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Dataset:
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Showing genes starting with "P"
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851 to 860 of 1032 Genes
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Entrez ID
Gene Symbol
Gene Name
Synonyms
Diseases
851
64881
PCDH20
Protocadherin 20
PCDH13
Breast cancer
852
64895
PAPOLG
Poly(A) polymerase gamma
-
Lupus erythematosus
853
6490
PMEL
Premelanosome protein
D12S53E, HMB-45, HMB45, ME20, ME20-M, ME20M, P1, P100, PMEL17, SI, SIL, SILV, gp100
Asthma
,
Melanoma
,
Polycystic ovary syndrome
854
649179
PRAMENP
PRAME N-terminal like, pseudogene
PRAMEF24P, PRAMEL
Bladder exstrophy
855
65018
PINK1
PTEN induced kinase 1
BRPK, PARK6
Abnormal male sexual function
,
Anxiety disorder
,
Dementia
,
Dementia of frontal lobe
,
Dysautonomia
,
Dyskinetic syndrome
,
Female sexual dysfunction
,
Gastroparesis
,
Glioblastoma
,
Hallucinations
,
Male sexual dysfunction
,
Mental depression
,
Neuroblastoma
,
Panic disorder
,
Parkinson disease
,
Parkinsonian disease
,
Ramsay hunt paralysis syndrome
,
Restless legs syndrome
,
Schizophrenia
,
Social communication disorder
View all (5 more)
856
65217
PCDH15
Protocadherin related 15
CDHR15, DFNB23, USH1F
Anxiety disorder
,
Autism
,
Bipolar disorder
,
Cataract
,
Cerebral cortical atrophy
,
Chronic obstructive pulmonary disease
,
Ciliopathies
,
Cochlear diseases
,
Congenital sensorineural hearing loss
,
Deafness
,
Developmental delay
,
Disorder of eye
,
Hallucinations
,
Hearing loss
,
Hemianopsia
,
Hereditary retinal dystrophy
,
Leukemia
,
Mental depression
,
Mental retardation
,
Motor delay
,
Non-syndromic sensorineural deafness
,
Nonsyndromic deafness
,
Nyctalopia
,
Pituitary adenoma
,
Rheumatoid arthritis
,
Rod-cone dystrophy
,
Schizophrenia
,
Subcortical cerebral atrophy
,
Usher syndrome
View all (14 more)
857
653247
PRB2
Proline rich protein BstNI subfamily 2
IB-9, PRPPRB1, Ps, cP7
Pancreatic carcinoma
858
653583
PHLDB3
Pleckstrin homology like domain family B member 3
-
Breast carcinoma
859
654433
PAX8-AS1
PAX8 antisense RNA 1
-
Congenital hypothyroidism
,
Ovarian adenocarcinoma
860
692312
PPAN-P2RY11
PPAN-P2RY11 readthrough
BXDC3, P2RY11, P2Y11, PPAN, SSF1, Ssf-1
Narcolepsy
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