Abstract is: Filamin A, alpha (FLNA) is a protein that in humans is encoded by the FLNA gene.
| P594 | Ensembl gene ID | ENSG00000196924 |
| P704 | Ensembl transcript ID | ENST00000360319 |
| ENST00000369850 | ||
| ENST00000369856 | ||
| ENST00000415241 | ||
| ENST00000420627 | ||
| ENST00000422373 | ||
| ENST00000438732 | ||
| ENST00000444578 | ||
| ENST00000462590 | ||
| ENST00000465144 | ||
| ENST00000466319 | ||
| ENST00000466325 | ||
| ENST00000474072 | ||
| ENST00000474358 | ||
| ENST00000490936 | ||
| ENST00000498411 | ||
| ENST00000498491 | ||
| ENST00000610817 | ||
| ENST00000673639 | ||
| ENST00000676696 | ||
| ENST00000678304 | ||
| P351 | Entrez Gene ID | 2316 |
| P2888 | exact match | http://identifiers.org/ncbigene/2316 |
| P646 | Freebase ID | /m/0gg8k9p |
| P353 | HGNC gene symbol | FLNA |
| P354 | HGNC ID | 3754 |
| P593 | HomoloGene ID | 1119 |
| P6366 | Microsoft Academic ID | 2779684405 |
| P492 | OMIM ID | 300017 |
| 300017 | ||
| P10283 | OpenAlex ID | C2779684405 |
| P639 | RefSeq RNA ID | NM_001110556 |
| NM_001456 | ||
| P2892 | UMLS CUI | C1414635 |
| P1057 | chromosome | human X chromosome | Q29867336 |
| P4196 | cytogenetic location | Xq28 | |
| P688 | encodes | Filamin A | Q21109662 |
| Filamin-A | Q21150431 | ||
| P5572 | expressed in | tibial arteries | Q7800442 |
| gastric mucosa | Q383249 | ||
| right coronary artery | Q429285 | ||
| popliteal artery | Q707468 | ||
| left coronary artery | Q744391 | ||
| ascending aorta | Q2349469 | ||
| saphenous vein | Q30015816 | ||
| body of uterus | Q66508550 | ||
| muscle layer of sigmoid colon | Q66511231 | ||
| Descending thoracic aorta | Q66592966 | ||
| P703 | found in taxon | Homo sapiens | Q15978631 |
| P2293 | genetic association | frontometaphyseal dysplasia | Q3042143 |
| Melnick–Needles syndrome | Q3508673 | ||
| otopalatodigital syndrome type 1 | Q3508782 | ||
| Heart valve dysplasia | Q5692507 | ||
| terminal osseous dysplasia with pigmentary defects | Q7702740 | ||
| periventricular nodular heterotopia | Q18553263 | ||
| intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked | Q55782410 | ||
| rare genetic intestinal disease | Q55785596 | ||
| X-linked cardiac valvular dysplasia | Q102293803 | ||
| P645 | genomic end | 153603006 | |
| 154374634 | |||
| P644 | genomic start | 153576892 | |
| 154348524 | |||
| P684 | ortholog | Flna | Q18295813 |
| Flna | Q24390969 | ||
| fln-1 | Q29688123 | ||
| cher | Q29711608 | ||
| P2548 | strand orientation | reverse strand | Q22809711 |
FileName: PBB GE FLNA 200859 x at fs.png
Description: Gene expression pattern of the FLNA gene.
Artist: AndrewGNF at English Wikipedia
Work is copyrighted.
License: CC BY-SA 3.0
Attribution is required.
FileName: PBB GE FLNA 213746 s at fs.png
Description: Gene expression pattern of the FLNA gene.
Artist: AndrewGNF at en.wikipedia
Work is copyrighted.
License: CC BY-SA 3.0
Attribution is required.
FileName: PBB GE FLNA 214752 x at fs.png
Description: Gene expression pattern of the FLNA gene.
Artist: AndrewGNF at en.wikipedia
Work is copyrighted.
License: CC BY-SA 3.0
Attribution is required.
| Q21414101 | hsa-let-7b-5p |
| Q27593879 | hsa-miR-1-3p |
| Q27594279 | hsa-miR-149-5p |
| Q27594358 | hsa-miR-155-5p |
| Q27593305 | hsa-miR-16-5p |
| Q27593625 | hsa-miR-193b-3p |
| Q27593207 | hsa-miR-196a-5p |
| Q27593187 | hsa-miR-200c-3p |
| Q27593329 | hsa-miR-20a-5p |
| Q27594593 | hsa-miR-218-5p |
| Q27595201 | hsa-miR-221-3p |
| Q27595203 | hsa-miR-222-3p |
| Q27593966 | hsa-miR-23a-3p |
| Q27595118 | hsa-miR-23b-3p |
| Q27595076 | hsa-miR-31-5p |
| Q27593710 | hsa-miR-324-5p |
| Q27593246 | hsa-miR-331-3p |
| Q27594724 | hsa-miR-378a-3p |
| Q27593639 | hsa-miR-484 |
| Q27593210 | hsa-miR-615-3p |
| Q27593582 | hsa-miR-7-5p |
| Q27593334 | hsa-miR-92a-3p |
| Q27592842 | hsa-miR-92b-3p |
| Q530142 | FG syndrome |
| Q5692507 | Heart valve dysplasia |
| Q3508673 | Melnick–Needles syndrome |
| Q102293803 | X-linked cardiac valvular dysplasia |
| Q3042143 | frontometaphyseal dysplasia |
| Q55782410 | intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked |
| Q3508782 | otopalatodigital syndrome type 1 |
| Q29982053 | otopalatodigital syndrome type 2 |
| Q18553263 | periventricular nodular heterotopia |
| Q55785596 | rare genetic intestinal disease |
| Q7702740 | terminal osseous dysplasia with pigmentary defects |
| Q30225359 | Androgen receptor signaling pathway |
| Q54989094 | Ebola virus pathway in host |
| Q30151288 | Focal adhesion |
| Q30225413 | Hypothesized pathways in pathogenesis of cardiovascular disease |
| Q30225540 | IL-4 signaling pathway |
| Q66104465 | Joubert syndrome |
| Q29891990 | MAPK signaling pathway |
| Q30225469 | Prolactin signaling pathway |
| Q101405121 | human mesangial cell | has marker | P8872 |
| cy | FLNA | wikipedia |
| FLNA | wikipedia | |
| FLNA | wikipedia | |
| Filamine A | wikipedia | |
| Філамін А, альфа-ізоформа | wikipedia |
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