Evidence Details for NUDT14


Gene Symbol: | NUDT14 ( UGPP,UGPPase ) |
---|---|
Gene Full Name: | nudix (nucleoside diphosphate linked moiety X)-type motif 14 |
Band: | 14q32.33 |
Quick Links | Entrez ID:256281; OMIM: 609219; Uniprot ID:NUD14_HUMAN; ENSEMBL ID: ENSG00000183828; HGNC ID: 20141 |
Relate to Another Database: | SFARIGene; denovo-db |


>NUDT14|256281|nucleotide
ATGGAGCGCATCGAGGGGGCGTCCGTGGGCCGCTGCGCCGCCTCACCCTACCTGCGGCCGCTCACGCTGCATTACCGCCAGAATGGTGCCCAGAAGTCCTGGGAC
TTCATGAAGACGCATGACAGCGTGACCGTTCTCTTATTCAACTCTTCTCGGAGGAGCCTGGTGTTGGTGAAGCAGTTCCGGCCAGCTGTGTATGCGGGTGAGGTG
GAGCGCCGCTTCCCAGGGTCCCTAGCAGCTGTAGACCAGGACGGGCCTCGGGAGCTACAGCCAGCCCTGCCCGGCTCAGCGGGGGTGACAGTTGAGCTGTGTGCC
GGCCTCGTGGACCAGCCTGGGCTCTCGCTGGAGGAAGTGGCTTGCAAGGAGGCTTGGGAGGAGTGTGGCTACCACTTGGCCCCCTCTGATCTGCGCCGGGTCGCC
ACATACTGGTCTGGAGTGGGACTGACTGGCTCCAGACAGACCATGTTCTACACAGAGGTGACAGATGCCCAGCGTAGCGGTCCAGGTGGGGGCCTGGTGGAGGAG
GGTGAGCTCATTGAGGTGGTGCACCTGCCCCTGGAAGGCGCCCAGGCCTTTGCAGACGACCCGGACATCCCCAAGACCCTCGGCGTCATCTTTGGTGTCTCATGG
TTCCTCAGCCAGGTGGCCCCCAACCTGGATCTCCAGTGA
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ATGGAGCGCATCGAGGGGGCGTCCGTGGGCCGCTGCGCCGCCTCACCCTACCTGCGGCCGCTCACGCTGCATTACCGCCAGAATGGTGCCCAGAAGTCCTGGGAC
TTCATGAAGACGCATGACAGCGTGACCGTTCTCTTATTCAACTCTTCTCGGAGGAGCCTGGTGTTGGTGAAGCAGTTCCGGCCAGCTGTGTATGCGGGTGAGGTG
GAGCGCCGCTTCCCAGGGTCCCTAGCAGCTGTAGACCAGGACGGGCCTCGGGAGCTACAGCCAGCCCTGCCCGGCTCAGCGGGGGTGACAGTTGAGCTGTGTGCC
GGCCTCGTGGACCAGCCTGGGCTCTCGCTGGAGGAAGTGGCTTGCAAGGAGGCTTGGGAGGAGTGTGGCTACCACTTGGCCCCCTCTGATCTGCGCCGGGTCGCC
ACATACTGGTCTGGAGTGGGACTGACTGGCTCCAGACAGACCATGTTCTACACAGAGGTGACAGATGCCCAGCGTAGCGGTCCAGGTGGGGGCCTGGTGGAGGAG
GGTGAGCTCATTGAGGTGGTGCACCTGCCCCTGGAAGGCGCCCAGGCCTTTGCAGACGACCCGGACATCCCCAAGACCCTCGGCGTCATCTTTGGTGTCTCATGG
TTCCTCAGCCAGGTGGCCCCCAACCTGGATCTCCAGTGA
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>NUDT14|256281|protein
MERIEGASVGRCAASPYLRPLTLHYRQNGAQKSWDFMKTHDSVTVLLFNSSRRSLVLVKQFRPAVYAGEVERRFPGSLAAVDQDGPRELQPALPGSAGVTVELCA
GLVDQPGLSLEEVACKEAWEECGYHLAPSDLRRVATYWSGVGLTGSRQTMFYTEVTDAQRSGPGGGLVEEGELIEVVHLPLEGAQAFADDPDIPKTLGVIFGVSW
FLSQVAPNLDLQ
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MERIEGASVGRCAASPYLRPLTLHYRQNGAQKSWDFMKTHDSVTVLLFNSSRRSLVLVKQFRPAVYAGEVERRFPGSLAAVDQDGPRELQPALPGSAGVTVELCA
GLVDQPGLSLEEVACKEAWEECGYHLAPSDLRRVATYWSGVGLTGSRQTMFYTEVTDAQRSGPGGGLVEEGELIEVVHLPLEGAQAFADDPDIPKTLGVIFGVSW
FLSQVAPNLDLQ
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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) | 0 (0) | 0 (0) | 0 (0) | 1 (1) | 0 (1) | 0 (0) | 0 (0) | 0 (0) | 1 (2) |












Microarray Studies: 1
Reference | Source | Tissue | #Subjects (% Women) |
ADI-R | ADOS | Endo- pheno | Diagnosis | Normal Controls (% Women) |
Fold Change | Up/ Down | P/Q value | |
---|---|---|---|---|---|---|---|---|---|---|---|---|
Voineagu, 2011_1 | Unknown | 16 frontal cortex(BA9) and 13 temporal cortex(BA41 | 16 (25.00%) | ![]() | ![]() | - | autism | 16 (6.25%) |
0.932605 | Down | 36.649 | |
|
Proteomics Studies:0
Reference | Source | Tissue | Platform | #Subjects (% Women) |
ADI-R | ADOS | Diagnosis | Normal Controls(% Women) | |
---|---|---|---|---|---|---|---|---|---|
No Evidence. |


Reference | Case Number | Family Number | de novo Number | Title |
---|---|---|---|---|
Iossifov I, 2014 | 2508 | - | 1194 | The contribution of de novo coding mutations to autism spectrum disorder. |






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