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RAP1BP1 RAP1B pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 100506390, updated on 17-Sep-2024

Summary

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Official Symbol
RAP1BP1provided by HGNC
Official Full Name
RAP1B pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:49780
See related
AllianceGenome:HGNC:49780
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

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See RAP1BP1 in Genome Data Viewer
Location:
9p22.1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (18717911..18718692, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (18731188..18731969, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (18717909..18718690, complement)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene ADAMTS like 1 Neighboring gene uncharacterized LOC102724102 Neighboring gene RN7SK pseudogene 258 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:18711541-18712126 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28218 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr9:18769932-18771131 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_107208 Neighboring gene uncharacterized LOC124902127 Neighboring gene uncharacterized LOC105375985

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

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

Other Names

  • RAP1B, member of RAS oncogene family pseudogene 1

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.

Genomic

  1. NG_030297.2 

    Range
    36..817
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000009.12 Reference GRCh38.p14 Primary Assembly

    Range
    18717911..18718692 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    18731188..18731969 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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