UCSF Pharmacogenetics of Membrane Transporters
Gene View
Common Name:KE4
HGNC Symbol:SLC39A7
HGNC Description:solute carrier family 39 (zinc transporter), member 7
HGNC ID:4927
Superfamily:SLC
Chromosome:Chr.6(+): 33168603-33172214 GRCh37
Location:6p21.3
OMIM:601416
OMIM Phenotype:None
Accessions:AF117221
Nucleotide RefSeq:NM_001077516
Protein RefSeq:NP_001070984
Entrez:7922
Ensembl:ENSG00000112473
Isoforms:8
Evidence:None
Tissues:None
Type:protein-coding
Sets:0
PharmGKB ID:PA29305
HPRD ID:09028
Substrates:None
Trivial Names:KE4, HKE4, ZIP7, RING5, H2-KE4, D6S115E, D6S2244E
Transcripts:NM_001077516.1 [Chr.6(+): 33168603-33172214 GRCh37]
NM_006979.2 [Chr.6(+): 33168603-33172214 GRCh37]
XM_005249406.1 [Chr.6(+): 33168649-33172214 GRCh37]
XM_005272892.1 [Chr.6(+): 4612483-4616048 GRCh37]
XM_005275047.1 [Chr.6(+): 4449956-4453521 GRCh37]
XM_005275182.1 [Chr.6(+): 4625965-4629530 GRCh37]
XM_005275305.1 [Chr.6(+): 4642410-4645975 GRCh37]
XM_005275477.1 [Chr.6(+): 4400864-4404437 GRCh37]
ENST00000374675 [Chr.6(+): 33168603-33172216 GRCh37]
ENST00000374677 [Chr.6(+): 33168650-33172216 GRCh37]
ENST00000444757 [Chr.6(+): 33168222-33170469 GRCh37]
ENST00000463972 [Chr.6(+): 33170032-33172216 GRCh37]

GTEx Expression by Gene and Transcript

The heat map summarizes relative expression by tissue type at two levels of tissue detail, e.g., 'Brain' and 'Brain - Amygdala'. Choose among four calculated expression values, including mean and median RPKM values, and quantile normalized (QN) distributions of these values. (Note that differences between some distributions are subtle.) The coloring is relative to the mean of all displayed values. All values are log base 2. (See also PMT GTEx Expression Plotting.) Click on a transcript or tissue to resort the data.

Tissues:
Expression values:
No expression data exists for SLC39A7.

Variant Data

View all PMT variants for SLC39A7 on UCSC Genome Browser
Showing SNP features for transcript:   
1000 Genomes  

20141104 phase 3 variant call set of the 20130502 sequence freeze and alignments for SNPs and short indels (indels > 255 and structural variants are not included here). This variant set contains 2504 individuals from 26 populations (mouse over population column heading for population sizes).
Showing gene variants in regions defined by NCBI RefSeq exons, putative promoter, and PMT resequencing assays.
Note: Frequencies are calculated directly from reported genotypes and may vary from consensus frequencies reported by the 1000 Genomes project, which relied on additional data and the GATK tool Variant Quality Score Recalibrator.
dbSNP build 142.
Array availability: I - found on Illumina Human1M-Duo BeadChip (2011-04-21)  A - found on Affymetrix Genome-Wide SNP Array 6.0 (2011-06-21)  
Download the SNP table data as a tab-delimited file.

Transmembrane prediction: TOPO2 image is not available.