NAV2 (neuron navigator 2) - Rat Genome Database

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Gene: NAV2 (neuron navigator 2) Homo sapiens
Analyze
Symbol: NAV2
Name: neuron navigator 2
RGD ID: 1320655
HGNC Page HGNC:15997
Description: Enables 3'-5' DNA helicase activity. Predicted to be involved in cerebellar cortex development. Predicted to act upstream of or within several processes, including cranial nerve development; sensory perception of smell; and sensory perception of sound. Located in nucleoplasm.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: FLJ10633; FLJ11030; FLJ23707; FLJ77876; HELAD1; helicase APC down-regulated 1; helicase, APC down-regulated 1; KIAA1419; POMFIL2; pore membrane and/or filament interacting like protein 2; pore membrane and/or filament-interacting-like protein 2; RAINB1; retinoic acid inducible gene in neuroblastoma 1; retinoic acid inducible in neuroblastoma 1; steerin-2; STEERIN2; unc-53 homolog 2; UNC53H2
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
GRCh381119,345,236 - 20,121,601 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1119,350,724 - 20,121,601 (+)EnsemblGRCh38hg38GRCh38
GRCh371119,366,783 - 20,143,147 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361119,691,488 - 20,099,723 (+)NCBINCBI36Build 36hg18NCBI36
Build 341119,691,487 - 20,099,722NCBI
Celera1119,505,019 - 20,275,779 (+)NCBICelera
Cytogenetic Map11p15.1NCBI
HuRef1119,056,089 - 19,826,507 (+)NCBIHuRef
CHM1_11119,371,529 - 20,143,061 (+)NCBICHM1_1
T2T-CHM13v2.01119,465,285 - 20,242,238 (+)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
(1->4)-beta-D-glucan  (ISO)
1,2-dichloroethane  (ISO)
17beta-estradiol  (EXP)
2,2',4,4',5,5'-hexachlorobiphenyl  (ISO)
2,2',5,5'-tetrachlorobiphenyl  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
2,3,7,8-Tetrachlorodibenzofuran  (ISO)
3,3',4,4',5-pentachlorobiphenyl  (ISO)
3-isobutyl-1-methyl-7H-xanthine  (EXP)
4,4'-sulfonyldiphenol  (ISO)
4-hydroxyphenyl retinamide  (ISO)
6-propyl-2-thiouracil  (ISO)
acetamide  (ISO)
acrolein  (EXP)
actinomycin D  (EXP)
aflatoxin B1  (EXP)
all-trans-retinoic acid  (EXP)
alpha-Zearalanol  (ISO)
ammonium chloride  (ISO)
amphetamine  (ISO)
arsane  (EXP)
arsenic atom  (EXP)
arsenite(3-)  (EXP)
benzo[a]pyrene  (EXP)
benzo[a]pyrene diol epoxide I  (EXP)
benzo[e]pyrene  (EXP)
beta-naphthoflavone  (EXP)
bisphenol A  (EXP,ISO)
bisphenol F  (EXP)
cadmium dichloride  (ISO)
caffeine  (EXP)
carbon nanotube  (ISO)
CGP 52608  (EXP)
chloroprene  (ISO)
chlorpyrifos  (ISO)
cisplatin  (EXP)
cobalt dichloride  (EXP,ISO)
copper(II) sulfate  (EXP)
coumarin  (EXP)
crocidolite asbestos  (EXP)
cyclosporin A  (EXP)
cytarabine  (EXP)
decabromodiphenyl ether  (ISO)
dexamethasone  (EXP)
dicrotophos  (EXP)
dimethylarsinous acid  (EXP)
diuron  (ISO)
dorsomorphin  (EXP)
elemental selenium  (EXP)
endosulfan  (ISO)
epoxiconazole  (ISO)
ethanol  (EXP)
folic acid  (ISO)
FR900359  (EXP)
gentamycin  (ISO)
glycidyl methacrylate  (EXP)
hydrogen peroxide  (EXP)
indometacin  (EXP)
isobutanol  (EXP)
leflunomide  (EXP)
lipopolysaccharide  (EXP)
manganese(II) chloride  (ISO)
methapyrilene  (EXP)
methoxychlor  (ISO)
methylmercury chloride  (EXP)
nickel atom  (EXP)
nickel dichloride  (EXP)
nitrofen  (ISO)
ozone  (EXP)
paracetamol  (EXP,ISO)
paraquat  (ISO)
PCB138  (ISO)
perfluorohexanesulfonic acid  (ISO)
perfluorononanoic acid  (EXP)
perfluorooctane-1-sulfonic acid  (ISO)
perfluorooctanoic acid  (ISO)
phenobarbital  (ISO)
phenylmercury acetate  (EXP)
PhIP  (EXP)
potassium dichromate  (ISO)
quercetin  (EXP)
raloxifene  (EXP)
S-(1,2-dichlorovinyl)-L-cysteine  (EXP)
SB 431542  (EXP)
selenium atom  (EXP)
silicon dioxide  (EXP,ISO)
sodium arsenite  (EXP)
Soman  (ISO)
succimer  (ISO)
tamoxifen  (EXP,ISO)
temozolomide  (EXP)
trichostatin A  (EXP)
triphenyl phosphate  (ISO)
triptonide  (ISO)
valproic acid  (EXP,ISO)
vinclozolin  (ISO)
vorinostat  (EXP)
zoledronic acid  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
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:8889549   PMID:10718198   PMID:10737800   PMID:11904404   PMID:12062803   PMID:12079279   PMID:12168954   PMID:12214280   PMID:12477932   PMID:14702039   PMID:15031288   PMID:15158073  
PMID:15489334   PMID:16189514   PMID:16964243   PMID:17081983   PMID:18029348   PMID:18937294   PMID:20379614   PMID:20936779   PMID:21873635   PMID:22174851   PMID:23251661   PMID:23703321  
PMID:24161943   PMID:25065758   PMID:25416956   PMID:25468996   PMID:25910212   PMID:26871637   PMID:27107014   PMID:28643014   PMID:28778446   PMID:29507755   PMID:30021884   PMID:30639242  
PMID:30945288   PMID:30997569   PMID:31586073   PMID:31602702   PMID:33931978   PMID:33961781   PMID:34079125   PMID:34591612   PMID:34732716   PMID:35271311   PMID:35748872   PMID:35944360  
PMID:36774506   PMID:36931259   PMID:38152138  


Genomics

Comparative Map Data
NAV2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381119,345,236 - 20,121,601 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1119,350,724 - 20,121,601 (+)EnsemblGRCh38hg38GRCh38
GRCh371119,366,783 - 20,143,147 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361119,691,488 - 20,099,723 (+)NCBINCBI36Build 36hg18NCBI36
Build 341119,691,487 - 20,099,722NCBI
Celera1119,505,019 - 20,275,779 (+)NCBICelera
Cytogenetic Map11p15.1NCBI
HuRef1119,056,089 - 19,826,507 (+)NCBIHuRef
CHM1_11119,371,529 - 20,143,061 (+)NCBICHM1_1
T2T-CHM13v2.01119,465,285 - 20,242,238 (+)NCBIT2T-CHM13v2.0
Nav2
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39748,608,796 - 49,259,838 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl748,558,464 - 49,259,838 (+)EnsemblGRCm39 Ensembl
GRCm38748,959,063 - 49,610,090 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl748,908,716 - 49,610,090 (+)EnsemblGRCm38mm10GRCm38
MGSCv37756,214,443 - 56,865,458 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36749,232,742 - 49,322,663 (+)NCBIMGSCv36mm8
Celera744,402,885 - 45,057,893 (+)NCBICelera
Cytogenetic Map7B4NCBI
cM Map731.23NCBI
Nav2
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81107,799,968 - 108,458,546 (+)NCBIGRCr8
mRatBN7.2198,957,629 - 99,322,339 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl198,663,759 - 99,322,337 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1104,312,514 - 104,676,412 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01112,784,424 - 113,148,333 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01106,106,631 - 106,470,586 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01104,575,765 - 104,941,554 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1104,576,589 - 104,941,552 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01105,340,947 - 105,994,390 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4199,041,044 - 99,410,077 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1199,329,852 - 99,330,326 (+)NCBI
Celera193,160,898 - 93,522,785 (+)NCBICelera
Cytogenetic Map1q22NCBI
Nav2
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_004955476613,512 - 996,535 (+)EnsemblChiLan1.0
ChiLan1.0NW_004955476614,215 - 996,450 (+)NCBIChiLan1.0ChiLan1.0
NAV2
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2921,649,387 - 22,419,749 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11121,974,896 - 22,379,610 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01119,370,095 - 20,143,255 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11119,288,369 - 20,055,758 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1119,288,598 - 20,055,758 (+)Ensemblpanpan1.1panPan2
NAV2
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12141,458,280 - 42,181,227 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2141,458,984 - 42,177,813 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2140,930,438 - 41,658,542 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.02142,575,579 - 43,302,697 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl2142,581,349 - 43,300,905 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.12141,906,748 - 42,305,151 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02141,760,150 - 42,480,872 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02142,137,560 - 42,861,640 (+)NCBIUU_Cfam_GSD_1.0
Nav2
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494742,807,521 - 43,503,750 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_004936654740,194 - 1,119,067 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_004936654740,270 - 1,119,065 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
NAV2
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl239,266,926 - 40,078,124 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1239,263,939 - 40,083,539 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2242,202,180 - 42,246,214 (-)NCBISscrofa10.2Sscrofa10.2susScr3
NAV2
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1144,887,172 - 45,648,260 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl144,887,169 - 45,214,703 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_023666038142,222,004 - 142,987,858 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Nav2
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462476611,170,921 - 11,414,050 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462476611,056,877 - 11,417,291 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in NAV2
179 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 11p15.1(chr11:17905089-19674505)x1 copy number loss See cases [RCV000052646] Chr11:17905089..19674505 [GRCh38]
Chr11:17926636..19696051 [GRCh37]
Chr11:17883212..19652627 [NCBI36]
Chr11:11p15.1		 pathogenic
GRCh38/hg38 11p15.5-13(chr11:202758-31726224)x3 copy number gain See cases [RCV000053613] Chr11:202758..31726224 [GRCh38]
Chr11:202758..31747772 [GRCh37]
Chr11:192758..31704348 [NCBI36]
Chr11:11p15.5-13		 pathogenic
NM_001111018.1(NAV2):c.1611G>A (p.Gln537=) single nucleotide variant Malignant melanoma [RCV000069289] Chr11:19934047 [GRCh38]
Chr11:19955593 [GRCh37]
Chr11:19912169 [NCBI36]
Chr11:11p15.1		 not provided
NM_001111018.1(NAV2):c.3706C>G (p.Arg1236Gly) single nucleotide variant Malignant melanoma [RCV000069290] Chr11:20045666 [GRCh38]
Chr11:20067212 [GRCh37]
Chr11:20023788 [NCBI36]
Chr11:11p15.1		 not provided
NM_001111018.1(NAV2):c.4057T>C (p.Ser1353Pro) single nucleotide variant Malignant melanoma [RCV000062184] Chr11:20049074 [GRCh38]
Chr11:20070620 [GRCh37]
Chr11:20027196 [NCBI36]
Chr11:11p15.1		 not provided
NM_001111018.1(NAV2):c.4058C>T (p.Ser1353Phe) single nucleotide variant Malignant melanoma [RCV000062185] Chr11:20049075 [GRCh38]
Chr11:20070621 [GRCh37]
Chr11:20027197 [NCBI36]
Chr11:11p15.1		 not provided
NM_001111018.1(NAV2):c.4059C>T (p.Ser1353=) single nucleotide variant Malignant melanoma [RCV000062186] Chr11:20049076 [GRCh38]
Chr11:20070622 [GRCh37]
Chr11:20027198 [NCBI36]
Chr11:11p15.1		 not provided
NM_001111018.1(NAV2):c.6711C>G (p.Asp2237Glu) single nucleotide variant Malignant melanoma [RCV000062187] Chr11:20107725 [GRCh38]
Chr11:20129271 [GRCh37]
Chr11:20085847 [NCBI36]
Chr11:11p15.1		 not provided
NM_001111018.1(NAV2):c.75+172631G>T single nucleotide variant Lung cancer [RCV000109903] Chr11:19523658 [GRCh38]
Chr11:19545205 [GRCh37]
Chr11:11p15.1		 uncertain significance
GRCh38/hg38 11p15.1(chr11:18526222-20748125)x3 copy number gain See cases [RCV000134932] Chr11:18526222..20748125 [GRCh38]
Chr11:18547769..20769671 [GRCh37]
Chr11:18504345..20726247 [NCBI36]
Chr11:11p15.1		 uncertain significance
GRCh38/hg38 11p15.1-13(chr11:20079474-34463996)x1 copy number loss See cases [RCV000142499] Chr11:20079474..34463996 [GRCh38]
Chr11:20101020..34485543 [GRCh37]
Chr11:20057596..34442119 [NCBI36]
Chr11:11p15.1-13		 pathogenic
GRCh37/hg19 11p15.1-13(chr11:18536224-31923308)x1 copy number loss Aniridia 1 [RCV000420782] Chr11:18536224..31923308 [GRCh37]
Chr11:11p15.1-13		 pathogenic
NM_145117.5(NAV2):c.2500C>T (p.Arg834Trp) single nucleotide variant Hirschsprung disease, susceptibility to, 1 [RCV000508683]|Inborn genetic diseases [RCV002518799] Chr11:19948935 [GRCh38]
Chr11:19970481 [GRCh37]
Chr11:11p15.1		 uncertain significance
GRCh37/hg19 11p15.5-12(chr11:230615-37698540)x3 copy number gain See cases [RCV000511561] Chr11:230615..37698540 [GRCh37]
Chr11:11p15.5-12		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470) copy number gain See cases [RCV000511729] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)x3 copy number gain See cases [RCV000510881] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
NM_145117.5(NAV2):c.3139A>G (p.Ile1047Val) single nucleotide variant Inborn genetic diseases [RCV003295696] Chr11:20044212 [GRCh38]
Chr11:20065758 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.1268G>A (p.Arg423Gln) single nucleotide variant Inborn genetic diseases [RCV003297827] Chr11:19933512 [GRCh38]
Chr11:19955058 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.3431G>C (p.Ser1144Thr) single nucleotide variant Inborn genetic diseases [RCV003272411] Chr11:20045199 [GRCh38]
Chr11:20066745 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.3850A>C (p.Ser1284Arg) single nucleotide variant Inborn genetic diseases [RCV003295580] Chr11:20045618 [GRCh38]
Chr11:20067164 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.5299T>A (p.Ser1767Thr) single nucleotide variant Inborn genetic diseases [RCV003263032] Chr11:20080183 [GRCh38]
Chr11:20101729 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.3835A>G (p.Ser1279Gly) single nucleotide variant Inborn genetic diseases [RCV003251503] Chr11:20045603 [GRCh38]
Chr11:20067149 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.3415G>A (p.Gly1139Arg) single nucleotide variant Inborn genetic diseases [RCV003242791] Chr11:20045183 [GRCh38]
Chr11:20066729 [GRCh37]
Chr11:11p15.1		 uncertain significance
GRCh37/hg19 11p15.5-14.3(chr11:230615-25584362)x3 copy number gain See cases [RCV000512225] Chr11:230615..25584362 [GRCh37]
Chr11:11p15.5-14.3		 pathogenic
GRCh37/hg19 11p15.5-13(chr11:230615-31995219)x3 copy number gain See cases [RCV000512477] Chr11:230615..31995219 [GRCh37]
Chr11:11p15.5-13		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:198510-134934063)x3 copy number gain not provided [RCV000737348] Chr11:198510..134934063 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:70864-134938470)x3 copy number gain not provided [RCV000749874] Chr11:70864..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
NM_145117.5(NAV2):c.2598C>T (p.Asp866=) single nucleotide variant not provided [RCV001609613] Chr11:19949033 [GRCh38]
Chr11:19970579 [GRCh37]
Chr11:11p15.1		 benign
NM_145117.5(NAV2):c.3514G>A (p.Ala1172Thr) single nucleotide variant not provided [RCV000962428] Chr11:20045282 [GRCh38]
Chr11:20066828 [GRCh37]
Chr11:11p15.1		 benign
NM_145117.5(NAV2):c.924C>T (p.His308=) single nucleotide variant not provided [RCV000884569] Chr11:19892587 [GRCh38]
Chr11:19914133 [GRCh37]
Chr11:11p15.1		 benign
NM_145117.5(NAV2):c.3978C>T (p.Ser1326=) single nucleotide variant not provided [RCV000962429] Chr11:20048803 [GRCh38]
Chr11:20070349 [GRCh37]
Chr11:11p15.1		 benign
GRCh37/hg19 11p15.1(chr11:18894624-19554521)x3 copy number gain not provided [RCV000849349] Chr11:18894624..19554521 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.1037C>T (p.Ser346Leu) single nucleotide variant Inborn genetic diseases [RCV003239869] Chr11:19933281 [GRCh38]
Chr11:19954827 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.1352C>T (p.Thr451Ile) single nucleotide variant Inborn genetic diseases [RCV003240019] Chr11:19933596 [GRCh38]
Chr11:19955142 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.3712C>G (p.Leu1238Val) single nucleotide variant Inborn genetic diseases [RCV003273450] Chr11:20045480 [GRCh38]
Chr11:20067026 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.3278A>G (p.Asp1093Gly) single nucleotide variant Inborn genetic diseases [RCV003273036] Chr11:20045046 [GRCh38]
Chr11:20066592 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.5852G>A (p.Arg1951Gln) single nucleotide variant Inborn genetic diseases [RCV003240925] Chr11:20093135 [GRCh38]
Chr11:20114681 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.5442G>A (p.Pro1814=) single nucleotide variant not provided [RCV001620152] Chr11:20083123 [GRCh38]
Chr11:20104669 [GRCh37]
Chr11:11p15.1		 benign
NM_145117.5(NAV2):c.2520T>C (p.His840=) single nucleotide variant NAV2-related condition [RCV003966242]|not provided [RCV001594649] Chr11:19948955 [GRCh38]
Chr11:19970501 [GRCh37]
Chr11:11p15.1		 benign
NM_145117.5(NAV2):c.5379G>A (p.Ala1793=) single nucleotide variant NAV2-related condition [RCV003915846]|not provided [RCV000954634] Chr11:20083060 [GRCh38]
Chr11:20104606 [GRCh37]
Chr11:11p15.1		 benign
NM_145117.5(NAV2):c.1710A>G (p.Lys570=) single nucleotide variant not provided [RCV001595802] Chr11:19933954 [GRCh38]
Chr11:19955500 [GRCh37]
Chr11:11p15.1		 benign
NM_145117.5(NAV2):c.6580del (p.Tyr2193_Ile2194insTer) deletion NAV2-related neurodevelopmental condition [RCV002253063] Chr11:20103660 [GRCh38]
Chr11:20125206 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.1675C>G (p.Pro559Ala) single nucleotide variant Inborn genetic diseases [RCV003101380]|See cases [RCV002253136] Chr11:19933919 [GRCh38]
Chr11:19955465 [GRCh37]
Chr11:11p15.1		 uncertain significance
GRCh37/hg19 11p15.5-13(chr11:235934-33826995)x3 copy number gain not provided [RCV001006372] Chr11:235934..33826995 [GRCh37]
Chr11:11p15.5-13		 pathogenic
NM_145117.5(NAV2):c.931+19G>A single nucleotide variant not provided [RCV001659650] Chr11:19892613 [GRCh38]
Chr11:19914159 [GRCh37]
Chr11:11p15.1		 benign
NM_145117.5(NAV2):c.6181+7G>T single nucleotide variant NAV2-related condition [RCV003984070]|not provided [RCV001688551] Chr11:20097752 [GRCh38]
Chr11:20119298 [GRCh37]
Chr11:11p15.1		 benign
NM_145117.5(NAV2):c.2577T>C (p.Asp859=) single nucleotide variant not provided [RCV001673960] Chr11:19949012 [GRCh38]
Chr11:19970558 [GRCh37]
Chr11:11p15.1		 benign
NM_145117.5(NAV2):c.5070C>T (p.Asp1690=) single nucleotide variant not provided [RCV001614808] Chr11:20077995 [GRCh38]
Chr11:20099541 [GRCh37]
Chr11:11p15.1		 benign
GRCh37/hg19 11p15.2-14.1(chr11:13970757-27565888)x3 copy number gain not provided [RCV001006388] Chr11:13970757..27565888 [GRCh37]
Chr11:11p15.2-14.1		 pathogenic
GRCh37/hg19 11p15.3-13(chr11:11053978-34732891)x3 copy number gain not provided [RCV001006387] Chr11:11053978..34732891 [GRCh37]
Chr11:11p15.3-13		 pathogenic
Single allele deletion Intellectual disability [RCV001293382] Chr11:118359328..118372573 [GRCh37]
Chr11:11p15.3-q23.3		 pathogenic
NM_145117.5(NAV2):c.3750C>T (p.Asp1250=) single nucleotide variant NAV2-related condition [RCV003984033]|not provided [RCV001655430] Chr11:20045518 [GRCh38]
Chr11:20067064 [GRCh37]
Chr11:11p15.1		 benign
NM_145117.5(NAV2):c.5011_5012del (p.Leu1672fs) microsatellite NAV2-related neurodevelopmental condition [RCV002253058] Chr11:20077577..20077578 [GRCh38]
Chr11:20099123..20099124 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.1000G>A (p.Gly334Ser) single nucleotide variant Inborn genetic diseases [RCV003296597] Chr11:19933244 [GRCh38]
Chr11:19954790 [GRCh37]
Chr11:11p15.1		 likely benign
GRCh37/hg19 11p15.5-14.2(chr11:230615-26881146)x3 copy number gain See cases [RCV002286351] Chr11:230615..26881146 [GRCh37]
Chr11:11p15.5-14.2		 pathogenic
NM_145117.5(NAV2):c.6848G>A (p.Arg2283Gln) single nucleotide variant Inborn genetic diseases [RCV003258396] Chr11:20107670 [GRCh38]
Chr11:20129216 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.4024T>A (p.Ser1342Thr) single nucleotide variant Inborn genetic diseases [RCV003259697] Chr11:20048849 [GRCh38]
Chr11:20070395 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.52G>A (p.Val18Met) single nucleotide variant Inborn genetic diseases [RCV003304907] Chr11:19713747 [GRCh38]
Chr11:19735293 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.4162G>A (p.Ala1388Thr) single nucleotide variant Inborn genetic diseases [RCV002990522] Chr11:20048987 [GRCh38]
Chr11:20070533 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.4294C>T (p.Leu1432Phe) single nucleotide variant Inborn genetic diseases [RCV002901585] Chr11:20049119 [GRCh38]
Chr11:20070665 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.1480C>T (p.Arg494Trp) single nucleotide variant Inborn genetic diseases [RCV002990379] Chr11:19933724 [GRCh38]
Chr11:19955270 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.2455G>A (p.Gly819Ser) single nucleotide variant Inborn genetic diseases [RCV002684043] Chr11:19948890 [GRCh38]
Chr11:19970436 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.4535G>A (p.Arg1512Gln) single nucleotide variant Inborn genetic diseases [RCV002841701] Chr11:20054133 [GRCh38]
Chr11:20075679 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.2755G>A (p.Gly919Arg) single nucleotide variant Inborn genetic diseases [RCV002688123] Chr11:19984234 [GRCh38]
Chr11:20005780 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.2104C>T (p.His702Tyr) single nucleotide variant Inborn genetic diseases [RCV002794452] Chr11:19939731 [GRCh38]
Chr11:19961277 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.3787G>A (p.Ala1263Thr) single nucleotide variant Inborn genetic diseases [RCV002997457] Chr11:20045555 [GRCh38]
Chr11:20067101 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.3266G>A (p.Arg1089His) single nucleotide variant Inborn genetic diseases [RCV002688078] Chr11:20045034 [GRCh38]
Chr11:20066580 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.5029A>G (p.Ile1677Val) single nucleotide variant Inborn genetic diseases [RCV002968500] Chr11:20077597 [GRCh38]
Chr11:20099143 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.4579C>T (p.Pro1527Ser) single nucleotide variant Inborn genetic diseases [RCV002684425] Chr11:20054177 [GRCh38]
Chr11:20075723 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.4517A>G (p.Asp1506Gly) single nucleotide variant Inborn genetic diseases [RCV002974224] Chr11:20054115 [GRCh38]
Chr11:20075661 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.1712G>T (p.Ser571Ile) single nucleotide variant Inborn genetic diseases [RCV002901584] Chr11:19933956 [GRCh38]
Chr11:19955502 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.996G>T (p.Glu332Asp) single nucleotide variant Inborn genetic diseases [RCV002734286] Chr11:19933240 [GRCh38]
Chr11:19954786 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.4618A>G (p.Thr1540Ala) single nucleotide variant Inborn genetic diseases [RCV002818289] Chr11:20054216 [GRCh38]
Chr11:20075762 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.6067G>A (p.Val2023Ile) single nucleotide variant Inborn genetic diseases [RCV002762759] Chr11:20097631 [GRCh38]
Chr11:20119177 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.4022C>T (p.Pro1341Leu) single nucleotide variant Inborn genetic diseases [RCV002661680] Chr11:20048847 [GRCh38]
Chr11:20070393 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.6455G>T (p.Cys2152Phe) single nucleotide variant Inborn genetic diseases [RCV002799359] Chr11:20103292 [GRCh38]
Chr11:20124838 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.988T>C (p.Ser330Pro) single nucleotide variant Inborn genetic diseases [RCV002693436] Chr11:19933232 [GRCh38]
Chr11:19954778 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.5239G>A (p.Val1747Ile) single nucleotide variant Inborn genetic diseases [RCV002797743] Chr11:20080123 [GRCh38]
Chr11:20101669 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.1850C>T (p.Ala617Val) single nucleotide variant Inborn genetic diseases [RCV002660380] Chr11:19934094 [GRCh38]
Chr11:19955640 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.6097C>T (p.Arg2033Cys) single nucleotide variant Inborn genetic diseases [RCV002705186] Chr11:20097661 [GRCh38]
Chr11:20119207 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.1769G>A (p.Arg590Gln) single nucleotide variant Inborn genetic diseases [RCV002693136] Chr11:19934013 [GRCh38]
Chr11:19955559 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.3706A>G (p.Thr1236Ala) single nucleotide variant Inborn genetic diseases [RCV002822357] Chr11:20045474 [GRCh38]
Chr11:20067020 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.6616C>T (p.Pro2206Ser) single nucleotide variant Inborn genetic diseases [RCV002738534] Chr11:20103696 [GRCh38]
Chr11:20125242 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.6737G>A (p.Arg2246Gln) single nucleotide variant Inborn genetic diseases [RCV002868426] Chr11:20105623 [GRCh38]
Chr11:20127169 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.962C>T (p.Pro321Leu) single nucleotide variant Inborn genetic diseases [RCV002659960] Chr11:19933206 [GRCh38]
Chr11:19954752 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.5723G>A (p.Arg1908Gln) single nucleotide variant Inborn genetic diseases [RCV002702286] Chr11:20092276 [GRCh38]
Chr11:20113822 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.5180G>C (p.Gly1727Ala) single nucleotide variant Inborn genetic diseases [RCV002708643] Chr11:20080064 [GRCh38]
Chr11:20101610 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.1819G>A (p.Gly607Ser) single nucleotide variant Inborn genetic diseases [RCV002665931] Chr11:19934063 [GRCh38]
Chr11:19955609 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.4712A>T (p.Asn1571Ile) single nucleotide variant Inborn genetic diseases [RCV002956522] Chr11:20055838 [GRCh38]
Chr11:20077384 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.824G>A (p.Arg275His) single nucleotide variant Inborn genetic diseases [RCV002892671] Chr11:19892487 [GRCh38]
Chr11:19914033 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.6621C>A (p.Asn2207Lys) single nucleotide variant Inborn genetic diseases [RCV002874660] Chr11:20103701 [GRCh38]
Chr11:20125247 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.6343A>G (p.Ile2115Val) single nucleotide variant Inborn genetic diseases [RCV002698196] Chr11:20101098 [GRCh38]
Chr11:20122644 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.6742C>T (p.Arg2248Cys) single nucleotide variant Inborn genetic diseases [RCV002930084] Chr11:20105628 [GRCh38]
Chr11:20127174 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.1591G>A (p.Glu531Lys) single nucleotide variant Inborn genetic diseases [RCV002709139] Chr11:19933835 [GRCh38]
Chr11:19955381 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.1700C>T (p.Pro567Leu) single nucleotide variant Inborn genetic diseases [RCV002699974] Chr11:19933944 [GRCh38]
Chr11:19955490 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.5495C>T (p.Ser1832Phe) single nucleotide variant Inborn genetic diseases [RCV002804786] Chr11:20083176 [GRCh38]
Chr11:20104722 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.4799G>A (p.Arg1600His) single nucleotide variant Inborn genetic diseases [RCV002709757] Chr11:20055925 [GRCh38]
Chr11:20077471 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.3214G>A (p.Ala1072Thr) single nucleotide variant Inborn genetic diseases [RCV002873285] Chr11:20044982 [GRCh38]
Chr11:20066528 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.2738A>T (p.Asn913Ile) single nucleotide variant Inborn genetic diseases [RCV002712735] Chr11:19984217 [GRCh38]
Chr11:20005763 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.2866G>A (p.Ala956Thr) single nucleotide variant Inborn genetic diseases [RCV002812813] Chr11:20036056 [GRCh38]
Chr11:20057602 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.1634A>G (p.Lys545Arg) single nucleotide variant Inborn genetic diseases [RCV002808055] Chr11:19933878 [GRCh38]
Chr11:19955424 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.908C>A (p.Pro303Gln) single nucleotide variant Inborn genetic diseases [RCV002896496] Chr11:19892571 [GRCh38]
Chr11:19914117 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.3911G>T (p.Gly1304Val) single nucleotide variant Inborn genetic diseases [RCV002809310] Chr11:20048736 [GRCh38]
Chr11:20070282 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.5128G>T (p.Ala1710Ser) single nucleotide variant Inborn genetic diseases [RCV002808367] Chr11:20078053 [GRCh38]
Chr11:20099599 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.740A>C (p.Gln247Pro) single nucleotide variant Inborn genetic diseases [RCV002878841] Chr11:19880097 [GRCh38]
Chr11:19901643 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.1593G>C (p.Glu531Asp) single nucleotide variant Inborn genetic diseases [RCV002808054] Chr11:19933837 [GRCh38]
Chr11:19955383 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.5300C>T (p.Ser1767Leu) single nucleotide variant Inborn genetic diseases [RCV002855310] Chr11:20080184 [GRCh38]
Chr11:20101730 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.1763G>A (p.Arg588Gln) single nucleotide variant Inborn genetic diseases [RCV002714661] Chr11:19934007 [GRCh38]
Chr11:19955553 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.497G>A (p.Gly166Glu) single nucleotide variant Inborn genetic diseases [RCV002674568] Chr11:19868983 [GRCh38]
Chr11:19890529 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.1604A>C (p.Lys535Thr) single nucleotide variant Inborn genetic diseases [RCV002835949] Chr11:19933848 [GRCh38]
Chr11:19955394 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.3505A>G (p.Met1169Val) single nucleotide variant Inborn genetic diseases [RCV002988207] Chr11:20045273 [GRCh38]
Chr11:20066819 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.4124A>G (p.His1375Arg) single nucleotide variant Inborn genetic diseases [RCV002808796] Chr11:20048949 [GRCh38]
Chr11:20070495 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.5180G>A (p.Gly1727Glu) single nucleotide variant Inborn genetic diseases [RCV002879184] Chr11:20080064 [GRCh38]
Chr11:20101610 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.674C>T (p.Pro225Leu) single nucleotide variant Inborn genetic diseases [RCV002768879] Chr11:19880031 [GRCh38]
Chr11:19901577 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.2459G>A (p.Arg820His) single nucleotide variant Inborn genetic diseases [RCV002678565] Chr11:19948894 [GRCh38]
Chr11:19970440 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.5898G>C (p.Glu1966Asp) single nucleotide variant Inborn genetic diseases [RCV002722634] Chr11:20093181 [GRCh38]
Chr11:20114727 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.3194G>T (p.Gly1065Val) single nucleotide variant Inborn genetic diseases [RCV002944381] Chr11:20044267 [GRCh38]
Chr11:20065813 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.1643A>T (p.Lys548Met) single nucleotide variant Inborn genetic diseases [RCV002655988] Chr11:19933887 [GRCh38]
Chr11:19955433 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.643G>A (p.Gly215Arg) single nucleotide variant Inborn genetic diseases [RCV002680523]|not provided [RCV003491304] Chr11:19880000 [GRCh38]
Chr11:19901546 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.3482G>A (p.Arg1161Gln) single nucleotide variant Inborn genetic diseases [RCV003277882] Chr11:20045250 [GRCh38]
Chr11:20066796 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.6516C>A (p.His2172Gln) single nucleotide variant not provided [RCV003222717] Chr11:20103353 [GRCh38]
Chr11:20124899 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.3586C>A (p.Pro1196Thr) single nucleotide variant Inborn genetic diseases [RCV003212932] Chr11:20045354 [GRCh38]
Chr11:20066900 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.2420G>A (p.Arg807Gln) single nucleotide variant Inborn genetic diseases [RCV003176236] Chr11:19948855 [GRCh38]
Chr11:19970401 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.4538C>G (p.Ser1513Cys) single nucleotide variant Inborn genetic diseases [RCV003194065] Chr11:20054136 [GRCh38]
Chr11:20075682 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.1957G>A (p.Val653Ile) single nucleotide variant Inborn genetic diseases [RCV003188313] Chr11:19934201 [GRCh38]
Chr11:19955747 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.7000T>C (p.Trp2334Arg) single nucleotide variant Inborn genetic diseases [RCV003220664] Chr11:20114631 [GRCh38]
Chr11:20136177 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.1801C>A (p.Gln601Lys) single nucleotide variant Inborn genetic diseases [RCV003261617] Chr11:19934045 [GRCh38]
Chr11:19955591 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.7102A>G (p.Met2368Val) single nucleotide variant Inborn genetic diseases [RCV003302244] Chr11:20114733 [GRCh38]
Chr11:20136279 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.1327G>T (p.Glu443Ter) single nucleotide variant not provided [RCV003222716] Chr11:19933571 [GRCh38]
Chr11:19955117 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.5358G>C (p.Lys1786Asn) single nucleotide variant Inborn genetic diseases [RCV003200329] Chr11:20083039 [GRCh38]
Chr11:20104585 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.4280A>G (p.Asn1427Ser) single nucleotide variant Inborn genetic diseases [RCV003219581] Chr11:20049105 [GRCh38]
Chr11:20070651 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.107C>A (p.Pro36His) single nucleotide variant Inborn genetic diseases [RCV003219935] Chr11:19713802 [GRCh38]
Chr11:19735348 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.2477C>T (p.Pro826Leu) single nucleotide variant Inborn genetic diseases [RCV003304816] Chr11:19948912 [GRCh38]
Chr11:19970458 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.39A>C (p.Gly13=) single nucleotide variant NAV2-related condition [RCV003919097]|not provided [RCV003394779] Chr11:19713734 [GRCh38]
Chr11:19735280 [GRCh37]
Chr11:11p15.1		 likely benign
NM_145117.5(NAV2):c.2698C>T (p.Pro900Ser) single nucleotide variant NAV2-related condition [RCV003919098]|not provided [RCV003394782] Chr11:19984177 [GRCh38]
Chr11:20005723 [GRCh37]
Chr11:11p15.1		 likely benign
NM_145117.5(NAV2):c.6418-7A>G single nucleotide variant not provided [RCV003394785] Chr11:20103248 [GRCh38]
Chr11:20124794 [GRCh37]
Chr11:11p15.1		 likely benign
NM_145117.5(NAV2):c.933G>C (p.Glu311Asp) single nucleotide variant Inborn genetic diseases [RCV003371844] Chr11:19933177 [GRCh38]
Chr11:19954723 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.6362G>A (p.Arg2121Gln) single nucleotide variant Inborn genetic diseases [RCV003372133] Chr11:20101117 [GRCh38]
Chr11:20122663 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.3154A>G (p.Thr1052Ala) single nucleotide variant Inborn genetic diseases [RCV003373173] Chr11:20044227 [GRCh38]
Chr11:20065773 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.3272C>T (p.Pro1091Leu) single nucleotide variant Inborn genetic diseases [RCV003376979] Chr11:20045040 [GRCh38]
Chr11:20066586 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.1274C>T (p.Thr425Ile) single nucleotide variant Inborn genetic diseases [RCV003367189] Chr11:19933518 [GRCh38]
Chr11:19955064 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.4364C>T (p.Ser1455Leu) single nucleotide variant Inborn genetic diseases [RCV003370260] Chr11:20049189 [GRCh38]
Chr11:20070735 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.619C>T (p.Pro207Ser) single nucleotide variant Inborn genetic diseases [RCV003374245] Chr11:19879976 [GRCh38]
Chr11:19901522 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.1774G>A (p.Gly592Arg) single nucleotide variant Inborn genetic diseases [RCV003375198] Chr11:19934018 [GRCh38]
Chr11:19955564 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.2333C>G (p.Pro778Arg) single nucleotide variant Inborn genetic diseases [RCV003373174] Chr11:19948768 [GRCh38]
Chr11:19970314 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.1354G>A (p.Val452Met) single nucleotide variant Inborn genetic diseases [RCV003347147] Chr11:19933598 [GRCh38]
Chr11:19955144 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.5360A>G (p.Lys1787Arg) single nucleotide variant Inborn genetic diseases [RCV003368972] Chr11:20083041 [GRCh38]
Chr11:20104587 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.1320G>A (p.Glu440=) single nucleotide variant NAV2-related condition [RCV003929030]|not provided [RCV003394780] Chr11:19933564 [GRCh38]
Chr11:19955110 [GRCh37]
Chr11:11p15.1		 benign|likely benign
NM_145117.5(NAV2):c.4884A>C (p.Thr1628=) single nucleotide variant not provided [RCV003394784] Chr11:20062359 [GRCh38]
Chr11:20083905 [GRCh37]
Chr11:11p15.1		 likely benign
NM_145117.5(NAV2):c.2319C>T (p.Ser773=) single nucleotide variant NAV2-related condition [RCV003954123]|not provided [RCV003394781] Chr11:19948754 [GRCh38]
Chr11:19970300 [GRCh37]
Chr11:11p15.1		 benign|likely benign
NM_145117.5(NAV2):c.3156G>A (p.Thr1052=) single nucleotide variant not provided [RCV003394783] Chr11:20044229 [GRCh38]
Chr11:20065775 [GRCh37]
Chr11:11p15.1		 likely benign
NM_145117.5(NAV2):c.333C>T (p.Leu111=) single nucleotide variant NAV2-related condition [RCV003938909]|not provided [RCV003390025] Chr11:19832549 [GRCh38]
Chr11:19854095 [GRCh37]
Chr11:11p15.1		 benign|likely benign
NM_145117.5(NAV2):c.5953G>C (p.Gly1985Arg) single nucleotide variant not provided [RCV003390026] Chr11:20095708 [GRCh38]
Chr11:20117254 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.671C>T (p.Thr224Ile) single nucleotide variant NAV2-related condition [RCV003416719] Chr11:19880028 [GRCh38]
Chr11:19901574 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.4742A>G (p.Asp1581Gly) single nucleotide variant NAV2-related condition [RCV003410528] Chr11:20055868 [GRCh38]
Chr11:20077414 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.3115C>T (p.Arg1039Ter) single nucleotide variant NAV2-related condition [RCV003400071] Chr11:20044188 [GRCh38]
Chr11:20065734 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.396G>T (p.Lys132Asn) single nucleotide variant NAV2-related condition [RCV003402803] Chr11:19842881 [GRCh38]
Chr11:19864427 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.6098G>A (p.Arg2033His) single nucleotide variant not provided [RCV003488109] Chr11:20097662 [GRCh38]
Chr11:20119208 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.1454A>G (p.Asn485Ser) single nucleotide variant not provided [RCV003488114] Chr11:19933698 [GRCh38]
Chr11:19955244 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.26A>C (p.Lys9Thr) single nucleotide variant not provided [RCV003488111] Chr11:19713721 [GRCh38]
Chr11:19735267 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.2389G>A (p.Ala797Thr) single nucleotide variant not provided [RCV003488113] Chr11:19948824 [GRCh38]
Chr11:19970370 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.5209C>T (p.Arg1737Cys) single nucleotide variant not provided [RCV003488115] Chr11:20080093 [GRCh38]
Chr11:20101639 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.4714G>T (p.Ala1572Ser) single nucleotide variant not provided [RCV003488108] Chr11:20055840 [GRCh38]
Chr11:20077386 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.2821C>T (p.Leu941Phe) single nucleotide variant not provided [RCV003488110] Chr11:20036011 [GRCh38]
Chr11:20057557 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.2713G>A (p.Val905Met) single nucleotide variant not provided [RCV003488112] Chr11:19984192 [GRCh38]
Chr11:20005738 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.5377G>A (p.Ala1793Thr) single nucleotide variant not provided [RCV003488116] Chr11:20083058 [GRCh38]
Chr11:20104604 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.1617T>C (p.Ile539=) single nucleotide variant NAV2-related condition [RCV003939301] Chr11:19933861 [GRCh38]
Chr11:19955407 [GRCh37]
Chr11:11p15.1		 benign
NM_145117.5(NAV2):c.1532C>T (p.Thr511Met) single nucleotide variant NAV2-related condition [RCV003916860] Chr11:19933776 [GRCh38]
Chr11:19955322 [GRCh37]
Chr11:11p15.1		 benign
NM_145117.5(NAV2):c.5007A>G (p.Glu1669=) single nucleotide variant NAV2-related condition [RCV003961443] Chr11:20077575 [GRCh38]
Chr11:20099121 [GRCh37]
Chr11:11p15.1		 benign
NM_145117.5(NAV2):c.5917-8A>G single nucleotide variant NAV2-related condition [RCV003961615] Chr11:20095664 [GRCh38]
Chr11:20117210 [GRCh37]
Chr11:11p15.1		 benign
NM_145117.5(NAV2):c.326G>A (p.Arg109Lys) single nucleotide variant NAV2-related condition [RCV003979502] Chr11:19832542 [GRCh38]
Chr11:19854088 [GRCh37]
Chr11:11p15.1		 benign
NM_145117.5(NAV2):c.5934C>A (p.Leu1978=) single nucleotide variant NAV2-related condition [RCV003909708] Chr11:20095689 [GRCh38]
Chr11:20117235 [GRCh37]
Chr11:11p15.1		 likely benign
NM_145117.5(NAV2):c.170C>G (p.Pro57Arg) single nucleotide variant NAV2-related condition [RCV003917263] Chr11:19713865 [GRCh38]
Chr11:19735411 [GRCh37]
Chr11:11p15.1		 benign
NM_145117.5(NAV2):c.5934C>G (p.Leu1978=) single nucleotide variant NAV2-related condition [RCV003919479] Chr11:20095689 [GRCh38]
Chr11:20117235 [GRCh37]
Chr11:11p15.1		 benign
NM_145117.5(NAV2):c.6943G>A (p.Val2315Ile) single nucleotide variant NAV2-related condition [RCV003979167] Chr11:20107765 [GRCh38]
Chr11:20129311 [GRCh37]
Chr11:11p15.1		 benign
NM_145117.5(NAV2):c.5022C>T (p.Asn1674=) single nucleotide variant NAV2-related condition [RCV003944737] Chr11:20077590 [GRCh38]
Chr11:20099136 [GRCh37]
Chr11:11p15.1		 likely benign
NM_145117.5(NAV2):c.4356C>T (p.Thr1452=) single nucleotide variant NAV2-related condition [RCV003924563] Chr11:20049181 [GRCh38]
Chr11:20070727 [GRCh37]
Chr11:11p15.1		 likely benign
NM_145117.5(NAV2):c.6187G>A (p.Ala2063Thr) single nucleotide variant NAV2-related condition [RCV003979186] Chr11:20100942 [GRCh38]
Chr11:20122488 [GRCh37]
Chr11:11p15.1		 benign
NM_145117.5(NAV2):c.3054G>T (p.Glu1018Asp) single nucleotide variant NAV2-related condition [RCV003982276] Chr11:20044127 [GRCh38]
Chr11:20065673 [GRCh37]
Chr11:11p15.1		 benign
NM_145117.5(NAV2):c.5505A>C (p.Ser1835=) single nucleotide variant NAV2-related condition [RCV003982400] Chr11:20090871 [GRCh38]
Chr11:20112417 [GRCh37]
Chr11:11p15.1		 benign
NM_145117.5(NAV2):c.6112G>A (p.Glu2038Lys) single nucleotide variant NAV2-related condition [RCV003903847] Chr11:20097676 [GRCh38]
Chr11:20119222 [GRCh37]
Chr11:11p15.1		 likely benign
NM_145117.5(NAV2):c.1762C>T (p.Arg588Trp) single nucleotide variant NAV2-related condition [RCV003897270] Chr11:19934006 [GRCh38]
Chr11:19955552 [GRCh37]
Chr11:11p15.1		 likely benign
NM_145117.5(NAV2):c.84C>A (p.Pro28=) single nucleotide variant NAV2-related condition [RCV003931390] Chr11:19713779 [GRCh38]
Chr11:19735325 [GRCh37]
Chr11:11p15.1		 benign
NM_145117.5(NAV2):c.1404G>C (p.Gln468His) single nucleotide variant NAV2-related condition [RCV003979784] Chr11:19933648 [GRCh38]
Chr11:19955194 [GRCh37]
Chr11:11p15.1		 benign
NM_145117.5(NAV2):c.4070G>A (p.Ser1357Asn) single nucleotide variant NAV2-related condition [RCV003947304] Chr11:20048895 [GRCh38]
Chr11:20070441 [GRCh37]
Chr11:11p15.1		 likely benign
NM_145117.5(NAV2):c.51C>G (p.Pro17=) single nucleotide variant NAV2-related condition [RCV003959566] Chr11:19713746 [GRCh38]
Chr11:19735292 [GRCh37]
Chr11:11p15.1		 benign
NM_145117.5(NAV2):c.5767A>G (p.Met1923Val) single nucleotide variant NAV2-related condition [RCV003924162] Chr11:20092320 [GRCh38]
Chr11:20113866 [GRCh37]
Chr11:11p15.1		 benign
NM_145117.5(NAV2):c.4297A>G (p.Ile1433Val) single nucleotide variant NAV2-related condition [RCV003917106] Chr11:20049122 [GRCh38]
Chr11:20070668 [GRCh37]
Chr11:11p15.1		 benign
NM_145117.5(NAV2):c.1267C>T (p.Arg423Trp) single nucleotide variant NAV2-related condition [RCV003977239] Chr11:19933511 [GRCh38]
Chr11:19955057 [GRCh37]
Chr11:11p15.1		 likely benign
NM_145117.5(NAV2):c.155A>G (p.Tyr52Cys) single nucleotide variant NAV2-related condition [RCV003924376] Chr11:19713850 [GRCh38]
Chr11:19735396 [GRCh37]
Chr11:11p15.1		 likely benign
NM_145117.5(NAV2):c.3391G>A (p.Gly1131Ser) single nucleotide variant NAV2-related condition [RCV003924398] Chr11:20045159 [GRCh38]
Chr11:20066705 [GRCh37]
Chr11:11p15.1		 benign
NM_145117.5(NAV2):c.4769C>T (p.Ser1590Phe) single nucleotide variant NAV2-related condition [RCV003896950] Chr11:20055895 [GRCh38]
Chr11:20077441 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.2292G>A (p.Thr764=) single nucleotide variant NAV2-related condition [RCV003924508] Chr11:19948727 [GRCh38]
Chr11:19970273 [GRCh37]
Chr11:11p15.1		 benign
NM_145117.5(NAV2):c.985G>C (p.Ala329Pro) single nucleotide variant NAV2-related condition [RCV003904186] Chr11:19933229 [GRCh38]
Chr11:19954775 [GRCh37]
Chr11:11p15.1		 likely benign
NM_145117.5(NAV2):c.2051A>C (p.Glu684Ala) single nucleotide variant NAV2-related condition [RCV003904770] Chr11:19939678 [GRCh38]
Chr11:19961224 [GRCh37]
Chr11:11p15.1		 likely benign
NM_145117.5(NAV2):c.2768+9G>A single nucleotide variant NAV2-related condition [RCV003972244] Chr11:19984256 [GRCh38]
Chr11:20005802 [GRCh37]
Chr11:11p15.1		 benign
NM_145117.5(NAV2):c.4885-7T>C single nucleotide variant NAV2-related condition [RCV003979220] Chr11:20068179 [GRCh38]
Chr11:20089725 [GRCh37]
Chr11:11p15.1		 benign
NM_145117.5(NAV2):c.3384C>T (p.Ser1128=) single nucleotide variant NAV2-related condition [RCV003921998] Chr11:20045152 [GRCh38]
Chr11:20066698 [GRCh37]
Chr11:11p15.1		 likely benign
NM_145117.5(NAV2):c.6424C>T (p.Arg2142Cys) single nucleotide variant NAV2-related condition [RCV003937169] Chr11:20103261 [GRCh38]
Chr11:20124807 [GRCh37]
Chr11:11p15.1		 likely benign
NM_145117.5(NAV2):c.472G>T (p.Ala158Ser) single nucleotide variant Inborn genetic diseases [RCV003214527] Chr11:19868958 [GRCh38]
Chr11:19890504 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.2125C>A (p.Pro709Thr) single nucleotide variant Inborn genetic diseases [RCV003195857] Chr11:19939752 [GRCh38]
Chr11:19961298 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.2291C>T (p.Thr764Met) single nucleotide variant Inborn genetic diseases [RCV003342712]|not provided [RCV003491369] Chr11:19948726 [GRCh38]
Chr11:19970272 [GRCh37]
Chr11:11p15.1		 uncertain significance
NM_145117.5(NAV2):c.1880C>G (p.Thr627Ser) single nucleotide variant NAV2-related condition [RCV003937135] Chr11:19934124 [GRCh38]
Chr11:19955670 [GRCh37]
Chr11:11p15.1		 benign
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:11178
Count of miRNA genes:1188
Interacting mature miRNAs:1471
Transcripts:ENST00000311043, ENST00000349880, ENST00000360655, ENST00000396085, ENST00000396087, ENST00000525025, ENST00000525322, ENST00000526675, ENST00000527559, ENST00000528008, ENST00000528923, ENST00000530408, ENST00000533746, ENST00000533917, ENST00000534229, ENST00000534299, ENST00000540292
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
D11S1308  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371119,650,957 - 19,651,271UniSTSGRCh37
GRCh371119,650,961 - 19,651,197UniSTSGRCh37
Build 361119,607,537 - 19,607,773RGDNCBI36
Celera1119,783,679 - 19,783,915RGD
Celera1119,783,675 - 19,783,989UniSTS
Cytogenetic Map11p15.1UniSTS
HuRef1119,334,996 - 19,335,310UniSTS
HuRef1119,335,000 - 19,335,236UniSTS
Marshfield Genetic Map1124.73RGD
Genethon Genetic Map1128.1UniSTS
TNG Radiation Hybrid Map119518.0UniSTS
deCODE Assembly Map1129.89UniSTS
GeneMap99-GB4 RH Map1175.58UniSTS
Whitehead-RH Map1163.3UniSTS
Whitehead-YAC Contig Map11 UniSTS
NCBI RH Map11129.6UniSTS
D11S899  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371119,418,925 - 19,419,011UniSTSGRCh37
Build 361119,375,501 - 19,375,587RGDNCBI36
Celera1119,551,645 - 19,551,731RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,102,716 - 19,102,808UniSTS
Marshfield Genetic Map1123.12UniSTS
Marshfield Genetic Map1123.12RGD
Genethon Genetic Map1126.5UniSTS
TNG Radiation Hybrid Map119432.0UniSTS
deCODE Assembly Map1129.35UniSTS
Stanford-G3 RH Map11785.0UniSTS
GeneMap99-GB4 RH Map1173.59UniSTS
Whitehead-YAC Contig Map11 UniSTS
NCBI RH Map11128.4UniSTS
GeneMap99-G3 RH Map11785.0UniSTS
D11S4106  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371119,977,824 - 19,978,093UniSTSGRCh37
Build 361119,934,400 - 19,934,669RGDNCBI36
Celera1120,110,499 - 20,110,768RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,661,322 - 19,661,593UniSTS
Marshfield Genetic Map1124.73RGD
Marshfield Genetic Map1124.73UniSTS
Genethon Genetic Map1128.1UniSTS
deCODE Assembly Map1132.71UniSTS
Whitehead-YAC Contig Map11 UniSTS
D11S2034  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371119,376,749 - 19,376,913UniSTSGRCh37
GRCh371119,376,869 - 19,376,976UniSTSGRCh37
Build 361119,333,325 - 19,333,489RGDNCBI36
Celera1119,509,491 - 19,509,654RGD
Celera1119,509,610 - 19,509,717UniSTS
Cytogenetic Map11p15.1UniSTS
HuRef1119,060,680 - 19,060,787UniSTS
HuRef1119,060,561 - 19,060,724UniSTS
TNG Radiation Hybrid Map119417.0UniSTS
Stanford-G3 RH Map11770.0UniSTS
RH36118  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371119,532,474 - 19,532,576UniSTSGRCh37
Build 361119,489,050 - 19,489,152RGDNCBI36
Celera1119,665,203 - 19,665,305RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,216,245 - 19,216,347UniSTS
GeneMap99-GB4 RH Map1175.58UniSTS
NCBI RH Map11129.6UniSTS
RH45581  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371120,071,892 - 20,072,096UniSTSGRCh37
Build 361120,028,468 - 20,028,672RGDNCBI36
Celera1120,204,529 - 20,204,733RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,755,238 - 19,755,442UniSTS
GeneMap99-GB4 RH Map1167.52UniSTS
NCBI RH Map11128.4UniSTS
RH12576  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371119,734,011 - 19,734,130UniSTSGRCh37
Build 361119,690,587 - 19,690,706RGDNCBI36
Celera1119,866,749 - 19,866,868RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,418,070 - 19,418,189UniSTS
GeneMap99-GB4 RH Map1167.52UniSTS
NCBI RH Map11128.4UniSTS
RH91544  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371120,139,879 - 20,140,013UniSTSGRCh37
Build 361120,096,455 - 20,096,589RGDNCBI36
Celera1120,272,512 - 20,272,646RGD
Celera1151,074,523 - 51,074,657UniSTS
Cytogenetic Map11p15.1UniSTS
HuRef1119,823,240 - 19,823,374UniSTS
GeneMap99-GB4 RH Map1167.52UniSTS
RH26949  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371119,838,209 - 19,838,317UniSTSGRCh37
Build 361119,794,785 - 19,794,893RGDNCBI36
Celera1119,970,925 - 19,971,033RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,522,105 - 19,522,213UniSTS
RH79583  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371120,066,828 - 20,067,050UniSTSGRCh37
Build 361120,023,404 - 20,023,626RGDNCBI36
Celera1120,199,469 - 20,199,691RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,750,178 - 19,750,400UniSTS
RH102763  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371120,065,441 - 20,065,591UniSTSGRCh37
Build 361120,022,017 - 20,022,167RGDNCBI36
Celera1120,198,082 - 20,198,232RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,748,791 - 19,748,941UniSTS
GeneMap99-GB4 RH Map1175.48UniSTS
RH102804  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371119,733,502 - 19,733,587UniSTSGRCh37
Build 361119,690,078 - 19,690,163RGDNCBI36
Celera1119,866,240 - 19,866,325RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,417,561 - 19,417,646UniSTS
GeneMap99-GB4 RH Map1173.59UniSTS
RH120569  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371120,049,363 - 20,049,653UniSTSGRCh37
Build 361120,005,939 - 20,006,229RGDNCBI36
Celera1120,182,001 - 20,182,291RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,732,713 - 19,733,003UniSTS
TNG Radiation Hybrid Map119714.0UniSTS
RH119298  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371119,847,719 - 19,847,999UniSTSGRCh37
Build 361119,804,295 - 19,804,575RGDNCBI36
Celera1119,980,432 - 19,980,712RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,531,611 - 19,531,891UniSTS
TNG Radiation Hybrid Map119604.0UniSTS
RH123694  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371120,031,835 - 20,032,156UniSTSGRCh37
Build 361119,988,411 - 19,988,732RGDNCBI36
Celera1120,164,494 - 20,164,815RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,715,322 - 19,715,643UniSTS
TNG Radiation Hybrid Map119685.0UniSTS
G59204  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371119,968,000 - 19,968,270UniSTSGRCh37
Build 361119,924,576 - 19,924,846RGDNCBI36
Celera1120,100,668 - 20,100,938RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,651,491 - 19,651,761UniSTS
TNG Radiation Hybrid Map119755.0UniSTS
G62943  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371119,693,530 - 19,693,817UniSTSGRCh37
Build 361119,650,106 - 19,650,393RGDNCBI36
Celera1119,826,251 - 19,826,538RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,377,577 - 19,377,864UniSTS
TNG Radiation Hybrid Map119538.0UniSTS
G63449  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371119,875,240 - 19,875,521UniSTSGRCh37
Build 361119,831,816 - 19,832,097RGDNCBI36
Celera1120,007,961 - 20,008,241RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,559,139 - 19,559,419UniSTS
TNG Radiation Hybrid Map119616.0UniSTS
D11S2970  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371120,017,834 - 20,017,951UniSTSGRCh37
Build 361119,974,410 - 19,974,527RGDNCBI36
Celera1120,150,493 - 20,150,610RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,701,321 - 19,701,438UniSTS
D11S3091  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371119,483,781 - 19,483,889UniSTSGRCh37
Build 361119,440,357 - 19,440,465RGDNCBI36
Celera1119,616,490 - 19,616,598RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,167,556 - 19,167,664UniSTS
D11S3201  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371119,464,083 - 19,464,378UniSTSGRCh37
Build 361119,420,659 - 19,420,954RGDNCBI36
Celera1119,596,796 - 19,597,091RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,147,872 - 19,148,167UniSTS
D11S3272  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371119,707,605 - 19,707,909UniSTSGRCh37
Build 361119,664,181 - 19,664,485RGDNCBI36
Celera1119,840,336 - 19,840,640RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,391,662 - 19,391,966UniSTS
D11S3611  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371119,459,280 - 19,459,622UniSTSGRCh37
Build 361119,415,856 - 19,416,198RGDNCBI36
Celera1119,591,993 - 19,592,335RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,143,069 - 19,143,411UniSTS
GDB:312742  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371169,581,109 - 69,581,348UniSTSGRCh37
GRCh371119,907,797 - 19,909,383UniSTSGRCh37
Build 361169,290,290 - 69,290,529RGDNCBI36
Celera1120,040,509 - 20,042,095UniSTS
Celera1166,878,147 - 66,878,366RGD
Cytogenetic Map12qUniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map12q14.3UniSTS
HuRef1263,777,835 - 63,779,102UniSTS
HuRef1165,873,469 - 65,873,689UniSTS
SHGC-141815  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371119,940,860 - 19,941,134UniSTSGRCh37
Build 361119,897,436 - 19,897,710RGDNCBI36
Celera1120,073,545 - 20,073,819RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,624,323 - 19,624,597UniSTS
TNG Radiation Hybrid Map119647.0UniSTS
SHGC-144693  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371119,475,507 - 19,475,782UniSTSGRCh37
Build 361119,432,083 - 19,432,358RGDNCBI36
Celera1119,608,216 - 19,608,491RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,159,283 - 19,159,558UniSTS
TNG Radiation Hybrid Map119462.0UniSTS
SHGC-147968  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371119,474,825 - 19,475,097UniSTSGRCh37
Build 361119,431,401 - 19,431,673RGDNCBI36
Celera1119,607,534 - 19,607,806RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,158,601 - 19,158,873UniSTS
TNG Radiation Hybrid Map119452.0UniSTS
RH65895  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371120,142,947 - 20,143,070UniSTSGRCh37
Build 361120,099,523 - 20,099,646RGDNCBI36
Celera1120,275,579 - 20,275,702RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,826,307 - 19,826,430UniSTS
GeneMap99-GB4 RH Map1173.59UniSTS
NCBI RH Map11128.4UniSTS
D11S1075  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371119,486,570 - 19,486,796UniSTSGRCh37
Build 361119,443,146 - 19,443,372RGDNCBI36
Celera1119,619,279 - 19,619,505RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,170,345 - 19,170,571UniSTS
D11S1034  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371119,744,466 - 19,744,727UniSTSGRCh37
Build 361119,701,042 - 19,701,303RGDNCBI36
Celera1119,877,204 - 19,877,465RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,428,525 - 19,428,786UniSTS
SHGC-155714  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371119,383,258 - 19,383,528UniSTSGRCh37
Build 361119,339,834 - 19,340,104RGDNCBI36
Celera1119,515,999 - 19,516,269RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,067,069 - 19,067,339UniSTS
TNG Radiation Hybrid Map119428.0UniSTS
SHGC-31021  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371119,734,502 - 19,734,627UniSTSGRCh37
Build 361119,691,078 - 19,691,203RGDNCBI36
Celera1119,867,240 - 19,867,365RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,418,561 - 19,418,686UniSTS
Stanford-G3 RH Map11861.0UniSTS
GeneMap99-GB4 RH Map1167.52UniSTS
Whitehead-RH Map1163.5UniSTS
GeneMap99-G3 RH Map11861.0UniSTS
D11S2296E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371119,858,927 - 19,859,157UniSTSGRCh37
Build 361119,815,503 - 19,815,733RGDNCBI36
Celera1119,991,641 - 19,991,871RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,542,820 - 19,543,050UniSTS
GeneMap99-GB4 RH Map1173.59UniSTS
NCBI RH Map11129.6UniSTS
SHGC-33456  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371120,139,994 - 20,140,121UniSTSGRCh37
Build 361120,096,570 - 20,096,697RGDNCBI36
Celera1120,272,627 - 20,272,754RGD
Celera1151,074,415 - 51,074,542UniSTS
Cytogenetic Map11p15.1UniSTS
HuRef1119,823,355 - 19,823,482UniSTS
TNG Radiation Hybrid Map119802.0UniSTS
Stanford-G3 RH Map11911.0UniSTS
NCBI RH Map11134.9UniSTS
GeneMap99-G3 RH Map11911.0UniSTS
1654  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371119,496,106 - 19,496,190UniSTSGRCh37
Build 361119,452,682 - 19,452,766RGDNCBI36
Celera1119,628,853 - 19,628,937RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,179,897 - 19,179,981UniSTS
GeneMap99-GB4 RH Map1173.59UniSTS
D11S1062  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371119,900,145 - 19,900,368UniSTSGRCh37
Build 361119,856,721 - 19,856,944RGDNCBI36
Celera1120,032,860 - 20,033,083RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,583,637 - 19,583,860UniSTS
RH70190  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371119,373,120 - 19,373,245UniSTSGRCh37
Build 361119,329,696 - 19,329,821RGDNCBI36
Celera1119,505,870 - 19,505,995RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,056,940 - 19,057,065UniSTS
GeneMap99-GB4 RH Map1173.64UniSTS
NCBI RH Map11129.6UniSTS
STS-R52158  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371120,141,196 - 20,141,316UniSTSGRCh37
Build 361120,097,772 - 20,097,892RGDNCBI36
Celera1120,273,828 - 20,273,948RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,824,556 - 19,824,676UniSTS
GeneMap99-GB4 RH Map1175.58UniSTS
NCBI RH Map11129.6UniSTS
RH15864  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371119,858,476 - 19,858,635UniSTSGRCh37
Build 361119,815,052 - 19,815,211RGDNCBI36
Celera1119,991,190 - 19,991,349RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,542,369 - 19,542,528UniSTS
GeneMap99-GB4 RH Map1175.58UniSTS
NCBI RH Map11129.6UniSTS
D11S4273  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371119,988,458 - 19,988,601UniSTSGRCh37
Build 361119,945,034 - 19,945,177RGDNCBI36
Celera1120,121,125 - 20,121,268RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,671,966 - 19,672,109UniSTS
WI-12433  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371119,859,062 - 19,859,211UniSTSGRCh37
Build 361119,815,638 - 19,815,787RGDNCBI36
Celera1119,991,776 - 19,991,925RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,542,955 - 19,543,104UniSTS
GeneMap99-GB4 RH Map1165.18UniSTS
Whitehead-RH Map1164.6UniSTS
G09854  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371119,988,458 - 19,988,640UniSTSGRCh37
Build 361119,945,034 - 19,945,216RGDNCBI36
Celera1120,121,125 - 20,121,307RGD
Cytogenetic Map11p15.1UniSTS
HuRef1119,671,966 - 19,672,148UniSTS
RH70750  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371495,570,131 - 95,570,259UniSTSGRCh37
Build 361494,639,884 - 94,640,012RGDNCBI36
Celera1475,626,246 - 75,626,374RGD
Cytogenetic Map14q32.13UniSTS
Cytogenetic Map11p15.1UniSTS
HuRef1119,730,399 - 19,730,622UniSTS
GeneMap99-GB4 RH Map14255.86UniSTS
D11S4010  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map11p15.1UniSTS
HuRef1119,753,210 - 19,753,346UniSTS
Whitehead-RH Map1163.3UniSTS
Whitehead-YAC Contig Map11 UniSTS
NCBI RH Map11130.2UniSTS
D11S2034  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map11p15.1UniSTS
TNG Radiation Hybrid Map119417.0UniSTS
Stanford-G3 RH Map11770.0UniSTS
D11S1308  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map11p15.1UniSTS
Marshfield Genetic Map1124.73UniSTS
Genethon Genetic Map1128.1UniSTS
deCODE Assembly Map1129.89UniSTS
Whitehead-RH Map1163.3UniSTS
Whitehead-YAC Contig Map11 UniSTS
NCBI RH Map11130.7UniSTS


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 adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 1470 1376 940 191 63 168 2333 813 1360 140 527 1397 32 405 1546 2
Low 953 858 778 433 942 296 2006 1328 2344 276 914 203 139 799 1225 3 2
Below cutoff 8 745 6 836 17 46 7 3 12 9 17

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_030347 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001111018 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001111019 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001244963 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_145117 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_182964 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005253214 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006718364 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006718365 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006718366 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006718367 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006718368 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006718369 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011520444 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011520445 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011520446 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011520447 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011520448 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011520449 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011520450 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011520451 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011520453 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011520454 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017018520 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017018521 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017018522 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017018523 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017018524 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017018525 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017018526 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448758 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047427809 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047427810 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047427811 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047427812 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047427813 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047427814 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047427815 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047427816 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047427817 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047427818 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047427819 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047427820 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047427821 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047427822 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047427823 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047427824 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047427825 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047427826 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047427827 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047427828 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047427829 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047427830 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047427831 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047427833 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047427834 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047427835 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047427836 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047427837 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047427838 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370371 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370372 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370373 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370374 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370375 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370376 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370377 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370378 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370379 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370380 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370381 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370382 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370383 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370384 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370385 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370386 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370387 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370388 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370389 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370390 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370391 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370392 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370393 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370394 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370395 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370396 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370397 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370398 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370399 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370400 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370401 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370402 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370403 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370404 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370405 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370406 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370407 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370408 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370409 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370410 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370411 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370412 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370413 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370414 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370415 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA451836 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB037840 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB063115 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB063116 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC009549 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC015684 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC023950 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC090662 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC111163 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC113193 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF466143 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF466144 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ488102 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ488202 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ488203 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ488204 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ488205 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ488206 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ488207 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ488208 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK001892 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK074287 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK096037 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK290458 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK298346 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK307574 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC016054 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC107690 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC150290 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BE818973 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BI831180 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX459843 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX485661 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471064 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068267 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF511142 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  R23148 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000349880   ⟹   ENSP00000309577
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1119,712,837 - 20,121,601 (+)Ensembl
RefSeq Acc Id: ENST00000360655   ⟹   ENSP00000353871
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1119,350,724 - 20,121,598 (+)Ensembl
RefSeq Acc Id: ENST00000396085   ⟹   ENSP00000379394
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1119,712,837 - 20,121,601 (+)Ensembl
RefSeq Acc Id: ENST00000396087   ⟹   ENSP00000379396
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1119,713,597 - 20,118,574 (+)Ensembl
RefSeq Acc Id: ENST00000525025
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1120,107,245 - 20,114,680 (+)Ensembl
RefSeq Acc Id: ENST00000525322   ⟹   ENSP00000437136
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1120,022,838 - 20,080,184 (+)Ensembl
RefSeq Acc Id: ENST00000526675
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1120,027,554 - 20,044,995 (+)Ensembl
RefSeq Acc Id: ENST00000527559   ⟹   ENSP00000435395
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1119,713,335 - 20,121,598 (+)Ensembl
RefSeq Acc Id: ENST00000528008
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1119,931,765 - 19,933,719 (+)Ensembl
RefSeq Acc Id: ENST00000528923
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1120,114,383 - 20,118,282 (+)Ensembl
RefSeq Acc Id: ENST00000530408   ⟹   ENSP00000431276
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1120,022,845 - 20,044,991 (+)Ensembl
RefSeq Acc Id: ENST00000533746
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1120,104,211 - 20,118,581 (+)Ensembl
RefSeq Acc Id: ENST00000533917   ⟹   ENSP00000437316
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1120,022,556 - 20,118,603 (+)Ensembl
RefSeq Acc Id: ENST00000534229
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1119,777,802 - 19,880,127 (+)Ensembl
RefSeq Acc Id: ENST00000534299
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1120,027,255 - 20,044,991 (+)Ensembl
RefSeq Acc Id: ENST00000540292   ⟹   ENSP00000443489
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1119,713,335 - 20,121,598 (+)Ensembl
RefSeq Acc Id: ENST00000650578   ⟹   ENSP00000497502
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1119,813,718 - 19,832,601 (+)Ensembl
RefSeq Acc Id: NM_001111018   ⟹   NP_001104488
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,345,236 - 20,121,601 (+)NCBI
GRCh371119,372,271 - 20,143,147 (+)RGD
Celera1119,505,019 - 20,275,779 (+)RGD
HuRef1119,056,089 - 19,826,507 (+)ENTREZGENE
CHM1_11119,371,529 - 20,143,061 (+)NCBI
T2T-CHM13v2.01119,465,285 - 20,242,238 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001111019   ⟹   NP_001104489
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381120,022,556 - 20,121,601 (+)NCBI
GRCh371119,372,271 - 20,143,147 (+)RGD
Celera1119,505,019 - 20,275,779 (+)RGD
HuRef1119,056,089 - 19,826,507 (+)ENTREZGENE
CHM1_11120,044,004 - 20,143,061 (+)NCBI
T2T-CHM13v2.01120,143,177 - 20,242,238 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001244963   ⟹   NP_001231892
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,712,837 - 20,121,601 (+)NCBI
GRCh371119,372,271 - 20,143,147 (+)NCBI
HuRef1119,056,089 - 19,826,507 (+)NCBI
CHM1_11119,734,473 - 20,143,061 (+)NCBI
T2T-CHM13v2.01119,833,290 - 20,242,238 (+)NCBI
Sequence:
RefSeq Acc Id: NM_145117   ⟹   NP_660093
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,712,837 - 20,121,601 (+)NCBI
GRCh371119,372,271 - 20,143,147 (+)RGD
Build 361119,691,488 - 20,099,723 (+)NCBI Archive
Celera1119,505,019 - 20,275,779 (+)RGD
HuRef1119,056,089 - 19,826,507 (+)ENTREZGENE
CHM1_11119,734,473 - 20,143,061 (+)NCBI
T2T-CHM13v2.01119,833,290 - 20,242,238 (+)NCBI
Sequence:
RefSeq Acc Id: NM_182964   ⟹   NP_892009
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,712,837 - 20,121,601 (+)NCBI
GRCh371119,372,271 - 20,143,147 (+)RGD
Build 361119,691,488 - 20,099,723 (+)NCBI Archive
Celera1119,505,019 - 20,275,779 (+)RGD
HuRef1119,056,089 - 19,826,507 (+)ENTREZGENE
CHM1_11119,734,473 - 20,143,061 (+)NCBI
T2T-CHM13v2.01119,833,290 - 20,242,238 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005253214   ⟹   XP_005253271
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381120,023,090 - 20,121,601 (+)NCBI
GRCh371119,372,271 - 20,143,147 (+)NCBI
Sequence:
RefSeq Acc Id: XM_006718364   ⟹   XP_006718427
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,712,837 - 20,121,601 (+)NCBI
Sequence:
RefSeq Acc Id: XM_006718365   ⟹   XP_006718428
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,712,837 - 20,121,601 (+)NCBI
Sequence:
RefSeq Acc Id: XM_006718366   ⟹   XP_006718429
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,777,420 - 20,121,601 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011520444   ⟹   XP_011518746
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,712,837 - 20,121,601 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011520445   ⟹   XP_011518747
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,712,837 - 20,121,601 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011520446   ⟹   XP_011518748
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,712,837 - 20,121,601 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011520447   ⟹   XP_011518749
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,712,837 - 20,121,601 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011520448   ⟹   XP_011518750
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,712,837 - 20,121,601 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011520449   ⟹   XP_011518751
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,712,837 - 20,121,601 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011520450   ⟹   XP_011518752
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,712,837 - 20,121,601 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017018520   ⟹   XP_016874009
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,345,236 - 20,121,601 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017018521   ⟹   XP_016874010
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,712,837 - 20,121,601 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017018522   ⟹   XP_016874011
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,345,236 - 20,121,601 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017018524   ⟹   XP_016874013
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,712,837 - 20,121,601 (+)NCBI
Sequence:
RefSeq Acc Id: XM_024448758   ⟹   XP_024304526
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,349,908 - 20,121,601 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047427809   ⟹   XP_047283765
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,712,837 - 20,121,601 (+)NCBI
RefSeq Acc Id: XM_047427810   ⟹   XP_047283766
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,712,837 - 20,121,601 (+)NCBI
RefSeq Acc Id: XM_047427811   ⟹   XP_047283767
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,712,837 - 20,121,601 (+)NCBI
RefSeq Acc Id: XM_047427812   ⟹   XP_047283768
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,712,837 - 20,121,601 (+)NCBI
RefSeq Acc Id: XM_047427813   ⟹   XP_047283769
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,712,837 - 20,121,601 (+)NCBI
RefSeq Acc Id: XM_047427814   ⟹   XP_047283770
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,712,837 - 20,121,601 (+)NCBI
RefSeq Acc Id: XM_047427815   ⟹   XP_047283771
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,712,837 - 20,121,601 (+)NCBI
RefSeq Acc Id: XM_047427816   ⟹   XP_047283772
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,712,837 - 20,121,601 (+)NCBI
RefSeq Acc Id: XM_047427817   ⟹   XP_047283773
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,712,837 - 20,121,601 (+)NCBI
RefSeq Acc Id: XM_047427818   ⟹   XP_047283774
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,712,837 - 20,121,601 (+)NCBI
RefSeq Acc Id: XM_047427819   ⟹   XP_047283775
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,712,837 - 20,121,601 (+)NCBI
RefSeq Acc Id: XM_047427820   ⟹   XP_047283776
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,349,908 - 20,121,601 (+)NCBI
RefSeq Acc Id: XM_047427821   ⟹   XP_047283777
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,712,837 - 20,121,601 (+)NCBI
RefSeq Acc Id: XM_047427822   ⟹   XP_047283778
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,777,420 - 20,121,601 (+)NCBI
RefSeq Acc Id: XM_047427823   ⟹   XP_047283779
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,712,837 - 20,121,601 (+)NCBI
RefSeq Acc Id: XM_047427824   ⟹   XP_047283780
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,345,236 - 20,121,601 (+)NCBI
RefSeq Acc Id: XM_047427825   ⟹   XP_047283781
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,349,908 - 20,121,601 (+)NCBI
RefSeq Acc Id: XM_047427826   ⟹   XP_047283782
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,777,420 - 20,121,601 (+)NCBI
RefSeq Acc Id: XM_047427827   ⟹   XP_047283783
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,777,420 - 20,121,601 (+)NCBI
RefSeq Acc Id: XM_047427828   ⟹   XP_047283784
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,345,236 - 20,121,601 (+)NCBI
RefSeq Acc Id: XM_047427829   ⟹   XP_047283785
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,777,420 - 20,121,601 (+)NCBI
RefSeq Acc Id: XM_047427830   ⟹   XP_047283786
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,345,236 - 20,121,601 (+)NCBI
RefSeq Acc Id: XM_047427831   ⟹   XP_047283787
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,345,236 - 20,121,601 (+)NCBI
RefSeq Acc Id: XM_047427833   ⟹   XP_047283789
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,349,908 - 20,121,601 (+)NCBI
RefSeq Acc Id: XM_047427834   ⟹   XP_047283790
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,777,420 - 20,121,601 (+)NCBI
RefSeq Acc Id: XM_047427835   ⟹   XP_047283791
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,777,420 - 20,121,601 (+)NCBI
RefSeq Acc Id: XM_047427836   ⟹   XP_047283792
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,818,264 - 20,121,601 (+)NCBI
RefSeq Acc Id: XM_047427837   ⟹   XP_047283793
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381120,023,090 - 20,121,601 (+)NCBI
RefSeq Acc Id: XM_047427838   ⟹   XP_047283794
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381120,023,090 - 20,121,601 (+)NCBI
RefSeq Acc Id: XM_054370371   ⟹   XP_054226346
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,833,290 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370372   ⟹   XP_054226347
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,833,290 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370373   ⟹   XP_054226348
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,833,290 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370374   ⟹   XP_054226349
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,833,290 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370375   ⟹   XP_054226350
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,833,290 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370376   ⟹   XP_054226351
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,833,290 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370377   ⟹   XP_054226352
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,833,290 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370378   ⟹   XP_054226353
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,833,290 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370379   ⟹   XP_054226354
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,833,290 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370380   ⟹   XP_054226355
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,833,290 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370381   ⟹   XP_054226356
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,833,290 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370382   ⟹   XP_054226357
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,833,290 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370383   ⟹   XP_054226358
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,833,290 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370384   ⟹   XP_054226359
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,833,290 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370385   ⟹   XP_054226360
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,833,290 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370386   ⟹   XP_054226361
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,833,290 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370387   ⟹   XP_054226362
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,465,285 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370388   ⟹   XP_054226363
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,833,263 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370389   ⟹   XP_054226364
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,833,290 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370390   ⟹   XP_054226365
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,897,552 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370391   ⟹   XP_054226366
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,833,290 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370392   ⟹   XP_054226367
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,833,290 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370393   ⟹   XP_054226368
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,833,290 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370394   ⟹   XP_054226369
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,470,244 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370395   ⟹   XP_054226370
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,465,285 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370396   ⟹   XP_054226371
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,833,290 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370397   ⟹   XP_054226372
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,897,610 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370398   ⟹   XP_054226373
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,833,290 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370399   ⟹   XP_054226374
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,465,285 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370400   ⟹   XP_054226375
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,470,244 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370401   ⟹   XP_054226376
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,897,610 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370402   ⟹   XP_054226377
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,897,610 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370403   ⟹   XP_054226378
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,465,285 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370404   ⟹   XP_054226379
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,945,761 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370405   ⟹   XP_054226380
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,833,823 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370406   ⟹   XP_054226381
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,897,610 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370407   ⟹   XP_054226382
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,465,285 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370408   ⟹   XP_054226383
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,465,285 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370409   ⟹   XP_054226384
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,470,244 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370410   ⟹   XP_054226385
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,897,610 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370411   ⟹   XP_054226386
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,897,610 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370412   ⟹   XP_054226387
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01119,945,762 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370413   ⟹   XP_054226388
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01120,143,711 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370414   ⟹   XP_054226389
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01120,143,711 - 20,242,238 (+)NCBI
RefSeq Acc Id: XM_054370415   ⟹   XP_054226390
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01120,143,711 - 20,242,238 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001104488 (Get FASTA)   NCBI Sequence Viewer  
  NP_001104489 (Get FASTA)   NCBI Sequence Viewer  
  NP_001231892 (Get FASTA)   NCBI Sequence Viewer  
  NP_660093 (Get FASTA)   NCBI Sequence Viewer  
  NP_892009 (Get FASTA)   NCBI Sequence Viewer  
  XP_005253271 (Get FASTA)   NCBI Sequence Viewer  
  XP_006718427 (Get FASTA)   NCBI Sequence Viewer  
  XP_006718428 (Get FASTA)   NCBI Sequence Viewer  
  XP_006718429 (Get FASTA)   NCBI Sequence Viewer  
  XP_011518746 (Get FASTA)   NCBI Sequence Viewer  
  XP_011518747 (Get FASTA)   NCBI Sequence Viewer  
  XP_011518748 (Get FASTA)   NCBI Sequence Viewer  
  XP_011518749 (Get FASTA)   NCBI Sequence Viewer  
  XP_011518750 (Get FASTA)   NCBI Sequence Viewer  
  XP_011518751 (Get FASTA)   NCBI Sequence Viewer  
  XP_011518752 (Get FASTA)   NCBI Sequence Viewer  
  XP_016874009 (Get FASTA)   NCBI Sequence Viewer  
  XP_016874010 (Get FASTA)   NCBI Sequence Viewer  
  XP_016874011 (Get FASTA)   NCBI Sequence Viewer  
  XP_016874013 (Get FASTA)   NCBI Sequence Viewer  
  XP_024304526 (Get FASTA)   NCBI Sequence Viewer  
  XP_047283765 (Get FASTA)   NCBI Sequence Viewer  
  XP_047283766 (Get FASTA)   NCBI Sequence Viewer  
  XP_047283767 (Get FASTA)   NCBI Sequence Viewer  
  XP_047283768 (Get FASTA)   NCBI Sequence Viewer  
  XP_047283769 (Get FASTA)   NCBI Sequence Viewer  
  XP_047283770 (Get FASTA)   NCBI Sequence Viewer  
  XP_047283771 (Get FASTA)   NCBI Sequence Viewer  
  XP_047283772 (Get FASTA)   NCBI Sequence Viewer  
  XP_047283773 (Get FASTA)   NCBI Sequence Viewer  
  XP_047283774 (Get FASTA)   NCBI Sequence Viewer  
  XP_047283775 (Get FASTA)   NCBI Sequence Viewer  
  XP_047283776 (Get FASTA)   NCBI Sequence Viewer  
  XP_047283777 (Get FASTA)   NCBI Sequence Viewer  
  XP_047283778 (Get FASTA)   NCBI Sequence Viewer  
  XP_047283779 (Get FASTA)   NCBI Sequence Viewer  
  XP_047283780 (Get FASTA)   NCBI Sequence Viewer  
  XP_047283781 (Get FASTA)   NCBI Sequence Viewer  
  XP_047283782 (Get FASTA)   NCBI Sequence Viewer  
  XP_047283783 (Get FASTA)   NCBI Sequence Viewer  
  XP_047283784 (Get FASTA)   NCBI Sequence Viewer  
  XP_047283785 (Get FASTA)   NCBI Sequence Viewer  
  XP_047283786 (Get FASTA)   NCBI Sequence Viewer  
  XP_047283787 (Get FASTA)   NCBI Sequence Viewer  
  XP_047283789 (Get FASTA)   NCBI Sequence Viewer  
  XP_047283790 (Get FASTA)   NCBI Sequence Viewer  
  XP_047283791 (Get FASTA)   NCBI Sequence Viewer  
  XP_047283792 (Get FASTA)   NCBI Sequence Viewer  
  XP_047283793 (Get FASTA)   NCBI Sequence Viewer  
  XP_047283794 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226346 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226347 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226348 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226349 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226350 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226351 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226352 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226353 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226354 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226355 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226356 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226357 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226358 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226359 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226360 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226361 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226362 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226363 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226364 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226365 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226366 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226367 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226368 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226369 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226370 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226371 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226372 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226373 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226374 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226375 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226376 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226377 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226378 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226379 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226380 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226381 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226382 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226383 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226384 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226385 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226386 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226387 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226388 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226389 (Get FASTA)   NCBI Sequence Viewer  
  XP_054226390 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH16054 (Get FASTA)   NCBI Sequence Viewer  
  AAI50291 (Get FASTA)   NCBI Sequence Viewer  
  AAL96479 (Get FASTA)   NCBI Sequence Viewer  
  AAL96480 (Get FASTA)   NCBI Sequence Viewer  
  BAA91965 (Get FASTA)   NCBI Sequence Viewer  
  BAA92657 (Get FASTA)   NCBI Sequence Viewer  
  BAB85038 (Get FASTA)   NCBI Sequence Viewer  
  BAC00853 (Get FASTA)   NCBI Sequence Viewer  
  BAC00854 (Get FASTA)   NCBI Sequence Viewer  
  BAF83147 (Get FASTA)   NCBI Sequence Viewer  
  BAH12762 (Get FASTA)   NCBI Sequence Viewer  
  CAD32471 (Get FASTA)   NCBI Sequence Viewer  
  CAD32555 (Get FASTA)   NCBI Sequence Viewer  
  CAD32556 (Get FASTA)   NCBI Sequence Viewer  
  CAD32557 (Get FASTA)   NCBI Sequence Viewer  
  CAD32558 (Get FASTA)   NCBI Sequence Viewer  
  CAD32559 (Get FASTA)   NCBI Sequence Viewer  
  CAD32560 (Get FASTA)   NCBI Sequence Viewer  
  CAD32561 (Get FASTA)   NCBI Sequence Viewer  
  EAW68343 (Get FASTA)   NCBI Sequence Viewer  
  EAW68344 (Get FASTA)   NCBI Sequence Viewer  
  EAW68345 (Get FASTA)   NCBI Sequence Viewer  
  EAW68346 (Get FASTA)   NCBI Sequence Viewer  
  EAW68347 (Get FASTA)   NCBI Sequence Viewer  
  EAW68348 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000309577
  ENSP00000309577.6
  ENSP00000353871
  ENSP00000353871.4
  ENSP00000379394
  ENSP00000379394.1
  ENSP00000379396
  ENSP00000379396.3
  ENSP00000431276.1
  ENSP00000437136.1
  ENSP00000437316
  ENSP00000437316.1
  ENSP00000497502.1
GenBank Protein Q8IVL1 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_001104488   ⟸   NM_001111018
- Peptide Label: isoform 3
- UniProtKB: A7E2D6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_660093   ⟸   NM_145117
- Peptide Label: isoform 2
- UniProtKB: A7E2D6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_892009   ⟸   NM_182964
- Peptide Label: isoform 1
- UniProtKB: A7E2D6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001104489   ⟸   NM_001111019
- Peptide Label: isoform 4
- UniProtKB: Q8IVL1 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001231892   ⟸   NM_001244963
- Peptide Label: isoform 5
- UniProtKB: Q9NVM7 (UniProtKB/Swiss-Prot),   Q9NUZ6 (UniProtKB/Swiss-Prot),   Q96B30 (UniProtKB/Swiss-Prot),   Q8TEB3 (UniProtKB/Swiss-Prot),   Q8TDF0 (UniProtKB/Swiss-Prot),   Q8TDE9 (UniProtKB/Swiss-Prot),   Q8NHD0 (UniProtKB/Swiss-Prot),   Q8NHC9 (UniProtKB/Swiss-Prot),   Q8IVK8 (UniProtKB/Swiss-Prot),   Q8IVK7 (UniProtKB/Swiss-Prot),   Q8IVK6 (UniProtKB/Swiss-Prot),   Q8IVK5 (UniProtKB/Swiss-Prot),   Q8IVK4 (UniProtKB/Swiss-Prot),   Q8IVK3 (UniProtKB/Swiss-Prot),   A6NEC1 (UniProtKB/Swiss-Prot),   Q9P2C8 (UniProtKB/Swiss-Prot),   Q8IVL1 (UniProtKB/Swiss-Prot),   A7E2D6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005253271   ⟸   XM_005253214
- Peptide Label: isoform X41
- Sequence:
RefSeq Acc Id: XP_006718428   ⟸   XM_006718365
- Peptide Label: isoform X6
- UniProtKB: A7E2D6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_006718427   ⟸   XM_006718364
- Peptide Label: isoform X3
- UniProtKB: A7E2D6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_006718429   ⟸   XM_006718366
- Peptide Label: isoform X20
- UniProtKB: A7E2D6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011518746   ⟸   XM_011520444
- Peptide Label: isoform X1
- UniProtKB: A7E2D6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011518748   ⟸   XM_011520446
- Peptide Label: isoform X7
- UniProtKB: A7E2D6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011518747   ⟸   XM_011520445
- Peptide Label: isoform X2
- UniProtKB: A7E2D6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011518751   ⟸   XM_011520449
- Peptide Label: isoform X14
- UniProtKB: A7E2D6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011518749   ⟸   XM_011520447
- Peptide Label: isoform X8
- UniProtKB: A7E2D6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011518752   ⟸   XM_011520450
- Peptide Label: isoform X19
- UniProtKB: A7E2D6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011518750   ⟸   XM_011520448
- Peptide Label: isoform X10
- UniProtKB: A7E2D6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016874011   ⟸   XM_017018522
- Peptide Label: isoform X24
- UniProtKB: A7E2D6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016874009   ⟸   XM_017018520
- Peptide Label: isoform X17
- UniProtKB: A7E2D6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016874010   ⟸   XM_017018521
- Peptide Label: isoform X21
- UniProtKB: A7E2D6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016874013   ⟸   XM_017018524
- Peptide Label: isoform X33
- UniProtKB: A7E2D6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_024304526   ⟸   XM_024448758
- Peptide Label: isoform X17
- UniProtKB: A7E2D6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000431276   ⟸   ENST00000530408
RefSeq Acc Id: ENSP00000309577   ⟸   ENST00000349880
RefSeq Acc Id: ENSP00000353871   ⟸   ENST00000360655
RefSeq Acc Id: ENSP00000497502   ⟸   ENST00000650578
RefSeq Acc Id: ENSP00000437316   ⟸   ENST00000533917
RefSeq Acc Id: ENSP00000437136   ⟸   ENST00000525322
RefSeq Acc Id: ENSP00000435395   ⟸   ENST00000527559
RefSeq Acc Id: ENSP00000379396   ⟸   ENST00000396087
RefSeq Acc Id: ENSP00000379394   ⟸   ENST00000396085
RefSeq Acc Id: ENSP00000443489   ⟸   ENST00000540292
RefSeq Acc Id: XP_047283780   ⟸   XM_047427824
- Peptide Label: isoform X28
RefSeq Acc Id: XP_047283784   ⟸   XM_047427828
- Peptide Label: isoform X32
RefSeq Acc Id: XP_047283786   ⟸   XM_047427830
- Peptide Label: isoform X35
RefSeq Acc Id: XP_047283787   ⟸   XM_047427831
- Peptide Label: isoform X36
RefSeq Acc Id: XP_047283776   ⟸   XM_047427820
- Peptide Label: isoform X24
RefSeq Acc Id: XP_047283781   ⟸   XM_047427825
- Peptide Label: isoform X29
RefSeq Acc Id: XP_047283789   ⟸   XM_047427833
- Peptide Label: isoform X36
RefSeq Acc Id: XP_047283765   ⟸   XM_047427809
- Peptide Label: isoform X4
RefSeq Acc Id: XP_047283770   ⟸   XM_047427814
- Peptide Label: isoform X13
RefSeq Acc Id: XP_047283767   ⟸   XM_047427811
- Peptide Label: isoform X9
RefSeq Acc Id: XP_047283766   ⟸   XM_047427810
- Peptide Label: isoform X5
RefSeq Acc Id: XP_047283768   ⟸   XM_047427812
- Peptide Label: isoform X11
RefSeq Acc Id: XP_047283769   ⟸   XM_047427813
- Peptide Label: isoform X12
RefSeq Acc Id: XP_047283774   ⟸   XM_047427818
- Peptide Label: isoform X22
RefSeq Acc Id: XP_047283775   ⟸   XM_047427819
- Peptide Label: isoform X23
RefSeq Acc Id: XP_047283771   ⟸   XM_047427815
- Peptide Label: isoform X15
RefSeq Acc Id: XP_047283772   ⟸   XM_047427816
- Peptide Label: isoform X16
RefSeq Acc Id: XP_047283777   ⟸   XM_047427821
- Peptide Label: isoform X25
RefSeq Acc Id: XP_047283779   ⟸   XM_047427823
- Peptide Label: isoform X27
RefSeq Acc Id: XP_047283773   ⟸   XM_047427817
- Peptide Label: isoform X18
RefSeq Acc Id: XP_047283778   ⟸   XM_047427822
- Peptide Label: isoform X26
RefSeq Acc Id: XP_047283785   ⟸   XM_047427829
- Peptide Label: isoform X34
RefSeq Acc Id: XP_047283782   ⟸   XM_047427826
- Peptide Label: isoform X30
RefSeq Acc Id: XP_047283783   ⟸   XM_047427827
- Peptide Label: isoform X31
RefSeq Acc Id: XP_047283790   ⟸   XM_047427834
- Peptide Label: isoform X37
RefSeq Acc Id: XP_047283791   ⟸   XM_047427835
- Peptide Label: isoform X38
RefSeq Acc Id: XP_047283792   ⟸   XM_047427836
- Peptide Label: isoform X39
RefSeq Acc Id: XP_047283793   ⟸   XM_047427837
- Peptide Label: isoform X40
RefSeq Acc Id: XP_047283794   ⟸   XM_047427838
- Peptide Label: isoform X42
RefSeq Acc Id: XP_054226362   ⟸   XM_054370387
- Peptide Label: isoform X17
RefSeq Acc Id: XP_054226374   ⟸   XM_054370399
- Peptide Label: isoform X28
RefSeq Acc Id: XP_054226370   ⟸   XM_054370395
- Peptide Label: isoform X24
RefSeq Acc Id: XP_054226378   ⟸   XM_054370403
- Peptide Label: isoform X32
RefSeq Acc Id: XP_054226382   ⟸   XM_054370407
- Peptide Label: isoform X35
RefSeq Acc Id: XP_054226383   ⟸   XM_054370408
- Peptide Label: isoform X36
RefSeq Acc Id: XP_054226369   ⟸   XM_054370394
- Peptide Label: isoform X24
RefSeq Acc Id: XP_054226375   ⟸   XM_054370400
- Peptide Label: isoform X29
RefSeq Acc Id: XP_054226384   ⟸   XM_054370409
- Peptide Label: isoform X36
RefSeq Acc Id: XP_054226363   ⟸   XM_054370388
- Peptide Label: isoform X18
RefSeq Acc Id: XP_054226346   ⟸   XM_054370371
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054226351   ⟸   XM_054370376
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054226352   ⟸   XM_054370377
- Peptide Label: isoform X7
RefSeq Acc Id: XP_054226347   ⟸   XM_054370372
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054226349   ⟸   XM_054370374
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054226358   ⟸   XM_054370383
- Peptide Label: isoform X13
RefSeq Acc Id: XP_054226359   ⟸   XM_054370384
- Peptide Label: isoform X14
RefSeq Acc Id: XP_054226353   ⟸   XM_054370378
- Peptide Label: isoform X8
RefSeq Acc Id: XP_054226354   ⟸   XM_054370379
- Peptide Label: isoform X9
RefSeq Acc Id: XP_054226364   ⟸   XM_054370389
- Peptide Label: isoform X19
RefSeq Acc Id: XP_054226366   ⟸   XM_054370391
- Peptide Label: isoform X21
RefSeq Acc Id: XP_054226348   ⟸   XM_054370373
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054226350   ⟸   XM_054370375
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054226356   ⟸   XM_054370381
- Peptide Label: isoform X11
RefSeq Acc Id: XP_054226357   ⟸   XM_054370382
- Peptide Label: isoform X12
RefSeq Acc Id: XP_054226367   ⟸   XM_054370392
- Peptide Label: isoform X22
RefSeq Acc Id: XP_054226368   ⟸   XM_054370393
- Peptide Label: isoform X23
RefSeq Acc Id: XP_054226360   ⟸   XM_054370385
- Peptide Label: isoform X15
RefSeq Acc Id: XP_054226361   ⟸   XM_054370386
- Peptide Label: isoform X16
RefSeq Acc Id: XP_054226371   ⟸   XM_054370396
- Peptide Label: isoform X25
RefSeq Acc Id: XP_054226373   ⟸   XM_054370398
- Peptide Label: isoform X27
RefSeq Acc Id: XP_054226355   ⟸   XM_054370380
- Peptide Label: isoform X10
RefSeq Acc Id: XP_054226380   ⟸   XM_054370405
- Peptide Label: isoform X33
RefSeq Acc Id: XP_054226365   ⟸   XM_054370390
- Peptide Label: isoform X20
RefSeq Acc Id: XP_054226372   ⟸   XM_054370397
- Peptide Label: isoform X26
RefSeq Acc Id: XP_054226381   ⟸   XM_054370406
- Peptide Label: isoform X34
RefSeq Acc Id: XP_054226376   ⟸   XM_054370401
- Peptide Label: isoform X30
RefSeq Acc Id: XP_054226377   ⟸   XM_054370402
- Peptide Label: isoform X31
RefSeq Acc Id: XP_054226385   ⟸   XM_054370410
- Peptide Label: isoform X37
RefSeq Acc Id: XP_054226386   ⟸   XM_054370411
- Peptide Label: isoform X38
RefSeq Acc Id: XP_054226379   ⟸   XM_054370404
- Peptide Label: isoform X33
RefSeq Acc Id: XP_054226387   ⟸   XM_054370412
- Peptide Label: isoform X39
RefSeq Acc Id: XP_054226388   ⟸   XM_054370413
- Peptide Label: isoform X40
RefSeq Acc Id: XP_054226389   ⟸   XM_054370414
- Peptide Label: isoform X41
RefSeq Acc Id: XP_054226390   ⟸   XM_054370415
- Peptide Label: isoform X42
Protein Domains
Calponin-homology (CH)

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q8IVL1-F1-model_v2 AlphaFold Q8IVL1 1-2488 view protein structure

Promoters
RGD ID:7219833
Promoter ID:EPDNEW_H15662
Type:initiation region
Name:NAV2_1
Description:neuron navigator 2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H15663  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,345,254 - 19,345,314EPDNEW
RGD ID:7219835
Promoter ID:EPDNEW_H15663
Type:initiation region
Name:NAV2_2
Description:neuron navigator 2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H15662  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381119,350,804 - 19,350,864EPDNEW
RGD ID:6810072
Promoter ID:HG_ACW:11362
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:NAV2.IAPR07
Position:
Human AssemblyChrPosition (strand)Source
Build 361119,754,976 - 19,755,777 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:15997 AgrOrtholog
COSMIC NAV2 COSMIC
Ensembl Genes ENSG00000166833 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000349880 ENTREZGENE
  ENST00000349880.9 UniProtKB/Swiss-Prot
  ENST00000360655 ENTREZGENE
  ENST00000360655.8 UniProtKB/Swiss-Prot
  ENST00000396085 ENTREZGENE
  ENST00000396085.6 UniProtKB/Swiss-Prot
  ENST00000396087 ENTREZGENE
  ENST00000396087.7 UniProtKB/Swiss-Prot
  ENST00000525322.5 UniProtKB/TrEMBL
  ENST00000530408.1 UniProtKB/TrEMBL
  ENST00000533917 ENTREZGENE
  ENST00000533917.5 UniProtKB/Swiss-Prot
  ENST00000650578.1 UniProtKB/TrEMBL
Gene3D-CATH 1.10.418.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  3.40.50.300 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000166833 GTEx
HGNC ID HGNC:15997 ENTREZGENE
Human Proteome Map NAV2 Human Proteome Map
InterPro AAA+_ATPase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  CH-domain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  CH_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Nav/unc-53 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  P-loop_NTPase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:89797 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 89797 ENTREZGENE
OMIM 607026 OMIM
PANTHER NEURON NAVIGATOR 2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR12784 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam PF00307 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA31452 PharmGKB
PROSITE PS50021 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART AAA UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SM00033 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF47576 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF52540 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A3B3ISY2_HUMAN UniProtKB/TrEMBL
  A6NEC1 ENTREZGENE
  A7E2D6 ENTREZGENE, UniProtKB/TrEMBL
  B7SSU1_HUMAN UniProtKB/TrEMBL
  E9PLU3_HUMAN UniProtKB/TrEMBL
  E9PNV5_HUMAN UniProtKB/TrEMBL
  NAV2_HUMAN UniProtKB/Swiss-Prot
  Q8IVK3 ENTREZGENE
  Q8IVK4 ENTREZGENE
  Q8IVK5 ENTREZGENE
  Q8IVK6 ENTREZGENE
  Q8IVK7 ENTREZGENE
  Q8IVK8 ENTREZGENE
  Q8IVL1 ENTREZGENE
  Q8NHC9 ENTREZGENE
  Q8NHD0 ENTREZGENE
  Q8TDE9 ENTREZGENE
  Q8TDF0 ENTREZGENE
  Q8TEB3 ENTREZGENE
  Q96B30 ENTREZGENE
  Q9NUZ6 ENTREZGENE
  Q9NVM7 ENTREZGENE
  Q9P2C8 ENTREZGENE
UniProt Secondary A6NEC1 UniProtKB/Swiss-Prot
  Q8IVK3 UniProtKB/Swiss-Prot
  Q8IVK4 UniProtKB/Swiss-Prot
  Q8IVK5 UniProtKB/Swiss-Prot
  Q8IVK6 UniProtKB/Swiss-Prot
  Q8IVK7 UniProtKB/Swiss-Prot
  Q8IVK8 UniProtKB/Swiss-Prot
  Q8NHC9 UniProtKB/Swiss-Prot
  Q8NHD0 UniProtKB/Swiss-Prot
  Q8TDE9 UniProtKB/Swiss-Prot
  Q8TDF0 UniProtKB/Swiss-Prot
  Q8TEB3 UniProtKB/Swiss-Prot
  Q96B30 UniProtKB/Swiss-Prot
  Q9NUZ6 UniProtKB/Swiss-Prot
  Q9NVM7 UniProtKB/Swiss-Prot
  Q9P2C8 UniProtKB/Swiss-Prot