ELOVL1 (ELOVL fatty acid elongase 1) - Rat Genome Database

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Gene: ELOVL1 (ELOVL fatty acid elongase 1) Homo sapiens
Analyze
Symbol: ELOVL1
Name: ELOVL fatty acid elongase 1
RGD ID: 1349015
HGNC Page HGNC:14418
Description: Enables fatty acid elongase activity. Involved in fatty acid biosynthetic process and sphingolipid biosynthetic process. Located in endoplasmic reticulum.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: 3-keto acyl-CoA synthase ELOVL1; CGI-88; elongation of very long chain fatty acids (FEN1/Elo2, SUR4/Elo3, yeast)-like 1; elongation of very long chain fatty acids protein 1; ELOVL FA elongase 1; IKSHD; Ssc1; very long chain 3-ketoacyl-CoA synthase 1; very long chain 3-oxoacyl-CoA synthase 1; very long chain fatty acid elongase 1; very-long-chain 3-oxoacyl-CoA synthase 1
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
GRCh38143,363,401 - 43,368,011 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl143,363,398 - 43,368,074 (-)EnsemblGRCh38hg38GRCh38
GRCh37143,829,072 - 43,833,682 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36143,601,659 - 43,606,286 (-)NCBINCBI36Build 36hg18NCBI36
Build 34143,498,165 - 43,502,792NCBI
Celera142,111,226 - 42,115,853 (-)NCBICelera
Cytogenetic Map1p34.2NCBI
HuRef141,948,810 - 41,953,487 (-)NCBIHuRef
CHM1_1143,945,527 - 43,950,204 (-)NCBICHM1_1
T2T-CHM13v2.0143,233,949 - 43,238,559 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(-)-alpha-phellandrene  (EXP)
(-)-epigallocatechin 3-gallate  (EXP)
(1->4)-beta-D-glucan  (ISO)
1,2-dimethylhydrazine  (ISO)
17beta-estradiol  (EXP)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
2-bromohexadecanoic acid  (EXP)
2-hydroxypropanoic acid  (EXP)
4-hydroxyphenyl retinamide  (ISO)
6-(4-chlorophenyl)imidazo[2,1-b][1,3]thiazole-5-carbaldehyde O-(3,4-dichlorobenzyl)oxime  (EXP)
6-propyl-2-thiouracil  (ISO)
acrolein  (EXP)
acrylamide  (EXP)
alpha-phellandrene  (EXP)
alpha-pinene  (EXP)
amitrole  (ISO)
arsane  (EXP)
arsenic atom  (EXP)
benzalkonium chloride  (EXP)
benzo[a]pyrene  (ISO)
benzo[b]fluoranthene  (ISO)
Benzo[k]fluoranthene  (ISO)
beta-lapachone  (EXP)
bis(2-ethylhexyl) phthalate  (EXP,ISO)
bisphenol A  (ISO)
Bisphenol B  (EXP)
cadmium atom  (EXP)
cadmium dichloride  (EXP)
carbon nanotube  (ISO)
CGP 52608  (EXP)
chlormequat chloride  (ISO)
chloroprene  (ISO)
chlorpyrifos  (ISO)
copper(II) chloride  (EXP)
Cuprizon  (ISO)
cyclosporin A  (EXP)
cyproconazole  (ISO)
diazinon  (EXP)
Dibutyl phosphate  (EXP)
dibutyl phthalate  (ISO)
diuron  (ISO)
dorsomorphin  (EXP)
epoxiconazole  (ISO)
ethanol  (ISO)
fenamidone  (ISO)
fluoranthene  (ISO)
folic acid  (ISO)
fonofos  (EXP)
furan  (ISO)
genistein  (EXP)
gentamycin  (ISO)
GW 4064  (EXP)
GW 7647  (EXP)
hydrogen cyanide  (ISO)
indole-3-methanol  (ISO)
isoprenaline  (ISO)
isotretinoin  (EXP)
ivermectin  (EXP)
lead diacetate  (ISO)
obeticholic acid  (EXP)
ozone  (EXP,ISO)
paracetamol  (EXP)
parathion  (EXP,ISO)
perfluorooctane-1-sulfonic acid  (ISO)
perfluorooctanoic acid  (ISO)
phenobarbital  (ISO)
phenylmercury acetate  (EXP)
pirinixic acid  (ISO)
potassium chromate  (EXP)
potassium cyanide  (ISO)
progesterone  (EXP)
propiconazole  (ISO)
quercetin  (EXP)
rac-lactic acid  (EXP)
resveratrol  (ISO)
SB 431542  (EXP)
senecionine  (ISO)
sodium arsenate  (EXP)
sodium arsenite  (EXP)
sodium dodecyl sulfate  (EXP)
tamoxifen  (ISO)
terbufos  (EXP)
tetraphene  (ISO)
Theaflavin 3,3'-digallate  (ISO)
thiram  (EXP)
trichostatin A  (EXP)
triphenyl phosphate  (EXP)
valproic acid  (EXP,ISO)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component
endoplasmic reticulum  (IDA,IEA)
endoplasmic reticulum membrane  (IBA,IEA,NAS,TAS)
membrane  (HDA,IEA)

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:8125298   PMID:8944226   PMID:10810093   PMID:10970790   PMID:12477932   PMID:14702039   PMID:15342556   PMID:15489334   PMID:16712791   PMID:17353931   PMID:19946888   PMID:20166112  
PMID:20937905   PMID:21873635   PMID:22658674   PMID:23538298   PMID:23864651   PMID:24489110   PMID:25499606   PMID:26496610   PMID:26638075   PMID:28986522   PMID:29180619   PMID:29496980  
PMID:30487246   PMID:30804502   PMID:31091453   PMID:31527615   PMID:31617661   PMID:31732153   PMID:31741433   PMID:31871319   PMID:32513696   PMID:32628020   PMID:32707033   PMID:32807901  
PMID:33961781   PMID:34732716   PMID:35271311   PMID:35944360   PMID:36042349   PMID:36215168   PMID:37314216   PMID:37774976   PMID:37827155   PMID:38569033   PMID:38777146  


Genomics

Comparative Map Data
ELOVL1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38143,363,401 - 43,368,011 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl143,363,398 - 43,368,074 (-)EnsemblGRCh38hg38GRCh38
GRCh37143,829,072 - 43,833,682 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36143,601,659 - 43,606,286 (-)NCBINCBI36Build 36hg18NCBI36
Build 34143,498,165 - 43,502,792NCBI
Celera142,111,226 - 42,115,853 (-)NCBICelera
Cytogenetic Map1p34.2NCBI
HuRef141,948,810 - 41,953,487 (-)NCBIHuRef
CHM1_1143,945,527 - 43,950,204 (-)NCBICHM1_1
T2T-CHM13v2.0143,233,949 - 43,238,559 (-)NCBIT2T-CHM13v2.0
Elovl1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm394118,285,321 - 118,290,150 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl4118,285,290 - 118,290,150 (+)EnsemblGRCm39 Ensembl
GRCm384118,426,874 - 118,432,953 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl4118,428,093 - 118,432,953 (+)EnsemblGRCm38mm10GRCm38
MGSCv374118,100,698 - 118,105,521 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv364117,926,025 - 117,930,848 (+)NCBIMGSCv36mm8
Celera4117,153,631 - 117,158,454 (+)NCBICelera
Cytogenetic Map4D2.1NCBI
cM Map454.61NCBI
Elovl1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr85137,246,781 - 137,251,351 (+)NCBIGRCr8
mRatBN7.25131,961,478 - 131,965,961 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl5131,961,322 - 131,965,958 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx5134,670,003 - 134,673,190 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.05136,424,640 - 136,427,827 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.05136,447,038 - 136,450,225 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.05137,255,868 - 137,260,486 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl5137,255,908 - 137,260,483 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.05141,046,751 - 141,049,947 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.45138,909,438 - 138,912,186 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera5130,508,244 - 130,511,440 (+)NCBICelera
Cytogenetic Map5q36NCBI
Elovl1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049555372,945,509 - 2,950,146 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049555372,945,509 - 2,950,146 (-)NCBIChiLan1.0ChiLan1.0
ELOVL1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21183,424,960 - 183,446,629 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11182,566,350 - 182,588,012 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0142,664,818 - 42,686,475 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1144,044,693 - 44,064,111 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl144,044,693 - 44,048,769 (-)Ensemblpanpan1.1panPan2
ELOVL1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11516,798,305 - 16,803,071 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1516,798,370 - 16,802,899 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1516,925,313 - 16,930,087 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01516,965,026 - 16,969,802 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1516,965,100 - 16,969,969 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11516,757,503 - 16,762,275 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01516,826,506 - 16,831,275 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01516,900,074 - 16,904,850 (+)NCBIUU_Cfam_GSD_1.0
Elovl1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440505858,940,387 - 58,945,152 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493647424,764,718 - 24,769,947 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493647424,765,173 - 24,769,903 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ELOVL1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl6167,881,352 - 167,886,124 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.16167,881,357 - 167,886,125 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.26155,333,073 - 155,340,903 (+)NCBISscrofa10.2Sscrofa10.2susScr3
ELOVL1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12089,444,146 - 89,448,802 (+)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_02366603327,472,819 - 27,477,500 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Elovl1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248922,675,421 - 2,684,622 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248922,679,872 - 2,684,499 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in ELOVL1
40 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 1p34.2-34.1(chr1:40693289-44514104)x1 copy number loss See cases [RCV000050706] Chr1:40693289..44514104 [GRCh38]
Chr1:41158961..44979776 [GRCh37]
Chr1:40931548..44752363 [NCBI36]
Chr1:1p34.2-34.1		 pathogenic
GRCh38/hg38 1p34.3-33(chr1:39479787-47688131)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051817]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051817]|See cases [RCV000051817] Chr1:39479787..47688131 [GRCh38]
Chr1:39945459..48153803 [GRCh37]
Chr1:39718046..47926390 [NCBI36]
Chr1:1p34.3-33		 pathogenic
GRCh38/hg38 1p34.3-34.1(chr1:38222737-45636176)x3 copy number gain See cases [RCV000051803] Chr1:38222737..45636176 [GRCh38]
Chr1:38688409..46101848 [GRCh37]
Chr1:38460996..45874435 [NCBI36]
Chr1:1p34.3-34.1		 pathogenic
GRCh38/hg38 1p34.2-34.1(chr1:40462415-44668040)x1 copy number loss See cases [RCV000053837] Chr1:40462415..44668040 [GRCh38]
Chr1:40928087..45133712 [GRCh37]
Chr1:40700674..44906299 [NCBI36]
Chr1:1p34.2-34.1		 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 1p34.2-34.1(chr1:42914303-45001279)x1 copy number loss See cases [RCV000446029] Chr1:42914303..45001279 [GRCh37]
Chr1:1p34.2-34.1		 pathogenic
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
NC_000001.10:g.(?_33241563)_(46663513_?)dup duplication Charcot-Marie-Tooth disease dominant intermediate C [RCV000708276] Chr1:33241563..46663513 [GRCh37]
Chr1:1p35.1-34.1		 uncertain significance
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
GRCh37/hg19 1p36.22-21.1(chr1:103343285-103455144)x3 copy number gain Global developmental delay [RCV000787285] Chr1:103343285..103455144 [GRCh37]
Chr1:1p36.22-21.1		 uncertain significance
NM_022821.4(ELOVL1):c.494C>T (p.Ser165Phe) single nucleotide variant Ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features [RCV000808178]|not provided [RCV001856252] Chr1:43364448 [GRCh38]
Chr1:43830119 [GRCh37]
Chr1:1p34.2		 pathogenic
GRCh37/hg19 1p34.2-34.1(chr1:43787578-44221212)x3 copy number gain not provided [RCV000847475] Chr1:43787578..44221212 [GRCh37]
Chr1:1p34.2-34.1		 uncertain significance
GRCh37/hg19 1p34.2-34.1(chr1:43336799-44713202)x1 copy number loss not provided [RCV000850001] Chr1:43336799..44713202 [GRCh37]
Chr1:1p34.2-34.1		 pathogenic
NC_000001.10:g.(?_43392692)_(43870241_?)del deletion not provided [RCV001382501] Chr1:43392692..43870241 [GRCh37]
Chr1:1p34.2		 pathogenic
NC_000001.10:g.(?_33241563)_(46663513_?)dup duplication Charcot-Marie-Tooth disease, dominant intermediate C [RCV001308684] Chr1:33241563..46663513 [GRCh37]
Chr1:1p35.1-34.1		 uncertain significance
GRCh37/hg19 1p35.1-33(chr1:33285582-47891811) copy number gain not specified [RCV002052781] Chr1:33285582..47891811 [GRCh37]
Chr1:1p35.1-33		 pathogenic
NC_000001.10:g.(?_42922237)_(44395893_?)del deletion not provided [RCV001939188] Chr1:42922237..44395893 [GRCh37]
Chr1:1p34.2-34.1		 pathogenic
NM_022821.4(ELOVL1):c.376-2A>G single nucleotide variant Ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features [RCV002248361] Chr1:43364649 [GRCh38]
Chr1:43830320 [GRCh37]
Chr1:1p34.2		 pathogenic
NM_022821.4(ELOVL1):c.105C>T (p.Leu35=) single nucleotide variant ELOVL1-related disorder [RCV003916359]|not provided [RCV002191164] Chr1:43365318 [GRCh38]
Chr1:43830989 [GRCh37]
Chr1:1p34.2		 benign|likely benign
NM_022821.4(ELOVL1):c.375+17G>A single nucleotide variant not provided [RCV002094172] Chr1:43364721 [GRCh38]
Chr1:43830392 [GRCh37]
Chr1:1p34.2		 likely benign
NM_022821.4(ELOVL1):c.351C>G (p.Ser117=) single nucleotide variant not provided [RCV002082734] Chr1:43364762 [GRCh38]
Chr1:43830433 [GRCh37]
Chr1:1p34.2		 likely benign
NM_022821.4(ELOVL1):c.142C>T (p.Arg48Cys) single nucleotide variant not provided [RCV003120016]|not specified [RCV004245965] Chr1:43365281 [GRCh38]
Chr1:43830952 [GRCh37]
Chr1:1p34.2		 uncertain significance
NM_022821.4(ELOVL1):c.46+8G>A single nucleotide variant not provided [RCV003121176] Chr1:43365556 [GRCh38]
Chr1:43831227 [GRCh37]
Chr1:1p34.2		 likely benign
NM_022821.4(ELOVL1):c.143G>A (p.Arg48His) single nucleotide variant not provided [RCV003013726] Chr1:43365280 [GRCh38]
Chr1:43830951 [GRCh37]
Chr1:1p34.2		 uncertain significance
NM_022821.4(ELOVL1):c.326G>A (p.Arg109Gln) single nucleotide variant not provided [RCV002904333] Chr1:43364787 [GRCh38]
Chr1:43830458 [GRCh37]
Chr1:1p34.2		 uncertain significance
NM_022821.4(ELOVL1):c.648C>A (p.Ile216=) single nucleotide variant not provided [RCV002994262] Chr1:43364108 [GRCh38]
Chr1:43829779 [GRCh37]
Chr1:1p34.2		 likely benign
NM_022821.4(ELOVL1):c.46+19G>T single nucleotide variant not provided [RCV002617553] Chr1:43365545 [GRCh38]
Chr1:43831216 [GRCh37]
Chr1:1p34.2		 likely benign
NM_022821.4(ELOVL1):c.325C>T (p.Arg109Trp) single nucleotide variant not provided [RCV002726879] Chr1:43364788 [GRCh38]
Chr1:43830459 [GRCh37]
Chr1:1p34.2		 uncertain significance
NM_022821.4(ELOVL1):c.458G>C (p.Trp153Ser) single nucleotide variant not specified [RCV004179856] Chr1:43364565 [GRCh38]
Chr1:43830236 [GRCh37]
Chr1:1p34.2		 uncertain significance
NM_022821.4(ELOVL1):c.335G>C (p.Trp112Ser) single nucleotide variant not provided [RCV002866746] Chr1:43364778 [GRCh38]
Chr1:43830449 [GRCh37]
Chr1:1p34.2		 uncertain significance
NM_022821.4(ELOVL1):c.342C>T (p.Phe114=) single nucleotide variant not provided [RCV002976150] Chr1:43364771 [GRCh38]
Chr1:43830442 [GRCh37]
Chr1:1p34.2		 benign
NM_022821.4(ELOVL1):c.42C>T (p.His14=) single nucleotide variant not provided [RCV003100338] Chr1:43365568 [GRCh38]
Chr1:43831239 [GRCh37]
Chr1:1p34.2		 likely benign
NM_022821.4(ELOVL1):c.669C>G (p.Ser223=) single nucleotide variant not provided [RCV002979776] Chr1:43364087 [GRCh38]
Chr1:43829758 [GRCh37]
Chr1:1p34.2		 likely benign
NM_022821.4(ELOVL1):c.302G>A (p.Ser101Asn) single nucleotide variant not provided [RCV002953178] Chr1:43364944 [GRCh38]
Chr1:43830615 [GRCh37]
Chr1:1p34.2		 uncertain significance
NM_022821.4(ELOVL1):c.492C>T (p.Gly164=) single nucleotide variant not provided [RCV002619710] Chr1:43364450 [GRCh38]
Chr1:43830121 [GRCh37]
Chr1:1p34.2		 likely benign
NM_022821.4(ELOVL1):c.244A>G (p.Met82Val) single nucleotide variant not specified [RCV004150695] Chr1:43365002 [GRCh38]
Chr1:43830673 [GRCh37]
Chr1:1p34.2		 uncertain significance
NM_022821.4(ELOVL1):c.13G>A (p.Val5Met) single nucleotide variant ELOVL1-related disorder [RCV003961158]|not provided [RCV002890739] Chr1:43365597 [GRCh38]
Chr1:43831268 [GRCh37]
Chr1:1p34.2		 benign
NM_022821.4(ELOVL1):c.46+7C>T single nucleotide variant ELOVL1-related disorder [RCV003906329]|not provided [RCV002932847] Chr1:43365557 [GRCh38]
Chr1:43831228 [GRCh37]
Chr1:1p34.2		 benign
NM_022821.4(ELOVL1):c.482-20_482-17del deletion not provided [RCV002575537] Chr1:43364477..43364480 [GRCh38]
Chr1:43830148..43830151 [GRCh37]
Chr1:1p34.2		 likely benign
NM_022821.4(ELOVL1):c.787C>T (p.Arg263Cys) single nucleotide variant not provided [RCV002632469] Chr1:43363969 [GRCh38]
Chr1:43829640 [GRCh37]
Chr1:1p34.2		 likely benign
NM_022821.4(ELOVL1):c.238-6T>A single nucleotide variant not provided [RCV002630659] Chr1:43365014 [GRCh38]
Chr1:43830685 [GRCh37]
Chr1:1p34.2		 likely benign
NM_022821.4(ELOVL1):c.46+5G>A single nucleotide variant not provided [RCV003049036] Chr1:43365559 [GRCh38]
Chr1:43831230 [GRCh37]
Chr1:1p34.2		 uncertain significance
NM_022821.4(ELOVL1):c.498C>G (p.Phe166Leu) single nucleotide variant not provided [RCV003010087] Chr1:43364444 [GRCh38]
Chr1:43830115 [GRCh37]
Chr1:1p34.2		 uncertain significance
NM_022821.4(ELOVL1):c.166T>C (p.Phe56Leu) single nucleotide variant not provided [RCV003071930] Chr1:43365257 [GRCh38]
Chr1:43830928 [GRCh37]
Chr1:1p34.2		 uncertain significance
NM_022821.4(ELOVL1):c.724A>G (p.Ile242Val) single nucleotide variant not provided [RCV003049597] Chr1:43364032 [GRCh38]
Chr1:43829703 [GRCh37]
Chr1:1p34.2		 uncertain significance
NM_022821.4(ELOVL1):c.72G>C (p.Leu24=) single nucleotide variant not provided [RCV003050115] Chr1:43365351 [GRCh38]
Chr1:43831022 [GRCh37]
Chr1:1p34.2		 likely benign
NM_022821.4(ELOVL1):c.202T>G (p.Ser68Ala) single nucleotide variant not specified [RCV004251479] Chr1:43365221 [GRCh38]
Chr1:43830892 [GRCh37]
Chr1:1p34.2		 uncertain significance
Single allele inversion Bilateral polymicrogyria [RCV003459046] Chr1:33246132..61045156 [GRCh38]
Chr1:1p35.1-31.3		 likely pathogenic
NM_022821.4(ELOVL1):c.399A>G (p.Lys133=) single nucleotide variant not provided [RCV003828880] Chr1:43364624 [GRCh38]
Chr1:43830295 [GRCh37]
Chr1:1p34.2		 likely benign
NM_022821.4(ELOVL1):c.585T>G (p.Leu195=) single nucleotide variant not provided [RCV003661770] Chr1:43364357 [GRCh38]
Chr1:43830028 [GRCh37]
Chr1:1p34.2		 likely benign
NM_022821.4(ELOVL1):c.474T>G (p.Ile158Met) single nucleotide variant not provided [RCV003696974] Chr1:43364549 [GRCh38]
Chr1:43830220 [GRCh37]
Chr1:1p34.2		 uncertain significance
GRCh38/hg38 1p34.2(chr1:42278946-43598390) copy number loss Epilepsy syndrome [RCV003986075] Chr1:42278946..43598390 [GRCh38]
Chr1:1p34.2		 pathogenic
NM_022821.4(ELOVL1):c.768C>T (p.Thr256=) single nucleotide variant not provided [RCV003854187] Chr1:43363988 [GRCh38]
Chr1:43829659 [GRCh37]
Chr1:1p34.2		 likely benign
NM_022821.4(ELOVL1):c.95C>A (p.Thr32Asn) single nucleotide variant not provided [RCV003550516] Chr1:43365328 [GRCh38]
Chr1:43830999 [GRCh37]
Chr1:1p34.2		 uncertain significance
NM_022821.4(ELOVL1):c.85T>G (p.Leu29Val) single nucleotide variant not provided [RCV003568162] Chr1:43365338 [GRCh38]
Chr1:43831009 [GRCh37]
Chr1:1p34.2		 uncertain significance
NM_022821.4(ELOVL1):c.520G>A (p.Val174Met) single nucleotide variant not provided [RCV003675252] Chr1:43364422 [GRCh38]
Chr1:43830093 [GRCh37]
Chr1:1p34.2		 uncertain significance
NM_022821.4(ELOVL1):c.46+8G>C single nucleotide variant ELOVL1-related disorder [RCV003944525] Chr1:43365556 [GRCh38]
Chr1:43831227 [GRCh37]
Chr1:1p34.2		 likely benign
NM_022821.4(ELOVL1):c.458G>A (p.Trp153Ter) single nucleotide variant ELOVL1-related disorder [RCV003952141] Chr1:43364565 [GRCh38]
Chr1:43830236 [GRCh37]
Chr1:1p34.2		 uncertain significance
NM_022821.4(ELOVL1):c.664A>G (p.Met222Val) single nucleotide variant not specified [RCV004380368] Chr1:43364092 [GRCh38]
Chr1:43829763 [GRCh37]
Chr1:1p34.2		 uncertain significance
NC_000001.10:g.(?_42922237)_(43916151_?)del deletion not provided [RCV004579159] Chr1:42922237..43916151 [GRCh37]
Chr1:1p34.2		 pathogenic
NM_022821.4(ELOVL1):c.458G>T (p.Trp153Leu) single nucleotide variant not specified [RCV004624818] Chr1:43364565 [GRCh38]
Chr1:43830236 [GRCh37]
Chr1:1p34.2		 uncertain significance
NM_022821.4(ELOVL1):c.115G>A (p.Val39Met) single nucleotide variant not specified [RCV004624817] Chr1:43365308 [GRCh38]
Chr1:43830979 [GRCh37]
Chr1:1p34.2		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:4588
Count of miRNA genes:832
Interacting mature miRNAs:1006
Transcripts:ENST00000372458, ENST00000413844, ENST00000464204, ENST00000465321, ENST00000468865, ENST00000470769, ENST00000470968, ENST00000478481, ENST00000479439, ENST00000479686, ENST00000482302, ENST00000487209, ENST00000496932, ENST00000497050, ENST00000497569
Prediction methods:Microtar, Miranda, Rnahybrid
Result types:miRGate_prediction

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

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

Markers in Region
A004O43  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37143,829,092 - 43,829,238UniSTSGRCh37
Build 36143,601,679 - 43,601,825RGDNCBI36
Celera142,111,246 - 42,111,392RGD
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map1p34.1UniSTS
HuRef141,948,834 - 41,948,980UniSTS
GeneMap99-GB4 RH Map1129.36UniSTS
NCBI RH Map1294.0UniSTS
RH98782  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37143,828,647 - 43,828,820UniSTSGRCh37
Build 36143,601,234 - 43,601,407RGDNCBI36
Celera142,110,801 - 42,110,974RGD
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map1p34.1UniSTS
HuRef141,948,389 - 41,948,562UniSTS
RH12828  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37143,829,158 - 43,829,302UniSTSGRCh37
Build 36143,601,745 - 43,601,889RGDNCBI36
Celera142,111,312 - 42,111,456RGD
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map1p34.1UniSTS
HuRef141,948,900 - 41,949,044UniSTS
GeneMap99-GB4 RH Map1125.97UniSTS


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
pharyngeal arch
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2439 2788 2253 4974 1726 2351 6 624 1951 465 2270 7306 6472 53 3734 1 852 1744 1617 175 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001256399 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001256401 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001256402 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_022821 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_046117 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA635780 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF151846 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF336793 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK001653 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK130174 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK222498 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK298163 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL139289 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL537185 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC000618 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC095456 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM556982 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BP208926 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BP281965 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU180063 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU786323 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU857779 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CB149715 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471059 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068277 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MG766453 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000372458   ⟹   ENSP00000361536
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl143,363,401 - 43,368,011 (-)Ensembl
Ensembl Acc Id: ENST00000413844   ⟹   ENSP00000416024
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl143,363,398 - 43,368,074 (-)Ensembl
Ensembl Acc Id: ENST00000464204
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl143,363,756 - 43,368,007 (-)Ensembl
Ensembl Acc Id: ENST00000465321
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl143,364,544 - 43,368,003 (-)Ensembl
Ensembl Acc Id: ENST00000468865
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl143,363,728 - 43,365,268 (-)Ensembl
Ensembl Acc Id: ENST00000470769
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl143,363,875 - 43,366,587 (-)Ensembl
Ensembl Acc Id: ENST00000470968
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl143,363,771 - 43,368,025 (-)Ensembl
Ensembl Acc Id: ENST00000478481
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl143,364,347 - 43,365,214 (-)Ensembl
Ensembl Acc Id: ENST00000479439
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl143,364,542 - 43,366,329 (-)Ensembl
Ensembl Acc Id: ENST00000479686
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl143,364,560 - 43,367,616 (-)Ensembl
Ensembl Acc Id: ENST00000482302
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl143,364,015 - 43,367,416 (-)Ensembl
Ensembl Acc Id: ENST00000487209
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl143,363,836 - 43,367,999 (-)Ensembl
Ensembl Acc Id: ENST00000496932
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl143,364,576 - 43,367,965 (-)Ensembl
Ensembl Acc Id: ENST00000497050
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl143,364,050 - 43,367,738 (-)Ensembl
Ensembl Acc Id: ENST00000497569
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl143,363,994 - 43,367,104 (-)Ensembl
Ensembl Acc Id: ENST00000621943   ⟹   ENSP00000477602
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl143,363,398 - 43,367,738 (-)Ensembl
RefSeq Acc Id: NM_001256399   ⟹   NP_001243328
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38143,363,401 - 43,367,714 (-)NCBI
GRCh37143,829,068 - 43,833,745 (-)NCBI
HuRef141,948,810 - 41,953,487 (-)NCBI
CHM1_1143,945,527 - 43,949,868 (-)NCBI
T2T-CHM13v2.0143,233,949 - 43,238,262 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001256401   ⟹   NP_001243330
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38143,363,401 - 43,368,011 (-)NCBI
GRCh37143,829,068 - 43,833,745 (-)NCBI
HuRef141,948,810 - 41,953,487 (-)NCBI
CHM1_1143,945,527 - 43,950,204 (-)NCBI
T2T-CHM13v2.0143,233,949 - 43,238,559 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001256402   ⟹   NP_001243331
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38143,363,401 - 43,368,011 (-)NCBI
GRCh37143,829,068 - 43,833,745 (-)NCBI
HuRef141,948,810 - 41,953,487 (-)NCBI
CHM1_1143,945,527 - 43,950,204 (-)NCBI
T2T-CHM13v2.0143,233,949 - 43,238,559 (-)NCBI
Sequence:
RefSeq Acc Id: NM_022821   ⟹   NP_073732
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38143,363,401 - 43,368,011 (-)NCBI
GRCh37143,829,068 - 43,833,745 (-)NCBI
Build 36143,601,659 - 43,606,286 (-)NCBI Archive
Celera142,111,226 - 42,115,853 (-)RGD
HuRef141,948,810 - 41,953,487 (-)NCBI
CHM1_1143,945,527 - 43,950,204 (-)NCBI
T2T-CHM13v2.0143,233,949 - 43,238,559 (-)NCBI
Sequence:
RefSeq Acc Id: NR_046117
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38143,363,401 - 43,368,011 (-)NCBI
GRCh37143,829,068 - 43,833,745 (-)NCBI
HuRef141,948,810 - 41,953,487 (-)NCBI
CHM1_1143,945,527 - 43,950,204 (-)NCBI
T2T-CHM13v2.0143,233,949 - 43,238,559 (-)NCBI
Sequence:
RefSeq Acc Id: NP_073732   ⟸   NM_022821
- Peptide Label: isoform 1
- UniProtKB: Q9NVD9 (UniProtKB/Swiss-Prot),   Q8WXU3 (UniProtKB/Swiss-Prot),   Q5JUY3 (UniProtKB/Swiss-Prot),   Q53HT2 (UniProtKB/Swiss-Prot),   B4DP24 (UniProtKB/Swiss-Prot),   Q9Y396 (UniProtKB/Swiss-Prot),   Q9BW60 (UniProtKB/Swiss-Prot),   A0A3G2LMN0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001243331   ⟸   NM_001256402
- Peptide Label: isoform 3
- UniProtKB: Q9BW60 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001243330   ⟸   NM_001256401
- Peptide Label: isoform 2
- UniProtKB: A0A3G2LMN0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001243328   ⟸   NM_001256399
- Peptide Label: isoform 1
- UniProtKB: Q9NVD9 (UniProtKB/Swiss-Prot),   Q8WXU3 (UniProtKB/Swiss-Prot),   Q5JUY3 (UniProtKB/Swiss-Prot),   Q53HT2 (UniProtKB/Swiss-Prot),   B4DP24 (UniProtKB/Swiss-Prot),   Q9Y396 (UniProtKB/Swiss-Prot),   Q9BW60 (UniProtKB/Swiss-Prot),   A0A3G2LMN0 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSP00000477602   ⟸   ENST00000621943
Ensembl Acc Id: ENSP00000361536   ⟸   ENST00000372458
Ensembl Acc Id: ENSP00000416024   ⟸   ENST00000413844

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9BW60-F1-model_v2 AlphaFold Q9BW60 1-279 view protein structure

Promoters
RGD ID:6855228
Promoter ID:EPDNEW_H779
Type:initiation region
Name:ELOVL1_1
Description:ELOVL fatty acid elongase 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
GRCh38143,368,011 - 43,368,071EPDNEW
RGD ID:6785115
Promoter ID:HG_KWN:2355
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell_12Hour,   HeLa_S3,   Lymphoblastoid
Transcripts:OTTHUMT00000019497,   OTTHUMT00000019499
Position:
Human AssemblyChrPosition (strand)Source
Build 36143,604,046 - 43,604,546 (-)MPROMDB
RGD ID:6785114
Promoter ID:HG_KWN:2356
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:OTTHUMT00000019496,   OTTHUMT00000019498,   OTTHUMT00000019501,   OTTHUMT00000019502,   OTTHUMT00000019504,   OTTHUMT00000019505,   OTTHUMT00000019507,   OTTHUMT00000019508,   OTTHUMT00000019509,   UC001CIZ.1,   UC001CJA.1,   UC001CJC.1
Position:
Human AssemblyChrPosition (strand)Source
Build 36143,604,531 - 43,606,832 (-)MPROMDB
RGD ID:6852736
Promoter ID:EP74181
Type:initiation region
Name:HS_ELOVL1
Description:Elongation of very long chain fatty acids (FEN1/Elo2, SUR4/Elo3, 1ast)-like 1.
SO ACC ID:SO:0000170
Source:EPD (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Mammalian gene collection (MGC) full-length cDNA cloning
Position:
Human AssemblyChrPosition (strand)Source
Build 36143,606,259 - 43,606,319EPD

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:14418 AgrOrtholog
COSMIC ELOVL1 COSMIC
Ensembl Genes ENSG00000066322 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000372458 ENTREZGENE
  ENST00000372458.8 UniProtKB/Swiss-Prot
  ENST00000413844 ENTREZGENE
  ENST00000413844.3 UniProtKB/Swiss-Prot
  ENST00000621943 ENTREZGENE
  ENST00000621943.4 UniProtKB/Swiss-Prot
GTEx ENSG00000066322 GTEx
HGNC ID HGNC:14418 ENTREZGENE
Human Proteome Map ELOVL1 Human Proteome Map
InterPro ELO_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ELO_fam UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ELOVL1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:64834 UniProtKB/Swiss-Prot
NCBI Gene 64834 ENTREZGENE
OMIM 611813 OMIM
PANTHER ELONGATION OF VERY LONG CHAIN FATTY ACIDS PROTEIN 1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR11157 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam ELO UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA27760 PharmGKB
PROSITE ELO UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A3G2LMN0 ENTREZGENE, UniProtKB/TrEMBL
  B4DP24 ENTREZGENE
  ELOV1_HUMAN UniProtKB/Swiss-Prot
  Q502X7_HUMAN UniProtKB/TrEMBL
  Q53HT2 ENTREZGENE
  Q5JUY3 ENTREZGENE
  Q8WXU3 ENTREZGENE
  Q9BW60 ENTREZGENE
  Q9NVD9 ENTREZGENE
  Q9Y396 ENTREZGENE
UniProt Secondary B4DP24 UniProtKB/Swiss-Prot
  Q53HT2 UniProtKB/Swiss-Prot
  Q5JUY3 UniProtKB/Swiss-Prot
  Q8WXU3 UniProtKB/Swiss-Prot
  Q9NVD9 UniProtKB/Swiss-Prot
  Q9Y396 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2011-07-27 ELOVL1  ELOVL fatty acid elongase 1  ELOVL1  elongation of very long chain fatty acids (FEN1/Elo2, SUR4/Elo3, yeast)-like 1  Symbol and/or name change 5135510 APPROVED