Human (GRCh38.p14)
Description

gem nuclear organelle associated protein 4 [Source:HGNC Symbol;Acc:HGNC:15717]

Gene Synonyms

DKFZP434B131, DKFZP434D174, HC56, HCAP1, HHRF-1, P97

Location

Chromosome 17: 744,421-753,999 reverse strand.

GRCh38:CM000679.2

About this gene

This gene has 7 transcripts (splice variants), 197 orthologues and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000319004.6GEMIN4-20137441058aaENSP00000321706.5
 
Protein coding
CCDS45559P57678 NM_015721.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000576778.1GEMIN4-20747291047aaENSP00000459565.1
 
Protein coding
I3L2C7 -GENCODE basicTSL:NA
ENST00000437269.1GEMIN4-2021182184aaENSP00000392460.1
 
Protein coding
E7EN12 -GENCODE basicTSL:2
ENST00000570364.5GEMIN4-2031048271aaENSP00000461103.1
 
Protein coding
I3L4A4 -TSL:3CDS 3' incomplete
ENST00000573482.5GEMIN4-2041015296aaENSP00000460286.1
 
Protein coding
I3L399 -TSL:2CDS 3' incomplete
ENST00000574958.1GEMIN4-20567370aaENSP00000458896.1
 
Protein coding
I3L1J7 -TSL:3CDS 3' incomplete
ENST00000576383.1GEMIN4-206633189aaENSP00000461368.1
 
Protein coding
I3L4M4 -TSL:3CDS 3' incomplete