ZMP
rab11a
Ensembl ID:
ZFIN ID:
Description:
ras-related protein Rab-11A [Source:RefSeq peptide;Acc:NP_001007360]
Human Orthologue:
RAB11A
Human Description:
RAB11A, member RAS oncogene family [Source:HGNC Symbol;Acc:9760]
Mouse Orthologue:
Rab11a
Mouse Description:
RAB11a, member RAS oncogene family Gene [Source:MGI Symbol;Acc:MGI:1858202]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36627 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa36628 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa36627
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 |
---|---|---|---|---|---|
ENSDART00000060766 | Essential Splice Site | 79 | 215 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 18915983)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 19146206 |
GRCz11 | 18 | 19135272 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATCTGGGACACGGCAGGACAGGAGCGCTACCGAGCCATCACTTCAGCG[T/A]AAGACTTATTACAGATTCCAGTTTTAAAGTTTAACTGCCTGTTCATAGCA
Long Flanking Sequence:
AGTTGATATTTATTGTTATTGCTTTCATATATATTTGGGAGTCACGACCAAAACAACAAAGGATTCAAAGAAAAATATACTTTTTAGAAATTTTATTGAGCAGTAATTTAGAATATTGATTTTCATTGCTGACTTTATTGTTTAATGTTTTTTTATGTTTTAGTATTTTCTTCATCACAGAATCGTTTATTTAATCAGTGTAGTAGTTTGGAAAGACACAAGGCTTGAGTAAATAATGTGAGAAGCCTAATTTGTTATGTGATCTATGTCAGATATTACACCATGTTGTGTTTTATTTTGAAGTGGTCCTAATTGGAGACTCTGGTGTGGGGAAGAGTAACCTGCTGTCTCGTTTCACTCGCAATGAATTCAACCTCGAGAGCAAAAGCACTATTGGAGTGGAGTTCGCCACACGTAGCATTCAGGTGGATGGAAAGACCGTCAAGGCTCAGATCTGGGACACGGCAGGACAGGAGCGCTACCGAGCCATCACTTCAGCG[T/A]AAGACTTATTACAGATTCCAGTTTTAAAGTTTAACTGCCTGTTCATAGCAAAGATCTCTATAGAAGTTATTTTAATCTTGTGATATTCCTCCAAAACACAACTTAAACACAATGGCAAAGACAAACAATATTGTACACTGATATAGTTAAGCATATTTGAGACTATAGATTAATTAACACCTTTTTTTTTGACGTTACTGTGCAGAATGACACTTGTGCATTATCGTTGTGTAAGCATTTATTTCATGCATCATAAAACAGAAAAAAGAGGCTCTGGAGGGTACATCTTTGAGTTTTTGAGCAAAAATGTTTAAAATCCTTTACATAAAAAGCAGTTAACAGGCTTAACCCTAGGAATACTGGTGAGGCCAATTTTTTTAAGGTACATTAATTAATATGTTATTCATACTCCAAACAAAATTCATATATAGCCCTTTTATTTTCCATCTTCATTTGATTTGCTGGCTAACAGGTATTACCGTGGAGCTGTGGGGGCCCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36628
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000060766 | Essential Splice Site | 144 | 215 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 18916744)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 19146967 |
GRCz11 | 18 | 19136033 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCTGAGGCATTAATCCATACTCTTCCACTTTTTTGCAACCATATTTGC[A/T]GAGAAAAACGGTCTGTCCTTCCTAGAGACCTCAGCTTTGGATTCCACCAA
Long Flanking Sequence:
GAAAAAAGAGGCTCTGGAGGGTACATCTTTGAGTTTTTGAGCAAAAATGTTTAAAATCCTTTACATAAAAAGCAGTTAACAGGCTTAACCCTAGGAATACTGGTGAGGCCAATTTTTTTAAGGTACATTAATTAATATGTTATTCATACTCCAAACAAAATTCATATATAGCCCTTTTATTTTCCATCTTCATTTGATTTGCTGGCTAACAGGTATTACCGTGGAGCTGTGGGGGCCCTCCTAGTGTATGACATCGCCAAGCATCTGACCTATGAGAATGTGGAACGCTGGCTTAAGGAGCTCCGAGACCACGCAGACAGCAACATTGTCATCATGCTGGTGGGCAATAAAAGTGACTTGCGTCACCTTCGGGCTGTGCCCACTGACGAAGCACGTGCATTTGCAGGTTAGAGGTGAACCATTAACTTCTGATAGTGCTGCTTGTGTGTATTGCTGAGGCATTAATCCATACTCTTCCACTTTTTTGCAACCATATTTGC[A/T]GAGAAAAACGGTCTGTCCTTCCTAGAGACCTCAGCTTTGGATTCCACCAATGTAGAGACTGCTTTTCAGACCATCCTGACTGGTGAGTGTTCTTTCCAAAAACCTTTTTCAGCAGATACTTATCAGTGTGCAAGGTTAAGGATGGTAAACTTTTGTTTTTGTAATGGCAGCATTTTTCTTGAAGAAATACAGGCTTGAGGAAATGACTGTGTTAGTCTAAACTGGGAGAAAAAGAGATGGTAAATGATTGGCCGAAGGCCATATCCTTATGAATGACTCATCAAAAGCCCTGCCTTGGTCGGGTAGGTTTCTCTGGCCTGACGTGACTGCCATAGAGAGTTTCTGTCGTCTTTTGCTCCTCTGTTCAGCTCCTGGCATCTGCAGAGGAAGAACAAATAATAAATGTTTCAGAGGCATTGCTGTCAGTTGCGATGCTGTAATTGCATCGGCCCTGACATCCAGTAATAACAGCACGGATGTATGGCAAAACAAAGTTCATA
Associated Phenotype:
Not determined