| Type | Description |
|---|---|
| Definition | noggin |
| Date | Results | Publications |
|---|---|---|
| 2021-02-06 13:54:00 | Noggin regulates foregut progenitor cell programming, and misexpression leads to esophageal atresia. | 32427591 |
| 2021-02-02 13:24:00 | Multiple synostoses syndrome: Clinical report and retrospective analysis. | 32259393 |
| 2021-01-02 12:48:00 | Sp1 promotes dental pulp stem cell osteoblastic differentiation through regulating noggin. | 31904417 |
| 2020-09-05 13:56:00 | Exogenous noggin binds the BMP-2 receptor and induces alkaline phosphatase activity in osteoblasts. | 30887565 |
| 2020-02-15 12:43:00 | we identified a novel NOG mutation (c.690C > G/p.C230W) by target sequencing and helped the family to deliver a baby who did not carry the mutation. Our study expanded the spectrum of NOG mutations and contributed to genetic diagnosis and counseling of families with proximal symphalangism-1A | 31694554 |
| Type | IDs |
|---|---|
| Synonymous | SYM1, SYNS1, SYNS1A |
| Gene |
UniProtKB-ID:
NOGG_HUMAN
UniprotKB:
Q13253
UniParc:
UPI0000130342
EMBL:
U31202,
BC034027
Ensembl:
ENSG00000183691
KO:
hsa:9241
|
| Nucleutide sequences |
EMBL-CDS:
AAH34027.1,
AAA83259.1
Ensembl_TRS:
ENST00000332822
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000328181
RefSeq:
NP_005441.1
|
| Others |
UniRef100:
UniRef100_Q13253
UniRef90:
UniRef90_P97466
UniRef50:
UniRef50_P97466
UniGene:
Hs.248201
CCDS:
CCDS11589.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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| Location | {{protein.contigId}} ( {{protein.positionStart}}..{{protein.positionEnd}} , {{protein.orientation}} ) | |||||||
| 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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