1. Gene
  2. RAB36 - RAB36, member RAS oncogene family Gene

RAB36 - RAB36, member RAS oncogene family Gene

Homo sapiens
Gene ID: 9609 | Gene type: protein coding

About RAB36

Cytogenetic location: 22q11.23 Genomic coordinates (GRCh38): 22:23,145,324-23,169,280 (from NCBI)

This gene has 3 transcripts (splice variants), 175 orthologues and 68 paralogues. Broad expression in thyroid (RPKM 6.1), kidney (RPKM 2.1) and 17 other tissues.

Summary

Predicted to enable GTP binding activity and GTPase activity. Predicted to be involved in protein transport. Predicted to be located in Golgi membrane. [provided by Alliance of Genome Resources, Apr 2022]

RAB36 Products(3)

mRNA Protein Name
NM_001349877.1 NP_001336806.1 ras-related protein Rab-36 isoform 1
NM_001349878.1 NP_001336807.1 ras-related protein Rab-36 isoform 2
NM_004914.5 NP_004905.3 ras-related protein Rab-36 isoform 3

RAB36 Protein Structure

Ras

Ras: Ras family (125 - 285)

  • 0
  • 100
  • 200
  • 300
  • 333 a.a.
Protein Preferred Names Protein Names

ras-related protein Rab-36

small GTP-binding protein Rab36

Related Diseases

Diseases Alias
Ulna And Fibula, Absence Of, With Severe Limb Deficiency

Schinzel Phocomelia Syndrome

Aarrs

Limb/Pelvis-Hypoplasia/Aplasia Syndrome

LPHAS

Schinzel Type Phocomelia

Absence Of Ulna And Fibula With Severe Limb Deficiency

Al-Awadi/Raas-Rothschild Syndrome

Al Awadi-Raas-Rothschild Syndrome

Al-Awadi/Raas-Rothschild/Schinzel Phocomelia Syndrome

Aplasia/Hypoplasia Of Limbs And Pelvis

Congenital Absence Of Ulna And Fibula

Severe Limb Deficit

Phocomelia, Schinzel Type

Al-Awadi-Raas-Rothschild Syndrome

Ulna And Fibula Absence Of With Severe Limb Deficiency

Limb Pelvis Hypoplasia Aplasia Syndrome

Limb/Pelvis/Uterus-Hypoplasia/Aplasia Syndrome

Ulna And Fibula, Absence Of, With Sever Limb Deficiency

Thrombocytopenia-Absent Radius Syndrome

Tar Syndrome

Radial Aplasia-Thrombocytopenia Syndrome

Absent Radii And Thrombocytopenia

TAR

Chromosome 1q21.1 Deletion Syndrome, 200-Kb

Thrombocytopenia Absent Radius Syndrome

Thrombocytopenia Absent Radii

Chromosome 1q21.1 Deletion Syndrome

Thrombocytopenia With Absent Radii Syndrome

Radial Aplasia-Amegakaryocytic Thrombocytopenia

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Felis catus RAB36 VGNC VGNC:80474
Bos taurus RAB36 VGNC VGNC:59360
Canis familiaris RAB36 VGNC VGNC:49953
Mus musculus RAB36 MGD MGI:1924127
Rattus norvegicus RAB36 RGD RGD:1596098
Macaca mulatta RAB36 VGNC VGNC:81534