Homo sapiens (human): 633
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Entry
633 CDS
T01001
Symbol
BGN, DSPG1, MRLS, PG-S1, PGI, SEMDX, SLRR1A
Name
(RefSeq) biglycan
KO
K08118
biglycan
Organism
hsa
Homo sapiens (human)
Pathway
hsa04820
Cytoskeleton in muscle cells
Network
nt06539
Cytoskeleton in muscle cells
Element
N01814
Extracellular matrix - Basal lamina
Disease
H02187
Spondyloepimetaphyseal dysplasia
H02720
Meester-Loeys syndrome
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09142 Cell motility
04820 Cytoskeleton in muscle cells
633 (BGN)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00535 Proteoglycans [BR:
hsa00535
]
633 (BGN)
Proteoglycans [BR:
hsa00535
]
Extracellular matrix (ECM) proteoglycans
Small leucine-rich proteoglycan (SLRP) family
class I
633 (BGN)
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SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
LRR_8
LRR_4
LRR_1
LRRNT
LRR_9
LRR_14
LRR_5
Motif
Other DBs
NCBI-GeneID:
633
NCBI-ProteinID:
NP_001702
OMIM:
301870
HGNC:
1044
Ensembl:
ENSG00000182492
UniProt:
P21810
B4DNL4
LinkDB
All DBs
Position
X:153494980..153509546
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AA seq
368 aa
AA seq
DB search
MWPLWRLVSLLALSQALPFEQRGFWDFTLDDGPFMMNDEEASGADTSGVLDPDSVTPTYS
AMCPFGCHCHLRVVQCSDLGLKSVPKEISPDTTLLDLQNNDISELRKDDFKGLQHLYALV
LVNNKISKIHEKAFSPLRKLQKLYISKNHLVEIPPNLPSSLVELRIHDNRIRKVPKGVFS
GLRNMNCIEMGGNPLENSGFEPGAFDGLKLNYLRISEAKLTGIPKDLPETLNELHLDHNK
IQAIELEDLLRYSKLYRLGLGHNQIRMIENGSLSFLPTLRELHLDNNKLARVPSGLPDLK
LLQVVYLHSNNITKVGVNDFCPMGFGVKRAYYNGISLFNNPVPYWEVQPATFRCVTDRLA
IQFGNYKK
NT seq
1107 nt
NT seq
+upstream
nt +downstream
nt
atgtggcccctgtggcgcctcgtgtctctgctggccctgagccaggccctgccctttgag
cagagaggcttctgggacttcaccctggacgatgggccattcatgatgaacgatgaggaa
gcttcgggcgctgacacctcgggcgtcctggacccggactctgtcacacccacctacagc
gccatgtgtcctttcggctgccactgccacctgcgggtggttcagtgctccgacctgggt
ctgaagtctgtgcccaaagagatctcccctgacaccacgctgctggacctgcagaacaac
gacatctccgagctccgcaaggatgacttcaagggtctccagcacctctacgccctcgtc
ctggtgaacaacaagatctccaagatccatgagaaggccttcagcccactgcggaagctg
cagaagctctacatctccaagaaccacctggtggagatcccgcccaacctacccagctcc
ctggtggagctccgcatccacgacaaccgcatccgcaaggtgcccaagggagtgttcagc
gggctccggaacatgaactgcatcgagatgggcgggaacccactggagaacagtggcttt
gaacctggagccttcgatggcctgaagctcaactacctgcgcatctcagaggccaagctg
actggcatccccaaagacctccctgagaccctgaatgaactccacctagaccacaacaaa
atccaggccatcgaactggaggacctgcttcgctactccaagctgtacaggctgggccta
ggccacaaccagatcaggatgatcgagaacgggagcctgagcttcctgcccaccctccgg
gagctccacttggacaacaacaagttggccagggtgccctcagggctcccagacctcaag
ctcctccaggtggtctatctgcactccaacaacatcaccaaagtgggtgtcaacgacttc
tgtcccatgggcttcggggtgaagcgggcctactacaacggcatcagcctcttcaacaac
cccgtgccctactgggaggtgcagccggccactttccgctgcgtcactgaccgcctggcc
atccagtttggcaactacaaaaagtag
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