|Official Full Name||family with sequence similarity 161, member A|
|Background||This gene belongs to the FAM161 family. It is expressed mainly in the retina. Mouse studies suggested that this gene is involved in development of retinal progenitors during embryogenesis, and that its activity is restricted to mature photoreceptors after birth. Mutations in this gene cause autosomal recessive retinitis pigmentosa-28. Alternatively spliced transcript variants have been identified.|
|Synonyms||FAM161A; family with sequence similarity 161, member A; retinitis pigmentosa 28 (autosomal recessive) , RP28; protein FAM161A; FLJ13305; retinitis pigmentosa 28 (autosomal recessive); RP28; MGC129982; MGC129983|
|Species||Cat.#||Product name||Source (Host)||Tag||Protein Length||Price|
FAM161A involved in several pathways and played different roles in them. We selected most pathways FAM161A participated on our site, such as , which may be useful for your reference. Also, other proteins which involved in the same pathway with FAM161A were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.
|Pathway Name||Pathway Related Protein|
FAM161A has several biochemical functions, for example, protein binding. Some of the functions are cooperated with other proteins, some of the functions could acted by FAM161A itself. We selected most functions FAM161A had, and list some proteins which have the same functions with FAM161A. You can find most of the proteins on our site.
|protein binding||DVL2; PHF15; NAA11; C1QTNF1; NUDC; SEPSECS; EEF1B2; XPO5; TRIM6; CENPK|
FAM161A has direct interactions with proteins and molecules. Those interactions were detected by several methods such as yeast two hybrid, co-IP, pull-down and so on. We selected proteins and molecules interacted with FAM161A here. Most of them are supplied by our site. Hope this information will be useful for your research of FAM161A.
CCDC102B; FSD2; EHMT2; CADPS; 80125