Please wait while page loads....
Details of PRKCSH gene in Homo sapiens
IDs |
|---|
| Link outs |
Gene Name |
Alias |
Uniprot ID |
SwissProt ID |
NCBI gene ID |
ENSEMBL ID |
Description |
Source |
|
| PRKCSH | G19P1 | P14314 | GLU2B_HUMAN | 5589
| Q96D06
| Q9P0W9 | Polycystic liver |
Disease |
|---|
| Disease |
OMIM id |
| Polycystic liver disease (PCLD) [MIM:174050]: A hepatobiliary disease characterized by overgrowth of biliary epithelium and supportive connective tissue |
177060 |
Phenotypes
Abdominal distention, Abdominal symptom, Abnormal axial skeleton morphology, Abnormal bleeding, Abnormality of blood and blood-forming tissues, Abnormality of alkaline phosphatase activity, Abnormality of metabolism/homeostasis, Abnormality of skeletal morphology, Abnormality of the abdomen, Abnormality of the abdominal organs, Abnormality of the cardiovascular system, Abnormality of the genitourinary system, Abnormality of the kidney, Abnormality of the liver, Abnormality of the lung, Abnormality of the nervous system, Abnormality of the respiratory system, Abnormality of the skeletal system, Abnormality of the upper urinary tract, Abnormality of the urinary system, Abnormality of the vertebral column, All, Ascites, Autosomal dominant inheritance, Back pain, Cystic liver disease, Dyspnea, Elevated alkaline phosphatase, Functional respiratory abnormality, Hyperbilirubinemia, Increased total bilirubin, Mode of inheritance, Phenotypic abnormality, Polycystic liver disease, Renal cysts, Respiratory difficulties, Respiratory insufficiency.
Orthologs in other species |
|---|
| M. musculus |
D. melonogaster |
C. elegans |
S. purpuratus |
Fatal error: Uncaught TypeError: count(): Argument #1 ($var) must be of type Countable|array, string given in /var/www/html/dbin/cnsb/metazoa/php/gene_details.php:895
Stack trace:
#0 {main}
thrown in /var/www/html/dbin/cnsb/metazoa/php/gene_details.php on line 895
