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RNY1P16 RNY1 pseudogene 16 [ Homo sapiens (human) ]

Gene ID: 106480312, updated on 13-May-2022

Summary

Official Symbol
RNY1P16provided by HGNC
Official Full Name
RNY1 pseudogene 16provided by HGNC
Primary source
HGNC:HGNC:50879
See related
Ensembl:ENSG00000199933 AllianceGenome:HGNC:50879
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 RNY1P16 in Genome Data Viewer
Location:
12q23.2
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 12 NC_000012.12 (101719808..101719918)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 12 NC_060936.1 (101681035..101681145)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (102113586..102113696)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene myosin binding protein C1 Neighboring gene uncharacterized LOC105369937 Neighboring gene uncharacterized LOC124902996 Neighboring gene choline phosphotransferase 1 Neighboring gene uncharacterized LOC124902997 Neighboring gene synaptonemal complex protein 3

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_045811.1 

    Range
    101..211
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000012.12 Reference GRCh38.p14 Primary Assembly

    Range
    101719808..101719918
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060936.1 Alternate T2T-CHM13v2.0

    Range
    101681035..101681145
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)