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RNF14P1 RNF14 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 100129375, updated on 17-Sep-2024

Summary

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Official Symbol
RNF14P1provided by HGNC
Official Full Name
RNF14 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:54669
See related
AllianceGenome:HGNC:54669
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 RNF14P1 in Genome Data Viewer
Location:
2q22.1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (138411877..138413457, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 2 NC_060926.1 (138857596..138859176, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (139169447..139171027, complement)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon pseudogene 5 Neighboring gene IDI1 pseudogene 1 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 16593 Neighboring gene Sharpr-MPRA regulatory region 15192 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 11986 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 11987 Neighboring gene SPOPL divergent transcript Neighboring gene ATAC-STARR-seq lymphoblastoid active region 16594 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 16595 Neighboring gene speckle type BTB/POZ protein like

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 studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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Other Names

  • ring finger protein 14 pseudogene

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_021525.2 

    Range
    62..1642
    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_000002.12 Reference GRCh38.p14 Primary Assembly

    Range
    138411877..138413457 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060926.1 Alternate T2T-CHM13v2.0

    Range
    138857596..138859176 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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