AutismKB 2.0

Evidence Details for C12orf34


View Evidences View Variants View Annotations
Basic Information Top
Gene Symbol:C12orf34 ( FLJ14721 )
Gene Full Name: chromosome 12 open reading frame 34
Band: 12q24.11
Quick LinksEntrez ID:84915; OMIM: NA; Uniprot ID:CL034_HUMAN; ENSEMBL ID: ENSG00000139438; HGNC ID:
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>C12orf34|84915|nucleotide
ATGCTGGCCTGTCTGCAGAGGACCCAGAACGCCCCGGGCCAACACCTGGCCTGCCCGAGCAAGAGCCTGGAGCTGCGCAAGTGCGAGGCGGTGGCCAGCGCCATG
CATTCCTCCCGCTACCCGAGCCCAGCAGAACTGGACGCCTATGCCGAGAAGGTGGCCAACAGCCCGCTGTCCATCAAGATCTTCCCCACCAACATCCGTGTGCCC
CAGCACAAGCACCTCAGCCGCACAGTCAATGGCTATGACACCAGTGGCCAGCGCTACAGCCCCTACCCACAGCACACCGCTGGCTACCAGGGCCTTCTGGCCATT
GTCAAGGCCGCGGTTTCCTCCTCCAGCACGGCCGCACCAGCTGGGCCCGCCAAAAGTGTGCTCAAGAGCGCCGAGGGCAAGCGGACCAAGCTGTCACCGGCCGCC
GTGCAGGTGGGCATTGCGCCCTACCCAGTGCCCAGCACTCTGGGTCCCTTGGCCTACCCCAAGCCACCTGAGGCGCCTGCTCCACCACCCGGCCTGCCCGCAGCC
GCCACTGCCGCCTCCGTCATCCCCCTGCCGGGCCGGGGCCTGCCCCTGCCACCTTCCAACCTGCCCTCCATCCACAGCCTCCTGTACCAGCTCAACCAGCAGTGC
CAGGCCCCGGGCGCCGCACCCCCTGCCTGCCAGGGCATGGCTATTCCCCATCCCAGCCCTGCCAAGCACGGCCCAGTGCCCAGCTTCCCCAGCATGGCCTACTCG
GCTGCAGCCGGTCTGCCCGACTGCCGGAAAGGCACTGAGCTGGGCCAGGGAGCCACCCAAGCCTTGACGTTGGCTGGGGCCGCCAAGCCTGCAGGGTACGCAGAC
AGCGGCCTGGATTACCTGCTGTGGCCGCAGAAACCGCCCCCACCGCCGCCCCAGCCACTGCGTGCCTACAGTGGGAGCACGGTGGCCAGCAAGTCCCCTGAGGCT
TGCGGGGGCCGGGCATACGAGCGGGCCAGCGGGTCACCCCTCAACTGTGGCGTGGGGCTGCCCACCAGCTTCACCGTAGGCCAGTACTTTGCGGCCCCGTGGAAC
AGTGTGCTGGTGACACCCACCAGCGACTGCTACAACCCAGCGGCGGCGGTGGTGGTCACGGAGCTGGGGCCGGGGGCAGCCCGGGAGCTGGCTGGGCCCCCTGCA
Show »

>C12orf34|84915|protein
MLACLQRTQNAPGQHLACPSKSLELRKCEAVASAMHSSRYPSPAELDAYAEKVANSPLSIKIFPTNIRVPQHKHLSRTVNGYDTSGQRYSPYPQHTAGYQGLLAI
VKAAVSSSSTAAPAGPAKSVLKSAEGKRTKLSPAAVQVGIAPYPVPSTLGPLAYPKPPEAPAPPPGLPAAATAASVIPLPGRGLPLPPSNLPSIHSLLYQLNQQC
QAPGAAPPACQGMAIPHPSPAKHGPVPSFPSMAYSAAAGLPDCRKGTELGQGATQALTLAGAAKPAGYADSGLDYLLWPQKPPPPPPQPLRAYSGSTVASKSPEA
CGGRAYERASGSPLNCGVGLPTSFTVGQYFAAPWNSVLVTPTSDCYNPAAAVVVTELGPGAARELAGPPADALSGLPSKSVCNTSVLSSSLQSLEYLINDIRPPC
IKEQMLGKGYETVAVPRLLDHQHAHIRLPVYR
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 (1) 0 (0) 0 (0) 0 (0) 0 (1) 0 (0) 0 (0) 0 (0) 0 (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
Szatmari, 2007 Europe, North America SNP microarrayASD 1491 - - - - - 0
Linkage Studies Top