KEGG   Homo sapiens (human): 84816
Entry
84816             CDS       T01001                                 
Symbol
RTN4IP1, NIMP, OPA10
Name
(RefSeq) reticulon 4 interacting protein 1
  KO
K23164  reticulon-4-interacting protein 1, mitochondrial
Organism
hsa  Homo sapiens (human)
Disease
H01020  Optic atrophy
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:hsa03029]
    84816 (RTN4IP1)
Mitochondrial biogenesis [BR:hsa03029]
 Mitochondrial quality control factors
  Mitochondrial respiratory chain complex assembly factors
   Complex-I assembly factors
    84816 (RTN4IP1)
SSDB
Motif
Pfam: ADH_zinc_N_2 ADH_zinc_N ADH_N THF_DHG_CYH_C Methyltransf_24 Semialdhyde_dh ELFV_dehydrog Eno-Rase_NADH_b
Other DBs
NCBI-GeneID: 84816
NCBI-ProteinID: NP_116119
OMIM: 610502
HGNC: 18647
Ensembl: ENSG00000130347
UniProt: Q8WWV3
Structure
Position
6:complement(106570771..106630491)
AA seq 396 aa
MEFLKTCVLRRNACTAVCFWRSKVVQKPSVRRISTTSPRSTVMPAWVIDKYGKNEVLRFT
QNMMMPIIHYPNEVIVKVHAASVNPIDVNMRSGYGATALNMKRDPLHVKIKGEEFPLTLG
RDVSGVVMECGLDVKYFKPGDEVWAAVPPWKQGTLSEFVVVSGNEVSHKPKSLTHTQAAS
LPYVALTAWSAINKVGGLNDKNCTGKRVLILGASGGVGTFAIQVMKAWDAHVTAVCSQDA
SELVRKLGADDVIDYKSGSVEEQLKSLKPFDFILDNVGGSTETWAPDFLKKWSGATYVTL
VTPFLLNMDRLGIADGMLQTGVTVGSKALKHFWKGVHYRWAFFMASGPCLDDIAELVDAG
KIRPVIEQTFPFSKVPEAFLKVERGHARGKTVINVV
NT seq 1191 nt   +upstreamnt  +downstreamnt
atggaatttctgaagacttgtgtacttagaagaaatgcatgcactgcggtttgcttctgg
agaagcaaagttgtccaaaagccttcagttagaaggattagtactacctctcctaggagc
actgtcatgcctgcttgggtgatagataaatatgggaagaatgaagtgcttcgattcact
cagaacatgatgatgcctatcatacactatccaaatgaagtcattgtcaaagttcacgct
gccagtgtaaatcctatagacgttaatatgagaagtggttatggagctacagctttaaat
atgaagcgtgatcctttacacgtgaaaatcaaaggagaagaatttcctctgactctgggt
cgggatgtctctggcgtggtgatggaatgtgggcttgatgtgaaatacttcaagcctgga
gatgaggtctgggctgcagttcctccttggaaacaaggcactctttcagagtttgttgta
gtcagtgggaatgaggtctctcacaaacccaaatcactcactcatactcaagctgcctct
ttgccatatgtggctctcacagcctggtctgctataaacaaagttggtggcctgaatgac
aagaattgcacaggaaaacgtgttctaatcttaggcgcttcaggcggagttggtactttt
gctatacaggtaatgaaagcatgggatgctcatgtgacagcagtttgctcccaagatgcc
agtgaacttgtaaggaagcttggtgcagacgatgtaattgattacaaatctggaagtgtg
gaagagcagttgaaatccttaaaaccatttgattttatccttgataatgttggcggatcc
actgaaacatgggctccagattttctcaagaaatggtcaggagccacctatgtgactttg
gtgactcctttcctcctgaacatggaccgattgggcatagcagatggcatgttgcagaca
ggagtcactgtaggttcaaaggcattaaagcatttctggaaaggagtccattatcgctgg
gcatttttcatggccagtggcccatgtttagatgacattgcagaactggtggatgcggga
aagatccggccagttattgaacaaacctttcctttttctaaagttccagaagccttcctg
aaggtggaaagaggacacgcacgaggaaagactgtaattaatgttgtttaa

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (10)   
   KEGG ORTHOLOGY (1)   
   RefGene (3)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (1)   
   OC (1)   
Protein sequence (8)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (6)   
DNA sequence (22)   
   RefSeq(nuc) (6)   
   GenBank (8)   
   EMBL (8)   
3D Structure (1)   
   PDB (1)   
Protein domain (8)   
   Pfam (8)   
All databases (55)   

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