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_MANN_CTG1: 4,619,918-4,623,912 forward strand.

GRCh38:GL000253.2

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
ENST00000456261.6SLC39A7-2382409469aaENSP00000414145.2
 
Protein coding
A0A024RCX7 Q92504 -Ensembl CanonicalGENCODE basicTSL:1
ENST00000443773.6SLC39A7-2372153469aaENSP00000407093.2
 
Protein coding
A0A024RCX7 Q92504 -GENCODE basicTSL:1
ENST00000425069.5SLC39A7-2361015220aaENSP00000411819.1
 
Protein coding
A2AAT0 -TSL:5CDS 3' incomplete
ENST00000487655.1SLC39A7-2401496No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000460361.1SLC39A7-2391410No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000493496.5SLC39A7-2411105No protein-
 
Protein coding CDS not defined
--TSL:5