NKAIN2 (sodium/potassium transporting ATPase interacting 2) - Rat Genome Database

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Gene: NKAIN2 (sodium/potassium transporting ATPase interacting 2) Homo sapiens
Analyze
Symbol: NKAIN2
Name: sodium/potassium transporting ATPase interacting 2
RGD ID: 1349938
HGNC Page HGNC:16443
Description: Predicted to be involved in regulation of sodium ion transport. Predicted to be located in plasma membrane.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: FAM77B; MGC41924; Na(+)/K(+)-transporting ATPase subunit beta-1-interacting protein 2; Na+/K+ transporting ATPase interacting 2; NKAIP2; sodium/potassium-transporting ATPase subunit beta-1-interacting protein 2; T-cell lymphoma breakpoint-associated target protein 1; TCBA; TCBA1
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
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
GRCh386123,803,865 - 124,825,640 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl6123,803,865 - 124,825,640 (+)EnsemblGRCh38hg38GRCh38
GRCh376124,125,010 - 125,146,786 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 366124,166,768 - 125,188,485 (+)NCBINCBI36Build 36hg18NCBI36
Build 346124,166,987 - 125,188,485NCBI
Celera6124,869,958 - 125,891,802 (+)NCBICelera
Cytogenetic Map6q22.31NCBI
HuRef6121,702,429 - 122,723,736 (+)NCBIHuRef
CHM1_16124,388,612 - 125,410,248 (+)NCBICHM1_1
T2T-CHM13v2.06124,991,747 - 126,013,690 (+)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

Biological Process

Cellular Component

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders. Blokland GAM, etal., Biol Psychiatry. 2022 Jan 1;91(1):102-117. doi: 10.1016/j.biopsych.2021.02.972. Epub 2021 Mar 23.
2. Genome-wide association study identifies SIAH3 locus influencing the rate of ventricular enlargement in non-demented elders. Li X, etal., Aging (Albany NY). 2019 Nov 11;11(21):9862-9874. doi: 10.18632/aging.102435. Epub 2019 Nov 11.
3. NKAIN2 functions as a novel tumor suppressor in prostate cancer. Mao X, etal., Oncotarget. 2016 Sep 27;7(39):63793-63803. doi: 10.18632/oncotarget.11690.
4. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
5. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
6. High-resolution array CGH profiling identifies Na/K transporting ATPase interacting 2 (NKAIN2) as a predisposing candidate gene in neuroblastoma. Romania P, etal., PLoS One. 2013 Oct 25;8(10):e78481. doi: 10.1371/journal.pone.0078481. eCollection 2013.
7. Family-based association analysis of alcohol dependence in the COGA sample and replication in the Australian twin-family study. Wang KS, etal., J Neural Transm (Vienna). 2011 Sep;118(9):1293-9. doi: 10.1007/s00702-011-0628-3. Epub 2011 Mar 29.
Additional References at PubMed
PMID:11979551   PMID:12477932   PMID:14574404   PMID:14702039   PMID:15908570   PMID:16344560   PMID:17606467   PMID:19913121   PMID:20379614   PMID:20628086   PMID:20634892   PMID:21873635  
PMID:22589738   PMID:23534349   PMID:23535033   PMID:23894747   PMID:24024966   PMID:24569950   PMID:24999842   PMID:28381166  


Genomics

Comparative Map Data
NKAIN2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh386123,803,865 - 124,825,640 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl6123,803,865 - 124,825,640 (+)EnsemblGRCh38hg38GRCh38
GRCh376124,125,010 - 125,146,786 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 366124,166,768 - 125,188,485 (+)NCBINCBI36Build 36hg18NCBI36
Build 346124,166,987 - 125,188,485NCBI
Celera6124,869,958 - 125,891,802 (+)NCBICelera
Cytogenetic Map6q22.31NCBI
HuRef6121,702,429 - 122,723,736 (+)NCBIHuRef
CHM1_16124,388,612 - 125,410,248 (+)NCBICHM1_1
T2T-CHM13v2.06124,991,747 - 126,013,690 (+)NCBIT2T-CHM13v2.0
Nkain2
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391031,565,314 - 32,773,170 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1031,565,306 - 32,766,458 (-)EnsemblGRCm39 Ensembl
GRCm381031,689,310 - 32,897,174 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1031,689,310 - 32,890,462 (-)EnsemblGRCm38mm10GRCm38
MGSCv371031,409,125 - 32,609,721 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361031,378,735 - 32,579,264 (-)NCBIMGSCv36mm8
Celera1032,612,553 - 33,799,322 (-)NCBICelera
Cytogenetic Map10A4NCBI
cM Map1017.56NCBI
Nkain2
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8126,488,381 - 27,696,134 (+)NCBIGRCr8
mRatBN7.2124,668,627 - 25,877,051 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl124,669,462 - 25,877,064 (+)EnsemblmRatBN7.2 Ensembl
Rnor_6.0127,473,251 - 28,161,521 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl127,476,375 - 28,159,290 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0128,926,594 - 29,615,541 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
Celera123,895,595 - 24,572,547 (+)NCBICelera
Cytogenetic Map1p11NCBI
Nkain2
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554365,407,773 - 6,343,953 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049554365,407,642 - 6,345,015 (+)NCBIChiLan1.0ChiLan1.0
NKAIN2
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v25143,793,042 - 144,817,344 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan16141,700,135 - 142,776,468 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v06121,590,732 - 122,611,445 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.16125,713,030 - 126,732,080 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl6125,713,247 - 126,729,668 (+)Ensemblpanpan1.1panPan2
NKAIN2
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1163,091,956 - 63,857,512 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl162,910,841 - 63,858,164 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha163,719,503 - 64,668,404 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0163,115,179 - 64,065,713 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl163,115,326 - 64,065,725 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1163,047,299 - 63,997,590 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0162,836,039 - 63,786,131 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0163,484,826 - 64,435,218 (+)NCBIUU_Cfam_GSD_1.0
NKAIN2
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl138,014,255 - 39,040,605 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1138,014,252 - 39,040,215 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2142,053,739 - 42,198,706 (-)NCBISscrofa10.2Sscrofa10.2susScr3
NKAIN2
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11348,876,514 - 50,121,382 (-)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_02366604021,185,910 - 22,296,563 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Nkain2
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247986,687,807 - 7,619,303 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247986,685,647 - 7,619,436 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in NKAIN2
42 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_001040214.2(NKAIN2):c.55-181262G>T single nucleotide variant Lung cancer [RCV000096499] Chr6:124101744 [GRCh38]
Chr6:124422889 [GRCh37]
Chr6:6q22.31		 uncertain significance
NM_001040214.2(NKAIN2):c.55-103306T>A single nucleotide variant Lung cancer [RCV000096500] Chr6:124179700 [GRCh38]
Chr6:124500845 [GRCh37]
Chr6:6q22.31		 uncertain significance
NM_001040214.2(NKAIN2):c.192+374T>G single nucleotide variant Lung cancer [RCV000096502] Chr6:124283516 [GRCh38]
Chr6:124604662 [GRCh37]
Chr6:6q22.31		 uncertain significance
NM_001040214.2(NKAIN2):c.274-62168C>G single nucleotide variant Lung cancer [RCV000096503] Chr6:124596018 [GRCh38]
Chr6:124917164 [GRCh37]
Chr6:6q22.31		 uncertain significance
NM_001040214.2(NKAIN2):c.475-46818C>T single nucleotide variant Lung cancer [RCV000096504] Chr6:124744521 [GRCh38]
Chr6:125065667 [GRCh37]
Chr6:6q22.31		 uncertain significance
GRCh38/hg38 6q21-23.2(chr6:108944899-132067720)x1 copy number loss See cases [RCV000051196] Chr6:108944899..132067720 [GRCh38]
Chr6:109266102..132388860 [GRCh37]
Chr6:109372795..132430553 [NCBI36]
Chr6:6q21-23.2		 pathogenic
GRCh38/hg38 6q22.1-22.33(chr6:115601230-128514324)x1 copy number loss See cases [RCV000052196] Chr6:115601230..128514324 [GRCh38]
Chr6:115922394..128835469 [GRCh37]
Chr6:116029087..128877162 [NCBI36]
Chr6:6q22.1-22.33		 pathogenic
GRCh38/hg38 6q22.31(chr6:118975015-125713307)x1 copy number loss See cases [RCV000052197] Chr6:118975015..125713307 [GRCh38]
Chr6:119296180..126034453 [GRCh37]
Chr6:119337879..126076146 [NCBI36]
Chr6:6q22.31		 pathogenic
GRCh38/hg38 6q22.31(chr6:124116341-124499647)x1 copy number loss See cases [RCV000052198] Chr6:124116341..124499647 [GRCh38]
Chr6:124437486..124820793 [GRCh37]
Chr6:124479185..124862492 [NCBI36]
Chr6:6q22.31		 pathogenic
GRCh38/hg38 6q22.31(chr6:123206400-123959297)x3 copy number gain See cases [RCV000053387] Chr6:123206400..123959297 [GRCh38]
Chr6:123527545..124280442 [GRCh37]
Chr6:123569244..124322141 [NCBI36]
Chr6:6q22.31		 uncertain significance
GRCh38/hg38 6q22.31(chr6:123352392-123845516)x3 copy number gain See cases [RCV000136997] Chr6:123352392..123845516 [GRCh38]
Chr6:123673537..124166661 [GRCh37]
Chr6:123715236..124208360 [NCBI36]
Chr6:6q22.31		 uncertain significance
GRCh38/hg38 6q22.31-22.32(chr6:121829616-126154472)x1 copy number loss See cases [RCV000137174] Chr6:121829616..126154472 [GRCh38]
Chr6:122150762..126475618 [GRCh37]
Chr6:122192461..126517311 [NCBI36]
Chr6:6q22.31-22.32		 uncertain significance
GRCh38/hg38 6q22.31(chr6:123206400-123981401)x3 copy number gain See cases [RCV000137762] Chr6:123206400..123981401 [GRCh38]
Chr6:123527545..124302546 [GRCh37]
Chr6:123569244..124344245 [NCBI36]
Chr6:6q22.31		 likely benign
GRCh38/hg38 6q22.1-22.32(chr6:117607147-126699980)x3 copy number gain See cases [RCV000137726] Chr6:117607147..126699980 [GRCh38]
Chr6:117928310..127021125 [GRCh37]
Chr6:118035003..127062818 [NCBI36]
Chr6:6q22.1-22.32		 pathogenic
GRCh38/hg38 6q22.31(chr6:123206369-123959291)x3 copy number gain See cases [RCV000139579] Chr6:123206369..123959291 [GRCh38]
Chr6:123527514..124280436 [GRCh37]
Chr6:123569213..124322135 [NCBI36]
Chr6:6q22.31		 likely benign
GRCh38/hg38 6q13-24.1(chr6:74382807-142040500)x3 copy number gain See cases [RCV000139729] Chr6:74382807..142040500 [GRCh38]
Chr6:75092523..142361637 [GRCh37]
Chr6:75149243..142403330 [NCBI36]
Chr6:6q13-24.1		 pathogenic
GRCh38/hg38 6q21-22.31(chr6:106503719-125781219)x1 copy number loss See cases [RCV000141587] Chr6:106503719..125781219 [GRCh38]
Chr6:106951594..126102365 [GRCh37]
Chr6:107058287..126144058 [NCBI36]
Chr6:6q21-22.31		 pathogenic
GRCh38/hg38 6q22.31(chr6:123188343-124008918)x3 copy number gain See cases [RCV000143453] Chr6:123188343..124008918 [GRCh38]
Chr6:123509488..124330063 [GRCh37]
Chr6:123551187..124371762 [NCBI36]
Chr6:6q22.31		 uncertain significance
GRCh38/hg38 6q22.31(chr6:123206400-123959297)x3 copy number gain See cases [RCV000148083] Chr6:123206400..123959297 [GRCh38]
Chr6:123527545..124280442 [GRCh37]
Chr6:123569244..124322141 [NCBI36]
Chr6:6q22.31		 uncertain significance
GRCh38/hg38 6q22.31(chr6:123197871-124008917)x3 copy number gain See cases [RCV000143491] Chr6:123197871..124008917 [GRCh38]
Chr6:123519016..124330062 [GRCh37]
Chr6:123560715..124371761 [NCBI36]
Chr6:6q22.31		 uncertain significance
NM_001040214.2(NKAIN2):c.55-199612_55-129556dup duplication Normal pregnancy [RCV000161451] Chr6:124083394..124153450 [GRCh38]
Chr6:124404539..124474595 [GRCh37]
Chr6:6q22.31		 not provided
NM_001040214.2(NKAIN2):c.55-187304_55-129556dup duplication Small for gestational age [RCV000161452] Chr6:124095702..124153450 [GRCh38]
Chr6:124416847..124474595 [GRCh37]
Chr6:6q22.31		 not provided
GRCh37/hg19 6q22.31(chr6:123477056-124324549)x3 copy number gain See cases [RCV000515555] Chr6:123477056..124324549 [GRCh37]
Chr6:6q22.31		 uncertain significance
GRCh37/hg19 6q22.31(chr6:123539531-124324489)x4 copy number gain See cases [RCV000446396] Chr6:123539531..124324489 [GRCh37]
Chr6:6q22.31		 uncertain significance
GRCh37/hg19 6q22.31(chr6:124373571-124463314)x1 copy number loss See cases [RCV000447777] Chr6:124373571..124463314 [GRCh37]
Chr6:6q22.31		 uncertain significance
GRCh37/hg19 6q22.31(chr6:124494613-125184025)x3 copy number gain See cases [RCV000447799] Chr6:124494613..125184025 [GRCh37]
Chr6:6q22.31		 likely benign
GRCh37/hg19 6p25.3-q27(chr6:156975-170919482)x3 copy number gain See cases [RCV000512067] Chr6:156975..170919482 [GRCh37]
Chr6:6p25.3-q27		 pathogenic
GRCh37/hg19 6p25.3-q27(chr6:156975-170919482) copy number gain See cases [RCV000510595] Chr6:156975..170919482 [GRCh37]
Chr6:6p25.3-q27		 pathogenic
GRCh37/hg19 6q22.31-23.2(chr6:122612641-131564463)x1 copy number loss See cases [RCV000511386] Chr6:122612641..131564463 [GRCh37]
Chr6:6q22.31-23.2		 pathogenic
NM_001040214.3(NKAIN2):c.188C>A (p.Thr63Lys) single nucleotide variant not specified [RCV004316264] Chr6:124283138 [GRCh38]
Chr6:124604284 [GRCh37]
Chr6:6q22.31		 uncertain significance
GRCh37/hg19 6q21-23.2(chr6:112939290-132327952)x1 copy number loss Poly (ADP-Ribose) polymerase inhibitor response [RCV000626432] Chr6:112939290..132327952 [GRCh37]
Chr6:6q21-23.2		 drug response
GRCh37/hg19 6q22.31(chr6:123509362-124332260)x3 copy number gain not provided [RCV000682718] Chr6:123509362..124332260 [GRCh37]
Chr6:6q22.31		 likely benign|uncertain significance
GRCh37/hg19 6q22.31(chr6:124496938-125189118)x3 copy number gain not provided [RCV000682720] Chr6:124496938..125189118 [GRCh37]
Chr6:6q22.31		 uncertain significance
GRCh37/hg19 6q22.31(chr6:124691423-124984989)x3 copy number gain not provided [RCV000682721] Chr6:124691423..124984989 [GRCh37]
Chr6:6q22.31		 uncertain significance
Single allele duplication not provided [RCV000677970] Chr6:123539531..124463373 [GRCh37]
Chr6:6q22.31		 uncertain significance
GRCh37/hg19 6p25.3-q27(chr6:60107-171054786)x3 copy number gain not provided [RCV000745400] Chr6:60107..171054786 [GRCh37]
Chr6:6p25.3-q27		 pathogenic
GRCh37/hg19 6p25.3-q27(chr6:108666-170980171)x3 copy number gain not provided [RCV000745403] Chr6:108666..170980171 [GRCh37]
Chr6:6p25.3-q27		 pathogenic
GRCh37/hg19 6p25.3-q27(chr6:165632-170919470)x3 copy number gain not provided [RCV000745404] Chr6:165632..170919470 [GRCh37]
Chr6:6p25.3-q27		 pathogenic
GRCh37/hg19 6q22.31(chr6:124269067-124349384)x1 copy number loss not provided [RCV000746019] Chr6:124269067..124349384 [GRCh37]
Chr6:6q22.31		 benign
GRCh37/hg19 6q22.31(chr6:124427556-124471337)x3 copy number gain not provided [RCV000746020] Chr6:124427556..124471337 [GRCh37]
Chr6:6q22.31		 benign
GRCh37/hg19 6q22.31(chr6:124434003-124500739)x3 copy number gain not provided [RCV000746021] Chr6:124434003..124500739 [GRCh37]
Chr6:6q22.31		 benign
GRCh37/hg19 6q22.31(chr6:124633499-124661546)x1 copy number loss not provided [RCV000746022] Chr6:124633499..124661546 [GRCh37]
Chr6:6q22.31		 benign
NM_001040214.3(NKAIN2):c.617+10T>C single nucleotide variant not provided [RCV000921043] Chr6:124818478 [GRCh38]
Chr6:125139624 [GRCh37]
Chr6:6q22.31		 likely benign
Single allele duplication not provided [RCV000844964] Chr6:124373571..124778355 [GRCh37]
Chr6:6q22.31		 not provided
NM_001040214.3(NKAIN2):c.133A>G (p.Ile45Val) single nucleotide variant not specified [RCV004307764] Chr6:124283083 [GRCh38]
Chr6:124604229 [GRCh37]
Chr6:6q22.31		 uncertain significance
NM_001040214.3(NKAIN2):c.105A>G (p.Ala35=) single nucleotide variant not provided [RCV000956410] Chr6:124283055 [GRCh38]
Chr6:124604201 [GRCh37]
Chr6:6q22.31		 benign
GRCh37/hg19 6q22.31-22.33(chr6:120059951-130033233)x1 copy number loss not provided [RCV002472894] Chr6:120059951..130033233 [GRCh37]
Chr6:6q22.31-22.33		 uncertain significance
GRCh37/hg19 6q22.31(chr6:121646369-124675332)x3 copy number gain not provided [RCV002473858] Chr6:121646369..124675332 [GRCh37]
Chr6:6q22.31		 uncertain significance
GRCh37/hg19 6q22.31(chr6:124632709-124755323)x1 copy number loss not provided [RCV001259958] Chr6:124632709..124755323 [GRCh37]
Chr6:6q22.31		 uncertain significance
Single allele deletion Interstitial 6q microdeletion syndrome [RCV002280353] Chr6:115941808..133892653 [GRCh38]
Chr6:6q22.1-23.2		 pathogenic
GRCh37/hg19 6q22.31-22.33(chr6:125037475-129494795)x1 copy number loss not provided [RCV001834303] Chr6:125037475..129494795 [GRCh37]
Chr6:6q22.31-22.33		 pathogenic
GRCh37/hg19 6q22.31-22.33(chr6:122839432-128801386) copy number loss not specified [RCV002053616] Chr6:122839432..128801386 [GRCh37]
Chr6:6q22.31-22.33		 pathogenic
GRCh37/hg19 6q22.31(chr6:123858348-125320485)x1 copy number loss not provided [RCV002472875] Chr6:123858348..125320485 [GRCh37]
Chr6:6q22.31		 uncertain significance
NM_001040214.3(NKAIN2):c.472G>A (p.Ala158Thr) single nucleotide variant not specified [RCV004134967] Chr6:124658384 [GRCh38]
Chr6:124979530 [GRCh37]
Chr6:6q22.31		 uncertain significance
NM_001040214.3(NKAIN2):c.512G>C (p.Cys171Ser) single nucleotide variant not specified [RCV004113223] Chr6:124791376 [GRCh38]
Chr6:125112522 [GRCh37]
Chr6:6q22.31		 uncertain significance
GRCh37/hg19 6q22.31(chr6:119243634-126078530)x1 copy number loss not provided [RCV002509028] Chr6:119243634..126078530 [GRCh37]
Chr6:6q22.31		 not provided
NM_001040214.3(NKAIN2):c.13A>G (p.Ser5Gly) single nucleotide variant not specified [RCV004179419] Chr6:123804213 [GRCh38]
Chr6:124125358 [GRCh37]
Chr6:6q22.31		 uncertain significance
NM_001040214.3(NKAIN2):c.547G>T (p.Gly183Cys) single nucleotide variant not specified [RCV004080573] Chr6:124818398 [GRCh38]
Chr6:125139544 [GRCh37]
Chr6:6q22.31		 uncertain significance
GRCh38/hg38 6q21-23.1(chr6:113857248-130442177)x1 copy number loss Intellectual disability, autosomal dominant 55, with seizures [RCV003327704] Chr6:113857248..130442177 [GRCh38]
Chr6:6q21-23.1		 pathogenic
NM_001040214.3(NKAIN2):c.42T>G (p.Cys14Trp) single nucleotide variant not specified [RCV004357618] Chr6:123804242 [GRCh38]
Chr6:124125387 [GRCh37]
Chr6:6q22.31		 uncertain significance
GRCh37/hg19 6q22.31(chr6:123554219-125882578)x1 copy number loss not provided [RCV003482931] Chr6:123554219..125882578 [GRCh37]
Chr6:6q22.31		 uncertain significance
GRCh37/hg19 6q22.31(chr6:124918580-125201001)x4 copy number gain not provided [RCV003485348] Chr6:124918580..125201001 [GRCh37]
Chr6:6q22.31		 uncertain significance
GRCh37/hg19 6q22.31-23.3(chr6:120218852-137160850)x1 copy number loss not provided [RCV003482930] Chr6:120218852..137160850 [GRCh37]
Chr6:6q22.31-23.3		 pathogenic
GRCh37/hg19 6q22.31-22.33(chr6:124515654-130227224)x1 copy number loss not specified [RCV003986658] Chr6:124515654..130227224 [GRCh37]
Chr6:6q22.31-22.33		 uncertain significance
GRCh37/hg19 6q22.31-25.3(chr6:119840686-156623091)x3 copy number gain not specified [RCV003986631] Chr6:119840686..156623091 [GRCh37]
Chr6:6q22.31-25.3		 pathogenic
GRCh37/hg19 6q21-23.2(chr6:110546061-131896074)x3 copy number gain not specified [RCV003986625] Chr6:110546061..131896074 [GRCh37]
Chr6:6q21-23.2		 likely pathogenic
NM_001040214.3(NKAIN2):c.173G>A (p.Arg58Lys) single nucleotide variant not specified [RCV004493150] Chr6:124283123 [GRCh38]
Chr6:124604269 [GRCh37]
Chr6:6q22.31		 uncertain significance
GRCh37/hg19 6q21-22.31(chr6:109324789-124836619)x1 copy number loss not provided [RCV004577478] Chr6:109324789..124836619 [GRCh37]
Chr6:6q21-22.31		 pathogenic
NM_001040214.3(NKAIN2):c.619T>C (p.Ser207Pro) single nucleotide variant not specified [RCV004643736] Chr6:124823221 [GRCh38]
Chr6:125144367 [GRCh37]
Chr6:6q22.31		 uncertain significance
NM_001040214.3(NKAIN2):c.340G>A (p.Gly114Arg) single nucleotide variant not specified [RCV004643735] Chr6:124658252 [GRCh38]
Chr6:124979398 [GRCh37]
Chr6:6q22.31		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1196
Count of miRNA genes:758
Interacting mature miRNAs:848
Transcripts:ENST00000368416, ENST00000368417, ENST00000476571, ENST00000545433, ENST00000546092
Prediction methods:Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

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

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


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
597050260GWAS1146334_Huterine fibroid QTL GWAS1146334 (human)0.000009uterine fibroid6124823206124823207Human
597315743GWAS1411817_Hexecutive function measurement QTL GWAS1411817 (human)0.000008executive function measurement6124122624124122625Human
597106335GWAS1202409_Hpallidum volume change measurement, age at assessment QTL GWAS1202409 (human)0.0000002pallidum volume change measurement, age at assessment6123860740123860741Human
597227921GWAS1323995_Hcognitive function measurement QTL GWAS1323995 (human)0.000004cognitive function measurement6123837107123837108Human
597091485GWAS1187559_Hseasonal gut microbiome measurement QTL GWAS1187559 (human)0.000006seasonal gut microbiome measurement6123915139123915140Human
597338772GWAS1434846_Hdiastolic blood pressure QTL GWAS1434846 (human)0.000004diastolic blood pressurediastolic blood pressure (CMO:0000005)6123903314123903315Human
597020298GWAS1116372_HLDL peak particle diameter measurement, total fat intake measurement QTL GWAS1116372 (human)0.000005LDL peak particle diameter measurement, total fat intake measurementblood low density lipoprotein particle diameter (CMO:0002693)6124486668124486669Human
597144503GWAS1240577_HCOVID-19 QTL GWAS1240577 (human)0.0000005COVID-196124718735124718736Human
597319101GWAS1415175_Hisoeugenol sulfate measurement QTL GWAS1415175 (human)0.0000004isoeugenol sulfate measurement6124016238124016239Human
597024952GWAS1121026_Hcolorectal health QTL GWAS1121026 (human)0.000008colorectal health6123998565123998566Human
407020143GWAS669119_Hneurotic disorder QTL GWAS669119 (human)0.0000003neurotic disorder6124370091124370092Human
407040109GWAS689085_Hceliac disease QTL GWAS689085 (human)0.0000005celiac disease6124422361124422362Human
407377275GWAS1026251_Hpreterm premature rupture of the membranes, spontaneous preterm birth QTL GWAS1026251 (human)0.000003preterm premature rupture of the membranes, spontaneous preterm birth6124704154124704155Human
596973217GWAS1092736_Hbipolar disorder, schizophrenia, sex interaction measurement, major depressive disorder QTL GWAS1092736 (human)0.000004bipolar disorder, schizophrenia, sex interaction measurement, major depressive disorder6123991513123991514Human
407124849GWAS773825_HAlzheimer disease QTL GWAS773825 (human)0.0000006Alzheimer disease6124005082124005083Human
597351599GWAS1447673_Hbody height QTL GWAS1447673 (human)0.0000001body height (VT:0001253)body height (CMO:0000106)6124189782124189783Human
597333164GWAS1429238_Hsmoking initiation QTL GWAS1429238 (human)4e-16smoking initiation6123881758123881759Human
597341356GWAS1437430_Hnon-small cell lung carcinoma QTL GWAS1437430 (human)0.000007non-small cell lung carcinoma6124092050124092051Human
597030563GWAS1126637_Hbody mass index QTL GWAS1126637 (human)1e-10body mass indexbody mass index (BMI) (CMO:0000105)6124590388124590389Human
597062063GWAS1158137_Hsusceptibility to rubella infection measurement QTL GWAS1158137 (human)0.0000006susceptibility to rubella infection measurement6124349498124349499Human
597253280GWAS1349354_Hage at first sexual intercourse measurement QTL GWAS1349354 (human)5e-10age at first sexual intercourse measurement6124729847124729848Human
597333920GWAS1429994_HS-6-hydroxywarfarin to S-warfarin ratio measurement QTL GWAS1429994 (human)0.000002S-6-hydroxywarfarin to S-warfarin ratio measurement6123861365123861366Human
597188770GWAS1284844_Hmajor depressive disorder QTL GWAS1284844 (human)9e-11major depressive disorder6123971449123971450Human
596981935GWAS1101454_Hmemory performance QTL GWAS1101454 (human)0.00001memory performance6124810557124810558Human
597069226GWAS1165300_Hsusceptibility to urinary tract infection measurement QTL GWAS1165300 (human)0.000007susceptibility to urinary tract infection measurement6124145243124145244Human
597124522GWAS1220596_Hattention deficit hyperactivity disorder, substance abuse, antisocial behaviour measurement QTL GWAS1220596 (human)3e-09attention deficit hyperactivity disorder, substance abuse, antisocial behaviour measurement6124721359124721360Human
597102761GWAS1198835_Hgut microbiome measurement QTL GWAS1198835 (human)0.000009gut microbiome measurement6123821834123821835Human
597311909GWAS1407983_Hvaginal microbiome measurement QTL GWAS1407983 (human)0.000001vaginal microbiome measurement6123853094123853095Human
596981162GWAS1100681_Hmemory performance QTL GWAS1100681 (human)0.000008memory performance6124598830124598831Human
597224923GWAS1320997_Hpneumonia, COVID-19 QTL GWAS1320997 (human)0.000004pneumonia, COVID-196124641484124641485Human
597099486GWAS1195560_Hmalaria QTL GWAS1195560 (human)0.0000005malaria6124585841124585842Human
597287123GWAS1383197_Hbody weight QTL GWAS1383197 (human)3e-08body mass (VT:0001259)body weight (CMO:0000012)6124576550124576551Human
406958359GWAS607335_Heconomic and social preference QTL GWAS607335 (human)0.0000009economic and social preference6124750876124750877Human
597318084GWAS1414158_Hinsomnia QTL GWAS1414158 (human)1e-08insomnia6123937988123938024Human
597097929GWAS1194003_Hprotein measurement QTL GWAS1194003 (human)2e-08protein measurement6123863700123863701Human
596973258GWAS1092777_Hmajor depressive disorder QTL GWAS1092777 (human)9e-11major depressive disorder6123971449123971450Human
597318085GWAS1414159_Hinsomnia QTL GWAS1414159 (human)2e-08insomnia6123971449123971450Human
596973055GWAS1092574_Hbipolar disorder, schizophrenia, sex interaction measurement, major depressive disorder QTL GWAS1092574 (human)3e-08bipolar disorder, schizophrenia, sex interaction measurement, major depressive disorder6124005082124005083Human
596968447GWAS1087966_Hbody mass index QTL GWAS1087966 (human)2e-08body mass indexbody mass index (BMI) (CMO:0000105)6124590388124590389Human
406912559GWAS561535_Hunipolar depression, bipolar disorder, schizophrenia, sex interaction measurement QTL GWAS561535 (human)3e-08unipolar depression, bipolar disorder, schizophrenia, sex interaction measurement6124005082124005083Human
597309928GWAS1406002_Hbody mass index QTL GWAS1406002 (human)2e-08body mass indexbody mass index (BMI) (CMO:0000105)6124590388124590389Human
597462254GWAS1558328_Heducational attainment QTL GWAS1558328 (human)2e-08educational attainment6124740763124740764Human
597294829GWAS1390903_Hblood arsenic measurement QTL GWAS1390903 (human)0.000002blood arsenic measurement6123860982123860983Human
597327087GWAS1423161_Hbiliary atresia QTL GWAS1423161 (human)0.000004biliary atresia6123833691123833692Human
597104098GWAS1200172_Hreading and spelling ability QTL GWAS1200172 (human)0.000003reading and spelling ability6124823206124823207Human
407013176GWAS662152_Hbody mass index QTL GWAS662152 (human)4e-11body mass indexbody mass index (BMI) (CMO:0000105)6124603886124603887Human
597134828GWAS1230902_Hmemory performance QTL GWAS1230902 (human)0.00001memory performance6124810557124810558Human
406950973GWAS599949_Hfemoral neck bone mineral density QTL GWAS599949 (human)0.000001bone mineralization trait (VT:0002896)bone mineral density (CMO:0001226)6124443485124443486Human
597582304GWAS1639164_Hamyloid-beta measurement QTL GWAS1639164 (human)0.000003amyloid-beta measurement6124047990124047991Human
597124626GWAS1220700_Hmajor depressive disorder QTL GWAS1220700 (human)0.000004major depressive disorder6123971449123971450Human
597609243GWAS1666103_Hbenign neoplasm of adrenal gland QTL GWAS1666103 (human)2e-11benign neoplasm of adrenal gland6124037461124037462Human
597099281GWAS1195355_Hmalaria QTL GWAS1195355 (human)0.000002malaria6124585841124585842Human
597100572GWAS1196646_Hbody height QTL GWAS1196646 (human)6e-12body height (VT:0001253)body height (CMO:0000106)6124603886124603887Human
407158473GWAS807449_Hgut microbiome measurement QTL GWAS807449 (human)0.000003gut microbiome measurement6123812300123812301Human
597137432GWAS1233506_Hbone density QTL GWAS1233506 (human)2e-36bone mineral mass (VT:0005007)bone mineral density (CMO:0001226)6124238586124238587Human
597301269GWAS1397343_Hbody mass index QTL GWAS1397343 (human)1e-09body mass indexbody mass index (BMI) (CMO:0000105)6124590388124590389Human
407050449GWAS699425_Hoxalate measurement QTL GWAS699425 (human)0.0000002oxalate measurement6124076857124076858Human
597019143GWAS1115217_Hopioid dependence QTL GWAS1115217 (human)0.0000003opioid dependence6124215869124215870Human
406912983GWAS561959_Hunipolar depression, bipolar disorder, schizophrenia, sex interaction measurement QTL GWAS561959 (human)0.000004unipolar depression, bipolar disorder, schizophrenia, sex interaction measurement6123991513123991514Human
597173760GWAS1269834_Hleft ventricular mass index QTL GWAS1269834 (human)0.0000001left ventricular mass indexheart left ventricle weight to body weight ratio (CMO:0000530)6124040001124040002Human
597330947GWAS1427021_Hbody mass index QTL GWAS1427021 (human)2e-08body mass indexbody mass index (BMI) (CMO:0000105)6124603886124603887Human
597621252GWAS1678112_Hhypotension QTL GWAS1678112 (human)2e-12hypotension6124559100124559101Human
407029721GWAS678697_Hunipolar depression QTL GWAS678697 (human)9e-11unipolar depression6123971449123971450Human
597323781GWAS1419855_Hessential tremor QTL GWAS1419855 (human)0.000002essential tremor6124216800124216801Human
597247288GWAS1343362_Hbipolar disorder, sex interaction measurement QTL GWAS1343362 (human)0.000001bipolar disorder, sex interaction measurement6124005082124005083Human
406896354GWAS545330_HQRS duration QTL GWAS545330 (human)0.000003QRS durationQRS duration (CMO:0000267)6124629917124629918Human
407093223GWAS742199_Hventricular enlargement measurement QTL GWAS742199 (human)0.000004brain ventricle morphology trait (VT:0000822)6124330054124330055Human
407125475GWAS774451_Hschizophrenia QTL GWAS774451 (human)0.000004schizophrenia6124021518124021519Human
406978798GWAS627774_Hintelligence QTL GWAS627774 (human)0.000003intelligence6123816600123816601Human
407043053GWAS692029_Hperiodontitis QTL GWAS692029 (human)0.0000008periodontitis6124238586124238587Human
597446191GWAS1542265_HParkinson disease QTL GWAS1542265 (human)0.000003Parkinson disease6124786353124786354Human
597133347GWAS1229421_Hmemory performance QTL GWAS1229421 (human)0.000008memory performance6124598830124598831Human
597031713GWAS1127787_Hbody mass index QTL GWAS1127787 (human)6e-11metabolic syndromebody mass index (BMI) (CMO:0000105)6124603886124603887Human
597184291GWAS1280365_Hsmoking initiation QTL GWAS1280365 (human)1e-10smoking initiation6124193616124193617Human
596987473GWAS1106992_Hbody mass index QTL GWAS1106992 (human)1e-09body mass indexbody mass index (BMI) (CMO:0000105)6124590388124590389Human
597036625GWAS1132699_Hthird ventricle volume measurement QTL GWAS1132699 (human)0.000006third ventricle size trait (VT:0000827)brain ventricle morphological measurement (CMO:0001971)6124503656124503657Human
597334871GWAS1430945_HR-warfarin measurement QTL GWAS1430945 (human)0.000004R-warfarin measurement6123851604123851605Human
597321034GWAS1417108_Heducational attainment QTL GWAS1417108 (human)3e-08educational attainment6124147675124147676Human
597321035GWAS1417109_Heducational attainment QTL GWAS1417109 (human)6e-09educational attainment6124439370124439371Human
597326152GWAS1422226_Hbody mass index QTL GWAS1422226 (human)2e-10body mass indexbody mass index (BMI) (CMO:0000105)6124603886124603887Human
597321033GWAS1417107_Heducational attainment QTL GWAS1417107 (human)5e-08educational attainment6124028800124028801Human
597191499GWAS1287573_Hbody mass index QTL GWAS1287573 (human)5e-16body mass indexbody mass index (BMI) (CMO:0000105)6124603886124603887Human
596953664GWAS1073183_Hbody mass index QTL GWAS1073183 (human)1e-10body mass indexbody mass index (BMI) (CMO:0000105)6124590388124590389Human
597294156GWAS1390230_Hcardiac troponin T measurement QTL GWAS1390230 (human)0.000004cardiac troponin T measurementblood troponin T level (CMO:0001284)6124622165124622166Human
597321036GWAS1417110_Heducational attainment QTL GWAS1417110 (human)1e-12educational attainment6124442639124442640Human
597228111GWAS1324185_Hprotein measurement QTL GWAS1324185 (human)3e-10protein measurement6123863700123863701Human
597321037GWAS1417111_Heducational attainment QTL GWAS1417111 (human)0.0000003educational attainment6124642095124642096Human
597325888GWAS1421962_Hcolor vision disorder QTL GWAS1421962 (human)0.0000009color vision disorder6124595014124595015Human
407210904GWAS859880_Hintelligence QTL GWAS859880 (human)0.000005intelligence6124683704124683705Human
406940837GWAS589813_Hinsomnia measurement QTL GWAS589813 (human)1e-08sleep behavior trait (VT:0001501)6123971449123971450Human
406980265GWAS629241_Hhemoglobin measurement QTL GWAS629241 (human)4e-13hemoglobin measurementhemoglobin measurement (CMO:0000508)6124473056124473057Human
597184116GWAS1280190_Hsmoking initiation QTL GWAS1280190 (human)1e-16smoking initiation6123881758123881759Human
597263989GWAS1360063_Hschizophrenia QTL GWAS1360063 (human)0.0000001schizophrenia6124755018124755019Human
597184117GWAS1280191_Hsmoking initiation QTL GWAS1280191 (human)4e-16smoking initiation6123971449123971450Human
597275753GWAS1371827_Htestosterone measurement QTL GWAS1371827 (human)2e-08testosterone measurementserum testosterone level (CMO:0000568)6124082741124082742Human
597218665GWAS1314739_Hbipolar disorder, schizophrenia, sex interaction measurement, major depressive disorder QTL GWAS1314739 (human)3e-08bipolar disorder, schizophrenia, sex interaction measurement, major depressive disorder6124005082124005083Human
406966706GWAS615682_Hsleep quality QTL GWAS615682 (human)0.000004sleep quality6123877771123877772Human
597218669GWAS1314743_Hbipolar disorder, schizophrenia, sex interaction measurement, major depressive disorder QTL GWAS1314743 (human)0.000004bipolar disorder, schizophrenia, sex interaction measurement, major depressive disorder6123991513123991514Human
597239916GWAS1335990_HMyopia QTL GWAS1335990 (human)0.0000008Myopia6124732471124732472Human
407042750GWAS691726_Hperiodontitis QTL GWAS691726 (human)0.000002periodontitis6124084010124084011Human
597195623GWAS1291697_Hlean body mass QTL GWAS1291697 (human)4e-09body lean mass (VT:0010483)total body lean mass (CMO:0003950)6124603886124603887Human

Markers in Region
D6S408  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376125,098,980 - 125,099,158UniSTSGRCh37
Build 366125,140,679 - 125,140,857RGDNCBI36
Celera6125,844,010 - 125,844,188RGD
Cytogenetic Map6q21UniSTS
HuRef6122,675,959 - 122,676,137UniSTS
Marshfield Genetic Map6125.71RGD
Marshfield Genetic Map6125.71UniSTS
Genethon Genetic Map6124.2UniSTS
deCODE Assembly Map6125.52UniSTS
GeneMap99-GB4 RH Map6506.72UniSTS
Whitehead-RH Map6729.9UniSTS
Whitehead-YAC Contig Map6 UniSTS
D6S1639  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376125,080,692 - 125,080,880UniSTSGRCh37
Build 366125,122,391 - 125,122,579RGDNCBI36
Celera6125,825,723 - 125,825,911RGD
Cytogenetic Map6q21-q22UniSTS
Cytogenetic Map6q21UniSTS
HuRef6122,657,708 - 122,657,868UniSTS
Marshfield Genetic Map6124.11UniSTS
Marshfield Genetic Map6124.11RGD
Genethon Genetic Map6124.2UniSTS
Stanford-G3 RH Map65128.0UniSTS
Whitehead-YAC Contig Map6 UniSTS
GeneMap99-G3 RH Map65431.0UniSTS
SHGC-53538  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376124,203,562 - 124,203,809UniSTSGRCh37
Build 366124,245,261 - 124,245,508RGDNCBI36
Celera6124,948,458 - 124,948,705RGD
Cytogenetic Map6q21UniSTS
HuRef6121,780,758 - 121,781,005UniSTS
TNG Radiation Hybrid Map658240.0UniSTS
SHGC-77850  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376124,506,514 - 124,506,622UniSTSGRCh37
Build 366124,548,213 - 124,548,321RGDNCBI36
Celera6125,251,014 - 125,251,122RGD
Cytogenetic Map6q21UniSTS
HuRef6122,083,019 - 122,083,127UniSTS
TNG Radiation Hybrid Map660134.0UniSTS
SHGC-78097  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376124,653,807 - 124,654,106UniSTSGRCh37
Build 366124,695,506 - 124,695,805RGDNCBI36
Celera6125,398,312 - 125,398,611RGD
Cytogenetic Map6q21UniSTS
HuRef6122,230,374 - 122,230,673UniSTS
SHGC-80073  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376124,875,378 - 124,875,676UniSTSGRCh37
Build 366124,917,077 - 124,917,375RGDNCBI36
Celera6125,619,819 - 125,620,117RGD
Cytogenetic Map6q21UniSTS
HuRef6122,451,759 - 122,452,057UniSTS
TNG Radiation Hybrid Map660232.0UniSTS
SHGC-80603  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376124,831,993 - 124,832,299UniSTSGRCh37
Build 366124,873,692 - 124,873,998RGDNCBI36
Celera6125,576,532 - 125,576,838RGD
Cytogenetic Map6q21UniSTS
HuRef6122,408,478 - 122,408,784UniSTS
TNG Radiation Hybrid Map660213.0UniSTS
G62757  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376124,149,189 - 124,149,473UniSTSGRCh37
Build 366124,190,888 - 124,191,172RGDNCBI36
Celera6124,894,077 - 124,894,361RGD
Cytogenetic Map6q21UniSTS
HuRef6121,726,382 - 121,726,666UniSTS
TNG Radiation Hybrid Map658209.0UniSTS
G62675  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376124,603,269 - 124,603,596UniSTSGRCh37
Build 366124,644,968 - 124,645,295RGDNCBI36
Celera6125,347,770 - 125,348,097RGD
Cytogenetic Map6q21UniSTS
HuRef6122,179,773 - 122,180,100UniSTS
TNG Radiation Hybrid Map660168.0UniSTS
SHGC-111710  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376124,831,845 - 124,832,158UniSTSGRCh37
Build 366124,873,544 - 124,873,857RGDNCBI36
Celera6125,576,384 - 125,576,697RGD
Cytogenetic Map6q21UniSTS
HuRef6122,408,330 - 122,408,643UniSTS
TNG Radiation Hybrid Map660213.0UniSTS
SHGC-105740  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376124,135,567 - 124,135,896UniSTSGRCh37
Build 366124,177,266 - 124,177,595RGDNCBI36
Celera6124,880,457 - 124,880,786RGD
Cytogenetic Map6q21UniSTS
HuRef6121,712,762 - 121,713,091UniSTS
TNG Radiation Hybrid Map658212.0UniSTS
SHGC-141801  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376125,035,868 - 125,036,140UniSTSGRCh37
Build 366125,077,567 - 125,077,839RGDNCBI36
Celera6125,780,903 - 125,781,175RGD
Cytogenetic Map6q21UniSTS
HuRef6122,612,890 - 122,613,162UniSTS
TNG Radiation Hybrid Map660390.0UniSTS
SHGC-142534  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376125,065,833 - 125,066,105UniSTSGRCh37
Build 366125,107,532 - 125,107,804RGDNCBI36
Celera6125,810,861 - 125,811,133RGD
Cytogenetic Map6q21UniSTS
HuRef6122,642,847 - 122,643,119UniSTS
TNG Radiation Hybrid Map660411.0UniSTS
SHGC-1831  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376125,098,981 - 125,099,245UniSTSGRCh37
Build 366125,140,680 - 125,140,944RGDNCBI36
Celera6125,844,011 - 125,844,275RGD
Cytogenetic Map6q21UniSTS
HuRef6122,675,960 - 122,676,224UniSTS
TNG Radiation Hybrid Map660345.0UniSTS
SHGC-150790  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376125,080,620 - 125,080,896UniSTSGRCh37
Build 366125,122,319 - 125,122,595RGDNCBI36
Celera6125,825,651 - 125,825,927RGD
Cytogenetic Map6q21UniSTS
HuRef6122,657,636 - 122,657,884UniSTS
TNG Radiation Hybrid Map660428.0UniSTS
RH66670  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376124,379,997 - 124,380,116UniSTSGRCh37
Build 366124,421,696 - 124,421,815RGDNCBI36
Celera6125,124,827 - 125,124,946RGD
Cytogenetic Map6q21UniSTS
HuRef6121,957,095 - 121,957,214UniSTS
GeneMap99-GB4 RH Map6504.4UniSTS
RH15888  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376124,226,635 - 124,226,816UniSTSGRCh37
Build 366124,268,334 - 124,268,515RGDNCBI36
Celera6124,971,532 - 124,971,713RGD
Cytogenetic Map6q21UniSTS
HuRef6121,803,848 - 121,804,029UniSTS
GeneMap99-GB4 RH Map6502.97UniSTS
SHGC-112081  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376124,440,771 - 124,441,047UniSTSGRCh37
Build 366124,482,470 - 124,482,746RGDNCBI36
Celera6125,185,597 - 125,185,873RGD
Cytogenetic Map6q21UniSTS
HuRef6122,017,872 - 122,018,148UniSTS
TNG Radiation Hybrid Map660068.0UniSTS
SGC32046  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376124,877,079 - 124,877,212UniSTSGRCh37
Build 366124,918,778 - 124,918,911RGDNCBI36
Celera6125,621,520 - 125,621,653RGD
Cytogenetic Map6q21UniSTS
HuRef6122,453,460 - 122,453,593UniSTS
GeneMap99-GB4 RH Map6506.82UniSTS
Whitehead-RH Map6730.4UniSTS
GDB:314425  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376124,715,544 - 124,715,750UniSTSGRCh37
Build 366124,757,243 - 124,757,449RGDNCBI36
Celera6125,460,094 - 125,460,304RGD
Cytogenetic Map6q21UniSTS
HuRef6122,292,074 - 122,292,288UniSTS
D6S988  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376125,021,932 - 125,022,085UniSTSGRCh37
Build 366125,063,631 - 125,063,784RGDNCBI36
Celera6125,766,954 - 125,767,107RGD
Cytogenetic Map6q21UniSTS
HuRef6122,599,201 - 122,599,354UniSTS
RH41840  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376124,276,152 - 124,276,291UniSTSGRCh37
Build 366124,317,851 - 124,317,990RGDNCBI36
Celera6125,021,061 - 125,021,200RGD
Cytogenetic Map6q21UniSTS
HuRef6121,853,365 - 121,853,504UniSTS
GeneMap99-GB4 RH Map6504.3UniSTS
WI-19339  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376124,379,942 - 124,380,189UniSTSGRCh37
Build 366124,421,641 - 124,421,888RGDNCBI36
Celera6125,124,772 - 125,125,019RGD
Cytogenetic Map6q21UniSTS
HuRef6121,957,040 - 121,957,287UniSTS
GeneMap99-GB4 RH Map6504.3UniSTS
Whitehead-RH Map6729.4UniSTS
RH63718  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376124,207,120 - 124,207,264UniSTSGRCh37
Build 366124,248,819 - 124,248,963RGDNCBI36
Celera6124,952,016 - 124,952,160RGD
Cytogenetic Map6q21UniSTS
HuRef6121,784,320 - 121,784,464UniSTS
GeneMap99-GB4 RH Map6502.97UniSTS
RH15825  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376124,321,417 - 124,321,546UniSTSGRCh37
Build 366124,363,116 - 124,363,245RGDNCBI36
Celera6125,066,250 - 125,066,379RGD
Cytogenetic Map6q21UniSTS
HuRef6121,898,554 - 121,898,683UniSTS
GeneMap99-GB4 RH Map6504.3UniSTS
NCBI RH Map61505.5UniSTS
RH78368  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376125,146,517 - 125,146,677UniSTSGRCh37
Build 366125,188,216 - 125,188,376RGDNCBI36
Celera6125,891,533 - 125,891,693RGD
Cytogenetic Map6q21UniSTS
HuRef6122,723,467 - 122,723,627UniSTS
GeneMap99-GB4 RH Map6506.72UniSTS
G17066  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376124,605,519 - 124,605,865UniSTSGRCh37
Build 366124,647,218 - 124,647,564RGDNCBI36
Celera6125,350,022 - 125,350,368RGD
Cytogenetic Map6q21UniSTS
HuRef6122,182,025 - 122,182,371UniSTS
AFM199zh10  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376125,099,191 - 125,099,245UniSTSGRCh37
Celera6125,844,221 - 125,844,275UniSTS
Cytogenetic Map6q21UniSTS
HuRef6122,676,170 - 122,676,224UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
pharyngeal arch
renal system
reproductive system
respiratory system
sensory system
visual system
1193 2265 2775 2188 4827 1565 2019 3 482 1077 322 2165 5999 5522 35 3689 1 679 1615 1445 170 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_021365 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001040214 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001300737 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001300738 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001300740 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_153355 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011535501 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011535503 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017010318 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017010319 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024446340 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054354379 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054354380 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054354381 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054354382 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_007059213 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_007059214 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_007059215 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB070452 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK055326 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK308927 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK309385 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK309407 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK309802 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK310763 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK315886 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL035692 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL109842 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL121968 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL136081 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL136107 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL136224 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL354936 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL356278 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL356605 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL450343 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL451135 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL451183 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL512376 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC035062 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471051 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068272 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA220592 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB174077 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB503487 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF458265 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF458269 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF458273 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF458274 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF510268 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000368416   ⟹   ENSP00000357401
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl6123,804,141 - 124,658,958 (+)Ensembl
Ensembl Acc Id: ENST00000368417   ⟹   ENSP00000357402
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl6123,803,865 - 124,825,640 (+)Ensembl
Ensembl Acc Id: ENST00000476571
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl6123,804,141 - 124,391,044 (+)Ensembl
Ensembl Acc Id: ENST00000545433   ⟹   ENSP00000437798
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl6124,121,850 - 124,825,616 (+)Ensembl
Ensembl Acc Id: ENST00000546092   ⟹   ENSP00000440287
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl6124,283,004 - 124,283,271 (+)Ensembl
Ensembl Acc Id: ENST00000640160   ⟹   ENSP00000492855
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl6124,818,399 - 124,823,623 (+)Ensembl
RefSeq Acc Id: NM_001040214   ⟹   NP_001035304
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386123,803,865 - 124,825,640 (+)NCBI
GRCh376124,124,991 - 125,146,786 (+)NCBI
Build 366124,166,768 - 125,188,485 (+)NCBI Archive
Celera6124,869,958 - 125,891,802 (+)RGD
HuRef6121,702,429 - 122,723,736 (+)ENTREZGENE
CHM1_16124,388,534 - 125,410,248 (+)NCBI
T2T-CHM13v2.06124,991,747 - 126,013,690 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001300737   ⟹   NP_001287666
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386123,803,865 - 124,825,640 (+)NCBI
CHM1_16124,388,534 - 125,410,248 (+)NCBI
T2T-CHM13v2.06124,991,747 - 126,013,690 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001300738   ⟹   NP_001287667
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386123,803,865 - 124,825,640 (+)NCBI
CHM1_16124,388,534 - 125,410,248 (+)NCBI
T2T-CHM13v2.06124,991,747 - 126,013,690 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001300740   ⟹   NP_001287669
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386123,804,385 - 124,825,640 (+)NCBI
CHM1_16124,389,073 - 125,410,248 (+)NCBI
T2T-CHM13v2.06124,992,267 - 126,013,690 (+)NCBI
Sequence:
RefSeq Acc Id: NM_153355   ⟹   NP_699186
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386123,803,865 - 124,825,640 (+)NCBI
GRCh376124,124,991 - 125,146,786 (+)NCBI
Celera6124,869,958 - 125,891,802 (+)RGD
HuRef6121,702,429 - 122,723,736 (+)ENTREZGENE
CHM1_16124,388,534 - 125,410,248 (+)NCBI
T2T-CHM13v2.06124,991,747 - 126,013,690 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017010318   ⟹   XP_016865807
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386123,803,865 - 124,825,640 (+)NCBI
Sequence:
RefSeq Acc Id: XM_054354379   ⟹   XP_054210354
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.06124,991,747 - 126,013,690 (+)NCBI
RefSeq Acc Id: XM_054354380   ⟹   XP_054210355
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.06124,991,747 - 126,013,690 (+)NCBI
RefSeq Acc Id: XM_054354381   ⟹   XP_054210356
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.06124,991,747 - 126,013,690 (+)NCBI
RefSeq Acc Id: XM_054354382   ⟹   XP_054210357
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.06124,991,747 - 126,013,690 (+)NCBI
RefSeq Acc Id: XR_007059213
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386123,803,865 - 124,825,640 (+)NCBI
RefSeq Acc Id: XR_007059214
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386123,803,865 - 124,825,640 (+)NCBI
RefSeq Acc Id: XR_007059215
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386123,803,865 - 124,825,640 (+)NCBI
RefSeq Acc Id: NP_699186   ⟸   NM_153355
- Peptide Label: isoform 2
- UniProtKB: Q5VXU1 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001035304   ⟸   NM_001040214
- Peptide Label: isoform 1
- UniProtKB: Q8TF67 (UniProtKB/Swiss-Prot),   Q8IYR4 (UniProtKB/Swiss-Prot),   Q5VXU1 (UniProtKB/Swiss-Prot),   B3KNZ0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001287666   ⟸   NM_001300737
- Peptide Label: isoform 3
- UniProtKB: B3KNZ0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001287667   ⟸   NM_001300738
- Peptide Label: isoform 4
- UniProtKB: Q5VXU1 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001287669   ⟸   NM_001300740
- Peptide Label: isoform 5
- UniProtKB: A6NLV5 (UniProtKB/TrEMBL),   B0AZU5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016865807   ⟸   XM_017010318
- Peptide Label: isoform X1
- UniProtKB: B3KNZ0 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSP00000437798   ⟸   ENST00000545433
Ensembl Acc Id: ENSP00000440287   ⟸   ENST00000546092
Ensembl Acc Id: ENSP00000492855   ⟸   ENST00000640160
Ensembl Acc Id: ENSP00000357402   ⟸   ENST00000368417
Ensembl Acc Id: ENSP00000357401   ⟸   ENST00000368416
RefSeq Acc Id: XP_054210354   ⟸   XM_054354379
- Peptide Label: isoform X2
- UniProtKB: B3KNZ0 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054210357   ⟸   XM_054354382
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054210355   ⟸   XM_054354380
- Peptide Label: isoform X3
- UniProtKB: B3KNZ0 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054210356   ⟸   XM_054354381
- Peptide Label: isoform X1
- UniProtKB: B3KNZ0 (UniProtKB/TrEMBL)

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q5VXU1-F1-model_v2 AlphaFold Q5VXU1 1-208 view protein structure

Promoters
RGD ID:7209053
Promoter ID:EPDNEW_H10272
Type:initiation region
Name:NKAIN2_2
Description:sodium/potassium transporting ATPase interacting 2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H10273  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh386123,804,001 - 123,804,061EPDNEW
RGD ID:7209055
Promoter ID:EPDNEW_H10273
Type:initiation region
Name:NKAIN2_1
Description:sodium/potassium transporting ATPase interacting 2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H10272  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh386123,804,196 - 123,804,256EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:16443 AgrOrtholog
COSMIC NKAIN2 COSMIC
Ensembl Genes ENSG00000188580 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000368416.5 UniProtKB/Swiss-Prot
  ENST00000368417 ENTREZGENE
  ENST00000368417.6 UniProtKB/Swiss-Prot
  ENST00000640160.1 UniProtKB/TrEMBL
GTEx ENSG00000188580 GTEx
HGNC ID HGNC:16443 ENTREZGENE
Human Proteome Map NKAIN2 Human Proteome Map
InterPro Na/K-Atpase_Interacting UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:154215 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene NKAIN2 ENTREZGENE
OMIM 609758 OMIM
PANTHER PTHR13084 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SODIUM/POTASSIUM-TRANSPORTING ATPASE SUBUNIT BETA-1-INTERACTING PROTEIN 2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam NKAIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA162397563 PharmGKB
UniProt A0A1W2PRU3_HUMAN UniProtKB/TrEMBL
  A6NLV5 ENTREZGENE
  B0AZU5 ENTREZGENE, UniProtKB/TrEMBL
  B3KNZ0 ENTREZGENE, UniProtKB/TrEMBL
  NKAI2_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
  Q8IYR4 ENTREZGENE
  Q8TF67 ENTREZGENE
UniProt Secondary A6NLV5 UniProtKB/TrEMBL
  Q8IYR4 UniProtKB/Swiss-Prot
  Q8TF67 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2017-03-28 NKAIN2  sodium/potassium transporting ATPase interacting 2    Sodium/potassium transporting ATPase interacting 2  Symbol and/or name change 5135510 APPROVED
2016-12-13 NKAIN2  Sodium/potassium transporting ATPase interacting 2    Na+/K+ transporting ATPase interacting 2  Symbol and/or name change 5135510 APPROVED