Gene Summary

Name:
Ngfi-A binding protein 2
Synonyms:
N/A

IMPC Data Collections

IMPC Phenotype Summary

Significant
Not Significant
Not tested

Phenotypes

The IMPC applies a panel of phenotyping screens to characterise single-gene knockout mice by comparison to wild types. Click on the different tabs to visualise significant phenotypes identified by the IMPC, as well as all data that was measured.

Phenotype System Allele Zyg Sex Life Stage P Value
abnormal behavior Nab2tm1b(EUCOMM)Hmgu HOM   Early adult 6.37×10-06
decreased exploration in new environment Nab2tm1b(EUCOMM)Hmgu HOM Early adult 1.49×10-09
decreased locomotor activity Nab2tm1b(EUCOMM)Hmgu HOM Early adult 7.76×10-05
abnormal contextual conditioning behavior Nab2tm1b(EUCOMM)Hmgu HOM Early adult 2.65×10-05
hyperactivity Nab2tm1b(EUCOMM)Hmgu HOM Early adult 7.46×10-23
increased thigmotaxis Nab2tm1b(EUCOMM)Hmgu HOM   Early adult 6.63×10-06
abnormal cornea morphology Nab2tm1b(EUCOMM)Hmgu HOM Early adult 6.82×10-06
abnormal freezing behavior Nab2tm1b(EUCOMM)Hmgu HOM Early adult 3.68×10-05
abnormal cued conditioning behavior Nab2tm1b(EUCOMM)Hmgu HOM Early adult 4.46×10-14
decreased circulating HDL cholesterol level Nab2tm1b(EUCOMM)Hmgu HOM Early adult 2.64×10-07
abnormal gait Nab2tm1b(EUCOMM)Hmgu HOM Early adult 5.20×10-05
abnormal liver morphology Nab2tm1b(EUCOMM)Hmgu HOM Early adult 0.00
increased vertical activity Nab2tm1b(EUCOMM)Hmgu HOM Early adult 7.65×10-18
abnormal motor capabilities/coordination/movement Nab2tm1b(EUCOMM)Hmgu HOM Early adult 2.12×10-05
decreased circulating cholesterol level Nab2tm1b(EUCOMM)Hmgu HOM Early adult 3.10×10-07
increased anxiety-related response Nab2tm1b(EUCOMM)Hmgu HOM Early adult 8.16×10-05

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lacZ Expression

Expression data not available

Associated Images

Images submitted by IMPC centres for a selection of procedures. Each set of images is available to view in our image comparator.

Echo

M-Mode Images

14 Images

X-ray

XRay Images Whole Body Lateral Orientation

10 Images

Gross Pathology and Tissue Collection

Images

2 Images

X-ray

XRay Images Whole Body Dorso Ventral

10 Images

Human diseases caused by Nab2 mutations

The analysis uses data from IMPC, along with published data on other mouse mutants, in comparison to human disease reports in OMIM, Orphanet, and DECIPHER.

Phenotype comparisons summarize the similarity of mouse phenotypes with human disease phenotypes.

The table below shows human diseases associated to Nab2 by orthology or direct annotation.

Disease Similarity of
phenotypes
Matching phenotypes Source
Solitary Fibrous Tumor
Neoplasm of the liver, Hypophosphatemic rickets, Reduced C-peptide level, Abnormal peritoneum mor... ORPHA:2126

The table below shows human diseases predicted to be associated to Nab2 by phenotypic similarity.

Disease Similarity of
phenotypes
Matching phenotypes Source
Intellectual Developmental Disorder, Autosomal Recessive 3
Short attention span, Hyperactivity OMIM:608443
Potocki-Lupski syndrome (17p11.2 duplication syndrome)
Short attention span, Hyperactivity DECIPHER:19
Attention Deficit-Hyperactivity Disorder
Attention deficit hyperactivity disorder, Hyperactivity OMIM:143465
Spastic Tetraplegia, Thin Corpus Callosum, And Progressive Microcephaly
Inability to walk, Hyperactivity, Irritability OMIM:616657
Pandas
Depression, Abnormal fear-induced behavior, Oppositional defiant disorder, Emotional lability, Ob... ORPHA:66624
Familial Apolipoprotein Gene Cluster Deletion Syndrome
Hypotriglyceridemia, Hypocholesterolemia, Decreased circulating apolipoprotein A-I concentration,... OMIM:620058
Encephalopathy, Progressive, With Or Without Lipodystrophy
Mental deterioration, Hypertriglyceridemia, Hyperactivity, Ataxia, Hepatomegaly OMIM:615924
Bilateral Parasagittal Parieto-Occipital Polymicrogyria
Delirium, Aggressive behavior, Abnormal fear-induced behavior, Pseudobulbar paralysis ORPHA:208441
22q13 deletion syndrome (Phelan-Mcdermid syndrome)
Hyperactivity DECIPHER:20
Schizophrenia 15
Hyperactivity OMIM:613950
Intellectual Developmental Disorder, Autosomal Recessive 37
Bruxism, Aggressive behavior, Hyperactivity OMIM:615493
Ank3-Related Intellectual Disability-Sleep Disturbance Syndrome
Bruxism, Aggressive behavior, Hyperactivity ORPHA:356996
Megalencephalic Leukoencephalopathy With Subcortical Cysts 4, Remitting
Gait ataxia, Dysphagia, Hyperactivity, Impulsivity OMIM:620448
Hartnup Disorder
Attention deficit hyperactivity disorder, Emotional lability, Episodic ataxia, Hyperactivity OMIM:234500
Glycine Encephalopathy 1
Hyperglycinemia, Irritability, Aggressive behavior, Lethargy, Hyperactivity, Restlessness, Impuls... OMIM:605899
Developmental And Epileptic Encephalopathy 43
Attention deficit hyperactivity disorder, Hyperactivity, Impulsivity, Ataxia OMIM:617113
Juvenile Huntington Disease
Broad-based gait, Depression, Gait ataxia, Irritability, Hyperactivity, Ataxia, Dementia, Bradyki... ORPHA:248111
Lennox-Gastaut Syndrome
Mental deterioration, Falls, Irritability, Aggressive behavior, Hyperactivity ORPHA:2382
Phenylketonuria
Cataract, Depression, Self-mutilation, Irritability, Maternal hyperphenylalaninemia, Attention de... OMIM:261600
X-Linked Intellectual Disability-Psychosis-Macroorchidism Syndrome
Broad-based gait, Shuffling gait, Abnormal fear-induced behavior, Irritability, Aggressive behavi... ORPHA:3077
Hyperprolinemia, Type I
Hyperprolinemia, Aggressive behavior, Hyperactivity, Ataxia, Motor stereotypy OMIM:239500
Landau-Kleffner Syndrome
Memory impairment, Depression, Short attention span, Emotional lability, Gait ataxia, Aggressive ... ORPHA:98818
Intellectual Developmental Disorder, Autosomal Recessive 38
Recurrent hand flapping, Self-mutilation, Diminished ability to concentrate, Aggressive behavior,... OMIM:615516
Intellectual Developmental Disorder, X-Linked 72
Motor stereotypy, Hyperactivity OMIM:300271
Smith-Magenis syndrome
Motor stereotypy, Hyperactivity, Self-mutilation DECIPHER:8
Microcephaly, Seizures, And Developmental Delay
Hyperactivity, Ataxia OMIM:613402
Intellectual Developmental Disorder, Autosomal Dominant 67
Astigmatism, Attention deficit hyperactivity disorder, Motor tics, Hyperactivity, Compulsive beha... OMIM:619927
Intellectual Developmental Disorder, X-Linked 109
Stereotypical body rocking, Recurrent hand flapping, Agitation, Aggressive behavior, Hyperactivit... OMIM:309548
Intellectual Developmental Disorder, X-Linked, Syndromic, Houge Type
Attention deficit hyperactivity disorder, Hyperactivity, Impulsivity OMIM:301008
Intellectual Developmental Disorder, X-Linked 111
Phonic tics, Aggressive behavior, Hyperactivity, Compulsive behaviors, Unsteady gait OMIM:301107
Fraxe Intellectual Disability
Stereotypical body rocking, Recurrent hand flapping, Impulsivity, Aggressive behavior, Hyperactiv... ORPHA:100973
Citrullinemia Type Ii
Abnormal eating behavior, Hepatic steatosis, Hepatomegaly, Delirium, Restlessness, Mania, Hypopro... ORPHA:247585
Angelman Syndrome Due To Imprinting Defect In 15Q11-Q13
Iris hypopigmentation, Broad-based gait, Inappropriate laughter, Short attention span, Polyphagia... ORPHA:411515
Hyperlysinemia, Type I
Hypoornithinemia, Ectopia lentis, Short attention span, Hyperlysinemia, Cognitive impairment, Hyp... OMIM:238700
Gaucher Disease, Atypical, Due To Saposin C Deficiency
Hepatomegaly, Hypocholesterolemia, Hypersplenism, Splenomegaly OMIM:610539
Porphyria Due To Ala Dehydratase Deficiency
Depression, Abnormal fear-induced behavior, Difficulty walking, Confusion, Abnormal circulating p... ORPHA:100924
Neurodevelopmental Disorder With Absent Speech And Movement And Behavioral Abnormalities
Aggressive behavior, Hyperactivity, Ataxia OMIM:620270
Potocki-Lupski Syndrome
Hypocholesterolemia, Motor stereotypy, Hyperactivity, Oral-pharyngeal dysphagia OMIM:610883
Intellectual Developmental Disorder, Autosomal Recessive 75, With Neuropsychiatric Features And Variant Lissencephaly
Self-injurious behavior, Memory impairment, Inappropriate behavior, Aggressive behavior, Attentio... OMIM:619827
Neurodevelopmental Disorder With Motor And Speech Delay And Behavioral Abnormalities
Aggressive behavior, Broad-based gait, Motor stereotypy, Hyperactivity OMIM:619470
Developmental And Epileptic Encephalopathy 104
Self-injurious behavior, Hyperactivity, Agitation OMIM:619970
Morm Syndrome
Aggressive behavior, Hyperactivity, Cataract ORPHA:75858
Intellectual Developmental Disorder With Epilepsy, Behavioral Abnormalities, And Coarse Facies
Self-injurious behavior, Aggressive behavior, Hyperactivity OMIM:619031
Hypobetalipoproteinemia, Familial, 1
Ataxia, Decreased HDL cholesterol concentration, Hypocholesterolemia, Elevated circulating aspart... OMIM:615558
Neurodevelopmental Disorder With Epilepsy And Hypoplasia Of The Corpus Callosum
Inability to walk, Gait ataxia, Dysmetria, Gait disturbance, Hyperactivity OMIM:618090
Bile Acid Synthesis Defect, Congenital, 1
Intrahepatic cholestasis, Hepatic failure, Elevated circulating hepatic transaminase concentratio... OMIM:607765
Severe Neurodegenerative Syndrome With Lipodystrophy
Progressive psychomotor deterioration, Gait ataxia, Hypertriglyceridemia, Hepatic steatosis, Cirr... ORPHA:363400
Peroxisome Biogenesis Disorder 3B
Elevated circulating phytanic acid concentration, Hypocholesterolemia, Hepatomegaly, Ataxia, Stea... OMIM:266510
Chromosome 3Q29 Deletion Syndrome
Gait ataxia, Aggressive behavior, Motor stereotypy, Hyperactivity OMIM:609425
Microcephaly, Congenital Cataract, And Psoriasiform Dermatitis
Hypocholesterolemia, Decreased LDL cholesterol concentration, Developmental cataract, Decreased H... OMIM:616834
Maternal Uniparental Disomy Of Chromosome 4
Depression, Hypocholesterolemia, Abetalipoproteinemia, Elevated circulating creatine kinase conce... ORPHA:96180
Squalene Synthase Deficiency
Hypocholesterolemia, Irritability, Decreased LDL cholesterol concentration, Elevated circulating ... OMIM:618156
Developmental Delay, Language Impairment, And Ocular Abnormalities
Myopic astigmatism, Frequent temper tantrums, Aggressive behavior, Attention deficit hyperactivit... OMIM:620141
Guanidinoacetate Methyltransferase Deficiency
Self-injurious behavior, Aggressive behavior, Hyperactivity, Ataxia, Athetosis ORPHA:382
Succinic Semialdehyde Dehydrogenase Deficiency
Self-injurious behavior, Elevated circulating gamma-aminobutyric acid concentration, Aggressive b... OMIM:271980
Neurodevelopmental Disorder With Behavioral Abnormalities, Absent Speech, And Hypotonia
Self-injurious behavior, Inability to walk, Bruxism, Motor stereotypy, Hyperactivity, Paroxysmal ... OMIM:618718
Chylomicron Retention Disease
Hypoalbuminemia, Hypotriglyceridemia, Hypocholesterolemia, Decreased LDL cholesterol concentratio... OMIM:246700
Lodder-Merla Syndrome, Type 2, With Developmental Delay And With Or Without Cardiac Arrhythmia
Attention deficit hyperactivity disorder, Hyperactivity OMIM:617182
Abetalipoproteinemia
Hypoalbuminemia, Ataxia, Broad-based gait, Hypotriglyceridemia, Hepatic fibrosis, Elevated circul... ORPHA:14
Rasmussen Subacute Encephalitis
Memory impairment, Inability to walk, Emotional lability, Irritability, Attention deficit hyperac... ORPHA:1929
Late Infantile Neuronal Ceroid Lipofuscinosis
Mental deterioration, Inability to walk, Obsessive-compulsive trait, Low frustration tolerance, A... ORPHA:168491
Gm2 Gangliosidosis, Ab Variant
Inappropriate behavior, Abnormal fear-induced behavior, Cognitive impairment ORPHA:309246
Argininemia
Portal fibrosis, Micronodular cirrhosis, Cholestasis, Hyperammonemia, Hyperargininemia, Irritabil... OMIM:207800
Cntnap2-Related Developmental And Epileptic Encephalopathy
Mental deterioration, Abnormal temper tantrums, Low frustration tolerance, Self-mutilation, Stere... ORPHA:163681
Neurodevelopmental Disorder With Microcephaly And Movement Abnormalities
Gait ataxia, Self-mutilation, Hyperactivity, Paroxysmal bursts of laughter, Impulsivity, Waddling... OMIM:620445
Childhood-Onset Motor And Cognitive Regression Syndrome With Extrapyramidal Movement Disorder
Inability to walk, Gait ataxia, Aggressive behavior, Hyperactivity, Dysphagia, Impulsivity ORPHA:500180
Usmani-Riazuddin Syndrome, Autosomal Dominant
Self-injurious behavior, Depression, Aggressive behavior, Hyperactivity, Compulsive behaviors OMIM:619467
Neurodevelopmental Disorder With Microcephaly, Movement Abnormalities, And Seizures
Self-injurious behavior, Inability to walk, Aggressive behavior, Hyperactivity, Choreoathetosis OMIM:620023
X-Linked Cerebral Adrenoleukodystrophy
Mental deterioration, Memory impairment, Difficulty walking, Confusion, Inability to walk, Short ... ORPHA:139396
X-Linked Adrenoleukodystrophy
Disinhibition, Aggressive behavior, Attention deficit hyperactivity disorder, Gait disturbance, C... ORPHA:43
Infantile Neuroaxonal Dystrophy
Mental deterioration, Short attention span, Emotional lability, Unsteady gait, Gait disturbance, ... ORPHA:35069
Pitt-Hopkins-Like Syndrome 1
Aggressive behavior, Attention deficit hyperactivity disorder, Hyperactivity, Ataxia, Progressive... OMIM:610042
Developmental And Epileptic Encephalopathy 109
Crouch gait, Gait ataxia, Hyperactivity OMIM:620145
Pancreatic Lipase Deficiency
Steatorrhea, Hypocholesterolemia OMIM:614338
Intellectual Developmental Disorder, X-Linked 30
Short attention span, Aggressive behavior, Hyperactivity, Restlessness, Agitation OMIM:300558
Neurodevelopmental Disorder With Poor Growth And Behavioral Abnormalities
Depression, Short attention span, Aggressive behavior, Attention deficit hyperactivity disorder, ... OMIM:620242
Optic Atrophy 11
Stereotypical body rocking, Splenomegaly, Dysmetria, Attention deficit hyperactivity disorder, Hy... OMIM:617302
Angelman Syndrome Due To Maternal 15Q11Q13 Deletion
Iris hypopigmentation, Broad-based gait, Inappropriate laughter, Abnormal eating behavior, Short ... ORPHA:98794
X-Linked Intellectual Disability-Hypotonia-Movement Disorder Syndrome
Aggressive behavior, Broad-based gait, Hyperactivity ORPHA:457260
Intellectual Developmental Disorder, X-Linked, Syndromic, Pilorge Type
Hyperactivity, Inflexible adherence to routines OMIM:301076
Gomez-Lopez-Hernandez Syndrome
Self-injurious behavior, Depression, Cognitive impairment, Hyperactivity, Ataxia, Opacification o... OMIM:601853
Congenital Disorder Of Glycosylation, Type Il
Hypoalbuminemia, Hypocholesterolemia, Splenomegaly, Hepatomegaly OMIM:608776
Intellectual Developmental Disorder, X-Linked 107
Aggressive behavior, Attention deficit hyperactivity disorder, Hyperactivity OMIM:301013
Neurodegeneration With Brain Iron Accumulation 2B
Mental deterioration, Short attention span, Emotional lability, Dysmetria, Gait ataxia, Hyperacti... OMIM:610217
Pontocerebellar Hypoplasia, Hypotonia, And Respiratory Insufficiency Syndrome, Neonatal Lethal
Hepatomegaly, Hypocholesterolemia, Developmental cataract OMIM:618810
Dubowitz Syndrome
Megalocornea, Hypoplasia of the iris, Hypocholesterolemia, Short attention span, Hyperactivity, I... OMIM:223370
Female Restricted Epilepsy With Intellectual Disability
Abnormal eating behavior, Aggressive behavior, Hyperactivity, Compulsive behaviors, Impulsivity ORPHA:101039
Intellectual Developmental Disorder, X-Linked 77
Hyperactivity OMIM:300454
Congenital Disorder Of Glycosylation, Type Ia
Hypoalbuminemia, Hepatic fibrosis, Elevated circulating hepatic transaminase concentration, Hypoc... OMIM:212065
Myoclonic-Astatic Epilepsy
Abnormal emotion, Attention deficit hyperactivity disorder, Hyperactivity, Ataxia, Unsteady gait ORPHA:1942
Mucopolysaccharidosis, Type Iiib
Splenomegaly, Aggressive behavior, Hepatomegaly, Hyperactivity, Progressive neurologic deterioration OMIM:252920
Chylomicron Retention Disease
Elevated circulating hepatic transaminase concentration, Hypocholesterolemia, Hepatic steatosis, ... ORPHA:71
Symptomatic Form Of Fragile X Syndrome In Female Carriers
Self-injurious behavior, Abnormal temper tantrums, Depression, Short attention span, Recurrent ha... ORPHA:449291
Insensitivity To Pain, Congenital, With Anhidrosis
Keratitis, Corneal scarring, Emotional lability, Self-mutilation, Recurrent corneal erosions, Hyp... OMIM:256800
Neurodevelopmental Disorder With Movement Abnormalities, Abnormal Gait, And Autistic Features
Broad-based gait, Stereotypical body rocking, Unsteady gait, Tongue thrusting, Hyperactivity, Ata... OMIM:617865
Lattice Corneal Dystrophy Type I
Abnormal cornea morphology, Corneal scarring, Astigmatism, Subepithelial corneal opacities, Recur... ORPHA:98964
Graves Disease
Polyphagia, Hyperactivity, Irritability OMIM:275000
Norrie Disease
Cataract, Hypoplasia of the iris, Opacification of the corneal stroma, Aggressive behavior, Leuko... OMIM:310600
Dihydropyrimidinase Deficiency
Elevated circulating thymine concentration, Elevated circulating aspartate aminotransferase conce... OMIM:222748
X-Linked Creatine Transporter Deficiency
Self-mutilation, Hyperactivity, Abnormal circulating creatine concentration, Ataxia, Athetosis ORPHA:52503
Intellectual Developmental Disorder, Autosomal Dominant 45
Recurrent hand flapping, Attention deficit hyperactivity disorder, Motor stereotypy, Hyperactivity OMIM:617600
Dystonia, Dopa-Responsive, Due To Sepiapterin Reductase Deficiency
Depression, Abnormal circulating biopterin concentration, Abnormal circulating neopterin concentr... OMIM:612716
Congenital-Onset Steinert Myotonic Dystrophy
Cataract, Short attention span, Hyperactivity, Dysphagia, Bradyphrenia ORPHA:589821
Mucopolysaccharidosis, Type Iiic
Splenomegaly, Hyperactivity, Motor deterioration, Hepatomegaly, Dysphagia OMIM:252930
Neurodegeneration With Brain Iron Accumulation 1
Phonic tics, Mental deterioration, Depression, Akinesia, Obsessive-compulsive trait, Motor tics, ... OMIM:234200
Insulin-Like Growth Factor I Deficiency
Short attention span, Hyperactivity OMIM:608747
Angelman Syndrome
Self-injurious behavior, Keratoconus, Iris hypopigmentation, Broad-based gait, Inability to walk,... ORPHA:72
Generalized Eruptive Keratoacanthoma
Conjunctivitis, Abnormal cornea morphology, Dysphagia, Keratoconjunctivitis sicca ORPHA:411777
Intellectual Developmental Disorder, X-Linked, Syndromic, Billuart Type
Gait ataxia, Low frustration tolerance, Self-mutilation, Hyperactivity, Motor stereotypy OMIM:300486
Choreoacanthocytosis
Mental deterioration, Emotional lability, Hair-pulling, Loss of ambulation, Elevated circulating ... ORPHA:2388
Smith-Lemli-Opitz Syndrome
Hypoalbuminemia, Cataract, Cholestatic liver disease, Hypocholesterolemia, Elevated circulating 7... OMIM:270400
Hypomagnesemia, Seizures, And Impaired Intellectual Development 2
Hypokalemia, Hyperactivity, Self-biting, Hypomagnesemia OMIM:618314
Kaufman Oculocerebrofacial Syndrome
Hypocholesterolemia, Microcornea, Astigmatism OMIM:244450
Alg12-Cdg
Hyponatremia, Hypocholesterolemia, Elevated circulating hepatic transaminase concentration, Hypoa... ORPHA:79324
Tangier Disease
Hypocholesterolemia, Hepatosplenomegaly, Corneal opacity, Hypertriglyceridemia ORPHA:31150
Pituitary Adenoma 4, Acth-Secreting
Hypokalemia, Abnormal fear-induced behavior, Emotional lability OMIM:219090
Legius Syndrome
Cataract, Xanthelasma, Short attention span, Attention deficit hyperactivity disorder, Hyperactiv... ORPHA:137605
Secondary Intestinal Lymphangiectasia
Hypoalbuminemia, Secondary hyperaldosteronism, Reduced circulating transferrin concentration, Hyp... ORPHA:90363
Multiple Mitochondrial Dysfunctions Syndrome 7
Hypernatremia, Decreased liver function, Hyperglycinemia, Irritability, Impulsivity, Lethargy, Hy... OMIM:620423
Microcephaly 29, Primary, Autosomal Recessive
Ataxia, Emotional lability, Hyperactivity OMIM:620047
X-Linked Intellectual Disability-Acromegaly-Hyperactivity Syndrome
Aggressive behavior, Hyperactivity ORPHA:85327
Amoebic Keratitis
Cataract, Corneal perforation, Abnormal cornea morphology, Punctate opacification of the cornea, ... ORPHA:67043
Infantile Nephropathic Cystinosis
Abnormal cornea morphology, Polydipsia, Corneal crystals, Hypokalemia, Hypophosphatemia, Cognitiv... ORPHA:411629
Rubinstein-Taybi Syndrome Due To 16P13.3 Microdeletion
Self-injurious behavior, Cataract, Abnormal fear-induced behavior, Emotional lability, Aggressive... ORPHA:353281
Hereditary Sensory And Autonomic Neuropathy Type 4
Difficulty walking, Abnormal emotion, Corneal scarring, Short attention span, Self-mutilation, Hy... ORPHA:642
Histidinemia
Hyperactivity, Hyperhistidinemia ORPHA:2157
Cerebellar Dysfunction With Variable Cognitive And Behavioral Abnormalities
Broad-based gait, Gait ataxia, Astigmatism, Dysmetria, Aggressive behavior, Attention deficit hyp... OMIM:614756
Rubinstein-Taybi Syndrome Due To Ep300 Haploinsufficiency
Self-injurious behavior, Cataract, Abnormal fear-induced behavior, Corneal scarring, Emotional la... ORPHA:353284
Rubinstein-Taybi Syndrome Due To Crebbp Mutations
Self-injurious behavior, Cataract, Abnormal fear-induced behavior, Corneal scarring, Emotional la... ORPHA:353277
Solitary Fibrous Tumor
Neoplasm of the liver, Hypophosphatemic rickets, Reduced C-peptide level, Abnormal peritoneum mor... ORPHA:2126

Histopathology

Summary table of phenotypes displayed during the Histopathology procedure which are considered significant. Full histopathology data table, including submitted images, can be accessed by clicking any row in this table.

There is no histopathology data for Nab2

IMPC related publications

The table below lists publications which used either products generated by the IMPC or data produced by the phenotyping efforts of the IMPC. These publications have also been associated to Nab2.

No publications found that use IMPC mice or data for Nab2.

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MGI Allele Allele Type Produced
Nab2tm1(KOMP)Vlcg Reporter-tagged deletion allele (with selection cassette) ES Cells
Nab2tm1b(EUCOMM)Hmgu Reporter-tagged deletion allele (with selection cassette) Mice
Nab2tm2e(EUCOMM)Hmgu Targeted, non-conditional allele ES Cells
Nab2tm1a(EUCOMM)Hmgu KO first allele (reporter-tagged insertion with conditional potential) Mice, Targeting vectors, ES Cells
Nab2tm1e(EUCOMM)Hmgu Targeted, non-conditional allele ES Cells

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