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MRPS18CP4 MRPS18C pseudogene 4 [ Homo sapiens (human) ]

Gene ID: 349842, updated on 10-Oct-2023

Summary

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Official Symbol
MRPS18CP4provided by HGNC
Official Full Name
MRPS18C pseudogene 4provided by HGNC
Primary source
HGNC:HGNC:29745
See related
AllianceGenome:HGNC:29745
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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Location:
12p13.1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 12 NC_000012.12 (14237261..14237324)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 12 NC_060936.1 (14114109..14114172)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (14390195..14390258)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene glutamate ionotropic receptor NMDA type subunit 2B Neighboring gene uncharacterized LOC105369667 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr12:14138289-14139488 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 6037 Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr12:14279960-14280579 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr12:14304393-14304981 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 6038 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr12:14372961-14374160 Neighboring gene high mobility group nucleosome binding domain 1 pseudogene 23 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:14392159-14393098 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:14402328-14402842 Neighboring gene RNA, U6 small nuclear 491, pseudogene Neighboring gene G protein subunit alpha i2 pseudogene 1

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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Related articles in PubMed

  1. Identification and characterization of over 100 mitochondrial ribosomal protein pseudogenes in the human genome. Zhang Z, et al. Genomics, 2003 May. PMID 12706105

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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Other Names

  • mitochondrial ribosomal protein S18C pseudogene 4

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_002839.2 

    Range
    101..164
    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_000012.12 Reference GRCh38.p14 Primary Assembly

    Range
    14237261..14237324
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060936.1 Alternate T2T-CHM13v2.0

    Range
    14114109..14114172
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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