Evidence Details for ARPP21


Gene Symbol: | ARPP21 ( ARPP-21,FLJ32997,R3HDM3,RCS,TARPP ) |
---|---|
Gene Full Name: | cAMP-regulated phosphoprotein, 21kDa |
Band: | 3p22.3 |
Quick Links | Entrez ID:10777; OMIM: 605488; Uniprot ID:ARP21_HUMAN; ENSEMBL ID: ENSG00000172995; HGNC ID: 16968 |
Relate to Another Database: | SFARIGene; denovo-db |


>ARPP21|10777|nucleotide
ATGTCTGAGCAAGGAGACCTGAATCAGGCAATAGCAGAGGAAGGAGGGACTGAGCAGGAGACGGCCACTCCAGAGAACGGCATTGTTAAATCAGAAAGTCTGGAT
GAAGAGGAGAAACTGGAACTGCAGAGGCGGCTGGAGGCTCAGAATCAAGAAAGAAGAAAATCCAAGTCAGGAGCAGGAAAAGGTAAACTGACTCGCAGCCTTGCT
GTCTGTGAGGAATCTTCTGCCAGACCAGGAGGTGAAAGTCTTCAGGATCAGACTCTCTGA
Show »
ATGTCTGAGCAAGGAGACCTGAATCAGGCAATAGCAGAGGAAGGAGGGACTGAGCAGGAGACGGCCACTCCAGAGAACGGCATTGTTAAATCAGAAAGTCTGGAT
GAAGAGGAGAAACTGGAACTGCAGAGGCGGCTGGAGGCTCAGAATCAAGAAAGAAGAAAATCCAAGTCAGGAGCAGGAAAAGGTAAACTGACTCGCAGCCTTGCT
GTCTGTGAGGAATCTTCTGCCAGACCAGGAGGTGAAAGTCTTCAGGATCAGACTCTCTGA
Show »
>ARPP21|10777|protein
MSEQGDLNQAIAEEGGTEQETATPENGIVKSESLDEEEKLELQRRLEAQNQERRKSKSGAGKGKLTRSLAVCEESSARPGGESLQDQTL
Show »
MSEQGDLNQAIAEEGGTEQETATPENGIVKSESLDEEEKLELQRRLEAQNQERRKSKSGAGKGKLTRSLAVCEESSARPGGESLQDQTL
Show »


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) | 1 (1) | 0 (1) | 0 (0) | 0 (0) | 0 (0) | 1 (3) |






Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
Pinto, 2010 | - | SNP microarray, qPCR | ![]() | ![]() | ASD | - | - | - | - | 996 | 1287 | 2283 |






Microarray Studies: 1
Reference | Source | Tissue | #Subjects (% Women) |
ADI-R | ADOS | Endo- pheno | Diagnosis | Normal Controls (% Women) |
Fold Change | Up/ Down | P/Q value | |
---|---|---|---|---|---|---|---|---|---|---|---|---|
Voineagu, 2011_1 | Unknown | 16 frontal cortex(BA9) and 13 temporal cortex(BA41 | 16 (25.00%) | ![]() | ![]() | - | autism | 16 (6.25%) |
1.10598 | Up | 26.4019 | |
|
Proteomics Studies:0
Reference | Source | Tissue | Platform | #Subjects (% Women) |
ADI-R | ADOS | Diagnosis | Normal Controls(% Women) | |
---|---|---|---|---|---|---|---|---|---|
No Evidence. |


Reference | Case Number | Family Number | de novo Number | Title |
---|---|---|---|---|
Nilsson D, 2017 | 8 | - | 17 | Whole-Genome Sequencing of Cytogenetically Balanced Chromosome Translocations Identifies Potentially |






Contact 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.