ZMP
vps39
Ensembl ID:
ZFIN ID:
Description:
vam6/Vps39-like protein [Source:RefSeq peptide;Acc:NP_001107012]
Human Orthologue:
VPS39
Human Description:
vacuolar protein sorting 39 homolog (S. cerevisiae) [Source:HGNC Symbol;Acc:20593]
Mouse Orthologue:
Vps39
Mouse Description:
vacuolar protein sorting 39 (yeast) Gene [Source:MGI Symbol;Acc:MGI:2443189]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14550 | Nonsense | Available for shipment | Available now |
sa9171 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18429 | Nonsense | Available for shipment | Available now |
sa9687 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14550
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 |
---|---|---|---|---|---|
ENSDART00000113644 | Nonsense | 333 | 875 | 11 | 24 |
Genomic Location (Zv9):
Chromosome 17 (position 50614399)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 50005216 |
GRCz11 | 17 | 50084285 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCWCTTTTTGCAGAAAATGAAGGATGATTCCGATACAGACAAGAGGCAA[C/T]AGATCCATCACAWTCAGAACCTGTTTGCCTTCAACCTGTTCTGCCAGAAG
Long Flanking Sequence:
AATGAAATACCTACTTTACCACATCCAATCAGCTCGCAGGAGAAAAAAACTGGCCACGCCCACTGTCTTATTTCTTTTTCTCTAGGAACTGCGTCACAATACAAAAAAGTGGTTGCAGCTTCCGGTTCATGCAGACTTTAATGTTTAAAGCAATCTTGCACCCGGATGATGTTTAGCATCAGTGTTTTGTTGTAAGATGCACTGATTATCTTCCCCTCTCTAATTTCACAGGTCAAACGTTGTGTATGTCGCTAGCAATCATTTTGTCTGGCGTTTGGTCCCGGTGTCTATAGCCAGCCAGATACGGCAGCTGCTACAGGACAAACAGTTTGAACTGGCACTTCAGCTAGCGGTGAGAAACCTAAACTCTGGCTTTATTTCCTAGTAAATACCACATGCAGAGGGAACGATGTTTGTCATAGGCTAACCTTGCTTTTTTCTTACTATTTGTTCTCTTTTTGCAGAAAATGAAGGATGATTCCGATACAGACAAGAGGCAA[C/T]AGATCCATCACATTCAGAACCTGTTTGCCTTCAACCTGTTCTGCCAGAAGCGCTTTGATGACTCCATGCAGGGCTTTGCTAAGTTAGGGACAGGTGAGTGGACTTCATATGTACAGCACAGAATGACGGGTTTGATGTGCAGTACTTTATTTGGTAAATAGTATGAATGCTGAAAAACTGAAAATGCTGTGTAATTGTAGTTTATTATTATAATTTTTAAAATAATAATATCAAGTAAATTTGTTAGATGTTATAAACTTAACGTAAAGGCTAAATAGTTCAAAACTAAAAATGTATTTACTTCAAGCGGTTGTAAACCTTTATGAGTGAATCCTGTGACCATTGTCAAAAAATATTGGAAGTCAAAGGTTTCCAGCATTCTTCAAATTATCTATCTTCAGAAGAATGAAACTCATTAAAGTTTAAAACAAGGGTGAGTAAATAATGCCATAATTTTTGTATTTTTTTATTTTTGGGTCAATTATCACTTTAATATTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9171
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 |
---|---|---|---|---|---|
ENSDART00000113644 | Nonsense | 575 | 875 | 17 | 24 |
Genomic Location (Zv9):
Chromosome 17 (position 50627259)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 50018076 |
GRCz11 | 17 | 50097145 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACAGATTTTCACGGAGGACCTAACGGAGGTGGARACACTGCCCAGGGAT[C/T]AAGTGTTGAACTTTCTGAAGGAGGGCTTCAAGGAGYTGGCCATCCCATAY
Long Flanking Sequence:
GTTCATTCCGCTGTGGCAACCCTGGATTAATAGAGGGACTAAGCCGACAAGAAAATGAATACATGAATGGTCTTAATGAGGATTAGGCATATTTTATAAACATTTGCGATACTTGTTTATCCTGTTATTTCCAGTACTTTTTTTTTTCTTTTCTAAAGACCGAAGTCTACATGTCGTGAACCAATTAATATAAAATGTATTACACAATATAAATCAAAATAAAGCAAAAACATCAACAGTTTCAGATAAGAATCCTTGTTTCTTTCTCAACATGATGTTTATTTGTGTCTCTCTGCTCAGGATTGGAGAACCTGGGAATCATCTTTGAGTTTTCGCCGTGGGTGTTGAAGATTTGTCCAGAGGACGGCCTGAAGGTGAGATGAGCACCGTATAATCATAAGACATGTGTCCTCTGTGCTGATTTTGAAGAGTTGAGCCTGAGTTGCTGCTTACAGATTTTCACGGAGGACCTAACGGAGGTGGAGACACTGCCCAGGGAT[C/T]AAGTGTTGAACTTTCTGAAGGAGGGCTTCAAGGAGCTGGCCATCCCATACCTGGAGCACATCATTCACATGTGGGACGAGACGCGGCCTGAGTTTCACAACGTTCTGATCCAGCTCTACCTGGAGAAGGTGCAAGGGCTCATGAAGGCGTATCTCAACACACTGCCTGAAGGTCAGACATACAGTCGACTCACACCACTTTATTAGTTCCGGTTAGACATGTAACGATGAACCACAAACAGGCTGGATGATTTTCCAAAACTGTAATAATTTATTTAACTGTTCTAGGTCTTAAATATTTTTGCACAGGTCTTTTTTTTTTGCGATGTCCATGTAACGCTACATTTAATGCTCATTTAAATTCTTTTTGTTGTTGTTGCTTGGTTTTTGGGGTGTCGTAGTTCTTTATTTCACTAGTCCAATTGTAATTTGCGGTATTACAACTACAAAAAGGTCAACTTGCAATAGCCAATCAGCTTTCTGTTATTAAACTCAGTGTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18429
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 |
---|---|---|---|---|---|
ENSDART00000113644 | Nonsense | 697 | 875 | 19 | 24 |
Genomic Location (Zv9):
Chromosome 17 (position 50630306)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 50021123 |
GRCz11 | 17 | 50100192 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCGCTYCTTTTGGGACGTATGGGGAAACACGAGCAGGCTCTGTTCATCTA[T/A]GTCCACATCCTGAAGGACACRCGGAYGGCTGAAGAGTRAGTRAAGTCNNNNNNNNNNNNNNNNN
Long Flanking Sequence:
TACTTAATGGTCTTAAAAAGGTCTTAAAAGGTCTTAAATGTGACATTAAGATATCTGCAGAGACCCTGTATAAGACCTCTTTGTGCCCTCAGGCCTGAACTACTAAATGAATTTCTAGCACCACACACAATATATCCAGTATTTCCACTATGTATCCATAAACCTTTCTAAAAGGAGAGCTTTCCATCTTCACGAAAGTTTTGTGGATTGTGTGCAGGCATTCCAGCTGTAGCTGCAGGAAAAGAGAAAGGAGAGCTGGGCGAGTTCAGGAACAAACTTCTGTCTTTCCTGGAAGTTTCCAGCAGTTACGAGCCAGAGATACTCATCAGTGATTTCCCTTTCGACGGTGAGTCCAGAGGTCAGACAGATCACTCAATATGACATCTATGAGTACAACTGGATGATGAAATGTTGGTTTCCCGCTTTCTGTCAGGCCTGTTGGAGGAAAGAGCGCTTCTTTTGGGACGTATGGGGAAACACGAGCAGGCTCTGTTCATCTA[T/A]GTCCACATCCTGAAGGACACGCGGATGGCTGAAGAGTGAGTGAAGTCGTCTTTAGTGTCTGGCAGTCTTCTGCTTTTTGATATCAGCATTTACTTTTTTACCTGGTTAATACATTAATCATTGCAAAATTGTGGATACATTATAAACTGTAATGATAGAGAGCAAATGTATACACTCACCGGCCACTTTATTAGGTAAACCAACTACTCATTAATGCGAGTTTCTAATCAGCCAATCACTACTCAATGCATTTAGGCATGTAGACATGGTCAAGACGATCATCTGCAGTTCAAATCGAGCATCAGAATGGGGAAGAAAGAGGATTTAAGGGACTTTGAACGTGGCATGGTTGTTGGTGCCAGACGGGCTGCTCTGAGTATTTCAGAAACTGCTGATCTACTGGGATTTTCAGGCACAACCATTCGAAAAAGAGGAAATATCCAGTGAGCGGCAGTTCTGTGGATGCAAATGCCTTGATGCTAGAGGTCAGAGGAGAATGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9687
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113644 | Essential Splice Site | 774 | 875 | 21 | 24 |
Genomic Location (Zv9):
Chromosome 17 (position 50633473)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 50024290 |
GRCz11 | 17 | 50103359 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCGCTGAACRTCCTTCAGCTTCACCACAGCAAACTCAACACCACCAAAG[T/A]GAGCGTCCACCRCTAAATCCTAMTAGTGTTKTCRAAAGGACTGACTTCAA
Long Flanking Sequence:
GTATCTGTTTCTACAAAGAAAATCCAATGACCTAAAGATACACTGACTAATTTCATTTGTATTGTGTTTAGTATGTGAGAATCTGATAAATAAATAACAGTTTGAGAGTTGCAACATTCATCAGTATTAAACTATTGCATAATAATTGCTTAGTGGAAACGTATAGACGTGCAGAAATTATAAGTTCTCTTTGACGCATTGGATTGAATTGCTGTTTCATTTGCTAATGTTTATTCGGTTTAATTCACATCTTCGGATGGAAACAGCTTCTGTGGACCCACAACAGATGTATCTGTCTCGTGGTGACACATTTTCTGTGAACGTTAACAGATGGATTTTGTGTCTGCAGGTGTATCTGTCACTGCTGCGCATGTATCTGTCTCCTCCTGATGTTCATTTCCTCGGGCCCATTAAGATGGAGCTATGCGAGCCACAGGCAAACCTCCAGGCGGCGCTGAACGTCCTTCAGCTTCACCACAGCAAACTCAACACCACCAAAG[T/A]GAGCGTCCACCACTAAATCCTACTAGTGTTGTCAAAAGGACTGACTTCAATACCAGACGATACCTACATTTTAATAACGTCCATTTAACATAGGTCTGCCCGATTCTGGATAAAGTGAGAACGTTAATGTCTACGTTATTTATAACTTTACCACCTGTTATTCACAGCCTGTGCAGGTACTGTTTACTACAGTAGACCTCATCATTGGGTTATCCTCTCTGTGGTAATCAAACAGCTCACAGCCACGAATAAGTCATTACATGAAGATAGAAATGACATTTTTAGTTGAATTATACCATATTAATCCAGTATTCTGACTCTTTCAACACTATTTAGAGTCTGGCTGTGTTCACGTTACCGAGTAATGTATGTAAGATGATGTATTAAAAGACTTTTGCTATTACATGCTTTTCTCCAGACATTGGAAACAATCGGCTGACTCATAGCGTGGTGGGTCGAATTGAGATCACGATCTTTTAACGATTAATCATGCAGCCCTG
Associated Phenotype:
Not determined