Search results for FANCC

Showing 14 results out of 1,615 in All results

Reactions, pathways & diseases (38 results found)


Stable Id: REACT_18816
Type: Protein
Species: Homo sapiens

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Source: Reactome  ID: 419530

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Genomes (65 results found)

Fanconi anemia, complementation group C

Approved Symbol: FANCC
Approved Name: Fanconi anemia, complementation group C
Status: (Approved)
Aliases: FAC FA3
Locus Type: gene with protein product
Chromosome: 9q22.3

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Source: HGNC  ID: HGNC:3584

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Nucleotide sequences (106 results found)


Bos taurus (cattle) FANCC protein

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Source: Coding (Release)  ID: AAI42140


Danio rerio (zebrafish) fancc protein

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Source: Coding (Release)  ID: AAI25958

View all 106 results for Nucleotide sequences

Protein sequences (362 results found)



Fanconi anemia group C protein Protein FACC
Homo sapiens (Reviewed)
Secondary accession number(s): B1ALR8

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Source: UniProtKB  ID: FANCC_HUMAN

View all 362 results for Protein sequences

Macromolecular structures (1 results found)

Crystal structure of the BTB domain from FAZF/ZBTB32

Accession: 3m5b
TRANSCRIPTION x-ray diffraction entry at resolution 2

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Source: PDBe  ID: 3m5b

Gene expression (661 results found)


Homo sapiens FANCC, Fanconi anemia, complementation group C [Source:HGNC Symbol;Acc:HGNC:3584], is expressed in 4 baseline experiment(s); cell line: H1-hESC, SK-N-SH, HUVEC cell line, HSMM cell line, HMEC cell line, hMSC-AT cell line, GM12878, IMR-90, K562, NHEK cell line, MCF-7, BJ, HepG2, HeLa-S3 ...

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Source: Baseline Expression Atlas Genes  ID: ENSG00000158169

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Molecular interactions (41 results found)


BD-FANCE interacts with AD-FANCC in a yeast two-hybrid assay

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Source: IntAct Interactions  ID: EBI-1377978


BD-FANCC interacts with AD-FANCE in a yeast two-hybrid assay

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Source: IntAct Interactions  ID: EBI-1377990

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Protein families (3 results found)


awaiting family name
awaiting annotation

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Source: TreeFam  ID: TF330803

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Samples & ontologies (92 results found)


Sample Name: source GSM444469 1 Organism: Homo sapiens subtype: clear cell mutation: ADH6 mutation: FANCC mutation: TNFRSF19 mutation: VHL mutation: XRCC6

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Source: BioSamples  ID: SAMEA163345

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