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LOC112268140 loricrin-like [ Homo sapiens (human) ]

Gene ID: 112268140, updated on 15-Mar-2024

Summary

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Gene symbol
LOC112268140
Gene description
loricrin-like
Gene type
ncRNA
RefSeq status
PREDICTED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Orthologs
all
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Genomic context

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Location:
14q23.2
Exon count:
1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 14 NC_000014.9 (63542784..63544664)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 14 NC_060938.1 (57750182..57752062)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 14 NC_000014.8 (64009502..64011382)

Chromosome 14 - NC_000014.9Genomic Context describing neighboring genes Neighboring gene protein phosphatase 2 regulatory subunit B'epsilon Neighboring gene U6 spliceosomal RNA Neighboring gene ATAC-STARR-seq lymphoblastoid active region 8505 Neighboring gene uncharacterized LOC124900352 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr14:63950021-63950522 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr14:63950523-63951022 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 8506 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 8508 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 8507 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 5827 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 5828 Neighboring gene H3K27ac hESC enhancer GRCh37_chr14:64010147-64011138 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 8510 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:64030470-64031292 Neighboring gene ribosomal protein L31 pseudogene 5 Neighboring gene glycine C-acetyltransferase pseudogene 1

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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Related articles in PubMed

  1. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Strausberg RL, et al. Proc Natl Acad Sci U S A, 2002 Dec 24. PMID 12477932, Free PMC Article

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 variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

General gene information

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Homology

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_158218.1 RNA Sequence

    Status: PREDICTED

    Source sequence(s)
    AL136038

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_000014.9 Reference GRCh38.p14 Primary Assembly

    Range
    63542784..63544664
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060938.1 Alternate T2T-CHM13v2.0

    Range
    57750182..57752062
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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