TTC21B Products

Bioinformatics

Entrez	79809 Human
Uniprot	NP_079029 Human Q7Z4L5 Human
Product By Gene ID	79809
Alternate Names	ATD4 THM1 KIAA1992 tetratricopeptide repeat protein 21B JBTS11 TPR repeat protein 21B putative protein product of Nbla10696 tetratricopeptide repeat domain 21B

Diseases related to TTC21B

Discover more about diseases related to TTC21B.

Retinal Degeneration
Jeune Thoracic Dystrophy
Bardet-biedl Syndrome
Nephronophthisis
Kidney Diseases
Renal Dysplasia And Retinal Aplasia (disorder)
Familial Aplasia Of The Vermis
Nystagmus
Dysostoses
Curry-hall Syndrome
Meckel-gruber Syndrome
Complete Hearing Loss
Glioblastoma
Chronic Eosinophilic Leukemia
Cystic Kidney Diseases
Dystrophy
Short Rib-polydactyly Syndrome, Majewski Type
Usher Syndrome
Ciliary Motility Disorders

Pathways for TTC21B

View related products by pathway and learn more about each of the pathways below.

Transport
Intraflagellar Transport
Brain Development
Forebrain Development

Bioinformatics Tool for TTC21B

Discover related pathways, diseases and genes to TTC21B. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.