MIPOL1

MIPOL1
Identifiers
Aliases	MIPOL1, CCDC193, mirror-image polydactyly 1
External IDs	OMIM: 606850; MGI: 1920740; HomoloGene: 16340; GeneCards: MIPOL1; OMA:MIPOL1 - orthologs
Gene location (Human)
Chr.	Chromosome 14 (human)
End	37,552,361 bp
Gene location (Mouse)
Chr.	Chromosome 12 (mouse)
End	57,543,985 bp
RNA expression pattern
	Top expressed in
	Achilles tendon; ; testicle; ; sural nerve; ; epithelium of colon; ; left testis; ; gonad; ; right testis; ; popliteal artery; ; tibial arteries; ; ventricular zone;
	Top expressed in
	lumbar spinal ganglion; ; genital tubercle; ; tail of embryo; ; lumbar subsegment of spinal cord; ; transitional epithelium of urinary bladder; ; spermatid; ; zygote; ; embryo; ; ventricular zone; ; embryo;
	More reference expression data
	n/a
Orthologs
	145282
	73490
	ENSG00000151338
	ENSMUSG00000047022
	Q8TD10; Q4G0U7
	Q9D9F8
NM_001195296; NM_001195297; NM_138731; NM_001388067; NM_001388068;
	NM_001388069; NM_001388070; NM_001388071; NM_001388072; NM_001388073; NM_001388074; NM_001388075; NM_001388077
	NM_001164370
	NP_001182225; NP_001182226; NP_620059; NP_001182226.1; NP_620059.1
	n/a
	Wikidata
View/Edit Human	View/Edit Mouse

MIPOL1 (Mirror Image Polydactyly 1), also known as CCDC193 (Coiled-coil domain containing 193), is a protein that in humans is encoded by the MIPOL1 gene. Mutation of this gene is associated with mirror-image polydactyly (also known as Laurin-Sandrow syndrome.) in humans, which is a rare genetic condition characterized by mirror-image duplication of digits.