BRAFP1 BRAF pseudogene 1 [Homo sapiens (human)] - Gene

Summary

Official Symbol: BRAFP1provided by HGNC
Official Full Name: BRAF pseudogene 1provided by HGNC
Primary source: HGNC:HGNC:18615
See related: Ensembl:ENSG00000224775 MIM:300956; AllianceGenome:HGNC:18615
Gene type: pseudo
RefSeq status: INFERRED
Organism: Homo sapiens
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as: BRAF2; BRAFPS2
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Genomic context

Location:: Xq13.3

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	X	NC_000023.11 (75582654..75585917)
RS_2024_08	current	T2T-CHM13v2.0 (GCF_009914755.1)	X	NC_060947.1 (74016336..74019599)
RS_2024_09	previous assembly	GRCh37.p13 (GCF_000001405.25)	X	NC_000023.10 (74802489..74805752)

Chromosome X - NC_000023.11 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Submit: New GeneRIF Correction

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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Markers

Braf (e-PCR), detects polymorphism
- UniSTS:259512

Other Names

murine sarcoma viral (v-raf) oncogene homolog B1 oncogene
v-raf murine sarcoma viral oncogene homolog B pseudogene 1
v-raf murine sarcoma viral oncogene homolog B pseudogene 2
v-raf murine sarcoma viral oncogene homolog B1 pseudogene 1
v-raf murine sarcoma viral oncogene homolog B1 pseudogene 2

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.