Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 1590
HGNC: 2599
Ensembl: ENSG00000204338
Variants:
dbSNP: 1590
ClinVar: 1590
TCGA: ENSG00000204338
COSMIC: CYP21A1P
RNA/Proteins
Expression (GTEx)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 31229653 | 2019 | High-Throughput Screening for CYP21A1P-TNXA/TNXB Chimeric Genes Responsible for Ehlers-Danlos Syndrome in Patients with Congenital Adrenal Hyperplasia. | 17 |
| 31229653 | 2019 | High-Throughput Screening for CYP21A1P-TNXA/TNXB Chimeric Genes Responsible for Ehlers-Danlos Syndrome in Patients with Congenital Adrenal Hyperplasia. | 17 |
| 23313747 | 2013 | Variants of the CYP21A2 and CYP21A1P genes in congenital adrenal hyperplasia. | 3 |
| 23313747 | 2013 | Variants of the CYP21A2 and CYP21A1P genes in congenital adrenal hyperplasia. | 3 |
| 20970527 | 2011 | Chimeric CYP21A1P/CYP21A2 genes identified in Czech patients with congenital adrenal hyperplasia. | 13 |
| 21324303 | 2011 | Analysis of the CYP21A1P pseudogene: indication of mutational diversity and CYP21A2-like and duplicated CYP21A2 genes. | 9 |
| 20970527 | 2011 | Chimeric CYP21A1P/CYP21A2 genes identified in Czech patients with congenital adrenal hyperplasia. | 13 |
| 21324303 | 2011 | Analysis of the CYP21A1P pseudogene: indication of mutational diversity and CYP21A2-like and duplicated CYP21A2 genes. | 9 |
| 19135723 | 2009 | Great genotypic and phenotypic diversities associated with copy-number variations of complement C4 and RP-C4-CYP21-TNX (RCCX) modules: a comparison of Asian-Indian and European American populations. | 22 |
| 19201236 | 2009 | The gene founder effect of two spontaneous mutations in ethnic Chinese (Taiwanese) CAH patients with 21-hydroxylase deficiency. | 1 |
| 19505723 | 2009 | Linkage analysis of the C4A/C4B copy number variation and polymorphisms of the adjacent steroid 21-hydroxylase gene in a healthy population. | 3 |
| 19624807 | 2009 | A new CYP21A1P/CYP21A2 chimeric gene identified in an Italian woman suffering from classical congenital adrenal hyperplasia form. | 14 |
| 19135723 | 2009 | Great genotypic and phenotypic diversities associated with copy-number variations of complement C4 and RP-C4-CYP21-TNX (RCCX) modules: a comparison of Asian-Indian and European American populations. | 22 |
| 19201236 | 2009 | The gene founder effect of two spontaneous mutations in ethnic Chinese (Taiwanese) CAH patients with 21-hydroxylase deficiency. | 1 |
| 19505723 | 2009 | Linkage analysis of the C4A/C4B copy number variation and polymorphisms of the adjacent steroid 21-hydroxylase gene in a healthy population. | 3 |
Citation
Dessen P
CYP21A1P (cytochrome P450 family 21 subfamily A member 1, pseudogene)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/62247/cyp21a1p-(cytochrome-p450-family-21-subfamily-a-member-1-pseudogene)
