ACSL1 (acyl-CoA synthetase long chain family member 1) - Rat Genome Database
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Gene: ACSL1 (acyl-CoA synthetase long chain family member 1) Homo sapiens
Analyze
Symbol: ACSL1
Name: acyl-CoA synthetase long chain family member 1
RGD ID: 1342971
HGNC Page HGNC
Description: Exhibits long-chain fatty acid-CoA ligase activity. Involved in lipid biosynthetic process; long-chain fatty acid import into cell; and long-chain fatty acid metabolic process. Localizes to endoplasmic reticulum and mitochondrion. Biomarker of obesity.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: ACS1; acyl-CoA synthetase 1; acyl-CoA synthetase long-chain family member 1; arachidonate--CoA ligase; FACL1; FACL2; fatty-acid-Coenzyme A ligase, long-chain 1; fatty-acid-Coenzyme A ligase, long-chain 2; LACS; LACS 1; LACS 2; LACS1; LACS2; lignoceroyl-CoA synthase; long-chain acyl-CoA synthetase 1; long-chain acyl-CoA synthetase 2; long-chain fatty acid-CoA ligase 2; long-chain fatty-acid-coenzyme A ligase 1; long-chain-fatty-acid--CoA ligase 1; palmitoyl-CoA ligase 1; palmitoyl-CoA ligase 2; paltimoyl-CoA ligase 1; phytanate--CoA ligase
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl4184,755,595 - 184,826,818 (-)EnsemblGRCh38hg38GRCh38
GRCh384184,755,595 - 184,826,593 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh374185,676,749 - 185,747,215 (-)NCBIGRCh37GRCh37hg19GRCh37
GRCh374185,676,749 - 185,747,122 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 364185,913,743 - 185,984,209 (-)NCBINCBI36hg18NCBI36
Build 344186,051,898 - 186,122,364NCBI
Celera4183,005,275 - 183,075,742 (-)NCBI
Cytogenetic Map4q35.1NCBI
HuRef4181,430,075 - 181,478,058 (-)NCBIHuRef
CHM1_14185,652,944 - 185,723,638 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(+)-dexrazoxane  (ISO)
(+)-schisandrin B  (ISO)
(-)-epigallocatechin 3-gallate  (ISO)
(S)-nicotine  (EXP)
1,1-dichloroethene  (ISO)
1,2-dimethylhydrazine  (ISO)
1-naphthyl isothiocyanate  (ISO)
17alpha-ethynylestradiol  (ISO)
17beta-estradiol  (EXP)
2,2',4,4'-Tetrabromodiphenyl ether  (ISO)
2,3,3,3-tetrafluoro-2-(heptafluoropropoxy)propanoic acid  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
2,3-dimethoxynaphthalene-1,4-dione  (EXP)
2,4-dinitrotoluene  (ISO)
2,6-dinitrotoluene  (ISO)
3,3',4,4'-tetrachlorobiphenyl  (ISO)
3,3',5-triiodo-L-thyronine  (ISO)
3,4-methylenedioxymethamphetamine  (ISO)
3-chloropropane-1,2-diol  (ISO)
3-isobutyl-1-methyl-7H-xanthine  (EXP,ISO)
4,4'-diaminodiphenylmethane  (ISO)
4-(N-nitrosomethylamino)-1-(3-pyridyl)butan-1-one  (EXP)
4-nitroquinoline N-oxide  (ISO)
6-propyl-2-thiouracil  (ISO)
acetamide  (ISO)
aflatoxin B1  (EXP)
aflatoxin B2  (EXP)
all-trans-retinoic acid  (EXP)
ammonium chloride  (ISO)
antimony(0)  (EXP)
aristolochic acid  (ISO)
Aroclor 1254  (ISO)
arsenite(3-)  (EXP)
arsenous acid  (EXP)
benzene  (EXP)
benzo[a]pyrene  (EXP,ISO)
Benzo[k]fluoranthene  (ISO)
beta-D-glucosamine 6-sulfate  (ISO)
bexarotene  (ISO)
bezafibrate  (EXP,ISO)
bicalutamide  (EXP)
bis(2-ethylhexyl) phthalate  (EXP,ISO)
bisphenol A  (EXP,ISO)
bisphenol F  (EXP)
bromobenzene  (ISO)
butan-1-ol  (EXP)
cadmium atom  (ISO)
cadmium dichloride  (EXP,ISO)
carbamazepine  (EXP)
carbon nanotube  (ISO)
chloroacetaldehyde  (EXP)
chloroform  (ISO)
choline  (ISO)
chromium atom  (EXP)
cidofovir anhydrous  (EXP)
ciglitazone  (EXP)
ciprofibrate  (ISO)
cisplatin  (EXP)
clodronic acid  (EXP)
clofibrate  (ISO)
Clofop  (EXP)
cobalt dichloride  (ISO)
copper atom  (EXP,ISO)
copper(0)  (EXP,ISO)
copper(II) sulfate  (EXP)
cyclosporin A  (EXP,ISO)
cyproconazole  (ISO)
dehydroepiandrosterone  (ISO)
dexamethasone  (EXP,ISO)
diarsenic trioxide  (EXP)
dichlorine  (ISO)
dichloroacetic acid  (ISO)
dioscin  (ISO)
dioxygen  (EXP,ISO)
dipotassium bis[mu-tartrato(4-)]diantimonate(2-) trihydrate  (EXP)
diuron  (ISO)
dorsomorphin  (EXP)
doxorubicin  (EXP,ISO)
endosulfan  (ISO)
entacapone  (ISO)
entinostat  (EXP)
epoxiconazole  (ISO)
erythromycin estolate  (ISO)
ethanol  (ISO)
ethyl methanesulfonate  (EXP)
fenofibrate  (EXP,ISO)
fenoprofen  (ISO)
fenvalerate  (ISO)
flutamide  (ISO)
fumonisin B1  (ISO)
furan  (ISO)
gentamycin  (ISO)
glafenine  (ISO)
GW 7647  (ISO)
hexadecanoic acid  (EXP)
hydrogen peroxide  (EXP)
ibuprofen  (EXP,ISO)
ifosfamide  (EXP)
indometacin  (EXP)
iron atom  (ISO)
iron(0)  (ISO)
linalool  (EXP,ISO)
lithocholic acid  (ISO)
medroxyprogesterone acetate  (EXP)
menadione  (EXP)
mercury atom  (EXP)
mercury dibromide  (EXP)
mercury(0)  (EXP)
metformin  (ISO)
methoxyacetic acid  (EXP)
methyl methanesulfonate  (EXP)
Methylazoxymethanol acetate  (ISO)
methylmercury chloride  (EXP)
mitomycin C  (EXP)
mono(2-ethylhexyl) phthalate  (ISO)
N-nitrosodiethylamine  (ISO)
N-nitrosodimethylamine  (EXP,ISO)
nefazodone  (ISO)
nickel dichloride  (EXP,ISO)
niclosamide  (EXP)
nicotine  (EXP)
nimesulide  (ISO)
O-methyleugenol  (EXP)
obeticholic acid  (EXP)
ochratoxin A  (ISO)
oleic acid  (EXP)
osthole  (EXP)
oxaliplatin  (ISO)
ozone  (ISO)
panobinostat  (EXP)
paracetamol  (EXP,ISO)
paraquat  (ISO)
perfluorobutanesulfonic acid  (ISO)
perfluorodecanoic acid  (EXP)
perfluoroheptanoic acid  (EXP)
perfluorohexanesulfonic acid  (EXP,ISO)
perfluorohexanoic acid  (EXP)
perfluorononanoic acid  (EXP)
perfluorooctane-1-sulfonic acid  (ISO)
perfluorooctanoic acid  (EXP,ISO)
permethrin  (ISO)
phenobarbital  (ISO)
phenylmercury acetate  (EXP)
phlorizin  (ISO)
pirinixic acid  (EXP,ISO)
potassium dichromate  (EXP)
pravastatin  (ISO)
prednisolone  (EXP)
pregnenolone 16alpha-carbonitrile  (ISO)
progesterone  (EXP,ISO)
promegestone  (EXP)
propiconazole  (ISO)
protein kinase inhibitor  (EXP)
raloxifene  (EXP)
SB 431542  (EXP)
scopoletin  (ISO)
Senkirkine  (EXP)
silicon dioxide  (ISO)
sodium arsenite  (EXP,ISO)
sodium dichromate  (ISO)
sodium fluoride  (ISO)
sulforaphane  (EXP,ISO)
sulindac  (ISO)
tamoxifen  (EXP,ISO)
Tanshinone I  (EXP)
tauroursodeoxycholic acid  (ISO)
Tesaglitazar  (ISO)
tetrachloroethene  (ISO)
tetrachloromethane  (ISO)
tetracycline  (ISO)
thioacetamide  (ISO)
titanium dioxide  (ISO)
tolcapone  (EXP,ISO)
toluene  (EXP)
topotecan  (ISO)
tributylstannane  (ISO)
trichloroethene  (ISO)
trichostatin A  (EXP)
triclosan  (EXP)
troglitazone  (ISO)
tungsten  (ISO)
valproic acid  (EXP,ISO)
vancomycin  (ISO)
vinclozolin  (ISO)
zaragozic acid A  (ISO)
zinc atom  (ISO)
zinc(0)  (ISO)
zoledronic acid  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

References

Additional References at PubMed
PMID:1531127   PMID:1599407   PMID:1607358   PMID:2007410   PMID:2973813   PMID:7429333   PMID:7490105   PMID:7948012   PMID:8399326   PMID:8584017   PMID:8889548   PMID:8944226  
PMID:10548543   PMID:12477932   PMID:14702039   PMID:15292367   PMID:15489334   PMID:16054041   PMID:16834775   PMID:17255364   PMID:18660489   PMID:19946888   PMID:20176858   PMID:20620995  
PMID:20877624   PMID:21242590   PMID:21873635   PMID:21988832   PMID:22022213   PMID:22829935   PMID:22990118   PMID:23303383   PMID:23433401   PMID:23503661   PMID:24269233   PMID:24462768  
PMID:24503477   PMID:25592151   PMID:25915184   PMID:25921289   PMID:26711138   PMID:26728456   PMID:26972000   PMID:27173435   PMID:27499296   PMID:27992526   PMID:28132807   PMID:28498416  
PMID:28675297   PMID:28986522   PMID:29117863   PMID:29467282   PMID:30041843   PMID:30619736   PMID:30845379   PMID:31089396   PMID:31240132   PMID:31488013   PMID:31581558   PMID:31769755  
PMID:32218693   PMID:32521232   PMID:32694731  


Genomics

Comparative Map Data
ACSL1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl4184,755,595 - 184,826,818 (-)EnsemblGRCh38hg38GRCh38
GRCh384184,755,595 - 184,826,593 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh374185,676,749 - 185,747,215 (-)NCBIGRCh37GRCh37hg19GRCh37
GRCh374185,676,749 - 185,747,122 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 364185,913,743 - 185,984,209 (-)NCBINCBI36hg18NCBI36
Build 344186,051,898 - 186,122,364NCBI
Celera4183,005,275 - 183,075,742 (-)NCBI
Cytogenetic Map4q35.1NCBI
HuRef4181,430,075 - 181,478,058 (-)NCBIHuRef
CHM1_14185,652,944 - 185,723,638 (-)NCBICHM1_1
Acsl1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39846,924,074 - 46,989,088 (+)NCBIGRCm39mm39
GRCm38846,471,037 - 46,536,051 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl846,471,037 - 46,536,051 (+)EnsemblGRCm38mm10GRCm38
MGSCv37847,556,396 - 47,621,404 (+)NCBIGRCm37mm9NCBIm37
MGSCv36847,969,859 - 48,034,867 (+)NCBImm8
Celera849,153,706 - 49,218,586 (+)NCBICelera
Cytogenetic Map8B1.1NCBI
Acsl1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.21645,755,246 - 45,821,541 (-)NCBI
Rnor_6.0 Ensembl1648,937,456 - 49,003,246 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.01648,937,456 - 49,003,898 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.01648,653,023 - 48,719,250 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41649,036,892 - 49,081,416 (-)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.11649,036,966 - 49,081,491 (-)NCBI
Celera1643,758,263 - 43,802,634 (-)NCBICelera
Cytogenetic Map16q11NCBI
Acsl1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495540324,190,674 - 24,236,780 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495540324,190,674 - 24,235,354 (+)NCBIChiLan1.0ChiLan1.0
ACSL1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.14189,145,403 - 189,216,458 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl4189,145,403 - 189,198,646 (-)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v04176,920,811 - 176,991,495 (-)NCBIMhudiblu_PPA_v0panPan3
ACSL1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1 Ensembl1645,735,703 - 45,804,970 (+)EnsemblCanFam3.1canFam3CanFam3.1
CanFam3.11645,735,675 - 45,806,235 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
Acsl1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
SpeTri2.0NW_0049365544,425,518 - 4,484,853 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ACSL1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1545,866,851 - 46,090,099 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11545,866,858 - 45,936,327 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21552,526,606 - 52,595,992 (-)NCBISscrofa10.2Sscrofa10.2susScr3
ACSL1
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.17130,712,633 - 130,783,360 (-)NCBI
ChlSab1.1 Ensembl7130,712,308 - 130,763,756 (-)Ensembl
Acsl1
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462476915,503,757 - 15,584,741 (-)NCBI

Position Markers
SHGC-50256  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh374185,677,679 - 185,677,838UniSTSGRCh37
Build 364185,914,673 - 185,914,832RGDNCBI36
Celera4183,006,205 - 183,006,364RGD
Cytogenetic Map4q35UniSTS
HuRef4181,431,005 - 181,431,164UniSTS
TNG Radiation Hybrid Map4110136.0UniSTS
D4S3128  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh374185,678,096 - 185,678,270UniSTSGRCh37
Build 364185,915,090 - 185,915,264RGDNCBI36
Celera4183,006,622 - 183,006,796RGD
Cytogenetic Map4q35UniSTS
HuRef4181,431,422 - 181,431,596UniSTS
TNG Radiation Hybrid Map4110136.0UniSTS
Stanford-G3 RH Map49848.0UniSTS
NCBI RH Map41757.2UniSTS
GeneMap99-G3 RH Map49773.0UniSTS
WI-20005  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh374185,676,750 - 185,677,017UniSTSGRCh37
Build 364185,913,744 - 185,914,011RGDNCBI36
Celera4183,005,276 - 183,005,543RGD
Cytogenetic Map4q35UniSTS
HuRef4181,430,076 - 181,430,343UniSTS
GeneMap99-GB4 RH Map4681.63UniSTS
Whitehead-RH Map4744.9UniSTS
Bdy94e02  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh374185,677,737 - 185,677,921UniSTSGRCh37
Build 364185,914,731 - 185,914,915RGDNCBI36
Celera4183,006,263 - 183,006,447RGD
Cytogenetic Map4q35UniSTS
HuRef4181,431,063 - 181,431,247UniSTS
GeneMap99-GB4 RH Map4681.63UniSTS
GeneMap99-G3 RH Map49773.0UniSTS
ACSL1_3367  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh374185,676,632 - 185,677,465UniSTSGRCh37
Build 364185,913,626 - 185,914,459RGDNCBI36
Celera4183,005,158 - 183,005,991RGD
HuRef4181,429,959 - 181,430,791UniSTS
D10S16   No map positions available.
D10S16  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map2q11.2-q12UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map3p22UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map9p13.3-p12UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map5q21-q22UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map1q24.1UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map4q34UniSTS
Cytogenetic Map2p22-p21UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map1p36.23UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map16p13.13UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map11p15.3-p15.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map3q26UniSTS
Cytogenetic Map12p12.1-p11.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic MapXq23UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map5p15.1UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map17qterUniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map20q12-q13.12UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map5q31.2-q34UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map1pter-q31.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map3p23-p21UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map2q24UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16p13.1UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1p36.1-p34UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map15q21.1-q21.2UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map3p11.1UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map13q12UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic MapXq21UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map15q24.2UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map2q34UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map3p23UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map4q26UniSTS
Cytogenetic Map4p15.3UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map12q14.2UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map6q22.32UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map9p22.3UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map19qterUniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map17pUniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map2p13.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map3q26.2UniSTS

miRNA Target Status

Confirmed Target Of
miRNA GeneMature miRNAMethod NameResult TypeData TypeSupport TypePMID
MIR34Ahsa-miR-34a-5pMirtarbaseexternal_infoReporter assay;Proteomics//ProteomicsFunctional MTI21566225

Predicted Target Of
Summary Value
Count of predictions:4249
Count of miRNA genes:1064
Interacting mature miRNAs:1295
Transcripts:ENST00000281455, ENST00000437665, ENST00000454703, ENST00000503407, ENST00000504342, ENST00000504900, ENST00000505492, ENST00000506733, ENST00000507295, ENST00000513001, ENST00000513317, ENST00000515030
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.


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 1 235 3 3 234 3 110 49 1 3 121 49
Medium 2331 2670 1696 609 1643 451 4074 2047 2951 407 1371 1574 170 1083 2739 3
Low 101 84 24 12 70 10 172 98 773 11 79 34 3 1 1 2
Below cutoff 1 3 2 1 6 3 2

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001286708 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001286710 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001286711 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001381877 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001381878 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001381879 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001381880 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001381881 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001381882 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001381883 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001381884 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001381885 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001381886 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001381887 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001381888 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001381889 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001381890 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001995 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_167698 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_167702 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_167703 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_167704 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_167705 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_167706 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_167708 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_167709 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017007887 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC079257 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC084871 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK096117 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK292798 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK296550 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK296826 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK303486 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC026290 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC033479 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC050073 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BG680610 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BG773086 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BI461964 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM982557 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471056 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  D10040 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC344113 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ083028 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ083029 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HB881341 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HC938750 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  L09229 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000281455   ⟹   ENSP00000281455
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl4184,755,595 - 184,825,968 (-)Ensembl
RefSeq Acc Id: ENST00000454703   ⟹   ENSP00000407165
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl4184,755,595 - 184,826,119 (-)Ensembl
RefSeq Acc Id: ENST00000503407   ⟹   ENSP00000425098
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl4184,755,601 - 184,766,702 (-)Ensembl
RefSeq Acc Id: ENST00000504342   ⟹   ENSP00000425006
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl4184,757,021 - 184,812,259 (-)Ensembl
RefSeq Acc Id: ENST00000504900   ⟹   ENSP00000424935
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl4184,768,030 - 184,826,052 (-)Ensembl
RefSeq Acc Id: ENST00000505492   ⟹   ENSP00000425640
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl4184,768,328 - 184,773,873 (-)Ensembl
RefSeq Acc Id: ENST00000506733   ⟹   ENSP00000426491
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl4184,756,903 - 184,808,451 (-)Ensembl
RefSeq Acc Id: ENST00000507295   ⟹   ENSP00000426244
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl4184,756,781 - 184,826,034 (-)Ensembl
RefSeq Acc Id: ENST00000513001
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl4184,755,600 - 184,758,876 (-)Ensembl
RefSeq Acc Id: ENST00000513317   ⟹   ENSP00000426150
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl4184,757,047 - 184,805,788 (-)Ensembl
RefSeq Acc Id: ENST00000515030   ⟹   ENSP00000422607
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl4184,755,600 - 184,826,818 (-)Ensembl
RefSeq Acc Id: ENST00000622937   ⟹   ENSP00000485264
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl4184,755,596 - 184,808,601 (-)Ensembl
RefSeq Acc Id: NM_001286708   ⟹   NP_001273637
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh384184,755,595 - 184,812,251 (-)NCBI
HuRef4181,430,075 - 181,487,028 (-)NCBI
CHM1_14185,652,944 - 185,709,846 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001286710   ⟹   NP_001273639
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh384184,755,595 - 184,805,553 (-)NCBI
HuRef4181,430,075 - 181,487,028 (-)NCBI
CHM1_14185,652,944 - 185,703,375 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001286711   ⟹   NP_001273640
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh384184,755,595 - 184,825,968 (-)NCBI
HuRef4181,430,075 - 181,487,028 (-)NCBI
CHM1_14185,652,944 - 185,723,638 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001381877   ⟹   NP_001368806
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh384184,755,595 - 184,825,968 (-)NCBI
RefSeq Acc Id: NM_001381878   ⟹   NP_001368807
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh384184,755,595 - 184,825,968 (-)NCBI
RefSeq Acc Id: NM_001381879   ⟹   NP_001368808
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh384184,755,595 - 184,815,124 (-)NCBI
RefSeq Acc Id: NM_001381880   ⟹   NP_001368809
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh384184,755,595 - 184,815,124 (-)NCBI
RefSeq Acc Id: NM_001381881   ⟹   NP_001368810
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh384184,755,595 - 184,808,531 (-)NCBI
RefSeq Acc Id: NM_001381882   ⟹   NP_001368811
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh384184,755,595 - 184,805,553 (-)NCBI
RefSeq Acc Id: NM_001381883   ⟹   NP_001368812
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh384184,755,595 - 184,805,553 (-)NCBI
RefSeq Acc Id: NM_001381884   ⟹   NP_001368813
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh384184,755,595 - 184,825,968 (-)NCBI
RefSeq Acc Id: NM_001381885   ⟹   NP_001368814
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh384184,755,595 - 184,825,968 (-)NCBI
RefSeq Acc Id: NM_001381886   ⟹   NP_001368815
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh384184,755,595 - 184,808,531 (-)NCBI
RefSeq Acc Id: NM_001381887   ⟹   NP_001368816
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh384184,755,595 - 184,805,553 (-)NCBI
RefSeq Acc Id: NM_001381888   ⟹   NP_001368817
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh384184,755,595 - 184,808,531 (-)NCBI
RefSeq Acc Id: NM_001381889   ⟹   NP_001368818
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh384184,755,595 - 184,805,553 (-)NCBI
RefSeq Acc Id: NM_001381890   ⟹   NP_001368819
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh384184,755,595 - 184,805,553 (-)NCBI
RefSeq Acc Id: NM_001995   ⟹   NP_001986
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh384184,755,595 - 184,825,968 (-)NCBI
GRCh374185,676,749 - 185,747,215 (-)ENTREZGENE
GRCh374185,676,749 - 185,747,215 (-)NCBI
Build 364185,913,743 - 185,984,209 (-)NCBI Archive
HuRef4181,430,075 - 181,487,028 (-)NCBI
CHM1_14185,652,944 - 185,723,638 (-)NCBI
Sequence:
RefSeq Acc Id: NR_167698
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh384184,755,595 - 184,808,531 (-)NCBI
RefSeq Acc Id: NR_167702
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh384184,755,595 - 184,825,968 (-)NCBI
RefSeq Acc Id: NR_167703
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh384184,755,595 - 184,825,968 (-)NCBI
RefSeq Acc Id: NR_167704
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh384184,755,595 - 184,825,968 (-)NCBI
RefSeq Acc Id: NR_167705
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh384184,755,595 - 184,825,968 (-)NCBI
RefSeq Acc Id: NR_167706
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh384184,755,595 - 184,825,968 (-)NCBI
RefSeq Acc Id: NR_167708
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh384184,755,595 - 184,808,531 (-)NCBI
RefSeq Acc Id: NR_167709
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh384184,755,595 - 184,805,553 (-)NCBI
RefSeq Acc Id: XM_017007887   ⟹   XP_016863376
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh384184,755,595 - 184,826,593 (-)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001273637 (Get FASTA)   NCBI Sequence Viewer  
  NP_001273639 (Get FASTA)   NCBI Sequence Viewer  
  NP_001273640 (Get FASTA)   NCBI Sequence Viewer  
  NP_001368806 (Get FASTA)   NCBI Sequence Viewer  
  NP_001368807 (Get FASTA)   NCBI Sequence Viewer  
  NP_001368808 (Get FASTA)   NCBI Sequence Viewer  
  NP_001368809 (Get FASTA)   NCBI Sequence Viewer  
  NP_001368810 (Get FASTA)   NCBI Sequence Viewer  
  NP_001368811 (Get FASTA)   NCBI Sequence Viewer  
  NP_001368812 (Get FASTA)   NCBI Sequence Viewer  
  NP_001368813 (Get FASTA)   NCBI Sequence Viewer  
  NP_001368814 (Get FASTA)   NCBI Sequence Viewer  
  NP_001368815 (Get FASTA)   NCBI Sequence Viewer  
  NP_001368816 (Get FASTA)   NCBI Sequence Viewer  
  NP_001368817 (Get FASTA)   NCBI Sequence Viewer  
  NP_001368818 (Get FASTA)   NCBI Sequence Viewer  
  NP_001368819 (Get FASTA)   NCBI Sequence Viewer  
  NP_001986 (Get FASTA)   NCBI Sequence Viewer  
  XP_016863376 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAB00959 (Get FASTA)   NCBI Sequence Viewer  
  AAH26290 (Get FASTA)   NCBI Sequence Viewer  
  AAH50073 (Get FASTA)   NCBI Sequence Viewer  
  AAZ30711 (Get FASTA)   NCBI Sequence Viewer  
  AAZ30712 (Get FASTA)   NCBI Sequence Viewer  
  BAA00931 (Get FASTA)   NCBI Sequence Viewer  
  BAC04704 (Get FASTA)   NCBI Sequence Viewer  
  BAF85487 (Get FASTA)   NCBI Sequence Viewer  
  BAG64522 (Get FASTA)   NCBI Sequence Viewer  
  BAH12385 (Get FASTA)   NCBI Sequence Viewer  
  BAH12438 (Get FASTA)   NCBI Sequence Viewer  
  CBF64949 (Get FASTA)   NCBI Sequence Viewer  
  CBU89820 (Get FASTA)   NCBI Sequence Viewer  
  EAX04662 (Get FASTA)   NCBI Sequence Viewer  
  EAX04663 (Get FASTA)   NCBI Sequence Viewer  
  EAX04664 (Get FASTA)   NCBI Sequence Viewer  
  EAX04665 (Get FASTA)   NCBI Sequence Viewer  
  P33121 (Get FASTA)   NCBI Sequence Viewer  
Reference Sequences
RefSeq Acc Id: NP_001986   ⟸   NM_001995
- Peptide Label: isoform a
- UniProtKB: P33121 (UniProtKB/Swiss-Prot),   A8K9T3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001273637   ⟸   NM_001286708
- Peptide Label: isoform a
- UniProtKB: P33121 (UniProtKB/Swiss-Prot),   A8K9T3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001273639   ⟸   NM_001286710
- Peptide Label: isoform b
- UniProtKB: P33121 (UniProtKB/Swiss-Prot),   A8K9T3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001273640   ⟸   NM_001286711
- Peptide Label: isoform c
- UniProtKB: P33121 (UniProtKB/Swiss-Prot),   A8K9T3 (UniProtKB/TrEMBL),   B4E0R0 (UniProtKB/TrEMBL),   E7EPM6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016863376   ⟸   XM_017007887
- Peptide Label: isoform X1
- UniProtKB: P33121 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001368813   ⟸   NM_001381884
- Peptide Label: isoform b
RefSeq Acc Id: NP_001368814   ⟸   NM_001381885
- Peptide Label: isoform b
RefSeq Acc Id: NP_001368806   ⟸   NM_001381877
- Peptide Label: isoform a
RefSeq Acc Id: NP_001368807   ⟸   NM_001381878
- Peptide Label: isoform a
RefSeq Acc Id: NP_001368809   ⟸   NM_001381880
- Peptide Label: isoform a
RefSeq Acc Id: NP_001368808   ⟸   NM_001381879
- Peptide Label: isoform a
RefSeq Acc Id: NP_001368815   ⟸   NM_001381886
- Peptide Label: isoform b
RefSeq Acc Id: NP_001368810   ⟸   NM_001381881
- Peptide Label: isoform a
RefSeq Acc Id: NP_001368817   ⟸   NM_001381888
- Peptide Label: isoform e
RefSeq Acc Id: NP_001368811   ⟸   NM_001381882
- Peptide Label: isoform a
RefSeq Acc Id: NP_001368819   ⟸   NM_001381890
- Peptide Label: isoform f
RefSeq Acc Id: NP_001368816   ⟸   NM_001381887
- Peptide Label: isoform b
RefSeq Acc Id: NP_001368812   ⟸   NM_001381883
- Peptide Label: isoform a
RefSeq Acc Id: NP_001368818   ⟸   NM_001381889
- Peptide Label: isoform e
RefSeq Acc Id: ENSP00000425098   ⟸   ENST00000503407
RefSeq Acc Id: ENSP00000425006   ⟸   ENST00000504342
RefSeq Acc Id: ENSP00000485264   ⟸   ENST00000622937
RefSeq Acc Id: ENSP00000424935   ⟸   ENST00000504900
RefSeq Acc Id: ENSP00000425640   ⟸   ENST00000505492
RefSeq Acc Id: ENSP00000426491   ⟸   ENST00000506733
RefSeq Acc Id: ENSP00000281455   ⟸   ENST00000281455
RefSeq Acc Id: ENSP00000426244   ⟸   ENST00000507295
RefSeq Acc Id: ENSP00000407165   ⟸   ENST00000454703
RefSeq Acc Id: ENSP00000426150   ⟸   ENST00000513317
RefSeq Acc Id: ENSP00000422607   ⟸   ENST00000515030
Protein Domains
AMP-binding   AMP-binding_C

Promoters
RGD ID:6869010
Promoter ID:EPDNEW_H7670
Type:initiation region
Name:ACSL1_1
Description:acyl-CoA synthetase long-chain family member 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H7671  EPDNEW_H7673  EPDNEW_H7674  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh384184,805,553 - 184,805,613EPDNEW
RGD ID:6869012
Promoter ID:EPDNEW_H7671
Type:initiation region
Name:ACSL1_4
Description:acyl-CoA synthetase long-chain family member 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H7670  EPDNEW_H7673  EPDNEW_H7674  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh384184,812,248 - 184,812,308EPDNEW
RGD ID:6812473
Promoter ID:HG_ACW:61988
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:ACSL1.VGAPR07
Position:
Human AssemblyChrPosition (strand)Source
Build 364185,934,236 - 185,934,736 (-)MPROMDB
RGD ID:6802026
Promoter ID:HG_KWN:49579
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:UC003IWW.1
Position:
Human AssemblyChrPosition (strand)Source
Build 364185,961,334 - 185,961,834 (-)MPROMDB
RGD ID:6812472
Promoter ID:HG_ACW:61990
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3,   Lymphoblastoid
Transcripts:ACSL1.EAPR07,   ACSL1.IAPR07,   ACSL1.RAPR07,   ACSL1.VAAPR07
Position:
Human AssemblyChrPosition (strand)Source
Build 364185,963,541 - 185,964,041 (-)MPROMDB
RGD ID:6802024
Promoter ID:HG_KWN:49580
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:UC003IWT.1
Position:
Human AssemblyChrPosition (strand)Source
Build 364185,970,036 - 185,970,536 (-)MPROMDB
RGD ID:6812541
Promoter ID:HG_ACW:61993
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562,   Lymphoblastoid
Transcripts:ACSL1.KAPR07,   KLUGAR.AAPR07
Position:
Human AssemblyChrPosition (strand)Source
Build 364185,973,186 - 185,973,686 (-)MPROMDB
RGD ID:6802021
Promoter ID:HG_KWN:49581
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_001995,   UC003IWV.1
Position:
Human AssemblyChrPosition (strand)Source
Build 364185,983,971 - 185,985,027 (-)MPROMDB

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 4q34.3-35.1(chr4:181579626-186100199)x1 copy number loss See cases [RCV000050324] Chr4:181579626..186100199 [GRCh38]
Chr4:182500779..187021353 [GRCh37]
Chr4:182737773..187258347 [NCBI36]
Chr4:4q34.3-35.1
pathogenic
GRCh38/hg38 4q34.1-35.2(chr4:173599911-188624331)x1 copy number loss See cases [RCV000050771] Chr4:173599911..188624331 [GRCh38]
Chr4:174521062..189545485 [GRCh37]
Chr4:174757637..189782479 [NCBI36]
Chr4:4q34.1-35.2
pathogenic
GRCh38/hg38 4q32.2-35.2(chr4:162013220-189975519)x3 copy number gain See cases [RCV000050649] Chr4:162013220..189975519 [GRCh38]
Chr4:162934372..190828225 [GRCh37]
Chr4:163153822..191133668 [NCBI36]
Chr4:4q32.2-35.2
pathogenic
GRCh38/hg38 4q35.1-35.2(chr4:183528264-188624331)x1 copy number loss See cases [RCV000050665] Chr4:183528264..188624331 [GRCh38]
Chr4:184449417..189545485 [GRCh37]
Chr4:184686411..189782479 [NCBI36]
Chr4:4q35.1-35.2
pathogenic
GRCh38/hg38 4q34.2-35.2(chr4:175483683-189975519)x1 copy number loss See cases [RCV000051215] Chr4:175483683..189975519 [GRCh38]
Chr4:176404834..190828225 [GRCh37]
Chr4:176641828..191133668 [NCBI36]
Chr4:4q34.2-35.2
pathogenic
GRCh38/hg38 4q26-35.2(chr4:118065569-190042639)x3 copy number gain See cases [RCV000051785] Chr4:118065569..190042639 [GRCh38]
Chr4:118986724..190828225 [GRCh37]
Chr4:119206172..191200788 [NCBI36]
Chr4:4q26-35.2
pathogenic
GRCh38/hg38 4q27-35.2(chr4:121518223-190062270)x3 copy number gain See cases [RCV000051786] Chr4:121518223..190062270 [GRCh38]
Chr4:122439378..190828225 [GRCh37]
Chr4:122658828..191220419 [NCBI36]
Chr4:4q27-35.2
pathogenic
GRCh38/hg38 4q31.23-35.2(chr4:148356485-189548183)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051789]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051789]|See cases [RCV000051789] Chr4:148356485..189548183 [GRCh38]
Chr4:149277637..190469337 [GRCh37]
Chr4:149497087..190706331 [NCBI36]
Chr4:4q31.23-35.2
pathogenic
GRCh38/hg38 4q32.3-35.2(chr4:167218288-189975519)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051792]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051792]|See cases [RCV000051792] Chr4:167218288..189975519 [GRCh38]
Chr4:168139439..190828225 [GRCh37]
Chr4:168376014..191133668 [NCBI36]
Chr4:4q32.3-35.2
pathogenic
GRCh38/hg38 4q34.1-35.2(chr4:172200228-189975519)x3 copy number gain See cases [RCV000051804] Chr4:172200228..189975519 [GRCh38]
Chr4:173121379..190828225 [GRCh37]
Chr4:173357954..191133668 [NCBI36]
Chr4:4q34.1-35.2
pathogenic
GRCh38/hg38 4q34.3-35.2(chr4:179946068-189548183)x3 copy number gain See cases [RCV000051805] Chr4:179946068..189548183 [GRCh38]
Chr4:180867221..190469337 [GRCh37]
Chr4:181104215..190706331 [NCBI36]
Chr4:4q34.3-35.2
pathogenic
GRCh38/hg38 4q35.1(chr4:182990639-186013514)x3 copy number gain See cases [RCV000051806] Chr4:182990639..186013514 [GRCh38]
Chr4:183911792..186934668 [GRCh37]
Chr4:184148786..187171662 [NCBI36]
Chr4:4q35.1
pathogenic
GRCh38/hg38 4q32.1-35.2(chr4:158568335-189975660)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053325]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053325]|See cases [RCV000053325] Chr4:158568335..189975660 [GRCh38]
Chr4:159489487..190828225 [GRCh37]
Chr4:159708937..191133809 [NCBI36]
Chr4:4q32.1-35.2
pathogenic
GRCh38/hg38 4q32.3-35.2(chr4:163651681-189975519)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053327]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053327]|See cases [RCV000053327] Chr4:163651681..189975519 [GRCh38]
Chr4:164572833..190828225 [GRCh37]
Chr4:164792283..191133668 [NCBI36]
Chr4:4q32.3-35.2
pathogenic
GRCh38/hg38 4q32.3-35.2(chr4:164039530-189982708)x1 copy number loss See cases [RCV000053347] Chr4:164039530..189982708 [GRCh38]
Chr4:164960682..190828225 [GRCh37]
Chr4:165180132..191140857 [NCBI36]
Chr4:4q32.3-35.2
pathogenic
GRCh38/hg38 4q34.1-35.2(chr4:171507704-189869726)x1 copy number loss See cases [RCV000053349] Chr4:171507704..189869726 [GRCh38]
Chr4:172428855..190790881 [GRCh37]
Chr4:172665430..191027875 [NCBI36]
Chr4:4q34.1-35.2
pathogenic
GRCh38/hg38 4q34.1-35.2(chr4:172356988-189975519)x1 copy number loss See cases [RCV000053352] Chr4:172356988..189975519 [GRCh38]
Chr4:173278139..190828225 [GRCh37]
Chr4:173514714..191133668 [NCBI36]
Chr4:4q34.1-35.2
pathogenic
GRCh38/hg38 4q34.1-35.2(chr4:173754675-189343295)x1 copy number loss See cases [RCV000053353] Chr4:173754675..189343295 [GRCh38]
Chr4:174675826..190264449 [GRCh37]
Chr4:174912401..190501443 [NCBI36]
Chr4:4q34.1-35.2
pathogenic
GRCh38/hg38 4q35.1-35.2(chr4:183354112-190042639)x1 copy number loss See cases [RCV000053378] Chr4:183354112..190042639 [GRCh38]
Chr4:184275265..190828225 [GRCh37]
Chr4:184512259..191200788 [NCBI36]
Chr4:4q35.1-35.2
pathogenic
GRCh38/hg38 4q34.2-35.2(chr4:176263514-189975519)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053373]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053373]|See cases [RCV000053373] Chr4:176263514..189975519 [GRCh38]
Chr4:177184665..190828225 [GRCh37]
Chr4:177421659..191133668 [NCBI36]
Chr4:4q34.2-35.2
pathogenic
GRCh38/hg38 4q34.3-35.2(chr4:177442769-190042639)x1 copy number loss See cases [RCV000053374] Chr4:177442769..190042639 [GRCh38]
Chr4:178363923..190828225 [GRCh37]
Chr4:178600917..191200788 [NCBI36]
Chr4:4q34.3-35.2
pathogenic
GRCh38/hg38 4q34.3-35.2(chr4:179669472-189975660)x1 copy number loss See cases [RCV000053375] Chr4:179669472..189975660 [GRCh38]
Chr4:180590625..190828225 [GRCh37]
Chr4:180827619..191133809 [NCBI36]
Chr4:4q34.3-35.2
pathogenic
GRCh38/hg38 4q34.3-35.2(chr4:179945868-189975660)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053376]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053376]|See cases [RCV000053376] Chr4:179945868..189975660 [GRCh38]
Chr4:180867021..190828225 [GRCh37]
Chr4:181104015..191133809 [NCBI36]
Chr4:4q34.3-35.2
pathogenic
GRCh38/hg38 4q34.3-35.2(chr4:181455566-189975660)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053377]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053377]|See cases [RCV000053377] Chr4:181455566..189975660 [GRCh38]
Chr4:182376719..190828225 [GRCh37]
Chr4:182613713..191133809 [NCBI36]
Chr4:4q34.3-35.2
pathogenic
GRCh38/hg38 4q35.1-35.2(chr4:184327081-189975519)x3 copy number gain See cases [RCV000133708] Chr4:184327081..189975519 [GRCh38]
Chr4:185248234..190828225 [GRCh37]
Chr4:185485228..191133668 [NCBI36]
Chr4:4q35.1-35.2
pathogenic
GRCh38/hg38 4q35.1-35.2(chr4:184327081-189975519)x1 copy number loss See cases [RCV000133709] Chr4:184327081..189975519 [GRCh38]
Chr4:185248234..190896674 [GRCh37]
Chr4:185485228..191133668 [NCBI36]
Chr4:4q35.1-35.2
likely pathogenic|likely benign
GRCh38/hg38 4q35.1-35.2(chr4:184406972-188915538)x3 copy number gain See cases [RCV000134158] Chr4:184406972..188915538 [GRCh38]
Chr4:185328126..189836692 [GRCh37]
Chr4:185565120..190073686 [NCBI36]
Chr4:4q35.1-35.2
pathogenic
GRCh38/hg38 4q35.1-35.2(chr4:182437091-190018185)x1 copy number loss See cases [RCV000134276] Chr4:182437091..190018185 [GRCh38]
Chr4:183358244..190939340 [GRCh37]
Chr4:183595238..191176334 [NCBI36]
Chr4:4q35.1-35.2
pathogenic
GRCh38/hg38 4q34.3-35.2(chr4:180451652-190095391)x3 copy number gain See cases [RCV000135693] Chr4:180451652..190095391 [GRCh38]
Chr4:181372805..190828225 [GRCh37]
Chr4:181609799..191250527 [NCBI36]
Chr4:4q34.3-35.2
likely pathogenic
GRCh38/hg38 4q31.21-35.2(chr4:145042668-189975519)x3 copy number gain See cases [RCV000135845] Chr4:145042668..189975519 [GRCh38]
Chr4:145963820..190828225 [GRCh37]
Chr4:146183270..191133668 [NCBI36]
Chr4:4q31.21-35.2
pathogenic
GRCh38/hg38 4q34.1-35.2(chr4:173854560-189548183)x1 copy number loss See cases [RCV000136115] Chr4:173854560..189548183 [GRCh38]
Chr4:174775711..190469337 [GRCh37]
Chr4:175012286..190706331 [NCBI36]
Chr4:4q34.1-35.2
pathogenic
GRCh38/hg38 4q35.1-35.2(chr4:184239531-189975519)x1 copy number loss See cases [RCV000136942] Chr4:184239531..189975519 [GRCh38]
Chr4:185160684..190828225 [GRCh37]
Chr4:185397678..191133668 [NCBI36]
Chr4:4q35.1-35.2
pathogenic
GRCh38/hg38 4q34.3-35.2(chr4:177985956-189975519)x1 copy number loss See cases [RCV000137101] Chr4:177985956..189975519 [GRCh38]
Chr4:178907110..190828225 [GRCh37]
Chr4:179144104..191133668 [NCBI36]
Chr4:4q34.3-35.2
pathogenic
GRCh38/hg38 4q31.1-35.2(chr4:138510532-189963195)x3 copy number gain See cases [RCV000136810] Chr4:138510532..189963195 [GRCh38]
Chr4:139431686..190828225 [GRCh37]
Chr4:139651136..191121344 [NCBI36]
Chr4:4q31.1-35.2
pathogenic
GRCh38/hg38 4q32.3-35.2(chr4:166317587-190095391)x1 copy number loss See cases [RCV000137532] Chr4:166317587..190095391 [GRCh38]
Chr4:167238739..190828225 [GRCh37]
Chr4:167458189..191250527 [NCBI36]
Chr4:4q32.3-35.2
pathogenic
GRCh38/hg38 4q28.3-35.2(chr4:131985253-190095391)x3 copy number gain See cases [RCV000137721] Chr4:131985253..190095391 [GRCh38]
Chr4:132906408..190828225 [GRCh37]
Chr4:133125858..191250527 [NCBI36]
Chr4:4q28.3-35.2
pathogenic|likely benign
GRCh38/hg38 4q34.3-35.2(chr4:178014570-190095391)x1 copy number loss See cases [RCV000137343] Chr4:178014570..190095391 [GRCh38]
Chr4:178935724..190828225 [GRCh37]
Chr4:179172718..191250527 [NCBI36]
Chr4:4q34.3-35.2
pathogenic
GRCh38/hg38 4q34.3-35.2(chr4:178549472-190095391)x1 copy number loss See cases [RCV000137262] Chr4:178549472..190095391 [GRCh38]
Chr4:179470626..190828225 [GRCh37]
Chr4:179707620..191250527 [NCBI36]
Chr4:4q34.3-35.2
pathogenic
GRCh38/hg38 4q34.3-35.2(chr4:180574962-190095391)x1 copy number loss See cases [RCV000137345] Chr4:180574962..190095391 [GRCh38]
Chr4:181496115..190828225 [GRCh37]
Chr4:181733109..191250527 [NCBI36]
Chr4:4q34.3-35.2
pathogenic
GRCh38/hg38 4q35.1(chr4:184573059-185237739)x3 copy number gain See cases [RCV000137905] Chr4:184573059..185237739 [GRCh38]
Chr4:185494213..186158893 [GRCh37]
Chr4:185731207..186395887 [NCBI36]
Chr4:4q35.1
uncertain significance
GRCh38/hg38 4q34.1-35.2(chr4:174150183-188259055)x1 copy number loss See cases [RCV000137925] Chr4:174150183..188259055 [GRCh38]
Chr4:175071334..189180209 [GRCh37]
Chr4:175307909..189417203 [NCBI36]
Chr4:4q34.1-35.2
likely pathogenic
GRCh38/hg38 4q35.1-35.2(chr4:183072743-190095391)x1 copy number loss See cases [RCV000138668] Chr4:183072743..190095391 [GRCh38]
Chr4:183993896..190828225 [GRCh37]
Chr4:184230890..191250527 [NCBI36]
Chr4:4q35.1-35.2
pathogenic
GRCh38/hg38 4q28.1-35.1(chr4:125432943-185761887)x3 copy number gain See cases [RCV000138578] Chr4:125432943..185761887 [GRCh38]
Chr4:126354098..186683041 [GRCh37]
Chr4:126573548..186920035 [NCBI36]
Chr4:4q28.1-35.1
pathogenic|likely benign
GRCh38/hg38 4q33-35.2(chr4:169901205-190095391)x3 copy number gain See cases [RCV000138540] Chr4:169901205..190095391 [GRCh38]
Chr4:170822356..190828225 [GRCh37]
Chr4:171058931..191250527 [NCBI36]
Chr4:4q33-35.2
uncertain significance
GRCh38/hg38 4q33-35.2(chr4:169873508-190018185)x1 copy number loss See cases [RCV000140396] Chr4:169873508..190018185 [GRCh38]
Chr4:170794659..190939340 [GRCh37]
Chr4:171031234..191176334 [NCBI36]
Chr4:4q33-35.2
pathogenic
GRCh38/hg38 4q32.3-35.2(chr4:165281036-190018185)x1 copy number loss See cases [RCV000140414] Chr4:165281036..190018185 [GRCh38]
Chr4:166202188..190939340 [GRCh37]
Chr4:166421638..191176334 [NCBI36]
Chr4:4q32.3-35.2
pathogenic
GRCh38/hg38 4q34.3-35.2(chr4:179295511-190036318)x3 copy number gain See cases [RCV000140450] Chr4:179295511..190036318 [GRCh38]
Chr4:180216665..190957473 [GRCh37]
Chr4:180453659..191194467 [NCBI36]
Chr4:4q34.3-35.2
pathogenic
GRCh38/hg38 4q32.1-35.2(chr4:160757699-190091407)x3 copy number gain See cases [RCV000140982] Chr4:160757699..190091407 [GRCh38]
Chr4:161678851..191012562 [GRCh37]
Chr4:161898301..191246543 [NCBI36]
Chr4:4q32.1-35.2
pathogenic
GRCh38/hg38 4q32.3-35.2(chr4:167373716-190036318)x1 copy number loss See cases [RCV000141964] Chr4:167373716..190036318 [GRCh38]
Chr4:168294867..190957473 [GRCh37]
Chr4:168531442..191194467 [NCBI36]
Chr4:4q32.3-35.2
pathogenic
GRCh38/hg38 4q34.1-35.2(chr4:173989029-189975519)x1 copy number loss See cases [RCV000141490] Chr4:173989029..189975519 [GRCh38]
Chr4:174910180..190828225 [GRCh37]
Chr4:175146755..191133668 [NCBI36]
Chr4:4q34.1-35.2
pathogenic
GRCh38/hg38 4q35.1-35.2(chr4:182732498-187998523)x4 copy number gain See cases [RCV000141753] Chr4:182732498..187998523 [GRCh38]
Chr4:183653651..188919677 [GRCh37]
Chr4:183890645..189156671 [NCBI36]
Chr4:4q35.1-35.2
likely pathogenic
GRCh38/hg38 4q32.3-35.2(chr4:168970400-186936738)x1 copy number loss See cases [RCV000142368] Chr4:168970400..186936738 [GRCh38]
Chr4:169891551..187857892 [GRCh37]
Chr4:170128126..188094886 [NCBI36]
Chr4:4q32.3-35.2
pathogenic
GRCh38/hg38 4q34.3-35.1(chr4:181762338-185175891)x1 copy number loss See cases [RCV000142279] Chr4:181762338..185175891 [GRCh38]
Chr4:182683491..186097045 [GRCh37]
Chr4:182920485..186334039 [NCBI36]
Chr4:4q34.3-35.1
uncertain significance
GRCh38/hg38 4q34.1-35.2(chr4:172501374-190095332)x1 copy number loss See cases [RCV000143079] Chr4:172501374..190095332 [GRCh38]
Chr4:173422525..190828225 [GRCh37]
Chr4:173659100..191250468 [NCBI36]
Chr4:4q34.1-35.2
pathogenic
GRCh38/hg38 4q34.3-35.2(chr4:180717850-190095391)x3 copy number gain See cases [RCV000143010] Chr4:180717850..190095391 [GRCh38]
Chr4:181639003..190828225 [GRCh37]
Chr4:181875997..191250527 [NCBI36]
Chr4:4q34.3-35.2
pathogenic|likely benign
GRCh38/hg38 4q32.3-35.2(chr4:168119317-190095391)x3 copy number gain See cases [RCV000143331] Chr4:168119317..190095391 [GRCh38]
Chr4:169040468..190828225 [GRCh37]
Chr4:169277043..191250527 [NCBI36]
Chr4:4q32.3-35.2
pathogenic
GRCh38/hg38 4q33-35.2(chr4:170899124-190036318)x1 copy number loss See cases [RCV000143232] Chr4:170899124..190036318 [GRCh38]
Chr4:171820275..190957473 [GRCh37]
Chr4:172056850..191194467 [NCBI36]
Chr4:4q33-35.2
pathogenic
GRCh38/hg38 4q34.3-35.2(chr4:176756632-189621964)x1 copy number loss See cases [RCV000143626] Chr4:176756632..189621964 [GRCh38]
Chr4:177677786..190543118 [GRCh37]
Chr4:177914780..190780112 [NCBI36]
Chr4:4q34.3-35.2
likely pathogenic
GRCh38/hg38 4q28.3-35.2(chr4:134935616-190036318)x3 copy number gain See cases [RCV000143559] Chr4:134935616..190036318 [GRCh38]
Chr4:135856771..190957473 [GRCh37]
Chr4:136076221..191194467 [NCBI36]
Chr4:4q28.3-35.2
pathogenic
GRCh38/hg38 4q34.3-35.1(chr4:181579626-186100199)x1 copy number loss See cases [RCV000148272] Chr4:181579626..186100199 [GRCh38]
Chr4:182500779..187021353 [GRCh37]
Chr4:182737773..187258347 [NCBI36]
Chr4:4q34.3-35.1
pathogenic
GRCh37/hg19 4q34.1-35.2(chr4:176270886-190713650)x1 copy number loss See cases [RCV000239790] Chr4:176270886..190713650 [GRCh37]
Chr4:4q34.1-35.2
pathogenic
GRCh37/hg19 4q34.3-35.2(chr4:178243625-190713650)x1 copy number loss See cases [RCV000239851] Chr4:178243625..190713650 [GRCh37]
Chr4:4q34.3-35.2
pathogenic
GRCh37/hg19 4q26-35.2(chr4:119437495-190904301)x3 copy number gain See cases [RCV000240392] Chr4:119437495..190904301 [GRCh37]
Chr4:4q26-35.2
pathogenic
GRCh37/hg19 4q35.1-35.2(chr4:185381293-190957473)x1 copy number loss See cases [RCV000449363] Chr4:185381293..190957473 [GRCh37]
Chr4:4q35.1-35.2
pathogenic
GRCh37/hg19 4q35.1-35.2(chr4:185253508-190713591)x1 copy number loss See cases [RCV000449221] Chr4:185253508..190713591 [GRCh37]
Chr4:4q35.1-35.2
pathogenic
GRCh37/hg19 4q34.1-35.2(chr4:175550289-190838582)x1 copy number loss See cases [RCV000446613] Chr4:175550289..190838582 [GRCh37]
Chr4:4q34.1-35.2
pathogenic
GRCh37/hg19 4q32.3-35.2(chr4:167413365-190957473)x1 copy number loss See cases [RCV000446115] Chr4:167413365..190957473 [GRCh37]
Chr4:4q32.3-35.2
pathogenic
GRCh37/hg19 4q32.3-35.2(chr4:166735148-190957473)x3 copy number gain See cases [RCV000446531] Chr4:166735148..190957473 [GRCh37]
Chr4:4q32.3-35.2
pathogenic
GRCh37/hg19 4p16.3-q35.2(chr4:12440-190904441)x3 copy number gain See cases [RCV000446653] Chr4:12440..190904441 [GRCh37]
Chr4:4p16.3-q35.2
pathogenic
GRCh37/hg19 4q34.1-35.2(chr4:175749001-190957473)x1 copy number loss See cases [RCV000445881] Chr4:175749001..190957473 [GRCh37]
Chr4:4q34.1-35.2
pathogenic
GRCh37/hg19 4q34.1-35.2(chr4:175550289-190957473)x1 copy number loss See cases [RCV000448048] Chr4:175550289..190957473 [GRCh37]
Chr4:4q34.1-35.2
pathogenic
GRCh37/hg19 4q35.1(chr4:183959053-186858555)x3 copy number gain See cases [RCV000448219] Chr4:183959053..186858555 [GRCh37]
Chr4:4q35.1
uncertain significance
GRCh37/hg19 4q35.1-35.2(chr4:184852835-190957473)x1 copy number loss See cases [RCV000512074] Chr4:184852835..190957473 [GRCh37]
Chr4:4q35.1-35.2
likely pathogenic
GRCh37/hg19 4q32.3-35.2(chr4:166436844-190957473)x3 copy number gain See cases [RCV000510222] Chr4:166436844..190957473 [GRCh37]
Chr4:4q32.3-35.2
pathogenic
GRCh37/hg19 4p16.3-q35.2(chr4:68346-190957473) copy number gain See cases [RCV000510453] Chr4:68346..190957473 [GRCh37]
Chr4:4p16.3-q35.2
pathogenic
GRCh37/hg19 4q31.3-35.2(chr4:153890440-190957473)x3 copy number gain See cases [RCV000510713] Chr4:153890440..190957473 [GRCh37]
Chr4:4q31.3-35.2
pathogenic
GRCh37/hg19 4q25-35.2(chr4:109199664-189752726)x3 copy number gain See cases [RCV000511945] Chr4:109199664..189752726 [GRCh37]
Chr4:4q25-35.2
pathogenic
GRCh37/hg19 4q34.2-35.2(chr4:176306103-190957473)x3 copy number gain See cases [RCV000511078] Chr4:176306103..190957473 [GRCh37]
Chr4:4q34.2-35.2
pathogenic
GRCh37/hg19 4q35.1(chr4:184870144-186592638)x3 copy number gain See cases [RCV000510983] Chr4:184870144..186592638 [GRCh37]
Chr4:4q35.1
likely benign
GRCh37/hg19 4q22.1-35.2(chr4:93071152-190957473)x3 copy number gain See cases [RCV000510970] Chr4:93071152..190957473 [GRCh37]
Chr4:4q22.1-35.2
pathogenic
GRCh37/hg19 4q34.3-35.2(chr4:180702769-190957473)x3 copy number gain See cases [RCV000512153] Chr4:180702769..190957473 [GRCh37]
Chr4:4q34.3-35.2
pathogenic
GRCh37/hg19 4q32.1-35.2(chr4:156465633-190957473)x3 copy number gain See cases [RCV000512542] Chr4:156465633..190957473 [GRCh37]
Chr4:4q32.1-35.2
pathogenic
GRCh37/hg19 4p16.3-q35.2(chr4:68346-190957473)x3 copy number gain See cases [RCV000512241] Chr4:68346..190957473 [GRCh37]
Chr4:4p16.3-q35.2
pathogenic
GRCh37/hg19 4q32.1-35.2(chr4:159492464-190957473)x3 copy number gain not provided [RCV000682478] Chr4:159492464..190957473 [GRCh37]
Chr4:4q32.1-35.2
pathogenic
GRCh37/hg19 4q32.3-35.2(chr4:169969014-190957473)x1 copy number loss not provided [RCV000682484] Chr4:169969014..190957473 [GRCh37]
Chr4:4q32.3-35.2
pathogenic
GRCh37/hg19 4q34.1-35.2(chr4:175709188-190957473)x1 copy number loss not provided [RCV000682492] Chr4:175709188..190957473 [GRCh37]
Chr4:4q34.1-35.2
pathogenic
GRCh37/hg19 4q34.3-35.2(chr4:178771936-190957473)x3 copy number gain not provided [RCV000682495] Chr4:178771936..190957473 [GRCh37]
Chr4:4q34.3-35.2
pathogenic
GRCh37/hg19 4q35.1-35.2(chr4:185017749-190957473)x3 copy number gain not provided [RCV000682497] Chr4:185017749..190957473 [GRCh37]
Chr4:4q35.1-35.2
pathogenic
Single allele deletion not provided [RCV000677918] Chr4:176270886..190713650 [GRCh37]
Chr4:4q34.1-35.2
pathogenic
GRCh37/hg19 4q34.2-35.2(chr4:176493246-190957473)x1 copy number loss not provided [RCV000682493] Chr4:176493246..190957473 [GRCh37]
Chr4:4q34.2-35.2
pathogenic
GRCh37/hg19 4p16.3-q35.2(chr4:49450-190915650)x3 copy number gain not provided [RCV000743155] Chr4:49450..190915650 [GRCh37]
Chr4:4p16.3-q35.2
pathogenic
GRCh37/hg19 4q34.3-35.2(chr4:183157313-191028879)x1 copy number loss not provided [RCV000744206] Chr4:183157313..191028879 [GRCh37]
Chr4:4q34.3-35.2
pathogenic
GRCh37/hg19 4q35.1-35.2(chr4:184040122-187880098)x3 copy number gain not provided [RCV000744219] Chr4:184040122..187880098 [GRCh37]
Chr4:4q35.1-35.2
uncertain significance
GRCh37/hg19 4q35.1-35.2(chr4:185137253-190915650)x1 copy number loss not provided [RCV000744226] Chr4:185137253..190915650 [GRCh37]
Chr4:4q35.1-35.2
pathogenic
GRCh37/hg19 4p16.3-q35.2(chr4:49450-190963766)x3 copy number gain not provided [RCV000743156] Chr4:49450..190963766 [GRCh37]
Chr4:4p16.3-q35.2
pathogenic
GRCh37/hg19 4q35.1(chr4:185746607-185747538)x1 copy number loss not provided [RCV000744228] Chr4:185746607..185747538 [GRCh37]
Chr4:4q35.1
benign
GRCh37/hg19 4p16.3-q35.2(chr4:11525-191028879)x3 copy number gain not provided [RCV000743147] Chr4:11525..191028879 [GRCh37]
Chr4:4p16.3-q35.2
pathogenic
GRCh37/hg19 4q34.1-35.2(chr4:174610492-190427545) copy number loss not provided [RCV000767793] Chr4:174610492..190427545 [GRCh37]
Chr4:4q34.1-35.2
pathogenic
NM_001995.4(ACSL1):c.627A>G (p.Leu209=) single nucleotide variant not provided [RCV000969884] Chr4:184776613 [GRCh38]
Chr4:185697767 [GRCh37]
Chr4:4q35.1
benign
NM_001995.4(ACSL1):c.1518C>T (p.Gly506=) single nucleotide variant not provided [RCV000953526] Chr4:184763170 [GRCh38]
Chr4:185684324 [GRCh37]
Chr4:4q35.1
benign
GRCh37/hg19 4q34.3-35.2(chr4:178566256-190957473)x1 copy number loss not provided [RCV001005626] Chr4:178566256..190957473 [GRCh37]
Chr4:4q34.3-35.2
pathogenic
GRCh37/hg19 4q33-35.2(chr4:171663620-190431429) copy number loss not provided [RCV000767673] Chr4:171663620..190431429 [GRCh37]
Chr4:4q33-35.2
pathogenic
GRCh37/hg19 4q35.1-35.2(chr4:184648532-190957473)x1 copy number loss not provided [RCV000846185] Chr4:184648532..190957473 [GRCh37]
Chr4:4q35.1-35.2
pathogenic
GRCh37/hg19 4q32.3-35.2(chr4:166623890-190957473)x1 copy number loss not provided [RCV000845722] Chr4:166623890..190957473 [GRCh37]
Chr4:4q32.3-35.2
pathogenic
GRCh37/hg19 4q35.1-35.2(chr4:183245174-190948359)x1 copy number loss not provided [RCV000998343] Chr4:183245174..190948359 [GRCh37]
Chr4:4q35.1-35.2
likely pathogenic
GRCh37/hg19 4q35.1(chr4:184695117-185817439)x3 copy number gain not provided [RCV001005628] Chr4:184695117..185817439 [GRCh37]
Chr4:4q35.1
uncertain significance
GRCh37/hg19 4q32.3-35.2(chr4:169607746-190957473)x3 copy number gain not provided [RCV000847360] Chr4:169607746..190957473 [GRCh37]
Chr4:4q32.3-35.2
pathogenic
GRCh37/hg19 4q35.1(chr4:185399884-186542127)x3 copy number gain not provided [RCV000849196] Chr4:185399884..186542127 [GRCh37]
Chr4:4q35.1
uncertain significance
GRCh37/hg19 4q34.2-35.2(chr4:177189906-190816266)x1 copy number loss not provided [RCV000846268] Chr4:177189906..190816266 [GRCh37]
Chr4:4q34.2-35.2
pathogenic
GRCh37/hg19 4q34.3-35.2(chr4:179996712-190957473)x1 copy number loss not provided [RCV000849865] Chr4:179996712..190957473 [GRCh37]
Chr4:4q34.3-35.2
pathogenic
GRCh37/hg19 4q31.3-35.2(chr4:151174061-190957473)x3 copy number gain not provided [RCV000849098] Chr4:151174061..190957473 [GRCh37]
Chr4:4q31.3-35.2
pathogenic
NM_001995.4(ACSL1):c.1905C>T (p.Leu635=) single nucleotide variant not provided [RCV000890785] Chr4:184757686 [GRCh38]
Chr4:185678840 [GRCh37]
Chr4:4q35.1
benign
GRCh37/hg19 4q35.1(chr4:185211828-185748806)x3 copy number gain not provided [RCV001005629] Chr4:185211828..185748806 [GRCh37]
Chr4:4q35.1
uncertain significance
GRCh37/hg19 4q32.3-35.2(chr4:165010461-190957473)x1 copy number loss not provided [RCV001005612] Chr4:165010461..190957473 [GRCh37]
Chr4:4q32.3-35.2
pathogenic
GRCh37/hg19 4q34.3-35.2(chr4:179752903-187987047)x3 copy number gain not provided [RCV001005627] Chr4:179752903..187987047 [GRCh37]
Chr4:4q34.3-35.2
pathogenic
GRCh37/hg19 4q35.1(chr4:185745161-186099203)x3 copy number gain not provided [RCV001259892] Chr4:185745161..186099203 [GRCh37]
Chr4:4q35.1
uncertain significance

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:3569 AgrOrtholog
COSMIC ACSL1 COSMIC
Ensembl Genes ENSG00000151726 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000281455 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000407165 UniProtKB/TrEMBL
  ENSP00000422607 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000424935 UniProtKB/TrEMBL
  ENSP00000425006 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000425098 UniProtKB/TrEMBL
  ENSP00000425640 UniProtKB/TrEMBL
  ENSP00000426150 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000426244 ENTREZGENE, UniProtKB/TrEMBL
  ENSP00000426491 UniProtKB/TrEMBL
  ENSP00000485264 UniProtKB/TrEMBL
Ensembl Transcript ENST00000281455 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000454703 ENTREZGENE, UniProtKB/TrEMBL
  ENST00000503407 UniProtKB/TrEMBL
  ENST00000504342 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000504900 UniProtKB/TrEMBL
  ENST00000505492 UniProtKB/TrEMBL
  ENST00000506733 UniProtKB/TrEMBL
  ENST00000507295 ENTREZGENE, UniProtKB/TrEMBL
  ENST00000513317 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000515030 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000622937 UniProtKB/TrEMBL
Gene3D-CATH 3.40.50.12780 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000151726 GTEx
HGNC ID HGNC:3569 ENTREZGENE
Human Proteome Map ACSL1 Human Proteome Map
InterPro AMP-bd_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  AMP-binding UniProtKB/TrEMBL
  AMP-binding_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  AMP-dep_Synth/Lig UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  AMP-dep_Synthh-like_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:2180 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 2180 ENTREZGENE
OMIM 152425 OMIM
Pfam AMP-binding UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  AMP-binding_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA27966 PharmGKB
PRINTS AMPBINDING UniProtKB/TrEMBL
PROSITE AMP_BINDING UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A8K9T3 ENTREZGENE, UniProtKB/TrEMBL
  ACSL1_HUMAN UniProtKB/Swiss-Prot
  B4E0R0 ENTREZGENE, UniProtKB/TrEMBL
  B7Z3Z9_HUMAN UniProtKB/TrEMBL
  D6RER0_HUMAN UniProtKB/TrEMBL
  D6RG07_HUMAN UniProtKB/TrEMBL
  E7EPM6 ENTREZGENE, UniProtKB/TrEMBL
  H0Y9U7_HUMAN UniProtKB/TrEMBL
  H0Y9Z9_HUMAN UniProtKB/TrEMBL
  P33121 ENTREZGENE
  Q108N1_HUMAN UniProtKB/TrEMBL
  Q108N2_HUMAN UniProtKB/TrEMBL
UniProt Secondary B7Z452 UniProtKB/Swiss-Prot
  D3DP57 UniProtKB/Swiss-Prot
  E7EQJ5 UniProtKB/TrEMBL
  P41215 UniProtKB/Swiss-Prot
  Q8N8V7 UniProtKB/Swiss-Prot
  Q8TA99 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2017-06-20 ACSL1  acyl-CoA synthetase long chain family member 1    acyl-CoA synthetase long-chain family member 1  Symbol and/or name change 5135510 APPROVED
2011-08-17 ACSL1  acyl-CoA synthetase long-chain family member 1  ACSL1  acyl-CoA synthetase long-chain family member 1  Symbol and/or name change 5135510 APPROVED