Genomics England
GMS Panels
Panels
Genes and Entities
RSRC1
arginine and serine rich coiled-coil 1
OMIM:
613352
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Panel
Mode of inheritance
Details
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Intellectual disability - microarray and sequencing
Component of the following Super Panels:
- Childhood onset leukodystrophy
- Hypotonic infant
- Paediatric disorders
R-numbers:
R29
Signed-off version 5.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Intellectual developmental disorder, autosomal recessive 70 618402