AutismKB 2.0

Evidence Details for ID2


View Evidences View Variants View Annotations
Basic Information Top
Gene Symbol:ID2 ( GIG8,ID2A,ID2H,MGC26389,bHLHb26 )
Gene Full Name: inhibitor of DNA binding 2, dominant negative helix-loop-helix protein
Band: 2p25.1
Quick LinksEntrez ID:3398; OMIM: 600386; Uniprot ID:ID2_HUMAN; ENSEMBL ID: ENSG00000115738; HGNC ID: 5361
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>ID2|3398|nucleotide
ATGAAAGCCTTCAGTCCCGTGAGGTCCGTTAGGAAAAACAGCCTGTCGGACCACAGCCTGGGCATCTCCCGGAGCAAAACCCCTGTGGACGACCCGATGAGCCTG
CTATACAACATGAACGACTGCTACTCCAAGCTCAAGGAGCTGGTGCCCAGCATCCCCCAGAACAAGAAGGTGAGCAAGATGGAAATCCTGCAGCACGTCATCGAC
TACATCTTGGACCTGCAGATCGCCCTGGACTCGCATCCCACTATTGTCAGCCTGCATCACCAGAGACCCGGGCAGAACCAGGCGTCCAGGACGCCGCTGACCACC
CTCAACACGGATATCAGCATCCTGTCCTTGCAGGCTTCTGAATTCCCTTCTGAGTTAATGTCAAATGACAGCAAAGCACTGTGTGGCTGA







Show »

>ID2|3398|protein
MKAFSPVRSVRKNSLSDHSLGISRSKTPVDDPMSLLYNMNDCYSKLKELVPSIPQNKKVSKMEILQHVIDYILDLQIALDSHPTIVSLHHQRPGQNQASRTPLTT
LNTDISILSLQASEFPSELMSNDSKALCG



Show »

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 (0) 1 (1) 0 (1) 0 (0) 0 (0) 0 (0) 0 (0) 0 (0) 2 (2)
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Linkage Studies Top