Evidence Details for ARL6IP6


Gene Symbol: | ARL6IP6 ( MGC33864,PFAAP1 ) |
---|---|
Gene Full Name: | ADP-ribosylation-like factor 6 interacting protein 6 |
Band: | 2q23.3 |
Quick Links | Entrez ID:151188; OMIM: NA; Uniprot ID:AR6P6_HUMAN; ENSEMBL ID: ENSG00000177917; HGNC ID: 24048 |
Relate to Another Database: | SFARIGene; denovo-db |


>ARL6IP6|151188|nucleotide
ATGTCGTTTGCTGAGAGCGGGTGGCGGTCGGCTCTGCGGCGCCGCGGTCCCGGCACCCCGGGCCCTGTGGCTCGGCCATCGTATTCCTCCTTTACTCAGGGGGAC
AGCTGGGGTGAAGGCGAAGTCGACGAGGAGGAGGGATGCGACCAAGTGGCCCGCGACCTGCGGGCGGAGTTCTCGGCTGGGGCGTGGTCAGAGCCCAGAAAGCGC
TCGGTGCTCCCGCCGGACGGGAACGGGTCGCCCGTTCTGCCCGATAAGCGCAATGGTATCTTTCCCGCGGCCGCGGGCAGCAGAGCCCAGCCTCGGCGGTGGCCG
GTCCAGGTCCTCTCTATTCTCTGCTCGCTGCTCTTCGCCATTCTTCTCGCCTTCCTCCTCGCCATCGCCTACTTGATCGTTAAAGAGTTGCATGCTGAGAATTTG
AAAAATGAAGATGATGTAGACACTGGACTATTAGGATTCTGGACTCTACTTATAATATCCCTAACTGCTGGATTCTCCTGTTGCAGCTTTTCTTGGACAGTGACT
TACTTTGATTCTTTTGAACCAGGAATGTTTCCTCCTACTCCTCTTTCACCTGCCAGGTTCAAGAAACTGACTGGACATTCTTTCCACATGGGCTATAGCATGGCG
ATTTTGAATGGCATCGTAGCTGCTCTTACTGTAGCATGGTGCCTCATGTAA
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ATGTCGTTTGCTGAGAGCGGGTGGCGGTCGGCTCTGCGGCGCCGCGGTCCCGGCACCCCGGGCCCTGTGGCTCGGCCATCGTATTCCTCCTTTACTCAGGGGGAC
AGCTGGGGTGAAGGCGAAGTCGACGAGGAGGAGGGATGCGACCAAGTGGCCCGCGACCTGCGGGCGGAGTTCTCGGCTGGGGCGTGGTCAGAGCCCAGAAAGCGC
TCGGTGCTCCCGCCGGACGGGAACGGGTCGCCCGTTCTGCCCGATAAGCGCAATGGTATCTTTCCCGCGGCCGCGGGCAGCAGAGCCCAGCCTCGGCGGTGGCCG
GTCCAGGTCCTCTCTATTCTCTGCTCGCTGCTCTTCGCCATTCTTCTCGCCTTCCTCCTCGCCATCGCCTACTTGATCGTTAAAGAGTTGCATGCTGAGAATTTG
AAAAATGAAGATGATGTAGACACTGGACTATTAGGATTCTGGACTCTACTTATAATATCCCTAACTGCTGGATTCTCCTGTTGCAGCTTTTCTTGGACAGTGACT
TACTTTGATTCTTTTGAACCAGGAATGTTTCCTCCTACTCCTCTTTCACCTGCCAGGTTCAAGAAACTGACTGGACATTCTTTCCACATGGGCTATAGCATGGCG
ATTTTGAATGGCATCGTAGCTGCTCTTACTGTAGCATGGTGCCTCATGTAA
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>ARL6IP6|151188|protein
MSFAESGWRSALRRRGPGTPGPVARPSYSSFTQGDSWGEGEVDEEEGCDQVARDLRAEFSAGAWSEPRKRSVLPPDGNGSPVLPDKRNGIFPAAAGSRAQPRRWP
VQVLSILCSLLFAILLAFLLAIAYLIVKELHAENLKNEDDVDTGLLGFWTLLIISLTAGFSCCSFSWTVTYFDSFEPGMFPPTPLSPARFKKLTGHSFHMGYSMA
ILNGIVAALTVAWCLM
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MSFAESGWRSALRRRGPGTPGPVARPSYSSFTQGDSWGEGEVDEEEGCDQVARDLRAEFSAGAWSEPRKRSVLPPDGNGSPVLPDKRNGIFPAAAGSRAQPRRWP
VQVLSILCSLLFAILLAFLLAIAYLIVKELHAENLKNEDDVDTGLLGFWTLLIISLTAGFSCCSFSWTVTYFDSFEPGMFPPTPLSPARFKKLTGHSFHMGYSMA
ILNGIVAALTVAWCLM
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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 (2) | 0 (0) | 0 (0) | 0 (0) | 0 (3) |






Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
Gregory, 2009 | USA | aCGH | ![]() | ![]() | ASD | - | - | - | - | 119 | 54 | 173 |








Reference | Case Number | Family Number | de novo Number | Title |
---|---|---|---|---|
Jiang YH, 2013 | - | 32 | 39 | Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome seque |
Yuen RK, 2016 | 200 | - | 301 | Genome-wide characteristics of de novo mutations in autism. |






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