Homo sapiens (human): 10613
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Entry
10613 CDS
T01001
Symbol
ERLIN1, C10orf69, Erlin-1, KE04, KEO4, SPFH1, SPG62
Name
(RefSeq) ER lipid raft associated 1
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
]
10613 (ERLIN1)
Ubiquitin system [BR:
hsa04121
]
Ubiquitin ligases (E3)
Multi subunit type E3
ERAD complex
10613 (ERLIN1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Band_7
Catalase-rel
Ribosomal_L33
Motif
Other DBs
NCBI-GeneID:
10613
NCBI-ProteinID:
NP_001094096
OMIM:
611604
HGNC:
16947
Ensembl:
ENSG00000107566
UniProt:
O75477
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All DBs
Position
10:complement(100150094..100186029)
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AA seq
348 aa
AA seq
DB search
MNMTQARVLVAAVVGLVAVLLYASIHKIEEGHLAVYYRGGALLTSPSGPGYHIMLPFITT
FRSVQTTLQTDEVKNVPCGTSGGVMIYIDRIEVVNMLAPYAVFDIVRNYTADYDKTLIFN
KIHHELNQFCSAHTLQEVYIELFDQIDENLKQALQKDLNLMAPGLTIQAVRVTKPKIPEA
IRRNFELMEAEKTKLLIAAQKQKVVEKEAETERKKAVIEAEKIAQVAKIRFQQKVMEKET
EKRISEIEDAAFLAREKAKADAEYYAAHKYATSNKHKLTPEYLELKKYQAIASNSKIYFG
SNIPNMFVDSSCALKYSDIRTGRESSLPSKEALEPSGENVIQNKESTG
NT seq
1047 nt
NT seq
+upstream
nt +downstream
nt
atgaatatgactcaagcccgggttctggtggctgcagtggtggggttggtggctgtcctg
ctctacgcctccatccacaagattgaggagggccatctggctgtgtactacaggggagga
gctttactaactagccccagtggaccaggctatcatatcatgttgcctttcattactacg
ttcagatctgtgcagacaacactacaaactgatgaagttaaaaatgtgccttgtggaaca
agtggtggggtcatgatctatattgaccgaatagaagtggttaatatgttggctccttat
gcagtgtttgatatcgtgaggaactatactgcagattatgacaagaccttaatcttcaat
aaaatccaccatgagctgaaccagttctgcagtgcccacacacttcaggaagtttacatt
gaattgtttgatcaaatagatgaaaacctgaagcaagctctgcagaaagacttaaacctc
atggccccaggtctcactatacaggctgtgcgtgttacaaaacccaaaatcccagaagcc
ataagaagaaattttgagttaatggaggctgagaagacaaaactccttatagctgcacag
aaacaaaaggttgtggaaaaagaagctgagacagagaggaaaaaggcagttatagaagca
gagaagattgcacaagtggcaaaaattcggtttcagcagaaagtgatggaaaaagaaact
gaaaagcgcatttctgaaatcgaagatgctgcattcctggcccgagagaaagcgaaagca
gatgctgaatattatgctgcacacaaatatgccacctcaaacaagcacaagttgaccccg
gaatatctggagctcaaaaagtaccaggccattgcttctaacagtaagatctattttggc
agcaacatccctaacatgttcgtggactcctcatgtgctttgaaatattcagatattagg
actggaagagaaagctcactcccctctaaggaggctcttgaaccctctggagagaacgtc
atccaaaacaaagagagcacaggttga
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