KEGG   Homo sapiens (human): 11160
Entry
11160             CDS       T01001                                 
Symbol
ERLIN2, C8orf2, Erlin-2, NET32, SPFH2, SPG18, SPG18A, SPG18B
Name
(RefSeq) ER lipid raft associated 2
  KO
K23341  erlin
Organism
hsa  Homo sapiens (human)
Disease
H00266  Hereditary spastic paraplegia
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   04121 Ubiquitin system [BR:hsa04121]
    11160 (ERLIN2)
Ubiquitin system [BR:hsa04121]
 Ubiquitin ligases (E3)
  Multi subunit Ring-finger type E3
   ERAD complex
    11160 (ERLIN2)
SSDB
Motif
Pfam: Band_7 RapA_C Hint DUF4346 POR_N
Other DBs
NCBI-GeneID: 11160
NCBI-ProteinID: NP_009106
OMIM: 611605
HGNC: 1356
Ensembl: ENSG00000147475
UniProt: O94905 A0A384ME54
Position
8:37736634..37758422
AA seq 339 aa
MAQLGAVVAVASSFFCASLFSAVHKIEEGHIGVYYRGGALLTSTSGPGFHLMLPFITSYK
SVQTTLQTDEVKNVPCGTSGGVMIYFDRIEVVNFLVPNAVYDIVKNYTADYDKALIFNKI
HHELNQFCSVHTLQEVYIELFDQIDENLKLALQQDLTSMAPGLVIQAVRVTKPNIPEAIR
RNYELMESEKTKLLIAAQKQKVVEKEAETERKKALIEAEKVAQVAEITYGQKVMEKETEK
KISEIEDAAFLAREKAKADAECYTAMKIAEANKLKLTPEYLQLMKYKAIASNSKIYFGKD
IPNMFMDSAGSVSKQFEGLADKLSFGLEDEPLETATKEN
NT seq 1020 nt   +upstreamnt  +downstreamnt
atggctcagttgggagcagttgtggctgtggcttccagtttcttttgtgcatctctcttc
tcagctgtgcacaagatagaagagggacatattggggtatattacagaggcggtgccctg
ctgacttcgaccagcggccctggtttccatctcatgctccctttcatcacatcatataag
tctgtgcagaccacactccagacagatgaggtgaagaatgtaccttgtgggactagtggt
ggtgtgatgatctactttgacagaattgaagtggtgaacttcctggtcccgaacgcagtg
tatgatatagtgaagaactatactgctgactatgacaaggccctcatcttcaacaagatc
caccacgaactgaaccagttctgcagtgtgcacacgcttcaagaggtctacattgagctg
tttgatcagattgatgaaaatctcaaactggctttgcaacaggacctgacctccatggcc
cctgggctggtcattcaagctgtgcgggtaacaaagcccaacataccagaggcaatccgc
agaaactacgagttgatggaaagtgagaagacaaagcttctcattgccgcccagaaacag
aaggtggtggaaaaggaagcagagacagagcggaagaaggcgctcattgaggcagaaaaa
gtggcccaggtggctgagatcacctacgggcagaaggtgatggagaaggagactgagaag
aagatttcagaaattgaagatgctgcatttctggcccgggagaaggcaaaggcagatgct
gagtgctacactgctatgaaaatagccgaagccaataagctgaagctaacccctgaatat
ctgcagctgatgaagtacaaggccattgcttccaacagcaagatttactttggcaaagac
attcctaacatgttcatggactctgcgggcagtgtgagcaagcagtttgaggggctagct
gacaagctaagctttggcttagaagatgaacccttggagacggccactaaggagaattga

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (4)   
   KEGG DISEASE (1)   
   OMIM (3)   
Genome (1)   
   KEGG GENOME (1)   
Gene (18)   
   KEGG ORTHOLOGY (1)   
   RefGene (9)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (3)   
   OC (1)   
Protein sequence (12)   
   UniProt (2)   
   SWISS-PROT (1)   
   RefSeq(pep) (9)   
DNA sequence (53)   
   RefSeq(nuc) (9)   
   GenBank (22)   
   EMBL (22)   
Protein domain (5)   
   Pfam (5)   
All databases (95)   

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