Human Gene BRAF (ENST00000644969.2) from GENCODE V50
Description: B-Raf proto-oncogene, serine/threonine kinase, transcript variant 5 (from RefSeq NM_001374258.1)
Gencode Transcript: ENST00000644969.2
Gencode Gene: ENSG00000157764.16
Transcript (Including UTRs)
Position: hg38 chr7:140,719,337-140,924,929 Size: 205,593 Total Exon Count: 20 Strand: -
Coding Region
Position: hg38 chr7:140,726,494-140,924,703 Size: 198,210 Coding Exon Count: 20
Data last updated at UCSC: 2026-07-12 09:30:09
Sequence and Links to Tools and Databases
Primer design for this transcript
MalaCards Disease Associations
MalaCards Gene Search: BRAF
Diseases sorted by gene-association score: cardiofaciocutaneous syndrome * (1601), lung cancer * (1278), noonan syndrome 7 * (1229), colorectal cancer * (992), leopard syndrome 3 * (829), braf-related noonan syndrome * (500), noonan syndrome 1 * (385), hashimoto-pritzker syndrome * (350), classic hairy cell leukemia * (350), melanoma * (323), craniopharyngioma * (253), cardiomyopathy, hypertrophic, 4 * (231), ptpn11-related noonan syndrome * (231), pilocytic astrocytoma * (208), colonic benign neoplasm * (200), noonan syndrome with multiple lentigines * (175), lymphoma, non-hodgkin * (122), thyroid carcinoma somatic * (117), braf-related cardiofaciocutaneous syndrome * (100), braf-related leopard syndrome * (100), differentiated thyroid carcinoma * (88), adenocarcinoma (68), malignant melanoma, somatic * (45), thyroid cancer (35), spitz nevus (25), erdheim-chester disease (25), hodgkin lymphoma (25), sarcoma (24), hairy cell leukemia (22), thyroid cancer, nonmedullary, 1 (19), leopard syndrome (19), desmoplastic infantile astrocytoma/ganglioglioma (19), desmoplastic infantile astrocytoma (18), syringocystadenoma papilliferum (18), refractory hairy cell leukemia (18), myopericytoma (18), thyroid cancer, anaplastic (14), colorectal adenocarcinoma (14), pulmonic stenosis (13), papillary carcinoma (13), papillary craniopharyngioma (13), nevus of ota (13), granulomatous dermatitis (13), nephrotic syndrome, type 3 (13), metanephric adenoma (11), rhabdoid meningioma (10), pleomorphic xanthoastrocytoma (10), struma ovarii (9), lynch syndrome (9), adenofibroma (9), histiocytosis (8), adenoma (8), skin melanoma (8), hyperplastic polyposis syndrome (8), small intestinal adenocarcinoma (8), mature teratoma (8), pilocytic astrocytoma of cerebellum (8), mucosal melanoma (8), ganglioglioma (8), papillary tumor of the pineal region (7), juvenile myelomonocytic leukemia (7), lip cancer (7), amelanotic melanoma (7), cerebellar astrocytoma (7), uveal melanoma (6), villous adenoma (6), lymphoma (6), histiocytic sarcoma (6), nodular goiter (6), hereditary colorectal cancer (5), thyroid cancer, nonmedullary, 2 (5), letterer-siwe disease (5), familial colorectal cancer (5), giant cell glioblastoma (4), endometrial cancer (3), renal cell carcinoma (2), lung cancer susceptibility 3 (1)* = Manually curated disease association
Comparative Toxicogenomics Database (CTD)
The following chemicals interact with this gene
C471405
sorafenib
D000082
Acetaminophen
D000242
Cyclic AMP
C551177
PLX4032
D010634
Phenobarbital
C028474
1,4-bis(2-(3,5-dichloropyridyloxy))benzene
C111118
2',3,3',4',5-pentachloro-4-hydroxybiphenyl
C078765
2,3,5-(triglutathion-S-yl)hydroquinone
C023514
2,6-dinitrotoluene
C532162
2-(1H-indazol-4-yl)-6-(4-methanesulfonylpiperazin-1-ylmethyl)-4-morpholin-4-ylthieno(3,2-d)pyrimidine
more ... click here to view the complete list
RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
Microarray Expression Data
mRNA Secondary Structure of 3' and 5' UTRs
The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.
Orthologous Genes in Other Species
Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.
Descriptions from all associated GenBank mRNAs
HM053972 - Homo sapiens AGTRAP-BRAF fusion protein mRNA, complete cds.GU149303 - Homo sapiens SLC45A3-BRAF fusion protein mRNA, complete cds.BC038966 - Homo sapiens, Similar to v-raf murine sarcoma viral oncogene homolog B1, clone IMAGE:4391530, mRNA.M95712 - Homo sapiens B-raf protein (BRAF) mRNA, complete cds.BC101757 - Homo sapiens v-raf murine sarcoma viral oncogene homolog B1, mRNA (cDNA clone MGC:126806 IMAGE:8069263), complete cds.BC112079 - Homo sapiens v-raf murine sarcoma viral oncogene homolog B1, mRNA (cDNA clone MGC:138284 IMAGE:8327547), complete cds.M21001 - Human B-raf oncogene mRNA, 3' end.AK314346 - Homo sapiens cDNA, FLJ95109.KJ890780 - Synthetic construct Homo sapiens clone ccsbBroadEn_00174 BRAF gene, encodes complete protein.KR712180 - Synthetic construct Homo sapiens clone CCSBHm_00036663 BRAF (BRAF) mRNA, encodes complete protein.AB529216 - Synthetic construct DNA, clone: pF1KB5776, Homo sapiens BRAF gene for v-raf murine sarcoma viral oncogene homolog B1, without stop codon, in Flexi system.AK094023 - Homo sapiens cDNA FLJ36704 fis, clone UTERU2009335.AK098095 - Homo sapiens cDNA FLJ40776 fis, clone TRACH2005210.AK124257 - Homo sapiens cDNA FLJ42263 fis, clone TKIDN2014570.LP057483 - Sequence 1 from Patent EP2841598.LP057484 - Sequence 2 from Patent EP2841598.LP057523 - Sequence 41 from Patent EP2841598.LP057524 - Sequence 42 from Patent EP2841598.HM437233 - Homo sapiens serine/threonine-protein kinase B-raf variant (BRAF) mRNA, partial cds.JD560335 - Sequence 541359 from Patent EP1572962.DJ444894 - Combinatorial Methods and Compositions for Treatment of Melanoma.AJ276310 - Homo sapiens partial mRNA for B-Raf protein (B-raf gene), alternative exon 10.AK054801 - Homo sapiens cDNA FLJ30239 fis, clone BRACE2002081, weakly similar to B-RAF PROTO-ONCOGENE SERINE/THREONINE-PROTEIN KINASE.JD019544 - Sequence 568 from Patent EP1572962.JD032247 - Sequence 13271 from Patent EP1572962.
Biochemical and Signaling Pathways
Other Names for This Gene
Alternate Gene Symbols: A0A2R8Y8E0, A0A2R8Y8E0_HUMAN, BRAF , ENST00000644969.1, NM_001374258, uc285zzl.1, uc285zzl.2UCSC ID: ENST00000644969.2RefSeq Accession: NM_001374258.1
GeneReviews for This Gene
GeneReviews article(s) related to gene BRAF:cfc (Cardiofaciocutaneous Syndrome)leopard (Noonan Syndrome with Multiple Lentigines)noonan (Noonan Syndrome)
Methods, Credits, and Use Restrictions
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for details on how this gene model was made and data restrictions if any.