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FAM120AOS family with sequence similarity 120A opposite strand [ Homo sapiens (human) ]

Gene ID: 158293, updated on 23-Nov-2021

Summary

Official Symbol
FAM120AOSprovided by HGNC
Official Full Name
family with sequence similarity 120A opposite strandprovided by HGNC
Primary source
HGNC:HGNC:23389
See related
Ensembl:ENSG00000188938
Gene type
protein coding
RefSeq status
REVIEWED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
C9orf10OS
Summary
Differences in the expression level of this gene are associated with the survival rate of those with glioma. [provided by RefSeq, May 2017]
Expression
Ubiquitous expression in thyroid (RPKM 13.5), colon (RPKM 12.6) and 25 other tissues See more
Orthologs
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Genomic context

See FAM120AOS in Genome Data Viewer
Location:
9q22.31
Exon count:
5
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 9 NC_000009.12 (93443332..93453601, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (96205614..96215883, complement)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene RNA, U6 small nuclear 829, pseudogene Neighboring gene uncharacterized LOC107987097 Neighboring gene Sharpr-MPRA regulatory region 4009 Neighboring gene family with sequence similarity 120A Neighboring gene MIA SH3 domain ER export factor 2 pseudogene Neighboring gene PHD finger protein 2 Neighboring gene microRNA 548au

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

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Homology

Clone Names

  • FLJ31534

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables protein binding IPI
Inferred from Physical Interaction
more info
PubMed 

General protein information

Preferred Names
uncharacterized protein FAM120AOS
Names
FAM120A opposite strand protein

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.

Genomic

  1. NG_054727.1 RefSeqGene

    Range
    5001..12108
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. NM_001322224.3NP_001309153.1  uncharacterized protein FAM120AOS isoform 2

    Status: REVIEWED

    Description
    Transcript Variant: This variant (2) contains an alternate exon in the 5' UTR, lacks a portion of the 5' coding region, and initiates translation at an alternate start codon, compared to variant 1. The encoded isoform (2) has a shorter and distinct N-terminus, compared to isoform 1.
    Source sequence(s)
    AL353629, AL583839, AW016692
    Consensus CDS
    CCDS83385.1
    UniProtKB/TrEMBL
    E9PCY8
    Related
    ENSP00000414298.1, ENST00000423591.5
  2. NM_198841.4NP_942138.2  uncharacterized protein FAM120AOS isoform 1

    See identical proteins and their annotated locations for NP_942138.2

    Status: REVIEWED

    Description
    Transcript Variant: This variant (1) encodes the longer isoform (1).
    Source sequence(s)
    AK056096, AL353629, AL583839, AW016692, BC038803
    Consensus CDS
    CCDS6705.1
    UniProtKB/Swiss-Prot
    Q5T036
    Related
    ENSP00000364561.5, ENST00000375412.11

RNA

  1. NR_136229.2 RNA Sequence

    Status: REVIEWED

    Description
    Transcript Variant: This variant (3) uses an alternate splice site in the first exon, compared to variant 1. This variant is represented as non-coding because the predicted protein does not meet RefSeq quality criteria.
    Source sequence(s)
    AL353629, AL583839, AW016692
  2. NR_136230.2 RNA Sequence

    Status: REVIEWED

    Description
    Transcript Variant: This variant (4) uses an alternate splice site in the first exon and contains an alternate internal exon, compared to variant 1. This variant is represented as non-coding because the predicted protein does not meet RefSeq quality criteria.
    Source sequence(s)
    AL353629, AL583839, AW016692
  3. NR_136231.3 RNA Sequence

    Status: REVIEWED

    Description
    Transcript Variant: This variant (5) contains an alternate internal exon, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
    Source sequence(s)
    AL353629, AL583839, AW016692
  4. NR_136232.3 RNA Sequence

    Status: REVIEWED

    Description
    Transcript Variant: This variant (6) contains an alternate first exon and an alternate internal exon, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
    Source sequence(s)
    AL353629, AL583839, AW016692
  5. NR_136233.3 RNA Sequence

    Status: REVIEWED

    Description
    Transcript Variant: This variant (7) contains an alternate first exon, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
    Source sequence(s)
    AL353629, AL583839, AW016692
  6. NR_136234.3 RNA Sequence

    Status: REVIEWED

    Description
    Transcript Variant: This variant (8) contains an alternate first exon and an alternate internal exon, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
    Source sequence(s)
    AL353629, AL583839, AW016692
  7. NR_136235.3 RNA Sequence

    Status: REVIEWED

    Description
    Transcript Variant: This variant (9) contains an alternate first exon, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
    Source sequence(s)
    AL353629, AL583839, AW016692
  8. NR_136236.3 RNA Sequence

    Status: REVIEWED

    Description
    Transcript Variant: This variant (10) contains an alternate first exon, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
    Source sequence(s)
    AL353629, AL583839, AW016692
  9. NR_136237.3 RNA Sequence

    Status: REVIEWED

    Description
    Transcript Variant: This variant (11) contains an alternate first exon and an alternate internal exon, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
    Source sequence(s)
    AL353629, AL583839, AW016692
  10. NR_136238.3 RNA Sequence

    Status: REVIEWED

    Description
    Transcript Variant: This variant (12) contains an alternate first exon and an alternate internal exon, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
    Source sequence(s)
    AL353629, AL583839, AW016692

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_000009.12 Reference GRCh38.p13 Primary Assembly

    Range
    93443332..93453601 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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