Evidence Details for ALS2CL


Gene Symbol: | ALS2CL ( DKFZp686P238,MGC129698,RN49018 ) |
---|---|
Gene Full Name: | ALS2 C-terminal like |
Band: | 3p21.31 |
Quick Links | Entrez ID:259173; OMIM: 612402; Uniprot ID:AL2CL_HUMAN; ENSEMBL ID: ENSG00000178038; HGNC ID: 20605 |
Relate to Another Database: | SFARIGene; denovo-db |


>ALS2CL|259173|nucleotide
ATGTGCAACCCTGAGGAGGCAGCTCTGCTGCGGCTGGAGGAGGTCTTCTCAGCCACCCTCGCCCATGTCAACAGCCTTGTCCTCCAGCCCCTGCTCCCAGCCGCC
CCAGATCCCTCGGATCCCTGGGGCAGAGAGTGCCTGCGGCTCTTGCAACAGCTGCACAAGAGCTCCCAGCAACTCTGGGAGGTGACGGAGGAAAGCCTGCACTCA
CTGCAGGAGAGGCTGCGTTACCCGGACTCCACCGGTCTGGAGTCCCTGCTGCTGCTGCGAGGTGCTGACCGTGTACTGCAGGCCCACATAGAGTACATTGAGTCC
TACACAAGCTGCATGGTGGTGCAGGCCTTCCAGAAGGCAGCAAAGAGGAGAAGCGAGTACTGGCGGGGCCAGCGGAAGGCGCTGCGGCAGCTGCTTTCAGGTGTG
AGCTCAGAGGGCTCGGTGGGCGCATCGCTGGGCCAGGCCCTCCACCAGCCACTCGCCCATCACGTGCAACAGTACGTGCTCCTCCTGCTGAGCCTCGGGGACACC
ATTGGGGAGCATCACCCAACCCGGGAGCTGGTGGTGAACGCAGTCACCCTCTTTGGGAACCTGCAGTCCTTCATGAAGCAGGAGTTGGACCAGGCTGTGGCCACA
CAGGCTCTCTGGCACACCCTGAGAGGCCGGCTGAGGGATGTGCTCTGCACCCCTGCTCACAGACTCCTTCAGGACAGCCAGGACGTACCCGTGACGGTCGCACCG
TTGCGGGCTGAGCGTGTGCTGCTCTTTGATGATGCCCTCGTCCTGCTGCAGGGCCACAATGTCCACACCTTTGATCTGAAGCTGGTGTGGGTGGATCCTGGGCAG
GACGGGTGCACGTTTCACCTCCTCACGCCCGAAGAAGAGTTCTCCTTTTGTGCCAAGGACTCCCAGGGCCAGGCAGTCTGGCAGTGGAAGGTGACCTGGGCTGTT
CACCAGGCCCTGCATGGGAAGAAGGACTTCCCCGTGCTGGGGGCTGGCCTGGAGCCCTCCCAGCCTCCCGACTGCCGCTGCGCAGAATATACCTTCCAGGCAGAG
GGCCGGCTCTGCCAGGCCACCTACGAGGGCGAGTGGTGCAGGGGCCGGCCCCACGGCAAGGGAACCCTGAAATGGCCGGATGGGCGGAATCACGTGGGGAATTTC
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ATGTGCAACCCTGAGGAGGCAGCTCTGCTGCGGCTGGAGGAGGTCTTCTCAGCCACCCTCGCCCATGTCAACAGCCTTGTCCTCCAGCCCCTGCTCCCAGCCGCC
CCAGATCCCTCGGATCCCTGGGGCAGAGAGTGCCTGCGGCTCTTGCAACAGCTGCACAAGAGCTCCCAGCAACTCTGGGAGGTGACGGAGGAAAGCCTGCACTCA
CTGCAGGAGAGGCTGCGTTACCCGGACTCCACCGGTCTGGAGTCCCTGCTGCTGCTGCGAGGTGCTGACCGTGTACTGCAGGCCCACATAGAGTACATTGAGTCC
TACACAAGCTGCATGGTGGTGCAGGCCTTCCAGAAGGCAGCAAAGAGGAGAAGCGAGTACTGGCGGGGCCAGCGGAAGGCGCTGCGGCAGCTGCTTTCAGGTGTG
AGCTCAGAGGGCTCGGTGGGCGCATCGCTGGGCCAGGCCCTCCACCAGCCACTCGCCCATCACGTGCAACAGTACGTGCTCCTCCTGCTGAGCCTCGGGGACACC
ATTGGGGAGCATCACCCAACCCGGGAGCTGGTGGTGAACGCAGTCACCCTCTTTGGGAACCTGCAGTCCTTCATGAAGCAGGAGTTGGACCAGGCTGTGGCCACA
CAGGCTCTCTGGCACACCCTGAGAGGCCGGCTGAGGGATGTGCTCTGCACCCCTGCTCACAGACTCCTTCAGGACAGCCAGGACGTACCCGTGACGGTCGCACCG
TTGCGGGCTGAGCGTGTGCTGCTCTTTGATGATGCCCTCGTCCTGCTGCAGGGCCACAATGTCCACACCTTTGATCTGAAGCTGGTGTGGGTGGATCCTGGGCAG
GACGGGTGCACGTTTCACCTCCTCACGCCCGAAGAAGAGTTCTCCTTTTGTGCCAAGGACTCCCAGGGCCAGGCAGTCTGGCAGTGGAAGGTGACCTGGGCTGTT
CACCAGGCCCTGCATGGGAAGAAGGACTTCCCCGTGCTGGGGGCTGGCCTGGAGCCCTCCCAGCCTCCCGACTGCCGCTGCGCAGAATATACCTTCCAGGCAGAG
GGCCGGCTCTGCCAGGCCACCTACGAGGGCGAGTGGTGCAGGGGCCGGCCCCACGGCAAGGGAACCCTGAAATGGCCGGATGGGCGGAATCACGTGGGGAATTTC
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>ALS2CL|259173|protein
MCNPEEAALLRLEEVFSATLAHVNSLVLQPLLPAAPDPSDPWGRECLRLLQQLHKSSQQLWEVTEESLHSLQERLRYPDSTGLESLLLLRGADRVLQAHIEYIES
YTSCMVVQAFQKAAKRRSEYWRGQRKALRQLLSGVSSEGSVGASLGQALHQPLAHHVQQYVLLLLSLGDTIGEHHPTRELVVNAVTLFGNLQSFMKQELDQAVAT
QALWHTLRGRLRDVLCTPAHRLLQDSQDVPVTVAPLRAERVLLFDDALVLLQGHNVHTFDLKLVWVDPGQDGCTFHLLTPEEEFSFCAKDSQGQAVWQWKVTWAV
HQALHGKKDFPVLGAGLEPSQPPDCRCAEYTFQAEGRLCQATYEGEWCRGRPHGKGTLKWPDGRNHVGNFCQGLEHGFGIRLLPQASEDKFDCYKCHWREGSMCG
YGICEYSTDEVYKGYFQEGLRHGFGVLESGPQAPQPFRYTGHWERGQRSGYGIEEDGDRGERYIGMWQAGQRHGPGVMVTQAGVCYQGTFQADKTVGPGILLSED
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MCNPEEAALLRLEEVFSATLAHVNSLVLQPLLPAAPDPSDPWGRECLRLLQQLHKSSQQLWEVTEESLHSLQERLRYPDSTGLESLLLLRGADRVLQAHIEYIES
YTSCMVVQAFQKAAKRRSEYWRGQRKALRQLLSGVSSEGSVGASLGQALHQPLAHHVQQYVLLLLSLGDTIGEHHPTRELVVNAVTLFGNLQSFMKQELDQAVAT
QALWHTLRGRLRDVLCTPAHRLLQDSQDVPVTVAPLRAERVLLFDDALVLLQGHNVHTFDLKLVWVDPGQDGCTFHLLTPEEEFSFCAKDSQGQAVWQWKVTWAV
HQALHGKKDFPVLGAGLEPSQPPDCRCAEYTFQAEGRLCQATYEGEWCRGRPHGKGTLKWPDGRNHVGNFCQGLEHGFGIRLLPQASEDKFDCYKCHWREGSMCG
YGICEYSTDEVYKGYFQEGLRHGFGVLESGPQAPQPFRYTGHWERGQRSGYGIEEDGDRGERYIGMWQAGQRHGPGVMVTQAGVCYQGTFQADKTVGPGILLSED
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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 (0) | 0 (0) | 0 (0) | 1 (1) | 0 (0) | 0 (0) | 0 (1) | 0 (0) | 1 (2) |












Microarray Studies: 1
Reference | Source | Tissue | #Subjects (% Women) |
ADI-R | ADOS | Endo- pheno | Diagnosis | Normal Controls (% Women) |
Fold Change | Up/ Down | P/Q value | |
---|---|---|---|---|---|---|---|---|---|---|---|---|
Hu, 2009_1 | mixed | lymphoblastoid cell lines | 21 (-) | ![]() | ![]() | autism with nonaffected sib pairs | autism | 17 (-) |
1.16 | Up | - | |
|
Proteomics Studies:0
Reference | Source | Tissue | Platform | #Subjects (% Women) |
ADI-R | ADOS | Diagnosis | Normal Controls(% Women) | |
---|---|---|---|---|---|---|---|---|---|
No Evidence. |






Reference | Source | Platform | ADI-R | ADOS | Diagnosis | Family | Affected | Validation Method | ||
---|---|---|---|---|---|---|---|---|---|---|
Total | Simplex | Multiplex | ||||||||
Cukier HN, 2014 | - | Illumina HiSeq 2000 | ![]() | ![]() | ASD | 40 | - | - | 100 | HumanExome BeadChip or Sanger sequencing |


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