Evidence Details for PTMS


Gene Symbol: | PTMS ( ParaT ) |
---|---|
Gene Full Name: | parathymosin |
Band: | 12p13 |
Quick Links | Entrez ID:5763; OMIM: 168440; Uniprot ID:PTMS_HUMAN; ENSEMBL ID: ENSG00000159335; HGNC ID: 9629 |
Relate to Another Database: | SFARIGene; denovo-db |


>PTMS|5763|nucleotide
ATGTCGGAGAAAAGCGTGGAGGCAGCGGCCGAGTTGAGCGCCAAGGACCTGAAGGAGAAGAAGGAGAAGGTGGAGGAGAAGGCAAGCCGGAAAGAGCGAAAGAAA
GAAGTGGTGGAGGAGGAGGAGAACGGGGCTGAGGAGGAAGAAGAAGAAACTGCCGAGGATGGAGAGGAGGAAGATGAAGGGGAAGAAGAAGATGAGGAAGAAGAA
GAAGAGGATGATGAAGGGCCCGCGCTGAAGAGAGCTGCCGAAGAGGAGGATGAAGCGGATCCCAAACGGCAGAAGACAGAAAATGGGGCATCGGCGTGA
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ATGTCGGAGAAAAGCGTGGAGGCAGCGGCCGAGTTGAGCGCCAAGGACCTGAAGGAGAAGAAGGAGAAGGTGGAGGAGAAGGCAAGCCGGAAAGAGCGAAAGAAA
GAAGTGGTGGAGGAGGAGGAGAACGGGGCTGAGGAGGAAGAAGAAGAAACTGCCGAGGATGGAGAGGAGGAAGATGAAGGGGAAGAAGAAGATGAGGAAGAAGAA
GAAGAGGATGATGAAGGGCCCGCGCTGAAGAGAGCTGCCGAAGAGGAGGATGAAGCGGATCCCAAACGGCAGAAGACAGAAAATGGGGCATCGGCGTGA
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>PTMS|5763|protein
MSEKSVEAAAELSAKDLKEKKEKVEEKASRKERKKEVVEEEENGAEEEEEETAEDGEEEDEGEEEDEEEEEEDDEGPALKRAAEEEDEADPKRQKTENGASA
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MSEKSVEAAAELSAKDLKEKKEKVEEKASRKERKKEVVEEEENGAEEEEEETAEDGEEEDEGEEEDEEEEEEDDEGPALKRAAEEEDEADPKRQKTENGASA
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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) | 1 (1) | 0 (0) | 0 (0) | 0 (0) | 0 (1) | 0 (0) | 0 (0) | 0 (0) | 2 (2) |






Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
Zwaag, 2009 | - | SNP microarray | ![]() | ![]() | autism | - | - | - | - | 105 | 267 | 372 |








Reference | Case Number | Family Number | de novo Number | Title |
---|---|---|---|---|
De Rubeis S, 2014 | 2270 | - | 1702 | Synaptic, transcriptional and chromatin genes disrupted in autism |






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