Human (GRCh38.p14)
Description

G protein nucleolar 3 [Source:HGNC Symbol;Acc:HGNC:29931]

Gene Synonyms

C77032, E2IG3, MGC800, NS

Location

Chromosome 3: 52,681,156-52,694,497 forward strand.

GRCh38:CM000665.2

About this gene

This gene has 12 transcripts (splice variants), 208 orthologues and 6 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000418458.6GNL3-2021933549aaENSP00000395772.1
 
Protein coding
CCDS2861Q9BVP2-1 NM_014366.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P2TSL:1
ENST00000394799.6GNL3-2012041537aaENSP00000378278.2
 
Protein coding
CCDS43100Q9BVP2-2 -GENCODE basicAPPRIS ALT2TSL:2
ENST00000474423.1GNL3-20756796aaENSP00000419895.1
 
Protein coding
C9JYH9 -TSL:3CDS 3' incomplete
ENST00000479230.5GNL3-208547134aaENSP00000419734.1
 
Protein coding
C9JZT7 -TSL:4CDS 3' incomplete
ENST00000492349.5GNL3-210729138aaENSP00000420345.1
 
Nonsense mediated decay
B4DMU5 -TSL:2
ENST00000460073.1GNL3-203583No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000468146.5GNL3-205533No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000496254.5GNL3-2112118No protein-
 
Retained intron
--TSL:5
ENST00000484022.1GNL3-209668No protein-
 
Retained intron
--TSL:2
ENST00000462550.5GNL3-204597No protein-
 
Retained intron
--TSL:2
ENST00000497356.1GNL3-212523No protein-
 
Retained intron
--TSL:2
ENST00000468885.1GNL3-206263No protein-
 
Retained intron
--TSL:1