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RNF14P2 RNF14 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 116435284, updated on 10-Oct-2023

Summary

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Official Symbol
RNF14P2provided by HGNC
Official Full Name
RNF14 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:54670
See related
Ensembl:ENSG00000250594 AllianceGenome:HGNC:54670
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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See RNF14P2 in Genome Data Viewer
Location:
4q25
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (110264865..110265017, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (113567132..113567284, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (111186021..111186173, complement)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene ELOVL fatty acid elongase 6 Neighboring gene RNA, 7SL, cytoplasmic 275, pseudogene Neighboring gene Sharpr-MPRA regulatory region 3955 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 15628 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr4:111119352-111120144 Neighboring gene Sharpr-MPRA regulatory region 7468 Neighboring gene uncharacterized LOC124900759 Neighboring gene CRISPRi-validated cis-regulatory element chr4.2510 Neighboring gene heat shock factor binding protein 1 pseudogene 2 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 21816 Neighboring gene RNA, U6 small nuclear 205, pseudogene Neighboring gene zinc finger BED-type containing 1 pseudogene 1 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 15629 Neighboring gene Sharpr-MPRA regulatory region 5470 Neighboring gene uncharacterized LOC105377362

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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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 Variation Viewer (GRCh37.p13)

General gene information

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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_068490.1 

    Range
    101..253
    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_000004.12 Reference GRCh38.p14 Primary Assembly

    Range
    110264865..110265017 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060928.1 Alternate T2T-CHM13v2.0

    Range
    113567132..113567284 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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