HNRNPH1P2
pseudogene in the species Homo sapiens
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HNRNPH1P2
Summary
HNRNPH1P2 is a pseudogene[1].
Key Facts
- HNRNPH1P2's instance of is recorded as pseudogene[2].
- HNRNPH1P2's instance of is recorded as gene[3].
- HNRNPH1P2's subclass of is recorded as pseudogene[4].
- HNRNPH1P2's Entrez Gene ID is recorded as 100129368[5].
- HNRNPH1P2's HGNC gene symbol is recorded as HNRNPH1P2[6].
- HNRNPH1P2's HGNC ID is recorded as 48810[7].
- HNRNPH1P2's Ensembl gene ID is recorded as ENSG00000213924[8].
- HNRNPH1P2's genomic start is recorded as 143677153[9].
- HNRNPH1P2's genomic end is recorded as 143678362[10].
- HNRNPH1P2's found in taxon is recorded as Homo sapiens[11].
- HNRNPH1P2's Ensembl transcript ID is recorded as ENST00000396845[12].
- HNRNPH1P2's chromosome is recorded as human X chromosome[13].
- HNRNPH1P2's strand orientation is recorded as reverse strand[14].
- HNRNPH1P2's exact match is recorded as http://identifiers.org/ncbigene/100129368[15].
- HNRNPH1P2's UMLS CUI is recorded as C3813520[16].
- HNRNPH1P2's cytogenetic location is recorded as Xq27.3[17].
- HNRNPH1P2's expressed in is recorded as ganglionic eminence[18].