Evidence Details for PSPN
Basic Information Top
Gene Symbol: | PSPN ( PSP ) |
---|---|
Gene Full Name: | persephin |
Band: | 19p13.3 |
Quick Links | Entrez ID:5623; OMIM: 602921; Uniprot ID:PSPN_HUMAN; ENSEMBL ID: ENSG00000125650; HGNC ID: 9579 |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>PSPN|5623|nucleotide
ATGGCCGTAGGGAAGTTCCTGCTGGGCTCCCTGCTGCTCCTGTCCCTGCAGCTGGGACAGGGCTGGGGCCCCGATGCCCGTGGGGTTCCCGTGGCCGATGGAGAG
TTCTCGTCTGAACAGGTGGCAAAGGCTGGAGGGACCTGGCTGGGCACCCACCGCCCCCTTGCCCGCCTGCGCCGAGCCCTGTCTGGTCCATGCCAGCTGTGGAGC
CTGACCCTGTCCGTGGCAGAGCTAGGCCTGGGCTACGCCTCAGAGGAGAAGGTCATCTTCCGCTACTGCGCCGGCAGCTGCCCCCGTGGTGCCCGCACCCAGCAT
GGCCTGGCGCTGGCCCGGCTGCAGGGCCAGGGCCGAGCCCACGGCGGGCCCTGCTGCCGGCCCACTCGCTACACCGACGTGGCCTTCCTCGATGACCGCCACCGC
TGGCAGCGGCTGCCCCAGCTCTCGGCGGCTGCCTGCGGCTGTGGTGGCTGA
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ATGGCCGTAGGGAAGTTCCTGCTGGGCTCCCTGCTGCTCCTGTCCCTGCAGCTGGGACAGGGCTGGGGCCCCGATGCCCGTGGGGTTCCCGTGGCCGATGGAGAG
TTCTCGTCTGAACAGGTGGCAAAGGCTGGAGGGACCTGGCTGGGCACCCACCGCCCCCTTGCCCGCCTGCGCCGAGCCCTGTCTGGTCCATGCCAGCTGTGGAGC
CTGACCCTGTCCGTGGCAGAGCTAGGCCTGGGCTACGCCTCAGAGGAGAAGGTCATCTTCCGCTACTGCGCCGGCAGCTGCCCCCGTGGTGCCCGCACCCAGCAT
GGCCTGGCGCTGGCCCGGCTGCAGGGCCAGGGCCGAGCCCACGGCGGGCCCTGCTGCCGGCCCACTCGCTACACCGACGTGGCCTTCCTCGATGACCGCCACCGC
TGGCAGCGGCTGCCCCAGCTCTCGGCGGCTGCCTGCGGCTGTGGTGGCTGA
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>PSPN|5623|protein
MAVGKFLLGSLLLLSLQLGQGWGPDARGVPVADGEFSSEQVAKAGGTWLGTHRPLARLRRALSGPCQLWSLTLSVAELGLGYASEEKVIFRYCAGSCPRGARTQH
GLALARLQGQGRAHGGPCCRPTRYTDVAFLDDRHRWQRLPQLSAAACGCGG
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MAVGKFLLGSLLLLSLQLGQGWGPDARGVPVADGEFSSEQVAKAGGTWLGTHRPLARLRRALSGPCQLWSLTLSVAELGLGYASEEKVIFRYCAGSCPRGARTQH
GLALARLQGQGRAHGGPCCRPTRYTDVAFLDDRHRWQRLPQLSAAACGCGG
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Evidence summary Top
Click 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) | 0 (0) | 1 (1) | 0 (0) | 0 (0) | 0 (1) | 0 (1) | 0 (0) | 0 (0) | 2 (3) |
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Linkage Studies Top
Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
Schellenberg, 2006 | USA | microsatellite-based genomic screen | autism | 222 | - | 222 | - | - | - | - |
Low Scale Association Studies (by Ethnic Group) Top
Large Scale Expression Studies Top
NGS de novo Mutation Studies Top
Reference | Case Number | Family Number | de novo Number | Title |
---|---|---|---|---|
De Rubeis S, 2014 | 2270 | - | 1702 | Synaptic, transcriptional and chromatin genes disrupted in autism |
NGS Mosaic SNV Studies Top
Reference | Case Number | Family Number | Mosaic Number | Title |
---|---|---|---|---|
Lim ET, 2017 | - | 5947 | 376 | Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder |
NGS Other Studies Top
Low Scale Gene Studies Top
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