fam46ba

Ensembl ID:
ENSDARG00000039943
ZFIN ID:
ZDB-GENE-061110-129
Description:
hypothetical protein LOC777768 [Source:RefSeq peptide;Acc:NP_001071274]
Human Orthologue:
FAM46B
Human Description:
family with sequence similarity 46, member B [Source:HGNC Symbol;Acc:28273]
Mouse Orthologue:
Fam46b
Mouse Description:
family with sequence similarity 46, member B Gene [Source:MGI Symbol;Acc:MGI:2140500]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa8575 Nonsense Mutation detected in F1 DNA During 2014

Mutation Details

Allele Name:
sa8575
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 2014.
Mutation:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000058424 Nonsense 283 393 2 2
Genomic Location:
Chromosome 16 (position 36471464)
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
AGCGGTACATGTGCTCTCGGTTCTTCATTGACTTTCCAGACATCGGGGAG[C/T]AGCAGCGAAAACTRGAGGCGTACCTRCAGAATCACTTTGCCGGAATGGAR
Associated Phenotype:
Not determined

Register

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* quick link - http://q.sanger.ac.uk/ysesn9h6