Homo sapiens (human): 51412
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Entry
51412 CDS
T01001
Symbol
ACTL6B, ACTL6, BAF53B, DEE76, EIEE76, IDDSSAD, SMARCN2, arpNalpha
Name
(RefSeq) actin like 6B
KO
K11652
actin-like protein 6B
Organism
hsa
Homo sapiens (human)
Pathway
hsa03082
ATP-dependent chromatin remodeling
hsa04714
Thermogenesis
hsa05225
Hepatocellular carcinoma
Network
nt06529
Thermogenesis
Element
N01688
ADRB3-UCP1 signaling pathway
Disease
H00606
Early infantile epileptic encephalopathy
H02463
Syndromic intellectual developmental disorder
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09120 Genetic Information Processing
09126 Chromosome
03082 ATP-dependent chromatin remodeling
51412 (ACTL6B)
09150 Organismal Systems
09159 Environmental adaptation
04714 Thermogenesis
51412 (ACTL6B)
09160 Human Diseases
09162 Cancer: specific types
05225 Hepatocellular carcinoma
51412 (ACTL6B)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03021 Transcription machinery [BR:
hsa03021
]
51412 (ACTL6B)
03036 Chromosome and associated proteins [BR:
hsa03036
]
51412 (ACTL6B)
Transcription machinery [BR:
hsa03021
]
Eukaryotic type
RNA polymerase II system
Coactivators
BAF/PBAF complex
51412 (ACTL6B)
Chromosome and associated proteins [BR:
hsa03036
]
Eukaryotic type
Chromatin remodeling factors
BAF complex
51412 (ACTL6B)
PBAF complex
51412 (ACTL6B)
GBAF(ncBAF) complex
51412 (ACTL6B)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Actin
MreB_Mbl
Motif
Other DBs
NCBI-GeneID:
51412
NCBI-ProteinID:
NP_057272
OMIM:
612458
HGNC:
160
Ensembl:
ENSG00000077080
UniProt:
O94805
LinkDB
All DBs
Position
7:complement(100643097..100656448)
Genome browser
AA seq
426 aa
AA seq
DB search
MSGGVYGGDEVGALVFDIGSFSVRAGYAGEDCPKADFPTTVGLLAAEEGGGLELEGDKEK
KGKIFHIDTNALHVPRDGAEVMSPLKNGMIEDWECFRAILDHTYSKHVKSEPNLHPVLMS
EAPWNTRAKREKLTELMFEQYNIPAFFLCKTAVLTAFANGRSTGLVLDSGATHTTAIPVH
DGYVLQQGIVKSPLAGDFISMQCRELFQEMAIDIIPPYMIAAKEPVREGAPPNWKKKEKL
PQVSKSWHNYMCNEVIQDFQASVLQVSDSPYDEQVAAQMPTVHYEMPNGYNTDYGAERLR
IPEGLFDPSNVKGLSGNTMLGVGHVVTTSIGMCDIDIRPGLYGSVIVTGGNTLLQGFTDR
LNRELSQKTPPSMRLKLIASNSTMERKFSPWIGGSILASLGTFQQMWISKQEYEEGGKQC
VERKCP
NT seq
1281 nt
NT seq
+upstream
nt +downstream
nt
atgagcgggggcgtctacggcggagatgaggtgggggcgctggtctttgacattggctcc
ttctcagtccgcgctgggtacgctggggaggactgtcccaaggctgacttccccaccaca
gtggggctgctggccgcggaggaggggggcgggctggagctggagggggacaaagagaag
aaagggaagatcttccacatcgacaccaatgccctgcacgtgcctcgggatggagcggag
gtcatgtcgcccctcaagaatggcatgatcgaggactgggagtgcttccgagccatcctg
gatcacacctacagcaaacacgtcaagtctgagccaaacctgcacccagtgctcatgtcc
gaggctccgtggaacacacgggccaagcgggagaagctgacagagctgatgttcgagcag
tacaacattcctgccttcttcttatgcaagacggctgtgctcaccgcctttgcaaacggg
cggtccactggcctcgtgctggacagtggagccacccacaccacggccattccagtacat
gacggctacgttctgcagcaaggcatcgtcaagtcccctctggcaggggacttcatctcc
atgcagtgccgggagctgttccaggagatggccattgacatcatcccaccttacatgatc
gcagccaaggagcctgtccgggagggtgcccccccaaactggaagaagaaggagaagcta
ccccaggtctccaagtcctggcataactacatgtgtaatgaggtgatccaggacttccag
gcctccgtgctgcaggtctcagactccccctacgatgaacaggtggctgcacaaatgccc
acagtgcactacgagatgcccaatggctacaatacagactacggcgccgagcgactccgc
atccctgagggcctgtttgatccctcgaacgtcaagggcctgtcggggaacaccatgttg
ggtgtgggccacgtggtgaccaccagcatcggcatgtgtgacattgatattcgcccgggc
ctgtacgggagtgtcattgtcaccggcgggaacacactgctgcagggcttcactgacagg
ctcaatcgagagctttcccagaagaccccaccgagcatgcgactgaaactcattgccagc
aacagcaccatggagcgcaagttcagcccctggatcgggggttccatcctggcctcactg
ggcactttccagcagatgtggatctccaagcaggaatatgaggagggcgggaagcagtgc
gtggagcgaaagtgcccctga
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