MAP2 (microtubule associated protein 2) - Rat Genome Database

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Gene: MAP2 (microtubule associated protein 2) Homo sapiens
Analyze
Symbol: MAP2
Name: microtubule associated protein 2
RGD ID: 733668
HGNC Page HGNC:6839
Description: Enables dystroglycan binding activity. Involved in central nervous system neuron development and dendrite morphogenesis. Predicted to be located in several cellular components, including axon; cytoskeleton; and dendrite. Predicted to be part of microtubule associated complex. Predicted to be active in several cellular components, including cell body; glutamatergic synapse; and postsynapse. Biomarker of Huntington's disease; Lewy body dementia; and schizophrenia.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: DKFZp686I2148; MAP-2; MAP2A; MAP2B; MAP2C; microtubule-associated protein 2
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
GRCh382209,424,047 - 209,734,112 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p13 Ensembl2209,424,047 - 209,734,147 (+)EnsemblGRCh38hg38GRCh38
GRCh372210,288,771 - 210,598,836 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 362209,997,016 - 210,307,079 (+)NCBINCBI36Build 36hg18NCBI36
Build 342210,269,908 - 210,421,484NCBI
Celera2204,056,618 - 204,366,628 (+)NCBICelera
Cytogenetic Map2q34NCBI
HuRef2202,133,889 - 202,443,633 (+)NCBIHuRef
CHM1_12210,294,619 - 210,604,654 (+)NCBICHM1_1
T2T-CHM13v2.02209,904,237 - 210,214,222 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(20S)-ginsenoside Rg3  (ISO)
(S)-3,5-dihydroxyphenylglycine  (ISO)
(S)-colchicine  (EXP)
1,1-dichloroethene  (ISO)
1,2-dimethylhydrazine  (ISO)
1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine  (ISO)
1-naphthyl isothiocyanate  (ISO)
17alpha-ethynylestradiol  (ISO)
17beta-estradiol  (EXP)
17beta-hydroxy-5alpha-androstan-3-one  (EXP)
2,2',4,4',5,5'-hexachlorobiphenyl  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2,3,7,8-Tetrachlorodibenzofuran  (ISO)
2,5-hexanedione  (ISO)
2-hydroxypropanoic acid  (EXP)
2-methylcholine  (EXP)
3',5'-cyclic AMP  (EXP)
3,3',5,5'-tetrabromobisphenol A  (ISO)
3,4-methylenedioxymethamphetamine  (ISO)
3-isobutyl-1-methyl-7H-xanthine  (EXP)
3-methyladenine  (ISO)
5-fluorouracil  (EXP)
9-cis-retinoic acid  (EXP)
acrylamide  (ISO)
aflatoxin B1  (EXP,ISO)
agomelatine  (ISO)
aldicarb  (EXP)
all-trans-retinoic acid  (EXP,ISO)
aluminium sulfate (anhydrous)  (ISO)
amantadine  (EXP)
ammonia  (ISO)
ammonium chloride  (ISO)
antimycin A  (EXP)
antirheumatic drug  (EXP)
aristolochic acid A  (EXP)
Aroclor 1254  (ISO)
arsane  (EXP,ISO)
arsenic atom  (EXP,ISO)
arsenous acid  (EXP)
azoxystrobin  (EXP)
benzo[a]pyrene  (EXP,ISO)
Benzo[k]fluoranthene  (ISO)
bexarotene  (ISO)
bisphenol A  (EXP,ISO)
bucladesine  (EXP)
butanal  (EXP)
cadmium atom  (EXP)
calcidiol  (ISO)
Calpeptin  (ISO)
capsaicin  (EXP)
carbaryl  (EXP)
CGP 52608  (EXP)
chlordecone  (ISO)
chlorohydrocarbon  (ISO)
chloroquine  (ISO)
chlorpromazine  (ISO)
chlorpyrifos  (ISO)
choline  (ISO)
cisplatin  (EXP,ISO)
clobetasol  (ISO)
cobalt dichloride  (ISO)
cocaine  (ISO)
colforsin daropate hydrochloride  (EXP)
copper atom  (EXP)
copper(0)  (EXP)
Cuprizon  (ISO)
Cyclopamine  (ISO)
cyclosporin A  (EXP)
cypermethrin  (ISO)
cyproconazole  (ISO)
cytarabine  (EXP)
DAPT  (ISO)
DDT  (ISO)
deguelin  (EXP)
dexamethasone  (ISO)
diarsenic trioxide  (EXP)
dibutyl phthalate  (ISO)
dichlorvos  (ISO)
dieldrin  (EXP)
dihydrolipoic acid  (ISO)
diquat  (EXP)
diuron  (ISO)
dorsomorphin  (EXP)
doxorubicin  (EXP)
endosulfan  (ISO)
enzalutamide  (EXP)
ethanol  (ISO)
folic acid  (ISO)
gamma-hexachlorocyclohexane  (EXP)
gentamycin  (ISO)
ginsenoside Rb1  (ISO)
ginsenoside Rd  (ISO)
ginsenoside Re  (ISO)
ginsenoside Rg1  (ISO)
glutathione  (EXP)
glyphosate  (EXP)
haloperidol  (ISO)
heptachlor  (EXP)
hexachlorophene  (EXP)
hydrogen peroxide  (EXP)
isoniazide  (ISO)
ivermectin  (EXP)
kainic acid  (ISO)
L-ascorbic acid  (EXP,ISO)
L-methionine  (ISO)
lead diacetate  (ISO)
leflunomide  (EXP)
LY294002  (ISO)
maneb  (ISO)
manganese(II) chloride  (ISO)
melatonin  (ISO)
methamphetamine  (ISO)
methotrexate  (EXP)
methylmercury chloride  (EXP,ISO)
miconazole  (ISO)
morphine  (ISO)
N,N-diethyl-m-toluamide  (ISO)
N-acetyl-L-cysteine  (EXP,ISO)
N-nitrosodiethylamine  (ISO)
nickel dichloride  (EXP)
nicotinic acid  (ISO)
nimodipine  (ISO)
nitrofen  (ISO)
Nivalenol  (ISO)
olanzapine  (ISO)
oxaliplatin  (EXP)
ozone  (ISO)
panobinostat  (EXP)
paracetamol  (EXP,ISO)
paraquat  (ISO)
PD123319  (ISO)
permethrin  (ISO)
phenethyl isothiocyanate  (ISO)
phenylmercury acetate  (EXP)
physostigmine  (ISO)
picoxystrobin  (EXP)
poly(vinylpyrrolidone)  (ISO)
potassium chromate  (EXP)
potassium dichromate  (ISO)
progesterone  (EXP,ISO)
pyrimidifen  (EXP)
pyrroloquinoline quinone  (EXP)
rac-lactic acid  (EXP)
resveratrol  (ISO)
risperidone  (ISO)
rotenone  (EXP,ISO)
Salidroside  (ISO)
sarin  (ISO)
SB 431542  (EXP)
scopolamine  (EXP)
sevoflurane  (ISO)
silver atom  (EXP)
silver(0)  (EXP)
silver(1+) nitrate  (ISO)
sirolimus  (ISO)
sodium arsenate  (ISO)
sodium arsenite  (EXP,ISO)
streptozocin  (ISO)
sulforaphane  (EXP)
tetrachloromethane  (ISO)
thifluzamide  (EXP)
trichloroethene  (ISO)
trichostatin A  (EXP)
triclosan  (EXP)
triphenyl phosphate  (ISO)
triptonide  (ISO)
Tryptanthrine  (EXP)
valproic acid  (EXP,ISO)
valsartan  (ISO)
venlafaxine hydrochloride  (ISO)
WIN 55212-2  (ISO)
zoledronic acid  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. An experimental rat model of sporadic Alzheimer's disease and rescue of cognitive impairment with a neurotrophic peptide. Bolognin S, etal., Acta Neuropathol. 2012 Jan;123(1):133-51. Epub 2011 Nov 15.
2. A mouse model of term chorioamnionitis: unraveling causes of adverse neurological outcomes. Burd I, etal., Reprod Sci. 2011 Sep;18(9):900-7. Epub 2011 Mar 18.
3. Expression changes of parvalbumin and microtubule-associated protein 2 induced by chronic constriction injury in rat dorsal root ganglia. Cao MH, etal., Chin Med J (Engl). 2011 Jul;124(14):2184-90.
4. Compression alters kinase and phosphatase activity and tau and MAP2 phosphorylation transiently while inducing the fast adaptive dendritic remodeling of underlying cortical neurons. Chen LJ, etal., J Neurotrauma. 2010 Sep;27(9):1657-69.
5. Treatment of experimental spinal cord injury with 3beta-methoxy-pregnenolone. Duchossoy Y, etal., Brain Res. 2011 Jul 27;1403:57-66. Epub 2011 Jun 12.
6. Morphological Alteration and Reduction of MAP2-Immunoreactivity in Pyramidal Neurons of Cerebral Cortex in a Rat Model of Focal Cortical Compression. Furutani R and Kibayashi K, J Neurotrauma. 2012 Apr 10;29(6):1266-76. Epub 2011 Aug 5.
7. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
8. Cognitive impairment and changes of neuronal plasticity in rats of chronic cerebral hypoperfusion associated with cerebral arteriovenous malformations. Hai J, etal., Acta Neurol Belg. 2010 Jun;110(2):180-5.
9. Lewy body variant of Alzheimer's disease: selective neocortical loss of t-SNARE proteins and loss of MAP2 and alpha-synuclein in medial temporal lobe. Mukaetova-Ladinska EB, etal., ScientificWorldJournal. 2009 Dec 16;9:1463-75.
10. Microtubule-associated protein 2, an early blood marker of ischemic brain injury. Park D, etal., J Neurosci Res. 2012 Feb;90(2):461-7. doi: 10.1002/jnr.22769. Epub 2011 Sep 21.
11. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
12. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
13. Green Tea-EGCG reduces GFAP associated neuronal loss in HIV-1 Tat transgenic mice. Rrapo E, etal., Am J Transl Res. 2009 Jan 1;1(1):72-9.
14. Effects of perinatal asphyxia on rat striatal cytoskeleton. Saraceno GE, etal., Synapse. 2012 Jan;66(1):9-19. doi: 10.1002/syn.20978. Epub 2011 Oct 11.
15. A comparative study of MAP2 immunostaining in areas 9 and 17 in schizophrenia and Huntington chorea. Somenarain L and Jones LB, J Psychiatr Res. 2010 Aug;44(11):694-9. Epub 2010 Jan 22.
16. Post-ischemic hypothermia promotes generation of neural cells and reduces apoptosis by Bcl-2 in the striatum of neonatal rat brain. Xiong M, etal., Neurochem Int. 2011 May;58(6):625-33. Epub 2011 Feb 12.
17. BACE1 elevation is associated with aberrant limbic axonal sprouting in epileptic CD1 mice. Yan XX, etal., Exp Neurol. 2012 May;235(1):228-37. Epub 2012 Jan 11.
18. Functional improvement and neuroplastic effects of anodal transcranial direct current stimulation (tDCS) delivered 1day vs. 1week after cerebral ischemia in rats. Yoon KJ, etal., Brain Res. 2012 May 3;1452:61-72. Epub 2012 Mar 5.
Additional References at PubMed
PMID:1494913   PMID:1708129   PMID:1902666   PMID:2212989   PMID:2254332   PMID:2455776   PMID:2481044   PMID:2561973   PMID:2701845   PMID:2777757   PMID:3027087   PMID:3103857  
PMID:3200318   PMID:7479905   PMID:7556643   PMID:7591286   PMID:7820861   PMID:7854050   PMID:8294038   PMID:8624078   PMID:8631898   PMID:8990203   PMID:8997639   PMID:9384577  
PMID:9588626   PMID:10527895   PMID:10640627   PMID:10781592   PMID:10862698   PMID:11029056   PMID:11171103   PMID:11546790   PMID:11831386   PMID:11922706   PMID:12023276   PMID:12079519  
PMID:12082079   PMID:12477932   PMID:12605092   PMID:12629046   PMID:12775713   PMID:12879020   PMID:12890753   PMID:12927759   PMID:14594945   PMID:14604896   PMID:14702039   PMID:14759258  
PMID:15146346   PMID:15285794   PMID:15285795   PMID:15345747   PMID:15465982   PMID:15536091   PMID:15623521   PMID:15822905   PMID:16145685   PMID:16195780   PMID:16611822   PMID:16916793  
PMID:17081983   PMID:17326138   PMID:18073143   PMID:18341635   PMID:19009302   PMID:19165527   PMID:19309409   PMID:19369632   PMID:19701075   PMID:19880519   PMID:19913121   PMID:19953087  
PMID:20100193   PMID:20195357   PMID:20379614   PMID:20628086   PMID:20846339   PMID:21249135   PMID:21832049   PMID:21873635   PMID:22272295   PMID:22403409   PMID:22863883   PMID:22874672  
PMID:22985576   PMID:23077641   PMID:24069608   PMID:24124579   PMID:24163370   PMID:24587039   PMID:24780770   PMID:24825317   PMID:24977729   PMID:25400739   PMID:25497017   PMID:25569473  
PMID:25629269   PMID:25653352   PMID:25682157   PMID:25818630   PMID:25871823   PMID:25921289   PMID:26014048   PMID:26134402   PMID:26186194   PMID:26269332   PMID:26469323   PMID:26604067  
PMID:26609151   PMID:26637429   PMID:26638075   PMID:27098187   PMID:28386764   PMID:28514442   PMID:28611215   PMID:28895474   PMID:29480405   PMID:29925592   PMID:30021884   PMID:30997723  
PMID:31343991   PMID:31701227   PMID:31732726   PMID:31834144   PMID:32393512   PMID:32457219   PMID:32572922   PMID:32710889   PMID:33931805   PMID:33957083   PMID:33961781   PMID:34079125  
PMID:34285710   PMID:35013218   PMID:35139773   PMID:35229233   PMID:35244772   PMID:35356984   PMID:35987383   PMID:36215168  


Genomics

Comparative Map Data
MAP2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382209,424,047 - 209,734,112 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p13 Ensembl2209,424,047 - 209,734,147 (+)EnsemblGRCh38hg38GRCh38
GRCh372210,288,771 - 210,598,836 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 362209,997,016 - 210,307,079 (+)NCBINCBI36Build 36hg18NCBI36
Build 342210,269,908 - 210,421,484NCBI
Celera2204,056,618 - 204,366,628 (+)NCBICelera
Cytogenetic Map2q34NCBI
HuRef2202,133,889 - 202,443,633 (+)NCBIHuRef
CHM1_12210,294,619 - 210,604,654 (+)NCBICHM1_1
T2T-CHM13v2.02209,904,237 - 210,214,222 (+)NCBIT2T-CHM13v2.0
Map2
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39166,214,337 - 66,481,742 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl166,214,432 - 66,481,742 (+)EnsemblGRCm39 Ensembl
GRCm38166,175,202 - 66,442,583 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl166,175,273 - 66,442,583 (+)EnsemblGRCm38mm10GRCm38
MGSCv37166,221,903 - 66,489,157 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36166,108,521 - 66,375,797 (+)NCBIMGSCv36mm8
Celera166,699,319 - 66,964,492 (+)NCBICelera
Cytogenetic Map1C3NCBI
cM Map133.49NCBI
Map2
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.2967,723,422 - 67,981,886 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl967,723,371 - 67,979,809 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx976,387,776 - 76,469,106 (+)NCBIRnor_SHR
UTH_Rnor_SHRSP_BbbUtx_1.0981,515,139 - 81,596,514 (+)NCBIRnor_SHRSP
UTH_Rnor_WKY_Bbb_1.0979,899,162 - 79,986,857 (+)NCBIRnor_WKY
Rnor_6.0973,204,753 - 73,462,965 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl973,319,710 - 73,462,972 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0973,837,509 - 74,095,431 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4965,174,376 - 65,256,003 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1965,321,360 - 65,402,977 (+)NCBI
Celera965,377,941 - 65,459,391 (+)NCBICelera
RH 3.4 Map9593.2RGD
Cytogenetic Map9q32NCBI
Map2
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554575,678,436 - 5,875,024 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554575,678,826 - 5,816,114 (-)NCBIChiLan1.0ChiLan1.0
MAP2
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan12B112,061,728 - 112,372,130 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v02B96,681,268 - 96,991,650 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.12B215,085,476 - 215,395,439 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl2B215,314,857 - 215,391,728 (+)Ensemblpanpan1.1panPan2
MAP2
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.13717,316,899 - 17,611,360 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl3717,466,678 - 17,607,803 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha3718,197,871 - 18,492,089 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.03717,252,304 - 17,547,172 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl3717,260,892 - 17,545,422 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.13717,357,768 - 17,502,660 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.03717,171,196 - 17,465,399 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.03717,188,565 - 17,479,742 (+)NCBIUU_Cfam_GSD_1.0
Map2
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024405303165,843,181 - 166,122,293 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_004936845473,366 - 545,135 (-)EnsemblSpeTri2.0
SpeTri2.0NW_004936845475,406 - 752,600 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
MAP2
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl15112,236,119 - 112,462,929 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.115112,156,578 - 112,462,932 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.215124,033,358 - 124,184,546 (+)NCBISscrofa10.2Sscrofa10.2susScr3
MAP2
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11095,319,649 - 95,431,106 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1095,349,157 - 95,431,320 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_023666040103,915,685 - 104,226,077 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Map2
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247656,476,346 - 6,546,116 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247656,476,544 - 6,758,959 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in MAP2
76 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 2q32.3-37.3(chr2:194898783-236473913)x3 copy number gain See cases [RCV000051119] Chr2:194898783..236473913 [GRCh38]
Chr2:195763507..237382556 [GRCh37]
Chr2:195471752..237047295 [NCBI36]
Chr2:2q32.3-37.3		 pathogenic
GRCh38/hg38 2q33.1-34(chr2:198095810-211803453)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052603]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052603]|See cases [RCV000052603] Chr2:198095810..211803453 [GRCh38]
Chr2:198960534..212668178 [GRCh37]
Chr2:198668779..212376423 [NCBI36]
Chr2:2q33.1-34		 pathogenic
GRCh38/hg38 2q33.2-35(chr2:203010732-214671878)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052607]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052607]|See cases [RCV000052607] Chr2:203010732..214671878 [GRCh38]
Chr2:203875455..215536602 [GRCh37]
Chr2:203583700..215244847 [NCBI36]
Chr2:2q33.2-35		 pathogenic
GRCh38/hg38 2q32.2-37.3(chr2:188818195-242065208)x3 copy number gain See cases [RCV000052958] Chr2:188818195..242065208 [GRCh38]
Chr2:189682921..243007359 [GRCh37]
Chr2:189391166..242656032 [NCBI36]
Chr2:2q32.2-37.3		 pathogenic
GRCh38/hg38 2q32.2-37.3(chr2:190310736-241892770)x3 copy number gain See cases [RCV000052959] Chr2:190310736..241892770 [GRCh38]
Chr2:191175462..242834921 [GRCh37]
Chr2:190883707..242483594 [NCBI36]
Chr2:2q32.2-37.3		 pathogenic
GRCh38/hg38 2q32.3-37.3(chr2:193122313-241074980)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052960]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052960]|See cases [RCV000052960] Chr2:193122313..241074980 [GRCh38]
Chr2:193987039..242014395 [GRCh37]
Chr2:193695284..241663068 [NCBI36]
Chr2:2q32.3-37.3		 pathogenic
NM_002374.3(MAP2):c.4455C>T (p.Phe1485=) single nucleotide variant Malignant melanoma [RCV000060474] Chr2:209696984 [GRCh38]
Chr2:210561708 [GRCh37]
Chr2:210269953 [NCBI36]
Chr2:2q34		 not provided
NM_001039538.1(MAP2):c.263-8402G>T single nucleotide variant Lung cancer [RCV000091845] Chr2:209670170 [GRCh38]
Chr2:210534894 [GRCh37]
Chr2:2q34		 uncertain significance
GRCh38/hg38 2q33.3-34(chr2:207058886-211245603)x1 copy number loss See cases [RCV000139325] Chr2:207058886..211245603 [GRCh38]
Chr2:207923610..212110328 [GRCh37]
Chr2:207631855..211818573 [NCBI36]
Chr2:2q33.3-34		 pathogenic
GRCh38/hg38 2q31.3-36.2(chr2:180513793-224302848)x3 copy number gain See cases [RCV000139446] Chr2:180513793..224302848 [GRCh38]
Chr2:181378520..225167565 [GRCh37]
Chr2:181086765..224875809 [NCBI36]
Chr2:2q31.3-36.2		 pathogenic
GRCh38/hg38 2q33.3-34(chr2:204906843-210031449)x1 copy number loss See cases [RCV000139629] Chr2:204906843..210031449 [GRCh38]
Chr2:205771566..210896173 [GRCh37]
Chr2:205479811..210604418 [NCBI36]
Chr2:2q33.3-34		 pathogenic
GRCh38/hg38 2q32.3-35(chr2:192938826-215705052)x1 copy number loss See cases [RCV000141254] Chr2:192938826..215705052 [GRCh38]
Chr2:193803552..216569775 [GRCh37]
Chr2:193511797..216278020 [NCBI36]
Chr2:2q32.3-35		 pathogenic
GRCh38/hg38 2q33.1-34(chr2:199946494-209985195)x1 copy number loss See cases [RCV000141076] Chr2:199946494..209985195 [GRCh38]
Chr2:200811217..210849919 [GRCh37]
Chr2:200519462..210558164 [NCBI36]
Chr2:2q33.1-34		 pathogenic
GRCh38/hg38 2q32.2-37.3(chr2:189436149-241841232)x3 copy number gain See cases [RCV000142307] Chr2:189436149..241841232 [GRCh38]
Chr2:190300875..242783384 [GRCh37]
Chr2:190009120..242432057 [NCBI36]
Chr2:2q32.2-37.3		 pathogenic
GRCh38/hg38 2q33.1-34(chr2:199937273-210031924)x1 copy number loss See cases [RCV000143301] Chr2:199937273..210031924 [GRCh38]
Chr2:200801996..210896648 [GRCh37]
Chr2:200510241..210604893 [NCBI36]
Chr2:2q33.1-34		 pathogenic
NM_001375505.1(MAP2):c.2254G>T (p.Ala752Ser) single nucleotide variant not specified [RCV000239245] Chr2:209694424 [GRCh38]
Chr2:210559148 [GRCh37]
Chr2:2q34		 uncertain significance
GRCh37/hg19 2p25.3-q37.3(chr2:14238-243048760)x3 copy number gain not provided [RCV000752802] Chr2:14238..243048760 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
GRCh37/hg19 2q31.1-35(chr2:169829974-215521436)x3 copy number gain See cases [RCV000448271] Chr2:169829974..215521436 [GRCh37]
Chr2:2q31.1-35		 pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384) copy number gain See cases [RCV000512056] Chr2:12771..242783384 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)x3 copy number gain See cases [RCV000511212] Chr2:12771..242783384 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
GRCh37/hg19 2q34(chr2:209164383-210460943)x4 copy number gain not provided [RCV000682126] Chr2:209164383..210460943 [GRCh37]
Chr2:2q34		 uncertain significance
GRCh37/hg19 2q33.3-35(chr2:205169148-219149293)x3 copy number gain not provided [RCV000682166] Chr2:205169148..219149293 [GRCh37]
Chr2:2q33.3-35		 pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:15672-243101834)x3 copy number gain not provided [RCV000752804] Chr2:15672..243101834 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
Single allele deletion Trichorhinophalangeal dysplasia type I [RCV000735898] Chr2:209425211..211567929 [GRCh37]
Chr2:2q34		 uncertain significance
NM_001375505.1(MAP2):c.2927A>T (p.His976Leu) single nucleotide variant not provided [RCV000959838] Chr2:209695097 [GRCh38]
Chr2:210559821 [GRCh37]
Chr2:2q34		 benign
Single allele duplication Neurodevelopmental disorder [RCV000787403] Chr2:188926928..225298653 [GRCh37]
Chr2:2q32.1-36.2		 pathogenic
NM_001375505.1(MAP2):c.4522+2_4522+3insA insertion not provided [RCV001668845] Chr2:209697053..209697054 [GRCh38]
Chr2:210561777..210561778 [GRCh37]
Chr2:2q34		 benign
NM_001375505.1(MAP2):c.4614C>T (p.Arg1538=) single nucleotide variant not provided [RCV000901564] Chr2:209705609 [GRCh38]
Chr2:210570333 [GRCh37]
Chr2:2q34		 likely benign
NM_001375505.1(MAP2):c.2523G>A (p.Glu841=) single nucleotide variant not provided [RCV000971727] Chr2:209694693 [GRCh38]
Chr2:210559417 [GRCh37]
Chr2:2q34		 benign
NM_001375505.1(MAP2):c.526G>A (p.Asp176Asn) single nucleotide variant not provided [RCV000900473] Chr2:209692696 [GRCh38]
Chr2:210557420 [GRCh37]
Chr2:2q34		 benign
NM_001375505.1(MAP2):c.3498C>T (p.Ala1166=) single nucleotide variant not provided [RCV000967822] Chr2:209695668 [GRCh38]
Chr2:210560392 [GRCh37]
Chr2:2q34		 likely benign
NM_001375505.1(MAP2):c.2156G>A (p.Gly719Asp) single nucleotide variant not provided [RCV000882235] Chr2:209694326 [GRCh38]
Chr2:210559050 [GRCh37]
Chr2:2q34		 likely benign
NM_001375505.1(MAP2):c.1240G>T (p.Ala414Ser) single nucleotide variant not provided [RCV000959539] Chr2:209693410 [GRCh38]
Chr2:210558134 [GRCh37]
Chr2:2q34		 benign
NM_001375505.1(MAP2):c.4836C>G (p.Arg1612=) single nucleotide variant not provided [RCV000926312] Chr2:209710017 [GRCh38]
Chr2:210574741 [GRCh37]
Chr2:2q34		 likely benign
NM_001375505.1(MAP2):c.1405G>A (p.Glu469Lys) single nucleotide variant not provided [RCV000882234] Chr2:209693575 [GRCh38]
Chr2:210558299 [GRCh37]
Chr2:2q34		 likely benign
NM_001375505.1(MAP2):c.5280A>G (p.Gln1760=) single nucleotide variant not provided [RCV000885060] Chr2:209730193 [GRCh38]
Chr2:210594917 [GRCh37]
Chr2:2q34		 benign
NM_001375505.1(MAP2):c.2280T>C (p.Pro760=) single nucleotide variant not provided [RCV000946667] Chr2:209694450 [GRCh38]
Chr2:210559174 [GRCh37]
Chr2:2q34		 benign
NM_001375505.1(MAP2):c.105C>T (p.Gly35=) single nucleotide variant not provided [RCV000892055] Chr2:209653275 [GRCh38]
Chr2:210517999 [GRCh37]
Chr2:2q34		 likely benign
NM_001375505.1(MAP2):c.2463T>C (p.Ser821=) single nucleotide variant not provided [RCV000894597] Chr2:209694633 [GRCh38]
Chr2:210559357 [GRCh37]
Chr2:2q34		 likely benign
NM_001375505.1(MAP2):c.2457G>A (p.Leu819=) single nucleotide variant not provided [RCV000922771] Chr2:209694627 [GRCh38]
Chr2:210559351 [GRCh37]
Chr2:2q34		 likely benign
GRCh37/hg19 2q32.1-34(chr2:185697659-213002074) copy number loss Chromosome 2q32-q33 deletion syndrome [RCV002280608] Chr2:185697659..213002074 [GRCh37]
Chr2:2q32.1-34		 pathogenic
NM_001375505.1(MAP2):c.536A>G (p.Glu179Gly) single nucleotide variant not provided [RCV000959837] Chr2:209692706 [GRCh38]
Chr2:210557430 [GRCh37]
Chr2:2q34		 benign
NM_001375505.1(MAP2):c.54G>A (p.Pro18=) single nucleotide variant not provided [RCV000975418] Chr2:209653224 [GRCh38]
Chr2:210517948 [GRCh37]
Chr2:2q34		 likely benign
NM_001375505.1(MAP2):c.3108A>G (p.Gln1036=) single nucleotide variant not provided [RCV000917824] Chr2:209695278 [GRCh38]
Chr2:210560002 [GRCh37]
Chr2:2q34		 likely benign
NM_001375505.1(MAP2):c.3462A>G (p.Thr1154=) single nucleotide variant not provided [RCV000936941] Chr2:209695632 [GRCh38]
Chr2:210560356 [GRCh37]
Chr2:2q34		 likely benign
GRCh37/hg19 2q34(chr2:209900047-210377488)x3 copy number gain not provided [RCV000847437] Chr2:209900047..210377488 [GRCh37]
Chr2:2q34		 uncertain significance
GRCh37/hg19 2q24.2-34(chr2:163233162-211927188)x3 copy number gain not provided [RCV001005349] Chr2:163233162..211927188 [GRCh37]
Chr2:2q24.2-34		 pathogenic
NM_001375505.1(MAP2):c.24A>G (p.Glu8=) single nucleotide variant not provided [RCV000921652] Chr2:209653194 [GRCh38]
Chr2:210517918 [GRCh37]
Chr2:2q34		 likely benign
NM_001375505.1(MAP2):c.3387G>A (p.Glu1129=) single nucleotide variant not provided [RCV000952831] Chr2:209695557 [GRCh38]
Chr2:210560281 [GRCh37]
Chr2:2q34		 benign
NM_001375505.1(MAP2):c.1219G>T (p.Val407Phe) single nucleotide variant not provided [RCV000974047] Chr2:209693389 [GRCh38]
Chr2:210558113 [GRCh37]
Chr2:2q34		 benign
NM_001375505.1(MAP2):c.163G>A (p.Glu55Lys) single nucleotide variant not provided [RCV000954389] Chr2:209653333 [GRCh38]
Chr2:210518057 [GRCh37]
Chr2:2q34		 benign
NM_001375505.1(MAP2):c.5067G>T (p.Gly1689=) single nucleotide variant not provided [RCV000908602] Chr2:209710248 [GRCh38]
Chr2:210574972 [GRCh37]
Chr2:2q34		 benign
NM_001375505.1(MAP2):c.4031A>C (p.Lys1344Thr) single nucleotide variant not provided [RCV000909497] Chr2:209696201 [GRCh38]
Chr2:210560925 [GRCh37]
Chr2:2q34		 likely benign
NM_001375505.1(MAP2):c.117A>G (p.Glu39=) single nucleotide variant not provided [RCV000954890] Chr2:209653287 [GRCh38]
Chr2:210518011 [GRCh37]
Chr2:2q34		 likely benign
NM_001375505.1(MAP2):c.4587C>T (p.Asp1529=) single nucleotide variant not provided [RCV000910461] Chr2:209705582 [GRCh38]
Chr2:210570306 [GRCh37]
Chr2:2q34		 benign
NM_001375505.1(MAP2):c.3204A>G (p.Thr1068=) single nucleotide variant not provided [RCV000912178] Chr2:209695374 [GRCh38]
Chr2:210560098 [GRCh37]
Chr2:2q34		 likely benign
NM_001375505.1(MAP2):c.2345C>T (p.Ala782Val) single nucleotide variant not provided [RCV000890759] Chr2:209694515 [GRCh38]
Chr2:210559239 [GRCh37]
Chr2:2q34		 benign
NM_001375505.1(MAP2):c.2037T>C (p.Asp679=) single nucleotide variant not provided [RCV000956030] Chr2:209694207 [GRCh38]
Chr2:210558931 [GRCh37]
Chr2:2q34		 benign
GRCh37/hg19 2q33.2-34(chr2:204445619-212580788)x1 copy number loss not provided [RCV001258576] Chr2:204445619..212580788 [GRCh37]
Chr2:2q33.2-34		 pathogenic
GRCh37/hg19 2q31.2-37.3(chr2:178397959-243007457)x3 copy number gain See cases [RCV001263052] Chr2:178397959..243007457 [GRCh37]
Chr2:2q31.2-37.3		 pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:1-243199373) copy number gain Mosaic trisomy 2 [RCV002280628] Chr2:1..243199373 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
GRCh37/hg19 2q31.1-35(chr2:169829974-215521436) copy number gain not specified [RCV002053265] Chr2:169829974..215521436 [GRCh37]
Chr2:2q31.1-35		 pathogenic
NM_001375505.1(MAP2):c.5144G>A (p.Arg1715His) single nucleotide variant Inborn genetic diseases [RCV002543254]|not provided [RCV001839321] Chr2:209725779 [GRCh38]
Chr2:210590503 [GRCh37]
Chr2:2q34		 uncertain significance
GRCh37/hg19 2q34(chr2:209682592-210429755)x1 copy number loss not provided [RCV001827848] Chr2:209682592..210429755 [GRCh37]
Chr2:2q34		 uncertain significance
NC_000002.11:g.(?_203420070)_(211811277_?)del deletion Primary pulmonary hypertension [RCV002016799] Chr2:203420070..211811277 [GRCh37]
Chr2:2q33.2-34		 uncertain significance
NM_001375505.1(MAP2):c.2227del (p.Asp743fs) deletion MAP2-associated Neurodevelopmental Disorder [RCV002227803] Chr2:209694394 [GRCh38]
Chr2:210559118 [GRCh37]
Chr2:2q34		 uncertain significance
NM_001375505.1(MAP2):c.2629G>A (p.Val877Ile) single nucleotide variant Inborn genetic diseases [RCV002772141] Chr2:209694799 [GRCh38]
Chr2:210559523 [GRCh37]
Chr2:2q34		 uncertain significance
NM_001375505.1(MAP2):c.1601A>G (p.Gln534Arg) single nucleotide variant Inborn genetic diseases [RCV002970126] Chr2:209693771 [GRCh38]
Chr2:210558495 [GRCh37]
Chr2:2q34		 uncertain significance
NM_001375505.1(MAP2):c.3778C>A (p.Leu1260Met) single nucleotide variant Inborn genetic diseases [RCV002793316] Chr2:209695948 [GRCh38]
Chr2:210560672 [GRCh37]
Chr2:2q34		 uncertain significance
NM_001375505.1(MAP2):c.3317G>A (p.Ser1106Asn) single nucleotide variant Inborn genetic diseases [RCV002732942] Chr2:209695487 [GRCh38]
Chr2:210560211 [GRCh37]
Chr2:2q34		 uncertain significance
NM_001375505.1(MAP2):c.812C>T (p.Thr271Met) single nucleotide variant Inborn genetic diseases [RCV002902692] Chr2:209692982 [GRCh38]
Chr2:210557706 [GRCh37]
Chr2:2q34		 likely benign
NM_001375505.1(MAP2):c.4281A>C (p.Lys1427Asn) single nucleotide variant Rett syndrome [RCV002510646] Chr2:209696642 [GRCh38]
Chr2:210561366 [GRCh37]
Chr2:2q34		 uncertain significance
NM_001375505.1(MAP2):c.2987A>G (p.Tyr996Cys) single nucleotide variant Inborn genetic diseases [RCV002905719] Chr2:209695157 [GRCh38]
Chr2:210559881 [GRCh37]
Chr2:2q34		 uncertain significance
NM_001375505.1(MAP2):c.4333G>A (p.Val1445Ile) single nucleotide variant Inborn genetic diseases [RCV002906075] Chr2:209696694 [GRCh38]
Chr2:210561418 [GRCh37]
Chr2:2q34		 likely benign
NM_001375505.1(MAP2):c.739G>A (p.Val247Ile) single nucleotide variant Inborn genetic diseases [RCV002849111] Chr2:209692909 [GRCh38]
Chr2:210557633 [GRCh37]
Chr2:2q34		 uncertain significance
NM_001375505.1(MAP2):c.1102A>G (p.Ile368Val) single nucleotide variant Inborn genetic diseases [RCV002981375] Chr2:209693272 [GRCh38]
Chr2:210557996 [GRCh37]
Chr2:2q34		 likely benign
NM_001375505.1(MAP2):c.3220G>A (p.Ala1074Thr) single nucleotide variant Inborn genetic diseases [RCV002784181] Chr2:209695390 [GRCh38]
Chr2:210560114 [GRCh37]
Chr2:2q34		 uncertain significance
NM_001375505.1(MAP2):c.2188G>A (p.Asp730Asn) single nucleotide variant Inborn genetic diseases [RCV002759538] Chr2:209694358 [GRCh38]
Chr2:210559082 [GRCh37]
Chr2:2q34		 uncertain significance
NM_001375505.1(MAP2):c.1088A>G (p.Lys363Arg) single nucleotide variant Inborn genetic diseases [RCV002868380] Chr2:209693258 [GRCh38]
Chr2:210557982 [GRCh37]
Chr2:2q34		 uncertain significance
NM_001375505.1(MAP2):c.128G>A (p.Arg43Gln) single nucleotide variant Inborn genetic diseases [RCV002661132] Chr2:209653298 [GRCh38]
Chr2:210518022 [GRCh37]
Chr2:2q34		 uncertain significance
NM_001375505.1(MAP2):c.875T>G (p.Met292Arg) single nucleotide variant Inborn genetic diseases [RCV002910837] Chr2:209693045 [GRCh38]
Chr2:210557769 [GRCh37]
Chr2:2q34		 uncertain significance
NM_001375505.1(MAP2):c.2899A>G (p.Ser967Gly) single nucleotide variant Inborn genetic diseases [RCV002758717] Chr2:209695069 [GRCh38]
Chr2:210559793 [GRCh37]
Chr2:2q34		 uncertain significance
NM_001375505.1(MAP2):c.2582A>G (p.Asp861Gly) single nucleotide variant Inborn genetic diseases [RCV002768612] Chr2:209694752 [GRCh38]
Chr2:210559476 [GRCh37]
Chr2:2q34		 uncertain significance
NM_001375505.1(MAP2):c.4076T>C (p.Val1359Ala) single nucleotide variant Inborn genetic diseases [RCV002769587] Chr2:209696246 [GRCh38]
Chr2:210560970 [GRCh37]
Chr2:2q34		 uncertain significance
NM_001375505.1(MAP2):c.13C>T (p.Arg5Trp) single nucleotide variant Inborn genetic diseases [RCV002669768] Chr2:209653183 [GRCh38]
Chr2:210517907 [GRCh37]
Chr2:2q34		 uncertain significance
NM_001375505.1(MAP2):c.1401T>A (p.Asp467Glu) single nucleotide variant Inborn genetic diseases [RCV003203374] Chr2:209693571 [GRCh38]
Chr2:210558295 [GRCh37]
Chr2:2q34		 uncertain significance
NM_001375505.1(MAP2):c.3932T>G (p.Phe1311Cys) single nucleotide variant Inborn genetic diseases [RCV003195098] Chr2:209696102 [GRCh38]
Chr2:210560826 [GRCh37]
Chr2:2q34		 uncertain significance
NM_001375505.1(MAP2):c.3724C>A (p.Gln1242Lys) single nucleotide variant Inborn genetic diseases [RCV003205405] Chr2:209695894 [GRCh38]
Chr2:210560618 [GRCh37]
Chr2:2q34		 uncertain significance
NM_001375505.1(MAP2):c.3188A>G (p.Asp1063Gly) single nucleotide variant Inborn genetic diseases [RCV003186371] Chr2:209695358 [GRCh38]
Chr2:210560082 [GRCh37]
Chr2:2q34		 uncertain significance
NM_001375505.1(MAP2):c.3461C>T (p.Thr1154Ile) single nucleotide variant Inborn genetic diseases [RCV003175273] Chr2:209695631 [GRCh38]
Chr2:210560355 [GRCh37]
Chr2:2q34		 uncertain significance
NM_001375505.1(MAP2):c.1501G>A (p.Val501Ile) single nucleotide variant Inborn genetic diseases [RCV003188724] Chr2:209693671 [GRCh38]
Chr2:210558395 [GRCh37]
Chr2:2q34		 uncertain significance
NM_001375505.1(MAP2):c.4652G>A (p.Arg1551Gln) single nucleotide variant Inborn genetic diseases [RCV003211189] Chr2:209705647 [GRCh38]
Chr2:210570371 [GRCh37]
Chr2:2q34		 uncertain significance
NM_001375505.1(MAP2):c.4591G>A (p.Val1531Ile) single nucleotide variant Inborn genetic diseases [RCV003192781] Chr2:209705586 [GRCh38]
Chr2:210570310 [GRCh37]
Chr2:2q34		 uncertain significance
NM_001375505.1(MAP2):c.851T>C (p.Ile284Thr) single nucleotide variant Inborn genetic diseases [RCV003211507] Chr2:209693021 [GRCh38]
Chr2:210557745 [GRCh37]
Chr2:2q34		 uncertain significance
NM_001375505.1(MAP2):c.1175A>G (p.Lys392Arg) single nucleotide variant Inborn genetic diseases [RCV003200386] Chr2:209693345 [GRCh38]
Chr2:210558069 [GRCh37]
Chr2:2q34		 uncertain significance
NM_001375505.1(MAP2):c.5206G>A (p.Ala1736Thr) single nucleotide variant Inborn genetic diseases [RCV003208603] Chr2:209729900 [GRCh38]
Chr2:210594624 [GRCh37]
Chr2:2q34		 uncertain significance
NM_001375505.1(MAP2):c.2981T>A (p.Val994Glu) single nucleotide variant Inborn genetic diseases [RCV003215265] Chr2:209695151 [GRCh38]
Chr2:210559875 [GRCh37]
Chr2:2q34		 uncertain significance
NM_001375505.1(MAP2):c.3821C>A (p.Pro1274Gln) single nucleotide variant Inborn genetic diseases [RCV003186591] Chr2:209695991 [GRCh38]
Chr2:210560715 [GRCh37]
Chr2:2q34		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:4674
Count of miRNA genes:1237
Interacting mature miRNAs:1583
Transcripts:ENST00000199940, ENST00000360351, ENST00000361559, ENST00000392193, ENST00000392194, ENST00000445941, ENST00000447185, ENST00000452717, ENST00000461253, ENST00000464007, ENST00000471619, ENST00000473543, ENST00000475600, ENST00000478233, ENST00000481649, ENST00000482864
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

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

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

Markers in Region
D2S1369  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372210,543,979 - 210,544,248UniSTSGRCh37
Build 362210,252,224 - 210,252,493RGDNCBI36
Celera2204,311,779 - 204,312,044RGD
Cytogenetic Map2q34-q35UniSTS
HuRef2202,389,290 - 202,389,559UniSTS
Marshfield Genetic Map2206.13UniSTS
Marshfield Genetic Map2206.13RGD
TNG Radiation Hybrid Map2115728.0UniSTS
deCODE Assembly Map2206.51UniSTS
Whitehead-RH Map2975.9UniSTS
Whitehead-YAC Contig Map2 UniSTS
NCBI RH Map21553.1UniSTS
RH48276  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372210,352,358 - 210,352,509UniSTSGRCh37
Build 362210,060,603 - 210,060,754RGDNCBI36
Celera2204,120,177 - 204,120,328RGD
Cytogenetic Map2q34-q35UniSTS
HuRef2202,197,519 - 202,197,670UniSTS
GeneMap99-GB4 RH Map2650.64UniSTS
WI-14008  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372210,596,360 - 210,596,509UniSTSGRCh37
Build 362210,304,605 - 210,304,754RGDNCBI36
Celera2204,364,156 - 204,364,305RGD
Cytogenetic Map2q34-q35UniSTS
HuRef2202,441,161 - 202,441,310UniSTS
GeneMap99-GB4 RH Map2651.17UniSTS
Whitehead-RH Map2978.7UniSTS
NCBI RH Map21553.1UniSTS
SHGC-81013  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372210,445,681 - 210,445,957UniSTSGRCh37
Build 362210,153,926 - 210,154,202RGDNCBI36
Celera2204,213,493 - 204,213,769RGD
Cytogenetic Map2q34-q35UniSTS
HuRef2202,290,920 - 202,291,196UniSTS
TNG Radiation Hybrid Map2115796.0UniSTS
RH118485  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372210,426,432 - 210,426,636UniSTSGRCh37
Build 362210,134,677 - 210,134,881RGDNCBI36
Celera2204,194,238 - 204,194,442RGD
Cytogenetic Map2q34-q35UniSTS
HuRef2202,271,669 - 202,271,873UniSTS
TNG Radiation Hybrid Map2115796.0UniSTS
G62667  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372210,341,478 - 210,341,755UniSTSGRCh37
Build 362210,049,723 - 210,050,000RGDNCBI36
Celera2204,109,289 - 204,109,566RGD
Cytogenetic Map2q34-q35UniSTS
HuRef2202,186,630 - 202,186,907UniSTS
TNG Radiation Hybrid Map2115556.0UniSTS
GDB:197515  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372210,560,465 - 210,561,765UniSTSGRCh37
Build 362210,268,710 - 210,270,010RGDNCBI36
Celera2204,328,261 - 204,329,561RGD
Cytogenetic Map2q34-q35UniSTS
HuRef2202,405,260 - 202,406,560UniSTS
SHGC-155562  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372210,492,433 - 210,492,624UniSTSGRCh37
Build 362210,200,678 - 210,200,869RGDNCBI36
Celera2204,260,232 - 204,260,423RGD
Cytogenetic Map2q34-q35UniSTS
HuRef2202,337,749 - 202,337,940UniSTS
TNG Radiation Hybrid Map2115811.0UniSTS
D2S1366  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372210,447,749 - 210,447,962UniSTSGRCh37
Build 362210,155,994 - 210,156,207RGDNCBI36
Celera2204,215,545 - 204,215,760RGD
Cytogenetic Map2q34-q35UniSTS
HuRef2202,292,972 - 202,293,193UniSTS
Whitehead-RH Map2979.8UniSTS
Whitehead-YAC Contig Map2 UniSTS
D2S241E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372210,494,266 - 210,494,412UniSTSGRCh37
Build 362210,202,511 - 210,202,657RGDNCBI36
Celera2204,262,065 - 204,262,211RGD
HuRef2202,339,582 - 202,339,728UniSTS
RH66399  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372210,598,522 - 210,598,681UniSTSGRCh37
Build 362210,306,767 - 210,306,926RGDNCBI36
Celera2204,366,316 - 204,366,475RGD
Cytogenetic Map2q34-q35UniSTS
HuRef2202,443,321 - 202,443,480UniSTS
GeneMap99-GB4 RH Map2645.82UniSTS
GDB:372046  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372210,334,320 - 210,334,551UniSTSGRCh37
Build 362210,042,565 - 210,042,796RGDNCBI36
Celera2204,102,129 - 204,102,360RGD
Cytogenetic Map2q34-q35UniSTS
HuRef2202,179,470 - 202,179,701UniSTS
STS-U01828  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372210,595,158 - 210,595,350UniSTSGRCh37
Build 362210,303,403 - 210,303,595RGDNCBI36
Celera2204,362,954 - 204,363,146RGD
Cytogenetic Map2q34-q35UniSTS
HuRef2202,439,959 - 202,440,151UniSTS
SHGC-31054  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372210,555,850 - 210,555,984UniSTSGRCh37
Build 362210,264,095 - 210,264,229RGDNCBI36
Celera2204,323,646 - 204,323,780RGD
Cytogenetic Map2q34-q35UniSTS
Cytogenetic Map2q34UniSTS
HuRef2202,400,645 - 202,400,779UniSTS
GeneMap99-GB4 RH Map2647.82UniSTS
Whitehead-RH Map2975.7UniSTS
NCBI RH Map21553.1UniSTS
GeneMap99-G3 RH Map29098.0UniSTS
MAP2  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372210,598,633 - 210,598,782UniSTSGRCh37
Celera2204,366,427 - 204,366,576UniSTS
HuRef2202,443,432 - 202,443,581UniSTS


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
High 1 1
Medium 191 941 807 55 56 38 1595 181 3140 64 119 1013 21 7 1237
Low 1985 1277 810 477 521 336 2498 1716 577 320 1282 569 151 1 1195 1301 1
Below cutoff 209 755 106 90 1030 90 260 286 9 33 37 22 2 250 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_052836 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001039538 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001363910 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001363911 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001363913 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375474 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375493 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375494 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375495 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375496 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375497 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375498 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375499 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375500 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375501 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375502 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375503 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375504 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375505 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375506 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375507 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375508 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375509 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375510 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375526 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375527 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375528 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375529 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375530 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375531 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375532 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375533 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375534 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375535 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375536 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375537 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375538 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375539 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375540 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375541 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375542 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375543 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375544 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375545 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375546 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375548 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375551 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375552 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375553 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375554 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375555 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375556 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375557 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375558 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375559 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375583 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_002374 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_031845 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_031847 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_164694 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_164695 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_164696 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_164697 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_164698 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_164699 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005246565 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005246566 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011511195 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011511196 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011511197 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017004112 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017004113 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017004114 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017004116 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017004122 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017004128 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017004129 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017004130 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017004131 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017004138 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024452893 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024452894 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024452895 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024452896 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024452897 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024452899 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024452902 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024452906 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024452907 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047444386 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047444387 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047444388 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047444389 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047444390 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047444391 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047444392 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047444393 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342083 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342084 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342085 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342086 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342087 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342088 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342089 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342090 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342091 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342092 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342093 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342094 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342095 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342096 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342097 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342098 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342099 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342100 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342101 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342102 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342103 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342104 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342105 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342106 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054342107 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB209330 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC006385 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC019106 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC079833 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC108072 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF088065 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AH004878 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK055674 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK056148 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK291446 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK307603 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL833567 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AV718243 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC027583 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC038857 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC066648 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC110423 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC117123 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC143245 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX431335 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX474027 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX485448 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX490896 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471063 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CK903071 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068276 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ386449 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M25668 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  S76756 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U01828 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U89329 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U89330 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000199940   ⟹   ENSP00000199940
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2209,424,058 - 209,730,518 (+)Ensembl
RefSeq Acc Id: ENST00000360351   ⟹   ENSP00000353508
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2209,579,421 - 209,734,118 (+)Ensembl
RefSeq Acc Id: ENST00000361559   ⟹   ENSP00000355290
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2209,579,431 - 209,730,523 (+)Ensembl
RefSeq Acc Id: ENST00000392193   ⟹   ENSP00000376031
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2209,579,315 - 209,678,628 (+)Ensembl
RefSeq Acc Id: ENST00000392194   ⟹   ENSP00000376032
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2209,580,041 - 209,734,118 (+)Ensembl
RefSeq Acc Id: ENST00000445941   ⟹   ENSP00000409969
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2209,579,609 - 209,693,625 (+)Ensembl
RefSeq Acc Id: ENST00000447185   ⟹   ENSP00000392164
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2209,653,171 - 209,730,397 (+)Ensembl
RefSeq Acc Id: ENST00000452717   ⟹   ENSP00000388824
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2209,653,393 - 209,705,690 (+)Ensembl
RefSeq Acc Id: ENST00000461253
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2209,684,633 - 209,693,162 (+)Ensembl
RefSeq Acc Id: ENST00000464007
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2209,705,382 - 209,710,161 (+)Ensembl
RefSeq Acc Id: ENST00000471619
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2209,661,465 - 209,710,264 (+)Ensembl
RefSeq Acc Id: ENST00000473543
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2209,709,954 - 209,710,812 (+)Ensembl
RefSeq Acc Id: ENST00000475600
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2209,696,314 - 209,729,868 (+)Ensembl
RefSeq Acc Id: ENST00000478233
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2209,705,580 - 209,710,579 (+)Ensembl
RefSeq Acc Id: ENST00000481649
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2209,690,603 - 209,692,792 (+)Ensembl
RefSeq Acc Id: ENST00000482864
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2209,661,515 - 209,696,748 (+)Ensembl
RefSeq Acc Id: ENST00000673860   ⟹   ENSP00000501117
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2209,579,609 - 209,734,118 (+)Ensembl
RefSeq Acc Id: ENST00000682079   ⟹   ENSP00000507035
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2209,424,047 - 209,734,112 (+)Ensembl
RefSeq Acc Id: ENST00000704357   ⟹   ENSP00000515868
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2209,424,047 - 209,734,147 (+)Ensembl
RefSeq Acc Id: NM_001039538   ⟹   NP_001034627
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,424,047 - 209,734,112 (+)NCBI
GRCh372210,288,733 - 210,598,842 (+)NCBI
Build 362209,997,016 - 210,307,079 (+)NCBI Archive
HuRef2202,133,889 - 202,443,633 (+)ENTREZGENE
CHM1_12210,294,619 - 210,604,654 (+)NCBI
T2T-CHM13v2.02209,904,237 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001363910   ⟹   NP_001350839
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,424,047 - 209,734,112 (+)NCBI
T2T-CHM13v2.02209,904,237 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001363911   ⟹   NP_001350840
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,579,607 - 209,734,112 (+)NCBI
T2T-CHM13v2.02210,059,746 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001363913   ⟹   NP_001350842
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,579,332 - 209,734,112 (+)NCBI
T2T-CHM13v2.02210,059,471 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375474   ⟹   NP_001362403
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,424,047 - 209,734,112 (+)NCBI
T2T-CHM13v2.02209,904,237 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375493   ⟹   NP_001362422
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,424,047 - 209,734,112 (+)NCBI
T2T-CHM13v2.02209,904,237 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375494   ⟹   NP_001362423
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,424,047 - 209,710,814 (+)NCBI
T2T-CHM13v2.02209,904,237 - 210,190,927 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375495   ⟹   NP_001362424
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,424,047 - 209,734,112 (+)NCBI
T2T-CHM13v2.02209,904,237 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375496   ⟹   NP_001362425
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,424,047 - 209,734,112 (+)NCBI
T2T-CHM13v2.02209,904,237 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375497   ⟹   NP_001362426
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,424,047 - 209,734,112 (+)NCBI
T2T-CHM13v2.02209,904,237 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375498   ⟹   NP_001362427
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,424,047 - 209,734,112 (+)NCBI
T2T-CHM13v2.02209,904,237 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375499   ⟹   NP_001362428
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,424,047 - 209,734,112 (+)NCBI
T2T-CHM13v2.02209,904,237 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375500   ⟹   NP_001362429
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,424,047 - 209,710,814 (+)NCBI
T2T-CHM13v2.02209,904,237 - 210,190,927 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375501   ⟹   NP_001362430
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,424,047 - 209,734,112 (+)NCBI
T2T-CHM13v2.02209,904,237 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375502   ⟹   NP_001362431
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,424,047 - 209,734,112 (+)NCBI
T2T-CHM13v2.02209,904,237 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375503   ⟹   NP_001362432
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,424,047 - 209,734,112 (+)NCBI
T2T-CHM13v2.02209,904,237 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375504   ⟹   NP_001362433
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,424,047 - 209,734,112 (+)NCBI
T2T-CHM13v2.02209,904,237 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375505   ⟹   NP_001362434
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,424,047 - 209,734,112 (+)NCBI
T2T-CHM13v2.02209,904,237 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375506   ⟹   NP_001362435
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,424,047 - 209,734,112 (+)NCBI
T2T-CHM13v2.02209,904,237 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375507   ⟹   NP_001362436
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,424,047 - 209,734,112 (+)NCBI
T2T-CHM13v2.02209,904,237 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375508   ⟹   NP_001362437
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,424,047 - 209,734,112 (+)NCBI
T2T-CHM13v2.02209,904,237 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375509   ⟹   NP_001362438
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,579,332 - 209,734,112 (+)NCBI
T2T-CHM13v2.02210,059,471 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375510   ⟹   NP_001362439
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,579,332 - 209,734,112 (+)NCBI
T2T-CHM13v2.02210,059,471 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375526   ⟹   NP_001362455
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,579,332 - 209,734,112 (+)NCBI
T2T-CHM13v2.02210,059,471 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375527   ⟹   NP_001362456
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,579,332 - 209,734,112 (+)NCBI
T2T-CHM13v2.02210,059,471 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375528   ⟹   NP_001362457
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,579,332 - 209,734,112 (+)NCBI
T2T-CHM13v2.02210,059,471 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375529   ⟹   NP_001362458
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,579,332 - 209,734,112 (+)NCBI
T2T-CHM13v2.02210,059,471 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375530   ⟹   NP_001362459
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,579,607 - 209,734,112 (+)NCBI
T2T-CHM13v2.02210,059,746 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375531   ⟹   NP_001362460
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,579,607 - 209,734,112 (+)NCBI
T2T-CHM13v2.02210,059,746 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375532   ⟹   NP_001362461
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,579,607 - 209,734,112 (+)NCBI
T2T-CHM13v2.02210,059,746 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375533   ⟹   NP_001362462
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,579,607 - 209,734,112 (+)NCBI
T2T-CHM13v2.02210,059,746 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375534   ⟹   NP_001362463
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,579,607 - 209,734,112 (+)NCBI
T2T-CHM13v2.02210,059,746 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375535   ⟹   NP_001362464
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,579,607 - 209,734,112 (+)NCBI
T2T-CHM13v2.02210,059,746 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375536   ⟹   NP_001362465
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,579,607 - 209,734,112 (+)NCBI
T2T-CHM13v2.02210,059,746 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375537   ⟹   NP_001362466
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,579,607 - 209,734,112 (+)NCBI
T2T-CHM13v2.02210,059,746 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375538   ⟹   NP_001362467
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,579,607 - 209,734,112 (+)NCBI
T2T-CHM13v2.02210,059,746 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375539   ⟹   NP_001362468
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,579,607 - 209,734,112 (+)NCBI
T2T-CHM13v2.02210,059,746 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375540   ⟹   NP_001362469
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,579,607 - 209,734,112 (+)NCBI
T2T-CHM13v2.02210,059,746 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375541   ⟹   NP_001362470
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,579,607 - 209,734,112 (+)NCBI
T2T-CHM13v2.02210,059,746 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375542   ⟹   NP_001362471
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,579,607 - 209,734,112 (+)NCBI
T2T-CHM13v2.02210,059,746 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375543   ⟹   NP_001362472
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,579,607 - 209,734,112 (+)NCBI
T2T-CHM13v2.02210,059,746 - 210,214,222 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375544   ⟹   NP_001362473
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382209,579,607 - 209,734,112 (+)NCBI
T2T-CHM13v2.02210,059,746 - 210,214,222 (+)NCBI
Sequence: