Gene Summary

Name:
zinc finger protein 91
Synonyms:
A530054C17Rik,  Pzf,  9130014I08Rik

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
pallor Zfp91em1(IMPC)Tcp HOM E15.5 0.00
abnormal embryo size Zfp91em1(IMPC)Tcp HOM E9.5 0.00
abnormal embryo size Zfp91em1(IMPC)Tcp HOM E15.5 0.00
enlarged lymph nodes Zfp91em1(IMPC)Tcp HET Early adult 0.00
cataract Zfp91em1(IMPC)Tcp HET Early adult 1.84×10-05
decreased body length Zfp91em1(IMPC)Tcp HET Early adult 1.51×10-05
preweaning lethality, complete penetrance Zfp91em1(IMPC)Tcp HOM   Early adult 0.00
abnormal skin coloration Zfp91em1(IMPC)Tcp HOM E15.5 0.00
increased startle reflex Zfp91em1(IMPC)Tcp HET Early adult 1.10×10-06
edema Zfp91em1(IMPC)Tcp HOM E15.5 0.00

Download data as:  TSV  XLS

Select physiological systems to view:
Viewing: all phenotypes
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Viewing: all phenotypes

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.

Eye Morphology

Images Ophthalmoscopy

100 Images

Gross Morphology Embryo E14.5-E15.5

Images

44 Images

X-ray

XRay Images Skull Dorso Ventral Orientation

10 Images

Gross Pathology and Tissue Collection

Images

8 Images

Gross Morphology Embryo E9.5

Images

2 Images

X-ray

XRay Images Whole Body Lateral Orientation

10 Images

X-ray

XRay Images Whole Body Dorso Ventral

10 Images

Eye Morphology

Images Slit Lamp

12 Images

X-ray

XRay Images Skull Lateral Orientation

10 Images

MicroCT E14.5-E15.5

Embryo reconstruction

7 Images

Electrocardiogram (ECG)

Waveform Image

1 Images

Human diseases caused by Zfp91 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.

No human diseases associated to this gene by orthology or annotation.

The table below shows human diseases predicted to be associated to Zfp91 by phenotypic similarity.

Disease Similarity of
phenotypes
Matching phenotypes Source
Cataract 20, Multiple Types
Membranous cataract, Cataract OMIM:116100
Kaposi Sarcoma, Susceptibility To
Hypermelanotic macule, Edema OMIM:148000
Retinitis Pigmentosa 42
Pallor OMIM:612943
Hereditary Hyperferritinemia-Cataract Syndrome
Cataract ORPHA:163
Cataract 36
Cataract OMIM:613887
Cataract 18
Cataract OMIM:610019
Cataract 29
Cataract OMIM:115800
Corneal Dystrophy, Fuchs Endothelial, 3
Edema OMIM:613267
Retinitis Pigmentosa 81
Pallor OMIM:617871
Cataract 35
Cataract OMIM:609376
Hypertrophic Neuropathy And Cataract
Cataract OMIM:239900
Cataract And Congenital Ichthyosis
Cataract OMIM:212400
Lipedema
Edema OMIM:614103
Aniridia 3
Cataract OMIM:617142
Retinohepatoendocrinologic Syndrome
Pallor, Abnormality of skin pigmentation OMIM:268040
Corneal Dystrophy, Groenouw Type I
Nodular corneal dystrophy, Granular corneal dystrophy, Cataract, Punctate corneal dystrophy OMIM:121900
Retinitis Pigmentosa 60
Pallor OMIM:613983
Spastic Paraparesis And Deafness
Tremor, Cataract OMIM:312910
Hydrocephaly-Cerebellar Agenesis Syndrome
Cataract ORPHA:1397
Cataract 12, Multiple Types
Developmental cataract, Progressive cataract OMIM:611597
Osteoporosis-Oculocutaneous Hypopigmentation Syndrome
Pallor, Albinism, Hypopigmentation of the skin ORPHA:2786
Aldh18A1-Related De Barsy Syndrome
Cataract ORPHA:35664
Mastocytosis, Cutaneous
Hypermelanotic macule, Erythema, Edema OMIM:154800
Optic Atrophy 9
Pallor OMIM:616289
Trichomegaly
Cataract OMIM:190330
Retinitis Pigmentosa 27
Pallor, Macular edema OMIM:613750
Neutropenia, Severe Congenital, 9, Autosomal Dominant
Cataract, Splenomegaly OMIM:619813
Hereditary Persistence Of Fetal Hemoglobin-Beta-Thalassemia Syndrome
Pallor ORPHA:46532
Nathalie Syndrome
Cataract ORPHA:2663
Optic Atrophy 3, Autosomal Dominant
Tremor, Cataract OMIM:165300
Cataract-Microcornea Syndrome
Corneal opacity, Microcornea, Iris coloboma, Cataract, Corneal dystrophy ORPHA:1377
Acral Self-Healing Collodion Baby
Edema of the dorsum of feet, Lack of skin elasticity, Erythema, Palmoplantar scaling skin, Edema ... ORPHA:281127
Methylmalonic Acidemia With Homocystinuria, Type Cbld
Pallor ORPHA:79283
Myopathy, Mitochondrial Progressive, With Congenital Cataract And Developmental Delay
Cataract, Developmental cataract OMIM:613076
Cone-Rod Dystrophy 11
Pallor OMIM:610381
Peripheral Cone Dystrophy
Pallor OMIM:609021
X-Linked Sideroblastic Anemia
Pallor, Hyperpigmentation of the skin ORPHA:75563
Retinitis Pigmentosa 70
Pallor OMIM:615922
Breath-Holding Spells
Pallor OMIM:607578
Auditory Neuropathy And Optic Atrophy
Pallor OMIM:617717
Galactosemia Iv
Cataract OMIM:618881
Cataract 9, Multiple Types
Progressive cataract, Microcornea, Iris coloboma, Cataract, Developmental cataract OMIM:604219
Megalocornea
Lens subluxation, Mosaic corneal dystrophy, Megalocornea, Astigmatism, Iridodonesis, Cataract, Ir... OMIM:309300
Retinitis Pigmentosa 73
Pallor OMIM:616544
Hypoalphalipoproteinemia, Primary, 2
Cataract, Corneal arcus OMIM:618463
Anemia, Hypochromic Microcytic, With Iron Overload 2
Pallor, Cafe-au-lait spot OMIM:615234
Hb Bart'S Hydrops Fetalis
Pallor, Polyhydramnios, Oligohydramnios, Hydrops fetalis ORPHA:163596
Autoimmune Hemolytic Anemia, Cold Type
Pallor ORPHA:228312
Benign Paroxysmal Torticollis Of Infancy
Pallor ORPHA:71518
Chorea, Remitting, With Nystagmus And Cataract
Cataract OMIM:601372
Microphthalmia, Isolated, With Coloboma 3
Iris coloboma, Cataract OMIM:610092
Cataract 1, Multiple Types
Nuclear cataract, Posterior subcapsular cataract, Microcornea, Pulverulent cataract, Developmenta... OMIM:116200
Dermatitis, Atopic
Pallor, Dry skin, Facial erythema OMIM:603165
Anterior Segment Dysgenesis 8
Microphakia, Ectopia pupillae, Uveal ectropion, Hypoplasia of the iris, Cataract, Iris transillum... OMIM:617319
Galactosemia Ii
Cataract OMIM:230200
Lymphatic Malformation 11
Lymphedema, Pedal edema OMIM:619401
Optic Atrophy 1
Pallor OMIM:165500
Thanatophoric Dysplasia, Glasgow Variant
Hepatosplenomegaly, Cataract OMIM:273680
Acute Peripheral Arterial Occlusion
Pallor ORPHA:90064
Muscular Dystrophy, Congenital, With Infantile Cataract And Hypogonadism
Cataract OMIM:254000
Cataract 15, Multiple Types
Nuclear cataract, Lamellar cataract, Cataract, Developmental cataract, Cortical cataract OMIM:615274
Aniridia, Microcornea, And Spontaneously Reabsorbed Cataract
Cataract, Microcornea, Aniridia OMIM:106230
Iris Pigment Layer, Cleavage Of
Cataract OMIM:147610
Leber Congenital Amaurosis 14
Pallor OMIM:613341
Primary Lateral Sclerosis, Juvenile
Pallor OMIM:606353
Acute Myelomonocytic Leukemia
Pallor ORPHA:517
Cataract 47
Cataract, Microcornea OMIM:612018
Ectopia Lentis Et Pupillae
Cataract, Ectopia lentis, Persistent pupillary membrane OMIM:225200
Exfoliation Syndrome
Lens subluxation, Anisocoria, Mydriasis, Pseudoexfoliation, Cataract, Phakodonesis, Pigment depos... OMIM:177650
Hemoglobin D Disease
Pallor ORPHA:90039
Myoclonus, Intractable, Neonatal
Pallor OMIM:617235
Optic Atrophy 7 With Or Without Auditory Neuropathy
Pallor OMIM:612989
Cataract 10, Multiple Types
Posterior Y-sutural cataract, Developmental cataract, Zonular cataract OMIM:600881
Hemolytic Anemia Due To Glutathione Reductase Deficiency
Cataract OMIM:618660
Aniridia-Intellectual Disability Syndrome
Cataract, Ectopia lentis, Aniridia ORPHA:1068
Aniridia 2
Iris coloboma, Lens subluxation, Cataract, Aniridia OMIM:617141
Familial Focal Epilepsy With Variable Foci
Pallor ORPHA:98820
Coats Disease
Abnormal anterior chamber morphology, Aplasia/Hypoplasia of the iris, Cataract ORPHA:190
Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 2
Pallor OMIM:608423
Cataract 3, Multiple Types
Developmental cataract, Nuclear pulverulent cataract, Cerulean cataract, Sutural cataract OMIM:601547
Anterior Segment Dysgenesis 7
Buphthalmos, Microcornea, Cataract, Ocular anterior segment dysgenesis, Sclerocornea OMIM:269400
Aniridia-Ptosis-Intellectual Disability-Familial Obesity Syndrome
Corneal opacity, Aplasia/Hypoplasia of the iris, Cataract, Persistent pupillary membrane ORPHA:1067
Myelofibrosis
Pallor, Purpura OMIM:254450
Cataract 14, Multiple Types
Zonular cataract OMIM:601885
Pulmonary Edema Of Mountaineers, Susceptibility To
Pulmonary edema, Edema OMIM:178400
Kcnq2-Related Epileptic Encephalopathy
Facial erythema, Pallor, Cerebral edema ORPHA:439218
Peters Anomaly
Subcapsular cataract, Central opacification of the cornea, Thinning of Descemet membrane, Opacifi... ORPHA:708
Myopia, High, With Cataract And Vitreoretinal Degeneration
Lens subluxation, Cataract OMIM:614292
Non-Insulinoma Pancreatogenous Hypoglycemia Syndrome
Pallor ORPHA:276608
Wells Syndrome
Skin vesicle, Edema ORPHA:901
Pyruvate Kinase Deficiency Of Red Cells
Pallor, Intrauterine growth retardation, Nonimmune hydrops fetalis OMIM:266200
Lymphatic Malformation 8
Nonimmune hydrops fetalis, Polyhydramnios, Pleural effusion, Generalized edema, Pericardial effusion OMIM:618773
Spontaneous Periodic Hypothermia
Pallor ORPHA:29822
Microcornea, Rod-Cone Dystrophy, Cataract, And Posterior Staphyloma 1
Cataract, Microcornea OMIM:619082
Sea-Blue Histiocytosis
Hypopigmentation of the skin, Petechiae, Hyperpigmentation of the skin, Edema ORPHA:158029
Retinitis Pigmentosa 51
Pallor OMIM:613464
American Trypanosomiasis
Pallor, Edema, Periorbital edema ORPHA:3386
Proximal Myotonic Myopathy
Cataract ORPHA:606
Cataract 5, Multiple Types
Nuclear cataract, Zonular cataract, Anterior polar cataract, Lamellar cataract, Pulverulent cataract OMIM:116800
Autosomal Dominant Keratitis
Keratitis, Hypoplastic iris stroma, Corneal neovascularization, Opacification of the corneal stro... ORPHA:2334
Megaloblastic Anemia Due To Dihydrofolate Reductase Deficiency
Pallor OMIM:613839
Irida Syndrome
Pallor ORPHA:209981
Cyclic Vomiting Syndrome
Pallor OMIM:500007
Retinitis Pigmentosa 75
Pallor OMIM:617023
Amoebic Keratitis
Corneal perforation, Corneal ulceration, Abnormal cornea morphology, Abnormal anterior chamber mo... ORPHA:67043
Thiamine-Responsive Megaloblastic Anemia Syndrome
Pallor ORPHA:49827
Lymphatic Malformation 7
Pulmonary edema, Facial edema, Nonimmune hydrops fetalis, Lymphedema, Edema, Pericardial effusion OMIM:617300
Evans Syndrome
Pallor, Petechiae ORPHA:1959
Anterior Segment Dysgenesis 2
Congenital aphakia, Corneal opacity, Microcornea, Peters anomaly, Cataract, Posterior synechiae o... OMIM:610256
Retinitis Pigmentosa 84
Cataract OMIM:618220
Deafness-Lymphedema-Leukemia Syndrome
Pallor, Lymphedema ORPHA:3226
Hyperinsulinism Due To Ucp2 Deficiency
Pallor ORPHA:276556
Anemia, Congenital Dyserythropoietic, Type Ib
Pallor OMIM:615631
Autosomal Dominant Hyperinsulinism Due To Sur1 Deficiency
Pallor ORPHA:276575
Beta-Thalassemia
Skin ulcer, Pallor ORPHA:848
Anemia, Sideroblastic, 1
Anemic pallor OMIM:300751
Autosomal Dominant Hyperinsulinism Due To Kir6.2 Deficiency
Pallor ORPHA:276580
Hyperekplexia 3
Exaggerated startle response OMIM:614618
Hyperinsulinism Due To Hnf1A Deficiency
Pallor ORPHA:324575
Elliptocytosis 1
Pallor OMIM:611804
Isolated Aniridia
Peters anomaly, Cataract, Aniridia ORPHA:250923
Myopia 28, Autosomal Recessive
Cataract OMIM:619781
Anterior Segment Dysgenesis 1
Posterior polar cataract, Opacification of the corneal stroma, Microcornea, Peters anomaly, Ocula... OMIM:107250
Fanconi Anemia, Complementation Group I
Pallor, Cafe-au-lait spot, Intrauterine growth retardation OMIM:609053
Developmental And Epileptic Encephalopathy 8
Exaggerated startle response OMIM:300607
Myopathy, Lactic Acidosis, And Sideroblastic Anemia 1
Pallor OMIM:600462
Leishmaniasis
Skin ulcer, Pallor ORPHA:507
Drug-Induced Autoimmune Hemolytic Anemia
Pallor ORPHA:90037
Myopathic Ehlers-Danlos Syndrome
Pallor ORPHA:536516
Aniridia And Absent Patella
Cataract, Aniridia OMIM:106220
Primary Myelofibrosis
Pallor, Purpura, Ecchymosis, Petechiae ORPHA:824
Generalized Juvenile Polyposis/Juvenile Polyposis Coli
Anemic pallor, Edema ORPHA:329971
Cold Agglutinin Disease
Pallor ORPHA:56425
Renal Tubular Acidosis, Distal, 4, With Hemolytic Anemia
Pallor OMIM:611590
Hyperekplexia 2
Exaggerated startle response, Astigmatism OMIM:614619
Dravet Syndrome
Pallor ORPHA:33069
Autoimmune Hemolytic Anemia
Pallor ORPHA:98375
Dystonia, Juvenile-Onset
Leg dystonia, Oculogyric crisis, Cataract, Generalized dystonia OMIM:607371
Mixed-Type Autoimmune Hemolytic Anemia
Pallor ORPHA:90036
Cataract 30, Multiple Types
Diffuse nuclear cataract, Pulverulent cataract, Posterior polar cataract OMIM:116300
Lymphangiectasia, Pulmonary, Congenital
Facial edema, Chylothorax, Chylous ascites, Palpebral edema, Nonimmune hydrops fetalis, Polyhydra... OMIM:265300
Non-Functioning Paraganglioma
Pallor ORPHA:94080
Waldenström Macroglobulinemia
Pallor, Purpura, Pedal edema, Pleural effusion, Periorbital edema ORPHA:33226
Cone-Rod Dystrophy 8
Pallor OMIM:605549
Severe Combined Immunodeficiency With Sensitivity To Ionizing Radiation
Aplasia of the thymus, Splenomegaly, Generalized lymphadenopathy, Lymph node hypoplasia, Absent t... OMIM:602450
Beta-Ketothiolase Deficiency
Pallor, Dehydration, Edema ORPHA:134
Severe Congenital Hypochromic Anemia With Ringed Sideroblasts
Pallor, Cafe-au-lait spot ORPHA:300298
Superficial Epidermolytic Ichthyosis
Erythema, Edema ORPHA:455
Acquired Idiopathic Sideroblastic Anemia
Pallor ORPHA:75564
Cataract 31, Multiple Types
Nuclear cataract, Posterior subcapsular cataract, Anterior subcapsular cataract OMIM:605387
Vitreoretinal Degeneration, Snowflake Type
Corneal guttata, Cataract OMIM:193230
3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency
Pallor OMIM:246450
6-Pyruvoyl-Tetrahydropterin Synthase Deficiency
Pallor ORPHA:13
Blindness-Scoliosis-Arachnodactyly Syndrome
Microphakia, Lens subluxation, Cataract ORPHA:171844
Tay-Sachs Disease
Pallor OMIM:272800
Rheumatic Fever
Pallor, Erythema ORPHA:3099
Sepsis In Premature Infants
Pallor, Purpura, Edema, Petechiae ORPHA:90051
Autoimmune Hemolytic Anemia, Warm Type
Pallor ORPHA:90033
Refractory Anemia With Excess Blasts
Anemic pallor, Pedal edema ORPHA:86839
Idiopathic Pulmonary Hemosiderosis
Pallor ORPHA:99931
Hyperinsulinism Due To Hnf4A Deficiency
Pallor ORPHA:263455
Senior-Loken Syndrome 8
Pallor OMIM:616307
Hyperekplexia-Epilepsy Syndrome
Exaggerated startle response ORPHA:163985
Cataract 33, Multiple Types
Cortical cataract, Lamellar cataract, Nuclear cataract OMIM:611391
Coloboma, Ocular, Autosomal Recessive
Iris coloboma, Lens subluxation, Cataract OMIM:216820
Letterer-Siwe Disease
Pallor OMIM:246400
Dominant Beta-Thalassemia
Skin ulcer, Hyperpigmentation of the skin, Pallor ORPHA:231226
Plummer-Vinson Syndrome
Pallor ORPHA:54028
Congenital Dyserythropoietic Anemia Type Iii
Pallor ORPHA:98870
3-Hydroxy-3-Methylglutaric Aciduria
Pallor, Dehydration, Edema ORPHA:20
Childhood Absence Epilepsy
Pallor ORPHA:64280
Purine Nucleoside Phosphorylase Deficiency
Lymph node hypoplasia, Tremor, Splenomegaly OMIM:613179
Norrie Disease
Corneal opacity, Shallow anterior chamber, Buphthalmos, Opacification of the corneal stroma, Hypo... OMIM:310600
Fumarase Deficiency
Pallor OMIM:606812
Meige Disease
Lymph node hypoplasia, Absence of lymph node germinal center ORPHA:90186
Beta-Thalassemia Major
Skin ulcer, Hyperpigmentation of the skin, Pallor ORPHA:231214
Hereditary Folate Malabsorption
Pallor ORPHA:90045
Aromatic L-Amino Acid Decarboxylase Deficiency
Torticollis, Blepharospasm, Exaggerated startle response, Oculogyric crisis, Athetosis, Choreoath... OMIM:608643
Hereditary Spherocytosis
Skin ulcer, Pallor ORPHA:822
Fructose-1,6-Bisphosphatase Deficiency
Pallor ORPHA:348
Myopathy, Mitochondrial, And Ataxia
Pallor OMIM:617675
Pearson Marrow-Pancreas Syndrome
Pallor, Dehydration, Hydrops fetalis, Erythema OMIM:557000
Dehydrated Hereditary Stomatocytosis 1 With Or Without Pseudohyperkalemia And/Or Perinatal Edema
Pallor OMIM:194380
Rare Circulatory System Disease
Pallor ORPHA:98028
Beta-Thalassemia Intermedia
Skin ulcer, Pallor ORPHA:231222
Persistent Hyperplastic Primary Vitreous, Autosomal Recessive
Corneal opacity, Shallow anterior chamber, Buphthalmos, Microcornea, Iris coloboma, Cataract, Leu... OMIM:221900
Fanconi Anemia, Complementation Group C
Cafe-au-lait spot, Anemic pallor, Hyperpigmentation of the skin, Intrauterine growth retardation OMIM:227645
Fanconi Anemia, Complementation Group E
Cafe-au-lait spot, Anemic pallor, Hyperpigmentation of the skin OMIM:600901
Sporadic Pheochromocytoma/Secreting Paraganglioma
Pallor ORPHA:276621
Retinitis Pigmentosa And Erythrocytic Microcytosis
Pallor OMIM:616959
Incontinentia Pigmenti
Pallor, Abnormality of skin pigmentation, Erythema OMIM:308300
Anemia, Nonspherocytic Hemolytic, Due To G6Pd Deficiency
Pallor OMIM:300908
T-B+ Severe Combined Immunodeficiency Due To Gamma Chain Deficiency
Lymph node hypoplasia, Absent tonsils ORPHA:276
Fanconi Anemia, Complementation Group A
Cafe-au-lait spot, Anemic pallor, Abnormality of skin pigmentation OMIM:227650
Developmental And Epileptic Encephalopathy 68
Exaggerated startle response OMIM:618201
Severe Combined Immunodeficiency Due To Complete Rag1/2 Deficiency
Pallor ORPHA:331206
Imerslund-Gräsbeck Syndrome
Pallor ORPHA:35858
Aregenerative Anemia
Pallor ORPHA:101096
Aniridia 1
Corneal neovascularization, Ectopia pupillae, Opacification of the corneal stroma, Hypoplasia of ... OMIM:106210
Neurodevelopmental Disorder With Microcephaly, Epilepsy, And Hypomyelination
Exaggerated startle response OMIM:618367
Alternating Hemiplegia Of Childhood
Pallor, Dehydration ORPHA:2131
Non-Functioning Pituitary Adenoma
Pallor ORPHA:91349
Gm2 Gangliosidosis, Ab Variant
Dystonia, Exaggerated startle response ORPHA:309246
Infection-Related Hemolytic Uremic Syndrome
Pallor, Generalized edema, Pleural empyema, Edema ORPHA:544482
Adenohypophysitis
Pallor ORPHA:95512
Sheehan Syndrome
Pallor, Dry skin ORPHA:91355
Pituitary Apoplexy
Pallor ORPHA:95613
Systemic Mastocytosis With Associated Hematologic Neoplasm
Pallor ORPHA:98849
Panhypophysitis
Pallor ORPHA:95513
Deafness, Unilateral, With Delayed Endolymphatic Hydrops
Edema OMIM:612097
Prolactinoma
Pallor ORPHA:2965
Polycystic Kidney, Cataract, And Congenital Blindness
Microcoria, Cataract OMIM:263100
Hereditary Pheochromocytoma-Paraganglioma
Pallor ORPHA:29072
Idiopathic Hypereosinophilic Syndrome
Pallor, Joint swelling, Angioedema, Pleural effusion ORPHA:3260
Hyperekplexia 1
Exaggerated startle response OMIM:149400
Persistent Hyperplastic Primary Vitreous
Corneal opacity, Shallow anterior chamber, Buphthalmos, Microcornea, Cataract, Developmental cata... ORPHA:91495
Gm2-Gangliosidosis, Ab Variant
Dystonia, Exaggerated startle response OMIM:272750
Histiocytoid Cardiomyopathy
Pallor, Pulmonary edema ORPHA:137675
Stiff Person Spectrum Disorder
Exaggerated startle response ORPHA:3198
Spastic Tetraplegia And Axial Hypotonia, Progressive
Exaggerated startle response OMIM:618598
Autosomal Dominant Optic Atrophy And Cataract
Anterior cortical cataract, Resting tremor, Cerulean cataract, Posterior subcapsular cataract, Ca... ORPHA:67036
Degcags Syndrome
Pallor, Hypopigmentation of the skin, Polyhydramnios, Abnormality of skin pigmentation, Intrauter... OMIM:619488
Spastic Paraplegia, Optic Atrophy, And Neuropathy
Exaggerated startle response OMIM:609541
Spastic Paraplegia-Optic Atrophy-Neuropathy Syndrome
Exaggerated startle response ORPHA:320406
Esophageal Atresia
Pallor, Polyhydramnios ORPHA:1199
Stiff-Person Syndrome
Exaggerated startle response, Opisthotonus OMIM:184850
Fanconi Anemia, Complementation Group D2
Cafe-au-lait spot, Anemic pallor, Abnormality of skin pigmentation OMIM:227646
Sandhoff Disease
Hepatosplenomegaly, Exaggerated startle response OMIM:268800
Tsh-Secreting Pituitary Adenoma
Pallor, Pericardial effusion ORPHA:91347
Von Hippel-Lindau Disease
Pallor, Macular edema ORPHA:892
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 4
Cataract, Exaggerated startle response OMIM:253800
Diamond-Blackfan Anemia 1
Pallor, Intrauterine growth retardation OMIM:105650
Blackfan-Diamond Anemia
Pallor, Nonimmune hydrops fetalis ORPHA:124
Asparagine Synthetase Deficiency
Exaggerated startle response OMIM:615574
Agammaglobulinemia, X-Linked
Lymph node hypoplasia, Conjunctivitis OMIM:300755
Pura-Related Severe Neonatal Hypotonia-Seizures-Encephalopathy Syndrome Due To A Point Mutation
Dystonia, Exaggerated startle response ORPHA:438216
Multiple Endocrine Neoplasia Type 2
Pallor ORPHA:653
Tay-Sachs Disease
Tremor, Dystonia, Exaggerated startle response, Laryngeal dystonia ORPHA:845
Gm1 Gangliosidosis Type 1
Hepatosplenomegaly, Exaggerated startle response ORPHA:79255
Glycine Encephalopathy With Normal Serum Glycine
Exaggerated startle response OMIM:617301
Autosomal Recessive Malignant Osteopetrosis
Pallor ORPHA:667
Plaa-Associated Neurodevelopmental Disorder
Dystonia, Exaggerated startle response ORPHA:521426
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 3
Pallor OMIM:253280
Neurodevelopmental Disorder With Progressive Microcephaly, Spasticity, And Brain Anomalies
Exaggerated startle response OMIM:617527
Goodpasture Syndrome
Pallor OMIM:233450
Pura-Related Severe Neonatal Hypotonia-Seizures-Encephalopathy Syndrome
Exaggerated startle response, Dystonia ORPHA:438213
Congenital Total Pulmonary Venous Return Anomaly
Pallor ORPHA:99125
Neurodevelopmental-Craniofacial Syndrome With Variable Renal And Cardiac Abnormalities
Exaggerated startle response OMIM:619522

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 Zfp91

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 Zfp91.

No publications found that use IMPC mice or data for Zfp91.

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MGI Allele Allele Type Produced
Zfp91em1(IMPC)Tcp Exon Deletion Mice
Zfp91tm194308(L1L2_Bact_P) KO first allele (reporter-tagged insertion with conditional potential) Targeting vectors

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