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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_COX_CTG1: 4,611,950-4,615,944 forward strand.

GRCh38:GL000251.2

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
ENST00000418477.6SLC39A7-2322409469aaENSP00000416439.2
 
Protein coding
A0A024RCX7 Q92504 -Ensembl CanonicalGENCODE PrimaryGENCODE BasicTSL:1
ENST00000423043.6SLC39A7-2332153469aaENSP00000389623.2
 
Protein coding
A0A024RCX7 Q92504 -GENCODE BasicTSL:1
ENST00000429042.5SLC39A7-2341015220aaENSP00000404101.1
 
Protein coding
A2AAT0 -TSL:5CDS 3' incomplete
ENST00000486338.5SLC39A7-2371496No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000474514.1SLC39A7-2361410No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000465516.1SLC39A7-2351105No protein-
 
Protein coding CDS not defined
--TSL:5