ZMP
rab22a
Ensembl ID:
ZFIN ID:
Description:
ras-related protein Rab-22A [Source:RefSeq peptide;Acc:NP_991282]
Human Orthologue:
RAB22A
Human Description:
RAB22A, member RAS oncogene family [Source:HGNC Symbol;Acc:9764]
Mouse Orthologue:
Rab22a
Mouse Description:
RAB22A, member RAS oncogene family Gene [Source:MGI Symbol;Acc:MGI:105072]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa5387 | Nonsense | F2 line generated | Not yet available |
| sa7049 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa5387
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:
G > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000022581 | Nonsense | 59 | 196 | 3 | 7 |
The following transcripts of ENSDARG00000015807 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 49508512)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 49558193 |
| GRCz11 | 6 | 49556846 |
KASP Assay ID:
554-3544.1 (used for ordering genotyping assays)
KASP Sequence:
ATGACAAAGACTGTGCAATACCAAAAYGAGCTTCACAAATTCCTCATCTG[G/A]GACACAGCAGGACAAGAAAGGGTAAACAGTAACAATCACTACACACACAA
Long Flanking Sequence:
GTGTATGTGTCATAAAAATGTCAAACCTGGCTATTTATAACCTAATGCTATTTATAATCATGGCTATTCTACTTTTAGAGCAGTTGTTTTACTTTTATTATTATAAAACAAAGATTATTGGGGTATTTTGTTTGGAAAAAAATACAGTTTTACTATTCAGCATTTTTTGTGGCTATTTGTGAAATTGAATGGCAGTTTCTGGGTGAAAATGTATTTATTTTTTGCTCAGATTATTGAATTAACACTTGAAAACGTCTGAATTTATCTTATAAGTAGATCCACATAATAAATAGATTTAAATAGAGTAAAGCTGTATTAAACAAAGCTGAGAGTCTTATTAGCGTGCGTATGTGTTATAAACGTGAAAAACCCCCATGTCTAGATATATAGTTAATGCTATTTTTATTTTTTAATCATGCCTGTTTCGATTTTTTTTTTAGAGCATCGTTTATGACAAAGACTGTGCAATACCAAAATGAGCTTCACAAATTCCTCATCTG[G/A]GACACAGCAGGACAAGAAAGGGTAAACAGTAACAATCACTACACACACAAAGACACTGTGGTAACACATCAACAAGCTGACAGCCATTAAATACAATGTTTGCTCTGTTTCACTTCTGTTTTTGCGGTGTCTCTATAAATCCGACAGGGGGCAGTATTGCATGCAGGTTTCTTAAATGCGAGCATAAAAGGGACAGTTCGCTCAAAATTGAAAATTCAGTCATCATTTACTCAGTTTTCACTTGTTTCAAGTCAATTTAAGTTTTTTTTTCTGTTGAACACAAAAGAAGAAATTTTGAAGAATGTTGGAAACCTGTAACCATTGACTGCCATAGTGCTTTTATGGAAGTCAGTGGTTACAAGTTTTCAGCTTTCCTCAAAATATCTTCTTTTTTGTTTAATCAGAAACTCGCAAATCTCTTGAGTAAATAGCGAGTAAATGCTTATTTTTTGTGAACTATCCCTTTTATGTCATTGGAAAGCGTTCAGGCTTCTTAATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7049
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 |
|---|---|---|---|---|---|
| ENSDART00000022581 | Essential Splice Site | 90 | 196 | None | 7 |
The following transcripts of ENSDARG00000015807 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 49518311)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 49567992 |
| GRCz11 | 6 | 49566645 |
KASP Assay ID:
554-4107.1 (used for ordering genotyping assays)
KASP Sequence:
CTACAGAGGCTCTGCTGCGGCCATCATCGTCTATGACATCACTAAAGAGG[T/A]ACTGAAACATTTCTTCGTTATTACCACACAAATCTTTCTTCTGGTAAAGM
Long Flanking Sequence:
ATTTGCTCTTCAGTGTCTGAACTTTCAGCAGTGAAAATTAAACCACACTGACCTAAACTAAACTGAACTTCAACTGGACTGACACAGTTTCAATTTGCTCCAACTTCTATGTTAAGCTGCTTTGACACAATTTCCGTTGTTAAAGCACTATAGAAATGAAGATTAAGTAAATTGTGAGATCAAATTTTGAGAAAAAAATTATTTGACTTATTTTAATGGTTCAAATTAGCTTTCAGTAAATTCACTCCTTTAAACTCTCACACTTCATAAAAATATAATAAGCATTTGCAGAGATCAGCCTCTTTACTCATAAGAAAGTATGACTGGTTGTGATCAGTGATGATTAAATACTCCTTTTATTTGTTTGTTTTAAAGCACAGGCCATGTCTTTTCTCTCACATCTGCATGTTATCTGTTCCACTTTTAGTTTCGTGCTCTGGCTCCCATGTACTACAGAGGCTCTGCTGCGGCCATCATCGTCTATGACATCACTAAAGAGG[T/A]ACTGAAACATTTCTTCGTTATTACCACACAAATCTTTCTTCTGGTAAAGCTATTAAAAGGGATAGTTCACCCAGAAATCAGAGTTCTTTCATCATGTACTCAACTTCATGTCACTTCAACTACATAAGATATATATTTTTCCATGGAACACTAAAAGAGTTATGGGCTGAGGTAAGACTTTCAGTGAAGAGTGGGTTAAAGGAAGACTCCACTGTTTTTGTAAATAGGCTCATTTTACAACTCCTCTAGAGTTAAATGTTTGCGTTTTACTATTTTTTTTAATTCACTCAGCAGATCTCCAGGTCATGTAATAATGGCCATATGGTTTGTTGCAGTGTGGTATAATATAATATTTTTCTCCATTTCCACTATAAAAGGTACCAAAAAACTGAACCATATTGTACTGCCTTTTGGGTACCATTTTAAATAGTACCAGCACAGCAGAACAATACCAAAAGGATGGACTAAGACGCAGATTTTTAAATAGGCGTACACAGCTG
Associated Phenotype:
Not determined