KEGG   Homo sapiens (human): 8022
Entry
8022              CDS       T01001                                 
Symbol
LHX3, CPHD3, LIM3, M2-LHX3
Name
(RefSeq) LIM homeobox 3
  KO
K09374  LIM homeobox protein 3/4
Organism
hsa  Homo sapiens (human)
Disease
H00254  Growth hormone deficiency
H02036  Combined pituitary hormone deficiency
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    8022 (LHX3)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Helix-turn-helix
   Homeo domain LIM
    8022 (LHX3)
SSDB
Motif
Pfam: LIM Homeodomain Homeobox_KN Furin-like_2 Trm112p SARA_C
Other DBs
NCBI-GeneID: 8022
NCBI-ProteinID: NP_835258
OMIM: 600577
HGNC: 6595
Ensembl: ENSG00000107187
UniProt: Q9UBR4 F1T0D5
Position
9:complement(136196250..136205128)
AA seq 397 aa
MLLETGLERDRARPGAAAVCTLGGTREIPLCAGCDQHILDRFILKALDRHWHSKCLKCSD
CHTPLAERCFSRGESVYCKDDFFKRFGTKCAACQLGIPPTQVVRRAQDFVYHLHCFACVV
CKRQLATGDEFYLMEDSRLVCKADYETAKQREAEATAKRPRTTITAKQLETLKSAYNTSP
KPARHVREQLSSETGLDMRVVQVWFQNRRAKEKRLKKDAGRQRWGQYFRNMKRSRGGSKS
DKDSVQEGQDSDAEVSFPDEPSLAEMGPANGLYGSLGEPTQALGRPSGALGNFSLEHGGL
AGPEQYRELRPGSPYGVPPSPAAPQSLPGPQPLLSSLVYPDTSLGLVPSGAPGGPPPMRV
LAGNGPSSDLSTGSSGGYPDFPASPASWLDEVDHAQF
NT seq 1194 nt   +upstreamnt  +downstreamnt
atgctgctggaaacggggctcgagcgcgaccgagcgaggcccggggccgccgccgtctgc
accttgggcgggactcgggagatcccgctgtgcgctggctgtgaccagcacatcctggac
cgcttcatcctcaaggctctggaccgccactggcacagcaagtgtctcaagtgcagcgac
tgccacacgccactggccgagcgctgcttcagccgaggggagagcgtttactgcaaggac
gactttttcaagcgcttcgggaccaagtgcgccgcgtgccagctgggcatcccgcccacg
caggtggtgcgccgcgcccaggacttcgtgtaccacctgcactgctttgcctgcgtcgtg
tgcaagcggcagctggccacgggcgacgagttctacctcatggaggacagccggctcgtg
tgcaaggcggactacgaaaccgccaagcagcgagaggccgaggccacggccaagcggccg
cgcacgaccatcaccgccaagcagctggagacgctgaagagcgcttacaacacctcgccc
aagccggcgcgccacgtgcgcgagcagctctcgtccgagacgggcctggacatgcgcgtg
gtgcaggtttggttccagaaccgccgggccaaggagaagaggctgaagaaggacgccggc
cggcagcgctgggggcagtatttccgcaacatgaagcgctcccgcggcggctccaagtcg
gacaaggacagcgttcaggaggggcaggacagcgacgctgaggtctccttccccgatgag
ccttccttggcggaaatgggcccggccaatggcctctacgggagcttgggggaacccacc
caggccttgggccggccctcgggagccctgggcaacttctccctggagcatggaggcctg
gcaggcccagagcagtaccgagagctgcgtcccggcagcccctacggtgtccccccatcc
cccgccgccccgcagagcctccctggcccccagcccctcctctccagcctggtgtaccca
gacaccagcttgggccttgtgccctcgggagcccccggcgggcccccacccatgagggtg
ctggcagggaacggacccagttctgacctatccacggggagcagcgggggttaccccgac
ttccctgccagccccgcctcctggctggatgaggtagaccacgctcagttctga

  All links  
Disease (2)   
   OMIM (2)   
Gene (22)   
   RefGene (8)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (9)   
   OC (1)   
Protein sequence (8)   
   UniProt (2)   
   SWISS-PROT (1)   
   RefSeq(pep) (5)   
DNA sequence (31)   
   RefSeq(nuc) (5)   
   GenBank (13)   
   EMBL (13)   
Protein domain (6)   
   Pfam (6)   
All databases (69)   

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