SORT1 (sortilin 1) - Rat Genome Database

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Gene: SORT1 (sortilin 1) Homo sapiens
Analyze
Symbol: SORT1
Name: sortilin 1
RGD ID: 731682
HGNC Page HGNC:11186
Description: Enables several functions, including nerve growth factor binding activity; nerve growth factor receptor activity; and neurotensin receptor activity, non-G protein-coupled. Involved in several processes, including cell surface receptor signaling pathway; negative regulation of lipoprotein lipase activity; and post-Golgi vesicle-mediated transport. Located in several cellular components, including clathrin-coated pit; cytoplasmic vesicle; and perinuclear region of cytoplasm. Implicated in abdominal aortic aneurysm.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: 100 kDa NT receptor; glycoprotein 95; Gp95; LDLCQ6; neurotensin receptor 3; NT3; NTR3; sortilin
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
GRCh381109,309,575 - 109,397,918 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1109,309,568 - 109,397,918 (-)EnsemblGRCh38hg38GRCh38
GRCh371109,852,197 - 109,940,540 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361109,653,715 - 109,742,086 (-)NCBINCBI36Build 36hg18NCBI36
Build 341109,564,233 - 109,652,605NCBI
Celera1108,121,561 - 108,209,921 (-)NCBICelera
Cytogenetic Map1p13.3NCBI
HuRef1107,745,442 - 107,833,803 (-)NCBIHuRef
CHM1_11109,967,032 - 110,055,400 (-)NCBICHM1_1
T2T-CHM13v2.01109,342,381 - 109,430,699 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(1->4)-beta-D-glucan  (ISO)
1,2-dimethylhydrazine  (ISO)
17beta-estradiol  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2-hydroxypropanoic acid  (EXP)
2-methylcholine  (EXP)
3,4-methylenedioxymethamphetamine  (ISO)
3-chloropropane-1,2-diol  (ISO)
3-isobutyl-1-methyl-7H-xanthine  (EXP)
4,4'-diaminodiphenylmethane  (ISO)
4-hydroxyphenyl retinamide  (ISO)
6-propyl-2-thiouracil  (ISO)
acrylamide  (ISO)
aflatoxin B1  (ISO)
all-trans-retinoic acid  (EXP)
ammonium chloride  (ISO)
amphetamine  (ISO)
aristolochic acid A  (EXP)
bafilomycin A1  (ISO)
benzo[a]pyrene  (EXP,ISO)
beta-naphthoflavone  (ISO)
bisphenol A  (EXP,ISO)
Bisphenol B  (EXP)
bisphenol F  (EXP)
butan-1-ol  (EXP)
butanal  (EXP)
cadmium dichloride  (ISO)
cannabidiol  (EXP)
carbon nanotube  (ISO)
chloroquine  (ISO)
chlorpyrifos  (ISO)
cholesterol  (ISO)
cobalt dichloride  (EXP,ISO)
copper atom  (ISO)
copper(0)  (ISO)
copper(II) chloride  (EXP)
cycloheximide  (EXP,ISO)
cyclosporin A  (EXP)
DDE  (EXP)
dexamethasone  (EXP)
dibutyl phthalate  (ISO)
dioxygen  (ISO)
disodium selenite  (EXP)
doxorubicin  (EXP)
endosulfan  (ISO)
ethanol  (ISO)
etoposide  (EXP)
fenofibrate  (ISO)
fenthion  (ISO)
FR900359  (EXP)
furan  (ISO)
hexadecanoic acid  (EXP)
indole-3-methanol  (ISO)
indometacin  (EXP)
inulin  (ISO)
iron atom  (EXP)
iron(0)  (EXP)
isotretinoin  (EXP)
ivermectin  (EXP)
L-ascorbic acid  (ISO)
lead(0)  (ISO)
lipopolysaccharide  (EXP)
manganese atom  (EXP)
manganese(0)  (EXP)
manganese(II) chloride  (EXP)
methotrexate  (ISO)
methoxychlor  (ISO)
mitomycin C  (EXP)
N-benzyloxycarbonyl-L-leucyl-L-leucyl-L-leucinal  (ISO)
N-nitrosodiethylamine  (ISO)
nickel atom  (EXP)
orphenadrine  (ISO)
ozone  (ISO)
p-toluidine  (ISO)
paracetamol  (ISO)
paraquat  (ISO)
pentachlorophenol  (ISO)
perfluorooctane-1-sulfonic acid  (ISO)
perfluorooctanoic acid  (EXP,ISO)
phosgene  (ISO)
pirinixic acid  (ISO)
progesterone  (EXP)
protein kinase inhibitor  (EXP)
PX-866  (ISO)
rac-lactic acid  (EXP)
S-(1,2-dichlorovinyl)-L-cysteine  (EXP)
Se-methyl-L-selenocysteine  (EXP)
Se-methylselenocysteine  (EXP)
silicon dioxide  (EXP)
sodium arsenite  (ISO)
streptozocin  (ISO)
taurocholic acid  (ISO)
temozolomide  (EXP)
testosterone  (EXP)
tetrachloromethane  (ISO)
thioacetamide  (ISO)
titanium dioxide  (ISO)
trichostatin A  (EXP)
triptonide  (ISO)
troglitazone  (EXP)
tungsten  (ISO)
valproic acid  (EXP,ISO)
vincaleukoblastine  (EXP)
vinclozolin  (ISO)
vitamin E  (EXP)
wortmannin  (ISO)
Yessotoxin  (EXP)
zinc atom  (EXP)
zinc(0)  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

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

Human Phenotype
Autism  (IAGP)
Hypertension  (IAGP)
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
4. Transcriptomic characteristics of bronchoalveolar lavage fluid and peripheral blood mononuclear cells in COVID-19 patients. Xiong Y, etal., Emerg Microbes Infect. 2020 Dec;9(1):761-770. doi: 10.1080/22221751.2020.1747363.
5. A DAB2IP genotype: sex interaction is associated with abdominal aortic aneurysm expansion. Ye Z, etal., J Investig Med. 2017 Oct;65(7):1077-1082. doi: 10.1136/jim-2016-000404. Epub 2017 Jul 11.
Additional References at PubMed
PMID:8205478   PMID:9013611   PMID:9305862   PMID:9657377   PMID:9756851   PMID:9927419   PMID:10085125   PMID:10390649   PMID:11257441   PMID:11294867   PMID:11331584   PMID:11390366  
PMID:11499680   PMID:11821067   PMID:11859376   PMID:12209882   PMID:12360476   PMID:12419319   PMID:12477932   PMID:12482870   PMID:12598608   PMID:14657016   PMID:14702039   PMID:14985763  
PMID:15313463   PMID:15364913   PMID:15489334   PMID:15930396   PMID:15987945   PMID:15992544   PMID:16087676   PMID:16263699   PMID:16344560   PMID:16710414   PMID:16787399   PMID:17220298  
PMID:17353931   PMID:18029348   PMID:18088323   PMID:18191449   PMID:18193043   PMID:18193044   PMID:18258592   PMID:18603531   PMID:18624930   PMID:18687776   PMID:18713973   PMID:18817523  
PMID:19060906   PMID:19060910   PMID:19122660   PMID:19148283   PMID:19198609   PMID:19219422   PMID:19299407   PMID:19322201   PMID:19487539   PMID:19837406   PMID:19875813   PMID:20015111  
PMID:20031591   PMID:20036257   PMID:20048080   PMID:20085800   PMID:20159974   PMID:20167577   PMID:20339536   PMID:20383146   PMID:20570916   PMID:20584990   PMID:20613775   PMID:20628624  
PMID:20676133   PMID:20679960   PMID:20686565   PMID:20686566   PMID:20738937   PMID:20816088   PMID:20971364   PMID:21087763   PMID:21092856   PMID:21102451   PMID:21239051   PMID:21245145  
PMID:21261755   PMID:21347282   PMID:21357693   PMID:21378988   PMID:21378990   PMID:21466885   PMID:21521695   PMID:21730062   PMID:21873635   PMID:21909109   PMID:21949853   PMID:21966426  
PMID:22128158   PMID:22256600   PMID:22297619   PMID:22361451   PMID:22418572   PMID:22431521   PMID:22751103   PMID:22768187   PMID:22884962   PMID:23102784   PMID:23118302   PMID:23236149  
PMID:23283322   PMID:23318115   PMID:23438231   PMID:23485461   PMID:23535823   PMID:23660633   PMID:23704887   PMID:23895422   PMID:23910371   PMID:24070898   PMID:24097068   PMID:24128306  
PMID:24163244   PMID:24262325   PMID:24404198   PMID:24674750   PMID:24838608   PMID:24981860   PMID:25036637   PMID:25037567   PMID:25042869   PMID:25101658   PMID:25365768   PMID:25401472  
PMID:25542012   PMID:25609649   PMID:25805502   PMID:25854576   PMID:25921289   PMID:26085104   PMID:26261636   PMID:26297037   PMID:26331452   PMID:26370502   PMID:26375028   PMID:26464717  
PMID:26496610   PMID:26556286   PMID:26566674   PMID:26614389   PMID:26950419   PMID:26972000   PMID:27085161   PMID:27112212   PMID:27375898   PMID:27392867   PMID:27612602   PMID:27666481  
PMID:27834811   PMID:27838145   PMID:27846466   PMID:27880917   PMID:27943270   PMID:28279970   PMID:28388416   PMID:28433812   PMID:28541286   PMID:28768823   PMID:29037860   PMID:29084952  
PMID:29097363   PMID:29203673   PMID:29272741   PMID:29275103   PMID:29382723   PMID:29507755   PMID:29509190   PMID:29555433   PMID:29972886   PMID:29973585   PMID:30634965   PMID:30770901  
PMID:30833792   PMID:30909233   PMID:31073040   PMID:31104815   PMID:31608989   PMID:31767632   PMID:32077308   PMID:32125883   PMID:32296183   PMID:32357547   PMID:32526166   PMID:32614325  
PMID:32707033   PMID:32712736   PMID:32814053   PMID:32940806   PMID:33153264   PMID:33325631   PMID:33618683   PMID:33634506   PMID:33845483   PMID:33961781   PMID:34004257   PMID:34162830  
PMID:34470550   PMID:34709727   PMID:34781973   PMID:34784266   PMID:35192625   PMID:35241646   PMID:35271311   PMID:35337019   PMID:35403511   PMID:35469919   PMID:35500800   PMID:35563538  
PMID:35696571   PMID:35944360   PMID:36089417   PMID:36114006   PMID:36215168   PMID:36233189   PMID:36445845   PMID:36538041   PMID:37314216   PMID:37499664   PMID:37579565   PMID:37596305  
PMID:37616343   PMID:37673328   PMID:37913995   PMID:38070861   PMID:38095557   PMID:38297188   PMID:38334954   PMID:38339069   PMID:38694940   PMID:39382416  


Genomics

Comparative Map Data
SORT1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381109,309,575 - 109,397,918 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1109,309,568 - 109,397,918 (-)EnsemblGRCh38hg38GRCh38
GRCh371109,852,197 - 109,940,540 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361109,653,715 - 109,742,086 (-)NCBINCBI36Build 36hg18NCBI36
Build 341109,564,233 - 109,652,605NCBI
Celera1108,121,561 - 108,209,921 (-)NCBICelera
Cytogenetic Map1p13.3NCBI
HuRef1107,745,442 - 107,833,803 (-)NCBIHuRef
CHM1_11109,967,032 - 110,055,400 (-)NCBICHM1_1
T2T-CHM13v2.01109,342,381 - 109,430,699 (-)NCBIT2T-CHM13v2.0
Sort1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm393108,191,272 - 108,268,835 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl3108,191,398 - 108,268,827 (+)EnsemblGRCm39 Ensembl
GRCm383108,283,974 - 108,361,519 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl3108,284,082 - 108,361,511 (+)EnsemblGRCm38mm10GRCm38
MGSCv373108,087,050 - 108,164,429 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv363108,412,188 - 108,489,567 (+)NCBIMGSCv36mm8
Celera3110,641,971 - 110,695,148 (+)NCBICelera
Cytogenetic Map3F3NCBI
cM Map346.9NCBI
Sort1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr82198,609,466 - 198,690,481 (+)NCBIGRCr8
mRatBN7.22195,924,033 - 196,002,354 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl2195,924,099 - 196,002,354 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx2203,567,532 - 203,645,624 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.02201,449,641 - 201,527,742 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.02196,266,598 - 196,344,698 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.02211,078,092 - 211,156,312 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl2211,078,334 - 211,156,312 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.02230,546,773 - 230,626,278 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.42203,853,009 - 203,931,559 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.12203,816,049 - 203,890,296 (+)NCBI
Celera2188,569,202 - 188,647,900 (+)NCBICelera
Cytogenetic Map2q34NCBI
Sort1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495543512,730,270 - 12,819,029 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495543512,725,952 - 12,819,280 (-)NCBIChiLan1.0ChiLan1.0
SORT1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21117,906,698 - 117,994,934 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11117,066,633 - 117,154,840 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01111,687,119 - 111,775,339 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11110,850,311 - 110,888,690 (-)NCBIpanpan1.1PanPan1.1panPan2
SORT1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1642,454,091 - 42,521,251 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl642,453,942 - 42,516,740 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha645,228,326 - 45,295,415 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0642,784,113 - 42,848,096 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl642,783,933 - 42,851,871 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1642,517,324 - 42,583,603 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0642,474,716 - 42,541,652 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0642,909,755 - 42,976,918 (+)NCBIUU_Cfam_GSD_1.0
Sort1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440505819,210,972 - 19,281,426 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_004936704837,057 - 901,392 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_004936704832,651 - 901,658 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
SORT1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl4110,720,947 - 110,789,070 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.14110,721,110 - 110,791,406 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.24121,230,024 - 121,289,561 (+)NCBISscrofa10.2Sscrofa10.2susScr3
SORT1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12024,150,210 - 24,235,518 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2024,150,300 - 24,239,503 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366603834,220,514 - 34,309,885 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Sort1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247725,049,045 - 5,123,365 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247725,044,948 - 5,123,300 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in SORT1
44 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NC_000001.11:g.109274968G>T single nucleotide variant Low density lipoprotein cholesterol level quantitative trait locus 6 [RCV000007497] Chr1:109274968 [GRCh38]
Chr1:109817590 [GRCh37]
Chr1:1p13.3		 association
GRCh38/hg38 1p21.2-13.2(chr1:101618097-111703028)x1 copy number loss See cases [RCV000053879] Chr1:101618097..111703028 [GRCh38]
Chr1:102083653..112245650 [GRCh37]
Chr1:101856241..112047173 [NCBI36]
Chr1:1p21.2-13.2		 pathogenic
GRCh38/hg38 1p21.1-13.3(chr1:106074587-110144290)x1 copy number loss See cases [RCV000053881] Chr1:106074587..110144290 [GRCh38]
Chr1:106617209..110686912 [GRCh37]
Chr1:106418732..110488435 [NCBI36]
Chr1:1p21.1-13.3		 pathogenic
GRCh38/hg38 1p21.3-13.3(chr1:97410602-110670510)x1 copy number loss See cases [RCV000053877] Chr1:97410602..110670510 [GRCh38]
Chr1:97876158..111213132 [GRCh37]
Chr1:97648746..111014655 [NCBI36]
Chr1:1p21.3-13.3		 pathogenic
GRCh38/hg38 1p13.3(chr1:108970247-109794222)x3 copy number gain See cases [RCV000138606] Chr1:108970247..109794222 [GRCh38]
Chr1:109512869..110336844 [GRCh37]
Chr1:109314392..110138367 [NCBI36]
Chr1:1p13.3		 uncertain significance
GRCh38/hg38 1p21.1-12(chr1:104325484-119977655)x3 copy number gain See cases [RCV000142953] Chr1:104325484..119977655 [GRCh38]
Chr1:104868106..120471049 [GRCh37]
Chr1:104669629..120321801 [NCBI36]
Chr1:1p21.1-12		 pathogenic
GRCh38/hg38 1p21.1-13.2(chr1:105468292-112190626)x1 copy number loss See cases [RCV000142760] Chr1:105468292..112190626 [GRCh38]
Chr1:106010914..112733248 [GRCh37]
Chr1:105812437..112534771 [NCBI36]
Chr1:1p21.1-13.2		 pathogenic
GRCh37/hg19 1p36.12-12(chr1:20608823-120546301)x3 copy number loss not provided [RCV000762767] Chr1:20608823..120546301 [GRCh37]
Chr1:1p36.12-12		 likely benign
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3 copy number gain See cases [RCV000510383] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684) copy number gain See cases [RCV000510926] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1p13.3(chr1:109343840-109868178)x3 copy number gain See cases [RCV000510931] Chr1:109343840..109868178 [GRCh37]
Chr1:1p13.3		 uncertain significance
NM_002959.7(SORT1):c.740G>A (p.Gly247Glu) single nucleotide variant not specified [RCV004290380] Chr1:109350971 [GRCh38]
Chr1:109893593 [GRCh37]
Chr1:1p13.3		 uncertain significance
GRCh37/hg19 1p22.1-11.2(chr1:93837992-121343783)x3 copy number gain See cases [RCV000512354] Chr1:93837992..121343783 [GRCh37]
Chr1:1p22.1-11.2		 pathogenic
GRCh37/hg19 1p36.33-q44(chr1:47851-249228449)x3 copy number gain not provided [RCV000736295] Chr1:47851..249228449 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1p36.33-q44(chr1:82154-249218992)x3 copy number gain not provided [RCV000736305] Chr1:82154..249218992 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
NC_000001.11:g.(?_103175204)_(111410059_?)del deletion Autism [RCV000754122] Chr1:103175204..111410059 [GRCh38]
Chr1:1p21.1-13.2		 likely pathogenic
GRCh37/hg19 1p13.3(chr1:109832283-109871787)x1 copy number loss not provided [RCV000736645] Chr1:109832283..109871787 [GRCh37]
Chr1:1p13.3		 benign
GRCh37/hg19 1p22.1-13.3(chr1:94054724-111671707)x3 copy number gain not provided [RCV000749068] Chr1:94054724..111671707 [GRCh37]
Chr1:1p22.1-13.3		 pathogenic
NM_002959.7(SORT1):c.2237G>A (p.Ser746Asn) single nucleotide variant not provided [RCV000968528] Chr1:109316863 [GRCh38]
Chr1:109859485 [GRCh37]
Chr1:1p13.3		 benign
NM_002959.7(SORT1):c.543+8T>A single nucleotide variant not provided [RCV000966759] Chr1:109355359 [GRCh38]
Chr1:109897981 [GRCh37]
Chr1:1p13.3		 benign
Single allele deletion 1p13.3 deletion syndrome [RCV000786772] Chr1:107779092..111199205 [GRCh37]
Chr1:1p13.3		 likely pathogenic
GRCh37/hg19 1p13.3(chr1:109612444-109857815)x3 copy number gain not provided [RCV000848378] Chr1:109612444..109857815 [GRCh37]
Chr1:1p13.3		 uncertain significance
Single allele deletion not provided [RCV000844956] Chr1:108926313..111266497 [GRCh37]
Chr1:1p13.3		 not provided
GRCh37/hg19 1p13.3(chr1:109801239-109901996)x3 copy number gain not provided [RCV000845930] Chr1:109801239..109901996 [GRCh37]
Chr1:1p13.3		 uncertain significance
NC_000001.10:g.(?_108679275)_(111674176_?)del deletion Hereditary spastic paraplegia 63 [RCV003105726] Chr1:108679275..111674176 [GRCh37]
Chr1:1p13.3		 pathogenic
NM_002959.7(SORT1):c.1072G>T (p.Asp358Tyr) single nucleotide variant not provided [RCV000972576] Chr1:109342050 [GRCh38]
Chr1:109884672 [GRCh37]
Chr1:1p13.3		 benign
NM_002959.7(SORT1):c.333A>G (p.Ser111=) single nucleotide variant not provided [RCV000913015] Chr1:109369563 [GRCh38]
Chr1:109912185 [GRCh37]
Chr1:1p13.3		 likely benign
GRCh37/hg19 1p21.2-12(chr1:102021465-119737478) copy number loss Seizure [RCV001352640] Chr1:102021465..119737478 [GRCh37]
Chr1:1p21.2-12		 pathogenic
GRCh37/hg19 1p13.3(chr1:108346477-110177123)x1 copy number loss not provided [RCV001827629] Chr1:108346477..110177123 [GRCh37]
Chr1:1p13.3		 uncertain significance
GRCh37/hg19 1p21.3-13.2(chr1:95046805-114714931) copy number loss not specified [RCV002053503] Chr1:95046805..114714931 [GRCh37]
Chr1:1p21.3-13.2		 pathogenic
NM_002959.7(SORT1):c.1145G>A (p.Arg382Gln) single nucleotide variant not specified [RCV004295085] Chr1:109340843 [GRCh38]
Chr1:109883465 [GRCh37]
Chr1:1p13.3		 uncertain significance
GRCh37/hg19 1p13.3(chr1:109371874-109906234)x3 copy number gain not provided [RCV002474707] Chr1:109371874..109906234 [GRCh37]
Chr1:1p13.3		 uncertain significance
NM_002959.7(SORT1):c.1639A>C (p.Ile547Leu) single nucleotide variant not specified [RCV004183427] Chr1:109326996 [GRCh38]
Chr1:109869618 [GRCh37]
Chr1:1p13.3		 uncertain significance
NM_002959.7(SORT1):c.259G>C (p.Gly87Arg) single nucleotide variant not specified [RCV004136597] Chr1:109397634 [GRCh38]
Chr1:109940256 [GRCh37]
Chr1:1p13.3		 uncertain significance
NM_002959.7(SORT1):c.807T>G (p.Phe269Leu) single nucleotide variant not specified [RCV004128867] Chr1:109347508 [GRCh38]
Chr1:109890130 [GRCh37]
Chr1:1p13.3		 uncertain significance
NM_002959.7(SORT1):c.2441C>T (p.Ser814Phe) single nucleotide variant not specified [RCV004111793] Chr1:109314301 [GRCh38]
Chr1:109856923 [GRCh37]
Chr1:1p13.3		 uncertain significance
NM_002959.7(SORT1):c.808A>T (p.Thr270Ser) single nucleotide variant not specified [RCV004128868] Chr1:109347507 [GRCh38]
Chr1:109890129 [GRCh37]
Chr1:1p13.3		 uncertain significance
NM_002959.7(SORT1):c.284A>G (p.Lys95Arg) single nucleotide variant not specified [RCV004083998] Chr1:109397609 [GRCh38]
Chr1:109940231 [GRCh37]
Chr1:1p13.3		 uncertain significance
NM_002959.7(SORT1):c.853G>A (p.Glu285Lys) single nucleotide variant not specified [RCV004074038] Chr1:109345861 [GRCh38]
Chr1:109888483 [GRCh37]
Chr1:1p13.3		 uncertain significance
NM_002959.7(SORT1):c.28G>C (p.Gly10Arg) single nucleotide variant not specified [RCV004285319] Chr1:109397865 [GRCh38]
Chr1:109940487 [GRCh37]
Chr1:1p13.3		 uncertain significance
NM_002959.7(SORT1):c.991A>G (p.Thr331Ala) single nucleotide variant not specified [RCV004351669] Chr1:109342131 [GRCh38]
Chr1:109884753 [GRCh37]
Chr1:1p13.3		 uncertain significance
NM_002959.7(SORT1):c.271G>A (p.Asp91Asn) single nucleotide variant not specified [RCV004346498] Chr1:109397622 [GRCh38]
Chr1:109940244 [GRCh37]
Chr1:1p13.3		 uncertain significance
GRCh37/hg19 1p13.3-13.2(chr1:109483388-112293512)x1 copy number loss not provided [RCV003483272] Chr1:109483388..112293512 [GRCh37]
Chr1:1p13.3-13.2		 pathogenic
NM_002959.7(SORT1):c.370A>G (p.Ile124Val) single nucleotide variant not provided [RCV003406657] Chr1:109367478 [GRCh38]
Chr1:109910100 [GRCh37]
Chr1:1p13.3		 likely benign
NM_002959.7(SORT1):c.904A>G (p.Lys302Glu) single nucleotide variant not provided [RCV003406656] Chr1:109345810 [GRCh38]
Chr1:109888432 [GRCh37]
Chr1:1p13.3		 likely benign
NM_002959.7(SORT1):c.1340A>G (p.Glu447Gly) single nucleotide variant not provided [RCV003406655] Chr1:109336271 [GRCh38]
Chr1:109878893 [GRCh37]
Chr1:1p13.3		 likely benign
GRCh37/hg19 1p13.3-13.2(chr1:109700156-112176616)x1 copy number loss not specified [RCV003987183] Chr1:109700156..112176616 [GRCh37]
Chr1:1p13.3-13.2		 uncertain significance
NM_002959.7(SORT1):c.2289C>T (p.Ile763=) single nucleotide variant SORT1-related disorder [RCV003957174] Chr1:109314740 [GRCh38]
Chr1:109857362 [GRCh37]
Chr1:1p13.3		 likely benign
NM_002959.7(SORT1):c.594T>C (p.Phe198=) single nucleotide variant SORT1-related disorder [RCV003979831] Chr1:109354481 [GRCh38]
Chr1:109897103 [GRCh37]
Chr1:1p13.3		 benign
NM_002959.7(SORT1):c.544-5A>G single nucleotide variant SORT1-related disorder [RCV003924192] Chr1:109354536 [GRCh38]
Chr1:109897158 [GRCh37]
Chr1:1p13.3		 likely benign
NM_002959.7(SORT1):c.12C>G (p.Pro4=) single nucleotide variant SORT1-related disorder [RCV003976652] Chr1:109397881 [GRCh38]
Chr1:109940503 [GRCh37]
Chr1:1p13.3		 benign
NM_002959.7(SORT1):c.1682C>T (p.Thr561Met) single nucleotide variant SORT1-related disorder [RCV003961506] Chr1:109325051 [GRCh38]
Chr1:109867673 [GRCh37]
Chr1:1p13.3		 benign
NM_002959.7(SORT1):c.2241G>A (p.Pro747=) single nucleotide variant SORT1-related disorder [RCV003964036] Chr1:109316859 [GRCh38]
Chr1:109859481 [GRCh37]
Chr1:1p13.3		 likely benign
NM_002959.7(SORT1):c.1227C>T (p.Ser409=) single nucleotide variant SORT1-related disorder [RCV003937286] Chr1:109340761 [GRCh38]
Chr1:109883383 [GRCh37]
Chr1:1p13.3		 likely benign
NM_002959.7(SORT1):c.969A>C (p.Thr323=) single nucleotide variant SORT1-related disorder [RCV003974309] Chr1:109342153 [GRCh38]
Chr1:109884775 [GRCh37]
Chr1:1p13.3		 benign
NM_002959.7(SORT1):c.1620C>T (p.Ser540=) single nucleotide variant SORT1-related disorder [RCV003942164] Chr1:109327015 [GRCh38]
Chr1:109869637 [GRCh37]
Chr1:1p13.3		 benign
NM_002959.7(SORT1):c.1315C>T (p.His439Tyr) single nucleotide variant not specified [RCV004457470] Chr1:109336296 [GRCh38]
Chr1:109878918 [GRCh37]
Chr1:1p13.3		 uncertain significance
NM_002959.7(SORT1):c.523G>T (p.Gly175Cys) single nucleotide variant not specified [RCV004457475] Chr1:109355387 [GRCh38]
Chr1:109898009 [GRCh37]
Chr1:1p13.3		 uncertain significance
NM_002959.7(SORT1):c.83C>T (p.Pro28Leu) single nucleotide variant not specified [RCV004457476] Chr1:109397810 [GRCh38]
Chr1:109940432 [GRCh37]
Chr1:1p13.3		 uncertain significance
NM_002959.7(SORT1):c.932G>A (p.Arg311His) single nucleotide variant not specified [RCV004457478] Chr1:109345782 [GRCh38]
Chr1:109888404 [GRCh37]
Chr1:1p13.3		 uncertain significance
NM_002959.7(SORT1):c.863G>A (p.Arg288Lys) single nucleotide variant not specified [RCV004457477] Chr1:109345851 [GRCh38]
Chr1:109888473 [GRCh37]
Chr1:1p13.3		 uncertain significance
NM_002959.7(SORT1):c.1426A>G (p.Met476Val) single nucleotide variant not specified [RCV004457471] Chr1:109327547 [GRCh38]
Chr1:109870169 [GRCh37]
Chr1:1p13.3		 uncertain significance
NM_002959.7(SORT1):c.2240C>T (p.Pro747Leu) single nucleotide variant not specified [RCV004457473] Chr1:109316860 [GRCh38]
Chr1:109859482 [GRCh37]
Chr1:1p13.3		 uncertain significance
NM_002959.7(SORT1):c.1905T>G (p.Ile635Met) single nucleotide variant not specified [RCV004457472] Chr1:109323051 [GRCh38]
Chr1:109865673 [GRCh37]
Chr1:1p13.3		 uncertain significance
NM_002959.7(SORT1):c.44C>T (p.Pro15Leu) single nucleotide variant not specified [RCV004679205] Chr1:109397849 [GRCh38]
Chr1:109940471 [GRCh37]
Chr1:1p13.3		 uncertain significance
NM_002959.7(SORT1):c.2242G>C (p.Glu748Gln) single nucleotide variant not specified [RCV004679206] Chr1:109316858 [GRCh38]
Chr1:109859480 [GRCh37]
Chr1:1p13.3		 uncertain significance
NM_002959.7(SORT1):c.170G>A (p.Ser57Asn) single nucleotide variant not specified [RCV004670565] Chr1:109397723 [GRCh38]
Chr1:109940345 [GRCh37]
Chr1:1p13.3		 uncertain significance
NM_002959.7(SORT1):c.179T>G (p.Leu60Arg) single nucleotide variant not specified [RCV004670566] Chr1:109397714 [GRCh38]
Chr1:109940336 [GRCh37]
Chr1:1p13.3		 uncertain significance
NM_002959.7(SORT1):c.49G>C (p.Gly17Arg) single nucleotide variant not specified [RCV004670567] Chr1:109397844 [GRCh38]
Chr1:109940466 [GRCh37]
Chr1:1p13.3		 uncertain significance
NM_002959.7(SORT1):c.1106G>T (p.Gly369Val) single nucleotide variant not specified [RCV004670569] Chr1:109342016 [GRCh38]
Chr1:109884638 [GRCh37]
Chr1:1p13.3		 uncertain significance
NM_002959.7(SORT1):c.1799A>T (p.Tyr600Phe) single nucleotide variant not specified [RCV004670570] Chr1:109324934 [GRCh38]
Chr1:109867556 [GRCh37]
Chr1:1p13.3		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:3227
Count of miRNA genes:1229
Interacting mature miRNAs:1566
Transcripts:ENST00000256637, ENST00000466471, ENST00000471996, ENST00000482236, ENST00000483508, ENST00000485149, ENST00000493736, ENST00000495777, ENST00000538502
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

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

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


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
407257094GWAS906070_Htotal cholesterol measurement QTL GWAS906070 (human)4e-15total cholesterol measurementblood total cholesterol level (CMO:0000051)1109372187109372188Human
406903874GWAS552850_Hlow density lipoprotein cholesterol measurement QTL GWAS552850 (human)0.0000004low density lipoprotein cholesterol measurementblood low density lipoprotein cholesterol level (CMO:0000053)1109393147109393148Human
406912034GWAS561010_Hintelligence QTL GWAS561010 (human)1e-09intelligence1109343749109343750Human
407184678GWAS833654_Htotal cholesterol measurement QTL GWAS833654 (human)3e-11total cholesterol measurementblood total cholesterol level (CMO:0000051)1109390828109390829Human
407309794GWAS958770_Hlow density lipoprotein cholesterol measurement QTL GWAS958770 (human)7e-12low density lipoprotein cholesterol measurementblood low density lipoprotein cholesterol level (CMO:0000053)1109390828109390829Human
1300021BP45_HBlood pressure QTL 45 (human)1.770.00218Blood pressuresystolic1103389009129389009Human
407172521GWAS821497_Hblood protein measurement QTL GWAS821497 (human)4e-19blood protein measurementblood protein measurement (CMO:0000028)1109348511109348512Human
406897230GWAS546206_Hcreatinine measurement, glomerular filtration rate QTL GWAS546206 (human)8e-09creatinine measurement, glomerular filtration rateglomerular filtration rate (CMO:0000490)1109348511109348512Human
406913169GWAS562145_Hunipolar depression, bipolar disorder, schizophrenia, sex interaction measurement QTL GWAS562145 (human)0.000007unipolar depression, bipolar disorder, schizophrenia, sex interaction measurement1109354481109354482Human
407307796GWAS956772_Hlow density lipoprotein cholesterol measurement QTL GWAS956772 (human)2e-20low density lipoprotein cholesterol measurementblood low density lipoprotein cholesterol level (CMO:0000053)1109372187109372188Human
407200048GWAS849024_HAlzheimer disease QTL GWAS849024 (human)0.000005Alzheimer disease1109345810109345811Human
407238704GWAS887680_Hapolipoprotein B measurement QTL GWAS887680 (human)1e-13apolipoprotein B measurementblood apoliprotein B level (CMO:0000522)1109390828109390829Human
407347346GWAS996322_Hsortilin measurement QTL GWAS996322 (human)5e-12sortilin measurement1109334263109334264Human
407278832GWAS927808_Hbody height QTL GWAS927808 (human)3e-24body height (VT:0001253)body height (CMO:0000106)1109344569109344570Human
407012213GWAS661189_Hglomerular filtration rate QTL GWAS661189 (human)4e-15glomerular filtration rateglomerular filtration rate (CMO:0000490)1109358840109358841Human
407310911GWAS959887_Hlow density lipoprotein cholesterol measurement QTL GWAS959887 (human)2e-10low density lipoprotein cholesterol measurementblood low density lipoprotein cholesterol level (CMO:0000053)1109352134109352135Human
406903641GWAS552617_Htotal cholesterol measurement QTL GWAS552617 (human)0.000007total cholesterol measurementblood total cholesterol level (CMO:0000051)1109393147109393148Human
407166109GWAS815085_Happendicular lean mass QTL GWAS815085 (human)1e-17appendicular lean mass1109392703109392704Human
407185529GWAS834505_HAlzheimer disease QTL GWAS834505 (human)8e-09Alzheimer disease1109345810109345811Human
407240760GWAS889736_Hapolipoprotein B measurement QTL GWAS889736 (human)2e-14apolipoprotein B measurementblood apoliprotein B level (CMO:0000522)1109352134109352135Human
407268665GWAS917641_Hapolipoprotein B measurement QTL GWAS917641 (human)1e-30apolipoprotein B measurementblood apoliprotein B level (CMO:0000522)1109372187109372188Human

Markers in Region
AL034289  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371109,861,176 - 109,861,301UniSTSGRCh37
Build 361109,662,699 - 109,662,824RGDNCBI36
Celera1108,130,542 - 108,130,667RGD
Cytogenetic Map1p21.3-p13.1UniSTS
Cytogenetic Map1p13.3UniSTS
HuRef1107,754,428 - 107,754,553UniSTS
WI-14018  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371109,941,691 - 109,941,815UniSTSGRCh37
Build 361109,743,214 - 109,743,338RGDNCBI36
Celera1108,211,049 - 108,211,173RGD
Cytogenetic Map1p21.3-p13.1UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map1p13UniSTS
HuRef1107,834,931 - 107,835,055UniSTS
GeneMap99-GB4 RH Map1337.87UniSTS
GeneMap99-GB4 RH Map1337.19UniSTS
Whitehead-RH Map1390.8UniSTS
NCBI RH Map1831.1UniSTS
SORT1_8606  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371109,852,010 - 109,852,874UniSTSGRCh37
Build 361109,653,533 - 109,654,397RGDNCBI36
Celera1108,121,379 - 108,122,243RGD
HuRef1107,745,265 - 107,746,129UniSTS
SHGC-75268  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371109,852,450 - 109,852,626UniSTSGRCh37
Build 361109,653,973 - 109,654,149RGDNCBI36
Celera1108,121,819 - 108,121,995RGD
Cytogenetic Map1p21.3-p13.1UniSTS
Cytogenetic Map1p13.3UniSTS
HuRef1107,745,705 - 107,745,881UniSTS
TNG Radiation Hybrid Map159681.0UniSTS
GeneMap99-GB4 RH Map1337.59UniSTS
Whitehead-RH Map1401.2UniSTS
Whitehead-YAC Contig Map1 UniSTS
SHGC-75262  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371109,941,725 - 109,941,918UniSTSGRCh37
Build 361109,743,248 - 109,743,441RGDNCBI36
Celera1108,211,083 - 108,211,276RGD
Cytogenetic Map1p13UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map1p21.3-p13.1UniSTS
HuRef1107,834,965 - 107,835,158UniSTS
TNG Radiation Hybrid Map159726.0UniSTS
GeneMap99-GB4 RH Map1338.73UniSTS
SHGC-75270  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371109,853,990 - 109,854,127UniSTSGRCh37
Build 361109,655,513 - 109,655,650RGDNCBI36
Celera1108,123,359 - 108,123,496RGD
Cytogenetic Map1p21.3-p13.1UniSTS
Cytogenetic Map1p13.3UniSTS
HuRef1107,747,245 - 107,747,382UniSTS
TNG Radiation Hybrid Map159681.0UniSTS
GeneMap99-GB4 RH Map1337.93UniSTS
NCBI RH Map1831.1UniSTS
GDB:434012  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map19q13.13UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map2q31.2-q33.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map5q21UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map9q13-q21UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map17q25.2UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map7q21.3UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map1p21.3-p13.1UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map1p35-p34.3UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map12p13.1UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map6q22-q23UniSTS
Cytogenetic Map1q24-q25.3UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map1pter-q31.3UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map16p13UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16p12.1UniSTS
Cytogenetic Map10p11.1UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map2q11.2-q12UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic Map1p36-p35UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map4q13UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic MapXq21.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map6p12.3-p11.2UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map4p16UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map12q13.1-q13.2UniSTS
Cytogenetic Map1p31UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map6pter-p12.1UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map14q31UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2434 2788 2251 4966 1725 2350 6 622 1941 465 2268 7291 6460 53 3729 850 1740 1616 175 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_028280 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001205228 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_002959 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005271100 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005271101 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005271102 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006710812 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054338107 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054338108 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA782785 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI623426 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI695671 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK000757 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK023648 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK129918 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK130545 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK293118 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK301548 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK310147 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL117561 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL390252 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AU132384 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC023542 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC041982 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC053575 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BF591118 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ001031 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ774407 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX955818 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CB267773 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471122 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068277 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA023768 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB045034 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ525881 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HY003953 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JA738725 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000256637   ⟹   ENSP00000256637
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1109,309,575 - 109,397,918 (-)Ensembl
Ensembl Acc Id: ENST00000466471
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1109,326,806 - 109,336,302 (-)Ensembl
Ensembl Acc Id: ENST00000471996   ⟹   ENSP00000487674
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1109,369,530 - 109,397,861 (-)Ensembl
Ensembl Acc Id: ENST00000482236   ⟹   ENSP00000487712
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1109,354,485 - 109,393,357 (-)Ensembl
Ensembl Acc Id: ENST00000483508
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1109,366,783 - 109,369,589 (-)Ensembl
Ensembl Acc Id: ENST00000485149
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1109,313,801 - 109,316,927 (-)Ensembl
Ensembl Acc Id: ENST00000493736   ⟹   ENSP00000488262
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1109,350,947 - 109,389,899 (-)Ensembl
Ensembl Acc Id: ENST00000495777
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1109,368,478 - 109,369,589 (-)Ensembl
Ensembl Acc Id: ENST00000538502   ⟹   ENSP00000438597
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1109,309,568 - 109,393,357 (-)Ensembl
Ensembl Acc Id: ENST00000633956   ⟹   ENSP00000488662
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1109,355,441 - 109,392,988 (-)Ensembl
RefSeq Acc Id: NM_001205228   ⟹   NP_001192157
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381109,309,575 - 109,393,135 (-)NCBI
GRCh371109,852,187 - 109,940,563 (-)ENTREZGENE
HuRef1107,745,442 - 107,833,803 (-)ENTREZGENE
CHM1_11109,967,032 - 110,050,819 (-)NCBI
T2T-CHM13v2.01109,342,381 - 109,425,920 (-)NCBI
Sequence:
RefSeq Acc Id: NM_002959   ⟹   NP_002950
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381109,309,575 - 109,397,918 (-)NCBI
GRCh371109,852,187 - 109,940,563 (-)ENTREZGENE
Build 361109,653,715 - 109,742,086 (-)NCBI Archive
HuRef1107,745,442 - 107,833,803 (-)ENTREZGENE
CHM1_11109,967,032 - 110,055,404 (-)NCBI
T2T-CHM13v2.01109,342,381 - 109,430,699 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005271100   ⟹   XP_005271157
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381109,309,575 - 109,397,918 (-)NCBI
GRCh371109,852,187 - 109,940,563 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005271101   ⟹   XP_005271158
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381109,309,575 - 109,393,135 (-)NCBI
GRCh371109,852,187 - 109,940,563 (-)NCBI
Sequence:
RefSeq Acc Id: XM_054338107   ⟹   XP_054194082
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01109,342,381 - 109,430,699 (-)NCBI
RefSeq Acc Id: XM_054338108   ⟹   XP_054194083
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01109,342,381 - 109,425,920 (-)NCBI
RefSeq Acc Id: NP_002950   ⟸   NM_002959
- Peptide Label: isoform 1 preproprotein
- UniProtKB: C0JYZ0 (UniProtKB/Swiss-Prot),   B4DWI3 (UniProtKB/Swiss-Prot),   Q8IZ49 (UniProtKB/Swiss-Prot),   Q99523 (UniProtKB/Swiss-Prot),   A8KAQ3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001192157   ⟸   NM_001205228
- Peptide Label: isoform 2
- UniProtKB: A8KAQ3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005271157   ⟸   XM_005271100
- Peptide Label: isoform X1
- UniProtKB: A8KAQ3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005271158   ⟸   XM_005271101
- Peptide Label: isoform X2
- UniProtKB: A8KAQ3 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSP00000256637   ⟸   ENST00000256637
Ensembl Acc Id: ENSP00000488262   ⟸   ENST00000493736
Ensembl Acc Id: ENSP00000487712   ⟸   ENST00000482236
Ensembl Acc Id: ENSP00000438597   ⟸   ENST00000538502
Ensembl Acc Id: ENSP00000487674   ⟸   ENST00000471996
Ensembl Acc Id: ENSP00000488662   ⟸   ENST00000633956
RefSeq Acc Id: XP_054194082   ⟸   XM_054338107
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054194083   ⟸   XM_054338108
- Peptide Label: isoform X2
Protein Domains
Sortilin N-terminal   VPS10

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q99523-F1-model_v2 AlphaFold Q99523 1-831 view protein structure

Promoters
RGD ID:6856480
Promoter ID:EPDNEW_H1405
Type:initiation region
Name:SORT1_1
Description:sortilin 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381109,397,918 - 109,397,978EPDNEW
RGD ID:6786913
Promoter ID:HG_KWN:3982
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562
Transcripts:OTTHUMT00000317150
Position:
Human AssemblyChrPosition (strand)Source
Build 361109,733,946 - 109,734,947 (-)MPROMDB
RGD ID:6786914
Promoter ID:HG_KWN:3983
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562
Transcripts:OTTHUMT00000317149,   UC009WFB.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361109,736,946 - 109,737,446 (-)MPROMDB
RGD ID:6786912
Promoter ID:HG_KWN:3984
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid
Transcripts:OTTHUMT00000033179,   OTTHUMT00000317148
Position:
Human AssemblyChrPosition (strand)Source
Build 361109,741,936 - 109,742,747 (-)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:11186 AgrOrtholog
COSMIC SORT1 COSMIC
Ensembl Genes ENSG00000134243 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000256637 ENTREZGENE
  ENST00000256637.8 UniProtKB/Swiss-Prot
  ENST00000471996.1 UniProtKB/TrEMBL
  ENST00000482236.5 UniProtKB/TrEMBL
  ENST00000493736.5 UniProtKB/TrEMBL
  ENST00000538502 ENTREZGENE
  ENST00000538502.5 UniProtKB/Swiss-Prot
  ENST00000633956.1 UniProtKB/TrEMBL
Gene3D-CATH 2.10.70.80 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  2.130.10.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  3.30.60.270 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000134243 GTEx
HGNC ID HGNC:11186 ENTREZGENE
Human Proteome Map SORT1 Human Proteome Map
InterPro BNR_rpt UniProtKB/TrEMBL
  Sortilin_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Sortilin_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  VPS10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  VPS10-sortilin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  WD40/YVTN_repeat-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:6272 UniProtKB/Swiss-Prot
NCBI Gene 6272 ENTREZGENE
OMIM 602458 OMIM
PANTHER SORTILIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SORTILIN RELATED UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam BNR_6 UniProtKB/TrEMBL
  Sortilin-Vps10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Sortilin_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA36023 PharmGKB
SMART VPS10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP Oligoxyloglucan reducing end-specific cellobiohydrolase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A0J9YVU2_HUMAN UniProtKB/TrEMBL
  A0A0J9YVX1_HUMAN UniProtKB/TrEMBL
  A0A0J9YX61_HUMAN UniProtKB/TrEMBL
  A0A0J9YY30_HUMAN UniProtKB/TrEMBL
  A8KAQ3 ENTREZGENE, UniProtKB/TrEMBL
  B4DWI3 ENTREZGENE
  C0JYZ0 ENTREZGENE
  Q8IZ49 ENTREZGENE
  Q99523 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary B4DWI3 UniProtKB/Swiss-Prot
  C0JYZ0 UniProtKB/Swiss-Prot
  Q8IZ49 UniProtKB/Swiss-Prot