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Gene: Grcc10 MGI:1315201

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Gene Summary

Name:
gene rich cluster, C10 gene
Synonyms:
2310033H05Rik

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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, incomplete penetrance Grcc10tm1.1(KOMP)Vlcg HOM   Early adult 0.00
cyanosis Grcc10tm1.1(KOMP)Vlcg HOM E18.5 0.00

Download data as:  TSV  XLS

Select physiological systems to view:
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Viewing: all phenotypes

lacZ Expression

An assay measuring the expression of lacZ shows the tissue where the gene is expressed.

Anatomy Images Zygosity Mutant Expr
Adrenal gland  Section images heterozygote 100% (2 of 2)
Aorta  Section images heterozygote 100% (2 of 2)
Brain  Section images heterozygote 100% (2 of 2)
Brainstem  Section images heterozygote 100% (2 of 2)
Cartilage tissue  Section images heterozygote 100% (2 of 2)
Cerebellum  Section images heterozygote 100% (2 of 2)
Cerebral cortex  Section images heterozygote 100% (2 of 2)
Epididymis  Section images heterozygote 50% (1 of 2)
Eye  Section images heterozygote 100% (2 of 2)
Heart  Section images heterozygote 100% (2 of 2)
Hippocampus  Section images heterozygote 100% (2 of 2)
Hypothalamus  Section images heterozygote 100% (2 of 2)
Kidney  Section images heterozygote 100% (2 of 2)
Large intestine  Section images heterozygote 100% (2 of 2)
Lung  Section images heterozygote 100% (2 of 2)
Midbrain  Section images heterozygote 100% (2 of 2)
Olfactory lobe  Section images heterozygote 100% (2 of 2)
Ovary  Section images heterozygote 50% (1 of 2)
Oviduct  Section images heterozygote 50% (1 of 2)
Pancreas  Section images heterozygote 100% (2 of 2)
Pituitary gland  Section images heterozygote 100% (2 of 2)
Skin  Section images heterozygote 100% (2 of 2)
Small intestine  Section images heterozygote 100% (2 of 2)
Spinal cord  Section images heterozygote 100% (2 of 2)
Stomach  Section images heterozygote 100% (2 of 2)
Submandibular gland  Section images heterozygote 50% (1 of 2)
Testis  Section images heterozygote 50% (1 of 2)
Thalamus  Section images heterozygote 100% (2 of 2)
Thymus  Section images heterozygote 50% (1 of 2)
Thyroid gland  Section images heterozygote Ambiguous
Trachea  Section images heterozygote 100% (2 of 2)
Uterus  Section images heterozygote 50% (1 of 2)
Brown adipose tissue N/A heterozygote 0.0% (0 of 2)
Esophagus N/A heterozygote 0.0% (0 of 2)
Liver N/A heterozygote 0.0% (0 of 2)
Lower urinary tract N/A heterozygote Not available
Lymph node N/A heterozygote 0.0% (0 of 2)
Mammary gland N/A heterozygote 0.0% (0 of 2)
Peripheral nervous system N/A heterozygote 0.0% (0 of 2)
Peyer's patch N/A heterozygote 0.0% (0 of 2)
Prostate gland N/A heterozygote Not available
Skeletal muscle N/A heterozygote 0.0% (0 of 2)
Spleen N/A heterozygote 0.0% (0 of 2)
Striatum N/A heterozygote 0.0% (0 of 2)
Urinary bladder N/A heterozygote 0.0% (0 of 2)
Vascular system N/A heterozygote 0.0% (0 of 2)
Vesicular gland N/A heterozygote Not available
White adipose tissue N/A heterozygote 0.0% (0 of 2)

An assay measuring the expression of lacZ shows the tissue where the gene is expressed.

Anatomy Images Zygosity Mutant Expr
Embryo N/A heterozygote 100% (2 of 2)
Embryo N/A homozygote Ambiguous
Brain N/A heterozygote 50% (1 of 2)
Brain N/A homozygote Ambiguous
Dorsal root ganglion N/A heterozygote 0.0% (0 of 2)
Dorsal root ganglion N/A homozygote Ambiguous
Ear N/A heterozygote 0.0% (0 of 2)
Ear N/A homozygote Ambiguous
Eye N/A heterozygote 0.0% (0 of 2)
Eye N/A homozygote Ambiguous
Footplate N/A heterozygote 0.0% (0 of 2)
Footplate N/A homozygote Ambiguous
Forebrain N/A heterozygote 0.0% (0 of 2)
Forebrain N/A homozygote Ambiguous
Forelimb N/A heterozygote 0.0% (0 of 2)
Forelimb N/A homozygote Ambiguous
Fronto-nasal process N/A heterozygote Ambiguous
Fronto-nasal process N/A homozygote Ambiguous
Handplate N/A heterozygote 0.0% (0 of 2)
Handplate N/A homozygote Ambiguous
Head N/A heterozygote 100% (2 of 2)
Head N/A homozygote Ambiguous
Heart N/A heterozygote 0.0% (0 of 2)
Heart N/A homozygote Ambiguous
Hindbrain N/A heterozygote 50% (1 of 2)
Hindbrain N/A homozygote Ambiguous
Hindlimb N/A heterozygote 0.0% (0 of 2)
Hindlimb N/A homozygote Ambiguous
Liver N/A heterozygote 0.0% (0 of 2)
Liver N/A homozygote Ambiguous
Lung N/A heterozygote Ambiguous
Lung N/A homozygote Ambiguous
Mandibular process N/A heterozygote 0.0% (0 of 2)
Mandibular process N/A homozygote Ambiguous
Maxillary process N/A heterozygote 0.0% (0 of 2)
Maxillary process N/A homozygote Ambiguous
Midbrain N/A heterozygote 0.0% (0 of 2)
Midbrain N/A homozygote Ambiguous
Nose N/A heterozygote 100% (2 of 2)
Nose N/A homozygote Ambiguous
Oral cavity N/A heterozygote 0.0% (0 of 2)
Oral cavity N/A homozygote Ambiguous
Skin N/A heterozygote 0.0% (0 of 2)
Skin N/A homozygote Ambiguous
Spinal cord N/A heterozygote 50% (1 of 2)
Spinal cord N/A homozygote Ambiguous
Tail somite N/A heterozygote 0.0% (0 of 2)
Tail somite N/A homozygote Ambiguous
Tail N/A heterozygote 0.0% (0 of 2)
Tail N/A homozygote Ambiguous

Background staining occurs in wild type mice and embryos at an incidental rate.

Anatomy Background staining in controls (WT)
adrenal gland 0.0%
aorta 0.0%
brain 0.0%
brainstem 0.0%
brown adipose tissue 0.0%
cartilage tissue 0.0%
cerebellum 0.0%
cerebral cortex 0.0%
epididymis Unavailable
esophagus 0.0%
eye 0.0%
heart 0.0%
hippocampus 0.0%
hypothalamus 0.0%
kidney 0.0%
large intestine 0.0%
liver 0.0%
lower urinary tract 0.0%
lung 0.0%
lymph node 0.0%
mammary gland 0.0%
midbrain 0.0%
olfactory lobe 0.0%
ovary 0.0%
oviduct 0.0%
pancreas 0.0%
peripheral nervous system 0.0%
peyers patch 0.0%
pituitary gland 0.0%
prostate gland 0.0%
skeletal muscle 0.0%
skin 0.0%
small intestine 0.0%
spinal cord 0.0%
spleen 0.0%
stomach 0.0%
striatum 0.0%
submandibular gland 0.0%
testis 0.0%
thalamus 0.0%
thymus 0.0%
thyroid gland 0.0%
trachea 0.0%
urinary bladder
uterus 0.0%
vascular system 0.0%
vesicular gland Unavailable
white adipose tissue 0.0%

Background staining occurs in wild type mice and embryos at an incidental rate.

Background staining occurs in wild type embryos at a measurable rate.

Anatomy Background staining in controls(WT)
brain 0.0%
dorsal root ganglion Ambiguous
ear 0.0%
embryo 0.0%
eye 0.0%
footplate 0.0%
forebrain 0.0%
forelimb 0.0%
fronto-nasal process Ambiguous
handplate 0.0%
head 0.0%
heart 0.0%
hindbrain 0.0%
hindlimb 0.0%
liver 0.0%
lung 0.0%
mandibular process 0.0%
maxillary process 0.0%
midbrain 0.0%
nose Ambiguous
oral cavity 0.0%
skin 0.0%
spinal cord Ambiguous
tail 0.0%
tail somite group 0.0%

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 Forepaw

10 Images

View images
Adult LacZ

LacZ Images Section

32 Images

View images
X-ray

XRay Images Whole Body Lateral Orientation

10 Images

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Embryo LacZ

LacZ images wholemount

12 Images

View images
X-ray

XRay Images Whole Body Dorso Ventral

10 Images

View images
Download thumbnail Download
MicroCT E18.5

Embryo reconstruction

5 Images

View images
X-ray

XRay Images Skull Lateral Orientation

10 Images

View images
X-ray

XRay Images Skull Dorso Ventral Orientation

10 Images

View images
Eye Morphology

Images Slit Lamp

2 Images

View images
Sleep Wake

Wake state (bmp file)

9 Images

View images
PDF thumbnail PDF
Electroretinography 2

Rod and cone PDF

4 Images

View images
PDF thumbnail PDF
Auditory Brain Stem Response

Click-evoked + 6 to 30kHz tone waveforms (pdf format)

7 Images

View images

Human diseases caused by Grcc10 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 Grcc10 by orthology or direct annotation.

Disease Similarity of
phenotypes		 Matching phenotypes Source
Temtamy Syndrome
ORPHA:1777
Temtamy Syndrome
OMIM:218340

The table below shows human diseases predicted to be associated to Grcc10 by phenotypic similarity.

Disease Similarity of
phenotypes		 Matching phenotypes Source
Venular Insufficiency, Systemic
Cyanosis OMIM:192700
Sulfhemoglobinemia, Congenital
Cyanosis OMIM:185460
Diffuse Palmoplantar Keratoderma-Acrocyanosis Syndrome
Acrocyanosis ORPHA:86918
Methemoglobinemia, Beta Type
Cyanosis OMIM:617971
Methemoglobinemia, Alpha Type
Cyanosis OMIM:617973
Cryofibrinogenemia, Familial Primary
Acrocyanosis OMIM:123540
Breath-Holding Spells
Cyanosis OMIM:607578
Cyanosis, Transient Neonatal
Jaundice, Cyanosis OMIM:613977
Cleft Larynx, Posterior
Cyanosis OMIM:215800
Seizures, Benign Familial Infantile, 3
Cyanosis OMIM:607745
Bullous Dystrophy, Hereditary Macular Type
Acrocyanosis OMIM:302000
Obesity-Hypoventilation Syndrome
Cyanosis OMIM:257500
Seizures, Benign Familial Infantile, 1
Cyanosis OMIM:601764
Perching Syndrome
Cyanosis OMIM:617055
Peripheral Motor Neuropathy-Dysautonomia Syndrome
Acrocyanosis ORPHA:2400
Neuralgic Amyotrophy
Acrocyanosis ORPHA:2901
Laryngeal Abductor Paralysis
Cyanosis OMIM:150260
Cardiomyopathy-Hypotonia-Lactic Acidosis Syndrome
Cyanosis ORPHA:91130
Buerger Disease
Acrocyanosis ORPHA:36258
Phosphoserine Aminotransferase Deficiency
Cyanotic episode OMIM:610992
Tricuspid Atresia
Cyanosis ORPHA:1209
Classic Glucose Transporter Type 1 Deficiency Syndrome
Cyanosis ORPHA:71277
Mitochondrial Phosphate Carrier Deficiency
Cyanosis OMIM:610773
Benign Familial Infantile Epilepsy
Cyanosis ORPHA:306
Interstitial Pneumonitis, Desquamative, Familial
Cyanosis OMIM:263000
Methemoglobinemia Due To Deficiency Of Methemoglobin Reductase
Cyanosis OMIM:250800
Laryngotracheal Angioma
Cyanosis ORPHA:137935
Hypoadrenocorticism, Familial
Cyanosis OMIM:240200
Hereditary Methemoglobinemia
Cyanosis ORPHA:621
High Altitude Pulmonary Edema
Hypoxemia, Cyanosis ORPHA:330012
Chronic Pneumonitis Of Infancy
Hypoxemia, Cyanosis ORPHA:91359
Benign Familial Neonatal Epilepsy
Circumoral cyanosis ORPHA:1949
Congenital Pulmonary Lymphangiectasia
Cyanosis ORPHA:2414
Infant Acute Respiratory Distress Syndrome
Hypoxemia, Cyanosis ORPHA:70587
Acquired Methemoglobinemia
Hypoxemia, Cyanosis ORPHA:464453
Methemoglobinemia And Ambiguous Genitalia
Cyanosis OMIM:250790
Laryngotracheoesophageal Cleft
Cyanosis ORPHA:2004
Ethylmalonic Encephalopathy
Acrocyanosis, Petechiae ORPHA:51188
Congenital Fibrinogen Deficiency
Cyanosis, Bruising susceptibility, Subcutaneous hemorrhage ORPHA:335
Cryptogenic Organizing Pneumonia
Hypoxemia, Cyanosis ORPHA:1302
Restrictive Dermopathy 2
Cyanosis OMIM:619793
Congenital Heart Block
Cyanosis ORPHA:60041
Phosphoserine Aminotransferase Deficiency, Infantile/Juvenile Form
Cyanotic episode ORPHA:284417
Postsynaptic Congenital Myasthenic Syndromes
Cyanosis ORPHA:98913
Encephalopathy, Ethylmalonic
Acrocyanosis, Petechiae OMIM:602473
Pulmonary Alveolar Proteinosis, Acquired
Hypoxemia, Cyanosis OMIM:610910
Asbestos Intoxication
Hypoxemia, Cyanosis, Oxygen desaturation on exertion ORPHA:2302
Hsd10 Disease, Infantile Type
Cyanosis ORPHA:391428
Chiari Malformation Type Ii
Cyanosis OMIM:207950
Primary Pulmonary Hypoplasia
Hypoxemia, Cyanosis ORPHA:2257
Combined Oxidative Phosphorylation Defect Type 23
Cyanosis ORPHA:444013
Dravet Syndrome
Cyanotic episode ORPHA:33069
Isolated Right Ventricular Hypoplasia
Hypoxemia, Cyanosis ORPHA:439
Hyperimmunoglobulinemia D With Periodic Fever
Urticaria, Erythema, Acrocyanosis, Purpura ORPHA:343
Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic
Cyanosis OMIM:261680
Microcephaly, Cerebellar Hypoplasia, And Cardiac Conduction Defect Syndrome
Acrocyanosis OMIM:614407
Eosinophilic Fasciitis
Acrocyanosis ORPHA:3165
Acute Interstitial Pneumonia
Hypoxemia, Cyanosis ORPHA:79126
Choanal Atresia
Cyanosis ORPHA:137914
Acquired Purpura Fulminans
Acrocyanosis, Macular purpura ORPHA:49566
Fallot Complex-Intellectual Disability-Growth Delay Syndrome
Cyanosis ORPHA:3304
Congenitally Uncorrected Transposition Of The Great Arteries
Hypoxemia, Cyanosis ORPHA:860
Criss-Cross Heart
Cyanosis ORPHA:1461
Autoimmune Pulmonary Alveolar Proteinosis
Hypoxemia, Cyanosis ORPHA:747
Waardenburg Syndrome Type 3
Acrocyanosis ORPHA:896
Aicardi-Goutieres Syndrome 1
Erythema, Prolonged neonatal jaundice, Acrocyanosis, Petechiae, Purpura OMIM:225750
Hereditary Bullous Dystrophy, Macular Type
Acrocyanosis ORPHA:1867
Sepsis In Premature Infants
Jaundice, Cyanosis, Petechiae, Purpura ORPHA:90051
Tetrasomy 5P
Cyanosis ORPHA:3309
Neurodevelopmental Disorder With Impaired Language And Ataxia And With Or Without Seizures
Cyanosis OMIM:619580
Pulmonary Arteriovenous Malformation
Hypoxemia, Cyanosis, Telangiectasia ORPHA:2038
Severe Growth Deficiency-Strabismus-Extensive Dermal Melanocytosis-Intellectual Disability Syndrome
Cyanosis ORPHA:488627
Carnitine-Acylcarnitine Translocase Deficiency
Cyanosis ORPHA:159
Double Outlet Right Ventricle
Cyanosis ORPHA:3426
Surfactant Metabolism Dysfunction, Pulmonary, 1
Cyanosis OMIM:265120
Congenital Myasthenic Syndrome
Cyanosis ORPHA:590
Presynaptic Congenital Myasthenic Syndromes
Cyanosis ORPHA:98914
Pulmonary Capillary Hemangiomatosis
Hypoxemia, Cyanosis ORPHA:199241
Congenital Tricuspid Valve Dysplasia
Hypoxemia, Cyanosis ORPHA:555874
Kallmann Syndrome-Heart Disease Syndrome
Cyanosis ORPHA:2326
Fucosidosis
Acrocyanosis, Vascular skin abnormality ORPHA:349
Cardiac Valvular Dysplasia 2
Central cyanosis OMIM:620067
Surfactant Metabolism Dysfunction, Pulmonary, 2
Hypoxemia, Cyanosis OMIM:610913
Eosinophilic Granulomatosis With Polyangiitis
Urticaria, Acrocyanosis, Cutis marmorata, Purpura ORPHA:183
Surfactant Metabolism Dysfunction, Pulmonary, 3
Hypoxemia, Cyanosis OMIM:610921
Meckel Syndrome 14
Cyanosis OMIM:619879
Myasthenic Syndrome, Congenital, 21, Presynaptic
Cyanosis OMIM:617239
Ethylene Glycol Poisoning
Cyanosis ORPHA:31826
Heterotaxy, Visceral, 7, Autosomal
Cyanosis OMIM:616749
Structural Heart Defects And Renal Anomalies Syndrome
Cyanosis OMIM:617478
Complete Atrioventricular Septal Defect
Cyanosis ORPHA:1329
Telangiectasia, Hereditary Hemorrhagic, Type 4
Conjunctival telangiectasia, Cyanosis, Lip telangiectasia, Tongue telangiectasia, Nasal mucosa te... OMIM:610655
Myasthenia Gravis
Acrocyanosis ORPHA:589
Tarp Syndrome
Cyanosis ORPHA:2886
Telangiectasia, Hereditary Hemorrhagic, Type 2
Conjunctival telangiectasia, Cyanosis, Nail bed telangiectasia, Fingerpad telangiectases, Lip tel... OMIM:600376
Pulmonary Alveolar Microlithiasis
Hypoxemia, Cyanosis, Oxygen desaturation on exertion ORPHA:60025
Atrial Septal Defect, Ostium Primum Type
Cyanosis ORPHA:99106
Double Outlet Left Ventricle
Cyanosis ORPHA:3427
Atrial Septal Defect, Coronary Sinus Type
Cyanosis ORPHA:99104
Mitochondrial Complex I Deficiency, Nuclear Type 1
Cyanosis OMIM:252010
Glycogen Storage Disease Of Heart, Lethal Congenital
Cyanosis OMIM:261740
Histiocytoid Cardiomyopathy
Cyanosis ORPHA:137675
Poems Syndrome
Acrocyanosis ORPHA:2905
Neuropathy, Hereditary Sensory And Autonomic, Type Iii
Acrocyanosis OMIM:223900
Esophageal Atresia
Cyanosis ORPHA:1199
Encephalopathy, Acute, Infection-Induced, Susceptibility To, 9
Cyanosis OMIM:618426
Telangiectasia, Hereditary Hemorrhagic, Type 1
Conjunctival telangiectasia, Cyanosis, Telangiectasia of the skin, Nail bed telangiectasia, Finge... OMIM:187300
Hyperoxaluria, Primary, Type I
Acrocyanosis, Cutis marmorata OMIM:259900
Familial Dysautonomia
Acrocyanosis ORPHA:1764
Congenital Tracheomalacia
Cyanosis ORPHA:95430
Atrial Septal Defect, Ostium Secundum Type
Cyanosis ORPHA:99103
Unilateral Polymicrogyria
Cyanosis ORPHA:268943
Absence Of The Pulmonary Artery
Cyanosis, Hypocapnia ORPHA:980
Abnormal Origin Of Right Or Left Pulmonary Artery From The Aorta
Cyanosis ORPHA:99050
Heterotaxy, Visceral, 1, X-Linked
Cyanosis OMIM:306955
Pitt-Hopkins Syndrome
Acrocyanosis ORPHA:2896
Hutchinson-Gilford Progeria Syndrome
Premature skin wrinkling, Prominent superficial blood vessels, Generalized abnormality of skin, C... ORPHA:740
Primary Hyperoxaluria
Acrocyanosis, Cutis marmorata ORPHA:416
Dermatomyositis
Cutaneous photosensitivity, Acrocyanosis, Telangiectasia of the skin, Erythema ORPHA:221
Postinfectious Vasculitis
Palpable purpura, Acrocyanosis, Cutis marmorata, Vasculitis in the skin ORPHA:48435
Congenital Tracheal Stenosis
Cyanosis ORPHA:141127
Rapid-Onset Childhood Obesity-Hypothalamic Dysfunction-Hypoventilation-Autonomic Dysregulation Syndrome
Cyanosis ORPHA:293987
Aortic Arch Interruption
Cyanosis ORPHA:2299
Aicardi-Goutières Syndrome
Acrocyanosis, Cutis marmorata, Prolonged neonatal jaundice ORPHA:51
Cardiac Valvular Dysplasia 1
Cyanosis OMIM:212093
Classical Ehlers-Danlos Syndrome
Prematurely aged appearance, Poor wound healing, Ecchymosis, Acrocyanosis, Fragile skin, Bruising... ORPHA:287
Eisenmenger Syndrome
Hypoxemia, Cyanosis ORPHA:97214
Truncus Arteriosus
Cyanosis ORPHA:3384
Congenitally Corrected Transposition Of The Great Arteries
Cyanosis ORPHA:216694
Coffin-Lowry Syndrome
Acrocyanosis, Cutis marmorata OMIM:303600
Goodpasture Syndrome
Cyanosis OMIM:233450
Generalized Arterial Calcification Of Infancy
Cyanosis ORPHA:51608
Hypermobile Ehlers-Danlos Syndrome
Acrocyanosis ORPHA:285
Congenital Total Pulmonary Venous Return Anomaly
Cyanosis ORPHA:99125
Temtamy Syndrome
ORPHA:1777
Temtamy Syndrome
OMIM:218340

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 Grcc10

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 Grcc10.

No publications found that use IMPC mice or data for Grcc10.

Order Mouse and ES Cells

All available products are supplied via our member's centres or partnerships. When ordering a product from the IMPC you will be redirected to one of their websites or prompted to start an email.

MGI Allele Allele Type Produced
Grcc10tm1a(EUCOMM)Hmgu KO first allele (reporter-tagged insertion with conditional potential) Targeting vectors, ES Cells
Grcc10tm1(KOMP)Vlcg Reporter-tagged deletion allele (with selection cassette) Mice, ES Cells
Grcc10tm1.1(KOMP)Vlcg Reporter-tagged deletion allele (post Cre, with no selection cassette) Mice
Grcc10tm3(EUCOMM)Wtsi Reporter-tagged deletion allele (with selection cassette) Targeting vectors, ES Cells
Grcc10tm1e(EUCOMM)Hmgu Targeted, non-conditional allele ES Cells

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