KEGG   Homo sapiens (human): 9096
Entry
9096              CDS       T01001                                 
Symbol
TBX18, CAKUT2, PUJO
Name
(RefSeq) T-box transcription factor 18
  KO
K10183  T-box protein 18
Organism
hsa  Homo sapiens (human)
Disease
H01867  Congenital anomalies of kidney and urinary tract
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    9096 (TBX18)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Other transcription factors
   T-box
    9096 (TBX18)
SSDB
Motif
Pfam: T-box
Other DBs
NCBI-GeneID: 9096
NCBI-ProteinID: NP_001073977
OMIM: 604613
HGNC: 11595
Ensembl: ENSG00000112837
UniProt: O95935
Position
6:complement(84732496..84764598)
AA seq 607 aa
MAEKRRGSPCSMLSLKAHAFSVEALIGAEKQQQLQKKRRKLGAEEAAGAVDDGGCSRGGG
AGEKGSSEGDEGAALPPPAGATSGPARSGADLERGAAGGCEDGFQQGASPLASPGGSPKG
SPARSLARPGTPLPSPQAPRVDLQGAELWKRFHEIGTEMIITKAGRRMFPAMRVKISGLD
PHQQYYIAMDIVPVDNKRYRYVYHSSKWMVAGNADSPVPPRVYIHPDSPASGETWMRQVI
SFDKLKLTNNELDDQGHIILHSMHKYQPRVHVIRKDCGDDLSPIKPVPSGEGVKAFSFPE
TVFTTVTAYQNQQITRLKIDRNPFAKGFRDSGRNRMGLEALVESYAFWRPSLRTLTFEDI
PGIPKQGNASSSTLLQGTGNGVPATHPHLLSGSSCSSPAFHLGPNTSQLCSLAPADYSAC
ARSGLTLNRYSTSLAETYNRLTNQAGETFAPPRTPSYVGVSSSTSVNMSMGGTDGDTFSC
PQTSLSMQISGMSPQLQYIMPSPSSNAFATNQTHQGSYNTFRLHSPCALYGYNFSTSPKL
AASPEKIVSSQGSFLGSSPSGTMTDRQMLPPVEGVHLLSSGGQQSFFDSRTLGSLTLSSS
QVSAHMV
NT seq 1824 nt   +upstreamnt  +downstreamnt
atggccgagaagcgaaggggctcgccgtgcagcatgctaagcctcaaggcgcacgctttc
tcggtggaggcgctgatcggcgccgagaagcagcaacagcttcagaagaagcggcgaaaa
ctgggcgccgaagaggcggcgggggccgtggacgacggaggctgcagccgcggcggcggc
gcgggcgaaaagggttcttctgagggagacgaaggcgctgcgctcccgccgccggctggg
gcgacgtctgggccggctcggagtggcgcagacctggagcgcggagccgcgggcggctgt
gaggacggcttccagcagggagcttcccctctggcgtcaccgggaggctcccccaagggg
tctccggcgcgctccctggcccggcccgggacccctctgccctcgccgcaggccccgcgg
gtggatctgcagggagccgagctctggaagcgctttcatgagataggcactgagatgatc
atcaccaaggccggcaggcgcatgtttccagcaatgagagtgaagatctctggattagat
cctcaccagcaatattacattgccatggatattgtaccagtggacaacaaaagatacagg
tatgtttaccacagttcgaaatggatggtggcaggtaatgctgactcgcctgtgccaccc
cgtgtgtacattcatccagactcgcctgcctcgggggagacttggatgagacaagttatc
agcttcgacaagctgaagctcaccaacaatgaactggatgaccaaggccatattattctt
cattctatgcacaaataccaaccgcgagtgcacgtcatccgtaaagactgtggagacgat
ctttctcccatcaagcctgttccatccggggagggagtaaaggcattctcctttccagaa
actgtcttcacaaccgtcactgcctatcagaatcagcagattactcgcctgaagatagat
aggaatccatttgctaaaggcttccgagactccgggcgcaacagaatgggtttggaagcc
ttggtggaatcatatgcattctggcgaccatcactacggactctgacctttgaagatatc
cctggaattcccaagcaaggcaatgcaagttcctccaccttgctccaaggtactgggaat
ggcgttcctgccactcaccctcaccttttgtctggctcctcttgctcctctcctgccttc
catctggggcccaacaccagccagctgtgtagtctggcccctgctgactattctgcctgt
gcccgctcaggcctcaccctcaaccgatacagcacatctttggcagagacctacaacagg
ctcaccaaccaggctggtgagacctttgccccgcccaggactccctcctatgtgggcgtg
agcagcagcacctccgtgaacatgtccatgggtggcactgatggggacaccttcagctgc
ccacagaccagcttatccatgcagatttcgggaatgtccccccagctccagtatatcatg
ccatcaccctccagcaatgccttcgccactaaccagacccatcagggttcctataatact
tttagattacacagcccctgtgcactatatggatataacttctccacatcccccaaactg
gctgccagtcctgagaaaattgtttcttcccaaggaagtttcttggggtcctcaccgagt
gggaccatgacggatcggcagatgttgccccctgtggaaggagtgcacctgcttagcagt
gggggtcagcagagtttctttgactctaggaccctaggaagcttaactctgtcatcatct
caagtatctgcacatatggtctga

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (20)   
   KEGG ORTHOLOGY (1)   
   RefGene (13)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (1)   
   OC (1)   
Protein sequence (3)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (1)   
DNA sequence (11)   
   RefSeq(nuc) (1)   
   GenBank (5)   
   EMBL (5)   
Protein domain (1)   
   Pfam (1)   
All databases (41)   

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