ZMP
vps52
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate vacuolar protein sorting 52 (Yeast) (VSP52) [Source:UniProtKB/Tr
Human Orthologue:
VPS52
Human Description:
vacuolar protein sorting 52 homolog (S. cerevisiae) [Source:HGNC Symbol;Acc:10518]
Mouse Orthologue:
Vps52
Mouse Description:
vacuolar protein sorting 52 (yeast) Gene [Source:MGI Symbol;Acc:MGI:1330304]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43253 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa4801 | Essential Splice Site | F2 line generated | Not yet available |
sa23494 | Nonsense | Available for shipment | Available now |
sa18372 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa43253
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 |
---|---|---|---|---|---|
ENSDART00000047190 | Nonsense | 288 | 724 | 9 | 20 |
The following transcripts of ENSDARG00000009175 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 18328709)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 19173944 |
GRCz11 | 19 | 18636797 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCAGTTCCTGTTAGCCAATGAGAGAACAGTTGCAAAAGAGATCCGGGAC[G/T]AGTATGTGGATACCATGAGCAAAATCTACTTAAGTTACTTCAAGTCATAT
Long Flanking Sequence:
TCCATGACCTACTCAAAATGGATTTGTGACCCATTTTAAGTCACAAAAAACCAATTGAGAAACACTTTAATAGGAATACAAGAATACAAAATTTAGGTTTGTGTTGCAGTTTTTTAATTTTTAATTTTGATCACAGGCTGTCACAAAGATCCGGGAGTTCATCCTACAGAAAATTTACTCTTTTAGAAAGCCAATGACCAACTACCAGATCCCCCAGAACACATTACTCAAGTACAGGTACAAAACACACTCCTTTAAACTAAACCAAACAAAGACTTTGGTTACATCAGAACAAGCAACAGGGGTTATTAGTAAAATTTGTCCTGGTGAATAGCAATTATTAACTCTATTAAATTAAATTCTTAAATAATTAATTTATAGATATTTTATCAATACAATATGTTACACCCCCCTAAATATGTCTGTTTCTGATCATTTATAGGTTTTTCTACCAGTTCCTGTTAGCCAATGAGAGAACAGTTGCAAAAGAGATCCGGGAC[G/T]AGTATGTGGATACCATGAGCAAAATCTACTTAAGTTACTTCAAGTCATATAGTGGCAGACTGCTGAAAGTCCAGGTGAAATTGGTTTAAGATAGCAAAAGGTTTTCAAAATCTAAAAAAATTGTAAATTTGAAGAAAAAAATGTCCATGGAAGTCATTTTGTACAGGTTTAAATCCCAGGACAATATCTGAATGCATAAATTATGTATTCAGAATTGTAACGGAGACACTTACCAAGTAACTAAGACACTTACAAAGTATCAACTCAGATCTTCATAAAATGAATAGAAACATATTTAGCATTAAATAATTAATTCTAATAATTAATAGTCAATTCTCTGCTAAAAACTATTTGCCTTGAAAGTGTCATGAATTTAAACACAAGGAGGCTACTGTGTGTATAAAATATGATATTGTGTAGTCTTATAATGTGCATGTATGATGAAGCTAATGTAATATGCAAGATTATAATATCAAGTGGCTGTACAATTTAAATAACTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa4801
Status:
F2 line generated
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000047190 | Essential Splice Site | 332 | 724 | 10 | 20 |
The following transcripts of ENSDARG00000009175 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 18330062)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 19175297 |
GRCz11 | 19 | 18638150 |
KASP Assay ID:
554-3570.1 (used for ordering genotyping assays)
KASP Sequence:
GTTGCAGACAAAGATGATCTGATGGGAGTGGAAGATACAGCCAAAAAAGA[T/G]ATCCTTAACTGATTGCTGCCTATTTAGACATAAATGGCAATAGTGACATA
Long Flanking Sequence:
AAACATTCTCTGTCAACTCAAGGTATTTGAATAGAGAATTGACATGGCAAATGATGTAATAAGTTAATATTATTTGCTTCTTGCAAGAGAGAGCTGGTGCAATGAAGTTTAAGATGTATCATTGTTAATAGTAAAATAAATTCAAATAAATTTACAATATAGGAATAAGTTTGACAAGGGAGCTGAATTGAAACATCTGACAATGTAAATTGAAGTATAATAAAGTATTTCTAAACCTCAGCTCGTTAGCTGAAGGGACACTTCTACAGGCACTTACCATCCCACACTCTTAAATCGATGCACTTACATACTCTACATCTTAAAATTAATACAAATATAAAAGTAAAGGCATGCTCAAGGCTCAATGATGTTGTTGTTTTTGTTGTTGTTGTTGTTTTTTCAATTAGTCCTGTTTGTTCCTTCTTTCTCTCTATTCGTCAGTATGAAGATGTTGCAGACAAAGATGATCTGATGGGAGTGGAAGATACAGCCAAAAAAGA[T/G]ATCCTTAACTGATTGCTGCCTATTTAGACATAAATGGCAATAGTGACATACATACACCAAACCTATTGCACCACTGTTTTGGTATCTTTTAACCAATGTCTTATCACAATCACATAGAATTAGCATGCCAAGTAAATTTCAAGTCTTTTTCTATATTCTATTACAACGTGGTTGATTTCTTTAACTGCTCGGCAGGTTTTTTCTCTAAGCCTTCTCTCAAAAGTAGAAACACCATTTTTACTCTCGGCCAAAGGGGGGCAATATTGAGCCCCGCAGAGCTGGAGGGGCCCATACTAATCCCACATGCTGCTCAAAGAGGAGACTCCAGAGTAAGTGATCTATTGCTGTACAAATCTTCCAGTTGCTGCCATGGAAAAGATGCATTTCATACTTTTAATTTCATGCTATTCTTTCTTAGTCAAAGATAGAAACCTGGTAGAAGATAAAACAAGATAAAAACATGCAACAGTTTTTTTTAAAGACCTAGTGGAATTCACCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23494
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 |
---|---|---|---|---|---|
ENSDART00000047190 | Nonsense | 379 | 724 | 12 | 20 |
The following transcripts of ENSDARG00000009175 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 18330813)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 19176048 |
GRCz11 | 19 | 18638901 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAACAGTATTTTGTCTCACTCATTTCTCTTTGTCTCTGTCAGTACCCCTA[T/A]GAAACTCTCTTCCGCAGTCAGCACTATGCTTTGCTGGATAATGGCTGTCG
Long Flanking Sequence:
AAGGGGGGCAATATTGAGCCCCGCAGAGCTGGAGGGGCCCATACTAATCCCACATGCTGCTCAAAGAGGAGACTCCAGAGTAAGTGATCTATTGCTGTACAAATCTTCCAGTTGCTGCCATGGAAAAGATGCATTTCATACTTTTAATTTCATGCTATTCTTTCTTAGTCAAAGATAGAAACCTGGTAGAAGATAAAACAAGATAAAAACATGCAACAGTTTTTTTTAAAGACCTAGTGGAATTCACCACAGTATAAATGTTGCCAGCATCAAGATAGTTGAAAGCATATACCCAAATTAATTTGCAATGCAATAGGCTTGACAGCAAATGTAATTCTGTTCCCATCTTTCCAAGCTGTTTTACAATACGTGTACCTAAAAGTAGCATTTTAAAGCCAAAATAGGGTTTATATAAATGTTCATTTAGTAAATGTGTCTGTTTGTGGCTCATAACAGTATTTTGTCTCACTCATTTCTCTTTGTCTCTGTCAGTACCCCTA[T/A]GAAACTCTCTTCCGCAGTCAGCACTATGCTTTGCTGGATAATGGCTGTCGAGAATTCCTGTTCTTGTCTGATTTTTTCATGGTGGCAGGGAATTCAGCACTGGACTTGTTCAACAGCATTATGGGAAAAACACTCAGCATTTTTTTGGTACATTTATTCTCTTACTACAATCTGTGTATTTAAAGGAATGTCACATTACTGAGTATTTGTTTTCTTTTTTTTTCTTTTTTTTAGCATTCTCTAATTTTATTAATAATAGTTTTTTTTCTACCTGTAGAAGAATCTGTCTACATACTTGTCAGACTGTTACGATAGTATTGCAGTATTTCTCTGCATTCACATCATTCTGCGCTTCAGAGCCATCGTAGCCAAGAGGAATATCCCTGCACTTGACAAGTCAGTCCCTGTCAGTACAAACACATTCTTATACCCCTTATTGGTAGTTTTTTTTTTTTTTGATCAAAAATACACCATCAACAATTACTAAAAAAACTTAAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18372
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 |
---|---|---|---|---|---|
ENSDART00000047190 | Nonsense | 396 | 724 | 12 | 20 |
The following transcripts of ENSDARG00000009175 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 18330862)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 19176097 |
GRCz11 | 19 | 18638950 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGAAACTCTCTTCCGCAGTCAGCACTATGCTTTGCTGGATAATGGCTGT[C/T]GAGAATTCCTGTTCTTGTCTGATWTTTTCATGGTGGCAGGGAATTCAGCA
Long Flanking Sequence:
CCACATGCTGCTCAAAGAGGAGACTCCAGAGTAAGTGATCTATTGCTGTACAAATCTTCCAGTTGCTGCCATGGAAAAGATGCATTTCATACTTTTAATTTCATGCTATTCTTTCTTAGTCAAAGATAGAAACCTGGTAGAAGATAAAACAAGATAAAAACATGCAACAGTTTTTTTTAAAGACCTAGTGGAATTCACCACAGTATAAATGTTGCCAGCATCAAGATAGTTGAAAGCATATACCCAAATTAATTTGCAATGCAATAGGCTTGACAGCAAATGTAATTCTGTTCCCATCTTTCCAAGCTGTTTTACAATACGTGTACCTAAAAGTAGCATTTTAAAGCCAAAATAGGGTTTATATAAATGTTCATTTAGTAAATGTGTCTGTTTGTGGCTCATAACAGTATTTTGTCTCACTCATTTCTCTTTGTCTCTGTCAGTACCCCTATGAAACTCTCTTCCGCAGTCAGCACTATGCTTTGCTGGATAATGGCTGT[C/T]GAGAATTCCTGTTCTTGTCTGATTTTTTCATGGTGGCAGGGAATTCAGCACTGGACTTGTTCAACAGCATTATGGGAAAAACACTCAGCATTTTTTTGGTACATTTATTCTCTTACTACAATCTGTGTATTTAAAGGAATGTCACATTACTGAGTATTTGTTTTCTTTTTTTTTCTTTTTTTTAGCATTCTCTAATTTTATTAATAATAGTTTTTTTTCTACCTGTAGAAGAATCTGTCTACATACTTGTCAGACTGTTACGATAGTATTGCAGTATTTCTCTGCATTCACATCATTCTGCGCTTCAGAGCCATCGTAGCCAAGAGGAATATCCCTGCACTTGACAAGTCAGTCCCTGTCAGTACAAACACATTCTTATACCCCTTATTGGTAGTTTTTTTTTTTTTTGATCAAAAATACACCATCAACAATTACTAAAAAAACTTAAAAGAATTGTTTTGCTCTCGAATGTGCTTCTGGCTTGTTACTTTTCAAATATT
Associated Phenotype:
Not determined