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基因ID、名称查询：  
基因IDtaxidGeneDate
LocusTag		Symbol
Synonyms		Symbolfna
Fullnamefna		dbXrefschromosome
maplocation		descriptiongenetype
fnastatus		OtherdesignationsFeaturetype
1001877055972920210724
SLC7A6OS
11
solute carrier family 7 member 6 opposite strandprotein-coding
probable RNA polymerase II nuclear localization protein SLC7A6OS
1001877065972920211016
CYBASC3
Ensembl:ENSTGUG000000065075
cytochrome b, ascorbate dependent 3protein-coding
cytochrome b ascorbate-dependent protein 3
1001877075972920210531
NUS1
Ensembl:ENSTGUG000000118923
NUS1 dehydrodolichyl diphosphate synthase subunitprotein-coding
dehydrodolichyl diphosphate synthase complex subunit NUS1
100187708742520210527
Nrk1
1
nicotinamide riboside kinaseprotein-coding
100187709746020220616
Nrk1
GB53410
LG9
nicotinamide riboside kinaseprotein-coding
100187710960620170408
CRCS6
MIM:6122318
8q23
colorectal cancer, susceptibility to, 6unknown
100187711960620170408
CRCS7
MIM:61223211
11q23
colorectal cancer, susceptibility to, 7unknown
1001877123103320220514
mc1r
Ensembl:ENSTRUG0000001819213
melanocortin 1 receptorprotein-coding
melanocyte-stimulating hormone receptor
100187713968520220104
ADIPOR1
EnsemblRapid:ENSFCTG00005011664F1
adiponectin receptor 1protein-coding
adiponectin receptor protein 1
100187714961520211223
CRSP-3
Ensembl:ENSCAFG0084502328121
calcitonin receptor-stimulating peptide 3protein-coding
100187715961520211223
CRSP-4
Ensembl:ENSCAFG0084502666214
calcitonin receptor-stimulating peptide 4protein-coding
100187716960620220626
MIR1224
MIRN1224|mir-1224
MIR1224
microRNA 1224
MIM:611620|HGNC:HGNC:33923|Ensembl:ENSG00000221120|miRBase:MI0003764|AllianceGenome:HGNC:339233
3q27.1
microRNA 1224ncRNA
O
hsa-mir-1224
100187717960620170408
NNO3
MIM:6118972
2q11-q14
nanophthalmos 3unknown
100187718742520210527
LOC100187718
1
B-cell CLL/lymphoma 11-like proteinprotein-coding
100187719742520210527
140up
1
upstream of RpII140protein-coding
100187720742520210527
Lin
5
linesprotein-coding
100187721742520210527
LOC100187721
NASONIABASE:NV215735
cuticular proteinprotein-coding
100187722742520210527
LOC100187722
5
N-lysine methyltransferase SMYD2-likeprotein-coding
100187723742520210527
Rhbdd1
1
rhomboid domain containing 1protein-coding
100187724960620170408
DEL16P11.2
AUTS14|AUTS14A|C16DELp11.2|C16DUPp11.2|DUP16p11.2
MIM:61191316
16p11.2
autism, susceptibility to, 14unknown
100187725960620220513
LOC100187725
15
15q21.1
5-azacytidine induced 2 pseudogenepseudo
100187727982320220719
CDH3
Cadherin-3
CDH3
cadherin 3
VGNC:VGNC:96941|Ensembl:ENSSSCG000000231626
cadherin 3protein-coding
O
LOW QUALITY PROTEIN: cadherin-3|cadherin 15, M-cadherin (myotubule)|cadherin 15, type 1, M-cadherin (myotubule)
100187732742520210527
LOC100187732
1
uncharacterized LOC100187732protein-coding
uncharacterized protein LOC100187732
100187734742520210527
LOC100187734
1
uncharacterized LOC100187734protein-coding
uncharacterized protein LOC100187734
100187735982320220719
USP19
USP19
ubiquitin specific peptidase 19
VGNC:VGNC:94750|Ensembl:ENSSSCG0000001137513
ubiquitin specific peptidase 19protein-coding
O
ubiquitin carboxyl-terminal hydrolase 19
100187736707020210213
TcasGA2_TC007616
LOC100187736
LG4
uncharacterized LOC100187736protein-coding
uncharacterized protein LOC100187736|AUGUSTUS-3.0.2_07616|GLEAN_07616
100187737742520210527
Gemin7
2
gem (nuclear organelle) associated protein 7protein-coding
100187738707020210213
Gemin7
LG8
gem (nuclear organelle) associated protein 7protein-coding
100187739959820210724
PATR-DRB1
major histocompatibility complex, class II, DR beta 1protein-coding
100187740959820190324
PATR-DRB3
major histocompatibility complex, class II, DR beta 3protein-coding
100187741959820190324
PATR-DRB4
major histocompatibility complex, class II, DR beta 4protein-coding
100187749960620170402
ASDP
MIM:105563
anal sphincter dysplasiaunknown
100187761960620170402
AN
MIM:110350
blood group Ahonenunknown
100187828960620170402
HBD
MIM:146350
hypophosphatemic bone diseaseunknown
100187907960620190707
TRAP
MIM:190445
triiodothyronine receptor auxiliary proteinprotein-coding
100188011960620170402
DIP
MIM:263000
interstitial pneumonitis, desquamative, familialunknown
100188278960620170408
FECD2
FCD1
MIM:61015813
13pter-q12.13
corneal dystrophy, Fuchs endothelial 2unknown
100188314960620170408
AUTS12
MIM:61083821
21p13-q11
autism, susceptibility to, 12unknown
100188317960620170408
AUTS13
MIM:61090812
12q14.2
autism, susceptibility to, 13unknown
100188321960620190816
HYT8
MIM:61101418
18q21.2
hypertension, essential, susceptibility to, 8unknown
100188328960620170408
PNKD2
MIM:6111472
2q31
paroxysmal nonkinesigenic dyskinesia 2unknown
100188340960620170402
AOS
MIM:100300
Adams-Oliver syndromeunknown
100188397960620170402
HLP
MIM:144150
hyperkeratosis lenticularis perstansunknown
100188695960620170402
DA4
MIM:609128
arthrogryposis, distal, type 4unknown
100188748960620170408
STHAG5
MIM:61092610
10q
tooth agenesis, selective, 5unknown
100188754960620170408
AD14
MIM:6111541
1q25
Alzheimer disease 14unknown
100188765960620190816
CFTDX
MIM:300580X
Xq13.1-q22.1
Myopathy, congenital, with fiber-type disproportion, X-linkedunknown
100188767960620190816
AGSPX
MIM:300652X
Xp11.3-q12
Angio serpiginosumunknown
100188768960620190816
SCAX5
MIM:300703X
Xq25-q27.1
Spinocerebellar ataxia, X-linked 5unknown
100188769960620190816
HPCX2
MIM:300704X
Xp11.22
Prostate cancer, hereditary, X-linked 2unknown
1...156469...300902300903300904300905300906300907300908...300931...300960
 
 
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