Sox11 (SRY (sex determining region Y)-box 11) - Rat Genome Database

Send us a Message

Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Gene: Sox11 (SRY (sex determining region Y)-box 11) Mus musculus
Symbol: Sox11
Name: SRY (sex determining region Y)-box 11
RGD ID: 735735
Description: Exhibits DNA-binding transcription activator activity, RNA polymerase II-specific and cis-regulatory region sequence-specific DNA binding activity. Involved in several processes, including animal organ development; nervous system development; and regulation of gene expression. Localizes to nucleus. Is expressed in several structures, including alimentary system; brain; genitourinary system; limb; and sensory organ. Used to study Weissenbacher-Zweymuller syndrome. Human ortholog(s) of this gene implicated in Coffin-Siris syndrome 9. Orthologous to human SOX11 (SRY-box transcription factor 11); INTERACTS WITH 1,2-dichloroethane; 17beta-estradiol; 2,2',4,4',5,5'-hexachlorobiphenyl.
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: 1110038H03Rik; 6230403H02Rik; AI836553; end; end1; SRY-box containing gene 11; transcription factor SOX-11
RGD Orthologs
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Latest Assembly: GRCm38 - Mouse Genome Assembly GRCm38
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
GRCm391227,384,267 - 27,392,717 (-)NCBIGRCm39mm39
GRCm39 Ensembl1227,384,263 - 27,392,573 (-)Ensembl
GRCm381227,334,268 - 27,342,718 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1227,334,264 - 27,342,574 (-)EnsemblGRCm38mm10GRCm38
MGSCv371228,019,133 - 28,027,583 (-)NCBIGRCm37mm9NCBIm37
MGSCv361227,921,484 - 27,928,980 (-)NCBImm8
Celera1228,811,290 - 28,819,758 (-)NCBICelera
Cytogenetic Map12A2NCBI
JBrowse: View Region in Genome Browser (JBrowse)

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process
anatomical structure morphogenesis  (IBA)
cardiac ventricle formation  (IMP)
cell cycle checkpoint signaling  (ISO)
cell differentiation  (IBA)
cell population proliferation  (ISO)
closure of optic fissure  (IMP)
cornea development in camera-type eye  (IMP)
embryonic digestive tract morphogenesis  (IMP)
embryonic skeletal system morphogenesis  (IMP)
eyelid development in camera-type eye  (IMP)
glial cell development  (IMP)
glial cell proliferation  (IMP)
hard palate development  (IMP)
kidney development  (ISO)
lens morphogenesis in camera-type eye  (IMP)
limb bud formation  (IMP)
lung morphogenesis  (IMP)
multicellular organism development  (IEA)
negative regulation of cell death  (IMP)
negative regulation of gene expression  (IMP,ISO)
negative regulation of glial cell proliferation  (IMP,ISO)
negative regulation of lymphocyte proliferation  (ISO)
negative regulation of transcription by RNA polymerase II  (IBA,IDA,ISO)
negative regulation of transcription regulatory region DNA binding  (ISO)
nervous system development  (IEA)
neural crest cell development  (IMP)
neural tube formation  (IMP)
neuroepithelial cell differentiation  (IMP)
neuron differentiation  (IBA)
noradrenergic neuron differentiation  (IMP,ISO)
oligodendrocyte development  (ISO)
outflow tract morphogenesis  (IMP)
positive regulation of BMP signaling pathway  (IMP)
positive regulation of cell population proliferation  (IMP)
positive regulation of gene expression  (IMP,ISO)
positive regulation of hippo signaling  (IMP)
positive regulation of hormone secretion  (IMP)
positive regulation of lens epithelial cell proliferation  (IMP)
positive regulation of neurogenesis  (IDA)
positive regulation of neuron differentiation  (IDA,IMP,ISO)
positive regulation of ossification  (IMP,ISO)
positive regulation of osteoblast differentiation  (ISO)
positive regulation of stem cell proliferation  (ISO)
positive regulation of transcription by RNA polymerase II  (IBA,IDA,ISO)
positive regulation of transcription, DNA-templated  (IDA,IMP)
regulation of transcription, DNA-templated  (IBA)
regulation of transforming growth factor beta receptor signaling pathway  (ISO)
skeletal muscle cell differentiation  (IMP)
skeletal system development  (IMP)
soft palate development  (IMP)
somite development  (IMP)
spinal cord development  (IMP)
sympathetic nervous system development  (IMP)
ventricular septum morphogenesis  (IMP)

Cellular Component
nucleoplasm  (ISO)
nucleus  (IDA,ISO)
plasma membrane  (ISO)

Phenotype Annotations     Click to see Annotation Detail View

Mammalian Phenotype
abnormal axon fasciculation  (IAGP)
abnormal bone mineralization  (IAGP)
abnormal bone ossification  (IAGP)
abnormal bronchus morphology  (IAGP)
abnormal calcaneum morphology  (IAGP)
abnormal caudal vertebrae morphology  (IAGP)
abnormal cell death  (IAGP)
abnormal cerebellum morphology  (IAGP)
abnormal cerebral cortex morphology  (IAGP)
abnormal cortical ventricular zone morphology  (IAGP)
abnormal craniofacial morphology  (IAGP)
abnormal cranium morphology  (IAGP)
abnormal dentate gyrus morphology  (IAGP)
abnormal embryonic/fetal subventricular zone morphology  (IAGP)
abnormal eye development  (IAGP)
abnormal eyelid morphology  (IAGP)
abnormal heart development  (IAGP)
abnormal hippocampus CA2 region morphology  (IAGP)
abnormal hippocampus CA3 region morphology  (IAGP)
abnormal hippocampus morphology  (IAGP)
abnormal innervation pattern to muscle  (IAGP)
abnormal limb mesenchyme morphology  (IAGP)
abnormal lumbar vertebrae morphology  (IAGP)
abnormal lung development  (IAGP)
abnormal mandible morphology  (IAGP)
abnormal Meibomian gland morphology  (IAGP)
abnormal myocardium layer morphology  (IAGP)
abnormal nervous system development  (IAGP)
abnormal neural tube morphology  (IAGP)
abnormal neuron differentiation  (IAGP)
abnormal neuronal precursor proliferation  (IAGP)
abnormal notochord morphology  (IAGP)
abnormal olfactory bulb morphology  (IAGP)
abnormal palatal shelf elevation  (IAGP)
abnormal pancreas morphology  (IAGP)
abnormal phalanx morphology  (IAGP)
abnormal pharyngeal arch development  (IAGP)
abnormal pharyngeal arch mesenchyme morphology  (IAGP)
abnormal pterygoid process morphology  (IAGP)
abnormal retina morphology  (IAGP)
abnormal retinal bipolar cell morphology  (IAGP)
abnormal retinal outer plexiform layer morphology  (IAGP)
abnormal rib morphology  (IAGP)
abnormal secondary palate development  (IAGP)
abnormal semilunar valve morphology  (IAGP)
abnormal skeleton development  (IAGP)
abnormal stellate ganglion morphology  (IAGP)
abnormal sternebra morphology  (IAGP)
abnormal sternum ossification  (IAGP)
abnormal stomach pyloric region morphology  (IAGP)
abnormal sympathetic ganglion morphology  (IAGP)
abnormal sympathetic neuron innervation pattern  (IAGP)
abnormal talus morphology  (IAGP)
abnormal tongue morphology  (IAGP)
abnormal truncus arteriosus septation  (IAGP)
abnormal vertebrae morphology  (IAGP)
abnormal xiphoid process morphology  (IAGP)
absent limb buds  (IAGP)
absent optic nerve  (IAGP)
absent retinal ganglion cell  (IAGP)
absent retinal ganglion layer  (IAGP)
absent retinal inner plexiform layer  (IAGP)
absent spleen  (IAGP)
aphakia  (IAGP)
asymmetric sternocostal joints  (IAGP)
barrel chest  (IAGP)
blepharoptosis  (IAGP)
cardia bifida  (IAGP)
cleft palate  (IAGP)
cleft secondary palate  (IAGP)
cleft upper lip  (IAGP)
curly tail  (IAGP)
cyanosis  (IAGP)
decreased amacrine cell number  (IAGP)
decreased birth body size  (IAGP)
decreased birth weight  (IAGP)
decreased brain size  (IAGP)
decreased cell proliferation  (IAGP)
decreased embryo size  (IAGP)
decreased pulmonary respiratory rate  (IAGP)
decreased retinal ganglion cell number  (IAGP)
double outlet right ventricle  (IAGP)
edema  (IAGP)
embryonic growth arrest  (IAGP)
embryonic lethality during organogenesis, complete penetrance  (IAGP)
eyelids open at birth  (IAGP)
failure of heart looping  (IAGP)
heart valve hypoplasia  (IAGP)
impaired somite development  (IAGP)
incomplete embryo turning  (IAGP)
incomplete rostral neuropore closure  (IAGP)
increased neuron apoptosis  (IAGP)
increased retinal apoptosis  (IAGP)
increased rib number  (IAGP)
kinked neural tube  (IAGP)
kinked tail  (IAGP)
lethality throughout fetal growth and development, complete penetrance  (IAGP)
mandible hypoplasia  (IAGP)
maxilla hypoplasia  (IAGP)
micrognathia  (IAGP)
microphthalmia  (IAGP)
neonatal lethality, complete penetrance  (IAGP)
no abnormal phenotype detected  (IAGP)
omphalocele  (IAGP)
open neural tube  (IAGP)
optic nerve hypoplasia  (IAGP)
palatal shelves fail to meet at midline  (IAGP)
perinatal lethality, complete penetrance  (IAGP)
persistent truncus arteriosis  (IAGP)
postnatal lethality, complete penetrance  (IAGP)
pulmonary hypoplasia  (IAGP)
short mandible  (IAGP)
small cerebellum  (IAGP)
small hippocampus  (IAGP)
small lung  (IAGP)
small Meckel's cartilage  (IAGP)
small olfactory bulb  (IAGP)
small spleen  (IAGP)
small stomach  (IAGP)
small superior cervical ganglion  (IAGP)
sternebra fusion  (IAGP)
sternum hypoplasia  (IAGP)
thin cerebral cortex  (IAGP)
thin retinal ganglion layer  (IAGP)
thin retinal inner nuclear layer  (IAGP)
ventricular septal defect  (IAGP)
wavy neural tube  (IAGP)
wide cranial sutures  (IAGP)

Additional References at PubMed
PMID:7590241   PMID:7821514   PMID:8441686   PMID:8666406   PMID:8889548   PMID:8921394   PMID:9337129   PMID:10037800   PMID:10349636   PMID:10925158   PMID:11042159   PMID:11071752  
PMID:11076861   PMID:11793228   PMID:12447396   PMID:12477932   PMID:12815626   PMID:12923295   PMID:14573547   PMID:14681479   PMID:15163632   PMID:15172686   PMID:15226823   PMID:15254231  
PMID:15345747   PMID:15456859   PMID:15489334   PMID:15778864   PMID:16107646   PMID:16141072   PMID:16141073   PMID:16306355   PMID:16602821   PMID:16919269   PMID:17055661   PMID:17084361  
PMID:17515609   PMID:17623775   PMID:17697936   PMID:18287559   PMID:18403418   PMID:18423449   PMID:18505825   PMID:18640244   PMID:18725516   PMID:19030180   PMID:19133245   PMID:19272164  
PMID:19303107   PMID:19369396   PMID:19386638   PMID:19490090   PMID:19799774   PMID:19808959   PMID:20147379   PMID:20436479   PMID:20463296   PMID:20596238   PMID:20646169   PMID:20847309  
PMID:21117150   PMID:21267068   PMID:21527504   PMID:21677750   PMID:21731673   PMID:21873192   PMID:21873635   PMID:21880559   PMID:21985610   PMID:22024412   PMID:22085726   PMID:22331573  
PMID:22371338   PMID:22378879   PMID:22465478   PMID:22678282   PMID:22687574   PMID:23201825   PMID:23313252   PMID:23318640   PMID:23356643   PMID:23483698   PMID:23516376   PMID:23559562  
PMID:23649630   PMID:23888050   PMID:23933087   PMID:24115909   PMID:24154525   PMID:24310815   PMID:24589730   PMID:24722414   PMID:24859337   PMID:24886874   PMID:24952961   PMID:25043184  
PMID:25234735   PMID:25452386   PMID:25652387   PMID:25698749   PMID:25761772   PMID:25775587   PMID:26203155   PMID:26504244   PMID:26687222   PMID:26826126   PMID:26864488   PMID:27225767  
PMID:27241892   PMID:27600842   PMID:28053041   PMID:28118982   PMID:28215559   PMID:28411269   PMID:28429312   PMID:28641110   PMID:28641113   PMID:29031500   PMID:29180573   PMID:29459093  
PMID:29513653   PMID:29746989   PMID:29749639   PMID:29954934   PMID:29973868   PMID:30329130   PMID:30385877   PMID:30786278   PMID:30871468   PMID:30879763   PMID:31155355   PMID:31291246  
PMID:31351040   PMID:31492871  


Comparative Map Data
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
GRCm391227,384,267 - 27,392,717 (-)NCBIGRCm39mm39
GRCm39 Ensembl1227,384,263 - 27,392,573 (-)Ensembl
GRCm381227,334,268 - 27,342,718 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1227,334,264 - 27,342,574 (-)EnsemblGRCm38mm10GRCm38
MGSCv371228,019,133 - 28,027,583 (-)NCBIGRCm37mm9NCBIm37
MGSCv361227,921,484 - 27,928,980 (-)NCBImm8
Celera1228,811,290 - 28,819,758 (-)NCBICelera
Cytogenetic Map12A2NCBI
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
GRCh38.p13 Ensembl25,692,384 - 5,701,385 (+)EnsemblGRCh38hg38GRCh38
GRCh3825,692,384 - 5,701,385 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh3725,832,516 - 5,841,517 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 3625,750,250 - 5,758,968 (+)NCBINCBI36hg18NCBI36
Build 3425,783,396 - 5,792,114NCBI
Celera25,748,512 - 5,756,851 (+)NCBI
Cytogenetic Map2p25.2NCBI
HuRef25,676,397 - 5,685,112 (+)NCBIHuRef
CHM1_125,762,093 - 5,770,810 (+)NCBICHM1_1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
mRatBN7.2644,008,333 - 44,010,354 (-)NCBI
Rnor_6.0 Ensembl646,629,974 - 46,631,983 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.0646,629,967 - 46,631,988 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.0655,343,067 - 55,345,088 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4645,141,366 - 45,143,387 (-)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.1645,144,498 - 45,146,513 (-)NCBI
Celera643,252,857 - 43,254,878 (-)NCBICelera
Cytogenetic Map6q16NCBI
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
ChiLan1.0 EnsemblNW_0049554872,679,145 - 2,680,521 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554872,678,961 - 2,680,869 (-)NCBIChiLan1.0ChiLan1.0
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
PanPan1.12A5,840,399 - 5,841,762 (+)NCBIpanpan1.1PanPan1.1panPan2
Mhudiblu_PPA_v02A5,699,738 - 5,711,210 (+)NCBIMhudiblu_PPA_v0panPan3
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
Dog10K_Boxer_Tasha173,570,850 - 3,572,822 (+)NCBI
ROS_Cfam_1.0173,680,433 - 3,682,409 (+)NCBI
UMICH_Zoey_3.1173,573,068 - 3,575,034 (+)NCBI
UNSW_CanFamBas_1.0173,576,503 - 3,578,454 (+)NCBI
UU_Cfam_GSD_1.0173,580,950 - 3,582,922 (+)NCBI
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
HiC_Itri_2NW_0244050589,632,081 - 9,635,331 (-)NCBI
SpeTri2.0NW_004937107203,120 - 207,185 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
Sscrofa11.1 Ensembl3129,798,704 - 129,800,329 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.13129,797,438 - 129,800,568 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.23138,751,621 - 138,754,531 (-)NCBISscrofa10.2Sscrofa10.2susScr3
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
ChlSab1.114101,982,551 - 101,991,305 (-)NCBI
ChlSab1.1 Ensembl14101,989,895 - 101,991,220 (-)Ensembl
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
HetGla 1.0NW_0046248464,043,010 - 4,046,660 (-)NCBI

Position Markers
Mouse AssemblyChrPosition (strand)SourceJBrowse
GRCm381227,334,831 - 27,334,975UniSTSGRCm38
MGSCv371228,019,696 - 28,019,840UniSTSGRCm37
Celera1228,811,854 - 28,811,998UniSTS
Cytogenetic Map12A3UniSTS
Mouse AssemblyChrPosition (strand)SourceJBrowse
GRCm381227,339,910 - 27,340,639UniSTSGRCm38
MGSCv371228,024,775 - 28,025,504UniSTSGRCm37
Celera1228,816,946 - 28,817,679UniSTS
Cytogenetic Map12A3UniSTS
cM Map12 UniSTS
Mouse AssemblyChrPosition (strand)SourceJBrowse
GRCm381227,341,164 - 27,341,359UniSTSGRCm38
MGSCv371228,026,029 - 28,026,224UniSTSGRCm37
Celera1228,818,204 - 28,818,399UniSTS
Cytogenetic Map12A3UniSTS
Mouse AssemblyChrPosition (strand)SourceJBrowse
GRCm381227,336,039 - 27,336,234UniSTSGRCm38
MGSCv371228,020,904 - 28,021,099UniSTSGRCm37
Celera1228,813,060 - 28,813,255UniSTS
Cytogenetic Map12A3UniSTS
Mouse AssemblyChrPosition (strand)SourceJBrowse
GRCm381227,341,501 - 27,342,153UniSTSGRCm38
MGSCv371228,026,366 - 28,027,018UniSTSGRCm37
Celera1228,818,541 - 28,819,193UniSTS
Cytogenetic Map12A3UniSTS
Mouse AssemblyChrPosition (strand)SourceJBrowse
GRCm381227,342,073 - 27,342,223UniSTSGRCm38
MGSCv371228,026,938 - 28,027,088UniSTSGRCm37
Celera1228,819,113 - 28,819,263UniSTS
Cytogenetic Map12A3UniSTS
cM Map12 UniSTS
Mouse AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map12A3UniSTS
Mouse AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map12A3UniSTS
Mouse AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map12A3UniSTS

QTLs in Region (GRCm38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
4141296Femwf9_mfemur work to failure 9 (mouse)Not determined127870733Mouse
4141112Tglq2a_mtriglyceride QTL 2a (mouse)Not determined12127870733Mouse
4141436Chldq7_mcholesterol and HDL QTL 7 (mouse)Not determined12127870733Mouse
9850128Tglq5_mtriglyceride QTL 5 (mouse)Not determined12127870733Mouse
12910983Pifs1_mpeptide-induced fatal syndrome 1 (mouse)12130383077Mouse
1301925Ath6_matherosclerosis 6 (mouse)Not determined12132708755Mouse
1301207Circp1_mcircadian photosensitivity 1 (mouse)Not determined12133380338Mouse
4141660Nbwa1_mNZB and NZW autoimmunity 1 (mouse)Not determined1229013334290301Mouse
26884410Bzwq15_mbi-zygomatic width QTL 15, 16 week (mouse)12360000029700000Mouse
4142234Tmc1m3_mTmc1 modifier 3 (mouse)Not determined12536844076984429Mouse
1301163Eae16_msusceptibility to experimental allergic encephalomyelitis 16 (mouse)Not determined12767315941673302Mouse
13208568Bmiq11_mbody mass index QTL 11 (mouse)12800000040000000Mouse
1301037Cd4ts5_mCD4 T cell subset 5 (mouse)Not determined12830244542302582Mouse
1301723Fcsa7_mfemoral cross-sectional area 7 (mouse)Not determined12944100543441113Mouse
27226753Femd7_mfemur midshaft diameter 7, 10 week (mouse)12950000084100000Mouse
14746972Manh72_mmandible shape 72 (mouse)121056528244565282Mouse
10401249Bglu15_mblood glucose level 15 (mouse)Not determined121057064344570810Mouse
13207568Tcq14_mtotal cholesterol QTL 14 (mouse)121161000097210000Mouse
4141516slwr_mslowlearner (mouse)Not determined1234247646342615Mouse
10043977Obq34_mobesity QTL 34 (mouse)Not determined121509733249097332Mouse
1558978Cplaq10_mcircadian period of locomotor activity 10 (mouse)Not determined121529102578993590Mouse
26884413Bzwq9_mbi-zygomatic width QTL 9, 10 week (mouse)121610000047700000Mouse
1301574Lmblgq5_mlimb length QTL 5 (mouse)Not determined121754644680910109Mouse
15039339Nmrs29_mNAFLD-associated magnetic resonance shift 29 (mouse)121777585351775853Mouse
10043848Hdlq90_mHDL QTL 90 (mouse)Not determined121778994051790082Mouse
1300870Ath18_matherosclerosis 18 (mouse)Not determined121820996752210068Mouse
12904956Edlmmq10_mextensor digitorum longus muscle mass QTL 10 (mouse)121968983453689834Mouse
1302172Skts5_mskin tumor susceptibility 5 (mouse)Not determined122209886756099017Mouse

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:195
Count of miRNA genes:141
Interacting mature miRNAs:156
Prediction methods:Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (
For more information about miRGate, see PMID:25858286 or access the full paper here.



Nucleotide Sequences
RefSeq Transcripts NM_009234 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB108675 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC158383 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF009414 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK004158 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK012222 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK012306 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK017690 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK018080 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK020994 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK021300 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK086263 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK086326 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK146514 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK165005 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK165693 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC053503 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC062095 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC078643 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BK001484 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  Z18960 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENSMUST00000079063   ⟹   ENSMUSP00000078070
RefSeq Status:
Mouse AssemblyChrPosition (strand)Source
GRCm38.p6 Ensembl1227,334,264 - 27,342,574 (-)Ensembl
RefSeq Acc Id: NM_009234   ⟹   NP_033260
RefSeq Status: VALIDATED
Mouse AssemblyChrPosition (strand)Source
GRCm391227,384,267 - 27,392,717 (-)NCBI
GRCm381227,334,268 - 27,342,718 (-)ENTREZGENE
MGSCv371228,019,133 - 28,027,583 (-)RGD
Celera1228,811,290 - 28,819,758 (-)RGD
Reference Sequences
RefSeq Acc Id: NP_033260   ⟸   NM_009234
- UniProtKB: Q7M6Y2 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSMUSP00000078070   ⟸   ENSMUST00000079063
Protein Domains
HMG box

RGD ID:8678040
Promoter ID:EPDNEW_M17051
Type:initiation region
Description:Mus musculus SRY -box 11 , mRNA.
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database,
Experiment Methods:Single-end sequencing.
Mouse AssemblyChrPosition (strand)Source
GRCm381227,342,704 - 27,342,764EPDNEW
RGD ID:6823437
Promoter ID:MM_KWN:11382
SO ACC ID:SO:0000170
Tissues & Cell Lines:Brain,   ES_Cell
Mouse AssemblyChrPosition (strand)Source
MGSCv361228,026,416 - 28,027,592 (-)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene MGI:98359 AgrOrtholog
Ensembl Genes ENSMUSG00000063632 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Protein ENSMUSP00000078070 ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENSMUST00000079063 ENTREZGENE, UniProtKB/Swiss-Prot
Gene3D-CATH UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
InterPro HMG_box_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  HMG_box_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SOX-11 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SOX-11/4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report mmu:20666 UniProtKB/Swiss-Prot
PANTHER PTHR10270:SF113 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam HMG_box UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PhenoGen Sox11 PhenoGen
PIRSF SOX-12/11/4a UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE HMG_BOX_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART HMG UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF47095 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Q7M6Y2 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary O35178 UniProtKB/Swiss-Prot
  O89036 UniProtKB/Swiss-Prot
  Q04889 UniProtKB/Swiss-Prot
  Q80XF0 UniProtKB/Swiss-Prot

Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2013-11-26 Sox11  SRY (sex determining region Y)-box 11    SRY-box containing gene 11  Symbol and/or name change 5135510 APPROVED