1. Gene
  2. CR1 - complement C3b/C4b receptor 1 (Knops blood group) Gene

CR1 - complement C3b/C4b receptor 1 (Knops blood group) Gene

中文名称:补体 C3b/C4b 受体 1 (诺普斯血型)

种属: Homo sapiens

同用名: KN; C3BR; C4BR; CD35

基因 ID: 1378 | 基因类型: protein coding

关于 CR1

Cytogenetic location: 1q32.2 Genomic coordinates (GRCh38): 1:207,496,157-207,641,765 (from NCBI)

This gene has 12 transcripts (splice variants), 87 orthologues, 39 paralogues and is associated with 2 phenotypes. Biased expression in appendix (RPKM 18.3), spleen (RPKM 14.7) and 10 other tissues.

功能概要

该基因是补体激活受体 (RCA) 家族的成员,位于 1 号染色体的“RCA 簇”区域。基因组在该位点具有多态性,具有编码不同亚型的等位基因特异性剪接变体,基于存在/缺少长同源重复序列 (LHR) 。该基因编码在红细胞、白细胞、肾小球足细胞和脾脏滤泡树突细胞上发现的单体单程 I 型膜糖蛋白。 Knops 血型系统是位于该蛋白质上的抗原系统。该蛋白质介导细胞与具有激活补体的颗粒和免疫复合物的结合。这种蛋白质表达的减少和/或这种基因的突变与胆囊癌、系膜毛细血管性肾小球肾炎、系统性红斑狼疮、结节病和阿尔茨海默病有关。该基因的突变也与恶性疟原虫玫瑰花结的减少有关,从而提供针对严重疟疾的保护。[RefSeq 提供,2020 年 5 月]

This gene is a member of the receptors of complement activation (RCA) family and is located in the 'cluster RCA' region of chromosome 1. The genome is polymorphic at this locus with allele-specific splice variants encoding different isoforms, based on the presence/absence of long homologous repeats (LHRs). The gene encodes a monomeric single-pass type I membrane glycoprotein found on erythrocytes, leukocytes, glomerular podocytes, and splenic follicular dendritic cells. The Knops blood group system is a system of antigens located on this protein. The protein mediates cellular binding to particles and immune complexes that have activated complement. Decreases in expression of this protein and/or mutations in this gene have been associated with gallbladder carcinomas, mesangiocapillary glomerulonephritis, systemic lupus erythematosus, sarcoidosis and Alzheimer's disease. Mutations in this gene have also been associated with a reduction in Plasmodium falciparum rosetting, conferring protection against severe malaria. [provided by RefSeq, May 2020]

CR1 基因产物(3)

mRNA Protein Name
NM_000573.4 NP_000564.2 complement receptor type 1 isoform F precursor
NM_000651.6 NP_000642.3 complement receptor type 1 isoform S precursor
NM_001381851.1 NP_001368780.1 complement receptor type 1 isoform 3 precursor
基因本体论
  • 分子功能
  • 生物过程
  • 细胞组分
分子功能 GO 注释 逻辑证据 参考文献 来源
enables complement component C3b binding IDA
IDA: 通过直接分析推断
2972794 GOA
enables complement component C3b receptor activity IDA
IDA: 通过直接分析推断
2972794 GOA
enables complement component C4b binding IDA
IDA: 通过直接分析推断
2972794 GOA
enables complement component C4b receptor activity IDA
IDA: 通过直接分析推断
2972794 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
18684861 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
acts upstream of or within ATP export IDA
IDA: 通过直接分析推断
24022490 GOA
involved in complement activation, alternative pathway IMP
IMP: 通过突变表型推断
11981823 GOA
involved in complement receptor mediated signaling pathway IDA
IDA: 通过直接分析推断
16360013 GOA
involved in immune complex clearance by erythrocytes IDA
IDA: 通过直接分析推断
24022490 GOA
involved in negative regulation of T cell proliferation IDA
IDA: 通过直接分析推断
16360013 GOA
acts upstream of negative regulation of activation of membrane attack complex IDA
IDA: 通过直接分析推断
31862673 GOA
involved in negative regulation of complement activation IDA
IDA: 通过直接分析推断
31862673 GOA
involved in negative regulation of complement activation, alternative pathway IDA
IDA: 通过直接分析推断
10531307 GOA
involved in negative regulation of complement activation, classical pathway IDA
IDA: 通过直接分析推断
6910481 GOA
involved in negative regulation of complement-dependent cytotoxicity IDA
IDA: 通过直接分析推断
31862673 GOA
acts upstream of negative regulation of immunoglobulin production IDA
IDA: 通过直接分析推断
22962438 GOA
acts upstream of or within negative regulation of interleukin-2 production IDA
IDA: 通过直接分析推断
16360013 GOA
acts upstream of negative regulation of plasma cell differentiation IDA
IDA: 通过直接分析推断
22962438 GOA
involved in negative regulation of serine-type endopeptidase activity IDA
IDA: 通过直接分析推断
6910481 GOA
acts upstream of or within negative regulation of type II interferon production IDA
IDA: 通过直接分析推断
16360013 GOA
involved in plasma membrane organization IDA
IDA: 通过直接分析推断
24022490 GOA
involved in positive regulation of activation of membrane attack complex IMP
IMP: 通过突变表型推断
11981823 GOA
involved in positive regulation of cell population proliferation IDA
IDA: 通过直接分析推断
25742728 GOA
involved in positive regulation of regulatory T cell differentiation IDA
IDA: 通过直接分析推断
25742728 GOA
involved in positive regulation of serine-type endopeptidase activity IDA
IDA: 通过直接分析推断
2972794 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in cell surface IDA
IDA: 通过直接分析推断
2972794 GOA
located in cytoskeleton IDA
IDA: 通过直接分析推断
18684861 GOA
located in plasma membrane IDA
IDA: 通过直接分析推断
6910481 GOA
located in plasma membrane raft IDA
IDA: 通过直接分析推断
24022490 GOA
EXP:通过实验结果推断 IDA:通过直接分析推断 IPI:通过物理相互作用推断 IMP:通过突变表型推断 IGI:通过遗传相互作用推断 IEP:通过表达模式推断

CR1 蛋白结构

Sushi

Sushi: Sushi repeat (SCR repeat) (43 - 99)

Sushi

Sushi: Sushi repeat (SCR repeat) (104 - 161)

Sushi

Sushi: Sushi repeat (SCR repeat) (166 - 232)

Sushi

Sushi: Sushi repeat (SCR repeat) (238 - 293)

Sushi

Sushi: Sushi repeat (SCR repeat) (297 - 353)

Sushi

Sushi: Sushi repeat (SCR repeat) (375 - 416)

Sushi

Sushi: Sushi repeat (SCR repeat) (421 - 487)

Sushi

Sushi: Sushi repeat (SCR repeat) (493 - 549)

Sushi

Sushi: Sushi repeat (SCR repeat) (554 - 611)

Sushi

Sushi: Sushi repeat (SCR repeat) (616 - 682)

Sushi

Sushi: Sushi repeat (SCR repeat) (688 - 743)

Sushi

Sushi: Sushi repeat (SCR repeat) (747 - 803)

Sushi

Sushi: Sushi repeat (SCR repeat) (825 - 866)

Sushi

Sushi: Sushi repeat (SCR repeat) (871 - 937)

Sushi

Sushi: Sushi repeat (SCR repeat) (943 - 999)

Sushi

Sushi: Sushi repeat (SCR repeat) (1004 - 1061)

Sushi

Sushi: Sushi repeat (SCR repeat) (1066 - 1132)

Sushi

Sushi: Sushi repeat (SCR repeat) (1138 - 1193)

Sushi

Sushi: Sushi repeat (SCR repeat) (1197 - 1253)

Sushi

Sushi: Sushi repeat (SCR repeat) (1274 - 1316)

Sushi

Sushi: Sushi repeat (SCR repeat) (1321 - 1387)

Sushi

Sushi: Sushi repeat (SCR repeat) (1396 - 1452)

Sushi

Sushi: Sushi repeat (SCR repeat) (1457 - 1514)

Sushi

Sushi: Sushi repeat (SCR repeat) (1519 - 1585)

Sushi

Sushi: Sushi repeat (SCR repeat) (1591 - 1646)

Sushi

Sushi: Sushi repeat (SCR repeat) (1650 - 1706)

Sushi

Sushi: Sushi repeat (SCR repeat) (1718 - 1769)

Sushi

Sushi: Sushi repeat (SCR repeat) (1774 - 1840)

Sushi

Sushi: Sushi repeat (SCR repeat) (1848 - 1900)

Sushi

Sushi: Sushi repeat (SCR repeat) (1923 - 1965)

  • 0
  • 400
  • 800
  • 1200
  • 1600
  • 2039 a.a.
蛋白主名 其他名称

complement receptor type 1

C3-binding protein

CR1 蛋白互作信息

分类
蛋白名称 蛋白编号 互作蛋白 互作蛋白种属 互作蛋白编号 实验方法 参考文献
种属内
CR1 P17927 FCN3 Homo sapiens O75636
SPR
23460739
种属内
CR1 P17927 MBL2 Homo sapiens P11226
SPR
23460739
种属内
CR1 P17927 FCN2 Homo sapiens Q15485
SPR
23460739
种属间: 跨种属相互作用 种属内: 同种属相互作用

CR1 抗体

目录号 产品名 应用 反应物种
HY-P81583 CD35 Antibody (YA1328) IHC-P Human

关联疾病

疾病名称 别名
Malaria

Malaria, Susceptibility To

Malaria, Resistance To

Malaria, Cerebral

Cerebral Malaria

Malaria, Severe, Susceptibility To

Malaria, Severe, Resistance To

Malaria, Cerebral, Susceptibility To

Induced Malaria

Malaria, Vivax, Protection Against

Malaria, Severe

Malaria, Cerebral, Reduced Risk Of

Malaria, Protection Against

Resistance To Malaria Due To G6pd Deficiency

Malaria Due To G6pd Deficiency

Malarial Encephalitis

CM

Malaria Cerebral

Susceptibility To Malaria

Acute Pernicious Fever

Aestivo-Autumnal Fever

Aestivo Autumnal Malaria

Chagres Fever

Continued Malaria Fever

Estivo-Autumnal Fever

Estivo-Autumnal Malaria

Estivo-Autumnal Malarial Fever

Falciparum Fever

Malignant Tertian Fever

Malignant Tertian Malaria

Pernicious Intermittent Fever

Pernicious Malaria

Quotidian Malaria

Subtertian Fever

Subtertian Malaria Fever

Subtertian Malignant Tertian Malaria

Tropical Malaria

Algid Malaria

Bilious Haemoglobinuric Fever

Black Water Fever

Blackwater Fever

Malarial Blackwater Fever

Severe Malarial Falciparum

West African Fever

Malarial Haematinuria

Haemoglobinuric Fever

Haemoglobinuric Malaria

Severe Plasmodium Falciparum Malaria

Malarial Haemoglobinuria

Malarial Haematuria

Falciparum Malaria [Malignant Tertian]

Malaria Tropica

Malarial Shock

Chagres Virus Disease

Malignant Malaria

Mtm - [Malignant Tertian Malaria]

Tm -[Malignant Tertian Malaria]

Panama Fever

St - [Subtertian Malaria]

Malarial Quotidian

Benign Tertian Malaria

Tertian Ague

Vivax Fever

Plasmodium Vivax Malaria Nos

Btm - [Benign Tertian Malaria]

Bt - [Benign Tertian Malaria]

Vivax Malaria

Benign Tertian Vivax Malaria

Tertian Malaria

Quartan Malaria

Quartan Ague

Quartan Fever

Plasmodium Malariae Malaria Nos

Quartan Malarial

Malaria By Plasmodium Malariae

Malariae Malaria

Ovale Tertian Malaria

Plasmodium Ovale Fever

Malaria Fever By Plasmodium Ovale

Ovale Malaria

Malaria By Plasmodium Ovale

Malarial Ovale

Marsh Fever

Remittent Congestive Fever

Coastal Fever

Remittent Gastric Fever

Miasmatic Fever

Congestive Remittent Fever

Intermittent Fever

Jungle Fever

Paludism

Cameroon Fever

Ague

Corsican Fever

Intermittent Bilious Fever

Disease Due To Plasmodiidae

Malarial Fever

Plasmodiosis

Remittent Fever

Roman Fever

Malaria Fever Nos

Malaria Nos

Paludal Fever

Clinically Diagnosed Malaria

Clinically Diagnosed Malaria Without Parasitological Confirmation

Congestive Fever

Malarial Cachexia

Marsh Cachexia

Paludal Cachexia

Recurrent Malaria

Remittent Malaria

Follicular Dendritic Cell Sarcoma

Dendritic Cell Sarcoma

Dendritic Cell Sarcoma, Follicular

Follicular Dendritic Cell Tumour

Dendritic Cell Sarcoma, Interdigitating

Dendritic Cell Sarcoma, Not Otherwise Specified

Plasmodium Falciparum Malaria

Falciparum Malaria

Malaria, Falciparum

Malaria Fever, Subtertian

Malignant Tertian Fever

Malaria Falciparum

Cerebral Malaria Nos

Cerebral Malaria

Complement Factor I Deficiency

Complement Component 3 Inactivator Deficiency

C3 Inactivator Deficiency

Hereditary Factor I Deficiency Disease

C3 Glomerulopathy 2

CFID

C3g2

Immunodeficiency With Factor I Anomaly

Complete Factor I Deficiency

CFI DEFICIENCY

Deficiency, Complement Factor I

Complement Factor I Deficiency

Deficiency Of Factor 1

Hereditary Fibrinogen Deficiency

Deficiency Of Fibrinogen

Congenital Fibrinogenopenia

Glomerulonephritis

Bright'S Disease

Arthus Reaction

Arthus Phenomenon

Arthus Type Urticaria

Parapharyngeal Meningioma

Primary Parapharyngeal Meningioma

Histiocytic And Dendritic Cell Cancer

Histiocytic And Dendritic Cell

Castleman Disease

Angiofollicular Ganglionic Hyperplasia

Angiofollicular Lymph Hyperplasia

Giant Lymph Node Hyperplasia

Castleman'S Disease

Angiofollicular Lymph Node Hyperplasia

Lymphoid Hamartoma

Benign Giant Lymphoma

Angiolymphoid Hyperplasia

Hemoglobinuria
Lupus Erythematosus

Lupus

Lupus Vulgaris

Lupus Erythematosus, Discoid

Lupus Erythematosus, Systemic

Subacute Cutaneous Lupus

Le - [Lupus Erythematosus]

Systemic Lupus Erythematosus

Lupus Nephritis

SLE

Disseminated Lupus Erythematosus

Systemic Lupus Erythematosus, Susceptibility To

Lupus Erythematosus, Systemic

Lupus Nephritis, Susceptibility To

Libman-Sacks Disease

Systemic Lupus Erythematosus Susceptibility To

Sle - Lupus Erythematosus, Systemic

Le Syndrome

Lupus

Lupus Erythematosus Systemic

Lupus Erythematosus, Systemic, Susceptibility To

Lupus Vulgaris

Lupus Erythematosus, Discoid

Lupus Erythematosus

Systemic Lupus Erythematosus Nos

Sle - [Systemic Lupus Erythematosus]

Mycetoma

Madura Foot

Mycetoma Of Foot

Combined Oxidative Phosphorylation Deficiency 33

COXPD33

Interdigitating Dendritic Cell Sarcoma

Interdigitating Cell Sarcoma

Dendritic Cell Sarcoma, Interdigitating

Reticulum Cell Sarcoma

Myasthenia Gravis

MG

Acquired Myasthenia

Autoimmune Myasthenia Gravis

Erb-Goldflam Disease

Mg - [Myasthenia Gravis]

Myasthenia Gravis Nos

Myasthenia

Afibrinogenemia, Congenital

Congenital Afibrinogenemia

Afibrinogenemia

Factor I Deficiency

Familial Afibrinogenemia

Hypofibrinogenemia, Congenital

Fibrinogen Deficiency

Afibrinogenemia Congenital

CAFBN

Congenital Hypofibrinogenemia

Hypofibrinogenemia

Complement Factor I Deficiency

Follicular Lymphoma

Lymphoma, Follicular

Lymphoma Follicular

Brill-Symmers' Disease

Large Cell Follicular Non-Hodgkin Lymphoma

Diffuse Follicle Centre Lymphoma

Diffuse Follicular Lymphoma Nos

Follicular Nodular Non-Hodgkin Lymphoma, Unspecified

Follicular Large Cell Cleaved Or Noncleaved Lymphoma

Large Cell Follicular Noncleaved Lymphoma

Follicular Lymphoma With Or Without Diffuse Areas

Histiocytic Follicular Lymphoma

Histiocytic Nodular Lymphoma

Histiocytic Nodular Malignant Lymphoma

Large Cell Follicular Lymphoma

Large Cell Noncleaved Follicular Lymphoma

Large Cell Noncleaved Follicular Malignant Lymphoma

Nodular Reticulum Cell Sarcoma

Noncleaved Follicular Lymphoma

Peritonitis

Retractile Mesenteritis

Sclerosing Mesenteritis

Acute Generalized Peritonitis

Primary Bacterial Peritonitis

Idiopathic Sclerosing Mesenteritis

Mesenteric Panniculitis

Peritoneal Retractile Mesenteritis

Liposclerotic Mesenteritis

Mesenteric Fibromatosis

Mesenteric Lipodystrophy

Mesenteric Lipogranuloma

Fibromatosis, Abdominal

Peritoneum Inflammation

Peritonitis Of Undetermined Cause

Peritonitis Of Unspecified Cause

Pelviperitonitis

Pelvic Peritonitis, Nos

Generalised Peritonitis Nos

Abdominal Peritonitis

Acute Idiopathic Peritonitis

Acute Lesser Sac Peritonitis

Acute Peritoneal Inflammation

Diffuse Peritonitis

Peritoneal Inflammation

Acute Primary Peritonitis

Pneumococcal Peritonitis

Hemolytic Anemia

Anemia, Hemolytic

Anemia Hemolytic

Anaemia Due To Other Disorders Of Glutathione Metabolism

Chronic Non Spherocytic Anaemia

G6pd - [Glucose-6-Phosphate Dehydrogenase Deficiency] Anaemia

Anaemia Due To Glucose-6-Phosphate Dehydrogenase Deficiency

Glucose-6-Phosphate Dehydrogenase Deficiency With Anaemia

Glucose-6-Phosphate Dehydrogenase Deficiency Anaemia

Favism Anaemia

Haemolytic Anaemia Due Tog6pd Deficiency

Favism

Pentose Phosphate Pathway Disorder Anaemia

Anaemia Due To Pentose Phosphate Pathway Defect

Spinal Cord Lymphoma

Lymphoma Of The Spinal Cord

Spinal Cord Cancer

Spine Lymphoma

Spinal Cord--Cancer

Hereditary Angioedema

Hereditary Angioneurotic Edema

Hereditary Angioedema Type 1

Hane

Angioedema, Hereditary

Hae

Angioedemas, Hereditary

Deficiency Of C1 Esterase Inhibitor

C1 Esterase Inhibitor Deficiency

C1 Inhibitor Deficiency

Familial Angioneurotic Edema

Hereditary Bradykinine-Induced Angioedema

Hereditary Non Histamine-Induced Angioedema

Hae 1

Hae-I

Hereditary Angioneurotic Edema Type 1

Hereditary C1 Esterase Inhibitor Deficiency - Deficient Factor

Hereditary Angioedema Types I And Ii

Hereditary Angioneurotic Oedema

Familial Angioedema

Hae - [Hereditary Angioneurotic Oedema]

Bannister Disease, Hereditary

Quincke Disease Or Oedema

Hereditary Quincke Oedema

Vulvar Angiokeratoma

Fordyce Angiokeratoma Of Vulva

Angiokeratoma Of Vulva

Granulomatous Gastritis
Langerhans Cell Sarcoma

Malignant Langerhans Cell Sarcoma

Complement Component 3 Deficiency

C3 Deficiency

Ureteral Lymphoma

Lymphoma Of Ureter

Ureter Lymphoma

Membranous Nephropathy

Membranous Glomerulonephritis

Glomerulonephritis, Membranous

Idiopathic Membranous Nephropathy

Idiopathic Membranous Glomerulonephritis

MBNP

Membranous Nephropathy, Susceptibility To

Extramembranous Glomerulonephritis

Mgn

Membranous Gn

Primary Membranous Glomerulonephritis

Primary Membranous Nephropathy

Nephropathy Membranous

Endobronchial Leiomyoma
Adult Respiratory Distress Syndrome

Acute Respiratory Distress Syndrome

Ards

Non-Cardiogenic Pulmonary Edema

Acute Lung Injury

Respiratory Distress Syndrome, Adult

Shock Lung

Acute Respiratory Distress

Respiratory Distress Syndrome

Adult Rds

Ali

Increased-Permeability Pulmonary Edema

Stiff Lung

Respiratory Distress Syndrome Adult

Rheumatoid Arthritis

RA

Arthritis, Rheumatoid

Rheumatoid Arthritis, Susceptibility To

Arthritis Or Polyarthritis, Rheumatic

Atrophic Arthritis

Rheumatism Arthritis

Rheumatoid Polyarthritis

Hypersensitivity Reaction Type Iii Disease

Immune Complex Diseases

Immune Complex Disease

Type Iii Hypersensitivity Reaction Disease

Focal Segmental Glomerulosclerosis

Familial Idiopathic Steroid-Resistant Nephrotic Syndrome

Focal Glomerulosclerosis

Fsgs

Segmental Glomerulosclerosis

Glomerulosclerosis, Focal Segmental

Fgs

Focal Glomerular Sclerosis

Familial Idiopathic Nephrotic Syndrome

Focal Sclerosis With Hyalinosis

Glomerulosclerosis, Focal

Glomerulosclerosis Focal

Glomerulosclerosis, Segmental, Focal

Focal Segmental Glomerulosclerosis, Not Otherwise Specified

Alzheimer Disease 4

AD4

Alzheimer Disease-4

Alzheimer'S Disease 4

Alzheimer Disease, Familial, 4

Alzheimer Disease, Familial4

Alzheimer'S Disease 4, Early Onset

Alzheimer Disease, Type 4

Hemolytic Uremic Syndrome, Atypical 1

Atypical Hemolytic-Uremic Syndrome

Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 1

Atypical Hemolytic Uremic Syndrome

Hemolytic Uremic Syndrome, Atypical, Susceptibility To

Ahus

AHUS1

Hemolytic-Uremic Syndrome

Ahus 1

Ahus, Susceptibility To, 1

Hemolytic Uremic Syndrome, Atypical

Non-Shiga-Like Toxin-Associated Hus

Non-Stx-Hus

Nonenteropathic Hus

Atypical Hus

Shiga Toxin-Associated Hemolytic Uremic Syndrome

D+ Hus

Ehec-Hus

Hemolytic Uremic Syndrome Associated With Shiga Toxin-Producing Escherichia Coli

Hemolytic Uremic Syndrome With Diarrhea

Stec-Hus

Shiga-Like Toxin-Associated Hus

Stx-Hus

Typical Hus

Typical Hemolytic Uremic Syndrome

Atypical Hemolytic Uremic Syndrome With Anti-Factor H Antibodies

Atypical Hus With Anti-Factor H Antibodies

Ahus With Anti-Factor H Antibodies

Ahus With Neutralizing Autoantibodies Against Factor H

Hemolytic Uremic Syndrome Atypical 1

Atypical Hemolytic Uremic Syndrome With H Factor Anomaly

D Hus

Hemolytic-Uremic Syndrome Without Diarrhea

Hemolytic-Uremic Syndrome, Atypical, Type 1

Hemolytic Uremic Syndrome, Typical

Inflammatory Myofibroblastic Tumor

Inflammatory Fibrosarcoma

Common Variable Immunodeficiency

Cvid

Common Variable Agammaglobulinemia

Common Variable Immune Deficiency

Acquired Hypogammaglobulinemia

Hypogamma-Globulinemia, Acquired

Idiopathic Immunoglobulin Deficiency

Primary Antibody Deficiency

Primary Hypogammaglobulinemia

Acquired Agammaglobulinemia

Sporadic Hypogammaglobulinemia

Common Variable Hypogamma-Globulinemia

Immunoglobulin Deficiency, Late-Onset

Common Variable Hypogammaglobulinemia

Immunodeficiency, Common Variable

Deficiency Anemia

Anemia

Deficiency Anemias

Anaemia

Membranoproliferative Glomerulonephritis

Mesangiocapillary Glomerulonephritis

Dense Deposit Disease

Membranoproliferative Glomerulonephritis Type 2

Primary Membranoproliferative Glomerulonephritis

Mesangiocapillary Glomerulonephritis, Type Ii

Glomerulonephritis, Membranoproliferative

Chronic Glomerulonephritis, Lobular

Lobular Glomerulonephritis

Ddd

Glomerulonephritis Membranoproliferative Type 2

Mpgn 2

Membranoproliferative Glomerulonephritis Type Ii

Mesangiocapillary Glomerulonephritis Type 2

Mpgn

Primary Mpgn

Glomerulonephritis Membranoproliferative

Membranoproliferative Glomerulonephritis, Type Ii

Interstitial Lung Disease 2

Idiopathic Pulmonary Fibrosis

Ipf

Fibrocystic Pulmonary Dysplasia

Pulmonary Fibrosis, Idiopathic

Pulmonary Fibrosis, Idiopathic, Susceptibility To

Cryptogenic Fibrosing Alveolitis

ILD2

Idiopathic Pulmonary Fibrosis, Familial

Fibrosing Alveolitis, Cryptogenic

Uip

Fibrosing Alveolitis

Interstitial Pneumonitis, Usual

Familial Idiopathic Pulmonary Fibrosis

Idiopathic Fibrosing Alveolitis, Chronic Form

Usual Interstitial Pneumonia

Fibrosing Alveolitis Cryptogenic

Hamman-Rich Disease

Idiopathic Pulmonary Fibrosis Familial

Interstitial Pneumonitis Usual

Fibrosis Idiopathic Pulmonary

Fibrosis, Pulmonary, Idiopathic

Hamman-Rich Syndrome

Chronic Idiopathic Pulmonary Fibrosis

Acute Interstitial Pneumonia

Interstitial Pulmonary Fibrosis

Ipf - [Idiopathic Pulmonary Fibrosis]

Idiopathic Lung Fibrosis

Fibrosing Lung Disease

Pulmonary Fibrosis Nos

Fibrosing Pneumonitis

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

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

Alzheimer Disease, Familial, 1

Alzheimer Disease

Alzheimer'S Disease

Presenile And Senile Dementia

AD1

Alzheimer Disease, Susceptibility To

Alzheimer Disease, Late-Onset, Susceptibility To

Alzheimer Disease 1, Familial

AD

Familial Alzheimer Disease

Alzheimer Disease, Late-Onset

Alzheimers Dementia

Alzheimer Dementia

Alzheimer Sclerosis

Alzheimer Syndrome

Alzheimer-Type Dementia

Dat

Primary Senile Degenerative Dementia

Sdat

Alzheimer Disease 1

Autosomal Dominant Alzheimer Disease

Early-Onset Alzheimer Disease With Cerebral Amyloid Angiopathy

Late Onset Alzheimer Disease

Alzheimers Disease

Alzheimer Disease, Early-Onset, With Cerebral Amyloid Angiopathy

Late-Onset Alzheimers Disease

Alzheimer'S Disease Pathway Kegg

Dementia Due To Alzheimer'S Disease

Alzheimer Disease Type 1

Alzheimers

疾病名称 别名
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

直系同源

种属 基因名 来源 基因 ID
Canis familiaris CR1 NCBI
Macaca fascicularis CR1 NCBI NCBI:102117401
Mus musculus CR1 NCBI
Rattus norvegicus CR1 NCBI