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FAM157C family with sequence similarity 157 member C [ Homo sapiens (human) ]

Gene ID: 100996541, updated on 23-Nov-2021

Summary

Official Symbol
FAM157Cprovided by HGNC
Official Full Name
family with sequence similarity 157 member Cprovided by HGNC
Primary source
HGNC:HGNC:34081
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 bone marrow (RPKM 9.8), appendix (RPKM 2.9) and 3 other tissues See more
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Genomic context

See FAM157C in Genome Data Viewer
Location:
16q24.3
Exon count:
4
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 16 NC_000016.10 (90102264..90177606)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 16 NC_000016.9 (90168672..90244014)

Chromosome 16 - NC_000016.10Genomic Context describing neighboring genes Neighboring gene PR/SET domain 7 Neighboring gene uncharacterized LOC105376786 Neighboring gene tubulin beta 8 class VIII pseudogene 7 Neighboring gene uncharacterized LOC105376781 Neighboring gene RNA, U6 small nuclear 355, pseudogene Neighboring gene putative uncharacterized protein FLJ44672 Neighboring gene septin 14 pseudogene 16 Neighboring gene capicua transcriptional repressor pseudogene 25 Neighboring gene long intergenic non-protein coding RNA 2193 Neighboring gene uncharacterized LOC107987240

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

General gene information

Other Names

  • family with sequence similarity 157 member C (non-protein coding)

Clone Names

  • FLJ35239, DKFZp434B2016

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_126161.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC133919, BX459292, DA670997, DB461851

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000016.10 Reference GRCh38.p13 Primary Assembly

    Range
    90102264..90177606
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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