Type | Description |
---|---|
Definition | doublecortin domain containing 2 |
Date | Results | Publications |
---|---|---|
2021-03-20 13:31:00 | Do Genes Associated with Dyslexia of Chinese Characters Evolve Neutrally? | 32560373 |
2021-01-09 13:26:00 | Nephronophthisis due to a novel DCDC2 variant in a patient from African-Caribbean descent: A case report. | 31821705 |
2020-10-31 13:12:00 | Effect of READ1 on latent profiles of reading disorder and comorbid attention and language impairment subtypes. | 31411106 |
2020-08-13 18:51:00 | DCDC2 READ1 regulatory element: how temporal processing differences may shape language. | 32486976 |
2020-07-04 10:44:00 | Our findings add further evidence to support the hypothesis of a DCDC2 contribution to inter-individual variation in distinct indicators of reading (dis)ability in transparent languages (i.e., reading accuracy and speed), suggesting a potential pleiotropic effect | 29803723 |
Type | IDs |
---|---|
Synonymous | DCDC2A, DFNB66, NPHP19, NSC, RU2, RU2S |
Gene |
UniProtKB-ID:
DCDC2_HUMAN
UniprotKB:
Q9UHG0
UniParc:
UPI000013DA24,
UPI0000458AA9
EMBL:
AL359389,
AL359713,
BC050704,
FO393410,
AL133043,
AF181720,
AF181721,
AB032980
Ensembl:
ENSG00000146038
KO:
hsa:51473
|
Nucleutide sequences |
EMBL-CDS:
AAH50704.1,
AAF23612.1,
AAF23610.1,
BAA86468.2,
CAB61371.1
Ensembl_TRS:
ENST00000378454,
ENST00000378450
|
Protein sequencees |
Ensembl_PRO:
ENSP00000367711,
ENSP00000367715
RefSeq:
NP_057440.2,
NP_001182539.1
|
Others |
UniRef100:
UniRef100_Q9UHG0
UniRef90:
UniRef90_Q9UHG0
UniRef50:
UniRef50_Q9UHG0
UniGene:
Hs.61345
CCDS:
CCDS4550.1
|
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Refseq |
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Conserved domain | Region: {{conservedDomain.region == '' || conservedDomain.region == null ? "-": conservedDomain.region}} GFID: {{conservedDomain.gfid == '' || conservedDomain.gfid == null ? "-": conservedDomain.gfid}} Family: {{conservedDomain.family == '' || conservedDomain.family == null ? "-": conservedDomain.family}} CDD: {{conservedDomain.cdd}} - |
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