Eulemur rufifrons (Bennett's brown lemur): 138378486
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Entry
138378486 CDS
T11398
Name
(RefSeq) bcl-2-like protein 1 isoform X1
KO
K04570
Bcl-2-like 1 (apoptosis regulator Bcl-X)
Organism
eruf Eulemur rufifrons (Bennett's brown lemur)
Pathway
eruf01521
EGFR tyrosine kinase inhibitor resistance
eruf01524
Platinum drug resistance
eruf04014
Ras signaling pathway
eruf04064
NF-kappa B signaling pathway
eruf04115
p53 signaling pathway
eruf04137
Mitophagy - animal
eruf04140
Autophagy - animal
eruf04151
PI3K-Akt signaling pathway
eruf04210
Apoptosis
eruf04215
Apoptosis - multiple species
eruf04621
NOD-like receptor signaling pathway
eruf04630
JAK-STAT signaling pathway
eruf05012
Parkinson disease
eruf05014
Amyotrophic lateral sclerosis
eruf05022
Pathways of neurodegeneration - multiple diseases
eruf05145
Toxoplasmosis
eruf05162
Measles
eruf05166
Human T-cell leukemia virus 1 infection
eruf05168
Herpes simplex virus 1 infection
eruf05170
Human immunodeficiency virus 1 infection
eruf05200
Pathways in cancer
eruf05202
Transcriptional misregulation in cancer
eruf05212
Pancreatic cancer
eruf05220
Chronic myeloid leukemia
eruf05222
Small cell lung cancer
eruf05225
Hepatocellular carcinoma
eruf05417
Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:
eruf00001
]
09130 Environmental Information Processing
09132 Signal transduction
04014 Ras signaling pathway
138378486
04630 JAK-STAT signaling pathway
138378486
04064 NF-kappa B signaling pathway
138378486
04151 PI3K-Akt signaling pathway
138378486
09140 Cellular Processes
09141 Transport and catabolism
04140 Autophagy - animal
138378486
04137 Mitophagy - animal
138378486
09143 Cell growth and death
04210 Apoptosis
138378486
04215 Apoptosis - multiple species
138378486
04115 p53 signaling pathway
138378486
09150 Organismal Systems
09151 Immune system
04621 NOD-like receptor signaling pathway
138378486
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
138378486
05202 Transcriptional misregulation in cancer
138378486
09162 Cancer: specific types
05212 Pancreatic cancer
138378486
05225 Hepatocellular carcinoma
138378486
05220 Chronic myeloid leukemia
138378486
05222 Small cell lung cancer
138378486
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
138378486
05170 Human immunodeficiency virus 1 infection
138378486
05162 Measles
138378486
05168 Herpes simplex virus 1 infection
138378486
09174 Infectious disease: parasitic
05145 Toxoplasmosis
138378486
09164 Neurodegenerative disease
05012 Parkinson disease
138378486
05014 Amyotrophic lateral sclerosis
138378486
05022 Pathways of neurodegeneration - multiple diseases
138378486
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
138378486
09176 Drug resistance: antineoplastic
01521 EGFR tyrosine kinase inhibitor resistance
138378486
01524 Platinum drug resistance
138378486
09180 Brite Hierarchies
09181 Protein families: metabolism
01009 Protein phosphatases and associated proteins [BR:
eruf01009
]
138378486
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins [BR:
eruf03036
]
138378486
09183 Protein families: signaling and cellular processes
02000 Transporters [BR:
eruf02000
]
138378486
Protein phosphatases and associated proteins [BR:
eruf01009
]
Protein serine/threonine phosphatases
Phosphoprotein phosphatases (PPPs)
Protein phosphatase-1
PP1-interacting proteins (PIPs)
138378486
Chromosome and associated proteins [BR:
eruf03036
]
Eukaryotic type
Centrosome formation proteins
Other centrosome associated proteins
138378486
Transporters [BR:
eruf02000
]
Other transporters
Pores ion channels [TC:
1
]
138378486
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Bcl-2
BH4
Bcl-2_3
Motif
Other DBs
NCBI-GeneID:
138378486
NCBI-ProteinID:
XP_069319917
LinkDB
All DBs
Position
30:complement(119375119..119375826)
Genome browser
AA seq
235 aa
AA seq
DB search
MSQSSWELVVDFLSYKLSQKGYSWNQFGDVEENKTAAPEGIRSEMATPRAINDNPSRHVA
DSPAVNAAIGRSSSLDALREEIPIAAVKQTLKEAGDEFERWYRRAFGDLMSELHVTPETA
FPIFEQVVEELFSDDINWGRIVALFSFGGALCVESKDKEMQLLTSEIAIWMVAYLNDNIE
PWIQENGGWDAFVKIYGKNAAVKRWRGQEGFNRWFLMGMMTVTGVVLLGLFFSRK
NT seq
708 nt
NT seq
+upstream
nt +downstream
nt
atgtctcagagcagctgggagctggtggttgactttctctcctacaagctttcccagaaa
ggatacagctggaatcagtttggcgatgtggaggagaacaagactgcggccccagaaggg
attaggtcggagatggcgacccccagggccattaatgacaacccatcccggcacgtggcg
gacagccctgcagtgaatgcagccattggtcgcagcagcagtttggatgccctccgggag
gagatccccatagcagcagtgaagcaaacactgaaggaggcgggcgatgagtttgaacgg
tggtaccggcgggcattcggtgacctgatgtccgagctccacgtcaccccagagacagca
tttccgatcttcgaacaggtagtggaagaactcttctcggatgacataaactggggtcgc
attgtggcccttttctcctttggcggggccctgtgcgtggaaagcaaagacaaggaaatg
caactattgactagtgagatcgcaatttggatggtcgcttacctgaatgacaacatcgag
ccatggatccaggagaacggcggctgggacgctttcgtgaaaatctacgggaagaatgca
gcagtcaagagatggagaggccaggaaggcttcaaccgctggttcctgatgggtatgatg
actgtgactggtgtggttctgctgggcttgttcttcagcaggaaatga
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