Full data view for gene TULP1

This database is one of the "Eye disease" gene variant databases.
Information The variants shown are described using the NM_003322.3 transcript reference sequence.

4 entries on 1 page. Showing entries 1 - 4.
Legend   How to query  

Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+?/. - c.1081C>T r.(?) p.(Arg361*) Maternal (confirmed) - likely pathogenic (recessive) g.35473549G>A g.35505772G>A - - TULP1_000112 - PubMed: Thompson 2017 - - Germline - - - - - DNA SEQ - - retinal disease Fam2175 PubMed: Thompson 2017 family, 2 affected - - Australia - - - - - 2 LOVD
+?/. - c.1081C>T r.(?) p.(Arg361*) Parent #1 - likely pathogenic g.35473549G>A g.35505772G>A TULP1, variant 1: c.1081C>T/p.R361*, variant 2: c.1258C>A/p.R420S - TULP1_000112 solved, compound heterozygous PubMed: Weisschuh 2020 - - Germline yes - - - - DNA SEQ-NG blood RET2 targeted sequencing panel - see paper retinal disease 386 PubMed: Weisschuh 2020 Filing key number: 127, autosomal recessive retinitis pigmentosa, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+?/. - c.1081C>T r.(?) p.(Arg361*) Parent #1 - likely pathogenic g.35473549G>A g.35505772G>A TULP1, variant 1: c.1081C>T/p.R361*, variant 2: c.1258C>A/p.R420S - TULP1_000112 solved, compound heterozygous PubMed: Weisschuh 2020 - - Germline yes - - - - DNA SEQ blood Sanger sequencing retinal disease 387 PubMed: Weisschuh 2020 Filing key number: 127, autosomal recessive retinitis pigmentosa, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
+?/. - c.1081C>T r.(?) p.(Arg361*) Both (homozygous) - likely pathogenic g.35473549G>A g.35505772G>A TULP1 c.1081C>T, p.Arg361* - TULP1_000112 homozygous PubMed: Guo 2015 - - Germline yes - - - - DNA SEQ, SEQ-NG - 135 of the most common LCA-causing variations, followed by sequencing of 61 regions in 14 causative genes in LCA, whole exome sequencing retinal disease II-3 PubMed: Guo 2015 parents first cousins F yes Australia Italian - - - - 1 LOVD
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.