Human (GRCh38.p14)
Description

solute carrier family 39 member 7 [Source:HGNC Symbol;Acc:HGNC:4927]

Gene Synonyms

D6S2244E, H2-KE4, HKE4, KE4, RING5, ZIP7

Location

Scaffold HSCHR6_MHC_MCF_CTG1: 4,636,398-4,640,392 forward strand.

GRCh38:GL000254.2

View this gene on the primary assembly.

About this gene

This gene has 6 transcripts (splice variants), 1 gene allele and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000431735.6SLC39A7-2252409469aaENSP00000410656.2
 
Protein coding
A0A024RCX7 Q92504 -Ensembl CanonicalGENCODE basicTSL:1
ENST00000441953.6SLC39A7-2262153469aaENSP00000413027.2
 
Protein coding
A0A024RCX7 Q92504 -GENCODE basicTSL:1
ENST00000414757.5SLC39A7-2241015220aaENSP00000390246.1
 
Protein coding
A2AAT0 -TSL:5CDS 3' incomplete
ENST00000462670.1SLC39A7-2271496No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000468378.1SLC39A7-2281410No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000491795.5SLC39A7-2291105No protein-
 
Protein coding CDS not defined
--TSL:5