KEGG   Homo sapiens (human): 79576
Entry
79576             CDS       T01001                                 
Symbol
NKAP, MRXSHD
Name
(RefSeq) NFKB activating protein
  KO
K25931  NF-kappa-B-activating protein
Organism
hsa  Homo sapiens (human)
Disease
H00658  X-linked syndromic intellectual developmental disorder
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03041 Spliceosome [BR:hsa03041]
    79576 (NKAP)
Spliceosome [BR:hsa03041]
 Other splicing related proteins
  Spliceosome associated proteins (SAPs)
   RNA binding proteins (RBPs)
    79576 (NKAP)
SSDB
Motif
Pfam: Nkap_C NKAP SR-25
Other DBs
NCBI-GeneID: 79576
NCBI-ProteinID: NP_078804
OMIM: 300766
HGNC: 29873
Ensembl: ENSG00000101882
UniProt: Q8N5F7
Structure
Position
X:complement(119920672..119943751)
AA seq 415 aa
MAPVSGSRSPDREASGSGGRRRSSSKSPKPSKSARSPRGRRSRSHSCSRSGDRNGLTHQL
GGLSQGSRNQSYRSRSRSRSRERPSAPRGIPFASASSSVYYGSYSRPYGSDKPWPSLLDK
EREESLRQKRLSERERIGELGAPEVWGLSPKNPEPDSDEHTPVEDEEPKKSTTSASTSEE
EKKKKSSRSKERSKKRRKKKSSKRKHKKYSEDSDSDSDSETDSSDEDNKRRAKKAKKKEK
KKKHRSKKYKKKRSKKSRKESSDSSSKESQEEFLENPWKDRTKAEEPSDLIGPEAPKTLT
SQDDKPLNYGHALLPGEGAAMAEYVKAGKRIPRRGEIGLTSEEIASFECSGYVMSGSRHR
RMEAVRLRKENQIYSADEKRALASFNQEERRKRENKILASFREMVYRKTKGKDDK
NT seq 1248 nt   +upstreamnt  +downstreamnt
atggctccggtgtccggctcacgcagcccggatagggaggcctcgggctcggggggaaga
cgtcgcagttcgtcgaagagtccgaagcccagcaaatctgcccgctccccgcggggccgc
cgctctcgctcgcactcttgctctcggtccggggaccggaatggactcacccatcagctg
ggtggcctcagccaaggctcccgaaaccagtcctaccgctcacgctcgcggtcgcgttct
agagagcggccctctgcgccccggggcatccccttcgcttctgcctcctcgtcagtctat
tacggcagctactcgcgcccctacgggagcgacaagccttggcctagcctcctcgacaag
gagagggaggagagcctgcggcagaagagattaagtgagagagagagaattggagaattg
ggagctcctgaagtatggggactttctccaaagaatcctgaaccagattctgatgaacat
acaccagtggaggatgaagagccaaagaaaagcactacttcagcttctacttcagaagaa
gaaaaaaagaagaagtctagccgttcaaaagaaaggtccaagaaaaggagaaagaaaaaa
tcatcgaaaagaaaacataagaagtattctgaagatagcgacagtgactctgattctgaa
acagactccagtgatgaagataacaaaaggagagcaaagaaagccaagaaaaaggaaaag
aagaagaaacacagatcgaagaaatataagaaaaagaggtctaagaagagcagaaaagag
tccagtgattcaagctctaaagaatcccaagaagagtttctggaaaatccctggaaggat
cgaacaaaggctgaagaaccatcagatttaattggcccagaggctccaaaaacacttacc
tctcaagatgataaacctttgaactatggccatgctctgttacctggtgaaggtgcagct
atggctgaatatgtaaaagctggaaaacgtatcccacgaagaggtgaaattggcttgaca
agtgaagaaattgcatcatttgaatgctcaggttatgtaatgagtggtagcaggcatcgc
cgaatggaggctgtgcgactgcgaaaagagaaccagatctacagtgctgatgagaagaga
gcccttgcatcctttaaccaagaagagagacgaaagagagagaacaagattctggccagt
tttcgagaaatggtttacagaaagaccaaagggaaggatgacaaataa

  All links  
Disease (2)   
   OMIM (2)   
Gene (32)   
   RefGene (19)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (8)   
   OC (1)   
Protein sequence (3)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (1)   
DNA sequence (23)   
   RefSeq(nuc) (1)   
   GenBank (11)   
   EMBL (11)   
3D Structure (4)   
   PDB (4)   
Protein domain (3)   
   Pfam (3)   
All databases (67)   

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