Ttc21b omim
WebFeb 18, 2024 · Title: A homozygous missense mutation in the ciliary gene TTC21B causes familial FSGS. TTC21B contributes pathogenic alleles to approximately 5% of ciliopathy cases. Our data illustrate how genetic lesions can be both causally associated with diverse ciliopathies and interact in trans with other disease-causing genes. WebJan 30, 2024 · Tubulointerstitial kidney diseaseGene: TTC21B. Green List (high evidence) TTC21B (tetratricopeptide repeat domain 21B) EnsemblGeneIds (GRCh38): …
Ttc21b omim
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Webttc21b ID ZDB-GENE-031010-34 Name tetratricopeptide repeat domain 21B Symbol ttc21b Nomenclature History Previous Names. sb:cb947; Type protein_coding_gene ... OMIM … WebJan 23, 2011 · Nicholas Katsanis and colleagues show that biallelic mutations in TTC21B, encoding the retrograde intraflagellar transport protein IFT139, are associated with diverse ciliopathy phenotypes in humans.
WebMar 4, 2024 · TTC21B mutation is associated with glomerular and cystic kidney diseases. Exome sequencing and further CRB2 analysis revealed that both siblings are compound … WebSep 26, 2016 · The variant found in TTC21B gene in the R98-443 case could also act as a modifier of the phenotype 19 although the high frequency of this variant in the population makes it unlikely.
WebTTC21B 199 tests. Also known as: ATD4, CFAP60, FAP60, FLA17, IFT139, IFT139B, JBTS11, NPHP12, Nbla10696, SRTD4, THM1, TTC21B ... (HPO) and OMIM. For more information about the disease, please go to the disease information page. Imported from Human Phenotype Ontology (HPO) Show all Hide all. Abnormality of the genitourinary system. WebNM_024753.5(TTC21B):c.2758-2A>G AND Nephronophthisis 12 Clinical significance: Pathogenic (Last evaluated: Mar 1, 2011) Review status: (0/4) 0 stars out of maximum of 4 stars
WebJul 2, 2024 · OMIM 612014 Clinvar variants Variants in TTC21B Penetrance None Panels with this gene. Limb disorders Severe Paediatric Disorders Tubulointerstitial kidney disease Unexplained kidney failure in young people Structural eye disease Skeletal dysplasia Glaucoma (developmental) Skeletal ciliopathies Childhood onset dystonia, chorea or …
WebMalaCards based summary: Nephronophthisis 12, also known as joubert syndrome 11, is related to end stage renal disease and ciliopathy. An important gene associated with Nephronophthisis 12 is TTC21B (Tetratricopeptide Repeat Domain 21B), and among its related pathways/superpathways are Signaling by Hedgehog and Organelle biogenesis … how to setup viteWebMar 21, 2024 · GeneCards Summary for TTC21B Gene. TTC21B (Tetratricopeptide Repeat Domain 21B) is a Protein Coding gene. Diseases associated with TTC21B include … how to setup virtual desktop quest 2WebDiscover Ttc21b's significant phenotypes, expression, images, histopathology and more. Data for gene Ttc21b is all freely available for download. Cite IMPC; Help; IMPC Cloud; ... OMIM:263630: Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 13: how to setup obs to stream twitchWebFeb 17, 2015 · TETRATRICOPEPTIDE REPEAT DOMAIN-CONTAINING PROTEIN 21B; TTC21B (OMIM - 612014) Genes & Proteins . Cytoplasmic dynein 2 intermediate chain 1 (UniProt - Q8WVS4) Similar Articles . To arrive at the top five similar articles we use a word-weighted algorithm to compare words from the Title and Abstract of each citation. how to setup incognito switchWebTTC21B - Explore an overview of TTC21B, with a histogram displaying coding mutations, ... OMIM 612014 Transcript ENST00000243344.7 Genome Browsers Ensembl, UCSC Copy Number CONAN NCBI Entrez Gene 79809 CCDS CCDS33315.1 UniProt Q7Z4L5 Pfam Q7Z4L5 Atlas Genetic Oncology n/a HGNC 25660. Drug resistance. how to setup wifi on tvWebMay 6, 2024 · TTC21B:tetratricopeptide repeat domain 21B [Gene - OMIM - HGNC] Variant type: single nucleotide variant Cytogenetic location: 2q24.3 Genomic location: Chr2: 165884002 (on Assembly GRCh38) Chr2: 166740512 (on Assembly GRCh37) Preferred name: NM_024753.5(TTC21B):c.3476C>T (p.Ala1159Val) how to setup vscode for salesforceWebNephronophthisis-20 is an autosomal recessive tubulointerstitial nephritis characterized by progressive renal fibrosis resulting in end-stage renal failure. The age at onset is relatively … how to setup wifi extender netgear