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GCOM2 GRINL1B complex locus 2 (pseudogene) [ Homo sapiens (human) ]

Gene ID: 339970, updated on 8-Oct-2017
Official Symbol
GCOM2provided by HGNC
Official Full Name
GRINL1B complex locus 2 (pseudogene)provided by HGNC
Primary source
HGNC:HGNC:15712
See related
MIM:608311
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
GLURR2; GRINL1B
Location:
4q13.2
Annotation release Status Assembly Chr Location
108 current GRCh38.p7 (GCF_000001405.33) 4 NC_000004.12 (68038416..68042511)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (68904134..68908238)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene transmembrane protease, serine 11G, pseudogene Neighboring gene RNA, U6 small nuclear 95, pseudogene Neighboring gene transmembrane protease, serine 11F Neighboring gene uncharacterized LOC550113 Neighboring gene synaptotagmin 14 pseudogene 1 Neighboring gene solute carrier family 47 member 2 pseudogene

GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

Products Interactant Other Gene Complex Source Pubs Description

Markers

Other Names

  • glutamate receptor, ionotropic, N-methyl D-aspartate-like 1B

Gene Ontology Provided by GOA

Function Evidence Code Pubs
molecular_function ND
No biological Data available
more info
 
Process Evidence Code Pubs
biological_process ND
No biological Data available
more info
 
maintenance of ER location IBA
Inferred from Biological aspect of Ancestor
more info
 
Component Evidence Code Pubs
DNA-directed RNA polymerase II, holoenzyme IBA
Inferred from Biological aspect of Ancestor
more info
 
cellular_component ND
No biological Data available
more info
 

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_009901.2 

    Range
    101..4196
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 108 details...Open this link in a new tab

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

Reference GRCh38.p7 Primary Assembly

Genomic

  1. NC_000004.12 Reference GRCh38.p7 Primary Assembly

    Range
    68038416..68042511
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate CHM1_1.1

Genomic

  1. NC_018915.2 Alternate CHM1_1.1

    Range
    68941140..68945235
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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