NEU3 (neuraminidase 3) - Rat Genome Database

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Gene: NEU3 (neuraminidase 3) Homo sapiens
Analyze
Symbol: NEU3
Name: neuraminidase 3
RGD ID: 1347886
HGNC Page HGNC:7760
Description: Enables exo-alpha-(2->3)-sialidase activity and exo-alpha-(2->8)-sialidase activity. Involved in several processes, including ganglioside catabolic process; negative regulation of clathrin-dependent endocytosis; and positive regulation of epidermal growth factor receptor signaling pathway. Acts upstream of or within carbohydrate metabolic process. Located in bounding membrane of organelle and plasma membrane.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: FLJ12388; ganglioside sialidase; ganglioside sialidasedis; membrane sialidase; N-acetyl-alpha-neuraminidase 3; neuraminidase 3 (membrane sialidase); neuraminidase 3, membrane sialidase; SIAL3; sialidase 3 (membrane sialidase); sialidase-3
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381174,980,515 - 75,020,676 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1174,988,279 - 75,018,893 (+)EnsemblGRCh38hg38GRCh38
GRCh371174,699,689 - 74,721,952 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361174,377,598 - 74,396,391 (+)NCBINCBI36Build 36hg18NCBI36
Build 341174,376,826 - 74,396,389NCBI
Celera1172,006,517 - 72,025,314 (+)NCBICelera
Cytogenetic Map11q13.4NCBI
HuRef1170,996,749 - 71,016,487 (+)NCBIHuRef
CHM1_11174,583,347 - 74,602,139 (+)NCBICHM1_1
T2T-CHM13v2.01174,910,079 - 74,957,510 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Pathway Annotations     Click to see Annotation Detail View
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. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
3. SMPDB Annotation Import Pipeline Pipeline to import SMPDB annotations from SMPDB into RGD
4. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:8892864   PMID:10405317   PMID:10861246   PMID:11298736   PMID:12011038   PMID:12149448   PMID:12477932   PMID:12487819   PMID:12530538   PMID:12730204   PMID:14702039   PMID:15146197  
PMID:15179041   PMID:15342556   PMID:15847605   PMID:15885103   PMID:16241905   PMID:16344560   PMID:16428383   PMID:16751776   PMID:16765317   PMID:17028199   PMID:17292733   PMID:17334392  
PMID:17827720   PMID:18023981   PMID:18339327   PMID:18651674   PMID:18820643   PMID:18953356   PMID:19588508   PMID:19686243   PMID:20511247   PMID:20518744   PMID:20800603   PMID:21675735  
PMID:21681193   PMID:21873635   PMID:21895867   PMID:22403397   PMID:22903576   PMID:22989879   PMID:23139422   PMID:25408341   PMID:25652216   PMID:25803810   PMID:25810027   PMID:25922362  
PMID:26186194   PMID:26251452   PMID:26470851   PMID:26987901   PMID:27344026   PMID:28514442   PMID:28646141   PMID:28760640   PMID:29088281   PMID:29507755   PMID:30466783   PMID:32102576  
PMID:32393512   PMID:32576593   PMID:32869836   PMID:33233823   PMID:33961781   PMID:34048709   PMID:35675020   PMID:35899930  


Genomics

Comparative Map Data
NEU3
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381174,980,515 - 75,020,676 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1174,988,279 - 75,018,893 (+)EnsemblGRCh38hg38GRCh38
GRCh371174,699,689 - 74,721,952 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361174,377,598 - 74,396,391 (+)NCBINCBI36Build 36hg18NCBI36
Build 341174,376,826 - 74,396,389NCBI
Celera1172,006,517 - 72,025,314 (+)NCBICelera
Cytogenetic Map11q13.4NCBI
HuRef1170,996,749 - 71,016,487 (+)NCBIHuRef
CHM1_11174,583,347 - 74,602,139 (+)NCBICHM1_1
T2T-CHM13v2.01174,910,079 - 74,957,510 (+)NCBIT2T-CHM13v2.0
Neu3
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39799,460,646 - 99,477,579 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl799,460,646 - 99,477,624 (-)EnsemblGRCm39 Ensembl
GRCm38799,811,434 - 99,828,457 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl799,811,439 - 99,828,417 (-)EnsemblGRCm38mm10GRCm38
MGSCv377106,959,949 - 106,976,927 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36799,685,522 - 99,702,500 (-)NCBIMGSCv36mm8
Celera7100,136,642 - 100,153,663 (-)NCBICelera
Cytogenetic Map7E1NCBI
cM Map754.15NCBI
Neu3
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81163,549,834 - 163,560,997 (-)NCBIGRCr8
mRatBN7.21154,137,732 - 154,148,879 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1154,050,855 - 154,148,813 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1162,132,680 - 162,143,804 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01169,312,813 - 169,323,937 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01162,186,360 - 162,197,489 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01164,803,574 - 164,814,777 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1164,803,574 - 164,814,651 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01171,006,216 - 171,017,255 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41157,172,027 - 157,183,064 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11157,250,432 - 157,261,470 (-)NCBI
Celera1152,223,019 - 152,234,091 (-)NCBICelera
Cytogenetic Map1q32NCBI
Neu3
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495541416,788,171 - 16,798,535 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495541416,783,996 - 16,798,368 (-)NCBIChiLan1.0ChiLan1.0
NEU3
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2975,918,466 - 75,940,916 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11176,961,185 - 76,983,624 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01170,047,878 - 70,070,303 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11173,353,332 - 73,373,270 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1173,353,332 - 73,373,270 (+)Ensemblpanpan1.1panPan2
NEU3
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12123,456,424 - 23,484,872 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2123,213,985 - 23,250,034 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.02123,651,315 - 23,687,393 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl2123,663,243 - 23,677,038 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.12123,449,567 - 23,485,563 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02123,646,010 - 23,682,029 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02123,563,652 - 23,599,693 (-)NCBIUU_Cfam_GSD_1.0
Neu3
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494762,297,867 - 62,315,348 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049364983,897,485 - 3,910,115 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049364983,897,511 - 3,915,013 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
NEU3
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl99,315,334 - 9,334,918 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.199,315,263 - 9,333,878 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2910,407,329 - 10,423,135 (+)NCBISscrofa10.2Sscrofa10.2susScr3
NEU3
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1166,220,472 - 66,243,163 (+)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_02366604359,567,996 - 59,590,439 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Neu3
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046248172,107,893 - 2,133,626 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in NEU3
33 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 11q13.4-14.1(chr11:71923251-79662025)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052684]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052684]|See cases [RCV000052684] Chr11:71923251..79662025 [GRCh38]
Chr11:71634297..79373069 [GRCh37]
Chr11:71311945..79050717 [NCBI36]
Chr11:11q13.4-14.1		 pathogenic
GRCh38/hg38 11q13.4-13.5(chr11:71928796-77064521)x1 copy number loss See cases [RCV000052708] Chr11:71928796..77064521 [GRCh38]
Chr11:71639842..76751808 [GRCh37]
Chr11:71317490..76453216 [NCBI36]
Chr11:11q13.4-13.5		 pathogenic
GRCh38/hg38 11q13.4-14.1(chr11:71969881-78232895)x1 copy number loss See cases [RCV000052709] Chr11:71969881..78232895 [GRCh38]
Chr11:71680927..77943941 [GRCh37]
Chr11:71358575..77621589 [NCBI36]
Chr11:11q13.4-14.1		 pathogenic
GRCh37/hg19 11p13-q25(chr11:32799481-134938470)x3 copy number gain MISSED ABORTION [RCV002282973] Chr11:32799481..134938470 [GRCh37]
Chr11:11p13-q25		 pathogenic
NM_006656.6(NEU3):c.473G>A (p.Arg158His) single nucleotide variant Inborn genetic diseases [RCV003244781] Chr11:75005579 [GRCh38]
Chr11:74716624 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_006656.6(NEU3):c.506G>A (p.Cys169Tyr) single nucleotide variant Inborn genetic diseases [RCV003311448] Chr11:75005612 [GRCh38]
Chr11:74716657 [GRCh37]
Chr11:11q13.4		 uncertain significance
GRCh37/hg19 11q13.4(chr11:74580424-75099464)x3 copy number gain See cases [RCV000448058] Chr11:74580424..75099464 [GRCh37]
Chr11:11q13.4		 uncertain significance
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_006656.6(NEU3):c.173G>A (p.Arg58Gln) single nucleotide variant Inborn genetic diseases [RCV003247828] Chr11:74994587 [GRCh38]
Chr11:74705632 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_006656.6(NEU3):c.1330C>A (p.Leu444Met) single nucleotide variant Inborn genetic diseases [RCV003299894] Chr11:75006436 [GRCh38]
Chr11:74717481 [GRCh37]
Chr11:11q13.4		 uncertain significance
GRCh37/hg19 11q13.4-23.3(chr11:71588805-116680918)x3 copy number gain not provided [RCV000683374] Chr11:71588805..116680918 [GRCh37]
Chr11:11q13.4-23.3		 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_006656.6(NEU3):c.56C>T (p.Ser19Phe) single nucleotide variant Inborn genetic diseases [RCV003247962] Chr11:74989116 [GRCh38]
Chr11:74700161 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_006656.6(NEU3):c.316C>G (p.Leu106Val) single nucleotide variant Marfanoid habitus and intellectual disability [RCV000850411] Chr11:75005422 [GRCh38]
Chr11:74716467 [GRCh37]
Chr11:11q13.4		 uncertain significance
Single allele deletion Intellectual disability [RCV001293382] Chr11:118359328..118372573 [GRCh37]
Chr11:11p15.3-q23.3		 pathogenic
NC_000011.9:g.(?_71146421)_(75283128_?)dup duplication 3-methylglutaconic aciduria, type VIIB [RCV003122786] Chr11:71146421..75283128 [GRCh37]
Chr11:11q13.4-13.5		 uncertain significance
NM_006656.6(NEU3):c.1373T>C (p.Phe458Ser) single nucleotide variant Inborn genetic diseases [RCV002753927] Chr11:75006479 [GRCh38]
Chr11:74717524 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_006656.6(NEU3):c.548G>T (p.Gly183Val) single nucleotide variant Inborn genetic diseases [RCV002783041] Chr11:75005654 [GRCh38]
Chr11:74716699 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_006656.6(NEU3):c.440G>A (p.Arg147His) single nucleotide variant Inborn genetic diseases [RCV002869625] Chr11:75005546 [GRCh38]
Chr11:74716591 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_006656.6(NEU3):c.451G>A (p.Val151Met) single nucleotide variant Inborn genetic diseases [RCV002924559] Chr11:75005557 [GRCh38]
Chr11:74716602 [GRCh37]
Chr11:11q13.4		 likely benign
NM_006656.6(NEU3):c.364C>T (p.Pro122Ser) single nucleotide variant Inborn genetic diseases [RCV002821286] Chr11:75005470 [GRCh38]
Chr11:74716515 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_006656.6(NEU3):c.196C>A (p.Pro66Thr) single nucleotide variant Inborn genetic diseases [RCV002845743] Chr11:74994610 [GRCh38]
Chr11:74705655 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_006656.6(NEU3):c.213C>G (p.Phe71Leu) single nucleotide variant Inborn genetic diseases [RCV002888674] Chr11:74994627 [GRCh38]
Chr11:74705672 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_006656.6(NEU3):c.200C>G (p.Pro67Arg) single nucleotide variant Inborn genetic diseases [RCV002850410] Chr11:74994614 [GRCh38]
Chr11:74705659 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_006656.6(NEU3):c.472C>T (p.Arg158Cys) single nucleotide variant Inborn genetic diseases [RCV002931622] Chr11:75005578 [GRCh38]
Chr11:74716623 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_006656.6(NEU3):c.1354G>A (p.Gly452Ser) single nucleotide variant Inborn genetic diseases [RCV002803749] Chr11:75006460 [GRCh38]
Chr11:74717505 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_006656.6(NEU3):c.389G>A (p.Ser130Asn) single nucleotide variant Inborn genetic diseases [RCV002770006] Chr11:75005495 [GRCh38]
Chr11:74716540 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_006656.6(NEU3):c.172C>T (p.Arg58Trp) single nucleotide variant Inborn genetic diseases [RCV002672350] Chr11:74994586 [GRCh38]
Chr11:74705631 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_006656.6(NEU3):c.959G>A (p.Arg320Gln) single nucleotide variant Inborn genetic diseases [RCV002669973] Chr11:75006065 [GRCh38]
Chr11:74717110 [GRCh37]
Chr11:11q13.4		 likely benign
NM_006656.6(NEU3):c.833G>A (p.Arg278Gln) single nucleotide variant Inborn genetic diseases [RCV002940502] Chr11:75005939 [GRCh38]
Chr11:74716984 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_006656.6(NEU3):c.422G>T (p.Arg141Leu) single nucleotide variant Inborn genetic diseases [RCV003203904] Chr11:75005528 [GRCh38]
Chr11:74716573 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_006656.6(NEU3):c.359T>G (p.Met120Arg) single nucleotide variant Inborn genetic diseases [RCV003186294] Chr11:75005465 [GRCh38]
Chr11:74716510 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_006656.6(NEU3):c.803C>T (p.Ala268Val) single nucleotide variant Inborn genetic diseases [RCV003199991] Chr11:75005909 [GRCh38]
Chr11:74716954 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_006656.6(NEU3):c.22C>A (p.Pro8Thr) single nucleotide variant Inborn genetic diseases [RCV003209760] Chr11:74989082 [GRCh38]
Chr11:74700127 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_006656.6(NEU3):c.679T>C (p.Cys227Arg) single nucleotide variant Inborn genetic diseases [RCV003285237] Chr11:75005785 [GRCh38]
Chr11:74716830 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_006656.6(NEU3):c.959G>C (p.Arg320Pro) single nucleotide variant Inborn genetic diseases [RCV003309623] Chr11:75006065 [GRCh38]
Chr11:74717110 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_006656.6(NEU3):c.382C>A (p.Gln128Lys) single nucleotide variant Inborn genetic diseases [RCV003357074] Chr11:75005488 [GRCh38]
Chr11:74716533 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_006656.6(NEU3):c.438G>C (p.Glu146Asp) single nucleotide variant Inborn genetic diseases [RCV003345287] Chr11:75005544 [GRCh38]
Chr11:74716589 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_006656.6(NEU3):c.439C>G (p.Arg147Gly) single nucleotide variant Inborn genetic diseases [RCV003345288] Chr11:75005545 [GRCh38]
Chr11:74716590 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_006656.6(NEU3):c.1317G>C (p.Glu439Asp) single nucleotide variant Inborn genetic diseases [RCV003350396] Chr11:75006423 [GRCh38]
Chr11:74717468 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_006656.6(NEU3):c.1361A>G (p.Asn454Ser) single nucleotide variant Inborn genetic diseases [RCV003373746] Chr11:75006467 [GRCh38]
Chr11:74717512 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_006656.6(NEU3):c.1298G>A (p.Arg433His) single nucleotide variant Inborn genetic diseases [RCV003370758] Chr11:75006404 [GRCh38]
Chr11:74717449 [GRCh37]
Chr11:11q13.4		 uncertain significance
NM_006656.6(NEU3):c.1364C>G (p.Pro455Arg) single nucleotide variant Inborn genetic diseases [RCV003368839] Chr11:75006470 [GRCh38]
Chr11:74717515 [GRCh37]
Chr11:11q13.4		 uncertain significance
GRCh37/hg19 11q12.2-13.5(chr11:59923608-76272324)x3 copy number gain not provided [RCV003484842] Chr11:59923608..76272324 [GRCh37]
Chr11:11q12.2-13.5		 pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2193
Count of miRNA genes:880
Interacting mature miRNAs:1013
Transcripts:ENST00000294064, ENST00000526068, ENST00000529024, ENST00000531509, ENST00000531619, ENST00000532963, ENST00000534628, ENST00000544263, ENST00000545272
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
G63715  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371174,699,169 - 74,699,481UniSTSGRCh37
Build 361174,376,817 - 74,377,129RGDNCBI36
Celera1172,005,736 - 72,006,048RGD
Cytogenetic Map11q13.5UniSTS
HuRef1170,995,968 - 70,996,280UniSTS
TNG Radiation Hybrid Map1133741.0UniSTS
D11S3116  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371174,713,743 - 74,713,948UniSTSGRCh37
Build 361174,391,391 - 74,391,596RGDNCBI36
Celera1172,020,311 - 72,020,516RGD
Cytogenetic Map11q13.5UniSTS
HuRef1171,011,484 - 71,011,689UniSTS
SHGC-107164  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371174,700,376 - 74,700,566UniSTSGRCh37
Build 361174,378,024 - 74,378,214RGDNCBI36
Celera1172,006,943 - 72,007,133RGD
Cytogenetic Map11q13.5UniSTS
HuRef1170,997,175 - 70,997,365UniSTS
TNG Radiation Hybrid Map1133750.0UniSTS


Expression


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

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 130 54 363 21 727 22 898 599 407 53 698 310 8 10 655
Low 2308 2897 1337 581 1198 421 3458 1584 3321 347 753 1296 167 1 1194 2133 6 2
Below cutoff 1 40 26 22 26 22 14 6 19 9 7

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001367860 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001367861 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001367862 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001367863 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001367864 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001367865 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001367866 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001367867 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_006656 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047426298 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047426299 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047426300 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047426301 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047426302 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047426303 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047426304 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367518 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367519 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367520 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367521 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367522 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367523 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367524 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB008185 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK022450 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK290442 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK303540 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP001992 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC136397 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC144059 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BP352846 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX108543 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471076 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CN429425 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068267 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB099096 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB240271 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ590342 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  Y18563 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000294064   ⟹   ENSP00000294064
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1174,988,933 - 75,010,907 (+)Ensembl
RefSeq Acc Id: ENST00000526068   ⟹   ENSP00000436540
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1174,988,925 - 74,990,163 (+)Ensembl
RefSeq Acc Id: ENST00000529024   ⟹   ENSP00000434474
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1174,988,698 - 75,018,893 (+)Ensembl
RefSeq Acc Id: ENST00000531509   ⟹   ENSP00000432097
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1174,988,279 - 75,007,084 (+)Ensembl
RefSeq Acc Id: ENST00000531619   ⟹   ENSP00000436118
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1174,988,943 - 75,005,469 (+)Ensembl
RefSeq Acc Id: ENST00000532963   ⟹   ENSP00000434907
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1174,988,934 - 75,006,834 (+)Ensembl
RefSeq Acc Id: ENST00000534628   ⟹   ENSP00000434754
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1174,988,944 - 74,995,043 (+)Ensembl
RefSeq Acc Id: NM_001367860   ⟹   NP_001354789
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381174,988,644 - 75,010,907 (+)NCBI
T2T-CHM13v2.01174,918,200 - 74,940,457 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001367861   ⟹   NP_001354790
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381174,988,644 - 74,995,038 (+)NCBI
T2T-CHM13v2.01174,918,200 - 74,924,594 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001367862   ⟹   NP_001354791
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381174,988,933 - 74,995,038 (+)NCBI
T2T-CHM13v2.01174,918,489 - 74,924,594 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001367863   ⟹   NP_001354792
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381174,988,644 - 75,010,907 (+)NCBI
T2T-CHM13v2.01174,918,200 - 74,940,457 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001367864   ⟹   NP_001354793
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381174,988,933 - 75,010,907 (+)NCBI
T2T-CHM13v2.01174,918,489 - 74,940,457 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001367865   ⟹   NP_001354794
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381174,988,644 - 75,010,907 (+)NCBI
T2T-CHM13v2.01174,918,200 - 74,940,457 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001367866   ⟹   NP_001354795
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381174,988,933 - 75,010,907 (+)NCBI
T2T-CHM13v2.01174,918,489 - 74,940,457 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001367867   ⟹   NP_001354796
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381174,988,933 - 74,990,158 (+)NCBI
T2T-CHM13v2.01174,918,489 - 74,919,714 (+)NCBI
Sequence:
RefSeq Acc Id: NM_006656   ⟹   NP_006647
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381174,988,933 - 75,010,907 (+)NCBI
GRCh371174,699,950 - 74,718,743 (+)ENTREZGENE
Build 361174,377,598 - 74,396,391 (+)NCBI Archive
HuRef1170,996,749 - 71,016,487 (+)ENTREZGENE
CHM1_11174,583,347 - 74,602,139 (+)NCBI
T2T-CHM13v2.01174,918,489 - 74,940,457 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047426298   ⟹   XP_047282254
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381174,980,515 - 75,010,907 (+)NCBI
RefSeq Acc Id: XM_047426299   ⟹   XP_047282255
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381175,000,807 - 75,010,907 (+)NCBI
RefSeq Acc Id: XM_047426300   ⟹   XP_047282256
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381174,996,857 - 75,010,907 (+)NCBI
RefSeq Acc Id: XM_047426301   ⟹   XP_047282257
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381174,994,909 - 75,010,907 (+)NCBI
RefSeq Acc Id: XM_047426302   ⟹   XP_047282258
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381174,988,933 - 75,020,676 (+)NCBI
RefSeq Acc Id: XM_047426303   ⟹   XP_047282259
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381174,988,644 - 75,020,676 (+)NCBI
RefSeq Acc Id: XM_047426304   ⟹   XP_047282260
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381174,980,515 - 74,990,158 (+)NCBI
RefSeq Acc Id: XM_054367518   ⟹   XP_054223493
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01174,910,079 - 74,940,457 (+)NCBI
RefSeq Acc Id: XM_054367519   ⟹   XP_054223494
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01174,930,355 - 74,940,457 (+)NCBI
RefSeq Acc Id: XM_054367520   ⟹   XP_054223495
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01174,926,410 - 74,940,457 (+)NCBI
RefSeq Acc Id: XM_054367521   ⟹   XP_054223496
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01174,924,465 - 74,940,457 (+)NCBI
RefSeq Acc Id: XM_054367522   ⟹   XP_054223497
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01174,918,489 - 74,957,510 (+)NCBI
RefSeq Acc Id: XM_054367523   ⟹   XP_054223498
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01174,918,200 - 74,957,510 (+)NCBI
RefSeq Acc Id: XM_054367524   ⟹   XP_054223499
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01174,910,079 - 74,919,714 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001354789 (Get FASTA)   NCBI Sequence Viewer  
  NP_001354790 (Get FASTA)   NCBI Sequence Viewer  
  NP_001354791 (Get FASTA)   NCBI Sequence Viewer  
  NP_001354792 (Get FASTA)   NCBI Sequence Viewer  
  NP_001354793 (Get FASTA)   NCBI Sequence Viewer  
  NP_001354794 (Get FASTA)   NCBI Sequence Viewer  
  NP_001354795 (Get FASTA)   NCBI Sequence Viewer  
  NP_001354796 (Get FASTA)   NCBI Sequence Viewer  
  NP_006647 (Get FASTA)   NCBI Sequence Viewer  
  XP_047282254 (Get FASTA)   NCBI Sequence Viewer  
  XP_047282255 (Get FASTA)   NCBI Sequence Viewer  
  XP_047282256 (Get FASTA)   NCBI Sequence Viewer  
  XP_047282257 (Get FASTA)   NCBI Sequence Viewer  
  XP_047282258 (Get FASTA)   NCBI Sequence Viewer  
  XP_047282259 (Get FASTA)   NCBI Sequence Viewer  
  XP_047282260 (Get FASTA)   NCBI Sequence Viewer  
  XP_054223493 (Get FASTA)   NCBI Sequence Viewer  
  XP_054223494 (Get FASTA)   NCBI Sequence Viewer  
  XP_054223495 (Get FASTA)   NCBI Sequence Viewer  
  XP_054223496 (Get FASTA)   NCBI Sequence Viewer  
  XP_054223497 (Get FASTA)   NCBI Sequence Viewer  
  XP_054223498 (Get FASTA)   NCBI Sequence Viewer  
  XP_054223499 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAI36398 (Get FASTA)   NCBI Sequence Viewer  
  AAI44060 (Get FASTA)   NCBI Sequence Viewer  
  BAA82611 (Get FASTA)   NCBI Sequence Viewer  
  BAF83131 (Get FASTA)   NCBI Sequence Viewer  
  BAG51074 (Get FASTA)   NCBI Sequence Viewer  
  BAG64566 (Get FASTA)   NCBI Sequence Viewer  
  CAB96131 (Get FASTA)   NCBI Sequence Viewer  
  EAW74953 (Get FASTA)   NCBI Sequence Viewer  
  EAW74954 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000294064
  ENSP00000294064.4
  ENSP00000432097
  ENSP00000432097.1
  ENSP00000434474
  ENSP00000434474.1
  ENSP00000434754
  ENSP00000434754.1
  ENSP00000434907
  ENSP00000434907.1
  ENSP00000436118
  ENSP00000436118.1
  ENSP00000436540
  ENSP00000436540.1
GenBank Protein Q9UQ49 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_006647   ⟸   NM_006656
- Peptide Label: isoform a
- UniProtKB: Q9NQE1 (UniProtKB/Swiss-Prot),   A8K327 (UniProtKB/Swiss-Prot),   Q9UQ49 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001354789   ⟸   NM_001367860
- Peptide Label: isoform a
- UniProtKB: Q9UQ49 (UniProtKB/Swiss-Prot),   Q9NQE1 (UniProtKB/Swiss-Prot),   A8K327 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: NP_001354794   ⟸   NM_001367865
- Peptide Label: isoform d
RefSeq Acc Id: NP_001354792   ⟸   NM_001367863
- Peptide Label: isoform c
- UniProtKB: E9PMZ3 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001354790   ⟸   NM_001367861
- Peptide Label: isoform b
- UniProtKB: E9PNK1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001354795   ⟸   NM_001367866
- Peptide Label: isoform e
- UniProtKB: E9PR25 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001354793   ⟸   NM_001367864
- Peptide Label: isoform c
- UniProtKB: E9PMZ3 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001354791   ⟸   NM_001367862
- Peptide Label: isoform b
- UniProtKB: E9PNK1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001354796   ⟸   NM_001367867
- Peptide Label: isoform f
- UniProtKB: E9PI40 (UniProtKB/TrEMBL)
RefSeq Acc Id: ENSP00000294064   ⟸   ENST00000294064
RefSeq Acc Id: ENSP00000436118   ⟸   ENST00000531619
RefSeq Acc Id: ENSP00000432097   ⟸   ENST00000531509
RefSeq Acc Id: ENSP00000434907   ⟸   ENST00000532963
RefSeq Acc Id: ENSP00000434754   ⟸   ENST00000534628
RefSeq Acc Id: ENSP00000436540   ⟸   ENST00000526068
RefSeq Acc Id: ENSP00000434474   ⟸   ENST00000529024
RefSeq Acc Id: XP_047282254   ⟸   XM_047426298
- Peptide Label: isoform X1
RefSeq Acc Id: XP_047282260   ⟸   XM_047426304
- Peptide Label: isoform X5
RefSeq Acc Id: XP_047282259   ⟸   XM_047426303
- Peptide Label: isoform X4
RefSeq Acc Id: XP_047282258   ⟸   XM_047426302
- Peptide Label: isoform X4
RefSeq Acc Id: XP_047282257   ⟸   XM_047426301
- Peptide Label: isoform X3
- UniProtKB: B4E0V4 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047282256   ⟸   XM_047426300
- Peptide Label: isoform X3
- UniProtKB: B4E0V4 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047282255   ⟸   XM_047426299
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054223493   ⟸   XM_054367518
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054223499   ⟸   XM_054367524
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054223498   ⟸   XM_054367523
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054223497   ⟸   XM_054367522
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054223496   ⟸   XM_054367521
- Peptide Label: isoform X3
- UniProtKB: B4E0V4 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054223495   ⟸   XM_054367520
- Peptide Label: isoform X3
- UniProtKB: B4E0V4 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054223494   ⟸   XM_054367519
- Peptide Label: isoform X2
Protein Domains
Sialidase

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9UQ49-F1-model_v2 AlphaFold Q9UQ49 1-428 view protein structure

Promoters
RGD ID:6789160
Promoter ID:HG_KWN:13730
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000294064,   UC001OVV.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361174,377,334 - 74,377,834 (+)MPROMDB
RGD ID:7221555
Promoter ID:EPDNEW_H16523
Type:initiation region
Name:NEU3_1
Description:neuraminidase 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381174,988,933 - 74,988,993EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:7760 AgrOrtholog
COSMIC NEU3 COSMIC
Ensembl Genes ENSG00000162139 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000294064 ENTREZGENE
  ENST00000294064.9 UniProtKB/Swiss-Prot
  ENST00000526068 ENTREZGENE
  ENST00000526068.1 UniProtKB/TrEMBL
  ENST00000529024 ENTREZGENE
  ENST00000529024.1 UniProtKB/TrEMBL
  ENST00000531509 ENTREZGENE
  ENST00000531509.5 UniProtKB/Swiss-Prot
  ENST00000531619 ENTREZGENE
  ENST00000531619.1 UniProtKB/TrEMBL
  ENST00000532963 ENTREZGENE
  ENST00000532963.1 UniProtKB/TrEMBL
  ENST00000534628 ENTREZGENE
  ENST00000534628.1 UniProtKB/TrEMBL
Gene3D-CATH 2.120.10.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000162139 GTEx
HGNC ID HGNC:7760 ENTREZGENE
Human Proteome Map NEU3 Human Proteome Map
InterPro Sialidase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Sialidase_fam UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Sialidase_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:10825 UniProtKB/Swiss-Prot
NCBI Gene 10825 ENTREZGENE
OMIM 604617 OMIM
PANTHER PTHR10628 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR10628:SF23 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam BNR_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA31562 PharmGKB
Superfamily-SCOP SSF50939 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A8K327 ENTREZGENE
  B4E0V4 ENTREZGENE, UniProtKB/TrEMBL
  E9PI40 ENTREZGENE, UniProtKB/TrEMBL
  E9PMZ3 ENTREZGENE, UniProtKB/TrEMBL
  E9PNK1 ENTREZGENE, UniProtKB/TrEMBL
  E9PR25 ENTREZGENE, UniProtKB/TrEMBL
  NEUR3_HUMAN UniProtKB/Swiss-Prot
  Q9NQE1 ENTREZGENE
  Q9UQ49 ENTREZGENE
UniProt Secondary A8K327 UniProtKB/Swiss-Prot
  Q9NQE1 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-07-05 NEU3  neuraminidase 3  NEU3  neuraminidase 3, membrane sialidase  Symbol and/or name change 5135510 APPROVED
2016-06-28 NEU3  neuraminidase 3, membrane sialidase  NEU3  neuraminidase 3 (membrane sialidase)  Symbol and/or name change 5135510 APPROVED
2015-11-24 NEU3  neuraminidase 3 (membrane sialidase)  NEU3  sialidase 3 (membrane sialidase)  Symbol and/or name change 5135510 APPROVED