Evidence Details for AGBL1
Basic Information Top
| Gene Symbol: | AGBL1 ( FLJ32310,MGC149239 ) |
|---|---|
| Gene Full Name: | ATP/GTP binding protein-like 1 |
| Band: | 15q25.3 |
| Quick Links | Entrez ID:123624; OMIM: NA; Uniprot ID:CBPC4_HUMAN; ENSEMBL ID: ENSG00000166748; HGNC ID: 26504 |
| Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top>AGBL1|123624|nucleotide
ATGATCAGCAAGGGTGGCAGTGAAGCTCTTCTGCAGACCCTGGTAGACACAGCGAGGACAGCTCCTCCAGACTATGACATCCTCCTGCCTCTCTTCCGGCTGCTG
GCCAAAGTTGGCCTAAGAGATAAAAAGATTGGACGGAAGGCCCTAGAATTGGAAGCACTTGATGTGACATTGATTCTGGCCAGGAAGAACCTATCCCATGGCCAG
AATCTCCTCCACTGTCTCTGGGCTCTGCGTGTGTTTGCCTCCAGTGTCTCCATGGGAGCCATGCTGGGAATTAATGGAGCCATGGAACTGCTTTTCAAGGTTATT
ACTCCTTACACCCGAAAGCGCACCCAAGCAATCAGGGCAGCCACTGAAGTTTTGGCAGCATTGCTGAAATCCAAGTCGAACGGCCGCAGAGCAGTGAACCGAGGC
TACGTCACCAGCCTGCTCGGGCTGCACCAGGACTGGCACAGCCATGACACAGCCAACGCCTACGTGCAGATCCGACGGGGCTTGCTGCTCTGCCTCAGGCACATT
GCTGCCCTCCGGTCCGGCAGGGAGGCCTTCCTGGCAGCACAGGGCATGGAGATCCTCTTCAGCACCACACAGAACTGCCTGGATGACAAGAGCATGGAGCCCGTC
ATCTCTGTGGTGCTTCAGATCCTGAGGCAGTGCTACCCTACGAGTCCACTTCCCTTGGTCACAGCCAGCAGTGCCTATGCCTTCCCGGTCCCCGGGTGCATCACC
ACTGAACCTCCACATGATCTACCTGAAGAGGATTTTGAAGATGATGGCGATGATGAAGTGGACAAAGACTCTGATACTGAAGATGGGAAAGTGGAAGATGATGAC
TTGGAAACAGACGTGAACAAGCTGAGTTCCAAACCTGGTCTTGACCGACCTGAAGAGGAACTGATGCAATATGAGGTGATGTGTCTTGAGCTCTCCTATAGCTTT
GAGGAACTGCAGTCCAAACTTGGAGATGATTTGAACTCTGAAAAGACTCAGTATGCCAATCACCACCACATTCCAGCCGCTGCCTCCTCAAAACAGCATTGCTAC
AGCAAGGACCAAAGCTCCTGTGGGCAAGAAAGAGAATATGCTGTCCAGACTTCCCTTCTGTGCAGGGTGAAGACGGGAAGGTCCACTGTGCATCTAGGCTCCAAA
Show »
ATGATCAGCAAGGGTGGCAGTGAAGCTCTTCTGCAGACCCTGGTAGACACAGCGAGGACAGCTCCTCCAGACTATGACATCCTCCTGCCTCTCTTCCGGCTGCTG
GCCAAAGTTGGCCTAAGAGATAAAAAGATTGGACGGAAGGCCCTAGAATTGGAAGCACTTGATGTGACATTGATTCTGGCCAGGAAGAACCTATCCCATGGCCAG
AATCTCCTCCACTGTCTCTGGGCTCTGCGTGTGTTTGCCTCCAGTGTCTCCATGGGAGCCATGCTGGGAATTAATGGAGCCATGGAACTGCTTTTCAAGGTTATT
ACTCCTTACACCCGAAAGCGCACCCAAGCAATCAGGGCAGCCACTGAAGTTTTGGCAGCATTGCTGAAATCCAAGTCGAACGGCCGCAGAGCAGTGAACCGAGGC
TACGTCACCAGCCTGCTCGGGCTGCACCAGGACTGGCACAGCCATGACACAGCCAACGCCTACGTGCAGATCCGACGGGGCTTGCTGCTCTGCCTCAGGCACATT
GCTGCCCTCCGGTCCGGCAGGGAGGCCTTCCTGGCAGCACAGGGCATGGAGATCCTCTTCAGCACCACACAGAACTGCCTGGATGACAAGAGCATGGAGCCCGTC
ATCTCTGTGGTGCTTCAGATCCTGAGGCAGTGCTACCCTACGAGTCCACTTCCCTTGGTCACAGCCAGCAGTGCCTATGCCTTCCCGGTCCCCGGGTGCATCACC
ACTGAACCTCCACATGATCTACCTGAAGAGGATTTTGAAGATGATGGCGATGATGAAGTGGACAAAGACTCTGATACTGAAGATGGGAAAGTGGAAGATGATGAC
TTGGAAACAGACGTGAACAAGCTGAGTTCCAAACCTGGTCTTGACCGACCTGAAGAGGAACTGATGCAATATGAGGTGATGTGTCTTGAGCTCTCCTATAGCTTT
GAGGAACTGCAGTCCAAACTTGGAGATGATTTGAACTCTGAAAAGACTCAGTATGCCAATCACCACCACATTCCAGCCGCTGCCTCCTCAAAACAGCATTGCTAC
AGCAAGGACCAAAGCTCCTGTGGGCAAGAAAGAGAATATGCTGTCCAGACTTCCCTTCTGTGCAGGGTGAAGACGGGAAGGTCCACTGTGCATCTAGGCTCCAAA
Show »
>AGBL1|123624|protein
MISKGGSEALLQTLVDTARTAPPDYDILLPLFRLLAKVGLRDKKIGRKALELEALDVTLILARKNLSHGQNLLHCLWALRVFASSVSMGAMLGINGAMELLFKVI
TPYTRKRTQAIRAATEVLAALLKSKSNGRRAVNRGYVTSLLGLHQDWHSHDTANAYVQIRRGLLLCLRHIAALRSGREAFLAAQGMEILFSTTQNCLDDKSMEPV
ISVVLQILRQCYPTSPLPLVTASSAYAFPVPGCITTEPPHDLPEEDFEDDGDDEVDKDSDTEDGKVEDDDLETDVNKLSSKPGLDRPEEELMQYEVMCLELSYSF
EELQSKLGDDLNSEKTQYANHHHIPAAASSKQHCYSKDQSSCGQEREYAVQTSLLCRVKTGRSTVHLGSKKNPGVNLYQNVQSNSLRRDSSESEIPDIQASPKAD
AWDVDAIFCPRMSASFSNSTRTREVVKVIDKLLQTHLKRVPFHDPYLYMAKARRTSSVVDFKMMAFPDVWGHCPPPTTQPMLERKCGVQRIRIFEDIRRLIQPSD
Show »
MISKGGSEALLQTLVDTARTAPPDYDILLPLFRLLAKVGLRDKKIGRKALELEALDVTLILARKNLSHGQNLLHCLWALRVFASSVSMGAMLGINGAMELLFKVI
TPYTRKRTQAIRAATEVLAALLKSKSNGRRAVNRGYVTSLLGLHQDWHSHDTANAYVQIRRGLLLCLRHIAALRSGREAFLAAQGMEILFSTTQNCLDDKSMEPV
ISVVLQILRQCYPTSPLPLVTASSAYAFPVPGCITTEPPHDLPEEDFEDDGDDEVDKDSDTEDGKVEDDDLETDVNKLSSKPGLDRPEEELMQYEVMCLELSYSF
EELQSKLGDDLNSEKTQYANHHHIPAAASSKQHCYSKDQSSCGQEREYAVQTSLLCRVKTGRSTVHLGSKKNPGVNLYQNVQSNSLRRDSSESEIPDIQASPKAD
AWDVDAIFCPRMSASFSNSTRTREVVKVIDKLLQTHLKRVPFHDPYLYMAKARRTSSVVDFKMMAFPDVWGHCPPPTTQPMLERKCGVQRIRIFEDIRRLIQPSD
Show »
Evidence summary TopClick 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 (1) | 1 (3) | 0 (0) | 0 (0) | 0 (0) | 0 (1) | 0 (0) | 1 (1) | 0 (0) | 10 (6) |
Syndromic Autism Gene TopGenome-Wide Association Studies (By Ethnic Group) Top Family Based Association Studies: 1
| Reference | Stage | Platform | #Families | Affecteds | Result | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| #Subjects (% Women) |
ADI-R | ADOS | Diagnosis | Age (range) |
IQ (range) |
||||||
| CAUCASIAN | |||||||||||
| 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 | |||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| #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 | ||||||
| Bonati, 2005 | - | FISH | | | autism | - | - | - | - | 1 | - | 1 |
| Szatmari, 2007 | Europe, North America | SNP microarray | | | ASD | 1491 | - | - | - | - | - | 0 |
| Pinto, 2010 | - | SNP microarray, qPCR | | | ASD | - | - | - | - | 996 | 1287 | 2283 |
Linkage Studies TopLow Scale Association Studies (by Ethnic Group) TopLarge Scale Expression Studies TopNGS de novo Mutation Studies TopNGS Mosaic SNV Studies TopNGS Other Studies Top| Reference | Source | Platform | ADI-R | ADOS | Diagnosis | Family | Affected | Validation Method | ||
|---|---|---|---|---|---|---|---|---|---|---|
| Total | Simplex | Multiplex | ||||||||
| Novarino G, 2012 | USA | - | | | - | 2 | - | 2 | - | - |
Low Scale Gene Studies TopContact Us if you are an author of a study regarding this gene and do not find your study in this table or find errors in the representation of your study details.