CDK5 - cyclin dependent kinase 5 Gene

Also Known as LIS7; PSSALRE

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 1020

About CDK5

Cytogenetic location: 7q36.1 Genomic coordinates (GRCh38): 7:151,053,815-151,057,897 (from NCBI)

This gene has 5 transcripts (splice variants), 167 orthologues, 26 paralogues and is associated with 1 phenotype. Ubiquitous expression in brain (RPKM 18.5), adrenal (RPKM 6.8) and 25 other tissues.

Summary

This gene encodes a proline-directed serine/threonine kinase that is a member of the cyclin-dependent kinase family of proteins. Unlike Other members of the family, the protein encoded by this gene does not directly control cell cycle regulation. Instead the protein, which is predominantly expressed at high levels in mammalian postmitotic central nervous system neurons, functions in diverse processes such as synaptic plasticity and neuronal migration through phosphorylation of proteins required for cytoskeletal organization, endocytosis and exocytosis, and Apoptosis. In humans, an allelic variant of the gene that results in undetectable levels of the protein has been associated with lethal autosomal recessive lissencephaly-7. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2015]

CDK5 Products (2)

mRNA Protein Name
NM_004935.4 NP_004926.1 cyclin-dependent kinase 5 isoform 1
NM_001164410.3 NP_001157882.1 cyclin-dependent kinase 5 isoform 2
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
8090221 GOA
enables protein serine/threonine kinase activity IDA
IDA: Inferred from direct assay
20357208 GOA
Biological Process GO Annotation Evidence References Source
involved in negative regulation of DNA-templated transcription IMP
IMP: Inferred from mutant phenotype
20357208 GOA
involved in negative regulation of proteolysis IMP
IMP: Inferred from mutant phenotype
24548080 GOA
involved in oligodendrocyte differentiation IDA
IDA: Inferred from direct assay
18042622 GOA
involved in peptidyl-serine phosphorylation IDA
IDA: Inferred from direct assay
21145489 GOA
involved in phosphorylation IDA
IDA: Inferred from direct assay
20357208 GOA
Cellular Component GO Annotation Evidence References Source
part of cyclin-dependent protein kinase holoenzyme complex IPI
IPI: Inferred from physical interaction
16039528 GOA
part of protein kinase 5 complex IPI
IPI: Inferred from physical interaction
15689152 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

CDK5 Protein Structure

Pkinase

Pkinase: Protein kinase domain (4 - 286)

  • 0
  • 100
  • 200
  • 292 a.a.
Protein Preferred Names Protein Names

cyclin-dependent kinase 5

  • TPKII catalytic subunit

  • cell division protein kinase 5

  • cyclin-dependent-like kinase 5

  • epididymis secretory sperm binding protein

  • protein kinase CDK5 splicing

  • serine/threonine-protein kinase PSSALRE

  • tau protein kinase II catalytic subunit

CDK5 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
CDK5 Q00535 CCNI Homo sapiens Q14094 32296183
Intra
CDK5 Q00535 CCNI Homo sapiens Q14094 32296183
Intra
CDK5 Q00535 CCNI Homo sapiens Q14094 32296183
Intra
CDK5 Q00535 CCNI Homo sapiens Q14094 25852190
Intra
CDK5 Q00535 SPDYE4 Homo sapiens A6NLX3 32296183
Intra
CDK5 Q00535 SPDYE4 Homo sapiens A6NLX3 32296183
Intra
CDK5 Q00535 BDNF Homo sapiens P23560-2 32814053
Intra
CDK5 Q00535 BDNF Homo sapiens P23560-2 32814053
Intra
CDK5 Q00535 BDNF Homo sapiens P23560-2 32814053
Intra
CDK5 Q00535 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
CDK5 Q00535 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
CDK5 Q00535 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
CDK5 Q00535 TBP Homo sapiens P20226 32814053
Intra
CDK5 Q00535 TBP Homo sapiens P20226 32814053
Intra
CDK5 Q00535 TBP Homo sapiens P20226 32814053
Intra
CDK5 Q00535 CCND3 Homo sapiens P30281
TAP
23602568
Intra
CDK5 Q00535 CCND3 Homo sapiens P30281
TAP
23455922
Intra
CDK5 Q00535 CCND3 Homo sapiens P30281 32296183
Intra
CDK5 Q00535 CCND3 Homo sapiens P30281 32296183
Intra
CDK5 Q00535 CDKN1A Homo sapiens P38936
TAP
23455922
Intra
CDK5 Q00535 CDKN1A Homo sapiens P38936
SPR
15890360
Intra
CDK5 Q00535 CDKN1A Homo sapiens P38936
TAP
23602568
Intra
CDK5 Q00535 CCNC Homo sapiens P24863 25852190
Intra
CDK5 Q00535 PPIA Homo sapiens P62937 32814053
Intra
CDK5 Q00535 PPIA Homo sapiens P62937 32814053
Intra
CDK5 Q00535 PPIA Homo sapiens P62937 32814053
Intra
CDK5 Q00535 CCNB1 Homo sapiens P14635 25852190
Intra
CDK5 Q00535 CCNB1 Homo sapiens P14635
TAP
23602568
Intra
CDK5 Q00535 CCNB1 Homo sapiens P14635 33961781
Intra
CDK5 Q00535 CCNB1 Homo sapiens P14635
TAP
23455922
Intra
CDK5 Q00535 CCNB1 Homo sapiens P14635 28514442
Intra
CDK5 Q00535 CCNB1 Homo sapiens P14635 32707033
Intra
CDK5 Q00535 CCNB1 Homo sapiens P14635 35271311
Intra
CDK5 Q00535 CDKN1B Homo sapiens P46527 15890360
Intra
CDK5 Q00535 CDKN1B Homo sapiens P46527 25852190
Intra
CDK5 Q00535 CDKN1B Homo sapiens P46527
TAP
23602568
Intra
CDK5 Q00535 CDKN1B Homo sapiens P46527 33961781
Intra
CDK5 Q00535 CDKN1B Homo sapiens P46527
TAP
23455922
Intra
CDK5 Q00535 CDKN1B Homo sapiens P46527 28514442
Intra
CDK5 Q00535 CDKN1B Homo sapiens P46527 32707033
Intra
CDK5 Q00535 CABLES1 Homo sapiens Q8TDN4 33961781
Intra
CDK5 Q00535 CABLES1 Homo sapiens Q8TDN4
TAP
23602568
Intra
CDK5 Q00535 CABLES1 Homo sapiens Q8TDN4
TAP
23455922
Intra
CDK5 Q00535 CABLES1 Homo sapiens Q8TDN4 28514442
Intra
CDK5 Q00535 CABLES1 Homo sapiens Q8TDN4 32707033
Intra
CDK5 Q00535 CABLES1 Homo sapiens Q8TDN4 20559324
Intra
CDK5 Q00535 CABLES1 Homo sapiens Q8TDN4 25852190
Intra
CDK5 Q00535 SPDYA Homo sapiens Q5MJ70 32296183
Intra
CDK5 Q00535 SPDYA Homo sapiens Q5MJ70 32296183
Intra
CDK5 Q00535 SPDYA Homo sapiens Q5MJ70 32296183
Intra
CDK5 Q00535 CDK5R1 Homo sapiens Q15078
TAP
23602568
Intra
CDK5 Q00535 CDK5R1 Homo sapiens Q15078 33961781
Intra
CDK5 Q00535 CDK5R1 Homo sapiens Q15078 14521924
Intra
CDK5 Q00535 CDK5R1 Homo sapiens Q15078 20133653
Intra
CDK5 Q00535 CDK5R1 Homo sapiens Q15078 15689152
Intra
CDK5 Q00535 CDK5R1 Homo sapiens Q15078 20133653
Intra
CDK5 Q00535 CDK5R1 Homo sapiens Q15078 21220307
Intra
CDK5 Q00535 HOOK1 Homo sapiens Q9UJC3 32814053
Intra
CDK5 Q00535 HOOK1 Homo sapiens Q9UJC3 32814053
Intra
CDK5 Q00535 HOOK1 Homo sapiens Q9UJC3 32814053
Intra
CDK5 Q00535 CCND2 Homo sapiens P30279
TAP
23602568
Intra
CDK5 Q00535 CCND2 Homo sapiens P30279 27107012
Intra
CDK5 Q00535 CCND2 Homo sapiens P30279 25416956
Intra
CDK5 Q00535 CCND2 Homo sapiens P30279 26871637
Intra
CDK5 Q00535 CCND2 Homo sapiens P30279
TAP
23455922
Intra
CDK5 Q00535 CCND2 Homo sapiens P30279 32296183
Intra
CDK5 Q00535 CCND2 Homo sapiens P30279 26871637
Intra
CDK5 Q00535 CCND2 Homo sapiens P30279 32707033
Intra
CDK5 Q00535 CCND2 Homo sapiens P30279 26871637
Intra
CDK5 Q00535 CCND2 Homo sapiens P30279 32296183
Intra
CDK5 Q00535 PPARG Homo sapiens P37231-2 22078880
Intra
CDK5 Q00535 PPARG Homo sapiens P37231-2
Y2H
22078880
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant CDK5 Proteins

Cat. No. Product Name Accession Purity
HY-P72298 CDK5 Protein, Human (P.pastoris, His) Q00535 (M1-P292) ≥ 90%, as determined by reducing SDS-PAGE.

CDK5 Antibodies

Cat. No. Product Name Application Reactivity
HY-P80078 CDK5 Antibody (YA512) WB, IHC-P, FC, IP Human, Mouse, Rat
HY-P80613 CDK5 Antibody (YA796) WB, ICC/IF Human, Mouse, Rat, Monkey
HY-P84450 CDK5 Antibody (YA4147) WB, IHC-P, ICC/IF, FC, ELISA Human, Rat, Monkey
HY-P84450A CDK5 Antibody (YA4147)(PBS only) WB, IHC-P, ICC/IF, FC, ELISA Human, Rat, Monkey
HY-P85533 CDK5(N-term) Antibody (YA5225) WB, ICC/IF Human, Mouse, Rat, Monkey
HY-P85693 CDK5 Antibody (YA5385) IHC-P, WB Human, Mouse, Rat

Related Diseases

Diseases Alias
Congenital Nervous System Abnormality
  • Congenital Neurologic Anomaly

  • Congenital Nervous System Disorder

Diabetes Mellitus
  • Diabetes

Supranuclear Palsy, Progressive, 1
  • Progressive Supranuclear Palsy

  • Steele-Richardson-Olszewski Syndrome

  • Supranuclear Palsy, Progressive

  • Psp

  • Progressive Supranuclear Ophthalmoplegia

  • PSNP1

  • Familial Progressive Supranuclear Palsy

  • Richardson'S Syndrome

  • Psp Syndrome

  • Progressive Supranuclear Palsy 1

  • Supranuclear Palsy Progressive

  • Ophthalmoplegia, Supranuclear, Progressive

  • Steele-Richardson-Olszewksi Syndrome

Mild Cognitive Impairment
Lissencephaly 7 With Cerebellar Hypoplasia
  • LIS7

  • Lissencephaly 7, With Cerebellar Hypoplasia

  • Lissencephaly, Type 7, With Cerebellar Hypoplasia

Scrapie
Giant Axonal Neuropathy 2
Peripheral Nervous System Disease
  • Peripheral Neuropathy

  • Peripheral Nerve Disease

  • Peripheral Nerve Disorders

  • Neuropathy, Peripheral

  • Peripheral Neuropathy Due To Vitamin Pyridoxine Hyperalimentation

Pick Disease Of Brain
  • Pick Disease

  • Pick Disease Of The Brain

  • Lobar Atrophy Of Brain

  • Dementia With Lobar Atrophy And Neuronal Cytoplasmic Inclusions

  • Pick'S Disease

  • Behavioral Variant Of Frontotemporal Dementia

  • Dementia In Pick'S Disease

  • Lobar Atrophy Of The Brain

  • Bvftd

  • Bv-Ftd

  • PIDB

  • Picks Disease

Purulent Acute Otitis Media
  • Acute Suppurative Otitis Media

  • Acute Or Subacute Suppurative Otitis Media

  • Acute Or Subacute Purulent Otitis Media

Alzheimer Disease 9
  • AD9

  • Alzheimer'S Disease 9

  • Alzheimer Disease 9, Susceptibility To

  • Alzheimer Disease 9, Late-Onset

  • Alzheimer'S Disease 9, Late Onset

  • {Alzheimer Disease 9, Susceptibility To}

Dyslexia
Stroke, Ischemic
  • Cerebral Infarction

  • Stroke

  • Ischemic Stroke

  • Cerebrovascular Accident

  • Cerebral Infarction, Susceptibility To

  • Stroke, Ischemic, Susceptibility To

  • Cerebral Infarct

  • Ischemic Stroke, Susceptibility To

  • Stroke, Susceptibility To

  • Cva - Cerebral Infarction

  • ISCHSTR

  • Ischemic Cerebrovascular Accident

Hypothyroidism, Congenital, Nongoitrous, 6
  • CHNG6

  • Congenital Nongoitrous Hypothyroidism 6

  • Hypothyroidism, Congenital, Non-Goitrous, 6

  • Hypothyroidism, Congenital, Nongoitrous, Type 6

Neuroblastoma
  • Nb

  • Neuroblastoma, Susceptibility To

  • Neuroblastomas

  • Central Neuroblastoma

Lissencephaly 1
  • LIS1

  • Classic Lissencephaly

  • Ils

  • Subcortical Laminar Heterotopia

  • Lissencephaly Due To Lis1 Mutation

  • Lissencephaly Sequence, Isolated

  • Lissencephaly, Classic

  • Pafah1b1-Related Lissencephaly

  • Classical Lissencephaly

  • Lissencephaly Type 1

  • Lissencephaly-1

  • Subcortical Band Heterotopia

  • Double Cortex

  • Lissencephaly Classic

  • Lissencephaly Sequence Isolated

  • Isolated Lissencephaly Sequence

  • Type 1 Lissencephaly

  • Lissencephaly Syndrome Type 1

  • SBH

  • Sclh

  • Lissencephaly, Type 1

  • Type I Lissencephaly

Alzheimer Disease, Familial, 1
  • Alzheimer Disease

  • Alzheimer'S Disease

  • Presenile And Senile Dementia

  • AD1

  • Alzheimer Disease, Susceptibility To

  • Alzheimer Disease, Late-Onset, Susceptibility To

  • Alzheimer Disease 1, Familial

  • AD

  • Familial Alzheimer Disease

  • Alzheimer Disease, Late-Onset

  • Alzheimers Dementia

  • Alzheimer Dementia

  • Alzheimer Sclerosis

  • Alzheimer Syndrome

  • Alzheimer-Type Dementia

  • Dat

  • Primary Senile Degenerative Dementia

  • Sdat

  • Alzheimer Disease 1

  • Autosomal Dominant Alzheimer Disease

  • Early-Onset Alzheimer Disease With Cerebral Amyloid Angiopathy

  • Late Onset Alzheimer Disease

  • Alzheimers Disease

  • Alzheimer Disease, Early-Onset, With Cerebral Amyloid Angiopathy

  • Late-Onset Alzheimers Disease

  • Alzheimer'S Disease Pathway Kegg

  • Dementia Due To Alzheimer'S Disease

  • Alzheimer Disease Type 1

  • Alzheimers

Ischemia
  • Acute Coronary Syndrome

Schizophrenia
  • SCZD

  • Schizophrenia With Or Without An Affective Disorder

  • Schizophrenia 12

  • Schizophrenia, Susceptibility To

  • Schizophrenia-1

  • Dementia Praecox

  • Schizophrenia 1

Toxic Encephalopathy
  • Neurotoxicity

  • Neurotoxicity Syndromes

  • Neurotoxicity Syndrome

  • Encephalopathy, Toxic

Amyotrophic Lateral Sclerosis 1
  • Amyotrophic Lateral Sclerosis

  • ALS

  • Lou Gehrig Disease

  • Amyotrophic Lateral Sclerosis Type 1

  • Charcot Disease

  • ALS1

  • Amyotrophic Lateral Sclerosis, Susceptibility To

  • Fals

  • Lou Gehrig'S Disease

  • Mnd

  • Motor Neuron Disease

  • Familial Amyotrophic Lateral Sclerosis

  • Amyotrophic Lateral Sclerosis 1, Familial

  • Amyotrophic Lateral Sclerosis 1, Autosomal Dominant

  • Motor Neuron Disease, Bulbar

  • Motor Neurone Disease

  • Amyotrophic Lateral Sclerosis With Dementia

  • Dementia With Amyotrophic Lateral Sclerosis

  • Motor Neuron Disease, Amyotrophic Lateral Sclerosis

  • Sclerosis, Lateral, Amyotrophic

  • Sclerosis, Lateral, Amyotrophic, Type 1

  • Amyotrophic Sclerosis

  • Als - [Amyotrophic Lateral Sclerosis]

  • Wasting Palsy

  • Amyotrophic Paralysis

  • Amyotrophy Lateral Sclerosis

  • Wasting Paralysis

  • Spinal Progressive Amyotrophy

  • Progressive Atrophic Paralysis

Primary Microcephaly
  • True Microcephaly

  • Microcephaly, Primary

Cerebellar Hypoplasia
Multiple System Atrophy 1
  • Multiple System Atrophy

  • Shy-Drager Syndrome

  • Msa

  • MSA1

  • Multiple System Atrophy 1, Susceptibility To

  • Sporadic Olivopontocerebellar Atrophy

  • Multisystem Atrophy

  • Msa1, Susceptibility To

  • Multiple System Atrophy, Susceptibility To

  • Opca

  • Progressive Autonomic Failure With Multiple System Atrophy

  • Sds

Movement Disease
  • Movement Disorders

  • Movement Disorder

Band Heterotopia
  • Subcortical Band Heterotopia

  • Double Cortex Syndrome

  • Subcortical Laminar Heterotopia

  • Double Cortex

  • Band Heterotopia Of Brain

  • BH

  • Heco

  • Heterotopic Cortex

  • Familial Band Heterotopia

  • Dc

  • Dc Syndrome

  • Heterotopia, Subcortical Band

  • Sbh

  • Sclh

  • Bhy

Motor Neuron Disease
  • Anterior Horn Cell Disease

  • Motor Neuron Diseases

  • Mnd - [Motor Neurone Disease]

  • Lou Gehrig Disease

  • Creeping Palsy

  • Creeping Paralysis

  • Bulbar Motor Neuron Disease

  • Bulbar Syndrome

  • Anterior Horn Cell Disorder

  • Hereditary Motor Neuron Disease

Frontotemporal Dementia
  • Pallidopontonigral Degeneration

  • Frontotemporal Lobar Degeneration

  • Semantic Dementia

  • FTD

  • Frontotemporal Lobe Dementia

  • Multiple System Tauopathy With Presenile Dementia

  • Dementia, Frontotemporal

  • Frontotemporal Dementia With Parkinsonism

  • Mstd

  • Frontotemporal Lobar Degeneration With Tau Inclusions

  • Ftld With Tau Inclusions

  • Dementia, Frontotemporal, With Parkinsonism

  • Fldem

  • Ftdp17

  • Disinhibition-Dementia-Parkinsonism-Amyotrophy Complex

  • Ddpac

  • Wilhelmsen-Lynch Disease

  • Wld

  • Ppnd

  • Dementia, Frontotemporal, With Or Without Parkinsonism

  • Semantic Primary Progressive Aphasia

  • Semantic Variant Ppa

  • Wilhemsen-Lynch Disease

  • Frontotemporal Dementia-Amyotrophic Lateral Sclerosis

  • Frontotemporal Dementia And Parkinsonism Linked To Chromosome 17

  • Ftd-Als

  • Ftld

  • Pick Complex

  • Pick Disease Of The Brain

  • Frontotemporal Dementia With Parkinsonism-17

  • Grn-Related Frontotemporal Dementia

  • Frontotemporal Dementia With Motor Neuron Disease

  • Dementia In Fronto-Temporal Lobar Degeneration

  • Ftd - [Frontotemporal Dementia]

  • Temple Dementia

  • Frontal Lobe Dementia

Dementia, Lewy Body
  • Lewy Body Dementia

  • Lewy Body Disease

  • Diffuse Lewy Body Disease

  • Dementia With Lewy Bodies

  • DLB

  • Autosomal Dominant Diffuse Lewy Body Disease

  • Cortical Lewy Body Disease

  • Dementia, Lewy Body, Susceptibility To

  • Lewy Body Dementia, Susceptibility To

  • Senile Dementia Of The Lewy Body Type

  • Dementia Of The Lewy Body Type

  • Lbd

  • Diffuse Lewy Body Disease With Gaze Palsy

  • Dysphasic Dementia Hereditary

  • Lewy Body Type Senile Dementia

  • Lewy Body Variant Of Alzheimer Disease

  • Lewy Bodies

  • Lewy Body

  • Dlbd - [Diffuse Lewy Body Disease]

  • Clbd - [Cortical Lewy Body Disease]

Lung Cancer
  • Lung Carcinoma

  • Non-Small Cell Lung Carcinoma

  • Lung Cancer, Protection Against

  • Lung Cancer, Susceptibility To

  • Adenocarcinoma Of Lung, Somatic

  • Nonsmall Cell Lung Cancer

  • Adenocarcinoma Of Lung, Response To Tyrosine Kinase Inhibitor In

  • Lung Neoplasm

  • Carcinoma Of Lung

  • Lung Non-Small Cell Carcinoma

  • Non-Small Cell Lung Cancer

  • Nsclc

  • Lung Neoplasms

  • Malignant Neoplasm Of Lung

  • Alveolar Cell Carcinoma

  • Nonsmall Cell Lung Cancer, Somatic

  • Nonsmall Cell Lung Cancer, Response To Tyrosine Kinase Inhibitor In

  • Nonsmall Cell Lung Cancer, Susceptibility To

  • Lung Cancer, Somatic

  • Lung Cancer, Resistance To

  • Cancer Of Lung

  • Cancer Of Bronchus

  • Cancer Of The Lung

  • Lung Malignancies

  • Lung Malignant Tumors

  • Malignant Lung Tumor

  • Malignant Tumor Of Lung

  • Pulmonary Cancer

  • Pulmonary Carcinoma

  • Pulmonary Neoplasms

  • Respiratory Carcinoma

  • LNCR

  • Adenocarcinoma Of Lung

  • Neoplasm Of Lung

  • Cancer Lung

  • Carcinoma Non-Small Cell Lung

  • Carcinoma, Non-Small-Cell Lung

  • Lung Cancers

  • Lung Carcinomas

  • Cancer, Lung

  • Cancer, Lung, Non-Small Cell

  • Primary Malignant Neoplasm Of Lung

  • Bronchioloalveolar Adenocarcinoma

Primary Autosomal Recessive Microcephaly
  • Autosomal Recessive Primary Microcephaly

  • Mcph

  • True Microcephaly

  • Microcephalia Vera

  • Microcephaly Vera

  • Microcephaly Primary Hereditary

  • Microcephaly, Primary, Autosomal Recessive

  • Primary Microcephaly

Parkinson Disease, Late-Onset
  • Parkinson Disease

  • Parkinson'S Disease

  • PD

  • PARK

  • Parkinson Disease, Susceptibility To

  • Late Onset Parkinson'S Disease

  • Late Onset Parkinson Disease

  • Paralysis Agitans

  • Primary Parkinsonism

  • Idiopathic Parkinson Disease

  • Parkinson'S

  • Parkinson Disease, Late-Onset, Susceptibility To

  • Parkinson Disease, Age Of Onset, Modifier

  • Lewy Body Parkinson Disease

  • Idiopathic Parkinson'S Disease

  • Pd - [Parkinson Disease]

  • Parkinson Disease Nos

  • Parkinson, Nos

  • Primary Parkinson Disease

Miller-Dieker Lissencephaly Syndrome
  • Miller-Dieker Syndrome

  • Mds

  • MDLS

  • Miller Dieker Syndrome

  • Classical Lissencephaly Syndrome

  • Lissencephaly Due To 17p13.3 Deletion

  • Monosomy 17p13.3

  • Telomeric Deletion 17p

  • Classical Lissencephaly

Lissencephaly
  • Pachygyria

  • Broad Gyri Of Cerebrum

  • Large Gyri Of Cerebrum

  • Macrogyria

Epilepsy
  • Epilepsy Syndrome

  • Epileptic Syndrome

  • Epilepsies

  • Symptomatic Epilepsies

  • Post Traumatic Epilepsy

  • Traumatic Epilepsy

  • Traumatic Epileptic

  • Epilepsy Due To Hippocampal Sclerosis

  • Epilepsy With Ammon'S Horn Sclerosis

  • Epilepsy Due To Cortical Dysplasia

  • Epilepsy Due To Neuronal Migration Disorders

Nervous System Disease
  • Abnormality Of The Nervous System

  • Nervous System Diseases

  • Nervous System Disorder

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
Canis familiaris CDK5 VGNC VGNC:51795
Felis catus CDK5 VGNC VGNC:60700
Mus musculus CDK5 MGD MGI:101765
Macaca mulatta CDK5 VGNC VGNC:80858
Rattus norvegicus CDK5 RGD RGD:70514
Bos taurus CDK5 VGNC VGNC:27127
Others CDK5 NCBI