Homo sapiens (human): 9275
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Entry
9275 CDS
T01001
Symbol
BCL7B, SMARCJ2
Name
(RefSeq) BAF chromatin remodeling complex subunit BCL7B
KO
K25605
B-cell CLL/lymphoma 7 protein
Organism
hsa
Homo sapiens (human)
Pathway
hsa03082
ATP-dependent chromatin remodeling
Disease
H01439
Williams-Beuren syndrome
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09120 Genetic Information Processing
09126 Chromosome
03082 ATP-dependent chromatin remodeling
9275 (BCL7B)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins [BR:
hsa03036
]
9275 (BCL7B)
Chromosome and associated proteins [BR:
hsa03036
]
Eukaryotic type
Chromatin remodeling factors
BAF complex
9275 (BCL7B)
PBAF complex
9275 (BCL7B)
GBAF(ncBAF) complex
9275 (BCL7B)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
BCL_N
Motif
Other DBs
NCBI-GeneID:
9275
NCBI-ProteinID:
NP_001698
OMIM:
605846
HGNC:
1005
Ensembl:
ENSG00000106635
UniProt:
Q9BQE9
LinkDB
All DBs
Position
7:complement(73536356..73557690)
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AA seq
202 aa
AA seq
DB search
MSGRSVRAETRSRAKDDIKKVMAAIEKVRKWEKKWVTVGDTSLRIFKWVPVTDSKEKEKS
KSNSSAAREPNGFPSDASANSSLLLEFQDENSNQSSVSDVYQLKVDSSTNSSPSPQQSES
LSPAHTSDFRTDDSQPPTLGQEILEEPSLPSSEVADEPPTLTKEEPVPLETQVVEEEEDS
GAPPLKRFCVDQPTVPQTASES
NT seq
609 nt
NT seq
+upstream
nt +downstream
nt
atgtcgggccggtcggtccgggcggagacccgcagccgggccaaggacgacatcaagaag
gtgatggcggccatcgagaaagtgcggaaatgggagaagaagtgggtgactgtgggtgac
acgtccctgaggatatttaagtgggttcctgtgacagacagcaaggagaaagaaaagtca
aaatcgaacagttcagcagcccgagaacctaatggctttccttctgatgcctcagccaat
tcctctctccttcttgaattccaggacgaaaacagcaaccagagttccgtgtctgacgtc
tatcagcttaaggtggacagcagcaccaactcaagccccagcccccagcagagtgagtcc
ctgagcccagcacacacctccgacttccgcacggatgactcccagcccccaacgctgggc
caggagatcctggaggagccctccctgccctcctcggaagttgctgatgaacctcctacc
ctcaccaaggaagaaccagttccactagagacacaggtcgttgaggaagaggaagactca
ggtgccccgcccctgaagcgcttctgtgtggaccaacccacagtgccgcagacggcgtca
gaaagctag
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