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FAM242D family with sequence similarity 242 member D [ Homo sapiens (human) ]

Gene ID: 112488742, updated on 10-Oct-2023

Summary

Official Symbol
FAM242Dprovided by HGNC
Official Full Name
family with sequence similarity 242 member Dprovided by HGNC
Primary source
HGNC:HGNC:53874
See related
AllianceGenome:HGNC:53874
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

Location:
9q13
Exon count:
3
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (61615821..61626913)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (44823659..44834751)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene splicing factor 45-like Neighboring gene uncharacterized LOC105379437 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:44767663-44768162 Neighboring gene RNA, 7SL, cytoplasmic 722, pseudogene Neighboring gene family with sequence similarity 27 member C

Genomic regions, transcripts, and products

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_170271.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL935212
  2. NR_170272.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL935212
  3. NR_170273.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL935212

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
    61615821..61626913
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)