KEGG   Homo sapiens (human): 51008
Entry
51008             CDS       T01001                                 
Symbol
ASCC1, ASC1p50, CGI-18, SMABF2, p50
Name
(RefSeq) activating signal cointegrator 1 complex subunit 1 isoform a
  KO
K18666  activating signal cointegrator complex subunit 1
Organism
hsa  Homo sapiens (human)
Disease
H01901  Barrett esophagus
H02238  Spinal muscular atrophy with congenital bone fractures
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09190 Not Included in Pathway or Brite
  09192 Unclassified: genetic information processing
   99973 Transcription
    51008 (ASCC1)
SSDB
Motif
Pfam: AKAP7_NLS KH_1 KH_PNO1_2nd HVSL ApeA_NTD1 YozF
Other DBs
NCBI-GeneID: 51008
NCBI-ProteinID: NP_001185728
OMIM: 614215
HGNC: 24268
UniProt: Q8N9N2
Structure
Position
10:complement(72096032..72217134)
AA seq 400 aa
MEVLRPQLIRIDGRNYRKNPVQEQTYQHEEDEEDFYQGSMECADEPCDAYEVEQTPQGFR
STLRAPSLLYNLIHLNTSNDCGFQKITLDCQNIYTWKSRHIVGKRGDTRKKIEMETKTSI
SIPKPGQDGEIVITGQHRNGVISARTRIDVLLDTFRRKQPFTHFLAFFLNEVEVQEGFLR
FQEEVLAKCSMDHGVDSSIFQNPKKLHLTIGMLVLLSEEEIQQTCEMLQQCKEEFINDIS
GGKPLEVEMAGIEYMNDDPGMVDVLYAKVHMKDGSNRLQELVDRVLERFQASGLIVKEWN
SVKLHATVMNTLFRKDPNAEGRYNLYTAEGKYIFKERESFDGRNILKSFALLPRLEYNDA
ISAHCNLCLPGSSDSPASASQVAGITGVSDAYSQSLPGKS
NT seq 1203 nt   +upstreamnt  +downstreamnt
atggaagttctgcgtccacagcttataagaattgatggccggaattacaggaagaatcca
gtccaagaacagacctatcaacatgaagaagatgaagaggacttctatcaaggctccatg
gagtgtgctgatgagccctgtgatgcctacgaggtggagcagaccccacaaggattccgg
tctactttgagggcccccagcttgctctataatctcattcacttgaacacatcaaacgac
tgtgggttccagaagataactttggattgtcagaatatttatacttggaagtccaggcat
atagttggaaagagaggggacactaggaagaaaatagaaatggagaccaaaacttctatt
agcattcctaaacctggacaagacggggaaattgtaatcactggccagcatcgaaatggt
gtaatttcagcccgaacacggattgatgttcttttggacacttttcgaagaaagcagccc
ttcactcacttccttgcctttttcctcaatgaagttgaggttcaggaaggattcctgaga
ttccaggaggaagtactggcgaagtgctccatggatcatggggttgacagcagcattttc
cagaatcctaaaaagcttcatctaactattgggatgttggtgcttttgagtgaggaagag
atccagcagacatgtgagatgctacagcagtgtaaagaggaattcattaatgatatttct
gggggtaaacccctagaagtggagatggcagggatagaatacatgaatgatgatcctggc
atggtggatgttctttacgccaaagtccatatgaaagatggctccaacaggctacaagaa
ttagttgatcgagtgctggaacgttttcaggcatctggactaatagtgaaagagtggaat
agtgtgaaactgcatgctacagttatgaatacactattcaggaaagaccccaatgctgaa
ggcaggtacaatctctacacagcggaaggcaaatatatcttcaaggaaagagaatcattt
gatggccgaaatattttaaagagctttgccttgttgcccaggctggagtacaatgatgca
atctccgctcactgcaacctgtgcctcccgggttcaagtgattctcctgcctcagcctcc
caagtagctgggattacaggtgtctctgatgcatattctcagagcctaccaggaaaatcc
tag

  All links  
Disease (3)   
   OMIM (3)   
Gene (22)   
   RefGene (10)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   RIKEN BRC-DNA (8)   
   OC (1)   
Protein sequence (45)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (43)   
DNA sequence (81)   
   RefSeq(nuc) (45)   
   GenBank (18)   
   EMBL (18)   
3D Structure (1)   
   PDB (1)   
Protein domain (6)   
   Pfam (6)   
All databases (158)   

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