Homo sapiens (human): 2213
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Entry
2213 CDS
T01001
Symbol
FCGR2B, CD32, CD32B, FCG2, FCGR2, FCGR2C, FcGRIIB, FcRII-c, FcgammaRIIb, IGFR2
Name
(RefSeq) Fc gamma receptor IIb
KO
K12560
low affinity immunoglobulin gamma Fc receptor II-b
Organism
hsa
Homo sapiens (human)
Pathway
hsa04145
Phagosome
hsa04380
Osteoclast differentiation
hsa04662
B cell receptor signaling pathway
hsa04666
Fc gamma R-mediated phagocytosis
hsa05150
Staphylococcus aureus infection
hsa05152
Tuberculosis
hsa05162
Measles
Disease
H00080
Systemic lupus erythematosus
H00361
Malaria
Drug target
Valziflocept:
D11339
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09141 Transport and catabolism
04145 Phagosome
2213 (FCGR2B)
09150 Organismal Systems
09151 Immune system
04662 B cell receptor signaling pathway
2213 (FCGR2B)
04666 Fc gamma R-mediated phagocytosis
2213 (FCGR2B)
09158 Development and regeneration
04380 Osteoclast differentiation
2213 (FCGR2B)
09160 Human Diseases
09172 Infectious disease: viral
05162 Measles
2213 (FCGR2B)
09171 Infectious disease: bacterial
05150 Staphylococcus aureus infection
2213 (FCGR2B)
05152 Tuberculosis
2213 (FCGR2B)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04131 Membrane trafficking [BR:
hsa04131
]
2213 (FCGR2B)
09183 Protein families: signaling and cellular processes
04090 CD molecules [BR:
hsa04090
]
2213 (FCGR2B)
Membrane trafficking [BR:
hsa04131
]
Endocytosis
Phagocytosis
Fc receptors
2213 (FCGR2B)
CD molecules [BR:
hsa04090
]
Proteins
2213 (FCGR2B)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Ig_2
Ig_3
ig
Ig_4
I-set
V-set
Ig_5
Big_7
V-set_CD47
C2-set_2
KIAA1549
ECSCR
Protocadherin
Adeno_E3_CR2
Motif
Other DBs
NCBI-GeneID:
2213
NCBI-ProteinID:
NP_003992
OMIM:
604590
HGNC:
3618
Ensembl:
ENSG00000072694
UniProt:
P31994
Structure
PDB
LinkDB
All DBs
Position
1:161647243..161678654
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AA seq
310 aa
AA seq
DB search
MGILSFLPVLATESDWADCKSPQPWGHMLLWTAVLFLAPVAGTPAAPPKAVLKLEPQWIN
VLQEDSVTLTCRGTHSPESDSIQWFHNGNLIPTHTQPSYRFKANNNDSGEYTCQTGQTSL
SDPVHLTVLSEWLVLQTPHLEFQEGETIVLRCHSWKDKPLVKVTFFQNGKSKKFSRSDPN
FSIPQANHSHSGDYHCTGNIGYTLYSSKPVTITVQAPSSSPMGIIVAVVTGIAVAAIVAA
VVALIYCRKKRISALPGYPECREMGETLPEKPANPTNPDEADKVGAENTITYSLLMHPDA
LEEPDDQNRI
NT seq
933 nt
NT seq
+upstream
nt +downstream
nt
atgggaatcctgtcattcttacctgtccttgccactgagagtgactgggctgactgcaag
tccccccagccttggggtcatatgcttctgtggacagctgtgctattcctggctcctgtt
gctgggacacctgcagctcccccaaaggctgtgctgaaactcgagccccagtggatcaac
gtgctccaggaggactctgtgactctgacatgccgggggactcacagccctgagagcgac
tccattcagtggttccacaatgggaatctcattcccacccacacgcagcccagctacagg
ttcaaggccaacaacaatgacagcggggagtacacgtgccagactggccagaccagcctc
agcgaccctgtgcatctgactgtgctttctgagtggctggtgctccagacccctcacctg
gagttccaggagggagaaaccatcgtgctgaggtgccacagctggaaggacaagcctctg
gtcaaggtcacattcttccagaatggaaaatccaagaaattttcccgttcggatcccaac
ttctccatcccacaagcaaaccacagtcacagtggtgattaccactgcacaggaaacata
ggctacacgctgtactcatccaagcctgtgaccatcactgtccaagctcccagctcttca
ccgatggggatcattgtggctgtggtcactgggattgctgtagcggccattgttgctgct
gtagtggccttgatctactgcaggaaaaagcggatttcagctctcccaggataccctgag
tgcagggaaatgggagagaccctccctgagaaaccagccaatcccactaatcctgatgag
gctgacaaagttggggctgagaacacaatcacctattcacttctcatgcacccggatgct
ctggaagagcctgatgaccagaaccgtatttag
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