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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_QBL_CTG1: 4,394,849-4,398,843 forward strand.

GRCh38:GL000255.2

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
ENST00000383213.8SLC39A7-2202409469aaENSP00000372700.4
 
Protein coding
A0A024RCX7 Q92504 -Ensembl CanonicalGENCODE PrimaryGENCODE BasicTSL:1
ENST00000383214.8SLC39A7-2212153469aaENSP00000372701.4
 
Protein coding
A0A024RCX7 Q92504 -GENCODE BasicTSL:1
ENST00000414916.5SLC39A7-2221015220aaENSP00000416566.1
 
Protein coding
A2AAT0 -TSL:5CDS 3' incomplete
ENST00000486373.5SLC39A7-2241496No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000491702.1SLC39A7-2251105No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000478834.1SLC39A7-2231410No protein-
 
Retained intron
--TSL:2