MTSS1 (MTSS I-BAR domain containing 1) - Rat Genome Database

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Gene: MTSS1 (MTSS I-BAR domain containing 1) Homo sapiens
Analyze
Symbol: MTSS1
Name: MTSS I-BAR domain containing 1
RGD ID: 1320466
HGNC Page HGNC
Description: Exhibits actin monomer binding activity; identical protein binding activity; and signaling receptor binding activity. Predicted to be involved in several processes, including actin filament polymerization; adherens junction maintenance; and renal system development. Localizes to actin cytoskeleton; PARTICIPATES IN Hedgehog signaling pathway; INTERACTS WITH 14-Deoxy-11,12-didehydroandrographolide; 17beta-estradiol; 2,2',4,4'-Tetrabromodiphenyl ether.
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: DKFZp781P2223; FLJ44694; KIAA0429; metastasis suppressor 1; metastasis suppressor protein 1; metastasis suppressor YGL-1; MIM; MIMA; MIMB; missing in metastasis protein; MTSS1, I-BAR domain containing
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl8124,550,784 - 124,728,473 (-)EnsemblGRCh38hg38GRCh38
GRCh38.p13 Ensembl8124,550,790 - 124,728,429 (-)EnsemblGRCh38hg38GRCh38
GRCh388124,550,784 - 124,728,473 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh378125,563,025 - 125,740,714 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 368125,632,206 - 125,809,911 (-)NCBINCBI36hg18NCBI36
Build 348125,632,211 - 125,809,840NCBI
Celera8121,751,140 - 121,928,858 (-)NCBI
Cytogenetic Map8q24.13NCBI
HuRef8120,888,491 - 121,064,564 (-)NCBIHuRef
CHM1_18125,603,254 - 125,781,001 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(+)-schisandrin B  (ISO)
1,2-dichloroethane  (ISO)
1,2-dimethylhydrazine  (ISO)
14-Deoxy-11,12-didehydroandrographolide  (EXP)
17alpha-ethynylestradiol  (ISO)
17beta-estradiol  (EXP)
2,2',4,4'-Tetrabromodiphenyl ether  (EXP)
2,2',5,5'-tetrachlorobiphenyl  (ISO)
2,3',4,4',5-Pentachlorobiphenyl  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2-butoxyethanol  (ISO)
2-methylcholine  (EXP)
4,4'-diaminodiphenylmethane  (ISO)
4-amino-2,6-dinitrotoluene  (ISO)
4-hydroxynon-2-enal  (ISO)
4-hydroxyphenyl retinamide  (ISO)
5-aza-2'-deoxycytidine  (EXP)
6-propyl-2-thiouracil  (ISO)
8-Br-cAMP  (EXP)
acrolein  (EXP)
aflatoxin B1  (EXP,ISO)
alpha-pinene  (EXP)
antirheumatic drug  (EXP)
Aroclor 1254  (ISO)
asbestos  (EXP)
benzo[a]pyrene  (EXP,ISO)
bisphenol A  (EXP,ISO)
Brodifacoum  (ISO)
bromobenzene  (ISO)
buspirone  (ISO)
C60 fullerene  (ISO)
calcitriol  (EXP)
carbon nanotube  (EXP,ISO)
chloroprene  (ISO)
chromium(6+)  (EXP)
ciguatoxin CTX1B  (ISO)
copper(II) sulfate  (EXP)
crocidolite asbestos  (ISO)
cyclosporin A  (EXP,ISO)
dibenz[a,h]anthracene  (ISO)
diclofenac  (ISO)
dioxygen  (EXP)
dorsomorphin  (EXP)
doxorubicin  (EXP)
endosulfan  (ISO)
ethanol  (ISO)
furan  (ISO)
gold atom  (EXP)
gold(0)  (EXP)
isoprenaline  (ISO)
levonorgestrel  (EXP)
lipopolysaccharide  (ISO)
medroxyprogesterone acetate  (EXP)
mercury dibromide  (EXP)
methapyrilene  (ISO)
methylmercury chloride  (EXP)
nefazodone  (ISO)
nickel sulfate  (EXP)
O-methyleugenol  (EXP)
oxaliplatin  (ISO)
ozone  (EXP)
p-chloromercuribenzoic acid  (EXP)
paracetamol  (EXP,ISO)
pentachlorophenol  (ISO)
phenformin  (ISO)
phenobarbital  (ISO)
pirinixic acid  (ISO)
potassium chromate  (EXP)
propiconazole  (ISO)
quercetin  (EXP)
rotenone  (ISO)
SB 431542  (EXP)
silicon dioxide  (EXP)
sodium arsenate  (ISO)
sodium arsenite  (EXP)
Soman  (ISO)
succimer  (ISO)
tamoxifen  (ISO)
tanespimycin  (EXP)
testosterone undecanoate  (EXP)
tetrachloromethane  (ISO)
titanium dioxide  (ISO)
topotecan  (ISO)
trichostatin A  (EXP)
triclosan  (EXP)
troglitazone  (ISO)
tungsten  (ISO)
valproic acid  (EXP)

Molecular Pathway Annotations     Click to see Annotation Detail View
References

Additional References at PubMed
PMID:8889548   PMID:9455477   PMID:12082544   PMID:12477932   PMID:12482861   PMID:12570871   PMID:14702039   PMID:14752106   PMID:15146197   PMID:15383276   PMID:15488640   PMID:15489334  
PMID:15545630   PMID:15684034   PMID:15688017   PMID:16169070   PMID:16280553   PMID:16344560   PMID:16921485   PMID:17442377   PMID:19328678   PMID:20080650   PMID:20201926   PMID:20379614  
PMID:20712855   PMID:21196400   PMID:21696600   PMID:21909138   PMID:21927027   PMID:21965727   PMID:22020285   PMID:22100162   PMID:22455847   PMID:22479308   PMID:22681717   PMID:22721729  
PMID:23017832   PMID:23350348   PMID:23382691   PMID:23383207   PMID:23474751   PMID:23852458   PMID:24318128   PMID:24632752   PMID:24684796   PMID:25287652   PMID:25332235   PMID:25385572  
PMID:25625275   PMID:25783158   PMID:25996952   PMID:26119942   PMID:26198729   PMID:26316204   PMID:26621336   PMID:27164937   PMID:27181205   PMID:27634022   PMID:27693783   PMID:28068324  
PMID:28146435   PMID:28159994   PMID:28264927   PMID:28739745   PMID:29175021   PMID:29218652   PMID:29453719   PMID:29497041   PMID:30246429   PMID:30808710   PMID:30945288   PMID:30949866  
PMID:31541465   PMID:31545491   PMID:32052679   PMID:32645138  


Genomics

Comparative Map Data
MTSS1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl8124,550,784 - 124,728,473 (-)EnsemblGRCh38hg38GRCh38
GRCh38.p13 Ensembl8124,550,790 - 124,728,429 (-)EnsemblGRCh38hg38GRCh38
GRCh388124,550,784 - 124,728,473 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh378125,563,025 - 125,740,714 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 368125,632,206 - 125,809,911 (-)NCBINCBI36hg18NCBI36
Build 348125,632,211 - 125,809,840NCBI
Celera8121,751,140 - 121,928,858 (-)NCBI
Cytogenetic Map8q24.13NCBI
HuRef8120,888,491 - 121,064,564 (-)NCBIHuRef
CHM1_18125,603,254 - 125,781,001 (-)NCBICHM1_1
Mtss1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391558,813,083 - 58,955,805 (-)NCBIGRCm39mm39
GRCm39 Ensembl1558,813,083 - 58,953,854 (-)Ensembl
GRCm381558,941,234 - 59,083,956 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1558,941,234 - 59,082,005 (-)EnsemblGRCm38mm10GRCm38
MGSCv371558,772,789 - 58,913,581 (-)NCBIGRCm37mm9NCBIm37
MGSCv361558,773,330 - 58,912,072 (-)NCBImm8
Celera1560,471,026 - 60,611,759 (-)NCBICelera
Cytogenetic Map15D1NCBI
Mtss1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.2790,488,751 - 90,628,007 (-)NCBI
Rnor_6.0 Ensembl798,820,812 - 98,960,837 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.0798,820,799 - 98,960,878 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.0799,419,324 - 99,558,069 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4795,808,266 - 95,947,927 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.1795,753,976 - 95,979,992 (+)NCBI
Celera787,254,103 - 87,391,446 (-)NCBICelera
Cytogenetic Map7q33NCBI
Mtss1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049555403,204,367 - 3,346,026 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049555403,204,357 - 3,346,026 (-)NCBIChiLan1.0ChiLan1.0
MTSS1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.18123,987,583 - 124,164,827 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl8123,987,577 - 124,032,339 (-)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v08121,235,545 - 121,413,037 (-)NCBIMhudiblu_PPA_v0panPan3
MTSS1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11322,633,001 - 22,794,960 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1322,635,230 - 22,794,453 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1322,598,451 - 22,760,081 (-)NCBI
ROS_Cfam_1.01322,974,900 - 23,136,665 (-)NCBI
UMICH_Zoey_3.11322,695,751 - 22,857,455 (-)NCBI
UNSW_CanFamBas_1.01322,805,300 - 22,967,342 (-)NCBI
UU_Cfam_GSD_1.01323,048,188 - 23,210,026 (-)NCBI
Mtss1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440530315,537,415 - 15,690,947 (+)NCBI
SpeTri2.0NW_00493647022,963,498 - 23,117,923 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
MTSS1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl414,933,324 - 15,105,406 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1414,933,290 - 15,103,256 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2415,692,248 - 15,759,809 (+)NCBISscrofa10.2Sscrofa10.2susScr3
MTSS1
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.18119,114,241 - 119,297,945 (-)NCBI
ChlSab1.1 Ensembl8119,114,078 - 119,297,943 (-)Ensembl
Mtss1
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462473530,512,474 - 30,659,727 (+)NCBI

Position Markers
D8S1799  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378125,576,771 - 125,577,010UniSTSGRCh37
Build 368125,645,952 - 125,646,191RGDNCBI36
Celera8121,764,886 - 121,765,125RGD
Cytogenetic Map8p22UniSTS
HuRef8120,902,233 - 120,902,488UniSTS
Marshfield Genetic Map8133.64UniSTS
Marshfield Genetic Map8133.64RGD
Genethon Genetic Map8132.4UniSTS
Stanford-G3 RH Map83806.0UniSTS
GeneMap99-GB4 RH Map8476.51UniSTS
Whitehead-YAC Contig Map8 UniSTS
NCBI RH Map81461.6UniSTS
GeneMap99-G3 RH Map83896.0UniSTS
D17S825E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378125,565,110 - 125,565,283UniSTSGRCh37
Build 368125,634,291 - 125,634,464RGDNCBI36
Celera8121,753,225 - 121,753,398RGD
Cytogenetic Map8p22UniSTS
HuRef8120,890,576 - 120,890,749UniSTS
TNG Radiation Hybrid Map860842.0UniSTS
Stanford-G3 RH Map83815.0UniSTS
NCBI RH Map81461.6UniSTS
GeneMap99-G3 RH Map83905.0UniSTS
A008N08  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378125,699,969 - 125,700,070UniSTSGRCh37
Build 368125,769,150 - 125,769,251RGDNCBI36
Celera8121,888,085 - 121,888,186RGD
Cytogenetic Map8p22UniSTS
HuRef8121,023,800 - 121,023,901UniSTS
GeneMap99-GB4 RH Map8476.51UniSTS
NCBI RH Map81461.6UniSTS
RH46986  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378125,729,289 - 125,729,439UniSTSGRCh37
Build 368125,798,470 - 125,798,620RGDNCBI36
Celera8121,917,406 - 121,917,556RGD
Cytogenetic Map8p22UniSTS
HuRef8121,053,107 - 121,053,257UniSTS
GeneMap99-GB4 RH Map8474.57UniSTS
NCBI RH Map81459.3UniSTS
SGC30260  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378125,563,044 - 125,563,171UniSTSGRCh37
Build 368125,632,225 - 125,632,352RGDNCBI36
Celera8121,751,159 - 121,751,286RGD
Cytogenetic Map8p22UniSTS
HuRef8120,888,510 - 120,888,637UniSTS
GeneMap99-GB4 RH Map8478.86UniSTS
Whitehead-RH Map8638.4UniSTS
A009Q06  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378125,586,362 - 125,586,536UniSTSGRCh37
GRCh37264,322,953 - 64,323,185UniSTSGRCh37
Build 36264,176,457 - 64,176,689RGDNCBI36
Celera264,168,211 - 64,168,443RGD
Celera8121,774,482 - 121,774,656UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map2p13.3UniSTS
HuRef8120,911,843 - 120,912,017UniSTS
HuRef264,062,730 - 64,062,962UniSTS
GeneMap99-GB4 RH Map8476.41UniSTS
NCBI RH Map81461.6UniSTS
RH80990  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378125,591,184 - 125,591,400UniSTSGRCh37
Build 368125,660,365 - 125,660,581RGDNCBI36
Celera8121,779,304 - 121,779,520RGD
Cytogenetic Map8p22UniSTS
HuRef8120,915,325 - 120,915,541UniSTS
GeneMap99-GB4 RH Map8474.09UniSTS
D8S58  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378125,696,125 - 125,696,295UniSTSGRCh37
Build 368125,765,306 - 125,765,476RGDNCBI36
Celera8121,884,241 - 121,884,411RGD
Cytogenetic Map8p22UniSTS
HuRef8121,019,954 - 121,020,124UniSTS
SHGC-150814  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378125,576,796 - 125,577,043UniSTSGRCh37
Build 368125,645,977 - 125,646,224RGDNCBI36
Celera8121,764,911 - 121,765,158RGD
Cytogenetic Map8p22UniSTS
HuRef8120,902,258 - 120,902,521UniSTS
TNG Radiation Hybrid Map860853.0UniSTS
TNG Radiation Hybrid Map1040995.0UniSTS
RH46386  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378125,697,388 - 125,697,506UniSTSGRCh37
Build 368125,766,569 - 125,766,687RGDNCBI36
Celera8121,885,504 - 121,885,622RGD
Cytogenetic Map8p22UniSTS
HuRef8121,021,218 - 121,021,337UniSTS
GeneMap99-GB4 RH Map8471.5UniSTS
RH69480  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378125,573,028 - 125,573,238UniSTSGRCh37
Build 368125,642,209 - 125,642,419RGDNCBI36
Celera8121,761,143 - 121,761,353RGD
Cytogenetic Map8p22UniSTS
HuRef8120,898,494 - 120,898,704UniSTS
GeneMap99-GB4 RH Map8477.8UniSTS
RH18269  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378125,646,703 - 125,646,872UniSTSGRCh37
Build 368125,715,884 - 125,716,053RGDNCBI36
Celera8121,834,820 - 121,834,989RGD
Cytogenetic Map8p22UniSTS
HuRef8120,970,826 - 120,970,995UniSTS
GeneMap99-GB4 RH Map8474.48UniSTS
NCBI RH Map81474.0UniSTS
STS-H91255  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378125,692,343 - 125,692,563UniSTSGRCh37
Build 368125,761,524 - 125,761,744RGDNCBI36
Celera8121,880,460 - 121,880,680RGD
Cytogenetic Map8p22UniSTS
HuRef8121,016,173 - 121,016,393UniSTS
GeneMap99-GB4 RH Map8476.51UniSTS
WI-21130  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378125,698,773 - 125,698,970UniSTSGRCh37
Build 368125,767,954 - 125,768,151RGDNCBI36
Celera8121,886,889 - 121,887,086RGD
Cytogenetic Map8p22UniSTS
HuRef8121,022,604 - 121,022,801UniSTS
GeneMap99-GB4 RH Map8471.67UniSTS
Whitehead-RH Map8631.9UniSTS
RH68595  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378125,622,883 - 125,623,057UniSTSGRCh37
Build 368125,692,064 - 125,692,238RGDNCBI36
Celera8121,811,000 - 121,811,174RGD
Cytogenetic Map8p22UniSTS
HuRef8120,947,019 - 120,947,193UniSTS
GeneMap99-GB4 RH Map8476.51UniSTS
NCBI RH Map81461.6UniSTS
D8S2132  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378125,660,589 - 125,660,730UniSTSGRCh37
Build 368125,729,770 - 125,729,911RGDNCBI36
Celera8121,848,706 - 121,848,847RGD
Cytogenetic Map8p22UniSTS
HuRef8120,984,711 - 120,984,852UniSTS
D8S1357E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378125,565,194 - 125,565,289UniSTSGRCh37
Build 368125,634,375 - 125,634,470RGDNCBI36
Celera8121,753,309 - 121,753,404RGD
Cytogenetic Map8p22UniSTS
HuRef8120,890,660 - 120,890,755UniSTS
GeneMap99-GB4 RH Map8477.8UniSTS
G32763  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378125,586,362 - 125,586,536UniSTSGRCh37
Celera8121,774,482 - 121,774,656UniSTS
Cytogenetic Map8p22UniSTS
HuRef8120,911,843 - 120,912,017UniSTS

miRNA Target Status

Confirmed Target Of
miRNA GeneMature miRNAMethod NameResult TypeData TypeSupport TypePMID
MIR23Ahsa-miR-23a-3pOncomiRDBexternal_infoNANA22628407
MIR135A1hsa-miR-135a-5pOncomiRDBexternal_infoNANA23017832
MIR135A1hsa-miR-135a-5pOncomiRDBexternal_infoNANA21888875
MIR182hsa-miR-182-5pMirtarbaseexternal_infoLuciferase reporter assayFunctional MTI22322863
MIR182hsa-miR-182-5pMirtarbaseexternal_infoLuciferase reporter assayFunctional MTI23383207
MIR182hsa-miR-182-5pOncomiRDBexternal_infoNANA22681717
MIR135A2hsa-miR-135a-5pOncomiRDBexternal_infoNANA23017832
MIR135A2hsa-miR-135a-5pOncomiRDBexternal_infoNANA21888875

Predicted Target Of
Summary Value
Count of predictions:5364
Count of miRNA genes:1190
Interacting mature miRNAs:1510
Transcripts:ENST00000325064, ENST00000354184, ENST00000378017, ENST00000395508, ENST00000431961, ENST00000472084, ENST00000518547, ENST00000519168, ENST00000519226, ENST00000519671, ENST00000520094, ENST00000520771, ENST00000522118, ENST00000522162, ENST00000522722, ENST00000523179, ENST00000523587, ENST00000524090, ENST00000524243, ENST00000529463
Prediction methods:Microtar, 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 (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High 1
Medium 1397 1415 1326 547 726 429 3786 1595 2952 329 1099 1123 123 1173 2480 1
Low 1014 1567 393 74 1170 33 561 588 737 85 342 471 47 31 308 1 1
Below cutoff 20 3 5 2 50 3 7 10 28 5 12 16 4 1 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001282971 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001282974 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001363294 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001363295 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001363296 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001363297 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001363298 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001363299 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001363300 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001363301 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001363302 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_014751 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005251111 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005251113 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006716700 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006716701 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006716702 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006716703 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006716704 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006716705 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006716706 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011517403 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011517404 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011517407 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017014086 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017014087 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017014088 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017014089 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017014090 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017014091 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017014092 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017014101 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024447351 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB007889 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC090198 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC090922 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF086645 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF116674 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI041104 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ710067 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK027015 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK126651 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK126989 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK295681 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK302036 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK310792 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC023998 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU145296 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU674412 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BY993850 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471060 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CN348724 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA225605 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA227466 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA447614 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA451172 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA785323 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA790325 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EF560715 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HY339502 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF458837 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF495754 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U50573 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000325064   ⟹   ENSP00000322804
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8124,552,813 - 124,728,273 (-)Ensembl
RefSeq Acc Id: ENST00000378017   ⟹   ENSP00000367256
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8124,550,790 - 124,728,018 (-)Ensembl
RefSeq Acc Id: ENST00000431961   ⟹   ENSP00000393606
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8124,552,888 - 124,568,841 (-)Ensembl
RefSeq Acc Id: ENST00000472084
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8124,699,090 - 124,728,018 (-)Ensembl
RefSeq Acc Id: ENST00000518547   ⟹   ENSP00000429064
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8124,550,790 - 124,728,429 (-)Ensembl
RefSeq Acc Id: ENST00000519168   ⟹   ENSP00000428685
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8124,552,800 - 124,565,727 (-)Ensembl
RefSeq Acc Id: ENST00000519226
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8124,562,967 - 124,566,209 (-)Ensembl
RefSeq Acc Id: ENST00000519671
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8124,589,665 - 124,619,479 (-)Ensembl
RefSeq Acc Id: ENST00000520094
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8124,555,813 - 124,557,995 (-)Ensembl
RefSeq Acc Id: ENST00000520771
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8124,550,976 - 124,556,572 (-)Ensembl
RefSeq Acc Id: ENST00000522118   ⟹   ENSP00000428145
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8124,557,688 - 124,568,821 (-)Ensembl
RefSeq Acc Id: ENST00000522162   ⟹   ENSP00000429752
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8124,568,428 - 124,727,616 (-)Ensembl
RefSeq Acc Id: ENST00000522722
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8124,556,261 - 124,564,802 (-)Ensembl
RefSeq Acc Id: ENST00000523179   ⟹   ENSP00000428348
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8124,555,799 - 124,568,538 (-)Ensembl
RefSeq Acc Id: ENST00000523587
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8124,552,890 - 124,563,427 (-)Ensembl
RefSeq Acc Id: ENST00000524090   ⟹   ENSP00000428319
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8124,552,902 - 124,568,804 (-)Ensembl
RefSeq Acc Id: ENST00000524243
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8124,698,039 - 124,727,998 (-)Ensembl
RefSeq Acc Id: ENST00000529463
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8124,585,087 - 124,673,513 (-)Ensembl
RefSeq Acc Id: NM_001282971   ⟹   NP_001269900
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388124,550,784 - 124,728,473 (-)NCBI
HuRef8120,888,477 - 121,064,582 (-)NCBI
CHM1_18125,603,254 - 125,781,001 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001282974   ⟹   NP_001269903
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388124,550,784 - 124,728,473 (-)NCBI
HuRef8120,888,477 - 121,064,582 (-)NCBI
CHM1_18125,603,254 - 125,781,001 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001363294   ⟹   NP_001350223
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388124,550,784 - 124,728,473 (-)NCBI
RefSeq Acc Id: NM_001363295   ⟹   NP_001350224
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388124,550,784 - 124,728,473 (-)NCBI
RefSeq Acc Id: NM_001363296   ⟹   NP_001350225
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388124,550,784 - 124,728,473 (-)NCBI
RefSeq Acc Id: NM_001363297   ⟹   NP_001350226
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388124,550,784 - 124,728,473 (-)NCBI
RefSeq Acc Id: NM_001363298   ⟹   NP_001350227
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388124,550,784 - 124,728,473 (-)NCBI
RefSeq Acc Id: NM_001363299   ⟹   NP_001350228
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388124,550,784 - 124,728,473 (-)NCBI
RefSeq Acc Id: NM_001363300   ⟹   NP_001350229
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388124,550,784 - 124,728,473 (-)NCBI
RefSeq Acc Id: NM_001363301   ⟹   NP_001350230
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388124,550,784 - 124,728,473 (-)NCBI
RefSeq Acc Id: NM_001363302   ⟹   NP_001350231
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388124,550,784 - 124,728,473 (-)NCBI
RefSeq Acc Id: NM_014751   ⟹   NP_055566
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388124,550,784 - 124,728,473 (-)NCBI
GRCh378125,563,025 - 125,740,730 (-)ENTREZGENE
GRCh378125,563,025 - 125,740,730 (-)NCBI
Build 368125,632,206 - 125,809,911 (-)NCBI Archive
HuRef8120,888,477 - 121,064,582 (-)NCBI
CHM1_18125,603,254 - 125,781,001 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005251111   ⟹   XP_005251168
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388124,550,784 - 124,728,440 (-)NCBI
GRCh378125,563,025 - 125,740,730 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005251113   ⟹   XP_005251170
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388124,550,784 - 124,728,440 (-)NCBI
GRCh378125,563,025 - 125,740,730 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006716700   ⟹   XP_006716763
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388124,550,784 - 124,728,411 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006716701   ⟹   XP_006716764
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388124,550,784 - 124,728,440 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006716702   ⟹   XP_006716765
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388124,550,784 - 124,728,440 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006716703   ⟹   XP_006716766
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388124,550,784 - 124,728,440 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006716704   ⟹   XP_006716767
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388124,550,784 - 124,728,440 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006716705   ⟹   XP_006716768
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388124,550,784 - 124,728,440 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006716706   ⟹   XP_006716769
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388124,550,784 - 124,728,440 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011517403   ⟹   XP_011515705
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388124,550,784 - 124,727,616 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011517404   ⟹   XP_011515706
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388124,550,784 - 124,685,088 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011517407   ⟹   XP_011515709
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388124,550,784 - 124,564,802 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017014086   ⟹   XP_016869575
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388124,550,784 - 124,728,440 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017014087   ⟹   XP_016869576
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388124,550,784 - 124,728,411 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017014088   ⟹   XP_016869577
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388124,550,784 - 124,728,440 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017014089   ⟹   XP_016869578
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388124,550,784 - 124,728,411 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017014090   ⟹   XP_016869579
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388124,550,784 - 124,642,630 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017014091   ⟹   XP_016869580
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388124,550,784 - 124,727,584 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017014092   ⟹   XP_016869581
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388124,550,784 - 124,728,440 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017014101   ⟹   XP_016869590
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388124,550,971 - 124,673,581 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024447351   ⟹   XP_024303119
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388124,550,784 - 124,565,635 (-)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001269900 (Get FASTA)   NCBI Sequence Viewer  
  NP_001269903 (Get FASTA)   NCBI Sequence Viewer  
  NP_001350223 (Get FASTA)   NCBI Sequence Viewer  
  NP_001350224 (Get FASTA)   NCBI Sequence Viewer  
  NP_001350225 (Get FASTA)   NCBI Sequence Viewer  
  NP_001350226 (Get FASTA)   NCBI Sequence Viewer  
  NP_001350227 (Get FASTA)   NCBI Sequence Viewer  
  NP_001350228 (Get FASTA)   NCBI Sequence Viewer  
  NP_001350229 (Get FASTA)   NCBI Sequence Viewer  
  NP_001350230 (Get FASTA)   NCBI Sequence Viewer  
  NP_001350231 (Get FASTA)   NCBI Sequence Viewer  
  NP_055566 (Get FASTA)   NCBI Sequence Viewer  
  XP_005251168 (Get FASTA)   NCBI Sequence Viewer  
  XP_005251170 (Get FASTA)   NCBI Sequence Viewer  
  XP_006716763 (Get FASTA)   NCBI Sequence Viewer  
  XP_006716764 (Get FASTA)   NCBI Sequence Viewer  
  XP_006716765 (Get FASTA)   NCBI Sequence Viewer  
  XP_006716766 (Get FASTA)   NCBI Sequence Viewer  
  XP_006716767 (Get FASTA)   NCBI Sequence Viewer  
  XP_006716768 (Get FASTA)   NCBI Sequence Viewer  
  XP_006716769 (Get FASTA)   NCBI Sequence Viewer  
  XP_011515705 (Get FASTA)   NCBI Sequence Viewer  
  XP_011515706 (Get FASTA)   NCBI Sequence Viewer  
  XP_011515709 (Get FASTA)   NCBI Sequence Viewer  
  XP_016869575 (Get FASTA)   NCBI Sequence Viewer  
  XP_016869576 (Get FASTA)   NCBI Sequence Viewer  
  XP_016869577 (Get FASTA)   NCBI Sequence Viewer  
  XP_016869578 (Get FASTA)   NCBI Sequence Viewer  
  XP_016869579 (Get FASTA)   NCBI Sequence Viewer  
  XP_016869580 (Get FASTA)   NCBI Sequence Viewer  
  XP_016869581 (Get FASTA)   NCBI Sequence Viewer  
  XP_016869590 (Get FASTA)   NCBI Sequence Viewer  
  XP_024303119 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAF15947 (Get FASTA)   NCBI Sequence Viewer  
  AAF71094 (Get FASTA)   NCBI Sequence Viewer  
  AAH23998 (Get FASTA)   NCBI Sequence Viewer  
  ABQ59025 (Get FASTA)   NCBI Sequence Viewer  
  BAA24859 (Get FASTA)   NCBI Sequence Viewer  
  BAC86629 (Get FASTA)   NCBI Sequence Viewer  
  BAC86779 (Get FASTA)   NCBI Sequence Viewer  
  BAH12152 (Get FASTA)   NCBI Sequence Viewer  
  BAH13614 (Get FASTA)   NCBI Sequence Viewer  
  EAW92069 (Get FASTA)   NCBI Sequence Viewer  
  EAW92070 (Get FASTA)   NCBI Sequence Viewer  
  EAW92071 (Get FASTA)   NCBI Sequence Viewer  
  EAW92072 (Get FASTA)   NCBI Sequence Viewer  
  EAW92073 (Get FASTA)   NCBI Sequence Viewer  
  EAW92074 (Get FASTA)   NCBI Sequence Viewer  
  O43312 (Get FASTA)   NCBI Sequence Viewer  
Reference Sequences
RefSeq Acc Id: NP_055566   ⟸   NM_014751
- Peptide Label: isoform 2
- UniProtKB: O43312 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_005251170   ⟸   XM_005251113
- Peptide Label: isoform X11
- Sequence:
RefSeq Acc Id: XP_005251168   ⟸   XM_005251111
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: NP_001269903   ⟸   NM_001282974
- Peptide Label: isoform 3
- UniProtKB: O43312 (UniProtKB/Swiss-Prot),   A5YM41 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001269900   ⟸   NM_001282971
- Peptide Label: isoform 1
- UniProtKB: O43312 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_006716764   ⟸   XM_006716701
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: XP_006716767   ⟸   XM_006716704
- Peptide Label: isoform X16
- Sequence:
RefSeq Acc Id: XP_006716763   ⟸   XM_006716700
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_006716769   ⟸   XM_006716706
- Peptide Label: isoform X26
- Sequence:
RefSeq Acc Id: XP_006716766   ⟸   XM_006716703
- Peptide Label: isoform X15
- Sequence:
RefSeq Acc Id: XP_006716768   ⟸   XM_006716705
- Peptide Label: isoform X18
- Sequence:
RefSeq Acc Id: XP_006716765   ⟸   XM_006716702
- Peptide Label: isoform X5
- Sequence:
RefSeq Acc Id: XP_011515705   ⟸   XM_011517403
- Peptide Label: isoform X12
- Sequence:
RefSeq Acc Id: XP_011515706   ⟸   XM_011517404
- Peptide Label: isoform X14
- Sequence:
RefSeq Acc Id: XP_011515709   ⟸   XM_011517407
- Peptide Label: isoform X30
- Sequence:
RefSeq Acc Id: XP_016869575   ⟸   XM_017014086
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: XP_016869578   ⟸   XM_017014089
- Peptide Label: isoform X8
- Sequence:
RefSeq Acc Id: XP_016869581   ⟸   XM_017014092
- Peptide Label: isoform X13
- Sequence:
RefSeq Acc Id: XP_016869577   ⟸   XM_017014088
- Peptide Label: isoform X7
- Sequence:
RefSeq Acc Id: XP_016869576   ⟸   XM_017014087
- Peptide Label: isoform X6
- Sequence:
RefSeq Acc Id: XP_016869580   ⟸   XM_017014091
- Peptide Label: isoform X10
- Sequence:
RefSeq Acc Id: XP_016869579   ⟸   XM_017014090
- Peptide Label: isoform X9
- Sequence:
RefSeq Acc Id: XP_016869590   ⟸   XM_017014101
- Peptide Label: isoform X28
- Sequence:
RefSeq Acc Id: XP_024303119   ⟸   XM_024447351
- Peptide Label: isoform X29
- Sequence:
RefSeq Acc Id: NP_001350230   ⟸   NM_001363301
- Peptide Label: isoform 11
RefSeq Acc Id: NP_001350223   ⟸   NM_001363294
- Peptide Label: isoform 4
RefSeq Acc Id: NP_001350227   ⟸   NM_001363298
- Peptide Label: isoform 8
RefSeq Acc Id: NP_001350231   ⟸   NM_001363302
- Peptide Label: isoform 12
RefSeq Acc Id: NP_001350229   ⟸   NM_001363300
- Peptide Label: isoform 10
RefSeq Acc Id: NP_001350224   ⟸   NM_001363295
- Peptide Label: isoform 5
RefSeq Acc Id: NP_001350226   ⟸   NM_001363297
- Peptide Label: isoform 7
RefSeq Acc Id: NP_001350228   ⟸   NM_001363299
- Peptide Label: isoform 9
RefSeq Acc Id: NP_001350225   ⟸   NM_001363296
- Peptide Label: isoform 6
RefSeq Acc Id: ENSP00000429064   ⟸   ENST00000518547
RefSeq Acc Id: ENSP00000428685   ⟸   ENST00000519168
RefSeq Acc Id: ENSP00000367256   ⟸   ENST00000378017
RefSeq Acc Id: ENSP00000322804   ⟸   ENST00000325064
RefSeq Acc Id: ENSP00000428145   ⟸   ENST00000522118
RefSeq Acc Id: ENSP00000429752   ⟸   ENST00000522162
RefSeq Acc Id: ENSP00000428348   ⟸   ENST00000523179
RefSeq Acc Id: ENSP00000428319   ⟸   ENST00000524090
RefSeq Acc Id: ENSP00000393606   ⟸   ENST00000431961
Protein Domains
IMD   WH2

Promoters
RGD ID:7214155
Promoter ID:EPDNEW_H12823
Type:initiation region
Name:MTSS1_1
Description:MTSS1, I-BAR domain containing
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh388124,728,473 - 124,728,533EPDNEW
RGD ID:6806884
Promoter ID:HG_KWN:62056
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   K562,   Lymphoblastoid
Transcripts:UC003YRH.2
Position:
Human AssemblyChrPosition (strand)Source
Build 368125,637,266 - 125,638,717 (-)MPROMDB
RGD ID:6806487
Promoter ID:HG_KWN:62059
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:NB4
Transcripts:NM_014751,   OTTHUMT00000109623,   UC003YRJ.2,   UC003YRL.2
Position:
Human AssemblyChrPosition (strand)Source
Build 368125,809,701 - 125,810,201 (-)MPROMDB

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 8q24.13(chr8:124125245-125337217)x3 copy number gain See cases [RCV000050762] Chr8:124125245..125337217 [GRCh38]
Chr8:125137486..126349459 [GRCh37]
Chr8:125206667..126418641 [NCBI36]
Chr8:8q24.13
pathogenic
GRCh38/hg38 8q23.3-24.3(chr8:113580402-145054634)x3 copy number gain See cases [RCV000050638] Chr8:113580402..145054634 [GRCh38]
Chr8:114592631..146280020 [GRCh37]
Chr8:114661807..146250824 [NCBI36]
Chr8:8q23.3-24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145049449)x3 copy number gain See cases [RCV000051206] Chr8:241530..145049449 [GRCh38]
Chr8:191530..146274835 [GRCh37]
Chr8:181530..146245639 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q24.13(chr8:124377953-124575712)x1 copy number loss See cases [RCV000052791] Chr8:124377953..124575712 [GRCh38]
Chr8:125390194..125587953 [GRCh37]
Chr8:125459375..125657134 [NCBI36]
Chr8:8q24.13
uncertain significance
GRCh38/hg38 8q22.1-24.3(chr8:95606052-145054775)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053677]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053677]|See cases [RCV000053677] Chr8:95606052..145054775 [GRCh38]
Chr8:96618280..146280161 [GRCh37]
Chr8:96687456..146250965 [NCBI36]
Chr8:8q22.1-24.3
pathogenic
GRCh38/hg38 8q24.13-24.3(chr8:124514090-145054634)x3 copy number gain See cases [RCV000053678] Chr8:124514090..145054634 [GRCh38]
Chr8:125526331..146280020 [GRCh37]
Chr8:125595512..146250824 [NCBI36]
Chr8:8q24.13-24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:244417-145054775)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]|See cases [RCV000053604] Chr8:244417..145054775 [GRCh38]
Chr8:194417..146280161 [GRCh37]
Chr8:184417..146250965 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3 copy number gain See cases [RCV000053602] Chr8:241530..145054634 [GRCh38]
Chr8:191530..146280020 [GRCh37]
Chr8:181530..146250824 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q23.3-24.21(chr8:113288454-126716087)x1 copy number loss See cases [RCV000054301] Chr8:113288454..126716087 [GRCh38]
Chr8:114300683..127728332 [GRCh37]
Chr8:114369859..127797514 [NCBI36]
Chr8:8q23.3-24.21
pathogenic
GRCh38/hg38 8q24.13-24.21(chr8:122454392-128513076)x3 copy number gain See cases [RCV000133620] Chr8:122454392..128513076 [GRCh38]
Chr8:123466631..129525322 [GRCh37]
Chr8:123535812..129594504 [NCBI36]
Chr8:8q24.13-24.21
pathogenic
GRCh38/hg38 8q22.1-24.3(chr8:94682154-145068656)x3 copy number gain See cases [RCV000134353] Chr8:94682154..145068656 [GRCh38]
Chr8:95694382..146294042 [GRCh37]
Chr8:95763558..146264846 [NCBI36]
Chr8:8q22.1-24.3
pathogenic
GRCh38/hg38 8q21.3-24.23(chr8:86300584-137022587)x3 copy number gain See cases [RCV000135621] Chr8:86300584..137022587 [GRCh38]
Chr8:87312813..138034830 [GRCh37]
Chr8:87381929..138104012 [NCBI36]
Chr8:8q21.3-24.23
pathogenic|likely pathogenic
GRCh38/hg38 8q24.13-24.3(chr8:124498498-145068712)x3 copy number gain See cases [RCV000137346] Chr8:124498498..145068712 [GRCh38]
Chr8:125510739..146294098 [GRCh37]
Chr8:125579920..146264902 [NCBI36]
Chr8:8q24.13-24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241605-145054781)x3 copy number gain See cases [RCV000138643] Chr8:241605..145054781 [GRCh38]
Chr8:191605..146280167 [GRCh37]
Chr8:181605..146250971 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q21.3-24.3(chr8:87931152-145068712)x3 copy number gain See cases [RCV000138551] Chr8:87931152..145068712 [GRCh38]
Chr8:88943380..146294098 [GRCh37]
Chr8:89012496..146264902 [NCBI36]
Chr8:8q21.3-24.3
pathogenic
GRCh38/hg38 8q21.13-24.3(chr8:77480050-145068712)x3 copy number gain See cases [RCV000139036] Chr8:77480050..145068712 [GRCh38]
Chr8:78392286..146294098 [GRCh37]
Chr8:78554841..146264902 [NCBI36]
Chr8:8q21.13-24.3
pathogenic
GRCh38/hg38 8q22.1-24.3(chr8:97382873-145070385)x3 copy number gain See cases [RCV000140447] Chr8:97382873..145070385 [GRCh38]
Chr8:98395101..146295771 [GRCh37]
Chr8:98464277..146266575 [NCBI36]
Chr8:8q22.1-24.3
pathogenic
GRCh38/hg38 8q11.1-24.3(chr8:46031340-139285494)x3 copy number gain See cases [RCV000139539] Chr8:46031340..139285494 [GRCh38]
Chr8:46942962..140297737 [GRCh37]
Chr8:47062127..140366919 [NCBI36]
Chr8:8q11.1-24.3
pathogenic
GRCh38/hg38 8q22.3-24.3(chr8:100867343-145070385)x3 copy number gain See cases [RCV000141694] Chr8:100867343..145070385 [GRCh38]
Chr8:101879571..146295771 [GRCh37]
Chr8:101948747..146266575 [NCBI36]
Chr8:8q22.3-24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:208048-145070385)x3 copy number gain See cases [RCV000141808] Chr8:208048..145070385 [GRCh38]
Chr8:158048..146295771 [GRCh37]
Chr8:148048..146266575 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8p21.3-q24.3(chr8:21291522-145070385)x3 copy number gain See cases [RCV000142021] Chr8:21291522..145070385 [GRCh38]
Chr8:21149033..146295771 [GRCh37]
Chr8:21193313..146266575 [NCBI36]
Chr8:8p21.3-q24.3
pathogenic
GRCh38/hg38 8q22.3-24.3(chr8:103306336-145068712)x3 copy number gain See cases [RCV000142810] Chr8:103306336..145068712 [GRCh38]
Chr8:104318564..146294098 [GRCh37]
Chr8:104387740..146264902 [NCBI36]
Chr8:8q22.3-24.3
pathogenic|likely pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:226452-145068712)x3 copy number gain See cases [RCV000142858] Chr8:226452..145068712 [GRCh38]
Chr8:176452..146294098 [GRCh37]
Chr8:166452..146264902 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q21.13-24.3(chr8:78614077-145054634)x3 copy number gain See cases [RCV000142597] Chr8:78614077..145054634 [GRCh38]
Chr8:79526312..146280020 [GRCh37]
Chr8:79688867..146250824 [NCBI36]
Chr8:8q21.13-24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3 copy number gain See cases [RCV000148092] Chr8:241530..145054634 [GRCh38]
Chr8:191530..146280020 [GRCh37]
Chr8:181530..146250824 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q21.2-24.3(chr8:85765999-145070385)x3 copy number gain See cases [RCV000143659] Chr8:85765999..145070385 [GRCh38]
Chr8:86778228..146295771 [GRCh37]
Chr8:86863079..146266575 [NCBI36]
Chr8:8q21.2-24.3
pathogenic
GRCh38/hg38 8q24.13-24.3(chr8:124514090-145054634)x3 copy number gain See cases [RCV000148117] Chr8:124514090..145054634 [GRCh38]
Chr8:125526331..146280020 [GRCh37]
Chr8:125595512..146250824 [NCBI36]
Chr8:8q24.13-24.3
pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158991-146280828)x3 copy number gain See cases [RCV000447507] Chr8:158991..146280828 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
GRCh37/hg19 8q22.1-24.3(chr8:98432250-146222672)x4 copy number gain See cases [RCV000448954] Chr8:98432250..146222672 [GRCh37]
Chr8:8q22.1-24.3
pathogenic
GRCh37/hg19 8q24.13-24.21(chr8:125539280-128129372)x1 copy number loss See cases [RCV000510509] Chr8:125539280..128129372 [GRCh37]
Chr8:8q24.13-24.21
uncertain significance
GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771) copy number gain See cases [RCV000510234] Chr8:158049..146295771 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
GRCh37/hg19 8q21.3-24.3(chr8:93047482-141355635)x3 copy number gain See cases [RCV000511761] Chr8:93047482..141355635 [GRCh37]
Chr8:8q21.3-24.3
pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771)x3 copy number gain See cases [RCV000511095] Chr8:158049..146295771 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
GRCh37/hg19 8q21.2-24.3(chr8:86841154-146295771)x3 copy number gain See cases [RCV000511002] Chr8:86841154..146295771 [GRCh37]
Chr8:8q21.2-24.3
pathogenic
GRCh37/hg19 8q21.2-24.3(chr8:86841228-142689874)x3 copy number gain See cases [RCV000510854] Chr8:86841228..142689874 [GRCh37]
Chr8:8q21.2-24.3
pathogenic
GRCh37/hg19 8q23.3-24.3(chr8:114853126-146295771)x3 copy number gain See cases [RCV000512401] Chr8:114853126..146295771 [GRCh37]
Chr8:8q23.3-24.3
pathogenic
GRCh37/hg19 8p23.1-q24.3(chr8:12490999-146295771)x3 copy number gain See cases [RCV000512169] Chr8:12490999..146295771 [GRCh37]
Chr8:8p23.1-q24.3
pathogenic
GRCh37/hg19 8q24.12-24.3(chr8:121694649-146295771)x3 copy number gain not provided [RCV000683044] Chr8:121694649..146295771 [GRCh37]
Chr8:8q24.12-24.3
pathogenic
GRCh37/hg19 8q24.13-24.3(chr8:125496223-146295771)x3 copy number gain not provided [RCV000845705] Chr8:125496223..146295771 [GRCh37]
Chr8:8q24.13-24.3
pathogenic
Single allele deletion Trichorhinophalangeal dysplasia type I [RCV000735900] Chr8:114508086..129040004 [GRCh37]
Chr8:8q23.3-24.21
pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:164984-146293414)x3 copy number gain not provided [RCV000747254] Chr8:164984..146293414 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:10213-146293414)x3 copy number gain not provided [RCV000747248] Chr8:10213..146293414 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
NM_014751.5(MTSS1):c.619-571G>A single nucleotide variant Mitochondrial complex 1 deficiency, nuclear type 24 [RCV000988115] Chr8:124567749 [GRCh38]
Chr8:125579990 [GRCh37]
Chr8:8q24.13
benign
GRCh37/hg19 8q24.13(chr8:125310755-125983817)x3 copy number gain not provided [RCV000848433] Chr8:125310755..125983817 [GRCh37]
Chr8:8q24.13
uncertain significance
GRCh37/hg19 8q24.13-24.22(chr8:124120772-135265846)x1 copy number loss not provided [RCV000848438] Chr8:124120772..135265846 [GRCh37]
Chr8:8q24.13-24.22
pathogenic
GRCh37/hg19 8q24.12-24.3(chr8:122193546-146295771)x3 copy number gain not provided [RCV000849762] Chr8:122193546..146295771 [GRCh37]
Chr8:8q24.12-24.3
pathogenic
NM_014751.5(MTSS1):c.1036-28C>T single nucleotide variant Mitochondrial complex 1 deficiency, nuclear type 24 [RCV000988114] Chr8:124557903 [GRCh38]
Chr8:125570144 [GRCh37]
Chr8:8q24.13
benign
GRCh37/hg19 8q24.13-24.21(chr8:123074293-131113892)x1 copy number loss not provided [RCV000848164] Chr8:123074293..131113892 [GRCh37]
Chr8:8q24.13-24.21
pathogenic
GRCh37/hg19 8p12-q24.3(chr8:31936551-146295771)x3 copy number gain not provided [RCV000848192] Chr8:31936551..146295771 [GRCh37]
Chr8:8p12-q24.3
pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3 copy number gain not provided [RCV000848478] Chr8:158048..146295771 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
GRCh37/hg19 8q24.13(chr8:124878368-126737708)x3 copy number gain not provided [RCV001006141] Chr8:124878368..126737708 [GRCh37]
Chr8:8q24.13
uncertain significance
GRCh37/hg19 8q24.13(chr8:125584474-126043912)x1 copy number loss not provided [RCV001006142] Chr8:125584474..126043912 [GRCh37]
Chr8:8q24.13
uncertain significance
GRCh37/hg19 8q24.12-24.3(chr8:121042467-146295771)x3 copy number gain not provided [RCV001006140] Chr8:121042467..146295771 [GRCh37]
Chr8:8q24.12-24.3
pathogenic

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:20443 AgrOrtholog
COSMIC MTSS1 COSMIC
Ensembl Genes ENSG00000170873 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000322804 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000367256 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000393606 UniProtKB/Swiss-Prot
  ENSP00000428145 UniProtKB/TrEMBL
  ENSP00000428319 UniProtKB/TrEMBL
  ENSP00000428348 UniProtKB/TrEMBL
  ENSP00000428685 UniProtKB/TrEMBL
  ENSP00000429064 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000429752 UniProtKB/TrEMBL
Ensembl Transcript ENST00000325064 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000378017 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000431961 UniProtKB/Swiss-Prot
  ENST00000518547 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000519168 UniProtKB/TrEMBL
  ENST00000522118 UniProtKB/TrEMBL
  ENST00000522162 UniProtKB/TrEMBL
  ENST00000523179 UniProtKB/TrEMBL
  ENST00000524090 UniProtKB/TrEMBL
Gene3D-CATH 1.20.1270.60 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000170873 GTEx
HGNC ID HGNC:20443 ENTREZGENE
Human Proteome Map MTSS1 Human Proteome Map
InterPro AH/BAR_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  I-BAR_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MIM UniProtKB/Swiss-Prot
  MIM/ABBA UniProtKB/Swiss-Prot
  MTSS1 UniProtKB/TrEMBL
  MTSS1/MTSS2 UniProtKB/TrEMBL
  WH2_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:9788 UniProtKB/Swiss-Prot
NCBI Gene 9788 ENTREZGENE
OMIM 608486 OMIM
PANTHER PTHR15708 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR15708:SF10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam IMD UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  WH2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134892011 PharmGKB
PROSITE IMD UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  WH2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF103657 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A5YM41 ENTREZGENE, UniProtKB/TrEMBL
  E5RJX3_HUMAN UniProtKB/TrEMBL
  E7EWW5_HUMAN UniProtKB/TrEMBL
  H0YAZ8_HUMAN UniProtKB/TrEMBL
  H0YB53_HUMAN UniProtKB/TrEMBL
  H0YBL3_HUMAN UniProtKB/TrEMBL
  MTSS1_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
UniProt Secondary J3KNK6 UniProtKB/Swiss-Prot
  Q8TCA2 UniProtKB/Swiss-Prot
  Q96RX2 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2019-01-29 MTSS1  MTSS I-BAR domain containing 1    MTSS1, I-BAR domain containing  Symbol and/or name change 5135510 APPROVED
2016-08-02 MTSS1  MTSS1, I-BAR domain containing    metastasis suppressor 1  Symbol and/or name change 5135510 APPROVED