Genesⓘ

Dataset:
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "G"
501 to 510 of 533 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

501
Galanin receptor 2
GAL2-R, GALNR2, GALR-2
Involutional depression, Involutional paraphrenia, Mental depression, Psychosis

502
Gamma-glutamyl hydrolase
GATD10, GH
Urinary bladder cancer, Bladder neoplasm, Colorectal cancer, Colorectal neoplasms, Rheumatoid arthritis

503
Glycogenin 2
GN-2, GN2
Glycogen storage disease

504
Galactosidase beta 1 like 2
MST114, MSTP114
Leukemia

505
G protein-coupled receptor class C group 5 member A
GPCR5A, PEIG-1, RAI3, RAIG1, TIG1
Malignant melanoma of skin, Melanoma, Rheumatoid arthritis

506
GUSB pseudogene 11
-
Cholecystolithiasis, Cholelithiasis

507
Golgin, RAB6 interacting
GO, NTKLBP1, SCYL1BP1
Acquired kyphoscoliosis, Alopecia, male pattern, Androgenetic alopecia, Congenital camptodactyly, Congenital kyphoscoliosis, Congenital pectus carinatum, Cutis laxa, Developmental delay, Dwarfism, Geroderma osteodysplastica, Hypoplasia of the maxilla, Malocclusion, Mental retardation, Microcephaly, Microcornea
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508
Glial cells missing transcription factor 2
FIH2, GCMB, HRPT4, hGCMb
Cataract, Chondrocalcinosis, Congenital hypoparathyroidism, Hypercalcemia, Hyperparathyroidism, Hyperphosphatemia, Hypocalcemic seizures, Hypoparathyroidism, Nephrocalcinosis, Osteopenia, Osteoporosis, Parathyroid adenoma, Parathyroid agenesis, Phosphate diabetes, Renal insufficiency

509
G protein-coupled receptor 50
H9, Mel1c
Autism spectrum disorder, Bipolar disorder, Mood disorder, Schizophrenia, Seasonal affective disorder

510
Glucose-6-phosphatase catalytic subunit 3
SCN4, UGRP
Anemia, Atrial septal defect, Clinodactyly, Congenital hypoplasia of thymus, Congenital neutropenia, Congenital pectus carinatum, Cor triatriatum, Cryptorchidism, Dursun syndrome, Erythroid hypoplasia, High palate, Lymphopenia, Microcephaly, Monocytosis, Neutropenia
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