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Gene: Zfp91 MGI:104854

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Gene Summary

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

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IMPC Data Collections

IMPC Phenotype Summary

Significant
Not Significant
Not tested

View all our phenotype data below

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
preweaning lethality, complete penetrance Zfp91em1(IMPC)Tcp HOM   Early adult 0.00
edema Zfp91em1(IMPC)Tcp HOM E15.5 0.00
abnormal embryo size Zfp91em1(IMPC)Tcp HOM E9.5 0.00
enlarged lymph nodes Zfp91em1(IMPC)Tcp HET Early adult 0.00
abnormal skin coloration Zfp91em1(IMPC)Tcp HOM E15.5 0.00
increased startle reflex Zfp91em1(IMPC)Tcp HET Early adult 1.03×10-06
abnormal embryo size Zfp91em1(IMPC)Tcp HOM E15.5 0.00
pallor Zfp91em1(IMPC)Tcp HOM E15.5 0.00
decreased body length Zfp91em1(IMPC)Tcp HET Early adult 1.18×10-05
cataract Zfp91em1(IMPC)Tcp HET Early adult 1.81×10-05

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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.

X-ray

XRay Images Skull Dorso Ventral Orientation

10 Images

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Gross Morphology Embryo E14.5-E15.5

Images

44 Images

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Eye Morphology

Images Ophthalmoscopy

100 Images

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Eye Morphology

Images Slit Lamp

12 Images

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Gross Pathology and Tissue Collection

Images

8 Images

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Electrocardiogram (ECG)

Waveform Image

1 Images

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X-ray

XRay Images Skull Lateral Orientation

10 Images

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Download thumbnail Download
MicroCT E14.5-E15.5

Embryo reconstruction

7 Images

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X-ray

XRay Images Whole Body Dorso Ventral

10 Images

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X-ray

XRay Images Whole Body Lateral Orientation

10 Images

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Gross Morphology Embryo E9.5

Images

2 Images

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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
Kaposi Sarcoma, Susceptibility To
Hypermelanotic macule, Edema OMIM:148000
Hereditary Hyperferritinemia-Cataract Syndrome
Cataract ORPHA:163
Cataract 36
Cataract OMIM:613887
Cataract 29
Cataract OMIM:115800
Cataract 35
Cataract OMIM:609376
Hypertrophic Neuropathy And Cataract
Cataract OMIM:239900
Cataract And Congenital Ichthyosis
Cataract OMIM:212400
Corneal Dystrophy, Groenouw Type I
Cataract, Granular corneal dystrophy, Punctate corneal dystrophy, Nodular corneal dystrophy OMIM:121900
Spastic Paraparesis And Deafness
Tremor, Cataract OMIM:312910
Cataract 42
Cataract, Developmental cataract OMIM:115900
Hydrocephaly-Cerebellar Agenesis Syndrome
Cataract ORPHA:1397
Neutropenia, Severe Congenital, 9, Autosomal Dominant
Cataract, Splenomegaly OMIM:619813
Cataract 12, Multiple Types
Developmental cataract, Progressive cataract OMIM:611597
Osteoporosis-Oculocutaneous Hypopigmentation Syndrome
Hypopigmentation of the skin, Albinism, Pallor ORPHA:2786
Aldh18A1-Related De Barsy Syndrome
Cataract ORPHA:35664
Mastocytosis, Cutaneous
Hypermelanotic macule, Erythema, Edema OMIM:154800
Trichomegaly
Cataract OMIM:190330
Optic Atrophy 3, Autosomal Dominant
Tremor, Cataract OMIM:165300
Hereditary Persistence Of Fetal Hemoglobin-Beta-Thalassemia Syndrome
Pallor ORPHA:46532
Nathalie Syndrome
Cataract ORPHA:2663
Cataract-Microcornea Syndrome
Cataract, Iris coloboma, Corneal dystrophy, Corneal opacity, Microcornea ORPHA:1377
Acral Self-Healing Collodion Baby
Erythema, Palmoplantar scaling skin, Lack of skin elasticity, Edema of the dorsum of feet, Edema ... ORPHA:281127
Methylmalonic Acidemia With Homocystinuria, Type Cbld
Pallor ORPHA:79283
Cone-Rod Dystrophy 11
Pallor OMIM:610381
X-Linked Sideroblastic Anemia
Hyperpigmentation of the skin, Pallor ORPHA:75563
Peripheral Cone Dystrophy
Pallor OMIM:609021
Myopathy, Mitochondrial Progressive, With Congenital Cataract And Developmental Delay
Cataract, Developmental cataract OMIM:613076
Breath-Holding Spells
Pallor OMIM:607578
Hb Bart'S Hydrops Fetalis
Polyhydramnios, Pallor, Oligohydramnios, Hydrops fetalis ORPHA:163596
Galactosemia Iv
Cataract OMIM:618881
Cataract 9, Multiple Types
Cataract, Iris coloboma, Developmental cataract, Progressive cataract, Microcornea OMIM:604219
Megalocornea
Cataract, Megalocornea, Astigmatism, Iridodonesis, Mosaic corneal dystrophy, Decreased corneal th... OMIM:309300
Autoimmune Hemolytic Anemia, Cold Type
Pallor ORPHA:228312
Hypoalphalipoproteinemia, Primary, 2
Cataract, Corneal arcus OMIM:618463
Benign Paroxysmal Torticollis Of Infancy
Pallor ORPHA:71518
Dermatitis, Atopic
Dry skin, Facial erythema, Pallor OMIM:603165
Microphthalmia, Isolated, With Coloboma 3
Cataract, Iris coloboma OMIM:610092
Chorea, Remitting, With Nystagmus And Cataract
Cataract OMIM:601372
Anterior Segment Dysgenesis 8
Cataract, Ectopia pupillae, Ectopia lentis, Iridodonesis, Microphakia, Persistent pupillary membr... OMIM:617319
Galactosemia Ii
Cataract OMIM:230200
Optic Atrophy 1
Pallor OMIM:165500
Acute Peripheral Arterial Occlusion
Pallor ORPHA:90064
Cataract 11, Multiple Types
Cataract, Developmental cataract OMIM:610623
Lymphatic Malformation 11
Lymphedema, Pedal edema OMIM:619401
Thanatophoric Dysplasia, Glasgow Variant
Cataract, Hepatosplenomegaly OMIM:273680
Exfoliation Syndrome
Cataract, Mydriasis, Phakodonesis, Abnormal lens morphology, Iris hypoperfusion, Anisocoria, Pigm... OMIM:177650
Muscular Dystrophy, Congenital, With Infantile Cataract And Hypogonadism
Cataract OMIM:254000
Aniridia, Microcornea, And Spontaneously Reabsorbed Cataract
Cataract, Aniridia, Microcornea OMIM:106230
Leber Congenital Amaurosis 14
Pallor OMIM:613341
Cataract 10, Multiple Types
Zonular cataract, Nuclear cataract, Posterior Y-sutural cataract, Developmental cataract OMIM:600881
Acute Myelomonocytic Leukemia
Pallor ORPHA:517
Iris Pigment Layer, Cleavage Of
Cataract OMIM:147610
Cataract 50 With Or Without Glaucoma
Cataract, Persistent pupillary membrane OMIM:620253
Cataract 47
Cataract, Microcornea OMIM:612018
Cataract 1, Multiple Types
Nuclear cataract, Pulverulent cataract, Microcornea, Posterior subcapsular cataract OMIM:116200
Optic Atrophy 7 With Or Without Auditory Neuropathy
Pallor OMIM:612989
Hemoglobin D Disease
Pallor ORPHA:90039
Primary Lateral Sclerosis, Juvenile
Pallor OMIM:606353
Hemolytic Anemia Due To Glutathione Reductase Deficiency
Cataract OMIM:618660
Aniridia-Intellectual Disability Syndrome
Cataract, Ectopia lentis, Aniridia ORPHA:1068
Familial Focal Epilepsy With Variable Foci
Pallor ORPHA:98820
Anterior Segment Dysgenesis 7
Cataract, Iris coloboma, Buphthalmos, Anterior synechiae of the anterior chamber, Sclerocornea, C... OMIM:269400
Aniridia 2
Cataract, Lens subluxation, Aniridia, Iris coloboma OMIM:617141
Cataract 3, Multiple Types
Cerulean cataract, Sutural cataract, Developmental cataract, Nuclear pulverulent cataract OMIM:601547
Cataract 14, Multiple Types
Zonular cataract OMIM:601885
Kcnq2-Related Epileptic Encephalopathy
Facial erythema, Pallor, Cerebral edema ORPHA:439218
Coats Disease
Cataract, Abnormal anterior chamber morphology, Aplasia/Hypoplasia of the iris ORPHA:190
Myopathy, Lactic Acidosis, And Sideroblastic Anemia 2
Pallor OMIM:613561
Myelofibrosis
Purpura, Pallor OMIM:254450
Ectopia Lentis Et Pupillae
Cataract, Ectopia pupillae, Ectopia lentis, Persistent pupillary membrane, Iris transillumination... OMIM:225200
Aniridia-Ptosis-Intellectual Disability-Familial Obesity Syndrome
Cataract, Corneal opacity, Persistent pupillary membrane, Aplasia/Hypoplasia of the iris ORPHA:1067
Peters Anomaly
Subcapsular cataract, Thinning of Descemet membrane, Anterior synechiae of the anterior chamber, ... ORPHA:708
Non-Insulinoma Pancreatogenous Hypoglycemia Syndrome
Pallor ORPHA:276608
Pulmonary Edema Of Mountaineers, Susceptibility To
Pulmonary edema, Edema OMIM:178400
Lymphatic Malformation 8
Nonimmune hydrops fetalis, Polyhydramnios, Pericardial effusion, Pleural effusion, Generalized edema OMIM:618773
Spontaneous Periodic Hypothermia
Pallor ORPHA:29822
Pyruvate Kinase Deficiency Of Red Cells
Nonimmune hydrops fetalis, Intrauterine growth retardation, Pallor OMIM:266200
Cataract 5, Multiple Types
Zonular cataract, Pulverulent cataract, Lamellar cataract, Anterior polar cataract, Nuclear cataract OMIM:116800
Anemia, Hypochromic Microcytic, With Iron Overload 2
Pallor, Cafe-au-lait spot OMIM:615234
Intellectual Developmental Disorder, Autosomal Recessive 54
Exaggerated startle response OMIM:617028
Microcornea, Rod-Cone Dystrophy, Cataract, And Posterior Staphyloma 1
Cataract, Microcornea OMIM:619082
Irida Syndrome
Pallor ORPHA:209981
American Trypanosomiasis
Periorbital edema, Pallor, Edema ORPHA:3386
Proximal Myotonic Myopathy
Cataract ORPHA:606
Lymphatic Malformation 7
Nonimmune hydrops fetalis, Increased nuchal translucency, Edema, Facial edema, Pulmonary edema, L... OMIM:617300
Retinitis Pigmentosa 51
Pallor OMIM:613464
Autosomal Dominant Keratitis
Cataract, Hypoplastic iris stroma, Limbal stem cell deficiency, Abnormal corneal limbus morpholog... ORPHA:2334
Cataract 20, Multiple Types
Membranous cataract, Cortical cataract, Sutural cataract, Lamellar cataract OMIM:116100
Cyclic Vomiting Syndrome
Pallor OMIM:500007
Thiamine-Responsive Megaloblastic Anemia Syndrome
Pallor ORPHA:49827
Evans Syndrome
Pallor, Petechiae ORPHA:1959
Anterior Segment Dysgenesis 2
Cataract, Congenital aphakia, Anterior segment of eye aplasia, Posterior synechiae of the anterio... OMIM:610256
Peroxisome Biogenesis Disorder 11B
Cataract, Hepatosplenomegaly OMIM:614885
Deafness-Lymphedema-Leukemia Syndrome
Lymphedema, Pallor ORPHA:3226
Amoebic Keratitis
Cataract, Corneal perforation, Corneal ulceration, Abnormal corneal epithelium morphology, Puncta... ORPHA:67043
Hyperinsulinism Due To Ucp2 Deficiency
Pallor ORPHA:276556
Anemia, Congenital Dyserythropoietic, Type Ib
Pallor OMIM:615631
Myopia 28, Autosomal Recessive
Cataract OMIM:619781
Autosomal Dominant Hyperinsulinism Due To Sur1 Deficiency
Pallor ORPHA:276575
Anemia, Sideroblastic, 1
Anemic pallor OMIM:300751
Autosomal Dominant Hyperinsulinism Due To Kir6.2 Deficiency
Pallor ORPHA:276580
Beta-Thalassemia
Pallor, Skin ulcer ORPHA:848
Hyperinsulinism Due To Hnf1A Deficiency
Pallor ORPHA:324575
Isolated Aniridia
Cataract, Aniridia, Peters anomaly ORPHA:250923
Leishmaniasis
Pallor, Skin ulcer ORPHA:507
Elliptocytosis 1
Pallor OMIM:611804
Fanconi Anemia, Complementation Group I
Pallor, Intrauterine growth retardation, Cafe-au-lait spot OMIM:609053
Drug-Induced Autoimmune Hemolytic Anemia
Pallor ORPHA:90037
Retinitis Pigmentosa 75
Pallor OMIM:617023
Hyperekplexia 2
Exaggerated startle response, Astigmatism OMIM:614619
Anterior Segment Dysgenesis 1
Opacification of the corneal stroma, Posterior polar cataract, Microcornea, Peters anomaly, Ocula... OMIM:107250
Myopathic Ehlers-Danlos Syndrome
Pallor ORPHA:536516
Generalized Juvenile Polyposis/Juvenile Polyposis Coli
Anemic pallor, Edema ORPHA:329971
Primary Myelofibrosis
Purpura, Pallor, Petechiae, Ecchymosis ORPHA:824
Renal Tubular Acidosis, Distal, 4, With Hemolytic Anemia
Pallor OMIM:611590
Aniridia And Absent Patella
Cataract, Aniridia OMIM:106220
Dravet Syndrome
Pallor ORPHA:33069
Cataract 39, Multiple Types
Developmental cataract, Anterior polar cataract, Lamellar cataract OMIM:615188
Cold Agglutinin Disease
Pallor ORPHA:56425
Aniridia 3
Cataract, Aniridia OMIM:617142
Megaloblastic Anemia Due To Dihydrofolate Reductase Deficiency
Pallor OMIM:613839
Non-Functioning Paraganglioma
Pallor ORPHA:94080
Autoimmune Hemolytic Anemia
Pallor ORPHA:98375
Mixed-Type Autoimmune Hemolytic Anemia
Pallor ORPHA:90036
Lymphangiectasia, Pulmonary, Congenital
Nonimmune hydrops fetalis, Chylous ascites, Edema, Polyhydramnios, Facial edema, Palpebral edema,... OMIM:265300
Beta-Ketothiolase Deficiency
Dehydration, Pallor, Edema ORPHA:134
Cataract 30, Multiple Types
Posterior polar cataract, Pulverulent cataract, Diffuse nuclear cataract OMIM:116300
Cone-Rod Dystrophy 8
Pallor OMIM:605549
Waldenström Macroglobulinemia
Periorbital edema, Purpura, Pleural effusion, Pallor, Pedal edema ORPHA:33226
Severe Combined Immunodeficiency With Sensitivity To Ionizing Radiation
Generalized lymphadenopathy, Absent tonsils, Splenomegaly, Lymph node hypoplasia, Aplasia of the ... OMIM:602450
Acquired Idiopathic Sideroblastic Anemia
Pallor ORPHA:75564
Severe Congenital Hypochromic Anemia With Ringed Sideroblasts
Pallor, Cafe-au-lait spot ORPHA:300298
Myopathy, Lactic Acidosis, And Sideroblastic Anemia 1
Pallor OMIM:600462
3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency
Pallor OMIM:246450
Tay-Sachs Disease
Pallor OMIM:272800
Vitreoretinal Degeneration, Snowflake Type
Cataract, Corneal guttata OMIM:193230
Cataract 31, Multiple Types
Nuclear cataract, Anterior subcapsular cataract, Posterior subcapsular cataract OMIM:605387
6-Pyruvoyl-Tetrahydropterin Synthase Deficiency
Pallor ORPHA:13
Sepsis In Premature Infants
Purpura, Edema, Pallor, Petechiae ORPHA:90051
Rheumatic Fever
Erythema, Pallor ORPHA:3099
Blindness-Scoliosis-Arachnodactyly Syndrome
Cataract, Lens subluxation, Microphakia ORPHA:171844
Hyperekplexia-Epilepsy Syndrome
Exaggerated startle response ORPHA:163985
Idiopathic Pulmonary Hemosiderosis
Pallor ORPHA:99931
Autoimmune Hemolytic Anemia, Warm Type
Pallor ORPHA:90033
Refractory Anemia With Excess Blasts
Anemic pallor, Pedal edema ORPHA:86839
Cataract 15, Multiple Types
Nuclear cataract, Cortical cataract, Lamellar cataract OMIM:615274
Cataract 33, Multiple Types
Nuclear cataract, Cortical cataract, Lamellar cataract OMIM:611391
Congenital Hyperinsulinism Due To Hnf4A Deficiency
Pallor ORPHA:263455
Senior-Loken Syndrome 8
Pallor OMIM:616307
Coloboma, Ocular, Autosomal Recessive
Cataract, Lens subluxation, Iris coloboma OMIM:216820
3-Hydroxy-3-Methylglutaric Aciduria
Dehydration, Pallor, Edema ORPHA:20
Plummer-Vinson Syndrome
Pallor ORPHA:54028
Letterer-Siwe Disease
Pallor OMIM:246400
Dominant Beta-Thalassemia
Hyperpigmentation of the skin, Pallor, Skin ulcer ORPHA:231226
Congenital Dyserythropoietic Anemia Type Iii
Pallor ORPHA:98870
Aromatic L-Amino Acid Decarboxylase Deficiency
Limb dystonia, Torticollis, Blepharospasm, Limb tremor, Oculogyric crisis, Athetosis, Exaggerated... OMIM:608643
Childhood Absence Epilepsy
Pallor ORPHA:64280
Purine Nucleoside Phosphorylase Deficiency
Tremor, Lymph node hypoplasia, Splenomegaly OMIM:613179
Hereditary Folate Malabsorption
Pallor ORPHA:90045
Fumarase Deficiency
Polyhydramnios, Pallor, Ascites OMIM:606812
Beta-Thalassemia Intermedia
Pallor, Skin ulcer ORPHA:231222
Beta-Thalassemia Major
Hyperpigmentation of the skin, Pallor, Skin ulcer ORPHA:231214
Myopathy, Mitochondrial, And Ataxia
Pallor OMIM:617675
Hereditary Spherocytosis
Pallor, Skin ulcer ORPHA:822
Meige Disease
Lymph node hypoplasia, Absence of lymph node germinal center ORPHA:90186
Fructose-1,6-Bisphosphatase Deficiency
Pallor ORPHA:348
Developmental And Epileptic Encephalopathy 68
Exaggerated startle response OMIM:618201
Norrie Disease
Cataract, Buphthalmos, Shallow anterior chamber, Hypoplasia of the iris, Corneal opacity, Opacifi... OMIM:310600
Developmental And Epileptic Encephalopathy 8
Exaggerated startle response OMIM:300607
Rare Circulatory System Disease
Pallor ORPHA:98028
Pearson Marrow-Pancreas Syndrome
Erythema, Dehydration, Pallor, Hydrops fetalis OMIM:557000
Dehydrated Hereditary Stomatocytosis 1 With Or Without Pseudohyperkalemia And/Or Perinatal Edema
Pallor OMIM:194380
Sandhoff Disease, Infantile Form
Hepatosplenomegaly, Exaggerated startle response ORPHA:309155
Incontinentia Pigmenti
Erythema, Pallor, Abnormality of skin pigmentation OMIM:308300
Fanconi Anemia, Complementation Group C
Hyperpigmentation of the skin, Intrauterine growth retardation, Cafe-au-lait spot, Anemic pallor OMIM:227645
Fanconi Anemia, Complementation Group E
Hyperpigmentation of the skin, Anemic pallor, Cafe-au-lait spot OMIM:600901
Sporadic Pheochromocytoma/Secreting Paraganglioma
Pallor ORPHA:276621
Persistent Hyperplastic Primary Vitreous, Autosomal Recessive
Cataract, Iris coloboma, Buphthalmos, Persistent pupillary membrane, Shallow anterior chamber, Po... OMIM:221900
Anemia, Nonspherocytic Hemolytic, Due To G6Pd Deficiency
Pallor OMIM:300908
Hyperekplexia 3
Exaggerated startle response OMIM:614618
Fanconi Anemia, Complementation Group A
Anemic pallor, Cafe-au-lait spot, Abnormality of skin pigmentation OMIM:227650
Severe Combined Immunodeficiency Due To Complete Rag1/2 Deficiency
Pallor ORPHA:331206
T-B+ Severe Combined Immunodeficiency Due To Gamma Chain Deficiency
Lymph node hypoplasia, Absent tonsils ORPHA:276
Imerslund-Gräsbeck Syndrome
Pallor ORPHA:35858
Aregenerative Anemia
Pallor ORPHA:101096
Retinitis Pigmentosa And Erythrocytic Microcytosis
Pallor OMIM:616959
Gm2 Gangliosidosis, Ab Variant
Exaggerated startle response, Dystonia ORPHA:309246
Aniridia 1
Cataract, Ectopia pupillae, Ectopia lentis, Corneal erosion, Anterior subcapsular cataract, Hypop... OMIM:106210
Non-Functioning Pituitary Adenoma
Pallor ORPHA:91349
Alternating Hemiplegia Of Childhood
Dehydration, Pallor ORPHA:2131
Adenohypophysitis
Pallor ORPHA:95512
Panhypophysitis
Pallor ORPHA:95513
Infection-Related Hemolytic Uremic Syndrome
Pleural empyema, Generalized edema, Pallor, Edema ORPHA:544482
Pituitary Apoplexy
Pallor ORPHA:95613
Sheehan Syndrome
Dry skin, Pallor ORPHA:91355
Stiff Person Spectrum Disorder
Exaggerated startle response ORPHA:3198
Systemic Mastocytosis With Associated Hematologic Neoplasm
Pallor ORPHA:98849
Neurodevelopmental Disorder With Cerebellar Atrophy And With Or Without Seizures
Tremor, Exaggerated startle response, Truncal titubation OMIM:618056
Prolactinoma
Pallor ORPHA:2965
Hereditary Pheochromocytoma-Paraganglioma
Pallor ORPHA:29072
Spastic Paraplegia, Optic Atrophy, And Neuropathy
Exaggerated startle response OMIM:609541
Hyperekplexia 1
Exaggerated startle response OMIM:149400
Spastic Paraplegia-Optic Atrophy-Neuropathy Syndrome
Exaggerated startle response ORPHA:320406
Spastic Tetraplegia And Axial Hypotonia, Progressive
Exaggerated startle response OMIM:618598
Idiopathic Hypereosinophilic Syndrome
Pleural effusion, Angioedema, Pallor, Joint swelling ORPHA:3260
Histiocytoid Cardiomyopathy
Pulmonary edema, Pallor ORPHA:137675
Stiff-Person Syndrome
Exaggerated startle response, Opisthotonus OMIM:184850
Neurodevelopmental Disorder With Speech Impairment And With Or Without Seizures
Exaggerated startle response OMIM:620114
Persistent Hyperplastic Primary Vitreous
Cataract, Buphthalmos, Persistent pupillary membrane, Shallow anterior chamber, Corneal opacity, ... ORPHA:91495
Autosomal Dominant Optic Atrophy And Cataract
Cataract, Cerulean cataract, Posterior cortical cataract, Anterior subcapsular cataract, Postural... ORPHA:67036
Degcags Syndrome
Polyhydramnios, Intrauterine growth retardation, Hypopigmentation of the skin, Pallor, Abnormalit... OMIM:619488
Gm2-Gangliosidosis, Ab Variant
Exaggerated startle response, Dystonia OMIM:272750
Esophageal Atresia
Polyhydramnios, Pallor ORPHA:1199
Leukodystrophy, Hypomyelinating, 13
Exaggerated startle response OMIM:616881
Sandhoff Disease
Hepatosplenomegaly, Exaggerated startle response OMIM:268800
Sudden Infant Death With Dysgenesis Of The Testes Syndrome
Exaggerated startle response OMIM:608800
Fanconi Anemia, Complementation Group D2
Anemic pallor, Cafe-au-lait spot, Abnormality of skin pigmentation OMIM:227646
Tay-Sachs Disease
Hepatosplenomegaly, Tremor, Exaggerated startle response, Laryngeal dystonia, Dystonia ORPHA:845
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 4
Cataract, Exaggerated startle response OMIM:253800
Pura-Related Severe Neonatal Hypotonia-Seizures-Encephalopathy Syndrome Due To A Point Mutation
Exaggerated startle response, Dystonia ORPHA:438216
Diamond-Blackfan Anemia 1
Spina bifida occulta, Intrauterine growth retardation, Pallor OMIM:105650
Tsh-Secreting Pituitary Adenoma
Pericardial effusion, Pallor ORPHA:91347
Von Hippel-Lindau Disease
Pallor, Macular edema ORPHA:892
Gm1 Gangliosidosis Type 1
Hepatosplenomegaly, Exaggerated startle response, Dystonia ORPHA:79255
Asparagine Synthetase Deficiency
Exaggerated startle response OMIM:615574
Neurodevelopmental Disorder With Or Without Seizures And Gait Abnormalities
Exaggerated startle response OMIM:617864
Diamond-Blackfan Anemia
Nonimmune hydrops fetalis, Pallor ORPHA:124
Agammaglobulinemia, X-Linked
Conjunctivitis, Lymph node hypoplasia OMIM:300755
Glycine Encephalopathy With Normal Serum Glycine
Exaggerated startle response OMIM:617301
Multiple Endocrine Neoplasia Type 2
Pallor ORPHA:653
Plaa-Associated Neurodevelopmental Disorder
Exaggerated startle response, Dystonia ORPHA:521426
Developmental And Epileptic Encephalopathy 49
Exaggerated startle response OMIM:617281
Autosomal Recessive Malignant Osteopetrosis
Pallor ORPHA:667
Neurodevelopmental Disorder With Progressive Microcephaly, Spasticity, And Brain Anomalies
Exaggerated startle response OMIM:617527
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 3
Pallor OMIM:253280
Goodpasture Syndrome
Pallor OMIM:233450
Neurodevelopmental Disorder With Microcephaly, Epilepsy, And Hypomyelination
Exaggerated startle response OMIM:618367
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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