LOC564932

Ensembl ID:
ENSDARG00000075803
Human Orthologue:
SLC41A2
Human Description:
solute carrier family 41, member 2 [Source:HGNC Symbol;Acc:31045]
Mouse Orthologue:
Slc41a2
Mouse Description:
solute carrier family 41, member 2 Gene [Source:MGI Symbol;Acc:MGI:2442940]

Alleles

There are 2 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa16306 Nonsense Available for shipment Available now
sa38103 Nonsense Mutation detected in F1 DNA During 2016

Mutation Details

Allele Name:
sa16306
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109702 Nonsense 90 494 1 10
Genomic Location:
Chromosome 25 (position 29643534)
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
KCCACACAATATCCWGGAGATGCCCAGTGAGTCAATCAGGGCCATGGTTT[T/A]ACAGATTTTGTTTCCATTCCTGCTTGCGGGTTTTGGAACGGTGCTGGCTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38103
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 > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109702 Nonsense 325 494 7 10
Genomic Location:
Chromosome 25 (position 29660307)
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
CTTTTTGTGATGGAGGAACTGTATTTTTTTTTCCTCAAGCCTTGGAGGAT[T/A]AATTCTGGACCGAACAATCACAAATCCAAAGCTCGATGGTCTTGTTCTAT
Associated Phenotype:
Not determined

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