Homo sapiens (human): 440738
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Entry
440738 CDS
T01001
Symbol
MAP1LC3C, ATG8J, LC3C
Name
(RefSeq) microtubule associated protein 1 light chain 3 gamma
KO
K10435
microtubule-associated protein 1 light chain
Organism
hsa
Homo sapiens (human)
Pathway
hsa04137
Mitophagy - animal
hsa04140
Autophagy - animal
hsa04216
Ferroptosis
hsa04371
Apelin signaling pathway
hsa04621
NOD-like receptor signaling pathway
hsa05014
Amyotrophic lateral sclerosis
hsa05022
Pathways of neurodegeneration - multiple diseases
hsa05131
Shigellosis
hsa05167
Kaposi sarcoma-associated herpesvirus infection
Network
nt06164
Kaposi sarcoma-associated herpesvirus (KSHV)
nt06182
Shigella
nt06464
Amyotrophic lateral sclerosis
nt06466
Pathways of neurodegeneration
nt06532
Autophagy
nt06536
Mitophagy
Element
N00156
Autophagy-vesicle nucleation/elongation/maturation, LC3-II formation
N01137
PINK-Parkin-mediated autophagosome formation
N01139
Mutation-inactivated p62 to PINK-Parkin-mediated autophagosome formation
N01140
TBK1-mediated autophagosome formation
N01141
Mutation-inactivated TBK1 to TBK1-mediated autophagosome formation
N01716
Autophagy-vesicle nucleation/elongation/maturation, sequestosome-1-like receptor
N01721
Autophagosome and lysosome fusion, tethering factor
N01722
Autophagosome and lysosome fusion, tethering factor, GRASP55
N01756
PINK-Parkin-independent ubiquitin-mediated mitophagy
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04371 Apelin signaling pathway
440738 (MAP1LC3C)
09140 Cellular Processes
09141 Transport and catabolism
04140 Autophagy - animal
440738 (MAP1LC3C)
04137 Mitophagy - animal
440738 (MAP1LC3C)
09143 Cell growth and death
04216 Ferroptosis
440738 (MAP1LC3C)
09150 Organismal Systems
09151 Immune system
04621 NOD-like receptor signaling pathway
440738 (MAP1LC3C)
09160 Human Diseases
09172 Infectious disease: viral
05167 Kaposi sarcoma-associated herpesvirus infection
440738 (MAP1LC3C)
09171 Infectious disease: bacterial
05131 Shigellosis
440738 (MAP1LC3C)
09164 Neurodegenerative disease
05014 Amyotrophic lateral sclerosis
440738 (MAP1LC3C)
05022 Pathways of neurodegeneration - multiple diseases
440738 (MAP1LC3C)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04131 Membrane trafficking [BR:
hsa04131
]
440738 (MAP1LC3C)
03029 Mitochondrial biogenesis [BR:
hsa03029
]
440738 (MAP1LC3C)
09183 Protein families: signaling and cellular processes
04812 Cytoskeleton proteins [BR:
hsa04812
]
440738 (MAP1LC3C)
Membrane trafficking [BR:
hsa04131
]
Autophagy
Mitophagy
Other mitophagy associated proteins
440738 (MAP1LC3C)
Mitochondrial biogenesis [BR:
hsa03029
]
Mitochondrial quality control factors
Mitophagy factors
Other mitophagy factors
440738 (MAP1LC3C)
Cytoskeleton proteins [BR:
hsa04812
]
Eukaryotic cytoskeleton proteins
Microtubules
Tubulin-binding proteins
Microtubule-associated proteins (MAPs)
440738 (MAP1LC3C)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
ATG8
APG12
Motif
Other DBs
NCBI-GeneID:
440738
NCBI-ProteinID:
NP_001004343
OMIM:
609605
HGNC:
13353
Ensembl:
ENSG00000197769
UniProt:
Q9BXW4
Structure
PDB
PDBj
LinkDB
All DBs
Position
1:complement(241995490..242001393)
Genome browser
AA seq
147 aa
AA seq
DB search
MPPPQKIPSVRPFKQRKSLAIRQEEVAGIRAKFPNKIPVVVERYPRETFLPPLDKTKFLV
PQELTMTQFLSIIRSRMVLRATEAFYLLVNNKSLVSMSATMAEIYRDYKDEDGFVYMTYA
SQETFGCLESAAPRDGSSLEDRPCNPL
NT seq
444 nt
NT seq
+upstream
nt +downstream
nt
atgccgcctccacagaaaatcccaagcgtcagacccttcaagcagaggaaaagcttggca
atcagacaagaggaagttgctggaatccgggcaaagttccccaacaaaatcccggtggta
gtggagcgctaccccagggagacgttcctgcccccgctggacaaaaccaagttcctggtc
ccgcaggagctgaccatgacccagttcctcagcatcatccggagccgcatggtcctgaga
gccacggaagccttttacttgctggtgaacaacaagagcctggtcagcatgagcgcaacc
atggcagagatctacagagactacaaggatgaggatggcttcgtgtacatgacctacgcc
tcccaggagacatttggctgcctggagtcagcagcccccagggatgggagcagccttgag
gacagaccctgcaatcctctctag
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integrated database retrieval system