1. Gene
  2. CBL - Cbl proto-oncogene Gene

CBL - Cbl proto-oncogene Gene

中文名称:Cbl 原癌基因

种属: Homo sapiens

同用名: CBL2; NSLL; C-CBL; RNF55; FRA11B

基因 ID: 867 | 基因类型: protein coding

关于 CBL

Cytogenetic location: 11q23.3 Genomic coordinates (GRCh38): 11:119,206,339-119,308,149 (from NCBI)

This gene has 6 transcripts (splice variants), 264 orthologues, 2 paralogues and is associated with 119 phenotypes. Broad expression in testis (RPKM 12.3), lymph node (RPKM 6.0) and 23 other tissues.

功能概要

该基因是编码无名指 E3 泛素连接酶的原癌基因。编码的蛋白质是蛋白酶体降解靶向底物所需的酶之一。这种蛋白质介导泛素从泛素结合酶 (E2) 转移到特定底物。该蛋白质还包含一个 N 端磷酸酪氨酸结合结构域,使其能够与许多酪氨酸磷酸化底物相互作用并靶向它们进行蛋白酶体降解。因此,它作为许多信号转导通路的负调节剂发挥作用。已发现该基因在许多癌症中发生突变或易位,包括急性髓性白血病,并且 5' UTR 中 CGG 重复序列的扩增与 Jacobsen 综合征有关。该基因的突变也是努南综合征样疾病的原因。[RefSeq 提供,2016 年 7 月]

This gene is a proto-oncogene that encodes a RING finger E3 ubiquitin Ligase. The encoded protein is one of the Enzymes required for targeting substrates for degradation by the Proteasome. This protein mediates the transfer of ubiquitin from ubiquitin conjugating Enzymes (E2) to specific substrates. This protein also contains an N-terminal phosphotyrosine binding domain that allows it to interact with numerous tyrosine-phosphorylated substrates and target them for Proteasome degradation. As such it functions as a negative regulator of many signal transduction pathways. This gene has been found to be mutated or translocated in many cancers including acute myeloid leukaemia, and expansion of CGG repeats in the 5' UTR has been associated with Jacobsen syndrome. Mutations in this gene are also the cause of Noonan syndrome-like disorder. [provided by RefSeq, Jul 2016]

CBL 基因产物(1)

mRNA Protein Name
NM_005188.4 NP_005179.2 E3 ubiquitin-protein ligase CBL
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 SH3 domain binding IPI
IPI: 通过物理相互作用推断
9447983 GOA
enables ephrin receptor binding IPI
IPI: 通过物理相互作用推断
18034775 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
5668240 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in Golgi apparatus IDA
IDA: 通过直接分析推断
29237719 GOA
located in cilium IDA
IDA: 通过直接分析推断
29237719 GOA
located in plasma membrane IDA
IDA: 通过直接分析推断
15465819 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

CBL 蛋白结构

Cbl_N

Cbl_N: CBL proto-oncogene N-terminal domain 1 (48 - 176)

Cbl_N2

Cbl_N2: CBL proto-oncogene N-terminus, EF hand-like domain (178 - 262)

Cbl_N3

Cbl_N3: CBL proto-oncogene N-terminus, SH2-like domain (264 - 349)

zf-C3HC4_3

zf-C3HC4_3: Zinc finger, C3HC4 type (RING finger) (380 - 424)

UBA

UBA: UBA/TS-N domain (861 - 892)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 906 a.a.
蛋白主名 其他名称

E3 ubiquitin-protein ligase CBL

Cas-Br-M (murine) ecotropic retroviral transforming sequence

CBL 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
CBL P22681 NTRK1 Homo sapiens P04629 21570973
种属内
CBL P22681 MET Homo sapiens P08581 11894096
种属内
CBL P22681 MET Homo sapiens P08581
PLA
25241761
种属内
CBL P22681 MET Homo sapiens P08581
ITC
18273061
种属内
CBL P22681 MET Homo sapiens P08581 21163258
种属内
CBL P22681 MET Homo sapiens P08581 18273061
种属内
CBL P22681 MET Homo sapiens P08581
SPR
21163258
种属内
CBL P22681 ZAP70 Homo sapiens P43403
SPR
22266821
种属内
CBL P22681 ZAP70 Homo sapiens P43403 22266821
种属内
CBL P22681 MAPK8 Homo sapiens P45983 16982329
种属内
CBL P22681 EGFR Homo sapiens P00533 23799367
种属内
CBL P22681 EGFR Homo sapiens P00533
IF
16914641
种属内
CBL P22681 EGFR Homo sapiens P00533
ITC
18273061
种属内
CBL P22681 EGFR Homo sapiens P00533 15962011
种属内
CBL P22681 EGFR Homo sapiens P00533 18273061
种属内
CBL P22681 EGFR Homo sapiens P00533 7657591
种属内
CBL P22681 EGFR Homo sapiens P00533 23799367
种属内
CBL P22681 EGFR Homo sapiens P00533 20562913
种属内
CBL P22681 EGFR Homo sapiens P00533 8662998
种属内
CBL P22681 CD2AP Homo sapiens Q9Y5K6 17020880
种属内
CBL P22681 CD2AP Homo sapiens Q9Y5K6 11067845
种属内
CBL P22681 CD2AP Homo sapiens Q9Y5K6 11067845
种属内
CBL P22681 CD2AP Homo sapiens Q9Y5K6 17020880
种属内
CBL P22681 CD2AP Homo sapiens Q9Y5K6 25036637
种属内
CBL P22681 YWHAH Homo sapiens Q04917 25036637
种属内
CBL P22681 SH3KBP1 Homo sapiens Q96B97
Y2H
10679202
种属内
CBL P22681 SH3KBP1 Homo sapiens Q96B97 16407834
种属内
CBL P22681 SH3KBP1 Homo sapiens Q96B97 11894095
种属内
CBL P22681 SH3KBP1 Homo sapiens Q96B97 10679202
种属内
CBL P22681 SH3KBP1 Homo sapiens Q96B97 12177062
种属内
CBL P22681 SH3KBP1 Homo sapiens Q96B97 11894095
种属内
CBL P22681 SH3KBP1 Homo sapiens Q96B97
ITC
19268472
种属内
CBL P22681 SH3KBP1 Homo sapiens Q96B97 10679202
种属内
CBL P22681 SH3KBP1 Homo sapiens Q96B97 11894095
种属内
CBL P22681 SH3KBP1 Homo sapiens Q96B97 15962011
种属内
CBL P22681 SH3KBP1 Homo sapiens Q96B97 14596919
种属内
CBL P22681 SH3KBP1 Homo sapiens Q96B97
Y2H
11894095
种属内
CBL P22681 SH3KBP1 Homo sapiens Q96B97 25036637
种属内
CBL P22681 SH3KBP1 Homo sapiens Q96B97 20711168
种属内
CBL P22681 PIK3R2 Homo sapiens O00459
TAP
19380743
种属内
CBL P22681 YWHAZ Homo sapiens P63104 11697890
种属内
CBL P22681 UBE2D2 Homo sapiens P62837
SPR
22266821
种属内
CBL P22681 UBE2D2 Homo sapiens P62837 22266821
种属内
CBL P22681 SPRY4 Homo sapiens Q9C004 18273061
种属内
CBL P22681 SPRY4 Homo sapiens Q9C004
ITC
18273061
种属内
CBL P22681 SPRY4 Homo sapiens Q9C004 18273061
种属内
CBL P22681 YWHAE Homo sapiens P62258 25036637
种属内
CBL P22681 YWHAE Homo sapiens P62258 36931259
种属内
CBL P22681 YWHAE Homo sapiens P62258 11697890
种属内
CBL P22681 YWHAB Homo sapiens P31946 11157475
种属内
CBL P22681 YWHAG Homo sapiens P61981 11697890
种属内
CBL P22681 YWHAQ Homo sapiens P27348 15094368
种属内
CBL P22681 YWHAQ Homo sapiens P27348 9092538
种属内
CBL P22681 GRB2 Homo sapiens P62993 23799367
种属内
CBL P22681 GRB2 Homo sapiens P62993 25036637
种属内
CBL P22681 GRB2 Homo sapiens P62993 25814554
种属内
CBL P22681 GRB2 Homo sapiens P62993
TAP
19380743
种属内
CBL P22681 GRB2 Homo sapiens P62993 15677445
种属内
CBL P22681 F2RL1 Homo sapiens P55085 15708858
种属内
CBL P22681 HTT Homo sapiens P42858 32814053
种属内
CBL P22681 HTT Homo sapiens P42858 32814053
种属内
CBL P22681 HTT Homo sapiens P42858 32814053
种属内
CBL P22681 SFN Homo sapiens P31947 11697890
种属内
CBL P22681 ITSN1 Homo sapiens Q15811 16914641
种属内
CBL P22681 ITSN1 Homo sapiens Q15811
IF
16914641
种属内
CBL P22681 ITSN1 Homo sapiens Q15811 16914641
种属内
CBL P22681 ITSN1 Homo sapiens Q15811 16914641
种属内
CBL P22681 SRC Homo sapiens P12931 16636290
种属内
CBL P22681 SRC Homo sapiens P12931 17094785
种属内
CBL P22681 SRC Homo sapiens P12931 17094785
种属内
CBL P22681 ARHGEF7 Homo sapiens Q14155 16407834
种属内
CBL P22681 SPRY2 Homo sapiens O43597 18273061
种属内
CBL P22681 SPRY2 Homo sapiens O43597 18273061
种属内
CBL P22681 SPRY2 Homo sapiens O43597 16893902
种属内
CBL P22681 SPRY2 Homo sapiens O43597 12815057
种属内
CBL P22681 SPRY2 Homo sapiens O43597 15962011
种属内
CBL P22681 SH2B2 Homo sapiens O14492 15737992
种属内
CBL P22681 SH2B2 Homo sapiens O14492 18273061
种属内
CBL P22681 SYK Homo sapiens P43405 18273061
种属内
CBL P22681 SYK Homo sapiens P43405 15556646
种属内
CBL P22681 SYK Homo sapiens P43405 8621719
种属内
CBL P22681 SYK Homo sapiens P43405
ITC
18273061
种属内
CBL P22681 PIK3R1 Homo sapiens P27986 16219545
种属内
CBL P22681 PIK3R1 Homo sapiens P27986
TAP
19380743
种属内
CBL P22681 PIK3R1 Homo sapiens P27986 16982329
种属内
CBL P22681 PIK3R1 Homo sapiens P27986 9890970
种属内
CBL P22681 PIK3R1 Homo sapiens P27986 15556646
种属内
CBL P22681 PIK3R1 Homo sapiens P27986 7642581
种属内
CBL P22681 PIK3R1 Homo sapiens P27986
Y2H
9160881
种属内
CBL P22681 PIK3R1 Homo sapiens P27986 8621719
种属内
CBL P22681 PIK3R3 Homo sapiens Q92569 25814554
种属内
CBL P22681 CRK Homo sapiens P46108
TAP
19380743
种属内
CBL P22681 CRK Homo sapiens P46108 25814554
种属内
CBL P22681 CRK Homo sapiens P46108 8524328
种属内
CBL P22681 CRKL Homo sapiens P46109 15556646
种属内
CBL P22681 CRKL Homo sapiens P46109 15556646
种属内
CBL P22681 CRKL Homo sapiens P46109 8626543
种属内
CBL P22681 ATXN1 Homo sapiens P54253 32814053
种属内
CBL P22681 ATXN1 Homo sapiens P54253 32814053
种属内
CBL P22681 ATXN1 Homo sapiens P54253 32814053
种属内
CBL P22681 HCK Homo sapiens P08631-2 10092522
种属间
CBL P22681 PLCG1 Sus scrofa F1SDV6 17372230
种属间
CBL P22681 lpqN Mycobacterium tuberculosis A0A0H3L6J6 30118682
种属间: 跨种属相互作用 种属内: 同种属相互作用

CBL 抗体

目录号 产品名 应用 反应物种
HY-P81294 Phospho-CBL (Tyr774) Antibody (YA1014) WB, IP Human, Rat
HY-P81294A Phospho-CBL (Ser669) Antibody (YA1015) WB Human
HY-P82647 CBL Antibody (YA2392) WB, ICC/IF, IP Human

关联疾病

疾病名称 别名
Noonan Syndrome-Like Disorder With Or Without Juvenile Myelomonocytic Leukemia

NSLL

Cbl Syndrome

Noonan Syndrome-Like Disorder With Juvenile Myelomonocytic Leukemia

Cbl Mutation-Associated Syndrome

Noonan Syndrome-Like Disorder With Jmml

Juvenile Myelomonocytic Leukemia

Leukemia, Juvenile Myelomonocytic

JMML

Leukemia, Juvenile Myelomonocytic, Somatic

Juvenile Chronic Myelomonocytic Leukemia

Juvenile Chronic Myelogenous Leukemia

Leukemia, Myelomonocytic, Juvenile

Juvenile Myelomonocytic Leukaemia Without Mention Of Remission

Fragile Site 11b

FRA11B

Pseudo-Turner Syndrome

Noonan Syndrome

Noonan Syndrome And Noonan-Related Syndrome
Noonan Syndrome 1

Noonan Syndrome

NS1

Male Turner Syndrome

Female Pseudo-Turner Syndrome

Turner Phenotype With Normal Karyotype

Noonan Syndrome With Pigmented Villonodular Synovitis

Turner'S Phenotype, Karyotype Normal

Familial Turner Syndrome

Noonan'S Syndrome

Noonan-Ehmke Syndrome

Ns

Pseudo-Ullrich-Turner Syndrome

Turner Syndrome In Female With X Chromosome

Turner-Like Syndrome

Ullrich-Noonan Syndrome

Noonan-Like/Multiple Giant Cell Lesion Syndrome

Noonan Syndrome-Like Disorder With Multiple Giant Cell Lesions

Pterygium Colli Syndrome

Noonan Syndrome, Type 1

Turner Syndrome, Male

Rhabdomyosarcoma
Rasopathy

Ras/Mitogen-Activated Protein Kinase Syndrome

Aggressive Systemic Mastocytosis

Asm

Lymphadenopathic Mastocytosis With Eosinophilia

Ovarian Germ Cell Cancer

Ovarian Germ Cell Tumor

Malignant Germ Cell Tumor Of Ovary

Germ Cell Neoplasm Of Ovary

Germ Cell Tumor Of Ovary

Mogct

Malignant Ovarian Germ Cell Tumor

Malignant Ovarian Germ Cell Neoplasm

Jacobsen Syndrome

Chromosome 11q Deletion Syndrome

Partial 11q Monosomy Syndrome

Jacobsen Distal 11q Deletion Syndrome

JBS

11q Partial Monosomy Syndrome

Chromosome 11q Deletion

11q Deletion

11q Monosomy

Deletion 11q

Monosomy 11q

Partial Monosomy 11q

11q Deletion Disorder

11q Deletion Syndrome

11q Terminal Deletion Disorder

11q- Deletion Syndrome

11q23 Deletion Disorder

Jacobsen Thrombocytopenia

11q Terminal Deletion Syndrome

Del(11)(Q23.3)

Del(11)(Qter)

Distal Deletion 11q

Distal Monosomy 11q

Monosomy 11qter

Telomeric Deletion 11q

Paris-Trousseau Thrombocytopenia

Hematologic Cancer

Hematologic Neoplasm

Hematologic Neoplasms

Hematologic Malignancies

Blood Cancer

Hematologic Malignancy

Hematological Tumors

Hematopoietic And Lymphoid System Tumor

Hematopoietic Cancer

Hematopoietic Neoplasm

Hematopoietic Tumors

Malignant Hematopoietic Neoplasm

Liquid Tumor

Hematopoietic Neoplasms

Thanatophoric Dysplasia, Type I

Thanatophoric Dysplasia

Thanatophoric Dwarfism

Thanatophoric Dysplasia Type 1

TD1

Td

Thanatophoric Short Stature

Thanatophoric Dwarfism Type 1

Thanatophoric Dysplasia Type I

Platyspondylic Lethal Skeletal Dysplasia, San Diego Type

Lethal Short-Limbed Platyspondylic Dwarfism, San Diego Type

Skeletal Dysplasia, San Diego Type

Plsd San Diego Type

Thanatophoric Dwarfism 1

Dwarfism Thanatophoric

Dwarf, Thanatophoric

Thanatophoric Dysplasia 1

Lethal Short-Limbed Platyspondylic Dwarfism San Diego Type

Platyspondylic Lethal Skeletal Dysplasia San Diego Type

Thanatophoric Dwarf

Thanatophoric Dwarfism Or Short Stature

Thanatophoric Dwarfism Syndrome

Td - [Thanatophoric Dwarfism]

Saethre-Chotzen Syndrome

SCS

Acs3

Acs Iii

Chotzen Syndrome

Acrocephaly, Skull Asymmetry, And Mild Syndactyly

Acrocephalosyndactyly Type 3

Acrocephalosyndactyly, Type Iii

Acrocephalosyndactyly Type Iii

Saethre-Chotzen Syndrome With Or Without Eyelid Anomalies

Auralcephalosyndactyly

Acs 3

Acrocephalo-Syndactyly, Type 3

Blepharophimosis,Epicanthus Inversus, And Ptosis 3

Aural Cephalosyndactyly

Kurczynski-Casperson Syndrome

Acrocephalosyndactyly Iii

Dysostosis Craniofacialis With Hypertelorism

Saethre-Chotzen Syndrome, With/Without Eyelid Anomalies

Sakati Syndrome

Systemic Mastocytosis

Systemic Mast Cell Disease

Systemic Tissue Mast Cell Disease

Mastocytosis, Systemic

Smcd - Systemic Mast Cell Disease

Smcd

Mast Cell Disease, Systemic

Systemic Mast-Cell Disease

Systemic Mastocytoses

Mastocytosis Systemic

Corneal Dystrophy, Subepithelial Mucinous

Smcd - [Systemic Mast Cell Disease]

Lymphoma

Lymphoid Cancer

Lymphomas

Lymphoid Cancers

Lymphoid Neoplasm

Lymphoma Nos

Nhl - [Non-Hodgkin Lymphoma]

Non-Hodgkin Lymphoma

Non-Hodgkin Lymphoma, Nos

Non-Hodgkin Malignant Lymphoma Nos

Wiskott-Aldrich Syndrome

WAS

Eczema-Thrombocytopenia-Immunodeficiency Syndrome

Immunodeficiency 2

Aldrich Syndrome

Imd2

Wiskott-Aldrich Syndrome 1

Was1

Wiskott Syndrome

Wiskott Aldrich Syndrome

Eczema Thrombocytopenia Immunodeficiency Syndrome

Imd 2

Vitamin B12 Deficiency

Cobalamin Deficiency

Hypocobalaminemia

Vitamin B 12 Deficiency

Cyanocobalamin Deficiency

Deficiency Of Vitamin B12

Vitamin Metabolic Disorder
Brill-Zinsser Disease

Recrudescent Typhus

Brill Disease

Brill Zinsser Disease

Brill'S Disease

Latent Typhus

Sporadic Typhus

Typhus, Epidemic Louse-Borne

Recrudescent Typhus Due To Rickettsia Prowazekii

Recrudescent Typhus Fever

Recrudescent Brill-Zinsser Typhus Due To Rickettsia Prowazekii

Recrudescent Brill Disease

Recrudescent Typhus Fever Due To Rickettsia Prowazekii

Pernicious Anemia

Anemia, Pernicious

Anemia Pernicious

Pernicious Anaemia

Addison'S Anaemia

Biermer'S Anaemia

Biermer'S Anemia

Acquired Pernicious Anemia

Addison-Biermer Anemia

Addisonian Anemia

Biermer Anemia

Biermer'S Disease

Juvenile Onset Pernicious Anemia

Biermer Disease

Biermer-Addison Disease

Megaloblastic Anemia

Imerslund-Grasbeck Syndrome

Igs

Defect Of Enterocyte Intrinsic Factor Receptor

Enterocyte Cobalamin Malabsorption

Familial Megaloblastic Anemia

Megaloblastic Anemia 1

Selective Cobalamin Malabsorption With Proteinuria

Imerslund-Gräsbeck Syndrome

Anemia, Megaloblastic

Grasbeck-Imerslund Syndrome

Megaloblastic Anaemia

Mga1 Norwegian Type

Recessive Hereditary Megaloblastic Anaemia 1

Recessive Hereditary Megaloblastic Anemia 1

Rh-Mga1

Gräsbeck-Imerslund Disease

Pernicious Anemia, Juvenile, Due To Selective Intestinal Malabsorption Of Vitamin B12, With Proteinuria

Juvenile Pernicious Anemia With Proteinuria Due To Selective Intestinal Malabsorption Of Vitamin B12

Anemia Megaloblastic

Megaloblastic Anemia Due To Inborn Errors Of Metabolism

3-@Methylglutaconic Aciduria, Type I

Methylmalonic Acidemia

Methylmalonic Aciduria

Mma

Acidemia, Methylmalonic

Isolated Methylmalonic Acidemia

Leukemia, Chronic Myeloid

Chronic Myeloid Leukemia

Chronic Myelogenous Leukemia

CML

Chronic Granulocytic Leukemia

Leukemia, Philadelphia Chromosome-Positive, Resistant To Imatinib

Chronic Myeloid Leukaemia

Chronic Granulocytic Leukaemia

Chronic Myelogenous Leukaemia

Myeloid Leukemia, Chronic

Leukemia, Chronic Myelogenous

Leukemia, Chronic Myeloid, Philadelphia Chromosome Positive, Somatic

Cml - Chronic Myelogenous Leukemia

Cgl

Chronic Myelocytic Leukemia

Leukemia, Chronic Myeloid, Atypical

ACML

Atypical Chronic Myeloid Leukemia Bcr-Abl1 Negative

Myeloid Leukemia Chronic

Leukemia, Myeloid, Chronic

Leukemia, Myeloid, Chronic, Atypical, Bcr-Abl Negative

Cml- [Chronic Myeloid Leukaemia]

Cgl - [Chronic Granulocytic Leukaemia]

Chronic Myelocytic Leukaemia

Glioblastoma

Glioblastoma Multiforme

Gbm

Adult Glioblastoma Multiforme

Grade Iv Adult Astrocytic Tumor

Primary Glioblastoma Multiforme

Spongioblastoma Multiforme

Adult Glioblastoma

Primary Glioblastoma

Myelodysplastic Syndrome

Myelodysplastic Syndromes

Myelodysplasia

MDS

Myelodysplastic Syndrome Included

Myelodysplastic Syndrome, Susceptibility To, Included

Myelodysplastic Syndrome, Somatic

Myelodysplastic Syndrome, Susceptibility To

Craniosynostosis

Premature Closure Of Cranial Sutures

Craniostenosis

Craniosynostosis Syndrome

Cso

Craniosynostoses

Congenital Ossification Of Cranial Sutures

Congenital Ossification Of Sutures Of Skull

Craniostosis

Imperfect Fusion Of Skull

Congenital Imperfect Closure Skull

Imperfect Closure Skull

Premature Closure Cranium Sutures

Deficiency Of Craniofacial Axis

Myelodysplastic/Myeloproliferative Neoplasm

Myelodysplastic-Myeloproliferative Diseases

Myelodysplastic/Myeloproliferative Disease

Myelodysplastic Myeloproliferative Cancer

Myelodysplastic Myeloproliferative Disease

Myeloproliferative/Myelodysplastic Syndromes

Ptosis

Blepharoptosis

Drooping Eyelid

Droopy Eyelid

Ptosis Of Eyelid

Paralysis Of Levator Palpebrae Superioris

Methylmalonic Aciduria And Homocystinuria, Cbld Type

Homocystinuria, Cbld Type, Variant 1

Methylmalonic Aciduria And Homocystinuria Type Cbld

Vitamin B12-Responsive Methylmalonic Acidemia, Type Cbldv2

MAHCD

Methylmalonic Acidemia And Homocystinuria, Cbld Type

Methylmalonic Aciduria, Cblh Type, Formerly

Methylmalonic Acidemia, Cblh Type, Formerly

Methylmalonic Aciduria, Cbld Type, Variant 2

Cobalamin D Deficiency

Methylcobalamin Deficiency Type Cbldv1

Functional Methionine Synthase Deficiency Type Cbldv1

Vitamin B12-Responsive Methylmalonic Aciduria, Type Cbldv2

Methylmalonic Acidemia With Homocystinuria, Type Cbld

Cbld Defect

Cobalamin D Defect

Combined Defect In Adenosylcobalamin And Methylcobalamin Synthesis, Type Cbld

Methylmalonic Aciduria With Homocystinuria, Type Cbld

Homocystinuria Cbld Variant 1

Methylmalonic Acidemia And Homocystinuria Cbld Type

Methylmalonic Aciduria And Homocystinuria Cbld-Combined

Methylmalonic Aciduria And Homocystinuria Cbld Original

Methylmalonic Aciduria Cbld Variant 2

Aciduria, Methylmalonic, And Homocystinuria, Cbld Type

Deficiency Anemia

Anemia

Deficiency Anemias

Anaemia

Breast Cancer

Breast Carcinoma

Male Breast Cancer

Breast Cancer, Familial

Malignant Neoplasm Of Breast

Breast Cancer, Susceptibility To

Breast Cancer, Early-Onset

Malignant Tumor Of Breast

Carcinoma Of Male Breast

Breast Cancer, Invasive Ductal

Breast Cancer, Protection Against

Breast Cancer, Somatic

Breast Cancer, Male

Breast Cancer, Lobular, Somatic

Breast Tumor

Mammary Cancer

Mammary Tumor

Malignant Neoplasm Of Male Breast

Mammary Carcinoma

Male Breast Carcinoma

Familial Cancer Of Breast

Invasive Ductal Breast Carcinoma

Breast Cancer Susceptibility

Breast Cancer, Male, Susceptibility To

Breast Cancer, Early-Onset, Susceptibility To

Malignant Tumor Of The Breast

Mammary Neoplasm

Primary Breast Cancer

Neoplasm Of Male Breast

Carcinoma Of Breast

Breast Cancer In Men

Familial Breast Cancer

Cancer Of Breast

BC

Breast Cancer Familial

Breast Cancer Familial Male

Breast Cancer, Familial Male

Breast Male Carcinoma

Breast Neoplasms

Breast Neoplasms, Male

Mammary Tumors

Mammary Carcinomas

Cancer, Breast

Cancer, Breast, Susceptibility

Invasive Breast Ductal Carcinoma

Breast Neoplasm

Susceptibility To Breast Cancer

Mammary Neoplasms

Animal Mammary Neoplasms

Primary Malignant Neoplasm Of Breast

Infiltrating Ductal Carcinoma Of Breast

Infiltrating Duct Carcinoma Of Unspecified Site

Infiltrating Ductular Carcinoma Of Unspecified Site

Invasive Breast Carcinoma Of No Special Type

Microinvasive Carcinoma Of Breast

Carcinoma With Apocrine Differentiation

T-Cell Acute Lymphoblastic Leukemia

T-Cell Leukemia

Acute T Cell Leukemia

Precursor T Lymphoblastic Leukemia

Precursor T-Lymphoblastic Lymphoma/Leukemia

T Acute Lymphoblastic Leukemia

T-Cell Acute Lymphocytic Leukaemia

T-Cell Lymphoblastic Leukemia/Lymphoma

Leukemia T-Cell

Leukemia, T-Cell

Leukemia, Acute, Lymphoblastic, T-Cell

Leukemia, T-Cell Acute Lymphoblastic

Leukemia, Acute T-Cell

Precursor T-Cell Lymphoblastic Leukemia-Lymphoma

Precursor T-Cell Lymphoblastic Lymphoma

Precursor T Cell Lymphoblastic Leukemia/Lymphoblastic Lymphoma

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
Mus musculus CBL MGD MGI:88279
Macaca mulatta CBL VGNC VGNC:70554
Rattus norvegicus CBL RGD RGD:1561386
Canis familiaris CBL VGNC VGNC:38758
Felis catus CBL VGNC VGNC:108361
Bos taurus CBL VGNC VGNC:26808
Others CBL NCBI