CXorf67
Protein-coding gene in humans
From Wikipedia, the free encyclopedia
Uncharacterized protein CXorf67 is a protein that in humans is encoded by the CXorf67 gene. The Accession Number for the human gene is NM_203407.[3] Aliases include MGC47837 and LOC340602.[4] The gene is located on the positive strand of the X chromosome at Xp11.22.[4] The mRNA is 1939 base pairs long and contains 1 exon and no introns.[5]
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| Aliases | EZHIP, chromosome X open reading frame 67, CXorf67, EZH inhibitory protein, KIP75, CATACOMB | ||||||||||||||||||||||||||||||||||||||||||||||||||
| External IDs | GeneCards: EZHIP; OMA:EZHIP - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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Expression
![](#/media/File:"Expression_of_CXorf67_during_human_preimplantation_embryonic_development".png)
Expression of CXorf67 in humans is generally low in all tissues. Higher RNA expression has been reported in the testis and placenta and relatively higher nuclear protein expression has been observed in the placenta, testis and ovarian follicles.[6]
Protein
The translated human CXorf67 protein is 503 amino acids in length.[5] The protein has a molecular weight of 51.9 kdal and an isoelectric point of 10.432[7]
Interactions
Protein interaction of CXorf67 with UBC (polyubiquitin-C) in humans was identified using a two-hybrid screening.[8] Currently no other protein interactions have been identified in humans.