KEGG   Homo sapiens (human): 4784
Entry
4784              CDS       T01001                                 
Symbol
NFIX, CTF, MALNS, MRSHSS, NF-I/X, NF1-X, NF1A, SOTOS2
Name
(RefSeq) nuclear factor I X
  KO
K09171  nuclear factor I/X
Organism
hsa  Homo sapiens (human)
Disease
H00718  Sotos syndrome
H01834  Marshall-Smith syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    4784 (NFIX)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Other basic domains
   NF-1
    4784 (NFIX)
SSDB
Motif
Pfam: CTF_NFI NfI_DNAbd_pre-N MH1
Other DBs
NCBI-GeneID: 4784
NCBI-ProteinID: NP_002492
OMIM: 164005
HGNC: 7788
Ensembl: ENSG00000008441
UniProt: Q14938
Structure
Position
19:12995475..13098796
AA seq 441 aa
MYSPYCLTQDEFHPFIEALLPHVRAFSYTWFNLQARKRKYFKKHEKRMSKDEERAVKDEL
LGEKPEIKQKWASRLLAKLRKDIRPEFREDFVLTITGKKPPCCVLSNPDQKGKIRRIDCL
RQADKVWRLDLVMVILFKGIPLESTDGERLYKSPQCSNPGLCVQPHHIGVTIKELDLYLA
YFVHTPESGQSDSSNQQGDADIKPLPNGHLSFQDCFVTSGVWNVTELVRVSQTPVATASG
PNFSLADLESPSYYNINQVTLGRRSITSPPSTSTTKRPKSIDDSEMESPVDDVFYPGTGR
SPAAGSSQSSGWPNDVDAGPASLKKSGKLDFCSALSSQGSSPRMAFTHHPLPVLAGVRPG
SPRATASALHFPSTSIIQQSSPYFTHPTIRYHHHHGQDSLKEFVQFVCSDGSGQATGQHS
QRQAPPLPTGLSASDPGTATF
NT seq 1326 nt   +upstreamnt  +downstreamnt
atgtactccccgtactgcctcacccaggatgagttccacccgttcatcgaggcactgctg
cctcacgtccgcgctttctcctacacctggttcaacctgcaggcgcggaagcgcaagtac
ttcaagaagcatgaaaagcggatgtcgaaggacgaggagcgggcggtgaaggacgagctg
ctgggcgagaagcccgagatcaagcagaagtgggcatcccggctgctggccaagctgcgc
aaggacatccggcccgagttccgcgaggacttcgtgctgaccatcacgggcaagaagccc
ccctgctgcgtgctctccaaccccgaccagaagggcaagatccggcggattgactgcctg
cgccaggctgacaaggtgtggcggctggacctggtcatggtgattttgtttaaggggatc
cccctggaaagtactgatggggagcggctctacaagtcgcctcagtgctcgaaccccggc
ctgtgcgtccagccacatcacattggagtcacaatcaaagaactggatctttatctggct
tactttgtccacactccggaatccggacaatcagatagttcaaaccagcaaggagatgcg
gacatcaaaccactgcccaacgggcacttaagtttccaggactgttttgtgacttccggg
gtctggaatgtgacggagctggtgagagtatcacagactcctgttgcaacagcatcaggg
cccaacttctccctggcggacctggagagtcccagctactacaacatcaaccaggtgacc
ctggggcggcggtccatcacctcccctccttccaccagcaccaccaagcgccccaagtcc
atcgatgacagtgagatggagagccctgttgatgacgtgttctatcccgggacaggccgt
tccccagcagctggcagcagccagtccagcgggtggcccaacgatgtggatgcaggcccg
gcttctctaaagaagtcaggaaagctggacttctgcagtgccctctcctctcagggcagc
tccccgcgcatggctttcacccaccacccgctgcctgtgcttgctggagtcagaccaggg
agcccccgggccacagcatcagccctgcacttcccctccacgtccatcatccagcagtcg
agcccgtatttcacgcacccgaccatccgctaccaccaccaccacgggcaggactcactg
aaggagtttgtgcagtttgtgtgctcggatggctcgggccaggccaccggacagcattcg
caacgacaggcgcctcctctgccaaccggtttgtcagcatcggaccccgggacggcaact
ttctga

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Ontology (2)   
   KEGG BRITE (2)   
Disease (5)   
   KEGG DISEASE (2)   
   OMIM (3)   
Genome (1)   
   KEGG GENOME (1)   
Gene (8)   
   KEGG ORTHOLOGY (1)   
   RefGene (2)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   OC (1)   
Protein sequence (20)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (18)   
DNA sequence (48)   
   RefSeq(nuc) (18)   
   GenBank (15)   
   EMBL (15)   
3D Structure (2)   
   PDB (2)   
Protein domain (3)   
   Pfam (3)   
All databases (89)   

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