RHOXF1P1
pseudogene in the species Homo sapiens
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RHOXF1P1
Summary
RHOXF1P1 is a pseudogene[1].
Key Facts
- RHOXF1P1's instance of is recorded as pseudogene[2].
- RHOXF1P1's subclass of is recorded as pseudogene[3].
- RHOXF1P1's Entrez Gene ID is recorded as 101928941[4].
- RHOXF1P1's HGNC gene symbol is recorded as RHOXF1P1[5].
- RHOXF1P1's HGNC ID is recorded as 51580[6].
- RHOXF1P1's OMIM ID is recorded as 300973[7].
- RHOXF1P1's Ensembl gene ID is recorded as ENSG00000234493[8].
- RHOXF1P1's RefSeq RNA ID is recorded as NR_131250[9].
- RHOXF1P1's genomic start is recorded as 119978713[10].
- RHOXF1P1's genomic end is recorded as 120025138[11].
- RHOXF1P1's found in taxon is recorded as Homo sapiens[12].
- RHOXF1P1's Ensembl transcript ID is recorded as ENST00000635473[13].
- RHOXF1P1's Ensembl transcript ID is recorded as ENST00000454625[14].
- RHOXF1P1's Ensembl transcript ID is recorded as ENST00000649154[15].
- RHOXF1P1's chromosome is recorded as human X chromosome[16].
- RHOXF1P1's strand orientation is recorded as reverse strand[17].
- RHOXF1P1's exact match is recorded as http://identifiers.org/ncbigene/101928941[18].
- RHOXF1P1's UMLS CUI is recorded as C4085623[19].
- RHOXF1P1's cytogenetic location is recorded as Xq24[20].