Yeast Systematic Name | Yeast Symbol | SGDID | Analog Name | Analog Description | EC | Organism | Disease | Structure | Uniprot | Human ID | Human Symbol | HHsearch Probability | HHsearch E_value | HHsearch P_value | HHsearch Score | Flag Disease related | Flag Homo sapiens | Flag Mus musculus | Flag Danio rerio | Flag Drosophila melanogaster | Flag Caenorhabditis elegans | Flag Arabidopsis thaliana | Flag Escherichia coli |
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YPL006W | NCR1 | SGDID:S000005927 | PTCH1 PTCH |
Protein patched homolog 1 (PTC) (PTC1) |
Homo sapiens | Heart Disease,Physical Disorder,Small Intestine Leiomyoma,Spina Bifida Occulta,Squamous Cell Carcinoma,Retinitis Pigmentosa,Thyroid Gland Cancer,Cerebellum Cancer,Chromosome 9q Deletion,Metatypical Basal Cell Carcinoma,Micronodular Basal Cell Carcinoma,Fibroepithelial Basal Cell Carcinoma,Clear Cell Basal Cell Carcinoma,Follicular Basal Cell Carcinoma,Cystic Basal Cell Carcinoma,Microform Holoprosencephaly,Septopreoptic Holoprosencephaly,Thyroid Gland Anaplastic Carcinoma,Tinea Capitis,Congenital Hydrocephalus,Benign Teratoma,B-Lymphoblastic Leukemia/Lymphoma,Internal Auditory Canal Lipoma,Skin Tag,Holoprosencephaly,Infratentorial Cancer,Semilobar Holoprosencephaly,Overgrowth Syndrome,Keratocystic Odontogenic Tumor,Midline Interhemispheric Variant Of Holoprosencephaly,Lobar Holoprosencephaly,Alobar Holoprosencephaly,Precocious Puberty,Testicular Thecoma,Neuroblastoma,Multiple Endocrine Neoplasia, Type Iib,Inherited Cancer-Predisposing Syndrome,Leiomyoma,Congenital Nervous System Abnormality,Basal Cell Carcinoma,Colobomatous Microphthalmia,Basosquamous Carcinoma,Schilbach-Rott Syndrome,Basal Cell Nevus Syndrome,Benign Struma Ovarii,Monosomy 9q22.3,Ovary Leiomyosarcoma,Brain Cancer,Brachydactyly, Type A1,Laryngeal Neuroendocrine Tumor,Microphthalmia,Hepatocellular Carcinoma,9q22.3 Microdeletion,Skin Benign Neoplasm,Ellis-Van Creveld Syndrome,Microcephaly,Fraser Syndrome 3,Hydrocephalus,Basal Cell Carcinoma, Multiple,Basaloid Follicular Hamartoma,Embryonal Rhabdomyosarcoma,Rhabdomyosarcoma,Calcifying Epithelial Odontogenic Tumor,Germinoma,Holoprosencephaly 5,Polydactyly, Postaxial, Type A1,Polydactyly, Preaxial Ii,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A,Greig Cephalopolysyndactyly Syndrome,Cleft Palate, Isolated,Axenfeld-Rieger Syndrome,Skin Carcinoma,Coloboma Of Macula,Gastric Cancer,Polydactyly,West Syndrome,Contractures, Pterygia, And Spondylocarpotarsal Fusion Syndrome 1a,Central Nervous System Cancer,Anterior Segment Dysgenesis 5,Integumentary System Disease,Skin Disease,Holoprosencephaly, Recurrent Infections, And Monocytosis,Craniopharyngioma,Basal Cell Carcinoma, Infundibulocystic,Adult Medulloblastoma,Melanotic Medulloblastoma,Childhood Medulloblastoma,Nodular Medulloblastoma,Holoprosencephaly 7,Holoprosencephaly 9,Thyroid Gland Follicular Carcinoma,Skeletal Muscle Cancer,Muscle Cancer,Brooke-Spiegler Syndrome,Neural Tube Defects,Split-Foot Deformity With Mandibulofacial Dysostosis,Basal Cell Carcinoma 1,Multiple Self-Healing Squamous Epithelioma,Orofacial Cleft,Brachydactyly,Chromosome 2q35 Duplication Syndrome,Birt-Hogg-Dube Syndrome,Holoprosencephaly 11,Tumor Predisposition Syndrome,Hashimoto Thyroiditis,Hirschsprung Disease 1,Fibroma,Brachydactyly, Type A1, B,Ameloblastoma,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Meckel Syndrome, Type 1,Meningioma, Familial,Focal Dermal Hypoplasia,Pallister-Hall Syndrome,Joubert Syndrome 24,Solitary Median Maxillary Central Incisor,Cerebellar Medulloblastoma,Connective Tissue Benign Neoplasm,Hereditary Leiomyomatosis And Renal Cell Cancer,Li-Fraumeni Syndrome,Medulloblastoma,Nivelon-Nivelon-Mabille Syndrome,Tumoral Calcinosis, Hyperphosphatemic, Familial, 1,Joubert Syndrome 1,Pancreatic Cancer,Peters-Plus Syndrome |
6e1h_b | Q13635 | ENSG00000185920 | PTCH1 | 100.00 | 8.30E-60 | 5.80E-64 | 618.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YPL006W | NCR1 | SGDID:S000005927 | NPC1_N |
Niemann-Pick C1 N terminus |
pfam Domain | PF16414 | 100.00 | 2.70E-59 | 1.90E-63 | 486.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |