Homo sapiens (human): 284361
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Entry
284361 CDS
T01001
Symbol
EMC10, C19orf63, HSM1, HSS1, NEDDFAS
Name
(RefSeq) ER membrane protein complex subunit 10
KO
K23570
ER membrane protein complex subunit 10
Organism
hsa
Homo sapiens (human)
Disease
H02535
Neurodevelopmental disorder with dysmorphic facies
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04131 Membrane trafficking [BR:
hsa04131
]
284361 (EMC10)
Membrane trafficking [BR:
hsa04131
]
Endoplasmic reticulum (ER) - Golgi transport
Others
ER membrane protein complex
284361 (EMC10)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
ECM10
Motif
Other DBs
NCBI-GeneID:
284361
NCBI-ProteinID:
NP_996261
OMIM:
614545
HGNC:
27609
Ensembl:
ENSG00000161671
UniProt:
Q5UCC4
Structure
PDB
PDBj
LinkDB
All DBs
Position
19:50476507..50490871
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AA seq
262 aa
AA seq
DB search
MAAASAGATRLLLLLLMAVAAPSRARGSGCRAGTGARGAGAEGREGEACGTVGLLLEHSF
EIDDSANFRKRGSLLWNQQDGTLSLSQRQLSEEERGRLRDVAALNGLYRVRIPRRPGALD
GLEAGGYVSSFVPACSLVESHLSDQLTLHVDVAGNVVGVSVVTHPGGCRGHEVEDVDLEL
FNTSVQLQPPTTAPGPETAAFIERLEMEQAQKAKNPQEQKSFFAKYWMYIIPVVLFLMMS
GAPDTGGQGGGGGGGGGGGSGR
NT seq
789 nt
NT seq
+upstream
nt +downstream
nt
atggcggcagccagcgctggggcaacccggctgctcctgctcttgctgatggcggtagca
gcgcccagtcgagcccggggcagcggctgccgggccgggactggtgcgcgaggggctggg
gcggaaggtcgagagggcgaggcctgtggcacggtggggctgctgctggagcactcattt
gagatcgatgacagtgccaacttccggaagcggggctcactgctctggaaccagcaggat
ggtaccttgtccctgtcacagcggcagctcagcgaggaggagcggggccgactccgggat
gtggcagccctgaatggcctgtaccgggtccggatcccaaggcgacccggggccctggat
ggcctggaagctggtggctatgtctcctcctttgtccctgcgtgctccctggtggagtcg
cacctgtcggaccagctgaccctgcacgtggatgtggccggcaacgtggtgggcgtgtcg
gtggtgacgcaccccgggggctgccggggccatgaggtggaggacgtggacctggagctg
ttcaacacctcggtgcagctgcagccgcccaccacagccccaggccctgagacggcggcc
ttcattgagcgcctggagatggaacaggcccagaaggccaagaacccccaggagcagaag
tccttcttcgccaaatactggatgtacatcattcccgtcgtcctgttcctcatgatgtca
ggagcgccagacaccgggggccagggtgggggtgggggtgggggtggtggtgggggtagt
ggccggtga
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