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  2. BRIDGE_SPEED_NEURO_20170705
  3. RUNX2
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BRIDGE_SPEED_NEURO_20170705

Gene: RUNX2

Green List (high evidence)
RUNX2 (runt related transcription factor 2)
EnsemblGeneIds (GRCh38): ENSG00000124813
EnsemblGeneIds (GRCh37): ENSG00000124813
OMIM: 600211, Gene2Phenotype
RUNX2 is in 7 panels

2 reviews

BRIDGE consortium (NIHRBR-RD)

Green List (high evidence)

This is a pertinent gene from the NIHR BioResource - Rare Diseases Study (NIHRBR-RD) BRIDGE Study : SPEED (Specialist Pathology: Evaluating Exomes in Diagnostics) which covers epilepsies, movement and microcephaly disorders, this gene is on the SPEED_NEURO_20170705 gene list. Evidences used for SPEED NEURO gene list: in_ddg2p_20141118_conf;in_ddg2p_20141118_conf;in_ddg2p_201507;in_ddg2p_201507_conf;in_ddg2p_2_4_2017;in_ddg2p_2_4_2017_conf;in_UKGTN_v12 . Main mutation mechanism : Loss of function
Created: 28 Jul 2017, 10:42 a.m.

Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown

Publications

Created: 2 Aug 2017, 6:47 p.m.

Panel version: 0.191

Louise Daugherty (Genomics England Curator)

Comment on phenotypes: corrected format issue
Created: 31 Jul 2017, 2:14 p.m.
Created: 31 Jul 2017, 2:14 p.m.

Panel version: 0.145

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Green
  • BRIDGE study SPEED NEURO Tier1 Gene
Phenotypes
  • Cleidocranial dysplasia, 119600
  • Cleidocranial dysplasia, forme fruste, with brachydactyly, 119600
  • Cleidocranial dysplasia, forme fruste, dental anomalies only, 119600
  • Metaphyseal dysplasia with maxillary hypoplasia with or without brachydactyly, 156510
OMIM
600211
Clinvar variants
Variants in RUNX2
Penetrance
Complete
Panels with this gene

History Filter Activity

31 Jul 2017, Gel status: 4

Set Phenotypes

Louise Daugherty (Genomics England Curator)

Phenotypes for RUNX2 were set to Cleidocranial dysplasia, 119600; Cleidocranial dysplasia, forme fruste, with brachydactyly, 119600; Cleidocranial dysplasia, forme fruste, dental anomalies only, 119600; Metaphyseal dysplasia with maxillary hypoplasia with or without brachydactyly, 156510

27 Jul 2017, Gel status: 0

Created

Louise Daugherty (Genomics England Curator)

RUNX2 was created by LouiseD

27 Jul 2017, Gel status: 4

Added New Source

Louise Daugherty (Genomics England Curator)

RUNX2 was added to BRIDGE_SPEED_NEURO_20170705panel. Sources: BRIDGE study SPEED NEURO Tier1 Gene,Expert Review Green