Homo sapiens (human): 7123
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Entry
7123 CDS
T01001
Symbol
CLEC3B, MCDR4, TN, TNA
Name
(RefSeq) C-type lectin domain family 3 member B
KO
K17520
C-type lectin domain family 3 member B
Organism
hsa
Homo sapiens (human)
Disease
H01770
Macular dystrophy
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04091 Lectins [BR:
hsa04091
]
7123 (CLEC3B)
Lectins [BR:
hsa04091
]
C-Type lectins
Others
7123 (CLEC3B)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Lectin_C
Chordopox_A33R
DUF2304
Motif
Other DBs
NCBI-GeneID:
7123
NCBI-ProteinID:
NP_003269
OMIM:
187520
HGNC:
11891
Ensembl:
ENSG00000163815
UniProt:
P05452
Structure
PDB
PDBj
LinkDB
All DBs
Position
3:45026303..45036071
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AA seq
202 aa
AA seq
DB search
MELWGAYLLLCLFSLLTQVTTEPPTQKPKKIVNAKKDVVNTKMFEELKSRLDTLAQEVAL
LKEQQALQTVCLKGTKVHMKCFLAFTQTKTFHEASEDCISRGGTLGTPQTGSENDALYEY
LRQSVGNEAEIWLGLNDMAAEGTWVDMTGARIAYKNWETEITAQPDGGKTENCAVLSGAA
NGKWFDKRCRDQLPYICQFGIV
NT seq
609 nt
NT seq
+upstream
nt +downstream
nt
atggagctctggggggcctacctcctcctctgcctcttctccctcctgacccaggtcacc
accgagccaccaacccagaagcccaagaagattgtaaatgccaagaaagatgttgtgaac
acaaagatgtttgaggagctcaagagccgtctggacaccctggcccaggaggtggccctg
ctgaaggagcagcaggccctgcagacggtctgcctgaaggggaccaaggtgcacatgaaa
tgctttctggccttcacccagacgaagaccttccacgaggccagcgaggactgcatctcg
cgcgggggcaccctgggcacccctcagactggctcggagaacgacgccctgtatgagtac
ctgcgccagagcgtgggcaacgaggccgagatctggctgggcctcaacgacatggcggcc
gagggcacctgggtggacatgaccggcgcccgcatcgcctacaagaactgggagactgag
atcaccgcgcaacccgatggcggcaagaccgagaactgcgcggtcctgtcaggcgcggcc
aacggcaagtggttcgacaagcgctgccgcgatcagctgccctacatctgccagttcggg
atcgtgtag
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