lsm14b

Ensembl ID:
ENSDARG00000025386
ZFIN ID:
ZDB-GENE-040426-779
Description:
LSM14 homolog B-like [Source:RefSeq peptide;Acc:NP_956465]
Human Orthologue:
LSM14B
Human Description:
LSM14B, SCD6 homolog B (S. cerevisiae) [Source:HGNC Symbol;Acc:15887]
Mouse Orthologue:
Lsm14b
Mouse Description:
LSM14 homolog B (SCD6, S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI:3040677]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa4212 Missense, Nonsense Mutation detected in F1 DNA During 2014

Mutation Details

Allele Name:
sa4212
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:
G > T
Consequence:
Missense, Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000034707 Nonsense 186 380 4 9
ENSDART00000055116 Missense 138 145 5 5
Genomic Location:
Chromosome 23 (position 576805)
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
AGCAGCAGAAGAAGAGTCTGGRTGGAGGACAGCAGGGTGGAGCRCAGAGA[G/T]GAGCCAGAGCACAGAGAGGAGGTACACTGTCAAATCACCGTTTATTAGCT
Associated Phenotype:
Not determined

Register

If you would like to be informed when the status of this gene changes (for example, a new allele is generated or an allele is made available for distribution) then please enter your details below:

* quick link - http://q.sanger.ac.uk/fhh3wkwa