PRSS47P
protein-coding gene in the species Homo sapiens
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PRSS47P
Summary
PRSS47P is a pseudogene[1].
Key Facts
- PRSS47P's instance of is recorded as pseudogene[2].
- PRSS47P's subclass of is recorded as protein-coding gene[3].
- PRSS47P's Entrez Gene ID is recorded as 138652[4].
- PRSS47P's HGNC gene symbol is recorded as PRSS47P[5].
- PRSS47P's HGNC ID is recorded as 37326[6].
- PRSS47P's Ensembl gene ID is recorded as ENSG00000276717[7].
- PRSS47P's RefSeq RNA ID is recorded as NM_001350291[8].
- PRSS47P's genomic start is recorded as 92177235[9].
- PRSS47P's genomic end is recorded as 92191156[10].
- PRSS47P's found in taxon is recorded as Homo sapiens[11].
- PRSS47P's Ensembl transcript ID is recorded as ENST00000672321[12].
- PRSS47P's Ensembl transcript ID is recorded as ENST00000611097[13].
- PRSS47P's chromosome is recorded as human chromosome 9[14].
- PRSS47P's strand orientation is recorded as reverse strand[15].
- PRSS47P's exact match is recorded as http://identifiers.org/ncbigene/138652[16].
- PRSS47P's UMLS CUI is recorded as C2828576[17].
- PRSS47P's cytogenetic location is recorded as 9q22.31[18].
- PRSS47P's expressed in is recorded as ovary[19].
- PRSS47P's expressed in is recorded as gallbladder[20].
- PRSS47P's expressed in is recorded as endometrium[21].
- PRSS47P's expressed in is recorded as multicellular organism[22].