NTRK3 (neurotrophic receptor tyrosine kinase 3) - Rat Genome Database

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Gene: NTRK3 (neurotrophic receptor tyrosine kinase 3) Homo sapiens
Analyze
Symbol: NTRK3
Name: neurotrophic receptor tyrosine kinase 3
RGD ID: 1354062
HGNC Page HGNC:8033
Description: Enables neurotrophin receptor activity and p53 binding activity. Involved in several processes, including positive regulation of cell migration; positive regulation of positive chemotaxis; and regulation of protein phosphorylation. Part of receptor complex. Implicated in adenoid cystic carcinoma; colorectal cancer; and stomach cancer. Biomarker of invasive ductal carcinoma and pancreatic ductal carcinoma.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: ETS related protein-neurotrophic receptor tyrosine kinase fusion protein; ETV6-NTRK3 fusion; gp145(trkC); GP145-TrkC; neurotrophic tyrosine kinase, receptor, type 3; neurotrophin 3 receptor; neurotrophin 3 receptor truncated isoform; NT-3 growth factor receptor; trk-C; TRKC; trkC tyrosine kinase; tyrosine kinase receptor C
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
GRCh381587,859,751 - 88,256,739 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1587,859,751 - 88,256,791 (-)EnsemblGRCh38hg38GRCh38
GRCh371588,402,982 - 88,799,970 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361586,220,992 - 86,600,665 (-)NCBINCBI36Build 36hg18NCBI36
Build 341586,220,991 - 86,600,665NCBI
Celera1564,821,267 - 65,200,916 (-)NCBICelera
Cytogenetic Map15q25.3NCBI
HuRef1564,532,241 - 64,911,404 (-)NCBIHuRef
CHM1_11588,261,800 - 88,641,816 (-)NCBICHM1_1
T2T-CHM13v2.01585,614,323 - 86,011,407 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(+)-pilocarpine  (ISO)
17beta-estradiol  (EXP,ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
3,4-methylenedioxymethamphetamine  (ISO)
4,4'-sulfonyldiphenol  (EXP,ISO)
4-hydroxyphenyl retinamide  (ISO)
aflatoxin B1  (EXP)
all-trans-retinoic acid  (EXP)
alpha-Zearalanol  (ISO)
amiodarone  (EXP)
ammonium chloride  (ISO)
androgen antagonist  (ISO)
antirheumatic drug  (EXP)
arsane  (EXP)
arsenic atom  (EXP)
arsenite(3-)  (EXP)
arsenous acid  (EXP)
atrazine  (EXP,ISO)
belinostat  (EXP)
benzalkonium chloride  (EXP)
benzo[a]pyrene  (EXP,ISO)
bis(2-ethylhexyl) phthalate  (EXP)
bisphenol A  (ISO)
bisphenol F  (ISO)
butanal  (EXP)
Butylparaben  (ISO)
C60 fullerene  (ISO)
cadmium dichloride  (EXP,ISO)
calcitriol  (EXP)
calcium silicate  (ISO)
chlorpyrifos  (ISO)
choline  (ISO)
cisplatin  (ISO)
corticosterone  (ISO)
crocidolite asbestos  (EXP)
Cuprizon  (ISO)
diarsenic trioxide  (EXP)
diazinon  (ISO)
dieldrin  (ISO)
doxorubicin  (EXP)
enzacamene  (ISO)
ethyl methanesulfonate  (EXP)
folic acid  (ISO)
fonofos  (EXP)
fulvestrant  (EXP)
L-methionine  (ISO)
manganese atom  (EXP,ISO)
manganese(0)  (EXP,ISO)
manganese(II) chloride  (EXP,ISO)
mercury atom  (EXP)
mercury(0)  (EXP)
methylmercury chloride  (EXP)
N-nitrosodiethylamine  (ISO)
nickel atom  (EXP,ISO)
nitrofen  (ISO)
paracetamol  (EXP,ISO)
parathion  (EXP)
pentobarbital  (ISO)
perfluorooctanoic acid  (ISO)
phenobarbital  (ISO)
ponatinib  (EXP)
potassium dichromate  (ISO)
progesterone  (EXP)
resveratrol  (EXP)
rotenone  (EXP)
sarin  (EXP)
scopolamine  (ISO)
silicon dioxide  (EXP)
terbufos  (EXP)
thimerosal  (ISO)
titanium dioxide  (EXP,ISO)
triclosan  (EXP)
trimethyltin  (ISO)
triptonide  (ISO)
valproic acid  (EXP,ISO)
venlafaxine hydrochloride  (ISO)

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process
axon extension involved in regeneration  (ISO)
axon guidance  (IEA)
cell differentiation  (IEA)
cell surface receptor protein tyrosine kinase signaling pathway  (IDA,IEA,TAS)
cellular response to nerve growth factor stimulus  (IBA,IEA)
cellular response to retinoic acid  (ISO)
circadian rhythm  (ISO)
cochlea development  (ISO)
dendrite self-avoidance  (IEA)
heart development  (IMP)
homophilic cell adhesion via plasma membrane adhesion molecules  (IEA)
lens fiber cell differentiation  (ISO)
mechanoreceptor differentiation  (ISO)
myelination in peripheral nervous system  (ISO)
negative regulation of astrocyte differentiation  (ISO)
negative regulation of protein phosphorylation  (IDA)
nervous system development  (IEA)
neuron fate specification  (ISO)
neuron migration  (ISO)
neuronal action potential propagation  (ISO)
neurotrophin signaling pathway  (IEA)
positive regulation of apoptotic process  (ISO)
positive regulation of axon extension involved in regeneration  (ISO)
positive regulation of cell migration  (IDA)
positive regulation of cell population proliferation  (IDA)
positive regulation of ERK1 and ERK2 cascade  (IBA)
positive regulation of gene expression  (IDA)
positive regulation of neuron projection development  (IBA,IEA,ISO)
positive regulation of peptidyl-serine phosphorylation  (IDA)
positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction  (IBA)
positive regulation of positive chemotaxis  (IDA)
positive regulation of protein phosphorylation  (TAS)
positive regulation of synapse assembly  (ISO)
postsynaptic density assembly  (ISO)
regulation of neural precursor cell proliferation  (ISO)
regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction  (IEA)
regulation of presynapse assembly  (ISO)
response to axon injury  (ISO)
response to corticosterone  (ISO)
response to ethanol  (ISO)
signal transduction  (IEA)

Cellular Component
axon  (IBA,IEA)
cytoplasm  (ISO)
glutamatergic synapse  (ISO)
membrane  (IEA)
plasma membrane  (IBA,IEA,TAS)
postsynaptic membrane  (ISO)
receptor complex  (IBA,IDA,IEA)

Molecular Pathway Annotations     Click to see Annotation Detail View
Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. Detection of aberrant methylated SEPT9 and NTRK3 genes in sporadic colorectal cancer patients as a potential diagnostic biomarker. Behrouz Sharif S, etal., Oncol Lett. 2016 Dec;12(6):5335-5343. doi: 10.3892/ol.2016.5327. Epub 2016 Oct 31.
2. Long non-coding RNA LINC00978 promotes cell proliferation and tumorigenesis via regulating microRNA-497/NTRK3 axis in gastric cancer. Bu JY, etal., Int J Biol Macromol. 2019 Feb 15;123:1106-1114. doi: 10.1016/j.ijbiomac.2018.11.162. Epub 2018 Nov 17.
3. Genome-wide analysis identifies critical DNA methylations within NTRKs genes in colorectal cancer. Chen Z, etal., J Transl Med. 2021 Feb 16;19(1):73. doi: 10.1186/s12967-021-02740-6.
4. Target tissue production and axonal transport of neurotrophin-3 are reduced in streptozotocin-diabetic rats. Fernyhough P, etal., Diabetologia. 1998 Mar;41(3):300-6.
5. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
6. Gene expression alterations of neurotrophins, their receptors and prohormone convertases in a rat model of spinal cord contusion. Hajebrahimi Z, etal., Neurosci Lett. 2008 Aug 29;441(3):261-6. Epub 2008 Jun 21.
7. TrkC signaling is activated in adenoid cystic carcinoma and requires NT-3 to stimulate invasive behavior. Ivanov SV, etal., Oncogene. 2013 Aug 8;32(32):3698-710. doi: 10.1038/onc.2012.377. Epub 2012 Oct 1.
8. TrkC plays an essential role in breast tumor growth and metastasis. Jin W, etal., Carcinogenesis. 2010 Nov;31(11):1939-47. doi: 10.1093/carcin/bgq180. Epub 2010 Aug 28.
9. Neurotrophins and Trk receptors in human pancreatic ductal adenocarcinoma: expression patterns and effects on in vitro invasive behavior. Miknyoczki SJ, etal., Int J Cancer. 1999 May 5;81(3):417-27.
10. Ethanol exposure alters neurotrophin receptor expression in the rat central nervous system: Effects of prenatal exposure. Moore DB, etal., J Neurobiol. 2004 Jul;60(1):101-13. doi: 10.1002/neu.20009.
11. Ethanol exposure alters neurotrophin receptor expression in the rat central nervous system: Effects of neonatal exposure. Moore DB, etal., J Neurobiol. 2004 Jul;60(1):114-26. doi: 10.1002/neu.20010.
12. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
13. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
14. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
15. RGD HPO Phenotype Annotation Pipeline RGD automated import pipeline for human HPO-to-gene-to-disease annotations
16. Expression of Trk tyrosine kinase receptor is a biologic marker for cell proliferation and perineural invasion of human pancreatic ductal adenocarcinoma. Sakamoto Y, etal., Oncol Rep. 2001 May-Jun;8(3):477-84.
17. Somatic mutations of GUCY2F, EPHA3, and NTRK3 in human cancers. Wood LD, etal., Hum Mutat. 2006 Oct;27(10):1060-1.
18. Alterations in neurotrophin and neurotrophin receptor gene expression patterns in the rat central nervous system following perinatal Borna disease virus infection. Zocher M, etal., J Neurovirol. 2000 Dec;6(6):462-77.
Additional References at PubMed
PMID:1326636   PMID:1653651   PMID:7657612   PMID:7806211   PMID:7823156   PMID:7828539   PMID:8344249   PMID:8619474   PMID:8621424   PMID:8889548   PMID:8895847   PMID:9110174  
PMID:9195161   PMID:9197281   PMID:9462753   PMID:9488719   PMID:9648868   PMID:9778053   PMID:9856458   PMID:9927421   PMID:9973222   PMID:10027399   PMID:10092678   PMID:10764727  
PMID:11157096   PMID:11205744   PMID:11877382   PMID:12006576   PMID:12034707   PMID:12210087   PMID:12237455   PMID:12399943   PMID:12450792   PMID:12471037   PMID:12477932   PMID:12927579  
PMID:14668342   PMID:14702039   PMID:15167446   PMID:15167895   PMID:15198123   PMID:15247919   PMID:15312164   PMID:15513915   PMID:15932601   PMID:16344560   PMID:16537434   PMID:16647839  
PMID:16648236   PMID:16786155   PMID:16826429   PMID:16862449   PMID:17971243   PMID:18068631   PMID:18179783   PMID:18203754   PMID:18293376   PMID:18319596   PMID:18336001   PMID:18347002  
PMID:18367154   PMID:18428117   PMID:18616610   PMID:18639687   PMID:18713973   PMID:19011601   PMID:19036963   PMID:19040714   PMID:19086053   PMID:19156760   PMID:19179422   PMID:19187638  
PMID:19344762   PMID:19351817   PMID:19370765   PMID:19417027   PMID:19453261   PMID:19556619   PMID:19598235   PMID:19680743   PMID:19893451   PMID:19953569   PMID:20078941   PMID:20160348  
PMID:20219210   PMID:20379614   PMID:20554328   PMID:20565848   PMID:21070662   PMID:21102451   PMID:21139137   PMID:21295543   PMID:21392742   PMID:21401966   PMID:21552290   PMID:21617231  
PMID:21728718   PMID:21788388   PMID:21832049   PMID:21873635   PMID:21988832   PMID:22265740   PMID:22343487   PMID:22388998   PMID:22404213   PMID:22939624   PMID:23332094   PMID:23341610  
PMID:23382219   PMID:23416450   PMID:23453885   PMID:23598414   PMID:23727532   PMID:23832765   PMID:23869086   PMID:23874207   PMID:24034695   PMID:24145651   PMID:24327398   PMID:24603864  
PMID:24722188   PMID:25196463   PMID:25456394   PMID:25624497   PMID:25772499   PMID:25921289   PMID:26055783   PMID:26216473   PMID:26291510   PMID:26410934   PMID:26459250   PMID:26492182  
PMID:26606880   PMID:26647767   PMID:26652865   PMID:26884591   PMID:27259007   PMID:27282352   PMID:27351280   PMID:27477320   PMID:27631515   PMID:27763904   PMID:27826991   PMID:27974047  
PMID:28097808   PMID:28100780   PMID:28125451   PMID:28181547   PMID:28215291   PMID:28402394   PMID:28455963   PMID:28514442   PMID:28683589   PMID:28695340   PMID:28719467   PMID:28746220  
PMID:29046324   PMID:29391602   PMID:29553955   PMID:29911254   PMID:30187166   PMID:30366959   PMID:30520818   PMID:30898150   PMID:31127997   PMID:31268127   PMID:31479159   PMID:31569361  
PMID:31871300   PMID:32034283   PMID:32278476   PMID:32315394   PMID:32513696   PMID:32707033   PMID:32880785   PMID:32931153   PMID:32968185   PMID:33046021   PMID:33074583   PMID:33290352  
PMID:33301751   PMID:33524004   PMID:33627781   PMID:33758144   PMID:33894748   PMID:33899788   PMID:33961781   PMID:34378283   PMID:34445205   PMID:35152631   PMID:35384245   PMID:35536742  
PMID:35737155   PMID:36171207   PMID:36931259   PMID:37272057   PMID:37415052   PMID:37697438   PMID:38593276  


Genomics

Comparative Map Data
NTRK3
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381587,859,751 - 88,256,739 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1587,859,751 - 88,256,791 (-)EnsemblGRCh38hg38GRCh38
GRCh371588,402,982 - 88,799,970 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361586,220,992 - 86,600,665 (-)NCBINCBI36Build 36hg18NCBI36
Build 341586,220,991 - 86,600,665NCBI
Celera1564,821,267 - 65,200,916 (-)NCBICelera
Cytogenetic Map15q25.3NCBI
HuRef1564,532,241 - 64,911,404 (-)NCBIHuRef
CHM1_11588,261,800 - 88,641,816 (-)NCBICHM1_1
T2T-CHM13v2.01585,614,323 - 86,011,407 (-)NCBIT2T-CHM13v2.0
Ntrk3
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39777,825,711 - 78,228,865 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl777,825,707 - 78,387,760 (-)EnsemblGRCm39 Ensembl
GRCm38778,179,986 - 78,581,034 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl778,175,959 - 78,738,012 (-)EnsemblGRCm38mm10GRCm38
MGSCv37785,337,000 - 85,722,724 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36778,066,072 - 78,451,488 (-)NCBIMGSCv36mm8
Celera775,610,791 - 75,991,488 (-)NCBICelera
Cytogenetic Map7D2NCBI
cM Map744.01NCBI
Ntrk3
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81141,526,192 - 141,913,575 (-)NCBIGRCr8
mRatBN7.21132,116,472 - 132,503,849 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1132,132,849 - 132,503,286 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1140,038,778 - 140,410,193 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01147,208,513 - 147,579,935 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01140,126,320 - 140,497,270 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01139,890,537 - 140,262,503 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1139,890,560 - 140,262,503 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01140,868,261 - 141,239,954 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41133,925,530 - 134,302,139 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11134,003,872 - 134,380,482 (-)NCBI
Celera1124,206,109 - 124,576,015 (-)NCBICelera
Cytogenetic Map1q31NCBI
Ntrk3
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495541616,652,791 - 17,018,188 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495541616,652,931 - 17,018,188 (+)NCBIChiLan1.0ChiLan1.0
NTRK3
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21677,421,258 - 77,808,559 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11581,101,703 - 81,513,473 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01566,566,219 - 66,953,279 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11585,776,819 - 86,157,209 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1585,776,832 - 86,157,204 (-)Ensemblpanpan1.1panPan2
NTRK3
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1351,131,470 - 51,491,112 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl351,138,751 - 51,513,024 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha353,770,192 - 54,150,627 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0351,548,386 - 51,933,727 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl351,554,220 - 51,933,726 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1351,071,744 - 51,456,495 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0351,281,270 - 51,665,830 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0351,620,674 - 52,005,592 (-)NCBIUU_Cfam_GSD_1.0
Ntrk3
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024408640132,042,602 - 132,426,830 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493648313,909,109 - 14,291,887 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493648313,912,904 - 14,291,881 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
NTRK3
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1191,535,301 - 191,925,327 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11191,535,262 - 191,941,675 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21212,938,371 - 213,258,768 (+)NCBISscrofa10.2Sscrofa10.2susScr3
NTRK3
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1296,441,824 - 6,831,029 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl296,447,256 - 6,830,526 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366605940,018,915 - 40,410,728 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Ntrk3
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462476815,252,354 - 15,619,601 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462476815,239,111 - 15,619,979 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in NTRK3
85 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_001012338.2(NTRK3):c.1585+16988C>A single nucleotide variant Lung cancer [RCV000099736] Chr15:88015869 [GRCh38]
Chr15:88559100 [GRCh37]
Chr15:15q25.3
uncertain significance
NM_001012338.2(NTRK3):c.1204+1710G>A single nucleotide variant Lung cancer [RCV000099737] Chr15:88133391 [GRCh38]
Chr15:88676622 [GRCh37]
Chr15:15q25.3
uncertain significance
NM_001012338.2(NTRK3):c.465-2012T>C single nucleotide variant Lung cancer [RCV000099738] Chr15:88139573 [GRCh38]
Chr15:88682804 [GRCh37]
Chr15:15q25.3
uncertain significance
NM_001012338.2(NTRK3):c.464+167C>A single nucleotide variant Lung cancer [RCV000099739] Chr15:88147168 [GRCh38]
Chr15:88690399 [GRCh37]
Chr15:15q25.3
uncertain significance
NM_001012338.2(NTRK3):c.396-14100G>C single nucleotide variant Lung cancer [RCV000099740] Chr15:88161503 [GRCh38]
Chr15:88704734 [GRCh37]
Chr15:15q25.3
uncertain significance
GRCh38/hg38 15q24.2-26.3(chr15:75307767-101723215)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052346]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052346]|See cases [RCV000052346] Chr15:75307767..101723215 [GRCh38]
Chr15:75600108..102263418 [GRCh37]
Chr15:73387161..100080941 [NCBI36]
Chr15:15q24.2-26.3
pathogenic
GRCh38/hg38 15q24.3-26.3(chr15:77543797-101843411)x3 copy number gain See cases [RCV000052347] Chr15:77543797..101843411 [GRCh38]
Chr15:77836139..102383614 [GRCh37]
Chr15:75623194..100201137 [NCBI36]
Chr15:15q24.3-26.3
pathogenic
GRCh38/hg38 15q25.2-26.3(chr15:84169153-101904929)x3 copy number gain See cases [RCV000052352] Chr15:84169153..101904929 [GRCh38]
Chr15:84837905..102445132 [GRCh37]
Chr15:82628909..100262655 [NCBI36]
Chr15:15q25.2-26.3
pathogenic
NM_001012338.2(NTRK3):c.2071C>T (p.Leu691=) single nucleotide variant Malignant melanoma [RCV000070936] Chr15:87929253 [GRCh38]
Chr15:88472484 [GRCh37]
Chr15:86273488 [NCBI36]
Chr15:15q25.3
not provided
NM_001012338.2(NTRK3):c.2049G>A (p.Arg683=) single nucleotide variant Malignant melanoma [RCV000070937] Chr15:87929275 [GRCh38]
Chr15:88472506 [GRCh37]
Chr15:86273510 [NCBI36]
Chr15:15q25.3
not provided
GRCh38/hg38 15q25.2-26.3(chr15:83711377-101843270)x3 copy number gain See cases [RCV000135858] Chr15:83711377..101843270 [GRCh38]
Chr15:84380129..102383473 [GRCh37]
Chr15:82171133..100200996 [NCBI36]
Chr15:15q25.2-26.3
pathogenic
GRCh38/hg38 15q25.3-26.3(chr15:87904735-101843270)x3 copy number gain See cases [RCV000135568] Chr15:87904735..101843270 [GRCh38]
Chr15:88447966..102383473 [GRCh37]
Chr15:86248970..100200996 [NCBI36]
Chr15:15q25.3-26.3
pathogenic
GRCh38/hg38 15q25.2-26.3(chr15:82859676-101810992)x3 copy number gain See cases [RCV000136849] Chr15:82859676..101810992 [GRCh38]
Chr15:83528428..102351195 [GRCh37]
Chr15:81325482..100168718 [NCBI36]
Chr15:15q25.2-26.3
pathogenic
GRCh38/hg38 15q25.3-26.3(chr15:85826665-101920998)x4 copy number gain See cases [RCV000137264] Chr15:85826665..101920998 [GRCh38]
Chr15:86369896..102461201 [GRCh37]
Chr15:84170900..100278724 [NCBI36]
Chr15:15q25.3-26.3
pathogenic
GRCh38/hg38 15q25.3-26.3(chr15:85397539-101888909)x3 copy number gain See cases [RCV000141899] Chr15:85397539..101888909 [GRCh38]
Chr15:85940770..102429112 [GRCh37]
Chr15:83741774..100246635 [NCBI36]
Chr15:15q25.3-26.3
pathogenic
GRCh38/hg38 15q22.2-26.3(chr15:59828460-101920998)x3 copy number gain See cases [RCV000142915] Chr15:59828460..101920998 [GRCh38]
Chr15:60120659..102461201 [GRCh37]
Chr15:57907951..100278724 [NCBI36]
Chr15:15q22.2-26.3
pathogenic
GRCh38/hg38 15q23-26.3(chr15:72154949-101920998)x3 copy number gain See cases [RCV000143019] Chr15:72154949..101920998 [GRCh38]
Chr15:72447290..102461201 [GRCh37]
Chr15:70234344..100278724 [NCBI36]
Chr15:15q23-26.3
pathogenic
GRCh37/hg19 15q24.2-26.3(chr15:76061144-102429112)x3 copy number gain See cases [RCV000511332] Chr15:76061144..102429112 [GRCh37]
Chr15:15q24.2-26.3
pathogenic
GRCh37/hg19 15q22.31-26.3(chr15:64637227-102509910)x3 copy number gain See cases [RCV000240602] Chr15:64637227..102509910 [GRCh37]
Chr15:15q22.31-26.3
pathogenic
GRCh37/hg19 15q22.1-26.3(chr15:59297293-102480888)x3 copy number gain not provided [RCV000415836] Chr15:59297293..102480888 [GRCh37]
Chr15:15q22.1-26.3
likely pathogenic
GRCh37/hg19 15q25.2-26.3(chr15:85089467-102495441)x3 copy number gain See cases [RCV000449119] Chr15:85089467..102495441 [GRCh37]
Chr15:15q25.2-26.3
pathogenic
GRCh37/hg19 15q15.1-26.3(chr15:41745084-102354798)x4 copy number gain See cases [RCV000447123] Chr15:41745084..102354798 [GRCh37]
Chr15:15q15.1-26.3
pathogenic
GRCh37/hg19 15q25.3(chr15:88309119-88512556)x1 copy number loss See cases [RCV000446181] Chr15:88309119..88512556 [GRCh37]
Chr15:15q25.3
uncertain significance
GRCh37/hg19 15q25.1-26.3(chr15:80648093-102429112)x3 copy number gain See cases [RCV000445705] Chr15:80648093..102429112 [GRCh37]
Chr15:15q25.1-26.3
pathogenic
GRCh37/hg19 15q11.2-26.3(chr15:20733395-102511616)x4 copy number gain See cases [RCV000447765] Chr15:20733395..102511616 [GRCh37]
Chr15:15q11.2-26.3
pathogenic
GRCh37/hg19 15q25.3-26.3(chr15:86148286-102511616)x3 copy number gain See cases [RCV000448044] Chr15:86148286..102511616 [GRCh37]
Chr15:15q25.3-26.3
pathogenic
GRCh37/hg19 15q25.3-26.1(chr15:88295992-94215607)x1 copy number loss See cases [RCV000448680] Chr15:88295992..94215607 [GRCh37]
Chr15:15q25.3-26.1
pathogenic
GRCh37/hg19 15q11.2-26.3(chr15:22770422-102429112)x3 copy number gain See cases [RCV000510717] Chr15:22770422..102429112 [GRCh37]
Chr15:15q11.2-26.3
pathogenic
GRCh37/hg19 15q11.2-26.3(chr15:22770422-102429112) copy number gain See cases [RCV000512019] Chr15:22770422..102429112 [GRCh37]
Chr15:15q11.2-26.3
pathogenic
GRCh37/hg19 15q25.3-26.3(chr15:86899001-98734014)x3 copy number gain See cases [RCV000511629] Chr15:86899001..98734014 [GRCh37]
Chr15:15q25.3-26.3
likely pathogenic
NM_001012338.3(NTRK3):c.1052A>T (p.Glu351Val) single nucleotide variant not specified [RCV004312723] Chr15:88135253 [GRCh38]
Chr15:88678484 [GRCh37]
Chr15:15q25.3
uncertain significance
Single allele duplication not provided [RCV000677926] Chr15:31115047..102354857 [GRCh37]
Chr15:15q13.2-26.3
pathogenic
GRCh37/hg19 15q23-26.3(chr15:71329220-102270758)x3 copy number gain not provided [RCV000683703] Chr15:71329220..102270758 [GRCh37]
Chr15:15q23-26.3
pathogenic
GRCh37/hg19 15q24.3-26.3(chr15:77479244-102429112)x3 copy number gain not provided [RCV000683710] Chr15:77479244..102429112 [GRCh37]
Chr15:15q24.3-26.3
pathogenic
GRCh37/hg19 15q25.3(chr15:87321162-88860904)x3 copy number gain not provided [RCV000683717] Chr15:87321162..88860904 [GRCh37]
Chr15:15q25.3
uncertain significance
GRCh37/hg19 15q25.3-26.3(chr15:88385150-102461162)x3 copy number gain not provided [RCV000738864] Chr15:88385150..102461162 [GRCh37]
Chr15:15q25.3-26.3
pathogenic
GRCh37/hg19 15q11.1-26.3(chr15:20071673-102461162)x3 copy number gain not provided [RCV000751156] Chr15:20071673..102461162 [GRCh37]
Chr15:15q11.1-26.3
pathogenic
GRCh37/hg19 15q11.1-26.3(chr15:20016811-102493540)x3 copy number gain not provided [RCV000751155] Chr15:20016811..102493540 [GRCh37]
Chr15:15q11.1-26.3
pathogenic
NM_001012338.3(NTRK3):c.*197AT[12] microsatellite not provided [RCV001708055] Chr15:87876716..87876717 [GRCh38]
Chr15:88419947..88419948 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.660C>T (p.Thr220=) single nucleotide variant not provided [RCV000919527] Chr15:88136572 [GRCh38]
Chr15:88679803 [GRCh37]
Chr15:15q25.3
likely benign
NM_001012338.3(NTRK3):c.465-151C>A single nucleotide variant not provided [RCV001708567] Chr15:88137712 [GRCh38]
Chr15:88680943 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.249-221T>A single nucleotide variant not provided [RCV001609238] Chr15:88184520 [GRCh38]
Chr15:88727751 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.1396+120C>G single nucleotide variant not provided [RCV001690516] Chr15:88126151 [GRCh38]
Chr15:88669382 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.396-150AAG[14] microsatellite not provided [RCV001678825] Chr15:88147506..88147511 [GRCh38]
Chr15:88690737..88690742 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.1818G>T (p.Val606=) single nucleotide variant not provided [RCV000926548] Chr15:87933083 [GRCh38]
Chr15:88476314 [GRCh37]
Chr15:15q25.3
likely benign
NM_001012338.3(NTRK3):c.1665C>T (p.Ala555=) single nucleotide variant NTRK3-related disorder [RCV003910622]|not provided [RCV000892674] Chr15:87940674 [GRCh38]
Chr15:88483905 [GRCh37]
Chr15:15q25.3
benign|likely benign
NM_001012338.3(NTRK3):c.1488C>A (p.Ala496=) single nucleotide variant not provided [RCV000879389] Chr15:88032954 [GRCh38]
Chr15:88576185 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.1503G>A (p.Val501=) single nucleotide variant NTRK3-related disorder [RCV003936013]|not provided [RCV000966338] Chr15:88032939 [GRCh38]
Chr15:88576170 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.1089G>A (p.Leu363=) single nucleotide variant not provided [RCV000983671] Chr15:88135216 [GRCh38]
Chr15:88678447 [GRCh37]
Chr15:15q25.3
likely benign
NM_001012338.3(NTRK3):c.1205-4G>A single nucleotide variant not provided [RCV000929365] Chr15:88128738 [GRCh38]
Chr15:88671969 [GRCh37]
Chr15:15q25.3
likely benign
NM_001012338.3(NTRK3):c.2094C>T (p.Phe698=) single nucleotide variant not provided [RCV000903112] Chr15:87929230 [GRCh38]
Chr15:88472461 [GRCh37]
Chr15:15q25.3
likely benign
NM_001012338.3(NTRK3):c.1704T>C (p.Leu568=) single nucleotide variant NTRK3-related disorder [RCV003940833]|not provided [RCV000899364] Chr15:87940635 [GRCh38]
Chr15:88483866 [GRCh37]
Chr15:15q25.3
benign|likely benign
NM_001012338.3(NTRK3):c.765+9C>G single nucleotide variant not provided [RCV000964346] Chr15:88136458 [GRCh38]
Chr15:88679689 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.309C>T (p.Thr103=) single nucleotide variant not provided [RCV000954294] Chr15:88184239 [GRCh38]
Chr15:88727470 [GRCh37]
Chr15:15q25.3
likely benign
NM_001012338.3(NTRK3):c.84C>G (p.Ser28=) single nucleotide variant not provided [RCV000916674] Chr15:88256070 [GRCh38]
Chr15:88799301 [GRCh37]
Chr15:15q25.3
likely benign
NM_001012338.3(NTRK3):c.802T>C (p.Leu268=) single nucleotide variant NTRK3-related disorder [RCV003962922]|not provided [RCV000974583] Chr15:88136004 [GRCh38]
Chr15:88679235 [GRCh37]
Chr15:15q25.3
benign|likely benign
NM_001012338.3(NTRK3):c.678= (p.Asn226=) variation not provided [RCV000974584] Chr15:88136554 [GRCh38]
Chr15:88679785 [GRCh37]
Chr15:15q25.3
likely benign
GRCh37/hg19 15q25.2-26.1(chr15:83883823-92165844) copy number loss not provided [RCV000767759] Chr15:83883823..92165844 [GRCh37]
Chr15:15q25.2-26.1
pathogenic
NM_001012338.3(NTRK3):c.1495G>A (p.Asp499Asn) single nucleotide variant Premature ovarian insufficiency [RCV000766169] Chr15:88032947 [GRCh38]
Chr15:88576178 [GRCh37]
Chr15:15q25.3
uncertain significance
NM_001012338.3(NTRK3):c.61G>T (p.Val21Phe) single nucleotide variant NTRK3-related disorder [RCV003940703]|not provided [RCV000892087] Chr15:88256093 [GRCh38]
Chr15:88799324 [GRCh37]
Chr15:15q25.3
likely benign
NM_001012338.3(NTRK3):c.1229-273G>C single nucleotide variant not provided [RCV001686877] Chr15:88127499 [GRCh38]
Chr15:88670730 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.465-195A>T single nucleotide variant not provided [RCV001659126] Chr15:88137756 [GRCh38]
Chr15:88680987 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.2334+164del deletion not provided [RCV001639499] Chr15:87880106 [GRCh38]
Chr15:88423337 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.396-150AAG[9] microsatellite not provided [RCV001719181] Chr15:88147506..88147526 [GRCh38]
Chr15:88690737..88690757 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.396-150AAG[17] microsatellite not provided [RCV001710224] Chr15:88147505..88147506 [GRCh38]
Chr15:88690736..88690737 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.1716+260T>C single nucleotide variant not provided [RCV001639790] Chr15:87940363 [GRCh38]
Chr15:88483594 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.*99G>A single nucleotide variant not provided [RCV001616038] Chr15:87876836 [GRCh38]
Chr15:88420067 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.395+244C>T single nucleotide variant not provided [RCV001656674] Chr15:88183174 [GRCh38]
Chr15:88726405 [GRCh37]
Chr15:15q25.3
benign
t(2;15)(q23.1;q25.3) translocation Glioblastoma [RCV001532882] Chr2:2q23.1-23.2 uncertain significance
NM_001012338.3(NTRK3):c.1752T>C (p.Asp584=) single nucleotide variant not provided [RCV000940056] Chr15:87933149 [GRCh38]
Chr15:88476380 [GRCh37]
Chr15:15q25.3
likely benign
NM_001012338.3(NTRK3):c.1896T>C (p.His632=) single nucleotide variant NTRK3-related disorder [RCV003913023]|not provided [RCV000911817] Chr15:87929428 [GRCh38]
Chr15:88472659 [GRCh37]
Chr15:15q25.3
likely benign
NM_001012338.3(NTRK3):c.1586-40804T>C single nucleotide variant not provided [RCV001719200] Chr15:87981557 [GRCh38]
Chr15:88524788 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.1229-301A>C single nucleotide variant not provided [RCV001636457] Chr15:88127527 [GRCh38]
Chr15:88670758 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.1488C>G (p.Ala496=) single nucleotide variant NTRK3-related disorder [RCV003975817]|not provided [RCV001657306] Chr15:88032954 [GRCh38]
Chr15:88576185 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.908-52A>G single nucleotide variant not provided [RCV001597643] Chr15:88135449 [GRCh38]
Chr15:88678680 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.2134-110T>C single nucleotide variant not provided [RCV001596237] Chr15:87885845 [GRCh38]
Chr15:88429076 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.1586-39051G>A single nucleotide variant not provided [RCV001657600] Chr15:87979804 [GRCh38]
Chr15:88523035 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.1293+280A>T single nucleotide variant not provided [RCV001719187] Chr15:88126882 [GRCh38]
Chr15:88670113 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.1585+202G>A single nucleotide variant not provided [RCV001719215] Chr15:88032655 [GRCh38]
Chr15:88575886 [GRCh37]
Chr15:15q25.3
benign
GRCh37/hg19 15q25.3-26.3(chr15:87189245-102429112)x1 copy number loss not provided [RCV001006718] Chr15:87189245..102429112 [GRCh37]
Chr15:15q25.3-26.3
pathogenic
NM_001012338.3(NTRK3):c.248+325T>A single nucleotide variant not provided [RCV001621753] Chr15:88255581 [GRCh38]
Chr15:88798812 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.2175+223G>T single nucleotide variant not provided [RCV001682608] Chr15:87885471 [GRCh38]
Chr15:88428702 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.248+320dup duplication not provided [RCV001677114] Chr15:88255577..88255578 [GRCh38]
Chr15:88798808..88798809 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.2133+252T>C single nucleotide variant not provided [RCV001698882] Chr15:87928939 [GRCh38]
Chr15:88472170 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.1586-39049C>A single nucleotide variant not provided [RCV001609706] Chr15:87979802 [GRCh38]
Chr15:88523033 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.573C>T (p.Asn191=) single nucleotide variant not provided [RCV001611495] Chr15:88137453 [GRCh38]
Chr15:88680684 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.2134-175T>C single nucleotide variant not provided [RCV001669628] Chr15:87885910 [GRCh38]
Chr15:88429141 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.1717-271G>A single nucleotide variant not provided [RCV001682374] Chr15:87933455 [GRCh38]
Chr15:88476686 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.396-150AAG[15] microsatellite not provided [RCV001671694] Chr15:88147506..88147508 [GRCh38]
Chr15:88690737..88690739 [GRCh37]
Chr15:15q25.3
benign
GRCh37/hg19 15q25.3-26.3(chr15:86962053-102531392)x1 copy number loss See cases [RCV001263026] Chr15:86962053..102531392 [GRCh37]
Chr15:15q25.3-26.3
pathogenic
NC_000015.9:g.(?_32964879)_(91358519_?)dup duplication Bloom syndrome [RCV001343104]|Familial colorectal cancer [RCV001325176] Chr15:32964879..91358519 [GRCh37]
Chr15:15q13.3-26.1
uncertain significance
NM_001012338.3(NTRK3):c.1396+339A>G single nucleotide variant not provided [RCV001534455] Chr15:88125932 [GRCh38]
Chr15:88669163 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.1889+77T>G single nucleotide variant not provided [RCV001694590] Chr15:87932935 [GRCh38]
Chr15:88476166 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.2334+38G>A single nucleotide variant not provided [RCV001655019] Chr15:87880232 [GRCh38]
Chr15:88423463 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.396-150AAG[13] microsatellite not provided [RCV001674542] Chr15:88147506..88147514 [GRCh38]
Chr15:88690737..88690745 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.323+120G>C single nucleotide variant not provided [RCV001696152] Chr15:88184105 [GRCh38]
Chr15:88727336 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.1396+310C>T single nucleotide variant not provided [RCV001687433] Chr15:88125961 [GRCh38]
Chr15:88669192 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.395+63C>T single nucleotide variant not provided [RCV001652718] Chr15:88183355 [GRCh38]
Chr15:88726586 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.623-260C>T single nucleotide variant not provided [RCV001538845] Chr15:88136869 [GRCh38]
Chr15:88680100 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.278C>T (p.Thr93Met) single nucleotide variant Neonatal cardiomyopathy [RCV003326013]|not specified [RCV002250159] Chr15:88184270 [GRCh38]
Chr15:88727501 [GRCh37]
Chr15:15q25.3
benign|uncertain significance
GRCh37/hg19 15q25.3-26.2(chr15:88465861-94411846)x1 copy number loss not provided [RCV001795547] Chr15:88465861..94411846 [GRCh37]
Chr15:15q25.3-26.2
pathogenic
t(12;15)(p13;q25) variation Glioma [RCV001824996] Chr15:15q25.3 pathogenic
NM_001012338.3(NTRK3):c.1868G>C (p.Gly623Ala) single nucleotide variant Entrectinib resistance [RCV001824997] Chr15:87933033 [GRCh38]
Chr15:88476264 [GRCh37]
Chr15:15q25.3
other
NM_001012338.3(NTRK3):c.1868G>A (p.Gly623Glu) single nucleotide variant Cabozantinib resistance [RCV001824998] Chr15:87933033 [GRCh38]
Chr15:88476264 [GRCh37]
Chr15:15q25.3
other
GRCh37/hg19 15q25.3(chr15:88066217-88595279) copy number gain not specified [RCV002052486] Chr15:88066217..88595279 [GRCh37]
Chr15:15q25.3
uncertain significance
NM_001012338.3(NTRK3):c.131A>G (p.Asn44Ser) single nucleotide variant not specified [RCV004310411] Chr15:88256023 [GRCh38]
Chr15:88799254 [GRCh37]
Chr15:15q25.3
uncertain significance
NM_001012338.3(NTRK3):c.137G>C (p.Arg46Pro) single nucleotide variant not specified [RCV004148012] Chr15:88256017 [GRCh38]
Chr15:88799248 [GRCh37]
Chr15:15q25.3
uncertain significance
GRCh37/hg19 15q24.3-26.3(chr15:77512817-102035027)x3 copy number gain not provided [RCV002475797] Chr15:77512817..102035027 [GRCh37]
Chr15:15q24.3-26.3
pathogenic
NM_001012338.3(NTRK3):c.887G>T (p.Ser296Ile) single nucleotide variant not specified [RCV004112781] Chr15:88135919 [GRCh38]
Chr15:88679150 [GRCh37]
Chr15:15q25.3
uncertain significance
NM_001012338.3(NTRK3):c.1835C>A (p.Pro612His) single nucleotide variant not specified [RCV004107779] Chr15:87933066 [GRCh38]
Chr15:88476297 [GRCh37]
Chr15:15q25.3
uncertain significance
NM_001012338.3(NTRK3):c.806C>T (p.Thr269Met) single nucleotide variant not specified [RCV004131666] Chr15:88136000 [GRCh38]
Chr15:88679231 [GRCh37]
Chr15:15q25.3
uncertain significance
NM_001012338.3(NTRK3):c.83C>T (p.Ser28Phe) single nucleotide variant not specified [RCV004183318] Chr15:88256071 [GRCh38]
Chr15:88799302 [GRCh37]
Chr15:15q25.3
uncertain significance
NM_001012338.3(NTRK3):c.755A>G (p.Asn252Ser) single nucleotide variant not specified [RCV004168299] Chr15:88136477 [GRCh38]
Chr15:88679708 [GRCh37]
Chr15:15q25.3
uncertain significance
NM_001012338.3(NTRK3):c.41G>A (p.Arg14Gln) single nucleotide variant not specified [RCV004239425] Chr15:88256113 [GRCh38]
Chr15:88799344 [GRCh37]
Chr15:15q25.3
uncertain significance
NM_001012338.3(NTRK3):c.1166A>G (p.Gln389Arg) single nucleotide variant not specified [RCV004176915] Chr15:88135139 [GRCh38]
Chr15:88678370 [GRCh37]
Chr15:15q25.3
uncertain significance
GRCh37/hg19 15q22.33-26.1(chr15:67358491-91644328)x3 copy number gain not provided [RCV003222839] Chr15:67358491..91644328 [GRCh37]
Chr15:15q22.33-26.1
pathogenic
NM_001012338.3(NTRK3):c.2380G>A (p.Val794Ile) single nucleotide variant not specified [RCV004287313] Chr15:87877075 [GRCh38]
Chr15:88420306 [GRCh37]
Chr15:15q25.3
uncertain significance
GRCh37/hg19 15q25.2-26.3(chr15:84228005-102264590)x3 copy number gain not provided [RCV003222840] Chr15:84228005..102264590 [GRCh37]
Chr15:15q25.2-26.3
pathogenic
NM_001012338.3(NTRK3):c.2297A>G (p.Tyr766Cys) single nucleotide variant not specified [RCV004256798] Chr15:87880307 [GRCh38]
Chr15:88423538 [GRCh37]
Chr15:15q25.3
uncertain significance
GRCh37/hg19 15q24.1-26.3(chr15:75165490-102520892)x3 copy number gain See cases [RCV003329502] Chr15:75165490..102520892 [GRCh37]
Chr15:15q24.1-26.3
pathogenic
NM_001012338.3(NTRK3):c.1459G>A (p.Gly487Ser) single nucleotide variant not specified [RCV004346401] Chr15:88032983 [GRCh38]
Chr15:88576214 [GRCh37]
Chr15:15q25.3
uncertain significance
NM_001012338.3(NTRK3):c.1765G>A (p.Ala589Thr) single nucleotide variant not specified [RCV004342240] Chr15:87933136 [GRCh38]
Chr15:88476367 [GRCh37]
Chr15:15q25.3
uncertain significance
GRCh37/hg19 15q25.3(chr15:88273612-88754445)x3 copy number gain not provided [RCV003485077] Chr15:88273612..88754445 [GRCh37]
Chr15:15q25.3
uncertain significance
NM_001012338.3(NTRK3):c.1686G>A (p.Pro562=) single nucleotide variant NTRK3-related disorder [RCV003907414] Chr15:87940653 [GRCh38]
Chr15:88483884 [GRCh37]
Chr15:15q25.3
likely benign
NM_001012338.3(NTRK3):c.930G>T (p.Leu310=) single nucleotide variant NTRK3-related disorder [RCV003912053] Chr15:88135375 [GRCh38]
Chr15:88678606 [GRCh37]
Chr15:15q25.3
likely benign
NM_001012338.3(NTRK3):c.2256T>C (p.Asp752=) single nucleotide variant not provided [RCV003885260] Chr15:87880348 [GRCh38]
Chr15:88423579 [GRCh37]
Chr15:15q25.3
likely benign
NM_001012338.3(NTRK3):c.516G>A (p.Gln172=) single nucleotide variant NTRK3-related disorder [RCV003963873] Chr15:88137510 [GRCh38]
Chr15:88680741 [GRCh37]
Chr15:15q25.3
likely benign
NM_001012338.3(NTRK3):c.1173C>T (p.Ile391=) single nucleotide variant NTRK3-related disorder [RCV003911724] Chr15:88135132 [GRCh38]
Chr15:88678363 [GRCh37]
Chr15:15q25.3
likely benign
NM_001012338.3(NTRK3):c.1035C>G (p.Ser345=) single nucleotide variant NTRK3-related disorder [RCV003944118] Chr15:88135270 [GRCh38]
Chr15:88678501 [GRCh37]
Chr15:15q25.3
likely benign
NM_001012338.3(NTRK3):c.1767C>T (p.Ala589=) single nucleotide variant NTRK3-related disorder [RCV003979691] Chr15:87933134 [GRCh38]
Chr15:88476365 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.-1G>A single nucleotide variant NTRK3-related disorder [RCV003929487] Chr15:88256154 [GRCh38]
Chr15:88799385 [GRCh37]
Chr15:15q25.3
likely benign
NM_001012338.3(NTRK3):c.1933C>T (p.Arg645Cys) single nucleotide variant NTRK3-related disorder [RCV003954490] Chr15:87929391 [GRCh38]
Chr15:88472622 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.1458C>T (p.His486=) single nucleotide variant NTRK3-related disorder [RCV003976465] Chr15:88032984 [GRCh38]
Chr15:88576215 [GRCh37]
Chr15:15q25.3
benign
NM_001012338.3(NTRK3):c.1164C>G (p.Asn388Lys) single nucleotide variant not specified [RCV004496043] Chr15:88135141 [GRCh38]
Chr15:88678372 [GRCh37]
Chr15:15q25.3
uncertain significance
NM_001012338.3(NTRK3):c.1678C>G (p.Leu560Val) single nucleotide variant not specified [RCV004496047] Chr15:87940661 [GRCh38]
Chr15:88483892 [GRCh37]
Chr15:15q25.3
uncertain significance
NM_001012338.3(NTRK3):c.1211C>T (p.Thr404Met) single nucleotide variant not specified [RCV004496044] Chr15:88128728 [GRCh38]
Chr15:88671959 [GRCh37]
Chr15:15q25.3
uncertain significance
NM_001012338.3(NTRK3):c.148G>T (p.Asp50Tyr) single nucleotide variant not specified [RCV004496046] Chr15:88256006 [GRCh38]
Chr15:88799237 [GRCh37]
Chr15:15q25.3
uncertain significance
NM_001012338.3(NTRK3):c.140G>A (p.Arg47Gln) single nucleotide variant not specified [RCV004496045] Chr15:88256014 [GRCh38]
Chr15:88799245 [GRCh37]
Chr15:15q25.3
uncertain significance
NM_001012338.3(NTRK3):c.1690A>C (p.Lys564Gln) single nucleotide variant not specified [RCV004496048] Chr15:87940649 [GRCh38]
Chr15:88483880 [GRCh37]
Chr15:15q25.3
uncertain significance
miRNA Target Status

Confirmed Target Of
miRNA GeneMature miRNAMethod NameResult TypeData TypeSupport TypePMID
MIR128-2hsa-miR-128Mirecordsexternal_infoNANA19370765
MIR128-1hsa-miR-128-3pMirtarbaseexternal_infoLuciferase reporter assayFunctional MTI19370765
MIR128-1hsa-miR-128-3pMirtarbaseexternal_infoLuciferase reporter assayFunctional MTI21143953
MIR151Ahsa-miR-151a-3pMirtarbaseexternal_infoLuciferase reporter assayFunctional MTI21143953
MIR625hsa-miR-625-5pMirtarbaseexternal_infoLuciferase reporter assayFunctional MTI19370765
MIR625hsa-miR-625-5pMirecordsexternal_infoNANA19370765
MIR509-3hsa-miR-509-3pMirtarbaseexternal_infoLuciferase reporter assayFunctional MTI19370765
MIR509-3hsa-miR-509-3pMirtarbaseexternal_infoLuciferase reporter assayFunctional MTI21143953
MIR509-3hsa-miR-509-3pMirecordsexternal_infoNANA19370765
MIR125B1hsa-miR-125b-5pMirtarbaseexternal_infoLuciferase reporter assay//Western blot//Reporter Functional MTI17483472
MIR345hsa-miR-345-5pMirtarbaseexternal_infoLuciferase reporter assayNon-Functional MTI19370765
MIR125B1hsa-miR-125b-5pOncomiRDBexternal_infoNANA17483472
MIR765hsa-miR-765Mirtarbaseexternal_infoLuciferase reporter assayFunctional MTI19370765
MIR765hsa-miR-765Mirecordsexternal_infoNANA19370765
MIR617hsa-miR-617Mirtarbaseexternal_infoLuciferase reporter assayNon-Functional MTI19370765
MIR330hsa-miR-330-3pMirtarbaseexternal_infoLuciferase reporter assayNon-Functional MTI19370765
MIR485hsa-miR-485-3pMirtarbaseexternal_infoLuciferase reporter assayFunctional MTI19370765
MIR485hsa-miR-485-3pMirecordsexternal_infoNANA19370765
MIR125B2hsa-miR-125b-5pMirtarbaseexternal_infoLuciferase reporter assay//Western blot//Reporter Functional MTI17483472
MIR198hsa-miR-198Mirtarbaseexternal_infoLuciferase reporter assayNon-Functional MTI19370765
MIR125B2hsa-miR-125b-5pOncomiRDBexternal_infoNANA17483472
MIR125Ahsa-miR-125a-5pOncomiRDBexternal_infoNANA18973228
MIR125Ahsa-miR-125a-5pOncomiRDBexternal_infoNANA17483472
MIR185hsa-miR-185-5pMirtarbaseexternal_infoLuciferase reporter assayFunctional MTI21143953
MIR384hsa-miR-384Mirtarbaseexternal_infoLuciferase reporter assayNon-Functional MTI19370765
MIR125Ahsa-miR-125a-5pMirtarbaseexternal_infoLuciferase reporter assay//Western blotFunctional MTI17483472
MIR125Ahsa-miR-125a-5pMirtarbaseexternal_infoLuciferase reporter assayFunctional MTI19179615
MIR125Ahsa-miR-125a-5pMirtarbaseexternal_infoLuciferase reporter assayFunctional MTI18973228

Predicted Target Of
Summary Value
Count of predictions:7275
Count of miRNA genes:1361
Interacting mature miRNAs:1858
Transcripts:ENST00000317501, ENST00000355254, ENST00000357724, ENST00000360948, ENST00000394480, ENST00000537300, ENST00000540489, ENST00000542733, ENST00000557856, ENST00000557897, ENST00000558306, ENST00000558576, ENST00000558676, ENST00000559067, ENST00000559188, ENST00000559680, ENST00000559764, ENST00000560017, ENST00000560201, ENST00000560739
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
RH78103  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371588,520,709 - 88,520,869UniSTSGRCh37
Build 361586,321,713 - 86,321,873RGDNCBI36
Celera1564,921,989 - 64,922,149RGD
Cytogenetic Map15q25UniSTS
HuRef1564,632,983 - 64,633,143UniSTS
GeneMap99-GB4 RH Map15319.19UniSTS
NCBI RH Map15690.8UniSTS
SHGC-30089  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371588,723,766 - 88,723,915UniSTSGRCh37
Build 361586,524,770 - 86,524,919RGDNCBI36
Celera1565,125,040 - 65,125,189RGD
Cytogenetic Map15q25UniSTS
HuRef1564,835,795 - 64,835,944UniSTS
TNG Radiation Hybrid Map1535568.0UniSTS
GeneMap99-G3 RH Map153225.0UniSTS
SGC30075  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371588,420,019 - 88,420,168UniSTSGRCh37
Build 361586,221,023 - 86,221,172RGDNCBI36
Celera1564,821,298 - 64,821,447RGD
Cytogenetic Map15q25UniSTS
HuRef1564,532,272 - 64,532,421UniSTS
GeneMap99-GB4 RH Map15319.19UniSTS
Whitehead-RH Map15334.1UniSTS
NCBI RH Map15627.9UniSTS
RH102137  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371588,796,198 - 88,796,368UniSTSGRCh37
Build 361586,597,202 - 86,597,372RGDNCBI36
Celera1565,197,453 - 65,197,623RGD
Cytogenetic Map15q25.3UniSTS
Cytogenetic Map15q25UniSTS
HuRef1564,908,203 - 64,908,373UniSTS
GeneMap99-GB4 RH Map15319.19UniSTS
RH122735  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371588,669,966 - 88,670,247UniSTSGRCh37
Build 361586,470,970 - 86,471,251RGDNCBI36
Celera1565,071,239 - 65,071,520RGD
Cytogenetic Map15q25UniSTS
HuRef1564,782,232 - 64,782,513UniSTS
TNG Radiation Hybrid Map1535546.0UniSTS
RH122647  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371588,744,822 - 88,745,098UniSTSGRCh37
Build 361586,545,826 - 86,546,102RGDNCBI36
Celera1565,146,094 - 65,146,370RGD
Cytogenetic Map15q25UniSTS
HuRef1564,856,849 - 64,857,125UniSTS
TNG Radiation Hybrid Map1535583.0UniSTS
RH122586  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371588,493,737 - 88,494,024UniSTSGRCh37
Build 361586,294,741 - 86,295,028RGDNCBI36
Celera1564,895,023 - 64,895,310RGD
Cytogenetic Map15q25UniSTS
HuRef1564,606,019 - 64,606,306UniSTS
TNG Radiation Hybrid Map1535459.0UniSTS
RH119005  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371588,670,696 - 88,671,027UniSTSGRCh37
Build 361586,471,700 - 86,472,031RGDNCBI36
Celera1565,071,969 - 65,072,300RGD
Cytogenetic Map15q25UniSTS
HuRef1564,782,962 - 64,783,293UniSTS
D15S99  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371588,435,263 - 88,435,389UniSTSGRCh37
Build 361586,236,267 - 86,236,393RGDNCBI36
Celera1564,836,539 - 64,836,673RGD
Cytogenetic Map15q25UniSTS
HuRef1564,547,529 - 64,547,655UniSTS
D18S99  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371588,582,330 - 88,582,435UniSTSGRCh37
Build 361586,383,334 - 86,383,439RGDNCBI36
Celera1564,983,606 - 64,983,711RGD
Cytogenetic Map15q25UniSTS
HuRef1564,694,601 - 64,694,704UniSTS
D15S171  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371588,582,330 - 88,582,448UniSTSGRCh37
Build 361586,383,334 - 86,383,452RGDNCBI36
Celera1564,983,606 - 64,983,724RGD
Cytogenetic Map15q25UniSTS
HuRef1564,694,601 - 64,694,717UniSTS
SHGC-112537  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371588,661,965 - 88,662,274UniSTSGRCh37
Build 361586,462,969 - 86,463,278RGDNCBI36
Celera1565,063,238 - 65,063,547RGD
Cytogenetic Map15q25UniSTS
HuRef1564,774,231 - 64,774,540UniSTS
TNG Radiation Hybrid Map1535537.0UniSTS
SHGC-89268  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371588,511,185 - 88,511,510UniSTSGRCh37
Build 361586,312,189 - 86,312,514RGDNCBI36
Celera1564,912,465 - 64,912,790RGD
Cytogenetic Map15q25UniSTS
HuRef1564,623,457 - 64,623,782UniSTS
TNG Radiation Hybrid Map1535462.0UniSTS
SHGC-144703  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371588,563,647 - 88,563,944UniSTSGRCh37
Build 361586,364,651 - 86,364,948RGDNCBI36
Celera1564,964,925 - 64,965,222RGD
Cytogenetic Map15q25UniSTS
HuRef1564,675,920 - 64,676,217UniSTS
TNG Radiation Hybrid Map1535484.0UniSTS
SHGC-154732  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371588,722,419 - 88,722,736UniSTSGRCh37
Build 361586,523,423 - 86,523,740RGDNCBI36
Celera1565,123,693 - 65,124,010RGD
Cytogenetic Map15q25UniSTS
HuRef1564,834,448 - 64,834,765UniSTS
TNG Radiation Hybrid Map1535562.0UniSTS
SHGC-156073  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371588,767,318 - 88,767,602UniSTSGRCh37
Build 361586,568,322 - 86,568,606RGDNCBI36
Celera1565,168,579 - 65,168,863RGD
Cytogenetic Map15q25UniSTS
HuRef1564,879,329 - 64,879,613UniSTS
TNG Radiation Hybrid Map1535599.0UniSTS
BE106688  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371588,420,022 - 88,420,182UniSTSGRCh37
Build 361586,221,026 - 86,221,186RGDNCBI36
Celera1564,821,301 - 64,821,461RGD
HuRef1564,532,275 - 64,532,435UniSTS
PMC311040P17  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371588,762,096 - 88,762,223UniSTSGRCh37
Build 361586,563,100 - 86,563,227RGDNCBI36
Celera1565,163,357 - 65,163,484RGD
Cytogenetic Map15q25UniSTS
HuRef1564,874,107 - 64,874,234UniSTS
PMC311040P20  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371588,651,792 - 88,652,037UniSTSGRCh37
Build 361586,452,796 - 86,453,041RGDNCBI36
Celera1565,053,065 - 65,053,310RGD
Cytogenetic Map15q25UniSTS
HuRef1564,764,057 - 64,764,302UniSTS
PMC311040P21  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371588,713,882 - 88,714,097UniSTSGRCh37
Build 361586,514,886 - 86,515,101RGDNCBI36
Celera1565,115,156 - 65,115,371RGD
Cytogenetic Map15q25UniSTS
HuRef1564,825,911 - 64,826,126UniSTS
PMC311040P6  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371588,733,429 - 88,733,754UniSTSGRCh37
Build 361586,534,433 - 86,534,758RGDNCBI36
Celera1565,134,703 - 65,135,028RGD
Cytogenetic Map15q25UniSTS
HuRef1564,845,458 - 64,845,783UniSTS
PMC311040P8  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371588,797,821 - 88,798,085UniSTSGRCh37
Build 361586,598,825 - 86,599,089RGDNCBI36
Celera1565,199,076 - 65,199,340RGD
Cytogenetic Map15q25.3UniSTS
Cytogenetic Map15q25UniSTS
HuRef1564,909,826 - 64,910,090UniSTS
D15S550  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371588,586,348 - 88,586,661UniSTSGRCh37
Build 361586,387,352 - 86,387,665RGDNCBI36
Celera1564,987,625 - 64,987,938RGD
Cytogenetic Map15q25UniSTS
HuRef1564,698,618 - 64,698,931UniSTS
D15S1230  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371588,564,510 - 88,564,668UniSTSGRCh37
Build 361586,365,514 - 86,365,672RGDNCBI36
Celera1564,965,788 - 64,965,946RGD
Cytogenetic Map15q25UniSTS
HuRef1564,676,783 - 64,676,941UniSTS
Whitehead-YAC Contig Map15 UniSTS
D15S930  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371588,493,065 - 88,493,219UniSTSGRCh37
Build 361586,294,069 - 86,294,223RGDNCBI36
Celera1564,894,351 - 64,894,505RGD
Cytogenetic Map15q25UniSTS
HuRef1564,605,347 - 64,605,501UniSTS
Whitehead-RH Map15335.8UniSTS
Whitehead-YAC Contig Map15 UniSTS
NCBI RH Map15627.9UniSTS


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 21 1227 25 1 2 1 859 14 821 3 58 8 1 72 807
Low 1639 572 1039 182 381 20 2521 947 2864 218 1106 1236 163 1 1079 1251 1
Below cutoff 631 1150 576 363 949 362 910 1196 28 143 171 199 2 53 730 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_029619 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001007156 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001012338 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001243101 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001320134 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001320135 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375810 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375811 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375812 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375813 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375814 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_002530 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006720545 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006720548 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006720549 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006720550 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011521638 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017022240 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017022241 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017022242 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017022243 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017022244 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017022245 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017022248 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017022250 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017022251 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017022252 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017022254 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024449933 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024449934 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024449935 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024449936 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047432602 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047432603 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047432604 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054378054 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054378055 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054378056 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054378057 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054378058 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054378059 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054378060 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054378061 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054378062 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054378063 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054378064 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054378065 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054378066 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054378067 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054378068 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054378069 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054378070 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054378071 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054378072 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054378073 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001751292 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001751293 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_002957645 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008488951 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008488952 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008488953 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC009711 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC011966 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC021677 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF052184 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF058389 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF058390 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF125808 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI613045 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ224521 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK094929 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK297160 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK302504 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK309695 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK313646 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL109700 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL134171 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY065844 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC013693 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC128249 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BG741347 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BI962878 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM675026 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM887782 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ893817 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BT007291 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CB053605 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CD370531 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471101 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CK903553 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068263 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA789502 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ323597 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HY003065 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KJ534904 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KJ534905 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KJ534906 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KJ535052 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  S76475 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  S76476 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U05012 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

RefSeq Acc Id: ENST00000317501   ⟹   ENSP00000318328
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1587,977,364 - 88,256,739 (-)Ensembl
RefSeq Acc Id: ENST00000355254   ⟹   ENSP00000347397
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1587,876,757 - 88,256,731 (-)Ensembl
RefSeq Acc Id: ENST00000357724   ⟹   ENSP00000350356
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1587,876,757 - 88,256,731 (-)Ensembl
RefSeq Acc Id: ENST00000360948   ⟹   ENSP00000354207
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1587,876,757 - 88,256,731 (-)Ensembl
RefSeq Acc Id: ENST00000394480   ⟹   ENSP00000377990
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1587,859,751 - 88,256,747 (-)Ensembl
RefSeq Acc Id: ENST00000540489   ⟹   ENSP00000444673
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1587,979,345 - 88,256,731 (-)Ensembl
RefSeq Acc Id: ENST00000542733   ⟹   ENSP00000437773
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1587,916,273 - 88,205,933 (-)Ensembl
RefSeq Acc Id: ENST00000557856   ⟹   ENSP00000453959
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1587,876,791 - 88,256,177 (-)Ensembl
RefSeq Acc Id: ENST00000557897
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1588,072,601 - 88,126,361 (-)Ensembl
RefSeq Acc Id: ENST00000558306   ⟹   ENSP00000480693
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1587,979,054 - 88,127,191 (-)Ensembl
RefSeq Acc Id: ENST00000558576   ⟹   ENSP00000473315
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1587,916,262 - 87,933,090 (-)Ensembl
RefSeq Acc Id: ENST00000558676   ⟹   ENSP00000453511
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1587,926,656 - 88,256,179 (-)Ensembl
RefSeq Acc Id: ENST00000559067
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1588,255,906 - 88,256,768 (-)Ensembl
RefSeq Acc Id: ENST00000559188   ⟹   ENSP00000473656
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1588,137,461 - 88,252,622 (-)Ensembl
RefSeq Acc Id: ENST00000559680
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1587,931,082 - 87,940,735 (-)Ensembl
RefSeq Acc Id: ENST00000559764
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1588,131,969 - 88,136,478 (-)Ensembl
RefSeq Acc Id: ENST00000560017   ⟹   ENSP00000473475
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1588,072,551 - 88,135,938 (-)Ensembl
RefSeq Acc Id: ENST00000560201
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1587,977,367 - 87,978,803 (-)Ensembl
RefSeq Acc Id: ENST00000560739
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1588,072,424 - 88,099,265 (-)Ensembl
RefSeq Acc Id: ENST00000626019   ⟹   ENSP00000486784
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1587,876,789 - 88,256,153 (-)Ensembl
RefSeq Acc Id: ENST00000629765   ⟹   ENSP00000485864
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1587,859,751 - 88,256,739 (-)Ensembl
RefSeq Acc Id: ENST00000695462   ⟹   ENSP00000511942
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1587,876,803 - 88,256,791 (-)Ensembl
RefSeq Acc Id: ENST00000695463   ⟹   ENSP00000511943
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1587,977,391 - 88,256,768 (-)Ensembl
RefSeq Acc Id: NM_001007156   ⟹   NP_001007157
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381587,977,364 - 88,256,739 (-)NCBI
GRCh371588,419,948 - 88,800,026 (-)NCBI
Build 361586,321,599 - 86,600,665 (-)NCBI Archive
HuRef1564,532,241 - 64,911,404 (-)NCBI
CHM1_11588,362,437 - 88,641,816 (-)NCBI
T2T-CHM13v2.01585,732,007 - 86,011,346 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001012338   ⟹   NP_001012338
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381587,859,751 - 88,256,739 (-)NCBI
GRCh371588,419,948 - 88,800,026 (-)NCBI
Build 361586,220,992 - 86,600,665 (-)NCBI Archive
HuRef1564,532,241 - 64,911,404 (-)NCBI
CHM1_11588,261,800 - 88,641,816 (-)NCBI
T2T-CHM13v2.01585,614,325 - 86,011,346 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001243101   ⟹   NP_001230030
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381587,859,751 - 88,256,739 (-)NCBI
HuRef1564,532,241 - 64,911,404 (-)NCBI
CHM1_11588,261,800 - 88,641,816 (-)NCBI
T2T-CHM13v2.01585,614,325 - 86,011,346 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001320134   ⟹   NP_001307063
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381587,977,364 - 88,256,169 (-)NCBI
CHM1_11588,362,437 - 88,641,254 (-)NCBI
T2T-CHM13v2.01585,732,007 - 86,010,776 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001320135   ⟹   NP_001307064
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381587,916,262 - 88,205,974 (-)NCBI
CHM1_11588,301,337 - 88,591,041 (-)NCBI
T2T-CHM13v2.01585,670,896 - 85,960,597 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001375810   ⟹   NP_001362739
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381587,859,751 - 88,256,179 (-)NCBI
T2T-CHM13v2.01585,614,325 - 86,010,786 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001375811   ⟹   NP_001362740
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381587,859,751 - 88,256,179 (-)NCBI
T2T-CHM13v2.01585,614,325 - 86,010,786 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001375812   ⟹   NP_001362741
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381587,859,751 - 88,256,179 (-)NCBI
T2T-CHM13v2.01585,614,325 - 86,010,786 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001375813   ⟹   NP_001362742
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381587,977,364 - 88,256,179 (-)NCBI
T2T-CHM13v2.01585,732,007 - 86,010,786 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001375814   ⟹   NP_001362743
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381587,977,364 - 88,256,179 (-)NCBI
T2T-CHM13v2.01585,732,007 - 86,010,786 (-)NCBI
Sequence:
RefSeq Acc Id: NM_002530   ⟹   NP_002521
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381587,859,751 - 88,256,739 (-)NCBI
GRCh371588,419,948 - 88,800,026 (-)NCBI
Build 361586,220,992 - 86,600,665 (-)NCBI Archive
HuRef1564,532,241 - 64,911,404 (-)NCBI
CHM1_11588,261,800 - 88,641,816 (-)NCBI
T2T-CHM13v2.01585,614,325 - 86,011,346 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006720545   ⟹   XP_006720608
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381587,916,262 - 88,256,179 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006720548   ⟹   XP_006720611
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381588,031,286 - 88,256,739 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006720549   ⟹   XP_006720612
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381588,072,424 - 88,256,179 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006720550   ⟹   XP_006720613
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381588,072,424 - 88,256,179 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011521638   ⟹   XP_011519940
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381588,072,424 - 88,256,179 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017022240   ⟹   XP_016877729
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381587,859,751 - 88,256,739 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017022241   ⟹   XP_016877730
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381587,859,751 - 88,190,259 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017022242   ⟹   XP_016877731
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381587,917,028 - 88,256,179 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017022243   ⟹   XP_016877732
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381587,859,751 - 88,205,974 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017022244   ⟹   XP_016877733
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381587,859,751 - 88,252,614 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017022245   ⟹   XP_016877734
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381587,859,751 - 88,252,614 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017022250   ⟹   XP_016877739
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381588,098,498 - 88,256,179 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017022251   ⟹   XP_016877740
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381587,859,751 - 88,132,583 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017022252   ⟹   XP_016877741
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381587,859,751 - 88,132,583 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017022254   ⟹   XP_016877743
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381587,859,751 - 88,256,179 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024449934   ⟹   XP_024305702
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381587,977,364 - 88,256,739 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024449935   ⟹   XP_024305703
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381588,011,214 - 88,256,179 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047432602   ⟹   XP_047288558
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381587,977,364 - 88,256,739 (-)NCBI
RefSeq Acc Id: XM_047432603   ⟹   XP_047288559
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381587,977,364 - 88,256,739 (-)NCBI
RefSeq Acc Id: XM_047432604   ⟹   XP_047288560
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381588,072,601 - 88,256,179 (-)NCBI
RefSeq Acc Id: XM_054378054   ⟹   XP_054234029
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01585,628,869 - 86,011,400 (-)NCBI
RefSeq Acc Id: XM_054378055   ⟹   XP_054234030
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01585,628,869 - 85,944,878 (-)NCBI
RefSeq Acc Id: XM_054378056   ⟹   XP_054234031
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01585,671,662 - 86,010,786 (-)NCBI
RefSeq Acc Id: XM_054378057   ⟹   XP_054234032
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01585,628,869 - 86,010,233 (-)NCBI
RefSeq Acc Id: XM_054378058   ⟹   XP_054234033
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01585,628,869 - 85,960,597 (-)NCBI
RefSeq Acc Id: XM_054378059   ⟹   XP_054234034
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01585,628,869 - 85,990,741 (-)NCBI
RefSeq Acc Id: XM_054378060   ⟹   XP_054234035
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01585,670,896 - 86,010,786 (-)NCBI
RefSeq Acc Id: XM_054378061   ⟹   XP_054234036
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01585,732,007 - 86,011,397 (-)NCBI
RefSeq Acc Id: XM_054378062   ⟹   XP_054234037
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01585,732,007 - 86,011,397 (-)NCBI
RefSeq Acc Id: XM_054378063   ⟹   XP_054234038
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01585,732,007 - 86,011,407 (-)NCBI
RefSeq Acc Id: XM_054378064   ⟹   XP_054234039
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01585,765,854 - 86,010,786 (-)NCBI
RefSeq Acc Id: XM_054378065   ⟹   XP_054234040
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01585,782,329 - 86,011,397 (-)NCBI
RefSeq Acc Id: XM_054378066   ⟹   XP_054234041
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01585,827,067 - 86,010,786 (-)NCBI
RefSeq Acc Id: XM_054378067   ⟹   XP_054234042
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01585,827,067 - 86,010,786 (-)NCBI
RefSeq Acc Id: XM_054378068   ⟹   XP_054234043
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01585,853,140 - 86,010,786 (-)NCBI
RefSeq Acc Id: XM_054378069   ⟹   XP_054234044
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01585,827,067 - 86,010,786 (-)NCBI
RefSeq Acc Id: XM_054378070   ⟹   XP_054234045
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01585,827,244 - 86,010,786 (-)NCBI
RefSeq Acc Id: XM_054378071   ⟹   XP_054234046
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01585,628,869 - 85,887,216 (-)NCBI
RefSeq Acc Id: XM_054378072   ⟹   XP_054234047
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01585,628,869 - 85,887,216 (-)NCBI
RefSeq Acc Id: XM_054378073   ⟹   XP_054234048
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01585,628,869 - 86,010,786 (-)NCBI
RefSeq Acc Id: XR_001751292
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381587,859,751 - 88,256,179 (-)NCBI
Sequence:
RefSeq Acc Id: XR_001751293
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381588,098,516 - 88,256,179 (-)NCBI
Sequence:
RefSeq Acc Id: XR_002957645
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381588,098,515 - 88,256,179 (-)NCBI
Sequence:
RefSeq Acc Id: XR_008488951
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01585,614,323 - 86,010,786 (-)NCBI
RefSeq Acc Id: XR_008488952
Type: NON-CODING
Position:
Human AssemblyChrPos