U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

LOC730098 uncharacterized LOC730098 [ Homo sapiens (human) ]

Gene ID: 730098, updated on 5-Oct-2022

Summary

Gene symbol
LOC730098
Gene description
uncharacterized LOC730098
See related
Ensembl:ENSG00000187186
Gene type
protein coding
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 testis (RPKM 19.5), brain (RPKM 2.1) and 6 other tissues See more
Orthologs
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

See LOC730098 in Genome Data Viewer
Location:
9p13.3
Exon count:
4
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (34664163..34666045, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (34682692..34684574, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (34664160..34666042, complement)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124902146 Neighboring gene interleukin 11 receptor subunit alpha Neighboring gene galactose-1-phosphate uridylyltransferase Neighboring gene C-C motif chemokine ligand 27 Neighboring gene PHD finger protein 24 Neighboring gene C-C motif chemokine ligand 19

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 protein information

Preferred Names
uncharacterized protein LOC730098

NCBI Reference Sequences (RefSeq)

NEW Try the new Transcript table

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.

mRNA and Protein(s)

  1. NM_001320037.2NP_001306966.1  uncharacterized protein LOC730098

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) represents the shorter transcript. Both variants 1 and 2 encode the same protein.
    Source sequence(s)
    AK296005, AL162231, HY158194
    Consensus CDS
    CCDS83357.1
    UniProtKB/TrEMBL
    B7Z3J9
    Related
    ENSP00000452132.1, ENST00000544078.2
  2. NM_001320038.2NP_001306967.1  uncharacterized protein LOC730098

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) retains an intron in the 5' UTR compared to variant 1. Both variants 1 and 2 encode the same protein.
    Source sequence(s)
    AK296005, AL162231, BC066358
    Consensus CDS
    CCDS83357.1
    UniProtKB/TrEMBL
    B7Z3J9
    Related
    ENSP00000457701.1, ENST00000421828.7

RNA

  1. NR_135148.2 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (3) retains an intron compared to variant 1. This variant is represented as non-coding because the predicted protein does not meet RefSeq quality criteria.
    Source sequence(s)
    AK296005, AL162231, BM695963, DB061900, HY030992

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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
    34664163..34666045 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    34682692..34684574 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)