Format

Send to:

Choose Destination

LIN28AP2 LIN28A pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 100287388, updated on 23-Nov-2021

Summary

Official Symbol
LIN28AP2provided by HGNC
Official Full Name
LIN28A pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:38056
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

See LIN28AP2 in Genome Data Viewer
Location:
13q31.2
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 13 NC_000013.11 (87379466..87380684, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (88031721..88032939, complement)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105370301 Neighboring gene ubiquitin B pseudogene 5 Neighboring gene uncharacterized LOC105370302 Neighboring gene MIR4500 host gene Neighboring gene microRNA 4500 Neighboring gene SLIT and NTRK like family member 5

Genomic regions, transcripts, and products

NCBI Reference Sequences (RefSeq)

NEW Try the new Transcript table

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_022998.1 

    Range
    101..1319
    Download
    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_000013.11 Reference GRCh38.p13 Primary Assembly

    Range
    87379466..87380684 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Support Center