INF2

Summary

INF2 is a gene^[1]. INF2 is known by 8 alternative names across languages and contexts.^[2]

Key Facts

• INF2's instance of is recorded as gene^[3].
• INF2 is a type of protein-coding gene^[4].
• INF2's HomoloGene ID is recorded as 82406^[5].
• INF2's genomic start is recorded as 105155943^[6].
• INF2's genomic start is recorded as 104681146^[7].
• INF2's genomic end is recorded as 104722535^[8].
• INF2's genomic end is recorded as 105185942^[9].
• INF2's ortholog is recorded as Inf2^[10].
• INF2's ortholog is recorded as Inf2^[11].
• INF2's encodes is recorded as Inverted formin 2^[12].
• INF2's encodes is recorded as Inverted formin-2^[13].
• INF2's found in taxon is recorded as Homo sapiens^[14].
• INF2's chromosome is recorded as human chromosome 14^[15].
• INF2's genetic association is recorded as focal segmental glomerulosclerosis 5^[16].
• INF2's genetic association is recorded as Charcot-Marie-Tooth disease dominant intermediate E^[17].
• INF2's genetic association is recorded as focal segmental glomerulosclerosis^[18].
• INF2's genetic association is recorded as familial idiopathic steroid-resistant nephrotic syndrome^[19].
• INF2's strand orientation is recorded as forward strand^[20].
• INF2's exact match is recorded as http://identifiers.org/ncbigene/64423^[21].

Why It Matters

INF2 is known by 8 alternative names across languages and contexts.^[2]