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FMO9P flavin containing dimethylaniline monoxygenase 9, pseudogene [ Homo sapiens (human) ]

Gene ID: 116123, updated on 1-Jun-2020

Summary

Official Symbol
FMO9Pprovided by HGNC
Official Full Name
flavin containing dimethylaniline monoxygenase 9, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:32210
See related
Ensembl:ENSG00000215834
Gene type
pseudo
RefSeq status
PROVISIONAL
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Expression
Biased expression in urinary bladder (RPKM 4.8) and esophagus (RPKM 0.3) See more

Genomic context

See FMO9P in Genome Data Viewer
Location:
1q24.1
Exon count:
7
Annotation release Status Assembly Chr Location
109.20200522 current GRCh38.p13 (GCF_000001405.39) 1 NC_000001.11 (166603916..166625238)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (166573153..166594475)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene long intergenic non-protein coding RNA 1675 Neighboring gene flavin containing dimethylaniline monoxygenase 7, pseudogene Neighboring gene flavin containing dimethylaniline monoxygenase 8, pseudogene Neighboring gene flavin containing dimethylaniline monoxygenase 10, pseudogene Neighboring gene ribosomal protein L4 pseudogene 2

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

Markers

Other Names

  • RP11-45J16.2
  • flavin containing monooxygenase 9, pseudogene

Clone Names

  • MGC23941

NCBI Reference Sequences (RefSeq)

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_002925.2 RNA Sequence

    Status: PROVISIONAL

    Source sequence(s)
    BC014341
    Related
    ENST00000477875.6

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000001.11 Reference GRCh38.p13 Primary Assembly

    Range
    166603916..166625238
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_138784.1: Suppressed sequence

    Description
    NM_138784.1: This RefSeq was permanently suppressed because this locus represents a pseudogene rather than a protein coding gene.
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