NBPF17P (NBPF member 17, pseudogene)
|
Gene
Gene information from NCBI Gene database.
|
|
| Entrez ID | 401967 |
| Gene name | NBPF member 17, pseudogene |
| Gene symbol | NBPF17P |
| Synonyms (NCBI Gene) |
NBPF23NBPF23P
|
| Chromosome | 1 |
| Chromosome location | 1q21.1 |
| Summary | This gene is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1. This gene family has experienced its greatest expansion within the |
|
Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
|
|||||||
|
|||||||
|
Related Genes
Genes most often co-reported with NBPF17P across shared curated disease and pathway associations.
0
|
|
|
Diseases Linked via Similar Genes
Diseases curated for genes most similar to NBPF17P (see Related Genes above), that are NOT already directly curated for NBPF17P itself -- a lead worth checking, not a confirmed association.
0
|
|