Homo sapiens (human): 23197
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Entry
23197 CDS
T01001
Symbol
FAF2, ETEA, UBXD8, UBXN3B
Name
(RefSeq) Fas associated factor family member 2
KO
K18726
FAS-associated factor 2
Organism
hsa
Homo sapiens (human)
Network
nt06464
Amyotrophic lateral sclerosis
nt06466
Pathways of neurodegeneration
nt06536
Mitophagy
Element
N01137
PINK-Parkin-mediated autophagosome formation
N01138
Mutation-inactivated OPTN to PINK-Parkin-mediated autophagosome formation
N01139
Mutation-inactivated p62 to PINK-Parkin-mediated autophagosome formation
N01756
PINK-Parkin-independent ubiquitin-mediated mitophagy
N01757
PINK-Parkin-independent ubiquitin-mediated mitophagy, ubiquitin E3 ligase
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03019 Messenger RNA biogenesis [BR:
hsa03019
]
23197 (FAF2)
Messenger RNA biogenesis [BR:
hsa03019
]
Eukaryotic type
mRNA surveillance and transport factors
Transport factors
Ran-mediated transport factors
23197 (FAF2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
FAF1
UBA_4
UBX
Thioredoxin_7
PEHE
Motif
Other DBs
NCBI-GeneID:
23197
NCBI-ProteinID:
NP_055428
OMIM:
616935
HGNC:
24666
Ensembl:
ENSG00000113194
UniProt:
Q96CS3
Structure
PDB
LinkDB
All DBs
Position
5:176448385..176510074
Genome browser
AA seq
445 aa
AA seq
DB search
MAAPEERDLTQEQTEKLLQFQDLTGIESMDQCRHTLEQHNWNIEAAVQDRLNEQEGVPSV
FNPPPSRPLQVNTADHRIYSYVVSRPQPRGLLGWGYYLIMLPFRFTYYTILDIFRFALRF
IRPDPRSRVTDPVGDIVSFMHSFEEKYGRAHPVFYQGTYSQALNDAKRELRFLLVYLHGD
DHQDSDEFCRNTLCAPEVISLINTRMLFWACSTNKPEGYRVSQALRENTYPFLAMIMLKD
RRMTVVGRLEGLIQPDDLINQLTFIMDANQTYLVSERLEREERNQTQVLRQQQDEAYLAS
LRADQEKERKKREERERKRRKEEEVQQQKLAEERRRQNLQEEKERKLECLPPEPSPDDPE
SVKIIFKLPNDSRVERRFHFSQSLTVIHDFLFSLKESPEKFQIEANFPRRVLPCIPSEEW
PNPPTLQEAGLSHTEVLFVQDLTDE
NT seq
1338 nt
NT seq
+upstream
nt +downstream
nt
atggcggcgcctgaggagcgggatctaacccaggagcagacagagaagctgctgcagttt
caggatctcactggcatcgaatctatggatcagtgtcgccataccttggaacagcataac
tggaacatagaggctgctgtacaggacagattgaatgagcaagagggcgtacctagtgtt
ttcaacccacctccatcacgacccctgcaggttaatacagctgaccacaggatctacagc
tatgttgtctcaagacctcaaccaagggggctgcttggatggggttattacttgataatg
cttccattccggtttacctattacacgatacttgatatatttaggtttgctcttcgtttt
atacggcctgaccctcgcagccgggtcactgaccccgttggggacattgtttcatttatg
cactcttttgaagagaaatatgggagggcacaccctgtcttctaccagggaacgtacagc
caggcacttaacgatgccaaaagggagcttcgctttcttttggtttatcttcatggagat
gatcaccaggactctgatgagttttgtcgcaacacactctgtgcacctgaagttatttca
ctaataaacactaggatgctcttctgggcatgctctacaaacaaacctgagggatacagg
gtctcacaggctttacgagagaacacctatccattcctggccatgattatgctgaaggat
cgaaggatgactgtggtgggacggctagaaggcctcattcaacctgatgacctcattaac
caactgacatttatcatggatgctaaccagacttacctggtgtcagaacgcctagaaagg
gaagaaagaaaccagacccaagtgctgagacaacagcaggatgaggcctacctggcctct
ctcagagctgaccaggagaaagaaagaaagaaacgggaggagcgggagcgtaagcggcgg
aaggaggaggaggtgcaacagcaaaagttggcagaggagagacggcggcagaatttacag
gaggaaaaggaaaggaagttggaatgcctgccccctgaaccttcccctgatgaccctgaa
agtgtcaagatcatcttcaaattacctaatgattctcgagtagagagacgattccacttt
tcacagtctctaacagtaatccacgacttcttattctccttgaaggaaagcccagaaaag
tttcagattgaagccaattttcccaggcgagtgctgccctgcatcccttcagaggagtgg
cccaatccccctacgctacaggaggccggactcagccacacagaagttctttttgttcag
gacctaactgacgaatga
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