSDART00000137998 None None 213 None 7
ENSDART00000138378 Nonsense 783 1343 17 27

The following transcripts of ENSDARG00000092419 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 22 (position 25326512)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 24826418
GRCz11 22 24854042
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCTCTTAAAGCTTTGCAGGAAGGAGTTGCCTTCCAGTATGCCAAACCTT[T/A]GCTTGCAGCTGAAGTGCGTCGTATCTTGCCAACTGCAGTTGGTGTGCCCA
Long Flanking Sequence:
TGTGAGAACTGGAGGAATCCATGAGGCCCTTCTAAAATCTTCTGCTGCAGATGAAAGTGTTGACCGTATCACAAAGATTAAGCGTACACTGAAGGCAGTAAGTGTTCATGTCTGTCATATCACATCATTTTACACTTTTATAATAAACATGAAATAGGCTAAATATATATGACTTCTGTCTCTTCCAGCTTGCAAACTGGAAGGCCTTGCCAACCGATAGACCCCTTGCTTCAGCCTATGTCAAAGTATTTGGACAAGAAGTGGCTTATGTCAACTTTGACAAAACCATCATTGAAGAAGCCATACCGGTATTGTAGTGTAGTAACTATATGCTTGATATTGACAATCTTGAACTTTGATTTCTTTTGGTGCCTACAATTAGAATTAAGCTTCTAATAAAAACTATCCTCAGATGGTTTCTGGACCCAAACCACGTGCACTGCTGAAGGAGGCTCTTAAAGCTTTGCAGGAAGGAGTTGCCTTCCAGTATGCCAAACCTT[T/A]GCTTGCAGCTGAAGTGCGTCGTATCTTGCCAACTGCAGTTGGTGTGCCCATGGAGTTCAGTTTGTACACTGCTGCTGTTGCTGCTGCATCTGTCAATGGTAAATTTTTGCCTCAGAATTTCTATATCCTTTATTCAGATATGGGGGGGGGGGTCACTTCCTAGGTTTGATGTTGTTCTGTTGACCTTTTAAGTTCAGGCCACTATTACACCTCCTCTCCCTGAGAAATTGGAGTCCATGACTCTTGATCAACTGAAGAGGACTGATGTTCAGTTCCAAGCTGAAGCTAGACCAAGGTACAGTTTTGCAGCTACATCCACTCAGATGTGACTTAATGTACACAACAACACTTTTAAAACAATCTTTCTTATTTTTTATTTCAGTGTTGCTCTCCAGACATTTGCTGTGATGGGAGTTAACACTGCCTTCATACAAGCTGCTGTTATGGCGAGAGGAAAGATCCGTACAATTGCCCCTGGAAAAGTGGCAGCAAGAGCAGAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39376
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000078216 Essential Splice Site 816 1358 17 28
ENSDART00000137998 None None 213 None 7
ENSDART00000138378 Essential Splice Site 816 1343 17 27

The following transcripts of ENSDARG00000092419 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 22 (position 25326412)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 24826318
GRCz11 22 24853942
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGAGTTCAGTTTGTACACTGCTGCTGTTGCTGCTGCATCTGTCAATGG[T/C]AAATTTTTGCCTCAGAATTTCTATATCCTTTATTCAGATATGGGGGGGGG
Long Flanking Sequence:
AGTGTTCATGTCTGTCATATCACATCATTTTACACTTTTATAATAAACATGAAATAGGCTAAATATATATGACTTCTGTCTCTTCCAGCTTGCAAACTGGAAGGCCTTGCCAACCGATAGACCCCTTGCTTCAGCCTATGTCAAAGTATTTGGACAAGAAGTGGCTTATGTCAACTTTGACAAAACCATCATTGAAGAAGCCATACCGGTATTGTAGTGTAGTAACTATATGCTTGATATTGACAATCTTGAACTTTGATTTCTTTTGGTGCCTACAATTAGAATTAAGCTTCTAATAAAAACTATCCTCAGATGGTTTCTGGACCCAAACCACGTGCACTGCTGAAGGAGGCTCTTAAAGCTTTGCAGGAAGGAGTTGCCTTCCAGTATGCCAAACCTTTGCTTGCAGCTGAAGTGCGTCGTATCTTGCCAACTGCAGTTGGTGTGCCCATGGAGTTCAGTTTGTACACTGCTGCTGTTGCTGCTGCATCTGTCAATGG[T/C]AAATTTTTGCCTCAGAATTTCTATATCCTTTATTCAGATATGGGGGGGGGGGTCACTTCCTAGGTTTGATGTTGTTCTGTTGACCTTTTAAGTTCAGGCCACTATTACACCTCCTCTCCCTGAGAAATTGGAGTCCATGACTCTTGATCAACTGAAGAGGACTGATGTTCAGTTCCAAGCTGAAGCTAGACCAAGGTACAGTTTTGCAGCTACATCCACTCAGATGTGACTTAATGTACACAACAACACTTTTAAAACAATCTTTCTTATTTTTTATTTCAGTGTTGCTCTCCAGACATTTGCTGTGATGGGAGTTAACACTGCCTTCATACAAGCTGCTGTTATGGCGAGAGGAAAGATCCGTACAATTGCCCCTGGAAAAGTGGCAGCAAGAGCAGACATTCTCAAGGGCAACTACAAGGTGGAGACTCTGCCTGTTGAACTTCCTGAACACATTGCTTCAGCAAGGTAATGACATTTCTGTACACATTTTGTTATGA
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa29794
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000078216 Essential Splice Site 816 1358 18 28
ENSDART00000137998 None None 213 None 7
ENSDART00000138378 Essential Splice Site 816 1343 18 27

The following transcripts of ENSDARG00000092419 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 22 (position 25326320)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 24826226
GRCz11 22 24853850
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGGGGGGGGGTCACTTCCTAGGTTTGATGTTGTTCTGTTGACCTTTTAA[G/T]TTCAGGCCACTATTACACCTCCTCTCCCTGAGAAATTGGAGTCCATGACT
Long Flanking Sequence:
CAAACTGGAAGGCCTTGCCAACCGATAGACCCCTTGCTTCAGCCTATGTCAAAGTATTTGGACAAGAAGTGGCTTATGTCAACTTTGACAAAACCATCATTGAAGAAGCCATACCGGTATTGTAGTGTAGTAACTATATGCTTGATATTGACAATCTTGAACTTTGATTTCTTTTGGTGCCTACAATTAGAATTAAGCTTCTAATAAAAACTATCCTCAGATGGTTTCTGGACCCAAACCACGTGCACTGCTGAAGGAGGCTCTTAAAGCTTTGCAGGAAGGAGTTGCCTTCCAGTATGCCAAACCTTTGCTTGCAGCTGAAGTGCGTCGTATCTTGCCAACTGCAGTTGGTGTGCCCATGGAGTTCAGTTTGTACACTGCTGCTGTTGCTGCTGCATCTGTCAATGGTAAATTTTTGCCTCAGAATTTCTATATCCTTTATTCAGATATGGGGGGGGGGGTCACTTCCTAGGTTTGATGTTGTTCTGTTGACCTTTTAA[G/T]TTCAGGCCACTATTACACCTCCTCTCCCTGAGAAATTGGAGTCCATGACTCTTGATCAACTGAAGAGGACTGATGTTCAGTTCCAAGCTGAAGCTAGACCAAGGTACAGTTTTGCAGCTACATCCACTCAGATGTGACTTAATGTACACAACAACACTTTTAAAACAATCTTTCTTATTTTTTATTTCAGTGTTGCTCTCCAGACATTTGCTGTGATGGGAGTTAACACTGCCTTCATACAAGCTGCTGTTATGGCGAGAGGAAAGATCCGTACAATTGCCCCTGGAAAAGTGGCAGCAAGAGCAGACATTCTCAAGGGCAACTACAAGGTGGAGACTCTGCCTGTTGAACTTCCTGAACACATTGCTTCAGCAAGGTAATGACATTTCTGTACACATTTTGTTATGAATACTGTTTTGTGAAATGCAATTAACTGTTCATGCTTCGACAGCTTTGAGACTCTTGCTGTGGTCAGAAACATTGAAGATCACAGTGCTGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9666
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000078216 Nonsense 903 1358 19 28
ENSDART00000137998 None None 213 None 7
ENSDART00000138378 Nonsense 903 1343 19 27

The following transcripts of ENSDARG00000092419 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 22 (position 25325972)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 24825878
GRCz11 22 24853502
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAAGAGCAGACATTCTCAAGGGCAACTACAAGGTGGAGACTCTGCCTGTT[G/T]AACTTCCTGAACACATTGCTTCAGCAAGGTAATGACATTTCTGTAMACAT
Long Flanking Sequence:
TGGTGTGCCCATGGAGTTCAGTTTGTACACTGCTGCTGTTGCTGCTGCATCTGTCAATGGTAAATTTTTGCCTCAGAATTTCTATATCCTTTATTCAGATATGGGGGGGGGGGTCACTTCCTAGGTTTGATGTTGTTCTGTTGACCTTTTAAGTTCAGGCCACTATTACACCTCCTCTCCCTGAGAAATTGGAGTCCATGACTCTTGATCAACTGAAGAGGACTGATGTTCAGTTCCAAGCTGAAGCTAGACCAAGGTACAGTTTTGCAGCTACATCCACTCAGATGTGACTTAATGTACACAACAACACTTTTAAAACAATCTTTCTTATTTTTTATTTCAGTGTTGCTCTCCAGACATTTGCTGTGATGGGAGTTAACACTGCCTTCATACAAGCTGCTGTTATGGCGAGAGGAAAGATCCGTACAATTGCCCCTGGAAAAGTGGCAGCAAGAGCAGACATTCTCAAGGGCAACTACAAGGTGGAGACTCTGCCTGTT[G/T]AACTTCCTGAACACATTGCTTCAGCAAGGTAATGACATTTCTGTACACATTTTGTTATGAATACTGTTTTGTGAAATGCAATTAACTGTTCATGCTTCGACAGCTTTGAGACTCTTGCTGTGGTCAGAAACATTGAAGATCACAGTGCTGAAAGGTCTATTCCCTTGGTACCTGAGTTGTCTCTGCAAAATTCTCAGACATCTTCTGCTGGTGATTTGGTAAGCTTTGAATGCACACATAGACAAATGAAACCATGCTATTATTAAAGCTTATACATAAAAATGTTCTTCTATTTCAGTCCACTGAGATGTCATCTGCTGCTTCAGTGAGAGCTTCTGCTCCATTTGACAGAACCCTTTGTTATTCCTGCCCATATATTCAAGTTAAAGGATGTGTTGAGGTGCACTCTTACAATGCTGCTTTTATCAGAAATTCTACTCTGTTCTACATAATTGGACAGCACTCAGCCCATGTTGCAGTGGCAAGAGGTGAGAAGATAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa24182
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000078216 Nonsense 1177 1358 25 28
ENSDART00000137998 None None 213 None 7
ENSDART00000138378 Nonsense 1162 1343 24 27

The following transcripts of ENSDARG00000092419 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 22 (position 25324600)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 24824506
GRCz11 22 24852130
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGATCTTCCACCTGTTTTTGCTATCATCGCCCGTGCTGTTAGAGATGAC[C/T]AGAAGCTTCTGGGCTACCAACTGGCTGCTTACTTTGACAAACCAACTGCA
Long Flanking Sequence:
AAACACTTAAAGTTCTGTATTATTCAAGTAGCCACAATAAATCTGAAAATTCATAACATTTATATATTTAAAGATTTAAAGTTGTGTTTTTTAAGTAGCAATGTGTAATAATTTCATAATTTAATTTGTTTATTTTTATATACATTTTCAGACTGCCACCATCATAGAGCCTTTCAAGAAATTCCACAAAGATCGGGTAAACATGAAAAACTTTTATTACTACTATAATTACCTAATTTATTGTTTAAAACTTACTAAATGTTTTGCTTGCAGTACTTGGCTCACCATAGTGCCACAAAGGATACTAGCAGTGGAAGTGCTGCAGCTAGCTTTGAGCAAATGCAGAAACAGGTTAGTCTCAGCTCTTTGCCCATGAAGCAAACCCAAATATGAAATATGCCCTATTTCATGTTTTATTTGTTTTATCCTTTCAGAATAGATTCCTTGGAAATGATCTTCCACCTGTTTTTGCTATCATCGCCCGTGCTGTTAGAGATGAC[C/T]AGAAGCTTCTGGGCTACCAACTGGCTGCTTACTTTGACAAACCAACTGCAAGAGTGCAACTGATAGCTTCCTCTATTGCTGAAAATGACAACAGGAAGATCTGTGCCGATGGTGCACTACTGAGCAAGCACAAAGTCACTGTAAGACTAGAAATTTGTCATTTTTGCCCTCAACATCAGTACCTTGTTATGAACTCAAATGTTTTTTTAGGGCAAGTTTTCTTGGGGTGCGGAGTGCAAACAGTATGCAGTCTTTGCTAAAGCTGAAGCTGGTGTCCTGGGTGAATTCCCTGCTGCACGTCTAGAAGTGGAATGGGAGAGACTGCCAATAATTGTCACCACCTATGCCAAAAAGTAATGATTATTAGCACTGAACAACAAATCTATAGTGTAGAACATGTACATGATTTGATCATTTGGTCTTCCCTGTTATTCACCTCCTAAATAGGCTGTGTAAGCACATCCTTAAGGCAGCATATGACACGGGATTCAGGTTTGAAA
Associated Phenotype:
Not determined