U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

RBM17P4 RNA binding motif protein 17 pseudogene 4 [ Homo sapiens (human) ]

Gene ID: 100128974, updated on 10-Oct-2023

Summary

Go to the top of the page Help
Official Symbol
RBM17P4provided by HGNC
Official Full Name
RNA binding motif protein 17 pseudogene 4provided by HGNC
Primary source
HGNC:HGNC:50369
See related
AllianceGenome:HGNC:50369
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

Go to the top of the page Help
Location:
15q14
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 15 NC_000015.10 (35298047..35299593, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 15 NC_060939.1 (33103367..33104913, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 15 NC_000015.9 (35590248..35591794, complement)

Chromosome 15 - NC_000015.10Genomic Context describing neighboring genes Neighboring gene diphthamine biosynthesis 6 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:35537116-35537669 Neighboring gene H3K27ac hESC enhancer GRCh37_chr15:35544243-35544742 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr15:35545952-35546470 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr15:35546471-35546990 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr15:35548334-35549533 Neighboring gene acidic nuclear phosphoprotein 32 family member A pseudogene 1 Neighboring gene H3K27ac hESC enhancer GRCh37_chr15:35555863-35556362 Neighboring gene Sharpr-MPRA regulatory region 14069 Neighboring gene nuclear transport factor 2 pseudogene 6 Neighboring gene microRNA 3942 Neighboring gene heterogeneous nuclear ribonucleoprotein A1 pseudogene 45

Genomic regions, transcripts, and products

Go to the top of the page Help

Go to nucleotide: Graphics FASTA GenBank

Bibliography

Go to the top of the pageHelp

GeneRIFs: Gene References Into Functions

Phenotypes

Go to the top of the page Help

Review eQTL and phenotype association data in this region using PheGenI

Variation

Go to the top of the page Help

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

Go to the top of the page Help

Markers

NCBI Reference Sequences (RefSeq)

Go to the top of the page Help

NEW Try the new Transcript table

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_009947.2 

    Range
    101..1647
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000015.10 Reference GRCh38.p14 Primary Assembly

    Range
    35298047..35299593 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060939.1 Alternate T2T-CHM13v2.0

    Range
    33103367..33104913 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.

Molecular Biology Databases