KEGG   Homo sapiens (human): 4781
Entry
4781              CDS       T01001                                 
Symbol
NFIB, CTF, HMGIC/NFIB, MACID, NF-I/B, NF1-B, NFI-B, NFI-RED, NFIB2, NFIB3
Name
(RefSeq) nuclear factor I B
  KO
K09169  nuclear factor I/B
Organism
hsa  Homo sapiens (human)
Disease
H02652  Macrocephaly, acquired, with impaired intellectual development
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    4781 (NFIB)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Other basic domains
   NF-1
    4781 (NFIB)
SSDB
Motif
Pfam: CTF_NFI NfI_DNAbd_pre-N MH1
Other DBs
NCBI-GeneID: 4781
NCBI-ProteinID: NP_005587
OMIM: 600728
HGNC: 7785
Ensembl: ENSG00000147862
UniProt: O00712 Q5VW28
Position
9:complement(14081843..14532077)
AA seq 420 aa
MMYSPICLTQDEFHPFIEALLPHVRAIAYTWFNLQARKRKYFKKHEKRMSKDEERAVKDE
LLSEKPEIKQKWASRLLAKLRKDIRQEYREDFVLTVTGKKHPCCVLSNPDQKGKIRRIDC
LRQADKVWRLDLVMVILFKGIPLESTDGERLMKSPHCTNPALCVQPHHITVSVKELDLFL
AYYVQEQDSGQSGSPSHNDPAKNPPGYLEDSFVKSGVFNVSELVRVSRTPITQGTGVNFP
IGEIPSQPYYHDMNSGVNLQRSLSSPPSSKRPKTISIDENMEPSPTGDFYPSPSSPAAGS
RTWHERDQDMSSPTTMKKPEKPLFSSASPQDSSPRLSTFPQHHHPGIPGVAHSVISTRTP
PPPSPLPFPTQAILPPAPSSYFSHPTIRYPPHLNPQDTLKNYVPSYDPSSPQTSQSWYLG
NT seq 1263 nt   +upstreamnt  +downstreamnt
atgatgtattctcccatctgtctcactcaggatgaatttcacccattcatcgaggcactt
cttccacatgtccgtgcaattgcctatacttggttcaacctgcaggctcgaaaacgcaag
tactttaaaaagcatgagaagcgaatgtcaaaggatgaagaaagagcagtcaaagatgag
cttctcagtgaaaagcctgaaatcaaacagaagtgggcatccaggctccttgccaaactg
cgcaaagatattcgccaggagtatcgagaggactttgtgctcaccgtgactggcaagaag
cacccgtgctgtgtcttatccaatcccgaccagaagggtaagattaggagaatcgactgc
ctgcgacaggcagacaaagtctggcgtctggatctagtcatggtgatcctgttcaaaggc
atccccttggaaagtaccgatggagagcggctcatgaaatccccacattgcacaaaccca
gcactttgtgtccagccacatcatatcacagtatcagttaaggagcttgatttgtttttg
gcatactacgtgcaggagcaagattctggacaatcaggaagtccaagccacaatgatcct
gccaagaatcctccaggttaccttgaggatagttttgtaaaatctggagtcttcaatgta
tcagaacttgtaagagtatccagaacgcccataacccagggaactggagtcaacttccca
attggagaaatcccaagccaaccatactatcatgacatgaactcgggggtcaatcttcag
aggtctctgtcttctccaccaagcagcaaaagacccaaaactatatccatagatgaaaat
atggaaccaagtcctacaggagacttttacccctctccaagttcaccagctgctggaagt
cgaacatggcacgaaagagatcaagatatgtcttctccgactactatgaagaagcctgaa
aagccattgttcagctctgcatctccacaggattcttccccaagactgagcactttcccc
cagcaccaccatcccggaatacctggagttgcacacagtgtcatctcaactcgaactcca
cctccaccttcaccgttgccatttccaacacaagctatccttcctccagccccatcgagc
tacttttctcatccaacaatcagatatcctccccacctgaatcctcaggatactctgaag
aactatgtaccttcttatgacccatccagtccacaaaccagccagtcctggtacctgggc
tag

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Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (17)   
   KEGG ORTHOLOGY (1)   
   RefGene (8)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (3)   
   OC (1)   
Protein sequence (31)   
   UniProt (2)   
   SWISS-PROT (1)   
   RefSeq(pep) (28)   
DNA sequence (80)   
   RefSeq(nuc) (32)   
   GenBank (24)   
   EMBL (24)   
Protein domain (3)   
   Pfam (3)   
All databases (137)   

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