CACNA1D

Summary

CACNA1D is a gene^[1]. CACNA1D ranks in the top 2% of gene entities by monthly Wikipedia readership (17 views/month).^[2]

Key Facts

• CACNA1D's instance of is recorded as gene^[3].
• CACNA1D is a type of protein-coding gene^[4].
• CACNA1D's HomoloGene ID is recorded as 578^[5].
• CACNA1D's genomic start is recorded as 53328963^[6].
• CACNA1D's genomic start is recorded as 53528683^[7].
• CACNA1D's genomic end is recorded as 53813733^[8].
• CACNA1D's genomic end is recorded as 53847760^[9].
• CACNA1D's ortholog is recorded as Cacna1d^[10].
• CACNA1D's ortholog is recorded as Cacna1d^[11].
• CACNA1D's ortholog is recorded as cacna1da^[12].
• CACNA1D's ortholog is recorded as Ca-alpha1D^[13].
• CACNA1D's ortholog is recorded as egl-19^[14].
• CACNA1D's encodes is recorded as Calcium voltage-gated channel subunit alpha1 D^[15].
• CACNA1D's encodes is recorded as Voltage-dependent L-type calcium channel subunit alpha-1D^[16].
• CACNA1D's found in taxon is recorded as Homo sapiens^[17].
• CACNA1D's chromosome is recorded as human chromosome 3^[18].
• CACNA1D's genetic association is recorded as refractive error^[19].
• CACNA1D's genetic association is recorded as sinoatrial node dysfunction and deafness^[20].
• CACNA1D's genetic association is recorded as arterial hypertension^[21].

Why It Matters

CACNA1D ranks in the top 2% of gene entities by monthly Wikipedia readership (17 views/month).^[2] CACNA1D is known by 8 alternative names across languages and contexts.^[22]