Gene id |
100529264 |
Gene Summary Diseases PubMed |
Gene Summary
|
Gene Symbol |
RAB4B-EGLN2 Gene UCSC Ensembl |
Aliases |
EGLN2, EIT-6, EIT6, HIF-PH1, HPH-1, HPH-3, PHD1, RERT-lncRNA |
Gene name |
RAB4B-EGLN2 readthrough (NMD candidate) |
Alternate names |
Egl nine homolog 2, Estrogen-induced tag 6, HIF-prolyl hydroxylase 1, Hypoxia-inducible factor prolyl hydroxylase 1, Prolyl hydroxylase domain-containing protein 1, RAB4B-EGLN2 readthrough (non-protein coding), RAB4B-EGLN2 readthrough long non-coding RNA, |
Gene location |
19q13.2 (40778218: 40808440) Exons: 12 NC_000019.10
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Gene summary(Entrez) |
This locus represents naturally occurring read-through transcription between the neighboring RAB4B (RAB4B, member RAS oncogene family) and EGLN2 (egl nine homolog 2) genes on chromosome 19. The read-through transcript is a candidate for nonsense-mediated
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OMIM |
0 |
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Associated diseases |
References |
Teratozoospermia | MIK: 17327269 |
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PMID |
Condition |
Mutation |
Ethnicity |
Population details |
Infertility_type |
Associated_genes |
Abstract |
17327269 |
Teratozoos permia
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19 (6 controls , 13 cases)
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Male infertility |
GSE6872 analyzed by GEO2R (cutoff 1.5 fold)
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Show abstract |
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