E Homo sapiens | Intermembrane lipid transfer protein VPS13B [VPS13B]
Description | vacuolar protein sorting 13 homolog B [Source:HGNC Symbol;Acc:HGNC:2183]; transcript_id=ENST00000358544.6 |
Organism | HUMAN - Homo sapiens |
Locus | [ Chromosome 8 ]: 99013789 ... 99875666 |
Number of exons | 61 |
Exons | join(99013789..99013935, 99038423..99038566, 99096312..99096432, 99102953..99103120, 99111098..99111279, 99115700..99115874, 99121177..99121445, 99134632..99134727, 99135015..99135137, 99135596..99135733, 99136665..99136752, 99142974..99143165, 99147841..99148010, 99156549..99156743, 99170039..99170163, 99192876..99193057, 99274198..99274332, 99275081..99275254, 99384208..99384317, 99391557..99391704, 99431537..99431664, 99442401..99442635, 99467414..99467634, 99481599..99481802, 99501687..99501858, 99502836..99502950, 99507770..99507911, 99511104..99511512, 99520899..99521010, 99556450..99556653, 99575658..99575784, 99577490..99577633, 99641811..99642498, 99661354..99661491, 99699525..99699932, 99717171..99717373, 99720345..99720552, 99720863..99721047, 99766774..99766970, 99776775..99776956, 99778682..99779031, 99784315..99784476, 99809375..99809530, 99817540..99817803, 99818451..99818534, 99818713..99818888, 99819412..99819582, 99819921..99820122, 99821294..99821482, 99823832..99823978, 99832369..99832652, 99835197..99835324, 99835539..99835738, 99848776..99848894, 99853451..99854256, 99859304..99859480, 99861776..99861946, 99868289..99868465, 99870785..99870887, 99871448..99871697, 99875418..99875666) |