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Fasl Gene Detail
Summary
  • Symbol
    Fasl
  • Name
    Fas ligand (TNF superfamily, member 6)
  • Synonyms
    APT1LG1, CD178, CD95L, Fasl, Fas-L, Tnfsf6
  • Feature Type
    protein coding gene
  • IDs
    MGI:99255
    NCBI Gene: 14103
  • Gene Overview
    MyGene.info: FASLG
  • Alliance
    gene page
Location & Maps
more
  • Sequence Map
    Chr1:161780689-161788495 bp, - strand
  • From VEGA annotation of GRCm38

    Mouse Genome Browser
  • Download
    Sequence
      7807 bp   ±  kb flank

  • Genome Browsers
    VEGA | Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome 1, 69.95 cM
  • Mapping Data
    22 experiments
Homology
more
  • Human Ortholog
    FASLG, Fas ligand
  • Vertebrate Orthologs
    10
  • Human Ortholog
    FASLG, Fas ligand
    Orthology source: HomoloGene, HGNC
  • Synonyms
    ALPS1B, APT1LG1, APTL, CD178, CD95L, CD95-L, FASL, TNFSF6, TNLG1A
  • Links
    NCBI Gene ID: 356
    neXtProt AC: NX_P48023
    UniProt: P48023

  • Chr Location
    1q24.3; chr1:172659008-172666873 (+)  GRCh38.p7
Human Diseases
more
  • Diseases
    2 with Fasl mouse models; 2 with human FASLG associations

Human Disease Mouse Models
      
IDs
 View 1 model
      
IDs
 View 3 models
      
IDs
Click on a disease name to see all genes associated with that disease.

  • Mutations/Alleles
    2 with disease annotations
  • References
    6 with disease annotations
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    94 phenotypes from 12 alleles in 18 genetic backgrounds
    26 phenotypes from multigenic genotypes
    1 images
    361 phenotype references
Phenotype Overview

adipose tissue
behavior/neurological
cardiovascular system
cellular
craniofacial
digestive/alimentary system
embryo
endocrine/exocrine glands
growth/size/body
hearing/vestibular/ear
hematopoietic system
homeostasis/metabolism
integument
immune system
limbs/digits/tail
liver/biliary system
mortality/aging
muscle
nervous system
pigmentation
renal/urinary system
reproductive system
respiratory system
skeleton
taste/olfaction
neoplasm
vision/eye

Click cells to view annotations.
Mice homozygous for a spontaneous allele, knock-out allele, or allele producting only the soluble isoform exhibit premature death due to the development of systemic lupus erythematosus, autoimmune glomerulonephritis, hepatomegaly, lymphadenopathy, and hypergammaglobulinaemia.
Gene Ontology
(GO)
Classifications
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  • All GO Annotations
    47
  • GO References
    15
Molecular Function

carbohydrate derivative binding
cytoskeletal protein binding
DNA binding
enzyme regulator
hydrolase
ligase
lipid binding
oxidoreductase
receptor binding
RNA binding
transcription
transferase
transporter
Biological Process

nucleic acid-templated transcription
carbohydrate derivative metabolism
cell death
cell differentiation
cell proliferation
cellular component organization
establishment of localization
homeostatic process
immune system process
lipid metabolic process
protein metabolic process
response to stimulus
signaling
system development
Cellular Component

cell projection
cytoplasmic vesicle
cytoskeleton
cytosol
endoplasmic reticulum
endosome
extracellular region
Golgi apparatus
mitochondrion
non-membrane-bounded organelle
nucleus
organelle envelope
organelle lumen
plasma membrane
synapse
vacuole
Click cells to view annotations.
Expression
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Expression Overview

early conceptus
embryo ectoderm
embryo endoderm
embryo mesoderm
embryo mesenchyme
extraembryonic component
alimentary system
auditory system
branchial arches
cardiovascular system
connective tissue
endocrine system
exocrine system
hemolymphoid system
integumental system
limbs
liver and biliary system
musculoskeletal system
nervous system
olfactory system
reproductive system
respiratory system
urinary system
visual system
Click cells to view annotations.


  • Assay Results
    155
  • Tissues
    87
  • cDNA Data
    31
  • Literature Summary
    18
Interactions
less
Sequences &
Gene Models
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Representative SequencesLengthStrain/SpeciesFlank
genomic OTTMUSG00000050992 VEGA Gene Model | MGI Sequence Detail 7807 C57BL/6J ±  kb
transcript OTTMUST00000129297 VEGA | MGI Sequence Detail 1937 Not Applicable  
polypeptide OTTMUSP00000069474 VEGA | MGI Sequence Detail 279 Not Applicable  
For the selected sequence
Polymorphisms
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  • SNPs within 2kb
    159 from dbSNP Build 142
  • PCR
    2
  • RFLP
    1
Protein
Information
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  • UniProt
    5 Sequences
  • Protein Ontology
    PR:000000095 tumor necrosis factor ligand superfamily member 6
    (term hierarchy)
  • InterPro Domains
    IPR028326 Tumor necrosis factor ligand superfamily member 6
    IPR006053 Tumour necrosis factor
    IPR021184 Tumour necrosis factor, conserved site
    IPR006052 Tumour necrosis factor domain
    IPR008983 Tumour necrosis factor-like domain superfamily
Molecular
Reagents
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  • All nucleic 39
    Genomic 4
    cDNA 31
    Primer pair 4

    Microarray probesets 4
Other
Accession IDs
less
MGD-MRK-10104, MGD-MRK-16013
References
more
  • Summaries
    All 544
    Developmental Gene Expression 18
    Diseases 6
    Gene Ontology 15
    Phenotypes 361
  • Earliest
    J:7306 Roths JB, et al., A new mutation, gld, that produces lymphoproliferation and autoimmunity in C3H/HeJ mice. J Exp Med. 1984 Jan 1;159(1):1-20
  • Latest
    J:254062 Chen S, et al., CNS Macrophages Control Neurovascular Development via CD95L. Cell Rep. 2017 May 16;19(7):1378-1393
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
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Send questions and comments to User Support. 		last database update
04/17/2018
MGI 6.11 		The Jackson Laboratory