ARAF - A-Raf proto-oncogene, serine/threonine kinase Gene

Also Known as PKS2; A-RAF; ARAF1; RAFA1

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 369

About ARAF

Cytogenetic location: Xp11.3 Genomic coordinates (GRCh38): X:47,561,205-47,571,908 (from NCBI)

This gene has 5 transcripts (splice variants), 191 orthologues, 23 paralogues and is associated with 79 phenotypes. Ubiquitous expression in bone marrow (RPKM 16.5), spleen (RPKM 14.0) and 25 other tissues.

Summary

This proto-oncogene belongs to the Raf subfamily of the Ser/Thr protein kinase family, and maybe involved in cell growth and development. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jan 2012]

ARAF Products (3)

mRNA Protein Name
NM_001256196.2 NP_001243125.1 serine/threonine-protein kinase A-Raf isoform 2
NM_001256197.2 NP_001243126.1 serine/threonine-protein kinase A-Raf isoform 3
NM_001654.5 NP_001645.1 serine/threonine-protein kinase A-Raf isoform 1
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
11909642 GOA
enables protein serine/threonine kinase activity IDA
IDA: Inferred from direct assay
19667065 GOA
Biological Process GO Annotation Evidence References Source
involved in negative regulation of apoptotic process IDA
IDA: Inferred from direct assay
19667065 GOA
involved in positive regulation of peptidyl-serine phosphorylation IDA
IDA: Inferred from direct assay
19667065 GOA
involved in regulation of TOR signaling IMP
IMP: Inferred from mutant phenotype
22609986 GOA
involved in regulation of proteasomal ubiquitin-dependent protein catabolic process IMP
IMP: Inferred from mutant phenotype
22609986 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

ARAF Protein Structure

RBD

RBD: Raf-like Ras-binding domain (20 - 91)

C1_1

C1_1: Phorbol esters/diacylglycerol binding domain (C1 domain) (99 - 145)

Pkinase_Tyr

Pkinase_Tyr: Protein tyrosine kinase (311 - 565)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 606 a.a.
Protein Preferred Names Protein Names

serine/threonine-protein kinase A-Raf

  • A-Raf proto-oncogene serine/threonine-protein kinase

ARAF Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
ARAF P10398 MAP2K2 Homo sapiens P36507 32707033
Intra
ARAF P10398 MAP2K2 Homo sapiens P36507
Y2H
11909642
Intra
ARAF P10398 MAP2K2 Homo sapiens P36507
Y2H
21988832
Intra
ARAF P10398 MAP2K2 Homo sapiens P36507 25852190
Intra
ARAF P10398 YWHAZ Homo sapiens P63104 31980649
Intra
ARAF P10398 YWHAZ Homo sapiens P63104 32707033
Intra
ARAF P10398 YWHAZ Homo sapiens P63104 35271311
Intra
ARAF P10398 YWHAZ Homo sapiens P63104 25852190
Intra
ARAF P10398 YWHAZ Homo sapiens P63104 20052757
Intra
ARAF P10398 HRAS Homo sapiens P01112
Y2H
12620389
Intra
ARAF P10398 COPS3 Homo sapiens Q9UNS2
Y2H
12620389
Intra
ARAF P10398 HSP90AB1 Homo sapiens P08238 22939624
Intra
ARAF P10398 HSP90AB1 Homo sapiens P08238 31980649
Intra
ARAF P10398 HSP90AB1 Homo sapiens P08238 25036637
Intra
ARAF P10398 HSP90AB1 Homo sapiens P08238 32707033
Intra
ARAF P10398 TIMM50 Homo sapiens Q3ZCQ8 25852190
Intra
ARAF P10398 TIMM50 Homo sapiens Q3ZCQ8
Y2H
12620389
Intra
ARAF P10398 YWHAE Homo sapiens P62258 25852190
Intra
ARAF P10398 YWHAE Homo sapiens P62258 32707033
Intra
ARAF P10398 SFN Homo sapiens P31947 31980649
Intra
ARAF P10398 SFN Homo sapiens P31947 25852190
Intra
ARAF P10398 RRAS2 Homo sapiens P62070
Y2H
12620389
Intra
ARAF P10398 RABGGTB Homo sapiens P53611
Y2H
12620389
Intra
ARAF P10398 NELFCD Homo sapiens Q8IXH7
Y2H
12620389
Intra
ARAF P10398 NELFCD Homo sapiens Q8IXH7
Y2H
21988832
Intra
ARAF P10398 PRPF6 Homo sapiens O94906
Y2H
12620389
Intra
ARAF P10398 EFEMP1 Homo sapiens Q12805
Y2H
12620389
Intra
ARAF P10398 CPS1 Homo sapiens P31327
Y2H
12620389
Intra
ARAF P10398 ASS1 Homo sapiens P00966
Y2H
12620389
Intra
ARAF P10398 PBK Homo sapiens Q96KB5
Y2H
12620389
Intra
ARAF P10398 NUDT14 Homo sapiens O95848
Y2H
12620389
Intra
ARAF P10398 TIMM44 Homo sapiens O43615
Y2H
12620389
Intra
ARAF P10398 IRF7 Homo sapiens Q92985 21903422
Cross: Cross-species interaction Intra: Intraspecies interaction

ARAF Antibodies

Cat. No. Product Name Application Reactivity
HY-P80018 A-RAF Antibody (YA614) WB, ICC/IF, IHC-P, FC Human, Mouse
HY-P82928 A-RAF Antibody (YA2673) WB, IHC-P, ICC/IF, FC Human
HY-P82928A A-RAF Antibody (YA2673)(PBS only) WB, IHC-P Human

Related Diseases

Diseases Alias
Pallister-Killian Syndrome
  • PKS

  • Tetrasomy 12p, Mosaic

  • Isochromosome 12p Syndrome

  • Pallister-Killian Mosaic Syndrome

  • Chromosome 12, Isochromosome 12p Syndrome

  • Killian Teschler-Nicola Syndrome

  • Killian Syndrome

  • Pallister Killian Syndrome

  • Pallister Mosaic Syndrome

  • Teschler-Nicola Killian Syndrome

  • Teschler-Nicola/Killian Syndrome

  • Tetrasomy 12p

  • Isochromosome 12p Mosaicism

Skin Melanoma
  • Cutaneous Melanoma

  • Malignant Ear Melanoma

  • Malignant Lip Melanoma

  • Malignant Lower Limb Melanoma

  • Malignant Melanoma Of Ear And/Or External Auricular Canal

  • Malignant Melanoma Of Skin Of Lower Limb

  • Malignant Melanoma Of Skin Of Trunk Except Scrotum

  • Malignant Melanoma Of Skin Of Upper Limb

  • Malignant Neck Melanoma

  • Malignant Scalp Melanoma

  • Malignant Trunk Melanoma

  • Malignant Upper Limb Melanoma

  • Melanoma, Cutaneous Malignant

  • Melanoma

  • Malignant Melanoma Of Skin

  • Melanoma Nos

  • Malignant Mole, Meaning Melanoma Of Unspecified Site

  • Melanoma Of Unspecified Site

  • Cutaneous Malignant Melanoma

  • Mm - [Malignant Melanoma]

Mycobacterium Marinum
  • Mycobacterium Marinum Infection

  • Fish Tank Granuloma

  • M. Marinum

Renal Cell Carcinoma, Papillary, 1
  • Papillary Renal Cell Carcinoma

  • Hereditary Papillary Renal Cell Carcinoma

  • Papillary Renal Cell Carcinoma, Sporadic

  • Papillary Renal Cell Adenocarcinoma

  • RCCP

  • RCCP1

  • Renal Cell Carcinoma, Papillary

  • Renal Cell Carcinoma, Papillary, 1, Familial And Somatic

  • Chromophil Carcinoma Of Kidney

  • Papillary Kidney Carcinoma

  • Sporadic Papillary Renal Cell Carcinoma

  • Chromophil Renal Cell Carcinoma

  • Papillary Renal Carcinoma, Malignant -

  • Papillary Renal Cell Carcinoma, Bilateral -

  • Papillary Renal Cell Carcinoma, Familial -

  • Papillary Renal Cell Carcinoma, Multiple -

  • Papillary Renal Cell Carcinoma, Sporadic -

  • Renal Adenocarcinoma

  • Chromophil Rcc

  • Hprcc

  • Renal Cell Carcinoma Papillary

  • Chromophilic Renal Cell Carcinoma

  • Prcc

  • Carcinoma, Renal Cell, Papillary, Type 1

  • Type 1 Papillary Renal Cell Carcinoma

  • Renal Cell Carcinoma

  • Hereditary Papillary Renal Carcinoma

Lymphatic Malformation 12
  • Central Conducting Lymphatic Anomaly

  • LMPHM12

  • Ccla

  • Lymphatic Malformation-7

  • Doid:0081030

Histiocytosis
  • Chronic Histiocytosis X

  • Hand Schuller Christian Disease

  • Hand-Schüller-Christian Disease

  • Histiocytic Syndrome

  • Histiocytosis, Langerhans-Cell

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

Lung Cancer Susceptibility 3
  • Lung Adenocarcinoma

  • Adenocarcinoma Of Lung

  • LNCR3

  • Adenocarcinoma Of Lung, Susceptibility To

  • Bronchogenic Lung Adenocarcinoma

  • Nonsmall Cell Adenocarcinoma

  • Adenocarcinoma Lung

  • Lung Adenocarcinomas

  • Non-Small Cell Adenocarcinoma

Sarcoma
  • Connective And Soft Tissue Neoplasm

  • Tumor Of Soft Tissue And Skeleton

  • Sarcomas

  • Sarcoma - Category

Non-Langerhans-Cell Histiocytosis
  • Histiocytosis, Non-Langerhans-Cell

  • Non-Langerhans Cell Histiocytosis

Acneiform Dermatitis
  • Dermatitis Acneiform

Colorectal Cancer
  • Colon Cancer

  • Colorectal Carcinoma

  • Colon Carcinoma

  • Colorectal Cancer, Susceptibility To

  • Carcinoma Of Colon

  • CRC

  • Colorectal Cancer With Chromosomal Instability, Somatic

  • Colon Cancer, Somatic

  • Colon Cancer, Susceptibility To

  • Colonic Neoplasms

  • Colorectal Neoplasms

  • Colorectal Cancer, Somatic

  • Colon Cancer, Advanced, Somatic

  • Colonic Carcinoma

  • Colorectal Carcinomas

  • Colon Cancers

  • Colorectal Cancers

  • Cancer, Colorectal, Somatic

  • Cancer, Colon

  • Cancer, Colorectal, Susceptibility To

  • Colorectal Neoplasm

  • Colonic Neoplasm

  • Malignant Tumor Of Colon

Hawkinsinuria
  • 4-Alpha-Hydroxyphenylpyruvate Hydroxylase Deficiency

  • 4-Hppd Deficiency

  • 4-Hydroxyphenylpyruvic Acid Dioxygenase Deficiency

  • HWKS

  • HAWK

Melanoma
  • Malignant Melanoma

  • Cutaneous Melanoma

  • Naevocarcinoma

  • Malignant Melanomas

Skin Squamous Cell Carcinoma
  • Squamous Cell Carcinoma Of Skin

  • Epidermoid Skin Carcinoma

  • Squamous Cell Carcinoma Of The Skin

  • Squamous Cell Epithelioma Of Skin

  • Cutaneous Squamous Cell Carcinoma

  • Scc - [Squamous Cell Carcinoma] Of Skin

Rasopathy
  • Ras/Mitogen-Activated Protein Kinase Syndrome

Langerhans Cell Histiocytosis
  • Histiocytosis X

  • Lch

  • Langerhans Cell Granulomatosis

  • Langerhans-Cell Histiocytosis

  • Letterer-Siwe Disease

  • Hashimoto-Pritzger Disease

  • Histiocytosis, Langerhans-Cell

  • Langerhan'S Cell Histiocytosis

  • Letterer-Siwe Disease Involving Intra-Abdominal Lymph Nodes

  • Letterer-Siwe Disease Involving Intrapelvic Lymph Nodes

  • Letterer-Siwe Disease Involving Intrathoracic Lymph Nodes

  • Letterer-Siwe Disease Involving Lymph Nodes Of Axilla And Upper Limb

  • Letterer-Siwe Disease Involving Lymph Nodes Of Head, Face And Neck

  • Letterer-Siwe Disease Involving Lymph Nodes Of Head, Face, And Neck

  • Letterer-Siwe Disease Involving Lymph Nodes Of Inguinal Region And Lower Limb

  • Letterer-Siwe Disease Involving Lymph Nodes Of Multiple Sites

  • Letterer-Siwe Disease Involving Spleen

  • Letterer-Siwe Disease Of Intra-Abdominal Lymph Nodes

  • Letterer-Siwe Disease Of Intrapelvic Lymph Nodes

  • Letterer-Siwe Disease Of Intrathoracic Lymph Nodes

  • Letterer-Siwe Disease Of Lymph Nodes Of Axilla And Upper Limb

  • Letterer-Siwe Disease Of Lymph Nodes Of Axilla And/Or Upper Limb

  • Letterer-Siwe Disease Of Lymph Nodes Of Head, Face And Neck

  • Letterer-Siwe Disease Of Lymph Nodes Of Head, Face And/Or Neck

  • Letterer-Siwe Disease Of Lymph Nodes Of Inguinal Region Amd/Or Lower Limb

  • Letterer-Siwe Disease Of Lymph Nodes Of Inguinal Region And Lower Limb

  • Letterer-Siwe Disease Of Lymph Nodes Of Inguinal Region And/Or Lower Limb

  • Letterer-Siwe Disease Of Lymph Nodes Of Multiple Sites

  • Letterer-Siwe Disease Of Spleen

  • Familial Letterer-Siwe Disease

  • Langerhans-Cell Histiocytosis Nos

Cardiofaciocutaneous Syndrome 1
  • Cardiofaciocutaneous Syndrome

  • Cfc Syndrome

  • Cardio-Facio-Cutaneous Syndrome

  • CFC1

  • Cfcs

  • Cardio-Facial-Cutaneous Syndrome

  • Congenital Heart Defects Characteristic Facial Appearance Ectodermal Abnormalities And Growth Failure

  • Cardiofaciocutaneous Syndrome, Type 1

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

Noonan Syndrome With Multiple Lentigines
  • Leopard Syndrome

  • Multiple Lentigines Syndrome

  • Moynahan Syndrome

  • Cardiomyopathic Lentiginosis

  • Progressive Cardiomyopathic Lentiginosis

  • Cardio-Cutaneous Syndrome

  • Lentiginosis Profusa

  • Capute-Rimoin-Konigsmark-Esterly-Richardson Syndrome

  • Generalized Lentiginosis

  • Gorlin Syndrome Ii

  • Lentiginosis Profusa Syndrome

  • Lentigines, Electrocardiographic Conduction Abnormalities, Ocular Hypertelorism, Pulmonic Stenosis, Abnormal Genitalia, Retardation Of Growth, Deafnes

  • Diffuse Lentiginosis

  • Nsml

  • Familial Multiple Lentigines Syndrome

  • Alopecia-Epilepsy-Intellectual Disability Syndrome, Moynahan Type

  • Progressive Cardiomyopathic Lentiginosis Syndrome

  • Alopecia Epilepsy Oligophrenia Syndrome Of Moynahan

Ovarian Cancer
  • Ovarian Carcinoma

  • Ovarian Neoplasm

  • Malignant Tumour Of Ovary

  • Cancer Of The Ovary

  • Epithelial Ovarian Cancer

  • Neoplasm Of Ovary

  • Ovarian Neoplasms

  • Ovarian Cancers

  • Malignant Neoplasm Of Ovary

  • Primary Malignant Neoplasm Of Ovary

  • Ovarian Cancer, Somatic

  • Malignant Ovarian Tumor

  • Ovary Neoplasm

  • Primary Ovarian Cancer

  • Tumor Of The Ovary

  • Malignant Neoplasm Of The Ovary

  • Malignant Tumor Of The Ovary

  • Ovarian Malignant Tumor

  • OC

  • Ovarian Carcinomas

  • Cancer, Ovarian

  • Cancer Of Ovary

  • Ovary Cancer

  • Ca Ovary

Melanoma, Cutaneous Malignant 1
  • Familial Melanoma

  • Melanoma, Cutaneous Malignant, Susceptibility To, 1

  • Melanoma, Malignant

  • CMM1

  • Melanoma, Cutaneous Malignant

  • Cmm

  • Familial Atypical Mole-Malignant Melanoma Syndrome

  • Fammm

  • Melanoma, Familial

  • Mlm

  • Dysplastic Nevus Syndrome, Hereditary

  • Dns

  • B-K Mole Syndrome

  • Melanoma, Cutaneous Malignant, 1

  • Malignant Melanoma, Cutaneous

  • Melanoma, Cutaneous, Malignant, Susceptibility To, Type 1

  • Dysplastic Nevus Syndrome

  • Cutaneous Melanoma

  • Familial Atypical Mole Melanoma Syndrome

  • Hereditary Melanoma

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

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 ARAF VGNC VGNC:69997
Canis familiaris ARAF VGNC VGNC:38024
Rattus norvegicus ARAF RGD RGD:2148
Bos taurus ARAF VGNC VGNC:26054
Mus musculus ARAF MGD MGI:88065
Felis catus ARAF VGNC VGNC:67995
Others ARAF NCBI