|
Gene id |
260294 |
| Gene Summary Diseases PubMed |
Gene Summary
|
|
Gene Symbol |
NSUN5P2 Gene UCSC Ensembl |
|
Aliases |
NOL1R2, NSUN5C, WBSCR20B, WBSCR20C |
|
Gene name |
NSUN5 pseudogene 2 |
|
Alternate names |
NOL1/NOP2/Sun domain family, member 5C, NOP2/Sun RNA methyltransferase family member 5 pseudogene 2, NOP2/Sun domain family, member 5 pseudogene 2, NOP2/Sun domain family, member 5C (pseudogene), Williams Beuren syndrome chromosome region 20C, |
|
Gene location |
7q11.23 (72954762: 72948292) Exons: 11 NC_000007.14
|
|
Gene summary(Entrez) |
This locus represents a transcribed pseudogene of a nearby locus on chromosome 7, which encodes a putative methyltransferase. There is also a third closely related pseudogene locus in this region. There is extensive alternative splicing at this locus. [pr
|
|
OMIM |
131235 |
|
| Associated diseases |
References |
| Aberrant CpGs in Low Motility Sperm | MIK: 21674046 |
|
|
| PMID |
Condition |
Mutation |
Ethnicity |
Population details |
Infertility_type |
Associated_genes |
Abstract |
| 21674046 |
Aberrant C
pGs in Low
Motility
Sperm
|
|
|
18
|
Male infertility |
GSE26881
|
Show abstract |
|