Evidence Details for ZER1
Basic Information Top
Gene Symbol: | ZER1 ( C9orf60,Hzyg,RP11-545E17.4,ZYG,ZYG11BL ) |
---|---|
Gene Full Name: | zer-1 homolog (C. elegans) |
Band: | 9q34.11 |
Quick Links | Entrez ID:10444; OMIM: NA; Uniprot ID:ZER1_HUMAN; ENSEMBL ID: ENSG00000160445; HGNC ID: 30960 |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>ZER1|10444|nucleotide
ATGGCGTCCGACACTCCCGAGTCGCTGATGGCCCTCTGTACTGACTTCTGCTTGCGCAACCTGGATGGCACCCTGGGCTACCTGCTGGACAAGGAGACCCTGCGG
CTACATCCGGACATCTTCTTGCCCAGCGAGATCTGTGACCGGCTCGTCAATGAGTATGTGGAGCTGGTGAACGCTGCCTGTAACTTCGAGCCACACGAGAGCTTC
TTCAGCCTCTTTTCGGACCCCCGCAGCACCCGCCTCACGCGGATCCACCTCCGTGAGGACCTGGTGCAGGACCAGGACCTGGAGGCCATCCGCAAGCAGGACCTG
GTGGAGCTGTACCTGACTAACTGCGAGAAGCTGTCCGCCAAGAGCCTGCAGACACTGAGGAGCTTCAGCCACACCCTGGTGTCCTTGAGCCTCTTCGGCTGTACA
AACATTTTCTATGAGGAGGAGAACCCAGGGGGCTGTGAAGATGAGTACCTCGTCAACCCCACCTGCCAGGTGCTGGTTAAGGATTTCACCTTCGAGGGCTTCAGC
CGCCTCCGCTTCCTCAACTTGGGCCGCATGATTGATTGGGTCCCTGTGGAGTCCCTGCTGCGGCCGCTTAACTCCCTGGCTGCCTTGGACCTCTCAGGCATTCAG
ACGAGCGACGCCGCCTTCCTCACCCAGTGGAAAGACAGCCTGGTGTCCCTCGTCCTCTACAACATGGACCTGTCCGACGACCACATCCGGGTCATCGTGCAGCTG
CACAAGCTGCGACACCTGGACATCTCCCGAGACCGCCTCTCCAGCTACTACAAGTTCAAGCTGACTCGGGAGGTGCTGAGCCTCTTTGTGCAGAAGCTGGGGAAC
CTAATGTCCCTGGACATCTCTGGCCACATGATCCTAGAGAACTGCAGCATCTCCAAGATGGAAGAGGAAGCGGGGCAGACCAGCATTGAGCCTTCCAAGAGCAGC
ATCATACCTTTCCGGGCTCTGAAGAGGCCGCTGCAGTTCCTCGGGCTCTTTGAGAACTCTCTGTGCCGCCTCACGCACATTCCAGCCTACAAAGTAAGTGGTGAC
AAAAACGAAGAGCAGGTGCTGAATGCCATCGAGGCCTACACGGAGCACCGGCCTGAGATCACCTCGCGGGCCATCAACTTGCTTTTTGACATCGCCCGCATCGAG
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ATGGCGTCCGACACTCCCGAGTCGCTGATGGCCCTCTGTACTGACTTCTGCTTGCGCAACCTGGATGGCACCCTGGGCTACCTGCTGGACAAGGAGACCCTGCGG
CTACATCCGGACATCTTCTTGCCCAGCGAGATCTGTGACCGGCTCGTCAATGAGTATGTGGAGCTGGTGAACGCTGCCTGTAACTTCGAGCCACACGAGAGCTTC
TTCAGCCTCTTTTCGGACCCCCGCAGCACCCGCCTCACGCGGATCCACCTCCGTGAGGACCTGGTGCAGGACCAGGACCTGGAGGCCATCCGCAAGCAGGACCTG
GTGGAGCTGTACCTGACTAACTGCGAGAAGCTGTCCGCCAAGAGCCTGCAGACACTGAGGAGCTTCAGCCACACCCTGGTGTCCTTGAGCCTCTTCGGCTGTACA
AACATTTTCTATGAGGAGGAGAACCCAGGGGGCTGTGAAGATGAGTACCTCGTCAACCCCACCTGCCAGGTGCTGGTTAAGGATTTCACCTTCGAGGGCTTCAGC
CGCCTCCGCTTCCTCAACTTGGGCCGCATGATTGATTGGGTCCCTGTGGAGTCCCTGCTGCGGCCGCTTAACTCCCTGGCTGCCTTGGACCTCTCAGGCATTCAG
ACGAGCGACGCCGCCTTCCTCACCCAGTGGAAAGACAGCCTGGTGTCCCTCGTCCTCTACAACATGGACCTGTCCGACGACCACATCCGGGTCATCGTGCAGCTG
CACAAGCTGCGACACCTGGACATCTCCCGAGACCGCCTCTCCAGCTACTACAAGTTCAAGCTGACTCGGGAGGTGCTGAGCCTCTTTGTGCAGAAGCTGGGGAAC
CTAATGTCCCTGGACATCTCTGGCCACATGATCCTAGAGAACTGCAGCATCTCCAAGATGGAAGAGGAAGCGGGGCAGACCAGCATTGAGCCTTCCAAGAGCAGC
ATCATACCTTTCCGGGCTCTGAAGAGGCCGCTGCAGTTCCTCGGGCTCTTTGAGAACTCTCTGTGCCGCCTCACGCACATTCCAGCCTACAAAGTAAGTGGTGAC
AAAAACGAAGAGCAGGTGCTGAATGCCATCGAGGCCTACACGGAGCACCGGCCTGAGATCACCTCGCGGGCCATCAACTTGCTTTTTGACATCGCCCGCATCGAG
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>ZER1|10444|protein
MASDTPESLMALCTDFCLRNLDGTLGYLLDKETLRLHPDIFLPSEICDRLVNEYVELVNAACNFEPHESFFSLFSDPRSTRLTRIHLREDLVQDQDLEAIRKQDL
VELYLTNCEKLSAKSLQTLRSFSHTLVSLSLFGCTNIFYEEENPGGCEDEYLVNPTCQVLVKDFTFEGFSRLRFLNLGRMIDWVPVESLLRPLNSLAALDLSGIQ
TSDAAFLTQWKDSLVSLVLYNMDLSDDHIRVIVQLHKLRHLDISRDRLSSYYKFKLTREVLSLFVQKLGNLMSLDISGHMILENCSISKMEEEAGQTSIEPSKSS
IIPFRALKRPLQFLGLFENSLCRLTHIPAYKVSGDKNEEQVLNAIEAYTEHRPEITSRAINLLFDIARIERCNQLLRALKLVITALKCHKYDRNIQVTGSAALFY
LTNSEYRSEQSVKLRRQVIQVVLNGMESYQEVTVQRNCCLTLCNFSIPEELEFQYRRVNELLLSILNPTRQDESIQRIAVHLCNALVCQVDNDHKEAVGKMGFVV
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MASDTPESLMALCTDFCLRNLDGTLGYLLDKETLRLHPDIFLPSEICDRLVNEYVELVNAACNFEPHESFFSLFSDPRSTRLTRIHLREDLVQDQDLEAIRKQDL
VELYLTNCEKLSAKSLQTLRSFSHTLVSLSLFGCTNIFYEEENPGGCEDEYLVNPTCQVLVKDFTFEGFSRLRFLNLGRMIDWVPVESLLRPLNSLAALDLSGIQ
TSDAAFLTQWKDSLVSLVLYNMDLSDDHIRVIVQLHKLRHLDISRDRLSSYYKFKLTREVLSLFVQKLGNLMSLDISGHMILENCSISKMEEEAGQTSIEPSKSS
IIPFRALKRPLQFLGLFENSLCRLTHIPAYKVSGDKNEEQVLNAIEAYTEHRPEITSRAINLLFDIARIERCNQLLRALKLVITALKCHKYDRNIQVTGSAALFY
LTNSEYRSEQSVKLRRQVIQVVLNGMESYQEVTVQRNCCLTLCNFSIPEELEFQYRRVNELLLSILNPTRQDESIQRIAVHLCNALVCQVDNDHKEAVGKMGFVV
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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 (1) | 0 (0) | 0 (0) | 0 (0) | 0 (1) | 0 (0) | 0 (0) | 0 (0) | 0 (2) |
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 | ||||||
Gregory, 2009 | USA | aCGH | ASD | - | - | - | - | 119 | 54 | 173 |
Linkage Studies Top
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 |
---|---|---|---|---|
Takata A, 2018 | 262 | 262 | 322 | Integrative Analyses of De Novo Mutations Provide Deeper Biological Insights into Autism Spectrum Di |
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top
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