KEGG   Homo sapiens (human): 11198
Entry
11198             CDS       T01001                                 
Symbol
SUPT16H, CDC68, FACTP140, NEDDFAC, SPT16, SPT16/CDC68
Name
(RefSeq) SPT16 homolog, facilitates chromatin remodeling subunit
  KO
K25639  FACT complex subunit SPT16
Organism
hsa  Homo sapiens (human)
Disease
H02535  Neurodevelopmental disorder with dysmorphic facies
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03036 Chromosome and associated proteins [BR:hsa03036]
    11198 (SUPT16H)
Chromosome and associated proteins [BR:hsa03036]
 Eukaryotic type
  Nucleosome assembly factors
   Histone chaperones
    FACT complex
     11198 (SUPT16H)
SSDB
Motif
Pfam: SPT16 FACT-Spt16_Nlob Peptidase_M24 Rttp106-like_middle SPT16_C DUF1949
Other DBs
NCBI-GeneID: 11198
NCBI-ProteinID: NP_009123
OMIM: 605012
HGNC: 11465
Ensembl: ENSG00000092201
UniProt: Q9Y5B9
Structure
Position
14:complement(21351476..21384019)
AA seq 1047 aa
MAVTLDKDAYYRRVKRLYSNWRKGEDEYANVDAIVVSVGVDEEIVYAKSTALQTWLFGYE
LTDTIMVFCDDKIIFMASKKKVEFLKQIANTKGNENANGAPAITLLIREKNESNKSSFDK
MIEAIKESKNGKKIGVFSKDKFPGEFMKSWNDCLNKEGFDKIDISAVVAYTIAVKEDGEL
NLMKKAASITSEVFNKFFKERVMEIVDADEKVRHSKLAESVEKAIEEKKYLAGADPSTVE
MCYPPIIQSGGNYNLKFSVVSDKNHMHFGAITCAMGIRFKSYCSNLVRTLMVDPSQEVQE
NYNFLLQLQEELLKELRHGVKICDVYNAVMDVVKKQKPELLNKITKNLGFGMGIEFREGS
LVINSKNQYKLKKGMVFSINLGFSDLTNKEGKKPEEKTYALFIGDTVLVDEDGPATVLTS
VKKKVKNVGIFLKNEDEEEEEEEKDEAEDLLGRGSRAALLTERTRNEMTAEEKRRAHQKE
LAAQLNEEAKRRLTEQKGEQQIQKARKSNVSYKNPSLMPKEPHIREMKIYIDKKYETVIM
PVFGIATPFHIATIKNISMSVEGDYTYLRINFYCPGSALGRNEGNIFPNPEATFVKEITY
RASNIKAPGEQTVPALNLQNAFRIIKEVQKRYKTREAEEKEKEGIVKQDSLVINLNRSNP
KLKDLYIRPNIAQKRMQGSLEAHVNGFRFTSVRGDKVDILYNNIKHALFQPCDGEMIIVL
HFHLKNAIMFGKKRHTDVQFYTEVGEITTDLGKHQHMHDRDDLYAEQMEREMRHKLKTAF
KNFIEKVEALTKEELEFEVPFRDLGFNGAPYRSTCLLQPTSSALVNATEWPPFVVTLDEV
ELIHFERVQFHLKNFDMVIVYKDYSKKVTMINAIPVASLDPIKEWLNSCDLKYTEGVQSL
NWTKIMKTIVDDPEGFFEQGGWSFLEPEGEGSDAEEGDSESEIEDETFNPSEDDYEEEEE
DSDEDYSSEAEESDYSKESLGSEEESGKDWDELEEEARKADRESRYEEEEEQSRSMSRKR
KASVHSSGRGSNRGSRHSSAPPKKKRK
NT seq 3144 nt   +upstreamnt  +downstreamnt
atggctgtgactctggacaaagacgcttattatcggcgagtgaagagactgtacagcaat
tggcggaaaggagaagatgagtatgccaacgttgatgccattgttgtatcagtgggtgtt
gatgaagaaattgtttatgccaaatcaactgccttacagacatggctctttggttatgaa
ctaactgatactatcatggtcttttgtgatgacaaaatcatctttatggccagcaagaaa
aaagtggagttcttgaaacagattgccaacactaagggcaatgagaatgctaatggagcc
cctgccatcacactgctaatacgagaaaagaatgaaagtaataagagtagctttgacaaa
atgattgaagccattaaagaaagcaagaatggcaagaagattggagtgttcagcaaagac
aaattccctggagagttcatgaagagctggaatgactgcctcaacaaagaaggctttgac
aaaatagatatcagtgcagttgtggcatataccatcgctgtaaaggaggatggggagctc
aacctaatgaagaaagcagccagcatcacttctgaagtcttcaacaaattcttcaaggaa
agagtcatggaaatagttgatgcagatgagaaagttcgacacagcaaactggctgagtct
gtggaaaaggccattgaagagaaaaaataccttgctggggcagacccttctactgtggaa
atgtgttaccctcctatcattcagagtggtggcaactataatctcaagttcagtgtggtg
agtgacaagaatcatatgcactttggggctatcacttgtgccatgggtattcgcttcaag
tcttactgctccaaccttgttcgcactttgatggttgatccttctcaagaagttcaagaa
aattataactttttgctccagcttcaagaggagctgctgaaggaattaagacatggtgtg
aagatatgtgacgtgtataacgctgtcatggacgtggttaaaaagcagaagccagaactg
ctgaacaaaattaccaaaaacctagggtttgggatgggaattgaattccgtgaaggctcc
ctagtaatcaatagcaaaaatcaatacaaactgaagaaaggaatggttttcagcatcaat
ttaggattctcagacctgactaacaaggaggggaaaaagccagaagagaaaacctatgcc
ctgttcattggtgacacagtgcttgtggatgaggatggcccagctactgttctcacttct
gtgaagaagaaagtgaagaatgtggggattttcctaaagaatgaagatgaggaagaagag
gaggaggagaaagatgaggcagaggaccttttgggaagaggttctcgggcagcattactt
acagaaagaacaagaaatgaaatgactgcagaagagaagcgaagagcacatcagaaagaa
ctagcggctcaactcaatgaagaagcaaagaggcgattgactgaacaaaagggagaacag
cagattcagaaagctcgcaagtctaatgtgtcctataaaaacccatctctgatgcctaag
gaaccacatattcgggaaatgaagatctacatcgataagaaatatgagactgtaataatg
cccgtgtttggcattgcaacaccgtttcacattgccacaatcaagaatataagtatgtcc
gtggaaggagattatacttacttgcgaatcaacttttattgcccaggcagtgctctgggc
aggaatgaaggcaacatctttcctaaccctgaagcgacttttgtcaaggaaattacatac
cgagcatcaaatattaaggcacccggagaacagacagtaccagccttgaaccttcagaat
gctttccgaattattaaagaagtacagaaacgttataaaactcgagaagctgaagagaaa
gagaaggaggggattgtaaaacaagactcactggtgatcaatctaaaccggagtaatccg
aaactgaaagatctatacattcgcccaaatattgcccaaaagaggatgcaaggctcactg
gaggcccatgtcaatggcttccgcttcacatctgttcgaggagacaaagtggatattttg
tacaataatattaagcatgctttgttccagccctgtgatggagaaatgattattgtcttg
cactttcacctcaagaatgccatcatgtttgggaagaagcggcacacggatgtgcagttc
tacacagaagtgggagagataaccacggacttggggaaacatcagcatatgcatgaccga
gatgacctctatgctgagcagatggaacgagaaatgaggcacaaactgaaaacagccttt
aaaaatttcattgagaaagtagaggctctaactaaggaggaactggaatttgaagtgcct
tttagggacttgggatttaacggagctccctataggagtacctgcctccttcagcccact
agtagtgcgctggtaaatgctacggaatggccaccttttgtggtgacattggatgaggta
gagctgatccactttgagcgggtccagtttcacctgaagaactttgatatggtaatcgtc
tacaaggactacagcaagaaagtgaccatgatcaacgccattcctgtagcctctcttgac
cccatcaaggaatggttgaattcctgcgacctgaaatacacagaaggagtacagtccctc
aactggactaaaatcatgaagaccattgttgatgaccctgagggcttcttcgaacaaggt
ggctggtctttcctggagcctgagggtgaggggagtgatgctgaagaaggggattcagag
tctgaaattgaagatgagacttttaatccttcagaagatgactatgaagaggaagaggag
gacagtgatgaagattattcatcagaagcagaagagtcagactattctaaggagtcattg
ggtagtgaagaagagagtggaaaggattgggatgaactggaggaagaagcccgaaaagcg
gaccgagaaagtcgttacgaggaagaagaagaacaaagtcgaagtatgagccggaagagg
aaggcatctgtgcacagttcgggccgtggctctaaccgtggttccagacacagctctgca
ccccccaagaaaaagaggaagtaa

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (23)   
   KEGG ORTHOLOGY (1)   
   RefGene (13)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (4)   
   OC (1)   
Protein sequence (5)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (3)   
DNA sequence (25)   
   RefSeq(nuc) (3)   
   GenBank (11)   
   EMBL (11)   
3D Structure (9)   
   PDB (9)   
Protein domain (6)   
   Pfam (6)   
All databases (74)   

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