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Gene: Or8a1b MGI:1931271

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Not currently registered for phenotyping at IMPC

Phenotyping is currently not planned for a knockout strain of this gene.

Gene Summary

Name:
olfactory receptor family 8 subfamily A member 1B
Synonyms:
MOR171-3,  Olfr160,  M72,  GA_x6K02T2PVTD-31389446-31388517

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IMPC Data Collections

  • No Body Weight Data
  • No Embryo Imaging Data
  • No Viability Data

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.

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.

Phenotype associated images not available

Human diseases caused by Or8a1b 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 Or8a1b by phenotypic similarity.

Disease Similarity of
phenotypes		 Matching phenotypes Source
Leber Congenital Amaurosis 10
Hyposmia OMIM:611755
Hypogonadotropic Hypogonadism 17 With Or Without Anosmia
Hyposmia OMIM:615266
Anosmia For Butyl Mercaptan
Anosmia OMIM:270350
Isovaleric Acid, Inability To Smell
Anosmia OMIM:243450
Anosmia, Isolated Congenital, X-Linked
Anosmia OMIM:301700
Anosmia, Isolated Congenital
Anosmia OMIM:107200
Anosmia For Isobutyric Acid
Partial anosmia OMIM:207000
Hypogonadotropic Hypogonadism 21 With Or Without Anosmia
Hyposmia OMIM:615271
Musk, Inability To Smell
Anosmia OMIM:254150
Thumb Agenesis, Short Stature, And Immunodeficiency
Anosmia OMIM:274190
Aural Atresia, Congenital
Hyposmia OMIM:607842
Hypogonadotropic Hypogonadism 7 With Or Without Anosmia
Abnormality of the sense of smell OMIM:146110
Arrhinia-Choanal Atresia-Microphthalmia Syndrome
Aplasia/Hypoplasia involving the nose, Choanal atresia, Abnormality of the sense of smell ORPHA:1135
Apnea, Obstructive Sleep
Anosmia OMIM:107650
Hypogonadotropic Hypogonadism 9 With Or Without Anosmia
Hyposmia, Anosmia, Bifid nose OMIM:614838
Hypogonadotropic Hypogonadism 20 With Or Without Anosmia
Anosmia OMIM:615270
Hypogonadotropic Hypogonadism 14 With Or Without Anosmia
Anosmia OMIM:614858
Chondrodysplasia Punctata 1, X-Linked Recessive
Short nasal septum, Anosmia, Depressed nasal bridge, Short nose OMIM:302950
Leukoencephalopathy With Dystonia And Motor Neuropathy
Hyposmia OMIM:613724
Hypogonadotropic Hypogonadism 5 With Or Without Anosmia
Anosmia OMIM:612370
Body Mass Index Quantitative Trait Locus 19
Hyposmia, Anosmia OMIM:617885
Hypogonadotropic Hypogonadism 18 With Or Without Anosmia
Anosmia OMIM:615267
Hypogonadotropic Hypogonadism 6 With Or Without Anosmia
Hyposmia, Anosmia OMIM:612702
Hypogonadotropic Hypogonadism 4 With Or Without Anosmia
Hyposmia, Anosmia OMIM:610628
Hypogonadotropic Hypogonadism 2 With Or Without Anosmia
Hyposmia, Anosmia, Agenesis of corpus callosum, Choanal atresia OMIM:147950
Solitary Median Maxillary Central Incisor
Abnormal nasopharynx morphology, Midnasal stenosis, Choanal atresia, Anosmia, Holoprosencephaly, ... OMIM:147250
Gorlin Syndrome
Hydrocephalus, Wide nasal bridge, Abnormality of the sense of smell ORPHA:377
Peroxisome Biogenesis Disorder 9B
Anosmia, Total anosmia OMIM:614879
Hypogonadotropic Hypogonadism 3 With Or Without Anosmia
Hyposmia, Anosmia OMIM:244200
Hydrolethalus
Anencephaly, Hydrocephalus, Agenesis of corpus callosum, Abnormality of the sense of smell ORPHA:2189
Hyperostosis Cranialis Interna
Hyposmia, Anosmia OMIM:144755
Bardet-Biedl Syndrome 19
Hyposmia OMIM:615996
Indifference To Pain, Congenital, Autosomal Recessive
Hyposmia, Anosmia OMIM:243000
Hypogonadotropic Hypogonadism 15 With Or Without Anosmia
Anosmia OMIM:614880
Hypogonadotropic Hypogonadism 16 With Or Without Anosmia
Hyposmia, Anosmia OMIM:614897
Blepharophimosis With Ptosis, Syndactyly, And Short Stature
Anosmia, Wide nasal bridge OMIM:210745
Hypogonadotropic Hypogonadism 10 With Or Without Anosmia
Anosmia OMIM:614839
Hypogonadotropic Hypogonadism 13 With Or Without Anosmia
Anosmia OMIM:614842
Blepharophimosis-Ptosis-Esotropia-Syndactyly-Short Stature Syndrome
Anosmia ORPHA:2057
Huntington Disease
Abnormality of the sense of smell ORPHA:399
Hypogonadotropic Hypogonadism 25 With Anosmia
Anosmia OMIM:618841
Ventricular Extrasystoles With Syncopal Episodes-Perodactyly-Robin Sequence Syndrome
Abnormality of the sense of smell ORPHA:3201
Marcus-Gunn Syndrome
Choanal atresia, Abnormality of the sense of smell ORPHA:91412
Brachytelephalangy-Dysmorphism-Kallmann Syndrome
Abnormal nostril morphology, Short nose, Anosmia ORPHA:1295
Ciliary Dyskinesia, Primary, 1
Communicating hydrocephalus, Nasal polyposis, Anosmia, Chronic rhinitis OMIM:244400
Kleine-Levin Syndrome
Parosmia ORPHA:33543
Bardet-Biedl Syndrome 17
Hyposmia, Anosmia OMIM:615994
Hypogonadotropic Hypogonadism 22 With Or Without Anosmia
Anosmia OMIM:616030
Johnson Neuroectodermal Syndrome
Bulbous nose, Anosmia, Choanal atresia ORPHA:2316
Parkinson Disease 8, Autosomal Dominant
Hyposmia OMIM:607060
Hypogonadotropic Hypogonadism 12 With Or Without Anosmia
Anosmia OMIM:614841
Kufor-Rakeb Syndrome
Hyposmia, Anosmia OMIM:606693
Hypogonadotropic Hypogonadism 1 With Or Without Anosmia
Hyposmia, Anosmia OMIM:308700
Hypogonadotropic Hypogonadism 8 With Or Without Anosmia
Anosmia OMIM:614837
Refsum Disease, Classic
Anosmia OMIM:266500
Neuropathy, Hereditary Motor And Sensory, Type Via, With Optic Atrophy
Anosmia OMIM:601152
Hypogonadotropic Hypogonadism 23 With Or Without Anosmia
Abnormality of the sense of smell OMIM:228300
Polyendocrine-Polyneuropathy Syndrome
Abnormality of the sense of smell OMIM:616113
8Q21.11 Microdeletion Syndrome
Wide nose, Underdeveloped nasal alae, Abnormality of the sense of smell ORPHA:284160
Septo-Optic Dysplasia Spectrum
Anosmia, Agenesis of corpus callosum ORPHA:3157
Kallmann Syndrome With Spastic Paraplegia
Anosmia OMIM:308750
Neuropathy, Hereditary Sensory And Autonomic, Type Viii
Hyposmia OMIM:616488
Refsum Disease
Anosmia ORPHA:773
Holoprosencephaly
Encephalocele, Aplasia/Hypoplasia involving the nose, Anteverted nares, Choanal atresia, Hydrocep... ORPHA:2162
Acro-Renal-Mandibular Syndrome
Abnormality of the sense of smell ORPHA:958
Isolated Follicle Stimulating Hormone Deficiency
Anosmia ORPHA:52901
Campomelic Dysplasia
Depressed nasal bridge, Abnormality of the sense of smell ORPHA:140
Hyposmia-Nasal And Ocular Hypoplasia-Hypogonadotropic Hypogonadism Syndrome
Hyposmia, Anosmia, Absent nares, Single naris ORPHA:2250
Young-Onset Parkinson Disease
Hyposmia ORPHA:2828
Kallmann Syndrome
Hyposmia, Anosmia ORPHA:478
Kallmann Syndrome-Heart Disease Syndrome
Partial anosmia, Total anosmia ORPHA:2326
Moebius Syndrome
Abnormality of the sense of smell ORPHA:570
8P11.2 Deletion Syndrome
Anosmia, Depressed nasal bridge ORPHA:251066
Superficial Siderosis
Anosmia, Partial anosmia ORPHA:247245
Hereditary Late-Onset Parkinson Disease
Hyposmia ORPHA:411602
Meningioma
Hydrocephalus, Abnormality of the sense of smell ORPHA:2495
Waardenburg Syndrome, Type 2E
Anosmia OMIM:611584
Hypogonadotropic Hypogonadism 26 With Or Without Anosmia
Anosmia OMIM:619718
Waardenburg Syndrome, Type 4C
Anosmia OMIM:613266
Leopard Syndrome 1
Hyposmia, Spina bifida occulta, Depressed nasal ridge OMIM:151100
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, And Hirschsprung Disease
Anosmia OMIM:609136
Wilson Disease
Hyposmia OMIM:277900
Intellectual Developmental Disorder With Impaired Language And Dysmorphic Facies
Hyposmia OMIM:618653
Bosma Arhinia Microphthalmia Syndrome
Anosmia, Choanal atresia, Aplasia of the nose OMIM:603457
Occipital Horn Syndrome
Abnormality of the sense of smell ORPHA:198
Amoebiasis Due To Free-Living Amoebae
Hyposmia ORPHA:68
Charge Syndrome
Depressed nasal bridge, Choanal atresia, Aqueductal stenosis, Anosmia, Holoprosencephaly ORPHA:138
Lacrimoauriculodentodigital Syndrome
Anosmia, Choanal atresia ORPHA:2363
Charge Syndrome
Anosmia, Choanal atresia, Holoprosencephaly OMIM:214800

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 Or8a1b

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 Or8a1b.

No publications found that use IMPC mice or data for Or8a1b.

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