MX1 (MX dynamin like GTPase 1) - Rat Genome Database

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Gene: MX1 (MX dynamin like GTPase 1) Homo sapiens
Analyze
Symbol: MX1
Name: MX dynamin like GTPase 1
RGD ID: 1353561
HGNC Page HGNC
Description: Enables identical protein binding activity. Involved in antiviral innate immune response; interleukin-27-mediated signaling pathway; and negative regulation of viral genome replication. Located in cytosol; nuclear membrane; and perinuclear region of cytoplasm. Implicated in alopecia areata; avian influenza; liver disease; and prostate cancer. Biomarker of Human papillomavirus infectious disease.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: IFI-78K; IFI78; interferon inducible protein p78; interferon-induced GTP-binding protein Mx1; interferon-induced protein p78; interferon-inducible protein p78; interferon-regulated resistance GTP-binding protein MxA; lncMX1-215; MX; MX dynamin-like GTPase 1; MxA; myxoma resistance protein 1; myxovirus (influenza virus) resistance 1, interferon-inducible protein p78; myxovirus resistance protein 1
RGD Orthologs
Mouse
Rat
Bonobo
Dog
Pig
Green Monkey
Alliance Genes
More Info more info ...
Related Pseudogenes: AC006499.3   AC006499.5   AC006499.7  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl2141,420,020 - 41,470,071 (+)EnsemblGRCh38hg38GRCh38
GRCh382141,420,329 - 41,459,214 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh372142,792,485 - 42,831,141 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 362141,720,024 - 41,753,008 (+)NCBINCBI36hg18NCBI36
Build 342141,720,023 - 41,753,008NCBI
Celera2127,990,716 - 28,029,320 (+)NCBI
Cytogenetic Map21q22.3NCBI
HuRef2128,261,373 - 28,300,013 (+)NCBIHuRef
CHM1_12142,353,308 - 42,391,928 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(+)-schisandrin B  (ISO)
(-)-epigallocatechin 3-gallate  (EXP)
17alpha-ethynylestradiol  (ISO)
17beta-estradiol  (EXP,ISO)
17beta-estradiol 3-benzoate  (ISO)
2,2',4,4',5,5'-hexachlorobiphenyl  (EXP)
2,2',4,4'-Tetrabromodiphenyl ether  (EXP,ISO)
2,2',5,5'-tetrachlorobiphenyl  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
2,3,7,8-Tetrachlorodibenzofuran  (ISO)
2,4-dinitrotoluene  (ISO)
2-hydroxypropanoic acid  (EXP)
3,3',4,4',5-pentachlorobiphenyl  (ISO)
3,3',5,5'-tetrabromobisphenol A  (ISO)
3-phenylprop-2-enal  (EXP)
4,4'-diaminodiphenylmethane  (ISO)
4-hydroxynon-2-enal  (ISO)
5-aza-2'-deoxycytidine  (EXP)
6-propyl-2-thiouracil  (ISO)
6alpha-methylprednisolone  (EXP)
acetamide  (ISO)
acetylsalicylic acid  (EXP)
aconitine  (ISO)
acrolein  (EXP)
acrylamide  (ISO)
Actein  (ISO)
alpha-pinene  (EXP)
alvocidib  (ISO)
ammonium chloride  (ISO)
amphetamine  (ISO)
arsane  (EXP)
arsenic atom  (EXP)
arsenous acid  (EXP)
azathioprine  (EXP)
benzene  (EXP)
benzo[a]pyrene  (EXP,ISO)
bis(2-chloroethyl) sulfide  (EXP)
bis(2-ethylhexyl) phthalate  (EXP)
bisphenol A  (ISO)
bromobenzene  (ISO)
cadmium atom  (ISO)
cadmium dichloride  (ISO)
carbon nanotube  (ISO)
chromium(6+)  (EXP)
cisplatin  (ISO)
cobalt dichloride  (ISO)
copper atom  (EXP,ISO)
copper(0)  (EXP,ISO)
crocidolite asbestos  (ISO)
Cuprizon  (ISO)
cyclosporin A  (EXP)
decabromodiphenyl ether  (ISO)
diarsenic trioxide  (EXP)
dichloroacetic acid  (ISO)
diclofenac  (EXP)
dieldrin  (EXP,ISO)
diethyl maleate  (ISO)
dimethylarsinous acid  (EXP)
disulfiram  (EXP)
doxorubicin  (EXP,ISO)
elemental selenium  (EXP)
endosulfan  (ISO)
folic acid  (ISO)
formaldehyde  (EXP)
fragrance  (EXP)
Genipin  (ISO)
genistein  (EXP)
gentamycin  (ISO)
GW 4064  (ISO)
hydroquinone  (EXP)
iopamidol  (EXP)
lead diacetate  (ISO)
lipopolysaccharide  (EXP,ISO)
lucanthone  (EXP)
metam  (ISO)
metformin  (ISO)
methotrexate  (EXP)
methylarsonic acid  (EXP)
mitomycin C  (EXP)
N-acetyl-L-cysteine  (EXP)
N-Acetyl-S-(1,2-dichlorovinyl)-cysteine  (EXP)
N-nitrosodiethylamine  (ISO)
nickel atom  (EXP)
nickel sulfate  (EXP)
orphenadrine  (ISO)
oxaliplatin  (ISO)
ozone  (EXP)
paracetamol  (EXP,ISO)
paraquat  (ISO)
PCB138  (ISO)
pentachlorophenol  (ISO)
pentanal  (EXP)
perfluorooctanoic acid  (ISO)
phenformin  (ISO)
phenobarbital  (ISO)
phorbol 13-acetate 12-myristate  (ISO)
piroxicam  (EXP)
poly(I:C)  (EXP)
potassium chromate  (EXP)
prednisolone  (EXP)
pregnenolone 16alpha-carbonitrile  (ISO)
protein kinase inhibitor  (EXP)
rac-lactic acid  (EXP)
selenium atom  (EXP)
serpentine asbestos  (EXP)
silicon dioxide  (EXP,ISO)
silver atom  (ISO)
silver(0)  (ISO)
sodium arsenite  (EXP)
sodium aurothiomalate  (EXP)
Soman  (ISO)
sulindac sulfide  (EXP)
tamoxifen  (EXP)
tauroursodeoxycholic acid  (ISO)
temozolomide  (EXP)
tert-butyl hydroperoxide  (EXP,ISO)
testosterone  (ISO)
testosterone enanthate  (EXP)
tetrachloroethene  (EXP)
tetrachloromethane  (ISO)
thioacetamide  (ISO)
titanium dioxide  (ISO)
tofacitinib  (EXP)
topotecan  (ISO)
tremolite asbestos  (ISO)
trichostatin A  (EXP)
triclosan  (EXP)
Triptolide  (ISO)
valproic acid  (EXP)
vinclozolin  (ISO)
vitamin E  (EXP)
vorinostat  (EXP)
zidovudine  (EXP)
zinc atom  (ISO)
zinc(0)  (ISO)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
1. Ciminski K, etal., Emerg Microbes Infect. 2019;8(1):556-563. doi: 10.1080/22221751.2019.1599301.
2. Deeg CM, etal., J Exp Med. 2017 May 1;214(5):1239-1248. doi: 10.1084/jem.20161033. Epub 2017 Apr 10.
3. García-Álvarez M, etal., Sci Rep. 2017 Jan 31;7:41516. doi: 10.1038/srep41516.
4. Glymph S, etal., Infect Genet Evol. 2013 Jun;16:186-90. doi: 10.1016/j.meegid.2013.02.010. Epub 2013 Feb 22.
5. GOA_HUMAN data from the GO Consortium
6. Ivaska L, etal., J Infect. 2017 Apr;74(4):385-392. doi: 10.1016/j.jinf.2017.01.002. Epub 2017 Jan 7.
7. Jung HE, etal., Viruses. 2019 Jan 28;11(2). pii: v11020109. doi: 10.3390/v11020109.
8. Kolb E, etal., J Virol. 1992 Mar;66(3):1709-16. doi: 10.1128/JVI.66.3.1709-1716.1992.
9. Lee S, etal., Sci Immunol. 2019 Oct 25;4(40). pii: 4/40/eaau4643. doi: 10.1126/sciimmunol.aau4643.
10. Pipeline to import KEGG annotations from KEGG into RGD
11. RGD automated import pipeline for gene-chemical interactions
12. Saadeh D, etal., Clin Exp Dermatol. 2017 Dec;42(8):857-862. doi: 10.1111/ced.13187. Epub 2017 Jul 24.
13. Shaker OG, etal., Cell Biochem Biophys. 2015 Mar;71(2):617-25. doi: 10.1007/s12013-014-0241-9.
14. Tazi-Ahnini R, etal., Hum Genet. 2000 Jun;106(6):639-45. doi: 10.1007/s004390000318.
15. Toivonen L, etal., J Clin Virol. 2015 Jan;62:8-13. doi: 10.1016/j.jcv.2014.11.018. Epub 2014 Nov 18.
16. Zang F, etal., Epidemiol Infect. 2018 Feb;146(3):379-385. doi: 10.1017/S0950268817002928. Epub 2017 Dec 22.
17. Zhang X, etal., Hum Genet. 2014 Feb;133(2):187-97. doi: 10.1007/s00439-013-1367-3. Epub 2013 Oct 2.
Additional References at PubMed
PMID:1548781   PMID:1629950   PMID:1674496   PMID:2154602   PMID:2161946   PMID:2481229   PMID:2607176   PMID:3162334   PMID:8125298   PMID:8411374   PMID:8798556   PMID:9060610  
PMID:9093949   PMID:9389754   PMID:9735310   PMID:9933640   PMID:10590150   PMID:10830953   PMID:10971132   PMID:11716541   PMID:11805446   PMID:11847228   PMID:11880649   PMID:11911186  
PMID:11916975   PMID:12447867   PMID:12477932   PMID:12539042   PMID:12595530   PMID:12867637   PMID:12944978   PMID:14499622   PMID:14687945   PMID:14702039   PMID:14752052   PMID:14872030  
PMID:15047845   PMID:15063762   PMID:15117331   PMID:15135736   PMID:15163707   PMID:15221897   PMID:15355513   PMID:15489334   PMID:15602733   PMID:15757897   PMID:15766558   PMID:15850793  
PMID:16009940   PMID:16168514   PMID:16202617   PMID:16344560   PMID:16390004   PMID:16413306   PMID:16459719   PMID:16595158   PMID:16704297   PMID:16712791   PMID:16769349   PMID:16780588  
PMID:16792864   PMID:16824203   PMID:16843495   PMID:16894313   PMID:16978069   PMID:17075576   PMID:17126411   PMID:17177148   PMID:17307214   PMID:17374778   PMID:17407708   PMID:17570575  
PMID:17845304   PMID:17947524   PMID:18549400   PMID:18668195   PMID:18676680   PMID:18782441   PMID:18843779   PMID:19109387   PMID:19170196   PMID:19177264   PMID:19236454   PMID:19297326  
PMID:19299420   PMID:19434718   PMID:19462904   PMID:19625176   PMID:19625466   PMID:19635103   PMID:19692168   PMID:19744071   PMID:19817957   PMID:20019841   PMID:20237496   PMID:20309637  
PMID:20331378   PMID:20428112   PMID:20462354   PMID:20494980   PMID:20538602   PMID:20588308   PMID:20603636   PMID:20628624   PMID:20921509   PMID:20959021   PMID:21166595   PMID:21478870  
PMID:21645334   PMID:21832049   PMID:21859714   PMID:21873635   PMID:21900240   PMID:21918813   PMID:21935451   PMID:21962493   PMID:21992152   PMID:22340769   PMID:22507598   PMID:22531919  
PMID:22647704   PMID:22714910   PMID:22950423   PMID:22985419   PMID:22998463   PMID:23015724   PMID:23084925   PMID:23115279   PMID:23152507   PMID:23160781   PMID:23232524   PMID:23274784  
PMID:23382691   PMID:23529855   PMID:23831963   PMID:23848523   PMID:24032645   PMID:24049170   PMID:24212839   PMID:24314641   PMID:24421397   PMID:24438589   PMID:24448803   PMID:24553842  
PMID:24674141   PMID:24733382   PMID:24742347   PMID:24771638   PMID:24899177   PMID:25056900   PMID:25170834   PMID:25295396   PMID:25324306   PMID:25327819   PMID:25384438   PMID:25396411  
PMID:25416956   PMID:25447205   PMID:25829498   PMID:25868067   PMID:25905045   PMID:25930096   PMID:26116899   PMID:26175399   PMID:26446602   PMID:26507657   PMID:26618866   PMID:26815367  
PMID:26857498   PMID:27075916   PMID:27107014   PMID:27456948   PMID:27458866   PMID:27875556   PMID:28039312   PMID:28386647   PMID:28514442   PMID:28548099   PMID:28561372   PMID:28727764  
PMID:28744639   PMID:29330299   PMID:29417241   PMID:29509190   PMID:29530483   PMID:29770465   PMID:30471916   PMID:30555157   PMID:30667074   PMID:30833792   PMID:31444947   PMID:31484749  
PMID:31574080   PMID:32209695   PMID:32270034   PMID:32296183   PMID:32350677   PMID:32513696   PMID:32640729   PMID:32740454   PMID:32907985   PMID:34413236  


Genomics

Comparative Map Data
MX1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl2141,420,020 - 41,470,071 (+)EnsemblGRCh38hg38GRCh38
GRCh382141,420,329 - 41,459,214 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh372142,792,485 - 42,831,141 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 362141,720,024 - 41,753,008 (+)NCBINCBI36hg18NCBI36
Build 342141,720,023 - 41,753,008NCBI
Celera2127,990,716 - 28,029,320 (+)NCBI
Cytogenetic Map21q22.3NCBI
HuRef2128,261,373 - 28,300,013 (+)NCBIHuRef
CHM1_12142,353,308 - 42,391,928 (+)NCBICHM1_1
Mx1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391697,248,235 - 97,264,106 (-)NCBIGRCm39mm39
GRCm39 Ensembl1697,248,235 - 97,264,107 (-)Ensembl
GRCm381697,447,035 - 97,462,906 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1697,447,035 - 97,462,907 (-)EnsemblGRCm38mm10GRCm38
MGSCv371697,668,642 - 97,684,513 (-)NCBIGRCm37mm9NCBIm37
MGSCv361697,551,947 - 97,567,815 (-)NCBImm8
Celera1698,507,376 - 98,523,260 (-)NCBICelera
Cytogenetic Map16C4NCBI
cM Map1657.46NCBI
Mx1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.21136,799,659 - 36,825,209 (-)NCBImRatBN7.2
mRatBN7.2 Ensembl1136,799,660 - 36,823,507 (-)Ensembl
Rnor_6.01137,891,150 - 37,916,775 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1137,891,156 - 37,914,983 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01141,398,737 - 41,424,277 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41137,438,473 - 37,462,363 (-)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.11137,496,062 - 37,517,940 (-)NCBI
Celera1136,686,487 - 36,712,040 (-)NCBICelera
Cytogenetic Map11q12NCBI
MX1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.12141,089,711 - 41,123,019 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl2141,095,928 - 41,123,019 (+)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v02127,756,768 - 27,795,307 (+)NCBIMhudiblu_PPA_v0panPan3
MX1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.13135,898,206 - 35,929,802 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl3135,860,590 - 35,951,350 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha3135,060,087 - 35,084,645 (+)NCBI
ROS_Cfam_1.03135,419,440 - 35,447,820 (+)NCBI
UMICH_Zoey_3.13135,318,427 - 35,342,955 (+)NCBI
UNSW_CanFamBas_1.03135,297,561 - 35,322,100 (+)NCBI
UU_Cfam_GSD_1.03135,791,284 - 35,815,851 (+)NCBI
MX1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl13204,843,754 - 204,868,922 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.113204,843,049 - 204,868,927 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.213214,988,890 - 215,014,780 (-)NCBISscrofa10.2Sscrofa10.2susScr3
MX1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1285,333,327 - 85,368,179 (+)NCBIChlSab1.1chlSab2
ChlSab1.1 Ensembl285,338,530 - 85,368,507 (+)EnsemblChlSab1.1chlSab2
Vero_WHO_p1.0NW_02366605413,185,843 - 13,220,898 (+)NCBIVero_WHO_p1.0

Position Markers
D21S1260  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372142,796,042 - 42,796,251UniSTSGRCh37
GRCh372142,796,042 - 42,796,268UniSTSGRCh37
Build 362141,717,912 - 41,718,121RGDNCBI36
Celera2127,994,239 - 27,994,444RGD
Celera2127,994,239 - 27,994,461UniSTS
Cytogenetic Map21q22.3UniSTS
HuRef2128,264,896 - 28,265,101UniSTS
Marshfield Genetic Map2146.71RGD
Marshfield Genetic Map2146.71UniSTS
Genethon Genetic Map2151.6UniSTS
deCODE Assembly Map2156.33UniSTS
GeneMap99-GB4 RH Map21220.6UniSTS
Whitehead-RH Map21209.8UniSTS
Whitehead-YAC Contig Map21 UniSTS
NCBI RH Map21331.1UniSTS
SHGC-87654  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372142,830,750 - 42,830,892UniSTSGRCh37
Build 362141,752,620 - 41,752,762RGDNCBI36
Celera2128,028,929 - 28,029,071RGD
Cytogenetic Map21q22.3UniSTS
HuRef2128,299,622 - 28,299,764UniSTS
TNG Radiation Hybrid Map2116379.0UniSTS
GeneMap99-GB4 RH Map21227.15UniSTS
Whitehead-RH Map21234.2UniSTS
NCBI RH Map21344.1UniSTS
GDB:185157  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372142,830,681 - 42,830,952UniSTSGRCh37
Build 362141,752,551 - 41,752,822RGDNCBI36
Celera2128,028,860 - 28,029,131RGD
Cytogenetic Map21q22.3UniSTS
HuRef2128,299,553 - 28,299,824UniSTS
GDB:192322  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372142,830,857 - 42,831,078UniSTSGRCh37
Build 362141,752,727 - 41,752,948RGDNCBI36
Celera2128,029,036 - 28,029,257RGD
Cytogenetic Map21q22.3UniSTS
HuRef2128,299,729 - 28,299,950UniSTS
SHGC-2323  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372142,796,125 - 42,796,228UniSTSGRCh37
Build 362141,717,995 - 41,718,098RGDNCBI36
Celera2127,994,322 - 27,994,421RGD
Cytogenetic Map21q22.3UniSTS
HuRef2128,264,979 - 28,265,078UniSTS
TNG Radiation Hybrid Map2116367.0UniSTS
SHGC-6908  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372142,799,037 - 42,799,274UniSTSGRCh37
Build 362141,720,907 - 41,721,144RGDNCBI36
Celera2127,997,231 - 27,997,468RGD
Cytogenetic Map21q22.3UniSTS
HuRef2128,267,888 - 28,268,125UniSTS
TNG Radiation Hybrid Map2116371.0UniSTS
Stanford-G3 RH Map211451.0UniSTS
NCBI RH Map21359.6UniSTS
GeneMap99-G3 RH Map211451.0UniSTS
PMC154027P2  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372142,830,602 - 42,830,913UniSTSGRCh37
Build 362141,752,472 - 41,752,783RGDNCBI36
Celera2128,028,781 - 28,029,092RGD
Cytogenetic Map21q22.3UniSTS
HuRef2128,299,474 - 28,299,785UniSTS
PMC310729P8  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372142,808,458 - 42,808,814UniSTSGRCh37
Build 362141,730,328 - 41,730,684RGDNCBI36
Celera2128,006,654 - 28,007,010RGD
Cytogenetic Map21q22.3UniSTS
HuRef2128,277,318 - 28,277,674UniSTS
PMC310729P9  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372142,823,150 - 42,823,435UniSTSGRCh37
Build 362141,745,020 - 41,745,305RGDNCBI36
Celera2128,021,328 - 28,021,613RGD
Cytogenetic Map21q22.3UniSTS
HuRef2128,291,990 - 28,292,275UniSTS
PMC321570P12  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372142,830,746 - 42,830,946UniSTSGRCh37
Build 362141,752,616 - 41,752,816RGDNCBI36
Celera2128,028,925 - 28,029,125RGD
Cytogenetic Map21q22.3UniSTS
HuRef2128,299,618 - 28,299,818UniSTS
MX1_1629  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372142,830,487 - 42,831,141UniSTSGRCh37
Build 362141,752,357 - 41,753,011RGDNCBI36
Celera2128,028,666 - 28,029,320RGD
HuRef2128,299,359 - 28,300,013UniSTS
RH70302  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372142,830,807 - 42,830,964UniSTSGRCh37
Build 362141,752,677 - 41,752,834RGDNCBI36
Celera2128,028,986 - 28,029,143RGD
Cytogenetic Map21q22.3UniSTS
HuRef2128,299,679 - 28,299,836UniSTS
GeneMap99-GB4 RH Map21217.35UniSTS
SHGC-5964  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372142,830,907 - 42,831,137UniSTSGRCh37
Build 362141,752,777 - 41,753,007RGDNCBI36
Celera2128,029,086 - 28,029,316RGD
Cytogenetic Map21q22.3UniSTS
HuRef2128,299,779 - 28,300,009UniSTS
TNG Radiation Hybrid Map2116375.0UniSTS
Stanford-G3 RH Map211431.0UniSTS
NCBI RH Map21354.8UniSTS
GeneMap99-G3 RH Map211431.0UniSTS
MX1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372142,749,720 - 42,749,873UniSTSGRCh37
GRCh372142,807,768 - 42,807,921UniSTSGRCh37
Celera2127,947,948 - 27,948,101UniSTS
Celera2128,005,964 - 28,006,117UniSTS
HuRef2128,276,628 - 28,276,781UniSTS
HuRef2128,218,604 - 28,218,757UniSTS
D5S1597E  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map18q12.2UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map12q24.31-q24.32UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map13q33.3UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map20q13.1UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map20q12-q13.12UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map11p11.11UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map3q28UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic MapXp22.31UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map4q13UniSTS
Cytogenetic Map4q35.2UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map2p12-p11.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map15q21.1-q21.2UniSTS
Cytogenetic Map22q12-q13UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map10q26.1UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map15q11.2-q21.3UniSTS
Cytogenetic Map6q16.2UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:3782
Count of miRNA genes:1029
Interacting mature miRNAs:1269
Transcripts:ENST00000288383, ENST00000398598, ENST00000398600, ENST00000413778, ENST00000417963, ENST00000419044, ENST00000424365, ENST00000427464, ENST00000441677, ENST00000455164, ENST00000467510, ENST00000468506, ENST00000478268, ENST00000484465, ENST00000486275, ENST00000490220, ENST00000491110
Prediction methods:Microtar, Miranda, Rnahybrid
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 1 2 1 1 1
Medium 2090 1800 1291 302 1467 164 2295 924 2395 212 1005 1426 145 1060 1471 1
Low 338 1186 424 315 443 294 2057 1257 1306 203 429 150 28 1 144 1316 2 1
Below cutoff 8 1 10 6 36 7 1 13 15 4 20 31 2

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_027788 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001144925 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001178046 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001282920 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_002462 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005260978 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005260979 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005260980 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005260981 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005260982 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011529568 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011529570 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017028349 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017028350 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017028351 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017028352 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide A00209 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC005612 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF135187 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF168707 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF168708 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF208008 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF208009 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF208010 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK093008 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK096355 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK225885 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK315465 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL163285 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL773570 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL773577 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL773578 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP001610 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY186254 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC014222 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC032602 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC052255 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CB151486 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471079 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA351922 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA726666 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EB388095 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KC877894 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  L35664 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  L35666 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  L35669 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  L35671 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  L35672 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  L35673 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M30817 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M33882 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000288383   ⟹   ENSP00000288383
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,426,201 - 41,459,199 (+)Ensembl
RefSeq Acc Id: ENST00000398598   ⟹   ENSP00000381599
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,426,239 - 41,459,212 (+)Ensembl
RefSeq Acc Id: ENST00000398600   ⟹   ENSP00000381601
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,420,515 - 41,459,214 (+)Ensembl
RefSeq Acc Id: ENST00000413778   ⟹   ENSP00000408498
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,421,329 - 41,458,758 (+)Ensembl
RefSeq Acc Id: ENST00000417963   ⟹   ENSP00000402215
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,426,178 - 41,458,758 (+)Ensembl
RefSeq Acc Id: ENST00000419044   ⟹   ENSP00000392151
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,425,822 - 41,459,637 (+)Ensembl
RefSeq Acc Id: ENST00000424365   ⟹   ENSP00000400923
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,426,142 - 41,459,199 (+)Ensembl
RefSeq Acc Id: ENST00000427464   ⟹   ENSP00000410989
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,429,481 - 41,432,175 (+)Ensembl
RefSeq Acc Id: ENST00000441677   ⟹   ENSP00000393931
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,426,239 - 41,441,173 (+)Ensembl
RefSeq Acc Id: ENST00000455164   ⟹   ENSP00000410523
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,426,031 - 41,459,213 (+)Ensembl
RefSeq Acc Id: ENST00000467510
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,426,241 - 41,459,200 (+)Ensembl
RefSeq Acc Id: ENST00000468506
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,420,366 - 41,423,277 (+)Ensembl
RefSeq Acc Id: ENST00000478268
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,426,270 - 41,429,921 (+)Ensembl
RefSeq Acc Id: ENST00000484465
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,426,192 - 41,428,070 (+)Ensembl
RefSeq Acc Id: ENST00000486275
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,420,280 - 41,450,727 (+)Ensembl
RefSeq Acc Id: ENST00000490220
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,420,304 - 41,427,866 (+)Ensembl
RefSeq Acc Id: ENST00000491110
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,450,928 - 41,452,820 (+)Ensembl
RefSeq Acc Id: ENST00000619682   ⟹   ENSP00000478441
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,432,050 - 41,459,213 (+)Ensembl
RefSeq Acc Id: ENST00000679386   ⟹   ENSP00000505700
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,426,201 - 41,470,071 (+)Ensembl
RefSeq Acc Id: ENST00000679408   ⟹   ENSP00000505269
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,426,290 - 41,459,199 (+)Ensembl
RefSeq Acc Id: ENST00000679445   ⟹   ENSP00000505630
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,420,318 - 41,459,637 (+)Ensembl
RefSeq Acc Id: ENST00000679464   ⟹   ENSP00000505874
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,420,279 - 41,459,637 (+)Ensembl
RefSeq Acc Id: ENST00000679528
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,426,241 - 41,442,155 (+)Ensembl
RefSeq Acc Id: ENST00000679543   ⟹   ENSP00000505047
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,426,590 - 41,459,637 (+)Ensembl
RefSeq Acc Id: ENST00000679626   ⟹   ENSP00000506481
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,420,610 - 41,459,637 (+)Ensembl
RefSeq Acc Id: ENST00000679705   ⟹   ENSP00000506372
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,426,101 - 41,459,637 (+)Ensembl
RefSeq Acc Id: ENST00000679911   ⟹   ENSP00000505189
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,420,020 - 41,459,637 (+)Ensembl
RefSeq Acc Id: ENST00000680176   ⟹   ENSP00000506270
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,426,241 - 41,459,637 (+)Ensembl
RefSeq Acc Id: ENST00000680182   ⟹   ENSP00000506395
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,420,279 - 41,459,637 (+)Ensembl
RefSeq Acc Id: ENST00000680347   ⟹   ENSP00000506183
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,420,158 - 41,459,637 (+)Ensembl
RefSeq Acc Id: ENST00000680364   ⟹   ENSP00000505781
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,426,608 - 41,459,637 (+)Ensembl
RefSeq Acc Id: ENST00000680536   ⟹   ENSP00000505029
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,426,270 - 41,459,637 (+)Ensembl
RefSeq Acc Id: ENST00000680629   ⟹   ENSP00000506047
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,426,239 - 41,459,637 (+)Ensembl
RefSeq Acc Id: ENST00000680637
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,442,169 - 41,451,827 (+)Ensembl
RefSeq Acc Id: ENST00000680760   ⟹   ENSP00000506199
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,426,241 - 41,459,637 (+)Ensembl
RefSeq Acc Id: ENST00000680776   ⟹   ENSP00000506512
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,426,249 - 41,459,637 (+)Ensembl
RefSeq Acc Id: ENST00000680942   ⟹   ENSP00000505637
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,426,201 - 41,459,199 (+)Ensembl
RefSeq Acc Id: ENST00000680980
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,451,905 - 41,459,199 (+)Ensembl
RefSeq Acc Id: ENST00000681039   ⟹   ENSP00000506220
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,426,295 - 41,459,637 (+)Ensembl
RefSeq Acc Id: ENST00000681191   ⟹   ENSP00000505657
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,420,286 - 41,459,637 (+)Ensembl
RefSeq Acc Id: ENST00000681266   ⟹   ENSP00000506348
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,426,171 - 41,459,637 (+)Ensembl
RefSeq Acc Id: ENST00000681382
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,426,201 - 41,459,200 (+)Ensembl
RefSeq Acc Id: ENST00000681415   ⟹   ENSP00000506062
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,420,279 - 41,459,637 (+)Ensembl
RefSeq Acc Id: ENST00000681607   ⟹   ENSP00000505489
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,426,256 - 41,459,637 (+)Ensembl
RefSeq Acc Id: ENST00000681671   ⟹   ENSP00000506712
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,426,295 - 41,459,637 (+)Ensembl
RefSeq Acc Id: ENST00000681849   ⟹   ENSP00000505051
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,426,090 - 41,459,637 (+)Ensembl
RefSeq Acc Id: ENST00000681857   ⟹   ENSP00000505669
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,420,339 - 41,459,637 (+)Ensembl
RefSeq Acc Id: ENST00000681867   ⟹   ENSP00000506690
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,420,203 - 41,459,637 (+)Ensembl
RefSeq Acc Id: ENST00000681896   ⟹   ENSP00000505457
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,426,239 - 41,459,637 (+)Ensembl
RefSeq Acc Id: ENST00000681944   ⟹   ENSP00000505730
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2141,426,201 - 41,459,199 (+)Ensembl
RefSeq Acc Id: NM_001144925   ⟹   NP_001138397
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382141,420,558 - 41,459,214 (+)NCBI
GRCh372142,792,520 - 42,831,141 (+)ENTREZGENE
HuRef2128,261,339 - 28,300,013 (+)NCBI
CHM1_12142,353,274 - 42,391,928 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001178046   ⟹   NP_001171517
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382141,426,239 - 41,459,212 (+)NCBI
GRCh372142,792,520 - 42,831,141 (+)ENTREZGENE
HuRef2128,261,339 - 28,300,013 (+)NCBI
CHM1_12142,358,743 - 42,391,928 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001282920   ⟹   NP_001269849
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382141,432,050 - 41,459,214 (+)NCBI
HuRef2128,261,339 - 28,300,013 (+)NCBI
CHM1_12142,364,765 - 42,391,928 (+)NCBI
Sequence:
RefSeq Acc Id: NM_002462   ⟹   NP_002453
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382141,426,239 - 41,459,212 (+)NCBI
GRCh372142,792,520 - 42,831,141 (+)ENTREZGENE
Build 362141,720,024 - 41,753,008 (+)NCBI Archive
HuRef2128,261,339 - 28,300,013 (+)NCBI
CHM1_12142,358,743 - 42,391,928 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005260978   ⟹   XP_005261035
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382141,426,249 - 41,459,213 (+)NCBI
GRCh372142,792,520 - 42,831,141 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005260979   ⟹   XP_005261036
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382141,425,820 - 41,459,213 (+)NCBI
GRCh372142,792,520 - 42,831,141 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005260980   ⟹   XP_005261037
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382141,426,169 - 41,459,213 (+)NCBI
GRCh372142,792,520 - 42,831,141 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005260981   ⟹   XP_005261038
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382141,426,171 - 41,459,212 (+)NCBI
GRCh372142,792,520 - 42,831,141 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005260982   ⟹   XP_005261039
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382141,426,205 - 41,459,213 (+)NCBI
GRCh372142,792,520 - 42,831,141 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011529568   ⟹   XP_011527870
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382141,420,329 - 41,459,213 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011529570   ⟹   XP_011527872
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382141,432,055 - 41,448,816 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017028349   ⟹   XP_016883838
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382141,420,593 - 41,459,213 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017028350   ⟹   XP_016883839
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382141,425,820 - 41,459,213 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017028351   ⟹   XP_016883840
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382141,426,133 - 41,459,214 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017028352   ⟹   XP_016883841
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382141,426,249 - 41,459,214 (+)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001138397 (Get FASTA)   NCBI Sequence Viewer  
  NP_001171517 (Get FASTA)   NCBI Sequence Viewer  
  NP_001269849 (Get FASTA)   NCBI Sequence Viewer  
  NP_002453 (Get FASTA)   NCBI Sequence Viewer  
  XP_005261035 (Get FASTA)   NCBI Sequence Viewer  
  XP_005261036 (Get FASTA)   NCBI Sequence Viewer  
  XP_005261037 (Get FASTA)   NCBI Sequence Viewer  
  XP_005261038 (Get FASTA)   NCBI Sequence Viewer  
  XP_005261039 (Get FASTA)   NCBI Sequence Viewer  
  XP_011527870 (Get FASTA)   NCBI Sequence Viewer  
  XP_011527872 (Get FASTA)   NCBI Sequence Viewer  
  XP_016883838 (Get FASTA)   NCBI Sequence Viewer  
  XP_016883839 (Get FASTA)   NCBI Sequence Viewer  
  XP_016883840 (Get FASTA)   NCBI Sequence Viewer  
  XP_016883841 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAA36337 (Get FASTA)   NCBI Sequence Viewer  
  AAA36458 (Get FASTA)   NCBI Sequence Viewer  
  AAD43063 (Get FASTA)   NCBI Sequence Viewer  
  AAH14222 (Get FASTA)   NCBI Sequence Viewer  
  AAH32602 (Get FASTA)   NCBI Sequence Viewer  
  AAO31807 (Get FASTA)   NCBI Sequence Viewer  
  BAC04017 (Get FASTA)   NCBI Sequence Viewer  
  BAG37852 (Get FASTA)   NCBI Sequence Viewer  
  BAG53272 (Get FASTA)   NCBI Sequence Viewer  
  CAA00041 (Get FASTA)   NCBI Sequence Viewer  
  CAB90556 (Get FASTA)   NCBI Sequence Viewer  
  EAX09600 (Get FASTA)   NCBI Sequence Viewer  
  EAX09601 (Get FASTA)   NCBI Sequence Viewer  
  EAX09602 (Get FASTA)   NCBI Sequence Viewer  
  EAX09603 (Get FASTA)   NCBI Sequence Viewer  
  EAX09604 (Get FASTA)   NCBI Sequence Viewer  
  P20591 (Get FASTA)   NCBI Sequence Viewer  
Reference Sequences
RefSeq Acc Id: NP_001138397   ⟸   NM_001144925
- Peptide Label: isoform a
- UniProtKB: P20591 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_002453   ⟸   NM_002462
- Peptide Label: isoform a
- UniProtKB: P20591 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001171517   ⟸   NM_001178046
- Peptide Label: isoform a
- UniProtKB: P20591 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_005261036   ⟸   XM_005260979
- Peptide Label: isoform X1
- UniProtKB: P20591 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_005261037   ⟸   XM_005260980
- Peptide Label: isoform X1
- UniProtKB: P20591 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_005261038   ⟸   XM_005260981
- Peptide Label: isoform X1
- UniProtKB: P20591 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_005261039   ⟸   XM_005260982
- Peptide Label: isoform X1
- UniProtKB: P20591 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_005261035   ⟸   XM_005260978
- Peptide Label: isoform X1
- UniProtKB: P20591 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001269849   ⟸   NM_001282920
- Peptide Label: isoform b
- UniProtKB: P20591 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_011527870   ⟸   XM_011529568
- Peptide Label: isoform X1
- UniProtKB: P20591 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_011527872   ⟸   XM_011529570
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: XP_016883838   ⟸   XM_017028349
- Peptide Label: isoform X1
- UniProtKB: P20591 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_016883839   ⟸   XM_017028350
- Peptide Label: isoform X1
- UniProtKB: P20591 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_016883840   ⟸   XM_017028351
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_016883841   ⟸   XM_017028352
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: ENSP00000381601   ⟸   ENST00000398600
RefSeq Acc Id: ENSP00000381599   ⟸   ENST00000398598
RefSeq Acc Id: ENSP00000400923   ⟸   ENST00000424365
RefSeq Acc Id: ENSP00000410989   ⟸   ENST00000427464
RefSeq Acc Id: ENSP00000408498   ⟸   ENST00000413778
RefSeq Acc Id: ENSP00000410523   ⟸   ENST00000455164
RefSeq Acc Id: ENSP00000393931   ⟸   ENST00000441677
RefSeq Acc Id: ENSP00000402215   ⟸   ENST00000417963
RefSeq Acc Id: ENSP00000392151   ⟸   ENST00000419044
RefSeq Acc Id: ENSP00000288383   ⟸   ENST00000288383
RefSeq Acc Id: ENSP00000478441   ⟸   ENST00000619682
RefSeq Acc Id: ENSP00000505457   ⟸   ENST00000681896
RefSeq Acc Id: ENSP00000506395   ⟸   ENST00000680182
RefSeq Acc Id: ENSP00000505029   ⟸   ENST00000680536
RefSeq Acc Id: ENSP00000505657   ⟸   ENST00000681191
RefSeq Acc Id: ENSP00000506220   ⟸   ENST00000681039
RefSeq Acc Id: ENSP00000505874   ⟸   ENST00000679464
RefSeq Acc Id: ENSP00000505189   ⟸   ENST00000679911
RefSeq Acc Id: ENSP00000506062   ⟸   ENST00000681415
RefSeq Acc Id: ENSP00000506270   ⟸   ENST00000680176
RefSeq Acc Id: ENSP00000505781   ⟸   ENST00000680364
RefSeq Acc Id: ENSP00000505489   ⟸   ENST00000681607
RefSeq Acc Id: ENSP00000506372   ⟸   ENST00000679705
RefSeq Acc Id: ENSP00000506199   ⟸   ENST00000680760
RefSeq Acc Id: ENSP00000506512   ⟸   ENST00000680776
RefSeq Acc Id: ENSP00000506183   ⟸   ENST00000680347
RefSeq Acc Id: ENSP00000506481   ⟸   ENST00000679626
RefSeq Acc Id: ENSP00000506712   ⟸   ENST00000681671
RefSeq Acc Id: ENSP00000506690   ⟸   ENST00000681867
RefSeq Acc Id: ENSP00000505269   ⟸   ENST00000679408
RefSeq Acc Id: ENSP00000505047   ⟸   ENST00000679543
RefSeq Acc Id: ENSP00000505051   ⟸   ENST00000681849
RefSeq Acc Id: ENSP00000505700   ⟸   ENST00000679386
RefSeq Acc Id: ENSP00000506047   ⟸   ENST00000680629
RefSeq Acc Id: ENSP00000505730   ⟸   ENST00000681944
RefSeq Acc Id: ENSP00000505630   ⟸   ENST00000679445
RefSeq Acc Id: ENSP00000506348   ⟸   ENST00000681266
RefSeq Acc Id: ENSP00000505669   ⟸   ENST00000681857
RefSeq Acc Id: ENSP00000505637   ⟸   ENST00000680942
Protein Domains
Dynamin-type G   GED

Promoters
RGD ID:13602886
Promoter ID:EPDNEW_H27627
Type:initiation region
Name:MX1_4
Description:MX dynamin like GTPase 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H27624  EPDNEW_H27628  EPDNEW_H27629  EPDNEW_H27630  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh382141,420,318 - 41,420,378EPDNEW
RGD ID:13602888
Promoter ID:EPDNEW_H27628
Type:initiation region
Name:MX1_5
Description:MX dynamin like GTPase 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H27624  EPDNEW_H27627  EPDNEW_H27629  EPDNEW_H27630  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh382141,426,123 - 41,426,183EPDNEW
RGD ID:13602890
Promoter ID:EPDNEW_H27629
Type:initiation region
Name:MX1_1
Description:MX dynamin like GTPase 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H27624  EPDNEW_H27627  EPDNEW_H27628  EPDNEW_H27630  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh382141,426,241 - 41,426,301EPDNEW
RGD ID:13602894
Promoter ID:EPDNEW_H27630
Type:multiple initiation site
Name:MX1_3
Description:MX dynamin like GTPase 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H27624  EPDNEW_H27627  EPDNEW_H27628  EPDNEW_H27629  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh382141,427,260 - 41,427,320EPDNEW
RGD ID:6799493
Promoter ID:HG_KWN:40967
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   Lymphoblastoid,   NB4
Transcripts:OTTHUMT00000195161,   OTTHUMT00000195165,   OTTHUMT00000195166
Position:
Human AssemblyChrPosition (strand)Source
Build 362141,713,911 - 41,714,552 (+)MPROMDB
RGD ID:6799492
Promoter ID:HG_KWN:40969
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   K562,   Lymphoblastoid
Transcripts:NM_001178046,   OTTHUMT00000195162,   OTTHUMT00000195164,   OTTHUMT00000195168,   OTTHUMT00000195169,   OTTHUMT00000195170,   OTTHUMT00000195171,   OTTHUMT00000195172
Position:
Human AssemblyChrPosition (strand)Source
Build 362141,719,911 - 41,720,912 (+)MPROMDB
RGD ID:6799495
Promoter ID:HG_KWN:40970
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562,   Lymphoblastoid
Transcripts:OTTHUMT00000195173
Position:
Human AssemblyChrPosition (strand)Source
Build 362141,722,321 - 41,723,232 (+)MPROMDB
RGD ID:6799413
Promoter ID:HG_KWN:40971
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562,   Lymphoblastoid
Transcripts:ENST00000288383
Position:
Human AssemblyChrPosition (strand)Source
Build 362141,724,931 - 41,725,962 (+)MPROMDB
RGD ID:6799494
Promoter ID:HG_KWN:40973
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562,   Lymphoblastoid
Transcripts:OTTHUMT00000195174
Position:
Human AssemblyChrPosition (strand)Source
Build 362141,736,386 - 41,737,662 (+)MPROMDB
RGD ID:6799500
Promoter ID:HG_KWN:40974
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562,   Lymphoblastoid
Transcripts:OTTHUMT00000195175
Position:
Human AssemblyChrPosition (strand)Source
Build 362141,738,561 - 41,739,632 (+)MPROMDB
RGD ID:6812150
Promoter ID:HG_ACW:50662
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562
Transcripts:MX1.IAPR07,   PLOYPLAR.AAPR07-UNSPLICED
Position:
Human AssemblyChrPosition (strand)Source
Build 362141,741,921 - 41,742,421 (+)MPROMDB
RGD ID:6799499
Promoter ID:HG_KWN:40975
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000195176
Position:
Human AssemblyChrPosition (strand)Source
Build 362141,743,931 - 41,745,072 (+)MPROMDB

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46670405)x3 copy number gain See cases [RCV000050445] Chr21:7749532..46670405 [GRCh38]
Chr21:15499847..48090317 [GRCh37]
Chr21:14421718..46914745 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic|conflicting interpretations of pathogenicity|conflicting data from submitters
GRCh38/hg38 21q22.3(chr21:41285201-46670405)x1 copy number loss See cases [RCV000051022] Chr21:41285201..46670405 [GRCh38]
Chr21:42657128..48090317 [GRCh37]
Chr21:41578998..46914745 [NCBI36]
Chr21:21q22.3
pathogenic
GRCh38/hg38 21q22.13-22.3(chr21:37135738-42434515)x1 copy number loss See cases [RCV000051047] Chr21:37135738..42434515 [GRCh38]
Chr21:38508038..43854625 [GRCh37]
Chr21:37429908..42727694 [NCBI36]
Chr21:21q22.13-22.3
pathogenic
GRCh37/hg19 21q22.1-22.3(chr21:35527952-44298520)x1 copy number loss See cases [RCV000052807] Chr21:35527952..44298520 [GRCh37]
Chr21:34449822..43171589 [NCBI36]
Chr21:21q22.1-22.3
pathogenic
GRCh38/hg38 21q22.12-22.3(chr21:35027972-46670405)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052836]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052836]|See cases [RCV000052836] Chr21:35027972..46670405 [GRCh38]
Chr21:36400269..48090317 [GRCh37]
Chr21:35322139..46914745 [NCBI36]
Chr21:21q22.12-22.3
pathogenic
GRCh38/hg38 21q22.13-22.3(chr21:38273492-46670405)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052838]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052838]|See cases [RCV000052838] Chr21:38273492..46670405 [GRCh38]
Chr21:39645414..48090317 [GRCh37]
Chr21:38567284..46914745 [NCBI36]
Chr21:21q22.13-22.3
pathogenic
GRCh38/hg38 21q22.2-22.3(chr21:40127825-46670546)x1 copy number loss See cases [RCV000052839] Chr21:40127825..46670546 [GRCh38]
Chr21:41499752..48090458 [GRCh37]
Chr21:40421622..46914886 [NCBI36]
Chr21:21q22.2-22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46623792)x3 copy number gain See cases [RCV000053042] Chr21:7749532..46623792 [GRCh38]
Chr21:14595524..48043704 [GRCh37]
Chr21:13517395..46868132 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46623792)x3 copy number gain See cases [RCV000053043] Chr21:7749532..46623792 [GRCh38]
Chr21:14629063..48043704 [GRCh37]
Chr21:13550934..46868132 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46670546)x3 copy number gain See cases [RCV000053045] Chr21:7749532..46670546 [GRCh38]
Chr21:15499647..48090458 [GRCh37]
Chr21:14421518..46914886 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46661140)x3 copy number gain See cases [RCV000053065] Chr21:7749532..46661140 [GRCh38]
Chr21:15499647..48081052 [GRCh37]
Chr21:14421518..46905480 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46661140)x3 copy number gain See cases [RCV000053067] Chr21:7749532..46661140 [GRCh38]
Chr21:15499847..48081052 [GRCh37]
Chr21:14421718..46905480 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46670405)x3 copy number gain See cases [RCV000053068] Chr21:7749532..46670405 [GRCh38]
Chr21:20655360..48090317 [GRCh37]
Chr21:19577231..46914745 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46670405)x3 copy number gain See cases [RCV000053069] Chr21:7749532..46670405 [GRCh38]
Chr21:34423268..48090317 [GRCh37]
Chr21:33345138..46914745 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46623792)x3 copy number gain See cases [RCV000053039] Chr21:7749532..46623792 [GRCh38]
Chr21:14524963..48043704 [GRCh37]
Chr21:13446834..46868132 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46653090)x3 copy number gain See cases [RCV000053040] Chr21:7749532..46653090 [GRCh38]
Chr21:14539679..48073002 [GRCh37]
Chr21:13461550..46897430 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-42971047)x3 copy number gain See cases [RCV000133676] Chr21:7749532..42971047 [GRCh38]
Chr21:15499847..44391157 [GRCh37]
Chr21:14421718..43264226 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46653084)x3 copy number gain See cases [RCV000134727] Chr21:7749532..46653084 [GRCh38]
Chr21:15485038..48072996 [GRCh37]
Chr21:14406909..46897424 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21q11.2-22.3(chr21:7749532-46649831)x3 copy number gain See cases [RCV000134509] Chr21:7749532..46649831 [GRCh38]
Chr21:14577835..48069743 [GRCh37]
Chr21:13499706..46894171 [NCBI36]
Chr21:21q11.2-22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46670440)x3 copy number gain See cases [RCV000134119] Chr21:7749532..46670440 [GRCh38]
Chr21:15485038..48090352 [GRCh37]
Chr21:14406909..46914780 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21q22.11-22.3(chr21:7749532-46670346)x3 copy number gain See cases [RCV000135310] Chr21:7749532..46670346 [GRCh38]
Chr21:34111831..48090258 [GRCh37]
Chr21:33033702..46914686 [NCBI36]
Chr21:21q22.11-22.3
pathogenic
GRCh38/hg38 21q22.12-22.3(chr21:36206067-46670405)x3 copy number gain See cases [RCV000134972] Chr21:36206067..46670405 [GRCh38]
Chr21:37578365..48090317 [GRCh37]
Chr21:36500235..46914745 [NCBI36]
Chr21:21q22.12-22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46664250)x3 copy number gain See cases [RCV000134836] Chr21:7749532..46664250 [GRCh38]
Chr21:15485038..48084162 [GRCh37]
Chr21:14406909..46908590 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46670440)x3 copy number gain See cases [RCV000134842] Chr21:7749532..46670440 [GRCh38]
Chr21:15513244..48090352 [GRCh37]
Chr21:14435115..46914780 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46660999)x3 copy number gain See cases [RCV000135448] Chr21:7749532..46660999 [GRCh38]
Chr21:15499847..48080911 [GRCh37]
Chr21:14421718..46905339 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21q22.13-22.3(chr21:36519173-46670405)x3 copy number gain See cases [RCV000136142] Chr21:36519173..46670405 [GRCh38]
Chr21:37891471..48090317 [GRCh37]
Chr21:36813341..46914745 [NCBI36]
Chr21:21q22.13-22.3
pathogenic
GRCh38/hg38 21q22.12-22.3(chr21:34789953-46636538)x1 copy number loss See cases [RCV000136828] Chr21:34789953..46636538 [GRCh38]
Chr21:36162250..48056450 [GRCh37]
Chr21:35084120..46880878 [NCBI36]
Chr21:21q22.12-22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46671060)x3 copy number gain See cases [RCV000137255] Chr21:7749532..46671060 [GRCh38]
Chr21:35319225..48090972 [GRCh37]
Chr21:34241095..46915400 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46671060)x3 copy number gain See cases [RCV000137337] Chr21:7749532..46671060 [GRCh38]
Chr21:10697897..48090972 [GRCh37]
Chr21:1..46915400 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46671060)x3 copy number gain See cases [RCV000138216] Chr21:7749532..46671060 [GRCh38]
Chr21:10944001..48090972 [GRCh37]
Chr21:9965872..46915400 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21q22.13-22.3(chr21:37669628-46671060)x1 copy number loss See cases [RCV000138096] Chr21:37669628..46671060 [GRCh38]
Chr21:39041930..48090972 [GRCh37]
Chr21:37963800..46915400 [NCBI36]
Chr21:21q22.13-22.3
pathogenic
GRCh38/hg38 21q22.12-22.3(chr21:36066991-46671060)x3 copy number gain See cases [RCV000138164] Chr21:36066991..46671060 [GRCh38]
Chr21:37439289..48090972 [GRCh37]
Chr21:36361159..46915400 [NCBI36]
Chr21:21q22.12-22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46671060)x3 copy number gain See cases [RCV000138436] Chr21:7749532..46671060 [GRCh38]
Chr21:15451032..48090972 [GRCh37]
Chr21:14372903..46915400 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic|conflicting data from submitters
GRCh38/hg38 21q22.2-22.3(chr21:40296025-46670440)x1 copy number loss See cases [RCV000139158] Chr21:40296025..46670440 [GRCh38]
Chr21:41667952..48090352 [GRCh37]
Chr21:40589822..46914780 [NCBI36]
Chr21:21q22.2-22.3
pathogenic
GRCh38/hg38 21q11.2-22.3(chr21:7749532-46670346)x3 copy number gain See cases [RCV000140103] Chr21:7749532..46670346 [GRCh38]
Chr21:14577894..48090258 [GRCh37]
Chr21:13499765..46914686 [NCBI36]
Chr21:21q11.2-22.3
pathogenic
GRCh38/hg38 21q11.2-22.3(chr21:7749532-46698247)x3 copy number gain See cases [RCV000141346] Chr21:7749532..46698247 [GRCh38]
Chr21:14577835..48118159 [GRCh37]
Chr21:13499706..46942587 [NCBI36]
Chr21:21q11.2-22.3
pathogenic
GRCh38/hg38 21q21.3-22.3(chr21:7749532-46677460)x3 copy number gain See cases [RCV000141827] Chr21:7749532..46677460 [GRCh38]
Chr21:28285299..48097372 [GRCh37]
Chr21:27207170..46921800 [NCBI36]
Chr21:21q21.3-22.3
uncertain significance
GRCh38/hg38 21q22.2-22.3(chr21:38816399-46677460)x1 copy number loss See cases [RCV000142311] Chr21:38816399..46677460 [GRCh38]
Chr21:40188323..48097372 [GRCh37]
Chr21:39110193..46921800 [NCBI36]
Chr21:21q22.2-22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7817158-46670440)x1 copy number loss See cases [RCV000142427] Chr21:7817158..46670440 [GRCh38]
Chr21:15485038..48090352 [GRCh37]
Chr21:14406909..46914780 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21q11.2-22.3(chr21:7749532-46677460)x3 copy number gain See cases [RCV000143120] Chr21:7749532..46677460 [GRCh38]
Chr21:15006457..48097372 [GRCh37]
Chr21:13928328..46921800 [NCBI36]
Chr21:21q11.2-22.3
pathogenic
GRCh38/hg38 21q22.2-22.3(chr21:39375937-44246148)x1 copy number loss See cases [RCV000142650] Chr21:39375937..44246148 [GRCh38]
Chr21:40747863..45666031 [GRCh37]
Chr21:39669733..44490459 [NCBI36]
Chr21:21q22.2-22.3
pathogenic
GRCh38/hg38 21q11.2-22.3(chr21:7749532-46677460)x3 copy number gain See cases [RCV000143376] Chr21:7749532..46677460 [GRCh38]
Chr21:15006458..48097372 [GRCh37]
Chr21:13928329..46921800 [NCBI36]
Chr21:21q11.2-22.3
pathogenic
GRCh38/hg38 21q22.3(chr21:41368412-42556043)x3 copy number gain See cases [RCV000143383] Chr21:41368412..42556043 [GRCh38]
Chr21:42740339..43976153 [GRCh37]
Chr21:41662209..42849222 [NCBI36]
Chr21:21q22.3
likely benign|uncertain significance
GRCh38/hg38 21q11.2-22.3(chr21:7749532-46677460) copy number gain See cases [RCV000143160] Chr21:7749532..46677460 [GRCh38]
Chr21:14386013..48097372 [GRCh37]
Chr21:13307884..46921800 [NCBI36]
Chr21:21q11.2-22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46670405)x3 copy number gain See cases [RCV000148131] Chr21:7749532..46670405 [GRCh38]
Chr21:15499847..48090317 [GRCh37]
Chr21:14421718..46914745 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15538655-48080926)x1 copy number loss See cases [RCV000239948] Chr21:15538655..48080926 [GRCh37]
Chr21:21q11.2-22.3
pathogenic
GRCh37/hg19 21q22.2-22.3(chr21:39841248-44652723)x3 copy number gain See cases [RCV000239953] Chr21:39841248..44652723 [GRCh37]
Chr21:21q22.2-22.3
pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15410701-48090317)x3 copy number gain See cases [RCV000240397] Chr21:15410701..48090317 [GRCh37]
Chr21:21q11.2-22.3
pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15006457-43598570)x3 copy number gain See cases [RCV000446716] Chr21:15006457..43598570 [GRCh37]
Chr21:21q11.2-22.3
pathogenic
GRCh37/hg19 21q22.13-22.3(chr21:38790552-43619940)x1 copy number loss See cases [RCV000446516] Chr21:38790552..43619940 [GRCh37]
Chr21:21q22.13-22.3
pathogenic
GRCh37/hg19 21q22.2-22.3(chr21:42410406-48097372)x1 copy number loss See cases [RCV000448694] Chr21:42410406..48097372 [GRCh37]
Chr21:21q22.2-22.3
pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:14771770-48080867)x3 copy number gain See cases [RCV000447884] Chr21:14771770..48080867 [GRCh37]
Chr21:21q11.2-22.3
pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15285841-48097372)x3 copy number gain See cases [RCV000447729] Chr21:15285841..48097372 [GRCh37]
Chr21:21q11.2-22.3
pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15006457-44827632)x3 copy number gain See cases [RCV000448199] Chr21:15006457..44827632 [GRCh37]
Chr21:21q11.2-22.3
pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15006457-48097372)x3 copy number gain See cases [RCV000447749] Chr21:15006457..48097372 [GRCh37]
Chr21:21q11.2-22.3
pathogenic
GRCh37/hg19 21q22.13-22.3(chr21:38699545-48097372)x1 copy number loss See cases [RCV000510684] Chr21:38699545..48097372 [GRCh37]
Chr21:21q22.13-22.3
pathogenic
GRCh37/hg19 21q22.2-22.3(chr21:41254101-48097372)x1 copy number loss See cases [RCV000511808] Chr21:41254101..48097372 [GRCh37]
Chr21:21q22.2-22.3
pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15006458-48097372) copy number gain See cases [RCV000511589] Chr21:15006458..48097372 [GRCh37]
Chr21:21q11.2-22.3
pathogenic
GRCh37/hg19 21q22.3(chr21:42661850-43590844)x3 copy number gain See cases [RCV000511842] Chr21:42661850..43590844 [GRCh37]
Chr21:21q22.3
uncertain significance
GRCh37/hg19 21q22.13-22.3(chr21:37914123-48097372)x1 copy number loss See cases [RCV000510798] Chr21:37914123..48097372 [GRCh37]
Chr21:21q22.13-22.3
pathogenic
GRCh37/hg19 21q22.3(chr21:42805420-43176065)x3 copy number gain not provided [RCV000684141] Chr21:42805420..43176065 [GRCh37]
Chr21:21q22.3
uncertain significance
GRCh37/hg19 21q22.2-22.3(chr21:42335622-48097372)x1 copy number loss not provided [RCV000684165] Chr21:42335622..48097372 [GRCh37]
Chr21:21q22.2-22.3
pathogenic
NC_000021.9:g.(?_38981673)_(41568791_?)del deletion Autistic disorder of childhood onset [RCV000754228] Chr21:38981673..41568791 [GRCh38]
Chr21:21q22.2-22.3
likely pathogenic
GRCh37/hg19 21p11.2-q22.3(chr21:10827533-48100155)x3 copy number gain not provided [RCV000741419] Chr21:10827533..48100155 [GRCh37]
Chr21:21p11.2-q22.3
pathogenic
GRCh37/hg19 21q22.2-22.3(chr21:40364245-44169928)x1 copy number loss not provided [RCV000741567] Chr21:40364245..44169928 [GRCh37]
Chr21:21q22.2-22.3
pathogenic
GRCh37/hg19 21p11.2-q22.3(chr21:10699330-48117896)x3 copy number gain not provided [RCV000741413] Chr21:10699330..48117896 [GRCh37]
Chr21:21p11.2-q22.3
pathogenic
GRCh37/hg19 21p11.2-q22.3(chr21:10704198-48117896)x3 copy number gain not provided [RCV000741415] Chr21:10704198..48117896 [GRCh37]
Chr21:21p11.2-q22.3
pathogenic
GRCh37/hg19 21p11.2-q22.3(chr21:10824040-48090629)x3 copy number gain not provided [RCV000741418] Chr21:10824040..48090629 [GRCh37]
Chr21:21p11.2-q22.3
pathogenic
NM_002462.5(MX1):c.105+9C>G single nucleotide variant not provided [RCV000966093] Chr21:41432184 [GRCh38]
Chr21:42804111 [GRCh37]
Chr21:21q22.3
benign
NM_002462.5(MX1):c.1901G>C (p.Ser634Thr) single nucleotide variant not provided [RCV000966095] Chr21:41458670 [GRCh38]
Chr21:42830597 [GRCh37]
Chr21:21q22.3
benign
NM_002462.5(MX1):c.946G>A (p.Gly316Arg) single nucleotide variant not provided [RCV000882972] Chr21:41443804 [GRCh38]
Chr21:42815731 [GRCh37]
Chr21:21q22.3
benign
GRCh37/hg19 21q22.3(chr21:42714287-42943077)x1 copy number loss not provided [RCV000848855] Chr21:42714287..42943077 [GRCh37]
Chr21:21q22.3
uncertain significance
NM_002462.5(MX1):c.1692C>T (p.Phe564=) single nucleotide variant not provided [RCV000958785] Chr21:41452803 [GRCh38]
Chr21:42824730 [GRCh37]
Chr21:21q22.3
benign
NM_002462.5(MX1):c.1065G>A (p.Glu355=) single nucleotide variant not provided [RCV000966094] Chr21:41445504 [GRCh38]
Chr21:42817431 [GRCh37]
Chr21:21q22.3
benign
GRCh37/hg19 21q22.2-22.3(chr21:41537095-46914745) copy number loss not provided [RCV000767626] Chr21:41537095..46914745 [GRCh37]
Chr21:21q22.2-22.3
pathogenic
Single allele deletion Neurodevelopmental disorder [RCV000787405] Chr21:42300424..43682911 [GRCh37]
Chr21:21q22.2-22.3
uncertain significance
GRCh37/hg19 21q22.2-22.3(chr21:42044877-48100155)x3 copy number gain See cases [RCV001007433] Chr21:42044877..48100155 [GRCh37]
Chr21:21q22.2-22.3
pathogenic
GRCh37/hg19 21q22.13-22.3(chr21:39410438-45171756)x1 copy number loss not provided [RCV001007132] Chr21:39410438..45171756 [GRCh37]
Chr21:21q22.13-22.3
pathogenic
GRCh37/hg19 21q11.2-22.3(chr21:15006457-48097372)x3 copy number gain not provided [RCV000846937] Chr21:15006457..48097372 [GRCh37]
Chr21:21q11.2-22.3
pathogenic
NM_002462.5(MX1):c.402G>A (p.Ser134=) single nucleotide variant not provided [RCV000959640] Chr21:41437118 [GRCh38]
Chr21:42809045 [GRCh37]
Chr21:21q22.3
benign
NM_002462.5(MX1):c.942G>A (p.Glu314=) single nucleotide variant not provided [RCV000912915] Chr21:41443800 [GRCh38]
Chr21:42815727 [GRCh37]
Chr21:21q22.3
likely benign
GRCh37/hg19 21q22.3(chr21:42662220-42799124)x1 copy number loss not provided [RCV001259414] Chr21:42662220..42799124 [GRCh37]
Chr21:21q22.3
uncertain significance
GRCh37/hg19 21q11.2-22.3(chr21:14629063-48090317)x3 copy number gain See cases [RCV001263025] Chr21:14629063..48090317 [GRCh37]
Chr21:21q11.2-22.3
pathogenic

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:7532 AgrOrtholog
COSMIC MX1 COSMIC
Ensembl Genes ENSG00000157601 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000288383 UniProtKB/TrEMBL
  ENSP00000381599 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000381601 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000392151 ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ENSP00000400923 ENTREZGENE, UniProtKB/TrEMBL
  ENSP00000402215 ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ENSP00000408498 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ENSP00000410523 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000478441 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000505029 UniProtKB/Swiss-Prot
  ENSP00000505047 UniProtKB/Swiss-Prot
  ENSP00000505051 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000505189 UniProtKB/Swiss-Prot
  ENSP00000505269 ENTREZGENE, UniProtKB/TrEMBL
  ENSP00000505457 UniProtKB/Swiss-Prot
  ENSP00000505489 UniProtKB/Swiss-Prot
  ENSP00000505630 UniProtKB/Swiss-Prot
  ENSP00000505637 UniProtKB/TrEMBL
  ENSP00000505657 UniProtKB/Swiss-Prot
  ENSP00000505669 UniProtKB/Swiss-Prot
  ENSP00000505700 UniProtKB/TrEMBL
  ENSP00000505730 UniProtKB/TrEMBL
  ENSP00000505781 UniProtKB/Swiss-Prot
  ENSP00000505874 UniProtKB/Swiss-Prot
  ENSP00000506047 UniProtKB/Swiss-Prot
  ENSP00000506062 UniProtKB/Swiss-Prot
  ENSP00000506183 UniProtKB/Swiss-Prot
  ENSP00000506199 UniProtKB/Swiss-Prot
  ENSP00000506220 UniProtKB/Swiss-Prot
  ENSP00000506270 UniProtKB/Swiss-Prot
  ENSP00000506348 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000506372 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000506395 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000506481 UniProtKB/Swiss-Prot
  ENSP00000506512 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000506690 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000506712 UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000288383 UniProtKB/TrEMBL
  ENST00000398598 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000398600 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000413778 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ENST00000417963 ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ENST00000419044 ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ENST00000424365 ENTREZGENE, UniProtKB/TrEMBL
  ENST00000455164 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000619682 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000679386 UniProtKB/TrEMBL
  ENST00000679408 ENTREZGENE, UniProtKB/TrEMBL
  ENST00000679445 UniProtKB/Swiss-Prot
  ENST00000679464 UniProtKB/Swiss-Prot
  ENST00000679543 UniProtKB/Swiss-Prot
  ENST00000679626 UniProtKB/Swiss-Prot
  ENST00000679705 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000679911 UniProtKB/Swiss-Prot
  ENST00000680176 UniProtKB/Swiss-Prot
  ENST00000680182 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000680347 UniProtKB/Swiss-Prot
  ENST00000680364 UniProtKB/Swiss-Prot
  ENST00000680536 UniProtKB/Swiss-Prot
  ENST00000680629 UniProtKB/Swiss-Prot
  ENST00000680760 UniProtKB/Swiss-Prot
  ENST00000680776 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000680942 UniProtKB/TrEMBL
  ENST00000681039 UniProtKB/Swiss-Prot
  ENST00000681191 UniProtKB/Swiss-Prot
  ENST00000681266 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000681415 UniProtKB/Swiss-Prot
  ENST00000681607 UniProtKB/Swiss-Prot
  ENST00000681671 UniProtKB/Swiss-Prot
  ENST00000681849 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000681857 UniProtKB/Swiss-Prot
  ENST00000681867 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000681896 UniProtKB/Swiss-Prot
  ENST00000681944 UniProtKB/TrEMBL
GTEx ENSG00000157601 GTEx
HGNC ID HGNC:7532 ENTREZGENE
Human Proteome Map MX1 Human Proteome Map
InterPro Dynamin_central UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Dynamin_GTPase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Dynamin_GTPase_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Dynamin_SF UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  G_DYNAMIN_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GED UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GED_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  P-loop_NTPase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:4599 UniProtKB/Swiss-Prot
NCBI Gene 4599 ENTREZGENE
OMIM 147150 OMIM
PANTHER PTHR11566 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Dynamin_M UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Dynamin_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GED UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA31333 PharmGKB
PRINTS DYNAMIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE G_DYNAMIN_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  G_DYNAMIN_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GED UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART DYNc UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GED UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF52540 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A7P0T9I6_HUMAN UniProtKB/TrEMBL
  A0A7P0T9R0_HUMAN UniProtKB/TrEMBL
  A0A7P0Z4E0_HUMAN UniProtKB/TrEMBL
  F8W8T1_HUMAN UniProtKB/TrEMBL
  H9KVC3_HUMAN UniProtKB/TrEMBL
  H9KVC7_HUMAN UniProtKB/TrEMBL
  H9KVC9_HUMAN UniProtKB/TrEMBL
  H9KVD0_HUMAN UniProtKB/TrEMBL
  MX1_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
UniProt Secondary B2RDA5 UniProtKB/Swiss-Prot
  B3KU10 UniProtKB/Swiss-Prot
  C9IYV7 UniProtKB/Swiss-Prot
  C9J8D6 UniProtKB/Swiss-Prot
  C9JN19 UniProtKB/Swiss-Prot
  C9JN88 UniProtKB/Swiss-Prot
  C9JUL1 UniProtKB/Swiss-Prot
  C9JZS6 UniProtKB/Swiss-Prot
  D3DSI8 UniProtKB/Swiss-Prot
  Q86YP5 UniProtKB/Swiss-Prot
  Q96CI3 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-02-18 MX1  MX dynamin like GTPase 1    MX dynamin-like GTPase 1  Symbol and/or name change 5135510 APPROVED
2014-07-23 MX1  MX dynamin-like GTPase 1    myxovirus (influenza virus) resistance 1, interferon-inducible protein p78 (mouse)  Symbol and/or name change 5135510 APPROVED
2011-08-16 MX1  myxovirus (influenza virus) resistance 1, interferon-inducible protein p78 (mouse)  MX1  myxovirus (influenza virus) resistance 1, interferon-inducible protein p78 (mouse)  Symbol and/or name change 5135510 APPROVED