KEGG   Homo sapiens (human): 6603
Entry
6603              CDS       T01001                                 
Symbol
SMARCD2, BAF60B, CRACD2, PRO2451, Rsc6p, SGD2
Name
(RefSeq) SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 2
  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
H02024  Neutrophil specific granule deficiency
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09120 Genetic Information Processing
  09126 Chromosome
   03082 ATP-dependent chromatin remodeling
    6603 (SMARCD2)
 09150 Organismal Systems
  09159 Environmental adaptation
   04714 Thermogenesis
    6603 (SMARCD2)
 09160 Human Diseases
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    6603 (SMARCD2)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03021 Transcription machinery [BR:hsa03021]
    6603 (SMARCD2)
   03036 Chromosome and associated proteins [BR:hsa03036]
    6603 (SMARCD2)
Transcription machinery [BR:hsa03021]
 Eukaryotic type
  RNA polymerase II system
   Coactivators
    BAF/PBAF complex
     6603 (SMARCD2)
Chromosome and associated proteins [BR:hsa03036]
 Eukaryotic type
  Chromatin remodeling factors
   BAF complex
    6603 (SMARCD2)
   PBAF complex
    6603 (SMARCD2)
   GBAF(ncBAF) complex
    6603 (SMARCD2)
SSDB
Motif
Pfam: SWIB
Other DBs
NCBI-GeneID: 6603
NCBI-ProteinID: NP_001091896
OMIM: 601736
HGNC: 11107
Ensembl: ENSG00000108604
UniProt: Q92925
Position
17:complement(63832081..63842685)
AA seq 531 aa
MSGRGAGGFPLPPLSPGGGAVAAALGAPPPPAGPGMLPGPALRGPGPAGGVGGPGAAAFR
PMGPAGPAAQYQRPGMSPGNRMPMAGLQVGPPAGSPFGAAAPLRPGMPPTMMDPFRKRLL
VPQAQPPMPAQRRGLKRRKMADKVLPQRIRELVPESQAYMDLLAFERKLDQTIARKRMEI
QEAIKKPLTQKRKLRIYISNTFSPSKAEGDSAGTAGTPGGTPAGDKVASWELRVEGKLLD
DPSKQKRKFSSFFKSLVIELDKELYGPDNHLVEWHRMPTTQETDGFQVKRPGDLNVKCTL
LLMLDHQPPQYKLDPRLARLLGVHTQTRAAIMQALWLYIKHNQLQDGHEREYINCNRYFR
QIFSCGRLRFSEIPMKLAGLLQHPDPIVINHVISVDPNDQKKTACYDIDVEVDDPLKAQM
SNFLASTTNQQEIASLDVKIHETIESINQLKTQRDFMLSFSTDPQDFIQEWLRSQRRDLK
IITDVIGNPEEERRAAFYHQPWAQEAVGRHIFAKVQQRRQELEQVLGIRLT
NT seq 1596 nt   +upstreamnt  +downstreamnt
atgtcgggccgaggcgcgggcgggttcccgctgcccccgctaagccctggcggcggcgcc
gtggctgcggccctgggagcgccgcctccccccgcgggacccggcatgctgcccggaccg
gcgctccggggaccgggtccggcaggaggcgtggggggccccggggccgccgccttccgc
cccatgggccccgcgggccccgcggcgcagtaccagcgacctggcatgtcaccagggaac
cggatgcccatggctggcttgcaggtgggaccccctgctggctccccatttggtgcagca
gctccgcttcgacctggcatgccacccaccatgatggatccattccgaaaacgcctgctt
gtgccccaggcgcagcctcccatgcctgcccagcgccgggggttaaagaggaggaagatg
gcagataaggttctacctcagcgaatccgggagcttgttccagagtctcaggcgtacatg
gatctcttggcttttgagcggaagctggaccagaccattgctcgcaagcggatggagatc
caggaggccatcaaaaagcctctgacacaaaagcgaaagcttcggatctacatttccaat
acgttcagtcccagcaaggcggaaggcgatagtgcaggaactgcagggacccctggggga
accccagcaggggacaaggtggcttcctgggaactccgagtggaaggaaaactgctggat
gatcctagcaaacagaagaggaagttttcttcattctttaagagcctcgtcattgagctg
gacaaggagctgtacgggcctgacaatcacctggtggagtggcaccggatgcccaccacc
caggagacagatggcttccaagtaaaacggcctggagacctcaacgtcaagtgcaccctc
ctgctcatgctggatcatcagcctccccagtacaaattggacccccgattggcaaggctg
ctgggagtgcacacgcagacgagggccgccatcatgcaggccctgtggctttacatcaag
cacaaccagctgcaggatgggcacgagcgggagtacatcaactgcaaccgttacttccgc
cagatcttcagttgtggccgactccgtttctccgagattcccatgaagctggcagggttg
ctgcagcatccagaccccattgtcatcaaccatgtcattagtgtcgaccctaacgaccag
aagaagacagcctgttacgacatcgatgtggaggtggacgacccactgaaggcccaaatg
agcaattttctggcctctaccaccaatcagcaggagatcgcctcccttgatgtcaagatc
catgagaccattgagtccatcaaccagctgaagacccagagagatttcatgctcagtttt
agcaccgacccccaggacttcatccaggaatggctccgttcccagcgccgagacctcaag
atcatcactgatgtgattggaaatcctgaggaggagagacgagctgctttctaccaccag
ccctgggcccaggaagcagtaggcaggcacatctttgccaaggtgcagcagcgaaggcag
gaactggaacaggtgctgggaattcgcctgacctaa

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