Evidence Details for C1orf168

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Basic Information Top

Gene Symbol:	C1orf168 ( FLJ43208 )
Gene Full Name:	chromosome 1 open reading frame 168
Band:	1p32.2
Quick Links	Entrez ID:199920; OMIM: NA; Uniprot ID:CA168_HUMAN; ENSEMBL ID: ENSG00000187889; HGNC ID:
Relate to Another Database:	SFARIGene; denovo-db

Sequences Top

Nucleotide Sequence
Protein Sequence

>C1orf168|199920|nucleotide
ATGGAAGGGGAAGGGGTAAGAAACTTCAAGGAACTTCGAGCCAAATTTCAAAATCTTGATGCTCCACCTCTTCCAGGACCTATTAAATTCCCAGCAGGTGTTTCT
CCAAAGGGTGACATTGGAGGCACACAGTCAACTCAAATTTTGGCCAATGGGAAACCCCTCTCATCCAACCACAAGCAGCGCACACCATACTGTTCCAGTAGTGAG
TCCCAGCCTCTTCAACCTCAGAAAATAAAGTTGGCTCAGAAGAGTGAAATTCCAAAATGTTCTAACTCCCCAGGGCCTCTGGGAAAGTCTACTGTATGTTCTGCA
ACAAGTTCACAGAAGGCTTCTCTGCTGTTAGAGGTGACTCAATCAAATGTTGAGATAATCACTAAGGAAAAAGTAATGGTGGCCAATAGCTTCAGAAACAAACTC
TGGAACTGGGAGAAGGTTTCATCTCAGAAAAGTGAAATGTCTTCAGCCCTTCTCCTTGCCAACTATGGAAGTAAGGCCATCCATCTGGAAGGGCAAAAAGGCATG
GGGCTTACTCCAGAGGAACCCAGGAAAAAGCTGGAAACAAAAGGAGCCCAGACTCTTCCTTCCCAGAAGCACGTGGTGGCCCCCAAAATATTACATAACGTCTCT
GAAGATCCCTCTTTTGTAATTTCTCAACATATCAGAAAAAGCTGGGAAAACCCACCTCCTGAGAGGAGCCCGGCAAGCAGCCCCTGCCAGCCCATCTATGAGTGT
GAGCTTGCCAGTCAGGCCCCAGAAAAACAGCCAGATGTCAGGCATCACCACCTTCCCAAAACAAAGCCATTGCCCTCCATCGACTCCCTGGGTCCTCCTCCCCCA
AAGCCTTCAAGACCTCCCATCGTGAACCTCCAGGCCTTTCAGAGGCAGCCAGCTGCTGTTCCCAAGACTCAGGGGGAAGTGACTGTGGAAGAGGGCTCCCTGTCT
CCAGAGAGGCTTTTCAATGCAGAATTTGAAGAACCACATAATTACGAGGCAACAATTTCATATCTGAGACACTCTGGCAACTCCATTAACCTGTGCACTGCAAAA
GAAATTGCTGATCCAACTTATGAAGTTGGAATTGAAGAACTCCAAAAGCCTGGGAAGAATTTTCCCTATCCAGAACCTAGTGCTAAACATGAAGATAAAAAAATG
AAGGAAAAACAACCATGTGAATTGAAACCTAAAAACACAGAAAAGGAACCATATTCAAACCATGTTTTCAAGGTAGATGCCTGTGAAGGGACACCTGAAAAAATT
CAGATGACCAACGTCCACACAGGTAGAAGGAACATGTTGGCTGGAAAGCAAGAGGCCATGATTGACATCATCCAGACAAATCCCTGCCCTGAGGGCCCAAAGCTG
GCCAGGCACTCCCAAGGCCACTGTGGGCATCTGGAGGTTTTGGAGTCAACTAAAGAAACTCCAGACCTAGGGGTCTCTAAGACAAGTTCCATCTCGGAGGAGATA
TATGATGATGTCGAGTACTCCAGGAAAGAGGTACCGAAGCTGAACTACTCTAGCTCACTTGCCTCAAGTAGTGAAGAAAATAGAGAACTGTATGAAGATGTCTAC
AAAACAAAGAACAACTACCCAAAGATAGATTTAGATGGAAAAGAAGCACTCAAAAGACTGCAGCAATTCTTCAAGAAAGAAAAGGATAGATTTAAAATAAAGAAA
ACCAAGTCGAAAGAAAACTTAAGTGCATTTTCCATTTTGCTGCCTGATTTAGAACTTAAGTCTCAGGAAGTTATTATTTATGATGATGTAGACCTGAGTGAAAAA
GAGTCAAAAGATGAAGATAAACTGAAAATGTGGAAGCCCAAGTTTCTGACACCAAAGGAAAAAAAAGAGAAAAACGGTGCTGAAGAATCAGAAAGTTTCTCTCCT
AGAAATTTCTTCAAAACCAAGAAGCAAAACTTAGAAAAGAACAGAATGAAAAGAGAAGAAAAACTATTTAGAGAAAGGTTTAAGTACGACAAAGAGATTATTGTC
ATCAATACAGCAGTGGCCTGTTCCAATAATTCAAGAAATGGAATATTTGATTTGCCAATAAGTCCTGGAGAAGAATTGGAAGTCATTGATACCACCGAACAAAAT
CTAGTGATATGTCGTAATTCTAAAGGCAAATATGGATATGTGCTCATTGAACATCTAGATTTCAAGCATCAAAGTTGGTCACCTTAG
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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 (0)	0 (0)	0 (1)	0 (0)	0 (1)

Syndromic Autism Gene Top

Genome-Wide Association Studies(By Ethnic Group) Top

Reference	Stage	Platform	#Families	Affecteds	Result
#Subjects (% Women)	ADI-R	ADOS	Diagnosis	Age (range)	IQ (range)
No Evidence.

Reference	Stage	Platform	ASD Cases	Normal Controls	Result
#Subjects (% Women)	ADI-R	ADOS	Diagnosis	Age (range)	IQ	#Subjects (% Women)	Age (range)
No Evidence.

CNV Studies Top

Reference	Source	Method	ADI-R	ADOS	Diagnosis	Family	Individual
Total	Simplex	Multiplex	Control	Affected	Control	Total
No matched CNVs !

Linkage Studies Top

AutismKB 2.0

Evidence Details for C1orf168