ABCB4 - ATP binding cassette subfamily B member 4 Gene

Also Known as GBD1; ICP3; MDR2; MDR3; PGY3; ABC21; MDR2/3; PFIC-3

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 5244

About ABCB4

Cytogenetic location: 7q21.12 Genomic coordinates (GRCh38): 7:87,365,896-87,476,027 (from NCBI)

This gene has 12 transcripts (splice variants), 189 orthologues, 10 paralogues and is associated with 6 phenotypes. Biased expression in liver (RPKM 23.8), adrenal (RPKM 3.1) and 3 other tissues.

Summary

The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance as well as antigen presentation. This gene encodes a full transporter and member of the P-glycoprotein family of membrane proteins with phosphatidylcholine as its substrate. The function of this protein has not yet been determined; however, it may involve transport of Phospholipids from liver hepatocytes into bile. Alternative splicing of this gene results in several products of undetermined function. [provided by RefSeq, Jul 2008]

ABCB4 Products (3)

mRNA Protein Name
NM_000443.4 NP_000434.1 phosphatidylcholine translocator ABCB4 isoform A
NM_018849.3 NP_061337.1 phosphatidylcholine translocator ABCB4 isoform B
NM_018850.3 NP_061338.1 phosphatidylcholine translocator ABCB4 isoform C
Molecular Function GO Annotation Evidence References Source
enables ATPase-coupled transmembrane transporter activity IDA
IDA: Inferred from direct assay
17523162 GOA
enables ATPase-coupled transmembrane transporter activity IMP
IMP: Inferred from mutant phenotype
8898203 GOA
NOT enables ceramide floppase activity IDA
IDA: Inferred from direct assay
8898203 GOA
enables phosphatidylcholine floppase activity IDA
IDA: Inferred from direct assay
8898203 GOA
enables phosphatidylcholine floppase activity IMP
IMP: Inferred from mutant phenotype
24045840 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
19674157 GOA
Biological Process GO Annotation Evidence References Source
involved in cellular response to bile acid IDA
IDA: Inferred from direct assay
17523162 GOA
NOT involved in ceramide translocation IDA
IDA: Inferred from direct assay
8898203 GOA
involved in lipid homeostasis IDA
IDA: Inferred from direct assay
17523162 GOA
involved in phospholipid translocation IDA
IDA: Inferred from direct assay
8898203 GOA
involved in phospholipid translocation IMP
IMP: Inferred from mutant phenotype
24806754 GOA
involved in positive regulation of cholesterol transport IDA
IDA: Inferred from direct assay
17523162 GOA
involved in positive regulation of cholesterol transport IMP
IMP: Inferred from mutant phenotype
24045840 GOA
involved in positive regulation of phospholipid translocation IDA
IDA: Inferred from direct assay
17523162 GOA
involved in positive regulation of phospholipid transport IDA
IDA: Inferred from direct assay
8898203 GOA
involved in positive regulation of phospholipid transport IMP
IMP: Inferred from mutant phenotype
24045840 GOA
Cellular Component GO Annotation Evidence References Source
located in apical plasma membrane IDA
IDA: Inferred from direct assay
8898203 GOA
located in cytoplasm IDA
IDA: Inferred from direct assay
24045840 GOA
located in plasma membrane IDA
IDA: Inferred from direct assay
24045840 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

ABCB4 Protein Structure

ABC_membrane

ABC_membrane: ABC transporter transmembrane region (58 - 347)

ABC_tran

ABC_tran: ABC transporter (412 - 561)

ABC_membrane

ABC_membrane: ABC transporter transmembrane region (712 - 987)

ABC_tran

ABC_tran: ABC transporter (1052 - 1210)

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  • 1286 a.a.
Protein Preferred Names Protein Names

phosphatidylcholine translocator ABCB4

  • ATP-binding cassette sub-family B member 4

ABCB4 Antibodies

Cat. No. 상품명 신청 Reactivity
HY-P811289 ABCB4 Antibody WB, ICC/IF Human, Mouse

Related Diseases

Diseases Alias
Cholestasis, Progressive Familial Intrahepatic, 3
  • PFIC3

  • Cholestasis, Progressive Familial Intrahepatic 3

  • Mdr3 Deficiency

  • Progressive Familial Intrahepatic Cholestasis Type 3

  • Progressive Familial Intrahepatic Cholestasis 3

  • Progressive Familial Intrahepatic Cholestasis With Elevated Serum Gamma-Glutamyltransferase

  • Cholestasis, Progressive Familial Intrahepatic, With Elevated Serum Gamma-Glutamyltransferase

  • Progressive Familial Intrahepatic Cholestasis With Elevated Serum Gama-Glutamyltransferase

  • Cholestasis, Intrahepatic, Familial, Progressive, Type 3

Gallbladder Disease 1
  • Gallstones

  • GBD1

  • Lpac

  • Low Phospholipid-Associated Cholelithiasis

  • Cholecystitis

  • Cholelithiasis

  • Low Phospholipid Associated Cholelithiasis

  • Cholelithiasis, Low Phospholipid-Associated

  • Abcb4-Related Cholelithiasis

  • Gallbladder Disease, Type 1

  • Cholecystolithiasis

Cholestasis, Intrahepatic, Of Pregnancy 3
  • ICP3

  • Cholestasis, Intrahepatic, Of Pregnancy, 3

  • Intrahepatic Cholestasis Of Pregnancy 3

  • Pregnancy Related Cholestasis 3

  • Cholestasis Of Pregnancy, Intrahepatic 3

  • Cholestasis, Intrahepatic, Of Pregnancy, Type 3

Cholecystitis
  • Acute Cholecystitis

  • Chronic Cholecystitis

  • Acalculous Cholecystitis

  • Acute And Chronic Cholecystitis

  • Acute On Chronic Cholecystitis

  • Gallstone Cholecystitis

  • Cholecystitis, Acute

  • Calculus Of Gallbladder With Cholecystitis

  • Gallbladder Inflammation

  • Acute Cholecystitis Infection

  • Acute Acalculous Cholecystitis

  • Chronic Acalculous Cholecystitis

  • Nonfunctioning Gallbladder

Cholestasis, Progressive Familial Intrahepatic, 1
  • PFIC1

  • Byler Disease

  • Cholestasis, Progressive Familial Intrahepatic 1

  • Progressive Familial Intrahepatic Cholestasis 1

  • Progressive Familial Intrahepatic Cholestasis Type 1

  • Fic1 Deficiency

  • Byler'S Disease

  • Cholestasis, Fatal Intrahepatic

  • Progressive Familial Intrahepatic Cholestasis

  • Severe Atp8b1 Deficiency

  • Fatal Intrahepatic Cholestasis

  • Cholestasis, Intrahepatic, Familial, Progressive, Type 1

  • Progressive Intrahepatic Cholestasis

  • Cholestasis, Progressive Familial Intrahepatic 3

Cholestasis, Benign Recurrent Intrahepatic, 1
  • Benign Recurrent Intrahepatic Cholestasis

  • BRIC1

  • Summerskill Syndrome

  • Bric

  • Summerskill-Walshe-Tygstrup Syndrome

  • Cholestasis, Benign Recurrent Intrahepatic

  • Benign Recurrent Intrahepatic Cholestasis 1

  • Benign Recurrent Intrahepatic Cholestasis Type 1

  • Bric Type 1

  • Low Gamma-Gt Familial Intrahepatic Cholestasis

  • Recurrent Familial Intrahepatic Cholestasis

  • Cholestasis, Benign Recurrent Intrahepatic 1

  • Mild Atp8b1 Deficiency

  • Recurrent Familial Intrahepatic Cholestasis 1

  • Abcb11-Related Intrahepatic Cholestasis

  • Atp8b1-Related Intrahepatic Cholestasis

  • Cholestasis, Intrahepatic, Recurrent, Benign, Type 1

  • Progressive Intrahepatic Cholestasis

  • Cholestasis, Progressive Familial Intrahepatic 3

  • Bric - [Benign Recurrent Intrahepatic Cholestasis]

Progressive Familial Intrahepatic Cholestasis
  • Abcb4-Related Intrahepatic Cholestasis

  • Cholestasis, Progressive Familial Intrahepatic

  • Pfic

  • Byler Disease

  • Abcb11-Related Intrahepatic Cholestasis

  • Atp8b1-Related Intrahepatic Cholestasis

  • Bsep Deficiency

  • Byler Disease

  • Byler Syndrome

  • Fic1 Deficiency

  • Low Γ-Gt Familial Intrahepatic Cholestasis

  • Mdr3 Deficiency

  • Pfic

  • Cholestasis, Intrahepatic, Familial, Progressive

  • Pfic - [Progressive Familial Intrahepatic Cholestasis]

Cholelithiasis
Cholestasis
  • Obstruction Of Bile Duct

  • Bile Duct Obstruction

  • Bile Occlusion

  • Extrahepatic Biliary Obstruction

  • Extrahepatic Bile Duct Obstruction

  • Bile Stasis

  • Biliary Stasis

  • Obstructive Hyperbilirubinemia

  • Obstructed Jaundice

  • Bile Duct Obstructed

  • Bile Ductal Obstruction

  • Biliary Duct Obstruction

  • Obstructed Bile Ductal

  • Obstructed Biliary Duct

  • Obstructed Biliary Ductal

  • Jaundice Regurgitation

  • Obstructive Jaundice

  • Cholestatic Jaundice

  • Cholestatic Jaundice Syndrome

Intrahepatic Cholestasis Of Pregnancy
  • Recurrent Intrahepatic Cholestasis Of Pregnancy

  • Gravidic Intrahepatic Cholestasis

  • Pregnancy-Related Cholestasis

  • Icp

  • Pregnancy Related Cholestasis

  • Cholestasis, Intrahepatic Of Pregnancy

  • Familial Intrahepatic Cholestasis Of Pregnancy

  • Familial Recurrent Intrahepatic Cholestasis Of Pregnancy

  • Ricp

  • Obstetric Cholestasis

Cholangitis
  • Acute Cholangiolitis

  • Ascending Cholangitis

  • Cholangiolitis

  • Cholangitis Nos

  • Chronic Cholangiolitis

  • Hepatic Duct Inflammation

  • Acute Cholangitis

  • Bile Duct Inflammation

Intrahepatic Cholestasis
  • Cholestasis, Intrahepatic

  • Neonatal Intrahepatic Cholestasis

  • Cholestasis Intrahepatic

  • Cholestasis Of Pregnancy

Cholestasis, Progressive Familial Intrahepatic, 2
  • PFIC2

  • Cholestasis, Progressive Familial Intrahepatic 2

  • Progressive Familial Intrahepatic Cholestasis Type 2

  • Progressive Familial Intrahepatic Cholestasis 2

  • Bsep Deficiency

  • Recurrent Familial Intrahepatic Cholestasis 2

  • Benign Recurrent Intrahepatic Cholestasis 2

  • Severe Abcb11 Deficiency

  • Bric2

  • Cholestasis, Benign Recurrent Intrahepatic 2

  • Mild Abcb11 Deficiency

  • Cholestasis, Intrahepatic, Familial, Progressive, Type 2

Choledocholithiasis
Liver Disease
  • Liver Failure

  • Liver Diseases

  • Abnormality Of The Liver

  • Liver Dysfunction

  • Disorder Of Liver

  • Hepatic Disorder

  • Hepatic Disease

  • Disease Of Bilirubin Metabolism

  • Disorder Of Bilirubin Metabolism

  • Liver Decompensation

  • Liver Function Failure

  • Hepatic Failure Nos

  • Liver Failure Nos

  • End Stage Liver Disease

  • Decompensated Liver Failure

  • Decompensation Of Liver Function

  • Hepatic Decompensation

  • Hepatic Insufficiency

  • Liver Cell Necrosis With Hepatic Failure

  • Liver Insufficiency

  • Decompensated Liver Disease

  • End Stage Liver Failure

  • Liver Necrosis With Hepatic Failure

Gallbladder Disease
  • Gallbladder Diseases

  • Gall Bladder

  • Gall Bladder Diseases

  • Abnormal Gallbladder Function

Pericholangitis
Chronic Cholangitis
Alagille Syndrome 1
  • Alagille Syndrome

  • Arteriohepatic Dysplasia

  • Alagille-Watson Syndrome

  • Cholestasis With Peripheral Pulmonary Stenosis

  • Hepatic Ductular Hypoplasia

  • Alagille Syndrome Due To A Jag1 Point Mutation

  • ALGS1

  • Algs

  • Aws

  • Syndromic Bile Duct Paucity

  • Cardiovertebral Syndrome

  • Hepatofacioneurocardiovertebral Syndrome

  • Paucity Of Interlobular Bile Ducts

  • Watson-Miller Syndrome

  • Alagille Syndrome Due To 20p12 Microdeletion

  • Ahd

  • Hepatic Ductular Hypoplasia, Syndromatic

  • Watson Alagille Syndrome

  • Alagille'S Syndrome

  • Alagille Syndrome Due To Del(20)(P12)

  • Alagille Syndrome Due To Monosomy 20p12

  • Alagille-Watson Syndrome Due To Monosomy 20p12

  • Arteriohepatic Dysplasia Due To Monosomy 20p12

  • Syndromic Bile Duct Paucity Due To Monosomy 20p12

  • Alagille-Watson Syndrome Due To A Jag1 Point Mutation

  • Arteriohepatic Dysplasia Due To A Jag1 Point Mutation

  • Syndromic Bile Duct Paucity Due To A Jag1 Point Mutation

  • Alagille Syndrome, Type 1

Prolymphocytic Leukemia
  • Pll

  • Prolymphocytic Leukaemia

  • Leukemia Prolymphocytic

  • Leukemia, Prolymphocytic

Cholangitis, Primary Sclerosing
  • Primary Sclerosing Cholangitis

  • PSC

  • Sclerosing Cholangitis

  • Cholangitis, Sclerosing

  • Cholangitis Primary Sclerosing

  • Psc - [Primary Sclerosing Cholangitis]

Primary Biliary Cholangitis
  • Primary Biliary Cirrhosis

  • Biliary Liver Cirrhosis

  • Chronic Nonsuppurative Destructive Cholangitis

  • Familial Primary Biliary Cirrhosis

  • Pbc

  • Hanot Syndrome

  • Cholestatic Cirrhosis

  • Biliary Cirrhosis Primary

  • Liver Cirrhosis, Biliary

  • Hanot'S Cirrhosis

  • Biliary Cirrhosis

  • Pericholangiolic Biliary Cirrhosis

  • Tannhauser-Magendantz Syndrome

  • Hanot-Rossle Syndrome

  • Hypertrophic Cirrhosis

  • Todd Cirrhosis

  • Hanot Cirrhosis

  • Charcot Cirrhosis

  • Mahon-Tannhauser Syndrome

  • Toxic Cirrhosis

  • Hypertrophic Biliary Cirrhosis

  • Monolobular Cirrhosis

  • Unilobar Cirrhosis

  • Xanthomatous Biliary Cirrhosis

Suppurative Cholangitis
Biliary Atresia
  • Congenital Biliary Atresia

  • Isolated Biliary Atresia

  • Isolated Atresia Of Bile Ducts

  • Non-Syndromic Biliary Atresia

  • Atresia Of Bile Duct

  • Biliary Atresia, Congenital

  • Atresia Of Bile Ducts

  • Bile Duct Atresia

  • Congenital Bile Duct Atresia

  • Ba - [Biliary Atresia]

  • Impervious Bile Duct

  • Atresia Of Common Duct

  • Biliary Duct Atresia

  • Bile Ductal Atresia

  • Cystic Duct Atresia

Cholestasis, Progressive Familial Intrahepatic, 4
  • PFIC4

  • Progressive Familial Intrahepatic Cholestasis 4

  • Cholestasis, Progressive Familial Intrahepatic 4

  • Tjp2 Deficit

  • Progressive Familial Intrahepatic Cholestasis-4

  • 3-Beta-Hydroxy-Delta-5-C27-Steroid Oxidoreductase Deficiency

  • Progressive Familial Intrahepatic Cholestasis Type 4

  • Cholestasis, Intrahepatic, Familial, Progressive, Type 4

  • Bile Acid Synthesis Defect, Congenital, 1

Sclerosing Cholangitis
  • Fibrosing Cholangitis

  • Cholangitis, Sclerosing

  • Primary Sclerosing Cholangitis

Cholestasis, Benign Recurrent Intrahepatic, 2
  • BRIC2

  • Benign Recurrent Intrahepatic Cholestasis 2

  • Benign Recurrent Intrahepatic Cholestasis Type 2

  • Bric Type 2

  • Cholestasis, Intrahepatic, Recurrent, Benign, Type 2

  • Cholestasis, Benign Recurrent Intrahepatic 2

Bile Duct Cysts
  • Choledochal Cyst

  • Choledochal Cysts

  • Choledochocele

  • Biliary Cyst

  • Congenital Choledochal Cyst

  • Bile Duct Cyst

  • Congenital Cystic Dilatation Of The Biliary Tract

  • Congenital Bile Duct Dilatation

Common Bile Duct Disease
  • Common Bile Duct Diseases

Cholestasis, Progressive Familial Intrahepatic, 5
  • PFIC5

  • Progressive Familial Intrahepatic Cholestasis 5

  • Nr1h4 Deficiency

  • Progressive Familial Intrahepatic Cholestasis Type 5

  • Cholestasis, Intrahepatic, Familial, Progressive, Type 5

Bile Duct Disease
  • Bile Duct Diseases

  • Bile Duct Disorder

  • Disorder Of Bile Duct

Extrahepatic Cholestasis
  • Cholestasis, Extrahepatic

  • Extrahepatic Biliary Stasis

  • Extrahepatic Obstructive Biliary Disease

  • Cholestasis Extrahepatic

Caroli Disease
  • Caroli Disease Isolated

  • Congenital Polycystic Dilatation Of Intrahepatic Bile Ducts

  • Cystic Dilatation Of The Intrahepatic Biliary Tree

  • Caroli Syndrome

  • Carolis Disease

Biliary Tract Disease
  • Biliary Tract Diseases

  • Biliary Tract Abnormality

Acute Cholangitis
Ascending Cholangitis
Dubin-Johnson Syndrome
  • DJS

  • Chronic Idiopathic Jaundice

  • Jaundice, Chronic Idiopathic

  • Hyperbilirubinemia, Dubin-Johnson Type

  • Hyperbilirubinemia Ii

  • Hyperbilirubinemia Type 2

  • Conjugated Hyperbilirubinemia

  • Dubin-Sprinz Disease

  • Sprinz-Nelson Syndrome

  • Hblrdj

  • Dubin Johnson Syndrome

  • Hyperbilirubinemia 2

  • Black Liver-Jaundice Syndrome

  • Chronic Idiopathic Jaundice With Pigmented Liver

  • Dubin-Sprinz Syndrome

  • Hyperbilirubinaemia Type 2

  • Djs - [Dubin-Johnson Syndrome]

Cholecystolithiasis
Sitosterolemia
  • Phytosterolemia

  • Beta-Sitosterolemia

  • Plant Sterol Storage Disease

  • Phytosterolæmia

  • Sitosterolæmia

  • Retention Of Dietary Cholesterol And Abnormal Retention Of Non-Cholesterol Sterols In The Body

  • Phytosterolaemia

  • Sitosterolaemia

  • Sitosterolemia With Xanthomatosis

Developmental And Epileptic Encephalopathy 11
  • Epileptic Encephalopathy, Early Infantile, 11

  • DEE11

  • Eiee11

  • Developmental And Epileptic Encephalopathy, 11

  • Early Infantile Epileptic Encephalopathy 11

  • Encephalopathy, Developmental And Epileptic, Type 11

Tinea Unguium
  • Dermatophytosis Of Nail

  • Onychomycosis Due To Dermatophyte

  • Cellulitis And Abscess

  • Cellulitis And Abscess Of Buttock

  • Cellulitis And Abscess Of Face

  • Cellulitis And Abscess Of Finger

  • Cellulitis And Abscess Of Finger And Toe

  • Cellulitis And Abscess Of Gluteal Region

  • Cellulitis And Abscess Of Trunk

  • Cellulitis And Abscess Of Upper Arm And Forearm

  • Dermatophytic Onychia

  • Dermatophytic Onychomycosis

  • Onychomycosis

  • Ringworm Of Nails

  • Tinea Of Nail

Autoimmune Cholangitis
  • Autoimmune Cholangiopathy

Hepatic Vascular Disease
  • Vascular Disorder Of Liver

Hepatocellular Carcinoma
  • Liver Cancer

  • Primary Liver Cancer

  • HCC

  • Hepatoma

  • Malignant Neoplasm Of Liver

  • Liver Neoplasms

  • Cancer, Hepatocellular

  • Liver Cell Carcinoma

  • Lcc

  • Hepatoblastoma, Somatic

  • Hepatic Cancer

  • Primary Malignant Neoplasm Of Liver

  • Rare Tumor Of Liver And Intrahepatic Biliary Tract

  • Hepatocellular Carcinoma, Somatic

  • Hepatocellular Carcinoma, Childhood Type, Somatic

  • Hepatocellular Cancer, Somatic

  • Ca Liver - Primary

  • Hepatic Neoplasm

  • Malignant Hepato-Biliary Neoplasm

  • Malignant Neoplasm Of Liver, Not Specified As Primary Or Secondary

  • Malignant Neoplasm Of Liver, Primary

  • Malignant Tumor Of Liver

  • Neoplasm Of Liver

  • Non-Resectable Primary Hepatic Malignant Neoplasm

  • Resectable Malignant Neoplasm Of Liver

  • Resectable Malignant Neoplasm Of The Liver

  • Primary Liver Carcinoma

  • Primary Malignant Liver Neoplasm

  • Primary Cancer Of Liver

  • Primary Tumor Of The Liver

  • Rare Tumor Of Liver And Ibt

  • Hepatocellular Cancer

  • Neoplasm Of The Liver

  • Carcinoma, Hepatocellular

  • Hepatomas

  • Liver Neoplasm

  • Liver Carcinoma

  • Liver And Intrahepatic Biliary Tract Carcinoma

  • Malignant Hepatobiliary Neoplasm

  • Adult Primary Hepatocellular Carcinoma

  • Hepatoblastoma

  • Carcinoma Of Liver

  • Malignant Liver Tumour

  • Malignant Hepatic Tumour

Bilirubin Metabolic Disorder
  • Hyperbilirubinemia

  • Hereditary Hyperbilirubinemia

  • Hyperbilirubinemia, Hereditary

  • Hyperbilirubinaemia

Cystic Fibrosis
  • Mucoviscidosis

  • CF

  • Pseudomonas Aeruginosa, Susceptibility To Chronic Infection By, In Cystic Fibrosis

  • Pseudomonas Aeruginosa Chronic Infection By, In Cystic Fibrosis

  • Cystic Fibrosis Lung Disease, Modifier Of

  • Cystic Fibrosis Of Pancreas

  • Fibrocystic Disease Of Pancreas

  • Cf - [Cystic Fibrosis]

  • Cystic Fibrosis Nos

  • Fibrocystic Disease

  • Fibrocystic Disease Of The Pancreas

  • Mucoviscidosis Of Pancreas

  • Nonproliferative Fibrocystic Disease

  • Pancreatic Cystic Fibrosis

Polycystic Liver Disease
  • Autosomal Dominant Polycystic Liver Disease

  • Isolated Polycystic Liver Disease

  • Pcld

  • Congenital Cystic Liver Disease

  • Congenital Hepatic Cyst

  • Fibrocystic Liver Disease

  • Isolated Autosomal Dominant Polycystic Liver Disease

  • Adpcld

  • Liver Disease, Polycystic

  • Multiple Cysts Of Liver

  • Pld - [Polycystic Liver Disease]

  • Polycystic Liver Disorder

  • Polycystic Liver

  • Congenital Polycystic Disease Of Liver

  • Congenital Polycystic Liver Disease

Leukemia, Chronic Lymphocytic
  • Chronic Lymphocytic Leukemia

  • B-Cell Chronic Lymphocytic Leukemia

  • CLL

  • B-Cell Chronic Lymphoid Leukemia

  • Chronic Lymphatic Leukemia

  • Chronic Lymphocytic Leukaemia

  • Lymphoplasmacytic Leukemia

  • Small Lymphocytic Lymphoma

  • Leukemia, Chronic Lymphatic

  • B-Cell Chronic Lymphocytic Leukaemia

  • Chronic Lymphatic Leukaemia

  • Lymphoplasmacytic Leukaemia

  • B Cell Chronic Lymphocytic Leukemia

  • Chronic B-Cell Lymphocytic Leukemia

  • Leukemia, Lymphocytic, Chronic

  • B-Cll

  • Chronic Lymphoid Leukemia

  • Leukemia Lymphocytic Chronic

  • Lymphoma Small Lymphocytic

  • Leukemia, Lymphocytic, Chronic, B-Cell

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Macaca mulatta ABCB4 VGNC VGNC:108142
Canis familiaris ABCB4 VGNC VGNC:37434
Bos taurus ABCB4 VGNC VGNC:53628
Rattus norvegicus ABCB4 RGD RGD:620248
Mus musculus ABCB4 MGD MGI:97569
Others ABCB4 NCBI