ZMP
vtg4
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC678536 [Source:RefSeq peptide;Acc:NP_001038759]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11872 | Essential Splice Site | Available for shipment | Available now |
sa16928 | Essential Splice Site | Available for shipment | Available now |
sa10877 | Nonsense | Available for shipment | Available now |
sa37523 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39374 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12457 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11872
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000105237 | Essential Splice Site | 156 | 1358 | 5 | 28 |
ENSDART00000109411 | None | None | 1135 | None | 23 |
ENSDART00000114647 | Essential Splice Site | 156 | 1362 | 5 | 28 |
ENSDART00000136837 | Essential Splice Site | 161 | 1363 | 5 | 28 |
The following transcripts of ENSDARG00000078429 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 25263073)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 24762979 |
GRCz11 | 22 | 24790603 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTGAGRTATTTTGAATTCTGCWATCTCAYCATTTGACTTGTTCTTGAA[G/A]GCTGGAGCTCAGGGAGTGTGCAGRACACACTATGTCATCAATGAGGATCC
Long Flanking Sequence:
TTCTCCTCAGTGCCGTGACTGAGAACACCTACCTGATGAAGGTAATGACTATTATGAAATGAGGAAATTGTAGGTGTTCCAAAATGAAGGAACACTTAAAAATAAAATGTTAATAAACTTAGTTATAAAAATGTTACTTAAGCAATGATATATTCCCTTACAGCTTATGGATCCTCTACTCTACGAGTATGCTGGCACTTGGCCCAAGGATTCATTTGTCCCTGCCACTAAGCTCACCTCAGCACTGGCTGCTCAGCTTCAGATCCCCATCAAGTTTGAGTACGCTAATGGTGTGGTTGGCAAGGTTTTCGCCCCAGCAGGAGTCTCTCCAACAGTCATGAACCTGCACAGAGGTATCCTCAACATCCTTCAGCTCAACCTCAAGAAGACCCAGAACATCTACGAGCTGCAAGAGGTAAAAAAAAAAAAAAAAAAAACAATTTAGGACATTTCTGAGGTATTTTGAATTCTGCTATCTCACCATTTGACTTGTTCTTGAA[G/A]GCTGGAGCTCAGGGAGTGTGCAGGACACACTATGTCATCAATGAGGATCCAAAAACCAACCACATTATTGTCACCAAGTCTAAGGATCTGAGCCATTGCCAGGAGAGAATCATGAAGGATGTTGGCTTGGCATACACTGAGAGGTGTGCTGAATGCACAAAGGTAATGAAAACTGGATAATGAACATTTGAAATAATTCAAATATCTATCCACTATACATGTCAAGAGTCAAATAACTTAACTTTCTCTCAACAGAGGGTCAAGAGTCTGATTGAAACGGCTACTTATAACTACATCATGAAACCAGCTGACAATGGTGCACTGATCGCTGAGGCAACAGTTGAGGAAGTGTATCAGTTCTCACCCTTCAATGAGATTCATGGTGCTGCAATGATGGAAGCAAAGTATGATTGAGTGATTATTGAGATCTCATTTTTTAAAGCAAAGTAACAACACTCTAGACACATTCAACTAGAAAATTAAGTCAAAGTTTCAGAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16928
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 |
---|---|---|---|---|---|
ENSDART00000105237 | Essential Splice Site | 259 | 1358 | 7 | 28 |
ENSDART00000109411 | Essential Splice Site | 36 | 1135 | 2 | 23 |
ENSDART00000114647 | Essential Splice Site | 259 | 1362 | 7 | 28 |
ENSDART00000136837 | Essential Splice Site | 264 | 1363 | 7 | 28 |
The following transcripts of ENSDARG00000078429 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 25262559)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 24762465 |
GRCz11 | 22 | 24790089 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACATTCAACTAGAAAATTAAGTCAAAGTTTMAGAAAYAATGATTTGTTTC[A/T]GACAAACCTTGGCTTTTGTTGAGATTGAGAAGACCCCTGTCGTTCCATTC
Long Flanking Sequence:
GAGTGTGCAGGACACACTATGTCATCAATGAGGATCCAAAAACCAACCACATTATTGTCACCAAGTCTAAGGATCTGAGCCATTGCCAGGAGAGAATCATGAAGGATGTTGGCTTGGCATACACTGAGAGGTGTGCTGAATGCACAAAGGTAATGAAAACTGGATAATGAACATTTGAAATAATTCAAATATCTATCCACTATACATGTCAAGAGTCAAATAACTTAACTTTCTCTCAACAGAGGGTCAAGAGTCTGATTGAAACGGCTACTTATAACTACATCATGAAACCAGCTGACAATGGTGCACTGATCGCTGAGGCAACAGTTGAGGAAGTGTATCAGTTCTCACCCTTCAATGAGATTCATGGTGCTGCAATGATGGAAGCAAAGTATGATTGAGTGATTATTGAGATCTCATTTTTTAAAGCAAAGTAACAACACTCTAGACACATTCAACTAGAAAATTAAGTCAAAGTTTCAGAAATAATGATTTGTTTC[A/T]GACAAACCTTGGCTTTTGTTGAGATTGAGAAGACCCCTGTCGTTCCATTCAAAGCTGATTACATGCATCGTGGATCCCTGCAGTACGAGTTTGCAACTGAGATTCTTCAGACCCCCATTCAACTCATGAAGATCAGTGATGCACCTGCCCAGGTATAATTCACAGCATAAAATGCTTAATTTCTTAGTTTATGCACTTGATATATGATCCTTTTTGTAATTTTCCTAGATTGTCGAGGTCCTGAAGCACTTGGTTGCAAACAATAAAGACATGGTCCATGATGATGCTCCACTTAAGTTTGTTCAACTCGTCCAGCTCTTGCGTGTTGCCACCTTGGAGAAAATTGAGGCTATCTGGTCTCAGTTCAAGGACAAACCAGTTTACAGGTATAATTTGTTTACAATAAATTAATACAGTTTGAGCACAATTTGTCATTGTGAATATGTTTTAAATAATAATTTCCTCAGGCGCTGGCTTCTGGATGCTCTTCCTGCTGTTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10877
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 |
---|---|---|---|---|---|
ENSDART00000105237 | Nonsense | 649 | 1358 | 14 | 28 |
ENSDART00000109411 | Nonsense | 426 | 1135 | 9 | 23 |
ENSDART00000114647 | Nonsense | 649 | 1362 | 14 | 28 |
ENSDART00000136837 | Nonsense | 654 | 1363 | 14 | 28 |
The following transcripts of ENSDARG00000078429 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 25260781)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 24760687 |
GRCz11 | 22 | 24788311 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCTTTGTCCATTAAGCKCCTCTWATGATTGGRGCTGCTGGTAGTGCCTA[T/A]ATGATCAATGATGCTGCCACCATCYTGCCCAGAGCTGTTGTAGCTAAAGC
Long Flanking Sequence:
TTGGACAGGGCTCTCCACCCAGAGGTTCGTATGGTTGCTTGTATTGTGCTGTTTGAGGCCGAGCCTTCAGTGGCTCTCATCTCCAGTCTTGCTGGAGCTTTGAGGACTGAGCCAAACATGCATGTTGCAAGCTTTGCCTATTCCCACATCAAGTCCTTGACCAGAATCACTGCTCCTGATATGGCATATGTGTAAGAAAAACAAATAATTTCTAATTTTGGCATCACACGAAATGAGCCCAAGCCTGATTTAATCATGTTTATTCATTTTCAGTGCTGGTGCAGCTAATGTTGCCATCAAGCTTATGAACTGCAAGCTGGACAGACTTAACTACCGTTACAGCAGAGCTTTTAAGATGGACTATTATTATAGTAAGACTTTCAATTTCTATGAGGAAATTAACATATGCATTAAAATTGTTCTGATATAAAACATTGCAAACTTATTCTTATCTTTGTCCATTAAGCTCCTCTAATGATTGGAGCTGCTGGTAGTGCCTA[T/A]ATGATCAATGATGCTGCCACCATCCTGCCCAGAGCTGTTGTAGCTAAAGCTCGTGCCTACCTGGCTGGAGCCGCTGCTGATGTTGTTGAGGTGAACCCTTTAAGATTTATTTTCCAGATATCAGAATCACTGTTTAAATCTGTTTAATACAGTTTCACTAAATTGCTCCTTTTAAACAGTTTGGTGTGAGAACTGGAGGAATCCATGAAGCTCTTCTAAAATCTCCTGCTGCAGATGAAAGTGTTGACCGTATCACAAAGATTAAGCGTACACTGAGAGCAGTAAGTTTTAAGCTCCAGTGTATCTTAATTTTACACTTTTACTATAAACTTGAACTAGGCAAAAAGTATACATGATTTCTCTCTCATCAAGCTCACAAACTGGAAGGCCTTGCCAACTGATAAACCACTTGCTTCAGCCTATGTTAAAGTATTTGGACAAGAAGTGGCTTATGTCAACTTTGACAAGACCATCATTGAAGAAGCCATACCGGTATAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37523
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000105237 | Nonsense | 1152 | 1358 | 24 | 28 |
ENSDART00000109411 | Nonsense | 929 | 1135 | 19 | 23 |
ENSDART00000114647 | None | None | 1362 | None | 28 |
ENSDART00000136837 | Nonsense | 1157 | 1363 | 24 | 28 |
The following transcripts of ENSDARG00000078429 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 25257590)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 24757496 |
GRCz11 | 22 | 24785120 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAGTGCCACAAAGGATACTAGCAGTGGAAGCGCTGCAGCTAGCTTTGAA[C/T]AAATGCAGAAAAAGGTTAGTCTTAGCTCTTTGTCTATGAAACAAAACCCA
Long Flanking Sequence:
CTGAAGGACAAGCTTTCTTGTTGAAACTGAGGGAAATCCTGGACACTGAAGCTAAAAATGCACCCGTCTCTTCAGAAAGCAGCAGCAGCAGCAGTCGCAACAGCCGCAGCACCAGTAGCAGCAGCACCAGCACTAGCAGCAGCGGCAGCAGCAGCAGCAGCAGCAGCTCAAGCTCATCCATGTCCAGCTCTCGCATGTCTAAGGTAAAGACATGGGAAGTATTGTATAAAGCAGCCAAAATCTGTCTTAAAAAAAAAACAATAATAATAAAATAAATTAATAAAAATTGTATGTATTTTTAGACTGCCACCATAATGGAGCCTTTTAGGAAATTCCACAAAGATCGGGTAACTGTTCAAAACTCTATTGTTACTATTGATACTTAATTTTTGGGTTTCTTCAAAACTCACTAAGTTTTTTTTTTTTTTTTCTGTCAGTACTTGGCACCCCATAGTGCCACAAAGGATACTAGCAGTGGAAGCGCTGCAGCTAGCTTTGAA[C/T]AAATGCAGAAAAAGGTTAGTCTTAGCTCTTTGTCTATGAAACAAAACCCAAATAATATGTATGCTCCATTTTATGTTATATTAATGTTTTTTTTTTTTTGCTTTTGCTTTCAGAATAGATTCCTTGGAAATGATATTCCACCTGTGTTTGCTATCATCGCCCGTGCTGTTAGAGCTGACCAGAAGCTTCTGGGCTACCAACTGGCTGCTTACTTTGACAAACCAACTGCAAGAGTGCAACTCATAGCTTCCTCCATTGCAGAAAACGACAACATGAAGATCTGTGCTGATGGTGCTCTGCTGAGCAAGCACAAAGTTACTGTAAGACTGGAACATATGGCAAAATGTATTTCTCTACTTCAGTACCATTCTTTGAACTCAAATGTGATTTCAGGCCAAGTTTTCTTGGGGTGCGGAGTGCAAACAGTATGCAGTCTTTGCTAAAGCTGAAGCTGGTGTCCTGGGTGAATACCCTGCTGCACGTCTAGAAGTGGAATGGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39374
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 |
---|---|---|---|---|---|
ENSDART00000105237 | None | None | 1358 | None | 28 |
ENSDART00000109411 | None | None | 1135 | None | 23 |
ENSDART00000114647 | Nonsense | 1073 | 1362 | 22 | 28 |
ENSDART00000136837 | None | None | 1363 | None | 28 |
The following transcripts of ENSDARG00000078429 do not overlap with this mutation:
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 25205482)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 24705388 |
GRCz11 | 22 | 24733012 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTGAGGGAAATCCTGGACACTGAAGCTAAAAATGCACCTGTTTCTTCT[G/T]AAAGCAGCAGCAGTCGTAACAGTCGCAGCAGCAGCAGCCGCAGCACCAGC
Long Flanking Sequence:
GACATTTGTTTCAAACTACAAAGTGTAAATATGTTTTTTTCTTCTTCTTTTCAGTCATCTGAGATGTCATCTGTTGCTTCAGTAAGAGCTCCTGCTCCATTTGACAGAACCCTCTGTTATGCTGTCCCATACATTGAAATCAAGGGATGTGTTGAGGTGCACTCTCACAATGCTGCTTTTATCAGAAATTCCACTCTTTTCTACATAATTGGACACCACTCAGTCCGTGCTGCAGTGGCAAGAGGTAAGACAACAACATTAATAAAACTTGTTTTTATTTTTTCAGATAAAACTTAAATAATTTGTTTGTTGTTCTGGCTGTAGCTGAAGGTCCTGCAGTTGAAAGACTGGAGTTTGAAGTTCAAGTTGGTCCTAGAGCTGCTGAGAGGCTTGTTAAGCAAATCAACATCATTGATGATGATACTCCAGAAGGACAGGCTTTCTTGTTGAAACTGAGGGAAATCCTGGACACTGAAGCTAAAAATGCACCTGTTTCTTCT[G/T]AAAGCAGCAGCAGTCGTAACAGTCGCAGCAGCAGCAGCCGCAGCACCAGCACTAGCACCAGCTCAAGCTCAAGCTCAAGTTCAAGTTCAAGTTCAAGCTCAAGCTCCTCTATGTCCAGCTCTCGTATGTCTAAGGTAAAAACACTTAAAGTTCTGTATTATTCAAGTAGCCAAAATGCATCTGAAAATTCTAAACATGGCACTGCAGTGGCGCAGTAGTTAGTGCTGTCGCCTCACAGCAAGAAGATTGCTGGATCACTGGTTTGAGCCTCGGCTGGGTTTCTGTGTGGGGTTTGCATGTTCTCCCTGCTTTCGCATGGATTTCCTCCGGGTGCTCCGGTTTTCCCCACAGTCCAAAGACATGCAGTACAGGTGAATTGGGTAGGCTAAATTGTCCGTAGTGTATGAATGTGTGTGAATGAGTGTGTGTGAATGTTTCCAAGAGATGGGTTGCGGCCGGAAAGGCATACGCTGTGTAAAAACGTGCTGGATAAGTTGGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12457
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 |
---|---|---|---|---|---|
ENSDART00000105237 | None | None | 1358 | None | 28 |
ENSDART00000109411 | None | None | 1135 | None | 23 |
ENSDART00000114647 | Nonsense | 1154 | 1362 | 24 | 28 |
ENSDART00000136837 | None | None | 1363 | None | 28 |
The following transcripts of ENSDARG00000078429 do not overlap with this mutation:
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 25204708)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 24704614 |
GRCz11 | 22 | 24732238 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATAGCGCCACAAAGGATACTAGCAGTGGAAGTGCTGSAGCTAGCTTTGAR[C/T]AAATGCAGAAACAGGTTAGTCTCAGCTATTTGCCCMTGAAGCAAACCCAA
Long Flanking Sequence:
CTGGGTTTCTGTGTGGGGTTTGCATGTTCTCCCTGCTTTCGCATGGATTTCCTCCGGGTGCTCCGGTTTTCCCCACAGTCCAAAGACATGCAGTACAGGTGAATTGGGTAGGCTAAATTGTCCGTAGTGTATGAATGTGTGTGAATGAGTGTGTGTGAATGTTTCCAAGAGATGGGTTGCGGCCGGAAAGGCATACGCTGTGTAAAAACGTGCTGGATAAGTTGGCAGTTCATTCCGCTGTGGCGACCCCGGATTAATAAAGGGATTAAGCTGAAAAGAAAATGAATGAATGAATTCTAAACATTTTTTTTCAGACTGCCACCATCATTGAGCCTTTCAGGAAATTCCACAAAGATCGGGTAACATTAATAAACCTATAATTATATTATAATTACTTTTTTTTCTTTTCCAAAACTTATAAAATGTTTTGCTTGCAGTACTTGGCACACCATAGCGCCACAAAGGATACTAGCAGTGGAAGTGCTGCAGCTAGCTTTGAA[C/T]AAATGCAGAAACAGGTTAGTCTCAGCTATTTGCCCCTGAAGCAAACCCAAATATGAAATATGCCAAACTTCATGTTTTACGTTTTATCCTTTCAGAATAGATTCCTTGGAAATGATATTCCACCTGTTTTTGCTATCATCGCCCGTGCTGTTAGAGCTGACCAGAAGCTTCTGGGCTACCAACTGGCTGCTTACTTTGACAAACCAACTGCAAGAGTGCAACTGATAGTTTCCTCCATTGCTGAAAACGACAACATGAAGATCTGTGCTGATGGTGCTCTGTTGAGCAAGCACAAAGTTACTGTAAGACATTTGGAAAAATTAATTTCTCAATTTCAGTACCTTTGGTATGCTTTGAACAAAAATGTTCTTTTCAGGGCAAGTTTTCTTGGGGTGCGGAGTGCAAACAGTATGCAGTCTTTGCTAAAGCTGAAGCTGGTGTCCTGGGTGAATTCCCTGCTGCACGTCTAGAAGTGGAATGGGAGAGACTGCCAATAATTG
Associated Phenotype:
Not determined