Homo sapiens (human): 714
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Entry
714 CDS
T01001
Symbol
C1QC, C1Q-C, C1QD3, C1QG
Name
(RefSeq) complement C1q C chain
KO
K03988
complement C1q subcomponent subunit C
Organism
hsa
Homo sapiens (human)
Pathway
hsa04148
Efferocytosis
hsa04610
Complement and coagulation cascades
hsa04936
Alcoholic liver disease
hsa05020
Prion disease
hsa05133
Pertussis
hsa05142
Chagas disease
hsa05150
Staphylococcus aureus infection
hsa05171
Coronavirus disease - COVID-19
hsa05322
Systemic lupus erythematosus
Network
nt06164
Kaposi sarcoma-associated herpesvirus (KSHV)
nt06171
SARS coronavirus 2 (SARS-CoV-2)
nt06513
Complement cascade
nt06535
Efferocytosis
Element
N01314
SARS-CoV-2 S to classical pathway of complement cascade
N01487
Classical pathway of complement cascade, C4/C2 to C3 convertase formation
N01763
MEGF10-mediated recognition and engulfment
N01764
Calreticulin-LRP1 mediated recognition and engulfment
Disease
H00102
Classic complement pathway component defects
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09141 Transport and catabolism
04148 Efferocytosis
714 (C1QC)
09150 Organismal Systems
09151 Immune system
04610 Complement and coagulation cascades
714 (C1QC)
09160 Human Diseases
09172 Infectious disease: viral
05171 Coronavirus disease - COVID-19
714 (C1QC)
09171 Infectious disease: bacterial
05133 Pertussis
714 (C1QC)
05150 Staphylococcus aureus infection
714 (C1QC)
09174 Infectious disease: parasitic
05142 Chagas disease
714 (C1QC)
09163 Immune disease
05322 Systemic lupus erythematosus
714 (C1QC)
09164 Neurodegenerative disease
05020 Prion disease
714 (C1QC)
09167 Endocrine and metabolic disease
04936 Alcoholic liver disease
714 (C1QC)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04131 Membrane trafficking [BR:
hsa04131
]
714 (C1QC)
Membrane trafficking [BR:
hsa04131
]
Endocytosis
Phagocytosis
Opsonins
714 (C1QC)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
C1q
Collagen
BclA_C
Motif
Other DBs
NCBI-GeneID:
714
NCBI-ProteinID:
NP_001107573
OMIM:
120575
HGNC:
1245
Ensembl:
ENSG00000159189
UniProt:
P02747
A0A024RAA7
Structure
PDB
PDBj
LinkDB
All DBs
Position
1:22643633..22648108
Genome browser
AA seq
245 aa
AA seq
DB search
MDVGPSSLPHLGLKLLLLLLLLPLRGQANTGCYGIPGMPGLPGAPGKDGYDGLPGPKGEP
GIPAIPGIRGPKGQKGEPGLPGHPGKNGPMGPPGMPGVPGPMGIPGEPGEEGRYKQKFQS
VFTVTRQTHQPPAPNSLIRFNAVLTNPQGDYDTSTGKFTCKVPGLYYFVYHASHTANLCV
LLYRSGVKVVTFCGHTSKTNQVNSGGVLLRLQVGEEVWLAVNDYYDMVGIQGSDSVFSGF
LLFPD
NT seq
738 nt
NT seq
+upstream
nt +downstream
nt
atggacgtggggcccagctccctgccccaccttgggctgaagctgctgctgctcctgctg
ctgctgcccctcaggggccaagccaacacaggctgctacgggatcccagggatgcccggc
ctgcccggggcaccagggaaggatgggtacgacggactgccggggcccaagggggagcca
ggaatcccagccattcccgggatccgaggacccaaagggcagaagggagaacccggctta
cccggccatcctgggaaaaatggccccatgggaccccctgggatgccaggggtgcccggc
cccatgggcatccctggagagccaggtgaggagggcagatacaagcagaaattccagtca
gtgttcacggtcactcggcagacccaccagccccctgcacccaacagcctgatcagattc
aacgcggtcctcaccaacccgcagggagattatgacacgagcactggcaagttcacctgc
aaagtccccggcctctactactttgtctaccacgcgtcgcatacagccaacctgtgcgtg
ctgctgtaccgcagcggcgtcaaagtggtcaccttctgtggccacacgtccaaaaccaat
caggtcaactcgggcggtgtgctgctgaggttgcaggtgggcgaggaggtgtggctggct
gtcaatgactactacgacatggtgggcatccagggctctgacagcgtcttctccggcttc
ctgctcttccccgactag
DBGET
integrated database retrieval system
