Genomics England
GMS Panels
Panels
Genes and Entities

TENM3

teneurin transmembrane protein 3
OMIM: 610083
PanelMode of inheritanceDetails
3 panels
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 5.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Microphthalmia, syndromic 15, OMIM:615145, ?Microphthalmia, isolated, with coloboma 9, OMIM:615145, Microphthalmia, isolated, with coloboma 9, MONDO:0014059
Green
in Intellectual disability
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 8.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Microphthalmia, syndromic 15, OMIM:615145, ?Microphthalmia, isolated, with coloboma 9, OMIM:615145, Microphthalmia, isolated, with coloboma 9, MONDO:0014059
Green
in Structural eye disease
R-numbers: R36
Signed-off version 4.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Microphthalmia, syndromic 15, OMIM:615145, ?Microphthalmia, isolated, with coloboma 9, OMIM:615145, Microphthalmia, isolated, with coloboma 9, MONDO:0014059