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FTCD (formimidoyltransferase cyclodeaminase)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
10841
Gene nameGene Name - the full gene name approved by the HGNC.
Formimidoyltransferase cyclodeaminase
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
FTCD
SynonymsGene synonyms aliases
LCHC1
ChromosomeChromosome number
21
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
21q22.3
SummarySummary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is a bifunctional enzyme that channels 1-carbon units from formiminoglutamate, a metabolite of the histidine degradation pathway, to the folate pool. Mutations in this gene are associated with glutamate formiminotransferas
SNPsSNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs149266909 A>G,T Pathogenic Non coding transcript variant, coding sequence variant, stop gained, synonymous variant, genic downstream transcript variant, missense variant
rs200283734 G>A Conflicting-interpretations-of-pathogenicity Genic downstream transcript variant, missense variant, non coding transcript variant, coding sequence variant
rs398124234 ->C Pathogenic-likely-pathogenic, conflicting-interpretations-of-pathogenicity Frameshift variant, coding sequence variant, non coding transcript variant
rs777099958 ->C Conflicting-interpretations-of-pathogenicity Frameshift variant, genic downstream transcript variant, coding sequence variant, non coding transcript variant
miRNAmiRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT018835 hsa-miR-335-5p Microarray 18185580
MIRT715545 hsa-miR-483-3p HITS-CLIP 19536157
MIRT715544 hsa-miR-668-3p HITS-CLIP 19536157
MIRT715543 hsa-miR-4722-3p HITS-CLIP 19536157
MIRT715542 hsa-miR-6727-3p HITS-CLIP 19536157
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000139 Component Golgi membrane IDA 14697341
GO:0000139 Component Golgi membrane ISS
GO:0005515 Function Protein binding IPI 25416956, 32296183
GO:0005542 Function Folic acid binding IEA
GO:0005737 Component Cytoplasm TAS 10029623
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
UniProt ID O95954
Protein name Formimidoyltransferase-cyclodeaminase (Formiminotransferase-cyclodeaminase) (FTCD) (LCHC1) [Includes: Glutamate formimidoyltransferase (EC 2.1.2.5) (Glutamate formiminotransferase) (Glutamate formyltransferase); Formimidoyltetrahydrofolate cyclodeaminase
Protein function Folate-dependent enzyme, that displays both transferase and deaminase activity. Serves to channel one-carbon units from formiminoglutamate to the folate pool. ; Binds and promotes bundling of vimentin fila
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07837 FTCD_N
4 179
Formiminotransferase domain, N-terminal subdomain
Domain
PF02971 FTCD
181 324
Formiminotransferase domain
Domain
PF04961 FTCD_C
339 520
Formiminotransferase-cyclodeaminase
Family
Sequence
Sequence length 541
Interactions View interactions
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
 
KEGG
 
Reactome
  Histidine metabolism
One carbon pool by folate
Metabolic pathways
  Histidine catabolism
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Anemia Anemia, Megaloblastic rs118204044, rs118204045, rs118204046, rs121918330, rs869320719, rs869312029, rs121918332, rs869320724, rs767094129, rs786205058, rs786205059, rs137853119, rs137853120, rs137853121, rs1384933966, rs137853122, rs137853123, rs786205060, rs267607121, rs121908584, rs80338697, rs80338699, rs120074166, rs120074167, rs1050828, rs74575103, rs137852314, rs5030868, rs137852316, rs137852317, rs137852318, rs137852319, rs137852320, rs137852321, rs137852322, rs137852323, rs137852324, rs72554665, rs387906468, rs5030872, rs137852326, rs137852333, rs137852327, rs137852328, rs137852329, rs137852330, rs137852331, rs137852332, rs137852334, rs137852335, rs137852336, rs137852339, rs76645461, rs137852340, rs137852341, rs78478128, rs137852343, rs137852344, rs137852345, rs587776730, rs137852346, rs137852347, rs137852349, rs2070404412, rs2070350038, rs2070350009, rs137852303, rs137852304, rs33946267, rs34378160, rs33933298, rs11549407, rs35724775, rs34598529, rs41469945, rs267607201, rs80338694, rs80338696, rs387907018, rs398123546, rs78365220, rs587777100, rs587777101, rs483352840, rs869312752, rs765487627, rs1557229599, rs1557230040, rs1555524842, rs782090947, rs1358275550, rs1557229736, rs1557230573, rs1556323334, rs1233124208, rs1293528130, rs146864395, rs1595503440, rs1603411214, rs137852325, rs1575247302, rs1603411177, rs1336651679, rs782322505
Burkitt`s lymphoma Burkitt Lymphoma, Burkitt Leukemia rs28933407, rs121918683, rs121918684 23143597
Glutamate formiminotransferase deficiency Glutamate formiminotransferase deficiency rs398124234, rs149266909, rs374724805, rs8133955, rs775788856, rs140217223 12815595, 29178637, 25689098, 26633545
Age-related macular degeneration Age related macular degeneration rs2133900556, rs199474657, rs2274700, rs1410996, rs61750120, rs1800728, rs62654397, rs61749423, rs61751412, rs61749439, rs61751398, rs61752417, rs62645946, rs1801269, rs62646860, rs61750142, rs61750145, rs61750152, rs61751377, rs61753029, rs61751407, rs61751389, rs61750645, rs61750648, rs879255520, rs752147871, rs886044750, rs886044749, rs746541266, rs756840095, rs886044725, rs749526785, rs1057518955, rs1057518767, rs371489809, rs1064793014, rs1571264574, rs1659524475 31120506
Unknown
Disease name Disease term dbSNP ID References
African burkitt`s lymphoma African Burkitt`s lymphoma 23143597

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