Heterocephalus glaber (naked mole-rat): 101721536
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Entry
101721536 CDS
T02812
Name
(RefSeq) cytochrome c-like
KO
K08738
cytochrome c
Organism
hgl
Heterocephalus glaber (naked mole-rat)
Pathway
hgl00190
Oxidative phosphorylation
hgl01100
Metabolic pathways
hgl01524
Platinum drug resistance
hgl04115
p53 signaling pathway
hgl04210
Apoptosis
hgl04215
Apoptosis - multiple species
hgl04932
Non-alcoholic fatty liver disease
hgl05010
Alzheimer disease
hgl05012
Parkinson disease
hgl05014
Amyotrophic lateral sclerosis
hgl05016
Huntington disease
hgl05017
Spinocerebellar ataxia
hgl05020
Prion disease
hgl05022
Pathways of neurodegeneration - multiple diseases
hgl05132
Salmonella infection
hgl05134
Legionellosis
hgl05145
Toxoplasmosis
hgl05152
Tuberculosis
hgl05160
Hepatitis C
hgl05161
Hepatitis B
hgl05162
Measles
hgl05163
Human cytomegalovirus infection
hgl05164
Influenza A
hgl05167
Kaposi sarcoma-associated herpesvirus infection
hgl05168
Herpes simplex virus 1 infection
hgl05169
Epstein-Barr virus infection
hgl05170
Human immunodeficiency virus 1 infection
hgl05200
Pathways in cancer
hgl05210
Colorectal cancer
hgl05222
Small cell lung cancer
hgl05416
Viral myocarditis
hgl05417
Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:
hgl00001
]
09100 Metabolism
09102 Energy metabolism
00190 Oxidative phosphorylation
101721536
09140 Cellular Processes
09143 Cell growth and death
04210 Apoptosis
101721536
04215 Apoptosis - multiple species
101721536
04115 p53 signaling pathway
101721536
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
101721536
09162 Cancer: specific types
05210 Colorectal cancer
101721536
05222 Small cell lung cancer
101721536
09172 Infectious disease: viral
05170 Human immunodeficiency virus 1 infection
101721536
05161 Hepatitis B
101721536
05160 Hepatitis C
101721536
05164 Influenza A
101721536
05162 Measles
101721536
05168 Herpes simplex virus 1 infection
101721536
05163 Human cytomegalovirus infection
101721536
05167 Kaposi sarcoma-associated herpesvirus infection
101721536
05169 Epstein-Barr virus infection
101721536
09171 Infectious disease: bacterial
05132 Salmonella infection
101721536
05134 Legionellosis
101721536
05152 Tuberculosis
101721536
09174 Infectious disease: parasitic
05145 Toxoplasmosis
101721536
09164 Neurodegenerative disease
05010 Alzheimer disease
101721536
05012 Parkinson disease
101721536
05014 Amyotrophic lateral sclerosis
101721536
05016 Huntington disease
101721536
05017 Spinocerebellar ataxia
101721536
05020 Prion disease
101721536
05022 Pathways of neurodegeneration - multiple diseases
101721536
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
101721536
05416 Viral myocarditis
101721536
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
101721536
09176 Drug resistance: antineoplastic
01524 Platinum drug resistance
101721536
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Cytochrom_C
Cytochrome_CBB3
Cytochrom_C550
CCP_MauG
Motif
Other DBs
NCBI-GeneID:
101721536
NCBI-ProteinID:
XP_004857089
LinkDB
All DBs
Position
Un
AA seq
103 aa
AA seq
DB search
MGDVEKGKIFVQKCAQCHTVEKGGKHKTGPNLHGLFGRKTAQAVGFSYTDANKNKGITWG
EDTLMEYLRNPKKYIPGTKMIFRGIKKGERADLIAYLKKATNE
NT seq
312 nt
NT seq
+upstream
nt +downstream
nt
atgggtgatgttgagaaaggcaagatttttgtacagaagtgtgcccagtgccacactgtg
gaaaagggaggcaagcacaagactggcccaaatctccatggtctgtttgggcggaagaca
gcccaagctgttggattctcttacacagatgccaacaagaacaaaggcatcacctgggga
gaggatacattgatggagtacttgaggaatcccaagaagtacatccctggaacaaaaatg
atcttcaggggcattaagaagggagaaagagcagacttaatagcttacctcaaaaaagct
actaatgagtaa
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