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RAB9BP1 RAB9B, member RAS oncogene family pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 9366, updated on 11-Sep-2019

Summary

Official Symbol
RAB9BP1provided by HGNC
Official Full Name
RAB9B, member RAS oncogene family pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:9793
See related
Ensembl:ENSG00000232159
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
RAB9P1

Genomic context

See RAB9BP1 in Genome Data Viewer
Location:
5q21.2-q21.3
Exon count:
1
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) 5 NC_000005.10 (105099474..105100098)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 5 NC_000005.9 (104435175..104435799)

Chromosome 5 - NC_000005.10Genomic Context describing neighboring genes Neighboring gene RNA, U6 small nuclear 334, pseudogene Neighboring gene uncharacterized LOC105379111 Neighboring gene uncharacterized LOC105379110 Neighboring gene uncharacterized LOC107986439 Neighboring gene RNA, 5S ribosomal pseudogene 189

Genomic regions, transcripts, and products

Phenotypes

NHGRI GWAS Catalog

Description
Genome-wide association study identifies 8 novel loci associated with blood pressure responses to interventions in Han Chinese.
NHGRI GWA Catalog
Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan.
NHGRI GWA Catalog

General gene information

Markers

Other Names

  • RAB9, member RAS oncogene family, pseudogene 1
  • RAB9A, member RAS oncogene family pseudogene

NCBI Reference Sequences (RefSeq)

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.

RNA

  1. NR_000039.2 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC091987
    Related
    ENST00000519581.1

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109 details...Open this link in a new tab

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000005.10 Reference GRCh38.p13 Primary Assembly

    Range
    105099474..105100098
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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