Homo sapiens (human): 11235
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Entry
11235 CDS
T01001
Symbol
PDCD10, CCM3, TFAR15
Name
(RefSeq) programmed cell death 10
KO
K18269
programmed cell death protein 10
Organism
hsa
Homo sapiens (human)
Pathway
hsa04520
Adherens junction
Disease
H00534
Cerebral cavernous malformation
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04147 Exosome [BR:
hsa04147
]
11235 (PDCD10)
Exosome [BR:
hsa04147
]
Exosomal proteins
Exosomal proteins of other body fluids (saliva and urine)
11235 (PDCD10)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
PDC10_C
PDCD10_N
CREPT
Talin_IBS2B
Med11
DALR_1
DUF5344
SabA_adhesion
TFIIF_beta
SesA
YxiF
Motif
Other DBs
NCBI-GeneID:
11235
NCBI-ProteinID:
NP_009148
OMIM:
609118
HGNC:
8761
Ensembl:
ENSG00000114209
UniProt:
Q9BUL8
Structure
PDB
PDBj
LinkDB
All DBs
Position
3:complement(167683298..167734892)
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AA seq
212 aa
AA seq
DB search
MRMTMEEMKNEAETTSMVSMPLYAVMYPVFNELERVNLSAAQTLRAAFIKAEKENPGLTQ
DIIMKILEKKSVEVNFTESLLRMAADDVEEYMIERPEPEFQDLNEKARALKQILSKIPDE
INDRVRFLQTIKDIASAIKELLDTVNNVFKKYQYQNRRALEHQKKEFVKYSKSFSDTLKT
YFKDGKAINVFVSANRLIHQTNLILQTFKTVA
NT seq
639 nt
NT seq
+upstream
nt +downstream
nt
atgaggatgacaatggaagagatgaagaatgaagctgagaccacatccatggtttctatg
cccctctatgcagtcatgtatcctgtgtttaatgagctagaacgagtaaatctgtctgca
gcccagacactgagagccgctttcatcaaggctgaaaaagaaaatccaggtctcacacaa
gacatcattatgaaaattttagagaaaaaaagcgtggaagttaacttcacggagtccctt
cttcgtatggcagctgatgatgtagaagagtatatgattgaacgaccagagccagaattc
caagacctaaacgaaaaggcacgagcacttaaacaaattctcagtaagatcccagatgag
atcaatgacagagtgaggtttctgcagacaatcaaggatatagctagtgcaataaaagaa
cttcttgatacagtgaataatgtcttcaagaaatatcaataccagaaccgcagggcactt
gaacaccaaaagaaagaatttgtaaagtactccaaaagtttcagtgatactctgaaaacg
tattttaaagatggcaaggcaataaatgtgttcgtaagtgccaaccgactaattcatcaa
accaacttaatacttcagaccttcaaaactgtggcctga
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