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

MAX - MYC associated factor X Gene

Homo sapiens

Also known as bHLHd4

Gene ID: 4149 | Gene type: protein coding

About 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.

Summary

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 Products(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
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables DNA binding IDA
IDA: Inferred from direct assay
9399572 GOA
enables DNA-binding transcription factor activity, RNA polymerase II-specific IDA
IDA: Inferred from direct assay
8425218 GOA
enables DNA-binding transcription factor binding IPI
IPI: Inferred from physical interaction
15674325 GOA
contributes to DNA-binding transcription repressor activity, RNA polymerase II-specific IDA
IDA: Inferred from direct assay
8521822 GOA
enables DNA-binding transcription repressor activity, RNA polymerase II-specific IDA
IDA: Inferred from direct assay
26070438 GOA
enables E-box binding IMP
IMP: Inferred from mutant phenotype
16171389 GOA
contributes to RNA polymerase II transcription regulatory region sequence-specific DNA binding IDA
IDA: Inferred from direct assay
8425219 GOA
enables identical protein binding IPI
IPI: Inferred from physical interaction
9184233 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
9184233 GOA
enables sequence-specific double-stranded DNA binding IDA
IDA: Inferred from direct assay
28473536 GOA
Biological Process GO Annotation Evidence Reference Source
involved in negative regulation of transcription by RNA polymerase II IDA
IDA: Inferred from direct assay
8521822 GOA
involved in positive regulation of DNA-templated transcription IDA
IDA: Inferred from direct assay
8425218 GOA
involved in regulation of transcription by RNA polymerase II IDA
IDA: Inferred from direct assay
8425218 GOA
Cellular Component GO Annotation Evidence Reference Source
part of MLL1 complex IDA
IDA: Inferred from direct assay
15960975 GOA
part of Mad-Max complex IPI
IPI: Inferred from physical interaction
12553908 GOA
part of Myc-Max complex IPI
IPI: Inferred from physical interaction
12553908 GOA
part of RNA polymerase II transcription regulator complex IDA
IDA: Inferred from direct assay
8425219 GOA
located in chromatin IDA
IDA: Inferred from direct assay
12837246 GOA
located in nucleus IDA
IDA: Inferred from direct assay
10723141 GOA
part of protein-DNA complex IDA
IDA: Inferred from direct assay
9399572 GOA
part of protein-DNA complex IMP
IMP: Inferred from mutant phenotype
16171389 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

MAX Protein Structure

HLH

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

  • 0
  • 100
  • 160 a.a.
Protein Preferred Names Protein Names

protein max

class D basic helix-loop-helix protein 4

MAX Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
MAX P61244 UNC45A Homo sapiens Q9H3U1 31515488
Intra
MAX P61244 UNC45A Homo sapiens Q9H3U1 25416956
Intra
MAX P61244 VRK3 Homo sapiens Q8IV63
TAP
25609649
Intra
MAX P61244 MECP2 Homo sapiens P51608
TAP
25609649
Intra
MAX P61244 LIG3 Homo sapiens P49916
TAP
25609649
Intra
MAX P61244 FOXK2 Homo sapiens Q01167 25609649
Intra
MAX P61244 FOXK2 Homo sapiens Q01167
TAP
25609649
Intra
MAX P61244 MGA Homo sapiens Q8IWI9
TAP
27705803
Intra
MAX P61244 MGA Homo sapiens Q8IWI9 33961781
Intra
MAX P61244 MGA Homo sapiens Q8IWI9
TAP
25609649
Intra
MAX P61244 MGA Homo sapiens Q8IWI9
Y2H
21988832
Intra
MAX P61244 MGA Homo sapiens Q8IWI9
TAP
24981860
Intra
MAX P61244 MACROH2A1 Homo sapiens O75367
TAP
25609649
Intra
MAX P61244 TFAP2A Homo sapiens P05549
TAP
25609649
Intra
MAX P61244 EEF1D Homo sapiens P29692
TAP
25609649
Intra
MAX P61244 MYC Homo sapiens P01106 32296183
Intra
MAX P61244 MYC Homo sapiens P01106
PLA
24951594
Intra
MAX P61244 MYC Homo sapiens P01106 17418410
Intra
MAX P61244 MYC Homo sapiens P01106 20691906
Intra
MAX P61244 MYC Homo sapiens P01106 32296183
Intra
MAX P61244 MYC Homo sapiens P01106 33961781
Intra
MAX P61244 MYC Homo sapiens P01106 9184233
Intra
MAX P61244 MYC Homo sapiens P01106
TAP
27705803
Intra
MAX P61244 MYC Homo sapiens P01106
PLA
18620061
Intra
MAX P61244 MYC Homo sapiens P01106
Y2H
21988832
Intra
MAX P61244 MYC Homo sapiens P01106 20691906
Intra
MAX P61244 MYC Homo sapiens P01106
TAP
25609649
Intra
MAX P61244 MYC Homo sapiens P01106 12821782
Intra
MAX P61244 MYC Homo sapiens P01106 17157259
Intra
MAX P61244 L3MBTL2 Homo sapiens Q969R5 33961781
Intra
MAX P61244 L3MBTL2 Homo sapiens Q969R5
TAP
25609649
Intra
MAX P61244 L3MBTL2 Homo sapiens Q969R5
TAP
27705803
Intra
MAX P61244 PLEKHF2 Homo sapiens Q9H8W4 16189514
Intra
MAX P61244 PLEKHF2 Homo sapiens Q9H8W4 32296183
Intra
MAX P61244 PLEKHF2 Homo sapiens Q9H8W4 32296183
Intra
MAX P61244 PLEKHF2 Homo sapiens Q9H8W4 32296183
Intra
MAX P61244 E2F6 Homo sapiens O75461
TAP
27705803
Intra
MAX P61244 E2F6 Homo sapiens O75461 33961781
Intra
MAX P61244 E2F6 Homo sapiens O75461
TAP
25609649
Intra
MAX P61244 TFDP1 Homo sapiens Q14186
TAP
25609649
Intra
MAX P61244 TFDP1 Homo sapiens Q14186 33961781
Intra
MAX P61244 TFDP1 Homo sapiens Q14186
TAP
27705803
Intra
MAX P61244 MXI1 Homo sapiens P50539 25416956
Intra
MAX P61244 MXI1 Homo sapiens P50539 25416956
Intra
MAX P61244 MXI1 Homo sapiens P50539 25416956
Intra
MAX P61244 MXI1 Homo sapiens P50539
TAP
27705803
Intra
MAX P61244 MXI1 Homo sapiens P50539 33961781
Intra
MAX P61244 MXI1 Homo sapiens P50539 9184233
Intra
MAX P61244 MXI1 Homo sapiens P50539 16189514
Intra
MAX P61244 MXI1 Homo sapiens P50539
TAP
25609649
Intra
MAX P61244 MNT Homo sapiens Q99583 33961781
Intra
MAX P61244 MNT Homo sapiens Q99583
TAP
25609649
Intra
MAX P61244 MNT Homo sapiens Q99583
TAP
27705803
Intra
MAX P61244 MNT Homo sapiens Q99583 9184233
Intra
MAX P61244 MXD1 Homo sapiens Q05195
TAP
27705803
Intra
MAX P61244 MXD1 Homo sapiens Q05195 33961781
Intra
MAX P61244 XRCC1 Homo sapiens P18887
TAP
25609649
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant MAX Proteins

Cat. No. Product Name Accession Purity
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%

Related Diseases

Diseases Alias
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

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 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