| Dataset | MPO Gene-Phenotype Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | anomaly in the length of the interval between an R wave and the next R wave; the RR interval is the inverse of the heart rate (Mammalian Phenotype Ontology, MP_0010504) |
| External Link | http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010504 |
| Similar Terms | |
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8 gene mutations causing the abnormal rr interval phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol | Name |
|---|---|
| CACNA1D | calcium channel, voltage-dependent, L type, alpha 1D subunit |
| EGFR | epidermal growth factor receptor |
| GLA | galactosidase, alpha |
| KL | klotho |
| NUP155 | nucleoporin 155kDa |
| SCN10A | sodium channel, voltage gated, type X alpha subunit |
| SCN1A | sodium channel, voltage gated, type I alpha subunit |
| SMAD7 | SMAD family member 7 |
