MAP7 (microtubule associated protein 7) - Rat Genome Database

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Gene: MAP7 (microtubule associated protein 7) Homo sapiens
Analyze
Symbol: MAP7
Name: microtubule associated protein 7
RGD ID: 1318886
HGNC Page HGNC:6869
Description: Predicted to enable signaling receptor binding activity. Predicted to be involved in microtubule cytoskeleton organization; protein localization to plasma membrane; and response to osmotic stress. Predicted to act upstream of or within several processes, including glycosphingolipid metabolic process; male gonad development; and response to retinoic acid. Located in cytosol and microtubule cytoskeleton.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: dJ325F22.2 (microtubule-associated protein 7 (EMAP115, E-MAP-115)); E-MAP-115; EMAP115; ensconsin; epithelial microtubule-associated protein of 115 kDa; MAP-7; microtubule-associated protein 7
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh386136,342,734 - 136,550,422 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl6136,342,281 - 136,550,819 (-)EnsemblGRCh38hg38GRCh38
GRCh376136,663,872 - 136,871,560 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 366136,705,565 - 136,913,485 (-)NCBINCBI36Build 36hg18NCBI36
Build 346136,705,565 - 136,913,485NCBI
Celera6137,404,328 - 137,612,277 (-)NCBICelera
Cytogenetic Map6q23.3NCBI
HuRef6134,227,897 - 134,436,269 (-)NCBIHuRef
CHM1_16136,925,972 - 137,134,594 (-)NCBICHM1_1
T2T-CHM13v2.06137,530,867 - 137,738,614 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
17alpha-ethynylestradiol  (ISO)
17beta-hydroxy-17-methylestra-4,9,11-trien-3-one  (EXP)
17beta-hydroxy-5alpha-androstan-3-one  (EXP)
2,2',4,4',5,5'-hexachlorobiphenyl  (ISO)
2,2',5,5'-tetrachlorobiphenyl  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2,4-dinitrotoluene  (ISO)
2,6-dinitrotoluene  (ISO)
3,3',5,5'-tetrabromobisphenol A  (ISO)
3,4-methylenedioxymethamphetamine  (ISO)
4-hydroxyphenyl retinamide  (ISO)
5-aza-2'-deoxycytidine  (EXP)
6-propyl-2-thiouracil  (ISO)
acrolein  (EXP)
aflatoxin B1  (EXP)
all-trans-retinoic acid  (EXP)
alpha-pinene  (EXP)
amitrole  (ISO)
aristolochic acid A  (EXP)
arsenous acid  (EXP)
benzo[a]pyrene  (EXP)
bisphenol A  (EXP,ISO)
butanal  (EXP)
cadmium dichloride  (EXP,ISO)
calcitriol  (EXP)
carbamazepine  (EXP)
carbon nanotube  (ISO)
CGP 52608  (EXP)
chlorpyrifos  (ISO)
ciguatoxin CTX1B  (ISO)
cisplatin  (EXP)
cobalt dichloride  (EXP,ISO)
colforsin daropate hydrochloride  (EXP)
diarsenic trioxide  (EXP)
dibutyl phthalate  (ISO)
dorsomorphin  (EXP)
epoxiconazole  (ISO)
ethanol  (ISO)
etoposide  (EXP)
fenvalerate  (ISO)
flutamide  (ISO)
FR900359  (EXP)
gentamycin  (ISO)
inulin  (ISO)
isoprenaline  (ISO)
ivermectin  (EXP)
lead(0)  (EXP)
manganese(II) chloride  (ISO)
medroxyprogesterone acetate  (EXP)
mercury dibromide  (EXP)
methapyrilene  (ISO)
methotrexate  (EXP)
methylmercury chloride  (EXP)
mitomycin C  (EXP)
ozone  (EXP)
p-chloromercuribenzoic acid  (EXP)
paracetamol  (EXP,ISO)
PCB138  (ISO)
perfluorooctane-1-sulfonic acid  (ISO)
phenylmercury acetate  (EXP)
pirinixic acid  (ISO)
potassium dichromate  (EXP,ISO)
progesterone  (EXP)
SB 431542  (EXP)
senecionine  (ISO)
sevoflurane  (ISO)
sodium arsenate  (ISO)
sodium arsenite  (EXP)
tamoxifen  (ISO)
tetrachloromethane  (ISO)
thioacetamide  (ISO)
titanium dioxide  (ISO)
trichostatin A  (EXP)
triclosan  (EXP)
triphenyl phosphate  (EXP)
tungsten  (ISO)
valproic acid  (EXP)
vancomycin  (ISO)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:7490279   PMID:8408219   PMID:9989799   PMID:11719555   PMID:12477932   PMID:12755995   PMID:12845596   PMID:14517216   PMID:14574404   PMID:15218243   PMID:15489334   PMID:16344560  
PMID:16565220   PMID:16712791   PMID:16964243   PMID:17081983   PMID:18029348   PMID:18695889   PMID:19531213   PMID:19913121   PMID:20467437   PMID:20628086   PMID:21044950   PMID:21873635  
PMID:22863883   PMID:24778252   PMID:25281560   PMID:26167880   PMID:26170170   PMID:26186194   PMID:26496610   PMID:26638075   PMID:27018634   PMID:27173435   PMID:28089446   PMID:28514442  
PMID:28515276   PMID:28986522   PMID:29089450   PMID:29117863   PMID:29459360   PMID:29490077   PMID:29507755   PMID:29845934   PMID:29880710   PMID:29991511   PMID:30770434   PMID:30804502  
PMID:30833792   PMID:31010829   PMID:31091453   PMID:31527615   PMID:31586073   PMID:31753913   PMID:32296183   PMID:32446391   PMID:32807901   PMID:33060197   PMID:33397691   PMID:33449227  
PMID:33545068   PMID:33731348   PMID:33742100   PMID:33783327   PMID:33957083   PMID:33961781   PMID:34079125   PMID:34133714   PMID:34244482   PMID:34537242   PMID:34728620   PMID:35013218  
PMID:35050657   PMID:35140242   PMID:35271311   PMID:35446349   PMID:35633546   PMID:35676659   PMID:35696571   PMID:35777956   PMID:35831314   PMID:36261182   PMID:36526897   PMID:36574265  
PMID:36779422   PMID:36779763   PMID:36931259   PMID:37314216   PMID:37499664   PMID:37506885   PMID:37616343   PMID:38113892   PMID:38431715   PMID:38580884   PMID:38803224  


Genomics

Comparative Map Data
MAP7
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh386136,342,734 - 136,550,422 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl6136,342,281 - 136,550,819 (-)EnsemblGRCh38hg38GRCh38
GRCh376136,663,872 - 136,871,560 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 366136,705,565 - 136,913,485 (-)NCBINCBI36Build 36hg18NCBI36
Build 346136,705,565 - 136,913,485NCBI
Celera6137,404,328 - 137,612,277 (-)NCBICelera
Cytogenetic Map6q23.3NCBI
HuRef6134,227,897 - 134,436,269 (-)NCBIHuRef
CHM1_16136,925,972 - 137,134,594 (-)NCBICHM1_1
T2T-CHM13v2.06137,530,867 - 137,738,614 (-)NCBIT2T-CHM13v2.0
Map7
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391020,024,666 - 20,157,336 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1020,024,217 - 20,157,336 (+)EnsemblGRCm39 Ensembl
GRCm381020,148,920 - 20,281,590 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1020,148,471 - 20,281,590 (+)EnsemblGRCm38mm10GRCm38
MGSCv371019,868,726 - 20,001,396 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361019,838,430 - 19,970,122 (+)NCBIMGSCv36mm8
Celera1020,035,994 - 20,170,438 (+)NCBICelera
Cytogenetic Map10A3NCBI
cM Map109.75NCBI
Map7
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8116,730,000 - 16,857,173 (+)NCBIGRCr8
mRatBN7.2114,910,433 - 15,037,574 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl114,910,551 - 15,037,574 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx114,664,530 - 14,792,774 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0120,666,457 - 20,794,703 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0114,890,419 - 15,017,466 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0115,620,665 - 15,748,203 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl115,620,653 - 15,748,203 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0117,189,224 - 17,293,867 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4115,440,422 - 15,553,260 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1115,505,838 - 15,553,312 (+)NCBI
Celera113,364,562 - 13,469,230 (+)NCBICelera
Cytogenetic Map1p12NCBI
Map7
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0NW_004955439404,212 - 548,732 (+)NCBIChiLan1.0ChiLan1.0
MAP7
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v25156,309,178 - 156,520,010 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan16154,207,905 - 154,417,231 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v06134,102,927 - 134,312,296 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.16138,193,074 - 138,401,302 (-)NCBIpanpan1.1PanPan1.1panPan2
MAP7
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1128,933,422 - 29,101,944 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl128,934,761 - 29,101,896 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha129,812,265 - 29,984,694 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0129,089,524 - 29,262,570 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl129,089,108 - 29,262,496 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1128,975,666 - 29,148,139 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0128,860,490 - 29,033,011 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0129,159,126 - 29,332,118 (-)NCBIUU_Cfam_GSD_1.0
Map7
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024404946124,031,925 - 124,178,791 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365603,816,209 - 3,872,488 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365603,811,021 - 3,958,007 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
MAP7
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl127,606,036 - 27,782,747 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1127,606,021 - 27,782,754 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2131,195,099 - 31,237,583 (-)NCBISscrofa10.2Sscrofa10.2susScr3
MAP7
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11336,863,546 - 37,073,861 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1336,888,942 - 37,075,818 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660409,047,411 - 9,259,093 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Map7
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248861,216,878 - 1,360,123 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248861,194,440 - 1,359,644 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in MAP7
60 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 6q23.3(chr6:135249940-136439720)x1 copy number loss See cases [RCV000052200] Chr6:135249940..136439720 [GRCh38]
Chr6:135571078..136760858 [GRCh37]
Chr6:135612771..136802551 [NCBI36]
Chr6:6q23.3		 pathogenic
NM_001198608.1(MAP7):c.2227C>T (p.Pro743Ser) single nucleotide variant Malignant melanoma [RCV000067142] Chr6:136345934 [GRCh38]
Chr6:136667072 [GRCh37]
Chr6:136708765 [NCBI36]
Chr6:6q23.3		 not provided
NM_001198608.1(MAP7):c.2162C>T (p.Pro721Leu) single nucleotide variant Malignant melanoma [RCV000067143] Chr6:136345999 [GRCh38]
Chr6:136667137 [GRCh37]
Chr6:136708830 [NCBI36]
Chr6:6q23.3		 not provided
NM_001198608.1(MAP7):c.1251G>A (p.Glu417=) single nucleotide variant Malignant melanoma [RCV000067144] Chr6:136365823 [GRCh38]
Chr6:136686961 [GRCh37]
Chr6:136728654 [NCBI36]
Chr6:6q23.3		 not provided
GRCh38/hg38 6q23.3-25.3(chr6:135358150-155455117)x3 copy number gain See cases [RCV000136826] Chr6:135358150..155455117 [GRCh38]
Chr6:135679288..155776251 [GRCh37]
Chr6:135720981..155817943 [NCBI36]
Chr6:6q23.3-25.3		 pathogenic
GRCh38/hg38 6q13-24.1(chr6:74382807-142040500)x3 copy number gain See cases [RCV000139729] Chr6:74382807..142040500 [GRCh38]
Chr6:75092523..142361637 [GRCh37]
Chr6:75149243..142403330 [NCBI36]
Chr6:6q13-24.1		 pathogenic
GRCh38/hg38 6q23.2-27(chr6:133537271-165875545)x3 copy number gain See cases [RCV000143444] Chr6:133537271..165875545 [GRCh38]
Chr6:133858409..166289033 [GRCh37]
Chr6:133900102..166209023 [NCBI36]
Chr6:6q23.2-27		 pathogenic
NM_003980.6(MAP7):c.580G>A (p.Val194Ile) single nucleotide variant not specified [RCV004311593] Chr6:136383728 [GRCh38]
Chr6:136704866 [GRCh37]
Chr6:6q23.3		 uncertain significance
GRCh37/hg19 6p25.3-q27(chr6:156975-170919482)x3 copy number gain See cases [RCV000512067] Chr6:156975..170919482 [GRCh37]
Chr6:6p25.3-q27		 pathogenic
GRCh37/hg19 6q23.2-24.2(chr6:133077239-143761582)x1 copy number loss See cases [RCV000510451] Chr6:133077239..143761582 [GRCh37]
Chr6:6q23.2-24.2		 pathogenic
GRCh37/hg19 6p25.3-q27(chr6:156975-170919482) copy number gain See cases [RCV000510595] Chr6:156975..170919482 [GRCh37]
Chr6:6p25.3-q27		 pathogenic
NM_003980.6(MAP7):c.2125G>A (p.Val709Ile) single nucleotide variant not specified [RCV004282565] Chr6:136345970 [GRCh38]
Chr6:136667108 [GRCh37]
Chr6:6q23.3		 uncertain significance
GRCh37/hg19 6q23.3-24.3(chr6:135239633-146997510) copy number loss not provided [RCV000767713] Chr6:135239633..146997510 [GRCh37]
Chr6:6q23.3-24.3		 pathogenic
GRCh37/hg19 6q23.2-23.3(chr6:131388023-137469640)x1 copy number loss not provided [RCV000682724] Chr6:131388023..137469640 [GRCh37]
Chr6:6q23.2-23.3		 pathogenic
GRCh37/hg19 6q23.2-23.3(chr6:132002460-137160850)x1 copy number loss not provided [RCV000682725] Chr6:132002460..137160850 [GRCh37]
Chr6:6q23.2-23.3		 pathogenic
GRCh37/hg19 6p25.3-q27(chr6:60107-171054786)x3 copy number gain not provided [RCV000745400] Chr6:60107..171054786 [GRCh37]
Chr6:6p25.3-q27		 pathogenic
GRCh37/hg19 6p25.3-q27(chr6:108666-170980171)x3 copy number gain not provided [RCV000745403] Chr6:108666..170980171 [GRCh37]
Chr6:6p25.3-q27		 pathogenic
GRCh37/hg19 6p25.3-q27(chr6:165632-170919470)x3 copy number gain not provided [RCV000745404] Chr6:165632..170919470 [GRCh37]
Chr6:6p25.3-q27		 pathogenic
GRCh37/hg19 6q23.3(chr6:136839188-136852895)x0 copy number loss not provided [RCV000746053] Chr6:136839188..136852895 [GRCh37]
Chr6:6q23.3		 benign
NM_003980.6(MAP7):c.67+24406A>G single nucleotide variant not specified [RCV004317099] Chr6:136525936 [GRCh38]
Chr6:136847074 [GRCh37]
Chr6:6q23.3		 uncertain significance
GRCh37/hg19 6q23.3-24.1(chr6:135936688-140660269)x1 copy number loss not provided [RCV001249247] Chr6:135936688..140660269 [GRCh37]
Chr6:6q23.3-24.1		 not provided
GRCh37/hg19 6q23.2-24.1(chr6:133817341-140038401)x1 copy number loss not provided [RCV001005848] Chr6:133817341..140038401 [GRCh37]
Chr6:6q23.2-24.1		 pathogenic
NC_000006.11:g.(?_136482728)_(137540520_?)del deletion Immunodeficiency 27A [RCV001031275] Chr6:136482728..137540520 [GRCh37]
Chr6:6q23.3		 pathogenic
GRCh37/hg19 6q23.2-24.1(chr6:133810210-140046615)x1 copy number loss not provided [RCV001537931] Chr6:133810210..140046615 [GRCh37]
Chr6:6q23.2-24.1		 pathogenic
Single allele deletion Autoinflammatory syndrome, familial, Behcet-like [RCV002247731] Chr6:134838331..142160056 [GRCh38]
Chr6:6q23.3-24.1		 pathogenic
NM_003980.6(MAP7):c.770T>A (p.Ile257Asn) single nucleotide variant not specified [RCV001824216] Chr6:136372607 [GRCh38]
Chr6:136693745 [GRCh37]
Chr6:6q23.3		 benign
NM_003980.6(MAP7):c.1618C>G (p.Arg540Gly) single nucleotide variant not specified [RCV004224876] Chr6:136361088 [GRCh38]
Chr6:136682226 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.977G>A (p.Arg326His) single nucleotide variant not specified [RCV004095824] Chr6:136366339 [GRCh38]
Chr6:136687477 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.1595G>T (p.Arg532Leu) single nucleotide variant not specified [RCV004165557] Chr6:136361111 [GRCh38]
Chr6:136682249 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.1340C>T (p.Pro447Leu) single nucleotide variant not specified [RCV004156071] Chr6:136362636 [GRCh38]
Chr6:136683774 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.469C>G (p.His157Asp) single nucleotide variant not specified [RCV004230150] Chr6:136388450 [GRCh38]
Chr6:136709588 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.476G>A (p.Arg159His) single nucleotide variant not specified [RCV004083987] Chr6:136388443 [GRCh38]
Chr6:136709581 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.230G>A (p.Arg77Gln) single nucleotide variant not specified [RCV004240688] Chr6:136411634 [GRCh38]
Chr6:136732772 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.923C>A (p.Ser308Tyr) single nucleotide variant not specified [RCV004131903] Chr6:136366393 [GRCh38]
Chr6:136687531 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.752-6G>A single nucleotide variant not specified [RCV004080825] Chr6:136372631 [GRCh38]
Chr6:136693769 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.67+24434G>T single nucleotide variant not specified [RCV004175784] Chr6:136525908 [GRCh38]
Chr6:136847046 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.1594C>T (p.Arg532Cys) single nucleotide variant not specified [RCV004102508] Chr6:136361112 [GRCh38]
Chr6:136682250 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.431G>A (p.Arg144Gln) single nucleotide variant not specified [RCV004207970] Chr6:136388488 [GRCh38]
Chr6:136709626 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.356G>A (p.Arg119Gln) single nucleotide variant not specified [RCV004132886] Chr6:136389406 [GRCh38]
Chr6:136710544 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.211C>T (p.Arg71Trp) single nucleotide variant not specified [RCV004069177] Chr6:136411653 [GRCh38]
Chr6:136732791 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.692C>T (p.Thr231Met) single nucleotide variant not specified [RCV004170372] Chr6:136377814 [GRCh38]
Chr6:136698952 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.280C>G (p.Arg94Gly) single nucleotide variant not specified [RCV004106020] Chr6:136389482 [GRCh38]
Chr6:136710620 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.50C>T (p.Ala17Val) single nucleotide variant not specified [RCV004202736] Chr6:136550359 [GRCh38]
Chr6:136871497 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.359G>C (p.Arg120Thr) single nucleotide variant not specified [RCV004203913] Chr6:136389403 [GRCh38]
Chr6:136710541 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.1165C>T (p.Pro389Ser) single nucleotide variant not specified [RCV004082072] Chr6:136365843 [GRCh38]
Chr6:136686981 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.952A>G (p.Asn318Asp) single nucleotide variant not specified [RCV004108258] Chr6:136366364 [GRCh38]
Chr6:136687502 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.644G>A (p.Arg215His) single nucleotide variant not specified [RCV004228389] Chr6:136377862 [GRCh38]
Chr6:136699000 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.1034C>T (p.Pro345Leu) single nucleotide variant not specified [RCV004138043] Chr6:136365974 [GRCh38]
Chr6:136687112 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.73G>A (p.Asp25Asn) single nucleotide variant not specified [RCV004213449] Chr6:136421794 [GRCh38]
Chr6:136742932 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.1793A>G (p.Glu598Gly) single nucleotide variant not specified [RCV004174834] Chr6:136360707 [GRCh38]
Chr6:136681845 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.1568G>A (p.Arg523Lys) single nucleotide variant not specified [RCV004142453] Chr6:136361138 [GRCh38]
Chr6:136682276 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.1667G>A (p.Arg556His) single nucleotide variant not specified [RCV004095707] Chr6:136361039 [GRCh38]
Chr6:136682177 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.203G>A (p.Arg68Gln) single nucleotide variant not specified [RCV004297400] Chr6:136411661 [GRCh38]
Chr6:136732799 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.704C>T (p.Ser235Leu) single nucleotide variant not specified [RCV004252419] Chr6:136377802 [GRCh38]
Chr6:136698940 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.439A>G (p.Met147Val) single nucleotide variant not specified [RCV004258902] Chr6:136388480 [GRCh38]
Chr6:136709618 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.1690G>T (p.Ala564Ser) single nucleotide variant not specified [RCV004280798] Chr6:136361016 [GRCh38]
Chr6:136682154 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.1153C>A (p.Pro385Thr) single nucleotide variant not specified [RCV004249538] Chr6:136365855 [GRCh38]
Chr6:136686993 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.488G>A (p.Gly163Glu) single nucleotide variant not specified [RCV004278536] Chr6:136388431 [GRCh38]
Chr6:136709569 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.1994A>C (p.Gln665Pro) single nucleotide variant not specified [RCV004316319] Chr6:136356713 [GRCh38]
Chr6:136677851 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.1643G>C (p.Arg548Pro) single nucleotide variant not specified [RCV004350968] Chr6:136361063 [GRCh38]
Chr6:136682201 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.1886C>T (p.Ala629Val) single nucleotide variant not specified [RCV004366055] Chr6:136359846 [GRCh38]
Chr6:136680984 [GRCh37]
Chr6:6q23.3		 uncertain significance
GRCh37/hg19 6q22.31-23.3(chr6:120218852-137160850)x1 copy number loss not provided [RCV003482930] Chr6:120218852..137160850 [GRCh37]
Chr6:6q22.31-23.3		 pathogenic
NM_003980.6(MAP7):c.1843G>A (p.Ala615Thr) single nucleotide variant not provided [RCV003432057] Chr6:136359992 [GRCh38]
Chr6:136681130 [GRCh37]
Chr6:6q23.3		 likely benign
NM_003980.6(MAP7):c.318G>A (p.Arg106=) single nucleotide variant not provided [RCV003432058] Chr6:136389444 [GRCh38]
Chr6:136710582 [GRCh37]
Chr6:6q23.3		 likely benign
GRCh37/hg19 6q23.2-24.2(chr6:131569837-145572239)x3 copy number gain not specified [RCV003986663] Chr6:131569837..145572239 [GRCh37]
Chr6:6q23.2-24.2		 pathogenic
GRCh37/hg19 6q22.31-25.3(chr6:119840686-156623091)x3 copy number gain not specified [RCV003986631] Chr6:119840686..156623091 [GRCh37]
Chr6:6q22.31-25.3		 pathogenic
NM_003980.6(MAP7):c.962C>T (p.Ala321Val) single nucleotide variant not specified [RCV004408510] Chr6:136366354 [GRCh38]
Chr6:136687492 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.980C>T (p.Ser327Phe) single nucleotide variant not specified [RCV004408512] Chr6:136366336 [GRCh38]
Chr6:136687474 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.1022G>A (p.Gly341Asp) single nucleotide variant not specified [RCV004408513] Chr6:136365986 [GRCh38]
Chr6:136687124 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.1411G>A (p.Ala471Thr) single nucleotide variant not specified [RCV004408514] Chr6:136362565 [GRCh38]
Chr6:136683703 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.1412C>T (p.Ala471Val) single nucleotide variant not specified [RCV004408515] Chr6:136362564 [GRCh38]
Chr6:136683702 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.1579C>G (p.Arg527Gly) single nucleotide variant not specified [RCV004408517] Chr6:136361127 [GRCh38]
Chr6:136682265 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.1885G>T (p.Ala629Ser) single nucleotide variant not specified [RCV004408518] Chr6:136359847 [GRCh38]
Chr6:136680985 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.173C>T (p.Pro58Leu) single nucleotide variant not specified [RCV004408520] Chr6:136411691 [GRCh38]
Chr6:136732829 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.221G>A (p.Arg74His) single nucleotide variant not specified [RCV004408521] Chr6:136411643 [GRCh38]
Chr6:136732781 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.234G>C (p.Glu78Asp) single nucleotide variant not specified [RCV004408522] Chr6:136411630 [GRCh38]
Chr6:136732768 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.248C>G (p.Ala83Gly) single nucleotide variant not specified [RCV004408524] Chr6:136389514 [GRCh38]
Chr6:136710652 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.412C>T (p.Arg138Cys) single nucleotide variant not specified [RCV004408525] Chr6:136388507 [GRCh38]
Chr6:136709645 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.482C>G (p.Ser161Trp) single nucleotide variant not specified [RCV004408526] Chr6:136388437 [GRCh38]
Chr6:136709575 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.529C>A (p.Pro177Thr) single nucleotide variant not specified [RCV004408527] Chr6:136383779 [GRCh38]
Chr6:136704917 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.700C>T (p.His234Tyr) single nucleotide variant not specified [RCV004408528] Chr6:136377806 [GRCh38]
Chr6:136698944 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.91G>A (p.Asp31Asn) single nucleotide variant not specified [RCV004636519] Chr6:136421776 [GRCh38]
Chr6:136742914 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.320A>T (p.Lys107Met) single nucleotide variant not specified [RCV004636520] Chr6:136389442 [GRCh38]
Chr6:136710580 [GRCh37]
Chr6:6q23.3		 uncertain significance
NM_003980.6(MAP7):c.845C>G (p.Ser282Cys) single nucleotide variant not specified [RCV004642936] Chr6:136372532 [GRCh38]
Chr6:136693670 [GRCh37]
Chr6:6q23.3		 uncertain significance
NC_000006.11:g.(?_135606783)_(138202456_?)del deletion Peroxisome biogenesis disorder 9B [RCV004578717] Chr6:135606783..138202456 [GRCh37]
Chr6:6q23.3		 pathogenic
NM_003980.6(MAP7):c.1942G>A (p.Ala648Thr) single nucleotide variant not specified [RCV004642935] Chr6:136356765 [GRCh38]
Chr6:136677903 [GRCh37]
Chr6:6q23.3		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1194
Count of miRNA genes:450
Interacting mature miRNAs:505
Transcripts:ENST00000354570, ENST00000432797, ENST00000438100, ENST00000454590, ENST00000544465
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

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

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


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
407204720GWAS853696_Hlung cancer QTL GWAS853696 (human)0.000002lung cancer6136508794136508795Human
406930792GWAS579768_Hsoluble triggering receptor expressed on myeloid cells 2 measurement QTL GWAS579768 (human)4e-12soluble triggering receptor expressed on myeloid cells 2 measurement6136540261136540262Human
406894956GWAS543932_Hpursuit maintenance gain measurement QTL GWAS543932 (human)0.000008pursuit maintenance gain measurement6136547440136547441Human

Markers in Region
D6S1849  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376136,665,037 - 136,665,291UniSTSGRCh37
Build 366136,706,730 - 136,706,984RGDNCBI36
Celera6137,405,493 - 137,405,747RGD
Cytogenetic Map6q23.3UniSTS
HuRef6134,229,514 - 134,229,768UniSTS
GeneMap99-G3 RH Map65865.0UniSTS
STS-X73882  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376136,664,804 - 136,665,053UniSTSGRCh37
Build 366136,706,497 - 136,706,746RGDNCBI36
Celera6137,405,260 - 137,405,509RGD
Cytogenetic Map6q23.3UniSTS
HuRef6134,229,281 - 134,229,530UniSTS
GeneMap99-GB4 RH Map6545.68UniSTS
WI-20359  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376136,663,895 - 136,664,192UniSTSGRCh37
Build 366136,705,588 - 136,705,885RGDNCBI36
Celera6137,404,351 - 137,404,648RGD
Cytogenetic Map6q23.3UniSTS
HuRef6134,228,372 - 134,228,669UniSTS
GeneMap99-GB4 RH Map6545.68UniSTS
Whitehead-RH Map6767.5UniSTS
RH46709  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376136,663,894 - 136,664,036UniSTSGRCh37
Build 366136,705,587 - 136,705,729RGDNCBI36
Celera6137,404,350 - 137,404,492RGD
Cytogenetic Map6q23.3UniSTS
HuRef6134,228,371 - 134,228,513UniSTS
GeneMap99-GB4 RH Map6549.03UniSTS
SHGC-77904  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376136,823,130 - 136,823,424UniSTSGRCh37
Build 366136,864,823 - 136,865,117RGDNCBI36
Celera6137,563,619 - 137,563,913RGD
Cytogenetic Map6q23.3UniSTS
HuRef6134,387,445 - 134,387,739UniSTS
TNG Radiation Hybrid Map681493.0UniSTS
SHGC-86169  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376136,761,267 - 136,761,596UniSTSGRCh37
Build 366136,802,960 - 136,803,289RGDNCBI36
Celera6137,501,749 - 137,502,078RGD
Cytogenetic Map6q23.3UniSTS
HuRef6134,325,680 - 134,326,009UniSTS
TNG Radiation Hybrid Map681503.0UniSTS
RH123523  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376136,781,791 - 136,782,127UniSTSGRCh37
Build 366136,823,484 - 136,823,820RGDNCBI36
Celera6137,522,279 - 137,522,615RGD
Cytogenetic Map6q23.3UniSTS
HuRef6134,346,105 - 134,346,441UniSTS
TNG Radiation Hybrid Map681496.0UniSTS
SHGC-132897  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376136,688,631 - 136,688,933UniSTSGRCh37
Build 366136,730,324 - 136,730,626RGDNCBI36
Celera6137,429,091 - 137,429,393RGD
Cytogenetic Map6q23.3UniSTS
HuRef6134,253,112 - 134,253,414UniSTS
TNG Radiation Hybrid Map681532.0UniSTS
D6S1865  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376136,663,988 - 136,664,122UniSTSGRCh37
GRCh376136,664,032 - 136,664,211UniSTSGRCh37
Build 366136,705,725 - 136,705,904RGDNCBI36
Celera6137,404,488 - 137,404,667RGD
Celera6137,404,444 - 137,404,578UniSTS
Cytogenetic Map6q23.3UniSTS
HuRef6134,228,465 - 134,228,599UniSTS
HuRef6134,228,509 - 134,228,688UniSTS
Stanford-G3 RH Map65562.0UniSTS
NCBI RH Map61532.6UniSTS
GeneMap99-G3 RH Map65865.0UniSTS
MAP7_917  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376136,664,406 - 136,665,270UniSTSGRCh37
Build 366136,706,099 - 136,706,963RGDNCBI36
Celera6137,404,862 - 137,405,726RGD
HuRef6134,228,883 - 134,229,747UniSTS
AL020982  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376136,723,025 - 136,723,152UniSTSGRCh37
Build 366136,764,718 - 136,764,845RGDNCBI36
Celera6137,463,514 - 137,463,641RGD
Cytogenetic Map6q23.3UniSTS
HuRef6134,287,521 - 134,287,648UniSTS
D6S1258  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376136,666,319 - 136,666,495UniSTSGRCh37
Build 366136,708,012 - 136,708,188RGDNCBI36
Celera6137,406,775 - 137,406,951RGD
Cytogenetic Map6q23.3UniSTS
HuRef6134,230,796 - 134,230,972UniSTS
Whitehead-YAC Contig Map6 UniSTS
1736  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376136,813,524 - 136,813,611UniSTSGRCh37
Build 366136,855,217 - 136,855,304RGDNCBI36
Celera6137,554,013 - 137,554,100RGD
Cytogenetic Map6q23.3UniSTS
HuRef6134,377,839 - 134,377,926UniSTS
GeneMap99-GB4 RH Map6547.89UniSTS
NCBI RH Map61538.9UniSTS
D6S1494  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376136,790,154 - 136,790,267UniSTSGRCh37
Build 366136,831,847 - 136,831,960RGDNCBI36
Celera6137,530,644 - 137,530,757RGD
Cytogenetic Map6q23.3UniSTS
HuRef6134,354,470 - 134,354,583UniSTS
Whitehead-YAC Contig Map6 UniSTS
STS-M61959  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376136,688,684 - 136,688,766UniSTSGRCh37
Build 366136,730,377 - 136,730,459RGDNCBI36
Celera6137,429,144 - 137,429,226RGD
Cytogenetic Map6q23.3UniSTS
HuRef6134,253,165 - 134,253,247UniSTS
GeneMap99-GB4 RH Map6548.3UniSTS
NCBI RH Map61538.9UniSTS
RH63710  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376136,688,684 - 136,688,759UniSTSGRCh37
Build 366136,730,377 - 136,730,452RGDNCBI36
Celera6137,429,144 - 137,429,219RGD
Cytogenetic Map6q23.3UniSTS
HuRef6134,253,165 - 134,253,240UniSTS
GeneMap99-GB4 RH Map6548.8UniSTS
D6S323E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376136,688,703 - 136,688,859UniSTSGRCh37
Build 366136,730,396 - 136,730,552RGDNCBI36
Celera6137,429,163 - 137,429,319RGD
Cytogenetic Map6q23.3UniSTS
HuRef6134,253,184 - 134,253,340UniSTS
GeneMap99-G3 RH Map65861.0UniSTS
D6S1865  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map6q23.3UniSTS
GeneMap99-G3 RH Map65861.0UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2433 2787 2242 4960 1725 2343 4 622 1890 464 2265 7226 6398 52 3728 849 1730 1610 173 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001198608 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001198609 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001198611 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001198614 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001198615 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001198616 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001198617 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001198618 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001198619 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001388328 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001388329 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001388330 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001388331 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001388332 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001388333 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001388334 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001388335 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001388336 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001388337 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001388338 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001388339 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001388340 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001388341 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001388342 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001388343 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001388344 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001388345 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001388346 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001388347 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001388348 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001388349 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001388350 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001388351 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001388352 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001388353 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_003980 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011536243 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011536246 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047419515 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054356741 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054356742 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054356743 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB073649 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI344295 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ242501 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ242502 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ420541 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK294461 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK295749 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK296483 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK296556 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK299355 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK307873 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK311114 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK311227 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK311234 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK311236 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK311270 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK312789 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK316062 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK316529 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL023284 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL024508 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL042021 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL133511 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC025777 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BF792432 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CB162980 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CD557798 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471051 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068272 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA329576 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA341792 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC325462 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC332469 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X73882 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000354570   ⟹   ENSP00000346581
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl6136,342,734 - 136,550,422 (-)Ensembl
Ensembl Acc Id: ENST00000432797   ⟹   ENSP00000414879
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl6136,342,281 - 136,526,606 (-)Ensembl
Ensembl Acc Id: ENST00000438100   ⟹   ENSP00000400790
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl6136,343,819 - 136,525,983 (-)Ensembl
Ensembl Acc Id: ENST00000454590   ⟹   ENSP00000414712
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl6136,343,543 - 136,526,472 (-)Ensembl
Ensembl Acc Id: ENST00000544465   ⟹   ENSP00000445737
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl6136,343,782 - 136,466,875 (-)Ensembl
Ensembl Acc Id: ENST00000611373   ⟹   ENSP00000482998
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl6136,343,840 - 136,526,660 (-)Ensembl
Ensembl Acc Id: ENST00000616617   ⟹   ENSP00000483511
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl6136,342,281 - 136,550,819 (-)Ensembl
Ensembl Acc Id: ENST00000617204   ⟹   ENSP00000482335
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl6136,342,281 - 136,526,213 (-)Ensembl
Ensembl Acc Id: ENST00000618822   ⟹   ENSP00000482356
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl6136,342,281 - 136,550,819 (-)Ensembl
RefSeq Acc Id: NM_001198608   ⟹   NP_001185537
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,526,582 (-)NCBI
GRCh376136,663,419 - 136,871,957 (-)ENTREZGENE
HuRef6134,227,897 - 134,436,269 (-)ENTREZGENE
CHM1_16136,925,972 - 137,109,977 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,714,773 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001198609   ⟹   NP_001185538
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,526,582 (-)NCBI
GRCh376136,663,419 - 136,871,957 (-)ENTREZGENE
HuRef6134,227,897 - 134,436,269 (-)ENTREZGENE
CHM1_16136,925,972 - 137,109,977 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,714,773 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001198611   ⟹   NP_001185540
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,526,582 (-)NCBI
GRCh376136,663,419 - 136,871,957 (-)ENTREZGENE
HuRef6134,227,897 - 134,436,269 (-)ENTREZGENE
CHM1_16136,925,972 - 137,109,977 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,714,773 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001198614   ⟹   NP_001185543
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,526,582 (-)NCBI
GRCh376136,663,419 - 136,871,957 (-)ENTREZGENE
HuRef6134,227,897 - 134,436,269 (-)ENTREZGENE
CHM1_16136,925,972 - 137,110,370 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,714,773 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001198615   ⟹   NP_001185544
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,466,878 (-)NCBI
GRCh376136,663,419 - 136,871,957 (-)ENTREZGENE
HuRef6134,227,897 - 134,436,269 (-)ENTREZGENE
CHM1_16136,925,972 - 137,050,634 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,655,076 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001198616   ⟹   NP_001185545
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,550,422 (-)NCBI
GRCh376136,663,419 - 136,871,957 (-)ENTREZGENE
HuRef6134,227,897 - 134,436,269 (-)ENTREZGENE
CHM1_16136,925,972 - 137,134,594 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,738,614 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001198617   ⟹   NP_001185546
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,550,422 (-)NCBI
GRCh376136,663,419 - 136,871,957 (-)ENTREZGENE
HuRef6134,227,897 - 134,436,269 (-)ENTREZGENE
CHM1_16136,925,972 - 137,134,594 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,738,614 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001198618   ⟹   NP_001185547
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,526,582 (-)NCBI
GRCh376136,663,419 - 136,871,957 (-)ENTREZGENE
HuRef6134,227,897 - 134,436,269 (-)ENTREZGENE
CHM1_16136,925,972 - 137,110,370 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,714,773 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001198619   ⟹   NP_001185548
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,527,144 (-)NCBI
GRCh376136,663,419 - 136,871,957 (-)ENTREZGENE
HuRef6134,227,897 - 134,436,269 (-)ENTREZGENE
CHM1_16136,925,972 - 137,110,474 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,715,335 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001388328   ⟹   NP_001375257
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,526,582 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,714,773 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001388329   ⟹   NP_001375258
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,526,582 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,714,773 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001388330   ⟹   NP_001375259
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,527,144 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,715,335 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001388331   ⟹   NP_001375260
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,526,582 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,714,773 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001388332   ⟹   NP_001375261
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,527,144 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,715,335 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001388333   ⟹   NP_001375262
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,526,582 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,714,773 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001388334   ⟹   NP_001375263
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,550,422 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,738,614 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001388335   ⟹   NP_001375264
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,550,422 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,738,614 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001388336   ⟹   NP_001375265
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,526,582 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,714,773 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001388337   ⟹   NP_001375266
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,527,144 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,715,335 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001388338   ⟹   NP_001375267
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,526,582 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,714,773 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001388339   ⟹   NP_001375268
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,550,422 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,738,614 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001388340   ⟹   NP_001375269
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,526,582 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,714,773 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001388341   ⟹   NP_001375270
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,526,582 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,714,773 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001388342   ⟹   NP_001375271
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,550,422 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,738,614 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001388343   ⟹   NP_001375272
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,526,582 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,714,773 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001388344   ⟹   NP_001375273
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,526,582 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,714,773 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001388345   ⟹   NP_001375274
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,526,582 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,714,773 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001388346   ⟹   NP_001375275
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,526,582 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,714,773 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001388347   ⟹   NP_001375276
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,550,422 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,738,614 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001388348   ⟹   NP_001375277
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,526,582 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,714,773 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001388349   ⟹   NP_001375278
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,527,144 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,715,335 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001388350   ⟹   NP_001375279
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,526,582 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,714,773 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001388351   ⟹   NP_001375280
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,527,144 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,715,335 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001388352   ⟹   NP_001375281
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,550,422 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,738,614 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001388353   ⟹   NP_001375282
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,526,582 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,714,773 (-)NCBI
Sequence:
RefSeq Acc Id: NM_003980   ⟹   NP_003971
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,550,422 (-)NCBI
GRCh376136,663,419 - 136,871,957 (-)ENTREZGENE
Build 366136,705,565 - 136,913,485 (-)NCBI Archive
HuRef6134,227,897 - 134,436,269 (-)ENTREZGENE
CHM1_16136,925,972 - 137,134,594 (-)NCBI
T2T-CHM13v2.06137,530,867 - 137,738,614 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011536243   ⟹   XP_011534545
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,466,878 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011536246   ⟹   XP_011534548
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,466,878 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047419515   ⟹   XP_047275471
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,342,734 - 136,466,878 (-)NCBI
RefSeq Acc Id: XM_054356741   ⟹   XP_054212716
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.06137,530,867 - 137,655,076 (-)NCBI
RefSeq Acc Id: XM_054356742   ⟹   XP_054212717
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.06137,530,867 - 137,655,076 (-)NCBI
RefSeq Acc Id: XM_054356743   ⟹   XP_054212718
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.06137,530,867 - 137,655,076 (-)NCBI
Protein Sequences
Protein RefSeqs NP_001185537 (Get FASTA)   NCBI Sequence Viewer  
  NP_001185538 (Get FASTA)   NCBI Sequence Viewer  
  NP_001185540 (Get FASTA)   NCBI Sequence Viewer  
  NP_001185543 (Get FASTA)   NCBI Sequence Viewer  
  NP_001185544 (Get FASTA)   NCBI Sequence Viewer  
  NP_001185545 (Get FASTA)   NCBI Sequence Viewer  
  NP_001185546 (Get FASTA)   NCBI Sequence Viewer  
  NP_001185547 (Get FASTA)   NCBI Sequence Viewer  
  NP_001185548 (Get FASTA)   NCBI Sequence Viewer  
  NP_001375257 (Get FASTA)   NCBI Sequence Viewer  
  NP_001375258 (Get FASTA)   NCBI Sequence Viewer  
  NP_001375259 (Get FASTA)   NCBI Sequence Viewer  
  NP_001375260 (Get FASTA)   NCBI Sequence Viewer  
  NP_001375261 (Get FASTA)   NCBI Sequence Viewer  
  NP_001375262 (Get FASTA)   NCBI Sequence Viewer  
  NP_001375263 (Get FASTA)   NCBI Sequence Viewer  
  NP_001375264 (Get FASTA)   NCBI Sequence Viewer  
  NP_001375265 (Get FASTA)   NCBI Sequence Viewer  
  NP_001375266 (Get FASTA)   NCBI Sequence Viewer  
  NP_001375267 (Get FASTA)   NCBI Sequence Viewer  
  NP_001375268 (Get FASTA)   NCBI Sequence Viewer  
  NP_001375269 (Get FASTA)   NCBI Sequence Viewer  
  NP_001375270 (Get FASTA)   NCBI Sequence Viewer  
  NP_001375271 (Get FASTA)   NCBI Sequence Viewer  
  NP_001375272 (Get FASTA)   NCBI Sequence Viewer  
  NP_001375273 (Get FASTA)   NCBI Sequence Viewer  
  NP_001375274 (Get FASTA)   NCBI Sequence Viewer  
  NP_001375275 (Get FASTA)   NCBI Sequence Viewer  
  NP_001375276 (Get FASTA)   NCBI Sequence Viewer  
  NP_001375277 (Get FASTA)   NCBI Sequence Viewer  
  NP_001375278 (Get FASTA)   NCBI Sequence Viewer  
  NP_001375279 (Get FASTA)   NCBI Sequence Viewer  
  NP_001375280 (Get FASTA)   NCBI Sequence Viewer  
  NP_001375281 (Get FASTA)   NCBI Sequence Viewer  
  NP_001375282 (Get FASTA)   NCBI Sequence Viewer  
  NP_003971 (Get FASTA)   NCBI Sequence Viewer  
  XP_011534545 (Get FASTA)   NCBI Sequence Viewer  
  XP_011534548 (Get FASTA)   NCBI Sequence Viewer  
  XP_047275471 (Get FASTA)   NCBI Sequence Viewer  
  XP_054212716 (Get FASTA)   NCBI Sequence Viewer  
  XP_054212717 (Get FASTA)   NCBI Sequence Viewer  
  XP_054212718 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH25777 (Get FASTA)   NCBI Sequence Viewer  
  BAG35651 (Get FASTA)   NCBI Sequence Viewer  
  BAH11776 (Get FASTA)   NCBI Sequence Viewer  
  BAH12177 (Get FASTA)   NCBI Sequence Viewer  
  BAH12369 (Get FASTA)   NCBI Sequence Viewer  
  BAH12386 (Get FASTA)   NCBI Sequence Viewer  
  BAH13013 (Get FASTA)   NCBI Sequence Viewer  
  BAH14433 (Get FASTA)   NCBI Sequence Viewer  
  BAH14900 (Get FASTA)   NCBI Sequence Viewer  
  CAA52086 (Get FASTA)   NCBI Sequence Viewer  
  CAB88030 (Get FASTA)   NCBI Sequence Viewer  
  CAB88031 (Get FASTA)   NCBI Sequence Viewer  
  EAW47944 (Get FASTA)   NCBI Sequence Viewer  
  EAW47945 (Get FASTA)   NCBI Sequence Viewer  
  EAW47946 (Get FASTA)   NCBI Sequence Viewer  
  EAW47947 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000346581
  ENSP00000346581.2
  ENSP00000400790
  ENSP00000400790.2
  ENSP00000414712
  ENSP00000414712.1
  ENSP00000414879
  ENSP00000414879.2
  ENSP00000445737
  ENSP00000445737.1
  ENSP00000482335
  ENSP00000482335.1
  ENSP00000482356
  ENSP00000482356.1
  ENSP00000482998
  ENSP00000482998.1
  ENSP00000483511
  ENSP00000483511.1
GenBank Protein Q14244 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_001185546   ⟸   NM_001198617
- Peptide Label: isoform 7
- UniProtKB: B2R704 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001185545   ⟸   NM_001198616
- Peptide Label: isoform 6
- UniProtKB: B2R704 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_003971   ⟸   NM_003980
- Peptide Label: isoform 3
- UniProtKB: Q9NY82 (UniProtKB/Swiss-Prot),   Q8TAU5 (UniProtKB/Swiss-Prot),   Q7Z6S0 (UniProtKB/Swiss-Prot),   F5H1E2 (UniProtKB/Swiss-Prot),   E9PCP3 (UniProtKB/Swiss-Prot),   C9JPS0 (UniProtKB/Swiss-Prot),   B7Z9U7 (UniProtKB/Swiss-Prot),   B7Z5S7 (UniProtKB/Swiss-Prot),   B7Z400 (UniProtKB/Swiss-Prot),   B7Z290 (UniProtKB/Swiss-Prot),   Q9NY83 (UniProtKB/Swiss-Prot),   Q14244 (UniProtKB/Swiss-Prot),   B2R704 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001185548   ⟸   NM_001198619
- Peptide Label: isoform 8
- UniProtKB: B7Z3Y3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001185547   ⟸   NM_001198618
- Peptide Label: isoform 8
- UniProtKB: B7Z3Y3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001185543   ⟸   NM_001198614
- Peptide Label: isoform 1
- UniProtKB: B7ZB64 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001185540   ⟸   NM_001198611
- Peptide Label: isoform 4
- UniProtKB: B7ZB64 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001185537   ⟸   NM_001198608
- Peptide Label: isoform 1
- UniProtKB: B7ZB64 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001185538   ⟸   NM_001198609
- Peptide Label: isoform 2
- UniProtKB: A0A087WZ40 (UniProtKB/TrEMBL),   B7ZB64 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001185544   ⟸   NM_001198615
- Peptide Label: isoform 5
- UniProtKB: B2R704 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011534548   ⟸   XM_011536246
- Peptide Label: isoform X2
- UniProtKB: B2R704 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011534545   ⟸   XM_011536243
- Peptide Label: isoform X1
- UniProtKB: B2R704 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSP00000400790   ⟸   ENST00000438100
Ensembl Acc Id: ENSP00000445737   ⟸   ENST00000544465
Ensembl Acc Id: ENSP00000482998   ⟸   ENST00000611373
Ensembl Acc Id: ENSP00000414712   ⟸   ENST00000454590
Ensembl Acc Id: ENSP00000483511   ⟸   ENST00000616617
Ensembl Acc Id: ENSP00000482335   ⟸   ENST00000617204
Ensembl Acc Id: ENSP00000482356   ⟸   ENST00000618822
Ensembl Acc Id: ENSP00000346581   ⟸   ENST00000354570
Ensembl Acc Id: ENSP00000414879   ⟸   ENST00000432797
RefSeq Acc Id: NP_001375281   ⟸   NM_001388352
- Peptide Label: isoform 21
- UniProtKB: B7Z3Y3 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001375276   ⟸   NM_001388347
- Peptide Label: isoform 18
- UniProtKB: B2R704 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001375268   ⟸   NM_001388339
- Peptide Label: isoform 13
- UniProtKB: B2R704 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001375271   ⟸   NM_001388342
- Peptide Label: isoform 14
- UniProtKB: B2R704 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001375263   ⟸   NM_001388334
- Peptide Label: isoform 10
- UniProtKB: B2R704 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001375264   ⟸   NM_001388335
- Peptide Label: isoform 11
- UniProtKB: B2R704 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001375280   ⟸   NM_001388351
- Peptide Label: isoform 20
- UniProtKB: B7Z3Y3 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001375266   ⟸   NM_001388337
- Peptide Label: isoform 12
- UniProtKB: B7ZB64 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001375261   ⟸   NM_001388332
- Peptide Label: isoform 1
- UniProtKB: B7ZB64 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001375259   ⟸   NM_001388330
- Peptide Label: isoform 2
- UniProtKB: A0A087WZ40 (UniProtKB/TrEMBL),   B7ZB64 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001375278   ⟸   NM_001388349
- Peptide Label: isoform 8
- UniProtKB: B7Z3Y3 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001375277   ⟸   NM_001388348
- Peptide Label: isoform 8
- UniProtKB: B7Z3Y3 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001375270   ⟸   NM_001388341
- Peptide Label: isoform 4
- UniProtKB: B7ZB64 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001375262   ⟸   NM_001388333
- Peptide Label: isoform 1
- UniProtKB: B7ZB64 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001375258   ⟸   NM_001388329
- Peptide Label: isoform 2
- UniProtKB: A0A087WZ40 (UniProtKB/TrEMBL),   B7ZB64 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001375279   ⟸   NM_001388350
- Peptide Label: isoform 20
- UniProtKB: B7Z3Y3 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001375275   ⟸   NM_001388346
- Peptide Label: isoform 17
- UniProtKB: B7ZB64 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001375273   ⟸   NM_001388344
- Peptide Label: isoform 16
- UniProtKB: B7ZB64 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001375269   ⟸   NM_001388340
- Peptide Label: isoform 4
- UniProtKB: B7ZB64 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001375267   ⟸   NM_001388338
- Peptide Label: isoform 12
- UniProtKB: B7ZB64 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001375257   ⟸   NM_001388328
- Peptide Label: isoform 2
- UniProtKB: A0A087WZ40 (UniProtKB/TrEMBL),   B7ZB64 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001375272   ⟸   NM_001388343
- Peptide Label: isoform 15
- UniProtKB: B7ZB64 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001375274   ⟸   NM_001388345
- Peptide Label: isoform 17
- UniProtKB: B7ZB64 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001375265   ⟸   NM_001388336
- Peptide Label: isoform 12
- UniProtKB: B7ZB64 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001375282   ⟸   NM_001388353
- Peptide Label: isoform 22
RefSeq Acc Id: NP_001375260   ⟸   NM_001388331
- Peptide Label: isoform 9
- UniProtKB: B7ZB64 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047275471   ⟸   XM_047419515
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054212718   ⟸   XM_054356743
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054212717   ⟸   XM_054356742
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054212716   ⟸   XM_054356741
- Peptide Label: isoform X1

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q14244-F1-model_v2 AlphaFold Q14244 1-749 view protein structure

Promoters
RGD ID:7209229
Promoter ID:EPDNEW_H10360
Type:initiation region
Name:MAP7_1
Description:microtubule associated protein 7
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H10361  EPDNEW_H10362  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,550,419 - 136,550,479EPDNEW
RGD ID:7209231
Promoter ID:EPDNEW_H10361
Type:initiation region
Name:MAP7_3
Description:microtubule associated protein 7
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H10360  EPDNEW_H10362  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh386136,550,864 - 136,550,924EPDNEW
RGD ID:6804474
Promoter ID:HG_KWN:55149
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:NB4
Transcripts:UC010KGR.1,   UC010KGS.1,   UC010KGT.1,   UC010KGU.1,   UC010KGV.1
Position:
Human AssemblyChrPosition (strand)Source
Build 366136,889,246 - 136,889,746 (-)MPROMDB
RGD ID:6804438
Promoter ID:HG_KWN:55150
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell_12Hour,   HeLa_S3,   K562,   Lymphoblastoid
Transcripts:ENST00000345567,   NM_003980,   UC003QHA.1,   UC010KGQ.1
Position:
Human AssemblyChrPosition (strand)Source
Build 366136,913,116 - 136,913,616 (-)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:6869 AgrOrtholog
COSMIC MAP7 COSMIC
Ensembl Genes ENSG00000135525 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000354570 ENTREZGENE
  ENST00000354570.8 UniProtKB/Swiss-Prot
  ENST00000432797 ENTREZGENE
  ENST00000432797.6 UniProtKB/Swiss-Prot
  ENST00000438100 ENTREZGENE
  ENST00000438100.6 UniProtKB/Swiss-Prot
  ENST00000454590 ENTREZGENE
  ENST00000454590.5 UniProtKB/Swiss-Prot
  ENST00000544465 ENTREZGENE
  ENST00000544465.5 UniProtKB/Swiss-Prot
  ENST00000611373 ENTREZGENE
  ENST00000611373.1 UniProtKB/Swiss-Prot
  ENST00000616617 ENTREZGENE
  ENST00000616617.4 UniProtKB/Swiss-Prot
  ENST00000617204 ENTREZGENE
  ENST00000617204.4 UniProtKB/TrEMBL
  ENST00000618822 ENTREZGENE
  ENST00000618822.4 UniProtKB/Swiss-Prot
GTEx ENSG00000135525 GTEx
HGNC ID HGNC:6869 ENTREZGENE
Human Proteome Map MAP7 Human Proteome Map
InterPro MAP7_domain-containing UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MAP7_fam UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:9053 UniProtKB/Swiss-Prot
NCBI Gene 9053 ENTREZGENE
OMIM 604108 OMIM
PANTHER MICROTUBULE-ASSOCIATED PROTEIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR15073:SF4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam MAP7 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA30615 PharmGKB
UniProt A0A087WZ40 ENTREZGENE, UniProtKB/TrEMBL
  B2R704 ENTREZGENE, UniProtKB/TrEMBL
  B7Z290 ENTREZGENE
  B7Z3E1_HUMAN UniProtKB/TrEMBL
  B7Z3Y3 ENTREZGENE, UniProtKB/TrEMBL
  B7Z400 ENTREZGENE
  B7Z5S7 ENTREZGENE
  B7Z9U7 ENTREZGENE
  B7ZB64 ENTREZGENE, UniProtKB/TrEMBL
  C9JPS0 ENTREZGENE
  E9PCP3 ENTREZGENE
  F5H1E2 ENTREZGENE
  MAP7_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
  Q7Z6S0 ENTREZGENE
  Q8TAU5 ENTREZGENE
  Q9NY82 ENTREZGENE
  Q9NY83 ENTREZGENE
UniProt Secondary B7Z290 UniProtKB/Swiss-Prot
  B7Z400 UniProtKB/Swiss-Prot
  B7Z5S7 UniProtKB/Swiss-Prot
  B7Z9U7 UniProtKB/Swiss-Prot
  C9JPS0 UniProtKB/Swiss-Prot
  E9PCP3 UniProtKB/Swiss-Prot
  F5H1E2 UniProtKB/Swiss-Prot
  Q7Z6S0 UniProtKB/Swiss-Prot
  Q8TAU5 UniProtKB/Swiss-Prot
  Q9NY82 UniProtKB/Swiss-Prot
  Q9NY83 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-11-24 MAP7  microtubule associated protein 7    microtubule-associated protein 7  Symbol and/or name change 5135510 APPROVED