FAM196B

Ensembl ID:
ENSDARG00000086049
Description:
family with sequence similarity 196, member B [Source:HGNC Symbol;Acc:37271]
Human Orthologue:
FAM196B
Human Description:
family with sequence similarity 196, member B [Source:HGNC Symbol;Acc:37271]
Mouse Orthologue:
Fam196b
Mouse Description:
family with sequence similarity 196, member B Gene [Source:MGI Symbol;Acc:MGI:3643491]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa12219 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa12219
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000122067 Nonsense 337 508 1 3
Genomic Location:
Chromosome 14 (position 1487116)
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
GTGAGTCACAAGCCACGCCYACTCTCCCTCCCAAGAAAGGCTCGCAGGTC[A/T]AATCAAAACCAGCACTTCCAAAGCTTCTGATTGGCTCAAAGGCGGWGCCT
Associated Phenotype:
Not determined

Register

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* quick link - http://q.sanger.ac.uk/qv2bmjud