SMCHD1

Summary

SMCHD1 is a gene^[1].

Key Facts

• SMCHD1's instance of is recorded as gene^[2].
• SMCHD1 is a type of protein-coding gene^[3].
• SMCHD1's HomoloGene ID is recorded as 23665^[4].
• SMCHD1's genomic start is recorded as 2655737^[5].
• SMCHD1's genomic start is recorded as 2655726^[6].
• SMCHD1's genomic end is recorded as 2805017^[7].
• SMCHD1's genomic end is recorded as 2805015^[8].
• SMCHD1's ortholog is recorded as Smchd1^[9].
• SMCHD1's ortholog is recorded as Smchd1^[10].
• SMCHD1's ortholog is recorded as smchd1^[11].
• SMCHD1's encodes is recorded as Structural maintenance of chromosomes flexible hinge domain containing 1^[12].
• SMCHD1's found in taxon is recorded as Homo sapiens^[13].
• SMCHD1's chromosome is recorded as human chromosome 18^[14].
• SMCHD1's genetic association is recorded as BOSMA Arhinia Microphthalmia Syndrome^[15].
• SMCHD1's genetic association is recorded as Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome^[16].
• SMCHD1's genetic association is recorded as facioscapulohumeral muscular dystrophy^[17].
• SMCHD1's strand orientation is recorded as forward strand^[18].
• SMCHD1's exact match is recorded as http://identifiers.org/ncbigene/23347^[19].
• SMCHD1's cytogenetic location is recorded as 18p11.32^[20].
• SMCHD1's expressed in is recorded as Achilles tendon^[21].
• SMCHD1's expressed in is recorded as epithelium of colon^[22].
• SMCHD1's expressed in is recorded as blood^[23].
• SMCHD1's expressed in is recorded as bone marrow cell^[24].
• SMCHD1's expressed in is recorded as monocyte^[25].
• SMCHD1's expressed in is recorded as superficial temporal artery^[26].