Human (GRCh38.p14)
Description

nucleolar complex associated 4 homolog [Source:HGNC Symbol;Acc:HGNC:28461]

Gene Synonyms

MGC3162, NET49, NOC4, UTP19

Location

Scaffold HG2246_HG2248_HG2276_PATCH: 51,486-59,502 forward strand.

GRCh38:ML143361.1

View this gene on the primary assembly.

About this gene

This gene has 4 transcripts (splice variants) and 1 gene allele.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000672504.1NOC4L-2061650516aaENSP00000500901.1
 
Protein coding
Q9BVI4 -Ensembl CanonicalGENCODE basic
ENST00000672726.1NOC4L-2071009270aaENSP00000500165.1
 
Protein coding
--CDS 3' incomplete
ENST00000671978.1NOC4L-205669No protein-
 
Protein coding CDS not defined
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ENST00000673530.1NOC4L-208862No protein-
 
Retained intron
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