protein

Showing entry for Band 3 anion transport protein

General Target Information
BXGT Id	BXGT005935
Protein Name	Band 3 anion transport protein
Uniport Id	P02730
Gene	SLC4A1
Gene Id	6521
Domain	Band_3_cyto; HCO3_cotransp
Pfam	PF07565 PF00955
Organism	Homo sapiens (Human)

Target protein affiliated biological pathways

KEGG

Class	Subclass	KEGG Id	Pathway Name
5. Organismal Systems	5.5 Excretory system	hsa04966	Collecting duct acid secretion

Gene Ontology

GO Type	GO Id	Gene Ontology
Biological Process	GO:0006820	anion transport
Biological Process	GO:0015701	bicarbonate transport
Biological Process	GO:0007596	blood coagulation
Biological Process	GO:0006873	cellular ion homeostasis
Biological Process	GO:0006821	chloride transport
Biological Process	GO:0048821	erythrocyte development
Biological Process	GO:1904539	negative regulation of glycolytic process through fructose-6-phosphate
Biological Process	GO:0051354	negative regulation of oxidoreductase activity
Biological Process	GO:0035811	negative regulation of urine volume
Biological Process	GO:0045852	pH elevation
Biological Process	GO:0017121	plasma membrane phospholipid scrambling
Biological Process	GO:0072659	protein localization to plasma membrane
Biological Process	GO:0051453	regulation of intracellular pH
molecular function	GO:0015301	anion:anion antiporter activity
molecular function	GO:0008509	anion transmembrane transporter activity
molecular function	GO:0030506	ankyrin binding
molecular function	GO:0015106	bicarbonate transmembrane transporter activity
molecular function	GO:0015108	chloride transmembrane transporter activity
molecular function	GO:0030492	hemoglobin binding
molecular function	GO:0005452	inorganic anion exchanger activity
molecular function	GO:0042803	protein homodimerization activity
molecular function	GO:0043495	protein-membrane adaptor activity
cellular component	GO:0016323	basolateral plasma membrane
cellular component	GO:0072562	blood microparticle
cellular component	GO:0030863	cortical cytoskeleton
cellular component	GO:0009898	cytoplasmic side of plasma membrane
cellular component	GO:0070062	extracellular exosome
cellular component	GO:0016021	integral component of membrane
cellular component	GO:0005887	integral component of plasma membrane
cellular component	GO:0005886	plasma membrane
cellular component	GO:0030018	Z disc

Reactome

Pathway Id	Pathway Name
R-HSA-1237044	Erythrocytes take up carbon dioxide and release oxygen
R-HSA-1247673	Erythrocytes take up oxygen and release carbon dioxide
R-HSA-1480926	O2/CO2 exchange in erythrocytes
R-HSA-1643685	Disease
R-HSA-382551	Transport of small molecules
R-HSA-425381	Bicarbonate transporters
R-HSA-425393	Transport of inorganic cations/anions and amino acids/oligopeptides
R-HSA-425407	SLC-mediated transmembrane transport
R-HSA-5619050	Defective SLC4A1 causes hereditary spherocytosis type 4 (HSP4), distal renal tubular acidosis (dRTA) and dRTA with hemolytic anemia (dRTA-HA)
R-HSA-5619102	SLC transporter disorders
R-HSA-5619115	Disorders of transmembrane transporters

Target protein-related diseases

Disease

CUI Id	BXGD Id	Disease Name	Disease Class
C0000731	BXGD000002	Abdomen distended	Digestive System Diseases
C0000737	BXGD000005	Abdominal Pain	Pathological Conditions, Signs and Symptoms
C0001126	BXGD000025	Renal tubular acidosis	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0001418	BXGD000050	Adenocarcinoma	Neoplasms
C0002063	BXGD000099	Alkalosis	Nutritional and Metabolic Diseases
C0002871	BXGD000132	Anemia	Hemic and Lymphatic Diseases
C0002878	BXGD000137	Anemia, Hemolytic	Hemic and Lymphatic Diseases
C0002879	BXGD000138	Anemia, Hemolytic, Acquired	Hemic and Lymphatic Diseases
C0002880	BXGD000139	Autoimmune hemolytic anemia	Immune System Diseases; Hemic and Lymphatic Diseases
C0002881	BXGD000140	Anemia, Hemolytic, Congenital	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
C0002889	BXGD000146	Anemia, Microangiopathic	Hemic and Lymphatic Diseases
C0003123	BXGD000178	Anorexia	Pathological Conditions, Signs and Symptoms
C0003130	BXGD000183	Anoxia	Pathological Conditions, Signs and Symptoms
C0003864	BXGD000231	Arthritis	Musculoskeletal Diseases
C0004134	BXGD000256	Ataxia	Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0005283	BXGD000308	beta Thalassemia	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
C0005806	BXGD000337	Blood Group Incompatibility
C0006142	BXGD000374	Malignant neoplasm of breast	Neoplasms; Skin and Connective Tissue Diseases
C0006826	BXGD000408	Malignant Neoplasms	Neoplasms
C0007196	BXGD000453	Restrictive cardiomyopathy	Cardiovascular Diseases
C0007787	BXGD000487	Transient Ischemic Attack	Nervous System Diseases; Cardiovascular Diseases
C0007820	BXGD000491	Cerebrovascular Disorders	Nervous System Diseases; Cardiovascular Diseases
C0008350	BXGD000531	Cholelithiasis	Digestive System Diseases
C0009402	BXGD000605	Colorectal Carcinoma	Digestive System Diseases; Neoplasms
C0011175	BXGD000701	Dehydration	Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases
C0013336	BXGD000815	Dwarfism	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases
C0013390	BXGD000828	Dysmenorrhea	Pathological Conditions, Signs and Symptoms
C0013394	BXGD000830	Dyspareunia (female)	Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Mental Disorders; Behavior and Behavior Mechanisms
C0013902	BXGD000865	Elliptocytosis, Hereditary	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
C0015544	BXGD001003	Failure to Thrive	Pathological Conditions, Signs and Symptoms
C0015695	BXGD001013	Fatty Liver	Digestive System Diseases
C0015967	BXGD001030	Fever	Pathological Conditions, Signs and Symptoms
C0016663	BXGD001071	Pathological fracture	Wounds and Injuries
C0017636	BXGD001131	Glioblastoma	Neoplasms
C0018099	BXGD001172	Gout	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
C0018784	BXGD001220	Sensorineural Hearing Loss (disorder)	Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
C0018801	BXGD001226	Heart failure	Cardiovascular Diseases
C0018802	BXGD001227	Congestive heart failure	Cardiovascular Diseases
C0018939	BXGD001253	Hematological Disease	Hemic and Lymphatic Diseases
C0018952	BXGD001257	Extramedullary Hematopoiesis Function
C0019045	BXGD001269	Hemoglobinopathies	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
C0019069	BXGD001277	Hemophilia A	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
C0019158	BXGD001293	Hepatitis	Digestive System Diseases
C0019159	BXGD001294	Hepatitis A	Digestive System Diseases; Infections
C0019196	BXGD001301	Hepatitis C	Digestive System Diseases; Infections
C0019209	BXGD001305	Hepatomegaly	Pathological Conditions, Signs and Symptoms; Digestive System Diseases
C0019214	BXGD001307	Hepatosplenomegaly	Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Hemic and Lymphatic Diseases
C0020433	BXGD001379	Hyperbilirubinemia	Pathological Conditions, Signs and Symptoms
C0020538	BXGD001422	Hypertensive disease	Cardiovascular Diseases
C0020598	BXGD001440	Hypocalcemia	Nutritional and Metabolic Diseases
C0020621	BXGD001449	Hypokalemia	Nutritional and Metabolic Diseases
C0022346	BXGD001537	Icterus	Pathological Conditions, Signs and Symptoms
C0022610	BXGD001566	Kernicterus	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases; Nervous System Diseases; Hemic and Lymphatic Diseases
C0022650	BXGD001568	Kidney Calculi	Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0022658	BXGD001570	Kidney Diseases	Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0022661	BXGD001572	Kidney Failure, Chronic	Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0023380	BXGD001640	Lethargy	Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms
C0023440	BXGD001646	Acute Erythroblastic Leukemia	Neoplasms; Hemic and Lymphatic Diseases
C0023467	BXGD001658	Leukemia, Myelocytic, Acute	Neoplasms
C0023890	BXGD001713	Liver Cirrhosis	Pathological Conditions, Signs and Symptoms; Digestive System Diseases
C0023895	BXGD001717	Liver diseases	Digestive System Diseases
C0023903	BXGD001720	Liver neoplasms	Digestive System Diseases; Neoplasms
C0024131	BXGD001736	Lupus Vulgaris	Infections; Skin and Connective Tissue Diseases
C0024138	BXGD001738	Lupus Erythematosus, Discoid	Skin and Connective Tissue Diseases
C0024141	BXGD001740	Lupus Erythematosus, Systemic	Skin and Connective Tissue Diseases; Immune System Diseases
C0024530	BXGD001783	Malaria	Infections
C0024534	BXGD001784	Malaria, Cerebral	Infections; Nervous System Diseases
C0024623	BXGD001791	Malignant neoplasm of stomach	Digestive System Diseases; Neoplasms
C0025281	BXGD001848	Meniere Disease	Otorhinolaryngologic Diseases
C0027651	BXGD002009	Neoplasms	Neoplasms
C0027707	BXGD002024	Nephritis, Interstitial	Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0027709	BXGD002026	Nephrocalcinosis	Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0029810	BXGD002172	Other specified iron deficiency anemias	Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
C0030232	BXGD002197	Pallor	Pathological Conditions, Signs and Symptoms
C0030443	BXGD002224	Familial Periodic Paralysis	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases
C0030794	BXGD002254	Pelvic Pain	Pathological Conditions, Signs and Symptoms
C0032827	BXGD002376	Potassium Deficiency	Nutritional and Metabolic Diseases
C0033117	BXGD002396	Priapism	Male Urogenital Diseases
C0033626	BXGD002412	Protein Deficiency	Nutritional and Metabolic Diseases
C0035579	BXGD002560	Rickets	Nutritional and Metabolic Diseases; Musculoskeletal Diseases
C0037299	BXGD002685	Skin Ulcer	Skin and Connective Tissue Diseases
C0037889	BXGD002709	Hereditary spherocytosis	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
C0038002	BXGD002723	Splenomegaly	Pathological Conditions, Signs and Symptoms
C0038454	BXGD002760	Cerebrovascular accident	Nervous System Diseases; Cardiovascular Diseases
C0039585	BXGD002821	Androgen-Insensitivity Syndrome	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases
C0039730	BXGD002826	Thalassemia	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
C0041349	BXGD002920	Nephritis, Tubulointerstitial	Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0042875	BXGD003009	Vitamin E Deficiency	Nutritional and Metabolic Diseases
C0085593	BXGD003196	Chills	Pathological Conditions, Signs and Symptoms
C0150055	BXGD003401	Chronic pain	Pathological Conditions, Signs and Symptoms
C0151517	BXGD003431	Complete atrioventricular block	Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0151786	BXGD003475	Muscle Weakness	Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
C0162309	BXGD003934	Adrenoleukodystrophy	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Endocrine System Diseases
C0162701	BXGD003978	Polysomnography
C0202117	BXGD004074	Low density lipoprotein cholesterol measurement
C0202236	BXGD004086	Triglycerides measurement
C0206160	BXGD004166	Reticulocytosis	Pathological Conditions, Signs and Symptoms
C0206161	BXGD004167	Reticulocyte count (procedure)
C0206698	BXGD004248	Cholangiocarcinoma	Neoplasms
C0220668	BXGD004317	Congenital contractural arachnodactyly	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0220981	BXGD004348	Metabolic acidosis	Nutritional and Metabolic Diseases
C0221021	BXGD004368	Microangiopathic hemolytic anemia	Hemic and Lymphatic Diseases
C0221409	BXGD004460	Anemia, hereditary spherocytic hemolytic	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
C0231528	BXGD004496	Myalgia	Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
C0239946	BXGD005010	Fibrosis, Liver	Pathological Conditions, Signs and Symptoms; Digestive System Diseases
C0268435	BXGD005945	Renal Tubular Acidosis, Type II	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0272048	BXGD006297	stomatocytic anemia	Hemic and Lymphatic Diseases
C0272051	BXGD006298	Xerocytosis	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Immune System Diseases; Hemic and Lymphatic Diseases
C0278878	BXGD006609	Adult Glioblastoma	Neoplasms
C0279626	BXGD006657	Squamous cell carcinoma of esophagus	Digestive System Diseases; Neoplasms
C0280474	BXGD006748	Childhood Glioblastoma	Neoplasms
C0342208	BXGD007445	Multinodular goiter	Neoplasms; Endocrine System Diseases
C0346255	BXGD007805	Oncocytoma, renal	Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0349588	BXGD007933	Short stature
C0392525	BXGD008052	Nephrolithiasis	Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0398623	BXGD008202	Thrombophilia	Hemic and Lymphatic Diseases
C0409974	BXGD008401	Lupus Erythematosus	Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases; Immune System Diseases
C0423791	BXGD008509	Maculopapular Lesion	Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases; Immune System Diseases
C0427460	BXGD008616	Red cell distribution width determination
C0427480	BXGD008617	Elliptocytosis found
C0428474	BXGD008631	Serum LDL cholesterol measurement
C0456070	BXGD008863	Growth delay
C0472767	BXGD008918	Beta thalassemia intermedia	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
C0524909	BXGD009247	Hepatitis B, Chronic	Digestive System Diseases; Infections
C0524910	BXGD009248	Hepatitis C, Chronic	Digestive System Diseases; Infections
C0553681	BXGD009406	Hypofibrinogenemia
C0553720	BXGD009414	Spherocytosis
C0596263	BXGD009639	Carcinogenesis	Pathological Conditions, Signs and Symptoms; Neoplasms
C0596887	BXGD009648	mathematical ability
C0677598	BXGD009719	Stomatocytosis Result
C0678222	BXGD009749	Breast Carcinoma	Neoplasms; Skin and Connective Tissue Diseases
C0684275	BXGD009792	Hemophilia, NOS	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
C0687120	BXGD009837	Nephronophthisis	Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0699791	BXGD009867	Stomach Carcinoma	Digestive System Diseases; Neoplasms
C0740394	BXGD009989	Hyperuricemia	Pathological Conditions, Signs and Symptoms
C0746102	BXGD010136	Chronic lung disease	Respiratory Tract Diseases
C0850758	BXGD010909	Pelvic pain female	Pathological Conditions, Signs and Symptoms
C1261502	BXGD011856	Finding of Mean Corpuscular Hemoglobin
C1262483	BXGD011884	Hereditary stomatocytosis	Hemic and Lymphatic Diseases
C1266042	BXGD011938	Chromophobe Renal Cell Carcinoma	Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C1269955	BXGD012005	Tumor Cell Invasion
C1279412	BXGD012121	periodic paralysis (finding)	Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C1304746	BXGD012343	RDW - Red blood cell distribution width result
C1306459	BXGD012361	Primary malignant neoplasm	Neoplasms
C1306589	BXGD012369	Congenital dyserythropoietic anemia, type II	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
C1333177	BXGD012605	Lymphoproliferative Disorder of the Skin	Skin and Connective Tissue Diseases; Immune System Diseases; Hemic and Lymphatic Diseases
C1561643	BXGD013363	Chronic Kidney Diseases	Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C1608408	BXGD013434	Malignant transformation
C1621958	BXGD013468	Glioblastoma Multiforme	Neoplasms
C1623038	BXGD013475	Cirrhosis	Pathological Conditions, Signs and Symptoms
C1704380	BXGD013555	Distal Renal Tubular Acidosis	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C1832168	BXGD013806	BLOOD GROUP--FROESE
C1849478	BXGD015056	Increased red cell osmotic fragility
C1859778	BXGD015931	Postnatal growth retardation
C1861453	BXGD016049	Pseudohyperkalemia Cardiff	Nutritional and Metabolic Diseases
C1862190	BXGD016117	BLOOD GROUP--WRIGHT ANTIGEN
C1862191	BXGD016118	BLOOD GROUP--WALDNER TYPE
C1862322	BXGD016123	Ovalocytosis, Malaysian-Melanesian-Filipino Type	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
C1862324	BXGD016124	Elliptocytosis 4	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
C1864498	BXGD016233	RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C1969038	BXGD016749	RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA (disorder)	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Hemic and Lymphatic Diseases
C1969039	BXGD016750	Renal Tubular Acidosis, Distal, With Normal Red Cell Morphology	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C1969073	BXGD016753	Hyperchloremic metabolic acidosis
C1970028	BXGD016803	MALARIA, SUSCEPTIBILITY TO (finding)
C2239176	BXGD016965	Liver carcinoma	Digestive System Diseases; Neoplasms
C2315100	BXGD017021	Pediatric failure to thrive	Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Mental Disorders
C2316810	BXGD017030	Chronic kidney disease stage 5	Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C2347748	BXGD017041	Adult Erythroleukemia
C2675212	BXGD017280	Spherocytosis, Type 4	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
C2711227	BXGD017478	Steatohepatitis	Digestive System Diseases
C2747816	BXGD017577	Complicated malaria	Infections
C2919142	BXGD017867	Short Stature, CTCAE
C3714514	BXGD019409	Infection	Infections
C3841459	BXGD019798	Hb H disease
C3887638	BXGD019906	Failure to thrive in infant	Pathological Conditions, Signs and Symptoms
C3887650	BXGD019911	Adult Rickets	Nutritional and Metabolic Diseases; Musculoskeletal Diseases
C4015898	BXGD020242	RENAL TUBULAR ACIDOSIS, AUTOSOMAL DOMINANT
C4015903	BXGD020243	SWANN BLOOD GROUP ANTIGEN PHENOTYPE
C4015904	BXGD020244	ACANTHOCYTOSIS DUE TO BAND 3 HT
C4021553	BXGD020669	Periodic hypokalemic paresis
C4021768	BXGD020766	Abnormality of metabolism/homeostasis
C4022665	BXGD020950	Isothenuria
C4025184	BXGD021580	Spontaneous hemolytic crises	Hemic and Lymphatic Diseases
C4049392	BXGD021929	Chronic hepatitis C genotype 1
C4272578	BXGD022330	Autosomal Recessive Osteopetrosis	Musculoskeletal Diseases
C4316812	BXGD022704	Fibrinogen Deficiency	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
C4520840	BXGD023041	Erythroleukemia (Erythroid/Myeloid)	Neoplasms; Hemic and Lymphatic Diseases
C4528257	BXGD023159	Corpuscular Hemoglobin Concentration Mean
C4529962	BXGD023178	Fatty Liver Disease
C4531297	BXGD023215	Increased mean corpuscular hemoglobin concentration
C4699508	BXGD023637	Cardioembolism (high-risk/medium-risk)
C4699512	BXGD023639	Large-artery atherosclerosis (embolus/thrombosis)
C4722085	BXGD023788	Malignant neoplasm of colon and/or rectum

Target protein-related compounds

Compounds

BXGC Id	Compound Name	Strcuture	Molecular Weight
BXGC0004275	Acetaldehyde		44.05

The target protein-related foods

Foods

BXGF Id	Food Name	Scientific Name	Food Group	Number of compound^{? Number of compound in food, higher numbers indicate the food are more associated with the protein}