Homo sapiens (human): 29760
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Entry
29760 CDS
T01001
Symbol
BLNK, AGM4, BASH, BLNK-S, LY57, SLP-65, SLP65, bca
Name
(RefSeq) B cell linker
KO
K07371
B-cell linker protein
Organism
hsa
Homo sapiens (human)
Pathway
hsa04064
NF-kappa B signaling pathway
hsa04380
Osteoclast differentiation
hsa04662
B cell receptor signaling pathway
hsa05169
Epstein-Barr virus infection
hsa05340
Primary immunodeficiency
Network
nt06160
Human T-cell leukemia virus 1 (HTLV-1)
nt06165
Epstein-Barr virus (EBV)
nt06220
Calcium signaling (cancer)
nt06537
TCR/BCR signaling
Element
N00487
BCR-PLCG-Calcineurin signaling pathway
Disease
H00085
Agammaglobulinemias
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04064 NF-kappa B signaling pathway
29760 (BLNK)
09150 Organismal Systems
09151 Immune system
04662 B cell receptor signaling pathway
29760 (BLNK)
09158 Development and regeneration
04380 Osteoclast differentiation
29760 (BLNK)
09160 Human Diseases
09172 Infectious disease: viral
05169 Epstein-Barr virus infection
29760 (BLNK)
09163 Immune disease
05340 Primary immunodeficiency
29760 (BLNK)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
SH2
Motif
Other DBs
NCBI-GeneID:
29760
NCBI-ProteinID:
NP_037446
OMIM:
604515
HGNC:
14211
Ensembl:
ENSG00000095585
Pharos:
Q8WV28
(Tbio)
UniProt:
Q8WV28
Structure
PDB
PDBj
LinkDB
All DBs
Position
10:complement(96189171..96271569)
Genome browser
AA seq
456 aa
AA seq
DB search
MDKLNKITVPASQKLRQLQKMVHDIKNNEGGIMNKIKKLKVKAPPSVPRRDYASESPADE
EEQWSDDFDSDYENPDEHSDSEMYVMPAEENADDSYEPPPVEQETRPVHPALPFARGEYI
DNRSSQRHSPPFSKTLPSKPSWPSEKARLTSTLPALTALQKPQVPPKPKGLLEDEADYVV
PVEDNDENYIHPTESSSPPPEKAPMVNRSTKPNSSTPASPPGTASGRNSGAWETKSPPPA
APSPLPRAGKKPTTPLKTTPVASQQNASSVCEEKPIPAERHRGSSHRQEAVQSPVFPPAQ
KQIHQKPIPLPRFTEGGNPTVDGPLPSFSSNSTISEQEAGVLCKPWYAGACDRKSAEEAL
HRSNKDGSFLIRKSSGHDSKQPYTLVVFFNKRVYNIPVRFIEATKQYALGRKKNGEEYFG
SVAEIIRNHQHSPLVLIDSQNNTKDSTRLKYAVKVS
NT seq
1371 nt
NT seq
+upstream
nt +downstream
nt
atggacaagcttaataaaataaccgtccccgccagtcagaagttgaggcagcttcaaaag
atggtccatgatattaaaaacaatgaaggtggaataatgaataaaatcaaaaagctaaaa
gtcaaagcacctccaagtgttcctcgaagggactacgcttcagagagccctgctgacgaa
gaggagcagtggtccgatgactttgacagcgactatgaaaatccagatgagcactcggac
tcagagatgtacgtgatgcccgccgaggagaacgctgatgacagctacgagccgcctcca
gtagagcaggaaaccaggccggttcacccagccctgcccttcgccagaggcgagtatata
gacaatcgatcaagccagaggcattccccacccttcagcaagacacttcccagtaagccc
agctggccttcagagaaagcaaggctcacctccaccctgccggccctgactgctttgcag
aaacctcaagtcccacccaaacccaaaggcctccttgaggatgaggctgattatgtggtc
cccgtggaagataatgatgaaaactatattcatcccacagaaagcagttcacctccacct
gaaaaagctcccatggtgaatagatcaaccaagccaaattcctcaacgcccgcctctcct
ccaggaacagcttcaggtcgaaacagtggggcctgggaaaccaagtcacctccaccagct
gcaccatccccgttgccacgggccgggaaaaaaccaacgacaccactgaagacaactcca
gttgcctctcaacagaatgcttcaagtgtttgtgaagaaaaacctatacctgctgaacgc
caccgagggtcaagtcacagacaagaagctgtgcagtcaccagtgtttcctcctgcccag
aaacaaatccaccaaaaacccatacctctgccaagatttacagaagggggaaacccaact
gtggatgggcccctacccagcttttcatctaattccactatttcagaacaggaagctggc
gttctctgcaagccatggtatgctggagcctgtgatcgaaagtctgctgaagaggcattg
cacagatcaaacaaggatggatcatttcttattcggaaaagctctggccatgattccaaa
caaccatatacactagttgtattctttaataagcgagtatataatattcctgtgcgattt
attgaagcaacaaaacaatatgccttgggcagaaagaaaaatggtgaagagtactttgga
agtgttgctgaaatcatcaggaatcatcaacatagtcctttggttcttattgacagtcag
aataacacaaaagattccaccagactgaagtatgcagttaaagtttcataa
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