Busch Lab

ZMP

rab11a

Ensembl ID:
ENSDARG00000041450
ZFIN ID:
ZDB-GENE-041114-53
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.
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.
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