Gene entry
SHROOM4
shroom family member 4
- Chromosome
- X
- Cytoband
- Xp11.22
- Variants (rsID)
- 48
SHROOM4 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xp11.22). Its official name is “shroom family member 4”. The reference table lists 48 variants (rsID) for this gene.
Clinically classified variants
6 reference-table entries with clinical significance.
- rs111940781Benignsingle nucleotide variantHistory of neurodevelopmental disorder
- rs144727288Benignsingle nucleotide variantX-linked intellectual disability, Stocco dos Santos type
- rs148911180Benignsingle nucleotide variantHistory of neurodevelopmental disorder
- rs28362302Benignsingle nucleotide variantHistory of neurodevelopmental disorder
- rs189694750Conflicting interpretationssingle nucleotide variantX-linked intellectual disability, Stocco dos Santos type
- rs142052951Uncertain significancesingle nucleotide variantHistory of neurodevelopmental disorder
Other listed variants
- rs749193
- rs911089
- rs911090
- rs955368
- rs1474968
- rs2103996
- rs2153529
- rs2281571
- rs2295544
- rs2316200
- rs4074811
- rs4826619
- rs5915275
- rs5915279
- rs5915284
- rs5915291
- rs5915293
- rs5915304
- rs5915310
- rs5915313
- rs5915314
- rs5961149
- rs5961199
- rs5961202
- rs6521882
- rs7051751
- rs7058894
- rs9887134
- rs9887724
- rs12834851
- rs17281496
- rs17315269
- rs28362300
- rs28362303
- rs112386248
- rs146699010
- rs147825273
- rs147980063
- rs185285900
- rs200066869
- rs200079497
- rs201801889
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.