KEGG   Homo sapiens (human): 203190
Entry
203190            CDS       T01001                                 
Symbol
LGI3, IDDMDS, LGIL4
Name
(RefSeq) leucine rich repeat LGI family member 3
  KO
K19999  leucine-rich repeat LGI family member 3
Organism
hsa  Homo sapiens (human)
Disease
H02463  Syndromic intellectual developmental disorder
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   04131 Membrane trafficking [BR:hsa04131]
    203190 (LGI3)
Membrane trafficking [BR:hsa04131]
 SNARE
  SNARE associated proteins
   Syntaxin-binding proteins
    203190 (LGI3)
SSDB
Motif
Pfam: EPTP LRR_8 LRR_5 LRR_4 LRR_9 LRRCT LRR_1
Other DBs
NCBI-GeneID: 203190
NCBI-ProteinID: NP_644807
OMIM: 608302
HGNC: 18711
Ensembl: ENSG00000168481
UniProt: Q8N145
Position
8:complement(22146830..22156806)
AA seq 548 aa
MAGLRARGGPGPGLLALSALGFCLMLQVSAKRPPKTPPCPPSCSCTRDTAFCVDSKAVPR
NLPSEVISLTLVNAAFSEIQDGAFSHLPLLQFLLLNSNKFTLIGDNAFTGLSHLQYLFIE
NNDIWALSKFTFRGLKSLTHLSLANNNLQTLPRDIFRPLDILNDLDLRGNSLNCDCKVKW
LVEWLAHTNTTVAPIYCASPPRFQEHKVQDLPLREFDCITTDFVLYQTLAFPAVSAEPFL
YSSDLYLALAQPGVSACTILKWDYVERQLRDYDRIPAPSAVHCKPMVVDSQLYVVVAQLF
GGSYIYHWDPNTTRFTRLQDIDPQRVRKPNDLEAFRIDGDWYFAVADSSKAGATSLYRWH
QNGFYSHQALHPWHRDTDLEFVDGEGKPRLIVSSSSQAPVIYQWSRTQKQFVAQGEVTQV
PDAQAVKHFRAGRDSYLCLSRYIGDSKILRWEGTRFSEVQALPSRGSLALQPFLVGGRRY
LALGSDFSFTQIYQWDEGRQKFVRFQELAVQAPRAFCYMPAGDAQLLLAPSFKGQTLVYR
HIVVDLSA
NT seq 1647 nt   +upstreamnt  +downstreamnt
atggcggggctgcgggccagggggggcccggggccggggctgctggcgctctccgcgctc
ggcttctgcctcatgctgcaagtcagcgctaagaggccccccaagacgcccccctgcccg
cccagctgctcttgcaccagggacaccgccttctgcgtggactcaaaggcggtgcccagg
aacctgccctcggaggtcatctccctgaccctggtgaatgccgccttctcagagatccag
gatggagcgttctcccacctcccgctgctgcagttcttgttactcaactccaacaagttt
acactgattggagacaacgccttcacaggactgtcgcacctgcagtatctcttcattgag
aacaatgacatctgggcactatccaagttcaccttccgaggactcaagtccttgactcac
ctctcgctggccaacaataacctgcagacactgcccagagacatcttccggcccctggac
atcctgaatgacttggacctgcggggcaactcactcaactgtgactgcaaggtgaagtgg
ttggtggagtggctggcacacaccaacaccacggtggcacccatctactgcgccagcccg
ccccgcttccaggagcacaaggtgcaggacctgccgctgcgggagttcgattgcatcacc
acagattttgtgttgtaccagaccctggccttcccagcagtgtcggctgagcccttcctc
tactccagtgacctctatttggctctggcccagccaggagtcagtgcctgcaccatcctg
aagtgggactatgttgagcggcagcttcgagactatgatagaatcccagccccctctgca
gtgcactgcaagccgatggtggtggacagccagctgtacgtggtcgtggcccagctgttt
ggcggctcttacatttaccactgggatcccaacaccacgcgcttcaccaggctgcaagac
attgacccgcagcgcgtgcgcaagcctaacgacctagaagccttccgcatcgacggtgac
tggtactttgccgtggctgacagctccaaggcaggcgccaccagcctctaccgctggcac
cagaatggcttctactcccaccaggcactgcacccctggcaccgtgacaccgacctggag
tttgtggacggcgagggcaagccacggctgattgtgtccagcagctcccaggcacccgtc
atctatcagtggagtcgcacccagaagcagtttgtggcccagggtgaggtgacccaggtg
cctgatgcccaagctgtgaaacactttcgtgccggccgcgacagctacctgtgcctcagc
cgctacattggcgactccaagatcctgcgctgggagggtacccgcttctcggaggtgcag
gccctgccctcccggggctcgctggccctgcagcccttccttgtgggtggccgccgctac
ctggcactgggcagtgatttctccttcacccagatctaccagtgggatgagggacgacag
aagtttgtacggttccaggagctggctgtgcaggctcctcgggccttctgctacatgcct
gctggggacgcccagctactcctggcccccagcttcaagggacagacgctggtgtataga
cacattgtggtggatctcagtgcctag

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (11)   
   KEGG ORTHOLOGY (1)   
   RefGene (4)   
   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 (17)   
   RefSeq(nuc) (1)   
   GenBank (8)   
   EMBL (8)   
Protein domain (7)   
   Pfam (7)   
All databases (44)   

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