AutismKB 2.0

Evidence Details for TDRD1


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Basic Information Top
Gene Symbol:TDRD1 ( CT41.1,FLJ21082 )
Gene Full Name: tudor domain containing 1
Band: 10q25.3
Quick LinksEntrez ID:56165; OMIM: 605796; Uniprot ID:TDRD1_HUMAN; ENSEMBL ID: ENSG00000095627; HGNC ID: 11712
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>TDRD1|56165|nucleotide
ATGAGTGTTAAATCGCCATTTAATGTGATGTCAAGAAATAATTTGGAAGCACCTCCTTGTAAGATGACAGAGCCATTTAATTTTGAGAAAAATGAAAACAAGCTT
CCACCACATGAGTCTTTAAGAAGTCCTGGAACACTTCCTAACCACCCTAATTTCAGGCTGAAAAGCTCAGAGAATGGAAATAAAAAGAACAATTTTTTGCTTTGT
GAGCAAACCAAACAATATTTGGCTAGTCAGGAAGACAATTCAGTTTCTTCAAACCCGAATGGCATCAACGGAGAAGTAGTTGGCTCCAAAGGAGACAGGAAAAAA
TTGCCAGCAGGAAACTCAGTGTCACCACCAAGTGCTGAAAGTAATTCACCACCCAAAGAAGTGAATATTAAGCCTGGAAATAATGTACGTCCTGCAAAATCAAAA
AAACTAAACAAGTTGGTCGAGAATTCCTTGTCCATAAGTAATCCAGGGCTCTTCACCTCCTTAGGACCTCCTCTTCGGTCCACAACTTGCCATCGCTGTGGCCTA
TTTGGATCGCTGAGGTGCTCTCAGTGCAAGCAGACCTACTATTGCTCCACAGCATGTCAAAGAAGAGACTGGTCTGCACACAGCATCGTGTGCAGGCCTGTTCAG
CCAAATTTCCACAAACTTGAAAATAAATCATCTATTGAAACAAAGGATGTGGAGGTAAACAATAAGAGTGACTGTCCACTTGGAGTTACTAAGGAAATAGCCATT
TGGGCTGAGAGAATAATGTTTTCTGATTTGAGAAGTCTACAACTCAAGAAAACCATGGAAATAAAGGGTACGGTTACCGAATTCAAACACCCAGGGGACTTCTAC
GTGCAGTTATATTCTTCAGAAGTTTTAGAATACATGAACCAACTCTCTGCCAGCTTAAAAGAAACATATGCAAATGTGCATGAAAAAGACTATATTCCTGTTAAG
GGGGAAGTTTGTATTGCCAAGTACACTGTTGATCAGACCTGGAACAGAGCAATCATACAAAACGTTGATGTGCAGCAAAAGAAGGCACATGTCTTATATATTGAT
TATGGAAATGAAGAAATAATTCCATTAAACAGAATTTACCACCTCAACAGGAACATTGACTTGTTTCCTCCTTGTGCCATAAAGTGCTTTGTAGCCAATGTTATC
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>TDRD1|56165|protein
MSVKSPFNVMSRNNLEAPPCKMTEPFNFEKNENKLPPHESLRSPGTLPNHPNFRLKSSENGNKKNNFLLCEQTKQYLASQEDNSVSSNPNGINGEVVGSKGDRKK
LPAGNSVSPPSAESNSPPKEVNIKPGNNVRPAKSKKLNKLVENSLSISNPGLFTSLGPPLRSTTCHRCGLFGSLRCSQCKQTYYCSTACQRRDWSAHSIVCRPVQ
PNFHKLENKSSIETKDVEVNNKSDCPLGVTKEIAIWAERIMFSDLRSLQLKKTMEIKGTVTEFKHPGDFYVQLYSSEVLEYMNQLSASLKETYANVHEKDYIPVK
GEVCIAKYTVDQTWNRAIIQNVDVQQKKAHVLYIDYGNEEIIPLNRIYHLNRNIDLFPPCAIKCFVANVIPAEGNWSSDCIKATKPLLMEQYCSIKIVDILEEEV
VTFAVEVELPNSGKLLDHVLIEMGYGLKPSGQDSKKENADQSDPEDVGKMTTENNIVVDKSDLIPKVLTLNVGDEFCGVVAHIQTPEDFFCQQLQSGRKLAELQA
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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) 0 (0) 0 (0) 0 (0) 0 (0) 0 (0) 0 (0) 0 (0) 0 (0) (0)
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
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
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top

Contact Us if you are an author of a study regarding this gene and do not find your study in this table or find errors in the representation of your study details.

Simple Query:


  (e.g. CHD8)

Syndromic Genes

Non-syndromic Genes

AutismKB Statistics

  • Studies: 1,036
  • Genes: 1,379
  • CNVs/SVs: 5,420
  • SNVs/Indels: 11,669
  • de novo Mutations: 5,669
  • Mosaics: 789
  • Linkage Regions: 172
  • Paper Collected: 6/30/2018
  • Last Update: 8/26/2018