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LOC105376057 protein FRG1B-like [ Homo sapiens (human) ]

Gene ID: 105376057, updated on 10-Dec-2024

Summary

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Gene symbol
LOC105376057
Gene description
protein FRG1B-like
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

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See LOC105376057 in Genome Data Viewer
Location:
9p11.2
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (41212711..41218474)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (42076566..42082329, complement)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene forkhead box D4 like 6 Neighboring gene Zn regulated GTPase metalloprotein activator 1F Neighboring gene H3K27ac hESC enhancer GRCh37_chr9:69261657-69262230 Neighboring gene H3K27ac hESC enhancer GRCh37_chr9:69262231-69262802 Neighboring gene uncharacterized LOC124902162 Neighboring gene microRNA 4477a Neighboring gene RNA, 5S ribosomal pseudogene 530

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

General gene information

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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_042239.3 

    Range
    101..5864
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    GenBank, FASTA, Sequence Viewer (Graphics)

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_000009.12 Reference GRCh38.p14 Primary Assembly

    Range
    41212711..41218474
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    42076566..42082329 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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