RPSAP38
pseudogene in the species Homo sapiens
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RPSAP38
Summary
RPSAP38 is a pseudogene[1].
Key Facts
- RPSAP38's instance of is recorded as pseudogene[2].
- RPSAP38's instance of is recorded as gene[3].
- RPSAP38's subclass of is recorded as pseudogene[4].
- RPSAP38's Entrez Gene ID is recorded as 100130676[5].
- RPSAP38's HGNC gene symbol is recorded as RPSAP38[6].
- RPSAP38's HGNC ID is recorded as 35963[7].
- RPSAP38's Ensembl gene ID is recorded as ENSG00000239694[8].
- RPSAP38's genomic start is recorded as 41951313[9].
- RPSAP38's genomic end is recorded as 41952193[10].
- RPSAP38's found in taxon is recorded as Homo sapiens[11].
- RPSAP38's Ensembl transcript ID is recorded as ENST00000475442[12].
- RPSAP38's chromosome is recorded as human chromosome 5[13].
- RPSAP38's strand orientation is recorded as reverse strand[14].
- RPSAP38's exact match is recorded as http://identifiers.org/ncbigene/100130676[15].
- RPSAP38's UMLS CUI is recorded as C2680332[16].
- RPSAP38's cytogenetic location is recorded as 5p13.1[17].
- RPSAP38's expressed in is recorded as ganglionic eminence[18].
- RPSAP38's expressed in is recorded as duodenum[19].
- RPSAP38's expressed in is recorded as islet of Langerhans[20].