White adipose tissue

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Unknown (3481)
Genomics (1305)
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Proteomics (161)
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Models (33)
Methylation profiling (19)
Other (17)

Organisms

Mus musculus (1076)
Homo sapiens (263)
Rattus norvegicus (76)
Sus scrofa (29)
Bos taurus (9)
Ovis aries (8)
Drosophila melanogaster (6)
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synthetic construct (4)
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Mustela putorius furo (3)
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human oral metagenome (1)
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Anguilla anguilla (1)
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Aedes aegypti (1)
Salmo salar (1)
Oncorhynchus mykiss (1)
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Oryctolagus cuniculus cuniculus (1)

Organisms

Mus musculus (822)
Homo sapiens (118)
Rattus norvegicus (32)
Sus scrofa (10)
Oryctolagus cuniculus (5)
Bos taurus (5)
Ovis aries (4)
Mustela putorius furo (3)
Mus musculus musculus (3)
Macaca mulatta (3)
Sus scrofa domesticus (2)
Marmota marmota marmota (1)
Cricetulus griseus (1)
Lasiopodomys brandtii (1)
Ictidomys tridecemlineatus (1)
urogenital metagenome (1)
Mesocricetus auratus (1)
Anas platyrhynchos (1)
Coturnix japonica (1)
pig gut metagenome (1)
Mus musculus domesticus (1)
gut metagenome (1)
feces metagenome (1)
Arabidopsis thaliana (1)
mouse gut metagenome (1)
unidentified (1)

Repository

ENA (1179)
geo (879)
biostudies-arrayexpress (540)
pride (114)
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jPOST (12)
MetabolomicsWorkbench (7)
GNPS (2)
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GPMDB (1)
PAXDB (1)

Tissue

White adipose tissue (47)
Brown adipose tissue (23)
Liver (23)
Epididymal white adipose tissue (17)
Skeletal muscle (11)
Heart (9)
Lung (5)
Ovary (2)
Cerebellum (2)
White adipose tissue around intestine (1)
White adipose tissue around gonad (1)
Hypothalamus and thalamus (1)
Muscle (1)
Gastrocnemius (1)
Diaphragm (1)
Saliva-secreting gland (1)
Eye (1)
Embryonic tissue (1)
Olfactory bulb (1)
Inguinal fat pad (1)
Zone of skin (1)
Thymus (1)
Corpus callosum (1)
Brainstem (1)
Duodenum (1)
Visceral abdominal adipose tissue (1)
Colon (1)
Medulla oblongata (1)
Midbrain (1)
Stomach (1)

Disease

Obesity (13)
Type 2 diabetes mellitus (12)
Metabolic dysfunction-associated steatotic liver disease (3)
Apparently healthy (2)
Normal (2)
Type 1 diabetes mellitus (2)
Not Available (1)
Obesity (1)
Diabetes (1)
Abdominal aortic aneurysm (1)
Cachexia (1)
Cardiovascular system disease (1)
Chronic pain (1)
Crohn's disease (1)
Diabetes mellitus (1)
Disease free (1)
Disease of metabolism (1)
Lesion of sciatic nerve (1)
Overweight (1)

Technology Type

Mass Spectrometry (121)
Shotgun proteomics (60)
Bottom-up proteomics (25)
Mass spectrometry (18)
Data-independent acquisition (17)
Mass spectrometry assay (13)
Data-dependent acquisition (11)
ESI (7)
Gel-based experiment (6)
SWATH MS (6)
Affinity purification coupled with mass spectrometry proteomics (5)
NMR spectroscopy (2)
HDMSE (2)
Top-down proteomics (2)
Illumina HiSeq 2500, Illumina HiSeq 4000, ILLUMINA (1)
HiSeq X Ten (1)
MSE (1)

Instrument Platform

Illumina NovaSeq 6000 (22)
Illumina HiSeq 2500 (21)
Illumina HiSeq 4000 (14)
NextSeq 500 (14)
Illumina HiSeq 2000 (6)
NextSeq 550 (3)
Illumina NovaSeq X (2)
NA (2)
NextSeq 2000 (2)
Illumina HiSeq 3000 (2)
GeneTitan MultiChannel System (1)
GeneChip Clariom S mouse array cartridge and Affymetrix GeneTitan MultiChannel System (1)
GeneChip Pico Kit (Affymetrix/ThermoFisher) (1)
ReliaPrep RNA Miniprep System (Promega) (1)
Adipocyte Progenitor Isolation Kit (Miltenyi Biotec) (1)
I.DOT (Dispendix), C.WASH (CYTENA), Qubit Fluorometer (Thermo Fisher Scientific), Agilent TapeStation 4200 (1)
BD FACSDiscover S8 (1)
Python (1)
Nugen Ovation SPIA; Wafergen’s Apollo liquid handler; KAPA Hyper Prep Library Kit (1)
QIAGEN TissueLyser II (1)
Isoflurane euthanasia chamber (1)
10X Genomics Chromium Single Cell Kit (1)
BD Aria, 10X Chromium (1)
Computer (1)
10X Chromium Controller (1)
Dell T8310 (1)
HiSeq 2000 (1)
454 GS FLX (1)
Agilent Technologies SureScan Microarray Scanne (1)
Not applicable (1)

Publication Date

2025 (170)
2015 (130)
2026 (127)
2024 (125)
2022 (120)
2023 (101)
2014 (100)
2019 (89)
2021 (87)
2016 (82)
2020 (80)
2018 (75)
2012 (70)
2013 (69)
2011 (49)
2017 (44)
2010 (42)
2008 (35)
2009 (31)
2007 (26)
2006 (3)
2005 (2)
2004 (1)

UNIPROT ID/AC

10090.ENSMUSP00000005406 (1)
10090.ENSMUSP00000032399 (1)
10090.ENSMUSP00000036258 (1)
10090.ENSMUSP00000043341 (1)
10090.ENSMUSP00000050156 (1)
10090.ENSMUSP00000065295 (1)
10090.ENSMUSP00000069914 (1)
10090.ENSMUSP00000071496 (1)
10090.ENSMUSP00000071763 (1)
10090.ENSMUSP00000072521 (1)
10090.ENSMUSP00000072775 (1)
10090.ENSMUSP00000076538 (1)
10090.ENSMUSP00000078239 (1)
10090.ENSMUSP00000078339 (1)
10090.ENSMUSP00000078625 (1)
10090.ENSMUSP00000078670 (1)
10090.ENSMUSP00000078877 (1)
10090.ENSMUSP00000079127 (1)
10090.ENSMUSP00000079727 (1)
10090.ENSMUSP00000079907 (1)
10090.ENSMUSP00000079944 (1)
10090.ENSMUSP00000082867 (1)
10090.ENSMUSP00000087372 (1)
10090.ENSMUSP00000087466 (1)
10090.ENSMUSP00000087632 (1)
10090.ENSMUSP00000088014 (1)
10090.ENSMUSP00000089336 (1)
10090.ENSMUSP00000089648 (1)
10090.ENSMUSP00000090897 (1)
10090.ENSMUSP00000091659 (1)

CHEBI ID

CHEBI:18036 (33)
CHEBI:15435 (33)
CHEBI:17458 (33)
CHEBI:15430 (33)
CHEBI:29009 (33)
CHEBI:42504 (33)
CHEBI:15940 (33)
CHEBI:27485 (33)
CHEBI:27754 (33)
CHEBI:15630 (33)
CHEBI:27969 (33)
CHEBI:15763 (33)
CHEBI:15554 (33)
CHEBI:16600 (33)
CHEBI:16208 (33)
CHEBI:15553 (33)
CHEBI:17154 (33)
CHEBI:15927 (33)
CHEBI:28031 (33)
CHEBI:45919 (33)
CHEBI:17151 (33)
CHEBI:16929 (33)
CHEBI:16171 (33)
CHEBI:16110 (33)
CHEBI:15551 (33)
CHEBI:16870 (33)
CHEBI:28096 (33)
CHEBI:42394 (33)
CHEBI:15901 (33)
CHEBI:17636 (33)

Metabolite Name

Palmitoleic acid (5)
Azelaic acid (5)
Myristoylglycine (4)
Leucine (4)
Alanine (4)
Lactate (4)
Phthalic acid (4)
L-Histidine (4)
Suberic acid (4)
Creatine (4)
Menadione bisulfite (3)
Allyl chloride (3)
(+)-Prosopinine (3)
Soyasapogenol B 3-O-b-D-glucuronide (3)
Bortezomib (3)
Paroxetine (3)
6-Oxopiperidine-2-carboxylic acid (3)
N-Acetyl-L-methionine (3)
Lactic acid (3)
Trifluoroacetic acid (3)
Oxalic acid (3)
Alpha-Linolenic acid (3)
Glycine (3)
Lysine (3)
Glutamate (3)
Tyrosine (3)
Citrate (3)
Valine (3)
Isoleucine (3)
Leucine (3)

IsPrivate

False (33)

Model Flag

Non Kinetic (33)

First Public Date

2025 (192)
2024 (142)
2014 (129)
2026 (120)
2023 (99)
2022 (99)
2021 (74)
2020 (74)
2019 (70)
2018 (67)
2017 (47)
2015 (36)
2016 (26)
2013 (4)

Modification

4-tetrahydrothiazine-3-carboxylic acid (2)
15.994915 (1)
57.021464 (1)
Not available (1)

Study type

Transcription profiling by array (359)
RNA-seq of coding RNA (83)
ChIP-seq (23)
RNA-seq of coding RNA from single cells (17)
Methylation profiling by array (10)
Animal - High-throughput sequencing (7)
RNA-seq of non coding RNA (6)
Methylation profiling by high throughput sequencing (4)
Unknown experiment type (3)
MicroRNA profiling by high throughput sequencing (3)
RNA-seq of total RNA (3)
Animal - One-color microarray (2)
Animal - Single-cell sequencing (2)
Cell line - One-color microarray (2)
High-throughput sequencing (2)
Other (2)
Single nucleus RNA sequencing (2)
MicroRNA profiling by array (2)
Transcription profiling by SAGE (1)
Differential (1)
ChIP-chip by tiling array (1)
Human - Single-cell sequencing (1)
RNAi profiling by array (1)
Spatial transcriptomics by high-throughput sequencing (1)
ATAC-seq (1)
DNA-seq (1)

Release Date

2022 (393)
2021 (370)
2025 (330)
2020 (319)
2019 (285)
2024 (283)
2023 (282)
2017 (235)
2018 (232)
2016 (230)
2015 (219)
2014 (189)
2013 (136)
2012 (122)
2011 (84)
2010 (81)
2008 (60)
2009 (59)
2026 (57)
2007 (23)
2006 (8)
2005 (7)
2004 (6)
2003 (3)
1998 (3)
2002 (2)
2000 (2)

Lab affiliation

Emmy-Noether Research Group Cellular Proteomics and Metabolic Signaling Institute for Diabetes and Obesity Helmholtz Diabetes Center Germany (4)
FBI (2)
Hebei Key Laboratory of Metabolic Diseases (2)
Howard Hughes Medical Institute Beth Israel Deaconess Medical Center Harvard Medical School (2)
The Charles Perkins Centre, University of Sydney, Australia (2)
1) Department of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center (MDACC), Houston, TX 77030, USA 2) Proteomics Core Facility, Department of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center (MDACC), Houston, TX 77030, USA 3) Metabolomics Core Facility, Department of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center (MDACC), Houston, TX 77030, USA (1)
1) Department of Cancer Biology, Dana–Farber Cancer Institute, Boston, MA, USA. 2) Department of Cell Biology, Harvard Medical School, Boston, MA, USA. (1)
1Center for Medical Genetics, Ghent University Hospital, Ghent, 9000, Belgium 2Department of Biomolecular Medicine, Faculty of Medicine and Health Sciences, Ghent (1)
1Department of Biochemistry and Molecular Biomedicine, Faculty of Biology, University of Barcelona, Barcelona, Spain (1)
1Department of Biochemistry, School of Medicine, Case Western Reserve University, Cleveland, OH, 44106 (1)
Advanced Research Centre (ARC) College of Medical, Veterinary and Life Sciences University of Glasgow, Glasgow, UK. (1)
Analytical Biochemistry and Proteomics Unit (1)
Assoc. Prof. at Novo Nordisk Foundation Center for Basic Metabolic Research, University of Copenhagen, Copenhagen, Denmark (1)
Associate Member, St. Jude Faculty Developmental Neurobiology St. Jude Children's Research Hospital Memphis, TN-38105 (1)
Boston University School of Medicine (1)
CRG, UPF (1)
Capital institute of Pediatrics. (1)
Cell Biology and Physiology, Washington University in St. Louis (1)
Centre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Barcelona, Spain. Universitat Pompeu Fabra (UPF), Barcelona, Spain. (lab head) (1)
Chair of Proteomics and Bioanalytics, Technical University of Munich, Freising, Germany (1)
Charles Perkins Centre, School of Life and Environmental Sciences and Sydney Medical School, University of Sydney, Camperdown, NSW, Australia (1)
Charles Perkins Centre, School of Medical Sciences, University of Sydney, Sydney, Australia. (1)
Charles Perkins Centre, The University of Sydney (1)
Cologne Excellence Cluster on Cellular Stress Responses in Ageing-Associated Diseases (CECAD), Center for Molecular Medicine Cologne (CMMC), and Institute for Mitochondrial Diseases and Ageing, Medical Faculty, University of Cologne D-50931 Cologne, Germany. (1)
Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD) and Institute for Mitochondrial Diseases and Aging, Medical Faculty, University of Cologne, Cologne, Germany. (1)
Dep. of Health Sciences and Technology, ETH Zurich Schorenstrasse 16, 8603 Schwerzenbach, Switzerland (1)
Department Molecular Toxicology, Helmholtz Centre for Environmental Research GmBH - UFZ (1)
Department of Biochemistry and Molecular Biology, University of Southern Denmark, 5230 Odense M, Denmark (1)
Department of Biochemistry and Molecular Biology, University of Southern Denmark, Odense M, Denmark (1)
Department of Biology, University of Padova, Padua, Italy (1)

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Brown vs White adipose tissue

Not available

ORGANISM(S): Mus musculus

ST000562 | MetabolomicsWorkbench

A metabolomic study of adipose tissue in mice with a disruption of the circadian system

Adipose tissue functions in terms of energy homeostasis as a rheostat for blood triglyceride, regulating its concentration, in response to external stimuli. In addition it acts as a barometer to inform the central nervous system of energy levels which can vary dramatically between meals and accor...

2017-10-27 | MTBLS380 | MetaboLights

A metabolomic study of adipose tissue in mice with a disruption of the circadian system

2017-10-27 | MTBLS390 | MetaboLights

Hypothalamic SLC7A14 accounts for aging-reduced lipolysis in white adipose tissue

The central nervous system has been implicated in the age-induced reduction in adipose tissue lipolysis. SLC7A14 is a lysosomal membrane protein highly expressed in the brain. Herein, we investigated the possible role of hypothalamic SLC7A14 in the age-induced lipolysis reduction. In this study, ...

2024-07-23 | MTBLS9872 | MetaboLights

A metabolomic study of adipose tissue in mice with a disruption of the circadian system

2017-10-27 | MTBLS382 | MetaboLights

Nitrate-Sialin2 Axis Couples ER-Mitochondrial Calcium Signaling with Fatty Acid Metabolism to Drive White Adipose Browning

Nutrient cues shape adipose homeostasis; however, the mechanism by which inorganic signals engage organelle networks to drive white fat browning remains unclear. Here, we identify a nitrate-Sialin2 pathway that converts dietary nitrate into a spatially confined thermogenic program. Sialin2 localizes...

2026-05-17 | MTBLS14192 | MetaboLights

Brown and beige adipose tissue regulate systemic metabolism through a metabolite interorgan signaling axis

Brown and beige adipose tissue are emerging as distinct endocrine organs. These tissues are functionally associated with skeletal muscle, adipose tissue metabolism and systemic energy expenditure, suggesting an interorgan signaling network. Using metabolomics, we identify 3-methyl-2-oxovaleric acid,...

2022-03-03 | MTBLS2436 | MetaboLights

Subcutaneous white adipose tissue-derived extracellular vesicle maintains intestinal homeostasis via IgA biosynthesis in aging mice

To identify the potential iWAT-derived adipokines that regulate intestinal IgA biosynthesis, we conducted untargeted metabolomics in the serum of iFR and iSham mice. A total of 214 differential abundant metabolites were identified (log2FC >1 or <-1 and adjusted p-value <0.05) between the...

2025-09-05 | MTBLS12800 | MetaboLights

Mouse Brown Adipose Tissue Lipidomics under Cold and Dietary Fat Interventions

This study investigates lipidomic remodeling in mouse brown adipose tissue under a 2 × 3 experimental design involving environmental condition and dietary fatty acid composition. Mice were maintained at room temperature with ad libitum feeding or exposed to 4°C cold conditions with 70% calorie restr...

2026-06-01 | MTBLS14642 | MetaboLights

AdipoAtlas: A Reference Lipidome for Human White Adipose Tissue

Not available

ORGANISM(S): Homo sapiens

ST001738 | MetabolomicsWorkbench

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6342 Results

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