| Symbol
| XK
|
| Location
| Xp21.1
|
| Name
|
MC Leod blood group phenotype |
| Corresponding gene
|
XK
|
| related resource
| Blood Group Antigen Mutation Database
|
| Main clinical features
|
without evidence of for CNS or neuromuscular involment |
Genetic determination
| Related entries
| MCLDP
|
| Function/system disorder
| hematology |
| Type
| other
| |
| Name
| membrane transport protein of yet unknown function containing the Kx erythrocyte antigen
|
| Gene mutation | Chromosome rearrangement | Effect | Comments |
|
|---|
| missense
|
|
|
| |
| Genotype/Phenotype correlations
|
no clear phenotype-genotype correlation |