Homo sapiens (human): 1379
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Entry
1379 CDS
T01001
Symbol
CR1L
Name
(RefSeq) complement C3b/C4b receptor 1 like
KO
K04011
complement component (3b/4b) receptor 1
Organism
hsa
Homo sapiens (human)
Pathway
hsa04610
Complement and coagulation cascades
hsa04613
Neutrophil extracellular trap formation
hsa04640
Hematopoietic cell lineage
hsa05134
Legionellosis
hsa05140
Leishmaniasis
hsa05144
Malaria
hsa05152
Tuberculosis
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09150 Organismal Systems
09151 Immune system
04640 Hematopoietic cell lineage
1379 (CR1L)
04610 Complement and coagulation cascades
1379 (CR1L)
04613 Neutrophil extracellular trap formation
1379 (CR1L)
09160 Human Diseases
09171 Infectious disease: bacterial
05134 Legionellosis
1379 (CR1L)
05152 Tuberculosis
1379 (CR1L)
09174 Infectious disease: parasitic
05144 Malaria
1379 (CR1L)
05140 Leishmaniasis
1379 (CR1L)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04131 Membrane trafficking [BR:
hsa04131
]
1379 (CR1L)
09183 Protein families: signaling and cellular processes
04090 CD molecules [BR:
hsa04090
]
1379 (CR1L)
Membrane trafficking [BR:
hsa04131
]
Endocytosis
Phagocytosis
Integrins (complement receptors)
1379 (CR1L)
CD molecules [BR:
hsa04090
]
Proteins
1379 (CR1L)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Sushi
Motif
Other DBs
NCBI-GeneID:
1379
NCBI-ProteinID:
NP_783641
OMIM:
605886
HGNC:
2335
Ensembl:
ENSG00000197721
UniProt:
Q2VPA4
LinkDB
All DBs
Position
1:207645133..207723703
Genome browser
AA seq
569 aa
AA seq
DB search
MAPPVRLERPFPSRRFPGLLLAALVLLLSSFSDQCNVPEWLPFARPTNLTDDFEFPIGTY
LNYECRPGYSGRPFSIICLKNSVWTSAKDKCKRKSCRNPPDPVNGMAHVIKDIQFRSQIK
YSCPKGYRLIGSSSATCIISGNTVIWDNKTPVCDRIICGLPPTIANGDFTSISREYFHYG
SVVTYHCNLGSRGKKVFELVGEPSIYCTSKDDQVGIWSGPAPQCIIPNKCTPPNVENGIL
VSDNRSLFSLNEVVEFRCQPGFGMKGPSHVKCQALNKWEPELPSCSRVCQPPPDVLHAER
TQRDKDNFSPGQEVFYSCEPGYDLRGSTYLHCTPQGDWSPAAPRCEVKSCDDFLGQLPNG
HVLFPLNLQLGAKVDFVCDEGFQLKGSSASYCVLAGMESLWNSSVPVCERKSCETPPVPV
NGMVHVITDIHVGSRINYSCTTGHRLIGHSSAECILSGNTAHWSMKPPICQQIFCPNPPA
ILNGRHTGTPLGDIPYGKEVSYTCDPHPDRGMTFNLIGESTIRRTSEPHGNGVWSSPAPR
CELPVGAGSHDALIVGKFYEVFAEEFCHL
NT seq
1710 nt
NT seq
+upstream
nt +downstream
nt
atggcgcctcccgtccgtctcgagcgtccctttccttcccggcgctttcctgggttgctt
ctggcggccctggtgttgctgctgtcctccttctccgatcaatgcaatgtcccggaatgg
cttccatttgccaggcctaccaacctaactgatgactttgagtttcccattgggacatat
ctgaactatgaatgccgccctggttattccggaagaccgttttctatcatctgcctaaaa
aactcagtctggacaagtgctaaggacaagtgcaaacgtaaatcatgtcgtaatcctcca
gatcctgtgaatggcatggcacatgtgatcaaagacatccagttcagatcccaaattaaa
tattcttgtcctaaaggataccgactcattggttcctcgtctgccacatgcatcatctca
ggcaacactgtcatttgggataataaaacacctgtttgtgacagaattatttgtgggcta
ccccccaccatcgccaatggagatttcactagcatcagcagagagtattttcactatgga
tcagtggtgacctaccactgcaatcttggaagcagagggaaaaaggtgtttgagcttgtg
ggtgagccctccatatactgcaccagcaaagatgatcaagtgggcatctggagtggccca
gcccctcagtgcattatacctaacaaatgcacgcctccaaatgtggaaaatggaatattg
gtatctgacaacagaagcttattttccttaaatgaagttgtggagtttaggtgtcagcct
ggctttggcatgaaagggccctcccatgtgaagtgccaggccctgaacaaatgggagcca
gagttaccaagctgctccagggtatgtcagccacctccagatgtcctgcatgctgagcgt
acccaaagggacaaggacaacttttcacccgggcaggaagtgttctacagctgtgagccc
ggctacgacctcagaggatctacgtatttgcactgcacaccccagggagactggagccct
gcagcccccagatgtgaagtgaaatcctgtgatgacttcctgggccaacttcctaatggc
catgtgctatttccacttaatctccagcttggagcaaaagtggattttgtttgtgatgaa
ggatttcaattaaaaggcagctctgctagttactgtgttttggctggaatggaaagcctt
tggaatagcagtgttccagtgtgtgaacgtaaatcatgtgaaactcctccagttccagtg
aatggcatggtgcatgtgatcacagacatccatgttggatccagaatcaactattcttgt
actacagggcaccgactcattggtcactcatctgctgaatgtatcctctcgggcaatact
gcccattggagcatgaagccaccaatttgtcaacaaatcttttgtccaaatcctccagct
atccttaatgggagacacacaggaactccccttggagatattccctatggaaaagaagta
tcttacacatgtgacccccacccagacagagggatgaccttcaacctcattggggagagc
accatccgccgcacaagtgaacctcatgggaatggggtttggagcagccctgcccctcgc
tgtgaacttcctgttggtgctggttcacatgatgctcttatagttggtaagttttatgaa
gtgtttgctgaggaattctgtcatctttaa
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