MPP1 (membrane palmitoylated protein 1) - Rat Genome Database

Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Gene: MPP1 (membrane palmitoylated protein 1) Homo sapiens
Analyze
Symbol: MPP1
Name: membrane palmitoylated protein 1
RGD ID: 1347904
HGNC Page HGNC
Description: Predicted to have guanylate kinase activity. Predicted to be involved in regulation of neutrophil chemotaxis. Localizes to centriolar satellite and plasma membrane.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: 55 kDa erythrocyte membrane protein; AAG12; aging-associated gene 12; DXS552; DXS552E; EMP55; erythrocyte membrane protein p55; membrane protein, palmitoylated 1; membrane protein, palmitoylated 1, 55kDa; migration-related gene 1; MRG1; p55; palmitoylated erythrocyte membrane protein; PEMP
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 EnsemblX154,778,684 - 154,821,007 (-)EnsemblGRCh38hg38GRCh38
GRCh38X154,778,684 - 154,805,485 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X154,006,959 - 154,033,760 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36X153,660,162 - 153,686,957 (-)NCBINCBI36hg18NCBI36
Build 34X153,570,671 - 153,597,467NCBI
CeleraX154,165,522 - 154,192,359 (-)NCBI
Cytogenetic MapXq28NCBI
HuRefX142,550,319 - 142,577,036 (-)NCBIHuRef
CHM1_1X153,918,634 - 153,945,496 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
1,2-dichloroethane  (ISO)
1,2-dimethylhydrazine  (ISO)
17alpha-ethynylestradiol  (ISO)
17beta-estradiol  (EXP)
2,3',4,4',5-Pentachlorobiphenyl  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2-hydroxypropanoic acid  (EXP)
4-hydroxyphenyl retinamide  (ISO)
acrolein  (EXP)
all-trans-retinoic acid  (EXP)
alpha-pinene  (EXP)
antirheumatic drug  (EXP)
benzo[a]pyrene  (EXP,ISO)
bis(2-ethylhexyl) phthalate  (EXP,ISO)
bisphenol A  (EXP)
butanal  (EXP)
cadmium dichloride  (ISO)
carbon nanotube  (ISO)
CHIR 99021  (EXP)
cisplatin  (EXP)
clofibrate  (ISO)
cyclosporin A  (EXP)
dibutyl phthalate  (ISO)
dichloroacetic acid  (ISO)
dorsomorphin  (EXP)
doxorubicin  (EXP)
ethanol  (ISO)
finasteride  (ISO)
folic acid  (ISO)
methotrexate  (EXP)
N-methyl-N'-nitro-N-nitrosoguanidine  (ISO)
nefazodone  (ISO)
nimesulide  (ISO)
okadaic acid  (ISO)
ozone  (EXP)
p-toluidine  (ISO)
paracetamol  (EXP,ISO)
pentachlorophenol  (ISO)
perfluorohexanesulfonic acid  (ISO)
perfluorononanoic acid  (ISO)
perfluorooctane-1-sulfonic acid  (ISO)
perfluorooctanoic acid  (ISO)
phenobarbital  (ISO)
phenylmercury acetate  (EXP)
phorbol 13-acetate 12-myristate  (ISO)
pirinixic acid  (ISO)
potassium chromate  (EXP)
potassium dichromate  (EXP)
progesterone  (EXP)
propanal  (EXP)
propiconazole  (ISO)
rac-lactic acid  (EXP)
SB 431542  (EXP)
silicon dioxide  (EXP)
silver atom  (ISO)
silver(0)  (ISO)
sodium arsenate  (ISO)
sodium arsenite  (EXP)
sunitinib  (EXP)
tert-butyl hydroperoxide  (ISO)
tetrachloromethane  (ISO)
thalidomide  (ISO)
titanium dioxide  (ISO)
valproic acid  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
Schizophrenia  (IAGP)
References

Additional References at PubMed
PMID:1301163   PMID:1310897   PMID:1713685   PMID:7822301   PMID:8125298   PMID:8824805   PMID:9305870   PMID:11256614   PMID:12477932   PMID:14702039   PMID:15123239   PMID:15231747  
PMID:15489334   PMID:15952887   PMID:16169070   PMID:16189514   PMID:16344560   PMID:16741958   PMID:17584769   PMID:18952129   PMID:19144871   PMID:19738201   PMID:19946888   PMID:21509594  
PMID:21900206   PMID:21903422   PMID:23263863   PMID:23446634   PMID:23507198   PMID:25408337   PMID:25416956   PMID:26344197   PMID:26496610   PMID:26638075   PMID:26871637   PMID:27545878  
PMID:27621083   PMID:28380382   PMID:28514442   PMID:28653654   PMID:28865798   PMID:29146910   PMID:30397336   PMID:30442766   PMID:30463901   PMID:30639242   PMID:30862715   PMID:31091453  
PMID:31391242   PMID:31678930   PMID:32296183   PMID:32814053   PMID:33001583  


Genomics

Comparative Map Data
MPP1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 EnsemblX154,778,684 - 154,821,007 (-)EnsemblGRCh38hg38GRCh38
GRCh38X154,778,684 - 154,805,485 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X154,006,959 - 154,033,760 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36X153,660,162 - 153,686,957 (-)NCBINCBI36hg18NCBI36
Build 34X153,570,671 - 153,597,467NCBI
CeleraX154,165,522 - 154,192,359 (-)NCBI
Cytogenetic MapXq28NCBI
HuRefX142,550,319 - 142,577,036 (-)NCBIHuRef
CHM1_1X153,918,634 - 153,945,496 (-)NCBICHM1_1
Mpp1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39X74,153,339 - 74,174,622 (-)NCBIGRCm39mm39
GRCm39 EnsemblX74,153,339 - 74,174,622 (-)Ensembl
GRCm38X75,109,733 - 75,131,016 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 EnsemblX75,109,733 - 75,131,016 (-)EnsemblGRCm38mm10GRCm38
MGSCv37X72,355,072 - 72,376,288 (-)NCBIGRCm37mm9NCBIm37
MGSCv36X71,362,453 - 71,383,669 (-)NCBImm8
CeleraX66,514,557 - 66,535,775 (-)NCBICelera
Cytogenetic MapXA7.3NCBI
cM MapX38.15NCBI
Mpp1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Rnor_6.01148,450,213 - 148,458,945 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.01154,731,975 - 154,741,021 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
Celera1137,539,255 - 137,547,772 (+)NCBICelera
Cytogenetic Map1q31NCBI
Mpp1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_004955594831,098 - 846,866 (+)EnsemblChiLan1.0
ChiLan1.0NW_004955594831,100 - 846,438 (+)NCBIChiLan1.0ChiLan1.0
MPP1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.1X154,099,463 - 154,126,575 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 EnsemblX154,099,463 - 154,126,575 (-)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v0X144,258,416 - 144,285,658 (-)NCBIMhudiblu_PPA_v0panPan3
MPP1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1X122,851,667 - 122,878,865 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 EnsemblX122,851,667 - 122,879,394 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_TashaX107,845,285 - 107,872,081 (-)NCBI
ROS_Cfam_1.0X125,977,893 - 126,005,109 (-)NCBI
UMICH_Zoey_3.1X121,726,260 - 121,753,061 (-)NCBI
UNSW_CanFamBas_1.0X124,249,501 - 124,276,287 (-)NCBI
UU_Cfam_GSD_1.0X123,942,589 - 123,969,391 (-)NCBI
Mpp1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2X119,788,981 - 119,811,866 (-)NCBI
SpeTri2.0NW_004936927147,448 - 170,435 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
MPP1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 EnsemblX125,229,449 - 125,300,101 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1X125,230,412 - 125,252,384 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2X143,231,475 - 143,252,754 (+)NCBISscrofa10.2Sscrofa10.2susScr3
MPP1
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1X129,030,736 - 129,057,952 (-)NCBI
ChlSab1.1 EnsemblX129,030,735 - 129,044,777 (-)Ensembl
Mpp1
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_004624963445,559 - 467,976 (+)NCBI

Position Markers
RH123086  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,006,921 - 154,007,253UniSTSGRCh37
Build 36X153,660,115 - 153,660,447RGDNCBI36
CeleraX154,165,484 - 154,165,816RGD
Cytogenetic MapXq28UniSTS
HuRefX142,550,281 - 142,550,613UniSTS
D1S1800E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,006,999 - 154,007,132UniSTSGRCh37
Build 36X153,660,193 - 153,660,326RGDNCBI36
CeleraX154,165,562 - 154,165,695RGD
Cytogenetic MapXq28UniSTS
HuRefX142,550,359 - 142,550,492UniSTS
HSC269_(M1)  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,015,351 - 154,015,525UniSTSGRCh37
Build 36X153,668,545 - 153,668,719RGDNCBI36
CeleraX154,173,916 - 154,174,082RGD
Cytogenetic MapXq28UniSTS
ECD00022  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,008,967 - 154,009,927UniSTSGRCh37
Build 36X153,662,161 - 153,663,121RGDNCBI36
CeleraX154,167,530 - 154,168,490RGD
Cytogenetic MapXq28UniSTS
HuRefX142,552,610 - 142,553,569UniSTS
ECD00900  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,009,945 - 154,010,830UniSTSGRCh37
Build 36X153,663,139 - 153,664,024RGDNCBI36
CeleraX154,168,508 - 154,169,393RGD
Cytogenetic MapXq28UniSTS
HuRefX142,553,587 - 142,554,472UniSTS
ECD03021  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,018,906 - 154,019,715UniSTSGRCh37
Build 36X153,672,100 - 153,672,909RGDNCBI36
CeleraX154,177,463 - 154,178,272RGD
Cytogenetic MapXq28UniSTS
HuRefX142,562,437 - 142,563,246UniSTS
ECD03044  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,019,723 - 154,020,531UniSTSGRCh37
Build 36X153,672,917 - 153,673,725RGDNCBI36
CeleraX154,178,280 - 154,179,088RGD
Cytogenetic MapXq28UniSTS
HuRefX142,563,254 - 142,564,062UniSTS
ECD03634  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,033,895 - 154,034,683UniSTSGRCh37
Build 36X153,687,089 - 153,687,877RGDNCBI36
CeleraX154,192,452 - 154,193,240RGD
Cytogenetic MapXq28UniSTS
ECD06414  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,032,972 - 154,033,681UniSTSGRCh37
Build 36X153,686,166 - 153,686,875RGDNCBI36
CeleraX154,191,529 - 154,192,238RGD
Cytogenetic MapXq28UniSTS
HuRefX142,576,206 - 142,576,915UniSTS
ECD08845  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,006,611 - 154,007,255UniSTSGRCh37
Build 36X153,659,805 - 153,660,449RGDNCBI36
CeleraX154,165,174 - 154,165,818RGD
Cytogenetic MapXq28UniSTS
HuRefX142,549,971 - 142,550,615UniSTS
ECD09184  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,028,726 - 154,029,361UniSTSGRCh37
Build 36X153,681,920 - 153,682,555RGDNCBI36
CeleraX154,187,283 - 154,187,918RGD
Cytogenetic MapXq28UniSTS
ECD09272  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,027,380 - 154,028,013UniSTSGRCh37
Build 36X153,680,574 - 153,681,207RGDNCBI36
CeleraX154,185,937 - 154,186,570RGD
Cytogenetic MapXq28UniSTS
HuRefX142,570,911 - 142,571,544UniSTS
ECD09273  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,028,015 - 154,028,648UniSTSGRCh37
Build 36X153,681,209 - 153,681,842RGDNCBI36
CeleraX154,186,572 - 154,187,205RGD
Cytogenetic MapXq28UniSTS
HuRefX142,571,546 - 142,572,179UniSTS
ECD09391  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,007,333 - 154,007,963UniSTSGRCh37
Build 36X153,660,527 - 153,661,157RGDNCBI36
CeleraX154,165,896 - 154,166,526RGD
Cytogenetic MapXq28UniSTS
HuRefX142,550,693 - 142,551,323UniSTS
ECD10501  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,014,250 - 154,014,850UniSTSGRCh37
Build 36X153,667,444 - 153,668,044RGDNCBI36
CeleraX154,172,814 - 154,173,414RGD
Cytogenetic MapXq28UniSTS
HuRefX142,557,638 - 142,558,238UniSTS
ECD11134  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,013,108 - 154,013,689UniSTSGRCh37
Build 36X153,666,302 - 153,666,883RGDNCBI36
CeleraX154,171,671 - 154,172,253RGD
Cytogenetic MapXq28UniSTS
HuRefX142,556,495 - 142,557,077UniSTS
ECD11278  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,030,089 - 154,030,666UniSTSGRCh37
Build 36X153,683,283 - 153,683,860RGDNCBI36
CeleraX154,188,646 - 154,189,223RGD
Cytogenetic MapXq28UniSTS
HuRefX142,573,323 - 142,573,900UniSTS
ECD11809  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,030,702 - 154,031,263UniSTSGRCh37
Build 36X153,683,896 - 153,684,457RGDNCBI36
CeleraX154,189,259 - 154,189,820RGD
Cytogenetic MapXq28UniSTS
HuRefX142,573,936 - 142,574,497UniSTS
ECD13665  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,012,187 - 154,012,699UniSTSGRCh37
Build 36X153,665,381 - 153,665,893RGDNCBI36
CeleraX154,170,750 - 154,171,262RGD
Cytogenetic MapXq28UniSTS
HuRefX142,555,574 - 142,556,086UniSTS
ECD14147  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,011,637 - 154,012,137UniSTSGRCh37
Build 36X153,664,831 - 153,665,331RGDNCBI36
CeleraX154,170,200 - 154,170,700RGD
Cytogenetic MapXq28UniSTS
ECD15309  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,017,982 - 154,018,455UniSTSGRCh37
Build 36X153,671,176 - 153,671,649RGDNCBI36
CeleraX154,176,539 - 154,177,012RGD
Cytogenetic MapXq28UniSTS
HuRefX142,561,513 - 142,561,986UniSTS
ECD16825  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,024,714 - 154,025,138UniSTSGRCh37
Build 36X153,677,908 - 153,678,332RGDNCBI36
CeleraX154,183,271 - 154,183,695RGD
Cytogenetic MapXq28UniSTS
HuRefX142,568,245 - 142,568,669UniSTS
ECD17474  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,011,160 - 154,011,557UniSTSGRCh37
Build 36X153,664,354 - 153,664,751RGDNCBI36
CeleraX154,169,723 - 154,170,120RGD
Cytogenetic MapXq28UniSTS
ECD18670  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,032,142 - 154,032,493UniSTSGRCh37
Build 36X153,685,336 - 153,685,687RGDNCBI36
CeleraX154,190,699 - 154,191,050RGD
Cytogenetic MapXq28UniSTS
HuRefX142,575,376 - 142,575,727UniSTS
ECD18897  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,031,465 - 154,031,808UniSTSGRCh37
Build 36X153,684,659 - 153,685,002RGDNCBI36
CeleraX154,190,022 - 154,190,365RGD
Cytogenetic MapXq28UniSTS
HuRefX142,574,699 - 142,575,042UniSTS
ECD19028  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,013,795 - 154,014,132UniSTSGRCh37
Build 36X153,666,989 - 153,667,326RGDNCBI36
CeleraX154,172,359 - 154,172,696RGD
Cytogenetic MapXq28UniSTS
HuRefX142,557,183 - 142,557,520UniSTS
ECD20052  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,024,076 - 154,024,375UniSTSGRCh37
Build 36X153,677,270 - 153,677,569RGDNCBI36
CeleraX154,182,633 - 154,182,932RGD
Cytogenetic MapXq28UniSTS
HuRefX142,567,607 - 142,567,906UniSTS
ECD20274  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,023,413 - 154,023,703UniSTSGRCh37
Build 36X153,676,607 - 153,676,897RGDNCBI36
CeleraX154,181,970 - 154,182,260RGD
Cytogenetic MapXq28UniSTS
HuRefX142,566,944 - 142,567,234UniSTS
ECD22569  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,025,374 - 154,025,589UniSTSGRCh37
Build 36X153,678,568 - 153,678,783RGDNCBI36
CeleraX154,183,931 - 154,184,146RGD
Cytogenetic MapXq28UniSTS
HuRefX142,568,905 - 142,569,120UniSTS
ECD22976  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,020,976 - 154,021,178UniSTSGRCh37
Build 36X153,674,170 - 153,674,372RGDNCBI36
CeleraX154,179,533 - 154,179,735RGD
Cytogenetic MapXq28UniSTS
HuRefX142,564,507 - 142,564,709UniSTS
ECD24067  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,029,572 - 154,029,734UniSTSGRCh37
Build 36X153,682,766 - 153,682,928RGDNCBI36
CeleraX154,188,129 - 154,188,291RGD
Cytogenetic MapXq28UniSTS
REN90642  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,006,467 - 154,006,736UniSTSGRCh37
Build 36X153,659,661 - 153,659,930RGDNCBI36
CeleraX154,165,030 - 154,165,299RGD
Cytogenetic MapXq28UniSTS
HuRefX142,549,827 - 142,550,096UniSTS
REN90643  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,006,702 - 154,006,951UniSTSGRCh37
Build 36X153,659,896 - 153,660,145RGDNCBI36
CeleraX154,165,265 - 154,165,514RGD
Cytogenetic MapXq28UniSTS
HuRefX142,550,062 - 142,550,311UniSTS
REN90644  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,006,946 - 154,007,193UniSTSGRCh37
Build 36X153,660,140 - 153,660,387RGDNCBI36
CeleraX154,165,509 - 154,165,756RGD
Cytogenetic MapXq28UniSTS
HuRefX142,550,306 - 142,550,553UniSTS
REN90645  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,007,186 - 154,007,435UniSTSGRCh37
Build 36X153,660,380 - 153,660,629RGDNCBI36
CeleraX154,165,749 - 154,165,998RGD
Cytogenetic MapXq28UniSTS
HuRefX142,550,546 - 142,550,795UniSTS
REN90646  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,007,407 - 154,007,656UniSTSGRCh37
Build 36X153,660,601 - 153,660,850RGDNCBI36
CeleraX154,165,970 - 154,166,219RGD
Cytogenetic MapXq28UniSTS
HuRefX142,550,767 - 142,551,016UniSTS
REN90647  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,007,633 - 154,007,890UniSTSGRCh37
Build 36X153,660,827 - 153,661,084RGDNCBI36
CeleraX154,166,196 - 154,166,453RGD
Cytogenetic MapXq28UniSTS
HuRefX142,550,993 - 142,551,250UniSTS
REN90648  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,007,777 - 154,008,010UniSTSGRCh37
Build 36X153,660,971 - 153,661,204RGDNCBI36
CeleraX154,166,340 - 154,166,573RGD
Cytogenetic MapXq28UniSTS
HuRefX142,551,137 - 142,551,370UniSTS
REN90649  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,007,958 - 154,008,229UniSTSGRCh37
Build 36X153,661,152 - 153,661,423RGDNCBI36
CeleraX154,166,521 - 154,166,792RGD
Cytogenetic MapXq28UniSTS
HuRefX142,551,318 - 142,551,589UniSTS
REN90650  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,008,285 - 154,008,509UniSTSGRCh37
Build 36X153,661,479 - 153,661,703RGDNCBI36
CeleraX154,166,848 - 154,167,072RGD
Cytogenetic MapXq28UniSTS
REN90651  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,008,478 - 154,008,702UniSTSGRCh37
Build 36X153,661,672 - 153,661,896RGDNCBI36
CeleraX154,167,041 - 154,167,265RGD
Cytogenetic MapXq28UniSTS
HuRefX142,552,121 - 142,552,345UniSTS
REN90652  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,008,681 - 154,008,931UniSTSGRCh37
Build 36X153,661,875 - 153,662,125RGDNCBI36
CeleraX154,167,244 - 154,167,494RGD
Cytogenetic MapXq28UniSTS
HuRefX142,552,324 - 142,552,574UniSTS
REN90653  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,008,881 - 154,009,133UniSTSGRCh37
Build 36X153,662,075 - 153,662,327RGDNCBI36
CeleraX154,167,444 - 154,167,696RGD
Cytogenetic MapXq28UniSTS
HuRefX142,552,524 - 142,552,776UniSTS
REN90654  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,009,116 - 154,009,368UniSTSGRCh37
Build 36X153,662,310 - 153,662,562RGDNCBI36
CeleraX154,167,679 - 154,167,931RGD
Cytogenetic MapXq28UniSTS
HuRefX142,552,759 - 142,553,011UniSTS
REN90655  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,009,336 - 154,009,583UniSTSGRCh37
Build 36X153,662,530 - 153,662,777RGDNCBI36
CeleraX154,167,899 - 154,168,146RGD
Cytogenetic MapXq28UniSTS
HuRefX142,552,979 - 142,553,226UniSTS
REN90656  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,009,569 - 154,009,818UniSTSGRCh37
Build 36X153,662,763 - 153,663,012RGDNCBI36
CeleraX154,168,132 - 154,168,381RGD
Cytogenetic MapXq28UniSTS
HuRefX142,553,212 - 142,553,460UniSTS
REN90657  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,009,815 - 154,010,056UniSTSGRCh37
Build 36X153,663,009 - 153,663,250RGDNCBI36
CeleraX154,168,378 - 154,168,619RGD
Cytogenetic MapXq28UniSTS
HuRefX142,553,457 - 142,553,698UniSTS
REN90658  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,010,037 - 154,010,306UniSTSGRCh37
Build 36X153,663,231 - 153,663,500RGDNCBI36
CeleraX154,168,600 - 154,168,869RGD
Cytogenetic MapXq28UniSTS
HuRefX142,553,679 - 142,553,948UniSTS
REN90659  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,010,305 - 154,010,529UniSTSGRCh37
Build 36X153,663,499 - 153,663,723RGDNCBI36
CeleraX154,168,868 - 154,169,092RGD
Cytogenetic MapXq28UniSTS
HuRefX142,553,947 - 142,554,171UniSTS
REN90660  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,010,502 - 154,010,755UniSTSGRCh37
Build 36X153,663,696 - 153,663,949RGDNCBI36
CeleraX154,169,065 - 154,169,318RGD
Cytogenetic MapXq28UniSTS
HuRefX142,554,144 - 142,554,397UniSTS
REN90661  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,010,732 - 154,010,984UniSTSGRCh37
Build 36X153,663,926 - 153,664,178RGDNCBI36
CeleraX154,169,295 - 154,169,547RGD
Cytogenetic MapXq28UniSTS
HuRefX142,554,374 - 142,554,626UniSTS
REN90662  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,010,979 - 154,011,208UniSTSGRCh37
Build 36X153,664,173 - 153,664,402RGDNCBI36
CeleraX154,169,542 - 154,169,771RGD
Cytogenetic MapXq28UniSTS
HuRefX142,554,621 - 142,554,850UniSTS
REN90663  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,011,175 - 154,011,399UniSTSGRCh37
Build 36X153,664,369 - 153,664,593RGDNCBI36
CeleraX154,169,738 - 154,169,962RGD
Cytogenetic MapXq28UniSTS
REN90664  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,011,335 - 154,011,559UniSTSGRCh37
Build 36X153,664,529 - 153,664,753RGDNCBI36
CeleraX154,169,898 - 154,170,122RGD
Cytogenetic MapXq28UniSTS
REN90665  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,011,525 - 154,011,759UniSTSGRCh37
Build 36X153,664,719 - 153,664,953RGDNCBI36
CeleraX154,170,088 - 154,170,322RGD
Cytogenetic MapXq28UniSTS
REN90666  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,011,737 - 154,011,991UniSTSGRCh37
Build 36X153,664,931 - 153,665,185RGDNCBI36
CeleraX154,170,300 - 154,170,554RGD
Cytogenetic MapXq28UniSTS
HuRefX142,555,124 - 142,555,378UniSTS
REN90667  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,011,990 - 154,012,229UniSTSGRCh37
Build 36X153,665,184 - 153,665,423RGDNCBI36
CeleraX154,170,553 - 154,170,792RGD
Cytogenetic MapXq28UniSTS
HuRefX142,555,377 - 142,555,616UniSTS
REN90668  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,012,208 - 154,012,454UniSTSGRCh37
Build 36X153,665,402 - 153,665,648RGDNCBI36
CeleraX154,170,771 - 154,171,017RGD
Cytogenetic MapXq28UniSTS
HuRefX142,555,595 - 142,555,841UniSTS
REN90669  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,012,438 - 154,012,700UniSTSGRCh37
Build 36X153,665,632 - 153,665,894RGDNCBI36
CeleraX154,171,001 - 154,171,263RGD
Cytogenetic MapXq28UniSTS
HuRefX142,555,825 - 142,556,087UniSTS
REN90670  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,012,677 - 154,012,914UniSTSGRCh37
Build 36X153,665,871 - 153,666,108RGDNCBI36
CeleraX154,171,240 - 154,171,477RGD
Cytogenetic MapXq28UniSTS
HuRefX142,556,064 - 142,556,301UniSTS
REN90671  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,012,890 - 154,013,143UniSTSGRCh37
Build 36X153,666,084 - 153,666,337RGDNCBI36
CeleraX154,171,453 - 154,171,706RGD
Cytogenetic MapXq28UniSTS
HuRefX142,556,277 - 142,556,530UniSTS
REN90672  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,013,110 - 154,013,358UniSTSGRCh37
Build 36X153,666,304 - 153,666,552RGDNCBI36
CeleraX154,171,673 - 154,171,921RGD
Cytogenetic MapXq28UniSTS
HuRefX142,556,497 - 142,556,745UniSTS
REN90673  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,013,333 - 154,013,562UniSTSGRCh37
Build 36X153,666,527 - 153,666,756RGDNCBI36
CeleraX154,171,896 - 154,172,126RGD
Cytogenetic MapXq28UniSTS
HuRefX142,556,720 - 142,556,950UniSTS
REN90674  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,013,528 - 154,013,785UniSTSGRCh37
Build 36X153,666,722 - 153,666,979RGDNCBI36
CeleraX154,172,092 - 154,172,349RGD
Cytogenetic MapXq28UniSTS
HuRefX142,556,916 - 142,557,173UniSTS
REN90675  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,013,755 - 154,014,021UniSTSGRCh37
Build 36X153,666,949 - 153,667,215RGDNCBI36
CeleraX154,172,319 - 154,172,585RGD
Cytogenetic MapXq28UniSTS
HuRefX142,557,143 - 142,557,409UniSTS
REN90676  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,014,000 - 154,014,244UniSTSGRCh37
Build 36X153,667,194 - 153,667,438RGDNCBI36
CeleraX154,172,564 - 154,172,808RGD
Cytogenetic MapXq28UniSTS
HuRefX142,557,388 - 142,557,632UniSTS
REN90677  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,014,217 - 154,014,448UniSTSGRCh37
Build 36X153,667,411 - 153,667,642RGDNCBI36
CeleraX154,172,781 - 154,173,012RGD
Cytogenetic MapXq28UniSTS
HuRefX142,557,605 - 142,557,836UniSTS
REN90678  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,014,431 - 154,014,680UniSTSGRCh37
Build 36X153,667,625 - 153,667,874RGDNCBI36
CeleraX154,172,995 - 154,173,244RGD
Cytogenetic MapXq28UniSTS
HuRefX142,557,819 - 142,558,068UniSTS
REN90679  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,014,646 - 154,014,886UniSTSGRCh37
Build 36X153,667,840 - 153,668,080RGDNCBI36
CeleraX154,173,210 - 154,173,450RGD
Cytogenetic MapXq28UniSTS
HuRefX142,558,034 - 142,558,274UniSTS
REN90680  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,014,733 - 154,014,969UniSTSGRCh37
Build 36X153,667,927 - 153,668,163RGDNCBI36
CeleraX154,173,297 - 154,173,533RGD
Cytogenetic MapXq28UniSTS
REN90681  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,014,946 - 154,015,219UniSTSGRCh37
Build 36X153,668,140 - 153,668,413RGDNCBI36
CeleraX154,173,510 - 154,173,784RGD
Cytogenetic MapXq28UniSTS
REN90682  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,015,209 - 154,015,457UniSTSGRCh37
Build 36X153,668,403 - 153,668,651RGDNCBI36
CeleraX154,173,774 - 154,174,014RGD
Cytogenetic MapXq28UniSTS
REN90683  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,015,455 - 154,015,715UniSTSGRCh37
Build 36X153,668,649 - 153,668,909RGDNCBI36
CeleraX154,174,012 - 154,174,272RGD
Cytogenetic MapXq28UniSTS
HuRefX142,558,986 - 142,559,246UniSTS
REN90684  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,015,691 - 154,015,951UniSTSGRCh37
Build 36X153,668,885 - 153,669,145RGDNCBI36
CeleraX154,174,248 - 154,174,508RGD
Cytogenetic MapXq28UniSTS
HuRefX142,559,222 - 142,559,482UniSTS
REN90685  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,015,926 - 154,016,175UniSTSGRCh37
Build 36X153,669,120 - 153,669,369RGDNCBI36
CeleraX154,174,483 - 154,174,732RGD
Cytogenetic MapXq28UniSTS
HuRefX142,559,457 - 142,559,706UniSTS
REN90686  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,016,152 - 154,016,413UniSTSGRCh37
Build 36X153,669,346 - 153,669,607RGDNCBI36
CeleraX154,174,709 - 154,174,970RGD
Cytogenetic MapXq28UniSTS
HuRefX142,559,683 - 142,559,944UniSTS
REN90687  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,016,389 - 154,016,630UniSTSGRCh37
Build 36X153,669,583 - 153,669,824RGDNCBI36
CeleraX154,174,946 - 154,175,187RGD
Cytogenetic MapXq28UniSTS
HuRefX142,559,920 - 142,560,161UniSTS
REN90688  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,016,607 - 154,016,871UniSTSGRCh37
Build 36X153,669,801 - 153,670,065RGDNCBI36
CeleraX154,175,164 - 154,175,428RGD
Cytogenetic MapXq28UniSTS
HuRefX142,560,138 - 142,560,402UniSTS
REN90689  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,016,839 - 154,017,072UniSTSGRCh37
Build 36X153,670,033 - 153,670,266RGDNCBI36
CeleraX154,175,396 - 154,175,629RGD
Cytogenetic MapXq28UniSTS
HuRefX142,560,370 - 142,560,603UniSTS
REN90690  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,017,044 - 154,017,295UniSTSGRCh37
Build 36X153,670,238 - 153,670,489RGDNCBI36
CeleraX154,175,601 - 154,175,852RGD
Cytogenetic MapXq28UniSTS
HuRefX142,560,575 - 142,560,826UniSTS
REN90691  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,017,268 - 154,017,534UniSTSGRCh37
Build 36X153,670,462 - 153,670,728RGDNCBI36
CeleraX154,175,825 - 154,176,091RGD
Cytogenetic MapXq28UniSTS
HuRefX142,560,799 - 142,561,065UniSTS
REN90692  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,017,511 - 154,017,747UniSTSGRCh37
Build 36X153,670,705 - 153,670,941RGDNCBI36
CeleraX154,176,068 - 154,176,304RGD
Cytogenetic MapXq28UniSTS
HuRefX142,561,042 - 142,561,278UniSTS
REN90693  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,017,722 - 154,017,982UniSTSGRCh37
Build 36X153,670,916 - 153,671,176RGDNCBI36
CeleraX154,176,279 - 154,176,539RGD
Cytogenetic MapXq28UniSTS
HuRefX142,561,253 - 142,561,513UniSTS
REN90694  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,017,952 - 154,018,190UniSTSGRCh37
Build 36X153,671,146 - 153,671,384RGDNCBI36
CeleraX154,176,509 - 154,176,747RGD
Cytogenetic MapXq28UniSTS
HuRefX142,561,483 - 142,561,721UniSTS
REN90695  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,018,167 - 154,018,400UniSTSGRCh37
Build 36X153,671,361 - 153,671,594RGDNCBI36
CeleraX154,176,724 - 154,176,957RGD
Cytogenetic MapXq28UniSTS
HuRefX142,561,698 - 142,561,931UniSTS
REN90696  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,018,344 - 154,018,568UniSTSGRCh37
Build 36X153,671,538 - 153,671,762RGDNCBI36
CeleraX154,176,901 - 154,177,125RGD
Cytogenetic MapXq28UniSTS
HuRefX142,561,875 - 142,562,099UniSTS
REN90697  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,018,823 - 154,019,047UniSTSGRCh37
Build 36X153,672,017 - 153,672,241RGDNCBI36
CeleraX154,177,380 - 154,177,604RGD
Cytogenetic MapXq28UniSTS
HuRefX142,562,354 - 142,562,578UniSTS
REN90698  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,019,041 - 154,019,266UniSTSGRCh37
Build 36X153,672,235 - 153,672,460RGDNCBI36
CeleraX154,177,598 - 154,177,823RGD
Cytogenetic MapXq28UniSTS
HuRefX142,562,572 - 142,562,797UniSTS
REN90699  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,019,239 - 154,019,497UniSTSGRCh37
Build 36X153,672,433 - 153,672,691RGDNCBI36
CeleraX154,177,796 - 154,178,054RGD
Cytogenetic MapXq28UniSTS
HuRefX142,562,770 - 142,563,028UniSTS
REN90700  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,019,473 - 154,019,730UniSTSGRCh37
Build 36X153,672,667 - 153,672,924RGDNCBI36
CeleraX154,178,030 - 154,178,287RGD
Cytogenetic MapXq28UniSTS
HuRefX142,563,004 - 142,563,261UniSTS
REN90701  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,019,724 - 154,019,972UniSTSGRCh37
Build 36X153,672,918 - 153,673,166RGDNCBI36
CeleraX154,178,281 - 154,178,529RGD
Cytogenetic MapXq28UniSTS
HuRefX142,563,255 - 142,563,503UniSTS
REN90702  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,019,956 - 154,020,185UniSTSGRCh37
Build 36X153,673,150 - 153,673,379RGDNCBI36
CeleraX154,178,513 - 154,178,742RGD
Cytogenetic MapXq28UniSTS
HuRefX142,563,487 - 142,563,716UniSTS
REN90703  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,020,149 - 154,020,403UniSTSGRCh37
Build 36X153,673,343 - 153,673,597RGDNCBI36
CeleraX154,178,706 - 154,178,960RGD
Cytogenetic MapXq28UniSTS
HuRefX142,563,680 - 142,563,934UniSTS
REN90704  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,020,380 - 154,020,637UniSTSGRCh37
Build 36X153,673,574 - 153,673,831RGDNCBI36
CeleraX154,178,937 - 154,179,194RGD
Cytogenetic MapXq28UniSTS
HuRefX142,563,911 - 142,564,168UniSTS
REN90705  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,020,618 - 154,020,885UniSTSGRCh37
Build 36X153,673,812 - 153,674,079RGDNCBI36
CeleraX154,179,175 - 154,179,442RGD
Cytogenetic MapXq28UniSTS
HuRefX142,564,149 - 142,564,416UniSTS
REN90706  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,020,870 - 154,021,094UniSTSGRCh37
Build 36X153,674,064 - 153,674,288RGDNCBI36
CeleraX154,179,427 - 154,179,651RGD
Cytogenetic MapXq28UniSTS
HuRefX142,564,401 - 142,564,625UniSTS
REN90707  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,021,069 - 154,021,317UniSTSGRCh37
Build 36X153,674,263 - 153,674,511RGDNCBI36
CeleraX154,179,626 - 154,179,874RGD
Cytogenetic MapXq28UniSTS
REN90708  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,021,289 - 154,021,540UniSTSGRCh37
Build 36X153,674,483 - 153,674,734RGDNCBI36
CeleraX154,179,846 - 154,180,097RGD
Cytogenetic MapXq28UniSTS
HuRefX142,564,820 - 142,565,071UniSTS
REN90709  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,021,502 - 154,021,747UniSTSGRCh37
Build 36X153,674,696 - 153,674,941RGDNCBI36
CeleraX154,180,059 - 154,180,304RGD
Cytogenetic MapXq28UniSTS
HuRefX142,565,033 - 142,565,278UniSTS
REN90710  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,021,724 - 154,021,982UniSTSGRCh37
Build 36X153,674,918 - 153,675,176RGDNCBI36
CeleraX154,180,281 - 154,180,539RGD
Cytogenetic MapXq28UniSTS
HuRefX142,565,255 - 142,565,513UniSTS
REN90711  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,021,980 - 154,022,206UniSTSGRCh37
Build 36X153,675,174 - 153,675,400RGDNCBI36
CeleraX154,180,537 - 154,180,763RGD
Cytogenetic MapXq28UniSTS
HuRefX142,565,511 - 142,565,737UniSTS
REN90712  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,022,179 - 154,022,437UniSTSGRCh37
Build 36X153,675,373 - 153,675,631RGDNCBI36
CeleraX154,180,736 - 154,180,994RGD
Cytogenetic MapXq28UniSTS
HuRefX142,565,710 - 142,565,968UniSTS
REN90713  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,022,410 - 154,022,655UniSTSGRCh37
Build 36X153,675,604 - 153,675,849RGDNCBI36
CeleraX154,180,967 - 154,181,212RGD
Cytogenetic MapXq28UniSTS
HuRefX142,565,941 - 142,566,186UniSTS
REN90714  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,022,632 - 154,022,899UniSTSGRCh37
Build 36X153,675,826 - 153,676,093RGDNCBI36
CeleraX154,181,189 - 154,181,456RGD
Cytogenetic MapXq28UniSTS
HuRefX142,566,163 - 142,566,430UniSTS
REN90715  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,022,844 - 154,023,094UniSTSGRCh37
Build 36X153,676,038 - 153,676,288RGDNCBI36
CeleraX154,181,401 - 154,181,651RGD
Cytogenetic MapXq28UniSTS
HuRefX142,566,375 - 142,566,625UniSTS
REN90716  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,022,998 - 154,023,222UniSTSGRCh37
Build 36X153,676,192 - 153,676,416RGDNCBI36
CeleraX154,181,555 - 154,181,779RGD
Cytogenetic MapXq28UniSTS
HuRefX142,566,529 - 142,566,753UniSTS
REN90717  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,023,196 - 154,023,454UniSTSGRCh37
Build 36X153,676,390 - 153,676,648RGDNCBI36
CeleraX154,181,753 - 154,182,011RGD
Cytogenetic MapXq28UniSTS
HuRefX142,566,727 - 142,566,985UniSTS
REN90718  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,023,442 - 154,023,703UniSTSGRCh37
Build 36X153,676,636 - 153,676,897RGDNCBI36
CeleraX154,181,999 - 154,182,260RGD
Cytogenetic MapXq28UniSTS
HuRefX142,566,973 - 142,567,234UniSTS
REN90719  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,023,626 - 154,023,873UniSTSGRCh37
Build 36X153,676,820 - 153,677,067RGDNCBI36
CeleraX154,182,183 - 154,182,430RGD
Cytogenetic MapXq28UniSTS
HuRefX142,567,157 - 142,567,404UniSTS
REN90720  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,023,846 - 154,024,116UniSTSGRCh37
Build 36X153,677,040 - 153,677,310RGDNCBI36
CeleraX154,182,403 - 154,182,673RGD
Cytogenetic MapXq28UniSTS
HuRefX142,567,377 - 142,567,647UniSTS
REN90721  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,024,112 - 154,024,340UniSTSGRCh37
Build 36X153,677,306 - 153,677,534RGDNCBI36
CeleraX154,182,669 - 154,182,897RGD
Cytogenetic MapXq28UniSTS
HuRefX142,567,643 - 142,567,871UniSTS
REN90722  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,024,145 - 154,024,380UniSTSGRCh37
Build 36X153,677,339 - 153,677,574RGDNCBI36
CeleraX154,182,702 - 154,182,937RGD
Cytogenetic MapXq28UniSTS
HuRefX142,567,676 - 142,567,911UniSTS
REN90723  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,024,728 - 154,024,977UniSTSGRCh37
Build 36X153,677,922 - 153,678,171RGDNCBI36
CeleraX154,183,285 - 154,183,534RGD
Cytogenetic MapXq28UniSTS
HuRefX142,568,259 - 142,568,508UniSTS
REN90724  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,024,951 - 154,025,185UniSTSGRCh37
Build 36X153,678,145 - 153,678,379RGDNCBI36
CeleraX154,183,508 - 154,183,742RGD
Cytogenetic MapXq28UniSTS
HuRefX142,568,482 - 142,568,716UniSTS
REN90725  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,025,161 - 154,025,427UniSTSGRCh37
Build 36X153,678,355 - 153,678,621RGDNCBI36
CeleraX154,183,718 - 154,183,984RGD
Cytogenetic MapXq28UniSTS
HuRefX142,568,692 - 142,568,958UniSTS
REN90726  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,025,404 - 154,025,639UniSTSGRCh37
Build 36X153,678,598 - 153,678,833RGDNCBI36
CeleraX154,183,961 - 154,184,196RGD
Cytogenetic MapXq28UniSTS
HuRefX142,568,935 - 142,569,170UniSTS
REN90727  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,025,616 - 154,025,863UniSTSGRCh37
Build 36X153,678,810 - 153,679,057RGDNCBI36
CeleraX154,184,173 - 154,184,420RGD
Cytogenetic MapXq28UniSTS
HuRefX142,569,147 - 142,569,394UniSTS
REN90728  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,025,840 - 154,026,083UniSTSGRCh37
Build 36X153,679,034 - 153,679,277RGDNCBI36
CeleraX154,184,397 - 154,184,640RGD
Cytogenetic MapXq28UniSTS
HuRefX142,569,371 - 142,569,614UniSTS
REN90729  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,026,080 - 154,026,326UniSTSGRCh37
Build 36X153,679,274 - 153,679,520RGDNCBI36
CeleraX154,184,637 - 154,184,883RGD
Cytogenetic MapXq28UniSTS
HuRefX142,569,611 - 142,569,857UniSTS
REN90730  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,026,301 - 154,026,536UniSTSGRCh37
Build 36X153,679,495 - 153,679,730RGDNCBI36
CeleraX154,184,858 - 154,185,093RGD
Cytogenetic MapXq28UniSTS
HuRefX142,569,832 - 142,570,067UniSTS
REN90731  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,026,513 - 154,026,773UniSTSGRCh37
Build 36X153,679,707 - 153,679,967RGDNCBI36
CeleraX154,185,070 - 154,185,330RGD
Cytogenetic MapXq28UniSTS
HuRefX142,570,044 - 142,570,304UniSTS
REN90732  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,026,750 - 154,027,001UniSTSGRCh37
Build 36X153,679,944 - 153,680,195RGDNCBI36
CeleraX154,185,307 - 154,185,558RGD
Cytogenetic MapXq28UniSTS
HuRefX142,570,281 - 142,570,532UniSTS
REN90733  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,027,297 - 154,027,535UniSTSGRCh37
Build 36X153,680,491 - 153,680,729RGDNCBI36
CeleraX154,185,854 - 154,186,092RGD
Cytogenetic MapXq28UniSTS
HuRefX142,570,828 - 142,571,066UniSTS
REN90734  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,027,498 - 154,027,747UniSTSGRCh37
Build 36X153,680,692 - 153,680,941RGDNCBI36
CeleraX154,186,055 - 154,186,304RGD
Cytogenetic MapXq28UniSTS
HuRefX142,571,029 - 142,571,278UniSTS
REN90735  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,027,741 - 154,027,991UniSTSGRCh37
Build 36X153,680,935 - 153,681,185RGDNCBI36
CeleraX154,186,298 - 154,186,548RGD
Cytogenetic MapXq28UniSTS
HuRefX142,571,272 - 142,571,522UniSTS
REN90736  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,027,957 - 154,028,181UniSTSGRCh37
Build 36X153,681,151 - 153,681,375RGDNCBI36
CeleraX154,186,514 - 154,186,738RGD
Cytogenetic MapXq28UniSTS
HuRefX142,571,488 - 142,571,712UniSTS
REN90737  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,028,155 - 154,028,381UniSTSGRCh37
Build 36X153,681,349 - 153,681,575RGDNCBI36
CeleraX154,186,712 - 154,186,938RGD
Cytogenetic MapXq28UniSTS
HuRefX142,571,686 - 142,571,912UniSTS
REN90738  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,028,369 - 154,028,639UniSTSGRCh37
Build 36X153,681,563 - 153,681,833RGDNCBI36
CeleraX154,186,926 - 154,187,196RGD
Cytogenetic MapXq28UniSTS
HuRefX142,571,900 - 142,572,170UniSTS
REN90739  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,028,619 - 154,028,867UniSTSGRCh37
Build 36X153,681,813 - 153,682,061RGDNCBI36
CeleraX154,187,176 - 154,187,424RGD
Cytogenetic MapXq28UniSTS
HuRefX142,572,150 - 142,572,398UniSTS
REN90740  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,028,846 - 154,029,082UniSTSGRCh37
Build 36X153,682,040 - 153,682,276RGDNCBI36
CeleraX154,187,403 - 154,187,639RGD
Cytogenetic MapXq28UniSTS
HuRefX142,572,377 - 142,572,613UniSTS
REN90741  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,029,059 - 154,029,314UniSTSGRCh37
Build 36X153,682,253 - 153,682,508RGDNCBI36
CeleraX154,187,616 - 154,187,871RGD
Cytogenetic MapXq28UniSTS
HuRefX142,572,590 - 142,572,845UniSTS
REN90742  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,029,291 - 154,029,532UniSTSGRCh37
Build 36X153,682,485 - 153,682,726RGDNCBI36
CeleraX154,187,848 - 154,188,089RGD
Cytogenetic MapXq28UniSTS
REN90743  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,029,498 - 154,029,733UniSTSGRCh37
Build 36X153,682,692 - 153,682,927RGDNCBI36
CeleraX154,188,055 - 154,188,290RGD
Cytogenetic MapXq28UniSTS
REN90744  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,029,535 - 154,029,759UniSTSGRCh37
Build 36X153,682,729 - 153,682,953RGDNCBI36
CeleraX154,188,092 - 154,188,316RGD
Cytogenetic MapXq28UniSTS
REN90745  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,029,848 - 154,030,099UniSTSGRCh37
Build 36X153,683,042 - 153,683,293RGDNCBI36
CeleraX154,188,405 - 154,188,656RGD
Cytogenetic MapXq28UniSTS
HuRefX142,573,078 - 142,573,333UniSTS
REN90746  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,030,081 - 154,030,327UniSTSGRCh37
Build 36X153,683,275 - 153,683,521RGDNCBI36
CeleraX154,188,638 - 154,188,884RGD
Cytogenetic MapXq28UniSTS
HuRefX142,573,315 - 142,573,561UniSTS
REN90747  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,030,325 - 154,030,586UniSTSGRCh37
Build 36X153,683,519 - 153,683,780RGDNCBI36
CeleraX154,188,882 - 154,189,143RGD
Cytogenetic MapXq28UniSTS
HuRefX142,573,559 - 142,573,820UniSTS
REN90748  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,030,556 - 154,030,787UniSTSGRCh37
Build 36X153,683,750 - 153,683,981RGDNCBI36
CeleraX154,189,113 - 154,189,344RGD
Cytogenetic MapXq28UniSTS
HuRefX142,573,790 - 142,574,021UniSTS
REN90749  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,030,761 - 154,031,024UniSTSGRCh37
Build 36X153,683,955 - 153,684,218RGDNCBI36
CeleraX154,189,318 - 154,189,581RGD
Cytogenetic MapXq28UniSTS
HuRefX142,573,995 - 142,574,258UniSTS
REN90750  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,031,017 - 154,031,257UniSTSGRCh37
Build 36X153,684,211 - 153,684,451RGDNCBI36
CeleraX154,189,574 - 154,189,814RGD
Cytogenetic MapXq28UniSTS
HuRefX142,574,251 - 142,574,491UniSTS
REN90751  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,031,227 - 154,031,483UniSTSGRCh37
Build 36X153,684,421 - 153,684,677RGDNCBI36
CeleraX154,189,784 - 154,190,040RGD
Cytogenetic MapXq28UniSTS
HuRefX142,574,461 - 142,574,717UniSTS
REN90752  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,031,479 - 154,031,713UniSTSGRCh37
Build 36X153,684,673 - 153,684,907RGDNCBI36
CeleraX154,190,036 - 154,190,270RGD
Cytogenetic MapXq28UniSTS
HuRefX142,574,713 - 142,574,947UniSTS
REN90753  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,031,710 - 154,031,952UniSTSGRCh37
Build 36X153,684,904 - 153,685,146RGDNCBI36
CeleraX154,190,267 - 154,190,509RGD
Cytogenetic MapXq28UniSTS
HuRefX142,574,944 - 142,575,186UniSTS
REN90754  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,031,931 - 154,032,174UniSTSGRCh37
Build 36X153,685,125 - 153,685,368RGDNCBI36
CeleraX154,190,488 - 154,190,731RGD
Cytogenetic MapXq28UniSTS
HuRefX142,575,165 - 142,575,408UniSTS
REN90755  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,032,160 - 154,032,419UniSTSGRCh37
Build 36X153,685,354 - 153,685,613RGDNCBI36
CeleraX154,190,717 - 154,190,976RGD
Cytogenetic MapXq28UniSTS
HuRefX142,575,394 - 142,575,653UniSTS
REN90756  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,032,406 - 154,032,660UniSTSGRCh37
Build 36X153,685,600 - 153,685,854RGDNCBI36
CeleraX154,190,963 - 154,191,217RGD
Cytogenetic MapXq28UniSTS
HuRefX142,575,640 - 142,575,894UniSTS
REN90757  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,032,654 - 154,032,916UniSTSGRCh37
Build 36X153,685,848 - 153,686,110RGDNCBI36
CeleraX154,191,211 - 154,191,473RGD
Cytogenetic MapXq28UniSTS
HuRefX142,575,888 - 142,576,150UniSTS
REN90758  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,032,875 - 154,033,120UniSTSGRCh37
Build 36X153,686,069 - 153,686,314RGDNCBI36
CeleraX154,191,432 - 154,191,677RGD
Cytogenetic MapXq28UniSTS
HuRefX142,576,109 - 142,576,354UniSTS
REN90759  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,033,097 - 154,033,335UniSTSGRCh37
Build 36X153,686,291 - 153,686,529RGDNCBI36
CeleraX154,191,654 - 154,191,892RGD
Cytogenetic MapXq28UniSTS
HuRefX142,576,331 - 142,576,569UniSTS
REN90760  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,033,313 - 154,033,576UniSTSGRCh37
Build 36X153,686,507 - 153,686,770RGDNCBI36
CeleraX154,191,870 - 154,192,133RGD
Cytogenetic MapXq28UniSTS
HuRefX142,576,547 - 142,576,810UniSTS
REN90761  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,033,412 - 154,033,668UniSTSGRCh37
Build 36X153,686,606 - 153,686,862RGDNCBI36
CeleraX154,191,969 - 154,192,225RGD
Cytogenetic MapXq28UniSTS
HuRefX142,576,646 - 142,576,902UniSTS
REN90762  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,033,663 - 154,033,929UniSTSGRCh37
Build 36X153,686,857 - 153,687,123RGDNCBI36
CeleraX154,192,220 - 154,192,486RGD
Cytogenetic MapXq28UniSTS
HuRefX142,576,897 - 142,577,163UniSTS
REN90763  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,033,905 - 154,034,150UniSTSGRCh37
Build 36X153,687,099 - 153,687,344RGDNCBI36
CeleraX154,192,462 - 154,192,707RGD
Cytogenetic MapXq28UniSTS
HuRefX142,577,139 - 142,577,384UniSTS
REN90764  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,034,117 - 154,034,367UniSTSGRCh37
Build 36X153,687,311 - 153,687,561RGDNCBI36
CeleraX154,192,674 - 154,192,924RGD
Cytogenetic MapXq28UniSTS
HuRefX142,577,351 - 142,577,601UniSTS
REN90765  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,034,348 - 154,034,597UniSTSGRCh37
Build 36X153,687,542 - 153,687,791RGDNCBI36
CeleraX154,192,905 - 154,193,154RGD
Cytogenetic MapXq28UniSTS
REN90766  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,034,583 - 154,034,836UniSTSGRCh37
Build 36X153,687,777 - 153,688,030RGDNCBI36
CeleraX154,193,140 - 154,193,393RGD
Cytogenetic MapXq28UniSTS
REN90767  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,034,814 - 154,035,065UniSTSGRCh37
Build 36X153,688,008 - 153,688,259RGDNCBI36
CeleraX154,193,371 - 154,193,622RGD
Cytogenetic MapXq28UniSTS
REN90768  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,035,030 - 154,035,295UniSTSGRCh37
Build 36X153,688,224 - 153,688,489RGDNCBI36
CeleraX154,193,587 - 154,193,852RGD
Cytogenetic MapXq28UniSTS
REN90769  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,035,281 - 154,035,528UniSTSGRCh37
Build 36X153,688,475 - 153,688,722RGDNCBI36
CeleraX154,193,838 - 154,194,085RGD
Cytogenetic MapXq28UniSTS
REN90770  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,035,521 - 154,035,782UniSTSGRCh37
Build 36X153,688,715 - 153,688,976RGDNCBI36
CeleraX154,194,078 - 154,194,339RGD
Cytogenetic MapXq28UniSTS
HuRefX142,578,797 - 142,579,058UniSTS
stSG604287  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,007,360 - 154,008,504UniSTSGRCh37
Build 36X153,660,554 - 153,661,698RGDNCBI36
CeleraX154,165,923 - 154,167,067RGD
HuRefX142,550,720 - 142,552,147UniSTS
stSG604288  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,008,485 - 154,009,540UniSTSGRCh37
Build 36X153,661,679 - 153,662,734RGDNCBI36
CeleraX154,167,048 - 154,168,103RGD
HuRefX142,552,128 - 142,553,183UniSTS
stSG604289  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,009,521 - 154,010,626UniSTSGRCh37
Build 36X153,662,715 - 153,663,820RGDNCBI36
CeleraX154,168,084 - 154,169,189RGD
Cytogenetic MapXq28UniSTS
HuRefX142,553,164 - 142,554,268UniSTS
stSG604291  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,011,849 - 154,012,859UniSTSGRCh37
Build 36X153,665,043 - 153,666,053RGDNCBI36
CeleraX154,170,412 - 154,171,422RGD
HuRefX142,555,236 - 142,556,246UniSTS
stSG604292  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,012,840 - 154,014,092UniSTSGRCh37
Build 36X153,666,034 - 153,667,286RGDNCBI36
CeleraX154,171,403 - 154,172,656RGD
HuRefX142,556,227 - 142,557,480UniSTS
stSG604293  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,014,073 - 154,015,388UniSTSGRCh37
Build 36X153,667,267 - 153,668,582RGDNCBI36
CeleraX154,172,637 - 154,173,953RGD
HuRefX142,557,461 - 142,558,927UniSTS
stSG604294  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,014,866 - 154,016,124UniSTSGRCh37
Build 36X153,668,060 - 153,669,318RGDNCBI36
CeleraX154,173,430 - 154,174,681RGD
HuRefX142,558,254 - 142,559,655UniSTS
stSG604295  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,017,409 - 154,018,460UniSTSGRCh37
Build 36X153,670,603 - 153,671,654RGDNCBI36
CeleraX154,175,966 - 154,177,017RGD
HuRefX142,560,940 - 142,561,991UniSTS
stSG604296  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,018,443 - 154,019,762UniSTSGRCh37
Build 36X153,671,637 - 153,672,956RGDNCBI36
CeleraX154,177,000 - 154,178,319RGD
HuRefX142,561,974 - 142,563,293UniSTS
stSG604297  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,019,743 - 154,021,025UniSTSGRCh37
Build 36X153,672,937 - 153,674,219RGDNCBI36
CeleraX154,178,300 - 154,179,582RGD
HuRefX142,563,274 - 142,564,556UniSTS
stSG604298  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,020,565 - 154,021,927UniSTSGRCh37
Build 36X153,673,759 - 153,675,121RGDNCBI36
CeleraX154,179,122 - 154,180,484RGD
HuRefX142,564,096 - 142,565,458UniSTS
stSG604299  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,021,908 - 154,022,995UniSTSGRCh37
Build 36X153,675,102 - 153,676,189RGDNCBI36
CeleraX154,180,465 - 154,181,552RGD
HuRefX142,565,439 - 142,566,526UniSTS
stSG604300  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,022,976 - 154,024,336UniSTSGRCh37
Build 36X153,676,170 - 153,677,530RGDNCBI36
CeleraX154,181,533 - 154,182,893RGD
HuRefX142,566,507 - 142,567,867UniSTS
stSG604301  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,024,322 - 154,025,531UniSTSGRCh37
Build 36X153,677,516 - 153,678,725RGDNCBI36
CeleraX154,182,879 - 154,184,088RGD
HuRefX142,567,853 - 142,569,062UniSTS
stSG604302  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,027,343 - 154,028,389UniSTSGRCh37
Build 36X153,680,537 - 153,681,583RGDNCBI36
CeleraX154,185,900 - 154,186,946RGD
HuRefX142,570,874 - 142,571,920UniSTS
stSG604303  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,028,370 - 154,029,739UniSTSGRCh37
Build 36X153,681,564 - 153,682,933RGDNCBI36
CeleraX154,186,927 - 154,188,296RGD
HuRefX142,571,901 - 142,572,969UniSTS
stSG604304  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,030,089 - 154,031,208UniSTSGRCh37
Build 36X153,683,283 - 153,684,402RGDNCBI36
CeleraX154,188,646 - 154,189,765RGD
HuRefX142,573,323 - 142,574,442UniSTS
stSG604305  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,031,203 - 154,032,321UniSTSGRCh37
Build 36X153,684,397 - 153,685,515RGDNCBI36
CeleraX154,189,760 - 154,190,878RGD
HuRefX142,574,437 - 142,575,555UniSTS
stSG604306  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,032,404 - 154,033,681UniSTSGRCh37
Build 36X153,685,598 - 153,686,875RGDNCBI36
CeleraX154,190,961 - 154,192,238RGD
HuRefX142,575,638 - 142,576,915UniSTS
STS-M64925  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,007,269 - 154,007,436UniSTSGRCh37
Build 36X153,660,463 - 153,660,630RGDNCBI36
CeleraX154,165,832 - 154,165,999RGD
Cytogenetic MapXq28UniSTS
HuRefX142,550,629 - 142,550,796UniSTS
GeneMap99-GB4 RH MapX354.15UniSTS
DXS7022E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,006,999 - 154,007,133UniSTSGRCh37
Build 36X153,660,193 - 153,660,327RGDNCBI36
CeleraX154,165,562 - 154,165,696RGD
Cytogenetic MapXq28UniSTS
HuRefX142,550,359 - 142,550,493UniSTS
GeneMap99-GB4 RH MapX354.15UniSTS
DXS9740  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,007,125 - 154,007,418UniSTSGRCh37
Build 36X153,660,319 - 153,660,612RGDNCBI36
CeleraX154,165,688 - 154,165,981RGD
Cytogenetic MapXq28UniSTS
HuRefX142,550,485 - 142,550,778UniSTS
GeneMap99-G3 RH MapX4235.0UniSTS
UniSTS:68640  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,015,257 - 154,015,521UniSTSGRCh37
Build 36X153,668,451 - 153,668,715RGDNCBI36
CeleraX154,173,822 - 154,174,078RGD
MPP1__6146  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,006,874 - 154,007,561UniSTSGRCh37
Build 36X153,660,068 - 153,660,755RGDNCBI36
CeleraX154,165,437 - 154,166,124RGD
HuRefX142,550,234 - 142,550,921UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:4607
Count of miRNA genes:1266
Interacting mature miRNAs:1610
Transcripts:ENST00000369531, ENST00000369534, ENST00000393529, ENST00000393531, ENST00000413259, ENST00000417435, ENST00000428488, ENST00000439370, ENST00000453245, ENST00000462825, ENST00000471821, ENST00000475943, ENST00000482757, ENST00000488694, ENST00000488754, ENST00000491955, ENST00000493871, ENST00000494170
Prediction methods:Microtar, Miranda, Pita, 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
Medium 2096 2738 1560 431 1754 322 3614 1677 3297 355 1196 1449 115 1200 2370 4
Low 310 252 165 192 175 142 742 518 433 61 258 143 58 4 418 1 2
Below cutoff 23 1 1 13 1 1 3 3 5 19 1 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_015873 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001166460 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001166461 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001166462 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_002436 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011531167 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011531169 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024452385 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC109993 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK093702 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK223396 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK290246 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK303111 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK304538 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK310681 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK311541 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK312296 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK315957 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY423731 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY634686 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC002392 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471172 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA074686 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M64925 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M87059 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U39611 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000369531   ⟹   ENSP00000358544
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX154,789,989 - 154,805,498 (-)Ensembl
RefSeq Acc Id: ENST00000369534   ⟹   ENSP00000358547
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX154,778,684 - 154,805,485 (-)Ensembl
RefSeq Acc Id: ENST00000393529   ⟹   ENSP00000377163
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX154,784,031 - 154,821,007 (-)Ensembl
RefSeq Acc Id: ENST00000393531   ⟹   ENSP00000377165
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX154,779,153 - 154,805,397 (-)Ensembl
RefSeq Acc Id: ENST00000413259   ⟹   ENSP00000400155
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX154,778,686 - 154,805,527 (-)Ensembl
RefSeq Acc Id: ENST00000417435   ⟹   ENSP00000389321
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX154,786,214 - 154,805,527 (-)Ensembl
RefSeq Acc Id: ENST00000428488   ⟹   ENSP00000391701
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX154,785,057 - 154,805,485 (-)Ensembl
RefSeq Acc Id: ENST00000439370   ⟹   ENSP00000400700
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX154,778,726 - 154,805,456 (-)Ensembl
RefSeq Acc Id: ENST00000453245   ⟹   ENSP00000410888
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX154,781,754 - 154,805,485 (-)Ensembl
RefSeq Acc Id: ENST00000462825
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX154,783,377 - 154,799,815 (-)Ensembl
RefSeq Acc Id: ENST00000471821
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX154,791,631 - 154,805,468 (-)Ensembl
RefSeq Acc Id: ENST00000475943
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX154,784,701 - 154,805,477 (-)Ensembl
RefSeq Acc Id: ENST00000482757
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX154,778,723 - 154,781,596 (-)Ensembl
RefSeq Acc Id: ENST00000488694
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX154,786,366 - 154,792,422 (-)Ensembl
RefSeq Acc Id: ENST00000488754
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX154,785,084 - 154,791,195 (-)Ensembl
RefSeq Acc Id: ENST00000491955
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX154,778,686 - 154,783,234 (-)Ensembl
RefSeq Acc Id: ENST00000493871
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX154,783,653 - 154,786,225 (-)Ensembl
RefSeq Acc Id: ENST00000494170
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX154,782,709 - 154,805,441 (-)Ensembl
RefSeq Acc Id: NM_001166460   ⟹   NP_001159932
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X154,778,684 - 154,805,485 (-)NCBI
GRCh37X154,006,959 - 154,033,802 (-)ENTREZGENE
HuRefX142,550,319 - 142,577,036 (-)ENTREZGENE
CHM1_1X153,918,634 - 153,945,496 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001166461   ⟹   NP_001159933
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X154,778,684 - 154,805,485 (-)NCBI
GRCh37X154,006,959 - 154,033,802 (-)ENTREZGENE
HuRefX142,550,319 - 142,577,036 (-)ENTREZGENE
CHM1_1X153,918,634 - 153,945,496 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001166462   ⟹   NP_001159934
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X154,778,684 - 154,805,485 (-)NCBI
GRCh37X154,006,959 - 154,033,802 (-)ENTREZGENE
HuRefX142,550,319 - 142,577,036 (-)ENTREZGENE
CHM1_1X153,918,634 - 153,945,496 (-)NCBI
Sequence:
RefSeq Acc Id: NM_002436   ⟹   NP_002427
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X154,778,684 - 154,805,485 (-)NCBI
GRCh37X154,006,959 - 154,033,802 (-)ENTREZGENE
Build 36X153,660,162 - 153,686,957 (-)NCBI Archive
HuRefX142,550,319 - 142,577,036 (-)ENTREZGENE
CHM1_1X153,918,634 - 153,945,496 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011531167   ⟹   XP_011529469
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X154,778,684 - 154,805,485 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011531169   ⟹   XP_011529471
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X154,778,684 - 154,805,477 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024452385   ⟹   XP_024308153
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X154,778,684 - 154,805,477 (-)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_001159932   ⟸   NM_001166460
- Peptide Label: isoform 2
- UniProtKB: Q00013 (UniProtKB/Swiss-Prot),   B4E325 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001159933   ⟸   NM_001166461
- Peptide Label: isoform 3
- UniProtKB: Q00013 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_002427   ⟸   NM_002436
- Peptide Label: isoform 1
- UniProtKB: Q00013 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001159934   ⟸   NM_001166462
- Peptide Label: isoform 4
- UniProtKB: Q00013 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_011529469   ⟸   XM_011531167
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_011529471   ⟸   XM_011531169
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_024308153   ⟸   XM_024452385
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: ENSP00000400700   ⟸   ENST00000439370
RefSeq Acc Id: ENSP00000400155   ⟸   ENST00000413259
RefSeq Acc Id: ENSP00000410888   ⟸   ENST00000453245
RefSeq Acc Id: ENSP00000391701   ⟸   ENST00000428488
RefSeq Acc Id: ENSP00000389321   ⟸   ENST00000417435
RefSeq Acc Id: ENSP00000377163   ⟸   ENST00000393529
RefSeq Acc Id: ENSP00000377165   ⟸   ENST00000393531
RefSeq Acc Id: ENSP00000358547   ⟸   ENST00000369534
RefSeq Acc Id: ENSP00000358544   ⟸   ENST00000369531
Protein Domains
Guanylate kinase-like   PDZ   SH3

Promoters
RGD ID:6809054
Promoter ID:HG_KWN:68703
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562
Transcripts:OTTHUMT00000061189,   OTTHUMT00000127559
Position:
Human AssemblyChrPosition (strand)Source
Build 36X153,662,861 - 153,665,012 (-)MPROMDB
RGD ID:6809055
Promoter ID:HG_KWN:68704
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell_12Hour,   K562
Transcripts:OTTHUMT00000316146,   OTTHUMT00000316147
Position:
Human AssemblyChrPosition (strand)Source
Build 36X153,667,229 - 153,667,729 (-)MPROMDB
RGD ID:6809056
Promoter ID:HG_KWN:68705
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562
Transcripts:OTTHUMT00000316145
Position:
Human AssemblyChrPosition (strand)Source
Build 36X153,672,861 - 153,673,562 (-)MPROMDB
RGD ID:6809050
Promoter ID:HG_KWN:68706
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562
Transcripts:OTTHUMT00000061188
Position:
Human AssemblyChrPosition (strand)Source
Build 36X153,674,611 - 153,675,111 (-)MPROMDB
RGD ID:6809053
Promoter ID:HG_KWN:68707
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562,   Lymphoblastoid,   NB4
Transcripts:OTTHUMT00000316143
Position:
Human AssemblyChrPosition (strand)Source
Build 36X153,680,801 - 153,682,112 (-)MPROMDB
RGD ID:6808462
Promoter ID:HG_KWN:68708
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000369531,   NM_001166460,   NM_001166461,   NM_001166462,   OTTHUMT00000061186,   OTTHUMT00000061187,   OTTHUMT00000061191,   OTTHUMT00000316138,   OTTHUMT00000316139,   OTTHUMT00000316142,   UC004FMQ.1,   UC010NVH.1
Position:
Human AssemblyChrPosition (strand)Source
Build 36X153,686,821 - 153,687,321 (-)MPROMDB
RGD ID:13628674
Promoter ID:EPDNEW_H29575
Type:initiation region
Name:MPP1_1
Description:membrane palmitoylated protein 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X154,805,422 - 154,805,482EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 Xp22.33-q28(chrX:10701-156003242)x3 copy number gain See cases [RCV000133911] ChrX:10701..156003242 [GRCh38]
ChrX:60701..155232907 [GRCh37]
ChrX:701..154886101 [NCBI36]
ChrX:Xp22.33-q28
pathogenic|likely pathogenic|conflicting data from submitters
GRCh38/hg38 Xp22.33-q28(chrX:3092486-155699618)x2 copy number gain See cases [RCV000050889] ChrX:3092486..155699618 [GRCh38]
ChrX:3010527..154929279 [GRCh37]
ChrX:3020527..154582473 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xq28(chrX:150036146-156022206)x3 copy number gain See cases [RCV000050946] ChrX:150036146..156022206 [GRCh38]
ChrX:149298619..155251871 [GRCh37]
ChrX:148955035..154905065 [NCBI36]
ChrX:Xq28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:20140-155699618)x3 copy number gain See cases [RCV000050810] ChrX:20140..155699618 [GRCh38]
ChrX:70140..154929279 [GRCh37]
ChrX:10140..154582473 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:20140-155699618)x1 copy number loss See cases [RCV000050811] ChrX:20140..155699618 [GRCh38]
ChrX:70140..154929279 [GRCh37]
ChrX:10140..154582473 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10679-156022206)x1 copy number loss See cases [RCV000050699] ChrX:10679..156022206 [GRCh38]
ChrX:60679..155251871 [GRCh37]
ChrX:679..154905065 [NCBI36]
ChrX:Xp22.33-q28
pathogenic|conflicting interpretations of pathogenicity|conflicting data from submitters
GRCh38/hg38 Xq28(chrX:149989929-156022206)x3 copy number gain See cases [RCV000050657] ChrX:149989929..156022206 [GRCh38]
ChrX:149158160..155251871 [GRCh37]
ChrX:148908818..154905065 [NCBI36]
ChrX:Xq28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10679-156013167)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000050385]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000050385]|See cases [RCV000050385] ChrX:10679..156013167 [GRCh38]
ChrX:60679..155242832 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10679-156013167)x1 copy number loss Global developmental delay [RCV000050386]|See cases [RCV000050386] ChrX:10679..156013167 [GRCh38]
ChrX:60679..155242832 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10679-156022206)x3 copy number gain See cases [RCV000050697] ChrX:10679..156022206 [GRCh38]
ChrX:60679..155251871 [GRCh37]
ChrX:679..154905065 [NCBI36]
ChrX:Xp22.33-q28
pathogenic|conflicting interpretations of pathogenicity|conflicting data from submitters
GRCh38/hg38 Xq28(chrX:154791149-154931411)x2 copy number gain See cases [RCV000051070] ChrX:154791149..154931411 [GRCh38]
ChrX:153672618..153812880 [NCBI36]
ChrX:Xq28
uncertain significance
GRCh38/hg38 Xq23-28(chrX:115417992-156022206)x1 copy number loss See cases [RCV000051160] ChrX:115417992..156022206 [GRCh38]
ChrX:114652461..155251871 [GRCh37]
ChrX:114558717..154905065 [NCBI36]
ChrX:Xq23-28
pathogenic
GRCh38/hg38 Xq27.3-28(chrX:145879711-156022206)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051747]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051747]|See cases [RCV000051747] ChrX:145879711..156022206 [GRCh38]
ChrX:146715565..155251871 [GRCh37]
ChrX:144768921..154905065 [NCBI36]
ChrX:Xq27.3-28
pathogenic
GRCh38/hg38 Xq28(chrX:153296806-155699618)x1 copy number loss See cases [RCV000051750] ChrX:153296806..155699618 [GRCh38]
ChrX:152568327..154929279 [GRCh37]
ChrX:152215458..154582473 [NCBI36]
ChrX:Xq28
pathogenic
GRCh38/hg38 Xp11.21-q28(chrX:57372584-155996431)x1 copy number loss See cases [RCV000051665] ChrX:57372584..155996431 [GRCh38]
ChrX:57399017..155226096 [GRCh37]
ChrX:57415742..154879290 [NCBI36]
ChrX:Xp11.21-q28
pathogenic
GRCh38/hg38 Xq11.1-28(chrX:63279794-155939524)x1 copy number loss See cases [RCV000051666] ChrX:63279794..155939524 [GRCh38]
ChrX:62499671..155169188 [GRCh37]
ChrX:62416396..154822382 [NCBI36]
ChrX:Xq11.1-28
pathogenic
GRCh38/hg38 Xq23-28(chrX:116264813-155980575)x1 copy number loss See cases [RCV000051728] ChrX:116264813..155980575 [GRCh38]
ChrX:115396069..155210240 [GRCh37]
ChrX:115310097..154863434 [NCBI36]
ChrX:Xq23-28
pathogenic
GRCh38/hg38 Xq25-28(chrX:126537861-155996431)x1 copy number loss See cases [RCV000051729] ChrX:126537861..155996431 [GRCh38]
ChrX:125671844..155226096 [GRCh37]
ChrX:125499525..154879290 [NCBI36]
ChrX:Xq25-28
pathogenic
GRCh38/hg38 Xq22.1-28(chrX:100524562-155669954)x1 copy number loss See cases [RCV000051713] ChrX:100524562..155669954 [GRCh38]
ChrX:99779559..154785891 [GRCh37]
ChrX:99666215..154552809 [NCBI36]
ChrX:Xq22.1-28
pathogenic
GRCh38/hg38 Xq26.3-28(chrX:136956500-156020993)x1 copy number loss See cases [RCV000051732] ChrX:136956500..156020993 [GRCh38]
ChrX:136038659..155250658 [GRCh37]
ChrX:135866325..154903852 [NCBI36]
ChrX:Xq26.3-28
pathogenic
GRCh38/hg38 Xq27.1-28(chrX:140445228-155998166)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051746]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051746]|See cases [RCV000051746] ChrX:140445228..155998166 [GRCh38]
ChrX:139527393..155227831 [GRCh37]
ChrX:139355059..154881025 [NCBI36]
ChrX:Xq27.1-28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:26101-155999293)x3 copy number gain See cases [RCV000052322] ChrX:26101..155999293 [GRCh38]
ChrX:76101..155228958 [GRCh37]
ChrX:16101..154882152 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:2790845-155699618)x3 copy number gain See cases [RCV000052359] ChrX:2790845..155699618 [GRCh38]
ChrX:2708886..154929279 [GRCh37]
ChrX:2718886..154582473 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:237659-156022362)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052327]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052327]|See cases [RCV000052327] ChrX:237659..156022362 [GRCh38]
ChrX:154326..155252027 [GRCh37]
ChrX:94326..154905221 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:27245-155996431)x3 copy number gain See cases [RCV000052324] ChrX:27245..155996431 [GRCh38]
ChrX:77245..155226096 [GRCh37]
ChrX:17245..154879290 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:40704-156022362)x3 copy number gain See cases [RCV000052325] ChrX:40704..156022362 [GRCh38]
ChrX:90704..155252027 [GRCh37]
ChrX:30704..154905221 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xq28(chrX:153932045-155611794)x3 copy number gain See cases [RCV000052529] ChrX:153932045..155611794 [GRCh38]
ChrX:152850692..154494649 [NCBI36]
ChrX:Xq28
pathogenic
GRCh38/hg38 Xq28(chrX:152932818-156022206)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052490]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052490]|See cases [RCV000052490] ChrX:152932818..156022206 [GRCh38]
ChrX:152173071..155251871 [GRCh37]
ChrX:151852018..154905065 [NCBI36]
ChrX:Xq28
pathogenic
GRCh38/hg38 Xq28(chrX:153395425-155687381)x2 copy number gain See cases [RCV000052491] ChrX:153395425..155687381 [GRCh38]
ChrX:152314077..154570236 [NCBI36]
ChrX:Xq28
pathogenic
GRCh38/hg38 Xq25-28(chrX:123731372-155687381)x3 copy number gain See cases [RCV000052445] ChrX:123731372..155687381 [GRCh38]
ChrX:122865222..154917042 [GRCh37]
ChrX:122692903..154570236 [NCBI36]
ChrX:Xq25-28
pathogenic
GRCh38/hg38 Xq27.1-28(chrX:140226495-155687381)x2 copy number gain See cases [RCV000052471] ChrX:140226495..155687381 [GRCh38]
ChrX:139308651..154917042 [GRCh37]
ChrX:139136317..154570236 [NCBI36]
ChrX:Xq27.1-28
pathogenic
GRCh38/hg38 Xq27.1-28(chrX:141160282-155699618)x3 copy number gain See cases [RCV000052475] ChrX:141160282..155699618 [GRCh38]
ChrX:140254480..154929279 [GRCh37]
ChrX:140082146..154582473 [NCBI36]
ChrX:Xq27.1-28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:26102-155996431)x1 copy number loss Global developmental delay [RCV000052986]|Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052987]|Intellectual functioning disability [RCV000052988]|Global developmental delay [RCV000052989]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052987]|See cases [RCV000052986] ChrX:26102..155996431 [GRCh38]
ChrX:76102..155226096 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:14245-155999293)x1 copy number loss Hypoplastic left heart [RCV000052982]|See cases [RCV000052982] ChrX:14245..155999293 [GRCh38]
ChrX:64245..155228958 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:26102-155996431)x3 copy number gain Global developmental delay [RCV000052984]|Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052985]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052985]|See cases [RCV000052984] ChrX:26102..155996431 [GRCh38]
ChrX:76102..155226096 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xq28(chrX:154791149-155996431)x3 copy number gain See cases [RCV000054323] ChrX:154791149..155996431 [GRCh38]
ChrX:153672618..154879290 [NCBI36]
ChrX:Xq28
uncertain significance
NM_002436.3(MPP1):c.659C>T (p.Ser220Phe) single nucleotide variant Malignant melanoma [RCV000073131] ChrX:154786222 [GRCh38]
ChrX:154014497 [GRCh37]
ChrX:153667691 [NCBI36]
ChrX:Xq28
not provided
GRCh37/hg19 Xq28(chrX:153576750-154563104)x1 copy number loss See cases [RCV000663390] ChrX:153576750..154563104 [GRCh37]
ChrX:Xq28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10679-156022826)x4 copy number gain See cases [RCV000133654] ChrX:10679..156022826 [GRCh38]
ChrX:60679..155252491 [GRCh37]
ChrX:679..154905685 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xq27.1-28(chrX:139333024-155978689)x1 copy number loss See cases [RCV000133818] ChrX:139333024..155978689 [GRCh38]
ChrX:138415183..155208354 [GRCh37]
ChrX:138242849..154861548 [NCBI36]
ChrX:Xq27.1-28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10701-155978689)x1 copy number loss See cases [RCV000133792] ChrX:10701..155978689 [GRCh38]
ChrX:60701..155208354 [GRCh37]
ChrX:701..154861548 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10679-156013167)x3 copy number gain See cases [RCV000050385] ChrX:10679..156013167 [GRCh38]
ChrX:60679..155242832 [GRCh37]
ChrX:679..154896026 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10679-156013167)x1 copy number loss See cases [RCV000050386] ChrX:10679..156013167 [GRCh38]
ChrX:60679..155242832 [GRCh37]
ChrX:679..154896026 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:14245-155999293)x1 copy number loss See cases [RCV000052982] ChrX:14245..155999293 [GRCh38]
ChrX:64245..155228958 [GRCh37]
ChrX:4245..154882152 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:26102-155996431)x3 copy number gain See cases [RCV000052984] ChrX:26102..155996431 [GRCh38]
ChrX:76102..155226096 [GRCh37]
ChrX:16102..154879290 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:26102-155996431)x1 copy number loss See cases [RCV000052986] ChrX:26102..155996431 [GRCh38]
ChrX:76102..155226096 [GRCh37]
ChrX:16102..154879290 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xq27.3-28(chrX:144627217-155434735)x3 copy number gain See cases [RCV000133725] ChrX:144627217..155434735 [GRCh38]
ChrX:146715565..154664396 [GRCh37]
ChrX:143516380..154317590 [NCBI36]
ChrX:Xq27.3-28
pathogenic
GRCh38/hg38 Xq21.1-28(chrX:85123740-156022206)x3 copy number gain See cases [RCV000133744] ChrX:85123740..156022206 [GRCh38]
ChrX:84378746..155251871 [GRCh37]
ChrX:84265402..154905065 [NCBI36]
ChrX:Xq21.1-28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:20297-155999253)x3 copy number gain See cases [RCV000134564] ChrX:20297..155999253 [GRCh38]
ChrX:70297..155228918 [GRCh37]
ChrX:10297..154882112 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xq21.1-28(chrX:78605009-156016560)x1 copy number loss See cases [RCV000134570] ChrX:78605009..156016560 [GRCh38]
ChrX:77860506..155246225 [GRCh37]
ChrX:77747162..154899419 [NCBI36]
ChrX:Xq21.1-28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10701-156003242)x1 copy number loss See cases [RCV000133947] ChrX:10701..156003242 [GRCh38]
ChrX:60701..155232907 [GRCh37]
ChrX:701..154886101 [NCBI36]
ChrX:Xp22.33-q28
pathogenic|conflicting interpretations of pathogenicity|conflicting data from submitters
GRCh38/hg38 Xq11.1-28(chrX:62712230-155978888)x3 copy number gain See cases [RCV000134025] ChrX:62712230..155978888 [GRCh38]
ChrX:61931700..155208553 [GRCh37]
ChrX:61848425..154861747 [NCBI36]
ChrX:Xq11.1-28
pathogenic
GRCh38/hg38 Xp21.1-q28(chrX:37076284-156016920)x1 copy number loss See cases [RCV000135300] ChrX:37076284..156016920 [GRCh38]
ChrX:37094357..155246585 [GRCh37]
ChrX:37004278..154899779 [NCBI36]
ChrX:Xp21.1-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:20297-156026127)x1 copy number loss See cases [RCV000135321] ChrX:20297..156026127 [GRCh38]
ChrX:70297..155255792 [GRCh37]
ChrX:10297..154908986 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xq21.31-28(chrX:92222680-156016920)x1 copy number loss See cases [RCV000135307] ChrX:92222680..156016920 [GRCh38]
ChrX:91477679..155246585 [GRCh37]
ChrX:91364335..154899779 [NCBI36]
ChrX:Xq21.31-28
pathogenic
GRCh38/hg38 Xq13.2-28(chrX:74510116-156022206)x1 copy number loss See cases [RCV000134958] ChrX:74510116..156022206 [GRCh38]
ChrX:73729951..155251871 [GRCh37]
ChrX:73646676..154905065 [NCBI36]
ChrX:Xq13.2-28
pathogenic
GRCh38/hg38 Xq23-28(chrX:114533139-156022206)x1 copy number loss See cases [RCV000134947] ChrX:114533139..156022206 [GRCh38]
ChrX:113767592..155251871 [GRCh37]
ChrX:113673848..154905065 [NCBI36]
ChrX:Xq23-28
pathogenic
GRCh38/hg38 Xp21.1-q28(chrX:36237706-156022206)x1 copy number loss See cases [RCV000135552] ChrX:36237706..156022206 [GRCh38]
ChrX:36255823..155251871 [GRCh37]
ChrX:36165744..154905065 [NCBI36]
ChrX:Xp21.1-q28
pathogenic
GRCh38/hg38 Xq21.1-28(chrX:77369933-156013167)x1 copy number loss See cases [RCV000135454] ChrX:77369933..156013167 [GRCh38]
ChrX:76634813..155242832 [GRCh37]
ChrX:76507069..154896026 [NCBI36]
ChrX:Xq21.1-28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:40904-155998166)x1 copy number loss See cases [RCV000136478] ChrX:40904..155998166 [GRCh38]
ChrX:90904..155227831 [GRCh37]
ChrX:30904..154881025 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xq21.33-28(chrX:94462929-156001635)x3 copy number gain See cases [RCV000136552] ChrX:94462929..156001635 [GRCh38]
ChrX:93717928..155231300 [GRCh37]
ChrX:93604584..154884494 [NCBI36]
ChrX:Xq21.33-28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10701-156003229)x1 copy number loss See cases [RCV000136097] ChrX:10701..156003229 [GRCh38]
ChrX:60701..155232894 [GRCh37]
ChrX:701..154886088 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xq28(chrX:154679854-156003229)x1 copy number loss See cases [RCV000136031] ChrX:154679854..156003229 [GRCh38]
ChrX:153908131..155232894 [GRCh37]
ChrX:153561325..154886088 [NCBI36]
ChrX:Xq28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10001-156030895)x1 copy number loss See cases [RCV000136005] ChrX:10001..156030895 [GRCh38]
ChrX:60001..155260560 [GRCh37]
ChrX:1..154913754 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xq25-28(chrX:128473235-156003229)x1 copy number loss See cases [RCV000136095] ChrX:128473235..156003229 [GRCh38]
ChrX:127607213..155232894 [GRCh37]
ChrX:127434894..154886088 [NCBI36]
ChrX:Xq25-28
pathogenic
GRCh38/hg38 Xq27.1-28(chrX:140783390-155611114)x2 copy number gain See cases [RCV000135881] ChrX:140783390..155611114 [GRCh38]
ChrX:139865555..154785891 [GRCh37]
ChrX:139693221..154493969 [NCBI36]
ChrX:Xq27.1-28
pathogenic
GRCh38/hg38 Xq21.1-28(chrX:79093152-156003229)x1 copy number loss See cases [RCV000136083] ChrX:79093152..156003229 [GRCh38]
ChrX:78348649..155232894 [GRCh37]
ChrX:78235305..154886088 [NCBI36]
ChrX:Xq21.1-28
pathogenic
GRCh38/hg38 Xq27.2-28(chrX:141650284-156022206)x1 copy number loss See cases [RCV000136912] ChrX:141650284..156022206 [GRCh38]
ChrX:140738414..155251871 [GRCh37]
ChrX:140566080..154905065 [NCBI36]
ChrX:Xq27.2-28
pathogenic
GRCh38/hg38 Xq13.3-28(chrX:75086417-156022206)x1 copy number loss See cases [RCV000137113] ChrX:75086417..156022206 [GRCh38]
ChrX:74306252..155251871 [GRCh37]
ChrX:74222977..154905065 [NCBI36]
ChrX:Xq13.3-28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:2782275-155611794)x2 copy number gain See cases [RCV000136841] ChrX:2782275..155611794 [GRCh38]
ChrX:2700316..154785891 [GRCh37]
ChrX:2710316..154494649 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xq28(chrX:153322656-155522304)x2 copy number gain See cases [RCV000136716] ChrX:153322656..155522304 [GRCh38]
ChrX:152864376..154751965 [GRCh37]
ChrX:152241308..154405159 [NCBI36]
ChrX:Xq28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:2765636-155522304)x3 copy number gain See cases [RCV000136791] ChrX:2765636..155522304 [GRCh38]
ChrX:2683677..154751965 [GRCh37]
ChrX:2693677..154405159 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xq28(chrX:151750863-155522304)x1 copy number loss See cases [RCV000136718] ChrX:151750863..155522304 [GRCh38]
ChrX:150919335..154751965 [GRCh37]
ChrX:150669991..154405159 [NCBI36]
ChrX:Xq28
pathogenic
GRCh38/hg38 Xq28(chrX:153276277-156003242)x3 copy number gain See cases [RCV000137498] ChrX:153276277..156003242 [GRCh38]
ChrX:152465185..155232907 [GRCh37]
ChrX:152118379..154886101 [NCBI36]
ChrX:Xq28
pathogenic
GRCh38/hg38 Xq22.1-28(chrX:102197284-156003242)x1 copy number loss See cases [RCV000137415] ChrX:102197284..156003242 [GRCh38]
ChrX:101452257..155232907 [GRCh37]
ChrX:101338913..154886101 [NCBI36]
ChrX:Xq22.1-28
pathogenic
GRCh38/hg38 Xq11.1-28(chrX:62561604-156003242)x3 copy number gain See cases [RCV000137553] ChrX:62561604..156003242 [GRCh38]
ChrX:61781074..155232907 [GRCh37]
ChrX:61697799..154886101 [NCBI36]
ChrX:Xq11.1-28
pathogenic
GRCh38/hg38 Xq13.3-28(chrX:76604011-156022206)x1 copy number loss See cases [RCV000137138] ChrX:76604011..156022206 [GRCh38]
ChrX:75824420..155251871 [GRCh37]
ChrX:75740824..154905065 [NCBI36]
ChrX:Xq13.3-28
pathogenic
GRCh38/hg38 Xq26.3-28(chrX:137118983-156003242)x1 copy number loss See cases [RCV000137257] ChrX:137118983..156003242 [GRCh38]
ChrX:136201142..155232907 [GRCh37]
ChrX:136028808..154886101 [NCBI36]
ChrX:Xq26.3-28
pathogenic|uncertain significance
GRCh38/hg38 Xq25-28(chrX:123793526-156022206)x1 copy number loss See cases [RCV000137167] ChrX:123793526..156022206 [GRCh38]
ChrX:122927376..155251871 [GRCh37]
ChrX:122755057..154905065 [NCBI36]
ChrX:Xq25-28
pathogenic|uncertain significance
GRCh38/hg38 Xq28(chrX:154604412-154935279)x3 copy number gain See cases [RCV000137292] ChrX:154604412..154935279 [GRCh38]
ChrX:153485859..153816748 [NCBI36]
ChrX:Xq28
likely pathogenic
GRCh38/hg38 Xq21.33-28(chrX:95846285-156003242)x3 copy number gain See cases [RCV000138020] ChrX:95846285..156003242 [GRCh38]
ChrX:95101284..155232907 [GRCh37]
ChrX:94987940..154886101 [NCBI36]
ChrX:Xq21.33-28
pathogenic
GRCh38/hg38 Xq22.3-28(chrX:106127173-156003242)x1 copy number loss See cases [RCV000137887] ChrX:106127173..156003242 [GRCh38]
ChrX:105371166..155232907 [GRCh37]
ChrX:105257822..154886101 [NCBI36]
ChrX:Xq22.3-28
pathogenic
GRCh38/hg38 Xq27.3-28(chrX:143553831-156003229)x1 copy number loss See cases [RCV000138679] ChrX:143553831..156003229 [GRCh38]
ChrX:142641674..155232894 [GRCh37]
ChrX:142469340..154886088 [NCBI36]
ChrX:Xq27.3-28
pathogenic
GRCh38/hg38 Xq21.1-28(chrX:79911061-156003229)x1 copy number loss See cases [RCV000138787] ChrX:79911061..156003229 [GRCh38]
ChrX:79166568..155232894 [GRCh37]
ChrX:79053224..154886088 [NCBI36]
ChrX:Xq21.1-28
pathogenic
GRCh38/hg38 Xq22.3-28(chrX:106465610-156003242)x1 copy number loss See cases [RCV000138541] ChrX:106465610..156003242 [GRCh38]
ChrX:105708840..155232907 [GRCh37]
ChrX:105595496..154886101 [NCBI36]
ChrX:Xq22.3-28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:1085618-155699644)x1 copy number loss See cases [RCV000139278] ChrX:1085618..155699644 [GRCh38]
ChrX:1118268..154929305 [GRCh37]
ChrX:1038268..154582499 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xq21.1-28(chrX:82211310-156003229)x1 copy number loss See cases [RCV000139400] ChrX:82211310..156003229 [GRCh38]
ChrX:81466759..155232894 [GRCh37]
ChrX:81353415..154886088 [NCBI36]
ChrX:Xq21.1-28
pathogenic
GRCh38/hg38 Xq21.31-28(chrX:88339926-156003242)x1 copy number loss See cases [RCV000139351] ChrX:88339926..156003242 [GRCh38]
ChrX:87594927..155232907 [GRCh37]
ChrX:87481583..154886101 [NCBI36]
ChrX:Xq21.31-28
pathogenic|likely benign
GRCh38/hg38 Xq11.1-28(chrX:62712219-156003242)x3 copy number gain See cases [RCV000139416] ChrX:62712219..156003242 [GRCh38]
ChrX:61931689..155232907 [GRCh37]
ChrX:61848414..154886101 [NCBI36]
ChrX:Xq11.1-28
pathogenic|likely benign
GRCh38/hg38 Xp22.33-q28(chrX:251880-156004181)x3 copy number gain See cases [RCV000139888] ChrX:251880..156004181 [GRCh38]
ChrX:168547..155233846 [GRCh37]
ChrX:108547..154887040 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xq27.1-28(chrX:139530928-156003229)x1 copy number loss See cases [RCV000139724] ChrX:139530928..156003229 [GRCh38]
ChrX:138613087..155232894 [GRCh37]
ChrX:138440753..154886088 [NCBI36]
ChrX:Xq27.1-28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:2299223-155992188)x3 copy number gain See cases [RCV000141400] ChrX:2299223..155992188 [GRCh38]
ChrX:2217264..155221853 [GRCh37]
ChrX:2227264..154875047 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:20297-156016920)x3 copy number gain See cases [RCV000141401] ChrX:20297..156016920 [GRCh38]
ChrX:70297..155246585 [GRCh37]
ChrX:10297..154899779 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:251880-156004066)x4 copy number gain See cases [RCV000140786] ChrX:251880..156004066 [GRCh38]
ChrX:168547..155233731 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:251880-156004066)x1 copy number loss See cases [RCV000140787] ChrX:251880..156004066 [GRCh38]
ChrX:168547..155233731 [GRCh37]
ChrX:Xp22.33-q28
pathogenic|conflicting data from submitters
GRCh38/hg38 Xq21.1-28(chrX:82096719-156004066)x1 copy number loss See cases [RCV000141825] ChrX:82096719..156004066 [GRCh38]
ChrX:81352168..155233731 [GRCh37]
ChrX:81238824..154886925 [NCBI36]
ChrX:Xq21.1-28
pathogenic
GRCh38/hg38 Xq21.31-28(chrX:89557622-156004066)x1 copy number loss See cases [RCV000142016] ChrX:89557622..156004066 [GRCh38]
ChrX:88812621..155233731 [GRCh37]
ChrX:88699277..154886925 [NCBI36]
ChrX:Xq21.31-28
pathogenic
GRCh38/hg38 Xq24-28(chrX:119297670-156004066)x1 copy number loss See cases [RCV000141743] ChrX:119297670..156004066 [GRCh38]
ChrX:118431633..155233731 [GRCh37]
ChrX:118315661..154886925 [NCBI36]
ChrX:Xq24-28
pathogenic
GRCh38/hg38 Xq21.1-28(chrX:78187188-156004066)x1 copy number loss See cases [RCV000142337] ChrX:78187188..156004066 [GRCh38]
ChrX:77442685..155233731 [GRCh37]
ChrX:77329341..154886925 [NCBI36]
ChrX:Xq21.1-28
pathogenic
GRCh38/hg38 Xq24-28(chrX:118856574-156004066)x1 copy number loss See cases [RCV000142137] ChrX:118856574..156004066 [GRCh38]
ChrX:117990537..155233731 [GRCh37]
ChrX:117874565..154886925 [NCBI36]
ChrX:Xq24-28
pathogenic
GRCh38/hg38 Xq21.2-28(chrX:86626431-156004066)x1 copy number loss See cases [RCV000142037] ChrX:86626431..156004066 [GRCh38]
ChrX:85881434..155233731 [GRCh37]
ChrX:85768090..154886925 [NCBI36]
ChrX:Xq21.2-28
pathogenic
GRCh38/hg38 Xq22.3-28(chrX:106722296-156004066)x1 copy number loss See cases [RCV000142190] ChrX:106722296..156004066 [GRCh38]
ChrX:105965526..155233731 [GRCh37]
ChrX:105852182..154886925 [NCBI36]
ChrX:Xq22.3-28
pathogenic
GRCh38/hg38 Xq28(chrX:148951460-155434653)x2 copy number gain See cases [RCV000143002] ChrX:148951460..155434653 [GRCh38]
ChrX:148956425..154664314 [GRCh37]
ChrX:147840690..154317508 [NCBI36]
ChrX:Xq28
pathogenic
GRCh38/hg38 Xq28(chrX:154772625-154971051)x3 copy number gain See cases [RCV000143085] ChrX:154772625..154971051 [GRCh38]
ChrX:153654094..153852520 [NCBI36]
ChrX:Xq28
uncertain significance
GRCh38/hg38 Xq23-28(chrX:111050385-156022206)x1 copy number loss See cases [RCV000142577] ChrX:111050385..156022206 [GRCh38]
ChrX:110293613..155251871 [GRCh37]
ChrX:110180269..154905065 [NCBI36]
ChrX:Xq23-28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10701-156003229)x3 copy number gain See cases [RCV000142625] ChrX:10701..156003229 [GRCh38]
ChrX:60701..155232894 [GRCh37]
ChrX:701..154886088 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xq13.2-28(chrX:74684615-156004066)x1 copy number loss See cases [RCV000143424] ChrX:74684615..156004066 [GRCh38]
ChrX:73904450..155233731 [GRCh37]
ChrX:73821175..154886925 [NCBI36]
ChrX:Xq13.2-28
pathogenic
GRCh38/hg38 Xp11.22-q28(chrX:53144751-156003242)x1 copy number loss See cases [RCV000143349] ChrX:53144751..156003242 [GRCh38]
ChrX:53321095..155232907 [GRCh37]
ChrX:53190658..154886101 [NCBI36]
ChrX:Xp11.22-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:251879-156004066)x1 copy number loss See cases [RCV000143441] ChrX:251879..156004066 [GRCh38]
ChrX:168546..155233731 [GRCh37]
ChrX:108546..154886925 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:251879-156004066)x3 copy number gain See cases [RCV000143433] ChrX:251879..156004066 [GRCh38]
ChrX:168546..155233731 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:251880-156004066)x3 copy number gain See cases [RCV000143219] ChrX:251880..156004066 [GRCh38]
ChrX:168547..155233731 [GRCh37]
ChrX:108547..154886925 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xq13.3-28(chrX:76557425-156004066)x1 copy number loss See cases [RCV000143132] ChrX:76557425..156004066 [GRCh38]
ChrX:75777833..155233731 [GRCh37]
ChrX:75694237..154886925 [NCBI36]
ChrX:Xq13.3-28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10679-156022206)x3 copy number gain See cases [RCV000148141] ChrX:10679..156022206 [GRCh38]
ChrX:60679..155251871 [GRCh37]
ChrX:679..154905065 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10679-156022206)x1 copy number loss See cases [RCV000148135] ChrX:10679..156022206 [GRCh38]
ChrX:60679..155251871 [GRCh37]
ChrX:679..154905065 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:71267-155246643)x3 copy number gain See cases [RCV000240122] ChrX:71267..155246643 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xq11.1-28(chrX:62063537-155246643)x3 copy number gain See cases [RCV000240143] ChrX:62063537..155246643 [GRCh37]
ChrX:Xq11.1-28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:176426-155250222)x3 copy number gain See cases [RCV000239843] ChrX:176426..155250222 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:71267-155255839)x1 copy number loss See cases [RCV000239832] ChrX:71267..155255839 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.2-q28(chrX:13147668-155250222)x3 copy number gain See cases [RCV000239798] ChrX:13147668..155250222 [GRCh37]
ChrX:Xp22.2-q28
pathogenic
GRCh37/hg19 Xq28(chrX:153627408-154089925)x2 copy number gain See cases [RCV000240046] ChrX:153627408..154089925 [GRCh37]
ChrX:Xq28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:150002-155234036)x2 copy number gain See cases [RCV000240106] ChrX:150002..155234036 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:60701-155246271)x3 copy number gain See cases [RCV000239989] ChrX:60701..155246271 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:71267-155224766)x1 copy number loss See cases [RCV000239902] ChrX:71267..155224766 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:71267-155234036)x2 copy number gain See cases [RCV000239874] ChrX:71267..155234036 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:553069-155233731)x1 copy number loss See cases [RCV000446026] ChrX:553069..155233731 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xq28(chrX:153928244-154065414)x3 copy number gain See cases [RCV000240020] ChrX:153928244..154065414 [GRCh37]
ChrX:Xq28
uncertain significance
GRCh37/hg19 Xp22.33-q28(chrX:70297-155255839)x3 copy number gain See cases [RCV000239934] ChrX:70297..155255839 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:176426-155236656)x3 copy number gain See cases [RCV000240552] ChrX:176426..155236656 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:225816-155234036)x2 copy number gain See cases [RCV000240464] ChrX:225816..155234036 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:150002-155234036)x3 copy number gain See cases [RCV000240314] ChrX:150002..155234036 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xq27.3-28(chrX:142174780-155250222)x2 copy number gain See cases [RCV000240530] ChrX:142174780..155250222 [GRCh37]
ChrX:Xq27.3-28
pathogenic
GRCh37/hg19 Xq11.1-28(chrX:62063537-155250222)x3 copy number gain See cases [RCV000240148] ChrX:62063537..155250222 [GRCh37]
ChrX:Xq11.1-28
pathogenic
GRCh37/hg19 Xq25-28(chrX:121022022-155211482)x1 copy number loss See cases [RCV000240337] ChrX:121022022..155211482 [GRCh37]
ChrX:Xq25-28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:2707626-155250222)x2 copy number gain See cases [RCV000240541] ChrX:2707626..155250222 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168546-154930047)x3 copy number gain See cases [RCV000449437] ChrX:168546..154930047 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x3 copy number gain See cases [RCV000449330] ChrX:168546..155233731 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:70297-155255792) copy number loss See cases [RCV000449461] ChrX:70297..155255792 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xq21.33-28(chrX:94043221-155246585)x1 copy number loss See cases [RCV000449365] ChrX:94043221..155246585 [GRCh37]
ChrX:Xq21.33-28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:60701-155246225)x3 copy number gain See cases [RCV000446270] ChrX:60701..155246225 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xq13.1-28(chrX:68701338-155233731)x3 copy number gain See cases [RCV000446471] ChrX:68701338..155233731 [GRCh37]
ChrX:Xq13.1-28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:2703632-155233731)x1 copy number loss See cases [RCV000446712] ChrX:2703632..155233731 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:71267-155255792)x1 copy number loss See cases [RCV000446197] ChrX:71267..155255792 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:318707-155224707)x1 copy number loss See cases [RCV000446667] ChrX:318707..155224707 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xq28(chrX:152228560-154930047)x2 copy number gain See cases [RCV000447331] ChrX:152228560..154930047 [GRCh37]
ChrX:Xq28
pathogenic
GRCh37/hg19 Xq13.3-28(chrX:74787886-155233731)x1 copy number loss See cases [RCV000447490] ChrX:74787886..155233731 [GRCh37]
ChrX:Xq13.3-28
pathogenic
GRCh37/hg19 Xp11.1-q28(chrX:58140271-155046703)x3 copy number gain See cases [RCV000446151] ChrX:58140271..155046703 [GRCh37]
ChrX:Xp11.1-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x4 copy number gain See cases [RCV000446932] ChrX:168546..155233731 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168546-155196888)x3 copy number gain See cases [RCV000446310] ChrX:168546..155196888 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xq28(chrX:150253008-155233731)x1 copy number loss See cases [RCV000446761] ChrX:150253008..155233731 [GRCh37]
ChrX:Xq28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168546-155081533)x3 copy number gain See cases [RCV000447253] ChrX:168546..155081533 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168566-155233731)x1 copy number loss See cases [RCV000445720] ChrX:168566..155233731 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xq22.3-28(chrX:105694656-155224707)x1 copy number loss See cases [RCV000445891] ChrX:105694656..155224707 [GRCh37]
ChrX:Xq22.3-28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x1 copy number loss See cases [RCV000448393] ChrX:168546..155233731 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xq25-28(chrX:126773628-155233731)x1 copy number loss See cases [RCV000448724] ChrX:126773628..155233731 [GRCh37]
ChrX:Xq25-28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:70297-155255792)x4 copy number gain See cases [RCV000448034] ChrX:70297..155255792 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:70297-155246585)x1 copy number loss See cases [RCV000448652] ChrX:70297..155246585 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xq26.3-28(chrX:134114063-155233731)x1 copy number loss See cases [RCV000448865] ChrX:134114063..155233731 [GRCh37]
ChrX:Xq26.3-28
pathogenic
GRCh37/hg19 Xq28(chrX:151201777-154741703)x2 copy number gain See cases [RCV000510478] ChrX:151201777..154741703 [GRCh37]
ChrX:Xq28
pathogenic
GRCh37/hg19 Xp11.21-q28(chrX:55000501-155230750)x3 copy number gain See cases [RCV000511787] ChrX:55000501..155230750 [GRCh37]
ChrX:Xp11.21-q28
pathogenic
GRCh37/hg19 Xp21.2-q28(chrX:31088082-155233731)x1 copy number loss See cases [RCV000511413] ChrX:31088082..155233731 [GRCh37]
ChrX:Xp21.2-q28
pathogenic
GRCh37/hg19 Xq23-28(chrX:112474054-155233731)x1 copy number loss See cases [RCV000511572] ChrX:112474054..155233731 [GRCh37]
ChrX:Xq23-28
pathogenic
GRCh37/hg19 Xq24-28(chrX:116621104-155233731)x1 copy number loss See cases [RCV000511936] ChrX:116621104..155233731 [GRCh37]
ChrX:Xq24-28
pathogenic
GRCh37/hg19 Xq21.1-28(chrX:79862302-155233731)x1 copy number loss See cases [RCV000511482] ChrX:79862302..155233731 [GRCh37]
ChrX:Xq21.1-28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168547-155233731) copy number gain See cases [RCV000512020] ChrX:168547..155233731 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xq21.31-28(chrX:86900388-155233731)x1 copy number loss See cases [RCV000511490] ChrX:86900388..155233731 [GRCh37]
ChrX:Xq21.31-28
pathogenic
GRCh37/hg19 Xp11.21-q28(chrX:57511767-155233731)x3 copy number gain See cases [RCV000510826] ChrX:57511767..155233731 [GRCh37]
ChrX:Xp11.21-q28
pathogenic
GRCh37/hg19 Xp11.21-q28(chrX:56457791-155233731)x3 copy number gain See cases [RCV000511307] ChrX:56457791..155233731 [GRCh37]
ChrX:Xp11.21-q28
pathogenic
GRCh37/hg19 Xq27.3-28(chrX:146232592-155233731)x1 copy number loss See cases [RCV000511228] ChrX:146232592..155233731 [GRCh37]
ChrX:Xq27.3-28
pathogenic
GRCh37/hg19 Xq21.1-28(chrX:78230501-155233731)x1 copy number loss See cases [RCV000510820] ChrX:78230501..155233731 [GRCh37]
ChrX:Xq21.1-28
pathogenic
GRCh37/hg19 Xq28(chrX:151963528-155233731)x1 copy number loss See cases [RCV000510866] ChrX:151963528..155233731 [GRCh37]
ChrX:Xq28
pathogenic
GRCh37/hg19 Xq28(chrX:151311551-155233731)x1 copy number loss See cases [RCV000510920] ChrX:151311551..155233731 [GRCh37]
ChrX:Xq28
pathogenic
GRCh37/hg19 Xq26.3-28(chrX:133944147-155233731)x3 copy number gain See cases [RCV000511034] ChrX:133944147..155233731 [GRCh37]
ChrX:Xq26.3-28
pathogenic
GRCh37/hg19 Xq22.1-28(chrX:98495811-155233731)x1 copy number loss See cases [RCV000512372] ChrX:98495811..155233731 [GRCh37]
ChrX:Xq22.1-28
pathogenic
GRCh37/hg19 Xp11.21-q28(chrX:57415659-155233731)x3 copy number gain See cases [RCV000512173] ChrX:57415659..155233731 [GRCh37]
ChrX:Xp11.21-q28
pathogenic
GRCh37/hg19 Xq25-28(chrX:125733292-155233846)x1 copy number loss not provided [RCV000684386] ChrX:125733292..155233846 [GRCh37]
ChrX:Xq25-28
pathogenic
GRCh37/hg19 Xq27.1-28(chrX:138331745-155233731)x1 copy number loss not provided [RCV000684397] ChrX:138331745..155233731 [GRCh37]
ChrX:Xq27.1-28
pathogenic
GRCh37/hg19 Xq27.1-28(chrX:139504488-155233731)x1 copy number loss not provided [RCV000684401] ChrX:139504488..155233731 [GRCh37]
ChrX:Xq27.1-28
pathogenic
GRCh37/hg19 Xq27.2-28(chrX:140388077-155233731)x3 copy number gain not provided [RCV000684402] ChrX:140388077..155233731 [GRCh37]
ChrX:Xq27.2-28
pathogenic
GRCh37/hg19 Xq22.3-28(chrX:107823442-155233731)x1 copy number loss not provided [RCV000684373] ChrX:107823442..155233731 [GRCh37]
ChrX:Xq22.3-28
pathogenic
GRCh37/hg19 Xq21.31-28(chrX:91140025-155233731)x1 copy number loss not provided [RCV000684357] ChrX:91140025..155233731 [GRCh37]
ChrX:Xq21.31-28
pathogenic
GRCh37/hg19 Xq22.1-28(chrX:99324651-155233731)x1 copy number loss not provided [RCV000684363] ChrX:99324651..155233731 [GRCh37]
ChrX:Xq22.1-28
pathogenic
GRCh37/hg19 Xq28(chrX:153749360-155233731)x3 copy number gain not provided [RCV000684416] ChrX:153749360..155233731 [GRCh37]
ChrX:Xq28
pathogenic
GRCh37/hg19 Xq28(chrX:153904473-155090513)x0 copy number loss not provided [RCV000753943] ChrX:153904473..155090513 [GRCh37]
ChrX:Xq28
benign
GRCh37/hg19 Xq27.1-28(chrX:138750575-155246749)x1 copy number loss not provided [RCV000753810] ChrX:138750575..155246749 [GRCh37]
ChrX:Xq27.1-28
pathogenic
GRCh37/hg19 Xq27.1-28(chrX:139504958-155254881)x1 copy number loss not provided [RCV000753815] ChrX:139504958..155254881 [GRCh37]
ChrX:Xq27.1-28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:60814-155254881)x2 copy number gain not provided [RCV000753277] ChrX:60814..155254881 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xq13.2-28(chrX:73472626-155254881)x1 copy number loss not provided [RCV000753606] ChrX:73472626..155254881 [GRCh37]
ChrX:Xq13.2-28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:60262-155245765)x1 copy number loss not provided [RCV000753271] ChrX:60262..155245765 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:60262-155245765)x3 copy number gain not provided [RCV000753272] ChrX:60262..155245765 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:181779-155171702)x1 copy number loss not provided [RCV000753278] ChrX:181779..155171702 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
Single allele duplication Autistic disorder of childhood onset [RCV000754365] ChrX:1..156040895 [GRCh38]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:60814-155236712)x2 copy number gain not provided [RCV000753276] ChrX:60814..155236712 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xq11.1-28(chrX:61694576-155254881)x1 copy number loss not provided [RCV000753556] ChrX:61694576..155254881 [GRCh37]
ChrX:Xq11.1-28
pathogenic
GRCh37/hg19 Xq25-28(chrX:122757437-155208244)x1 copy number loss Premature ovarian insufficiency [RCV000852349] ChrX:122757437..155208244 [GRCh37]
ChrX:Xq25-28
likely pathogenic
NM_002436.4(MPP1):c.153G>A (p.Gly51=) single nucleotide variant not provided [RCV000880711] ChrX:154792235 [GRCh38]
ChrX:154020510 [GRCh37]
ChrX:Xq28
likely benign
NM_002436.4(MPP1):c.102+10C>T single nucleotide variant not provided [RCV000925968] ChrX:154805262 [GRCh38]
ChrX:154033537 [GRCh37]
ChrX:Xq28
benign
GRCh37/hg19 Xp11.1-q28(chrX:58455352-155233731)x1 copy number loss not provided [RCV000846274] ChrX:58455352..155233731 [GRCh37]
ChrX:Xp11.1-q28
pathogenic
NM_002436.4(MPP1):c.181G>T (p.Val61Phe) single nucleotide variant not provided [RCV000901882] ChrX:154792207 [GRCh38]
ChrX:154020482 [GRCh37]
ChrX:Xq28
benign
GRCh37/hg19 Xq26.3-28(chrX:134975270-155233945) copy number gain not provided [RCV000767679] ChrX:134975270..155233945 [GRCh37]
ChrX:Xq26.3-28
pathogenic
GRCh37/hg19 Xq28(chrX:153761240-155227607) copy number loss not provided [RCV000767811] ChrX:153761240..155227607 [GRCh37]
ChrX:Xq28
likely pathogenic
GRCh37/hg19 Xq22.3-28(chrX:104098124-155233731)x1 copy number loss not provided [RCV000846958] ChrX:104098124..155233731 [GRCh37]
ChrX:Xq22.3-28
pathogenic
GRCh37/hg19 Xq21.1-28(chrX:78444738-155233731)x1 copy number loss not provided [RCV001007318] ChrX:78444738..155233731 [GRCh37]
ChrX:Xq21.1-28
pathogenic
NC_000023.10:g.(?_152954020)_(154096327_?)del deletion Adrenoleukodystrophy [RCV000815921] ChrX:152954020..154096327 [GRCh37]
ChrX:Xq28
pathogenic
GRCh37/hg19 Xq28(chrX:153941568-154290231)x2 copy number gain not provided [RCV000846317] ChrX:153941568..154290231 [GRCh37]
ChrX:Xq28
uncertain significance
GRCh37/hg19 Xq25-28(chrX:122924044-155233731)x1 copy number loss not provided [RCV000849097] ChrX:122924044..155233731 [GRCh37]
ChrX:Xq25-28
pathogenic
GRCh37/hg19 Xq21.1-28(chrX:84387417-155233731)x1 copy number loss not provided [RCV001007322] ChrX:84387417..155233731 [GRCh37]
ChrX:Xq21.1-28
pathogenic
GRCh37/hg19 Xq21.32-28(chrX:92814516-155233731)x1 copy number loss not provided [RCV000845672] ChrX:92814516..155233731 [GRCh37]
ChrX:Xq21.32-28
pathogenic
GRCh37/hg19 Xp11.21-q28(chrX:54941868-155233731)x1 copy number loss not provided [RCV000848218] ChrX:54941868..155233731 [GRCh37]
ChrX:Xp11.21-q28
uncertain significance
GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x4 copy number gain not provided [RCV000846039] ChrX:168546..155233731 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xq24-28(chrX:118150047-155233731)x1 copy number loss not provided [RCV000847838] ChrX:118150047..155233731 [GRCh37]
ChrX:Xq24-28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x1 copy number loss not provided [RCV000848828] ChrX:168546..155233731 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
NM_002436.4(MPP1):c.246+10C>T single nucleotide variant not provided [RCV000896982] ChrX:154792132 [GRCh38]
ChrX:154020407 [GRCh37]
ChrX:Xq28
likely benign
NM_002436.4(MPP1):c.103-4G>A single nucleotide variant not provided [RCV000887376] ChrX:154792289 [GRCh38]
ChrX:154020564 [GRCh37]
ChrX:Xq28
benign
NM_002436.4(MPP1):c.866-8C>T single nucleotide variant not provided [RCV000911528] ChrX:154783515 [GRCh38]
ChrX:154011790 [GRCh37]
ChrX:Xq28
likely benign
GRCh37/hg19 Xq25-28(chrX:122132166-155097214) copy number loss Intellectual disability [RCV001249592] ChrX:122132166..155097214 [GRCh37]
ChrX:Xq25-28
likely pathogenic
GRCh37/hg19 Xq21.33-28(chrX:94264404-155233731)x1 copy number loss not provided [RCV001259012] ChrX:94264404..155233731 [GRCh37]
ChrX:Xq21.33-28
pathogenic
GRCh37/hg19 Xp11.21-q28(chrX:55507789-155198481)x3 copy number gain See cases [RCV001263024] ChrX:55507789..155198481 [GRCh37]
ChrX:Xp11.21-q28
pathogenic
GRCh37/hg19 Xp11.21-q28(chrX:56469080-155233731)x3 copy number gain not provided [RCV001281359] ChrX:56469080..155233731 [GRCh37]
ChrX:Xp11.21-q28
pathogenic

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:7219 AgrOrtholog
COSMIC MPP1 COSMIC
Ensembl Genes ENSG00000130830 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000358544 UniProtKB/TrEMBL
  ENSP00000358547 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000377163 UniProtKB/TrEMBL
  ENSP00000377165 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000389321 UniProtKB/TrEMBL
  ENSP00000391701 UniProtKB/TrEMBL
  ENSP00000400155 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000400700 UniProtKB/TrEMBL
  ENSP00000410888 UniProtKB/TrEMBL
Ensembl Transcript ENST00000369531 UniProtKB/TrEMBL
  ENST00000369534 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000393529 UniProtKB/TrEMBL
  ENST00000393531 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000413259 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000417435 UniProtKB/TrEMBL
  ENST00000428488 UniProtKB/TrEMBL
  ENST00000439370 UniProtKB/TrEMBL
  ENST00000453245 UniProtKB/TrEMBL
Gene3D-CATH 2.30.42.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000130830 GTEx
HGNC ID HGNC:7219 ENTREZGENE
Human Proteome Map MPP1 Human Proteome Map
InterPro GK/Ca_channel_bsu UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Guanylate_kin-like_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Guanylate_kinase_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MPP1_SH3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  P-loop_NTPase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PDZ UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PDZ_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SH3-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SH3_domain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:4354 UniProtKB/Swiss-Prot
NCBI Gene 4354 ENTREZGENE
OMIM 305360 OMIM
Pfam Guanylate_kin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PDZ UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SH3_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA30924 PharmGKB
PRINTS SH3DOMAIN UniProtKB/TrEMBL
PROSITE GUANYLATE_KINASE_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GUANYLATE_KINASE_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PDZ UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SH3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART GuKc UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PDZ UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SH3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF50044 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF50156 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF52540 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A6NFY0_HUMAN UniProtKB/TrEMBL
  A8MTH1_HUMAN UniProtKB/TrEMBL
  B4E325 ENTREZGENE, UniProtKB/TrEMBL
  C9J9J4_HUMAN UniProtKB/TrEMBL
  C9JB34_HUMAN UniProtKB/TrEMBL
  EM55_HUMAN UniProtKB/Swiss-Prot
  F8WC84_HUMAN UniProtKB/TrEMBL
  F8WDV6_HUMAN UniProtKB/TrEMBL
  Q00013 ENTREZGENE
UniProt Secondary B4DZV5 UniProtKB/Swiss-Prot
  G3XAI1 UniProtKB/Swiss-Prot
  Q2TSB6 UniProtKB/Swiss-Prot
  Q5J7V5 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-04-12 MPP1  membrane palmitoylated protein 1    membrane protein, palmitoylated 1  Symbol and/or name change 5135510 APPROVED
2015-11-17 MPP1  membrane protein, palmitoylated 1    membrane protein, palmitoylated 1, 55kDa  Symbol and/or name change 5135510 APPROVED