AutismKB 2.0

Evidence Details for ANKRD5


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Basic Information Top
Gene Symbol:ANKRD5 ( FLJ21669,dJ839B4.6 )
Gene Full Name: ankyrin repeat domain 5
Band: 20pter-q11.23
Quick LinksEntrez ID:63926; OMIM: NA; Uniprot ID:ANKR5_HUMAN; ENSEMBL ID: ENSG00000132623; HGNC ID:
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>ANKRD5|63926|nucleotide
ATGGCTTTAGCAGATAAGAGACTTGAGAACTTACAGATCTACAAAGTTCTTCAATGTGTGCGGAACAAAGACAAGAAGCAGATAGAGAAGCTGACCAAGCTTGGA
TACCCTGAACTAATCAATTATACAGAACCCATTAATGGACTTAGTGCTTTGCACTTAGCCTCAGTTTCCAATGATATTGATATGGTCAGCTTTCTCCTTGACCTT
GGTGCTCACCCTGATGTGCAAGACCGAATGGGCTGTACTCCCACAATGAGGGCTGCAGAACTGGGCCATGAATTGTCAATGGAAATATTAGCAAAGGCAAAGGCT
GATATGACTATAGTTGATAATGAAGGAAAAGGTGTTTTGTTTTACTGCATTTTACCGACTAAGCGGCATTATCGCTGTGCTCTGATCGCCCTTGAACATGGTGCA
GATGTCAACAATTCTACCTATGAAGGAAAGCCAATATTCCTTAGAGCTTGTGAAGATGCACATGATGTTAAAGATGTGTGCCTGACATTTTTGGAAAAAGGAGCC
AATCCTAATGCAATCAACTCATCCACAGGCCGCACAGCTTTAATGGAAGCGTCAAGAGAAGGGGTAGTGGAAATAGTTCGAGGCATATTGGAAAGAGGAGGTGAA
GTGAATGCATTTGACAACGACAGGCATCACGCTGCTCATTTTGCTGCTAAAGGAGGCTTTTTCGATATATTGAAGCTTCTTTTTGCCTACAATGGAGACGTGGGG
CTGATTTCGATAAATGGGAACACACCACTTCATTATGCTGCCATGGGTGGTTTTGCAGACTGCTGTAAATATATAGCTCAGCGAGGATGTGACCTGAAATGGAAG
AATTTAGATCATAAAACGCCCAGGGCTGTGGCTAAGGAAGGCGGCTTCAAAGCAGCAAGCAAAGAAATACGCCGAGCAGAGAGAATCGCTAATAAACTAGCCAGG
CCAGGAGCCAAAAATCCAAATCCACTGTGGGCCCTTAGACTGCACGATTGGTCCGTAGAACGTGAGGCTTTCCTCCGGGAAGCCTTTGCGGTTTTAGACAGGGGT
GATGGAAGCATCAGCAAGAACGACTTCGTGATGGTGTTGGAGGAAAGGCAGGATTATGCAAGCTCAGAACAGCTGGCTGCCATCGCTCACCTTCATGAGAAAACC
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>ANKRD5|63926|protein
MALADKRLENLQIYKVLQCVRNKDKKQIEKLTKLGYPELINYTEPINGLSALHLASVSNDIDMVSFLLDLGAHPDVQDRMGCTPTMRAAELGHELSMEILAKAKA
DMTIVDNEGKGVLFYCILPTKRHYRCALIALEHGADVNNSTYEGKPIFLRACEDAHDVKDVCLTFLEKGANPNAINSSTGRTALMEASREGVVEIVRGILERGGE
VNAFDNDRHHAAHFAAKGGFFDILKLLFAYNGDVGLISINGNTPLHYAAMGGFADCCKYIAQRGCDLKWKNLDHKTPRAVAKEGGFKAASKEIRRAERIANKLAR
PGAKNPNPLWALRLHDWSVEREAFLREAFAVLDRGDGSISKNDFVMVLEERQDYASSEQLAAIAHLHEKTRGGGVNINEFFKGTRYLNKSFVLGSYGPKKKEKGM
GKKGKKGKFVLPLPICVIPEYAFPRRQDGGPPYYMIETYKNVTDSSRFNRDHPPEHPIQDDSVWYIDDSEKVFSNINIITKAGDLASLKKAFESGIPVDMKDNYY
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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 (1) 0 (0) 0 (0) 0 (0) 0 (1) 0 (0) 0 (0) 0 (0) 2 (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
Sauter, 2003 - FISHautism - - - - 1 - 1
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
De Rubeis S, 2014 2270 - 1702 Synaptic, transcriptional and chromatin genes disrupted in autism
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top

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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