| ANKH | 
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| Identifiers | 
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| Aliases | ANKH, ANK, CCAL2, CMDJ, CPPDD, HANK, MANK, ANKH inorganic pyrophosphate transport regulator, SLC62A1 | 
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| External IDs | OMIM: 605145; MGI: 3045421; HomoloGene: 10664; GeneCards: ANKH; OMA:ANKH - orthologs | 
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| | Gene location (Mouse) | 
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 |  |  | Chr. | Chromosome 15 (mouse) | 
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 |  |  | Band | 15 B1|15 10.23 cM | Start | 27,466,763 bp | 
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 | End | 27,594,995 bp | 
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| | RNA expression pattern | 
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 | Bgee | | Human | Mouse (ortholog) | 
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 | | Top expressed in |  | tibia
 parotid gland
 inferior ganglion of vagus nerve
 Pons
 right ventricle
 Skeletal muscle tissue of biceps brachii
 subthalamic nucleus
 synovial joint
 superior vestibular nucleus
 Skeletal muscle tissue of rectus abdominis
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 | | Top expressed in |  | seminal vesicula
 right ventricle
 digastric muscle
 ankle
 temporal muscle
 lip
 muscle of thigh
 sternocleidomastoid muscle
 triceps brachii muscle
 deep cerebellar nuclei
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 |  | More reference expression data | 
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 | BioGPS |  | 
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| Wikidata | 
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Progressive ankylosis protein homolog (ANK ilosis H omolog) is a protein that in humans is encoded by the ANKH gene.
This gene encodes a multipass transmembrane protein that is expressed in joints and other tissues and controls pyrophosphate levels in cultured cells. Mutation at the mouse 'progressive ankylosis' (ank) locus causes a generalized, progressive form of arthritis accompanied by mineral deposition, formation of bony outgrowths, and joint destruction. The human homolog is virtually identical to the mouse protein and ANKH-mediated control of pyrophosphate levels has been suggested as a possible mechanism regulating tissue calcification and susceptibility to arthritis in higher animals.