KEGG   Homo sapiens (human): 51412
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)
SSDB
Motif
Pfam: Actin MreB_Mbl
Other DBs
NCBI-GeneID: 51412
NCBI-ProteinID: NP_057272
OMIM: 612458
HGNC: 160
Ensembl: ENSG00000077080
UniProt: O94805
Position
7:complement(100643097..100656448)
AA seq 426 aa
MSGGVYGGDEVGALVFDIGSFSVRAGYAGEDCPKADFPTTVGLLAAEEGGGLELEGDKEK
KGKIFHIDTNALHVPRDGAEVMSPLKNGMIEDWECFRAILDHTYSKHVKSEPNLHPVLMS
EAPWNTRAKREKLTELMFEQYNIPAFFLCKTAVLTAFANGRSTGLVLDSGATHTTAIPVH
DGYVLQQGIVKSPLAGDFISMQCRELFQEMAIDIIPPYMIAAKEPVREGAPPNWKKKEKL
PQVSKSWHNYMCNEVIQDFQASVLQVSDSPYDEQVAAQMPTVHYEMPNGYNTDYGAERLR
IPEGLFDPSNVKGLSGNTMLGVGHVVTTSIGMCDIDIRPGLYGSVIVTGGNTLLQGFTDR
LNRELSQKTPPSMRLKLIASNSTMERKFSPWIGGSILASLGTFQQMWISKQEYEEGGKQC
VERKCP
NT seq 1281 nt   +upstreamnt  +downstreamnt
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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