KEGG   Homo sapiens (human): 4774
Entry
4774              CDS       T01001                                 
Symbol
NFIA, BRMUTD, C1DELp32p31, CTF, DEL1P32P31, NF-I/A, NF1-A, NFI-A, NFI-L
Name
(RefSeq) nuclear factor 1 A-type isoform 1
  KO
K09168  nuclear factor I/A
Organism
hsa  Homo sapiens (human)
Disease
H02471  Brain malformations with urinary tract defects
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    4774 (NFIA)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Other basic domains
   NF-1
    4774 (NFIA)
SSDB
Motif
Pfam: CTF_NFI NfI_DNAbd_pre-N MH1
Other DBs
NCBI-GeneID: 4774
NCBI-ProteinID: NP_001128145
OMIM: 600727
HGNC: 7784
Ensembl: ENSP00000384523.3
UniProt: Q12857
Position
1:61077227..61462788
AA seq 509 aa
MYSPLCLTQDEFHPFIEALLPHVRAFAYTWFNLQARKRKYFKKHEKRMSKEEERAVKDEL
LSEKPEVKQKWASRLLAKLRKDIRPEYREDFVLTVTGKKPPCCVLSNPDQKGKMRRIDCL
RQADKVWRLDLVMVILFKGIPLESTDGERLVKSPQCSNPGLCVQPHHIGVSVKELDLYLA
YFVHAADSSQSESPSQPSDADIKDQPENGHLGFQDSFVTSGVFSVTELVRVSQTPIAAGT
GPNFSLSDLESSSYYSMSPGAMRRSLPSTSSTSSTKRLKSVEDEMDSPGEEPFYTGQGRS
PGSGSQSSGWHEVEPGMPSPTTLKKSEKSGFSSPSPSQTSSLGTAFTQHHRPVITGPRAS
PHATPSTLHFPTSPIIQQPGPYFSHPAIRYHPQETLKEFVQLVCPDAGQQAGQVGFLNPN
GSSQGKVHNPFLPTPMLPPPPPPPMARPVPLPVPDTKPPTTSTEGGAASPTSPTYSTPST
SPANRFVSVGPRDPSFVNIPQQTQSWYLG
NT seq 1530 nt   +upstreamnt  +downstreamnt
atgtattctccgctctgtctcacccaggatgaatttcatcctttcatcgaagcacttctg
ccccacgtccgagcctttgcctacacatggttcaacctgcaggcccgaaaacgaaaatac
ttcaaaaaacatgaaaagcgtatgtcaaaagaagaagagagagccgtgaaggatgaattg
ctaagtgaaaaaccagaggtcaagcagaagtgggcatctcgacttctggcaaagttgcgg
aaagatatccgacccgaatatcgagaggattttgttcttacagttacagggaaaaaacct
ccatgttgtgttctttccaacccagaccagaaaggcaagatgcgaagaattgactgcctc
cgccaggcagataaagtctggaggttggaccttgttatggtgattttgtttaaaggtatt
ccgctggaaagtactgatggcgagcgccttgtaaagtccccacaatgctctaatccaggg
ctctgtgtccaaccccatcacataggggtttctgttaaggaactcgatttatatttggca
tactttgtgcatgcagcagattcaagtcaatctgaaagtcccagccagccaagtgacgct
gacattaaggaccagccagaaaatggacatttgggcttccaggacagttttgtcacatca
ggtgtttttagtgtcactgagctagtaagagtgtcacagacaccaatagctgcaggaact
ggcccaaatttttctctctcagatttggaaagttcttcatactacagcatgagtccagga
gcaatgaggaggtctttacccagcacatcctctacgagctccacaaagcgcctcaagtct
gtggaggatgaaatggacagtcctggtgaggagccattttatacaggccaagggcgctcc
ccaggaagtggcagtcagtcaagtggatggcatgaagtggagccaggaatgccatctcca
accacactgaagaagtcggagaagtctggtttcagcagcccctccccttcacagacctcc
tccctgggaacggcgttcacacagcatcaccgacctgtcattacaggacccagagcaagt
ccgcatgcaacaccatcgactcttcatttcccgacatcacccattatccagcagcctggg
ccttacttctcacacccagccatccgctatcaccctcaggagacgctgaaagaatttgtc
caacttgtctgccctgatgctggtcagcaggctggacaggtggggttcctcaatcccaat
gggagcagccaaggcaaggtgcacaacccattccttcccaccccaatgttgccaccgcca
ccgccaccaccgatggccaggcctgtgcctctgccggtgccagacacaaagcctccaacc
acgtcaacagaaggaggtgcagcctcccccacgtcaccaacctactcgacacccagcacc
tcccccgcaaaccgattcgtcagtgttggaccacgggatccaagctttgtaaatatccct
caacagacacagtcctggtacctgggataa

  All links  
Disease (2)   
   OMIM (2)   
Gene (15)   
   RefGene (8)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (2)   
   OC (1)   
Protein sequence (6)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (4)   
DNA sequence (40)   
   RefSeq(nuc) (4)   
   GenBank (18)   
   EMBL (18)   
Protein domain (3)   
   Pfam (3)   
All databases (66)   

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