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Trait
Sloping forehead
Inclination of the anterior surface of the forehead from the vertical more than two standard deviations above the mean (objective); or apparently excessive posterior sloping of the forehead in a lateral view.
Summary
- Also called
- Inclined forehead, Receding forehead, Posteriorly sloping forehead
- Body system
- Abnormality of head or neck
AtlasWho We HelpOur ScienceProductsOutcomes
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This page as data
Add .json to the page's address, or ask for application/json, to read it as JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/sloping-forehead.json"
page <- fromJSON(url)
page$trait$nameSloping foreheadHP:0000340
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Get my Genome Test80 condition reports read genes linked to this trait
Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- Fanconi AnemiaReads 18 of these genesBRCA1BRCA2BRIP1ERCC4FANCAFANCBAbout this report →
- Autosomal Recessive Primary MicrocephalyReads 17 of these genesANKLE2ASPMCDK5RAP2CEP135CEP152KNL1About this report →
- Meckel SyndromeReads 10 of these genesKIF14B9D1B9D2MKS1RPGRIP1LTCTN2About this report →
- DNA Repair DiseaseReads 20 of these genesNBNBRCA1BRCA2BRIP1ERCC4FANCAAbout this report →
Show 76 more reports
- Joubert Syndrome And Related DisordersReads 16 of these genesB9D1B9D2CC2D2ACEP290CSPP1KIF7About this report →
- Epilepsy (Full Panel)Reads 23 of these genesPAK3PUM1RELNUGP2ARXCACNA1EAbout this report →
- Hereditary Breast and Ovarian Cancer (BRCA1/2)Reads 2 of these genesBRCA1BRCA2About this report →
- Mosaic Variegated Aneuploidy SyndromeReads 3 of these genesBUB1BCEP57TRIP13About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 9 of these genesCC2D2ACEP290CSPP1MKS1TMEM216TMEM231About this report →
- Pontocerebellar Hypoplasia (TSEN54 and MINPP1)Reads 5 of these genesCOASYTSEN2SEPSECSTSEN15TSEN54About this report →
- Inherited Neurodegenerative DisordersReads 21 of these genesACER3COASYTSEN2PYCR2WARS1CC2D2AAbout this report →
- Lissencephaly Spectrum DisordersReads 5 of these genesPSAT1KATNB1NDE1RELNARXAbout this report →
- Breast and Ovarian Cancer Genes Beyond BRCA1/2Reads 3 of these genesBRIP1PALB2RAD51CAbout this report →
- Hereditary Episodic AtaxiasReads 2 of these genesKCNA1SCN2AAbout this report →
- ARC Syndrome 1 (VPS33B)Reads 1 of these genesVPS33BAbout this report →
- ARC Syndrome 2 (VIPAS39)Reads 1 of these genesVIPAS39About this report →
- Asparagine Synthetase DeficiencyReads 1 of these genesASNSAbout this report →
- CEP290-Related CiliopathyReads 1 of these genesCEP290About this report →
- Dias-Logan SyndromeReads 1 of these genesBCL11AAbout this report →
- FANCM-Related Genomic Instability DisorderReads 1 of these genesFANCMAbout this report →
- Greig Cephalopolysyndactyly SyndromeReads 1 of these genesGLI3About this report →
- KAT6B-Related DisordersReads 1 of these genesKAT6BAbout this report →
- Keutel SyndromeReads 1 of these genesMGPAbout this report →
- Marshall-Smith SyndromeReads 1 of these genesNFIXAbout this report →
- MCPH1-Related Primary MicrocephalyReads 1 of these genesMCPH1About this report →
- Microcephalic Osteodysplastic Primordial Dwarfism Type IIReads 1 of these genesPCNTAbout this report →
- Microcephaly and Chorioretinopathy 1 (TUBGCP6)Reads 1 of these genesTUBGCP6About this report →
- NDE1-Related MicrolissencephalyReads 1 of these genesNDE1About this report →
- Orofaciodigital Syndrome Type 14Reads 1 of these genesC2CD3About this report →
- PALB2 related diseasesReads 1 of these genesPALB2About this report →
- Phenylketonuria (PKU)Reads 1 of these genesPAHAbout this report →
- Primary Failure of Tooth EruptionReads 1 of these genesPTH1RAbout this report →
- RNU4ATAC Spectrum DisorderReads 1 of these genesRNU4ATACAbout this report →
- RTTN-Related Microcephalic Primordial DwarfismReads 1 of these genesRTTNAbout this report →
- Saul-Wilson SyndromeReads 1 of these genesCOG4About this report →
- TARP SyndromeReads 1 of these genesRBM10About this report →
- TRIM8-Related Neurodevelopmental and Kidney DisorderReads 1 of these genesTRIM8About this report →
- VARS1-Related Neurodevelopmental DisorderReads 1 of these genesVARS1About this report →
- Warsaw Breakage SyndromeReads 1 of these genesDDX11About this report →
- Spinal Muscular AtrophyReads 5 of these genesTSEN2WARS1SEPSECSTSEN15TSEN54About this report →
- Congenital Muscular DystrophiesReads 5 of these genesFKRPFKTNLARGE1POMT1POMT2About this report →
- Intellectual DisabilityReads 12 of these genesASXL3EIF2S3METTL5TAF13PAK3CAMK2BAbout this report →
- Disorders of Glycine & Serine MetabolismReads 2 of these genesPSAT1PHGDHAbout this report →
- Cleidocranial DysplasiaReads 1 of these genesRUNX2About this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 3 of these genesGLI3CNOT1ZIC2About this report →
- Hirschsprung Disease & Related Enteric NeurocristopathiesReads 1 of these genesKIFBPAbout this report →
- Immuno-Osseous DysplasiasReads 1 of these genesRNU4ATACAbout this report →
- Monogenic Early-Onset OsteoporosisReads 1 of these genesCOPB2About this report →
- Congenital Disorders of GlycosylationReads 5 of these genesCOG4FKRPFKTNPOMT1POMT2About this report →
- Overgrowth Syndromes (Sotos, Weaver, Tatton-Brown-Rahman, Malan)Reads 1 of these genesNFIXAbout this report →
- Thiamine Transporter and Metabolism DisordersReads 1 of these genesSLC25A19About this report →
- GPI Anchor Biosynthesis DefectsReads 2 of these genesPIGPPIGQAbout this report →
- Leber Congenital Amaurosis & RPE65-Related RetinopathyReads 2 of these genesCEP290RPGRIP1About this report →
- Bardet-Biedl and Alström SyndromesReads 2 of these genesCEP290MKS1About this report →
- Syndromic Complex Neurodevelopmental DisorderReads 2 of these genesTBCKRNU4-2About this report →
- Female InfertilityReads 3 of these genesNUP107FANCMTRIP13About this report →
- Limb-Girdle Muscular DystrophyReads 2 of these genesFKRPFKTNAbout this report →
- Neurodegeneration with Brain Iron Accumulation (NBIA)Reads 1 of these genesCOASYAbout this report →
- Neuronal Ceroid LipofuscinosisReads 1 of these genesCTSDAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 4 of these genesSLC25A19SARS1WARS1PNKPAbout this report →
- Complex Cortical Dysplasia and Frontoparietal PolymicrogyriaReads 1 of these genesTUBGCP2About this report →
- Cutis LaxaReads 1 of these genesLTBP4About this report →
- Fatty Acid Oxidation & Carnitine Cycle DisordersReads 1 of these genesCPT2About this report →
- Primary Lymphoedema & Lymphatic MalformationsReads 1 of these genesKIF11About this report →
- Other Inherited LeukodystrophiesReads 2 of these genesACER3PYCR2About this report →
- Nephronophthisis and Senior-Løken SyndromeReads 1 of these genesTMEM67About this report →
- Ehlers-Danlos SyndromeReads 1 of these genesFKBP14About this report →
- Syndromic CraniosynostosisReads 1 of these genesIL11RAAbout this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 1 of these genesPYCR2About this report →
- Nephrotic SyndromeReads 1 of these genesNUP107About this report →
- Diabetes MellitusReads 1 of these genesEIF2S3About this report →
- Severe Combined ImmunodeficiencyReads 1 of these genesNHEJ1About this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 1 of these genesPUM1About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesPNKPAbout this report →
- Male InfertilityReads 1 of these genesFANCMAbout this report →
- Dilated CardiomyopathyReads 1 of these genesFKTNAbout this report →
- Other Inborn Errors of ImmunityReads 2 of these genesNHEJ1RELAbout this report →
- Lysosomal Storage DiseaseReads 1 of these genesCTSDAbout this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesWARS1About this report →
- Retinitis PigmentosaReads 1 of these genesCC2D2AAbout this report →
Read the genes linked to Sloping forehead, and the rest of your genome, with one test.
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Get my Genome Test201 genes linked to Sloping forehead
Changes in these genes cause rare conditions in which Sloping forehead is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| ACER3alkaline ceramidase 3 | Always | In 1 condition |
| ANKLE2ankyrin repeat and LEM domain containing 2 | Always | In 2 conditions |
| ASPMassembly factor for spindle microtubules | Always | In 2 conditions |
| ASXL3ASXL transcriptional regulator 3 | Always | In 1 condition |
| CDK5RAP2CDK5 regulatory subunit associated protein 2 | Always | In 2 conditions |
| CDK6cyclin dependent kinase 6 | Always | In 2 conditions |
| CENPEcentromere protein E | Always | In 2 conditions |
| CEP135centrosomal protein 135 | Always | In 2 conditions |
| CEP152centrosomal protein 152 | Always | In 2 conditions |
| COASYCoenzyme A synthase | Always | In 1 condition |
| CRNKL1crooked neck pre-mRNA splicing factor 1 | Always | In 1 condition |
| DDX11DEAD/H-box helicase 11 | Always | In 1 condition |
| FKBP14FKBP prolyl isomerase 14 | Always | In 1 condition |
| INTS11integrator complex subunit 11 | Always | In 1 condition |
| JKAMPJNK1/MAPK8 associated membrane protein | Always | In 1 condition |
| KNL1kinetochore scaffold 1 | Always | In 2 conditions |
| NBNnibrin | Always | In 2 conditions |
| NCAPD2non-SMC condensin I complex subunit D2 | Always | In 1 condition |
| NCAPHnon-SMC condensin I complex subunit H | Always | In 1 condition |
| NUP107nucleoporin 107 | Always | In 2 conditions |
| PSAT1phosphoserine aminotransferase 1 | Always | In 2 conditions |
| RBBP8RB binding protein 8, endonuclease | Always | In 1 condition |
| RNU4ATACRNA, U4atac small nuclear | Always | In 3 conditions |
| RRP7Aribosomal RNA processing 7 homolog A | Always | In 1 condition |
| SLC25A19solute carrier family 25 member 19 | Always | In 2 conditions |
| STAG2STAG2 cohesin complex component | Always | In 1 condition |
| STILSTIL centriolar assembly protein | Always | In 2 conditions |
| TSEN2tRNA splicing endonuclease subunit 2 | Always | In 2 conditions |
| UGGT1UDP-glucose glycoprotein glucosyltransferase 1 | Always | In 1 condition |
| WDR62WD repeat domain 62 | Always | In 2 conditions |
| CITcitron rho-interacting serine/threonine kinase | Very often (80–99%) | In 2 conditions |
| COPB2coat protein complex I subunit beta 2 | Very often (80–99%) | In 1 condition |
| CPAPcentrosome assembly and centriole elongation protein | Very often (80–99%) | In 1 condition |
| EIF2S3eukaryotic translation initiation factor 2 subunit gamma | Very often (80–99%) | In 1 condition |
| EMG1EMG1 N1-specific pseudouridine methyltransferase | Very often (80–99%) | In 1 condition |
| KAT6Blysine acetyltransferase 6B | Very often (80–99%) | In 1 condition |
| KIF14kinesin family member 14 | Very often (80–99%) | In 3 conditions |
| MCM7minichromosome maintenance complex component 7 | Very often (80–99%) | In 1 condition |
| MCPH1microcephalin 1 | Very often (80–99%) | In 1 condition |
| METTL5methyltransferase 5, N6-adenosine | Very often (80–99%) | In 1 condition |
Show 161 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| MFSD2AMFSD2 lysolipid transporter A, lysophospholipid | Very often (80–99%) | In 1 condition |
| NCAPD3non-SMC condensin II complex subunit D3 | Very often (80–99%) | In 1 condition |
| NHEJ1non-homologous end joining factor 1 | Very often (80–99%) | In 1 condition |
| NUP37nucleoporin 37 | Very often (80–99%) | In 1 condition |
| PDCD6IPprogrammed cell death 6 interacting protein | Very often (80–99%) | In 1 condition |
| PHC1polyhomeotic homolog 1 | Very often (80–99%) | In 1 condition |
| PTH1Rparathyroid hormone 1 receptor | Very often (80–99%) | In 1 condition |
| PYCR2pyrroline-5-carboxylate reductase 2 | Very often (80–99%) | In 1 condition |
| RUNX2RUNX family transcription factor 2 | Very often (80–99%) | In 1 condition |
| SARS1seryl-tRNA synthetase 1 | Very often (80–99%) | In 1 condition |
| SASS6SAS-6 centriolar assembly protein | Very often (80–99%) | In 1 condition |
| TAF13TATA-box binding protein associated factor 13 | Very often (80–99%) | In 1 condition |
| TRAPPC10trafficking protein particle complex subunit 10 | Very often (80–99%) | In 1 condition |
| TRAPPC14trafficking protein particle complex subunit 14 | Very often (80–99%) | In 1 condition |
| WARS1tryptophanyl-tRNA synthetase 1 | Very often (80–99%) | In 2 conditions |
| ZNF526zinc finger protein 526 | Very often (80–99%) | In 1 condition |
| ASNSasparagine synthetase (glutamine-hydrolyzing) | Often (30–79%) | In 1 condition |
| B9D1B9 domain containing 1 | Often (30–79%) | In 1 condition |
| B9D2B9 domain containing 2 | Often (30–79%) | In 1 condition |
| BCL11ABCL11 transcription factor A | Often (30–79%) | In 1 condition |
| C2CD3C2 domain containing 3 centriole elongation regulator | Often (30–79%) | In 1 condition |
| CC2D2Acoiled-coil and C2 domain containing 2A | Often (30–79%) | In 1 condition |
| CEP290centrosomal protein 290 | Often (30–79%) | In 1 condition |
| CEP295centrosomal protein 295 | Often (30–79%) | In 1 condition |
| COG4component of oligomeric golgi complex 4 | Often (30–79%) | In 1 condition |
| CSPP1centrosome and spindle pole associated protein 1 | Often (30–79%) | In 1 condition |
| EXOC2exocyst complex component 2 | Often (30–79%) | In 1 condition |
| EXOSC5exosome component 5 | Often (30–79%) | In 1 condition |
| FKRPfukutin related protein | Often (30–79%) | In 1 condition |
| FKTNfukutin | Often (30–79%) | In 1 condition |
| GLI3GLI family zinc finger 3 | Often (30–79%) | In 1 condition |
| GPKOWG-patch domain and KOW motifs | Often (30–79%) | In 1 condition |
| KATNB1katanin regulatory subunit B1 | Often (30–79%) | In 2 conditions |
| KIF7kinesin family member 7 | Often (30–79%) | In 1 condition |
| LARGE1LARGE xylosyl- and glucuronyltransferase 1 | Often (30–79%) | In 1 condition |
| MGPmatrix Gla protein | Often (30–79%) | In 1 condition |
| MKS1MKS transition zone complex subunit 1 | Often (30–79%) | In 2 conditions |
| NDE1nudE neurodevelopment protein 1 | Often (30–79%) | In 2 conditions |
| PAK3p21 (RAC1) activated kinase 3 | Often (30–79%) | In 1 condition |
| PHGDHphosphoglycerate dehydrogenase | Often (30–79%) | In 1 condition |
| PLK4polo like kinase 4 | Often (30–79%) | In 2 conditions |
| POMT1protein O-mannosyltransferase 1 | Often (30–79%) | In 1 condition |
| POMT2protein O-mannosyltransferase 2 | Often (30–79%) | In 1 condition |
| PUM1pumilio RNA binding family member 1 | Often (30–79%) | In 1 condition |
| QARS1glutaminyl-tRNA synthetase 1 | Often (30–79%) | In 1 condition |
| RBM10RNA binding motif protein 10 | Often (30–79%) | In 1 condition |
| RBSNrabenosyn, RAB effector | Often (30–79%) | In 1 condition |
| RELREL proto-oncogene, NF-kB subunit | Often (30–79%) | In 1 condition |
| RELNreelin | Often (30–79%) | In 2 conditions |
| RPGRIP1RPGR interacting protein 1 | Often (30–79%) | In 1 condition |
| RPGRIP1LRPGRIP1 like | Often (30–79%) | In 1 condition |
| RTTNrotatin | Often (30–79%) | In 1 condition |
| SC5Dsterol-C5-desaturase | Often (30–79%) | In 1 condition |
| SEPSECSSep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase | Often (30–79%) | In 1 condition |
| TCTN1tectonic family member 1 | Often (30–79%) | In 1 condition |
| TCTN2tectonic family member 2 | Often (30–79%) | In 1 condition |
| TCTN3tectonic family member 3 | Often (30–79%) | In 1 condition |
| TMEM107transmembrane protein 107 | Often (30–79%) | In 1 condition |
| TMEM216transmembrane protein 216 | Often (30–79%) | In 1 condition |
| TMEM231transmembrane protein 231 | Often (30–79%) | In 1 condition |
| TMEM237transmembrane protein 237 | Often (30–79%) | In 1 condition |
| TMEM67transmembrane protein 67 | Often (30–79%) | In 1 condition |
| TSEN15tRNA splicing endonuclease subunit 15 | Often (30–79%) | In 1 condition |
| TSEN34tRNA splicing endonuclease subunit 34 | Often (30–79%) | In 1 condition |
| TSEN54tRNA splicing endonuclease subunit 54 | Often (30–79%) | In 2 conditions |
| TUBGCP4tubulin gamma complex component 4 | Often (30–79%) | In 1 condition |
| TUBGCP6tubulin gamma complex component 6 | Often (30–79%) | In 2 conditions |
| TXNDC15thioredoxin domain containing 15 | Often (30–79%) | In 1 condition |
| VARS1valyl-tRNA synthetase 1 | Often (30–79%) | In 1 condition |
| WLSWnt ligand secretion mediator | Often (30–79%) | In 1 condition |
| XPO1exportin 1 | Often (30–79%) | In 1 condition |
| ADAT3adenosine deaminase tRNA specific 3 | Sometimes (5–29%) | In 1 condition |
| BRCA1BRCA1 DNA repair associated | Sometimes (5–29%) | In 1 condition |
| BRCA2BRCA2 DNA repair associated | Sometimes (5–29%) | In 1 condition |
| BRIP1BRCA1 interacting DNA helicase 1 | Sometimes (5–29%) | In 1 condition |
| BUB1BUB1 mitotic checkpoint serine/threonine kinase | Sometimes (5–29%) | In 1 condition |
| BUB1BBUB1 mitotic checkpoint serine/threonine kinase B | Sometimes (5–29%) | In 1 condition |
| BUB3BUB3 mitotic checkpoint protein | Sometimes (5–29%) | In 1 condition |
| CAMK2Bcalcium/calmodulin dependent protein kinase II beta | Sometimes (5–29%) | In 1 condition |
| CEP57centrosomal protein 57 | Sometimes (5–29%) | In 1 condition |
| CNOT1CCR4-NOT transcription complex subunit 1 | Sometimes (5–29%) | In 1 condition |
| CRELD1CRELD disulfide isomerase 1 | Sometimes (5–29%) | In 1 condition |
| CTSDcathepsin D | Sometimes (5–29%) | In 1 condition |
| ERCC4ERCC excision repair 4, endonuclease catalytic subunit | Sometimes (5–29%) | In 1 condition |
| FAAP100FA core complex associated protein 100 | Sometimes (5–29%) | In 1 condition |
| FANCAFA complementation group A | Sometimes (5–29%) | In 1 condition |
| FANCBFA complementation group B | Sometimes (5–29%) | In 1 condition |
| FANCCFA complementation group C | Sometimes (5–29%) | In 1 condition |
| FANCD2FA complementation group D2 | Sometimes (5–29%) | In 1 condition |
| FANCEFA complementation group E | Sometimes (5–29%) | In 1 condition |
| FANCFFA complementation group F | Sometimes (5–29%) | In 1 condition |
| FANCGFA complementation group G | Sometimes (5–29%) | In 1 condition |
| FANCIFA complementation group I | Sometimes (5–29%) | In 1 condition |
| FANCLFA complementation group L | Sometimes (5–29%) | In 1 condition |
| FANCMFA complementation group M | Sometimes (5–29%) | In 1 condition |
| IL11RAinterleukin 11 receptor subunit alpha | Sometimes (5–29%) | In 1 condition |
| KIF11kinesin family member 11 | Sometimes (5–29%) | In 2 conditions |
| KIFBPkinesin family binding protein | Sometimes (5–29%) | In 1 condition |
| LTBP4latent transforming growth factor beta binding protein 4 | Sometimes (5–29%) | In 1 condition |
| MAD2L2mitotic arrest deficient 2 like 2 | Sometimes (5–29%) | In 1 condition |
| NFIXnuclear factor I X | Sometimes (5–29%) | In 1 condition |
| PALB2partner and localizer of BRCA2 | Sometimes (5–29%) | In 1 condition |
| PCDHGC4protocadherin gamma subfamily C, 4 | Sometimes (5–29%) | In 1 condition |
| PTPMT1protein tyrosine phosphatase mitochondrial 1 | Sometimes (5–29%) | In 1 condition |
| RAD51RAD51 recombinase | Sometimes (5–29%) | In 1 condition |
| RAD51CRAD51 paralog C | Sometimes (5–29%) | In 1 condition |
| RFWD3ring finger and WD repeat domain 3 | Sometimes (5–29%) | In 1 condition |
| SLX4SLX4 structure-specific endonuclease subunit | Sometimes (5–29%) | In 1 condition |
| SMPD4sphingomyelin phosphodiesterase 4 | Sometimes (5–29%) | In 1 condition |
| TBCBtubulin folding cofactor B | Sometimes (5–29%) | In 1 condition |
| TBCKTBC1 domain containing kinase | Sometimes (5–29%) | In 2 conditions |
| TRIP12thyroid hormone receptor interactor 12 | Sometimes (5–29%) | In 1 condition |
| TRIP13thyroid hormone receptor interactor 13 | Sometimes (5–29%) | In 1 condition |
| TTI2TELO2 interacting protein 2 | Sometimes (5–29%) | In 2 conditions |
| TUBGCP2tubulin gamma complex component 2 | Sometimes (5–29%) | In 1 condition |
| UBE2Tubiquitin conjugating enzyme E2 T | Sometimes (5–29%) | In 1 condition |
| UFC1ubiquitin-fold modifier conjugating enzyme 1 | Sometimes (5–29%) | In 1 condition |
| UGP2UDP-glucose pyrophosphorylase 2 | Sometimes (5–29%) | In 1 condition |
| XRCC2X-ray repair cross complementing 2 | Sometimes (5–29%) | In 1 condition |
| ZIC2Zic family zinc finger 2 | Sometimes (5–29%) | In 1 condition |
| ARXaristaless related homeobox | Rarely (1–4%) | In 1 condition |
| CACNA1Ecalcium voltage-gated channel subunit alpha1 E | Rarely (1–4%) | In 1 condition |
| CASKcalcium/calmodulin dependent serine protein kinase | Rarely (1–4%) | In 1 condition |
| CDKL5cyclin dependent kinase like 5 | Rarely (1–4%) | In 1 condition |
| DMXL2Dmx like 2 | Rarely (1–4%) | In 1 condition |
| GNAO1G protein subunit alpha o1 | Rarely (1–4%) | In 1 condition |
| GRIN1glutamate ionotropic receptor NMDA type subunit 1 | Rarely (1–4%) | In 1 condition |
| GRM7glutamate metabotropic receptor 7 | Rarely (1–4%) | In 1 condition |
| KCNA1potassium voltage-gated channel subfamily A member 1 | Rarely (1–4%) | In 1 condition |
| LGI1leucine rich glioma inactivated 1 | Rarely (1–4%) | In 1 condition |
| NEUROD2neuronal differentiation 2 | Rarely (1–4%) | In 1 condition |
| PAHphenylalanine hydroxylase | Rarely (1–4%) | In 1 condition |
| PIGPphosphatidylinositol glycan anchor biosynthesis class P | Rarely (1–4%) | In 1 condition |
| PIGQphosphatidylinositol glycan anchor biosynthesis class Q | Rarely (1–4%) | In 1 condition |
| PNKPpolynucleotide kinase 3'-phosphatase | Rarely (1–4%) | In 1 condition |
| RHOBTB2Rho related BTB domain containing 2 | Rarely (1–4%) | In 1 condition |
| RNU4-2RNA, U4 small nuclear 2 | Rarely (1–4%) | In 1 condition |
| SCN1Bsodium voltage-gated channel beta subunit 1 | Rarely (1–4%) | In 1 condition |
| SCN2Asodium voltage-gated channel alpha subunit 2 | Rarely (1–4%) | In 1 condition |
| SIK1salt inducible kinase 1 | Rarely (1–4%) | In 1 condition |
| SLC25A22solute carrier family 25 member 22 | Rarely (1–4%) | In 1 condition |
| SLC32A1solute carrier family 32 member 1 | Rarely (1–4%) | In 1 condition |
| TRIM8tripartite motif containing 8 | Rarely (1–4%) | In 1 condition |
| ATRATR checkpoint kinase | Not recorded | In 1 condition |
| CCDC88Acoiled-coil and HOOK domain protein 88A | Not recorded | In 1 condition |
| CPT2carnitine palmitoyltransferase 2 | Not recorded | In 1 condition |
| DYNC1I2dynein cytoplasmic 1 intermediate chain 2 | Not recorded | In 1 condition |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Not recorded | In 1 condition |
| OCLNoccludin | Not recorded | In 1 condition |
| OSGEPO-sialoglycoprotein endopeptidase | Not recorded | In 1 condition |
| PARS2prolyl-tRNA synthetase 2, mitochondrial | Not recorded | In 1 condition |
| PCNTpericentrin | Not recorded | In 1 condition |
| PHF8PHD finger protein 8 | Not recorded | In 1 condition |
| PRUNE1prune exopolyphosphatase 1 | Not recorded | In 1 condition |
| SETBP1SET binding protein 1 | Not recorded | In 1 condition |
| STAMBPSTAM binding protein | Not recorded | In 1 condition |
| VIPAS39VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog | Not recorded | In 1 condition |
| VPS33BVPS33B late endosome and lysosome associated | Not recorded | In 1 condition |
| WDR73WD repeat domain 73 | Not recorded | In 1 condition |
| XRCC4X-ray repair cross complementing 4 | Not recorded | In 1 condition |
| ZNF335zinc finger protein 335 | Not recorded | In 1 condition |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
Broader traits
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.19-9814e911.
AtlasWho We HelpOur ScienceProductsOutcomes
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