Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
7031 to 7040 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

7031
La ribonucleoprotein 1B
LARP2
Periodontal disease, Periodontitis, Diabetes mellitus type 2

7032
La ribonucleoprotein 4
PP13296
Alzheimer disease, Androgenetic alopecia, Polycystic ovary syndrome, Diabetes mellitus type 2

7033
La ribonucleoprotein 4B
KIAA0217, LARP5
Atypical femoral fracture, Autism, Kidney disease, Colorectal cancer, Migraine, Prostate cancer

7034
La ribonucleoprotein 7, transcriptional regulator
ALAZS, HDCMA18P, PIP7S, hLARP7
Developmental and epileptic encephalopathy, Intellectual developmental disorder, Thyroid cancer

7035
Leucyl-tRNA synthetase 1
HSPC192, ILFS1, LARS, LEURS, LEUS, LFIS, LRS, PIG44, RNTLS, cLRS, hr025Cl
Alzheimer disease, Seizure, Global developmental delay, Liver failure, Microcytic anemia, Hearing loss

7036
Leucyl-tRNA synthetase 2, mitochondrial
HLASA, LEURS, PRLTS4, mtLeuRS
Eczema, Bipolar disorder, Gonadal dysgenesis, Hydrops with lactic acidosis and sideroblastic anemia, Inflammatory skin disease, Major depressive disorder, Metabolic syndrome, Mitochondrial myopathy, Premature ovarian failure, Perrault syndrome, Psoriasis, Schizophrenia, Scoliosis, Diabetes mellitus type 2, Xx gonadal dysgenesis syndrome

7037
LAS1 like ribosome biogenesis factor
Las1, Las1-like, MRXSWTS, WTS, dJ475B7.2
Autism, Global developmental delay, Hypogonadism, Insomnia, Intellectual developmental disorder, x-linked, Neurodevelopmental disorder, Partington syndrome, Spinal muscular atrophy, Wilson-turner syndrome, X-linked intellectual disability

7038
LIM and SH3 protein 1
Lasp-1, MLN50
Autism, Endometrial neoplasms, Schizophrenia

7039
Linker for activation of T cells
IMD52, LAT1, pp36
Alzheimer disease, Amyotrophic lateral sclerosis, Atrial fibrillation, Diffuse gastric adenocarcinoma, Gastric cancer, Immunodeficiency, Liver disease, Motor neuron disease, Sarcoidosis, Severe combined immunodeficiency

7040
Linker for activation of T cells family member 2
HSPC046, LAB, NTAL, WBSCR15, WBSCR5, WSCR5
Promyelocytic leukemia, Moyamoya disease, Systemic lupus erythematosus, Williams syndrome