Gene catalog
Every gene page Sniff builds
Two honest sections. First, the 15 morphology loci where Sniff measures allele frequency across the atlas (18,477 research dogs). Second, the 324 disease-linked genes with a real page: OMIA conditions, human counterparts where the ortholog is one-to-one, and cited records. We would rather list every page we have than hide the disease genes behind a trait-only directory.
339 pages total. Looking for a Dog10K position or a human variant? Use the variant lookup.
Trait loci · atlas frequencies
The 15 loci Sniff reads on every dog
Morphology SNPs behind body size, legs, coat, ear set, and brachycephaly. Each page shows breed frequencies, direction of effect, and the published caveats (FGF4 retrogene polarity, SMOC2 polygenicity for brachycephaly).
Body Size
- LCORL NCAPG/LCORL height locus chr3 chr3 · atlas 83%
- SMAD2 small vs giant strong differentiation chr7 chr7 · atlas 74%
- STC2 size locus chr4 chr4 · atlas 74%
- HMGA2 small breeds enriched at chr10:8-12Mb chr10 · atlas 56%
- IGF1 small breeds enriched for short-allele haplotype chr15 · atlas 55%
- ADAMTS17 height/eye locus chr3 chr3 · atlas 54%
Leg Length
- FGF4_retrogene_CFA12 chondrodystrophy insertion site; not annotated as gene chr12 · atlas 80%
- FGF4_retrogene_CFA18 chondrodysplasia insertion site; not annotated as gene chr18 · atlas 77%
Coat Furnishings
- RSPO2 wirehaired/furnished breeds chr13 · atlas 55%
Coat Length
- FGF5 long-hair allele chr32 · atlas 64%
Coat Curl
- KRT71 curly-coat variant; backbone coverage poor chr27 · atlas 91%
Coat Color
- MC1R recessive red e/e; Ensembl symbol fails; chr5 region chr5 · atlas 62%
Ear Type
- MSRB3 erect vs drop; size-confounded with HMGA2 chr10 chr10 · atlas 80%
Disease-linked genes · OMIA and human bridge
324 genes with a condition or human homolog
These pages exist when OMIA links a condition, or a human OMIM homolog is bridged, and we have something honest to say (no empty stubs). A gene-level view: identity, linked conditions, and the human counterpart when the ortholog is one-to-one. Not a frequency map for every gene yet; we abstain where we cannot interpret a number honestly.
- ABCA4 Stargardt Disease (Discovered in the Labrador Retriever) 1 OMIA
- ABCB1 MDR1 (Multidrug Resistance 1) Medication Sensitivity 1 OMIA
- ABCC9 Human homolog bridged
- ABHD5 Human homolog bridged
- ACADM Human homolog bridged
- ACADVL Human homolog bridged
- ACPT Human homolog bridged
- ACSL5 Human homolog bridged
- ADAM9 Human homolog bridged
- ADAMTS10 Primary Open Angle Glaucoma (Discovered in the Beagle; POAG) 1 OMIA
- ADAMTS2 Human homolog bridged
- ADAMTS20 Cleft Lip with/without Palate and Syndactyly (ADAMTS20-related) 1 OMIA
- ADAMTS3 Human homolog bridged
- ADAMTSL2 Musladin-Lueke syndrome (MLS) 1 OMIA
- AGL Glycogen Storage Disease, Type IIIa (GSD IIIa) 1 OMIA
- AKNA Recurrent Inflammatory Pulmonary Disease (Discovered in the Rough Collie) 1 OMIA
- ALDH5A1 Human homolog bridged
- ALOXE3 Human homolog bridged
- ALPL Hypophosphatasia (Discovered in the Karelian Bear Dog; ALPL-related) 1 OMIA
- AMHR2 Persistent Müllerian Duct Syndrome (PMDS) 1 OMIA
- AMPD2 Human homolog bridged
- ANLN Acute Respiratory Distress Syndrome (Discovered in the Dalmatian; ARDS) 1 OMIA
- ANO6 Canine Scott Syndrome (CSS) 1 OMIA
- AP3B1 Human homolog bridged
- APC Human homolog bridged
- APOE Human homolog bridged
- APRT Human homolog bridged
- ARHGEF10 Human homolog bridged
- ARSB Human homolog bridged
- ARSG Neuronal Ceroid Lipofuscinosis 4A (Discovered in the American Staffordshire Terrier; NCL4A) 1 OMIA
- ASPRV1 Human homolog bridged
- ATF2 Neonatal Encephalopathy with Seizures (NEWS) 1 OMIA
- ATG4D Lagotto Storage Disease (LSD) 1 OMIA
- ATP13A2 Neuronal Ceroid Lipofuscinosis 12 (Discovered in the Australian Cattle Dog) 1 OMIA
- ATP1B2 Spongy Degeneration with Cerebellar Ataxia (Discovered in the Belgian Malinois; ATP1B2-related SDCA2) 1 OMIA
- ATP2A2 Human homolog bridged
- ATP7A Human homolog bridged
- ATP7B Human homolog bridged
- BBS2 Bardet-Biedl syndrome 2 or Progressive Retinal Atrophy (Discovered in the Shetland Sheepdog; BBS2-PRA) 1 OMIA
- BBS4 Human homolog bridged
- BCAN Episodic Falling (EF) 1 OMIA
- BCR Human homolog bridged
- BEST1 Canine Multifocal Retinopathy 1 (Discovered in Mastiff-related breeds; CMR1) 3 OMIA
- BIN1 Centronuclear Myopathy (Discovered in the Great Dane; BIN1-related; CNM) 1 OMIA
- BLVRA Human homolog bridged
- BRAF Human homolog bridged
- C3 Complement 3 (C3) Deficiency 1 OMIA
- CAPN1 Spinocerebellar Ataxia (Late-Onset Ataxia; CAPN1-related; SCA/LOA) 1 OMIA
- CARD9 Human homolog bridged
- CARMIL2 Human homolog bridged
- CAT Hypocatalasia 1 OMIA
- CCDC39 Primary Ciliary Dyskinesia (Discovered in the Old English Sheepdog; CCDC39-related PCD) 1 OMIA
- CCDC66 Early-onset PRA (Discovered in the Portuguese Water Dog; EOPRA) 1 OMIA
- CHAT Congenital Myasthenic Syndrome (Discovered in the Old Danish Pointer; CMS) 1 OMIA
- CHRNE Congenital Myasthenic Syndrome (Discovered in the Heideterrier; CHRNE-related; CMS) 1 OMIA
- CLCN1 Myotonia Congenita (Discovered in the Australian Cattle Dog) 1 OMIA
- CLN5 Neuronal Ceroid Lipofuscinosis 5 (Discovered in the Border Collie; NCL5) 1 OMIA
- CLN6 Human homolog bridged
- CLN8 Neuronal Ceroid Lipofuscinosis 8 (Discovered in the Australian Shepherd; NCL8) 1 OMIA
- CNGA1 Progressive Retinal Atrophy (Discovered in the Shetland Sheepdog; CNGA1-PRA) 1 OMIA
- CNGA3 Cone Degeneration (Discovered in the German Shepherd Dog; CNGA3-related) 1 OMIA
- CNGB1 Progressive Retinal Atrophy (Discovered in the Papillon and Phalène; CNGB1-related; PAP1_PRA) 1 OMIA
- CNGB3 Cone Degeneration (Discovered in the Alaskan Malamute) 1 OMIA
- CNP Human homolog bridged
- CNTNAP1 Human homolog bridged
- COL11A2 Skeletal Dysplasia 2 (SD2) 1 OMIA
- COL1A1 Human homolog bridged
- COL1A2 Osteogenesis Imperfecta (Discovered in the Beagle; COL1A2-related; OI) 1 OMIA
- COL4A4 Familial Nephropathy (Discovered in the English Cocker Spaniel; FN) 1 OMIA
- COL4A5 X-Linked Hereditary Nephropathy (Discovered in the Samoyed; XLHN) 1 OMIA
- COL5A1 Human homolog bridged
- COL5A2 Human homolog bridged
- COL6A1 Muscular Dystrophy, Ullrich Type (Discovered in the Landseer) 1 OMIA
- COL6A3 Human homolog bridged
- COL7A1 Dystrophic Epidermolysis Bullosa (Discovered in the Golden Retriever) 1 OMIA
- COL9A2 Oculoskeletal Dysplasia (OSD2) 1 OMIA
- COMMD1 Human homolog bridged
- CRHR1 Pituitary-Dependent Hyperadrenocorticism (Discovered in Poodles) 1 OMIA
- CTSD Human homolog bridged
- CUBN Intestinal Cobalamin Malabsorption (Discovered in the Border Collie; CUBN-related) 1 OMIA
- CYB5R3 Human homolog bridged
- CYP1A2 Human homolog bridged
- CYP27B1 Human homolog bridged
- CYTB Human homolog bridged
- DIRAS1 Juvenile Myoclonic Epilepsy (Discovered in the Rhodesian Ridgeback; JME) 1 OMIA
- DLX6 Cleft Palate (DLX6-related) 1 OMIA
- DMD Muscular Dystrophy (Discovered in the Golden Retriever) 1 OMIA
- DNM1 Exercise-Induced Collapse (EIC) 1 OMIA
- DNM2 Human homolog bridged
- DSG1 Human homolog bridged
- DVL2 Human homolog bridged
- EDA X-Linked Ectodermal Dysplasia (XHED) 1 OMIA
- EFNB3 Human homolog bridged
- EMC1 Human homolog bridged
- ENAM Amelogenesis Imperfecta (Discovered in the Parson Russell Terrier; AI) 1 OMIA
- EXT2 Osteochondromatosis (Discovered in the American Staffordshire Terrier) 1 OMIA
- F11 Factor XI Deficiency 1 OMIA
- F7 Factor VII Deficiency 1 OMIA
- F8 Hemophilia A (Discovered in the German Shepherd Dog; F8 p.C548Y) 1 OMIA
- F9 Hemophilia B (Discovered in the Lhasa Apso) 1 OMIA
- FAM134B Sensory Neuropathy (Discovered in the Border Collie) 1 OMIA
- FAM161A Progressive Retinal Atrophy, Type III (Discovered in the Tibetan Spaniel and Tibetan Terrier; PRA type III; FAM161A-related) 1 OMIA
- FAM20C Dental Hypomineralisation (Discovered in the Border Collie) 1 OMIA
- FAM83G Hereditary Footpad Hyperkeratosis (Discovered in the Irish Terrier and Kromfohrländer) 1 OMIA
- FAM83H Human homolog bridged
- FAN1 Fanconi Syndrome 1 OMIA
- FAS Human homolog bridged
- FERMT3 Canine Leukocyte Adhesion Deficiency (CLAD), Type III 1 OMIA
- FGA Human homolog bridged
- FGF4 Chondrodystrophy and Intervertebral Disc Disease Risk (CDDY) 1 OMIA
- FGF4 RETROGENE ON CFA12 Human homolog bridged
- FLCN Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND) 1 OMIA
- FNIP2 Hypomyelination (Discovered in the Weimaraner) 1 OMIA
- FOXI3 Human homolog bridged
- FUCA1 Human homolog bridged
- FYCO1 Human homolog bridged
- G6PC Glycogen Storage Disease, Type Ia (GSD Ia) 1 OMIA
- GAA Human homolog bridged
- GALC Globoid Cell Leukodystrophy (Discovered in Terriers) 1 OMIA
- GATM Human homolog bridged
- GDNF Acral Mutilation Syndrome (AMS) 1 OMIA
- GFAP Alexander Disease (Discovered in the Labrador Retriever) 1 OMIA
- GJA9 Leonberger Polyneuropathy, Type 2 (LPN2) 1 OMIA
- GLB1 GM1 Gangliosidosis (Discovered in the Shiba) 1 OMIA
- GLRA1 Human homolog bridged
- GNAS Human homolog bridged
- GP9 Bernard-Soulier Syndrome (Discovered in the Cocker Spaniel) 1 OMIA
- GPR22 Human homolog bridged
- GRM1 Bandera's Neonatal Ataxia (BNAt) 1 OMIA
- GTPBP2 Human homolog bridged
- GUCY2D Human homolog bridged
- GUSB Mucopolysaccharidosis, Type VII (Discovered in the German Shepherd Dog; MPS VII) 1 OMIA
- HACD1 Centronuclear Myopathy (Discovered in the Labrador Retriever; HACD1-related; CNM) 1 OMIA
- HACE1 Human homolog bridged
- HAS2 Human homolog bridged
- HCRTR2 Narcolepsy (Discovered in the Labrador Retriever) 1 OMIA
- HES7 Spondylocostal Dysostosis (Discovered in the Miniature Schnauzer) 1 OMIA
- HEXA GM2 Gangliosidosis (Discovered in the Japanese Chin) 1 OMIA
- HEXB GM2 Gangliosidosis (Discovered in the Toy Poodle) 1 OMIA
- HSD17B3 Human homolog bridged
- HSF4 Human homolog bridged
- IFT122 Progressive Retinal Atrophy (Discovered in the Lapponian Herder; IFT122-PRA) 1 OMIA
- IGFBP5 Bald Thigh Syndrome (Discovered in Sighthounds) 1 OMIA
- IL2RG X-Linked Severe Combined Immunodeficiency (Discovered in the Basset Hound; XSCID) 1 OMIA
- IMPG2 Progressive Retinal Atrophy (Discovered in the Lhasa Apso; IMPG2-related PRA4) 1 OMIA
- INPP5E Cystic Renal Dysplasia and Hepatic Fibrosis (Discovered in the Norwich Terrier) 1 OMIA
- IQCB1 Cone-Rod Dystrophy 2 (Discovered in the Pit Bull Terrier; crd2) 1 OMIA
- ITGA10 Chondrodysplasia, Disproportionate Short-limbed (Discovered in the Norwegian Elkhound; ITGA10-related) 1 OMIA
- ITGA2B Glanzmann Thrombasthenia, Type I (Discovered in the Great Pyrenees) 1 OMIA
- ITPR1 Human homolog bridged
- ITPR3 Human homolog bridged
- JAK2 Human homolog bridged
- KCNIP4 Hereditary Ataxia (Discovered in the Norwegian Buhund; KCNIP4-related) 1 OMIA
- KCNJ10 Spinocerebellar Ataxia with Myokymia and/or Seizures (KCNJ10-related; SCA) 1 OMIA
- KCNQ1 Human homolog bridged
- KIT Human homolog bridged
- KITLG Human homolog bridged
- KLF7 Human homolog bridged
- KLKB1 Prekallikrein Deficiency 1 OMIA
- KRT1 Human homolog bridged
- KRT10 Epidermolytic Hyperkeratosis (Discovered in the Norfolk Terrier) 1 OMIA
- KRT16 Focal Non-Epidermolytic Palmoplantar Keratoderma (Discovered in the Dogue de Bordeaux) 1 OMIA
- L2HGDH L-2-Hydroxyglutaric Aciduria (Discovered in the Staffordshire Bull Terrier) 1 OMIA
- LAMA3 Human homolog bridged
- LAMB3 Human homolog bridged
- LAMP3 Lung Developmental Disease (Discovered in the Airedale Terrier) 1 OMIA
- LARGE Human homolog bridged
- LGI2 Benign Familial Juvenile Epilepsy (Discovered in the Lagotto Romagnolo; BFJE) 1 OMIA
- LHX3 Human homolog bridged
- LMBR1L Human homolog bridged
- LMNA Human homolog bridged
- LOC489707 Human homolog bridged
- LOC608697 Congenital Myasthenic Syndrome (Discovered in the Labrador Retriever) 1 OMIA
- LOXHD1 Nonsyndromic hearing loss (Discovered in the Rottweiler) 1 OMIA
- LRIT3 Human homolog bridged
- MAN2B1 Human homolog bridged
- MANBA Human homolog bridged
- MC5R Human homolog bridged
- MCHR2 Human homolog bridged
- MECR Human homolog bridged
- MERTK Progressive Retinal Atrophy (Discovered in the Swedish Vallhund; MERTK-related) 1 OMIA
- MFN2 Fetal Onset Neuroaxonal Dystrophy (FNAD) 1 OMIA
- MFSD8 Neuronal Ceroid Lipofuscinosis 7 (Discovered in the Chinese Crested Dog and Chihuahua; NCL7) 1 OMIA
- MITF Human homolog bridged
- MKLN1 Lethal Acrodermatitis (Discovered in the Bull Terrier; LAD) 1 OMIA
- MOCOS Xanthinuria, Type II (Discovered in the Cavalier King Charles Spaniel) 1 OMIA
- MPO Myeloperoxidase Deficiency (Discovered in the Italian Hound) 1 OMIA
- MPZ Human homolog bridged
- MSTN Muscular Hypertrophy (Double Muscling) 1 OMIA
- MTBP Shar-Pei Autoinflammatory Disease (SPAID) 1 OMIA
- MTM1 Myotubular Myopathy (Discovered in the Rottweiler) 1 OMIA
- MTMR2 Human homolog bridged
- MYH9 May-Hegglin Anomaly (MHA) 1 OMIA
- MYO5A Human homolog bridged
- MYO7A Deafness and Vestibular Dysfunction (Discovered in the Doberman Pinscher) 1 OMIA
- NAGLU Human homolog bridged
- NDP Human homolog bridged
- NDRG1 Early-Onset Progressive Polyneuropathy (Discovered in the Greyhound) 1 OMIA
- NDUFS7 Human homolog bridged
- NEB Nemaline Myopathy (Discovered in the American Bulldog; NEB-related) 1 OMIA
- NECAP1 Progressive Retinal Atrophy (Discovered in the Giant Schnauzer; NECAP1-related) 1 OMIA
- NHEJ1 Collie Eye Anomaly (CEA) 1 OMIA
- NHLRC1 Human homolog bridged
- NIPAL4 Ichthyosis (Discovered in the American Bulldog; NIPAL4-related) 1 OMIA
- NKX2-8 Human homolog bridged
- NME5 Primary Ciliary Dyskinesia (Discovered in the Alaskan Malamute; NME5-related; PCD) 1 OMIA
- NPHP4 Cone-Rod Dystrophy (Discovered in the Standard Wirehaired Dachshund; crd SWD) 1 OMIA
- NPHS1 Protein Losing Nephropathy (PLN; NPHS1-related) 1 OMIA
- NR3C1 Human homolog bridged
- NSDHL Congenital Cornification Disorder (Discovered in the Chihuahua) 1 OMIA
- OCA2 Human homolog bridged
- P2RY12 Bleeding disorder (Discovered in the Greater Swiss Mountain Dog; P2RY12-related) 1 OMIA
- P3H2 Human homolog bridged
- PCYT1A Human homolog bridged
- PCYT2 Human homolog bridged
- PDE6A Rod-Cone Dysplasia 3 (Discovered in the Cardigan Welsh Corgi; rcd3) 1 OMIA
- PDE6B Rod-Cone Dysplasia 1 (Discovered in the Irish Setter; rcd1) 3 OMIA
- PDGFRA Human homolog bridged
- PDK4 Dilated Cardiomyopathy risk factor (Discovered in the Doberman Pinscher; PDK4-related) 1 OMIA
- PDP1 Pyruvate Dehydrogenase Phosphatase 1 (PDP1) Deficiency 1 OMIA
- PFKM Glycogen storage disease VII (GSD VII) or Phosphofructokinase (PFK) Deficiency 1 OMIA
- PIGN Paroxysmal Dyskinesia (Discovered in the Irish Soft Coated Wheaten Terrier; PIGN-related; PxD) 1 OMIA
- PITRM1 Juvenile Encephalopathy (Discovered in the Parson Russell Terrier) 1 OMIA
- PKD1 Polycystic Kidney Disease (Discovered in the Bull Terrier) 1 OMIA
- PKLR Pyruvate Kinase (PK) Deficiency (Discovered in the Beagle) 1 OMIA
- PKP1 Human homolog bridged
- PLA2G6 Neuroaxonal Dystrophy (Discovered in the Papillon; PLA2G6-related; NAD) 1 OMIA
- PLEC Human homolog bridged
- PLG Ligneous Membranitis (Discovered in the Scottish Terrier) 1 OMIA
- PLP1 X-Linked Tremors (Discovered in the English Springer Spaniel) 1 OMIA
- PMEL Human homolog bridged
- PNPLA1 Ichthyosis (Discovered in the Golden Retriever) 1 OMIA
- PNPLA8 Human homolog bridged
- POMC Human homolog bridged
- POU1F1 Pituitary Dwarfism (Discovered in the Karelian Bear Dog; POU1F1-related) 1 OMIA
- PPT1 Neuronal Ceroid Lipofuscinosis 1 (Discovered in the Dachshund; NCL1) 1 OMIA
- PRCD Progressive Rod-Cone Degeneration (prcd-PRA) 1 OMIA
- PRKDC Autosomal Recessive Severe Combined Immunodeficiency (ARSCID) 1 OMIA
- PTEN Human homolog bridged
- PTPRQ Deafness and Vestibular Dysfunction (Discovered in the Doberman Pinscher; PTPRQ-related) 1 OMIA
- RAB24 Cerebellar Ataxia (Discovered in the Old English Sheepdog and the Gordon Setter) 1 OMIA
- RAB3GAP1 Polyneuropathy with Ocular Abnormalities and Neuronal Vacuolation (Discovered in the Black Russian Terrier and Rottweiler; POANV) 1 OMIA
- RAG1 Severe Combined Immunodeficiency (Discovered in the Frisian Water Dog) 1 OMIA
- RALGAPA1 Human homolog bridged
- RASGRP2 Thrombopathia (Discovered in the Eskimo Spitz) 1 OMIA
- RB1CC1 Human homolog bridged
- RBCK1 Human homolog bridged
- RBM20 Dilated Cardiomyopathy (Discovered in the Schnauzer; DCM) 1 OMIA
- RBP4 Microphthalmia (Discovered in the Soft-Coated Wheaten Terrier) 1 OMIA
- RD3 Human homolog bridged
- RELN Human homolog bridged
- RETN Human homolog bridged
- RHO Dominant Progressive Retinal Atrophy (DPRA) 1 OMIA
- RNF170 Human homolog bridged
- RPE65 Congenital Stationary Night Blindness (Discovered in the the Briard; CSNB) 1 OMIA
- RPGR X-Linked Progressive Retinal Atrophy 1 (XLPRA1) 2 OMIA
- RPGRIP1 Cone-Rod Dystrophy (cord1-PRA/crd4) 1 OMIA
- SACS Human homolog bridged
- SAG Progressive Retinal Atrophy (Discovered in the Basenji; SAG-related) 1 OMIA
- SBF2 Demyelinating Polyneuropathy (Discovered in the Miniature Schnauzer; SBF2-related) 1 OMIA
- SCARF2 Van den Ende-Gupta Syndrome (VDEGS) 1 OMIA
- SCN8A Neuronal Ceroid Lipofuscinosis 8 (Discovered in the Alpine Dachsbracke; NCL8) 1 OMIA
- SCN9A Human homolog bridged
- SDR9C7 Human homolog bridged
- SEL1L Progressive Early-Onset Cerebellar Ataxia (Discovered in the Finnish Hound; SEL1L-related) 1 OMIA
- SEPP1 Human homolog bridged
- SERAC1 Canine Multiple Systems Degeneration (Discovered in the Chinese Crested Dog; CMSD) 1 OMIA
- SERPINE1 Human homolog bridged
- SERPINH1 Osteogenesis Imperfecta (Discovered in the Dachshund; OI) 1 OMIA
- SETX Human homolog bridged
- SGCA Human homolog bridged
- SGCD Limb-girdle Muscular Dystrophy, Type 2F (Discovered in the Boston Terrier) 1 OMIA
- SGK3 Human homolog bridged
- SGSH Mucopolysaccharidosis, Type IIIA (Discovered in the New Zealand Huntaway; MPS IIIA) 1 OMIA
- SH3TC2 Human homolog bridged
- SHH Human homolog bridged
- SIX6 Congenital Eye Malformation (Discovered in the Golden Retriever) 1 OMIA
- SLC12A6 Hereditary Ataxia (Discovered the in Belgian Malinois; SLC12A6-related) 1 OMIA
- SLC13A1 Osteochondrodysplasia (Discovered in the Miniature Poodle) 1 OMIA
- SLC19A3 Alaskan Husky Encephalopathy (AHE), Subacute Necrotising Encephalopathy 1 OMIA
- SLC25A12 Inflammatory Myopathy (Discovered in the Dutch Shepherd Dog; SLC25A12-related) 1 OMIA
- SLC27A4 Ichthyosis (Discovered in the Great Dane; SLC27A4-related) 1 OMIA
- SLC2A9 Hyperuricosuria (HUU) 1 OMIA
- SLC35D1 Craniomandibular Osteopathy (Discovered in the Weimaraner; CMO) 1 OMIA
- SLC37A2 Craniomandibular Osteopathy (Discovered in the Cairn, Scottish and West Highland White Terrier) 1 OMIA
- SLC3A1 Cystinuria Type I-A (SLC3A1 p.I192V) 2 OMIA
- SLC45A2 Human homolog bridged
- SLC4A3 Progressive Retinal Atrophy (Discovered in the Golden Retriever; GR_PRA1) 1 OMIA
- SLC5A5 Congenital Dyshormonogenic Hypothyroidism with Goiter (Discovered in the Shih Tzu) 1 OMIA
- SLC6A3 Human homolog bridged
- SLC6A5 Human homolog bridged
- SLC7A10 Human homolog bridged
- SLC7A9 Cystinuria Type I-B (SLC7A9 p.A217T) 1 OMIA
- SNX14 Cerebellar Cortical Degeneration (Discovered in the Vizsla; CCD) 1 OMIA
- SOD1 Degenerative Myelopathy (DM) 1 OMIA
- SPATA7 Human homolog bridged
- SPTB Hereditary Elliptocytosis 1 OMIA
- SPTBN2 Neonatal Cerebellar Cortical Degeneration (SPTBN2-related; NCCD) 1 OMIA
- STK36 Human homolog bridged
- STK38L Early Retinal Degeneration (Discovered in the Norwegian Elkhound; erd) 1 OMIA
- SUV39H2 Hereditary Nasal Parakeratosis (Discovered in the Labrador Retriever; HNPK) 1 OMIA
- TECPR2 Neuroaxonal Dystrophy (Discovered in the Spanish Water Dog; NAD) 1 OMIA
- TG Human homolog bridged
- TGM1 Lamellar Ichthyosis (LI) 1 OMIA
- TNR Human homolog bridged
- TNXB Ehlers-Danlos Syndrome (Discovered in the Chihuahua and Poodle) 1 OMIA
- TPO Congenital Hypothyroidism (Discovered in the Toy Fox and Rat Terrier) 1 OMIA
- TPP1 Human homolog bridged
- TSEN54 Human homolog bridged
- TTC8 Progressive Retinal Atrophy (Discovered in the Golden Retriever; GR_PRA2) 1 OMIA
- TTN Dilated Cardiomyopathy risk factor (Discovered in the Doberman Pinscher; PDK4-related) 1 OMIA
- TTPA Human homolog bridged
- TUBB1 Macrothrombocytopenia (Discovered in the Norfolk and Cairn Terrier) 1 OMIA
- TYR Human homolog bridged
- TYRP1 Human homolog bridged
- UNC93B1 Human homolog bridged
- USH2A Human homolog bridged
- VDR Hereditary Vitamin D-Resistant Rickets Type II 1 OMIA
- VLDLR Dandy-Walker-Like Malformation (Discovered in the Eurasier; DWLM) 1 OMIA
- VPS11 Neuroaxonal Dystrophy (Discovered in the Rottweiler; VPS11-related) 1 OMIA
- VPS13B Trapped Neutrophil Syndrome (TNS) 1 OMIA
- VWF Von Willebrand's Disease, Type 1 (vWD 1) 3 OMIA
- XDH Xanthinuria, Type 1 (Discovered in mixed breed dogs) 1 OMIA
- YARS2 Human homolog bridged