RPL3P4 ribosomal protein L3 pseudogene 4 [Homo sapiens (human)] - Gene

Summary

Official Symbol: RPL3P4provided by HGNC
Official Full Name: ribosomal protein L3 pseudogene 4provided by HGNC
Primary source: HGNC:HGNC:19805
See related: Ensembl:ENSG00000232573 AllianceGenome:HGNC:19805
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

Location:: 14q32.2

Annotation release	Status	Assembly	Chr	Location
RS_2023_10	current	GRCh38.p14 (GCF_000001405.40)	14	NC_000014.9 (98972823..98973301, complement)
RS_2023_10	current	T2T-CHM13v2.0 (GCF_009914755.1)	14	NC_060938.1 (93204526..93205004, complement)
105.20220307	previous assembly	GRCh37.p13 (GCF_000001405.25)	14	NC_000014.8 (99439160..99439638, complement)

Chromosome 14 - NC_000014.9 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Submit: New GeneRIF Correction

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

ECD10839 (e-PCR)
- UniSTS:291878

ECD04035 (e-PCR)
- UniSTS:285114

REN46851 (e-PCR)
- UniSTS:371651

REN46852 (e-PCR)
- UniSTS:371652

REN46853 (e-PCR)
- UniSTS:371653

REN46854 (e-PCR)
- UniSTS:371654

REN46855 (e-PCR)
- UniSTS:371655

REN46856 (e-PCR)
- UniSTS:371656

REN46857 (e-PCR)
- UniSTS:371657

REN46858 (e-PCR)
- UniSTS:371658

REN46859 (e-PCR)
- UniSTS:371659

REN46860 (e-PCR)
- UniSTS:371660

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.