Gene Gene information from NCBI Gene database.
Entrez ID 125061
Gene name Arylformamidase
Gene symbol AFMID
Synonyms (NCBI Gene)
FKFKFKFA
Chromosome 17
Chromosome location 17q25.3
miRNA miRNA information provided by mirtarbase database.
345
miRTarBase ID miRNA Experiments Reference
MIRT441249 hsa-miR-374a-5p HITS-CLIP 22473208
MIRT441249 hsa-miR-374a-5p HITS-CLIP 22473208
MIRT771467 hsa-miR-1207-5p CLIP-seq
MIRT771468 hsa-miR-1262 CLIP-seq
MIRT771469 hsa-miR-2114 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
12
GO ID Ontology Definition Evidence Reference
GO:0004061 Function Arylformamidase activity IEA
GO:0005515 Function Protein binding IPI 32296183
GO:0005634 Component Nucleus IEA
GO:0005737 Component Cytoplasm IBA
GO:0005737 Component Cytoplasm IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
621151 20910 ENSG00000183077
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q63HM1
Protein name Kynurenine formamidase (KFA) (KFase) (EC 3.5.1.9) (Arylformamidase) (N-formylkynurenine formamidase) (FKF)
Protein function Catalyzes the hydrolysis of N-formyl-L-kynurenine to L-kynurenine, the second step in the kynurenine pathway of tryptophan degradation. Kynurenine may be further oxidized to nicotinic acid, NAD(H) and NADP(H). Required for elimination of toxic m
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07859 Abhydrolase_3 91 282 alpha/beta hydrolase fold Domain
Sequence
Sequence length 303
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG 
  Tryptophan metabolism
Glyoxylate and dicarboxylate metabolism
Metabolic pathways
Biosynthesis of cofactors
 
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
DIVERTICULAR DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Amyotrophic lateral sclerosis 1 Associate 34194442
★☆☆☆☆
Found in Text Mining only
Colorectal Neoplasms Stimulate 31416966
★☆☆☆☆
Found in Text Mining only
Leiomyoma Associate 35715314
★☆☆☆☆
Found in Text Mining only