Homo sapiens (human): 8905
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Entry
8905 CDS
T01001
Symbol
AP1S2, DC22, MRX59, MRXS21, MRXS5, MRXSF, PGS, SIGMA1B
Name
(RefSeq) AP-1 complex subunit sigma-2 isoform 2
KO
K12394
AP-1 complex subunit sigma 1/2
Organism
hsa
Homo sapiens (human)
Pathway
hsa04142
Lysosome biogenesis
hsa05170
Human immunodeficiency virus 1 infection
Network
nt06550
Lysosome biogenesis
Element
N02015
Lysosomal enzyme (LE) transport from the TGN to endosome
N02020
GCase transport from the ER to the lysosome
Disease
H03038
Pettigrew syndrome
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09141 Transport and catabolism
04142 Lysosome biogenesis
8905 (AP1S2)
09160 Human Diseases
09172 Infectious disease: viral
05170 Human immunodeficiency virus 1 infection
8905 (AP1S2)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04131 Membrane trafficking [BR:
hsa04131
]
8905 (AP1S2)
Membrane trafficking [BR:
hsa04131
]
Endosome - Golgi transport
Others
AP-1 complex
8905 (AP1S2)
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Clat_adaptor_s
DUF629
Motif
Other DBs
NCBI-GeneID:
8905
NCBI-ProteinID:
NP_003907
OMIM:
300629
HGNC:
560
UniProt:
P56377
Q549M9
LinkDB
All DBs
Position
X:complement(15825806..15854813)
Genome browser
AA seq
157 aa
AA seq
DB search
MQFMLLFSRQGKLRLQKWYVPLSDKEKKKITRELVQTVLARKPKMCSFLEWRDLKIVYKR
YASLYFCCAIEDQDNELITLEIIHRYVELLDKYFGSVCELDIIFNFEKAYFILDEFLLGG
EVQETSKKNVLKAIEQADLLQEEAETPRSVLEEIGLT
NT seq
474 nt
NT seq
+upstream
nt +downstream
nt
atgcagtttatgttgctttttagtcgtcagggaaagcttcgactgcaaaaatggtatgtc
ccactatcagacaaagagaagaaaaagatcacaagagaacttgttcagaccgttttagca
cggaaacctaaaatgtgcagcttccttgagtggcgagatctgaagattgtttacaaaaga
tatgctagtctgtatttttgctgtgctattgaggatcaggacaatgaactaattaccctg
gaaataattcatcgttatgtggaattacttgacaagtatttcggcagtgtctgtgaacta
gatatcatctttaattttgagaaggcttattttattttggatgagtttcttttgggaggg
gaagttcaggaaacatccaagaaaaatgtccttaaagcaattgagcaggctgatctactg
caggaggaagctgaaaccccacgtagtgttcttgaagaaattggactgacataa
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