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LOC124907158 uncharacterized LOC124907158 [ Homo sapiens (human) ]

Gene ID: 124907158, updated on 27-Aug-2024

Summary

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Gene symbol
LOC124907158
Gene description
uncharacterized LOC124907158
Gene type
pseudo
RefSeq status
MODEL
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Annotation information
Annotation category: not annotated on reference assembly
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Genomic context

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See LOC124907158 in Genome Data Viewer
Location:
chromosome: 13
Annotation release Status Assembly Chr Location
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (10955043..10955179)

Chromosome 13 - NC_060937.1Genomic Context describing neighboring genes Neighboring gene eukaryotic translation initiation factor 3 subunit F-like Neighboring gene uncharacterized LOC124907097 Neighboring gene B melanoma antigen Neighboring gene protein FRG1-like Neighboring gene uncharacterized LOC124907111

Genomic regions, transcripts, and products

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Genomic Sequence:
NC_060937.1 Chromosome 13 Alternate T2T-CHM13v2.0

Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

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

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060937.1 Alternate T2T-CHM13v2.0

    Range
    10955043..10955179
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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