1. Gene
  2. MAX - MYC associated factor X Gene

MAX - MYC associated factor X Gene

中文名称:MYC 相关因子 X

种属: Homo sapiens

同用名: bHLHd4

基因 ID: 4149 | 基因类型: protein coding

关于 MAX

Cytogenetic location: 14q23.3 Genomic coordinates (GRCh38): 14:65,006,101-65,102,695 (from NCBI)

This gene has 20 transcripts (splice variants), 283 orthologues and is associated with 89 phenotypes. Ubiquitous expression in spleen (RPKM 18.6), lymph node (RPKM 17.0) and 25 other tissues.

功能概要

由该基因编码的蛋白质是基本螺旋-环-螺旋亮氨酸拉链 (bHLHZ) 转录因子家族的成员。它能够与其他家族成员 (包括 Mad、Mxi1 和 Myc) 形成同二聚体和异二聚体。 Myc 是一种与细胞增殖、分化和凋亡有关的癌蛋白。同二聚体和异二聚体竞争共同的 DNA 靶位点 (E 盒) ,并且这些二聚体形式之间的重排提供了一个复杂的转录调节系统。据报道,该基因的突变与遗传性嗜铬细胞瘤有关。该基因的一个假基因位于 7 号染色体的长臂上。可变剪接导致多个转录本变体。[RefSeq 提供,2012 年 8 月]

The protein encoded by this gene is a member of the basic helix-loop-helix leucine zipper (bHLHZ) family of transcription factors. It is able to form homodimers and heterodimers with Other family members, which include Mad, Mxi1 and Myc. Myc is an oncoprotein implicated in cell proliferation, differentiation and Apoptosis. The homodimers and heterodimers compete for a common DNA target site (the E box) and rearrangement among these dimer forms provides a complex system of transcriptional regulation. Mutations of this gene have been reported to be associated with hereditary pheochromocytoma. A pseudogene of this gene is located on the long arm of chromosome 7. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]

MAX 基因产物(29)

mRNA Protein Name
NM_001271068.2 NP_001257997.1 protein max isoform g
NM_001271069.2 NP_001257998.1 protein max isoform h
NM_001320415.2 NP_001307344.1 protein max isoform i
NM_001407094.1 NP_001394023.1 protein max isoform a
NM_001407095.1 NP_001394024.1 protein max isoform b
NM_001407096.1 NP_001394025.1 protein max isoform j
NM_001407097.1 NP_001394026.1 protein max isoform j
NM_001407098.1 NP_001394027.1 protein max isoform k
NM_001407099.1 NP_001394028.1 protein max isoform l
NM_001407100.1 NP_001394029.1 protein max isoform l
NM_001407101.1 NP_001394030.1 protein max isoform l
NM_001407102.1 NP_001394031.1 protein max isoform l
NM_001407103.1 NP_001394032.1 protein max isoform c
NM_001407104.1 NP_001394033.1 protein max isoform c
NM_001407105.1 NP_001394034.1 protein max isoform i
NM_001407106.1 NP_001394035.1 protein max isoform i
NM_001407107.1 NP_001394036.1 protein max isoform i
NM_001407108.1 NP_001394037.1 protein max isoform m
NM_001407109.1 NP_001394038.1 protein max isoform m
NM_001407110.1 NP_001394039.1 protein max isoform m
NM_001407111.1 NP_001394040.1 protein max isoform n
NM_001407112.1 NP_001394041.1 protein max isoform n
NM_001407113.1 NP_001394042.1 protein max isoform g
NM_001407114.1 NP_001394043.1 protein max isoform o
NM_002382.5 NP_002373.3 protein max isoform a
NM_145112.3 NP_660087.1 protein max isoform b
NM_145113.3 NP_660088.1 protein max isoform c
NM_145114.3 NP_660089.1 protein max isoform d
NM_197957.4 NP_932061.1 protein max isoform f
基因本体论
  • 分子功能
  • 生物过程
  • 细胞组分
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in negative regulation of transcription by RNA polymerase II IDA
IDA: 通过直接分析推断
8521822 GOA
involved in positive regulation of DNA-templated transcription IDA
IDA: 通过直接分析推断
8425218 GOA
involved in regulation of transcription by RNA polymerase II IDA
IDA: 通过直接分析推断
8425218 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
part of MLL1 complex IDA
IDA: 通过直接分析推断
15960975 GOA
part of Mad-Max complex IPI
IPI: 通过物理相互作用推断
12553908 GOA
part of Myc-Max complex IPI
IPI: 通过物理相互作用推断
12553908 GOA
part of RNA polymerase II transcription regulator complex IDA
IDA: 通过直接分析推断
8425219 GOA
located in chromatin IDA
IDA: 通过直接分析推断
12837246 GOA
located in nucleus IDA
IDA: 通过直接分析推断
10723141 GOA
part of protein-DNA complex IDA
IDA: 通过直接分析推断
9399572 GOA
part of protein-DNA complex IMP
IMP: 通过突变表型推断
16171389 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

MAX 蛋白结构

HLH

HLH: Helix-loop-helix DNA-binding domain (24 - 74)

  • 0
  • 100
  • 160 a.a.
蛋白主名 其他名称

protein max

class D basic helix-loop-helix protein 4

MAX 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
MAX P61244 UNC45A Homo sapiens Q9H3U1
Y2H Array
31515488
种属内
MAX P61244 UNC45A Homo sapiens Q9H3U1
Y2H Prey Pooling
25416956
种属内
MAX P61244 VRK3 Homo sapiens Q8IV63
TAP
25609649
种属内
MAX P61244 MECP2 Homo sapiens P51608
TAP
25609649
种属内
MAX P61244 LIG3 Homo sapiens P49916
TAP
25609649
种属内
MAX P61244 FOXK2 Homo sapiens Q01167
Pull Down
25609649
种属内
MAX P61244 FOXK2 Homo sapiens Q01167
TAP
25609649
种属内
MAX P61244 MGA Homo sapiens Q8IWI9
TAP
27705803
种属内
MAX P61244 MGA Homo sapiens Q8IWI9
Anti Tag CoIP
33961781
种属内
MAX P61244 MGA Homo sapiens Q8IWI9
TAP
25609649
种属内
MAX P61244 MGA Homo sapiens Q8IWI9
Y2H
21988832
种属内
MAX P61244 MGA Homo sapiens Q8IWI9
TAP
24981860
种属内
MAX P61244 MACROH2A1 Homo sapiens O75367
TAP
25609649
种属内
MAX P61244 TFAP2A Homo sapiens P05549
TAP
25609649
种属内
MAX P61244 EEF1D Homo sapiens P29692
TAP
25609649
种属内
MAX P61244 MYC Homo sapiens P01106
Y2H Prey Pooling
32296183
种属内
MAX P61244 MYC Homo sapiens P01106
PLA
24951594
种属内
MAX P61244 MYC Homo sapiens P01106
Anti Bait CoIP
17418410
种属内
MAX P61244 MYC Homo sapiens P01106
Anti Tag CoIP
20691906
种属内
MAX P61244 MYC Homo sapiens P01106
Y2H Array
32296183
种属内
MAX P61244 MYC Homo sapiens P01106
Anti Tag CoIP
33961781
种属内
MAX P61244 MYC Homo sapiens P01106
Pull Down
9184233
种属内
MAX P61244 MYC Homo sapiens P01106
TAP
27705803
种属内
MAX P61244 MYC Homo sapiens P01106
PLA
18620061
种属内
MAX P61244 MYC Homo sapiens P01106
Y2H
21988832
种属内
MAX P61244 MYC Homo sapiens P01106
Anti Bait CoIP
20691906
种属内
MAX P61244 MYC Homo sapiens P01106
TAP
25609649
种属内
MAX P61244 MYC Homo sapiens P01106
Anti Bait CoIP
12821782
种属内
MAX P61244 MYC Homo sapiens P01106
Anti Bait CoIP
17157259
种属内
MAX P61244 L3MBTL2 Homo sapiens Q969R5
Anti Tag CoIP
33961781
种属内
MAX P61244 L3MBTL2 Homo sapiens Q969R5
TAP
25609649
种属内
MAX P61244 L3MBTL2 Homo sapiens Q969R5
TAP
27705803
种属内
MAX P61244 PLEKHF2 Homo sapiens Q9H8W4
Y2H Pooling
16189514
种属内
MAX P61244 PLEKHF2 Homo sapiens Q9H8W4
Validated Y2H
32296183
种属内
MAX P61244 PLEKHF2 Homo sapiens Q9H8W4
Y2H Array
32296183
种属内
MAX P61244 PLEKHF2 Homo sapiens Q9H8W4
Y2H Prey Pooling
32296183
种属内
MAX P61244 E2F6 Homo sapiens O75461
TAP
27705803
种属内
MAX P61244 E2F6 Homo sapiens O75461
Anti Tag CoIP
33961781
种属内
MAX P61244 E2F6 Homo sapiens O75461
TAP
25609649
种属内
MAX P61244 TFDP1 Homo sapiens Q14186
TAP
25609649
种属内
MAX P61244 TFDP1 Homo sapiens Q14186
Anti Tag CoIP
33961781
种属内
MAX P61244 TFDP1 Homo sapiens Q14186
TAP
27705803
种属内
MAX P61244 MXI1 Homo sapiens P50539
Y2H Prey Pooling
25416956
种属内
MAX P61244 MXI1 Homo sapiens P50539
Validated Y2H
25416956
种属内
MAX P61244 MXI1 Homo sapiens P50539
Y2H Array
25416956
种属内
MAX P61244 MXI1 Homo sapiens P50539
TAP
27705803
种属内
MAX P61244 MXI1 Homo sapiens P50539
Anti Tag CoIP
33961781
种属内
MAX P61244 MXI1 Homo sapiens P50539
Pull Down
9184233
种属内
MAX P61244 MXI1 Homo sapiens P50539
Y2H Pooling
16189514
种属内
MAX P61244 MXI1 Homo sapiens P50539
TAP
25609649
种属内
MAX P61244 MNT Homo sapiens Q99583
Anti Tag CoIP
33961781
种属内
MAX P61244 MNT Homo sapiens Q99583
TAP
25609649
种属内
MAX P61244 MNT Homo sapiens Q99583
TAP
27705803
种属内
MAX P61244 MNT Homo sapiens Q99583
Pull Down
9184233
种属内
MAX P61244 MXD1 Homo sapiens Q05195
TAP
27705803
种属内
MAX P61244 MXD1 Homo sapiens Q05195
Anti Tag CoIP
33961781
种属内
MAX P61244 XRCC1 Homo sapiens P18887
TAP
25609649
种属间: 跨种属相互作用 种属内: 同种属相互作用

重组 MAX 蛋白

目录号 产品名 蛋白编号 纯度
HY-P70388 MAX Protein, Human (His) P61244-2 (M1-S151) ≥95%
HY-P73832 MAX Protein, Human (sf9, His-GST) P61244-1/NP_002373 (M1-S160) ≥95%

关联疾病

疾病名称 别名
Hereditary Paraganglioma-Pheochromocytoma Syndromes

Hereditary Pheochromocytoma-Paraganglioma

Hereditary Paraganglioma-Pheochromocytoma

Familial Pheochromocytoma-Paraganglioma

Paragangliomas 2

Paragangliomas 3

Paragangliomas 4

Sdhx-Related Paraganglioma-Pheochromocytoma

Familial Paraganglioma Syndrome

Familial Paraganglioma-Pheochromocytoma Syndromes

Fpgl

Fpgl/Pheo

Paragangliomas 1

Paraganglioma

Pheochromocytoma

Pheochromocytoma, Susceptibility To

Phaeochromocytoma

Adrenal Gland Chromaffin Paraganglioma

Adrenal Gland Chromaffinoma

Adrenal Gland Paraganglioma

Adrenal Gland Pheochromocytoma

Chromaffin Paraganglioma Of The Adrenal Gland

Intraadrenal Paraganglioma

PCC

Chromaffin Cell Tumor

Medullary Chromaffinoma

Medullary Paraganglioma

Pheochromoblastoma

Pheochromocytomas

Chromaffin Cell Neoplasm

Pheochromocytoma, Malignant

Bap1 Tumor Predisposition Syndrome

Bap1-Related Tumor Predisposition Syndrome

Common Syndrome

Bap1 Cancer Syndrome

Bap1-Tpds

Cutaneous/Ocular Melanoma, Atypical Melanocytic Proliferations, And Other Internal Neoplasms

Tumor Predisposition Syndrome

Tumor Susceptibility Linked To Germline Bap1 Mutations

Cutaneous/Ocular Melanoma, Atypical Melanocytic Proliferations, Other Internal Neoplasms

Tumor Predisposition

Inherited Cancer-Predisposing Syndrome

Hereditary Cancer-Predisposing Syndrome

Paraganglioma

Chemodectoma

Glomus Body Tumor

Paragangliomas

Carotid Body Paraganglioma

Extra-Adrenal Paraganglioma

Spastic Paraplegia 84, Autosomal Recessive

SPG84

Hereditary Spastic Paraplegia 84

Spastic Paraplegia 84 Autosomal Recessive

Doid:0112347

Spastic Paraplegia 85, Autosomal Recessive

SPG85

Hereditary Spastic Paraplegia 85

Spastic Paraplegia 85 Autosomal Recessive

Doid:0112345

Spastic Paraplegia 86, Autosomal Recessive

SPG86

Hereditary Spastic Paraplegia 86

Spastic Paraplegia 86 Autosomal Recessive

Doid:0112342

Esophagus Leiomyoma

Leiomyoma Of Esophagus

Persistent Generalized Lymphadenopathy

Pgl

Persistant Generalized Lymphadenopathy

Multiple Endocrine Neoplasia, Type Iia

Multiple Endocrine Neoplasia Type 2a

Sipple Syndrome

Multiple Endocrine Neoplasia Type 2

MEN2A

Men2

Ptc Syndrome

Multiple Endocrine Neoplasia, Type 2

Multiple Endocrine Neoplasia Iia

Men 2a

Pheochromocytoma And Amyloid Producing Medullary Thyroid Carcinoma

Multiple Endocrine Neoplasia, Type 2a

Pheochromocytoma And Amyloid-Producing Medullary Thyroid Carcinoma

Multiple Endocrine Neoplasia Ii

Men2 Syndrome

Men-2a Syndrome

Multiple Neoplasia 2a

Multiple Neoplasia Type 2

Duodenal Somatostatinoma

Duodenal Delta Cell Somatostatin Producing Tumor

Duodenal Somatostatin-Producing Neuroendocrine Tumor

Sweeney-Cox Syndrome

SWCOS

Malignant Pheochromocytoma

Pheochromocytoma, Malignant

Adrenal Medulla Cancer

Adrenal Medulla Neoplasm

Adrenal Medulla Tumor

Malignant Neoplasm Of Adrenal Medulla

Malignant Tumor Of The Adrenal Medulla

Adrenal Medulla Carcinoma

Neoplasm Of Adrenal Medulla

Peripheral Nervous System Benign Neoplasm
Autonomic Nervous System Benign Neoplasm
Lung Cancer

Lung Carcinoma

Non-Small Cell Lung Carcinoma

Lung Cancer, Susceptibility To

Lung Cancer, Protection Against

Adenocarcinoma Of Lung, Somatic

Adenocarcinoma Of Lung, Response To Tyrosine Kinase Inhibitor In

Nonsmall Cell Lung Cancer

Lung Neoplasm

Carcinoma Of Lung

Lung Non-Small Cell Carcinoma

Non-Small Cell Lung Cancer

Nsclc

Lung Neoplasms

Malignant Neoplasm Of Lung

Alveolar Cell Carcinoma

Nonsmall Cell Lung Cancer, Somatic

Nonsmall Cell Lung Cancer, Response To Tyrosine Kinase Inhibitor In

Nonsmall Cell Lung Cancer, Susceptibility To

Lung Cancer, Somatic

Lung Cancer, Resistance To

Cancer Of Lung

Cancer Of Bronchus

Cancer Of The Lung

Lung Malignancies

Lung Malignant Tumors

Malignant Lung Tumor

Malignant Tumor Of Lung

Pulmonary Cancer

Pulmonary Carcinoma

Pulmonary Neoplasms

Respiratory Carcinoma

LNCR

Adenocarcinoma Of Lung

Neoplasm Of Lung

Cancer Lung

Carcinoma Non-Small Cell Lung

Carcinoma, Non-Small-Cell Lung

Lung Cancers

Lung Carcinomas

Cancer, Lung

Cancer, Lung, Non-Small Cell

Primary Malignant Neoplasm Of Lung

Bronchioloalveolar Adenocarcinoma

Paraganglioma And Gastric Stromal Sarcoma

Carney-Stratakis Syndrome

Paraganglioma And Gastrointestinal Stromal Tumor

Carney Dyad

Carney-Stratakis Dyad Of Paraganglioma And Gastric Stromal Sarcoma

Paraganglioma And Gist

Carney-Stratakis Dyad

Gist-Paraganglioma Dyad

PGGSS

Paraganglioma, Gastric Stromal Sarcoma

Gastrointestinal Stromal Tumors

Von Hippel-Lindau Syndrome

Von Hippel-Lindau Disease

Vhl

Vhl Syndrome

VHLS

Von Hippel-Lindau Syndrome, Modifier Of

Hippel Lindau Syndrome

Angiomatosis Retinae

Cerebelloretinal Angiomatosis, Familial

Hippel-Lindau Disease

Familial Cerebelloretinal Angiomatosis

Lindau Disease

VHLD

Williams-Beuren Syndrome

Williams Syndrome

WBS

Wms

Deletion 7q11.23

Monosomy 7q11.23

Chromosome 7q11.23 Deletion Syndrome, 1.5- To 1.8-Mb

Fanconi Schlesinger Syndrome

Beuren Syndrome

Elfin Facies Syndrome

Elfin Facies With Hypercalcemia

Hypercalcemia-Supravalvar Aortic Stenosis

Ws

Neurofibromatosis, Type I

Von Recklinghausen Disease

Neurofibromatosis 1

Neurofibromatosis, Type 1

NF1

Neurofibromatosis, Peripheral Type

Neurofibromatosis Type I

Neurofibromatosis Type 1 Due To Nf1 Mutation Or Intragenic Deletion

Familial Spinal Neurofibromatosis

Fsnf

Peripheral Neurofibromatosis

Von Recklinghausen'S Neurofibromatosis

Von Recklinghausen Disease Due To Nf1 Mutation Or Intragenic Deletion

Neurofibromatosis Peripheral Type

Von Recklinghausen Syndrome

Neurofibromatosis Type 1

Von Recklinghausen Neuropathy

Nf1 - [Neurofibromatosis Type 1]

Recklinghausen Disease

Neuroblastoma

Nb

Neuroblastoma, Susceptibility To

Neuroblastomas

Central Neuroblastoma

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
Macaca mulatta MAX VGNC VGNC:74667
Rattus norvegicus MAX RGD RGD:621101
Felis catus MAX VGNC VGNC:80920
Canis familiaris MAX VGNC VGNC:43045
Mus musculus MAX MGD MGI:96921
Bos taurus MAX VGNC VGNC:31269
Others MAX NCBI