PanelApp
  1. Genes and Genomic Entities
  2. TTC37

TTC37

tetratricopeptide repeat domain 37
OMIM: 614589, Gene2Phenotype

16 panels

Panel Reviews Mode of inheritance Details
16 panels

Green TTC37 in Vasculitis


Level 2: Immunological disorders
Version 0.93

0 reviews Unknown
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green

Red TTC37 in Cataract


Level 2: Ophthalmological disorders
Version 0.375

1 review Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services

Green TTC37 in Congenital Diarrhoea


Level 2: Gastroenterological disorders
Version 1.23

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Trichohepatoenteric syndrome 1, MIM# 222470

Green TTC37 in Inflammatory bowel disease


Level 2: Gastroenterological disorders
Version 0.126

Component of the following Super Panels:

  • Immunological disorders_SuperPanel

    		•  1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Trichohepatoenteric syndrome 1, MIM#222470
    • Colitis
    • Pancolitis
    • Inflammatory bowel disease-like phenotype
    • Very Early Onset Inflammatory Bowel Disease

    Green TTC37 in Mendeliome


    Version 1.3512

    		2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Trichohepatoenteric syndrome 1, MIM# 222470

    Green TTC37 in Predominantly Antibody Deficiency


    Level 2: Immunological disorders
    Version 1.4

    Component of the following Super Panels:

  • Immunological disorders_SuperPanel

    		•  1 review Unknown
    Sources
    • Expert Review Green
    • Melbourne Genomics Health Alliance Immunology Flagship
    • Victorian Clinical Genetics Services
    • Melbourne Genomics Health Alliance Immunology Flagship
    • Victorian Clinical Genetics Services
    • Expert Review Green

    Green TTC37 in Combined Immunodeficiency


    Level 2: Immunological disorders
    Version 1.138

    Component of the following Super Panels:

  • Immunological disorders_SuperPanel

    		•  1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Trichohepatoenteric syndrome 1, MIM# 222470
    • Respiratory infections
    • IUGR
    • Facial dysmorphic features
    • Wooly hair:Early-onset intractable diarrhoea
    • Liver cirrhosis
    • Platelet abnormalities

    Green TTC37 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.410

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Genetic Health Queensland
    Phenotypes
    • trichohepatoenteric syndrome 1 MONDO:0024541

    Green TTC37 in Mackenzie's Mission_Reproductive Carrier Screening


    Level 2: Screening
    Version 0.110

    		0 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Trichohepatoenteric syndrome 1, 222470 (3)

    Green TTC37 in Hair disorders


    Level 2: Dermatological disorders
    Version 0.81

    		2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert Review
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Trichohepatoenteric syndrome 1, MIM#222470

    Green TTC37 in Additional findings_Paediatric


    Level 2: Screening
    Version 0.278

    		0 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • BabySeq Category A gene
    • Expert Review Green
    Phenotypes
    • Trichohepatoenteric syndrome

    Green TTC37 in Liver Failure_Paediatric


    Level 2: Gastroenterological disorders
    Version 1.30

    Component of the following Super Panels:

  • Liverome Superpanel

    		•  1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Trichohepatoenteric syndrome 1, MIM# 222470

    Red TTC37 in Fetal anomalies


    Version 1.465

    		2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Genomics England PanelApp
    Phenotypes
    • Trichohepatoenteric syndrome 1, MIM# 222470

    Green TTC37 in Prepair 1000+


    Level 2: Screening
    Version 2.14

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Trichohepatoenteric syndrome 1 MIM#222470

    Red TTC37 in Genomic newborn screening: BabyScreen+


    Level 2: Screening
    Version 1.140

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • BabySeq Category A gene
    Phenotypes
    • Trichohepatoenteric syndrome 1, MIM#222470

    Green TTC37 in Prepair 500+


    Level 2: Screening
    Version 2.0

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Trichohepatoenteric syndrome 1 MIM#222470