AutismKB 2.0

Evidence Details for ST8SIA2


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Basic Information Top
Gene Symbol:ST8SIA2 ( HsT19690,MGC116854,MGC116857,SIAT8B,ST8SIA-II,STX )
Gene Full Name: ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2
Band: 15q26.1
Quick LinksEntrez ID:8128; OMIM: 602546; Uniprot ID:SIA8B_HUMAN; ENSEMBL ID: ENSG00000140557; HGNC ID: 10870
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>ST8SIA2|8128|nucleotide
ATGCAGCTGCAGTTCCGGAGCTGGATGCTGGCCGCGCTCACGCTGCTCGTGGTCTTCCTCATCTTCGCAGACATCTCAGAGATCGAAGAAGAAATCGGGAATTCG
GGAGGCAGAGGTACAATCAGATCAGCTGTGAACAGCTTACATAGCAAATCTAATAGAGCTGAAGTTGTAATAAACGGCTCCTCATCACCAGCTGTTGTTGACAGA
AGTAATGAAAGCATCAAGCACAACATCCAGCCAGCCTCGTCCAAATGGAGACATAACCAGACGCTCTCTCTGAGGATCAGGAAGCAGATTTTAAAGTTCTTGGAT
GCTGAAAAGGACATTTCTGTCCTAAAGGGAACCCTGAAGCCTGGAGATATTATTCATTACATCTTCGATCGAGACAGCACCATGAATGTGTCCCAGAACCTCTAC
GAGCTCCTCCCCAGGACTTCGCCACTGAAGAATAAGCACTTTGGGACTTGTGCCATCGTGGGCAACTCGGGGGTCTTGCTGAACAGCGGCTGTGGGCAGGAGATT
GACGCCCACAGCTTCGTCATCAGGTGCAACCTGGCCCCAGTACAGGAGTATGCCCGGGATGTGGGGCTCAAGACAGACCTGGTAACCATGAACCCCTCGGTCATC
CAGCGGGCCTTTGAGGACTTGGTCAATGCCACGTGGCGGGAGAAGCTGCTGCAACGGCTGCACAGCCTCAATGGCAGCATCCTGTGGATCCCTGCCTTCATGGCC
CGGGGCGGCAAGGAGCGTGTTGAGTGGGTCAACGAGCTTATCCTGAAGCACCACGTCAACGTGCGCACTGCATACCCCTCGCTGCGCCTGCTGCACGCCGTTCGC
GGATACTGGCTGACCAACAAAGTCCACATCAAAAGACCCACCACCGGCCTCTTGATGTATACCCTGGCCACACGTTTCTGCAAACAAATCTACCTCTACGGCTTC
TGGCCCTTTCCGCTGGATCAGAACCAGAACCCAGTCAAGTACCACTATTATGACAGCCTCAAGTATGGCTACACCTCCCAGGCCAGCCCGCATACCATGCCCTTG
GAGTTTAAGGCCCTCAAGAGCCTACATGAGCAGGGGGCTTTGAAACTGACTGTCGGCCAGTGCGATGGGGCCACGTAG
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>ST8SIA2|8128|protein
MQLQFRSWMLAALTLLVVFLIFADISEIEEEIGNSGGRGTIRSAVNSLHSKSNRAEVVINGSSSPAVVDRSNESIKHNIQPASSKWRHNQTLSLRIRKQILKFLD
AEKDISVLKGTLKPGDIIHYIFDRDSTMNVSQNLYELLPRTSPLKNKHFGTCAIVGNSGVLLNSGCGQEIDAHSFVIRCNLAPVQEYARDVGLKTDLVTMNPSVI
QRAFEDLVNATWREKLLQRLHSLNGSILWIPAFMARGGKERVEWVNELILKHHVNVRTAYPSLRLLHAVRGYWLTNKVHIKRPTTGLLMYTLATRFCKQIYLYGF
WPFPLDQNQNPVKYHYYDSLKYGYTSQASPHTMPLEFKALKSLHEQGALKLTVGQCDGAT

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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 1 (2) 1 (3) 1 (1) 0 (0) 0 (0) 0 (0) 0 (0) 0 (1) 0 (0) 8 (7)
Syndromic Autism Gene Top
Genome-Wide Association Studies (By Ethnic Group) Top
Family Based Association Studies: 2
Reference Stage Platform #Families Affecteds Result
#Subjects
(% Women)
ADI-R ADOS Diagnosis Age
(range)
IQ
(range)
CAUCASIAN
Anney, 2010_4 Replication Illumina Human 1M-single Infinium BeadChip 476 702
(-)
ASD -
-
-
-
Anney, 2010_3 Discovery Illumina Human 1M-single Infinium BeadChip 897 909
(-)
ASD -
-
-
-
Case Control Based Association Studies: 0
Reference Stage Platform ASD Cases Normal Controls Result
#Subjects
(% Women)
ADI-R ADOS Diagnosis Age
(range)
IQ #Subjects
(% Women)
Age
(range)
No Evidence.
CNV Studies Top
Reference Source Method ADI-R ADOS Diagnosis Family Individual
Total Simplex Multiplex Control Affected Control Total
Bonati, 2005 - FISHautism - - - - 1 - 1
Szatmari, 2007 Europe, North America SNP microarrayASD 1491 - - - - - 0
Kamien B, 2014 - aCGHautism 1 - - - 1 - 1
Linkage Studies Top
Reference Source Method ADI-R ADOS Diagnosis Family Individual
Total Simplex Multiplex Control Affected Control Total
Risch, 1999 USA microsatellite-based genomic screenPDD 90 - 90 - - - -
Low Scale Association Studies (by Ethnic Group) Top
Large Scale Expression Studies Top
NGS de novo Mutation Studies Top
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Reference Source Platform ADI-R ADOS Diagnosis Family Affected Validation Method
Total Simplex Multiplex
Doan RN, 2016 - ---ASD - - - - -
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