RAB39B

Summary

RAB39B is a gene^[1].

Key Facts

• RAB39B's instance of is recorded as gene^[2].
• RAB39B is a type of protein-coding gene^[3].
• RAB39B's HomoloGene ID is recorded as 62377^[4].
• RAB39B's genomic start is recorded as 154487526^[5].
• RAB39B's genomic start is recorded as 155258235^[6].
• RAB39B's genomic end is recorded as 154493874^[7].
• RAB39B's genomic end is recorded as 155264491^[8].
• RAB39B's ortholog is recorded as Rab39b^[9].
• RAB39B's ortholog is recorded as Rab39^[10].
• RAB39B's ortholog is recorded as rab-39^[11].
• RAB39B's ortholog is recorded as rab39ba^[12].
• RAB39B's ortholog is recorded as rab39bb^[13].
• RAB39B's encodes is recorded as RAB39B, member RAS oncogene family^[14].
• RAB39B's found in taxon is recorded as Homo sapiens^[15].
• RAB39B's chromosome is recorded as human X chromosome^[16].
• RAB39B's genetic association is recorded as early-onset parkinsonism-intellectual disability syndrome^[17].
• RAB39B's genetic association is recorded as non-syndromic X-linked intellectual disability^[18].
• RAB39B's strand orientation is recorded as reverse strand^[19].
• RAB39B's exact match is recorded as http://identifiers.org/ncbigene/116442^[20].
• RAB39B's cytogenetic location is recorded as Xq28^[21].
• RAB39B's expressed in is recorded as endothelial cell^[22].
• RAB39B's expressed in is recorded as Brodmann area 23^[23].
• RAB39B's expressed in is recorded as middle temporal gyrus^[24].
• RAB39B's expressed in is recorded as primary visual cortex^[25].
• RAB39B's expressed in is recorded as islet of Langerhans^[26].