Human Gene C3 (ENST00000245907.11_8) from GENCODE V47lift37
Description: complement C3 (from RefSeq NM_000064.4)
Gencode Transcript: ENST00000245907.11_8
Gencode Gene: ENSG00000125730.18_15
Transcript (Including UTRs)
Position: hg19 chr19:6,677,715-6,720,661 Size: 42,947 Total Exon Count: 41 Strand: -
Coding Region
Position: hg19 chr19:6,677,893-6,720,600 Size: 42,708 Coding Exon Count: 41
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: C3
Diseases sorted by gene-association score: c3 deficiency * (1675), hemolytic uremic syndrome, atypical 5 * (1256), macular degeneration, age-related, 9 * (980), c3-related atypical hemolytic-uremic syndrome * (100), macular degeneration, age-related, 1 * (36), hemolytic-uremic syndrome (30), membranoproliferative glomerulonephritis (24), complement deficiency (23), glomerulonephritis (23), arteriolosclerosis (21), c3 glomerulopathy (18), complement factor i deficiency (17), chronic monocytic leukemia (15), proliferative glomerulonephritis (13), dense deposit disease (13), eye disease (10), herpes simplex (9), tick-borne relapsing fever (9), acquired angioedema (9), c4a deficiency (9), hemoglobinuria (8), retinal drusen (8), pneumococcal meningitis (8), c1s deficiency (8), afibrinogenemia (8), afibrinogenemia, congenital (7), lyme disease (7), orthostatic proteinuria (7), gerstmann-straussler disease (7), paroxysmal nocturnal hemoglobinuria (7), hypersensitivity reaction type iii disease (7), systemic lupus erythematosus (6), phototoxic dermatitis (6), hypersensitivity vasculitis (6), neisseria meningitidis infection (6), lichen nitidus (6), membranous nephropathy (6), acute maxillary sinusitis (6), ascending cholangitis (6), lipoprotein lipase deficiency (6), dysbaric osteonecrosis (5), pediatric systemic lupus erythematosus (5), chronic maxillary sinusitis (5), lupus erythematosus (5), occupational dermatitis (5), henoch-schoenlein purpura (5), deafness, autosomal dominant 25 (5), lemierre's syndrome (5), rhizomelic chondrodysplasia punctata, type 2 (4), autoimmune disease of blood (4), obesity (3), vaccinia (3), heart disease (2)* = 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.
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.
Descriptions from all associated GenBank mRNAs
BC150299 - Homo sapiens cDNA clone IMAGE:8860379, containing frame-shift errors.BC063852 - Homo sapiens cDNA clone IMAGE:6184508, containing frame-shift errors.BC150179 - Homo sapiens complement component 3, mRNA (cDNA clone MGC:164898 IMAGE:40148091), complete cds.BC150200 - Homo sapiens complement component 3, mRNA (cDNA clone MGC:165040 IMAGE:40148812), complete cds.EU794602 - Homo sapiens epididymis secretory sperm binding protein Li 62p (HEL-S-62p) mRNA, complete cds.AK304071 - Homo sapiens cDNA FLJ57339 complete cds, highly similar to Complement C3 precursor.BC022897 - Homo sapiens cDNA clone IMAGE:4714760, containing frame-shift errors.K02765 - Human complement component C3 mRNA, alpha and beta subunits, complete cds.MP282919 - Sequence 74 from Patent EP3526328.AK094728 - Homo sapiens cDNA FLJ37409 fis, clone BRAMY2028516, highly similar to COMPLEMENT C3 PRECURSOR.FU269668 - COMPOSITIONS AND METHODS FOR REGULATING COMPLEMENT SYSTEM.FU269678 - COMPOSITIONS AND METHODS FOR REGULATING COMPLEMENT SYSTEM.FU269677 - COMPOSITIONS AND METHODS FOR REGULATING COMPLEMENT SYSTEM.FU269670 - COMPOSITIONS AND METHODS FOR REGULATING COMPLEMENT SYSTEM.FU269681 - COMPOSITIONS AND METHODS FOR REGULATING COMPLEMENT SYSTEM.FU269673 - COMPOSITIONS AND METHODS FOR REGULATING COMPLEMENT SYSTEM.FU269675 - COMPOSITIONS AND METHODS FOR REGULATING COMPLEMENT SYSTEM.FU269667 - COMPOSITIONS AND METHODS FOR REGULATING COMPLEMENT SYSTEM.KC493376 - Homo sapiens clone TB1 complement component 3 (C3) pseudogene mRNA, partial sequence.KC493377 - Homo sapiens clone TB2 complement component 3 (C3) pseudogene mRNA, partial sequence.FU269671 - COMPOSITIONS AND METHODS FOR REGULATING COMPLEMENT SYSTEM.AK299114 - Homo sapiens cDNA FLJ60818 complete cds, highly similar to Complement C3 precursor.M55658 - Human complement C3 protein mRNA, 5' flank.JD365117 - Sequence 346141 from Patent EP1572962.JD226698 - Sequence 207722 from Patent EP1572962.JD150363 - Sequence 131387 from Patent EP1572962.
Biochemical and Signaling Pathways
Other Names for This Gene
Alternate Gene Symbols: ENST00000245907.1, ENST00000245907.10, ENST00000245907.2, ENST00000245907.3, ENST00000245907.4, ENST00000245907.5, ENST00000245907.6, ENST00000245907.7, ENST00000245907.8, ENST00000245907.9, HEL-S-62p , NM_000064, uc317ers.1, uc317ers.2, V9HWA9, V9HWA9_HUMANUCSC ID: ENST00000245907.11_8RefSeq Accession: NM_000064.4
GeneReviews for This Gene
GeneReviews article(s) related to gene C3:husa (Genetic Atypical Hemolytic-Uremic Syndrome)mpgn (C3 Glomerulopathy)
Gene Model Information
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for a detailed description of the fields of the table above.
Methods, Credits, and Use Restrictions
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for details on how this gene model was made and data restrictions if any.