ARHGAP21 (Rho GTPase activating protein 21) - Rat Genome Database

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Gene: ARHGAP21 (Rho GTPase activating protein 21) Homo sapiens
Analyze
Symbol: ARHGAP21
Name: Rho GTPase activating protein 21
RGD ID: 1322263
HGNC Page HGNC:23725
Description: Predicted to enable GTPase activator activity. Involved in several processes, including establishment of Golgi localization; maintenance of Golgi location; and organelle transport along microtubule. Located in several cellular components, including Golgi apparatus; actin cytoskeleton; and cell junction.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: ARHGAP10; DKFZp761L0424; FLJ33323; FLJ90108; rho GTPase-activating protein 10; rho GTPase-activating protein 21; Rho-GTPase activating protein 10; rho-type GTPase-activating protein 21
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Related Pseudogenes: LOC643562   LOC729945  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381024,583,614 - 24,723,887 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p13 Ensembl1024,583,609 - 24,723,887 (-)EnsemblGRCh38hg38GRCh38
GRCh371024,872,543 - 25,012,816 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361024,912,549 - 25,052,550 (-)NCBINCBI36Build 36hg18NCBI36
Build 341024,912,550 - 25,052,550NCBI
Celera1024,564,446 - 24,712,895 (-)NCBICelera
Cytogenetic Map10p12.1NCBI
HuRef1024,534,090 - 24,673,492 (-)NCBIHuRef
CHM1_11024,872,464 - 25,013,653 (-)NCBICHM1_1
T2T-CHM13v2.01024,602,382 - 24,742,515 (-)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

Cellular Component

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:7829101   PMID:10718198   PMID:11238453   PMID:12056806   PMID:12477932   PMID:14702039   PMID:15161933   PMID:15778465   PMID:15793564   PMID:16385451   PMID:17347647   PMID:17620599  
PMID:19268501   PMID:20195357   PMID:20525016   PMID:21173159   PMID:21873635   PMID:22318733   PMID:22922005   PMID:23235160   PMID:23414517   PMID:25416956   PMID:25468996   PMID:25691070  
PMID:26053890   PMID:26186194   PMID:26496610   PMID:26638075   PMID:26673895   PMID:26972000   PMID:27609421   PMID:28380382   PMID:28514442   PMID:28718761   PMID:28749339   PMID:29212046  
PMID:29395067   PMID:29507755   PMID:29856495   PMID:30344098   PMID:30639242   PMID:31586073   PMID:31871319   PMID:32129710   PMID:32203420   PMID:33727037   PMID:33766124   PMID:33864728  
PMID:33916271   PMID:33961781   PMID:34079125   PMID:34591612   PMID:34702444   PMID:34709266   PMID:34732716   PMID:35271311   PMID:35337019   PMID:35844135   PMID:35944360   PMID:36676763  
PMID:36764390  


Genomics

Comparative Map Data
ARHGAP21
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381024,583,614 - 24,723,887 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p13 Ensembl1024,583,609 - 24,723,887 (-)EnsemblGRCh38hg38GRCh38
GRCh371024,872,543 - 25,012,816 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361024,912,549 - 25,052,550 (-)NCBINCBI36Build 36hg18NCBI36
Build 341024,912,550 - 25,052,550NCBI
Celera1024,564,446 - 24,712,895 (-)NCBICelera
Cytogenetic Map10p12.1NCBI
HuRef1024,534,090 - 24,673,492 (-)NCBIHuRef
CHM1_11024,872,464 - 25,013,653 (-)NCBICHM1_1
T2T-CHM13v2.01024,602,382 - 24,742,515 (-)NCBIT2T-CHM13v2.0
Arhgap21
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39220,852,746 - 20,973,761 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl220,852,730 - 20,973,692 (-)EnsemblGRCm39 Ensembl
GRCm38220,847,919 - 20,968,691 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl220,847,919 - 20,968,881 (-)EnsemblGRCm38mm10GRCm38
MGSCv37220,769,546 - 20,889,348 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36220,765,673 - 20,886,635 (-)NCBIMGSCv36mm8
Celera220,722,855 - 20,850,910 (-)NCBICelera
Cytogenetic Map2A3NCBI
Arhgap21
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.21783,348,673 - 83,472,202 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1783,348,673 - 83,472,444 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1786,828,401 - 86,951,837 (-)NCBIRnor_SHR
UTH_Rnor_SHRSP_BbbUtx_1.01790,663,807 - 90,787,236 (-)NCBIRnor_SHRSP
UTH_Rnor_WKY_Bbb_1.01784,680,722 - 84,804,160 (-)NCBIRnor_WKY
Rnor_6.01787,725,978 - 87,797,436 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1787,725,867 - 87,826,421 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01789,415,087 - 89,486,545 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41794,817,558 - 94,941,088 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11794,828,397 - 94,951,968 (-)NCBI
Celera1782,609,823 - 82,732,937 (-)NCBICelera
Cytogenetic Map17q12.3NCBI
Arhgap21
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0NW_0049554294,424,425 - 4,559,596 (+)NCBIChiLan1.0ChiLan1.0
ARHGAP21
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan11037,291,011 - 37,427,984 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01024,761,427 - 24,898,572 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11025,131,262 - 25,267,188 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1025,132,054 - 25,266,378 (-)Ensemblpanpan1.1panPan2
ARHGAP21
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.128,740,760 - 8,877,399 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl28,740,119 - 8,877,016 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha27,492,699 - 7,570,795 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.026,941,316 - 7,076,212 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl26,941,307 - 7,075,970 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.126,367,333 - 6,445,123 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.026,386,800 - 6,529,731 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.026,612,602 - 6,694,835 (+)NCBIUU_Cfam_GSD_1.0
Arhgap21
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440934424,183,514 - 24,257,210 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_004936484349,466 - 483,523 (-)EnsemblSpeTri2.0
SpeTri2.0NW_004936484348,671 - 393,993 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ARHGAP21
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1050,638,719 - 50,669,497 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11050,541,582 - 50,680,156 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21055,994,406 - 56,132,994 (+)NCBISscrofa10.2Sscrofa10.2susScr3
ARHGAP21
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1924,325,648 - 24,459,006 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl924,326,454 - 24,406,743 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366605130,261,895 - 30,397,345 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Arhgap21
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247964,201,438 - 4,321,507 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247964,201,335 - 4,321,307 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in ARHGAP21
68 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 10p12.2-12.1(chr10:24111341-25350640)x1 copy number loss See cases [RCV000133897] Chr10:24111341..25350640 [GRCh38]
Chr10:24400270..25639569 [GRCh37]
Chr10:24440276..25679575 [NCBI36]
Chr10:10p12.2-12.1		 pathogenic
GRCh38/hg38 10p15.3-12.1(chr10:90421-29058318)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053512]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053512]|See cases [RCV000053512] Chr10:90421..29058318 [GRCh38]
Chr10:224406..29347247 [GRCh37]
Chr10:126361..29387253 [NCBI36]
Chr10:10p15.3-12.1		 pathogenic
NM_020824.3(ARHGAP21):c.5631C>G (p.Asn1877Lys) single nucleotide variant Malignant melanoma [RCV000068898] Chr10:24584658 [GRCh38]
Chr10:24873587 [GRCh37]
Chr10:24913593 [NCBI36]
Chr10:10p12.1		 not provided
GRCh38/hg38 10p15.3-12.1(chr10:90205-26339978)x3 copy number gain See cases [RCV000138428] Chr10:90205..26339978 [GRCh38]
Chr10:224406..26628907 [GRCh37]
Chr10:126145..26668913 [NCBI36]
Chr10:10p15.3-12.1		 pathogenic
GRCh38/hg38 10p12.31-11.22(chr10:19088161-32732293)x3 copy number gain See cases [RCV000139427] Chr10:19088161..32732293 [GRCh38]
Chr10:19377090..33021221 [GRCh37]
Chr10:19417096..33061227 [NCBI36]
Chr10:10p12.31-11.22		 likely pathogenic
GRCh38/hg38 10p15.1-q11.22(chr10:4604734-48074662)x3 copy number gain See cases [RCV000141497] Chr10:4604734..48074662 [GRCh38]
Chr10:4646926..47531169 [GRCh37]
Chr10:4636926..47125152 [NCBI36]
Chr10:10p15.1-q11.22		 benign
NM_020824.4(ARHGAP21):c.3491T>G (p.Ile1164Arg) single nucleotide variant Abnormality of brain morphology [RCV000454179] Chr10:24596030 [GRCh38]
Chr10:24884959 [GRCh37]
Chr10:10p12.1		 likely pathogenic
GRCh37/hg19 10p15.3-11.23(chr10:100026-30278548)x3 copy number gain See cases [RCV000447131] Chr10:100026..30278548 [GRCh37]
Chr10:10p15.3-11.23		 pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:93297-135378918)x3 copy number gain See cases [RCV000448750] Chr10:93297..135378918 [GRCh37]
Chr10:10p15.3-q26.3		 pathogenic
NM_020824.4(ARHGAP21):c.1790_1791del (p.Arg597fs) deletion not provided [RCV000481010] Chr10:24620104..24620105 [GRCh38]
Chr10:24909033..24909034 [GRCh37]
Chr10:10p12.1		 uncertain significance
GRCh37/hg19 10p12.1(chr10:24628319-26747630)x1 copy number loss See cases [RCV000511762] Chr10:24628319..26747630 [GRCh37]
Chr10:10p12.1		 uncertain significance
GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143) copy number gain See cases [RCV000511389] Chr10:100027..135427143 [GRCh37]
Chr10:10p15.3-q26.3		 pathogenic|uncertain significance
GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143)x3 copy number gain See cases [RCV000510861] Chr10:100027..135427143 [GRCh37]
Chr10:10p15.3-q26.3		 pathogenic
GRCh37/hg19 10p15.3-q11.23(chr10:100026-50961640)x3 copy number gain See cases [RCV000510893] Chr10:100026..50961640 [GRCh37]
Chr10:10p15.3-q11.23		 pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:73232-135524321)x3 copy number gain not provided [RCV000749464] Chr10:73232..135524321 [GRCh37]
Chr10:10p15.3-q26.3		 pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:98087-135477883)x3 copy number gain not provided [RCV000749465] Chr10:98087..135477883 [GRCh37]
Chr10:10p15.3-q26.3		 pathogenic
NM_020824.4(ARHGAP21):c.1474A>G (p.Arg492Gly) single nucleotide variant not provided [RCV000963068] Chr10:24620421 [GRCh38]
Chr10:24909350 [GRCh37]
Chr10:10p12.1		 likely benign
NM_020824.4(ARHGAP21):c.3047G>C (p.Cys1016Ser) single nucleotide variant not provided [RCV000914312] Chr10:24600731 [GRCh38]
Chr10:24889660 [GRCh37]
Chr10:10p12.1		 likely benign
NM_020824.4(ARHGAP21):c.960A>C (p.Pro320=) single nucleotide variant not provided [RCV000926685] Chr10:24620935 [GRCh38]
Chr10:24909864 [GRCh37]
Chr10:10p12.1		 benign
NM_020824.4(ARHGAP21):c.3621T>C (p.Asp1207=) single nucleotide variant not provided [RCV000964312] Chr10:24595900 [GRCh38]
Chr10:24884829 [GRCh37]
Chr10:10p12.1		 benign
NM_020824.4(ARHGAP21):c.2295C>T (p.Thr765=) single nucleotide variant not provided [RCV000880993] Chr10:24619600 [GRCh38]
Chr10:24908529 [GRCh37]
Chr10:10p12.1		 benign
NM_020824.4(ARHGAP21):c.2156A>G (p.Gln719Arg) single nucleotide variant not provided [RCV000922441] Chr10:24619739 [GRCh38]
Chr10:24908668 [GRCh37]
Chr10:10p12.1		 likely benign
NM_020824.4(ARHGAP21):c.3361G>A (p.Gly1121Ser) single nucleotide variant not provided [RCV000971564] Chr10:24596856 [GRCh38]
Chr10:24885785 [GRCh37]
Chr10:10p12.1		 benign
NM_020824.4(ARHGAP21):c.2051C>G (p.Ser684Cys) single nucleotide variant not provided [RCV000949762] Chr10:24619844 [GRCh38]
Chr10:24908773 [GRCh37]
Chr10:10p12.1		 likely benign
NM_020824.4(ARHGAP21):c.1944C>T (p.Asp648=) single nucleotide variant not provided [RCV000927221] Chr10:24619951 [GRCh38]
Chr10:24908880 [GRCh37]
Chr10:10p12.1		 likely benign
NM_020824.4(ARHGAP21):c.5849G>C (p.Ser1950Thr) single nucleotide variant not provided [RCV000948368] Chr10:24584440 [GRCh38]
Chr10:24873369 [GRCh37]
Chr10:10p12.1		 benign
NM_020824.4(ARHGAP21):c.5858_5859del (p.Glu1953fs) microsatellite not provided [RCV000886088] Chr10:24584430..24584431 [GRCh38]
Chr10:24873359..24873360 [GRCh37]
Chr10:10p12.1		 likely benign
NM_020824.4(ARHGAP21):c.5304G>T (p.Arg1768=) single nucleotide variant not provided [RCV000896323] Chr10:24584985 [GRCh38]
Chr10:24873914 [GRCh37]
Chr10:10p12.1		 likely benign
NM_020824.4(ARHGAP21):c.1826G>A (p.Arg609Gln) single nucleotide variant not provided [RCV000964313] Chr10:24620069 [GRCh38]
Chr10:24908998 [GRCh37]
Chr10:10p12.1		 benign
NM_020824.4(ARHGAP21):c.954A>C (p.Thr318=) single nucleotide variant not provided [RCV000964314] Chr10:24620941 [GRCh38]
Chr10:24909870 [GRCh37]
Chr10:10p12.1		 benign
NM_020824.4(ARHGAP21):c.2296G>A (p.Gly766Arg) single nucleotide variant not provided [RCV000893405] Chr10:24619599 [GRCh38]
Chr10:24908528 [GRCh37]
Chr10:10p12.1		 likely benign
NM_020824.4(ARHGAP21):c.5395C>A (p.Arg1799=) single nucleotide variant not provided [RCV000914311] Chr10:24584894 [GRCh38]
Chr10:24873823 [GRCh37]
Chr10:10p12.1		 likely benign
NM_020824.4(ARHGAP21):c.3787-8_3832dup duplication not provided [RCV000964311] Chr10:24594993..24594994 [GRCh38]
Chr10:24883922..24883923 [GRCh37]
Chr10:10p12.1		 benign
NM_020824.4(ARHGAP21):c.1015C>T (p.Leu339=) single nucleotide variant not provided [RCV000931594] Chr10:24620880 [GRCh38]
Chr10:24909809 [GRCh37]
Chr10:10p12.1		 likely benign
NM_020824.4(ARHGAP21):c.1872T>C (p.Asn624=) single nucleotide variant not provided [RCV000908025] Chr10:24620023 [GRCh38]
Chr10:24908952 [GRCh37]
Chr10:10p12.1		 likely benign
NM_020824.4(ARHGAP21):c.4134C>A (p.Ser1378=) single nucleotide variant not provided [RCV000892284] Chr10:24591241 [GRCh38]
Chr10:24880170 [GRCh37]
Chr10:10p12.1		 likely benign
NM_020824.4(ARHGAP21):c.3495T>A (p.Val1165=) single nucleotide variant not provided [RCV000899317] Chr10:24596026 [GRCh38]
Chr10:24884955 [GRCh37]
Chr10:10p12.1		 benign
NM_020824.4(ARHGAP21):c.5785G>A (p.Val1929Met) single nucleotide variant not provided [RCV000889343] Chr10:24584504 [GRCh38]
Chr10:24873433 [GRCh37]
Chr10:10p12.1		 likely benign
GRCh37/hg19 10p15.3-q11.22(chr10:135655-47688677)x4 copy number gain Mosaic supernumerary isodicentric chromosome 10 [RCV001825164] Chr10:135655..47688677 [GRCh37]
Chr10:10p15.3-q11.22		 not provided
GRCh37/hg19 10p15.1-11.21(chr10:6273934-34732521) copy number gain not specified [RCV002052863] Chr10:6273934..34732521 [GRCh37]
Chr10:10p15.1-11.21		 pathogenic
NM_020824.4(ARHGAP21):c.2593C>T (p.Pro865Ser) single nucleotide variant Inborn genetic diseases [RCV002749667] Chr10:24607590 [GRCh38]
Chr10:24896519 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.5758C>A (p.Gln1920Lys) single nucleotide variant Inborn genetic diseases [RCV002837138] Chr10:24584531 [GRCh38]
Chr10:24873460 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.1529A>G (p.Asn510Ser) single nucleotide variant Inborn genetic diseases [RCV002945116] Chr10:24620366 [GRCh38]
Chr10:24909295 [GRCh37]
Chr10:10p12.1		 likely benign
NM_020824.4(ARHGAP21):c.4835C>T (p.Ala1612Val) single nucleotide variant Inborn genetic diseases [RCV002905329] Chr10:24585454 [GRCh38]
Chr10:24874383 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.4436C>A (p.Thr1479Asn) single nucleotide variant Inborn genetic diseases [RCV002907281] Chr10:24585853 [GRCh38]
Chr10:24874782 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.4655C>T (p.Thr1552Met) single nucleotide variant Inborn genetic diseases [RCV002901768] Chr10:24585634 [GRCh38]
Chr10:24874563 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.3116G>A (p.Ser1039Asn) single nucleotide variant Inborn genetic diseases [RCV002906055] Chr10:24600662 [GRCh38]
Chr10:24889591 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.3740A>G (p.Asn1247Ser) single nucleotide variant Inborn genetic diseases [RCV002687356] Chr10:24595163 [GRCh38]
Chr10:24884092 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.38A>G (p.Asp13Gly) single nucleotide variant Inborn genetic diseases [RCV002992402] Chr10:24721862 [GRCh38]
Chr10:25010791 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.5198T>C (p.Val1733Ala) single nucleotide variant Inborn genetic diseases [RCV002797984] Chr10:24585091 [GRCh38]
Chr10:24874020 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.1295G>A (p.Arg432His) single nucleotide variant Inborn genetic diseases [RCV002978144] Chr10:24620600 [GRCh38]
Chr10:24909529 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.2845A>G (p.Lys949Glu) single nucleotide variant Inborn genetic diseases [RCV002869685] Chr10:24601980 [GRCh38]
Chr10:24890909 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.1894C>T (p.His632Tyr) single nucleotide variant Inborn genetic diseases [RCV002757190] Chr10:24620001 [GRCh38]
Chr10:24908930 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.2431A>G (p.Thr811Ala) single nucleotide variant Inborn genetic diseases [RCV002783710] Chr10:24607895 [GRCh38]
Chr10:24896824 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.2558G>A (p.Arg853His) single nucleotide variant Inborn genetic diseases [RCV002759822] Chr10:24607768 [GRCh38]
Chr10:24896697 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.2899G>A (p.Gly967Ser) single nucleotide variant Inborn genetic diseases [RCV002707275] Chr10:24600879 [GRCh38]
Chr10:24889808 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.907T>C (p.Tyr303His) single nucleotide variant Inborn genetic diseases [RCV002757678] Chr10:24620988 [GRCh38]
Chr10:24909917 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.803A>G (p.Asn268Ser) single nucleotide variant Inborn genetic diseases [RCV002701998] Chr10:24621092 [GRCh38]
Chr10:24910021 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.1892C>T (p.Thr631Met) single nucleotide variant Inborn genetic diseases [RCV003003440] Chr10:24620003 [GRCh38]
Chr10:24908932 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.4962C>A (p.Phe1654Leu) single nucleotide variant Inborn genetic diseases [RCV002640980] Chr10:24585327 [GRCh38]
Chr10:24874256 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.1028G>A (p.Gly343Glu) single nucleotide variant Inborn genetic diseases [RCV002873120] Chr10:24620867 [GRCh38]
Chr10:24909796 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.3743G>A (p.Arg1248His) single nucleotide variant Inborn genetic diseases [RCV002742507] Chr10:24595160 [GRCh38]
Chr10:24884089 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.641T>C (p.Met214Thr) single nucleotide variant Inborn genetic diseases [RCV002854166] Chr10:24621254 [GRCh38]
Chr10:24910183 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.722G>C (p.Gly241Ala) single nucleotide variant Inborn genetic diseases [RCV002789205] Chr10:24621173 [GRCh38]
Chr10:24910102 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.3481A>G (p.Ile1161Val) single nucleotide variant Inborn genetic diseases [RCV002809593] Chr10:24596040 [GRCh38]
Chr10:24884969 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.2756G>T (p.Gly919Val) single nucleotide variant Inborn genetic diseases [RCV002807984] Chr10:24602069 [GRCh38]
Chr10:24890998 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.2146T>A (p.Leu716Ile) single nucleotide variant Inborn genetic diseases [RCV002935570] Chr10:24619749 [GRCh38]
Chr10:24908678 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.1609A>G (p.Arg537Gly) single nucleotide variant Inborn genetic diseases [RCV002669397] Chr10:24620286 [GRCh38]
Chr10:24909215 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.1021C>A (p.Pro341Thr) single nucleotide variant Inborn genetic diseases [RCV002672793] Chr10:24620874 [GRCh38]
Chr10:24909803 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.2003G>A (p.Arg668Lys) single nucleotide variant Inborn genetic diseases [RCV002792391] Chr10:24619892 [GRCh38]
Chr10:24908821 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.1877T>C (p.Leu626Pro) single nucleotide variant Inborn genetic diseases [RCV002808348] Chr10:24620018 [GRCh38]
Chr10:24908947 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.155C>G (p.Thr52Arg) single nucleotide variant Inborn genetic diseases [RCV002896578] Chr10:24670306 [GRCh38]
Chr10:24959235 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.881C>T (p.Pro294Leu) single nucleotide variant Inborn genetic diseases [RCV002674921] Chr10:24621014 [GRCh38]
Chr10:24909943 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.5186C>T (p.Ser1729Leu) single nucleotide variant Inborn genetic diseases [RCV002702316] Chr10:24585103 [GRCh38]
Chr10:24874032 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.2945C>T (p.Pro982Leu) single nucleotide variant Inborn genetic diseases [RCV002678920] Chr10:24600833 [GRCh38]
Chr10:24889762 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.5362G>A (p.Val1788Met) single nucleotide variant Inborn genetic diseases [RCV002652409] Chr10:24584927 [GRCh38]
Chr10:24873856 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.5575C>T (p.Arg1859Cys) single nucleotide variant Inborn genetic diseases [RCV003196581] Chr10:24584714 [GRCh38]
Chr10:24873643 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.647A>G (p.Gln216Arg) single nucleotide variant Inborn genetic diseases [RCV003189529] Chr10:24621248 [GRCh38]
Chr10:24910177 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.5744C>T (p.Pro1915Leu) single nucleotide variant Inborn genetic diseases [RCV003202121] Chr10:24584545 [GRCh38]
Chr10:24873474 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.4631C>G (p.Ser1544Cys) single nucleotide variant Inborn genetic diseases [RCV003211821] Chr10:24585658 [GRCh38]
Chr10:24874587 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.346G>A (p.Ala116Thr) single nucleotide variant Inborn genetic diseases [RCV003198170] Chr10:24635026 [GRCh38]
Chr10:24923955 [GRCh37]
Chr10:10p12.1		 uncertain significance
NM_020824.4(ARHGAP21):c.1613G>A (p.Arg538Gln) single nucleotide variant Inborn genetic diseases [RCV003214544] Chr10:24620282 [GRCh38]
Chr10:24909211 [GRCh37]
Chr10:10p12.1		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2030
Count of miRNA genes:1049
Interacting mature miRNAs:1251
Transcripts:ENST00000320481, ENST00000376410, ENST00000396432, ENST00000416305, ENST00000418033, ENST00000418325, ENST00000446003, ENST00000463892, ENST00000472150, ENST00000476067, ENST00000476499, ENST00000477190, ENST00000482792, ENST00000483114, ENST00000486374, ENST00000493154
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.

Markers in Region
RH65067  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37680,775,193 - 80,775,293UniSTSGRCh37
GRCh371024,874,534 - 24,874,634UniSTSGRCh37
Build 36680,831,912 - 80,832,012RGDNCBI36
Celera1024,567,857 - 24,567,957UniSTS
Celera1024,569,283 - 24,569,383UniSTS
Celera681,193,214 - 81,193,314RGD
Celera1024,567,287 - 24,567,387UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map10p12.3UniSTS
HuRef1024,536,084 - 24,536,184UniSTS
HuRef677,998,023 - 77,998,123UniSTS
RH66951  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371024,873,609 - 24,873,737UniSTSGRCh37
GRCh37680,774,270 - 80,774,398UniSTSGRCh37
Build 36680,830,989 - 80,831,117RGDNCBI36
Celera1024,565,517 - 24,565,645UniSTS
Celera681,192,291 - 81,192,419RGD
Celera1024,566,362 - 24,566,490UniSTS
Cytogenetic Map10p12.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map6q14.1UniSTS
HuRef1024,535,159 - 24,535,287UniSTS
HuRef677,997,100 - 77,997,228UniSTS
SHGC-144197  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371024,951,935 - 24,952,209UniSTSGRCh37
Build 361024,991,941 - 24,992,215RGDNCBI36
Celera1024,652,282 - 24,652,556RGD
Cytogenetic Map10p12.3UniSTS
Cytogenetic Map10p12.1UniSTS
HuRef1024,612,875 - 24,613,149UniSTS
TNG Radiation Hybrid Map1012749.0UniSTS
RH37461  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37680,776,439 - 80,776,622UniSTSGRCh37
GRCh371024,885,708 - 24,886,455UniSTSGRCh37
Build 36680,833,158 - 80,833,341RGDNCBI36
Celera1024,580,456 - 24,581,200UniSTS
Celera681,194,460 - 81,194,643RGD
Cytogenetic Map10p12.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map6q14.1UniSTS
HuRef677,999,269 - 77,999,452UniSTS
HuRef1024,547,279 - 24,548,026UniSTS
GeneMap99-GB4 RH Map6354.97UniSTS
NCBI RH Map6933.3UniSTS
RH45030  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371025,002,403 - 25,002,505UniSTSGRCh37
Build 361025,042,409 - 25,042,511RGDNCBI36
Celera1024,702,702 - 24,702,804RGD
Cytogenetic Map10p12.3UniSTS
Cytogenetic Map10p12.1UniSTS
HuRef1024,663,298 - 24,663,400UniSTS
GeneMap99-GB4 RH Map10147.42UniSTS
D10Ulb1  
Human AssemblyChrPosition (strand)SourceJBrowse
Celera1024,568,427 - 24,568,532UniSTS
Celera1024,568,997 - 24,569,388UniSTS
D10S275  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map13q12.13UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map1p35.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map14q22-q24UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map10p11UniSTS
Cytogenetic Map1p13.1UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map6q24UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map9q13-q21UniSTS
Cytogenetic Map3p25UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map9q22UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic MapXp22.2-p22.1UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map20pter-q11.23UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map10p12.3UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map3q26.3UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map1q24-q25.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map12q24.32UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q24.1UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map11p14.3UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map4q13UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map7p14.2UniSTS
Cytogenetic Map6q24.3UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map6q12-q13UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map2p14UniSTS
SHGC-146218  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map10p12.3UniSTS
Cytogenetic Map10p12.1UniSTS
RH68400  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map10p12.3UniSTS
Cytogenetic Map10p12.1UniSTS


Expression


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

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 2397 2004 1400 313 679 159 4077 1910 3692 276 1393 1577 166 1203 2611 4
Low 39 909 325 310 1171 305 279 285 40 142 62 35 7 1 1 177 1
Below cutoff 2 76 1 94 1 1 2 1 3 1 1 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001367447 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001367448 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001367449 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001367450 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001367451 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001367452 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001367453 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001367454 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001367455 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_020824 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_160021 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_160022 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_160023 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_160024 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_160025 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011519602 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011519603 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011519604 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011519605 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011519606 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011519607 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017016459 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448088 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047425556 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047425557 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047425559 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047425560 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047425561 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047425562 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047425563 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054366407 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054366408 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054366409 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054366410 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054366411 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054366412 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054366413 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054366414 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054366415 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054366416 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054366417 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054366418 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054366419 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001747160 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001747163 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_242701 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_930513 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB037845 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF480466 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK074589 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK090642 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK295649 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK297278 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK307604 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL355979 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL392104 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL834495 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AV709499 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AV709848 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC022931 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC118915 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BI491305 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ026288 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX537570 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471072 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068268 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000320481   ⟹   ENSP00000365604
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1024,584,387 - 24,721,990 (-)Ensembl
RefSeq Acc Id: ENST00000376410   ⟹   ENSP00000365592
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1024,583,617 - 24,723,233 (-)Ensembl
RefSeq Acc Id: ENST00000396432   ⟹   ENSP00000379709
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1024,583,614 - 24,723,887 (-)Ensembl
RefSeq Acc Id: ENST00000416305   ⟹   ENSP00000400566
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1024,629,524 - 24,721,866 (-)Ensembl
RefSeq Acc Id: ENST00000418033   ⟹   ENSP00000389940
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1024,586,033 - 24,595,960 (-)Ensembl
RefSeq Acc Id: ENST00000418325   ⟹   ENSP00000402761
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1024,594,970 - 24,596,043 (-)Ensembl
RefSeq Acc Id: ENST00000446003   ⟹   ENSP00000405018
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1024,596,822 - 24,723,240 (-)Ensembl
RefSeq Acc Id: ENST00000463892
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1024,722,012 - 24,722,760 (-)Ensembl
RefSeq Acc Id: ENST00000472150
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1024,670,339 - 24,723,247 (-)Ensembl
RefSeq Acc Id: ENST00000476067
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1024,607,444 - 24,607,878 (-)Ensembl
RefSeq Acc Id: ENST00000476499
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1024,629,014 - 24,722,034 (-)Ensembl
RefSeq Acc Id: ENST00000477190
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1024,585,920 - 24,590,042 (-)Ensembl
RefSeq Acc Id: ENST00000482792
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1024,591,345 - 24,595,036 (-)Ensembl
RefSeq Acc Id: ENST00000483114
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1024,620,879 - 24,622,842 (-)Ensembl
RefSeq Acc Id: ENST00000486374
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1024,583,614 - 24,621,369 (-)Ensembl
RefSeq Acc Id: ENST00000493154
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1024,597,469 - 24,607,871 (-)Ensembl
RefSeq Acc Id: ENST00000612832   ⟹   ENSP00000480005
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1024,583,609 - 24,723,668 (-)Ensembl
RefSeq Acc Id: ENST00000636789   ⟹   ENSP00000490396
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1024,585,930 - 24,622,834 (-)Ensembl
RefSeq Acc Id: ENST00000636842   ⟹   ENSP00000490730
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1024,629,996 - 24,706,630 (-)Ensembl
RefSeq Acc Id: ENST00000638156   ⟹   ENSP00000489905
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1024,583,631 - 24,602,103 (-)Ensembl
RefSeq Acc Id: ENST00000680286   ⟹   ENSP00000506388
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1024,583,614 - 24,706,630 (-)Ensembl
RefSeq Acc Id: NM_001367447   ⟹   NP_001354376
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381024,583,614 - 24,723,887 (-)NCBI
T2T-CHM13v2.01024,602,382 - 24,742,515 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001367448   ⟹   NP_001354377
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381024,583,614 - 24,723,221 (-)NCBI
T2T-CHM13v2.01024,602,382 - 24,741,849 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001367449   ⟹   NP_001354378
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381024,583,614 - 24,723,221 (-)NCBI
T2T-CHM13v2.01024,602,382 - 24,741,849 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001367450   ⟹   NP_001354379
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381024,583,614 - 24,723,221 (-)NCBI
T2T-CHM13v2.01024,602,382 - 24,741,849 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001367451   ⟹   NP_001354380
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381024,583,614 - 24,723,221 (-)NCBI
T2T-CHM13v2.01024,602,382 - 24,741,849 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001367452   ⟹   NP_001354381
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381024,583,614 - 24,723,221 (-)NCBI
T2T-CHM13v2.01024,602,382 - 24,741,849 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001367453   ⟹   NP_001354382
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381024,583,614 - 24,722,748 (-)NCBI
T2T-CHM13v2.01024,602,382 - 24,741,376 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001367454   ⟹   NP_001354383
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381024,583,614 - 24,722,748 (-)NCBI
T2T-CHM13v2.01024,602,382 - 24,741,376 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001367455   ⟹   NP_001354384
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381024,583,614 - 24,622,843 (-)NCBI
T2T-CHM13v2.01024,602,382 - 24,641,607 (-)NCBI
Sequence:
RefSeq Acc Id: NM_020824   ⟹   NP_065875
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381024,583,614 - 24,723,887 (-)NCBI
GRCh371024,872,538 - 25,012,597 (-)RGD
Build 361024,912,549 - 25,052,550 (-)NCBI Archive
Celera1024,564,446 - 24,712,895 (-)RGD
HuRef1024,534,090 - 24,673,492 (-)ENTREZGENE
CHM1_11024,872,464 - 25,013,653 (-)NCBI
T2T-CHM13v2.01024,602,382 - 24,742,515 (-)NCBI
Sequence:
RefSeq Acc Id: NR_160021
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381024,583,614 - 24,723,221 (-)NCBI
T2T-CHM13v2.01024,602,382 - 24,741,849 (-)NCBI
Sequence:
RefSeq Acc Id: NR_160022
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381024,583,614 - 24,723,221 (-)NCBI
T2T-CHM13v2.01024,602,382 - 24,741,849 (-)NCBI
Sequence:
RefSeq Acc Id: NR_160023
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381024,583,614 - 24,722,748 (-)NCBI
T2T-CHM13v2.01024,602,382 - 24,741,376 (-)NCBI
Sequence:
RefSeq Acc Id: NR_160024
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381024,583,614 - 24,622,843 (-)NCBI
T2T-CHM13v2.01024,602,382 - 24,641,607 (-)NCBI
Sequence:
RefSeq Acc Id: NR_160025
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381024,583,614 - 24,622,843 (-)NCBI
T2T-CHM13v2.01024,602,382 - 24,641,607 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011519602   ⟹   XP_011517904
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381024,583,614 - 24,723,887 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011519603   ⟹   XP_011517905
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381024,583,614 - 24,722,748 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011519604   ⟹   XP_011517906
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381024,583,614 - 24,723,221 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011519605   ⟹   XP_011517907
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381024,583,614 - 24,723,887 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011519606   ⟹   XP_011517908
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381024,583,614 - 24,653,258 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011519607   ⟹   XP_011517909
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381024,583,614 - 24,723,887 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047425556   ⟹   XP_047281512
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381024,583,614 - 24,722,748 (-)NCBI
RefSeq Acc Id: XM_047425557   ⟹   XP_047281513
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381024,583,614 - 24,723,221 (-)NCBI
RefSeq Acc Id: XM_047425559   ⟹   XP_047281515
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381024,590,206 - 24,723,887 (-)NCBI
RefSeq Acc Id: XM_047425560   ⟹   XP_047281516
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381024,583,614 - 24,723,887 (-)NCBI
RefSeq Acc Id: XM_047425561   ⟹   XP_047281517
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381024,583,614 - 24,723,887 (-)NCBI
RefSeq Acc Id: XM_047425562   ⟹   XP_047281518
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381024,583,614 - 24,723,221 (-)NCBI
RefSeq Acc Id: XM_047425563   ⟹   XP_047281519
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381024,590,206 - 24,723,887 (-)NCBI
RefSeq Acc Id: XM_054366407   ⟹   XP_054222382
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01024,602,382 - 24,742,515 (-)NCBI
RefSeq Acc Id: XM_054366408   ⟹   XP_054222383
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01024,602,382 - 24,741,376 (-)NCBI
RefSeq Acc Id: XM_054366409   ⟹   XP_054222384
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01024,602,382 - 24,741,849 (-)NCBI
RefSeq Acc Id: XM_054366410   ⟹   XP_054222385
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01024,602,382 - 24,742,515 (-)NCBI
RefSeq Acc Id: XM_054366411   ⟹   XP_054222386
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01024,602,382 - 24,741,376 (-)NCBI
RefSeq Acc Id: XM_054366412   ⟹   XP_054222387
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01024,602,382 - 24,741,849 (-)NCBI
RefSeq Acc Id: XM_054366413   ⟹   XP_054222388
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01024,602,382 - 24,672,057 (-)NCBI
RefSeq Acc Id: XM_054366414   ⟹   XP_054222389
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01024,602,382 - 24,742,515 (-)NCBI
RefSeq Acc Id: XM_054366415   ⟹   XP_054222390
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01024,608,974 - 24,742,515 (-)NCBI
RefSeq Acc Id: XM_054366416   ⟹   XP_054222391
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01024,602,382 - 24,742,515 (-)NCBI
RefSeq Acc Id: XM_054366417   ⟹   XP_054222392
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01024,602,382 - 24,742,515 (-)NCBI
RefSeq Acc Id: XM_054366418   ⟹   XP_054222393
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01024,602,382 - 24,741,849 (-)NCBI
RefSeq Acc Id: XM_054366419   ⟹   XP_054222394
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01024,608,974 - 24,742,515 (-)NCBI
Protein Sequences
Protein RefSeqs NP_001354376 (Get FASTA)   NCBI Sequence Viewer  
  NP_001354377 (Get FASTA)   NCBI Sequence Viewer  
  NP_001354378 (Get FASTA)   NCBI Sequence Viewer  
  NP_001354379 (Get FASTA)   NCBI Sequence Viewer  
  NP_001354380 (Get FASTA)   NCBI Sequence Viewer  
  NP_001354381 (Get FASTA)   NCBI Sequence Viewer  
  NP_001354382 (Get FASTA)   NCBI Sequence Viewer  
  NP_001354383 (Get FASTA)   NCBI Sequence Viewer  
  NP_001354384 (Get FASTA)   NCBI Sequence Viewer  
  NP_065875 (Get FASTA)   NCBI Sequence Viewer  
  XP_011517904 (Get FASTA)   NCBI Sequence Viewer  
  XP_011517905 (Get FASTA)   NCBI Sequence Viewer  
  XP_011517906 (Get FASTA)   NCBI Sequence Viewer  
  XP_011517907 (Get FASTA)   NCBI Sequence Viewer  
  XP_011517908 (Get FASTA)   NCBI Sequence Viewer  
  XP_011517909 (Get FASTA)   NCBI Sequence Viewer  
  XP_047281512 (Get FASTA)   NCBI Sequence Viewer  
  XP_047281513 (Get FASTA)   NCBI Sequence Viewer  
  XP_047281515 (Get FASTA)   NCBI Sequence Viewer  
  XP_047281516 (Get FASTA)   NCBI Sequence Viewer  
  XP_047281517 (Get FASTA)   NCBI Sequence Viewer  
  XP_047281518 (Get FASTA)   NCBI Sequence Viewer  
  XP_047281519 (Get FASTA)   NCBI Sequence Viewer  
  XP_054222382 (Get FASTA)   NCBI Sequence Viewer  
  XP_054222383 (Get FASTA)   NCBI Sequence Viewer  
  XP_054222384 (Get FASTA)   NCBI Sequence Viewer  
  XP_054222385 (Get FASTA)   NCBI Sequence Viewer  
  XP_054222386 (Get FASTA)   NCBI Sequence Viewer  
  XP_054222387 (Get FASTA)   NCBI Sequence Viewer  
  XP_054222388 (Get FASTA)   NCBI Sequence Viewer  
  XP_054222389 (Get FASTA)   NCBI Sequence Viewer  
  XP_054222390 (Get FASTA)   NCBI Sequence Viewer  
  XP_054222391 (Get FASTA)   NCBI Sequence Viewer  
  XP_054222392 (Get FASTA)   NCBI Sequence Viewer  
  XP_054222393 (Get FASTA)   NCBI Sequence Viewer  
  XP_054222394 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH22931 (Get FASTA)   NCBI Sequence Viewer  
  AAI18916 (Get FASTA)   NCBI Sequence Viewer  
  AAM22955 (Get FASTA)   NCBI Sequence Viewer  
  BAA92662 (Get FASTA)   NCBI Sequence Viewer  
  BAG59749 (Get FASTA)   NCBI Sequence Viewer  
  BAH12139 (Get FASTA)   NCBI Sequence Viewer  
  CAD39153 (Get FASTA)   NCBI Sequence Viewer  
  CAD97787 (Get FASTA)   NCBI Sequence Viewer  
  EAW86122 (Get FASTA)   NCBI Sequence Viewer  
  Q5T5U3 (Get FASTA)   NCBI Sequence Viewer  
Reference Sequences
RefSeq Acc Id: NP_065875   ⟸   NM_020824
- Peptide Label: isoform a
- UniProtKB: Q9P2C3 (UniProtKB/Swiss-Prot),   Q5T5U3 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_011517907   ⟸   XM_011519605
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_011517904   ⟸   XM_011519602
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_011517906   ⟸   XM_011519604
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_011517905   ⟸   XM_011519603
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_011517908   ⟸   XM_011519606
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: XP_011517909   ⟸   XM_011519607
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: NP_001354376   ⟸   NM_001367447
- Peptide Label: isoform b
- UniProtKB: A0A805TBS0 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001354381   ⟸   NM_001367452
- Peptide Label: isoform d
RefSeq Acc Id: NP_001354380   ⟸   NM_001367451
- Peptide Label: isoform b
- UniProtKB: A0A805TBS0 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001354377   ⟸   NM_001367448
- Peptide Label: isoform a
- UniProtKB: Q9P2C3 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: NP_001354379   ⟸   NM_001367450
- Peptide Label: isoform c
RefSeq Acc Id: NP_001354378   ⟸   NM_001367449
- Peptide Label: isoform c
RefSeq Acc Id: NP_001354383   ⟸   NM_001367454
- Peptide Label: isoform a
- UniProtKB: Q9P2C3 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: NP_001354382   ⟸   NM_001367453
- Peptide Label: isoform b
- UniProtKB: A0A805TBS0 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001354384   ⟸   NM_001367455
- Peptide Label: isoform e
RefSeq Acc Id: ENSP00000490730   ⟸   ENST00000636842
RefSeq Acc Id: ENSP00000490396   ⟸   ENST00000636789
RefSeq Acc Id: ENSP00000365604   ⟸   ENST00000320481
RefSeq Acc Id: ENSP00000489905   ⟸   ENST00000638156
RefSeq Acc Id: ENSP00000365592   ⟸   ENST00000376410
RefSeq Acc Id: ENSP00000480005   ⟸   ENST00000612832
RefSeq Acc Id: ENSP00000400566   ⟸   ENST00000416305
RefSeq Acc Id: ENSP00000402761   ⟸   ENST00000418325
RefSeq Acc Id: ENSP00000389940   ⟸   ENST00000418033
RefSeq Acc Id: ENSP00000405018   ⟸   ENST00000446003
RefSeq Acc Id: ENSP00000379709   ⟸   ENST00000396432
RefSeq Acc Id: ENSP00000506388   ⟸   ENST00000680286
RefSeq Acc Id: XP_047281517   ⟸   XM_047425561
- Peptide Label: isoform X7
RefSeq Acc Id: XP_047281516   ⟸   XM_047425560
- Peptide Label: isoform X6
RefSeq Acc Id: XP_047281518   ⟸   XM_047425562
- Peptide Label: isoform X7
RefSeq Acc Id: XP_047281513   ⟸   XM_047425557
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047281512   ⟸   XM_047425556
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047281519   ⟸   XM_047425563
- Peptide Label: isoform X8
RefSeq Acc Id: XP_047281515   ⟸   XM_047425559
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054222392   ⟸   XM_054366417
- Peptide Label: isoform X7
RefSeq Acc Id: XP_054222385   ⟸   XM_054366410
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054222391   ⟸   XM_054366416
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054222389   ⟸   XM_054366414
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054222382   ⟸   XM_054366407
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054222393   ⟸   XM_054366418
- Peptide Label: isoform X7
RefSeq Acc Id: XP_054222387   ⟸   XM_054366412
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054222384   ⟸   XM_054366409
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054222386   ⟸   XM_054366411
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054222383   ⟸   XM_054366408
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054222388   ⟸   XM_054366413
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054222394   ⟸   XM_054366419
- Peptide Label: isoform X8
RefSeq Acc Id: XP_054222390   ⟸   XM_054366415
- Peptide Label: isoform X5
Protein Domains
PDZ   PH   Rho-GAP

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q5T5U3-F1-model_v2 AlphaFold Q5T5U3 1-1958 view protein structure

Promoters
RGD ID:7217199
Promoter ID:EPDNEW_H14344
Type:initiation region
Name:ARHGAP21_2
Description:Rho GTPase activating protein 21
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H14345  EPDNEW_H14346  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381024,723,220 - 24,723,280EPDNEW
RGD ID:7217197
Promoter ID:EPDNEW_H14345
Type:initiation region
Name:ARHGAP21_3
Description:Rho GTPase activating protein 21
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H14344  EPDNEW_H14346  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381024,723,710 - 24,723,770EPDNEW
RGD ID:7217203
Promoter ID:EPDNEW_H14346
Type:initiation region
Name:ARHGAP21_1
Description:Rho GTPase activating protein 21
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H14345  EPDNEW_H14344  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381024,724,631 - 24,724,691EPDNEW
RGD ID:6787354
Promoter ID:HG_KWN:8889
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000376410,   ENST00000396432,   NM_020824,   OTTHUMT00000047235,   OTTHUMT00000047236,   OTTHUMT00000327385,   UC001ISC.1,   UC001ISD.1,   UC009XKL.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361025,051,776 - 25,053,602 (-)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:23725 AgrOrtholog
COSMIC ARHGAP21 COSMIC
Ensembl Genes ENSG00000107863 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000365592 ENTREZGENE
  ENSP00000365592.3 UniProtKB/TrEMBL
  ENSP00000379709 ENTREZGENE
  ENSP00000379709.2 UniProtKB/Swiss-Prot
  ENSP00000389940.1 UniProtKB/TrEMBL
  ENSP00000400566.1 UniProtKB/TrEMBL
  ENSP00000402761.1 UniProtKB/TrEMBL
  ENSP00000405018.1 UniProtKB/TrEMBL
  ENSP00000480005.1 UniProtKB/TrEMBL
  ENSP00000489905.1 UniProtKB/TrEMBL
  ENSP00000490396 ENTREZGENE
  ENSP00000490396.1 UniProtKB/TrEMBL
  ENSP00000506388 ENTREZGENE
  ENSP00000506388.1 UniProtKB/TrEMBL
Ensembl Transcript ENST00000376410 ENTREZGENE
  ENST00000376410.7 UniProtKB/TrEMBL
  ENST00000396432 ENTREZGENE
  ENST00000396432.7 UniProtKB/Swiss-Prot
  ENST00000416305.1 UniProtKB/TrEMBL
  ENST00000418033.5 UniProtKB/TrEMBL
  ENST00000418325.1 UniProtKB/TrEMBL
  ENST00000446003.5 UniProtKB/TrEMBL
  ENST00000486374 ENTREZGENE
  ENST00000612832.4 UniProtKB/TrEMBL
  ENST00000636789 ENTREZGENE
  ENST00000636789.1 UniProtKB/TrEMBL
  ENST00000638156.1 UniProtKB/TrEMBL
  ENST00000680286 ENTREZGENE
  ENST00000680286.1 UniProtKB/TrEMBL
Gene3D-CATH 1.10.555.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  1.20.5.220 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  2.30.29.30 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  2.30.42.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000107863 GTEx
HGNC ID HGNC:23725 ENTREZGENE
Human Proteome Map ARHGAP21 Human Proteome Map
InterPro PDZ UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PDZ_6 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PDZ_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PH-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PH_domain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Rho_GTPase_activation_prot UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RhoGAP_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:57584 UniProtKB/Swiss-Prot
NCBI Gene 57584 ENTREZGENE
OMIM 609870 OMIM
PANTHER PDZ DOMAIN-CONTAINING PROTEIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RHO GTPASE-ACTIVATING PROTEIN 21 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam PDZ_6 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PF00169 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RhoGAP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134973559 PharmGKB
PROSITE PDZ UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PH_DOMAIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RHOGAP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART PDZ UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RhoGAP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SM00233 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP PH domain-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF48350 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF50156 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A087WW76_HUMAN UniProtKB/TrEMBL
  A0A1B0GTZ9_HUMAN UniProtKB/TrEMBL
  A0A1B0GV73_HUMAN UniProtKB/TrEMBL
  A0A2X0SF83_HUMAN UniProtKB/TrEMBL
  A0A7P0TAS2_HUMAN UniProtKB/TrEMBL
  A0A805TBS0 ENTREZGENE, UniProtKB/TrEMBL
  E7ESW5_HUMAN UniProtKB/TrEMBL
  H0Y468_HUMAN UniProtKB/TrEMBL
  H0Y5T2_HUMAN UniProtKB/TrEMBL
  J3JSM9_HUMAN UniProtKB/TrEMBL
  L8EB25_HUMAN UniProtKB/TrEMBL
  Q5JSD8_HUMAN UniProtKB/TrEMBL
  Q5T5U3 ENTREZGENE
  Q9P2C3 ENTREZGENE
  RHG21_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary Q0VF98 UniProtKB/Swiss-Prot
  Q7Z3P7 UniProtKB/Swiss-Prot
  Q8N3A2 UniProtKB/Swiss-Prot
  Q8NI19 UniProtKB/Swiss-Prot
  Q8TBV5 UniProtKB/Swiss-Prot
  Q9P2C3 UniProtKB/Swiss-Prot