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RNY4P19 RNY4 pseudogene 19 [ Homo sapiens (human) ]

Gene ID: 100169834, updated on 25-Jan-2022

Summary

Official Symbol
RNY4P19provided by HGNC
Official Full Name
RNY4 pseudogene 19provided by HGNC
Primary source
HGNC:HGNC:34069
See related
Ensembl:ENSG00000199400 AllianceGenome:HGNC:34069
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 RNY4P19 in Genome Data Viewer
Location:
2q36.3
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 2 NC_000002.12 (230058231..230058324, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (230922947..230923040, complement)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene F-box protein 36 Neighboring gene RNA, U6 small nuclear 1027, pseudogene Neighboring gene uncharacterized LOC107985996 Neighboring gene solute carrier family 16 member 14 Neighboring gene uncharacterized LOC107985995 Neighboring gene uncharacterized LOC107985997

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_007997.1 

    Range
    101..194
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000002.12 Reference GRCh38.p13 Primary Assembly

    Range
    230058231..230058324 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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