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RNF138P2 ring finger protein 138 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 100419777, updated on 17-Sep-2024

Summary

Official Symbol
RNF138P2provided by HGNC
Official Full Name
ring finger protein 138 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:50775
See related
Ensembl:ENSG00000271194 AllianceGenome:HGNC:50775
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

See RNF138P2 in Genome Data Viewer
Location:
7p12.1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (53316205..53316719)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (53477970..53478484)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (53383898..53384412)

Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene POM121 transmembrane nucleoporin like 12 Neighboring gene ReSE screen-validated silencer GRCh37_chr7:53155076-53155272 Neighboring gene HAUS augmin like complex subunit 6 pseudogene 1 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:53286621-53287122 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:53383338-53383838 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:53383839-53384339 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr7:53394135-53394982 Neighboring gene uncharacterized LOC105375282 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:53452734-53453234 Neighboring gene RNA, U1 small nuclear 14, pseudogene Neighboring gene RN7SK pseudogene 218

Genomic regions, transcripts, and products

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_026566.1 

    Range
    101..615
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    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_000007.14 Reference GRCh38.p14 Primary Assembly

    Range
    53316205..53316719
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060931.1 Alternate T2T-CHM13v2.0

    Range
    53477970..53478484
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)