ZMP
vps33b
Ensembl ID:
ZFIN ID:
Description:
Vacuolar protein sorting-associated protein 33B [Source:UniProtKB/Swiss-Prot;Acc:Q58EN8]
Human Orthologue:
VPS33B
Human Description:
vacuolar protein sorting 33 homolog B (yeast) [Source:HGNC Symbol;Acc:12712]
Mouse Orthologue:
Vps33b
Mouse Description:
vacuolar protein sorting 33B (yeast) Gene [Source:MGI Symbol;Acc:MGI:2446237]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34177 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa31593 | Nonsense | Available for shipment | Available now |
sa9761 | Essential Splice Site | Available for shipment | Available now |
sa12663 | Essential Splice Site | Available for shipment | Available now |
sa27045 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34177
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065868 | Essential Splice Site | 59 | 617 | 3 | 24 |
Genomic Location (Zv9):
Chromosome 7 (position 51851769)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 50122005 |
GRCz11 | 7 | 50394781 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATTTGATGAGTCCTCTAGATCGAATTGCAAATGTCACAATCCTAAAGG[T/A]GTGTTATCTTATACAACAAGGTTTGGGAAATGATTTGCAGTTTATATAAT
Long Flanking Sequence:
TATTTTGGCTGAAATAAGTAAGGATTTGACGATTCTATTTGCTGACAAACGGTGTAAATAAAACACTAACCTGAGCTGCTGTATGAAACCAGCCTTATAGTGACATAAGCAGAATTGTGACAGGAGTTGTTTACATTCAGCATTCGGTACATGCAGCTTCCACATATCGGAGGGACAGAAATGCTTAAACACAAATGTTTTACATGTTTGTCCAGCTGTCAGGATCTGTCCATATGGCTCAGACAGAGAGGAGAGATGCTCCTGAACTGCCCGACTTCTCATTGCTCAAAAGACTGGCAAGAGACCAGCTCATCTTTCTGCTGGAGCAGGTGAACAAAATGTGCTCAAAAAAAGAAGCTTTTTCTTGTGTATTTTCATTGTTAAGTGCCAACATGTATTGTTGTTTTTGTTTTTACAGTTGCCAGGGAAGAAGGATTTATTTATTGATGCAGATTTGATGAGTCCTCTAGATCGAATTGCAAATGTCACAATCCTAAAGG[T/A]GTGTTATCTTATACAACAAGGTTTGGGAAATGATTTGCAGTTTATATAATTTTTTAGAAAGAAGCAATACACACACACACACACACACACACACACACACACACACACACACACACACACACATACACACACTAATAATTTAACATCCATATCTGATTTTGCCTTGTAGCAACATGAAGTCGACAAACTATACAAAGTTGAGCTTAAACCAATCGTCAGCAGTTCAGACCAGTAAGTAAATTCACATGTTCATTACGGGAATTTTGATTATACATGGGTTCTTCTTTAAAATATTCATATTCTCTCTCGTGTACAGGCTGTGCTTCCTCATACGTCCTAGAATACAAACTGTGAAGTGGATTTCAGGTTGGTACTGTTTGGAGTTACATGGCTATATGCAGTTGAATGCAAAATTATAATCCCATCTGTGAAAATTTTGTTATTAAATATTTTCCAAATGAGGGTTAGCACTGTCGTCTCACAGCAAGAATATCGCTGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31593
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 |
---|---|---|---|---|---|
ENSDART00000065868 | Nonsense | 155 | 617 | 8 | 24 |
Genomic Location (Zv9):
Chromosome 7 (position 51850025)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 50120261 |
GRCz11 | 7 | 50393037 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGATGAATGGAATTTCTACATTCTTCCTCTGGATGACGATATCCTCAGCT[T/A]AGAGCTGCCAGAGTTCTTCAGAGATAACTTTCTGGTATTGATGTTCTTGA
Long Flanking Sequence:
TACAGATTTAGTTAATTCAGACAAGGTAGCTGGACGATTCAGAAGATATAAGATCATATTTACCCCACAAAAGGTAACTAGTTTTTCTATAACTGCACTTTATAACTTATACCTGTATCCTGCACTTGCTGCTATTGCACTGCTGGTTAGACCTCAACTGCATTTCGTTGCATTGTACTTGTACATGTGTAATGACAATAAAGTTGAATCTAATCTAATTTAAATTTAAATTATCTTGTGCTTTGGTAATCATGTTTAAATGTGCTACATATTTATTTAGATTTCTGACTGTTAGGTTATGATCTTCTTTACAGTTTTATGCGTGTGAAACAGTTTTGGAGGAACAGGGTGTCTATGGAGGTGAGTTAAATGTGCTCAATGTTTCAAGCTTTATTTTTTAGCTACATTAGACAGACATTAACAAGGACACTCTTTCTCAGATGTTACAACCGATGAATGGAATTTCTACATTCTTCCTCTGGATGACGATATCCTCAGCT[T/A]AGAGCTGCCAGAGTTCTTCAGAGATAACTTTCTGGTATTGATGTTCTTGATGCCATACATTGTGTGCAAAATAACAACACTTTTTTTTTAAGTGTCATGTTTTGAACTTAAAGGGATAGTTCACCCCCAAATGAAAATGATATCATCGCTTGTTTAAAACCTGTTTGAGTTTCTTTATTCTGTTGAACACAAAAGAAGATATTTTGAGTAATGCTGACTGCTGGCACCCATTGACCTGCTATCCTTTATGAAAAAAAGAGCTTTACCTCGCATAAAAACAGATTAAATTCAATTCAAGTTAATTTGTATAGCGCTTTTTACAATAACTATTGTTCCAAAGCAGCATTACAAAAGGTGCCCATGAGGGAGAATGATGAGCTTATTATCATTTAGAGCGAACTATCCCTTTAATGCAGGGGTGTCCAAACGTTTTCTTATGAAGGGCCAAAATCCAAACTTCATTGAGGGCTGTGGGCCGAAGATAAAAATAGCAAACTGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9761
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065868 | Essential Splice Site | 232 | 617 | 10 | 24 |
Genomic Location (Zv9):
Chromosome 7 (position 51848612)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 50118848 |
GRCz11 | 7 | 50391624 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAAAGAAMAAGACAACCTGAATTTGCCAAAGTATTTCTTAWCGACAGAGG[T/G]CAGTAATTTGAAATCAGATGCATYTKCATTTTTTTCACTTGTGGAATTGT
Long Flanking Sequence:
TCCCAAATGCTCTCCTTCATTCTCCTTCTCTTCTTAGATAGAATGGTGGGCCAAATCAAAGGTTATCATGGGCCAACTTTGGCCCACAGGCCCAAGTTTGAACATCTCTGCTTAAATGCTTTGTTGAAGAGAAAAAAAAAAAACATGAATGATAACTTATGTGTTGGATATGTGCTTCACATTGTGTGTAAATAATAACGTTTGTATTTATAAGGAGGGAGACCAGCGCTGGGTGACCACTGGAGGGGGTGCTTTACATCTTTTACAGTCTGTCTATGGTTCCTTCTCAAAGGTTTATGGGATTGGAAGATGTGCCAAGGTGAGGATTAGTAGACAACTTTACCTTCAAAAAGTTTATATTTCAGTTGATGAAATGCAGATTTACATGCCATATGTCTTTCTATAAAGATGGTGTATGAATCCTGGAGGGAACTAATGGAGGAGGGTGAACAAAGAACAAGACAACCTGAATTTGCCAAAGTATTTCTTATCGACAGAGG[T/G]CAGTAATTTGAAATCAGATGCATCTTCATTTTTTTCACTTGTGGAATTGTGTCAGAGTTGAAATCTTTCGTTTTTGTGTCCACATTCAAGTAAACAAAATTTAATTTTATAAATGCAGAAATAATAATTATTTAAAGTGTTTAATTTAATGTTTCAAAACCCCTTTTTTTTCAAATAAAAAGTCAAAATATTATTACATCATCACTTTGCGTGACAGATCTATACATGTAATATTGAAACAATATTCTCATTCTGACATACATTTATCAAAATAAATAAAAGAATGAATTAAACTTAATGTGATTACATTTTATACGATTAAAAGTTTATTTTTGTTAAATAATATTTGTACAAATTTATGAGAGCAAAGATTTAAATGAACAATTGGTATTTATGGGCTGTACTGTACTGGGCTGTATGATCAAAATTGTATTTCACAGTATGAGAAGGTTTATTTCACTGTAACCATTTCTTTCACAAAATAGATATTCTAAAGGTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12663
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065868 | Essential Splice Site | 282 | 617 | 12 | 24 |
Genomic Location (Zv9):
Chromosome 7 (position 51846186)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 50116422 |
GRCz11 | 7 | 50389198 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACTTCCTCTGACAAGAGTATCAAAGTGATGYTTAACTCTCAAGATAAAG[T/G]AAGAGTCACACAGACRTCATTAAGTTGACCATGATTAGAAGCAGCTATGT
Long Flanking Sequence:
TTAGTAAATGCATTAATTGCACATTAACTAATAAACCTTATTGTAAAGTGTGACCTGTTAATCTTGGTAAAATTGTATAGTAATCATTATTCATTTGCTCAGAAAAAAAAACCCTTAAATTAAACAGGACACATTGTGGTGCAGAAAATATATATATATTTTTTGACCTAATTACAGTTTGCATAATTTTATTATAGTAATGGCAACTTATATACAGGTCTCTGCATTTTGCTGTTTTAGATGTGGATTTTGTTACTCCTCTCTGCTCTCAAGTGGTTTACGAGGGATTGGTGGATGACATTTTCAGAATAAAATGTAGTAAGTCATCAGAATTCGTTCACAACATGTTTAGCAAAAACATACTGAAATCTTTCATTCTCAGATCTTCAAGTTCATCCCTTGTCATTTGTTTATATTGTTAATAGGCAGTGTGGAGTTTGGCCCTGATGTCACTTCCTCTGACAAGAGTATCAAAGTGATGCTTAACTCTCAAGATAAAG[T/G]AAGAGTCACACAGACGTCATTAAGTTGACCATGATTAGAAGCAGCTATGTAAAAAAAAACTTTCTTTGTTTTGATTCATCAGGTGTTCAATGAAATAAGGAATGAACATTTTTCCAATGTGTTTGGCTTTTTAAGTCAGAAGGCTAAGAATCTTCAGACAGCATATGATGTAAGTGTCATGATGTAAGGCTACATATGGCGTGTGTTTTTGTAGTGCACATTAATGTAATAACATTTTGACATTTTAGCAGTGTGACAATAAAAAACAAAAATGCTAATTGTTAACAGAAACGGCGTGGGATGGACATCCAGCAGATGAAGGCGTTTGTTGCAGATGAGCTGAAAGGACTCAAACAGGAACATCGTCTTCTTAGTCTTCGTAGGTTTTGTATACACTACTATTAAAGATTTCTGAATTATAAATTAATACTTTTATTTAGCAAGGATTCGTTGAAAATGGTCAAAAGTGACTGTAAAATAATTTGTAGTGTTATATATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27045
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065868 | Essential Splice Site | 311 | 617 | 13 | 24 |
Genomic Location (Zv9):
Chromosome 7 (position 51846015)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 50116251 |
GRCz11 | 7 | 50389027 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTGGCTTTTTAAGTCAGAAGGCTAAGAATCTTCAGACAGCATATGATG[T/C]AAGTGTCATGATGTAAGGCTACATATGGCGTGTGTTTTTGTAGTGCACAT
Long Flanking Sequence:
TTACAGTTTGCATAATTTTATTATAGTAATGGCAACTTATATACAGGTCTCTGCATTTTGCTGTTTTAGATGTGGATTTTGTTACTCCTCTCTGCTCTCAAGTGGTTTACGAGGGATTGGTGGATGACATTTTCAGAATAAAATGTAGTAAGTCATCAGAATTCGTTCACAACATGTTTAGCAAAAACATACTGAAATCTTTCATTCTCAGATCTTCAAGTTCATCCCTTGTCATTTGTTTATATTGTTAATAGGCAGTGTGGAGTTTGGCCCTGATGTCACTTCCTCTGACAAGAGTATCAAAGTGATGCTTAACTCTCAAGATAAAGTAAGAGTCACACAGACGTCATTAAGTTGACCATGATTAGAAGCAGCTATGTAAAAAAAAACTTTCTTTGTTTTGATTCATCAGGTGTTCAATGAAATAAGGAATGAACATTTTTCCAATGTGTTTGGCTTTTTAAGTCAGAAGGCTAAGAATCTTCAGACAGCATATGATG[T/C]AAGTGTCATGATGTAAGGCTACATATGGCGTGTGTTTTTGTAGTGCACATTAATGTAATAACATTTTGACATTTTAGCAGTGTGACAATAAAAAACAAAAATGCTAATTGTTAACAGAAACGGCGTGGGATGGACATCCAGCAGATGAAGGCGTTTGTTGCAGATGAGCTGAAAGGACTCAAACAGGAACATCGTCTTCTTAGTCTTCGTAGGTTTTGTATACACTACTATTAAAGATTTCTGAATTATAAATTAATACTTTTATTTAGCAAGGATTCGTTGAAAATGGTCAAAAGTGACTGTAAAATAATTTGTAGTGTTATATATTAATGTTCCCGTGAAATTTGCATTTTTTTCATTTGATGTTTGACGTAATCTCAATTTAAAGATGTAGAGAGGGAGGGGCATAGAATAGCCCCTCCCCTTAAAAAACAGCCAATAGTGTTTTGTTTAATCACATCTCTGCCAGTGAGAGTGGTTGAGCTCAAGCGTATCAAATG
Associated Phenotype:
Not determined