Genes in panel

Likely inborn error of metabolism - targeted testing not possible

Gene: MCCC2

Green List (high evidence)

MCCC2 (methylcrotonoyl-CoA carboxylase 2)
EnsemblGeneIds (GRCh38): ENSG00000131844
EnsemblGeneIds (GRCh37): ENSG00000131844
OMIM: 609014, Gene2Phenotype
MCCC2 is in 8 panels

1 review

Sarah Leigh (Genomics England Curator)

Comment when marking as ready: Associated with phenotype in OMIM and as a confirmed Developmental Disorder Gene / G2P. At least 10 variants reported.
Created: 17 Jan 2017, 10:12 a.m.
Amber review assigned as this gene is Green on the V1 panel(s) named as a phenotype(s)
Created: 6 Jan 2017, 1:59 p.m.

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Intellectual disability


Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
  • London North GLH
  • Expert Review Green
  • 3-Methylcrotonyl-CoA carboxylase 2 deficiency, 210210
Clinvar variants
Variants in MCCC2
Panels with this gene

History Filter Activity

13 Feb 2019, Gel status: 4

Added New Source, Added New Source

Ivone Leong (Genomics England Curator)

Source NHS GMS was added to MCCC2. Source London North GLH was added to MCCC2.

9 Jan 2019, Gel status: 4

Set Phenotypes

Louise Daugherty (Genomics England Curator)

Phenotypes for gene: MCCC2 were changed from to 3-Methylcrotonyl-CoA carboxylase 2 deficiency, 210210

8 Jan 2019, Gel status: 4

Panel promoted to version 1.0

Ellen McDonagh (Genomics England Curator)

Ellen McDonagh: Comment on mode of pathogenici

16 Dec 2018, Gel status: 4

Created, Added New Source, Set mode of inheritance, Set publications

Ellen McDonagh (Genomics England Curator)

gene: MCCC2 was added gene: MCCC2 was added to Inborn errors of metabolism. Sources: Expert Review Green Mode of inheritance for gene: MCCC2 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: MCCC2 were set to 27604308