Protein BRAF

URN urn:agi-llid:673
Total Entities 0
Connectivity 1479
Name BRAF
Description Braf transforming gene
Notes 13 germline BRAF variants, 4 of which were silent mutations in coding regions & 9 nucleotide substitutions in introns, were found in melanoma patients and melanoma family, but none appeared statistically likely to be a melanoma susceptibility gene. 13 germline BRAF variants, 4 of which were silent mutations in coding regions & 9 nucleotide substitutions in introns, were found in melanoma patients and melanoma family, but none appeared statistically likely to be a melanoma susceptibility gene. 3 cell lines derived from human choroidal melanoma express B-Raf containing the V599E mutation and showed a 10-fold increase in endogenous B-RafV599E kinase activity and a constitutive activation of the MEK/ERK pathway that is independent of Ras. AKAP9-BRAF fusion was preferentially found in radiation-induced papillary carcinomas developing after a short latency, whereas BRAF point mutations were absent in this group. Although BRAF and NRAS mutations are likely to be important for the initiation and maintenance of some melanomas, other factors might be more significant for proliferation and prognosis in subgroups of aggressive melanoma. Anaplastic thyroid carcinomas which are derived from papillary carcinomas are due to BRAF and p53 mutations. B-Raf and ERK are activated by cyclic AMP after calcium restriction. B-Raf has a role in extracellular signal-regulated kinase (ERK) signaling in T cells and prevents antigen-presenting cell-induced anergy. B-Raf kinase activity regulation by tuberin and Rheb is mammalian target of rapamycin (mTOR)-independent. B-raf is involved in adhesion-independent ERK1/2 signaling in melanocytes. B-raf mutations surrounding Thr439 found in human cancers are unlikely to contribute to increased oncogenic properties of B-raf. BRAF has a role in in squamous cell carcinoma of the head and neck through uncommon mutations. BRAF is occasionally mutated in NHL, and BRAF mutation may contribute to tumor development in some NHLs. BRAF mutation may be acquired during development of metastasis but is not a significant factor for primary melanoma development and disease outcome. BRAF mutation occurs later in thyroid tumor progression and is restricted mainly to papillary thyroid carcinoma and anaplastic thyroid carcinoma. BRAF mutations are associated with conjunctival neoplasms. BRAF mutations are associated with proximal colon tumors with mismatch repair deficiency and MLH1 hypermethylation. BRAF mutations are frequently present in sporadic colorectal cancer with methylated hMLH1. BRAF mutations are rather rare in solitary cold adenomas and adenomatous nodules and do not explain the molecular etiology of ras mutation-negative cold thyroid nodules. BRAF mutations are restricted to papillary carcinomas and poorly differentiated and anaplastic carcinomas arising from papillary carcinomas. BRAF mutations in colorectal cancers occur only in tumours that do not carry mutations in a RAS gene known as KRAS, and BRAF mutation is linked to the proficiency of these tumours in repairing mismatched bases in DNA. BRAF mutations proved to be absent in tumors from hereditary nonpolyposis colorectal cancer syndrome (HNPCC) families with germline mutations in the MMR genes MLH1 and MSH2. BRAF mutations were seen in stomach neoplasms. BRAF mutations, which are present in a variety of other human cancers, do not seem to be involved in gastric cancer development. BRAF(V599E) is more common genetic alteration found to date in adult sporadic papillary thyroid carcinomas (PTCs). It is unique for this thyroid cancer histotype, and it might drive the development of PTCs of classic papillary subtype. BRAF(V599E) mutation is seven times higher in lesions with structural changes and 13 times higher in growing lesions as compared with lesions without changes. Both BRAF and FBXW7 mutations functionally activate kinase effectors important in pancreatic cancer and extend potential options for therapeutic targeting of kinases in treatment of phenotypically distinct pancreatic adenocarcinoma subsets. Data provide evidence that B-Raf is a positive regulator of T cell receptor-mediated sustained ERK activation, which is required for NFAT activation and the full production of IL-2. Data show that the the RET receptor (RET/PTC), Ras and BRAF function along a linear oncogenic signaling cascade in which RET/PTC induces RAS-dependent BRAF activation and RAS- and BRAF-dependent ERK activation. Data suggest that BRAF T1796A activating mutation is not common in primary uveal melanoma. Data suggest that Rit is involved in a novel pathway of neuronal development and regeneration by coupling specific trophic factor signals to sustained activation of the B-Raf/ERK and p38 MAP kinase cascades. Data suggest that SPRY2, an inhibitor of ERK signaling, may be bypassed in melanoma cells either by down-regulation of its expression in WT BRAF cells, or by the presence of the BRAF mutation. High frequency of BRAF mutations in nevi. High prevalence of BRAF mutations in thyroid cancer is genetic evidence for constitutive activation of the RET/PTC-RAS-BRAF signaling pathway in papillary thyroid carcinoma. In patients with papillary thyroid cancer, BRAF mutation is associated with poorer clinicopathological outcomes and independently predicts recurrence. In this study, this BRAF mutation was demonstrated in some conjunctival melanoma tissue samples, suggesting that some conjunctival melanomas may share biological features in common with cutaneous melanoma. KSHV-infected cell lines expressed higher levels of B-Raf and VEGF-A; B-Raf-induced VEGF-A expression was demonstrated to be sufficient to enhance tubule formation in endothelial cells. MEK1 interacts with B-Raf. Missense mutation is marker of colonic but not gastric cancer. Mucinous ovarian cancers without a KRAS mutation have not sustained alternative activation of this signaling pathway through mutation of the BRAF oncogene. Mutations are not detectable in plasma cell leukemia and multiple myeloma. Mutations in BRAF gene is associated with malignant melanomas. Mutations in the BRAF protooncogene (V599E)may be an alternative pathway of tumorigenesis of familial colorectal cancer. Mutations of BRAF are associated with extensive hMLH1 promoter methylation in sporadic colorectal carcinomas. Mutations of BRAF or KRAS oncogenes are early events in the serrated polyp neoplasia pathway. CpG island methylation plays a role in serrated polyp progression to colorectal carcinoma. Mutations of the BRAF gene are partly involved in the malignant transformation of the endometrium. Mutations were found in exon 15 in colorectal adenocarcinoma. Mutations within the BRAF gene are useful markers for the differential diagnosis between Spitz nevus and malignant melanoma. NRAS and BRAF mutations arise early during melanoma pathogenesis and are preserved throughout tumor progression. New enriched PCR-RFLP assay for detecting mutations of BRAF codon 599 mutation in pleural mesotheliomas. None of the cases of gastric cancer showed braf mutations. Our data indicate that BRAF gene mutations are rare to absent events in uveal melanoma of humans. Our findings of a high frequency of BRAF mutations at codon 599 in benign melanocytic lesions of the skin indicate that this mutation is not sufficient by itself for malignant transformation. RAS or BRAF mutations are detected in about 32% of all Barrett's adenocarcinomas; the disruption of the Raf/MEK/ERK (MAPK) kinase pathway is a frequent but also early event in the development of Barrett's adenocarcinoma. REVIEW: our understanding of B-RAF as an oncogene and of its role in cancer. Radiation-induced tumors have a low prevalence of BRAF point mutations and high prevalence of RET/PTC rearrangements. Role of BRAF mutation in facilitating metastasis and progression of papillary thyroid cancer in lymph nodes. Single-cell clones with efficient knockdown of (V 600 E)B-RAF could be propagated in the presence of basic fibroblast growth factor but underwent apoptosis or senescence-like growth arrest upon withdrawal of this growth factor. The BRAF(V599E) mutation appears to be an alternative event to RET/PTC rearrangement rather than to RAS mutations, which are rare in PTC. BRAF(V599E) may represent an alternative pathway to oncogenic MAPK activation in PTCs without RET/PTC activation. The V599E BRAF mutation appears to be a somatic mutation associated with melanoma development and/or progression in a proportion of affected individuals. The data of this study suggest that activating mutations of B-RAF are not a frequent event in gliomas; nevertheless, when present they are associated with high-grade malignant lesions. The estimated proportion of attributable risk of melanoma due to variants in BRAF is 1.6%, but the burden of disease associated with this variant is greater than that associated with the major melanoma locus (CDKN2A) which has a risk of 0.2%. The finding of tandem mutations in thin melanomas makes it more likely that they arise as a simultaneous rather than sequential event. The increasing frequency of BRAF mutations as a function of age could help account for the well documented but poorly understood observation that age is a relevant prognostic indicator for patients with papillary thyroid carcinoma. The lack or low prevalence of BRAF mutation in other thyroid neoplasms is consistent with the notion that other previously defined genetic alterations on the same signaling pathway are sufficient to cause tumorigenesis in most thyroid neoplasms. The results showed that conjunctival nevi, similar to skin nevi, have a high frequency of oncogenic BRAF mutations. These data suggest that MITF is an anti-proliferation factor that is down-regulated by B-RAF signaling and that this is a crucial event for the progression of melanomas that harbor oncogenic B-RAF. These results suggest that BRAF mutations do not have a role in tumorigenesis of neuroendocrine gastroenteropancreatic tumors. These results suggest that the BRAF mutation is unlikely to be involved in gastric carcinogenesis. These studies identify isoprenylcysteine carboxyl methyltransferase as a potential target for reducing the growth of K-Ras- and B-Raf-induced malignancies. Uceal melanomas arise independent of oncogenic BRAF and NRAS mutations. We found mutations in p53, K-ras, and BRAF genes in 35%, 30%, and 4% of tumors, respectively, and observed a minimal or no co-presence of these gene alterations. A novel Ras-independent ERK1/2 activation system in which p110gamma/Raf-1/MEK1/2 and PKA/B-Raf/MEK1/2 cooperate to activate ERK1/2. Activating BRAF mutations may be an important event in the development of papillary thyroid cancer. Activation of this gene may be one of the early events in the pathogenesis of some melanomas. Autoinhibition was negatively regulated by acidic substitutions at phosphorylation sites within the activation loop. CAMP activates ERK and increases proliferation of autosomal dominant polycystic kindey epithelial cells through the sequential phosphorylation of PKA, B-Raf and MAPK in a pathway separate from the classical receptor tyrosine kinase cascade. Copy number gain may represent another mechanism of BRAF activation in thyroid tumors. Determination of mutation specific gene expression profiles in papillary thyroid carcinoma. Gene is mutated in skin melanoma, but not in uveal melanomas. In contrast to cutaneous melanoma, BRAF does not appear to be involved in the pathogenesis of uveal melanoma. Mucosal melanomas of the head and neck do not frequently harbor an activating mutation of BRAF. Mutated in childhood acute lymphoblastic leukemia. Mutated in papillary thyroid cancer. Mutation of BRAF gene could be a potentially useful marker of prognosis of patients with advanced thyroid cancers. Mutations in the BRAF gene and to some extent in the N-ras gene represent early somatic events that occur in melanocytic nevi. Ovarian serous cystadenomas do not contain mutations in either BRAF or KRAS genes. Possible cooperation between BRAF activation and PTEN loss in melanoma development. Results demonstrate that the mutational status of BRAF and KRAS is distinctly different among histologic types of ovarian serous carcinoma, occurring most frequently in invasive micropapillary serous carcinomas and its precursors, serous borderline tumors. Somatic missense mutations in 66% of malignant melanomas and at lower frequency in a wide range of human cancers. Sustained BRAF(V600E) expression in human melanocytes induces cell cycle arrest, which is accompanied by the induction of both p16(INK4a) and senescence-associated acidic beta-galactosidase (SA-beta-Gal) activity, a commonly used senescence marker. We found 19 cases (38%) to harbor somatic B-raf exon 15 mutations.

GO Molecular Function MAP kinase kinase kinase activity
receptor signaling protein activity
transferase activity
transferase activity, transferring phosphorus-containing groups
kinase activity
protein kinase activity
protein serine-threonine kinase activity
mitogen-activated protein kinase kinase binding
protein heterodimerization activity
nucleotide binding
ATP binding
metal ion binding
calcium ion binding

GO Cellular Component membrane
cell body
plasma membrane
cytoplasm
cytosol
mitochondrion
nucleus
neuron projection

GO Biological Process myeloid progenitor cell differentiation
alpha-beta T cell differentiation
CD4-positive, alpha-beta T cell differentiation
positive T cell selection
MAPK cascade
activation of MAPKK activity
positive regulation of ERK1 and ERK2 cascade
visual learning
organ morphogenesis
somatic stem cell maintenance
cell differentiation
positive regulation of substrate adhesion-dependent cell spreading
positive regulation of stress fiber assembly
signal transduction
intracellular signal transduction
small GTPase mediated signal transduction
neurotrophin TRK receptor signaling pathway
fibroblast growth factor receptor signaling pathway
synaptic transmission
negative regulation of synaptic vesicle exocytosis
long-term synaptic potentiation
negative regulation of fibroblast migration
negative regulation of apoptotic process
negative regulation of endothelial cell apoptotic process
negative regulation of neuron apoptotic process
regulation of cell proliferation
response to cAMP
response to peptide hormone
cellular response to calcium ion
response to epidermal growth factor
positive regulation of peptidyl-serine phosphorylation
positive regulation of gene expression
protein phosphorylation
phosphorylation
protein heterooligomerization

Pathway Metastatic Colorectal Cancer Overview
Mechanism of Cetuximab Resistance in Colorectal Cancer
Multiple Myeloma Overview
Proteins Involved in Pathogenesis of Breast Cancer Related to ERBB2/VEGFR/Akt Signaling Pathway
Proteins Involved in Pathogenesis of Breast Cancer Related to IGF1R/Akt Signaling Pathway
Proteins Involved in Pathogenesis of Breast Cancer Related to ESR1 Signaling Pathway
Congenital Hypothyroidism Due to Thyroid-Stimulating Hormone Resistance
Graves Ophthalmopathy
Thyroid Dysfunction in Graves Disease
Primary Overt Hypothyroidism Overview
Clear Cell Ovarian Carcinoma
Proteins Involved in Pathogenesis of Clear Cell Ovarian Carcinoma
Mucinous Ovarian Carcinoma
High-grade Serous Ovarian Carcinoma
Proteins Involved in Pathogenesis of Mucinous Ovarian Carcinoma
Proteins Involved in Pathogenesis of High-grade Serous Ovarian Carcinoma
Endometrioid Ovarian Carcinoma
Proteins Involved in Pathogenesis of Endometrioid Ovarian Carcinoma
Ovarian Cancer Overview
Low-grade Serous Ovarian Carcinoma
Proteins Involved in Pathogenesis of Low-grade Serous Ovarian Carcinoma
Type I Endometrial Cancer (Endometrioid Endometrial Cancer)
Type II Endometrial Cancer (Clear-cell Endometrial Cancer and Papillary Serous Endometrial Cancer)
Endometrial Cancer Overview
Deregulation of Cell Cycle in Melanoma
Block of Apoptosis in Melanoma
Proteins Involved in Pathogenesis of Melanoma
Melanoma Overview
Cancer Overview
Contraction due Vasospasm
Smooth Muscle Cell Dysfunction in Pulmonary Arterial Hypertension
Secondary Glioblastoma
Proteins Involved in Pathogenesis of Glioma
Proteins Involved in Pathogenesis of Astrocytoma
Astrocytoma
ALK-Associated Neuroblastoma
Proteins Involved in Pathogenesis of Neuroblastoma
Neuroblastoma Overview
Growth Factor Signaling in Pancreatic Cancer
TGFBR Signaling in Pancreatic Cancer
Pancreatic Ductal Carcinoma
Proteins Involved in Pathogenesis of Pancreatic Cancer
Pancreatic Neuroendocrine Tumors
FSH Action in Polycystic Ovary Syndrome
Impaired Steroidogenesis in Polycystic Ovary Syndrome
Block of Ovulation in Polycystic Ovary Syndrome
Polycystic Ovary Syndrome Overview
Growth Factor Signaling in Hepatocellular Carcinoma
Proteins Involved in Pathogenesis of Hepatocellular Carcinoma
Hepatocellular Carcinoma Overview
Induction of Apoptosis and Immediate Early Gene Activation in Hippocampal Neurons Following Seizures
Myocardial Remodeling in Myocardial Ischemia
WHIM Syndrom Overview
ADRA2C/ADRB2 -> vasoconstriction
ADRB1 -> prostaglandin generation
ADRA2C/ADRB2 -> synaptic endocytosis
GABA(B)R -> postsynaptic inhibition
NMDA receptors -> Ca2+/CREB activation/PGE2 synthesis
P2RY11/13/14 -> IL8/10 production
HRH2/4 -> IL6/10 production
PTGIR -> IL6 production
HTR5 -> TNF production
HTR1 -> IL6 production
HTR7 -> IL6 production
HTR4/6/7 -> cation channels
CNR1/2 -> IL1B/2/4/6/10 production
Nociception-related DRD1/5 expression targets
EDNRA/B -> vascular motility
CHRM1 -> IL2 production
CHRNA7 -> NOS1 production
NPY1R -> CRH/POMC production
Regulation of potassium flux
Summarized nociception-related expression targets
Summarized vascular motility pathway
OPRK -> pain perception
FibronectinR -> AP-1/ELK-SRF/SREBF signaling
B-cell receptor -> AP-1 signaling
CholinergicRm -> CREB/ELK-SRF signaling
CannabinoidR -> AP-1/EGR signaling
NeuropeptideYR -> ATF/CREB signaling
SerotoninR1 -> FOS signaling
PTAFR -> AP-1/ATF1/CREB/ERK-SRF signaling
CholecystokininR -> ELK-SRF signaling
GRM1/5 -> CREB signaling
IL8R -> CREB/EGR signaling
EDG3/5 -> AP-1/ELK-SRF signaling
EndothelinRb -> AP-1/CREB/ELK-SRF signaling
ProstaglandinIR -> ATF1/ELK-SRF/CREB signaling
AdrenergicRb -> CREB signaling
TachykininR -> ELK-SRF signaling
VIPR -> CREB/CEBP signaling
AdrenergicRb -> STAT3 signaling
AngiotensinR -> CREB/ELK-SRF/TP53 signaling
DopamineR1 -> CREB/ELK-SRF signaling
SerotoninR4/6/7 -> NR3C signaling
FSHR -> CREB/ELK-SRF/GATA4 signaling
VasopressinR2 -> CREB/ELK-SRF/AP-1/EGR signaling
GlucagonR -> CREB/ELK-SRF/SP1 signaling
ThromboxaneR -> CREB signaling
CholinergicRn -> CREB signaling
Cyclosporine-Induced Nephrotoxicity
Clozapine-Induced Granulocytopenia
Fibronectin Expression Targets
Gamma Globulins Expression Targets
NPY Expression Targets
Dronabinol/Anandamide Expression Targets
Acetylcholine Expression Targets
Thromboxane A2 Expression Targets
Glutamate/Gq Expression Targets
CCK Expression Targets
GAST Expression Targets
S1P Expression Targets
TAC1 Expression Targets
PGE1 Expression Targets
Epinephrine/Gs Expression Targets
Noradrenaline/Gs Expression Targets
VIP Expression Targets
Dopamine/Gs Expression Targets
GCG Expression Targets
FSHR Expression Targets
AVP/Gs -> CREB/ELK-SRF/AP-1/EGR Expression Targets
Serotonin/Gs Expression Targets
CXCL1 Expression Targets
CXCL2 Expression Targets
CXCL3 Expression Targets
CXCL5 Expression Targets
CXCL6 Expression Targets
EDN1 Expression Targets
EDN3 Expression Targets
ADCYAP1 Expression Targets
AGT/TP53 Expression Targets
AGT/ELK-SRF Expression Targets
AGT/CREB Expression Targets
PAF/Gq -> AP-1/ATF1/CREB/ERK-SRF Expression Targets
non-small cell lung cancer pathway
colorectal cancer pathway
the extracellular signal-regulated Raf/Mek/Erk signaling pathway
the extracellular signal-regulated Raf-Mek-Erk signaling pathway
colorectal cancer pathway

Group Raf
Oncogenes
myeloid progenitor cell differentiation
alpha-beta T cell differentiation
CD4-positive, alpha-beta T cell differentiation
positive T cell selection
MAPK cascade
MAP kinase kinase kinase activity
activation of MAPKK activity
positive regulation of ERK1 and ERK2 cascade
visual learning
organ morphogenesis
somatic stem cell maintenance
cell differentiation
positive regulation of substrate adhesion-dependent cell spreading
positive regulation of stress fiber assembly
signal transduction
intracellular signal transduction
small GTPase mediated signal transduction
receptor signaling protein activity
neurotrophin TRK receptor signaling pathway
fibroblast growth factor receptor signaling pathway
synaptic transmission
negative regulation of synaptic vesicle exocytosis
long-term synaptic potentiation
negative regulation of fibroblast migration
negative regulation of apoptotic process
negative regulation of endothelial cell apoptotic process
negative regulation of neuron apoptotic process
regulation of cell proliferation
response to cAMP
response to peptide hormone
cellular response to calcium ion
response to epidermal growth factor
positive regulation of peptidyl-serine phosphorylation
positive regulation of gene expression
transferase activity
transferase activity, transferring phosphorus-containing groups
kinase activity
protein kinase activity
protein serine-threonine kinase activity
protein phosphorylation
phosphorylation
protein heterooligomerization
mitogen-activated protein kinase kinase binding
protein heterodimerization activity
nucleotide binding
ATP binding
metal ion binding
calcium ion binding
membrane
cell body
plasma membrane
cytoplasm
cytosol
mitochondrion
nucleus
neuron projection
Genes with Mutations Associated with Multiple Myeloma
Genes with Mutations Associated with Hashimoto's Thyroiditis
Genes with Mutations Associated with Ovarian Cancer
Genes with Mutations Associated with Endometrial Cancer
Genes with Mutations Associated with Melanoma
Genes with Mutations Associated with Hepatocellular Carcinoma
Disease Genes Identified in Syndromic Epilepsy
Genes with Mutations, Deletions, and Amplifications Associated with Astrocytoma
Genes with Mutations, Deletions, and Amplifications Associated with Glioma
Genes with Mutations Associated with Pancreatic Cancer
Secreted proteins
Biofluids assayable substances

LocusLink ID 673
109880
114486
58892
12187
52385
97330
330290
319686
232705

Cell Localization Cytoplasm
Nucleus
Cell membrane

GO ID 0005524
0005509
0004672
0004674
0005057
0000186
0071277
0008543
0043066
0048011
0009887
0070374
0010628
0033138
0006468
0070849
0007264
0007268
0005829
0005634
0005886
0004709
0016301
0046872
0031434
0000166
0046982
0016740
0016772
0043367
0000165
0046632
0030154
0035556
0060291
0002318
2000352
0010764
0043524
2000301
0016310
0043368
0051496
1900026
0051291
0042127
0051591
0043434
0007165
0035019
0008542
0044297
0005737
0016020
0005739
0043005
0006916
0023034
0005625
0019717
0005624
0008270
0003677
0007242
0006355
0005622
0004713
0050875
0019992
0005515

Alias NS7
BRAF1
RAFB1
B-RAF1
serine/threonine-protein kinase B-raf
94 kDa B-raf protein
proto-oncogene B-Raf
v-raf murine sarcoma viral oncogene homolog B1
murine sarcoma viral (v-raf) oncogene homolog B1
B-Raf proto-oncogene serine/threonine-protein kinase (p94)
B-raf
Braf2
Braf-2
C87398
AA120551
AA387315
AA473386
C230098H17
D6Ertd631e
9930012E13Rik
proto-oncogene proteins B-raf
KRAB_HUMAN
LOC232705
MGC126806
MGC138284
protein kinase B-Raf
FLJ95109
RAFB I
serine/threonine kinase B-Raf
v-raf murine sarcoma viral oncogene homolog B
kinase BRAF
Braf transforming gene
Braf-transforming gene
RIKEN cDNA 9930012E13 gene
EST AI447469
B Raf kinase
DNA segment, Chr 6, ERATO Doi 631, expressed
9930012E13
AI447469
Braf
BRAF I
B-Raf proto-oncogene serine/threonine-protein kinase (p94) (v-Raf murine sarcoma viral oncogene homolog B1)
B-Raf proto-oncogene serine/threonine-protein kinase
B-RAF I
p94
Braf transforming
BRAF-1
B-RAF-1
C87398s
B-RAF-1s
B-raf 1
Doi 631
expressed sequence C87398
B-RAF Is
Doi 631s
hypothetical protein C230098H17
B-Raf protein
BRAF_HUMAN
similar to B-Raf protein

Mouse chromosome position 6 18.43 cM
6 15.5 cM

OMIM ID 164757
115150
613707
211980
613706
OMIM:211980
OMIM:164757

Rat chromosome position 4q21-q22

Hugo ID 1097

Human chromosome position 7q34

Swiss-Prot Accession P15056
P28028
E9QNG9
Q3USE9
A4D1T4
B6HY61
B6HY62
B6HY63
B6HY64
B6HY65
B6HY66
Q13878
Q3MIN6
Q9UDP8
Q9Y6T3
F1M9C3
Q75MQ8
Q9JJU4
Q9JJU5
Q9JJU6
Q99MC6

PIR ID A40951
A57977

GenBank ID NC_000007
XM_005250047
XP_005250104
XM_005250046
XP_005250103
XM_005250045
XP_005250102
NM_004333
NP_004324
XR_242190
NG_007873
NC_018918
AC_000068
AC_000139
AACC02000020
ABBA01034086
ABBA01034087
ABBA01034088
ABBA01034089
ABBA01034090
ABBA01034091
AC006006
AAS00359
AC006344
AAD43193
AC006347
AAD15551
AC079339
AMYH02016910
AMYH02016911
CH236950
EAL24023
CH471070
EAW83964
EAW83965
EU600171
ACD11489
HB432546
CAZ68014
HC464558
CBK51920
X65187
CAA46301
AA252358
AA834931
AI203435
AK054801
AK094023
AK098095
AK124257
AK314346
AW971583
BC038966
BC101757
AAI01758
BC112079
AAI12080
BM263585
DB454480
DN996440
HM437233
ADN43065
M21001
AAA96495
M95712
AAA35609
P15056
NC_000072
NM_139294
NP_647455
XM_006505356
XP_006505419
XM_006505353
XP_006505416
XM_006505354
XP_006505417
XM_006505355
XP_006505418
XM_006505357
XP_006505420
XM_006505358
XP_006505421
XM_006505359
XP_006505422
XM_006505360
XP_006505423
XR_377406
XM_006505361
XP_006505424
XR_377407
XM_006505362
XP_006505425
AC_000028
AAHY01052815
AAHY01052816
AC122345
AC163109
AF454556
AAQ04690
AF454557
AAQ04691
AF454558
AAQ04692
AF454559
AAQ04693
AJ276307
CAB81555
AJ276308
CAB81556
AJ276309
CAB81557
AK036143
AK036798
AK046760
AK049095
AK051252
AK076310
AK082596
AK088830
AK135401
AK140431
BAE24384
AK164972
BC038063
BF466677
CK393545
S79859
AAB35395
P28028
DQ545840
NC_005103
XM_231692
XP_231692
XM_006236357
XP_006236419
XM_006236356
XP_006236418
XM_006236358
XP_006236420
XM_006236359
XP_006236421
AC_000072
XM_001070228
XP_001070228
XM_006224885
XP_006224947
XM_006224884
XP_006224946
XM_006224886
XP_006224948
XM_006224887
XP_006224949
AABR06030571
AABR06030572
AAHX01029688
AAHX01029689
AAHX01029690
AAHX01029691
AAHX01029692
CH473959
EDM15397
AF352172
AAK32708
FQ232056
NT_079596
NT_007914
NW_001839073
NW_923640
AC_000050
Q75MQ8
NT_039341
NW_001030802
Q9JJU4
Q9JJU5
Q9JJU6
NW_001084827
NW_047690
Q99MC6
AA120551
AA386732
AA387315
AA473386
AA607928
AA764286
AI447469
AI462537
AI508654
AI585848
AU015031
BB327307
BG064099
BG083084
BM217816
BQ175652
C87398
Q9UDP8

Unigene ID Hs.550061
Hs.600998
Hs.659507
Mm.245513
Mm.489691
Rn.205813
Mm.479647
Rn.223261
Mm.436728
Mm.392307
Mm.393751
Mm.394373
Mm.423115
Mm.477773
Rn.99177
Mm.29415
Hs.324250
Rn.92360
Hs.162967
Mm.320936

KEGG ID hsa:673
mmu:109880
rno:114486

Swiss-Prot ID BRAF_MOUSE
BRAF_HUMAN
BRAF1_HUMAN
BRAF1_MOUSE
A4D1T4_HUMAN

EC Number 2.7.11.1
2.7.1.-

Ensembl ID ENSG00000157764
ENSP00000288602
ENST00000288602
ENSMUSG00000002413
ENSMUSP00000002487
ENSMUST00000002487

Homologene ID 3197

Organism Homo sapiens
Mus musculus
Rattus norvegicus

MGI ID 88190
2442536
2141786
1889824
1277149

RGD ID 619908

MedScan ID 673

Primary Cell Localization Cytoplasm

IPI ID IPI00230719
IPI00816967
IPI00303797
IPI00668709
IPI00766596
IPI00373550

KEGG pathway Regulation of actin cytoskeleton
MAPK signaling pathway
Dorso-ventral axis formation
Focal adhesion

Microarray ID 161718_at
93870_at