Homo sapiens (human): 6253
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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)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Reticulon
Motif
Other DBs
NCBI-GeneID:
6253
NCBI-ProteinID:
NP_005610
OMIM:
603183
HGNC:
10468
Ensembl:
ENSG00000125744
UniProt:
O75298
Q6GMT0
A8K7F2
LinkDB
All DBs
Position
19:complement(45485294..45497047)
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AA seq
545 aa
AA seq
DB search
MGQVLPVFAHCKEAPSTASSTPDSTEGGNDDSDFRELHTAREFSEEDEEETTSQDWGTPR
ELTFSYIAFDGVVGSGGRRDSTARRPRPQGRSVSEPRDQHPQPSLGDSLESIPSLSQSPE
PGRRGDPDTAPPSERPLEDLRLRLDHLGWVARGTGSGEDSSTSSSTPLEDEEPQEPNRLE
TGEAGEELDLRLRLAQPSSPEVLTPQLSPGSGTPQAGTPSPSRSRDSNSGPEEPLLEEEE
KQWGPLEREPVRGQCLDSTDQLEFTVEPRLLGTAMEWLKTSLLLAVYKTVPILELSPPLW
TAIGWVQRGPTPPTPVLRVLLKWAKSPRSSGVPSLSLGADMGSKVADLLYWKDTRTSGVV
FTGLMVSLLCLLHFSIVSVAAHLALLLLCGTISLRVYRKVLQAVHRGDGANPFQAYLDVD
LTLTREQTERLSHQITSRVVSAATQLRHFFLVEDLVDSLKLALLFYILTFVGAIFNGLTL
LILGVIGLFTIPLLYRQHQAQIDQYVGLVTNQLSHIKAKIRAKIPGTGALASAAAAVSGS
KAKAE
NT seq
1638 nt
NT seq
+upstream
nt +downstream
nt
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
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