DNM1L (dynamin 1 like) - Rat Genome Database

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Gene: DNM1L (dynamin 1 like) Homo sapiens
Analyze
Symbol: DNM1L
Name: dynamin 1 like
RGD ID: 733618
HGNC Page HGNC
Description: Enables several functions, including GTP-dependent protein binding activity; enzyme binding activity; and protein homodimerization activity. Involved in several processes, including mitochondrion organization; protein-containing complex assembly; and regulation of mitochondrion organization. Acts upstream of with a positive effect on protein-containing complex assembly. Acts upstream of or within mitochondrion morphogenesis. Located in several cellular components, including mitochondrial outer membrane; perinuclear region of cytoplasm; and peroxisome. Part of protein-containing complex. Colocalizes with microtubule and mitochondrion-derived vesicle. Implicated in encephalopathy due to defective mitochondrial and peroxisomal fission 1 and optic atrophy 5. Biomarker of Alzheimer's disease and pulmonary fibrosis.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: DLP1; Dnm1p/Vps1p-like protein; DRP1; DVLP; DYMPLE; dynamin 1-like; dynamin family member proline-rich carboxyl-terminal domain less; dynamin-1-like protein; dynamin-like protein 4; dynamin-like protein IV; dynamin-related protein 1; DYNIV-11; EMPF; EMPF1; FLJ41912; HDYNIV; OPA5; VPS1
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 Ensembl1232,679,200 - 32,745,650 (+)EnsemblGRCh38hg38GRCh38
GRCh381232,679,296 - 32,745,650 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371232,832,235 - 32,898,584 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361232,723,491 - 32,788,621 (+)NCBINCBI36hg18NCBI36
Build 341232,723,490 - 32,787,810NCBI
Celera1212,653,086 - 12,719,281 (+)NCBI
Cytogenetic Map12p11.21NCBI
HuRef1232,584,423 - 32,651,060 (+)NCBIHuRef
CHM1_11232,798,646 - 32,865,086 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(+)-epicatechin-3-O-gallate  (EXP)
(-)-epigallocatechin 3-gallate  (EXP)
(S)-nicotine  (EXP)
17alpha-ethynylestradiol  (ISO)
17beta-estradiol  (EXP)
17beta-hydroxy-5alpha-androstan-3-one  (EXP)
2,2',4,4'-Tetrabromodiphenyl ether  (EXP,ISO)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
2,4-dinitrotoluene  (ISO)
2,6-dinitrotoluene  (ISO)
2-(3,4-dimethoxyphenyl)-5-\{[2-(3,4-dimethoxyphenyl)ethyl](methyl)amino\}-2-(propan-2-yl)pentanenitrile  (EXP)
2-methylcholine  (EXP)
3,4-methylenedioxymethamphetamine  (ISO)
3-chloropropane-1,2-diol  (EXP,ISO)
3-isobutyl-1-methyl-7H-xanthine  (EXP,ISO)
4,4'-diaminodiphenylmethane  (ISO)
4,4'-sulfonyldiphenol  (ISO)
4-amino-2,6-dinitrotoluene  (ISO)
4-DAMP(1+)  (ISO)
4-phenylbutyric acid  (EXP,ISO)
4-vinylcyclohexene dioxide  (ISO)
6-propyl-2-thiouracil  (ISO)
acetylleucyl-leucyl-norleucinal  (ISO)
acrolein  (EXP)
aflatoxin B1  (EXP)
aflatoxin B2  (EXP)
aldehydo-D-glucose  (EXP,ISO)
alpha-D-galactose  (EXP,ISO)
alpha-pinene  (EXP)
ammonium chloride  (ISO)
Aroclor 1254  (ISO)
arsenous acid  (ISO)
azide  (EXP,ISO)
benzo[a]pyrene  (EXP,ISO)
beta-naphthoflavone  (ISO)
bis(2-ethylhexyl) phthalate  (ISO)
bisphenol A  (EXP,ISO)
bisphenol F  (EXP)
C60 fullerene  (ISO)
CCCP  (EXP)
chlorpyrifos  (ISO)
cisplatin  (EXP,ISO)
cocaine  (ISO)
colforsin daropate hydrochloride  (EXP)
coumestrol  (EXP)
crocidolite asbestos  (ISO)
curcumin  (ISO)
cycloheximide  (EXP)
cyclosporin A  (EXP,ISO)
D-glucose  (EXP,ISO)
desferrioxamine B  (ISO)
dexamethasone  (EXP,ISO)
diallyl trisulfide  (EXP)
diarsenic trioxide  (ISO)
dicrotophos  (EXP)
dioxygen  (ISO)
dorsomorphin  (ISO)
doxorubicin  (EXP,ISO)
efavirenz  (EXP)
Enterolactone  (EXP)
enzyme inhibitor  (EXP)
ethanol  (ISO)
excitatory amino acid agonist  (ISO)
fenofibrate  (EXP)
fenvalerate  (ISO)
ferric ammonium citrate  (ISO)
ferulic acid  (ISO)
fructose  (EXP)
galactose  (EXP,ISO)
gallic acid  (EXP)
gallocatechin  (EXP)
Genipin  (ISO)
glucose  (EXP,ISO)
glycidol  (ISO)
hexadecanoic acid  (EXP)
homocysteine  (EXP)
hydrogen peroxide  (EXP)
indometacin  (EXP)
isoprenaline  (ISO)
Licarin A  (ISO)
mabuterol  (ISO)
mangiferin  (EXP)
melatonin  (EXP,ISO)
menadione  (ISO)
metformin  (ISO)
methoxychlor  (ISO)
N-(4-aminobutyl)-5-chloronaphthalene-2-sulfonamide  (ISO)
N-acetyl-L-cysteine  (ISO)
N-acetylsphingosine  (ISO)
N-methyl-4-phenylpyridinium  (EXP)
N-nitrosodiethylamine  (ISO)
nicotine  (EXP)
nitrogen dioxide  (ISO)
okadaic acid  (ISO)
oxidopamine  (EXP)
ozone  (EXP)
paracetamol  (EXP,ISO)
paraquat  (EXP,ISO)
perfluorooctane-1-sulfonic acid  (ISO)
phenylephrine  (ISO)
pirinixic acid  (ISO)
potassium dichromate  (ISO)
pyrroloquinoline quinone  (EXP,ISO)
regorafenib  (ISO)
resveratrol  (ISO)
rotenone  (EXP,ISO)
Salvianolic acid A  (ISO)
SB-239063  (ISO)
sevoflurane  (ISO)
silicon dioxide  (ISO)
simvastatin  (EXP)
sodium arsenite  (ISO)
sodium dichromate  (ISO)
streptozocin  (ISO)
sulforaphane  (EXP)
sulfur dioxide  (ISO)
tacrolimus hydrate  (EXP,ISO)
tamoxifen  (ISO)
tetrachloromethane  (ISO)
thapsigargin  (EXP)
thioacetamide  (ISO)
thymoquinone  (ISO)
trans-cinnamic acid  (ISO)
trifloxystrobin  (EXP)
Triptolide  (ISO)
triptonide  (ISO)
verapamil  (EXP)
vinclozolin  (ISO)
xestospongin C  (EXP)
zearalenone  (ISO)
zidovudine  (EXP,ISO)

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process
calcium ion transport  (IEA,ISO)
cellular response to lipid  (ISO)
cellular response to oxygen-glucose deprivation  (IEA,ISO)
cellular response to thapsigargin  (IEA,ISO)
dynamin family protein polymerization involved in mitochondrial fission  (IDA)
endoplasmic reticulum organization  (IMP)
heart contraction  (IEA)
intracellular distribution of mitochondria  (IMP,ISO)
membrane fusion  (IDA)
mitochondrial fission  (IBA,IDA,IEA,IMP)
mitochondrial fragmentation involved in apoptotic process  (IBA,IMP,ISO)
mitochondrial membrane fission  (IDA,IMP)
mitochondrion morphogenesis  (IMP,ISO)
mitochondrion organization  (IMP,ISO)
necroptotic process  (IMP)
negative regulation of mitochondrial fusion  (IEA)
peroxisome fission  (IDA,IEA,IMP)
positive regulation of apoptotic process  (IMP)
positive regulation of dendritic spine morphogenesis  (IEA,ISO)
positive regulation of intrinsic apoptotic signaling pathway  (IMP)
positive regulation of mitochondrial fission  (IMP,ISO,TAS)
positive regulation of neutrophil chemotaxis  (IMP)
positive regulation of protein secretion  (IDA)
positive regulation of release of cytochrome c from mitochondria  (IMP)
positive regulation of synaptic vesicle endocytosis  (IEA)
positive regulation of synaptic vesicle exocytosis  (IEA)
protein complex oligomerization  (IMP)
protein localization to mitochondrion  (IEA,ISO)
protein-containing complex assembly  (IDA)
regulation of ATP metabolic process  (IEA)
regulation of autophagy of mitochondrion  (IGI)
regulation of gene expression  (IEA,ISO)
regulation of mitochondrion organization  (IMP)
regulation of peroxisome organization  (IMP)
regulation of ubiquitin protein ligase activity  (IEA,ISO)
release of cytochrome c from mitochondria  (IMP)
response to flavonoid  (IEA,ISO)
response to hypobaric hypoxia  (IEA,ISO)
rhythmic process  (IEA)
synaptic vesicle endocytosis  (IEA)
synaptic vesicle recycling via endosome  (IEA)

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

Human Phenotype
Abnormal periventricular white matter morphology  (IAGP)
Abnormal pyramidal sign  (IAGP)
Abnormality of the mitochondrion  (IAGP)
Absent speech  (IAGP)
Areflexia  (IAGP)
Ataxia  (IAGP)
Atrophy/Degeneration affecting the brainstem  (IAGP)
Autosomal dominant inheritance  (IAGP)
Autosomal recessive inheritance  (IAGP)
Basal ganglia calcification  (IAGP)
Bilateral ptosis  (IAGP)
Bilateral tonic-clonic seizure  (IAGP)
Cataract  (IAGP)
Central scotoma  (IAGP)
Cerebellar atrophy  (IAGP)
Cerebral atrophy  (IAGP)
Color vision defect  (IAGP)
Corpus callosum atrophy  (IAGP)
Death in infancy  (IAGP)
Decreased fetal movement  (IAGP)
Deeply set eye  (IAGP)
Delayed menarche  (IAGP)
Dementia  (IAGP)
Developmental regression  (IAGP)
Diabetes mellitus  (IAGP)
Difficulty walking  (IAGP)
Diffuse cerebral atrophy  (IAGP)
Duane anomaly  (IAGP)
Dysphagia  (IAGP)
Dysphasia  (IAGP)
Elevated brain lactate level by MRS  (IAGP)
Encephalopathy  (IAGP)
Epileptic encephalopathy  (IAGP)
Failure to thrive  (IAGP)
Fatigue  (IAGP)
Feeding difficulties  (IAGP)
Focal impaired awareness seizure  (IAGP)
Gait disturbance  (IAGP)
Gastrostomy tube feeding in infancy  (IAGP)
Generalized hypotonia  (IAGP)
Generalized myoclonic seizure  (IAGP)
Global developmental delay  (IAGP)
Hallucinations  (IAGP)
Hemiparesis  (IAGP)
Horizontal nystagmus  (IAGP)
Hyperactive deep tendon reflexes  (IAGP)
Hypogonadism  (IAGP)
Hypothyroidism  (IAGP)
Inability to walk  (IAGP)
Increased serum lactate  (IAGP)
Lactic acidosis  (IAGP)
Macrocytic anemia  (IAGP)
Microcephaly  (IAGP)
Migraine  (IAGP)
Moderately reduced visual acuity  (IAGP)
Morning glory anomaly  (IAGP)
Myalgia  (IAGP)
Myopathy  (IAGP)
Nystagmus  (IAGP)
Obesity  (IAGP)
Oculogyric crisis  (IAGP)
Oculomotor apraxia  (IAGP)
Ophthalmoplegia  (IAGP)
Optic atrophy  (IAGP)
Pes cavus  (IAGP)
Pointed chin  (IAGP)
Progressive  (IAGP)
Ptosis  (IAGP)
Scapular winging  (IAGP)
Scoliosis  (IAGP)
Seizure  (IAGP)
Sensorimotor neuropathy  (IAGP)
Sensorineural hearing impairment  (IAGP)
Skeletal muscle atrophy  (IAGP)
Slow decrease in visual acuity  (IAGP)
Slowly progressive  (IAGP)
Spastic paraplegia  (IAGP)
Status epilepticus  (IAGP)
Strabismus  (IAGP)
Temporal optic disc pallor  (IAGP)
Tremor  (IAGP)
Tritanomaly  (IAGP)
Variable expressivity  (IAGP)
Weakness of facial musculature  (IAGP)
References

Additional References at PubMed
PMID:9348079   PMID:9422767   PMID:9472031   PMID:9570752   PMID:9731200   PMID:9742220   PMID:9786947   PMID:10749171   PMID:11514614   PMID:12477932   PMID:12499352   PMID:12499366  
PMID:12618434   PMID:12668660   PMID:12861026   PMID:14741701   PMID:15342556   PMID:15356267   PMID:15364948   PMID:15383276   PMID:15791210   PMID:15824135   PMID:16010987   PMID:16169070  
PMID:16874301   PMID:16936636   PMID:16999686   PMID:17301055   PMID:17332775   PMID:17408615   PMID:17460227   PMID:17553808   PMID:17606867   PMID:17682056   PMID:17718388   PMID:17721437  
PMID:17906671   PMID:18330356   PMID:18353969   PMID:18465792   PMID:18599615   PMID:18695047   PMID:18838687   PMID:19074440   PMID:19279012   PMID:19342591   PMID:19407830   PMID:19409380  
PMID:19492085   PMID:19525928   PMID:19638400   PMID:19946888   PMID:20103533   PMID:20179104   PMID:20379614   PMID:20428767   PMID:20436456   PMID:20467437   PMID:20467441   PMID:20649536  
PMID:20683914   PMID:20688057   PMID:20696759   PMID:20826455   PMID:20850011   PMID:21145355   PMID:21145461   PMID:21149567   PMID:21172823   PMID:21217774   PMID:21292769   PMID:21325626  
PMID:21336284   PMID:21459773   PMID:21508961   PMID:21525035   PMID:21615675   PMID:21654808   PMID:21701560   PMID:21816823   PMID:21822277   PMID:21840923   PMID:21873635   PMID:21903925  
PMID:21956116   PMID:21997870   PMID:22005465   PMID:22020994   PMID:22228096   PMID:22265414   PMID:22340708   PMID:22367970   PMID:22428580   PMID:22438978   PMID:22445325   PMID:22487795  
PMID:22511751   PMID:22583914   PMID:22595283   PMID:22639965   PMID:22745122   PMID:22863883   PMID:22955947   PMID:23027751   PMID:23028930   PMID:23185298   PMID:23283981   PMID:23284813  
PMID:23288151   PMID:23334860   PMID:23349293   PMID:23434681   PMID:23492771   PMID:23516518   PMID:23524851   PMID:23530241   PMID:23582339   PMID:23584531   PMID:23641925   PMID:23658835  
PMID:23667531   PMID:23713734   PMID:23813973   PMID:23921378   PMID:23977156   PMID:23979707   PMID:24080278   PMID:24121705   PMID:24206264   PMID:24252614   PMID:24282027   PMID:24302731  
PMID:24489003   PMID:24550280   PMID:24599962   PMID:24634514   PMID:24681098   PMID:24755420   PMID:24790094   PMID:24797263   PMID:24899388   PMID:24947026   PMID:25033890   PMID:25082190  
PMID:25174275   PMID:25320323   PMID:25326752   PMID:25332205   PMID:25446129   PMID:25482923   PMID:25487648   PMID:25544563   PMID:25591737   PMID:25658204   PMID:25658205   PMID:25659608  
PMID:25737280   PMID:25767741   PMID:25770210   PMID:25822260   PMID:25921289   PMID:26093086   PMID:26114658   PMID:26122121   PMID:26186194   PMID:26217791   PMID:26344197   PMID:26356820  
PMID:26358295   PMID:26381214   PMID:26384664   PMID:26446488   PMID:26496610   PMID:26518267   PMID:26577411   PMID:26578513   PMID:26598294   PMID:26604000   PMID:26609810   PMID:26618722  
PMID:26708942   PMID:26812016   PMID:26825290   PMID:26903540   PMID:26915633   PMID:26931468   PMID:26992161   PMID:27059175   PMID:27145208   PMID:27145933   PMID:27215606   PMID:27288452  
PMID:27301544   PMID:27328748   PMID:27349184   PMID:27495873   PMID:27509055   PMID:27545046   PMID:27599716   PMID:27660309   PMID:27746856   PMID:27799292   PMID:27816895   PMID:27831567  
PMID:27903607   PMID:27923790   PMID:27941873   PMID:28007911   PMID:28040727   PMID:28079887   PMID:28085543   PMID:28132464   PMID:28174288   PMID:28262828   PMID:28282614   PMID:28294974  
PMID:28347692   PMID:28363867   PMID:28388446   PMID:28423497   PMID:28514442   PMID:28607103   PMID:28646508   PMID:28675297   PMID:28700943   PMID:28757354   PMID:28818497   PMID:28969390  
PMID:28974722   PMID:28986522   PMID:29072687   PMID:29110115   PMID:29111377   PMID:29128334   PMID:29158231   PMID:29262528   PMID:29299163   PMID:29307555   PMID:29329364   PMID:29335339  
PMID:29361534   PMID:29397067   PMID:29444369   PMID:29464060   PMID:29478834   PMID:29541021   PMID:29568061   PMID:29725013   PMID:29768044   PMID:29802333   PMID:29864925   PMID:29877124  
PMID:29899447   PMID:29924999   PMID:30085106   PMID:30143522   PMID:30194290   PMID:30209302   PMID:30232469   PMID:30258050   PMID:30323195   PMID:30347228   PMID:30463901   PMID:30501006  
PMID:30542779   PMID:30566949   PMID:30581142   PMID:30591411   PMID:30604255   PMID:30619736   PMID:30629163   PMID:30711678   PMID:30767411   PMID:30890647   PMID:30914652   PMID:30940726  
PMID:30948266   PMID:30981110   PMID:31002345   PMID:31091453   PMID:31239323   PMID:31253394   PMID:31285421   PMID:31412251   PMID:31450774   PMID:31519766   PMID:31533986   PMID:31594818  
PMID:31639424   PMID:31723608   PMID:31744532   PMID:31755231   PMID:31756635   PMID:31760107   PMID:31770286   PMID:31838085   PMID:31873747   PMID:31907514   PMID:31908078   PMID:31914641  
PMID:31950832   PMID:31994339   PMID:32017930   PMID:32020220   PMID:32129710   PMID:32147668   PMID:32169612   PMID:32235678   PMID:32236517   PMID:32249652   PMID:32351292   PMID:32416067  
PMID:32448194   PMID:32573516   PMID:32636049   PMID:32694731   PMID:32767829   PMID:32777260   PMID:32786267   PMID:32877691   PMID:33049497   PMID:33171123   PMID:33219495   PMID:33236140  
PMID:33472166   PMID:33804169   PMID:33895866   PMID:33902225   PMID:34079125  


Genomics

Comparative Map Data
DNM1L
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1232,679,200 - 32,745,650 (+)EnsemblGRCh38hg38GRCh38
GRCh381232,679,296 - 32,745,650 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371232,832,235 - 32,898,584 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361232,723,491 - 32,788,621 (+)NCBINCBI36hg18NCBI36
Build 341232,723,490 - 32,787,810NCBI
Celera1212,653,086 - 12,719,281 (+)NCBI
Cytogenetic Map12p11.21NCBI
HuRef1232,584,423 - 32,651,060 (+)NCBIHuRef
CHM1_11232,798,646 - 32,865,086 (+)NCBICHM1_1
Dnm1l
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391616,130,092 - 16,176,902 (-)NCBIGRCm39mm39
GRCm39 Ensembl1616,130,094 - 16,176,823 (-)Ensembl
GRCm381616,312,228 - 16,359,038 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1616,312,230 - 16,358,959 (-)EnsemblGRCm38mm10GRCm38
MGSCv371616,312,326 - 16,359,123 (-)NCBIGRCm37mm9NCBIm37
MGSCv361616,225,811 - 16,272,608 (-)NCBImm8
Celera1616,883,274 - 16,930,064 (-)NCBICelera
Cytogenetic Map16A2NCBI
Dnm1l
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.21184,581,216 - 84,632,382 (+)NCBImRatBN7.2
Rnor_6.0 Ensembl1188,830,957 - 88,880,198 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.01188,830,968 - 88,882,271 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.01191,885,295 - 91,936,512 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41186,617,236 - 86,665,861 (-)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.11186,657,172 - 86,706,365 (-)NCBI
Celera1183,326,642 - 83,375,373 (+)NCBICelera
Cytogenetic Map11q23NCBI
Dnm1l
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049555053,023,018 - 3,081,680 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049555053,025,742 - 3,081,491 (-)NCBIChiLan1.0ChiLan1.0
DNM1L
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.11256,077,504 - 56,142,376 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1256,077,504 - 56,142,376 (-)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v01253,476,553 - 53,541,421 (-)NCBIMhudiblu_PPA_v0panPan3
DNM1L
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12716,161,855 - 16,211,983 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2716,163,357 - 16,211,957 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2730,213,206 - 30,264,757 (+)NCBI
ROS_Cfam_1.02716,342,630 - 16,394,291 (-)NCBI
UMICH_Zoey_3.12716,151,140 - 16,202,287 (-)NCBI
UNSW_CanFamBas_1.02716,183,766 - 16,235,121 (-)NCBI
UU_Cfam_GSD_1.02730,361,257 - 30,412,627 (+)NCBI
Dnm1l
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494576,743,024 - 76,799,054 (-)NCBI
SpeTri2.0NW_0049366073,576,357 - 3,632,423 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
FGD4
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1541,571,054 - 41,636,058 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2544,756,967 - 44,785,760 (+)NCBISscrofa10.2Sscrofa10.2susScr3
DNM1L
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11132,114,642 - 32,178,330 (+)NCBI
ChlSab1.1 Ensembl1132,114,675 - 32,177,661 (+)Ensembl
Vero_WHO_p1.0NW_0236660692,716,938 - 2,783,519 (-)NCBI
Dnm1l
(Heterocephalus glaber - naked mole-rat)
Naked Mole-rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046247783,391,690 - 3,475,548 (-)NCBI

Position Markers
SGC33422  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371232,879,719 - 32,879,845UniSTSGRCh37
Build 361232,770,986 - 32,771,112RGDNCBI36
Celera1212,700,416 - 12,700,542RGD
Cytogenetic Map12p11.21UniSTS
HuRef1232,632,132 - 32,632,258UniSTS
GeneMap99-GB4 RH Map12140.67UniSTS
Whitehead-RH Map12210.3UniSTS
RH48065  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371232,889,905 - 32,890,032UniSTSGRCh37
Build 361232,781,172 - 32,781,299RGDNCBI36
Celera1212,710,602 - 12,710,729RGD
Cytogenetic Map12p11.21UniSTS
HuRef1232,642,384 - 32,642,511UniSTS
GeneMap99-GB4 RH Map12140.36UniSTS
RH48067  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371232,889,905 - 32,890,059UniSTSGRCh37
Build 361232,781,172 - 32,781,326RGDNCBI36
Celera1212,710,602 - 12,710,756RGD
Cytogenetic Map12p11.21UniSTS
HuRef1232,642,384 - 32,642,538UniSTS
GeneMap99-GB4 RH Map12140.36UniSTS
G43506  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371232,896,867 - 32,896,995UniSTSGRCh37
Build 361232,788,134 - 32,788,262RGDNCBI36
Celera1212,717,564 - 12,717,692RGD
Cytogenetic Map12p11.21UniSTS
HuRef1232,649,344 - 32,649,472UniSTS
RH123679  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh373120,527,468 - 120,527,763UniSTSGRCh37
GRCh371232,876,229 - 32,876,835UniSTSGRCh37
Build 363122,010,158 - 122,010,453RGDNCBI36
Celera1212,696,927 - 12,697,533UniSTS
Celera3118,937,220 - 118,937,515RGD
Cytogenetic Map12p11.21UniSTS
HuRef3117,901,551 - 117,901,846UniSTS
HuRef1232,628,646 - 32,629,252UniSTS
TNG Radiation Hybrid Map367400.0UniSTS
G59502  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371232,896,888 - 32,896,988UniSTSGRCh37
Build 361232,788,155 - 32,788,255RGDNCBI36
Celera1212,717,585 - 12,717,685RGD
Cytogenetic Map12p11.21UniSTS
HuRef1232,649,365 - 32,649,465UniSTS
TNG Radiation Hybrid Map1215074.0UniSTS
DNM1L_7961  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371232,896,663 - 32,897,312UniSTSGRCh37
Build 361232,787,930 - 32,788,579RGDNCBI36
Celera1212,717,360 - 12,718,009RGD
HuRef1232,649,140 - 32,649,789UniSTS
SGC30841  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371232,898,072 - 32,898,179UniSTSGRCh37
Build 361232,789,339 - 32,789,446RGDNCBI36
Celera1212,718,769 - 12,718,876RGD
Cytogenetic Map12p11.21UniSTS
HuRef1232,650,548 - 32,650,655UniSTS
GeneMap99-GB4 RH Map12134.34UniSTS
Whitehead-RH Map12207.4UniSTS
RH15679  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371232,896,397 - 32,896,521UniSTSGRCh37
Build 361232,787,664 - 32,787,788RGDNCBI36
Celera1212,717,094 - 12,717,218RGD
Cytogenetic Map12p11.21UniSTS
HuRef1232,648,874 - 32,648,998UniSTS
GeneMap99-GB4 RH Map12136.46UniSTS
SHGC-2539  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371276,440,382 - 76,440,538UniSTSGRCh37
GRCh371232,876,818 - 32,876,974UniSTSGRCh37
Build 361232,768,085 - 32,768,241RGDNCBI36
Celera1212,697,516 - 12,697,672RGD
Celera1276,107,546 - 76,107,702UniSTS
Cytogenetic Map12q21.2UniSTS
Cytogenetic Map12p11.21UniSTS
HuRef1273,490,423 - 73,490,579UniSTS
HuRef1232,629,235 - 32,629,391UniSTS
GeneMap99-G3 RH Map121454.0UniSTS
A001X15  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371276,441,338 - 76,441,566UniSTSGRCh37
Build 361274,727,605 - 74,727,833RGDNCBI36
Celera1276,108,503 - 76,108,731RGD
Cytogenetic Map12q21.2UniSTS
Cytogenetic Map12p11.21UniSTS
HuRef1232,630,558 - 32,630,780UniSTS
HuRef1232,630,560 - 32,630,780UniSTS
HuRef1273,491,380 - 73,491,608UniSTS
GeneMap99-GB4 RH Map12316.89UniSTS
NCBI RH Map12548.5UniSTS
D12S2017  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371276,439,969 - 76,440,248UniSTSGRCh37
GRCh371232,876,092 - 32,876,682UniSTSGRCh37
Build 361274,726,236 - 74,726,515RGDNCBI36
Celera1212,696,790 - 12,697,380UniSTS
Celera1276,107,133 - 76,107,412RGD
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map12q21.2UniSTS
HuRef1273,490,010 - 73,490,289UniSTS
HuRef1232,628,509 - 32,629,099UniSTS
Whitehead-YAC Contig Map12 UniSTS
D11S3114  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map15q11.2-q21.3UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map10q11.1UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map9q21.12UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map5q23.1UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map7q21.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map11q13.1-q13.2UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map12p13.1UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map1p35-p34.3UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map12p12.2-p11.2UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map3q22.3UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map10q11.1-q24UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map7q31.1-q31.3UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic MapXq13.1-q21.1UniSTS
Cytogenetic Map20pter-q12UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic Map15q21-q22UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic Map1q41-q42.2UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map9p23UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map2q37.2UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map2q24.1UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map1q31-q32UniSTS
Cytogenetic Map6q24.1UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map3p26.1-p25.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map17q24-q25UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic MapXq21UniSTS
Cytogenetic Map6p12UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic Map19qUniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map22q12.3-q13.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map2q34UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map4q21UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map9p22.3UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map4p12UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map19q11UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map1p32.2-p32.1UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map4q13.2UniSTS
Cytogenetic Map4q31.23UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map14q24.2UniSTS
RH80030  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic MapXq26.1UniSTS
Cytogenetic Map17q21.2-q21.3UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map9p13UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map12q15-q21UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map2p22.2UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map11q22.2-q22.3UniSTS
Cytogenetic Map1p36-p35UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map10q26.13-q26.3UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map12q14.2UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map2q32.2UniSTS
D8S2279  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.1-p12UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map8p23UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map13q14.1-q14.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17p13.1-p12UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q23.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5q14.2UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map1p35.2UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map17q21.2-q21.3UniSTS
Cytogenetic Map5q32-q34UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map8p22-p21UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map3q25UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map14q31-q32.1UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map20p11.23-p11.21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map12q24.11UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map10q11.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map7q34-q35UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map6p25.1-p23UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map12p13.1UniSTS
Cytogenetic Map13q12.1UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map12p13.1-p12.3UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map3p21.2UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic MapXp21.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map9q21.12UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map7q33UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map12p13-p12UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map9q13-q21UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic MapXp11.2UniSTS
Cytogenetic Map19pUniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map11p15.3-p15.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map8q22UniSTS
Cytogenetic Map4p15.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map2p16.3UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map6q24.3UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map5q23.1UniSTS
Cytogenetic Map10q23.2UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map6q22.1UniSTS
Cytogenetic Map1q42.1UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map15q22.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map3p21-p12UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3p22-p21.33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map9q22UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map2q31.3UniSTS
Cytogenetic Map1q31UniSTS
Cytogenetic Map7q32-q33UniSTS
Cytogenetic Map7q21.1UniSTS
Cytogenetic Map14q23-q24.2UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map2p24-p21UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map12p11UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map17q25.2UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map10p12.33UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic MapXq25-q26UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map15q25UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map3q26.31UniSTS
Cytogenetic Map17q22-q23UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map3q26.2-q27UniSTS
Cytogenetic Map1q25.1-q25.2UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map5q21.3UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map14q12-q13UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic MapXq23UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map4q32-q34UniSTS
Cytogenetic MapXq25-q26.1UniSTS
Cytogenetic Map2p25-p24UniSTS
Cytogenetic Map2p25UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic MapXp22.2-p22.1UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map20q11.22-q12UniSTS
Cytogenetic Map4q34.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map12q13-q14UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map9q31.2UniSTS
Cytogenetic Map11q13.1-q13.2UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map21q21.2UniSTS
Cytogenetic Map10q24.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map8q21.1UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map1q32.2UniSTS
Cytogenetic Map4q21.3UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map2q36.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map11q22.1UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map4p15.32UniSTS
Cytogenetic Map18q12.2UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map1p35UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map20p12UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map9p22UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2p22.3UniSTS
Cytogenetic MapXq26.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map22q13.3UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map11p14UniSTS
Cytogenetic Map1p32.1UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map4q34.3UniSTS
Cytogenetic Map9p12UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map11q23.2UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map3p13UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map15q22-q24UniSTS
Cytogenetic Map8q23UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map13q33.1UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map4q31.3UniSTS
Cytogenetic Map15q21-q22UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map15q22.1-q22.31UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic MapXq13UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map14q32.1UniSTS
Cytogenetic Map16q12-q13UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map12q11-q12UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map8q24.21UniSTS
Cytogenetic Map12q13.1UniSTS
Cytogenetic Map12q22-q23.1UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map5q31.2-q34UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map6q24.2UniSTS
Cytogenetic Map22qUniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic MapXp22.12-p22.11UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map8p22-p21.3UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map1p36.12UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map7p14-p13UniSTS
Cytogenetic Map12q24.2UniSTS
Cytogenetic Map6p22.2UniSTS
Cytogenetic Map7q22-qterUniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map1q32.2-q41UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map5p15.1-p14.3UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map6q22-q23UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map3p12.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map2q24UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map3q28UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic MapXq22.2UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map7p15.1UniSTS
Cytogenetic Map2q37.2UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map14q32.13UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map16p13.1UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map20q13.2-q13.3UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map13q13.3UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map5q33.2UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map2q24.1UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map18p11.2UniSTS
Cytogenetic Map7p11.1UniSTS
Cytogenetic Map1q31-q32UniSTS
Cytogenetic Map2q12UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map2p24.2UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map6q24.1UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map17q11-q21UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map6p24-p22.3UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map3p26.1-p25.1UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map6q16.3UniSTS
Cytogenetic Map17q24-q25UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic MapXq27.1UniSTS
Cytogenetic Map8q12.3UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map4q35.2UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map3p11.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map2q21.2UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map18q12.3UniSTS
Cytogenetic Map18p11.3UniSTS
Cytogenetic Map17q11.1UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map13q12.3UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map12q14UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map2q32-q34UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map6q23-q24UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map6p12.3-p11.2UniSTS
Cytogenetic Map6q16.1-q16.3UniSTS
Cytogenetic Map22q11UniSTS
Cytogenetic Map7q31.2UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map3q25.2UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map3q23-q24UniSTS
Cytogenetic Map3q12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map3q22.3UniSTS
Cytogenetic Map7q21.3UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map22q12-q13UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map1q24.3UniSTS
Cytogenetic Map9q33.1UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map2p16.2UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map4q21UniSTS
Cytogenetic Map13q12.2UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map1q23UniSTS
Cytogenetic Map11q12-q13UniSTS
Cytogenetic Map11q13.3UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map11q12.1UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map8p21UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map10q26.1UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q33-q34UniSTS
Cytogenetic Map5q11.2-q13.2UniSTS
Cytogenetic Map13q32UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map5q22UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic MapXq13.3UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map3p26.3UniSTS
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map12q24.23UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic MapXp22.31UniSTS
Cytogenetic MapXp21.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3q24UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map14q11.2-q12UniSTS
Cytogenetic Map3p24UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map8q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map11cen-q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map1p35-p34UniSTS
Cytogenetic Map4p13-p12UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map9q31-q34UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q12.12UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1pUniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map2qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map5q14.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map9p21.1UniSTS
Cytogenetic Map9q34.2-q34.3UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:5344
Count of miRNA genes:1063
Interacting mature miRNAs:1318
Transcripts:ENST00000266481, ENST00000358214, ENST00000381000, ENST00000413295, ENST00000414834, ENST00000434676, ENST00000452533, ENST00000546649, ENST00000546757, ENST00000547078, ENST00000547312, ENST00000547548, ENST00000547640, ENST00000547719, ENST00000547932, ENST00000548151, ENST00000548671, ENST00000548750, ENST00000549157, ENST00000549701, ENST00000549926, ENST00000550011, ENST00000550093, ENST00000550154, ENST00000551076, ENST00000551476, ENST00000551643, ENST00000552743, ENST00000553031, ENST00000553257
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.


Expression


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

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 2402 2126 1436 342 1245 183 4346 2056 3563 391 1456 1608 175 1 1202 2783 6 2
Low 37 865 290 282 706 282 11 141 171 28 4 5 2 5
Below cutoff

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_012219 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001278463 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001278464 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001278465 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001278466 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001330380 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_005690 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_012062 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_012063 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011520543 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011520544 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017018663 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017018664 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017018665 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA236613 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB006965 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB209070 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC084824 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC087588 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF000430 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF061795 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF151685 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK123906 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK291094 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK293290 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK294533 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK298568 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK299926 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK302565 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK311606 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC024590 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC107763 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BF725436 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BP342434 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471116 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC377686 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000266481   ⟹   ENSP00000266481
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1232,679,303 - 32,744,350 (+)Ensembl
RefSeq Acc Id: ENST00000358214   ⟹   ENSP00000350948
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1232,679,292 - 32,744,428 (+)Ensembl
RefSeq Acc Id: ENST00000381000   ⟹   ENSP00000370388
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1232,679,323 - 32,745,549 (+)Ensembl
RefSeq Acc Id: ENST00000413295   ⟹   ENSP00000396030
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1232,679,320 - 32,731,383 (+)Ensembl
RefSeq Acc Id: ENST00000414834   ⟹   ENSP00000404160
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1232,679,200 - 32,745,650 (+)Ensembl
RefSeq Acc Id: ENST00000434676   ⟹   ENSP00000390090
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1232,679,320 - 32,731,061 (+)Ensembl
RefSeq Acc Id: ENST00000452533   ⟹   ENSP00000415131
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1232,679,200 - 32,745,552 (+)Ensembl
RefSeq Acc Id: ENST00000546649   ⟹   ENSP00000448936
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1232,679,320 - 32,743,656 (+)Ensembl
RefSeq Acc Id: ENST00000546757   ⟹   ENSP00000448105
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1232,701,415 - 32,744,087 (+)Ensembl
RefSeq Acc Id: ENST00000547078   ⟹   ENSP00000448802
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1232,731,486 - 32,738,296 (+)Ensembl
RefSeq Acc Id: ENST00000547312   ⟹   ENSP00000448610
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1232,679,320 - 32,743,581 (+)Ensembl
RefSeq Acc Id: ENST00000547548
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1232,713,247 - 32,722,772 (+)Ensembl
RefSeq Acc Id: ENST00000547640
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1232,739,845 - 32,742,684 (+)Ensembl
RefSeq Acc Id: ENST00000547719
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1232,706,867 - 32,708,206 (+)Ensembl
RefSeq Acc Id: ENST00000547932
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1232,679,320 - 32,718,718 (+)Ensembl
RefSeq Acc Id: ENST00000548151
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1232,733,453 - 32,737,306 (+)Ensembl
RefSeq Acc Id: ENST00000548671
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1232,679,301 - 32,713,346 (+)Ensembl
RefSeq Acc Id: ENST00000548750   ⟹   ENSP00000447788
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1232,679,336 - 32,720,795 (+)Ensembl
RefSeq Acc Id: ENST00000549157
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1232,737,977 - 32,740,467 (+)Ensembl
RefSeq Acc Id: ENST00000549701   ⟹   ENSP00000450399
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1232,679,301 - 32,745,650 (+)Ensembl
RefSeq Acc Id: ENST00000549926
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1232,679,708 - 32,713,324 (+)Ensembl
RefSeq Acc Id: ENST00000550011
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1232,679,316 - 32,706,102 (+)Ensembl
RefSeq Acc Id: ENST00000550093
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1232,731,469 - 32,738,151 (+)Ensembl
RefSeq Acc Id: ENST00000550154   ⟹   ENSP00000447013
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1232,679,320 - 32,713,330 (+)Ensembl
RefSeq Acc Id: ENST00000551076
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1232,679,316 - 32,711,003 (+)Ensembl
RefSeq Acc Id: ENST00000551476   ⟹   ENSP00000447845
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1232,679,320 - 32,713,319 (+)Ensembl
RefSeq Acc Id: ENST00000551643   ⟹   ENSP00000450401
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1232,679,320 - 32,708,224 (+)Ensembl
RefSeq Acc Id: ENST00000552743
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1232,733,566 - 32,738,171 (+)Ensembl
RefSeq Acc Id: ENST00000553031
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1232,740,154 - 32,743,583 (+)Ensembl
RefSeq Acc Id: ENST00000553257   ⟹   ENSP00000449089
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1232,679,287 - 32,743,782 (+)Ensembl
RefSeq Acc Id: NM_001278463   ⟹   NP_001265392
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381232,679,301 - 32,745,650 (+)NCBI
GRCh371232,832,134 - 32,898,584 (+)NCBI
HuRef1232,584,423 - 32,651,060 (+)NCBI
CHM1_11232,798,646 - 32,865,086 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001278464   ⟹   NP_001265393
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381232,679,301 - 32,745,650 (+)NCBI
HuRef1232,584,423 - 32,651,060 (+)NCBI
CHM1_11232,798,646 - 32,865,086 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001278465   ⟹   NP_001265394
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381232,679,301 - 32,745,650 (+)NCBI
HuRef1232,584,423 - 32,651,060 (+)NCBI
CHM1_11232,798,646 - 32,865,086 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001278466   ⟹   NP_001265395
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381232,679,301 - 32,745,650 (+)NCBI
GRCh371232,832,134 - 32,898,584 (+)NCBI
HuRef1232,584,423 - 32,651,060 (+)NCBI
CHM1_11232,798,646 - 32,865,086 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001330380   ⟹   NP_001317309
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381232,679,301 - 32,745,650 (+)NCBI
Sequence:
RefSeq Acc Id: NM_005690   ⟹   NP_005681
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381232,679,301 - 32,745,650 (+)NCBI
GRCh371232,832,134 - 32,898,584 (+)NCBI
Build 361232,723,491 - 32,787,809 (+)NCBI Archive
HuRef1232,584,423 - 32,651,060 (+)NCBI
CHM1_11232,798,646 - 32,865,086 (+)NCBI
Sequence:
RefSeq Acc Id: NM_012062   ⟹   NP_036192
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381232,679,301 - 32,745,650 (+)NCBI
GRCh371232,832,134 - 32,898,584 (+)NCBI
Build 361232,723,491 - 32,788,621 (+)NCBI Archive
HuRef1232,584,423 - 32,651,060 (+)NCBI
CHM1_11232,798,646 - 32,865,086 (+)NCBI
Sequence:
RefSeq Acc Id: NM_012063   ⟹   NP_036193
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381232,679,301 - 32,745,650 (+)NCBI
GRCh371232,832,134 - 32,898,584 (+)NCBI
Build 361232,723,491 - 32,787,813 (+)NCBI Archive
HuRef1232,584,423 - 32,651,060 (+)NCBI
CHM1_11232,798,646 - 32,865,086 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011520543   ⟹   XP_011518845
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381232,679,316 - 32,745,547 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011520544   ⟹   XP_011518846
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381232,679,320 - 32,745,547 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017018663   ⟹   XP_016874152
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381232,679,296 - 32,745,547 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017018664   ⟹   XP_016874153
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381232,679,320 - 32,745,547 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017018665   ⟹   XP_016874154
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381232,679,320 - 32,745,547 (+)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001265392 (Get FASTA)   NCBI Sequence Viewer  
  NP_001265393 (Get FASTA)   NCBI Sequence Viewer  
  NP_001265394 (Get FASTA)   NCBI Sequence Viewer  
  NP_001265395 (Get FASTA)   NCBI Sequence Viewer  
  NP_001317309 (Get FASTA)   NCBI Sequence Viewer  
  NP_005681 (Get FASTA)   NCBI Sequence Viewer  
  NP_036192 (Get FASTA)   NCBI Sequence Viewer  
  NP_036193 (Get FASTA)   NCBI Sequence Viewer  
  XP_011518845 (Get FASTA)   NCBI Sequence Viewer  
  XP_011518846 (Get FASTA)   NCBI Sequence Viewer  
  XP_016874152 (Get FASTA)   NCBI Sequence Viewer  
  XP_016874153 (Get FASTA)   NCBI Sequence Viewer  
  XP_016874154 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAC23724 (Get FASTA)   NCBI Sequence Viewer  
  AAC35283 (Get FASTA)   NCBI Sequence Viewer  
  AAD39541 (Get FASTA)   NCBI Sequence Viewer  
  AAH24590 (Get FASTA)   NCBI Sequence Viewer  
  AAI07764 (Get FASTA)   NCBI Sequence Viewer  
  BAA22193 (Get FASTA)   NCBI Sequence Viewer  
  BAD92307 (Get FASTA)   NCBI Sequence Viewer  
  BAF83783 (Get FASTA)   NCBI Sequence Viewer  
  BAG56814 (Get FASTA)   NCBI Sequence Viewer  
  BAG57740 (Get FASTA)   NCBI Sequence Viewer  
  BAG60761 (Get FASTA)   NCBI Sequence Viewer  
  BAG61760 (Get FASTA)   NCBI Sequence Viewer  
  BAG63828 (Get FASTA)   NCBI Sequence Viewer  
  EAW88519 (Get FASTA)   NCBI Sequence Viewer  
  EAW88520 (Get FASTA)   NCBI Sequence Viewer  
  EAW88521 (Get FASTA)   NCBI Sequence Viewer  
  EAW88522 (Get FASTA)   NCBI Sequence Viewer  
  EAW88523 (Get FASTA)   NCBI Sequence Viewer  
  EAW88524 (Get FASTA)   NCBI Sequence Viewer  
  EAW88525 (Get FASTA)   NCBI Sequence Viewer  
  EAW88526 (Get FASTA)   NCBI Sequence Viewer  
  EAW88527 (Get FASTA)   NCBI Sequence Viewer  
  O00429 (Get FASTA)   NCBI Sequence Viewer  
Reference Sequences
RefSeq Acc Id: NP_036192   ⟸   NM_012062
- Peptide Label: isoform 1
- UniProtKB: O00429 (UniProtKB/Swiss-Prot),   B4DYR6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_036193   ⟸   NM_012063
- Peptide Label: isoform 2
- UniProtKB: O00429 (UniProtKB/Swiss-Prot),   B4DYR6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_005681   ⟸   NM_005690
- Peptide Label: isoform 3
- UniProtKB: O00429 (UniProtKB/Swiss-Prot),   B4DYR6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001265393   ⟸   NM_001278464
- Peptide Label: isoform 5
- UniProtKB: O00429 (UniProtKB/Swiss-Prot),   B4DYR6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001265394   ⟸   NM_001278465
- Peptide Label: isoform 6
- UniProtKB: O00429 (UniProtKB/Swiss-Prot),   B4DYR6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001265395   ⟸   NM_001278466
- Peptide Label: isoform 7
- UniProtKB: O00429 (UniProtKB/Swiss-Prot),   B4DYR6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001265392   ⟸   NM_001278463
- Peptide Label: isoform 4
- UniProtKB: O00429 (UniProtKB/Swiss-Prot),   B4DYR6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011518845   ⟸   XM_011520543
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_011518846   ⟸   XM_011520544
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_016874152   ⟸   XM_017018663
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: XP_016874153   ⟸   XM_017018664
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: XP_016874154   ⟸   XM_017018665
- Peptide Label: isoform X5
- Sequence:
RefSeq Acc Id: NP_001317309   ⟸   NM_001330380
- Peptide Label: isoform 8
- UniProtKB: O00429 (UniProtKB/Swiss-Prot),   B4DYR6 (UniProtKB/TrEMBL),   G8JLD5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000266481   ⟸   ENST00000266481
RefSeq Acc Id: ENSP00000415131   ⟸   ENST00000452533
RefSeq Acc Id: ENSP00000396030   ⟸   ENST00000413295
RefSeq Acc Id: ENSP00000448936   ⟸   ENST00000546649
RefSeq Acc Id: ENSP00000404160   ⟸   ENST00000414834
RefSeq Acc Id: ENSP00000448105   ⟸   ENST00000546757
RefSeq Acc Id: ENSP00000448610   ⟸   ENST00000547312
RefSeq Acc Id: ENSP00000448802   ⟸   ENST00000547078
RefSeq Acc Id: ENSP00000447788   ⟸   ENST00000548750
RefSeq Acc Id: ENSP00000450399   ⟸   ENST00000549701
RefSeq Acc Id: ENSP00000447013   ⟸   ENST00000550154
RefSeq Acc Id: ENSP00000450401   ⟸   ENST00000551643
RefSeq Acc Id: ENSP00000447845   ⟸   ENST00000551476
RefSeq Acc Id: ENSP00000390090   ⟸   ENST00000434676
RefSeq Acc Id: ENSP00000370388   ⟸   ENST00000381000
RefSeq Acc Id: ENSP00000449089   ⟸   ENST00000553257
RefSeq Acc Id: ENSP00000350948   ⟸   ENST00000358214
Protein Domains
Dynamin-type G   GED

Promoters
RGD ID:7223599
Promoter ID:EPDNEW_H17545
Type:initiation region
Name:DNM1L_1
Description:dynamin 1 like
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
GRCh381232,679,320 - 32,679,380EPDNEW
RGD ID:6789870
Promoter ID:HG_KWN:15330
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_005690,   NM_012062,   NM_012063,   UC001RLG.2,   UC001RLH.2
Position:
Human AssemblyChrPosition (strand)Source
Build 361232,723,251 - 32,723,751 (+)MPROMDB

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_012062.5(DNM1L):c.25_28delinsCACT (p.Asn9_Lys10delinsHisTer) indel not provided [RCV000520809] Chr12:32679388..32679391 [GRCh38]
Chr12:32832322..32832325 [GRCh37]
Chr12:12p11.21
likely pathogenic
NM_012062.5(DNM1L):c.415G>A (p.Val139Ile) single nucleotide variant not specified [RCV000521133] Chr12:32710974 [GRCh38]
Chr12:32863908 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.1184C>A (p.Ala395Asp) single nucleotide variant Encephalopathy due to defective mitochondrial and peroxisomal fission 1 [RCV000006386] Chr12:32731118 [GRCh38]
Chr12:32884052 [GRCh37]
Chr12:12p11.21
pathogenic
GRCh38/hg38 12p13.33-11.1(chr12:77187-34380176)x3 copy number gain See cases [RCV000053660] Chr12:77187..34380176 [GRCh38]
Chr12:282465..34533111 [GRCh37]
Chr12:56614..34424378 [NCBI36]
Chr12:12p13.33-11.1
pathogenic
GRCh38/hg38 12p13.33-11.1(chr12:212976-33926913)x4 copy number gain See cases [RCV000053666] Chr12:212976..33926913 [GRCh38]
Chr12:322142..34079848 [GRCh37]
Chr12:192403..33971115 [NCBI36]
Chr12:12p13.33-11.1
pathogenic
GRCh38/hg38 12p11.21(chr12:32731855-32881857)x3 copy number gain See cases [RCV000053672] Chr12:32731855..32881857 [GRCh38]
Chr12:32884789..33034791 [GRCh37]
Chr12:32776056..32926058 [NCBI36]
Chr12:12p11.21
pathogenic
NM_012062.5(DNM1L):c.966C>T (p.Tyr322=) single nucleotide variant not provided [RCV000676346]|not specified [RCV000124755] Chr12:32722520 [GRCh38]
Chr12:32875454 [GRCh37]
Chr12:12p11.21
benign|likely benign
NM_012062.5(DNM1L):c.1470A>G (p.Glu490=) single nucleotide variant not provided [RCV000676347]|not specified [RCV000124756] Chr12:32733738 [GRCh38]
Chr12:32886672 [GRCh37]
Chr12:12p11.21
benign|likely benign
NM_012062.5(DNM1L):c.1968C>T (p.Leu656=) single nucleotide variant not provided [RCV000675860]|not specified [RCV000124757] Chr12:32740492 [GRCh38]
Chr12:32893426 [GRCh37]
Chr12:12p11.21
benign|likely benign
NM_012062.5(DNM1L):c.-32G>T single nucleotide variant not specified [RCV000124758] Chr12:32679332 [GRCh38]
Chr12:32832266 [GRCh37]
Chr12:12p11.21
benign
NM_012062.5(DNM1L):c.975C>T (p.Pro325=) single nucleotide variant not provided [RCV000876401]|not specified [RCV000603233] Chr12:32722529 [GRCh38]
Chr12:32875463 [GRCh37]
Chr12:12p11.21
likely benign
GRCh38/hg38 12p12.1-11.1(chr12:25263833-34064528)x1 copy number loss See cases [RCV000133858] Chr12:25263833..34064528 [GRCh38]
Chr12:25416767..34217463 [GRCh37]
Chr12:25308034..34108730 [NCBI36]
Chr12:12p12.1-11.1
pathogenic
GRCh38/hg38 12p11.21-11.1(chr12:32672401-33313056)x3 copy number gain See cases [RCV000135581] Chr12:32672401..33313056 [GRCh38]
Chr12:32825335..33465991 [GRCh37]
Chr12:32716602..33357258 [NCBI36]
Chr12:12p11.21-11.1
uncertain significance
GRCh38/hg38 12p13.33-11.1(chr12:121255-34603274)x3 copy number gain See cases [RCV000136611] Chr12:121255..34603274 [GRCh38]
Chr12:282465..34756209 [GRCh37]
Chr12:100682..34647476 [NCBI36]
Chr12:12p13.33-11.1
pathogenic
GRCh38/hg38 12p13.33-11.1(chr12:121271-34603261)x3 copy number gain See cases [RCV000139052] Chr12:121271..34603261 [GRCh38]
Chr12:282465..34756196 [GRCh37]
Chr12:100698..34647463 [NCBI36]
Chr12:12p13.33-11.1
pathogenic
GRCh38/hg38 12p13.33-11.1(chr12:54427-34608071)x4 copy number gain See cases [RCV000139787] Chr12:54427..34608071 [GRCh38]
Chr12:282465..34761006 [GRCh37]
Chr12:33854..34652273 [NCBI36]
Chr12:12p13.33-11.1
pathogenic
GRCh38/hg38 12p13.33-q24.33(chr12:121271-133196807)x3 copy number gain See cases [RCV000139555] Chr12:121271..133196807 [GRCh38]
Chr12:282465..133773393 [GRCh37]
Chr12:100698..132283466 [NCBI36]
Chr12:12p13.33-q24.33
pathogenic
GRCh38/hg38 12p11.21(chr12:32646222-32689862)x3 copy number gain See cases [RCV000141167] Chr12:32646222..32689862 [GRCh38]
Chr12:32799156..32842796 [GRCh37]
Chr12:32690423..32734063 [NCBI36]
Chr12:12p11.21
likely benign
GRCh38/hg38 12p13.33-11.1(chr12:64620-34682902)x4 copy number gain See cases [RCV000142149] Chr12:64620..34682902 [GRCh38]
Chr12:173786..34835837 [GRCh37]
Chr12:44047..34727104 [NCBI36]
Chr12:12p13.33-11.1
pathogenic
NM_012062.5(DNM1L):c.1207C>T (p.Arg403Cys) single nucleotide variant Encephalopathy due to defective mitochondrial and peroxisomal fission 1 [RCV000239677]|Inborn genetic diseases [RCV000622584]|Optic atrophy 5 [RCV000850522]|not provided [RCV000200196] Chr12:32731362 [GRCh38]
Chr12:32884296 [GRCh37]
Chr12:12p11.21
pathogenic|uncertain significance
NM_012062.5(DNM1L):c.1651G>A (p.Ala551Thr) single nucleotide variant not provided [RCV000200424] Chr12:32737919 [GRCh38]
Chr12:32890853 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.1639C>T (p.Pro547Ser) single nucleotide variant not provided [RCV000196481] Chr12:32737907 [GRCh38]
Chr12:32890841 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.1645C>T (p.Pro549Ser) single nucleotide variant not provided [RCV000196608] Chr12:32737913 [GRCh38]
Chr12:32890847 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.422A>G (p.Asn141Ser) single nucleotide variant not specified [RCV000197602] Chr12:32710981 [GRCh38]
Chr12:32863915 [GRCh37]
Chr12:12p11.21
likely benign|uncertain significance
NM_012062.5(DNM1L):c.1640C>T (p.Pro547Leu) single nucleotide variant not specified [RCV000198006] Chr12:32737908 [GRCh38]
Chr12:32890842 [GRCh37]
Chr12:12p11.21
likely pathogenic|likely benign
NM_012062.5(DNM1L):c.1885-15del deletion not provided [RCV001516215]|not specified [RCV000198062] Chr12:32740390 [GRCh38]
Chr12:32893324 [GRCh37]
Chr12:12p11.21
pathogenic|benign
NM_012062.5(DNM1L):c.2032G>A (p.Val678Met) single nucleotide variant not provided [RCV000198330] Chr12:32742626 [GRCh38]
Chr12:32895560 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.1649C>A (p.Ala550Asp) single nucleotide variant not specified [RCV000198556] Chr12:32737917 [GRCh38]
Chr12:32890851 [GRCh37]
Chr12:12p11.21
likely benign|uncertain significance
NM_012062.5(DNM1L):c.741-19G>A single nucleotide variant not provided [RCV000675858]|not specified [RCV000199039] Chr12:32720645 [GRCh38]
Chr12:32873579 [GRCh37]
Chr12:12p11.21
benign
NM_012062.5(DNM1L):c.1648G>A (p.Ala550Thr) single nucleotide variant not provided [RCV000199095] Chr12:32737916 [GRCh38]
Chr12:32890850 [GRCh37]
Chr12:12p11.21
likely benign|uncertain significance
NM_012062.5(DNM1L):c.1200+9G>A single nucleotide variant not provided [RCV000875990]|not specified [RCV000195467] Chr12:32731143 [GRCh38]
Chr12:32884077 [GRCh37]
Chr12:12p11.21
benign|likely benign
NM_012062.5(DNM1L):c.1834A>T (p.Ile612Phe) single nucleotide variant Encephalopathy due to defective mitochondrial and peroxisomal fission 1 [RCV000988809]|not specified [RCV000195517] Chr12:32740190 [GRCh38]
Chr12:32893124 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.305C>T (p.Thr102Met) single nucleotide variant Optic atrophy 5 [RCV000763842]|not provided [RCV000196424] Chr12:32708160 [GRCh38]
Chr12:32861094 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.-14G>A single nucleotide variant not specified [RCV000200010] Chr12:32679350 [GRCh38]
Chr12:32832284 [GRCh37]
Chr12:12p11.21
benign
NM_012062.4(DNM1L):c.1184C>G (p.Ala395Gly) single nucleotide variant not provided [RCV000200151] Chr12:32731118 [GRCh38]
Chr12:32884052 [GRCh37]
Chr12:12p11.21
likely pathogenic
GRCh37/hg19 12p13.33-11.1(chr12:148034-34178799)x4 copy number gain See cases [RCV000240164] Chr12:148034..34178799 [GRCh37]
Chr12:12p13.33-11.1
pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:1-133851895)x3 copy number gain See cases [RCV000258805] Chr12:1..133851895 [GRCh37]
Chr12:12p13.33-q24.33
pathogenic|likely pathogenic
NC_000012.11:g.(?_32786463)_(32832419_?)dup duplication Charcot-Marie-Tooth disease type 4 [RCV000547434] Chr12:32786463..32832419 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.2135A>C (p.Glu712Ala) single nucleotide variant not provided [RCV000756031] Chr12:32742729 [GRCh38]
Chr12:32895663 [GRCh37]
Chr12:12p11.21
uncertain significance
GRCh37/hg19 12p11.21-q13.12(chr12:31886971-50360461)x3 copy number gain See cases [RCV000207454] Chr12:31886971..50360461 [GRCh37]
Chr12:12p11.21-q13.12
pathogenic
NM_012062.5(DNM1L):c.1337G>T (p.Cys446Phe) single nucleotide variant Encephalopathy due to defective mitochondrial and peroxisomal fission 1 [RCV000237095] Chr12:32731492 [GRCh38]
Chr12:32884426 [GRCh37]
Chr12:12p11.21
likely pathogenic
NC_000012.11:g.(?_32729272)_(33049685_?)dup duplication Arrhythmogenic right ventricular dysplasia 9 [RCV000545183] Chr12:32576338..32896751 [GRCh38]
Chr12:32729272..33049685 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.1084G>A (p.Gly362Ser) single nucleotide variant Encephalopathy due to defective mitochondrial and peroxisomal fission 1 [RCV000239681] Chr12:32731018 [GRCh38]
Chr12:32883952 [GRCh37]
Chr12:12p11.21
pathogenic
NM_012062.5(DNM1L):c.619+13G>C single nucleotide variant not specified [RCV000606266] Chr12:32713384 [GRCh38]
Chr12:32866318 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.1085G>A (p.Gly362Asp) single nucleotide variant Encephalopathy due to defective mitochondrial and peroxisomal fission 1 [RCV000239637] Chr12:32731019 [GRCh38]
Chr12:32883953 [GRCh37]
Chr12:12p11.21
pathogenic|likely pathogenic
NM_012062.5(DNM1L):c.1048G>A (p.Gly350Arg) single nucleotide variant Encephalopathy due to defective mitochondrial and peroxisomal fission 1 [RCV000239649] Chr12:32722602 [GRCh38]
Chr12:32875536 [GRCh37]
Chr12:12p11.21
pathogenic|uncertain significance
NM_012062.5(DNM1L):c.346_347del (p.Glu116fs) deletion Encephalopathy due to defective mitochondrial and peroxisomal fission 1 [RCV000239652] Chr12:32708200..32708201 [GRCh38]
Chr12:32861134..32861135 [GRCh37]
Chr12:12p11.21
pathogenic
NM_012062.5(DNM1L):c.106A>G (p.Ser36Gly) single nucleotide variant Encephalopathy due to defective mitochondrial and peroxisomal fission 1 [RCV000239716]|not provided [RCV000384736] Chr12:32701418 [GRCh38]
Chr12:32854352 [GRCh37]
Chr12:12p11.21
pathogenic
NM_012062.5(DNM1L):c.251-1532dup duplication Encephalopathy due to defective mitochondrial and peroxisomal fission 1 [RCV000239719] Chr12:32705834..32705835 [GRCh38]
Chr12:32858768..32858769 [GRCh37]
Chr12:12p11.21
pathogenic
NM_012062.5(DNM1L):c.252G>A (p.Gly84=) single nucleotide variant not provided [RCV000675857]|not specified [RCV000246489] Chr12:32707368 [GRCh38]
Chr12:32860302 [GRCh37]
Chr12:12p11.21
benign
NM_012062.5(DNM1L):c.918A>G (p.Thr306=) single nucleotide variant not provided [RCV000675859]|not specified [RCV000249820] Chr12:32722472 [GRCh38]
Chr12:32875406 [GRCh37]
Chr12:12p11.21
benign
GRCh37/hg19 12p13.33-11.1(chr12:89061-34178799)x3 copy number gain See cases [RCV000240487] Chr12:89061..34178799 [GRCh37]
Chr12:12p13.33-11.1
pathogenic
NM_012062.5(DNM1L):c.251-7T>C single nucleotide variant not provided [RCV000927348]|not specified [RCV000243133] Chr12:32707360 [GRCh38]
Chr12:32860294 [GRCh37]
Chr12:12p11.21
likely benign
GRCh37/hg19 12p11.21(chr12:32896340-32906926)x3 copy number gain See cases [RCV000240377] Chr12:32896340..32906926 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.1080-16C>T single nucleotide variant not specified [RCV000245849] Chr12:32730998 [GRCh38]
Chr12:32883932 [GRCh37]
Chr12:12p11.21
benign
NM_012062.5(DNM1L):c.120A>C (p.Ser40=) single nucleotide variant not provided [RCV000675856]|not specified [RCV000250836] Chr12:32701432 [GRCh38]
Chr12:32854366 [GRCh37]
Chr12:12p11.21
benign
NM_012062.5(DNM1L):c.*535T>G single nucleotide variant Lethal Encephalopathy [RCV000301358] Chr12:32743945 [GRCh38]
Chr12:32896879 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.1866C>T (p.Ala622=) single nucleotide variant Lethal Encephalopathy [RCV000302055] Chr12:32740222 [GRCh38]
Chr12:32893156 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.*1624T>C single nucleotide variant Lethal Encephalopathy [RCV000309297] Chr12:32745034 [GRCh38]
Chr12:32897968 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.*128A>G single nucleotide variant Lethal Encephalopathy [RCV000292472] Chr12:32743538 [GRCh38]
Chr12:32896472 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.486T>C (p.Ile162=) single nucleotide variant Lethal Encephalopathy [RCV000295136] Chr12:32713238 [GRCh38]
Chr12:32866172 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.*1338C>T single nucleotide variant Lethal Encephalopathy [RCV000337535] Chr12:32744748 [GRCh38]
Chr12:32897682 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.*1110C>T single nucleotide variant Lethal Encephalopathy [RCV000276723] Chr12:32744520 [GRCh38]
Chr12:32897454 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.*21_*22delinsCT indel Lethal Encephalopathy [RCV000277306]|not provided [RCV000675861] Chr12:32743431..32743432 [GRCh38]
Chr12:32896365..32896366 [GRCh37]
Chr12:12p11.21
likely benign|uncertain significance
NM_012062.5(DNM1L):c.*1526T>C single nucleotide variant Lethal Encephalopathy [RCV000315022] Chr12:32744936 [GRCh38]
Chr12:32897870 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.*1401A>G single nucleotide variant Lethal Encephalopathy [RCV000278767] Chr12:32744811 [GRCh38]
Chr12:32897745 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.-25A>G single nucleotide variant not specified [RCV000420317] Chr12:32679339 [GRCh38]
Chr12:32832273 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.-16C>T single nucleotide variant Lethal Encephalopathy [RCV000319943] Chr12:32679348 [GRCh38]
Chr12:32832282 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.*1755T>C single nucleotide variant Lethal Encephalopathy [RCV000365990] Chr12:32745165 [GRCh38]
Chr12:32898099 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.*519T>G single nucleotide variant Lethal Encephalopathy [RCV000392605] Chr12:32743929 [GRCh38]
Chr12:32896863 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.*1193C>T single nucleotide variant Lethal Encephalopathy [RCV000271011] Chr12:32744603 [GRCh38]
Chr12:32897537 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.1269T>A (p.Arg423=) single nucleotide variant not provided [RCV000876055] Chr12:32731424 [GRCh38]
Chr12:32884358 [GRCh37]
Chr12:12p11.21
likely benign|uncertain significance
NM_012062.5(DNM1L):c.*1279G>A single nucleotide variant Lethal Encephalopathy [RCV000324791] Chr12:32744689 [GRCh38]
Chr12:32897623 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.1994+9T>G single nucleotide variant Lethal Encephalopathy [RCV000261605] Chr12:32740527 [GRCh38]
Chr12:32893461 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.*2206dup duplication Lethal Encephalopathy [RCV000262136] Chr12:32745614..32745615 [GRCh38]
Chr12:32898548..32898549 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.*1872G>A single nucleotide variant Lethal Encephalopathy [RCV000307721] Chr12:32745282 [GRCh38]
Chr12:32898216 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.1104T>C (p.Tyr368=) single nucleotide variant Lethal Encephalopathy [RCV000308934] Chr12:32731038 [GRCh38]
Chr12:32883972 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.*1120A>G single nucleotide variant Lethal Encephalopathy [RCV000331916] Chr12:32744530 [GRCh38]
Chr12:32897464 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.*1538del deletion Lethal Encephalopathy [RCV000405929] Chr12:32744948 [GRCh38]
Chr12:32897882 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.*1341A>G single nucleotide variant Lethal Encephalopathy [RCV000408045] Chr12:32744751 [GRCh38]
Chr12:32897685 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.*1899C>T single nucleotide variant Lethal Encephalopathy [RCV000360149] Chr12:32745309 [GRCh38]
Chr12:32898243 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.2157A>G (p.Ala719=) single nucleotide variant Lethal Encephalopathy [RCV000316875] Chr12:32743356 [GRCh38]
Chr12:32896290 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.*48T>C single nucleotide variant Lethal Encephalopathy [RCV000386779] Chr12:32743458 [GRCh38]
Chr12:32896392 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.*1980A>C single nucleotide variant Lethal Encephalopathy [RCV000267976] Chr12:32745390 [GRCh38]
Chr12:32898324 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.*1842A>G single nucleotide variant Lethal Encephalopathy [RCV000269074] Chr12:32745252 [GRCh38]
Chr12:32898186 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.*156A>C single nucleotide variant Lethal Encephalopathy [RCV000329191] Chr12:32743566 [GRCh38]
Chr12:32896500 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.*1239G>A single nucleotide variant Lethal Encephalopathy [RCV000380776] Chr12:32744649 [GRCh38]
Chr12:32897583 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_001040436.3(YARS2):c.*209G>C single nucleotide variant Hereditary Sideroblastic Anemia with Myopathy and Lactic Acidosis [RCV000392192]|Lethal Encephalopathy [RCV000322564]|Mitochondrial myopathy and sideroblastic anemia [RCV000305932]|Myopathy, lactic acidosis, and sideroblastic anemia 2 [RCV001114809] Chr12:32746995 [GRCh38]
Chr12:32899929 [GRCh37]
Chr12:12p11.21
benign|likely benign
NM_012062.5(DNM1L):c.*1415T>C single nucleotide variant Hereditary Sideroblastic Anemia with Myopathy and Lactic Acidosis [RCV000315133]|Lethal Encephalopathy [RCV000336275]|Mitochondrial myopathy and sideroblastic anemia [RCV000362773] Chr12:32744825 [GRCh38]
Chr12:32897759 [GRCh37]
Chr12:12p11.21
benign|likely benign
NM_001040436.3(YARS2):c.*643G>A single nucleotide variant Hereditary Sideroblastic Anemia with Myopathy and Lactic Acidosis [RCV000371457]|Lethal Encephalopathy [RCV000406313]|Mitochondrial myopathy and sideroblastic anemia [RCV000319068]|Myopathy, lactic acidosis, and sideroblastic anemia 2 [RCV001113407] Chr12:32746561 [GRCh38]
Chr12:32899495 [GRCh37]
Chr12:12p11.21
benign|likely benign
NM_012062.5(DNM1L):c.*1093T>C single nucleotide variant Hereditary Sideroblastic Anemia with Myopathy and Lactic Acidosis [RCV000371686]|Mitochondrial myopathy and sideroblastic anemia [RCV000324028] Chr12:32744503 [GRCh38]
Chr12:32897437 [GRCh37]
Chr12:12p11.21
benign
NM_012062.5(DNM1L):c.*393A>C single nucleotide variant Hereditary Sideroblastic Anemia with Myopathy and Lactic Acidosis [RCV000364831]|Lethal Encephalopathy [RCV000407287]|Mitochondrial myopathy and sideroblastic anemia [RCV000326445] Chr12:32743803 [GRCh38]
Chr12:32896737 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.1597-3_1597-2dup duplication Lethal Encephalopathy [RCV000305588] Chr12:32737861..32737862 [GRCh38]
Chr12:32890795..32890796 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.*1532A>G single nucleotide variant Lethal Encephalopathy [RCV000367373] Chr12:32744942 [GRCh38]
Chr12:32897876 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_001040436.3(YARS2):c.*360A>G single nucleotide variant Hereditary Sideroblastic Anemia with Myopathy and Lactic Acidosis [RCV000392181]|Lethal Encephalopathy [RCV000366716]|Mitochondrial myopathy and sideroblastic anemia [RCV000349712]|Myopathy, lactic acidosis, and sideroblastic anemia 2 [RCV001113413] Chr12:32746844 [GRCh38]
Chr12:32899778 [GRCh37]
Chr12:12p11.21
likely benign|uncertain significance
NM_012062.5(DNM1L):c.*1316T>C single nucleotide variant Lethal Encephalopathy [RCV000284807] Chr12:32744726 [GRCh38]
Chr12:32897660 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.*2014C>T single nucleotide variant Lethal Encephalopathy [RCV000320714] Chr12:32745424 [GRCh38]
Chr12:32898358 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_001040436.3(YARS2):c.*142T>C single nucleotide variant Hereditary Sideroblastic Anemia with Myopathy and Lactic Acidosis [RCV000317776]|Lethal Encephalopathy [RCV000316547]|Mitochondrial myopathy and sideroblastic anemia [RCV000260179]|Myopathy, lactic acidosis, and sideroblastic anemia 2 [RCV001114812] Chr12:32747062 [GRCh38]
Chr12:32899996 [GRCh37]
Chr12:12p11.21
likely benign|uncertain significance
NM_012062.5(DNM1L):c.*402A>G single nucleotide variant Lethal Encephalopathy [RCV000285716] Chr12:32743812 [GRCh38]
Chr12:32896746 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.456+9G>A single nucleotide variant Lethal Encephalopathy [RCV000389373] Chr12:32711024 [GRCh38]
Chr12:32863958 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.*1471_*1475dup duplication Lethal Encephalopathy [RCV000408029] Chr12:32744880..32744881 [GRCh38]
Chr12:32897814..32897815 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_001040436.3(YARS2):c.*230A>G single nucleotide variant Hereditary Sideroblastic Anemia with Myopathy and Lactic Acidosis [RCV000345484]|Lethal Encephalopathy [RCV000264971]|Mitochondrial myopathy and sideroblastic anemia [RCV000307018]|Myopathy, lactic acidosis, and sideroblastic anemia 2 [RCV001114808] Chr12:32746974 [GRCh38]
Chr12:32899908 [GRCh37]
Chr12:12p11.21
likely benign|uncertain significance
NM_012062.5(DNM1L):c.*1072G>C single nucleotide variant Lethal Encephalopathy [RCV000297763] Chr12:32744482 [GRCh38]
Chr12:32897416 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.-50C>A single nucleotide variant Lethal Encephalopathy [RCV000323522] Chr12:32679314 [GRCh38]
Chr12:32832248 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_001040436.3(YARS2):c.*191T>C single nucleotide variant Hereditary Sideroblastic Anemia with Myopathy and Lactic Acidosis [RCV000265965]|Lethal Encephalopathy [RCV000360920]|Mitochondrial myopathy and sideroblastic anemia [RCV000358095]|Myopathy, lactic acidosis, and sideroblastic anemia 2 [RCV001114810] Chr12:32747013 [GRCh38]
Chr12:32899947 [GRCh37]
Chr12:12p11.21
benign|likely benign
NM_001040436.3(YARS2):c.*162A>G single nucleotide variant Hereditary Sideroblastic Anemia with Myopathy and Lactic Acidosis [RCV000299975]|Lethal Encephalopathy [RCV000268326]|Mitochondrial myopathy and sideroblastic anemia [RCV000357124]|Myopathy, lactic acidosis, and sideroblastic anemia 2 [RCV001114811] Chr12:32747042 [GRCh38]
Chr12:32899976 [GRCh37]
Chr12:12p11.21
benign|likely benign
NM_012062.5(DNM1L):c.*271C>G single nucleotide variant Hereditary Sideroblastic Anemia with Myopathy and Lactic Acidosis [RCV000370573]|Mitochondrial myopathy and sideroblastic anemia [RCV000268977] Chr12:32743681 [GRCh38]
Chr12:32896615 [GRCh37]
Chr12:12p11.21
benign|likely benign
NM_012062.5(DNM1L):c.*22A>T single nucleotide variant Hereditary Sideroblastic Anemia with Myopathy and Lactic Acidosis [RCV000313747]|Mitochondrial myopathy and sideroblastic anemia [RCV000275050] Chr12:32743432 [GRCh38]
Chr12:32896366 [GRCh37]
Chr12:12p11.21
benign|likely benign
NM_012062.5(DNM1L):c.*600C>T single nucleotide variant Hereditary Sideroblastic Anemia with Myopathy and Lactic Acidosis [RCV000272290]|Lethal Encephalopathy [RCV000356136]|Mitochondrial myopathy and sideroblastic anemia [RCV000320339] Chr12:32744010 [GRCh38]
Chr12:32896944 [GRCh37]
Chr12:12p11.21
benign|likely benign
NM_001040436.3(YARS2):c.*126_*127del deletion Hereditary Sideroblastic Anemia with Myopathy and Lactic Acidosis [RCV000388515]|Lethal Encephalopathy [RCV000373541]|Mitochondrial myopathy and sideroblastic anemia [RCV000277846] Chr12:32747077..32747078 [GRCh38]
Chr12:32900011..32900012 [GRCh37]
Chr12:12p11.21
likely benign|uncertain significance
NM_012062.5(DNM1L):c.*1156G>C single nucleotide variant Hereditary Sideroblastic Anemia with Myopathy and Lactic Acidosis [RCV000336831]|Mitochondrial myopathy and sideroblastic anemia [RCV000279496] Chr12:32744566 [GRCh38]
Chr12:32897500 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.*420C>G single nucleotide variant Lethal Encephalopathy [RCV000340740] Chr12:32743830 [GRCh38]
Chr12:32896764 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_001040436.3(YARS2):c.*62G>A single nucleotide variant Hereditary Sideroblastic Anemia with Myopathy and Lactic Acidosis [RCV000387461]|Lethal Encephalopathy [RCV000281421]|Mitochondrial myopathy and sideroblastic anemia [RCV000330686]|Myopathy, lactic acidosis, and sideroblastic anemia 2 [RCV001114813] Chr12:32747142 [GRCh38]
Chr12:32900076 [GRCh37]
Chr12:12p11.21
likely benign|uncertain significance
NM_012062.5(DNM1L):c.*744A>T single nucleotide variant Hereditary Sideroblastic Anemia with Myopathy and Lactic Acidosis [RCV000285137]|Mitochondrial myopathy and sideroblastic anemia [RCV000377247] Chr12:32744154 [GRCh38]
Chr12:32897088 [GRCh37]
Chr12:12p11.21
benign|likely benign
NM_012062.5(DNM1L):c.*1242G>A single nucleotide variant Hereditary Sideroblastic Anemia with Myopathy and Lactic Acidosis [RCV000350379]|Lethal Encephalopathy [RCV000286166]|Mitochondrial myopathy and sideroblastic anemia [RCV000391184] Chr12:32744652 [GRCh38]
Chr12:32897586 [GRCh37]
Chr12:12p11.21
benign|likely benign
NM_012062.5(DNM1L):c.*275_*278dup duplication Lethal Encephalopathy [RCV000289448] Chr12:32743684..32743685 [GRCh38]
Chr12:32896618..32896619 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.*1315dup duplication Lethal Encephalopathy [RCV000376995] Chr12:32744713..32744714 [GRCh38]
Chr12:32897647..32897648 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_001040436.3(YARS2):c.1356A>G (p.Gln452=) single nucleotide variant Hereditary Sideroblastic Anemia with Myopathy and Lactic Acidosis [RCV000289715]|Lethal Encephalopathy [RCV000329729]|Mitochondrial myopathy and sideroblastic anemia [RCV000380699]|Myopathy, lactic acidosis, and sideroblastic anemia 2 [RCV001114814]|not provided [RCV000968251] Chr12:32747282 [GRCh38]
Chr12:32900216 [GRCh37]
Chr12:12p11.21
benign|likely benign
NM_012062.5(DNM1L):c.963C>T (p.Ser321=) single nucleotide variant not specified [RCV000605735] Chr12:32722517 [GRCh38]
Chr12:32875451 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.*2102_*2103dup duplication Lethal Encephalopathy [RCV000377771] Chr12:32745511..32745512 [GRCh38]
Chr12:32898445..32898446 [GRCh37]
Chr12:12p11.21
likely benign
NM_001040436.3(YARS2):c.*406C>T single nucleotide variant Hereditary Sideroblastic Anemia with Myopathy and Lactic Acidosis [RCV000292534]|Lethal Encephalopathy [RCV000309191]|Mitochondrial myopathy and sideroblastic anemia [RCV000389223]|Myopathy, lactic acidosis, and sideroblastic anemia 2 [RCV001113411] Chr12:32746798 [GRCh38]
Chr12:32899732 [GRCh37]
Chr12:12p11.21
benign|likely benign
NM_012062.5(DNM1L):c.*1213G>T single nucleotide variant Hereditary Sideroblastic Anemia with Myopathy and Lactic Acidosis [RCV000391164]|Mitochondrial myopathy and sideroblastic anemia [RCV000293050] Chr12:32744623 [GRCh38]
Chr12:32897557 [GRCh37]
Chr12:12p11.21
benign|likely benign
NM_012062.5(DNM1L):c.1356+5C>T single nucleotide variant not specified [RCV000600540] Chr12:32731516 [GRCh38]
Chr12:32884450 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.*335_*338dup duplication Lethal Encephalopathy [RCV000344382] Chr12:32743743..32743744 [GRCh38]
Chr12:32896677..32896678 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.*21G>C single nucleotide variant Hereditary Sideroblastic Anemia with Myopathy and Lactic Acidosis [RCV000300893]|Mitochondrial myopathy and sideroblastic anemia [RCV000367296] Chr12:32743431 [GRCh38]
Chr12:32896365 [GRCh37]
Chr12:12p11.21
benign|likely benign
NM_012062.5(DNM1L):c.1135G>A (p.Glu379Lys) single nucleotide variant Encephalopathy due to defective mitochondrial and peroxisomal fission 1 [RCV000414839] Chr12:32731069 [GRCh38]
Chr12:32884003 [GRCh37]
Chr12:12p11.21
likely pathogenic
GRCh37/hg19 12p13.33-q11(chr12:173786-37869301)x3 copy number gain See cases [RCV000449191] Chr12:173786..37869301 [GRCh37]
Chr12:12p13.33-q11
pathogenic
GRCh37/hg19 12p13.33-11.1(chr12:173786-34835837)x3 copy number gain See cases [RCV000447551] Chr12:173786..34835837 [GRCh37]
Chr12:12p13.33-11.1
pathogenic
NM_012062.5(DNM1L):c.436G>A (p.Asp146Asn) single nucleotide variant not provided [RCV000443148]|not specified [RCV001002556] Chr12:32710995 [GRCh38]
Chr12:32863929 [GRCh37]
Chr12:12p11.21
likely pathogenic
NM_012062.5(DNM1L):c.1302G>T (p.Leu434=) single nucleotide variant not specified [RCV000417834] Chr12:32731457 [GRCh38]
Chr12:32884391 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.1535T>C (p.Ile512Thr) single nucleotide variant not provided [RCV000431728] Chr12:32733803 [GRCh38]
Chr12:32886737 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.138G>A (p.Val46=) single nucleotide variant not specified [RCV000428282] Chr12:32701450 [GRCh38]
Chr12:32854384 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.-48A>G single nucleotide variant not specified [RCV000439253] Chr12:32679316 [GRCh38]
Chr12:32832250 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.740+3T>C single nucleotide variant not specified [RCV000443266] Chr12:32718766 [GRCh38]
Chr12:32871700 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.1079+10A>G single nucleotide variant not provided [RCV000878944]|not specified [RCV000436462] Chr12:32722643 [GRCh38]
Chr12:32875577 [GRCh37]
Chr12:12p11.21
benign
NM_012062.5(DNM1L):c.666G>C (p.Ala222=) single nucleotide variant not specified [RCV000443872] Chr12:32718689 [GRCh38]
Chr12:32871623 [GRCh37]
Chr12:12p11.21
likely benign
GRCh37/hg19 12p13.33-11.1(chr12:189578-34756150) copy number gain See cases [RCV000446017] Chr12:189578..34756150 [GRCh37]
Chr12:12p13.33-11.1
pathogenic
NM_012062.5(DNM1L):c.95G>C (p.Gly32Ala) single nucleotide variant not provided [RCV000439994] Chr12:32679458 [GRCh38]
Chr12:32832392 [GRCh37]
Chr12:12p11.21
likely pathogenic
NM_012062.5(DNM1L):c.2082C>T (p.Ser694=) single nucleotide variant not provided [RCV000918991]|not specified [RCV000423494] Chr12:32742676 [GRCh38]
Chr12:32895610 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.1722delinsAGGTTTTTCAGGTGCATCA (p.Gly576_Val577insPheSerGlyAlaSerGly) indel not specified [RCV000480466] Chr12:32740078 [GRCh38]
Chr12:32893012 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.1065T>G (p.Ile355Met) single nucleotide variant not provided [RCV000481156] Chr12:32722619 [GRCh38]
Chr12:32875553 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.1292G>A (p.Cys431Tyr) single nucleotide variant not provided [RCV000484397] Chr12:32731447 [GRCh38]
Chr12:32884381 [GRCh37]
Chr12:12p11.21
likely pathogenic
NM_012062.5(DNM1L):c.*3_*7delinsGT indel not specified [RCV000482065] Chr12:32743413..32743417 [GRCh38]
Chr12:32896347..32896351 [GRCh37]
Chr12:12p11.21
likely benign
GRCh37/hg19 12p11.22-11.1(chr12:29579030-34835837)x3 copy number gain See cases [RCV000512134] Chr12:29579030..34835837 [GRCh37]
Chr12:12p11.22-11.1
likely pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)x3 copy number gain See cases [RCV000510482] Chr12:173787..133777902 [GRCh37]
Chr12:12p13.33-q24.33
pathogenic
NM_012062.5(DNM1L):c.1750C>G (p.Pro584Ala) single nucleotide variant not provided [RCV000498231] Chr12:32740106 [GRCh38]
Chr12:32893040 [GRCh37]
Chr12:12p11.21
uncertain significance
GRCh37/hg19 12p11.22-q12(chr12:29123400-40956186)x3 copy number gain See cases [RCV000512027] Chr12:29123400..40956186 [GRCh37]
Chr12:12p11.22-q12
likely pathogenic
GRCh37/hg19 12p11.21(chr12:32787628-32835751)x4 copy number gain See cases [RCV000511722] Chr12:32787628..32835751 [GRCh37]
Chr12:12p11.21
likely benign
GRCh37/hg19 12p13.33-11.1(chr12:565369-34835837)x3 copy number gain See cases [RCV000511580] Chr12:565369..34835837 [GRCh37]
Chr12:12p13.33-11.1
likely pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902) copy number gain See cases [RCV000511643] Chr12:173787..133777902 [GRCh37]
Chr12:12p13.33-q24.33
pathogenic
NC_000012.11:g.26370251_54361538inv inversion not specified [RCV000714265] Chr12:26370251..54361538 [GRCh37]
Chr12:12p12.1-q13.13
uncertain significance
NM_012062.5(DNM1L):c.1588C>T (p.Arg530Ter) single nucleotide variant not provided [RCV000578881] Chr12:32737153 [GRCh38]
Chr12:32890087 [GRCh37]
Chr12:12p11.21
likely pathogenic
NM_012062.5(DNM1L):c.1647C>T (p.Pro549=) single nucleotide variant not specified [RCV000604678] Chr12:32737915 [GRCh38]
Chr12:32890849 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.5A>C (p.Glu2Ala) single nucleotide variant Optic atrophy 5 [RCV000515453] Chr12:32679368 [GRCh38]
Chr12:32832302 [GRCh37]
Chr12:12p11.21
pathogenic
NM_012062.5(DNM1L):c.575C>A (p.Ala192Glu) single nucleotide variant Optic atrophy 5 [RCV000515455] Chr12:32713327 [GRCh38]
Chr12:32866261 [GRCh37]
Chr12:12p11.21
pathogenic
NM_012062.5(DNM1L):c.1708-4del deletion not specified [RCV000601545] Chr12:32740055 [GRCh38]
Chr12:32892989 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.1083C>T (p.Cys361=) single nucleotide variant not specified [RCV000605850] Chr12:32731017 [GRCh38]
Chr12:32883951 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.1596+9_1596+10del deletion not specified [RCV000613065] Chr12:32737170..32737171 [GRCh38]
Chr12:32890104..32890105 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.250+7T>A single nucleotide variant not specified [RCV000616368] Chr12:32701569 [GRCh38]
Chr12:32854503 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.1597-19del deletion not specified [RCV000608496] Chr12:32737841 [GRCh38]
Chr12:32890775 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.1708-8T>G single nucleotide variant not specified [RCV000608501] Chr12:32740056 [GRCh38]
Chr12:32892990 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.1356+11G>T single nucleotide variant not specified [RCV000614629] Chr12:32731522 [GRCh38]
Chr12:32884456 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.388A>G (p.Ile130Val) single nucleotide variant not provided [RCV000676345] Chr12:32710947 [GRCh38]
Chr12:32863881 [GRCh37]
Chr12:12p11.21
uncertain significance
GRCh37/hg19 12p13.33-11.1(chr12:173786-34835837)x2,3 copy number gain not provided [RCV000683478] Chr12:173786..34835837 [GRCh37]
Chr12:12p13.33-11.1
pathogenic
GRCh37/hg19 12p13.33-11.1(chr12:173786-34835837)x3 copy number gain not provided [RCV000683479] Chr12:173786..34835837 [GRCh37]
Chr12:12p13.33-11.1
pathogenic
GRCh37/hg19 12p13.33-q11(chr12:173786-37869107)x3 copy number gain not provided [RCV000683480] Chr12:173786..37869107 [GRCh37]
Chr12:12p13.33-q11
pathogenic
NM_012062.5(DNM1L):c.2072A>G (p.Tyr691Cys) single nucleotide variant Encephalopathy due to defective mitochondrial and peroxisomal fission 1 [RCV000757997]|Optic atrophy 5 [RCV000850546] Chr12:32742666 [GRCh38]
Chr12:32895600 [GRCh37]
Chr12:12p11.21
pathogenic|likely pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:191619-133777645)x3 copy number gain not provided [RCV000750246] Chr12:191619..133777645 [GRCh37]
Chr12:12p13.33-q24.33
pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:621220-133779118)x3 copy number gain not provided [RCV000750253] Chr12:621220..133779118 [GRCh37]
Chr12:12p13.33-q24.33
pathogenic
NM_012062.5(DNM1L):c.1002C>T (p.Leu334=) single nucleotide variant not provided [RCV000876308] Chr12:32722556 [GRCh38]
Chr12:32875490 [GRCh37]
Chr12:12p11.21
likely benign
GRCh37/hg19 12p13.33-q11(chr12:274676-37869301)x4 copy number gain not provided [RCV001006470] Chr12:274676..37869301 [GRCh37]
Chr12:12p13.33-q11
pathogenic
NM_012062.5(DNM1L):c.1255C>T (p.Arg419Trp) single nucleotide variant not specified [RCV000785123] Chr12:32731410 [GRCh38]
Chr12:32884344 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.171T>C (p.Ile57=) single nucleotide variant not provided [RCV000921605] Chr12:32701483 [GRCh38]
Chr12:32854417 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.1674+36T>A single nucleotide variant not provided [RCV000830843] Chr12:32737978 [GRCh38]
Chr12:32890912 [GRCh37]
Chr12:12p11.21
benign
NM_012062.5(DNM1L):c.1597-121T>C single nucleotide variant not provided [RCV000835766] Chr12:32737744 [GRCh38]
Chr12:32890678 [GRCh37]
Chr12:12p11.21
benign
NM_012062.5(DNM1L):c.619+98T>C single nucleotide variant not provided [RCV000832903] Chr12:32713469 [GRCh38]
Chr12:32866403 [GRCh37]
Chr12:12p11.21
benign
NM_012062.5(DNM1L):c.620-96G>A single nucleotide variant not provided [RCV000832904] Chr12:32718547 [GRCh38]
Chr12:32871481 [GRCh37]
Chr12:12p11.21
benign
NM_012062.5(DNM1L):c.2155-125_2155-124del deletion not provided [RCV000832905] Chr12:32743229..32743230 [GRCh38]
Chr12:32896163..32896164 [GRCh37]
Chr12:12p11.21
benign
NM_012062.5(DNM1L):c.103-198A>G single nucleotide variant not provided [RCV000838067] Chr12:32701217 [GRCh38]
Chr12:32854151 [GRCh37]
Chr12:12p11.21
benign
NM_012062.5(DNM1L):c.1708-124A>C single nucleotide variant not provided [RCV000836183] Chr12:32739940 [GRCh38]
Chr12:32892874 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.370-39T>C single nucleotide variant not provided [RCV000832902] Chr12:32710890 [GRCh38]
Chr12:32863824 [GRCh37]
Chr12:12p11.21
benign
NM_012062.5(DNM1L):c.620-88G>A single nucleotide variant not provided [RCV000834840] Chr12:32718555 [GRCh38]
Chr12:32871489 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.1995-133G>A single nucleotide variant not provided [RCV000834894] Chr12:32742456 [GRCh38]
Chr12:32895390 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.1994+263G>T single nucleotide variant not provided [RCV000840352] Chr12:32740781 [GRCh38]
Chr12:32893715 [GRCh37]
Chr12:12p11.21
benign
NM_012062.5(DNM1L):c.103-267C>T single nucleotide variant not provided [RCV000840366] Chr12:32701148 [GRCh38]
Chr12:32854082 [GRCh37]
Chr12:12p11.21
benign
NM_012062.5(DNM1L):c.250+262T>C single nucleotide variant not provided [RCV000840367] Chr12:32701824 [GRCh38]
Chr12:32854758 [GRCh37]
Chr12:12p11.21
benign
NM_012062.5(DNM1L):c.619+252G>A single nucleotide variant not provided [RCV000840368] Chr12:32713623 [GRCh38]
Chr12:32866557 [GRCh37]
Chr12:12p11.21
benign
NM_012062.5(DNM1L):c.2154+273G>A single nucleotide variant not provided [RCV000840377] Chr12:32743021 [GRCh38]
Chr12:32895955 [GRCh37]
Chr12:12p11.21
benign
NM_012062.5(DNM1L):c.1915C>T (p.Arg639Trp) single nucleotide variant Encephalopathy due to defective mitochondrial and peroxisomal fission 1 [RCV000988810] Chr12:32740439 [GRCh38]
Chr12:32893373 [GRCh37]
Chr12:12p11.21
likely pathogenic
NM_012062.5(DNM1L):c.250+106G>A single nucleotide variant not provided [RCV000830743] Chr12:32701668 [GRCh38]
Chr12:32854602 [GRCh37]
Chr12:12p11.21
benign
NM_012062.5(DNM1L):c.250+191G>T single nucleotide variant not provided [RCV000840765] Chr12:32701753 [GRCh38]
Chr12:32854687 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.370-163A>G single nucleotide variant not provided [RCV000838287] Chr12:32710766 [GRCh38]
Chr12:32863700 [GRCh37]
Chr12:12p11.21
benign
NM_012062.5(DNM1L):c.1597-114C>T single nucleotide variant not provided [RCV000835516] Chr12:32737751 [GRCh38]
Chr12:32890685 [GRCh37]
Chr12:12p11.21
benign
NM_012062.5(DNM1L):c.28A>T (p.Lys10Ter) single nucleotide variant Obesity [RCV000787973] Chr12:32679391 [GRCh38]
Chr12:32832325 [GRCh37]
Chr12:12p11.21
likely pathogenic
NM_012062.5(DNM1L):c.103-149A>G single nucleotide variant not provided [RCV000835704] Chr12:32701266 [GRCh38]
Chr12:32854200 [GRCh37]
Chr12:12p11.21
benign
NM_012062.5(DNM1L):c.1596+66C>T single nucleotide variant not provided [RCV000835705] Chr12:32737227 [GRCh38]
Chr12:32890161 [GRCh37]
Chr12:12p11.21
benign
NM_012062.5(DNM1L):c.1596+9dup duplication not provided [RCV000827659] Chr12:32737163..32737164 [GRCh38]
Chr12:32890097..32890098 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.1994+176C>T single nucleotide variant not provided [RCV000840767] Chr12:32740694 [GRCh38]
Chr12:32893628 [GRCh37]
Chr12:12p11.21
likely benign
GRCh37/hg19 12p11.21(chr12:31453473-33040145)x3 copy number gain not provided [RCV000849278] Chr12:31453473..33040145 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.251-1540C>G single nucleotide variant Hereditary spastic paraplegia 8 [RCV000785088] Chr12:32705827 [GRCh38]
Chr12:32858761 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.457-228C>T single nucleotide variant not provided [RCV000830988] Chr12:32712981 [GRCh38]
Chr12:32865915 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.103-215C>T single nucleotide variant not provided [RCV000840764] Chr12:32701200 [GRCh38]
Chr12:32854134 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.1995-319A>T single nucleotide variant not provided [RCV000840769] Chr12:32742270 [GRCh38]
Chr12:32895204 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.2154+186C>T single nucleotide variant not provided [RCV000840770] Chr12:32742934 [GRCh38]
Chr12:32895868 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.2155-216G>A single nucleotide variant not provided [RCV000840771] Chr12:32743138 [GRCh38]
Chr12:32896072 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.872+187C>T single nucleotide variant not provided [RCV000837692] Chr12:32720982 [GRCh38]
Chr12:32873916 [GRCh37]
Chr12:12p11.21
benign
NM_012062.5(DNM1L):c.370-238A>G single nucleotide variant not provided [RCV000838176] Chr12:32710691 [GRCh38]
Chr12:32863625 [GRCh37]
Chr12:12p11.21
benign
NM_012062.5(DNM1L):c.619+211A>T single nucleotide variant not provided [RCV000838177] Chr12:32713582 [GRCh38]
Chr12:32866516 [GRCh37]
Chr12:12p11.21
benign
NM_012062.5(DNM1L):c.620-251T>C single nucleotide variant not provided [RCV000838178] Chr12:32718392 [GRCh38]
Chr12:32871326 [GRCh37]
Chr12:12p11.21
benign
NM_012062.5(DNM1L):c.740+163G>A single nucleotide variant not provided [RCV000838179] Chr12:32718926 [GRCh38]
Chr12:32871860 [GRCh37]
Chr12:12p11.21
benign
NM_012062.5(DNM1L):c.1596+248G>A single nucleotide variant not provided [RCV000838181] Chr12:32737409 [GRCh38]
Chr12:32890343 [GRCh37]
Chr12:12p11.21
benign
NM_012062.5(DNM1L):c.1080-59A>G single nucleotide variant not provided [RCV000838504] Chr12:32730955 [GRCh38]
Chr12:32883889 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.619+94G>A single nucleotide variant not provided [RCV000832751] Chr12:32713465 [GRCh38]
Chr12:32866399 [GRCh37]
Chr12:12p11.21
benign
GRCh37/hg19 12p13.33-11.1(chr12:173786-34496628)x3 copy number gain not provided [RCV000847209] Chr12:173786..34496628 [GRCh37]
Chr12:12p13.33-11.1
pathogenic
NM_012062.5(DNM1L):c.763_764dup (p.Lys256fs) duplication Optic atrophy 5 [RCV000850504] Chr12:32720685..32720686 [GRCh38]
Chr12:32873619..32873620 [GRCh37]
Chr12:12p11.21
pathogenic
GRCh37/hg19 12p11.21(chr12:32783056-32836046)x3 copy number gain not provided [RCV000847676] Chr12:32783056..32836046 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.1571T>C (p.Leu524Ser) single nucleotide variant Encephalopathy due to defective mitochondrial and peroxisomal fission 1 [RCV000988807] Chr12:32737136 [GRCh38]
Chr12:32890070 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.108C>T (p.Ser36=) single nucleotide variant not provided [RCV000994885] Chr12:32701420 [GRCh38]
Chr12:32854354 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.1091C>A (p.Ala364Asp) single nucleotide variant not provided [RCV000994886] Chr12:32731025 [GRCh38]
Chr12:32883959 [GRCh37]
Chr12:12p11.21
likely pathogenic
NM_012062.5(DNM1L):c.1108T>C (p.Phe370Leu) single nucleotide variant Encephalopathy due to defective mitochondrial and peroxisomal fission 1 [RCV000988806] Chr12:32731042 [GRCh38]
Chr12:32883976 [GRCh37]
Chr12:12p11.21
likely pathogenic
NM_012062.5(DNM1L):c.1374T>C (p.Pro458=) single nucleotide variant not provided [RCV000962454] Chr12:32731871 [GRCh38]
Chr12:32884805 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.251-9T>C single nucleotide variant not provided [RCV000919449] Chr12:32707358 [GRCh38]
Chr12:32860292 [GRCh37]
Chr12:12p11.21
likely benign
NM_012062.5(DNM1L):c.344C>G (p.Thr115Arg) single nucleotide variant Encephalopathy due to defective mitochondrial and peroxisomal fission 1 [RCV001198068]|Inborn genetic diseases [RCV001266847] Chr12:32708199 [GRCh38]
Chr12:32861133 [GRCh37]
Chr12:12p11.21
likely pathogenic|uncertain significance
NM_012062.5(DNM1L):c.1822A>C (p.Lys608Gln) single nucleotide variant Encephalopathy due to defective mitochondrial and peroxisomal fission 1 [RCV000988808] Chr12:32740178 [GRCh38]
Chr12:32893112 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.759CAA[1] (p.Asn254del) microsatellite not provided [RCV001093214] Chr12:32720680..32720682 [GRCh38]
Chr12:32873614..32873616 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.1649C>T (p.Ala550Val) single nucleotide variant not provided [RCV001066764] Chr12:32737917 [GRCh38]
Chr12:32890851 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.115A>G (p.Ser39Gly) single nucleotide variant Encephalopathy due to defective mitochondrial and peroxisomal fission 1 [RCV001251095] Chr12:32701427 [GRCh38]
Chr12:32854361 [GRCh37]
Chr12:12p11.21
pathogenic|likely pathogenic
NM_012062.5(DNM1L):c.1087G>A (p.Gly363Ser) single nucleotide variant Encephalopathy due to defective mitochondrial and peroxisomal fission 1 [RCV001253719] Chr12:32731021 [GRCh38]
Chr12:32883955 [GRCh37]
Chr12:12p11.21
likely pathogenic
NM_012062.5(DNM1L):c.505C>T (p.Leu169Phe) single nucleotide variant Encephalopathy due to defective mitochondrial and peroxisomal fission 1 [RCV001333650] Chr12:32713257 [GRCh38]
Chr12:32866191 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.1228G>A (p.Glu410Lys) single nucleotide variant Encephalopathy due to defective mitochondrial and peroxisomal fission 1 [RCV001271120]|Inborn genetic diseases [RCV001265935] Chr12:32731383 [GRCh38]
Chr12:32884317 [GRCh37]
Chr12:12p11.21
pathogenic|likely pathogenic
GRCh37/hg19 12p11.21(chr12:32874959-33060511)x3 copy number gain not provided [RCV001258513] Chr12:32874959..33060511 [GRCh37]
Chr12:12p11.21
uncertain significance
NC_000012.11:g.(?_32772622)_(33049675_?)dup duplication Arrhythmogenic right ventricular dysplasia 9 [RCV001374111] Chr12:32772622..33049675 [GRCh37]
Chr12:12p11.21
uncertain significance
NM_012062.5(DNM1L):c.1099T>C (p.Cys367Arg) single nucleotide variant not provided [RCV001377566] Chr12:32731033 [GRCh38]
Chr12:32883967 [GRCh37]
Chr12:12p11.21
likely pathogenic

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:2973 AgrOrtholog
COSMIC DNM1L COSMIC
Ensembl Genes ENSG00000087470 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000266481 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000350948 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000370388 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000390090 UniProtKB/TrEMBL
  ENSP00000396030 UniProtKB/TrEMBL
  ENSP00000404160 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000415131 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000447013 UniProtKB/TrEMBL
  ENSP00000447788 UniProtKB/TrEMBL
  ENSP00000447845 UniProtKB/TrEMBL
  ENSP00000448105 UniProtKB/TrEMBL
  ENSP00000448610 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000448802 UniProtKB/TrEMBL
  ENSP00000448936 UniProtKB/TrEMBL
  ENSP00000449089 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000450399 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000450401 UniProtKB/TrEMBL
Ensembl Transcript ENST00000266481 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000358214 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000381000 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000413295 UniProtKB/TrEMBL
  ENST00000414834 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000434676 UniProtKB/TrEMBL
  ENST00000452533 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000546649 UniProtKB/TrEMBL
  ENST00000546757 UniProtKB/TrEMBL
  ENST00000547078 UniProtKB/TrEMBL
  ENST00000547312 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000548750 UniProtKB/TrEMBL
  ENST00000549701 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000550154 UniProtKB/TrEMBL
  ENST00000551476 UniProtKB/TrEMBL
  ENST00000551643 UniProtKB/TrEMBL
  ENST00000553257 ENTREZGENE, UniProtKB/Swiss-Prot
Gene3D-CATH 2.30.29.30 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000087470 GTEx
HGNC ID HGNC:2973 ENTREZGENE
Human Proteome Map DNM1L Human Proteome Map
InterPro DNM1L U