rab3db

Ensembl ID:
ENSDARG00000043607
ZFIN ID:
ZDB-GENE-040718-428
Description:
ras-related protein Rab-3B [Source:RefSeq peptide;Acc:NP_001002679]
Human Orthologue:
RAB3D
Human Description:
RAB3D, member RAS oncogene family [Source:HGNC Symbol;Acc:9779]
Mouse Orthologue:
Rab3d
Mouse Description:
RAB3D, member RAS oncogene family Gene [Source:MGI Symbol;Acc:MGI:97844]

Alleles

There are 2 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa31313 Essential Splice Site Mutation detected in F1 DNA During 2016
sa12251 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa31313
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2016.
Mutation:
T > C
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000064031 Essential Splice Site 78 220 2 5
Genomic Location (Zv9):
Chromosome 3 (position 13580586)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 14374038
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
GGTCAAAACCGTTTTTAGGAACAACAAGAGGATTAAACTACAAATCTGGG[T/C]AAGTTTGACGATCACGTGATCAGTCTAACATCTTAAACTAAAAGCAGAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12251
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000064031 Nonsense 118 220 4 5
Genomic Location (Zv9):
Chromosome 3 (position 13569663)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 14384961
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
TTTTTTNAATACTGATTGAGAGTGTTTAGTGTTTCTGTCCYGACTGTGTAG[G/A]GCCACGCAGATCAAGACGTACTCGTGGGACAAYGCTCAGGTGATTCTGGT
Associated Phenotype:
Not determined

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