AutismKB 2.0

Evidence Details for FAM111B


View Evidences View Variants View Annotations
Basic Information Top
Gene Symbol:FAM111B ( CANP )
Gene Full Name: family with sequence similarity 111, member B
Band: 11q12.1
Quick LinksEntrez ID:374393; OMIM: NA; Uniprot ID:F111B_HUMAN; ENSEMBL ID: ENSG00000189057; HGNC ID: 24200
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>FAM111B|374393|nucleotide
ATGAAGCAGACACATGCTGACACACCTGTTGATCATTGTCTATCTGGCATAAGAAAGTGTAGCAGCACCTTTAAGCTTAAAAGTGAAGTCAACAAGCATGAAACA
GCCCTTGAAATGCAGAATCCAAATTTGAACAATAAAGAATGTTGTTTCACCTTTACGTTGAATGGAAACTCCAGAAAATTAGACCGTAGTGTGTTTACAGCATAT
GGTAAACCCAGCGAGAGTATCTACTCAGCCCTGAGTGCTAATGACTATTTCAGTGAAAGGATAAAGAATCAGTTTAATAAGAACATTATTGTTTATGAAGAAAAG
ACAATAGATGGACATATAAATTTAGGAATGCCTCTCAAGTGCCTGCCTAGTGATTCTCATTTTAAAATTACATTTGGTCAAAGAAAGAGTAGCAAAGAAGATGGA
CACATATTACGCCAATGTGAAAATCCAAACATGGAATGCATTCTTTTTCATGTTGTTGCTATAGGAAGGACAAGAAAGAAGATTGTTAAGATCAACGAACTTCAT
GAAAAAGGAAGTAAACTTTGTATTTATGCCTTGAAGGGTGAGACTATTGAAGGAGCCTTATGCAAGGATGGCCGTTTTCGGTCTGACATAGGTGAATTTGAATGG
AAACTAAAGGAAGGTCATAAGAAAATTTATGGAAAACAGTCCATGGTGGATGAAGTATCTGGAAAAGTCTTAGAAATGGACATTTCAAAAAAAAAAGCATTACAA
CAGAAAGATATCCATAAAAAAATTAAACAGAATGAAAGTGCCACTGATGAAATTAATCACCAGAGTCTGATACAGTCTAAGAAAAAAGTCCACAAACCAAAGAAA
GATGGAGAGACCAAAGATGTAGAACACAGCAGAGAGCAAATTCTCCCACCTCAGGATCTAAGCCATTATATTAAAGATAAAACTCGCCAGACAATTCCCAGGATT
AGAAATTATTACTTTTGTAGTTTGCCCCGAAAATATAGGCAAATAAACTCACAAGTTAGACGGAGGCCGCATCTGGGTAGGCGGTATGCTATTAATCTGGATGTC
CAAAAGGAGGCAATTAATCTCTTAAAGAATTATCAAACGTTGAATGAAGCCATAATGCATCAGTATCCGAATTTTAAAGAGGAGGCACAGTGGGTAAGAAAATAT
Show »

>FAM111B|374393|protein
MKQTHADTPVDHCLSGIRKCSSTFKLKSEVNKHETALEMQNPNLNNKECCFTFTLNGNSRKLDRSVFTAYGKPSESIYSALSANDYFSERIKNQFNKNIIVYEEK
TIDGHINLGMPLKCLPSDSHFKITFGQRKSSKEDGHILRQCENPNMECILFHVVAIGRTRKKIVKINELHEKGSKLCIYALKGETIEGALCKDGRFRSDIGEFEW
KLKEGHKKIYGKQSMVDEVSGKVLEMDISKKKALQQKDIHKKIKQNESATDEINHQSLIQSKKKVHKPKKDGETKDVEHSREQILPPQDLSHYIKDKTRQTIPRI
RNYYFCSLPRKYRQINSQVRRRPHLGRRYAINLDVQKEAINLLKNYQTLNEAIMHQYPNFKEEAQWVRKYFREEQKRMNLSPAKQFNIYKKDFGKMTANSVSVAT
CEQLTYYSKSVGFMQWDNNGNTGNATCFVFNGGYIFTCRHVVHLMVGKNTHPSLWPDIISKCAKVTFTYTEFCPTPDNWFSIEPWLKVSNENLDYAILKLKENGN
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 (0) 0 (0) 0 (1) 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
Levy, 2011 Simons Simplex Collection aCGH--ASD 915 915 - - - - -
Linkage Studies Top