Symbol
Name
ID

Abcd1
ATP-binding cassette, sub-family D member 1
MGI:1349215

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes

Spastic paraplegia

Bulbar palsy

Abnormal cerebral white matter morphology

Neurodegeneration

Limb ataxia

Truncal ataxia

Incoordination

Slurred speech

Paraparesis

Loss of speech

Psychosis

Atypical behavior

Attention deficit hyperactivity disorder

Mental deterioration

Dementia

Polyneuropathy

Seizure

Impaired vibration sensation at ankles

Disease(s) Associated with ABCD1

adrenoleukodystrophy

Mouse Phenotypes		abnormal microglial cell morphology	abnormal astrocyte morphology	astrocytosis	abnormal Schwann cell morphology	abnormal spinal cord morphology	axon degeneration	abnormal nervous system physiology	abnormal myelination	abnormal nerve conduction
Availability	Mouse Genotype	abnormal microglial cell morphology	abnormal astrocyte morphology	astrocytosis	abnormal Schwann cell morphology	abnormal spinal cord morphology	axon degeneration	abnormal nervous system physiology	abnormal myelination	abnormal nerve conduction
	Abcd1^tm1Kds/Abcd1^tm1Kds
	Abcd1^tm1Kds/Y

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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