Format

Send to:

Choose Destination

LENG9 leukocyte receptor cluster member 9 [ Homo sapiens (human) ]

Gene ID: 94059, updated on 24-Nov-2021

Summary

Official Symbol
LENG9provided by HGNC
Official Full Name
leukocyte receptor cluster member 9provided by HGNC
Primary source
HGNC:HGNC:16306
See related
Ensembl:ENSG00000275183
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
Orthologs
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

See LENG9 in Genome Data Viewer
Location:
19q13.42
Exon count:
1
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 19 NC_000019.10 (54461732..54463778, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 19 NC_000019.9 (54972912..54974961, complement)

Chromosome 19 - NC_000019.10Genomic Context describing neighboring genes Neighboring gene tweety family member 1 Neighboring gene Sharpr-MPRA regulatory region 3780 Neighboring gene LENG8 antisense RNA 1 Neighboring gene leukocyte receptor cluster member 8 Neighboring gene CDC42 effector protein 5 Neighboring gene leukocyte associated immunoglobulin like receptor 2

Genomic regions, transcripts, and products

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Homology

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables metal ion binding IEA
Inferred from Electronic Annotation
more info
 

General protein information

Preferred Names
leukocyte receptor cluster member 9
Names
leukocyte receptor cluster (LRC) member 9

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_001301782.2NP_001288711.1  leukocyte receptor cluster member 9

    Status: VALIDATED

    Source sequence(s)
    AC245884, CA450132
    Consensus CDS
    CCDS77358.1
    UniProtKB/TrEMBL
    A0A087WVD1
    Related
    ENSP00000479355.1, ENST00000611161.2
    Conserved Domains (3) summary
    smart00356
    Location:2439
    ZnF_C3H1; zinc finger
    pfam10469
    Location:297477
    AKAP7_NLS; AKAP7 2'5' RNA ligase-like domain
    cl00661
    Location:87138
    DUF504; Protein of unknown function (DUF504)

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_000019.10 Reference GRCh38.p13 Primary Assembly

    Range
    54461732..54463778 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p13 ALT_REF_LOCI_1

Genomic

  1. NW_003571054.1 Reference GRCh38.p13 ALT_REF_LOCI_1

    Range
    368246..370292 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p13 ALT_REF_LOCI_7

Genomic

  1. NW_003571060.1 Reference GRCh38.p13 ALT_REF_LOCI_7

    Range
    366388..369424 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_045181401.1XP_045037336.1  leukocyte receptor cluster member 9 isoform X1

Reference GRCh38.p13 ALT_REF_LOCI_9

Genomic

  1. NT_187693.1 Reference GRCh38.p13 ALT_REF_LOCI_9

    Range
    443986..447030 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_045181402.1XP_045037337.1  leukocyte receptor cluster member 9 isoform X2

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_198988.2: Suppressed sequence

    Description
    NM_198988.2: This RefSeq was removed because there were mismatches and indels compared to available sequence data. One of the mismatches resulted in the use of an upstream start codon, which is not supported by available homology data.
Support Center