AutismKB 2.0

Evidence Details for FAM117B


View Evidences View Variants View Annotations
Basic Information Top
Gene Symbol:FAM117B ( ALS2CR13,DKFZp686H01244,FLJ38771 )
Gene Full Name: family with sequence similarity 117, member B
Band: 2q33.2
Quick LinksEntrez ID:150864; OMIM: NA; Uniprot ID:F117B_HUMAN; ENSEMBL ID: ENSG00000138439; HGNC ID: 14440
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>FAM117B|150864|nucleotide
ATGTCCCAGCGGGTGAGGCGCAATGGGTCCCCCACGCCGGCCGGCTCCCTTGGGGGTGGTGCGGTGGCCACGGCCGGGGGACCCGGGAGCCGCTTGCAGCCCATG
AGGGCGACGGTTCCGTTCCAGCTGAAGCAGCAGCAGCAGCAGCAACATGGCAGCCCCACGCGGAGCGGCGGCGGCGGCGGCGGCAACAACAACGGTGGCTGCTGT
GGTGGCGCCTCAGGCCCCGCAGGCGGCGGCGGCGGCGGTGGCCCGCGCACCGCCTCGCGCAGCACCAGCCCCACGCGCGGCGGCGGGAACGCGGCCGCGCGCACC
AGCCCCACGGTGGCCACGCAGACGGGCGCGTCCGCGACGTCCACGCGAGGCACCAGCCCCACGCGCAGCGCCGCGCCTGGAGCTCGCGGGAGCCCCCCACGGCCG
CCGCCGCCGCCGCCGCTGCTGGGCACCGTGTCGTCGCCCAGCTCGTCGCCCACCCACCTGTGGACCGGCGAGGTGAGCGCGGCCCCACCCCCAGCCCGCGTCCGG
CATCGGAGGAGGTCTCCGGAGCAGAGCCGAAGCTCGCCGGAGAAGAGGAGCCCCAGCGCCCCGGTTTGCAAAGCAGGTGACAAAACACGACAGCCTTCTTCAAGC
CCCTCCAGTATTATCCGACGCACTTCCTCCCTGGATACTCTTGCTGCACCGTATCTTGCTGGACACTGGCCTCGGGATAGCCATGGGCAAGCTGCACCTTGCATG
AGGGACAAAGCTACACAGACAGAGAGTGCATGGGCTGAAGAATACTCTGAAAAGAAGAAAGGGTCTCACAAGCGCTCAGCATCTTGGGGCAGTACAGATCAACTT
AAGGAGATTGCAAAATTACGCCAGCAGTTGCAGAGAAGTAAACACAGCAGTCGGCATCATCGAGATAAAGAAAGACAGTCTCCATTTCATGGCAACCATGCAGCT
ATTAACCAGTGTCAGGCTCCTGTTCCAAAGAGTGCACTTATTCCTGTAATTCCCATCACCAAATCAACAGGCTCCCGGTTCCGGAATAGCGTGGAAGGATTGAAT
CAGGAGATTGAAATAATAATTAAAGAGACTGGGGAAAAGGAAGAGCAACTTATACCGCAAGATATTCCAGATGGCCATCGTGCTCCACCCCCCCTTGTACAGAGA
Show »

>FAM117B|150864|protein
MSQRVRRNGSPTPAGSLGGGAVATAGGPGSRLQPMRATVPFQLKQQQQQQHGSPTRSGGGGGGNNNGGCCGGASGPAGGGGGGGPRTASRSTSPTRGGGNAAART
SPTVATQTGASATSTRGTSPTRSAAPGARGSPPRPPPPPPLLGTVSSPSSSPTHLWTGEVSAAPPPARVRHRRRSPEQSRSSPEKRSPSAPVCKAGDKTRQPSSS
PSSIIRRTSSLDTLAAPYLAGHWPRDSHGQAAPCMRDKATQTESAWAEEYSEKKKGSHKRSASWGSTDQLKEIAKLRQQLQRSKHSSRHHRDKERQSPFHGNHAA
INQCQAPVPKSALIPVIPITKSTGSRFRNSVEGLNQEIEIIIKETGEKEEQLIPQDIPDGHRAPPPLVQRSSSTRSIDTQTPGGADRGSNNSSRSQSVSPTSFLT
ISNEGSEESPCSADDLLVDPRDKENGNNSPLPKYATSPKPNNSYMFKREPPEGCERVKVFEECSPKQLHEIPAFYCPDKNKVNFIPKSGSAFCLVSILKPLLPTP
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 (1) 0 (0) 0 (0) 0 (0) 0 (1)
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Linkage Studies Top