Evidence Details for FAM13A

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Basic Information Top

Gene Symbol:	FAM13A ( FAM13A1,FLJ34562,MGC105131 )
Gene Full Name:	family with sequence similarity 13, member A
Band:	4q22.1
Quick Links	Entrez ID:10144; OMIM: 613299; Uniprot ID:FA13A_HUMAN; ENSEMBL ID: ENSG00000138640; HGNC ID: 19367
Relate to Another Database:	SFARIGene; denovo-db

Sequences Top

Nucleotide Sequence
Protein Sequence

>FAM13A|10144|nucleotide
ATGGCTTGTGAAATCATGCCTCTGCAAAGTTCACAGGAAGATGAAAGACCTCTGTCACCTTTCTATTTGAGTGCTCATGTACCCCAAGTCAGCAATGTGTCTGCA
ACCGGAGAACTCTTAGAAAGAACCATCCGATCAGCTGTAGAACAACATCTTTTTGATGTTAATAACTCTGGAGGTCAAAGTTCAGAGGACTCAGAATCTGGAACA
CTATCAGCATCTTCTGCCACATCTGCCAGACAGCGCCGCCGCCAGTCCAAGGAGCAGGATGAAGTTCGACATGGGAGAGACAAGGGACTTATCAACAAAGAAAAT
ACTCCTTCTGGGTTCAACCACCTTGATGATTGTATTTTGAATACTCAGGAAGTCGAAAAGGTACACAAAAATACTTTTGGTTGTGCTGGAGAAAGGAGCAAGCCT
AAACGTCAGAAATCCAGTACTAAACTTTCTGAGCTTCATGACAATCAGGACGGTCTTGTGAATATGGAAAGTCTCAATTCCACACGATCTCATGAGAGAACTGGA
CCTGATGATTTTGAATGGATGTCTGATGAAAGGAAAGGAAATGAAAAAGATGGTGGACACACTCAGCATTTTGAGAGCCCCACAATGAAGATCCAGGAGCATCCC
AGCCTATCTGACACCAAACAGCAGAGAAATCAAGATGCCGGTGACCAGGAGGAGAGCTTTGTCTCCGAAGTGCCCCAGTCGGACCTGACTGCATTGTGTGATGAA
AAGAACTGGGAAGAGCCTATCCCTGCTTTCTCCTCCTGGCAGCGGGAGAACAGTGACTCTGATGAAGCCCACCTCTCGCCGCAGGCTGGGCGCCTGATCCGTCAG
CTGCTGGACGAAGACAGCGACCCCATGCTCTCTCCTCGGTTCTACGCTTATGGGCAGAGCAGGCAATACCTGGATGACACAGAAGTGCCTCCTTCCCCACCAAAC
TCCCATTCTTTCATGAGGCGGCGAAGCTCCTCTCTGGGGTCCTATGATGATGAGCAAGAGGACCTGACACCTGCCCAGCTCACACGAAGGATTCAGAGCCTTAAA
AAGAAGATCCGGAAGTTTGAAGATAGATTCGAAGAAGAGAAGAAGTACAGACCTTCCCACAGTGACAAAGCAGCCAATCCGGAGGTTCTGAAATGGACAAATGAC
CTTGCCAAATTCCGGAGACAACTTAAAGAATCAAAACTAAAGATATCTGAAGAGGACCTAACTCCCAGGATGCGGCAGCGAAGCAACACACTCCCCAAGAGTTTT
GGTTCCCAACTTGAGAAAGAAGATGAGAAGAAGCAAGAGCTGGTGGATAAAGCAATAAAGCCCAGTGTTGAAGCCACATTGGAATCTATTCAGAGGAAGCTCCAG
GAGAAGCGAGCGGAAAGCAGCCGCCCTGAGGACATTAAGGATATGACCAAAGACCAGATTGCTAATGAGAAAGTGGCTCTGCAGAAAGCTCTGTTATATTATGAA
AGCATTCATGGACGGCCGGTAACAAAGAACGAACGGCAGGTGATGAAGCCACTATACGACAGGTACCGGCTGGTCAAACAGATCCTCTCCCGAGCTAACACCATA
CCCATCATTGGTTCCCCCTCCAGCAAGCGGAGAAGCCCTTTGCTGCAGCCAATTATCGAGGGCGAAACTGCTTCCTTCTTCAAGGAGATAAAGGAAGAAGAGGAG
GGGTCAGAAGACGATAGCAATGTGAAGCCAGACTTCATGGTCACTCTGAAAACCGATTTCAGTGCACGATGCTTTCTGGACCAATTCGAAGATGACGCTGATGGA
TTTATTTCCCCAATGGATGATAAAATACCATCAAAATGCAGCCAGGACACAGGGCTTTCAAATCTCCATGCTGCCTCAATACCTGAACTCCTGGAACACCTCCAG
GAAATGAGAGAAGAAAAGAAAAGGATTCGAAAGAAACTTCGGGATTTTGAAGACAACTTTTTCAGACAGAATGGAAGAAATGTCCAGAAGGAAGACCGCACTCCT
ATGGCTGAAGAATACAGTGAATATAAGCACATAAAGGCGAAACTGAGGCTCCTGGAGGTGCTCATCAGCAAGAGAGACACTGATTCCAAGTCCATGTGA
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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 (3)	0 (1)	1 (1)	0 (0)	0 (0)	0 (0)	0 (0)	0 (0)	0 (0)	2 (5)

Syndromic Autism Gene Top

Genome-Wide Association Studies (By Ethnic Group) Top

Family Based Association Studies: 3

Reference	Stage	Platform	#Families	Affecteds						Result
Reference	Stage	Platform	#Families	#Subjects (% Women)	ADI-R	ADOS	Diagnosis	Age (range)	IQ (range)	Result
CAUCASIAN
Salyakina, 2010_2	Replication	Illumina HumanHap 550K BeadChip	110	- (-)			AS	- (3-21)	- >70
Salyakina, 2010_1	Discovery	Illumina HumanHap 550K BeadChip	124	- (-)			AS	- (3-21)	- >70
Hussman, 2011_1	Discovery	Illumina Infinium Human 1 M beadship	597	- (-)			ASD	- -	- -

Case Control Based Association Studies: 0

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

CNV Studies Top

Reference	Source	Method	ADI-R	ADOS	Diagnosis	Family				Individual
Reference	Source	Method	ADI-R	ADOS	Diagnosis	Total	Simplex	Multiplex	Control	Affected	Control	Total
Jacquemont, 2006	France	aCGH			ASD	-	-	-	-	29	-	29

Linkage Studies Top

AutismKB 2.0

Evidence Details for FAM13A