KEGG   Homo sapiens (human): 6253
Entry
6253              CDS       T01001                                 
Symbol
RTN2, HMNR11, NSP2, NSPL1, NSPLI, SPG12
Name
(RefSeq) reticulon 2
  KO
K20722  reticulon-2
Organism
hsa  Homo sapiens (human)
Disease
H00266  Hereditary spastic paraplegia
H00856  Distal hereditary motor neuropathies
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   04131 Membrane trafficking [BR:hsa04131]
    6253 (RTN2)
   03036 Chromosome and associated proteins [BR:hsa03036]
    6253 (RTN2)
Membrane trafficking [BR:hsa04131]
 Endoplasmic reticulum (ER) - Golgi transport
  Others
   Others
    6253 (RTN2)
Chromosome and associated proteins [BR:hsa03036]
 Eukaryotic type
  Centrosome formation proteins
   Spindle formation proteins
    6253 (RTN2)
SSDB
Motif
Pfam: Reticulon
Other DBs
NCBI-GeneID: 6253
NCBI-ProteinID: NP_005610
OMIM: 603183
HGNC: 10468
Ensembl: ENSG00000125744
UniProt: O75298 Q6GMT0 A8K7F2
LinkDB
Position
19:complement(45485294..45497047)
AA seq 545 aa
MGQVLPVFAHCKEAPSTASSTPDSTEGGNDDSDFRELHTAREFSEEDEEETTSQDWGTPR
ELTFSYIAFDGVVGSGGRRDSTARRPRPQGRSVSEPRDQHPQPSLGDSLESIPSLSQSPE
PGRRGDPDTAPPSERPLEDLRLRLDHLGWVARGTGSGEDSSTSSSTPLEDEEPQEPNRLE
TGEAGEELDLRLRLAQPSSPEVLTPQLSPGSGTPQAGTPSPSRSRDSNSGPEEPLLEEEE
KQWGPLEREPVRGQCLDSTDQLEFTVEPRLLGTAMEWLKTSLLLAVYKTVPILELSPPLW
TAIGWVQRGPTPPTPVLRVLLKWAKSPRSSGVPSLSLGADMGSKVADLLYWKDTRTSGVV
FTGLMVSLLCLLHFSIVSVAAHLALLLLCGTISLRVYRKVLQAVHRGDGANPFQAYLDVD
LTLTREQTERLSHQITSRVVSAATQLRHFFLVEDLVDSLKLALLFYILTFVGAIFNGLTL
LILGVIGLFTIPLLYRQHQAQIDQYVGLVTNQLSHIKAKIRAKIPGTGALASAAAAVSGS
KAKAE
NT seq 1638 nt   +upstreamnt  +downstreamnt
atggggcaggtcctgccggtcttcgcccactgcaaagaagctccgtctacagcctcctca
actcctgattccacagaaggagggaacgacgactctgattttcgagagctgcacacagcc
cgggaattctcagaggaggacgaggaggagaccacgtcgcaggactggggcaccccccgg
gagctgaccttctcctacatcgcctttgatggtgtagtgggctccgggggccgcagggat
tcaactgcccgccgcccccgcccccagggccgctcagtctcggaaccacgagaccagcac
cctcagcccagcctgggcgacagcttggagagcatccccagcctgagccaatccccggag
cctggacgacggggtgatcctgacaccgcgcctccatccgagcgccctctggaagacctg
aggcttcggttggaccatctgggctgggtggcccggggaacgggatccggggaggactct
tccaccagcagctccaccccgctggaagacgaagaaccccaagaacccaacagattggag
acaggagaagctggggaagaactggacctacgactccgacttgctcagccctcatcgccc
gaggtcttgactccccagctcagtccgggctctgggacaccccaggccggtactccgtcc
ccatcccgatcgcgagattcgaactctgggcccgaagagccattgctggaagaggaagaa
aagcagtgggggccactggagcgagagccagtaaggggacagtgcctcgatagcacggac
caattagaattcacggtggagccacgccttctaggaacagctatggaatggttaaagaca
tcattgcttttggctgtttacaagacggttccaattttggaattgtccccacctctgtgg
acagccattggctgggtccaaaggggccccaccccccctactcctgtcctccgggttcta
ctgaagtgggcaaaatccccgagaagcagcggtgtccccagcctctcactcggagccgat
atggggagtaaagtggcggacctgctgtactggaaggacacgaggacgtcaggagtggtc
ttcacaggcctgatggtctccctcctctgcctcctgcactttagcatcgtgtccgtggcc
gcgcacttggctctgttgctgctctgcggcaccatctctctcagggtttaccgcaaagtg
ctgcaggccgtgcaccggggggatggagccaaccctttccaggcctacctggatgtggac
ctcaccctgactcgggagcagacggaacgtttgtcccaccagatcacctcccgcgtggtc
tcggcggccacgcagctgcggcacttcttcctggtagaagacctcgtggattccctcaag
ctggccctcctcttctacatcttgaccttcgtgggtgccatcttcaatggtttgactctt
ctcattctgggagtgattggtctattcaccatccccctgctgtaccggcagcaccaggct
cagatcgaccaatatgtggggttggtgaccaatcagttgagccacatcaaagctaagatc
cgagctaaaatcccagggaccggagccctggcctctgcagcagccgcagtctccggatcc
aaagccaaagccgaatga

DBGET integrated database retrieval system