Homo sapiens (human): 8905
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Entry
8905 CDS
T01001
Symbol
AP1S2, DC22, MRX59, MRXS21, MRXS5, MRXSF, PGS, SIGMA1B
Name
(RefSeq) adaptor related protein complex 1 subunit sigma 2
KO
K12394
AP-1 complex subunit sigma 1/2
Organism
hsa
Homo sapiens (human)
Pathway
hsa04142
Lysosome
hsa05170
Human immunodeficiency virus 1 infection
Disease
H00658
X-linked syndromic intellectual developmental disorder
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09141 Transport and catabolism
04142 Lysosome
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)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Clat_adaptor_s
DUF629
PulA_N1
Motif
Other DBs
NCBI-GeneID:
8905
NCBI-ProteinID:
NP_003907
OMIM:
300629
HGNC:
560
Ensembl:
ENSG00000182287
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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