Human Gene FASLG (ENST00000367721.3_4) from GENCODE V47lift37
Description: Fas ligand, transcript variant 1 (from RefSeq NM_000639.3)
Gencode Transcript: ENST00000367721.3_4
Gencode Gene: ENSG00000117560.8_8
Transcript (Including UTRs)
Position: hg19 chr1:172,628,243-172,636,016 Size: 7,774 Total Exon Count: 4 Strand: +
Coding Region
Position: hg19 chr1:172,628,342-172,635,156 Size: 6,815 Coding Exon Count: 4
Data last updated at UCSC: 2024-08-22 23:36:26
Sequence and Links to Tools and Databases
Primer design for this transcript
MalaCards Disease Associations
MalaCards Gene Search: FASLG
Diseases sorted by gene-association score: autoimmune lymphoproliferative syndrome * (1705), faslg-related autoimmune lymphoproliferative syndrome * (200), lung cancer * (167), silicosis (29), lymphoproliferative syndrome (24), hypersensitivity syndrome, carbamazepine-induced (18), t-cell large granular lymphocyte leukemia (16), chronic inflammatory demyelinating polyneuritis (15), hashimoto thyroiditis (11), chronic venous leg ulcers (10), lymphocytic gastritis (10), breast medullary carcinoma (10), erythema multiforme (10), myelopathy, htlv-1-associated (10), chediak-higashi syndrome (10), pneumoconiosis (9), lymphopenia (9), autoimmune lymphoproliferative syndrome, type iii (8), brain glioma (8), viral hepatitis (8), lymphomatoid papulosis (8), sjogren's syndrome (8), cartilage-hair hypoplasia (8), nontoxic goiter (8), thyroiditis (8), type ii mixed cryoglobulinemia (7), acute graft versus host disease (7), graves' disease (7), acute t cell leukemia (7), acute myocarditis (7), hepatitis (6), alopecia areata (6), epstein-barr virus-associated gastric carcinoma (6), fuchs' endothelial dystrophy (6), bile duct carcinoma (6), lymphadenitis (5), hepatocellular carcinoma (5), photokeratitis (5), systemic lupus erythematosus (5), choriocarcinoma of the testis (5), idiopathic neutropenia (5), colorectal cancer (5), chronic nk-cell lymphocytosis (4), chorioretinal scar (4), neutropenia (4), acute hemorrhagic leukoencephalitis (4), sialolithiasis (4), central nervous system tuberculosis (4), stomach cancer (4), malignant glioma (4), granulomatous hepatitis (4), b-cell expansion with nfkb and t-cell anergy (4), aplastic anemia (3), esophageal cancer (3), ovarian cancer, somatic (2), eye disease (2), malaria (1), pulmonary fibrosis, idiopathic (1), diabetes mellitus, insulin-dependent (1)* = Manually curated disease association
Comparative Toxicogenomics Database (CTD)
Common Gene Haplotype Alleles
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RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
Microarray Expression Data
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mRNA Secondary Structure of 3' and 5' UTRs
The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.
Protein Domain and Structure Information
InterPro Domains: Graphical view of domain structure IPR008064 - Fas_ligand
IPR006052 - TNF
IPR006053 - TNF_a/b/c
IPR021184 - TNF_CS
IPR008983 - Tumour_necrosis_fac-like
Pfam Domains: PF00229 - TNF(Tumour Necrosis Factor) family
SCOP Domains: 49842 - TNF-like
ModBase Predicted Comparative 3D Structure on Q53ZZ1
The pictures above may be empty if there is no ModBase structure for the protein. The ModBase structure frequently covers just a fragment of the protein. You may be asked to log onto ModBase the first time you click on the pictures. It is simplest after logging in to just click on the picture again to get to the specific info on that model.
Orthologous Genes in Other Species
Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.
Gene Ontology (GO) Annotations with Structured Vocabulary
Descriptions from all associated GenBank mRNAs
D38122 - Homo sapiens mRNA for Fas ligand, complete cds.E11157 - cDNA encoding human Fas ligand.AK314874 - Homo sapiens cDNA, FLJ95775, Homo sapiens tumor necrosis factor (ligand) superfamily, member 6(TNFSF6), mRNA.HI635191 - Sequence 41038 from Patent EP2242854.HV708946 - JP 2012506450-A/44: Methods for treating eye disorders.JA482178 - Sequence 161 from Patent WO2011072091.JE980470 - Sequence 161 from Patent EP2862929.KJ948655 - Homo sapiens mutant tumor necrosis factor family member 6 (FASLG) mRNA, complete cds.X89102 - H.sapiens mRNA for fasligand.BC017502 - Homo sapiens Fas ligand (TNF superfamily, member 6), mRNA (cDNA clone MGC:23109 IMAGE:4849770), complete cds.JD077865 - Sequence 58889 from Patent EP1572962.U08137 - Human Fas ligand mRNA, complete cds.E11354 - Human cDNA encoding Fas antigen binding protein.AF288573 - Homo sapiens FasL isoform mRNA, complete cds.U11821 - Human Fas ligand (FasL) mRNA, complete cds.AB528416 - Synthetic construct DNA, clone: pF1KB6314, Homo sapiens FASLG gene for Fas ligand, without stop codon, in Flexi system.DQ896147 - Synthetic construct Homo sapiens clone IMAGE:100010607; FLH193394.01L; RZPDo839F1068D Fas ligand (TNF superfamily, member 6) (FASLG) gene, encodes complete protein.DQ893466 - Synthetic construct clone IMAGE:100006096; FLH193398.01X; RZPDo839F1078D Fas ligand (TNF superfamily, member 6) (FASLG) gene, encodes complete protein.CU675998 - Synthetic construct Homo sapiens gateway clone IMAGE:100023387 5' read FASLG mRNA.KJ890694 - Synthetic construct Homo sapiens clone ccsbBroadEn_00088 FASLG gene, encodes complete protein.KR710526 - Synthetic construct Homo sapiens clone CCSBHm_00013802 FASLG (FASLG) mRNA, encodes complete protein.E11156 - cDNA encoding human Fas ligand.E11347 - Human cDNA encoding Fas antigen binding protein.AY225406 - Homo sapiens FAS ligand (TNFSF6) mRNA, complete cds.AY858799 - Homo sapiens CD95 ligand (FASLG) mRNA, complete cds.JD056227 - Sequence 37251 from Patent EP1572962.E11350 - Human cDNA encoding Fas antigen binding protein.JD440482 - Sequence 421506 from Patent EP1572962.JD112774 - Sequence 93798 from Patent EP1572962.JD374484 - Sequence 355508 from Patent EP1572962.JD354209 - Sequence 335233 from Patent EP1572962.JD086830 - Sequence 67854 from Patent EP1572962.JD269237 - Sequence 250261 from Patent EP1572962.JD188486 - Sequence 169510 from Patent EP1572962.
Biochemical and Signaling Pathways
Other Names for This Gene
Alternate Gene Symbols: ENST00000367721.1, ENST00000367721.2, FASLG , hCG_37643 , NM_000639, Q53ZZ1, Q53ZZ1_HUMAN, TNFSF6 , TNLG1A , uc318gdl.1, uc318gdl.2UCSC ID: ENST00000367721.3_4RefSeq Accession: NM_000639.3
Protein: Q53ZZ1
GeneReviews for This Gene
GeneReviews article(s) related to gene FASLG:alps (Autoimmune Lymphoproliferative Syndrome)
Gene Model Information
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Methods, Credits, and Use Restrictions
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for details on how this gene model was made and data restrictions if any.