ZMP
rab3gap2
Ensembl ID:
ZFIN IDs:
Description:
rab3 GTPase-activating protein non-catalytic subunit [Source:RefSeq peptide;Acc:NP_001004528]
Human Orthologue:
RAB3GAP2
Human Description:
RAB3 GTPase activating protein subunit 2 (non-catalytic) [Source:HGNC Symbol;Acc:17168]
Mouse Orthologue:
Rab3gap2
Mouse Description:
RAB3 GTPase activating protein subunit 2 Gene [Source:MGI Symbol;Acc:MGI:1916043]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9042 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18323 | Nonsense | Available for shipment | Available now |
sa17477 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa9042
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064806 | Nonsense | 178 | 1373 | 7 | 37 |
ENSDART00000105503 | Splice Site | None | 1270 | None | 35 |
ENSDART00000126201 | Nonsense | 178 | 1143 | 7 | 37 |
Genomic Location (Zv9):
Chromosome 17 (position 25469672)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 25609591 |
GRCz11 | 17 | 25627982 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTATTTTTTNNATCTATGTGTATGTGTAGAGTGGAGTTCTTCTATTAGCA[C/T]AGTTGTTGCATGAAGATCCTGTGCTGCGCCTGAAATGTCGGACTTATGAG
Long Flanking Sequence:
CATTGGAAATACTAAGAAATGTTTGTTTCGCATCAAATCAGCATATAAGAGTAATATCCAAAGGTTAGTGTTGCACTGAAGACTGAAGTAAACTGTTGACAAATCAGCTTTGACATGACAGAAATAAATTACATTATTATAATTTAATAAAATAAACAGCTGTGTTTTAGTTTTATTTACAGTACCTCTATTTCCCTGCATTTTTGATCCAATAAATGCTGCCTTGCTGATCATAAAGGAAAAAAAAATAGATTTTGATCTTTTGCATGGTAGGTAGTGGGCTCATTGTCTGTCTGTATGTTCAGGAGTTCAACCGGCCGGCCCGATTGGACCTGTATTGTGGTTGGATTCAGCTCAGGTTATGTCCGTTTCTACACAGAGGTACTTCATTCATTCAAATTAATTCAGACTTTGTAATTATTATTTTGCCACAGTAGACAACCTATTGGTATTATTTTTTTATCTATGTGTATGTGTAGAGTGGAGTTCTTCTATTAGCA[C/T]AGTTGTTGCATGAAGATCCTGTGCTGCGCCTGAAATGTCGGACTTATGAGATTCCACGTCATCCTGGAGTAACAGAACAGGTACCAATACCTCTCATGCTGACTCCTGTGTGTAGTTCTATGCAAAACATTTAATATCCAATTGTTAGCATGGTAAAACTTTATATCTCTGCCACATGCATTTTCAGTGATCTGATTCTGAACACAAGTGGTCAACCGATATGCTTTACCATTTCCACCTGGAATTGATATATATTCCCTCTTTTTTTTTCTTTTTTAAATGTCATTTTATTTTTTTTATTGTAAAAATTCAAGTAAAATAAGCAAAAAAATTAGATTGGTTGAATTATTGATAAATTAATCAACAGATTAATCAGTGTAAAATAAATAAATATTCATTAGTGGCAGTCAAGAATAGACAAGGTTAAAATGATTTAGAGTCACCTAAAATTAGAGCTGTTCATCGAGTGTCGTAAGGTTGATGAAAACCAGGTGTAAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18323
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 |
---|---|---|---|---|---|
ENSDART00000064806 | Nonsense | 1004 | 1373 | 28 | 37 |
ENSDART00000105503 | Nonsense | 942 | 1270 | 25 | 35 |
ENSDART00000126201 | Nonsense | 975 | 1143 | 26 | 37 |
Genomic Location (Zv9):
Chromosome 17 (position 25459427)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 25599346 |
GRCz11 | 17 | 25617737 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
NNNNNNNNNNNNNNNNNNNNNNNAATCTMCTGATGTGCTKTTTGCTCACTG[T/A]AGCTGGGAAAATGTGGTGCAGTGGAACAAAGACCCAGAGGTAAAAACTTG
Long Flanking Sequence:
GAACTATCATTATGTGTTTTAACTGATATTTAAAATGTTTCAGGAAATAAAATAAAATCATCCACATCAAACCAGTGAACAGTAAAGTTGTAAGGTACATATAAGAGTAAATTAATAGATATTTTTTTTATATAGTTTTTGTTTGACTTTAAGGTGGTGTAGCAGACTGTGTTTCAAAGCTGATCTTCAGACAAGGTGTTTCTCCTGATGTCCTGAGGGAGATCCTACAGCAGAGGAGAGAGAATGAGCCCACGCAACAGCCTTTACTGCAACGTGGAGAGGGCAAACTAGAGGGTAACTTCAATATGTGACTCAGACCATTAAAAAAAACATTTCCATAGTAGTTTCCATTTATAAAAGTTTATTTATGCCATGTGTGGGTGTTTTGTGTATGTCTGAATCTCAGCATCTGTTTGTATGCATGTCGTTTCAGAGCTGCTGGAGTGTGTGTGTCAGCGCTTTCCAAACTCTCTATCTCCTGATGTGCTGTTTGCTCACTG[T/A]AGCTGGGAAAATGTGGTGCAGTGGAACAAAGACCCAGAGGTAAAAACTTGAAACATTCTCAACATTTTGCTCATAGGCAGGGCCAGACAATATAGCAGACATTAGCATGTTTAAATTAAAGATTTGGAGGGTTTTTTTTACCTACAGAACAAGTGTGATTCTAGTAACAGCATCTTCTATTTTTAGTTCTGTTCCAAGTGCACAAGGTGTTCAACATGTTGTAATATGTATGAACATTATGTAAAATAAATGATAAATATCTTTGCAGAAAATAAATGAGATTTGAAATATTATACAAATCAGTGTAAACTTAACTTAATCAAACTTAATCAGTGTTGTGCTAGTTACTGAAAAATAGCACTAGTTACAGTTACTCTATTCAAAAAGTAACTCAATTACTTTATCGGTTACTTAAACCAAAAAAGTAATGCATTACCGTTAAAAGTAACTTTTAAGTTACTTTTCCAAAGAACATTCGTAATGCTCCCATCATTGCCCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17477
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 |
---|---|---|---|---|---|
ENSDART00000064806 | Essential Splice Site | 1324 | 1373 | None | 37 |
ENSDART00000105503 | Essential Splice Site | 1220 | 1270 | None | 35 |
ENSDART00000126201 | Essential Splice Site | None | 1143 | None | 37 |
Genomic Location (Zv9):
Chromosome 17 (position 25452954)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 25592873 |
GRCz11 | 17 | 25611264 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTGCTGGCTCGTCTGCCACCCACCCTCTGCACGTGGCTGAAGGCTATGG[T/A]GAGAACACGCACACACTGCACACYTCTCAAMAGATCACATCATTTGCCAC
Long Flanking Sequence:
ATCTCTTATTGTAGAGTTATTTTAAATAAAGAACTTTATATCGTTTTTCTTTCTTTTTGTATGTTTTGCAATTTGTGTTTTTTAAAATTCTTTAATTTTTCTTTATTTTTGTCATTTTTCTTCCTATTTTTAGGTTTTTTTTTTCATTTCTTTTATGTGATAGAGTTTTTCTTCCTGGTATTTTGTCTTGCTTTTTATGCAGTTTTTAATTTGTTTAATGTCTAAAATGTCTCAAATTTAATTTCTTATTAAAATGTTTTCTACATTTTGTGATGGTATTTTAGTTGTTTCTGTTGCTGATTTAGTATTTATATTATTTGTGGTGATGTCTCAGGTGATGATGGAGGTGCAGGACAAGGATGTTCTGGGCTCTCAGCTGCTGGTGTTGACGGGTCAGAGACTCTCTTTCTCTCTGCTTCACTCCCAGTCACAAACCAAACCCAACATGGAGCTGCTGGCTCGTCTGCCACCCACCCTCTGCACGTGGCTGAAGGCTATGG[T/A]GAGAACACGCACACACTGCACACTTCTCAACAGATCACATCATTTGCCACTTACCAGCTTCATGGTTTGTGTGTTTTTAGGACCCCAGTGAGCTTCGCTGTCCTTCAGTACCTCTTTCCCAGAGCAGTCGACTGATCAGCAAGGTCATCGAGATGCTCCCCGAAAACCATGCGCAGTACAGCCTTGCCCTCCATCTTCTGGAGGCTGTGGACTCTTTACACCAAGAGCCCTGATTTTTGAAAGAATGAAAATTATGTTTTTAATTATTATTATTGTTATTATGGACTCGAAAACTTTCCTAGACCTGGAAAACAATGCGGTCAGCAGCATACATAAATGCGTCATCATCGGTAATCTGCTTAACACAGCAAGTTTTAATTTCCCCTCCTACTTGTCACTAACATCAAGAACACTAGCACCTCTTGAGGATGTGCTTTCCCACAATGCCTGTGCACAATGAATGCGTCACAAATAAAGGGCCCGAGTCTCTAGTGTCTAGA
Associated Phenotype:
Not determined