STEAP3 (STEAP3 metalloreductase)
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Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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55240 |
Gene nameGene Name - the full gene name approved by the HGNC.
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STEAP3 metalloreductase |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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STEAP3 |
SynonymsGene synonyms aliases
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AHMIO2, STMP3, TSAP6, dudlin-2, dudulin-2, pHyde |
ChromosomeChromosome number
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2 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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2q14.2 |
SummarySummary of gene provided in NCBI Entrez Gene.
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This gene encodes a multipass membrane protein that functions as an iron transporter. The encoded protein can reduce both iron (Fe3+) and copper (Cu2+) cations. This protein may mediate downstream responses to p53, including promoting apoptosis. Deficienc |
miRNAmiRNA information provided by mirtarbase database.
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
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UniProt ID |
Q658P3 |
Protein name |
Metalloreductase STEAP3 (EC 1.16.1.-) (Dudulin-2) (Six-transmembrane epithelial antigen of prostate 3) (Tumor suppressor-activated pathway protein 6) (hTSAP6) (pHyde) (hpHyde) |
Protein function |
Integral membrane protein that functions as a NADPH-dependent ferric-chelate reductase, using NADPH from one side of the membrane to reduce a Fe(3+) chelate that is bound on the other side of the membrane (PubMed:26205815). Mediates sequential t |
PDB |
2VNS
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2VQ3
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Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF03807 |
F420_oxidored |
30 → 117 |
NADP oxidoreductase coenzyme F420-dependent |
Family |
PF01794 |
Ferric_reduct |
259 → 406 |
Ferric reductase like transmembrane component |
Family |
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Sequence |
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Sequence length |
488 |
Interactions |
View interactions |
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
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Associated diseases
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Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Anemia |
Anemia, Anemia, Hypochromic Microcytic, With Iron Overload, ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 2 |
rs118204044, rs118204045, rs118204046, rs121918330, rs869320719, rs869312029, rs121918332, rs869320724, rs767094129, rs786205058, rs786205059, rs137853119, rs137853120, rs137853121, rs1384933966, rs137853122, rs137853123, rs786205060, rs267607121, rs121908584, rs80338697, rs80338699, rs120074166, rs120074167, rs1050828, rs74575103, rs137852314, rs5030868, rs137852316, rs137852317, rs137852318, rs137852319, rs137852320, rs137852321, rs137852322, rs137852323, rs137852324, rs72554665, rs387906468, rs5030872, rs137852326, rs137852333, rs137852327, rs137852328, rs137852329, rs137852330, rs137852331, rs137852332, rs137852334, rs137852335, rs137852336, rs137852339, rs76645461, rs137852340, rs137852341, rs78478128, rs137852343, rs137852344, rs137852345, rs587776730, rs137852346, rs137852347, rs137852349, rs2070404412, rs2070350038, rs2070350009, rs137852303, rs137852304, rs33946267, rs34378160, rs33933298, rs11549407, rs35724775, rs34598529, rs41469945, rs267607201, rs80338694, rs80338696, rs387907018, rs398123546, rs78365220, rs587777100, rs587777101, rs483352840, rs869312752, rs765487627, rs1557229599, rs1557230040, rs1555524842, rs782090947, rs1358275550, rs1557229736, rs1557230573, rs1556323334, rs1233124208, rs1293528130, rs146864395, rs1595503440, rs1603411214, rs137852325, rs1575247302, rs1603411177, rs1336651679, rs782322505 |
22031863 |
Azoospermia |
Azoospermia |
rs200969445, rs144567652, rs765353898 |
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Hypothyroidism |
Hypothyroidism |
rs869320723, rs121908862, rs121908863, rs121908865, rs121908866, rs121908867, rs121908870, rs121908871, rs121908872, rs2140110277, rs121908881, rs121908884, rs121908885, rs786205080, rs1586182912, rs121917847, rs104893655, rs104893657, rs104893658, rs104893659, rs104893660, rs104893656, rs121917719, rs786204790, rs189261858, rs879255608, rs868197660, rs879255609, rs1586744173, rs1586182837, rs771222349, rs1587618417, rs1601844140, rs760832986, rs780982673, rs1603336347, rs1691155605 |
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Renal carcinoma |
Renal Cell Carcinoma |
rs121913668, rs121913670, rs121913243, rs786202724 |
31231134 |
Severe congenital hypochromic anemia with ringed sideroblasts |
Severe congenital hypochromic anemia with ringed sideroblasts |
rs587776963 |
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Dysplastic erythropoesis |
Dysplastic erythropoesis |
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Hypochromic anemia |
Hypochromic anemia |
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Hypogonadism |
Hypogonadism |
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