:Template:Vesicular transport protein disorders

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| name = Vesicular transport protein disorders

| title = Inherited disorders of trafficking / vesicular transport proteins

| state = {{{state|autocollapse}}}

| listclass = hlist

| group1 = Vesicle formation

| list1 = {{Navbox|child

| group1 = Lysosome/Melanosome:

| list1 =

• HPS1–HPS7
• Hermansky–Pudlak syndrome
• LYST
• Chédiak–Higashi syndrome

| group2 = COPII:

| list2 =

• SEC23A
• Cranio-lenticulo-sutural dysplasia

| list3 =

• COG7
• CDOG IIE

| group4 = APC:

| list4 =

• AP1S2
• X-linked intellectual disability
• AP3B1
• Hermansky–Pudlak syndrome 2
• AP4M1
• CPSQ3

}}

| group2 = Rab

| list2 = {{Navbox|child

| list1 =

• ARL6
• BBS3

| list2 =

• RAB27A
• Griscelli syndrome 2

| group3 Signal transducing adaptor protein:

| list3 =

• CHM
• Choroideremia
• MLPH
• Griscelli syndrome 3

}}

| group3 = Cytoskeleton

| list3 = {{Navbox|child

| group1 = Myosin:

| list1 =

• MYO5A
• Griscelli syndrome 1

| group2 = Microtubule:

| list2 =

• SPG4
• Hereditary spastic paraplegia 4

| group3 = Kinesin:

| list3 =

• KIF5A
• Hereditary spastic paraplegia 10

| group4 = Spectrin:

| list4 =

• SPTBN2
• Spinocerebellar ataxia 5

}}

| group4 = Vesicle fusion

| list4 = {{Navbox|child

| group1 = Synaptic vesicle:

| list1 =

• SNAP29
• CEDNIK syndrome
• STX11
• Hemophagocytic lymphohistiocytosis 4

| group2 = Caveolae:

| list2 =

• CAV1
• Congenital generalized lipodystrophy 3
• CAV3
• Limb-girdle muscular dystrophy 2B, Long QT syndrome 9

| group3 = Vacuolar protein sorting:

| list3 =

• VPS33B
• ARC syndrome
• VPS13B
• Cohen syndrome

| list4 =

• DYSF
• Distal muscular dystrophy

}}

| belowstyle = padding:0;

| below = See also vesicular transport proteins

}}

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Category:Biochemistry templates