|
321
|
|
|
Lamin tail domain containing 1 |
IFLTD1, LMNARS1, PAS1C1 |
|
|
322
|
|
|
Leucine rich repeat LGI family member 4 |
AMC1, AMCNMY, LGIL3 |
Arthrogryposis multiplex congenita, Arthrogryposis multiplex congenita, neurogenic, with myelin defect, Congenital camptodactyly, Congenital clubfoot, Developmental delay, Distal arthrogryposis, Elbow flexion contracture, Esotropia, High palate, Hip contracture, Hypomyelination neuropathy-arthrogryposis syndrome, Mental retardation, Micrognathism, Neurogenic arthrogryposis multiplex congenita, Pena shokeir syndrome, Ptosis, Vertical talusView all (2 more) |
|
323
|
|
|
Leucine rich repeat neuronal 4 |
C20orf75, NLRR-4, NLRR4, dJ1056H1.1 |
|
|
324
|
|
|
LON peptidase N-terminal domain and ring finger 2 |
RNF192 |
|
|
325
|
|
|
Lebercilin LCA5 |
C6orf152 |
Amaurosis, Blindness, Cataract, Ciliopathies, Congenital cerebral hernia, Developmental delay, Disorder of eye, Hemiplegia/hemiparesis, Hyperopia, Keratoconus, Leber congenital amaurosis, Malformation of cortical development, Mental retardation, Multiple congenital anomalies, Nystagmus, Retinal dystrophyView all (1 more) |
|
326
|
|
|
Lysophosphatidic acid receptor 1 |
EDG2, Gpcr26, LPA1, Mrec1.3, VZG1, edg-2, rec.1.3, vzg-1 |
Breast cancer, Mammary neoplasms, Breast carcinoma, Cacosmia, Colonic neoplasms, Colorectal adenoma, Colorectal cancer, Colorectal neoplasms, Leukemia, Marfan syndrome, Myeloid leukemia, Olfaction disorders, Prostatic neoplasms, Prostate cancer, Schizophrenia |
|
327
|
|
|
Long intergenic non-protein coding RNA 311 |
NCRNA00311, TMEM148 |
|
|
328
|
|
|
Lactate dehydrogenase D |
DLACD, DLD |
|
|
329
|
|
|
Long intergenic non-protein coding RNA 528 |
C22orf37 |
|
|
330
|
|
|
Lipase H |
AH, ARWH2, HYPT7, LAH2, LPDLR, PLA1B, mPA-PLA1 |
|
