Gene entry
MYT1L
myelin transcription factor 1 like
- Chromosome
- 2
- Cytoband
- 2p25.3
- Variants (rsID)
- 146
MYT1L is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2p25.3). Its official name is “myelin transcription factor 1 like”. The reference table lists 146 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs869320675Pathogenicsingle nucleotide variantIntellectual disability, autosomal dominant 39
Other listed variants
- rs891878
- rs891879
- rs919718
- rs1368233
- rs1862113
- rs1978703
- rs2042142
- rs2241685
- rs2668831
- rs3748985
- rs3748986
- rs4344956
- rs4473412
- rs4621187
- rs4853946
- rs4853947
- rs6548054
- rs6548123
- rs6709211
- rs6710116
- rs6721182
- rs6728613
- rs6737578
- rs6755567
- rs7580137
- rs7582260
- rs7592630
- rs7596980
- rs9808135
- rs9973708
- rs10153948
- rs10175467
- rs10181980
- rs10185662
- rs10190125
- rs10191292
- rs10495486
- rs11127292
- rs11681135
- rs11685526
- rs11690181
- rs11887279
- rs11888121
- rs11893101
- rs12052817
- rs12474490
- rs12998803
- rs13006826
- rs13034507
- rs13382326
- rs13389557
- rs13404264
- rs13414323
- rs13419681
- rs17039334
- rs17039361
- rs17039365
- rs17039395
- rs17039400
- rs17039421
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.
