LOC100331662

Ensembl ID:
ENSDARG00000077748
Human Orthologues:
SLC35E2, SLC35E2B
Human Descriptions:
solute carrier family 35, member E2 [Source:HGNC Symbol;Acc:20863]
solute carrier family 35, member E2B [Source:HGNC Symbol;Acc:33941]
Mouse Orthologue:
Slc35e2
Mouse Description:
solute carrier family 35, member E2 Gene [Source:MGI Symbol;Acc:MGI:2444240]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa30448 Essential Splice Site Mutation detected in F1 DNA During 2017

Mutation Details

Allele Name:
sa30448
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 2017.
Mutation:
T > C
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000041466 Essential Splice Site 74 350 1 9
Genomic Location (Zv9):
Chromosome Zv9_NA917 (position 13800)
Other Location(s):
Assembly Chromosome Position
GRCz10 KN150423.1 3807
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
ACTCTGGTACTTCTTCAGCTTCTGCACACTCTTCCTCAACAAATACATCC[T/C]CTCACTGCTGGAGGGAGAACCCAGCATGCTGGGTGAGTAGTACACACACA
Associated Phenotype:
Not determined

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