Gene entry
CNTLN
centlein
- Chromosome
- 9
- Cytoband
- 9p22.2
- Variants (rsID)
- 63
CNTLN is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9p22.2). Its official name is “centlein”. The reference table lists 63 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs144166918Not classifiedmissense_variant
Other listed variants
- rs1160340
- rs1442514
- rs2145665
- rs2180903
- rs2197153
- rs2208488
- rs2248136
- rs2441995
- rs2441998
- rs2593382
- rs2754322
- rs3808782
- rs3808794
- rs3824393
- rs4961441
- rs4961534
- rs7866391
- rs7874426
- rs10121841
- rs10756885
- rs10810790
- rs10962914
- rs10963050
- rs10963072
- rs10963115
- rs10963119
- rs16935412
- rs17827290
- rs41303219
- rs71504855
- rs73414434
- rs75161660
- rs75732155
- rs75938007
- rs78273820
- rs79402320
- rs79692494
- rs79693262
- rs111619383
- rs112351052
- rs113101231
- rs117027046
- rs117086232
- rs117098120
- rs117289052
- rs117358426
- rs117586320
- rs117859318
- rs117877396
- rs118064288
- rs143643420
- rs149916783
- rs150204922
- rs151228950
- rs183127118
- rs184852991
- rs187296474
- rs199893965
- rs200069430
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.