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LOC124906187 uncharacterized LOC124906187 [ Homo sapiens (human) ]

Gene ID: 124906187, updated on 27-Aug-2024

Summary

Gene symbol
LOC124906187
Gene description
uncharacterized LOC124906187
Gene type
pseudo
RefSeq status
MODEL
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 LOC124906187 in Genome Data Viewer
Location:
2q11.2
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (100577469..100577557)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 2 NC_060926.1 (101036194..101036282)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene ARPP19 pseudogene 2 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr2:101154295-101154846 Neighboring gene H3K27ac hESC enhancer GRCh37_chr2:101178200-101178996 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 11816 Neighboring gene phosducin like 3 Neighboring gene high mobility group nucleosomal binding domain 2 pseudogene 22 Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr2:101220203-101220846 Neighboring gene long intergenic non-protein coding RNA 1849

Genomic regions, transcripts, and products

NCBI Reference Sequences (RefSeq)

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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
    100577469..100577557
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060926.1 Alternate T2T-CHM13v2.0

    Range
    101036194..101036282
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)