FAM179B

Ensembl ID:
ENSDARG00000039197
Description:
family with sequence similarity 179, member B [Source:HGNC Symbol;Acc:19959]
Human Orthologue:
FAM179B
Human Description:
family with sequence similarity 179, member B [Source:HGNC Symbol;Acc:19959]
Mouse Orthologue:
Fam179b
Mouse Description:
family with sequence similarity 179, member B Gene [Source:MGI Symbol;Acc:MGI:2684313]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa38189 Nonsense Mutation detected in F1 DNA During 2017

Mutation Details

Allele Name:
sa38189
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:
C > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000057266 Nonsense 146 578 5 13
Genomic Location (Zv9):
Chromosome Zv9_NA429 (position 54618)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 627303
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
TATGTGTTTGTGTGTGTTGTTTTCAGGAGCGCCGCAGCACGTGTCCAAGT[C/A]GTGTGGTCTGCGTGAGATGTCAGAGGGTGTGATTGGACGAGGTGTGTGTT
Associated Phenotype:
Not determined

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