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LOC105379252 family with sequence similarity 95 member B1-like [ Homo sapiens (human) ]

Gene ID: 105379252, updated on 10-Oct-2023

Summary

Gene symbol
LOC105379252
Gene description
family with sequence similarity 95 member B1-like
See related
Ensembl:ENSG00000290970
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Expression
Biased expression in testis (RPKM 17.6), spleen (RPKM 1.7) and 3 other tissues See more
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Genomic context

Location:
9q21.11
Exon count:
5
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (66047085..66052734, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (79742705..79748352)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (43027663..43033312, complement)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene calponin 2 pseudogene Neighboring gene zinc finger protein 114 pseudogene Neighboring gene cytochrome P450 family 4 subfamily F member 59, pseudogene Neighboring gene sorting nexin 18 pseudogene 4 Neighboring gene ankyrin repeat domain 20 family member A3, pseudogene Neighboring gene RNA, U6 small nuclear 538, pseudogene

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

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.

RNA

  1. NR_136310.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL669942
    Related
    ENST00000610972.4

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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
    66047085..66052734 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    79742705..79748352
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)