Evidence Details for ZNF385D
Basic Information Top
Gene Symbol: | ZNF385D ( FLJ22419,ZNF659 ) |
---|---|
Gene Full Name: | zinc finger protein 385D |
Band: | 3p24.3 |
Quick Links | Entrez ID:79750; OMIM: NA; Uniprot ID:Z385D_HUMAN; ENSEMBL ID: ENSG00000151789; HGNC ID: 26191 |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>ZNF385D|79750|nucleotide
ATGAGAAACATAATGTATTTTGGTGGTACATGCCAGAGTCCTGCTCTCCCGGCCCTTGTCCGTCCACCAGCCCCTCCTTTGCAACCATCGCTGGATATTAAACCA
TTTCTTCCCTTTCCTCTTGACACTGCAGCTGCAGTCAACCTCTTCCCCAATTTCAATGCGATGGACCCGATTCAGAAAGCTGTAATAAACCATACATTCGGGGTT
CCTCTTCCCCACCGAAGAAAGCAAATCATATCATGCAACATTTGCCAGTTGAGATTTAATTCTGATAGCCAGGCTGCGGCCCACTACAAAGGCACGAAACATGCC
AAGAAGCTCAAAGCACTGGAAGCCATGAAAAATAAGCAGAAATCTGTAACTGCCAAGGACAGCGCAAAGACTACCTTCACCTCCATCACTACCAATACCATCAAT
ACCAGCTCTGACAAAACAGACGGTACTGCAGGGACACCAGCAATATCAACGACGACAACTGTGGAAATCCGCAAAAGCAGTGTTATGACAACTGAGATCACCTCT
AAAGTGGAAAAAAGCCCAACGACAGCCACTGGCAATAGCTCATGTCCTTCTACTGAGACCGAGGAAGAAAAGGCAAAACGGCTTCTTTACTGTTCGCTATGCAAG
GTTGCTGTCAACTCTGCCTCGCAGCTGGAGGCGCACAACAGTGGTACTAAGCACAAAACCATGTTAGAAGCCCGGAATGGAAGTGGCACTATCAAAGCCTTTCCT
AGGGCAGGAGTGAAAGGCAAAGGACCTGTTAATAAAGGAAACACAGGCCTCCAAAATAAAACATTTCACTGTGAAATCTGTGATGTGCACGTCAACTCGGAAACG
CAACTTAAACAGCACATTAGCAGTAGAAGGCACAAAGACAGAGCTGCTGGGAAGCCCCCGAAACCTAAATACAGTCCTTACAACAAACTACAGAAGACAGCACAT
CCACTGGGGGTAAAATTAGTATTTTCAAAAGAACCTTCAAAGCCATTGGCTCCACGAATTCTACCAAATCCTCTAGCAGCTGCAGCAGCCGCAGCAGCAGTGGCA
GTGAGTTCCCCCTTCAGTCTTCGAACTGCTCCAGCAGCAACACTGTTCCAGACTTCCGCGCTTCCTCCGGCACTCCTGCGGCCAGCTCCTGGACCCATTCGGACC
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ATGAGAAACATAATGTATTTTGGTGGTACATGCCAGAGTCCTGCTCTCCCGGCCCTTGTCCGTCCACCAGCCCCTCCTTTGCAACCATCGCTGGATATTAAACCA
TTTCTTCCCTTTCCTCTTGACACTGCAGCTGCAGTCAACCTCTTCCCCAATTTCAATGCGATGGACCCGATTCAGAAAGCTGTAATAAACCATACATTCGGGGTT
CCTCTTCCCCACCGAAGAAAGCAAATCATATCATGCAACATTTGCCAGTTGAGATTTAATTCTGATAGCCAGGCTGCGGCCCACTACAAAGGCACGAAACATGCC
AAGAAGCTCAAAGCACTGGAAGCCATGAAAAATAAGCAGAAATCTGTAACTGCCAAGGACAGCGCAAAGACTACCTTCACCTCCATCACTACCAATACCATCAAT
ACCAGCTCTGACAAAACAGACGGTACTGCAGGGACACCAGCAATATCAACGACGACAACTGTGGAAATCCGCAAAAGCAGTGTTATGACAACTGAGATCACCTCT
AAAGTGGAAAAAAGCCCAACGACAGCCACTGGCAATAGCTCATGTCCTTCTACTGAGACCGAGGAAGAAAAGGCAAAACGGCTTCTTTACTGTTCGCTATGCAAG
GTTGCTGTCAACTCTGCCTCGCAGCTGGAGGCGCACAACAGTGGTACTAAGCACAAAACCATGTTAGAAGCCCGGAATGGAAGTGGCACTATCAAAGCCTTTCCT
AGGGCAGGAGTGAAAGGCAAAGGACCTGTTAATAAAGGAAACACAGGCCTCCAAAATAAAACATTTCACTGTGAAATCTGTGATGTGCACGTCAACTCGGAAACG
CAACTTAAACAGCACATTAGCAGTAGAAGGCACAAAGACAGAGCTGCTGGGAAGCCCCCGAAACCTAAATACAGTCCTTACAACAAACTACAGAAGACAGCACAT
CCACTGGGGGTAAAATTAGTATTTTCAAAAGAACCTTCAAAGCCATTGGCTCCACGAATTCTACCAAATCCTCTAGCAGCTGCAGCAGCCGCAGCAGCAGTGGCA
GTGAGTTCCCCCTTCAGTCTTCGAACTGCTCCAGCAGCAACACTGTTCCAGACTTCCGCGCTTCCTCCGGCACTCCTGCGGCCAGCTCCTGGACCCATTCGGACC
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>ZNF385D|79750|protein
MRNIMYFGGTCQSPALPALVRPPAPPLQPSLDIKPFLPFPLDTAAAVNLFPNFNAMDPIQKAVINHTFGVPLPHRRKQIISCNICQLRFNSDSQAAAHYKGTKHA
KKLKALEAMKNKQKSVTAKDSAKTTFTSITTNTINTSSDKTDGTAGTPAISTTTTVEIRKSSVMTTEITSKVEKSPTTATGNSSCPSTETEEEKAKRLLYCSLCK
VAVNSASQLEAHNSGTKHKTMLEARNGSGTIKAFPRAGVKGKGPVNKGNTGLQNKTFHCEICDVHVNSETQLKQHISSRRHKDRAAGKPPKPKYSPYNKLQKTAH
PLGVKLVFSKEPSKPLAPRILPNPLAAAAAAAAVAVSSPFSLRTAPAATLFQTSALPPALLRPAPGPIRTAHTPVLFAPY
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MRNIMYFGGTCQSPALPALVRPPAPPLQPSLDIKPFLPFPLDTAAAVNLFPNFNAMDPIQKAVINHTFGVPLPHRRKQIISCNICQLRFNSDSQAAAHYKGTKHA
KKLKALEAMKNKQKSVTAKDSAKTTFTSITTNTINTSSDKTDGTAGTPAISTTTTVEIRKSSVMTTEITSKVEKSPTTATGNSSCPSTETEEEKAKRLLYCSLCK
VAVNSASQLEAHNSGTKHKTMLEARNGSGTIKAFPRAGVKGKGPVNKGNTGLQNKTFHCEICDVHVNSETQLKQHISSRRHKDRAAGKPPKPKYSPYNKLQKTAH
PLGVKLVFSKEPSKPLAPRILPNPLAAAAAAAAVAVSSPFSLRTAPAATLFQTSALPPALLRPAPGPIRTAHTPVLFAPY
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Evidence summary Top
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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 (2) | 0 (0) | 0 (0) | 1 (1) | 0 (2) | 0 (0) | 0 (0) | 0 (0) | 3 (5) |
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
Zwaag, 2009 | - | SNP microarray | autism | - | - | - | - | 105 | 267 | 372 | ||
Pinto, 2010 | - | SNP microarray, qPCR | ASD | - | - | - | - | 996 | 1287 | 2283 |
Linkage Studies Top
Low Scale Association Studies (by Ethnic Group) Top
Large Scale Expression Studies Top
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%) |
0.848224 | Down | 2.19157 | |||
|
Proteomics Studies:0
Reference | Source | Tissue | Platform | #Subjects (% Women) |
ADI-R | ADOS | Diagnosis | Normal Controls(% Women) | |
---|---|---|---|---|---|---|---|---|---|
No Evidence. |
NGS de novo Mutation Studies Top
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. |
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top
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