ZMP
vtg7
Ensembl ID:
ZFIN ID:
Description:
vitellogenin 7 [Source:RefSeq peptide;Acc:NP_001096141]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24183 | Nonsense | Available for shipment | Available now |
sa9666 | Nonsense | Available for shipment | Available now |
sa24182 | Nonsense | Available for shipment | Available now |
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.
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 |
---|---|---|---|---|---|
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:
sa9666
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 |
---|---|---|---|---|---|
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.
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 |
---|---|---|---|---|---|
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