ARHGAP28 (Rho GTPase activating protein 28) - Rat Genome Database

Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Advanced Search (OLGA)
Gene: ARHGAP28 (Rho GTPase activating protein 28) Homo sapiens
Analyze
Symbol: ARHGAP28
Name: Rho GTPase activating protein 28
RGD ID: 1347841
HGNC Page HGNC:25509
Description: Predicted to enable GTPase activator activity. Predicted to be involved in negative regulation of stress fiber assembly; regulation of actin filament polymerization; and regulation of small GTPase mediated signal transduction. Located in cell junction and nucleoplasm. Implicated in allergic disease. Biomarker of meningioma.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: DKFZp686A2038; FLJ10312; FLJ27160; rho GTPase-activating protein 28; rho-type GTPase-activating protein 28
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38186,729,716 - 6,915,716 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl186,729,716 - 6,915,716 (+)EnsemblGRCh38hg38GRCh38
GRCh37186,729,715 - 6,915,715 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36186,824,484 - 6,905,715 (+)NCBINCBI36Build 36hg18NCBI36
Celera186,719,871 - 6,801,101 (+)NCBICelera
Cytogenetic Map18p11.31NCBI
HuRef186,797,814 - 6,879,176 (+)NCBIHuRef
CHM1_1186,834,188 - 6,915,740 (+)NCBICHM1_1
T2T-CHM13v2.0186,890,201 - 7,076,260 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component
cell junction  (IDA)
cytoplasm  (IBA)
cytosol  (TAS)
membrane  (IEA)
nucleoplasm  (IDA)

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. Microarray gene expression profiling in meningiomas: differential expression according to grade or histopathological subtype. Fèvre-Montange M, etal., Int J Oncol. 2009 Dec;35(6):1395-407. doi: 10.3892/ijo_00000457.
2. Class II Human Leukocyte Antigen Variants Associate With Risk of Pegaspargase Hypersensitivity. Liu Y, etal., Clin Pharmacol Ther. 2021 Sep;110(3):794-802. doi: 10.1002/cpt.2241. Epub 2021 Apr 21.
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
4. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Strausberg RL, etal., Proc Natl Acad Sci U S A. 2002 Dec 24;99(26):16899-903. Epub 2002 Dec 11.
Additional References at PubMed
PMID:10718198   PMID:14702039   PMID:15489334   PMID:16177791   PMID:18029348   PMID:21873635   PMID:23251661   PMID:24832863   PMID:25211221   PMID:25277244   PMID:26514267   PMID:29507755  
PMID:30021884   PMID:35256949   PMID:37689310  


Genomics

Comparative Map Data
ARHGAP28
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38186,729,716 - 6,915,716 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl186,729,716 - 6,915,716 (+)EnsemblGRCh38hg38GRCh38
GRCh37186,729,715 - 6,915,715 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36186,824,484 - 6,905,715 (+)NCBINCBI36Build 36hg18NCBI36
Celera186,719,871 - 6,801,101 (+)NCBICelera
Cytogenetic Map18p11.31NCBI
HuRef186,797,814 - 6,879,176 (+)NCBIHuRef
CHM1_1186,834,188 - 6,915,740 (+)NCBICHM1_1
T2T-CHM13v2.0186,890,201 - 7,076,260 (+)NCBIT2T-CHM13v2.0
Arhgap28
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391768,149,701 - 68,311,185 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1768,149,708 - 68,311,115 (-)EnsemblGRCm39 Ensembl
GRCm381767,842,706 - 68,004,197 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1767,842,713 - 68,004,120 (-)EnsemblGRCm38mm10GRCm38
MGSCv371768,192,046 - 68,353,448 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361767,747,658 - 67,909,003 (-)NCBIMGSCv36mm8
Celera1772,140,076 - 72,305,462 (-)NCBICelera
Cytogenetic Map17E1.1- E1.2NCBI
cM Map1738.9NCBI
Arhgap28
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr89115,277,849 - 115,444,789 (-)NCBIGRCr8
mRatBN7.29107,832,584 - 107,998,030 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl9107,833,330 - 107,998,000 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx9116,224,487 - 116,389,795 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.09121,346,716 - 121,512,016 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.09119,690,382 - 119,855,688 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.09116,057,229 - 116,222,440 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl9116,058,610 - 116,222,440 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.09115,545,230 - 115,711,949 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.49106,996,258 - 107,162,388 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera9104,992,570 - 105,156,417 (-)NCBICelera
Cytogenetic Map9q38NCBI
Arhgap28
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554024,418,201 - 4,490,146 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554024,417,978 - 4,531,683 (-)NCBIChiLan1.0ChiLan1.0
ARHGAP28
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21731,531,407 - 31,761,519 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11817,224,000 - 17,454,112 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0187,366,986 - 7,548,782 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1189,686,547 - 9,870,372 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl189,690,107 - 9,775,270 (-)Ensemblpanpan1.1panPan2
ARHGAP28
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1773,023,681 - 73,260,093 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl773,055,118 - 73,257,375 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha772,418,137 - 72,667,855 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0773,075,625 - 73,312,589 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl773,107,066 - 73,310,284 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1772,779,563 - 73,016,360 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0772,807,839 - 73,044,981 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0773,102,267 - 73,339,846 (+)NCBIUU_Cfam_GSD_1.0
Arhgap28
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494469,583,693 - 69,796,899 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_004936670129,160 - 312,275 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_004936670186,141 - 315,613 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ARHGAP28
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl6100,494,652 - 100,655,708 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.16100,494,385 - 100,681,008 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2693,656,579 - 93,818,607 (-)NCBISscrofa10.2Sscrofa10.2susScr3
ARHGAP28
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11865,783,800 - 65,971,262 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1865,808,866 - 65,973,180 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366605040,693,936 - 40,889,236 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Arhgap28
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462477016,179,216 - 16,344,247 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462477016,179,225 - 16,343,299 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in ARHGAP28
56 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 18p11.32-11.21(chr18:148963-13715860)x1 copy number loss See cases [RCV000051027] Chr18:148963..13715860 [GRCh38]
Chr18:148963..13715859 [GRCh37]
Chr18:138963..13705859 [NCBI36]
Chr18:18p11.32-11.21		 pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:148963-14081888)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051153]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051153]|See cases [RCV000051153] Chr18:148963..14081888 [GRCh38]
Chr18:148963..14081887 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:148963-14081888)x1 copy number loss See cases [RCV000051154] Chr18:148963..14081888 [GRCh38]
Chr18:148963..14081887 [GRCh37]
Chr18:138963..14071887 [NCBI36]
Chr18:18p11.32-11.21		 pathogenic
GRCh38/hg38 18p11.32-q23(chr18:148963-80252149)x3 copy number gain See cases [RCV000051048] Chr18:148963..80252149 [GRCh38]
Chr18:148963..78010032 [GRCh37]
Chr18:138963..76111023 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:1919684-15325188)x3 copy number gain See cases [RCV000052535] Chr18:1919684..15325188 [GRCh38]
Chr18:1919685..15325187 [GRCh37]
Chr18:1909685..15315187 [NCBI36]
Chr18:18p11.32-11.21		 pathogenic
GRCh38/hg38 18p11.31-11.21(chr18:3389362-14082029)x3 copy number gain See cases [RCV000052536] Chr18:3389362..14082029 [GRCh38]
Chr18:3389360..14082028 [GRCh37]
Chr18:3379360..14072028 [NCBI36]
Chr18:18p11.31-11.21		 pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:10001-15380684)x3 copy number gain See cases [RCV000052499] Chr18:10001..15380684 [GRCh38]
Chr18:10001..15380683 [GRCh37]
Chr18:1..15370683 [NCBI36]
Chr18:18p11.32-11.21		 pathogenic
GRCh38/hg38 18p11.32-q23(chr18:53345-80209986)x3 copy number gain See cases [RCV000052501] Chr18:53345..80209986 [GRCh38]
Chr18:53345..77967869 [GRCh37]
Chr18:43345..76068860 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh38/hg38 18p11.32-q11.1(chr18:53345-20948503)x3 copy number gain See cases [RCV000052504] Chr18:53345..20948503 [GRCh38]
Chr18:53345..18528464 [GRCh37]
Chr18:43345..16782462 [NCBI36]
Chr18:18p11.32-q11.1		 pathogenic
GRCh38/hg38 18p11.32-q23(chr18:148763-80252290)x3 copy number gain See cases [RCV000052507] Chr18:148763..80252290 [GRCh38]
Chr18:148763..78010173 [GRCh37]
Chr18:138763..76111164 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh38/hg38 18p11.32-q11.1(chr18:148963-21040153)x3 copy number gain See cases [RCV000052513] Chr18:148963..21040153 [GRCh38]
Chr18:148963..18620114 [GRCh37]
Chr18:138963..16874112 [NCBI36]
Chr18:18p11.32-q11.1		 pathogenic
GRCh38/hg38 18p11.32-q23(chr18:148963-80244381)x3 copy number gain See cases [RCV000052514] Chr18:148963..80244381 [GRCh38]
Chr18:148963..78002264 [GRCh37]
Chr18:138963..76103255 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:131700-14226905)x1 copy number loss See cases [RCV000053461] Chr18:131700..14226905 [GRCh38]
Chr18:131700..14226904 [GRCh37]
Chr18:121700..14216904 [NCBI36]
Chr18:18p11.32-11.21		 pathogenic
GRCh38/hg38 18p11.31-11.23(chr18:6881457-8124873)x3 copy number gain See cases [RCV000053598] Chr18:6881457..8124873 [GRCh38]
Chr18:6881456..8124871 [GRCh37]
Chr18:6871456..8114871 [NCBI36]
Chr18:18p11.31-11.23		 benign
GRCh38/hg38 18p11.32-11.31(chr18:53344-7029134)x1 copy number loss See cases [RCV000053455] Chr18:53344..7029134 [GRCh38]
Chr18:53344..7029133 [GRCh37]
Chr18:43344..7019133 [NCBI36]
Chr18:18p11.32-11.31		 pathogenic
GRCh38/hg38 18p11.32-11.22(chr18:112259-9135777)x1 copy number loss See cases [RCV000053456] Chr18:112259..9135777 [GRCh38]
Chr18:112259..9135775 [GRCh37]
Chr18:102259..9125775 [NCBI36]
Chr18:18p11.32-11.22		 pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:112259-14122522)x1 copy number loss See cases [RCV000053457] Chr18:112259..14122522 [GRCh38]
Chr18:112259..14122521 [GRCh37]
Chr18:102259..14112521 [NCBI36]
Chr18:18p11.32-11.21		 pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:131700-15121055)x1 copy number loss See cases [RCV000053458] Chr18:131700..15121055 [GRCh38]
Chr18:131700..15121054 [GRCh37]
Chr18:121700..15111054 [NCBI36]
Chr18:18p11.32-11.21		 pathogenic
GRCh38/hg38 18p11.32-11.22(chr18:131700-10536767)x1 copy number loss See cases [RCV000053781] Chr18:131700..10536767 [GRCh38]
Chr18:131700..10536764 [GRCh37]
Chr18:121700..10526764 [NCBI36]
Chr18:18p11.32-11.22		 pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:148963-13530126)x1 copy number loss See cases [RCV000053784] Chr18:148963..13530126 [GRCh38]
Chr18:148963..13530125 [GRCh37]
Chr18:138963..13520125 [NCBI36]
Chr18:18p11.32-11.21		 pathogenic
GRCh38/hg38 18p11.32-11.22(chr18:148963-8572827)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053786]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053786]|See cases [RCV000053786] Chr18:148963..8572827 [GRCh38]
Chr18:148963..8572825 [GRCh37]
Chr18:138963..8562825 [NCBI36]
Chr18:18p11.32-11.22		 pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:148963-13068104)x1 copy number loss See cases [RCV000053787] Chr18:148963..13068104 [GRCh38]
Chr18:148963..13068103 [GRCh37]
Chr18:138963..13058103 [NCBI36]
Chr18:18p11.32-11.21		 pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:148963-14081888)x3 copy number gain See cases [RCV000051153] Chr18:148963..14081888 [GRCh38]
Chr18:148963..14081887 [GRCh37]
Chr18:138963..14071887 [NCBI36]
Chr18:18p11.32-11.21		 pathogenic
GRCh38/hg38 18p11.32-q23(chr18:149089-80234391)x3 copy number gain See cases [RCV000134110] Chr18:149089..80234391 [GRCh38]
Chr18:149089..77992274 [GRCh37]
Chr18:139089..76093265 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:148963-14081888)x4 copy number gain See cases [RCV000135515] Chr18:148963..14081888 [GRCh38]
Chr18:148963..14081887 [GRCh37]
Chr18:138963..14071887 [NCBI36]
Chr18:18p11.32-11.21		 pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:2425507-11904118)x3 copy number gain See cases [RCV000136590] Chr18:2425507..11904118 [GRCh38]
Chr18:2425506..11904117 [GRCh37]
Chr18:2415506..11894117 [NCBI36]
Chr18:18p11.32-11.21		 pathogenic
GRCh38/hg38 18p11.32-11.22(chr18:180229-10762632)x1 copy number loss See cases [RCV000136860] Chr18:180229..10762632 [GRCh38]
Chr18:180229..10762630 [GRCh37]
Chr18:170229..10752630 [NCBI36]
Chr18:18p11.32-11.22		 pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:148963-10900517)x1 copy number loss See cases [RCV000137105] Chr18:148963..10900517 [GRCh38]
Chr18:148963..10900515 [GRCh37]
Chr18:138963..10890515 [NCBI36]
Chr18:18p11.32-11.21		 pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:118760-14089410)x4 copy number gain See cases [RCV000137456] Chr18:118760..14089410 [GRCh38]
Chr18:118760..14089409 [GRCh37]
Chr18:108760..14079409 [NCBI36]
Chr18:18p11.32-11.21		 pathogenic|conflicting data from submitters
GRCh38/hg38 18p11.32-11.21(chr18:118760-14089410)x1 copy number loss See cases [RCV000137457] Chr18:118760..14089410 [GRCh38]
Chr18:118760..14089409 [GRCh37]
Chr18:108760..14079409 [NCBI36]
Chr18:18p11.32-11.21		 pathogenic
GRCh38/hg38 18p11.31-11.23(chr18:6894970-7577151)x3 copy number gain See cases [RCV000137626] Chr18:6894970..7577151 [GRCh38]
Chr18:6894969..7577149 [GRCh37]
Chr18:6884969..7567149 [NCBI36]
Chr18:18p11.31-11.23		 uncertain significance
GRCh38/hg38 18p11.32-11.21(chr18:133157-14089410)x1 copy number loss See cases [RCV000138101] Chr18:133157..14089410 [GRCh38]
Chr18:133157..14089409 [GRCh37]
Chr18:123157..14079409 [NCBI36]
Chr18:18p11.32-11.21		 pathogenic
GRCh38/hg38 18p11.32-q23(chr18:118760-80254946)x3 copy number gain See cases [RCV000138656] Chr18:118760..80254946 [GRCh38]
Chr18:118760..78012829 [GRCh37]
Chr18:108760..76113817 [NCBI36]
Chr18:18p11.32-q23		 pathogenic|conflicting data from submitters
GRCh38/hg38 18p11.31-11.23(chr18:6299210-7244644)x3 copy number gain See cases [RCV000139425] Chr18:6299210..7244644 [GRCh38]
Chr18:6299209..7244642 [GRCh37]
Chr18:6289209..7234642 [NCBI36]
Chr18:18p11.31-11.23		 uncertain significance
GRCh38/hg38 18p11.32-q23(chr18:149089-80254936)x3 copy number gain See cases [RCV000139397] Chr18:149089..80254936 [GRCh38]
Chr18:149089..78012819 [GRCh37]
Chr18:139089..76113807 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh38/hg38 18p11.32-11.22(chr18:118760-8999132)x1 copy number loss See cases [RCV000139022] Chr18:118760..8999132 [GRCh38]
Chr18:118760..8999130 [GRCh37]
Chr18:108760..8989130 [NCBI36]
Chr18:18p11.32-11.22		 pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:136226-15175006) copy number gain See cases [RCV000140442] Chr18:136226..15175006 [GRCh38]
Chr18:136226..15175005 [GRCh37]
Chr18:126226..15165005 [NCBI36]
Chr18:18p11.32-11.21		 pathogenic
GRCh38/hg38 18p11.31-11.23(chr18:6913063-7354636)x3 copy number gain See cases [RCV000140201] Chr18:6913063..7354636 [GRCh38]
Chr18:6913062..7354634 [GRCh37]
Chr18:6903062..7344634 [NCBI36]
Chr18:18p11.31-11.23		 uncertain significance
GRCh38/hg38 18p11.32-11.21(chr18:14316-14206225)x3 copy number gain See cases [RCV000141427] Chr18:14316..14206225 [GRCh38]
Chr18:14316..14206224 [GRCh37]
Chr18:4316..14196224 [NCBI36]
Chr18:18p11.32-11.21		 pathogenic
GRCh38/hg38 18p11.32-11.31(chr18:85432-7094700)x1 copy number loss See cases [RCV000141428] Chr18:85432..7094700 [GRCh38]
Chr18:85432..7094699 [GRCh37]
Chr18:75432..7084699 [NCBI36]
Chr18:18p11.32-11.31		 pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:118760-15024003)x1 copy number loss See cases [RCV000141086] Chr18:118760..15024003 [GRCh38]
Chr18:118760..15024002 [GRCh37]
Chr18:108760..15014002 [NCBI36]
Chr18:18p11.32-11.21		 pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:48782-14978076)x1 copy number loss See cases [RCV000141627] Chr18:48782..14978076 [GRCh38]
Chr18:48782..14978075 [GRCh37]
Chr18:38782..14968075 [NCBI36]
Chr18:18p11.32-11.21		 pathogenic
GRCh38/hg38 18p11.32-q23(chr18:136227-80256240)x3 copy number gain See cases [RCV000142244] Chr18:136227..80256240 [GRCh38]
Chr18:136227..78014123 [GRCh37]
Chr18:126227..76115097 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh38/hg38 18p11.31-11.22(chr18:6913068-9146867)x3 copy number gain See cases [RCV000142491] Chr18:6913068..9146867 [GRCh38]
Chr18:6913067..9146865 [GRCh37]
Chr18:6903067..9136865 [NCBI36]
Chr18:18p11.31-11.22		 uncertain significance
GRCh38/hg38 18p11.32-11.21(chr18:958974-11954935)x1 copy number loss See cases [RCV000142225] Chr18:958974..11954935 [GRCh38]
Chr18:958975..11954934 [GRCh37]
Chr18:948975..11944934 [NCBI36]
Chr18:18p11.32-11.21		 pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:136226-15198991)x4 copy number gain See cases [RCV000143434] Chr18:136226..15198991 [GRCh38]
Chr18:136226..15198990 [GRCh37]
Chr18:126226..15188990 [NCBI36]
Chr18:18p11.32-11.21		 pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:118760-12642431)x3 copy number gain See cases [RCV000143194] Chr18:118760..12642431 [GRCh38]
Chr18:118760..12642430 [GRCh37]
Chr18:108760..12632430 [NCBI36]
Chr18:18p11.32-11.21		 uncertain significance
GRCh38/hg38 18p11.32-q23(chr18:136226-80256240)x3 copy number gain See cases [RCV000143218] Chr18:136226..80256240 [GRCh38]
Chr18:136226..78014123 [GRCh37]
Chr18:126226..76115097 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh38/hg38 18p11.32-q23(chr18:148963-80252149)x3 copy number gain See cases [RCV000148072] Chr18:148963..80252149 [GRCh38]
Chr18:148963..78010032 [GRCh37]
Chr18:138963..76111023 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:136226-14337134)x3 copy number gain See cases [RCV000143477] Chr18:136226..14337134 [GRCh38]
Chr18:136226..14337133 [GRCh37]
Chr18:126226..14327133 [NCBI36]
Chr18:18p11.32-11.21		 pathogenic
GRCh38/hg38 18p11.32-11.21(chr18:148963-14081888)x1 copy number loss See cases [RCV000148129] Chr18:148963..14081888 [GRCh38]
Chr18:148963..14081887 [GRCh37]
Chr18:138963..14071887 [NCBI36]
Chr18:18p11.32-11.21		 pathogenic
GRCh38/hg38 18p11.32-11.31(chr18:148963-6731495)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053785]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053785]|See cases [RCV000053785] Chr18:148963..6731495 [GRCh38]
Chr18:148963..6731494 [GRCh37]
Chr18:138963..6721494 [NCBI36]
Chr18:18p11.32-11.31		 pathogenic
GRCh37/hg19 18p11.32-q23(chr18:163323-78005236)x3 copy number gain See cases [RCV000240130] Chr18:163323..78005236 [GRCh37]
Chr18:18p11.32-q23		 pathogenic
GRCh37/hg19 18p11.32-11.21(chr18:136226-15157836)x4 copy number gain See cases [RCV000449034] Chr18:136226..15157836 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
GRCh37/hg19 18p11.32-11.21(chr18:163323-14103971)x1 copy number loss See cases [RCV000239938] Chr18:163323..14103971 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
GRCh37/hg19 18p11.32-11.21(chr18:163323-15102598)x4 copy number gain See cases [RCV000240029] Chr18:163323..15102598 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
GRCh37/hg19 18p11.32-11.21(chr18:14316-15328499)x1 copy number loss See cases [RCV000240281] Chr18:14316..15328499 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
GRCh37/hg19 18p11.32-11.22(chr18:416490-8638370)x3 copy number gain See cases [RCV000240439] Chr18:416490..8638370 [GRCh37]
Chr18:18p11.32-11.22		 pathogenic
GRCh37/hg19 18p11.32-11.22(chr18:14316-10784606)x1 copy number loss See cases [RCV000240555] Chr18:14316..10784606 [GRCh37]
Chr18:18p11.32-11.22		 pathogenic
GRCh37/hg19 18p11.32-11.21(chr18:13034-15375878)x1 copy number loss See cases [RCV000599143] Chr18:13034..15375878 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
GRCh37/hg19 18p11.32-11.22(chr18:136226-9789368)x3 copy number gain See cases [RCV000446104] Chr18:136226..9789368 [GRCh37]
Chr18:18p11.32-11.22		 pathogenic
GRCh37/hg19 18p11.31-11.23(chr18:6850839-8084746)x3 copy number gain See cases [RCV000446926] Chr18:6850839..8084746 [GRCh37]
Chr18:18p11.31-11.23		 uncertain significance
GRCh37/hg19 18p11.31-11.21(chr18:4465872-15198990)x3 copy number gain See cases [RCV000447359] Chr18:4465872..15198990 [GRCh37]
Chr18:18p11.31-11.21		 pathogenic
GRCh37/hg19 18p11.32-q23(chr18:136226-78014123)x3 copy number gain See cases [RCV000446047] Chr18:136226..78014123 [GRCh37]
Chr18:18p11.32-q23		 pathogenic
GRCh37/hg19 18p11.32-q23(chr18:163323-78005185)x3 copy number gain See cases [RCV000445851] Chr18:163323..78005185 [GRCh37]
Chr18:18p11.32-q23		 pathogenic
GRCh37/hg19 18p11.32-11.21(chr18:136226-15198990)x4 copy number gain See cases [RCV000445796] Chr18:136226..15198990 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
GRCh37/hg19 18p11.31(chr18:6595124-6942942)x3 copy number gain See cases [RCV000448701] Chr18:6595124..6942942 [GRCh37]
Chr18:18p11.31		 uncertain significance
GRCh37/hg19 18p11.32-11.21(chr18:136226-14983938)x1 copy number loss See cases [RCV000449008] Chr18:136226..14983938 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
GRCh37/hg19 18p11.32-q11.1(chr18:136226-18534784)x4 copy number gain See cases [RCV000447836] Chr18:136226..18534784 [GRCh37]
Chr18:18p11.32-q11.1		 pathogenic
GRCh37/hg19 18p11.32-q11.2(chr18:136226-21657790)x3 copy number gain See cases [RCV000512118] Chr18:136226..21657790 [GRCh37]
Chr18:18p11.32-q11.2		 pathogenic
GRCh37/hg19 18p11.31-11.23(chr18:5000126-7135797)x1 copy number loss See cases [RCV000510579] Chr18:5000126..7135797 [GRCh37]
Chr18:18p11.31-11.23		 uncertain significance
GRCh37/hg19 18p11.32-11.22(chr18:2737126-9660466)x3 copy number gain See cases [RCV000511962] Chr18:2737126..9660466 [GRCh37]
Chr18:18p11.32-11.22		 pathogenic
GRCh37/hg19 18p11.32-11.21(chr18:136226-15198990)x3 copy number gain See cases [RCV000511520] Chr18:136226..15198990 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic|uncertain significance
GRCh37/hg19 18p11.32-11.21(chr18:136226-15157836)x1 copy number loss See cases [RCV000511826] Chr18:136226..15157836 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
GRCh37/hg19 18p11.32-q11.1(chr18:136226-18521285)x4 copy number gain See cases [RCV000511949] Chr18:136226..18521285 [GRCh37]
Chr18:18p11.32-q11.1		 pathogenic
GRCh37/hg19 18p11.32-q21.1(chr18:136227-46171053)x3 copy number gain See cases [RCV000511857] Chr18:136227..46171053 [GRCh37]
Chr18:18p11.32-q21.1		 pathogenic
GRCh37/hg19 18p11.32-q23(chr18:136227-78014123) copy number gain See cases [RCV000511189] Chr18:136227..78014123 [GRCh37]
Chr18:18p11.32-q23		 pathogenic
GRCh37/hg19 18p11.32-11.21(chr18:13034-15026309)x1 copy number loss See cases [RCV000515578] Chr18:13034..15026309 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
NM_001366230.1(ARHGAP28):c.2120C>T (p.Ala707Val) single nucleotide variant not specified [RCV004308292] Chr18:6912084 [GRCh38]
Chr18:6912083 [GRCh37]
Chr18:18p11.31		 uncertain significance
GRCh37/hg19 18p11.32-11.21(chr18:136226-15198990)x1 copy number loss See cases [RCV000512537] Chr18:136226..15198990 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
GRCh37/hg19 18p11.32-11.21(chr18:1-15157836)x1 copy number loss See cases [RCV000512162] Chr18:1..15157836 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
Single allele duplication not provided [RCV000677916] Chr18:416490..8638370 [GRCh37]
Chr18:18p11.32-11.22		 pathogenic
GRCh37/hg19 18p11.31-11.23(chr18:6834650-7298492)x3 copy number gain not provided [RCV000683999] Chr18:6834650..7298492 [GRCh37]
Chr18:18p11.31-11.23		 uncertain significance
GRCh37/hg19 18p11.32-11.23(chr18:136226-8057394)x1 copy number loss not provided [RCV000684044] Chr18:136226..8057394 [GRCh37]
Chr18:18p11.32-11.23		 pathogenic
GRCh37/hg19 18p11.32-11.22(chr18:136226-10074733)x1 copy number loss not provided [RCV000684046] Chr18:136226..10074733 [GRCh37]
Chr18:18p11.32-11.22		 pathogenic
GRCh37/hg19 18p11.32-11.21(chr18:136226-12767079)x1 copy number loss not provided [RCV000684048] Chr18:136226..12767079 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
GRCh37/hg19 18p11.32-11.21(chr18:958974-15181666)x3 copy number gain not provided [RCV000684051] Chr18:958974..15181666 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
GRCh37/hg19 18p11.32-11.21(chr18:136226-15157836)x4 copy number gain not provided [RCV000684052] Chr18:136226..15157836 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
GRCh37/hg19 18p11.32-11.21(chr18:136226-15198989)x1 copy number loss not provided [RCV000684053] Chr18:136226..15198989 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
GRCh37/hg19 18p11.32-11.21(chr18:136226-15198990)x4 copy number gain not provided [RCV000684054] Chr18:136226..15198990 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
GRCh37/hg19 18p11.31-11.23(chr18:6913061-8087455)x3 copy number gain not provided [RCV000684020] Chr18:6913061..8087455 [GRCh37]
Chr18:18p11.31-11.23		 uncertain significance
GRCh37/hg19 18p11.32-q23(chr18:12842-78015180)x3 copy number gain not provided [RCV000752245] Chr18:12842..78015180 [GRCh37]
Chr18:18p11.32-q23		 pathogenic
GRCh37/hg19 18p11.32-q23(chr18:13034-78015180)x3 copy number gain not provided [RCV000752246] Chr18:13034..78015180 [GRCh37]
Chr18:18p11.32-q23		 pathogenic
GRCh37/hg19 18p11.32-11.21(chr18:124335-14139006)x1 copy number loss not provided [RCV000752249] Chr18:124335..14139006 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
NM_001366230.1(ARHGAP28):c.2048G>A (p.Cys683Tyr) single nucleotide variant not provided [RCV000947870] Chr18:6908977 [GRCh38]
Chr18:6908976 [GRCh37]
Chr18:18p11.31		 benign
GRCh37/hg19 18p11.32-11.21(chr18:136304-15143714)x1 copy number loss not provided [RCV001006952] Chr18:136304..15143714 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
GRCh37/hg19 18p11.32-11.21(chr18:13034-15330525)x1 copy number loss See cases [RCV001007421] Chr18:13034..15330525 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
GRCh37/hg19 18p11.32-q11.1(chr18:136226-18529578)x1 copy number loss not provided [RCV001006954] Chr18:136226..18529578 [GRCh37]
Chr18:18p11.32-q11.1		 pathogenic
GRCh37/hg19 18p11.31-11.23(chr18:6525965-7310448)x3 copy number gain not provided [RCV001006937] Chr18:6525965..7310448 [GRCh37]
Chr18:18p11.31-11.23		 likely benign
GRCh37/hg19 18p11.31-11.23(chr18:6741973-7388381)x3 copy number gain not provided [RCV000846773] Chr18:6741973..7388381 [GRCh37]
Chr18:18p11.31-11.23		 uncertain significance
NM_001366230.1(ARHGAP28):c.1839C>T (p.Leu613=) single nucleotide variant not specified [RCV004298334] Chr18:6890534 [GRCh38]
Chr18:6890533 [GRCh37]
Chr18:18p11.31		 likely benign
GRCh37/hg19 18p11.31(chr18:6834650-7075088)x1 copy number loss not provided [RCV001006936] Chr18:6834650..7075088 [GRCh37]
Chr18:18p11.31		 uncertain significance
GRCh37/hg19 18p11.32-11.21(chr18:971295-11250447)x1 copy number loss not provided [RCV001006944] Chr18:971295..11250447 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
GRCh37/hg19 18p11.32-11.21(chr18:136226-15175005)x1 copy number loss not provided [RCV001006953] Chr18:136226..15175005 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
GRCh37/hg19 18p11.31-11.23(chr18:6875693-7304952)x3 copy number gain See cases [RCV001194518] Chr18:6875693..7304952 [GRCh37]
Chr18:18p11.31-11.23		 uncertain significance
GRCh37/hg19 18p11.32-11.21(chr18:136226-13894429)x1 copy number loss not provided [RCV001006947] Chr18:136226..13894429 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
GRCh37/hg19 18p11.31(chr18:6691690-6983454)x3 copy number gain not provided [RCV001258698] Chr18:6691690..6983454 [GRCh37]
Chr18:18p11.31		 uncertain significance
GRCh37/hg19 18p11.31-11.23(chr18:6858398-7305710)x3 copy number gain not provided [RCV001258700] Chr18:6858398..7305710 [GRCh37]
Chr18:18p11.31-11.23		 likely benign
GRCh37/hg19 18p11.32-11.21(chr18:136226-14632436)x1 copy number loss See cases [RCV002285056] Chr18:136226..14632436 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
GRCh37/hg19 18p11.31(chr18:6767055-7084385)x3 copy number gain not provided [RCV001258697] Chr18:6767055..7084385 [GRCh37]
Chr18:18p11.31		 uncertain significance
Single allele deletion Deletion of short arm of chromosome 18 [RCV001391667] Chr18:2656075..13885536 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
GRCh37/hg19 18p11.32-11.31(chr18:64996-6838315)x1 copy number loss not provided [RCV001537912] Chr18:64996..6838315 [GRCh37]
Chr18:18p11.32-11.31		 pathogenic
GRCh37/hg19 18p11.32-11.1(chr18:10501-15410398)x1 copy number loss Deletion of short arm of chromosome 18 [RCV001801193] Chr18:10501..15410398 [GRCh37]
Chr18:18p11.32-11.1		 pathogenic
GRCh37/hg19 18p11.32-q23(chr18:1-78077248) copy number gain Trisomy 18 [RCV002280660] Chr18:1..78077248 [GRCh37]
Chr18:18p11.32-q23		 pathogenic
Single allele deletion Intellectual disability [RCV001787257] Chr18:1262336..53254747 [GRCh37]
Chr18:18p11.32-q21.2		 pathogenic
GRCh37/hg19 18p11.32-11.21(chr18:136226-13655146) copy number loss not specified [RCV002052610] Chr18:136226..13655146 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
GRCh37/hg19 18p11.32-11.21(chr18:136226-14983938) copy number loss not specified [RCV002052612] Chr18:136226..14983938 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
GRCh37/hg19 18p11.32-11.21(chr18:136226-14384326) copy number gain not specified [RCV002052611] Chr18:136226..14384326 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
GRCh37/hg19 18p11.31-11.22(chr18:6834650-8978443) copy number gain not specified [RCV002052620] Chr18:6834650..8978443 [GRCh37]
Chr18:18p11.31-11.22		 uncertain significance
GRCh37/hg19 18p11.32-q12.1(chr18:136226-25252276)x3 copy number gain not provided [RCV001832915] Chr18:136226..25252276 [GRCh37]
Chr18:18p11.32-q12.1		 pathogenic
GRCh37/hg19 18p11.32-q23(chr18:136226-78014123) copy number gain not specified [RCV002052616] Chr18:136226..78014123 [GRCh37]
Chr18:18p11.32-q23		 pathogenic
GRCh37/hg19 18p11.31-11.23(chr18:3532742-7487522) copy number gain not specified [RCV002052618] Chr18:3532742..7487522 [GRCh37]
Chr18:18p11.31-11.23		 pathogenic
GRCh37/hg19 18p11.32-11.21(chr18:136226-15198990) copy number gain not specified [RCV002052613] Chr18:136226..15198990 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
GRCh37/hg19 18p11.32-11.21(chr18:136226-15198990) copy number loss not specified [RCV002052614] Chr18:136226..15198990 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
GRCh37/hg19 18p11.32-11.21(chr18:47390-14854037)x3 copy number gain not provided [RCV002276058] Chr18:47390..14854037 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
GRCh37/hg19 18p11.32-11.22(chr18:1-8638260)x1 copy number loss not provided [RCV002292972] Chr18:1..8638260 [GRCh37]
Chr18:18p11.32-11.22		 pathogenic
GRCh37/hg19 18p11.32-11.22(chr18:136226-10172941) copy number loss Deletion of short arm of chromosome 18 [RCV002280710] Chr18:136226..10172941 [GRCh37]
Chr18:18p11.32-11.22		 pathogenic
GRCh37/hg19 18p11.32-11.23(chr18:136226-7131132) copy number loss Deletion of short arm of chromosome 18 [RCV002280711] Chr18:136226..7131132 [GRCh37]
Chr18:18p11.32-11.23		 pathogenic
GRCh37/hg19 18p11.31(chr18:3824312-6983454)x1 copy number loss not provided [RCV002474913] Chr18:3824312..6983454 [GRCh37]
Chr18:18p11.31		 uncertain significance
GRCh37/hg19 18p11.31(chr18:6719041-7046603)x1 copy number loss not provided [RCV002472787] Chr18:6719041..7046603 [GRCh37]
Chr18:18p11.31		 uncertain significance
GRCh37/hg19 18p11.32-11.21(chr18:136227-11283184)x1 copy number loss not provided [RCV002472559] Chr18:136227..11283184 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
GRCh37/hg19 18p11.32-11.23(chr18:136227-7218594)x1 copy number loss not provided [RCV002472636] Chr18:136227..7218594 [GRCh37]
Chr18:18p11.32-11.23		 pathogenic
NM_001366230.1(ARHGAP28):c.2053A>G (p.Lys685Glu) single nucleotide variant not specified [RCV004332131] Chr18:6908982 [GRCh38]
Chr18:6908981 [GRCh37]
Chr18:18p11.31		 uncertain significance
NM_001366230.1(ARHGAP28):c.1468A>G (p.Lys490Glu) single nucleotide variant not specified [RCV004143250] Chr18:6887171 [GRCh38]
Chr18:6887170 [GRCh37]
Chr18:18p11.31		 uncertain significance
NM_001366230.1(ARHGAP28):c.1047T>G (p.Ile349Met) single nucleotide variant not specified [RCV004159256] Chr18:6873501 [GRCh38]
Chr18:6873500 [GRCh37]
Chr18:18p11.31		 uncertain significance
NM_001366230.1(ARHGAP28):c.1679A>G (p.Asn560Ser) single nucleotide variant not specified [RCV004228833] Chr18:6890030 [GRCh38]
Chr18:6890029 [GRCh37]
Chr18:18p11.31		 uncertain significance
NM_001366230.1(ARHGAP28):c.829A>G (p.Lys277Glu) single nucleotide variant not specified [RCV004132141] Chr18:6870607 [GRCh38]
Chr18:6870606 [GRCh37]
Chr18:18p11.31		 uncertain significance
NM_001366230.1(ARHGAP28):c.2102A>G (p.His701Arg) single nucleotide variant not specified [RCV004227686] Chr18:6912066 [GRCh38]
Chr18:6912065 [GRCh37]
Chr18:18p11.31		 uncertain significance
NM_001366230.1(ARHGAP28):c.1916C>T (p.Pro639Leu) single nucleotide variant not specified [RCV004088259] Chr18:6896512 [GRCh38]
Chr18:6896511 [GRCh37]
Chr18:18p11.31		 uncertain significance
NM_001366230.1(ARHGAP28):c.1607C>A (p.Ser536Tyr) single nucleotide variant not specified [RCV004146360] Chr18:6889958 [GRCh38]
Chr18:6889957 [GRCh37]
Chr18:18p11.31		 uncertain significance
NM_001366230.1(ARHGAP28):c.1108G>C (p.Val370Leu) single nucleotide variant not specified [RCV004070959] Chr18:6873562 [GRCh38]
Chr18:6873561 [GRCh37]
Chr18:18p11.31		 uncertain significance
NM_001366230.1(ARHGAP28):c.565C>T (p.His189Tyr) single nucleotide variant not specified [RCV004247038] Chr18:6851055 [GRCh38]
Chr18:6851054 [GRCh37]
Chr18:18p11.31		 uncertain significance
NM_001366230.1(ARHGAP28):c.1781C>T (p.Thr594Met) single nucleotide variant not specified [RCV004116561] Chr18:6890476 [GRCh38]
Chr18:6890475 [GRCh37]
Chr18:18p11.31		 uncertain significance
NM_001366230.1(ARHGAP28):c.1901G>A (p.Arg634Gln) single nucleotide variant not specified [RCV004230427] Chr18:6894887 [GRCh38]
Chr18:6894886 [GRCh37]
Chr18:18p11.31		 uncertain significance
NM_001366230.1(ARHGAP28):c.1892C>T (p.Ser631Leu) single nucleotide variant not specified [RCV004148718] Chr18:6894878 [GRCh38]
Chr18:6894877 [GRCh37]
Chr18:18p11.31		 uncertain significance
NM_001366230.1(ARHGAP28):c.1645A>G (p.Lys549Glu) single nucleotide variant not specified [RCV004188687] Chr18:6889996 [GRCh38]
Chr18:6889995 [GRCh37]
Chr18:18p11.31		 uncertain significance
NM_001366230.1(ARHGAP28):c.1007C>T (p.Ser336Phe) single nucleotide variant not specified [RCV004144442] Chr18:6873461 [GRCh38]
Chr18:6873460 [GRCh37]
Chr18:18p11.31		 uncertain significance
NM_001366230.1(ARHGAP28):c.1523G>C (p.Arg508Thr) single nucleotide variant not specified [RCV004103302] Chr18:6887226 [GRCh38]
Chr18:6887225 [GRCh37]
Chr18:18p11.31		 uncertain significance
GRCh37/hg19 18p11.32-11.1(chr18:1-15400035) copy number loss Deletion of short arm of chromosome 18 [RCV003159575] Chr18:1..15400035 [GRCh37]
Chr18:18p11.32-11.1		 pathogenic
NM_001366230.1(ARHGAP28):c.803C>T (p.Ala268Val) single nucleotide variant not specified [RCV004261817] Chr18:6868226 [GRCh38]
Chr18:6868225 [GRCh37]
Chr18:18p11.31		 uncertain significance
NM_001366230.1(ARHGAP28):c.1168C>G (p.Arg390Gly) single nucleotide variant not specified [RCV004277306] Chr18:6873731 [GRCh38]
Chr18:6873730 [GRCh37]
Chr18:18p11.31		 uncertain significance
GRCh38/hg38 18p11.32-11.21(chr18:158286-14124574)x1 copy number loss Deletion of short arm of chromosome 18 [RCV003327630] Chr18:158286..14124574 [GRCh38]
Chr18:18p11.32-11.21		 pathogenic
NM_001366230.1(ARHGAP28):c.830A>G (p.Lys277Arg) single nucleotide variant not specified [RCV004337799] Chr18:6870608 [GRCh38]
Chr18:6870607 [GRCh37]
Chr18:18p11.31		 uncertain significance
NM_001366230.1(ARHGAP28):c.885G>A (p.Met295Ile) single nucleotide variant not specified [RCV004337990] Chr18:6870663 [GRCh38]
Chr18:6870662 [GRCh37]
Chr18:18p11.31		 uncertain significance
NM_001366230.1(ARHGAP28):c.580G>T (p.Asp194Tyr) single nucleotide variant not specified [RCV004349238] Chr18:6851070 [GRCh38]
Chr18:6851069 [GRCh37]
Chr18:18p11.31		 uncertain significance
GRCh37/hg19 18p11.31-11.23(chr18:5689219-7964689)x3 copy number gain not provided [RCV003485171] Chr18:5689219..7964689 [GRCh37]
Chr18:18p11.31-11.23		 uncertain significance
GRCh37/hg19 18p11.32-q11.1(chr18:136227-18521285)x4 copy number gain not provided [RCV003485366] Chr18:136227..18521285 [GRCh37]
Chr18:18p11.32-q11.1		 pathogenic
GRCh37/hg19 18p11.32-11.22(chr18:136227-8513569)x1 copy number loss not provided [RCV003483329] Chr18:136227..8513569 [GRCh37]
Chr18:18p11.32-11.22		 pathogenic
GRCh37/hg19 18p11.32-11.21(chr18:136227-14585159)x1 copy number loss not provided [RCV003483328] Chr18:136227..14585159 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
NM_001366230.1(ARHGAP28):c.177C>G (p.Leu59=) single nucleotide variant not provided [RCV003423013] Chr18:6824816 [GRCh38]
Chr18:6824815 [GRCh37]
Chr18:18p11.31		 likely benign
GRCh37/hg19 18p11.31-11.23(chr18:6737164-7388708)x3 copy number gain not specified [RCV003987282] Chr18:6737164..7388708 [GRCh37]
Chr18:18p11.31-11.23		 uncertain significance
GRCh37/hg19 18p11.32-11.21(chr18:136226-15161581)x1 copy number loss not specified [RCV003987287] Chr18:136226..15161581 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
GRCh37/hg19 18p11.31-11.21(chr18:2922899-15198990)x3 copy number gain not specified [RCV003987271] Chr18:2922899..15198990 [GRCh37]
Chr18:18p11.31-11.21		 pathogenic
GRCh37/hg19 18p11.32-11.21(chr18:136227-15157836)x3 copy number gain not specified [RCV003986102] Chr18:136227..15157836 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
GRCh37/hg19 18p11.32-11.21(chr18:136226-14148354)x3 copy number gain not specified [RCV003987266] Chr18:136226..14148354 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
GRCh37/hg19 18p11.32-11.21(chr18:136226-14455323)x3 copy number gain not specified [RCV003987269] Chr18:136226..14455323 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
GRCh37/hg19 18p11.32-11.22(chr18:136226-10365982)x1 copy number loss not specified [RCV003987270] Chr18:136226..10365982 [GRCh37]
Chr18:18p11.32-11.22		 pathogenic
GRCh37/hg19 18p11.32-11.21(chr18:136226-14352648)x1 copy number loss not specified [RCV003987292] Chr18:136226..14352648 [GRCh37]
Chr18:18p11.32-11.21		 pathogenic
GRCh37/hg19 18p11.32-11.23(chr18:136227-8359829)x1 copy number loss not specified [RCV003987293] Chr18:136227..8359829 [GRCh37]
Chr18:18p11.32-11.23		 pathogenic
NM_001366230.1(ARHGAP28):c.1328A>G (p.Asp443Gly) single nucleotide variant not specified [RCV004422594] Chr18:6882174 [GRCh38]
Chr18:6882173 [GRCh37]
Chr18:18p11.31		 uncertain significance
NM_001366230.1(ARHGAP28):c.1873G>A (p.Val625Ile) single nucleotide variant not specified [RCV004422591] Chr18:6894859 [GRCh38]
Chr18:6894858 [GRCh37]
Chr18:18p11.31		 uncertain significance
NM_001366230.1(ARHGAP28):c.2018A>G (p.Gln673Arg) single nucleotide variant not specified [RCV004422592] Chr18:6896614 [GRCh38]
Chr18:6896613 [GRCh37]
Chr18:18p11.31		 uncertain significance
NM_001366230.1(ARHGAP28):c.1662A>C (p.Glu554Asp) single nucleotide variant not specified [RCV004422589] Chr18:6890013 [GRCh38]
Chr18:6890012 [GRCh37]
Chr18:18p11.31		 uncertain significance
NM_001366230.1(ARHGAP28):c.1505C>T (p.Ala502Val) single nucleotide variant not specified [RCV004422588] Chr18:6887208 [GRCh38]
Chr18:6887207 [GRCh37]
Chr18:18p11.31		 uncertain significance
NM_001366230.1(ARHGAP28):c.601G>A (p.Glu201Lys) single nucleotide variant not specified [RCV004422590] Chr18:6851091 [GRCh38]
Chr18:6851090 [GRCh37]
Chr18:18p11.31		 uncertain significance
NM_001366230.1(ARHGAP28):c.780G>C (p.Glu260Asp) single nucleotide variant not specified [RCV004422593] Chr18:6868203 [GRCh38]
Chr18:6868202 [GRCh37]
Chr18:18p11.31		 likely benign
NM_001366230.1(ARHGAP28):c.1734+46C>G single nucleotide variant ARHGAP28-related disorder [RCV003971675] Chr18:6890131 [GRCh38]
Chr18:6890130 [GRCh37]
Chr18:18p11.31		 likely benign
NM_001366230.1(ARHGAP28):c.2170A>G (p.Lys724Glu) single nucleotide variant not specified [RCV004662579] Chr18:6912134 [GRCh38]
Chr18:6912133 [GRCh37]
Chr18:18p11.31		 uncertain significance
NM_001366230.1(ARHGAP28):c.1699C>T (p.Arg567Cys) single nucleotide variant not specified [RCV004662565] Chr18:6890050 [GRCh38]
Chr18:6890049 [GRCh37]
Chr18:18p11.31		 uncertain significance
NM_001366230.1(ARHGAP28):c.847G>A (p.Ala283Thr) single nucleotide variant not specified [RCV004662571] Chr18:6870625 [GRCh38]
Chr18:6870624 [GRCh37]
Chr18:18p11.31		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:3845
Count of miRNA genes:1142
Interacting mature miRNAs:1428
Transcripts:ENST00000262227, ENST00000314319, ENST00000383472, ENST00000400091, ENST00000418986, ENST00000419673, ENST00000531294, ENST00000532723, ENST00000532996, ENST00000577524, ENST00000579245, ENST00000579689, ENST00000579796, ENST00000581099, ENST00000583410, ENST00000584287, ENST00000584387
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

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

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
597308507GWAS1404581_Herythrocyte count QTL GWAS1404581 (human)4e-08erythrocyte countred blood cell count (CMO:0000025)1867370926737093Human
597314008GWAS1410082_Hcortical surface area measurement QTL GWAS1410082 (human)2e-09cerebral cortex morphology trait (VT:0000788)tibia-fibula cortical bone total cross-sectional area (CMO:0001721)1867361266736127Human
597203580GWAS1299654_Hmacula measurement QTL GWAS1299654 (human)2e-14macula measurement1867307206730721Human
597193759GWAS1289833_Hbody mass index QTL GWAS1289833 (human)2e-09body mass indexbody mass index (BMI) (CMO:0000105)1868739556873956Human
597406332GWAS1502406_Hschizophrenia QTL GWAS1502406 (human)0.0000002schizophrenia1868977796897780Human
597204528GWAS1300602_Hcarotid plaque build QTL GWAS1300602 (human)0.000001carotid plaque build1868242206824221Human
597186320GWAS1282394_Hspontaneous preterm birth, parental genotype effect measurement QTL GWAS1282394 (human)0.000003spontaneous preterm birth, parental genotype effect measurement1868584276858428Human
597204721GWAS1300795_Hcarotid plaque build QTL GWAS1300795 (human)0.000003carotid plaque build1868242206824221Human
597066429GWAS1162503_Ht-tau:beta-amyloid 1-42 ratio measurement QTL GWAS1162503 (human)8e-08cerebral cortex integrity trait (VT:0010923)1867810176781018Human
597205075GWAS1301149_Hcarotid plaque build QTL GWAS1301149 (human)0.000005carotid plaque build1868269006826901Human
597129624GWAS1225698_Hcortical surface area measurement QTL GWAS1225698 (human)1e-08cerebral cortex morphology trait (VT:0000788)tibia-fibula cortical bone total cross-sectional area (CMO:0001721)1867361266736127Human
597326891GWAS1422965_Hcolor vision disorder QTL GWAS1422965 (human)0.000004color vision disorder1867597036759704Human
597115718GWAS1211792_Helectroencephalogram measurement QTL GWAS1211792 (human)0.000005electroencephalogram measurementbrain activity measurement (CMO:0001737)1868565316856532Human
597095076GWAS1191150_H3-hydroxypropylmercapturic acid measurement QTL GWAS1191150 (human)0.0000043-hydroxypropylmercapturic acid measurement1868944766894477Human
597204524GWAS1300598_Hcarotid plaque build QTL GWAS1300598 (human)0.0000005carotid plaque build1868242206824221Human
597039362GWAS1135436_Hrisk-taking behaviour QTL GWAS1135436 (human)5e-09risk-taking behaviour1868793546879355Human
597232292GWAS1328366_Hasparaginase hypersensitivity QTL GWAS1328366 (human)9e-09asparaginase hypersensitivity1867396256739626Human
597204903GWAS1300977_Hcarotid plaque build QTL GWAS1300977 (human)0.000002carotid plaque build1868242206824221Human

Markers in Region
RH92850  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37186,913,424 - 6,913,583UniSTSGRCh37
Build 36186,903,424 - 6,903,583RGDNCBI36
Celera186,798,810 - 6,798,969RGD
Cytogenetic Map18p11.31UniSTS
HuRef186,876,885 - 6,877,044UniSTS
GeneMap99-GB4 RH Map1844.1UniSTS
RH93927  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37186,914,376 - 6,914,565UniSTSGRCh37
Build 36186,904,376 - 6,904,565RGDNCBI36
Celera186,799,762 - 6,799,951RGD
Cytogenetic Map18p11.31UniSTS
HuRef186,877,837 - 6,878,026UniSTS
GeneMap99-GB4 RH Map1844.1UniSTS
RH93818  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37186,915,249 - 6,915,429UniSTSGRCh37
Build 36186,905,249 - 6,905,429RGDNCBI36
Celera186,800,635 - 6,800,815RGD
Cytogenetic Map18p11.31UniSTS
HuRef186,878,710 - 6,878,890UniSTS
GeneMap99-GB4 RH Map1844.1UniSTS
RH103364  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37186,915,307 - 6,915,429UniSTSGRCh37
Build 36186,905,307 - 6,905,429RGDNCBI36
Celera186,800,693 - 6,800,815RGD
Cytogenetic Map18p11.31UniSTS
HuRef186,878,768 - 6,878,890UniSTS
GeneMap99-GB4 RH Map1842.36UniSTS
SHGC-105816  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37186,873,981 - 6,874,298UniSTSGRCh37
Build 36186,863,981 - 6,864,298RGDNCBI36
Celera186,759,368 - 6,759,685RGD
Cytogenetic Map18p11.31UniSTS
HuRef186,837,352 - 6,837,669UniSTS
TNG Radiation Hybrid Map183666.0UniSTS
AB072742  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37186,889,912 - 6,890,058UniSTSGRCh37
Build 36186,879,912 - 6,880,058RGDNCBI36
Celera186,775,299 - 6,775,445RGD
HuRef186,853,337 - 6,853,483UniSTS
D1S1423  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map10p12.1-p11.2UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map6p22.3-p21.32UniSTS
Cytogenetic Map6q22.33UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map7q11.2UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map9q12UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map18q22.1UniSTS
Cytogenetic Map13q12UniSTS
Cytogenetic Map10p14-p13UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map11q23-q24UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map22cen-q12.3UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map15q11.2-q21.3UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map3q25UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map4q28UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map1q41-q42UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map12p13.1-p12.3UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map1p13.1UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map7q33UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map11q24.1UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map3q13UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map1q42.1UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map12q24.2UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map8p23-p22UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map10p12.33UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map3q26UniSTS
Cytogenetic Map9p21.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map5q21.3UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map3q26.31UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic MapXq27.2UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map4q31UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q24.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map11q22.1UniSTS
Cytogenetic Map12q14.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map20q11.21-q11.23UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map21p11.1UniSTS
Cytogenetic Map1p35-p34.3UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map12q24.31-q24.32UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map14q32.1UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map4q31.23UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2p22.3UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map9p12UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map13q33.3UniSTS
Cytogenetic Map15q22-q24UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map4p15.31UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map20q13.1UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map4q26UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map15q22.1-q22.31UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map12q11-q12UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map4q24UniSTS
Cytogenetic Map1p32UniSTS
Cytogenetic Map3p21.1-p14.2UniSTS
Cytogenetic Map12q22-q23.1UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map6q24.2UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map16p13.13UniSTS
Cytogenetic Map10pter-q25.3UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map6p22.2UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map1q32.2-q41UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map22q11UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map11q13.1-q13.3UniSTS
Cytogenetic Map16p13UniSTS
Cytogenetic Map15q26UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map4p15.1-p14UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map5q33.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map7q32.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map9p13UniSTS
Cytogenetic Map2p24.2UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic Map6p24-p22.3UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map3q21-q24UniSTS
Cytogenetic Map4q13UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map4q34.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map13q13.3UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map1q31UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map8q24.12UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map10q24.2UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map6q25.2UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map3q23-q24UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map20pter-p12UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map7p14.2UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map18p11.22UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map14q22.2UniSTS
Cytogenetic Map20p11.22-p11.1UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map11q12-q13UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map10p11.21UniSTS
Cytogenetic Map6p22-p21UniSTS
Cytogenetic Map17q21.1-q21.3UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map4p15.32UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map12p13.2-p12.3UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map5q22.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map4p15.3UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map12q13.1-q13.2UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map1p31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map9p22.3UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map6q22.32UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map18q12.2UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map13q33.1UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map16p12.1UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map10q22.3-q23.2UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map4q21.3UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map3q12.1UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map2p13.2UniSTS
Cytogenetic Map3p12.3UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map3q11.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map6p24.2UniSTS
Cytogenetic Map20q13.33UniSTS
D1S1425  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map8q12.1UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map6q25.2-q25.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map2p23-p22UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map17q22-q23UniSTS
Cytogenetic Map2p11.1UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map2p12-p11.2UniSTS
Cytogenetic Map3q11.1UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map1p21.3UniSTS
Cytogenetic Map1q32.2UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic Map18p11.3-p11.2UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map21p11.1UniSTS
Cytogenetic Map12q24.31-q24.32UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map12p12.2-p11.2UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map17q22-q23.2UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map7q31.1-q31.3UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map3p21.1-p14.2UniSTS
Cytogenetic Map2p24UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map12q24.32UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map15q11-q12UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map15q21.1-q21.2UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map12p13.33UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map4q31.21UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map10p15-p14UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map12q13.1-q13.2UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic Map6q22.32UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map3q12.1UniSTS
Cytogenetic Map15q24-q25UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map6pter-p12.1UniSTS
Cytogenetic Map6q16UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map11q23.1-q23.2UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map16q24.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic MapXq21.1UniSTS
GDB:315881  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map8p23UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map17q12UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2408 2788 2236 4945 1675 2290 5 574 1144 415 2266 6421 5659 51 3711 845 1726 1605 172 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001010000 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001366230 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001366231 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001410873 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005258146 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047437794 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047437795 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047437796 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047437797 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047437798 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047437799 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047437800 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047437801 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047437803 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319100 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319101 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319102 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319103 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319104 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319105 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319106 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319107 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319108 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054319109 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB037735 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI435330 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK001174 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK024298 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK130670 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK289791 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK302026 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK308259 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP005205 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP005210 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC033668 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC065274 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BG720645 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX648684 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471113 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068260 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC401238 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000262227   ⟹   ENSP00000262227
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl186,788,494 - 6,898,719 (+)Ensembl
Ensembl Acc Id: ENST00000314319   ⟹   ENSP00000313506
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl186,837,193 - 6,915,700 (+)Ensembl
Ensembl Acc Id: ENST00000383472   ⟹   ENSP00000372964
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl186,729,716 - 6,915,716 (+)Ensembl
Ensembl Acc Id: ENST00000419673   ⟹   ENSP00000392660
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl186,834,475 - 6,915,716 (+)Ensembl
Ensembl Acc Id: ENST00000531294   ⟹   ENSP00000437262
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl186,834,480 - 6,912,415 (+)Ensembl
Ensembl Acc Id: ENST00000532723   ⟹   ENSP00000433390
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl186,774,002 - 6,837,378 (+)Ensembl
Ensembl Acc Id: ENST00000532996   ⟹   ENSP00000435990
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl186,850,791 - 6,898,721 (+)Ensembl
Ensembl Acc Id: ENST00000577524   ⟹   ENSP00000463672
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl186,837,197 - 6,870,661 (+)Ensembl
Ensembl Acc Id: ENST00000579245
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl186,873,481 - 6,882,361 (+)Ensembl
Ensembl Acc Id: ENST00000579689   ⟹   ENSP00000463143
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl186,873,466 - 6,890,048 (+)Ensembl
Ensembl Acc Id: ENST00000579796
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl186,896,760 - 6,898,719 (+)Ensembl
Ensembl Acc Id: ENST00000581099   ⟹   ENSP00000462912
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl186,834,475 - 6,868,234 (+)Ensembl
Ensembl Acc Id: ENST00000583410   ⟹   ENSP00000464141
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl186,729,946 - 6,824,964 (+)Ensembl
Ensembl Acc Id: ENST00000584287   ⟹   ENSP00000464310
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl186,837,197 - 6,870,646 (+)Ensembl
Ensembl Acc Id: ENST00000584387   ⟹   ENSP00000462831
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl186,730,043 - 6,851,107 (+)Ensembl
RefSeq Acc Id: NM_001010000   ⟹   NP_001010000
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38186,834,485 - 6,915,716 (+)NCBI
GRCh37186,729,717 - 6,915,715 (+)NCBI
Build 36186,824,484 - 6,905,715 (+)NCBI Archive
Celera186,719,871 - 6,801,101 (+)RGD
HuRef186,797,814 - 6,879,176 (+)ENTREZGENE
CHM1_1186,834,188 - 6,915,740 (+)NCBI
T2T-CHM13v2.0186,995,049 - 7,076,260 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001366230   ⟹   NP_001353159
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38186,729,716 - 6,915,716 (+)NCBI
T2T-CHM13v2.0186,890,201 - 7,076,260 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001366231   ⟹   NP_001353160
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38186,729,716 - 6,898,721 (+)NCBI
T2T-CHM13v2.0186,890,201 - 7,059,286 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001410873   ⟹   NP_001397802
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38186,729,716 - 6,898,721 (+)NCBI
T2T-CHM13v2.0186,890,201 - 7,059,286 (+)NCBI
RefSeq Acc Id: XM_005258146   ⟹   XP_005258203
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38186,729,716 - 6,915,716 (+)NCBI
GRCh37186,729,717 - 6,915,715 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047437794   ⟹   XP_047293750
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38186,729,716 - 6,898,721 (+)NCBI
RefSeq Acc Id: XM_047437795   ⟹   XP_047293751
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38186,730,098 - 6,915,716 (+)NCBI
RefSeq Acc Id: XM_047437796   ⟹   XP_047293752
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38186,730,007 - 6,898,721 (+)NCBI
RefSeq Acc Id: XM_047437797   ⟹   XP_047293753
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38186,774,009 - 6,915,716 (+)NCBI
RefSeq Acc Id: XM_047437798   ⟹   XP_047293754
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38186,774,009 - 6,915,716 (+)NCBI
RefSeq Acc Id: XM_047437799   ⟹   XP_047293755
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38186,729,935 - 6,915,716 (+)NCBI
RefSeq Acc Id: XM_047437800   ⟹   XP_047293756
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38186,774,834 - 6,915,716 (+)NCBI
RefSeq Acc Id: XM_047437801   ⟹   XP_047293757
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38186,791,505 - 6,915,716 (+)NCBI
RefSeq Acc Id: XM_047437803   ⟹   XP_047293759
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38186,834,485 - 6,915,716 (+)NCBI
RefSeq Acc Id: XM_054319100   ⟹   XP_054175075
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0186,890,201 - 7,076,260 (+)NCBI
RefSeq Acc Id: XM_054319101   ⟹   XP_054175076
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0186,890,201 - 7,059,286 (+)NCBI
RefSeq Acc Id: XM_054319102   ⟹   XP_054175077
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0186,890,583 - 7,076,260 (+)NCBI
RefSeq Acc Id: XM_054319103   ⟹   XP_054175078
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0186,890,492 - 7,059,286 (+)NCBI
RefSeq Acc Id: XM_054319104   ⟹   XP_054175079
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0186,933,498 - 7,076,260 (+)NCBI
RefSeq Acc Id: XM_054319105   ⟹   XP_054175080
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0186,933,498 - 7,076,260 (+)NCBI
RefSeq Acc Id: XM_054319106   ⟹   XP_054175081
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0186,890,420 - 7,076,260 (+)NCBI
RefSeq Acc Id: XM_054319107   ⟹   XP_054175082
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0186,935,303 - 7,076,260 (+)NCBI
RefSeq Acc Id: XM_054319108   ⟹   XP_054175083
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0186,951,977 - 7,076,260 (+)NCBI
RefSeq Acc Id: XM_054319109   ⟹   XP_054175084
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0186,995,049 - 7,076,260 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001010000 (Get FASTA)   NCBI Sequence Viewer  
  NP_001353159 (Get FASTA)   NCBI Sequence Viewer  
  NP_001353160 (Get FASTA)   NCBI Sequence Viewer  
  NP_001397802 (Get FASTA)   NCBI Sequence Viewer  
  XP_005258203 (Get FASTA)   NCBI Sequence Viewer  
  XP_047293750 (Get FASTA)   NCBI Sequence Viewer  
  XP_047293751 (Get FASTA)   NCBI Sequence Viewer  
  XP_047293752 (Get FASTA)   NCBI Sequence Viewer  
  XP_047293753 (Get FASTA)   NCBI Sequence Viewer  
  XP_047293754 (Get FASTA)   NCBI Sequence Viewer  
  XP_047293755 (Get FASTA)   NCBI Sequence Viewer  
  XP_047293756 (Get FASTA)   NCBI Sequence Viewer  
  XP_047293757 (Get FASTA)   NCBI Sequence Viewer  
  XP_047293759 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175075 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175076 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175077 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175078 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175079 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175080 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175081 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175082 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175083 (Get FASTA)   NCBI Sequence Viewer  
  XP_054175084 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH33668 (Get FASTA)   NCBI Sequence Viewer  
  AAH65274 (Get FASTA)   NCBI Sequence Viewer  
  BAA91533 (Get FASTA)   NCBI Sequence Viewer  
  BAA92552 (Get FASTA)   NCBI Sequence Viewer  
  BAF82480 (Get FASTA)   NCBI Sequence Viewer  
  BAG63424 (Get FASTA)   NCBI Sequence Viewer  
  EAX01633 (Get FASTA)   NCBI Sequence Viewer  
  EAX01634 (Get FASTA)   NCBI Sequence Viewer  
  EAX01635 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000262227
  ENSP00000262227.3
  ENSP00000313506.3
  ENSP00000372964
  ENSP00000372964.4
  ENSP00000392660
  ENSP00000392660.2
  ENSP00000433390.1
  ENSP00000435990.1
  ENSP00000437262.1
  ENSP00000462831.1
  ENSP00000462912.1
  ENSP00000463143.1
  ENSP00000463672.1
  ENSP00000464141.1
  ENSP00000464310.1
GenBank Protein Q9P2N2 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_001010000   ⟸   NM_001010000
- Peptide Label: isoform a
- UniProtKB: E9PMX7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005258203   ⟸   XM_005258146
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: NP_001353159   ⟸   NM_001366230
- Peptide Label: isoform c
- UniProtKB: Q9P2N2 (UniProtKB/Swiss-Prot),   Q8N4T3 (UniProtKB/Swiss-Prot),   Q6P160 (UniProtKB/Swiss-Prot),   A8MU88 (UniProtKB/Swiss-Prot),   A8MQB7 (UniProtKB/Swiss-Prot),   Q9NW53 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: NP_001353160   ⟸   NM_001366231
- Peptide Label: isoform d
Ensembl Acc Id: ENSP00000462912   ⟸   ENST00000581099
Ensembl Acc Id: ENSP00000464141   ⟸   ENST00000583410
Ensembl Acc Id: ENSP00000462831   ⟸   ENST00000584387
Ensembl Acc Id: ENSP00000464310   ⟸   ENST00000584287
Ensembl Acc Id: ENSP00000437262   ⟸   ENST00000531294
Ensembl Acc Id: ENSP00000435990   ⟸   ENST00000532996
Ensembl Acc Id: ENSP00000433390   ⟸   ENST00000532723
Ensembl Acc Id: ENSP00000392660   ⟸   ENST00000419673
Ensembl Acc Id: ENSP00000463672   ⟸   ENST00000577524
Ensembl Acc Id: ENSP00000313506   ⟸   ENST00000314319
Ensembl Acc Id: ENSP00000463143   ⟸   ENST00000579689
Ensembl Acc Id: ENSP00000262227   ⟸   ENST00000262227
Ensembl Acc Id: ENSP00000372964   ⟸   ENST00000383472
RefSeq Acc Id: XP_047293750   ⟸   XM_047437794
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047293755   ⟸   XM_047437799
- Peptide Label: isoform X3
- UniProtKB: E9PMX7 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047293752   ⟸   XM_047437796
- Peptide Label: isoform X4
RefSeq Acc Id: XP_047293751   ⟸   XM_047437795
- Peptide Label: isoform X3
- UniProtKB: E9PMX7 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047293753   ⟸   XM_047437797
- Peptide Label: isoform X3
- UniProtKB: E9PMX7 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047293754   ⟸   XM_047437798
- Peptide Label: isoform X3
- UniProtKB: E9PMX7 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047293756   ⟸   XM_047437800
- Peptide Label: isoform X3
- UniProtKB: E9PMX7 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047293757   ⟸   XM_047437801
- Peptide Label: isoform X3
- UniProtKB: E9PMX7 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047293759   ⟸   XM_047437803
- Peptide Label: isoform X5
- UniProtKB: E9PMX7 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001397802   ⟸   NM_001410873
- Peptide Label: isoform e
RefSeq Acc Id: XP_054175075   ⟸   XM_054319100
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054175076   ⟸   XM_054319101
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054175081   ⟸   XM_054319106
- Peptide Label: isoform X3
- UniProtKB: E9PMX7 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054175078   ⟸   XM_054319103
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054175077   ⟸   XM_054319102
- Peptide Label: isoform X3
- UniProtKB: E9PMX7 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054175079   ⟸   XM_054319104
- Peptide Label: isoform X3
- UniProtKB: E9PMX7 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054175080   ⟸   XM_054319105
- Peptide Label: isoform X3
- UniProtKB: E9PMX7 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054175082   ⟸   XM_054319107
- Peptide Label: isoform X3
- UniProtKB: E9PMX7 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054175083   ⟸   XM_054319108
- Peptide Label: isoform X3
- UniProtKB: E9PMX7 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054175084   ⟸   XM_054319109
- Peptide Label: isoform X5
- UniProtKB: E9PMX7 (UniProtKB/TrEMBL)
Protein Domains
Rho-GAP

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9P2N2-F1-model_v2 AlphaFold Q9P2N2 1-729 view protein structure

Promoters
RGD ID:7236877
Promoter ID:EPDNEW_H24184
Type:initiation region
Name:ARHGAP28_1
Description:Rho GTPase activating protein 28
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H24185  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38186,729,716 - 6,729,776EPDNEW
RGD ID:7236879
Promoter ID:EPDNEW_H24185
Type:multiple initiation site
Name:ARHGAP28_2
Description:Rho GTPase activating protein 28
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H24184  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38186,834,485 - 6,834,545EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:25509 AgrOrtholog
COSMIC ARHGAP28 COSMIC
Ensembl Genes ENSG00000088756 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000262227 ENTREZGENE
  ENST00000262227.7 UniProtKB/Swiss-Prot
  ENST00000314319.7 UniProtKB/Swiss-Prot
  ENST00000383472 ENTREZGENE
  ENST00000383472.9 UniProtKB/Swiss-Prot
  ENST00000419673 ENTREZGENE
  ENST00000419673.6 UniProtKB/Swiss-Prot
  ENST00000531294.5 UniProtKB/TrEMBL
  ENST00000532723.5 UniProtKB/TrEMBL
  ENST00000532996.5 UniProtKB/Swiss-Prot
  ENST00000577524.5 UniProtKB/TrEMBL
  ENST00000579689.1 UniProtKB/TrEMBL
  ENST00000581099.5 UniProtKB/TrEMBL
  ENST00000583410.1 UniProtKB/TrEMBL
  ENST00000584287.5 UniProtKB/TrEMBL
  ENST00000584387.1 UniProtKB/TrEMBL
Gene3D-CATH 1.10.555.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000088756 GTEx
HGNC ID HGNC:25509 ENTREZGENE
Human Proteome Map ARHGAP28 Human Proteome Map
InterPro Rho_GTPase_activation_prot UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RhoGAP_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:79822 UniProtKB/TrEMBL
NCBI Gene 79822 ENTREZGENE
OMIM 610592 OMIM
PANTHER RHO GTPASE ACTIVATING PROTEIN 18,19-RELATED UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RHO GTPASE-ACTIVATING PROTEIN 28 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam RhoGAP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134915320 PharmGKB
PROSITE RHOGAP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART RhoGAP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF48350 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A8MQB7 ENTREZGENE
  A8MU88 ENTREZGENE
  B4DXL2_HUMAN UniProtKB/TrEMBL
  E9PL26_HUMAN UniProtKB/TrEMBL
  E9PMX7 ENTREZGENE, UniProtKB/TrEMBL
  J3KT69_HUMAN UniProtKB/TrEMBL
  J3KTC0_HUMAN UniProtKB/TrEMBL
  J3QKM0_HUMAN UniProtKB/TrEMBL
  J3QLR3_HUMAN UniProtKB/TrEMBL
  J3QRC2_HUMAN UniProtKB/TrEMBL
  Q6P160 ENTREZGENE
  Q8N4T3 ENTREZGENE
  Q9NW53 ENTREZGENE
  Q9P2N2 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary A8MQB7 UniProtKB/Swiss-Prot
  A8MU88 UniProtKB/Swiss-Prot
  Q6P160 UniProtKB/Swiss-Prot
  Q8N4T3 UniProtKB/Swiss-Prot
  Q9NW53 UniProtKB/Swiss-Prot