|Institutional Source||Beutler Lab|
|Gene Name||lysosomal trafficking regulator|
Ncbi RefSeq: NM_010748.2; MGI:107448
|Essential gene?||Possibly non essential (E-score: 0.318)|
|Stock #||R7871 (G1)|
|Chromosomal Location||13590397-13778803 bp(+) (GRCm38)|
|Type of Mutation||nonsense|
|DNA Base Change (assembly)||T to A at 13636052 bp (GRCm38)|
|Amino Acid Change||Leucine to Stop codon at position 769 (L769*)|
|Ref Sequence||ENSEMBL: ENSMUSP00000106188 (fasta)|
|Gene Model||predicted gene model for transcript(s): [ENSMUST00000110559]|
|AlphaFold||no structure available at present|
AA Change: L769*
AA Change: L769*
|Meta Mutation Damage Score||0.9756|
|Coding Region Coverage||
|Validation Efficiency||97% (64/66)|
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein that regulates intracellular protein trafficking in endosomes, and may be involved in pigmentation. Mutations in this gene are associated with Chediak-Higashi syndrome, a lysosomal storage disorder. Alternative splicing results in multiple transcript variants, though the full-length nature of some of these variants has not been determined. [provided by RefSeq, Apr 2013]
PHENOTYPE: Homozygous mice have a phenotype similar to human Chediak-Higashi syndrome patients, exhibiting lysosomal dysfunction with resultant protein storage; diluted coat color; abnormal melanogenesis; immune cell dysfunction resulting in increased susceptibility to bacterial, viral, and parasitic infections and decreased cytotoxic activity against tumor cells. [provided by MGI curators]
|Allele List at MGI||
All alleles(52) : Targeted(3) Gene trapped(34) Spontaneous(8) Chemically induced(6) Radiation induced(1)
|Other mutations in this stock||
|Other mutations in Lyst||
(F):5'- GCTCTGAAGACTTGCTGTGG -3'
(R):5'- TGTCCTCTAACTACCTCCAGAAAAG -3'
(F):5'- TGCATTAGAGGCTTATCAGAGC -3'
(R):5'- GTTGACAAACTAAAGTTCTTGATAGC -3'