AutismKB 2.0

Evidence Details for SMYD2


View Evidences View Variants View Annotations
Basic Information Top
Gene Symbol:SMYD2 ( HSKM-B,KMT3C,MGC119305,ZMYND14 )
Gene Full Name: SET and MYND domain containing 2
Band: 1q32.3
Quick LinksEntrez ID:56950; OMIM: 610663; Uniprot ID:SMYD2_HUMAN; ENSEMBL ID: ENSG00000143499; HGNC ID: 20982
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>SMYD2|56950|nucleotide
ATGAGGGCCGAGGGCCTCGGCGGCCTGGAGCGCTTCTGCAGCCCGGGCAAAGGCCGGGGGCTGCGGGCTCTGCAGCCCTTCCAGGTGGGGGACTTGCTGTTCTCC
TGCCCGGCCTATGCCTACGTGCTCACGGTCAACGAGCGGGGCAACCACTGCGAGTACTGCTTCACCAGGAAAGAAGGATTGTCCAAATGTGGAAGATGCAAGCAG
GCATTTTACTGCAATGTGGAGTGTCAGAAAGAAGATTGGCCCATGCACAAGCTGGAATGTTCTCCCATGGTTGTTTTTGGGGAAAACTGGAATCCCTCGGAGACT
GTAAGACTAACAGCAAGGATTCTGGCCAAACAGAAAATCCACCCAGAGAGAACACCTTCGGAAAAATTGTTAGCTGTGAAGGAGTTTGAATCACATCTGGATAAG
TTAGACAATGAGAAGAAGGATTTGATTCAGAGTGACATAGCTGCTCTCCATCACTTTTACTCCAAGCATCTCGGATTCCCTGACAATGATAGCCTCGTAGTACTC
TTTGCACAGGTTAACTGTAATGGCTTCACAATTGAAGATGAAGAACTTTCTCATTTGGGATCAGCGATATTTCCTGATGTTGCATTGATGAATCATAGCTGTTGC
CCCAATGTCATTGTGACCTACAAAGGGACCCTGGCAGAAGTCAGAGCTGTACAGGAAATCAAGCCGGGAGAGGAGGTTTTTACCAGCTATATTGATCTCCTGTAC
CCAACGGAAGATAGAAATGACCGGTTAAGAGATTCTTATTTCTTTACCTGTGAGTGCCAGGAGTGTACCACCAAGGACAAGGATAAGGCCAAGGTGGAAATCCGG
AAGCTCAGCGATCCCCCAAAGGCAGAAGCCATCCGAGACATGGTCAGATATGCACGCAACGTCATTGAAGAGTTCCGGAGGGCCAAGCACTATAAATCCCCTAGT
GAGCTGCTGGAGATCTGCGAGCTCAGCCAGGAGAAGATGAGCTCTGTGTTTGAGGACAGTAACGTGTACATGTTGCACATGATGTACCAGGCCATGGGTGTCTGC
TTGTACATGCAGGACTGGGAAGGAGCCCTGCAATATGGACAGAAAATCATTAAGCCCTACAGTAAGCACTATCCTTTGTACTCCCTCAACGTGGCCTCCATGTGG
Show »

>SMYD2|56950|protein
MRAEGLGGLERFCSPGKGRGLRALQPFQVGDLLFSCPAYAYVLTVNERGNHCEYCFTRKEGLSKCGRCKQAFYCNVECQKEDWPMHKLECSPMVVFGENWNPSET
VRLTARILAKQKIHPERTPSEKLLAVKEFESHLDKLDNEKKDLIQSDIAALHHFYSKHLGFPDNDSLVVLFAQVNCNGFTIEDEELSHLGSAIFPDVALMNHSCC
PNVIVTYKGTLAEVRAVQEIKPGEEVFTSYIDLLYPTEDRNDRLRDSYFFTCECQECTTKDKDKAKVEIRKLSDPPKAEAIRDMVRYARNVIEEFRRAKHYKSPS
ELLEICELSQEKMSSVFEDSNVYMLHMMYQAMGVCLYMQDWEGALQYGQKIIKPYSKHYPLYSLNVASMWLKLGRLYMGLEHKAAGEKALKKAIAIMEVAHGKDH
PYISEIKQEIESH
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) 0 (0) 0 (0) 1 (1) 0 (0) 0 (0) 0 (0) 0 (0) 1 (1)
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Linkage Studies Top