1. Gene
  2. SMO - smoothened, frizzled class receptor Gene

SMO - smoothened, frizzled class receptor Gene

Homo sapiens

Also known as Gx; CRJS; PHLS; SMOH; FZD11

Gene ID: 6608 | Gene type: protein coding

About SMO

Cytogenetic location: 7q32.1 Genomic coordinates (GRCh38): 7:129,188,633-129,213,545 (from NCBI)

This gene has 5 transcripts (splice variants), 204 orthologues, 15 paralogues and is associated with 118 phenotypes. Broad expression in ovary (RPKM 15.6), endometrium (RPKM 13.9) and 24 other tissues.

Summary

The protein encoded by this gene is a G protein-coupled receptor that interacts with the patched protein, a receptor for Hedgehog proteins. The encoded protein tranduces signals to other proteins after activation by a Hedgehog protein/patched protein complex. [provided by RefSeq, Jul 2010]

SMO Products(2)

mRNA Protein Name
NM_005631.5 NP_005622.1 smoothened homolog precursor
XM_047420759.1 XP_047276715.1 smoothened homolog isoform X1

SMO Protein Structure

Fz

Fz: Fz domain (70 - 176)

Frizzled

Frizzled: Frizzled/Smoothened family membrane region (220 - 554)

  • 0
  • 200
  • 400
  • 600
  • 787 a.a.
Protein Preferred Names Protein Names

smoothened homolog

frizzled family member 11

protein Gx

seven transmembrane helix receptor

smoothened, frizzled family receptor

smoothened, seven transmembrane spanning receptor

Related Diseases

Diseases Alias
Joubert Syndrome 32

JBTS32

Skull Base Meningioma

Meningioma Of The Skull Base

Medullomyoblastoma
Brain Meningioma

Intracranial Meningioma

Hirschsprung Disease 1

Hirschsprung Disease

Aganglionic Megacolon

Hscr

Congenital Megacolon

Colonic Aganglionosis

Hirschsprung Disease, Susceptibility To, 1

Hirschsprung Disease, Protection Against

Hirschsprung'S Disease

Congenital Intestinal Aganglionosis

HSCR1

Mgc

Pelvirectal Achalasia

Total Intestinal Aganglionosis

Megacolon, Aganglionic

Macrocolon

Hscr 1

Hirschsprung Disease Type 1

Hirschsprung Disease, Type 1

Congenital Dilatation Of Colon

Aganglionosis

Congenital Aganglionic Megacolon

Aganglionosis Of Colon

Bowel Aganglionosis

Colon Aganglionosis

Hirschsprung Megacolon

Pallister-Hall Syndrome

PHS

Hypothalamic Hamartomas

Hypothalamic Hamartoblastoma, Hypopituitarism, Imperforate Anus, And Postaxial Polydactyly

Hypothalamic Hamartoblastoma Syndrome

Hamartoma Of The Hypothalamus

Pallister Hall Syndrome

Hall-Pallister Syndrome

Hypothalamic Hamartoblastoma Hypopituitarism Imperforate Anus And Postaxial Polydactyly

Hamartoma, Hypothalamic

Holoprosencephaly

Holoprosencephaly Sequence

Hpe

Hpe - [Holoprosencephaly]

Alkaptonuria

Homogentisic Acid Oxidase Deficiency

Alcaptonuria

AKU

Deficiency Of Homogentisicase

Homogentisate 1,2-Dioxygenase Deficiency

Alkaptonuric Ochronosis

Homogentisic Acidura

Ochronosis, Hereditary

Hereditary Ochronosis

Ochronosis

Homogentisicaciduria

Deficiency Of Homogentisate Oxygenase

Cerebral Meningioma

Meningioma Of Cerebrum

Ameloblastoma

Adenoameloblastoma

Pallister-Hall-Like Syndrome

Hamartoma Of Hypothalamus

PHLS

Hypothalamic Hamartomas

Meningioma, Familial

Meningioma

Familial Meningioma

Meningioma, Familial, Susceptibility To

Meningeal Neoplasm

Meningeal Neoplasms

Meningiomas

Meningioma, Nf2-Related, Somatic

Meningioma, Sis-Related

Meningothelial Cell Tumor

Neoplasm Of The Meninges

Primary Meningeal Tumor

Familial Multiple Meningioma

MNGMA

Meningioma, Benign, No Icd-O Subtype

Intracranial Meningioma

Meningothelial Cell Neoplasm

Supratentorial Meningioma

Primary Neoplasm Of Spinal Meninges

Benign Intracranial Meningioma

Benign Meningioma

Meningeal Tumours

Meningeal Sarcoma Of Unspecified Site

Meningothelial Sarcoma Of Unspecified Site

Holoprosencephaly 7

HPE7

Holoprosencephaly-7

Holoprosencephaly, Type 7

Basal Cell Nevus Syndrome

Nevoid Basal Cell Carcinoma Syndrome

Gorlin Syndrome

Nbccs

BCNS

Gorlin-Goltz Syndrome

Multiple Basal Cell Nevi, Odontogenic Keratocysts, And Skeletal Anomalies

Cerebral Gigantism Jaw Cysts

Cramer Niederdellmann Syndrome

Gorlin Syndrome Or Gorlin-Goltz Syndrome

Naevoid Basal Cell Carcinoma Syndrome

Hydrolethalus Syndrome 2

HLS2

Hydrolethalus Syndrome, Type 2

Curry-Jones Syndrome

Craniofacial Malformations, Asymmetric, With Polysyndactyly And Abnormal Skin And Gut Development

CRJS

Curry-Jones Syndrome, Somatic Mosaic

Curry Jones Syndrome

Corpus Callosum Agenesis Polysyndactyly

Corpus Callosum Agenesis-Polysyndactyly Syndrome

Winter Shortland Temple Syndrome

Basal Cell Carcinoma

Basal Cell Cancer

Basal Cell Neoplasm

Basal Cell Carcinoma Of Skin

Malignant Basal Cell Tumor

Basal Cell Tumor

Epithelioma Basal Cell

Malignant Basal Cell Neoplasm

Rodent Ulcer

Carcinoma Basal Cell

Neoplasms, Basal Cell

Basal Cell Carcinomas

Experimental Organism Basal Cell Carcinoma

Nodulo-Ulcerative Basal Cell Carcinoma

Basalioma

Basal Cell Epithelioma Of Skin

Bcc - [Basal Cell Carcinoma] Of Skin

Rodent Ulcer Of Skin

Rodent Ulcer Of Unspecified Site

Basal Cell Epithelioma Of Unspecified Site

Lung Cancer

Lung Carcinoma

Non-Small Cell Lung Carcinoma

Lung Cancer, Protection Against

Lung Cancer, Susceptibility To

Adenocarcinoma Of Lung, Somatic

Nonsmall Cell Lung Cancer

Adenocarcinoma Of Lung, Response To Tyrosine Kinase Inhibitor In

Lung Neoplasm

Carcinoma Of Lung

Lung Non-Small Cell Carcinoma

Non-Small Cell Lung Cancer

Nsclc

Lung Neoplasms

Malignant Neoplasm Of Lung

Alveolar Cell Carcinoma

Nonsmall Cell Lung Cancer, Somatic

Nonsmall Cell Lung Cancer, Response To Tyrosine Kinase Inhibitor In

Nonsmall Cell Lung Cancer, Susceptibility To

Lung Cancer, Somatic

Lung Cancer, Resistance To

Cancer Of Lung

Cancer Of Bronchus

Cancer Of The Lung

Lung Malignancies

Lung Malignant Tumors

Malignant Lung Tumor

Malignant Tumor Of Lung

Pulmonary Cancer

Pulmonary Carcinoma

Pulmonary Neoplasms

Respiratory Carcinoma

LNCR

Adenocarcinoma Of Lung

Neoplasm Of Lung

Cancer Lung

Carcinoma Non-Small Cell Lung

Carcinoma, Non-Small-Cell Lung

Lung Cancers

Lung Carcinomas

Cancer, Lung

Cancer, Lung, Non-Small Cell

Primary Malignant Neoplasm Of Lung

Bronchioloalveolar Adenocarcinoma

Craniosynostosis

Premature Closure Of Cranial Sutures

Craniostenosis

Craniosynostosis Syndrome

Cso

Craniosynostoses

Congenital Ossification Of Cranial Sutures

Congenital Ossification Of Sutures Of Skull

Craniostosis

Imperfect Fusion Of Skull

Congenital Imperfect Closure Skull

Imperfect Closure Skull

Premature Closure Cranium Sutures

Deficiency Of Craniofacial Axis

Medulloblastoma

MDB

Cpnet

Localized Primitive Neuroectodermal Tumor

Classic Medulloblastoma

Desmoplastic/Nodular Medulloblastoma

Medulloblastoma With Extensive Nodularity

Desmoplastic Medulloblastoma

Medulloblastoma, Somatic

Medulloblastoma, Desmoplastic

Brain Medulloblastoma

Cns Pnet

Infratentorial Primitive Neuroectodermal Tumor

Mben

Medulloblastoma Desmoplastic

Neuroectodermal Tumors, Primitive

Medulloblastomas

Medulloblastoma, With Extensive Nodularity

Medulloblastoma Of Unspecified Site

Medullomyoblastoma Of Unspecified Site

Basal Cell Carcinoma 1

Basal Cell Carcinoma, Susceptibility To, 1

Basal Cell Carcinoma

BCC1

BCC

Multiple Basal Cell Carcinoma

Non-Syndromic Basal Cell Carcinoma

Carcinoma, Basal Cell, Susceptibility To, Type 1

Experimental Organism Basal Cell Carcinoma

Basal Cell Carcinoma, Multiple

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Canis familiaris SMO VGNC VGNC:46565
Mus musculus SMO MGD MGI:108075
Felis catus SMO VGNC VGNC:80721
Bos taurus SMO VGNC VGNC:35025
Rattus norvegicus SMO RGD RGD:3726
Macaca mulatta SMO VGNC VGNC:77658
Others SMO NCBI