AutismKB 2.0

Evidence Details for C10orf122


View Evidences View Variants View Annotations
Basic Information Top
Gene Symbol:C10orf122 ( FLJ27500,MGC157877,MGC157878,bA383C5.1 )
Gene Full Name: chromosome 10 open reading frame 122
Band: 10q26.13
Quick LinksEntrez ID:387718; OMIM: NA; Uniprot ID:CJ122_HUMAN; ENSEMBL ID: ENSG00000175018; HGNC ID:
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>C10orf122|387718|nucleotide
ATGACCAAAGGGCGACGCTTCAACCCACCTTCAGACAAGGATGGGAGATGGTTCCCTCACATCGGGCTAACGCAAAAGACACCAGAATCCATCACCAGTGCTACG
TCAAAAGAGCCCCAGAGTCCACACTTGCCTCGGCAAGCGGAGGGGAAGCTGCCGCCCATATACAAAGTCCGGGAGAAGCAAGCAGTGAATAACCAGTTCCCCTTC
TCCGTGCATGACAATCGGCACAGCTTGGAGAACTCTGGATGCTACCTTGACTCCGGCCTGGGACGTAAGAAGATCTCTCCAGATAAGAGGCAACATGTTTCAAGA
AATTTTAATCTCTGGGCATGTGACTATGTTCCATCTTGTCTTGATGGCTTTTCAAATAACCAAATATCATACGTATATAAAGAAGCCATGGTGGTCTCAAGCTTC
AGACGCTTTCCACGATGCTATAAAGAGATATGGAACGCTTTTACATTTCTTCCTGAGAGAAGCTATACAGAGGTTTTGAAAAAGAAGCCCAAAGTAAGGTTCACT
GTTGACAAAAAGGTTGTTTCTTCACTGGAGTCCTAA





Show »

>C10orf122|387718|protein
MTKGRRFNPPSDKDGRWFPHIGLTQKTPESITSATSKEPQSPHLPRQAEGKLPPIYKVREKQAVNNQFPFSVHDNRHSLENSGCYLDSGLGRKKISPDKRQHVSR
NFNLWACDYVPSCLDGFSNNQISYVYKEAMVVSSFRRFPRCYKEIWNAFTFLPERSYTEVLKKKPKVRFTVDKKVVSSLES



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