WSCD2

Summary

WSCD2 is a gene^[1].

Key Facts

• WSCD2's instance of is recorded as gene^[2].
• WSCD2 is a type of protein-coding gene^[3].
• WSCD2's HomoloGene ID is recorded as 35372^[4].
• WSCD2's ortholog is recorded as Wscd2^[5].
• WSCD2's ortholog is recorded as Wscd2^[6].
• WSCD2's ortholog is recorded as wscd2^[7].
• WSCD2's encodes is recorded as WSC domain containing 2^[8].
• WSCD2's encodes is recorded as WSC domain-containing protein 2^[9].
• WSCD2's found in taxon is recorded as Homo sapiens^[10].
• WSCD2's genetic association is recorded as bipolar disorder^[11].
• WSCD2's exact match is recorded as http://identifiers.org/ncbigene/9671^[12].
• WSCD2's cytogenetic location is recorded as 12q23.3^[13].
• WSCD2's expressed in is recorded as cerebellar cortex^[14].
• WSCD2's expressed in is recorded as cerebellar hemisphere^[15].
• WSCD2's expressed in is recorded as cerebellar vermis^[16].
• WSCD2's expressed in is recorded as middle temporal gyrus^[17].
• WSCD2's expressed in is recorded as tibia^[18].
• WSCD2's expressed in is recorded as islet of Langerhans^[19].
• WSCD2's expressed in is recorded as Brodmann area 23^[20].
• WSCD2's expressed in is recorded as right lobe of thyroid gland^[21].
• WSCD2's expressed in is recorded as Achilles tendon^[22].
• WSCD2's expressed in is recorded as left lobe of thyroid gland^[23].