WHSC1L2P

Summary

WHSC1L2P is a pseudogene^[1].

Key Facts

• WHSC1L2P's instance of is recorded as pseudogene^[2].
• WHSC1L2P's instance of is recorded as gene^[3].
• WHSC1L2P's subclass of is recorded as pseudogene^[4].
• WHSC1L2P's Entrez Gene ID is recorded as 100128016^[5].
• WHSC1L2P's HGNC gene symbol is recorded as WHSC1L2P^[6].
• WHSC1L2P's HGNC ID is recorded as 14647^[7].
• WHSC1L2P's Ensembl gene ID is recorded as ENSG00000267253^[8].
• WHSC1L2P's genomic start is recorded as 43718314^[9].
• WHSC1L2P's genomic end is recorded as 43720436^[10].
• WHSC1L2P's found in taxon is recorded as Homo sapiens^[11].
• WHSC1L2P's Ensembl transcript ID is recorded as ENST00000587110^[12].
• WHSC1L2P's chromosome is recorded as human chromosome 17^[13].
• WHSC1L2P's strand orientation is recorded as reverse strand^[14].
• WHSC1L2P's exact match is recorded as http://identifiers.org/ncbigene/100128016^[15].
• WHSC1L2P's UMLS CUI is recorded as C1422812^[16].
• WHSC1L2P's cytogenetic location is recorded as 17q21.31^[17].