Evidence Details for FAM117B
Basic Information Top
| Gene Symbol: | FAM117B ( ALS2CR13,DKFZp686H01244,FLJ38771 ) |
|---|---|
| Gene Full Name: | family with sequence similarity 117, member B |
| Band: | 2q33.2 |
| Quick Links | Entrez 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
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ATGTCCCAGCGGGTGAGGCGCAATGGGTCCCCCACGCCGGCCGGCTCCCTTGGGGGTGGTGCGGTGGCCACGGCCGGGGGACCCGGGAGCCGCTTGCAGCCCATG
AGGGCGACGGTTCCGTTCCAGCTGAAGCAGCAGCAGCAGCAGCAACATGGCAGCCCCACGCGGAGCGGCGGCGGCGGCGGCGGCAACAACAACGGTGGCTGCTGT
GGTGGCGCCTCAGGCCCCGCAGGCGGCGGCGGCGGCGGTGGCCCGCGCACCGCCTCGCGCAGCACCAGCCCCACGCGCGGCGGCGGGAACGCGGCCGCGCGCACC
AGCCCCACGGTGGCCACGCAGACGGGCGCGTCCGCGACGTCCACGCGAGGCACCAGCCCCACGCGCAGCGCCGCGCCTGGAGCTCGCGGGAGCCCCCCACGGCCG
CCGCCGCCGCCGCCGCTGCTGGGCACCGTGTCGTCGCCCAGCTCGTCGCCCACCCACCTGTGGACCGGCGAGGTGAGCGCGGCCCCACCCCCAGCCCGCGTCCGG
CATCGGAGGAGGTCTCCGGAGCAGAGCCGAAGCTCGCCGGAGAAGAGGAGCCCCAGCGCCCCGGTTTGCAAAGCAGGTGACAAAACACGACAGCCTTCTTCAAGC
CCCTCCAGTATTATCCGACGCACTTCCTCCCTGGATACTCTTGCTGCACCGTATCTTGCTGGACACTGGCCTCGGGATAGCCATGGGCAAGCTGCACCTTGCATG
AGGGACAAAGCTACACAGACAGAGAGTGCATGGGCTGAAGAATACTCTGAAAAGAAGAAAGGGTCTCACAAGCGCTCAGCATCTTGGGGCAGTACAGATCAACTT
AAGGAGATTGCAAAATTACGCCAGCAGTTGCAGAGAAGTAAACACAGCAGTCGGCATCATCGAGATAAAGAAAGACAGTCTCCATTTCATGGCAACCATGCAGCT
ATTAACCAGTGTCAGGCTCCTGTTCCAAAGAGTGCACTTATTCCTGTAATTCCCATCACCAAATCAACAGGCTCCCGGTTCCGGAATAGCGTGGAAGGATTGAAT
CAGGAGATTGAAATAATAATTAAAGAGACTGGGGAAAAGGAAGAGCAACTTATACCGCAAGATATTCCAGATGGCCATCGTGCTCCACCCCCCCTTGTACAGAGA
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>FAM117B|150864|protein
MSQRVRRNGSPTPAGSLGGGAVATAGGPGSRLQPMRATVPFQLKQQQQQQHGSPTRSGGGGGGNNNGGCCGGASGPAGGGGGGGPRTASRSTSPTRGGGNAAART
SPTVATQTGASATSTRGTSPTRSAAPGARGSPPRPPPPPPLLGTVSSPSSSPTHLWTGEVSAAPPPARVRHRRRSPEQSRSSPEKRSPSAPVCKAGDKTRQPSSS
PSSIIRRTSSLDTLAAPYLAGHWPRDSHGQAAPCMRDKATQTESAWAEEYSEKKKGSHKRSASWGSTDQLKEIAKLRQQLQRSKHSSRHHRDKERQSPFHGNHAA
INQCQAPVPKSALIPVIPITKSTGSRFRNSVEGLNQEIEIIIKETGEKEEQLIPQDIPDGHRAPPPLVQRSSSTRSIDTQTPGGADRGSNNSSRSQSVSPTSFLT
ISNEGSEESPCSADDLLVDPRDKENGNNSPLPKYATSPKPNNSYMFKREPPEGCERVKVFEECSPKQLHEIPAFYCPDKNKVNFIPKSGSAFCLVSILKPLLPTP
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MSQRVRRNGSPTPAGSLGGGAVATAGGPGSRLQPMRATVPFQLKQQQQQQHGSPTRSGGGGGGNNNGGCCGGASGPAGGGGGGGPRTASRSTSPTRGGGNAAART
SPTVATQTGASATSTRGTSPTRSAAPGARGSPPRPPPPPPLLGTVSSPSSSPTHLWTGEVSAAPPPARVRHRRRSPEQSRSSPEKRSPSAPVCKAGDKTRQPSSS
PSSIIRRTSSLDTLAAPYLAGHWPRDSHGQAAPCMRDKATQTESAWAEEYSEKKKGSHKRSASWGSTDQLKEIAKLRQQLQRSKHSSRHHRDKERQSPFHGNHAA
INQCQAPVPKSALIPVIPITKSTGSRFRNSVEGLNQEIEIIIKETGEKEEQLIPQDIPDGHRAPPPLVQRSSSTRSIDTQTPGGADRGSNNSSRSQSVSPTSFLT
ISNEGSEESPCSADDLLVDPRDKENGNNSPLPKYATSPKPNNSYMFKREPPEGCERVKVFEECSPKQLHEIPAFYCPDKNKVNFIPKSGSAFCLVSILKPLLPTP
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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

