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RBMXP1 RBMX pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 3186, updated on 17-Sep-2024

Summary

Official Symbol
RBMXP1provided by HGNC
Official Full Name
RBMX pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:9911
See related
AllianceGenome:HGNC:9911
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
HNRPG; HNRNP-G
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Genomic context

See RBMXP1 in Genome Data Viewer
Location:
6p12.3
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (48212918..48214969, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (48054686..48056737, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (48180654..48182705, complement)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene patched domain containing 4 Neighboring gene Sharpr-MPRA regulatory region 3755 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr6:48078458-48079657 Neighboring gene heterogeneous nuclear ribonucleoprotein A3 pseudogene 4 Neighboring gene uncharacterized LOC107986602 Neighboring gene MPRA-validated peak5834 silencer Neighboring gene NANOG hESC enhancer GRCh37_chr6:48732670-48733267 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr6:48794410-48795609 Neighboring gene PRR11 pseudogene 1

Genomic regions, transcripts, and products

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Other Names

  • Heterogeneous nuclear ribonucleoprotein polypeptide G
  • RNA binding motif protein, X chromosome, pseudogene 1
  • RNA binding motif protein, X-linked pseudogene 1
  • heterogeneous nuclear ribonucleoprotein G

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_001022.4 

    Range
    101..2152
    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_000006.12 Reference GRCh38.p14 Primary Assembly

    Range
    48212918..48214969 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060930.1 Alternate T2T-CHM13v2.0

    Range
    48054686..48056737 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)