| P594 | Ensembl gene ID | ENSG00000254527 |
| P704 | Ensembl transcript ID | ENST00000526818 |
| P351 | Entrez Gene ID | 106480230 |
| P2888 | exact match | http://identifiers.org/ncbigene/106480230 |
| P353 | HGNC gene symbol | ENPP7P12 |
| P354 | HGNC ID | 48697 |
| P2892 | UMLS CUI | C3815801 |
| P1057 | chromosome | human chromosome 8 | Q572848 |
| P4196 | cytogenetic location | 8p23.1 | |
| P5572 | expressed in | sural nerve | Q6135922 |
| corpus callosum | Q223851 | ||
| anterior pituitary | Q356002 | ||
| right coronary artery | Q429285 | ||
| bone marrow cells | Q66004840 | ||
| primary visual cortex | Q66531315 | ||
| right hemisphere of cerebellum | Q66590413 | ||
| epithelium of colon | Q66714209 | ||
| ascending aorta | Q2349469 | ||
| superior frontal gyrus | Q3064113 | ||
| P703 | found in taxon | Homo sapiens | Q15978631 |
| P645 | genomic end | 12206389 | |
| P644 | genomic start | 12205759 | |
| P2548 | strand orientation | reverse strand | Q22809711 |
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