1. Gene
  2. ERAS - ES cell expressed Ras Gene

ERAS - ES cell expressed Ras Gene

Homo sapiens

Also known as HRAS2; HRASP

Gene ID: 3266 | Gene type: protein coding

About ERAS

Cytogenetic location: Xp11.23 Genomic coordinates (GRCh38): X:48,826,513-48,829,869 (from NCBI)

This gene has 2 transcripts (splice variants), 72 orthologues and 35 paralogues. Low expression observed in reference dataset.

Summary

This gene encodes a constitutively active member of the small GTPase Ras protein family. The encoded protein activates the phosphatidylinositol 3-kinase signal transduction pathway in undifferentiated stem cells, but is not expressed in differentiated cells. This gene may be involved in Cancer and chemotherapy resistance. [provided by RefSeq, Dec 2012]

ERAS Products(1)

mRNA Protein Name
NM_181532.3 NP_853510.1 GTPase ERas precursor

ERAS Protein Structure

Ras

Ras: Ras family (43 - 200)

  • 0
  • 100
  • 200
  • 233 a.a.
Protein Preferred Names Protein Names

GTPase ERas

E-Ras

Related Diseases

Diseases Alias
Immunodeficiency 54

Natural Killer Cell Deficiency, Familial Isolated

Primary Immunodeficiency With Natural-Killer Cell Deficiency And Adrenal Insufficiency

IMD54

Nkcd

Natural Killer Cell And Glucocorticoid Deficiency With Dna Repair Defect

Nkgcd

Familial Isolated Natural Killer Cell Deficiency

Primary Immunodeficiency Due To Mcm4 Deficiency

Loose Anagen Hair Syndrome

Loose Anagen Syndrome

LAHS

Posterior Pituitary Gland Neoplasm

Posterior Pituitary Tumor

Neoplasm Of The Posterior Pituitary

Sarcoma

Connective And Soft Tissue Neoplasm

Tumor Of Soft Tissue And Skeleton

Sarcomas

Sarcoma - Category

Eccrine Papillary Adenocarcinoma

Digital Papillary Adenocarcinoma

Sweat Gland Adenocarcinoma

Digital Papillary Eccrine Carcinoma Of Skin

Apocrine Adenoma

Tubular Apocrine Adenoma

Eccrine Adenocarcinoma
Anorectal Stricture

Stenosis Of Rectum And Anus

Anorectal Malformations

Syringocystadenoma Papilliferum

Fistulous Vegetative Verrucous Hydradenoma

Papillary Syringadenoma

Naevus Syringocystadenomatosus Papilliferus

Papillary Syringocystadenoma

Scap

Syringadenoma Papilliferum

Papillary Hidradenoma

Spleen Angiosarcoma

Angiosarcoma Of Spleen

Splenic Hemangiosarcoma

Noonan Syndrome-Like Disorder With Loose Anagen Hair

Noonan-Like Syndrome With Loose Anagen Hair

Mazzanti Syndrome

Ns/Lah

Nevus, Epidermal

Epidermal Nevus

Woolly Hair Nevus

Epidermal Naevus

Epidermal Nevus Syndrome

Nevus, Keratinocytic, Nonepidermolytic

Epidermal Nevus, Somatic

Nevus, Epidermal, Somatic

Nevus Sebaceous Or Woolly Hair Nevus, Somatic

Nonepidermolytic Keratinocytic Nevus

Epidermal Hamartoma Syndrome

Wooly Hair Nevus

Keratinocytic Non-Epidermolytic Nevus

KNEN

Pigmented Moles

Organoid Nevus Phakomatosis

Nevus Sebaceous

Melanocytic Nevus

Melanocytic Nevus Of Skin

Costello Syndrome

Faciocutaneoskeletal Syndrome

Fcs Syndrome

Congenital Myopathy With Excess Of Muscle Spindles

CSTLO

CMEMS

Fcss

Myopathy, Congenital, With Excess Of Muscle Spindles

Familial Isolated Trichomegaly

Long Eyelashes

Tcmgly

Mongolian Spot

Mongolian Macula

Brain Compression

Compression Of Brain

Rasopathy

Ras/Mitogen-Activated Protein Kinase Syndrome

Schimmelpenning-Feuerstein-Mims Syndrome

Nevus Sebaceus Of Jadassohn

Organoid Nevus Phakomatosis

Linear Nevus Sebaceous Syndrome

Sfm Syndrome

Jadassohn Nevus Phakomatosis

Jnp

Schimmelpenning Syndrome

Solomon Syndrome

SFM

Linear Sebaceous Nevus Syndrome

Schimmelpenning-Feuerstein-Mims Syndrome, Somatic Mosaic

Nevus Sebaceus Syndrome

Organoid Nevus Syndrome

Schimmelpenning Feuerstein Mims Syndrome

Sebaceous Nevus Syndrome, Linear

Epidermal Nevus Syndrome, Formerly

Sebaceous Nevus Syndrome Linear

Linear Nevus Sebaceus Syndrome

Epidermal Nevus Syndrome

Ss

Nevus Sebaceous

Cardiofaciocutaneous Syndrome 1

Cardiofaciocutaneous Syndrome

Cfc Syndrome

Cardio-Facio-Cutaneous Syndrome

CFC1

Cfcs

Cardio-Facial-Cutaneous Syndrome

Congenital Heart Defects Characteristic Facial Appearance Ectodermal Abnormalities And Growth Failure

Cardiofaciocutaneous Syndrome, Type 1

Noonan Syndrome 1

Noonan Syndrome

NS1

Male Turner Syndrome

Female Pseudo-Turner Syndrome

Turner Phenotype With Normal Karyotype

Noonan Syndrome With Pigmented Villonodular Synovitis

Turner'S Phenotype, Karyotype Normal

Familial Turner Syndrome

Noonan'S Syndrome

Noonan-Ehmke Syndrome

Ns

Pseudo-Ullrich-Turner Syndrome

Turner Syndrome In Female With X Chromosome

Turner-Like Syndrome

Ullrich-Noonan Syndrome

Noonan-Like/Multiple Giant Cell Lesion Syndrome

Noonan Syndrome-Like Disorder With Multiple Giant Cell Lesions

Pterygium Colli Syndrome

Noonan Syndrome, Type 1

Turner Syndrome, Male

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
Rattus norvegicus ERAS RGD RGD:1585907
Bos taurus ERAS VGNC VGNC:28562
Mus musculus ERAS MGD MGI:2665023
Macaca mulatta ERAS VGNC VGNC:72256
Canis familiaris ERAS VGNC VGNC:40435
Macaca fascicularis ERAS NCBI
Others ERAS NCBI