KEGG   Homo sapiens (human): 6602
Entry
6602              CDS       T01001                                 
Symbol
SMARCD1, BAF60A, CRACD1, CSS11, Rsc6p
Name
(RefSeq) SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 1
  KO
K11650  SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D
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
H01403  Coffin-Siris syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09120 Genetic Information Processing
  09126 Chromosome
   03082 ATP-dependent chromatin remodeling
    6602 (SMARCD1)
 09150 Organismal Systems
  09159 Environmental adaptation
   04714 Thermogenesis
    6602 (SMARCD1)
 09160 Human Diseases
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    6602 (SMARCD1)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03021 Transcription machinery [BR:hsa03021]
    6602 (SMARCD1)
   03036 Chromosome and associated proteins [BR:hsa03036]
    6602 (SMARCD1)
Transcription machinery [BR:hsa03021]
 Eukaryotic type
  RNA polymerase II system
   Coactivators
    BAF/PBAF complex
     6602 (SMARCD1)
Chromosome and associated proteins [BR:hsa03036]
 Eukaryotic type
  Chromatin remodeling factors
   BAF complex
    6602 (SMARCD1)
   PBAF complex
    6602 (SMARCD1)
   GBAF(ncBAF) complex
    6602 (SMARCD1)
SSDB
Motif
Pfam: SWIB DivIC
Other DBs
NCBI-GeneID: 6602
NCBI-ProteinID: NP_003067
OMIM: 601735
HGNC: 11106
Ensembl: ENSG00000066117
UniProt: Q96GM5
Structure
Position
12:50085342..50100707
AA seq 515 aa
MAARAGFQSVAPSGGAGASGGAGAAAALGPGGTPGPPVRMGPAPGQGLYRSPMPGAAYPR
PGMLPGSRMTPQGPSMGPPGYGGNPSVRPGLAQSGMDQSRKRPAPQQIQQVQQQAVQNRN
HNAKKKKMADKILPQRIRELVPESQAYMDLLAFERKLDQTIMRKRLDIQEALKRPIKQKR
KLRIFISNTFNPAKSDAEDGEGTVASWELRVEGRLLEDSALSKYDATKQKRKFSSFFKSL
VIELDKDLYGPDNHLVEWHRTATTQETDGFQVKRPGDVNVRCTVLLMLDYQPPQFKLDPR
LARLLGIHTQTRPVIIQALWQYIKTHKLQDPHEREFVICDKYLQQIFESQRMKFSEIPQR
LHALLMPPEPIIINHVISVDPNDQKKTACYDIDVEVDDTLKTQMNSFLLSTASQQEIATL
DNKIHETIETINQLKTQREFMLSFARDPQGFINDWLQSQCRDLKTMTDVVGNPEEERRAE
FYFQPWAQEAVCRYFYSKVQQRRQELEQALGIRNT
NT seq 1548 nt   +upstreamnt  +downstreamnt
atggcggcccgggcgggtttccagtctgtggctccaagcggcggcgccggagcctcagga
ggggcgggcgcggctgctgccttgggcccgggcggaactccggggcctcctgtgcgaatg
ggcccggctccgggtcaagggctgtaccgctccccgatgcccggagcggcctatccgaga
ccaggtatgttgccaggcagccgaatgacacctcagggaccttccatgggaccccctggc
tatggggggaacccttcagtccgacctggcctggcccagtcagggatggatcagtcccgc
aagagacctgcccctcagcagatccagcaggtccagcagcaggcggtccaaaatcgaaac
cacaatgcaaagaaaaagaagatggctgacaaaattctacctcaaaggattcgtgaactg
gtaccagaatcccaggcctatatggatctcttggcttttgaaaggaaactggaccagact
atcatgaggaaacggctagatatccaagaggccttgaaacgtcccatcaagcaaaaacgg
aagctgcgaattttcatttctaacactttcaatccggctaagtcagatgccgaggatggg
gaagggacggtggcttcctgggagcttcgggtagaaggacggctcctggaggattcagcc
ttgtccaaatatgatgccactaaacaaaagaggaagttctcttccttttttaagtccttg
gtgattgaactggacaaagacctgtatgggccagacaaccatctggtagaatggcacagg
accgccactacccaggagaccgatggctttcaggtgaagcggccgggagacgtgaatgta
cggtgtactgtcctactgatgctggattaccagcctccccagtttaaattagacccccgc
ctagctcgactcctgggcatccatacccagactcgtccagtgatcatccaagcactgtgg
caatatattaagacacataagctccaggaccctcacgagcgggagtttgtcatctgtgac
aagtacctgcagcagatctttgagtctcaacgtatgaagttttcagagatccctcagcgg
ctccatgccttgcttatgccaccagaacctatcatcattaatcatgtcatcagtgttgac
ccgaatgatcagaaaaagacagcttgttatgacattgatgttgaagtggatgacaccttg
aagacccagatgaattcttttctgctgtccactgccagccaacaggagattgctactcta
gacaacaagatccatgagacaatagaaaccatcaaccagctgaagactcagcgggagttc
atgctgagctttgccagagaccctcagggtttcatcaatgactggcttcagtcccagtgc
agggacctcaagacaatgactgatgtggtgggtaacccagaggaggagcgccgagctgag
ttctacttccagccctgggctcaggaggctgtgtgccgatacttctactccaaggtgcag
cagagacgacaagaattagagcaagccctgggaatccggaatacatag

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