Evidence Details for NBPF22P
Basic Information Top
| Gene Symbol: | NBPF22P ( MGC48637 ) |
|---|---|
| Gene Full Name: | neuroblastoma breakpoint family, member 22 (pseudogene) |
| Band: | 5q14.3 |
| Quick Links | Entrez ID:285622; OMIM: NA; Uniprot ID:; ENSEMBL ID: ; HGNC ID: 28731 |
| Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top Evidence summary TopClick the link of the category-specific score to view different category of evidences. The categories without any evidences are hidden by default.
| Evidences | Syndromic Gene | GWAS | CNV | Linkage | Association | Expression | NGS de novo | NGS Mosaic | NGS Other | Low-Scale Gene Studies | Total |
|---|---|---|---|---|---|---|---|---|---|---|---|
| Score (No. of Studies) | No | 0 (0) | 1 (1) | 0 (0) | 0 (0) | 0 (0) | 0 (1) | 0 (0) | 0 (0) | 0 (0) | 2 (2) |
Syndromic Autism Gene TopGenome-Wide Association Studies(By Ethnic Group) TopCNV Studies Top| Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
| Ezugha, 2010 | - | aCGH |  | | autism | - | - | - | - | 1 | - | 1 |
Linkage Studies Top