| Type | Description |
|---|---|
| Definition | laminin subunit gamma 3 |
| Date | Results | Publications |
|---|---|---|
| 2020-02-01 12:38:00 | LAMC3 mutation causes structural and functional impairments in visual attention networks. | 29626609 |
| 2019-11-09 12:38:00 | These data demonstrate a unique temporal and spatial expression for laminins and reveal a novel role for laminin gamma3 during human retinogenesis. | 29795281 |
| 2019-10-05 12:14:00 | Study reports a novel mutation in LAMC3 associated with generalized polymicrogyria of the cortex and epilepsy. Study identified a homozygous nonsense mutation in LAMC3: c.3190C>T (p.Gln1064*). | 29247375 |
| 2017-09-09 10:38:00 | LAMC3 gene variation is associated with oral cavity and pharyngeal cancer. | 27749845 |
| 2016-11-12 11:05:00 | We found statistically significant association with AAO for three genes (WRN, NTN4 and LAMC3) with common associated variants. | 26394601 |
| Type | IDs |
|---|---|
| Synonymous | OCCM |
| Gene |
UniProtKB-ID:
LAMC3_HUMAN,
Q8N2D6_HUMAN
UniprotKB:
Q9Y6N6,
Q8N2D6
UniParc:
UPI000013D6D3,
UPI000003B0F5
EMBL:
AL583807,
AF041835,
AK075536,
AL355872,
AB208887
Ensembl:
ENSG00000050555
KO:
hsa:10319
|
| Nucleutide sequences |
EMBL-CDS:
BAD92124.1,
AAD36991.1,
BAC11679.1
Ensembl_TRS:
ENST00000361069
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000354360
RefSeq:
XP_011516423.1,
NP_006050.3,
XP_006716984.1
|
| Others |
UniRef100:
UniRef100_Q9Y6N6,
UniRef100_Q8N2D6
UniRef90:
UniRef90_Q8N2D6,
UniRef90_Q9Y6N6
UniRef50:
UniRef50_Q8N2D6,
UniRef50_Q9Y6N6
UniGene:
Hs.201805
CCDS:
CCDS6938.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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