1. Gene
  2. IKZF1 - IKAROS family zinc finger 1 Gene

IKZF1 - IKAROS family zinc finger 1 Gene

中文名称:IKAROS 家族锌指 1

种属: Homo sapiens

同用名: IK1; LYF1; LyF-1; CVID13; IKAROS; PPP1R92; PRO0758; ZNFN1A1; Hs.54452

基因 ID: 10320 | 基因类型: protein coding

关于 IKZF1

Cytogenetic location: 7p12.2 Genomic coordinates (GRCh38): 7:50,303,455-50,405,101 (from NCBI)

This gene has 22 transcripts (splice variants), 209 orthologues, 11 paralogues and is associated with 106 phenotypes. Biased expression in lymph node (RPKM 13.3), appendix (RPKM 8.6) and 10 other tissues.

功能概要

该基因编码的转录因子属于与染色质重塑相关的锌指 DNA 结合蛋白家族。这种蛋白质的表达仅限于胎儿和成人的造血淋巴细胞生成系统,它作为淋巴细胞分化的调节剂发挥作用。已经针对该基因描述了几种编码不同亚型的可变剪接转录物变体。大多数同种型共享一个共同的 C 末端结构域,其中包含异二聚化或同二聚化以及与其他蛋白质相互作用所需的两个锌指基序。然而,同种型在结合 DNA 的 N 末端锌指基序的数量和核定位信号的存在方面有所不同,从而导致具有和不具有 DNA 结合特性的成员。只有少数亚型包含必需的三个或更多 N 末端锌基序,这些基序赋予与靶基因启动子中特定核心 DNA 序列元素的高亲和力结合。非 DNA 结合亚型主要存在于细胞质中,被认为起着显性失活因子的作用。一些显性失活亚型的过度表达与 B 细胞恶性肿瘤有关,例如急性淋巴细胞白血病 (ALL) 。[RefSeq 提供,2014 年 5 月]

This gene encodes a transcription factor that belongs to the family of zinc-finger DNA-binding proteins associated with chromatin remodeling. The expression of this protein is restricted to the fetal and adult hemo-lymphopoietic system, and it functions as a regulator of lymphocyte differentiation. Several alternatively spliced transcript variants encoding different isoforms have been described for this gene. Most isoforms share a common C-terminal domain, which contains two zinc finger motifs that are required for hetero- or homo-dimerization, and for interactions with Other proteins. The isoforms, however, differ in the number of N-terminal zinc finger motifs that bind DNA and in nuclear localization signal presence, resulting in members with and without DNA-binding properties. Only a few isoforms contain the requisite three or more N-terminal zinc motifs that confer high affinity binding to a specific core DNA sequence element in the promoters of target genes. The non-DNA-binding isoforms are largely found in the cytoplasm, and are thought to function as dominant-negative factors. Overexpression of some dominant-negative isoforms have been associated with B-cell malignancies, such as acute lymphoblastic leukemia (ALL). [provided by RefSeq, May 2014]

IKZF1 基因产物(18)

mRNA Protein Name
NM_001220765.3 NP_001207694.1 DNA-binding protein Ikaros isoform 2
NM_001220767.2 NP_001207696.1 DNA-binding protein Ikaros isoform 4
NM_001220768.2 NP_001207697.1 DNA-binding protein Ikaros isoform 5
NM_001220770.2 NP_001207699.1 DNA-binding protein Ikaros isoform 7
NM_001220771.2 NP_001207700.1 DNA-binding protein Ikaros isoform 8
NM_001291837.2 NP_001278766.1 DNA-binding protein Ikaros isoform 2
NM_001291838.2 NP_001278767.1 DNA-binding protein Ikaros isoform 3
NM_001291839.2 NP_001278768.1 DNA-binding protein Ikaros isoform 6
NM_001291840.1 NP_001278769.1 DNA-binding protein Ikaros isoform Ik-6
NM_001291841.1 NP_001278770.1 DNA-binding protein Ikaros isoform Ik-7
NM_001291842.1 NP_001278771.1 DNA-binding protein Ikaros isoform Ik-7(del)
NM_001291843.1 NP_001278772.1 DNA-binding protein Ikaros isoform Ik-8
NM_001291844.1 NP_001278773.1 DNA-binding protein Ikaros isoform Ik-8(del)
NM_001291845.2 NP_001278774.1 DNA-binding protein Ikaros isoform 15
NM_001291846.2 NP_001278775.1 DNA-binding protein Ikaros isoform 16
NM_001291847.2 NP_001278776.1 DNA-binding protein Ikaros isoform 16
NM_001410879.1 NP_001397808.1 DNA-binding protein Ikaros isoform 17
NM_006060.6 NP_006051.1 DNA-binding protein Ikaros isoform 1
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 DNA binding IDA
IDA: 通过直接分析推断
21548011 GOA
enables identical protein binding IPI
IPI: 通过物理相互作用推断
32296183 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
15491138 GOA
enables protein domain specific binding IPI
IPI: 通过物理相互作用推断
15491138 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in erythrocyte differentiation IMP
IMP: 通过突变表型推断
17934067 GOA
involved in lymphocyte differentiation IMP
IMP: 通过突变表型推断
17934067 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in nucleus IDA
IDA: 通过直接分析推断
21548011 GOA
located in pericentric heterochromatin IDA
IDA: 通过直接分析推断
21548011 GOA
part of protein-containing complex IDA
IDA: 通过直接分析推断
23071339 GOA
part of protein-containing complex IMP
IMP: 通过突变表型推断
15491138 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

IKZF1 蛋白结构

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (132 - 155)

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (159 - 182)

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (188 - 211)

  • 0
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  • 400
  • 519 a.a.
蛋白主名 其他名称

DNA-binding protein Ikaros

CLL-associated antigen KW-6

IKZF1 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
IKZF1 Q13422 CTBP1 Homo sapiens Q13363-2 25416956
种属内
IKZF1 Q13422 CTBP2 Homo sapiens P56545-3 25416956
种属内
IKZF1 Q13422 CTBP2 Homo sapiens P56545-3 25416956
种属内
IKZF1 Q13422 a8k932_human Homo sapiens A8K932 25416956
种属内
IKZF1 Q13422 a8k932_human Homo sapiens A8K932 25416956
种属内
IKZF1 Q13422 a8k932_human Homo sapiens A8K932 25416956
种属内
IKZF1 Q13422 UBE2I Homo sapiens Q7KZS0 25416956
种属内
IKZF1 Q13422 FAM74A4 Homo sapiens Q5TZK3 25416956
种属内
IKZF1 Q13422 SHFL Homo sapiens Q9NUL5 25416956
种属内
IKZF1 Q13422 PNKP Homo sapiens Q96T60 25416956
种属内
IKZF1 Q13422 PNKP Homo sapiens Q96T60 25416956
种属内
IKZF1 Q13422 ISCU Homo sapiens Q9H1K1 25416956
种属内
IKZF1 Q13422 PRKAB2 Homo sapiens O43741 25416956
种属内
IKZF1 Q13422 PRKAB2 Homo sapiens O43741 25416956
种属内
IKZF1 Q13422 RAD51D Homo sapiens O75771 31515488
种属内
IKZF1 Q13422 ZMAT2 Homo sapiens Q96NC0 25416956
种属内
IKZF1 Q13422 MCRS1 Homo sapiens Q96EZ8 25416956
种属内
IKZF1 Q13422 MCRS1 Homo sapiens Q96EZ8 33961781
种属内
IKZF1 Q13422 DDX6 Homo sapiens P26196 25416956
种属内
IKZF1 Q13422 BYSL Homo sapiens Q13895 25416956
种属内
IKZF1 Q13422 PSMA4 Homo sapiens P25789 25416956
种属内
IKZF1 Q13422 PSMA1 Homo sapiens P25786 25416956
种属内
IKZF1 Q13422 PSMA1 Homo sapiens P25786 25416956
种属内
IKZF1 Q13422 PSMA1 Homo sapiens P25786 25416956
种属内
IKZF1 Q13422 LSM4 Homo sapiens Q9Y4Z0 25416956
种属内
IKZF1 Q13422 LSM4 Homo sapiens Q9Y4Z0 25416956
种属内
IKZF1 Q13422 SPATC1L Homo sapiens Q9H0A9 25416956
种属内
IKZF1 Q13422 GLRX3 Homo sapiens O76003 25416956
种属内
IKZF1 Q13422 NOC4L Homo sapiens Q9BVI4 25416956
种属内
IKZF1 Q13422 MORF4L1 Homo sapiens Q9UBU8 25416956
种属内
IKZF1 Q13422 MORF4L1 Homo sapiens Q9UBU8 25416956
种属内
IKZF1 Q13422 MORF4L2 Homo sapiens Q15014 25416956
种属内
IKZF1 Q13422 CKS1B Homo sapiens P61024 25416956
种属内
IKZF1 Q13422 CKS1B Homo sapiens P61024 25416956
种属内
IKZF1 Q13422 AP1M1 Homo sapiens Q9BXS5 25416956
种属内
IKZF1 Q13422 SNW1 Homo sapiens Q13573 25416956
种属内
IKZF1 Q13422 SNW1 Homo sapiens Q13573 25416956
种属内
IKZF1 Q13422 FGF12 Homo sapiens P61328 25416956
种属内
IKZF1 Q13422 ALKBH3 Homo sapiens Q96Q83 29892012
种属内
IKZF1 Q13422 ALKBH3 Homo sapiens Q96Q83 31515488
种属内
IKZF1 Q13422 ALKBH3 Homo sapiens Q96Q83 25416956
种属内
IKZF1 Q13422 PIN1 Homo sapiens Q13526 25416956
种属内
IKZF1 Q13422 PIN1 Homo sapiens Q13526 25416956
种属内
IKZF1 Q13422 MTA1 Homo sapiens Q13330 33961781
种属内
IKZF1 Q13422 MTA1 Homo sapiens Q13330 25416956
种属内
IKZF1 Q13422 MTA1 Homo sapiens Q13330 25416956
种属内
IKZF1 Q13422 C8orf33 Homo sapiens Q9H7E9 25416956
种属内
IKZF1 Q13422 C1orf174 Homo sapiens Q8IYL3 31515488
种属内
IKZF1 Q13422 C1orf174 Homo sapiens Q8IYL3 25416956
种属内
IKZF1 Q13422 FAM161A Homo sapiens Q3B820 25416956
种属内
IKZF1 Q13422 FAM161A Homo sapiens Q3B820 25416956
种属内
IKZF1 Q13422 FAM161A Homo sapiens Q3B820 25416956
种属内
IKZF1 Q13422 RWDD2B Homo sapiens P57060
Y2H
21516116
种属内
IKZF1 Q13422 SDCBP Homo sapiens O00560 25416956
种属内
IKZF1 Q13422 SDCBP Homo sapiens O00560 25416956
种属内
IKZF1 Q13422 SDCBP Homo sapiens O00560 25416956
种属内
IKZF1 Q13422 CTBP2 Homo sapiens P56545 33961781
种属内
IKZF1 Q13422 CTBP2 Homo sapiens P56545
Y2H
21516116
种属内
IKZF1 Q13422 CTBP2 Homo sapiens P56545 25416956
种属内
IKZF1 Q13422 CTBP2 Homo sapiens P56545 25416956
种属内
IKZF1 Q13422 FRMD6 Homo sapiens Q96NE9 25416956
种属内
IKZF1 Q13422 FRMD6 Homo sapiens Q96NE9 25416956
种属内
IKZF1 Q13422 FRMD6 Homo sapiens Q96NE9 25416956
种属内
IKZF1 Q13422 FAM50B Homo sapiens Q9Y247 25416956
种属内
IKZF1 Q13422 FAM50B Homo sapiens Q9Y247
Y2H
21516116
种属内
IKZF1 Q13422 ARMC7 Homo sapiens Q9H6L4 25416956
种属内
IKZF1 Q13422 SYT17 Homo sapiens Q9BSW7 25416956
种属内
IKZF1 Q13422 SYT17 Homo sapiens Q9BSW7 25416956
种属内
IKZF1 Q13422 ZNF581 Homo sapiens Q9P0T4 25416956
种属内
IKZF1 Q13422 ATOSB Homo sapiens Q7L5A3 25416956
种属内
IKZF1 Q13422 ATOSB Homo sapiens Q7L5A3 29892012
种属内
IKZF1 Q13422 ATOSB Homo sapiens Q7L5A3 31515488
种属内
IKZF1 Q13422 GMCL2 Homo sapiens Q8NEA9 25416956
种属内
IKZF1 Q13422 GMCL2 Homo sapiens Q8NEA9 25416956
种属内
IKZF1 Q13422 SCNM1 Homo sapiens Q9BWG6 25416956
种属内
IKZF1 Q13422 SCNM1 Homo sapiens Q9BWG6 25416956
种属内
IKZF1 Q13422 DYRK2 Homo sapiens Q92630 25416956
种属内
IKZF1 Q13422 DYRK2 Homo sapiens Q92630 25416956
种属内
IKZF1 Q13422 DYRK2 Homo sapiens Q92630 25416956
种属内
IKZF1 Q13422 WTAP Homo sapiens Q15007 25416956
种属内
IKZF1 Q13422 WTAP Homo sapiens Q15007 25416956
种属内
IKZF1 Q13422 WTAP Homo sapiens Q15007 33961781
种属内
IKZF1 Q13422 WTAP Homo sapiens Q15007 25416956
种属内
IKZF1 Q13422 MAD2L2 Homo sapiens Q9UI95 25416956
种属内
IKZF1 Q13422 AEN Homo sapiens Q8WTP8 25416956
种属内
IKZF1 Q13422 AIRIM Homo sapiens Q9NX04 25416956
种属内
IKZF1 Q13422 AIRIM Homo sapiens Q9NX04 25416956
种属间: 跨种属相互作用 种属内: 同种属相互作用

IKZF1 抗体

目录号 产品名 应用 反应物种
HY-P81282 Ikaros Antibody (YA987) WB, IP Human
HY-P81282A Ikaros Antibody (YA988) IHC-P Human

关联疾病

疾病名称 别名
Immunodeficiency, Common Variable, 13

Pancytopenia Due To Ikzf1 Mutations

CVID13

Common Variable Immunodeficiency 13

Cid Due To Ikaros Deficiency

Combined Immunodeficiency Due To Ikaros Deficiency

Diamond-Blackfan Anemia-Like

DBAL

Severe Cutaneous Adverse Reaction

Stevens-Johnson Syndrome

Toxic Epidermal Necrolysis

Drug-Induced Stevens Johnson Syndrome

Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum

Susceptibility To Severe Cutaneous Adverse Reaction

Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis

Lyell'S Syndrome

Lyell Syndrome

Severe Cutaneous Adverse Reaction, Susceptibility To

Hypersensitivity Syndrome, Carbamazepine-Induced, Susceptibility To

Hypersensitivity Syndrome, Carbamazepine-Induced

Stevens-Johnson Syndrome, Susceptibility To

Toxic Epidermal Necrolysis, Susceptibility To

Sjs/Ten

Susceptibility To Severe Cutaneous Adverse Reaction Ity To

Mycoplasma-Induced Stevens Johnson Syndrome

Dermatostomatitis, Stevens Johnson Type

Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis Spectrum

Sjs-Ten

Toxic Epidermolysis

SJS

Dermatostomatitis Stevens Johnson Type

Ten

Sjs/Ten - [Stevens-Johnson Syndrome And Toxic Epidermal Necrolysis]

Ten - [Toxic Epidermal Necrolysis]

B-Cell Adult Acute Lymphocytic Leukemia

Adult B Acute Lymphoblastic Leukemia

Adult B Acute Lymphoblastic Leukaemia

Adult B-Cell Acute Lymphoblastic Leukaemia

Adult B-Cell Acute Lymphoblastic Leukemia

Adult B-Cell Lymphocytic Leukaemia

Adult B-Cell Lymphocytic Leukemia

Adult B-Lymphoblastic Leukaemia

Adult B-Lymphoblastic Leukemia

B-Cell Adult Acute Lymphocytic Leukaemia

B-Cell Adult Acute Lymphoblastic Leukemia

B-Lymphoblastic Leukemia/Lymphoma With Recurrent Genetic Abnormality
Leukemia

Leukemias

Leukaemia, Unspecified, Without Mention Of Remission

Aleukemic Leukaemia

Chronic Leukaemia

Subacute Leukaemia

Leukaemia Disorder

Leukaemia Nos

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

Intellectual Developmental Disorder, Autosomal Dominant 33

MRD33

Autosomal Dominant Non-Syndromic Intellectual Disability 33

Mental Retardation, Autosomal Dominant 33

Autosomal Dominant Intellectual Developmental Disorder 33

Autosomal Dominant Mental Retardation 33

Mental Retardation, Autosomal Dominant, Type 33

B-Lymphoblastic Leukemia/Lymphoma, Bcr-Abl1-Like

B Lymphoblastic Leukemia/Lymphoma, Bcr-Abl1-Like

B-All Bcr-Abl1-Like

B-Lymphoblastic Leukemia/Lymphoma With Iamp21

B-All With Iamp21

Intrachromosomal Amplification Of Chromosome 21

Pancytopenia
B-Lymphoblastic Leukemia/Lymphoma With Bcr-Abl1

B-All With Bcr-Abl1

B-Lymphoblastic Leukemia/Lymphoma With T(9

22)(Q34.1

Q11.2)

Bcr-Abl1

B Lymphoblastic Leukemia/Lymphoma With T(9

22)(Q34.1

Q11.2)

Bcr-Abl1

Leukemia, Acute Lymphoblastic

Acute Lymphoblastic Leukemia

ALL

Acute Lymphocytic Leukemia

Leukemia, Acute Lymphocytic, Susceptibility To, 1

Acute Lymphoblastic Leukaemia

Precursor Lymphoblastic Lymphoma/Leukemia

Precursor Lymphoid Neoplasm

Leukemia, Acute Lymphoblastic, Susceptibility To

B-Cell Acute Lymphoblastic Leukemia

Leukemia, Acute Lymphocytic 1

Acute Lymphocytic Leukaemia

Acute Lymphoblastic Leukemia/Lymphoma

All1

Childhood Acute Lymphoblastic Leukemia

Leukemia Acute Lymphoblastic 1

Leukemia Acute Lymphoblastic B-Hyperdiploid

Leukemia Acute Lymphocytic

Leukemia Acute Lymphocytic 1

Leukemia B-Cell Acute Lymphoblastic

Leukemia T-Cell Acute Lymphoblastic

Leukemia, Acute Lymphoblastic, 3

ALL3

Lymphoblastic Leukemia Acute

Leukemia, Acute, Lymphoblastic

Precursor Cell Lymphoblastic Leukemia Lymphoma

Leukemia, Lymphocytic, Acute, L1

Leukemia, Acute Lymphoblastic, Susceptibility To, 3

Combined Immunodeficiency

Combined T Cell And B Cell Immunodeficiency

Congenital Combined Immunodeficiency

Syndrome With Combined Immunodeficiency

Combined T And B Cell Immunodeficiency

Combined Immunity Deficiency

Combined Immunodeficiency Syndrome

Combined T-Cell And B-Cell Immunodeficiency

Lymphopenic Agammaglobulinaemia

Lymphopenia

Lymphocytopenia

Adult Acute Lymphocytic Leukemia

Adult Acute Lymphoid Leukemia

Adult All

Childhood Acute Lymphocytic Leukemia

Childhood Acute Lymphoblastic Leukemia

Childhood All

Pediatric Acute Lymphoblastic Leukemia

Lymphoblastic Leukemia Acute Childhood

B-Cell Lymphoma

Lymphoma, B-Cell

B-Cell Lymphomas

B-Cell Lymphocytic Neoplasm

Lymphoma B-Cell

B-Cell Lymphoma Nos

Joubert Syndrome 6

JBTS6

Joubert Syndrome, Type 6

Trichorhinophalangeal Syndrome, Type I

Trichorhinophalangeal Dysplasia Type I

TRPS1

Trichorhinophalangeal Syndrome Type I

Trps I

Trichorhinophalangeal Syndrome Type 1

Type I Trichorhinophalangeal Syndrome

Giedion Syndrome

Trp Syndrome

Tricho-Rhino-Phalangeal Syndrome 1

Trichorhinophalangeal Syndrome, Type Iii

B-Lymphoblastic Leukemia/Lymphoma With Etv6-Runx1

B-All With Etv6-Runx1

B-Lymphoblastic Leukemia/Lymphoma With T(12

21)(P13.2

Q22.1)

Etv6-Runx1

B Lymphoblastic Leukemia/Lymphoma With T(12

21)(P13.2

Q22.1)

Etv6-Runx1

Childhood B-Cell Acute Lymphoblastic Leukemia

B-Cell Childhood Acute Lymphoblastic Leukemia

B-Lymphoblastic Leukemia/Lymphoma

B Lymphoblastic Leukemia/Lymphoma

B-All

Precursor B Lymphoblastic Lymphoma/Leukemia

C-All

Lymphoblastic Lymphoma, Nos

Common Precursor B All

Lymphoblastic B-Cell Lymphoma

Pro-B All

B-Precursor Lymphoma

Lbl - [Lymphoblastic Lymphoma]

Childhood Leukemia
Precursor T-Cell Acute Lymphoblastic Leukemia

T-All

Precursor T-Cell Acute Lymphoblastic Leukemia/Lymphoma

Precursor T-Cell Acute Lymphocytic Leukemia

Precursor T-Cell Acute Lymphocytic Leukemia/Lymphoma

Precursor T-Cell Lymphoblastic Leukemia-Lymphoma

Adult T-Cell Lymphoma/Leukemia

Dendritic Cell Deficiency
Down Syndrome

Trisomy 21

Complete Trisomy 21 Syndrome

Down'S Syndrome

Trisomy 21 Syndrome

Down'S Syndrome - Trisomy 21

Downs Syndrome

G Trisomy

47,Xx,+21

47,Xy,+21

Trisomy G

Down Syndrome, Susceptibility To

Chromosome 21 Trisomy

Trisomy 21 Nos

Abnormal Autosomes 21

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

Agammaglobulinemia 4, Autosomal Recessive

Agammaglobulinemia 4

AGM4

Agammaglobulinemia, Autosomal Recessive, Due To Blnk Defect

B Cell Linker Protein Deficiency

B-Cell Linker Protein Deficiency

Blnk Deficiency

Agammaglobulinemia Autosomal Recessive Due To Blnk Defect

Agammaglobulinemia, Type 4, Autosomal Recessive

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

Trichorhinophalangeal Syndrome, Type Ii

Langer-Giedion Syndrome

Lgs

Trichorhinophalangeal Syndrome Type Ii

Trichorhinophalangeal Syndrome Type 2

TRPS2

Monosomy 8q24.1

Chromosome 8q24.1 Deletion Syndrome

Deletion 8q24.1

Giedion-Langer Syndrome

Trichorhinophalangeal Dysplasia Type Ii

Langer Giedion Syndrome

Trps 2

Tricho-Rhino-Phalangeal Syndrome Type Ii

Trichorhinophalangeal Syndrome With Exostosis

Trps Ii

Tricho-Rhino-Phalangeal Syndrome 2

8q24.1 Microdeletion Syndrome

8q24.1 Deletion Syndrome

Autosomal Recessive Intellectual Developmental Disorder

Mental Retardation, Autosomal Recessive

Autosomal Recessive Mental Retardation

Autosomal Recessive Non-Syndromic Mental Retardation

Autosomal Recessive Non-Syndromic Intellectual Disability

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]

Lymphoma, Non-Hodgkin, Familial

Non-Hodgkin Lymphoma

Lymphoma, Non-Hodgkin

NHL

Lymphoma, Non-Hodgkin, Somatic

Lymphoma, Follicular, Somatic

Familial Non-Hodgkin Lymphoma

Lymphoma Non-Hodgkins

Follicular Lymphoma, Somatic

Lymphosarcoma

Non-Hodgkins Lymphoma

Chromosomal Duplication Syndrome
Myelodysplastic Syndrome

Myelodysplastic Syndromes

Myelodysplasia

MDS

Myelodysplastic Syndrome Included

Myelodysplastic Syndrome, Susceptibility To, Included

Myelodysplastic Syndrome, Somatic

Myelodysplastic Syndrome, Susceptibility To

Leukemia, Acute Myeloid

Acute Myeloid Leukemia

Leukemia, Acute Myelogenous

Acute Myelogenous Leukemia

AML

Leukemia, Acute Myeloid, Susceptibility To

Acute Myeloblastic Leukemia

Leukemia, Acute Myeloid, Reduced Survival In, Somatic

Acute Myeloid Leukaemia

Leukemia, Myelocytic, Acute

Therapy Related Acute Myeloid Leukemia And Myelodysplastic Syndrome

Secondary Aml

Acute Myelocytic Leukemia

Acute Myeloid Leukemia, Somatic

Leukemia, Acute Myeloid, Somatic

Myeloid Leukemia, Acute, M4/M4eo Subtype, Somatic

Acute Myeloblastic Leukaemia

Acute Myelogenous Leukaemia

Aml - Acute Myeloid Leukemia

Acute Myeloid Leukemia With Cebpa Somatic Mutations

Aml With Cebpa Somatic Mutations

Inherited Acute Myeloid Leukemia

Familial Aml

Inherited Aml

Pure Familial Aml

Pure Familial Acute Myeloid Leukemia

Secondary Acute Myeloid Leukemia

Therapy-Related Aml And Myelodysplastic Syndrome

Acute Myeloid Leukemia, Secondary

Acute Non-Lymphoblastic Leukemia

Acute Non-Lymphocytic Leukemia

Acute Biphenotypic Leukemia

Acute Undifferentiated Leukemia

Acute Myeloblastic Leukaemia With Multilineage Dysplasia

Acute Myeloid Leukaemia With Multilineage Dysplasia Without Mention Of Remission

Acute Myeloid Leukaemia With Myelodysplasia-Related Features

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
Rattus norvegicus IKZF1 RGD RGD:1562979
Macaca mulatta IKZF1 VGNC VGNC:73585
Canis familiaris IKZF1 VGNC VGNC:41923
Bos taurus IKZF1 VGNC VGNC:30103
Mus musculus IKZF1 MGD MGI:1342540
Felis catus IKZF1 VGNC VGNC:102613