Transferrin receptor 2

Mammalian protein found in Homo sapiens From Wikipedia, the free encyclopedia

Transferrin receptor 2 (TfR2) is a protein that in humans is encoded by the TFR2 gene.[5][6] This protein is involved in the uptake of transferrin-bound iron into cells by endocytosis, although its role is minor compared to transferrin receptor 1.

AliasesTFR2, HFE3, TFRC2, transferrin receptor 2
End100,642,779 bp[1]
Quick facts TFR2, Identifiers ...
TFR2
Identifiers
AliasesTFR2, HFE3, TFRC2, transferrin receptor 2
External IDsOMIM: 604720; MGI: 1354956; HomoloGene: 2428; GeneCards: TFR2; OMA:TFR2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001206855
NM_003227

NM_001289507
NM_001289509
NM_001289511
NM_015799
NM_001359206

RefSeq (protein)

NP_001193784
NP_003218

NP_001276436
NP_001276438
NP_001276440
NP_056614
NP_001346135

Location (UCSC)Chr 7: 100.62 – 100.64 MbChr 5: 137.57 – 137.59 Mb
PubMed search[3][4]
Wikidata
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Function

This gene is a member of the transferrin receptor-like family and encodes a single-pass type II membrane protein with a protease associated (PA) domain, an M28 peptidase domain and a transferrin receptor-like dimerization domain. This protein mediates cellular uptake of transferrin-bound iron and mutations in this gene have been associated with hereditary hemochromatosis type III. Alternatively spliced variants which encode different protein isoforms have been described; however, not all variants have been fully characterized.[7]

See also

References

Further reading

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