DGKB (diacylglycerol kinase beta) - Rat Genome Database

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Gene: DGKB (diacylglycerol kinase beta) Homo sapiens
Analyze
Symbol: DGKB
Name: diacylglycerol kinase beta
RGD ID: 731815
HGNC Page HGNC
Description: Enables diacylglycerol kinase activity and lipid binding activity. Involved in glycerolipid metabolic process and lipid phosphorylation. Located in cytosol and plasma membrane.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: 90 kDa diacylglycerol kinase; DAG kinase beta; DAGK2; DGK; DGK-BETA; diacylglycerol kinase, beta; diacylglycerol kinase, beta 90kDa; diglyceride kinase beta; KIAA0718
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
GRCh38.p13 Ensembl714,145,049 - 14,974,777 (-)EnsemblGRCh38hg38GRCh38
GRCh38714,145,049 - 14,974,858 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37714,184,674 - 15,014,483 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36714,153,770 - 14,847,413 (-)NCBINCBI36hg18NCBI36
Build 34713,988,847 - 14,654,128NCBI
Celera714,163,789 - 14,859,377 (-)NCBI
Cytogenetic Map7p21.2NCBI
HuRef714,066,966 - 14,764,852 (-)NCBIHuRef
CHM1_1714,184,411 - 14,880,671 (-)NCBICHM1_1
CRA_TCAGchr7v2714,235,562 - 14,932,596 (-)NCBI
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 Function

Molecular Pathway Annotations     Click to see Annotation Detail View
Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

Additional References at PubMed
PMID:7689223   PMID:9872452   PMID:11719522   PMID:12477932   PMID:12690205   PMID:12853948   PMID:14702039   PMID:15489334   PMID:16344560   PMID:17353931   PMID:18062770   PMID:19176441  
PMID:19913121   PMID:20081858   PMID:20185807   PMID:20379614   PMID:20419449   PMID:20490451   PMID:20571754   PMID:20628086   PMID:20677014   PMID:20889853   PMID:21493725   PMID:21873635  
PMID:22399527   PMID:22581228   PMID:22627129   PMID:23776197   PMID:23814057   PMID:24324551   PMID:24509480   PMID:24695318   PMID:25187374   PMID:27839966   PMID:28359772   PMID:30242153  


Genomics

Comparative Map Data
DGKB
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl714,145,049 - 14,974,777 (-)EnsemblGRCh38hg38GRCh38
GRCh38714,145,049 - 14,974,858 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37714,184,674 - 15,014,483 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36714,153,770 - 14,847,413 (-)NCBINCBI36hg18NCBI36
Build 34713,988,847 - 14,654,128NCBI
Celera714,163,789 - 14,859,377 (-)NCBI
Cytogenetic Map7p21.2NCBI
HuRef714,066,966 - 14,764,852 (-)NCBIHuRef
CHM1_1714,184,411 - 14,880,671 (-)NCBICHM1_1
CRA_TCAGchr7v2714,235,562 - 14,932,596 (-)NCBI
Dgkb
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391237,930,169 - 38,684,238 (+)NCBIGRCm39mm39
GRCm39 Ensembl1237,867,725 - 38,684,238 (+)Ensembl
GRCm381237,880,169 - 38,634,239 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1237,817,726 - 38,634,239 (+)EnsemblGRCm38mm10GRCm38
MGSCv371238,607,292 - 39,359,997 (+)NCBIGRCm37mm9NCBIm37
MGSCv361238,390,971 - 39,143,797 (+)NCBImm8
Celera1239,316,859 - 40,057,925 (+)NCBICelera
Cytogenetic Map12A3NCBI
Dgkb
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.2654,640,948 - 55,397,210 (+)NCBImRatBN7.2
mRatBN7.2 Ensembl654,641,614 - 55,397,043 (+)Ensembl
Rnor_6.0657,516,351 - 58,277,385 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl657,516,713 - 58,277,279 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0667,113,446 - 67,580,128 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
Rnor_5.0667,693,661 - 67,868,706 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4656,715,327 - 57,479,656 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.1656,718,452 - 57,482,782 (+)NCBI
Celera653,755,433 - 54,502,520 (+)NCBICelera
RH 3.4 Map6394.3RGD
Cytogenetic Map6q21NCBI
Dgkb
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495541017,676,930 - 18,243,869 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495541017,677,375 - 18,304,409 (-)NCBIChiLan1.0ChiLan1.0
DGKB
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.1714,142,951 - 14,896,676 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl714,165,933 - 14,969,825 (-)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v0714,803,023 - 15,638,280 (-)NCBIMhudiblu_PPA_v0panPan3
DGKB
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11428,916,630 - 29,609,138 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1428,918,351 - 29,537,303 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1428,434,629 - 29,133,432 (-)NCBI
ROS_Cfam_1.01428,827,965 - 29,521,435 (-)NCBI
UMICH_Zoey_3.11428,918,649 - 29,617,633 (-)NCBI
UNSW_CanFamBas_1.01428,647,672 - 29,348,080 (-)NCBI
UU_Cfam_GSD_1.01428,958,514 - 29,660,097 (-)NCBI
Dgkb
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440511873,288,180 - 74,005,408 (-)NCBI
SpeTri2.0NW_004936546964,387 - 1,615,928 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
DGKB
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl983,569,920 - 84,510,087 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1983,571,927 - 84,358,712 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2992,175,666 - 92,485,017 (-)NCBISscrofa10.2Sscrofa10.2susScr3
DGKB
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12143,176,715 - 43,929,833 (+)NCBI
ChlSab1.1 Ensembl2143,176,989 - 43,746,258 (+)Ensembl
Vero_WHO_p1.0NW_02366604260,567,411 - 61,318,935 (-)NCBI
Dgkb
(Heterocephalus glaber - naked mole-rat)
Naked Mole-rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462473915,185,294 - 15,821,293 (+)NCBI

Position Markers
G17150  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37714,567,799 - 14,567,996UniSTSGRCh37
Build 36714,534,324 - 14,534,521RGDNCBI36
Celera714,546,271 - 14,546,468RGD
Cytogenetic Map7p21.2UniSTS
HuRef714,450,931 - 14,451,128UniSTS
CRA_TCAGchr7v2714,619,485 - 14,619,682UniSTS
GDB:1317276  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37714,330,014 - 14,330,080UniSTSGRCh37
Build 36714,296,539 - 14,296,605RGDNCBI36
Celera714,308,867 - 14,308,933RGD
Cytogenetic Map7p21.2UniSTS
HuRef714,211,290 - 14,211,356UniSTS
CRA_TCAGchr7v2714,380,643 - 14,380,709UniSTS
G17164  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37714,763,068 - 14,763,186UniSTSGRCh37
Build 36714,729,593 - 14,729,711RGDNCBI36
Celera714,741,371 - 14,741,489RGD
Cytogenetic Map7p21.2UniSTS
HuRef714,646,715 - 14,646,833UniSTS
CRA_TCAGchr7v2714,814,585 - 14,814,703UniSTS
RH48035  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37714,291,472 - 14,291,661UniSTSGRCh37
Build 36714,257,997 - 14,258,186RGDNCBI36
Celera714,270,346 - 14,270,535RGD
Cytogenetic Map7p21.2UniSTS
HuRef714,172,853 - 14,173,042UniSTS
CRA_TCAGchr7v2714,342,121 - 14,342,310UniSTS
GeneMap99-GB4 RH Map776.96UniSTS
SHGC-78962  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37714,859,783 - 14,860,053UniSTSGRCh37
Build 36714,826,308 - 14,826,578RGDNCBI36
Celera714,838,083 - 14,838,353RGD
Cytogenetic Map7p21.2UniSTS
HuRef714,743,559 - 14,743,829UniSTS
CRA_TCAGchr7v2714,911,299 - 14,911,569UniSTS
TNG Radiation Hybrid Map750154.0UniSTS
SHGC-79897  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37714,363,321 - 14,363,447UniSTSGRCh37
Build 36714,329,846 - 14,329,972RGDNCBI36
Celera714,342,183 - 14,342,309RGD
Cytogenetic Map7p21.2UniSTS
HuRef714,244,631 - 14,244,757UniSTS
CRA_TCAGchr7v2714,413,961 - 14,414,087UniSTS
TNG Radiation Hybrid Map750214.0UniSTS
SHGC-79923  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37714,569,077 - 14,569,388UniSTSGRCh37
Build 36714,535,602 - 14,535,913RGDNCBI36
Celera714,547,549 - 14,547,860RGD
Cytogenetic Map7p21.2UniSTS
HuRef714,452,209 - 14,452,520UniSTS
CRA_TCAGchr7v2714,620,763 - 14,621,074UniSTS
TNG Radiation Hybrid Map750027.0UniSTS
RH120266  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37714,228,647 - 14,228,918UniSTSGRCh37
Build 36714,195,172 - 14,195,443RGDNCBI36
Celera714,207,765 - 14,208,036RGD
Cytogenetic Map7p21.2UniSTS
HuRef714,110,950 - 14,111,221UniSTS
CRA_TCAGchr7v2714,279,537 - 14,279,808UniSTS
TNG Radiation Hybrid Map750285.0UniSTS
RH120179  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37714,309,295 - 14,309,639UniSTSGRCh37
Build 36714,275,820 - 14,276,164RGDNCBI36
Celera714,288,155 - 14,288,499RGD
Cytogenetic Map7p21.2UniSTS
HuRef714,190,580 - 14,190,924UniSTS
CRA_TCAGchr7v2714,359,928 - 14,360,272UniSTS
TNG Radiation Hybrid Map750248.0UniSTS
RH120060  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37714,457,007 - 14,457,280UniSTSGRCh37
Build 36714,423,532 - 14,423,805RGDNCBI36
Celera714,435,493 - 14,435,766RGD
Cytogenetic Map7p21.2UniSTS
HuRef714,338,280 - 14,338,553UniSTS
CRA_TCAGchr7v2714,507,285 - 14,507,558UniSTS
TNG Radiation Hybrid Map749985.0UniSTS
RH122179  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37714,459,062 - 14,459,382UniSTSGRCh37
Build 36714,425,587 - 14,425,907RGDNCBI36
Celera714,437,548 - 14,437,868RGD
Cytogenetic Map7p21.2UniSTS
HuRef714,340,335 - 14,340,656UniSTS
CRA_TCAGchr7v2714,509,340 - 14,509,660UniSTS
TNG Radiation Hybrid Map749988.0UniSTS
DGKB_583  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37714,187,170 - 14,187,980UniSTSGRCh37
Build 36714,153,695 - 14,154,505RGDNCBI36
Celera714,166,286 - 14,167,096RGD
HuRef714,069,463 - 14,070,273UniSTS
CRA_TCAGchr7v2714,238,059 - 14,238,869UniSTS
GDB:1317914  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37714,309,261 - 14,309,329UniSTSGRCh37
Build 36714,275,786 - 14,275,854RGDNCBI36
Celera714,288,121 - 14,288,189RGD
Cytogenetic Map7p21.2UniSTS
HuRef714,190,546 - 14,190,614UniSTS
CRA_TCAGchr7v2714,359,894 - 14,359,962UniSTS
AFMB347YE1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37714,825,719 - 14,825,836UniSTSGRCh37
Build 36714,792,244 - 14,792,361RGDNCBI36
Celera714,804,019 - 14,804,136RGD
Cytogenetic Map7p21.2UniSTS
HuRef714,709,495 - 14,709,612UniSTS
CRA_TCAGchr7v2714,877,235 - 14,877,352UniSTS
Whitehead-YAC Contig Map7 UniSTS
D7S1533  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37714,508,670 - 14,508,774UniSTSGRCh37
Build 36714,475,195 - 14,475,299RGDNCBI36
Celera714,487,150 - 14,487,254RGD
Cytogenetic Map7p21.2UniSTS
HuRef714,389,937 - 14,390,041UniSTS
CRA_TCAGchr7v2714,558,952 - 14,559,056UniSTS
G17177  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37714,384,938 - 14,385,069UniSTSGRCh37
Build 36714,351,463 - 14,351,594RGDNCBI36
Celera714,363,801 - 14,363,932RGD
Cytogenetic Map7p21.2UniSTS
HuRef714,266,254 - 14,266,385UniSTS
CRA_TCAGchr7v2714,435,583 - 14,435,714UniSTS
GDB:1318446  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37714,196,771 - 14,196,869UniSTSGRCh37
Build 36714,163,296 - 14,163,394RGDNCBI36
Celera714,175,886 - 14,175,984RGD
Cytogenetic Map7p21.2UniSTS
HuRef714,079,063 - 14,079,161UniSTS
CRA_TCAGchr7v2714,247,659 - 14,247,757UniSTS
116XH6  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37714,408,177 - 14,408,302UniSTSGRCh37
Build 36714,374,702 - 14,374,827RGDNCBI36
Celera714,387,040 - 14,387,169RGD
Cytogenetic Map7p21.2UniSTS
HuRef714,289,822 - 14,289,951UniSTS
CRA_TCAGchr7v2714,458,838 - 14,458,963UniSTS
Whitehead-YAC Contig Map7 UniSTS
D7S2033  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37714,417,898 - 14,418,045UniSTSGRCh37
Build 36714,384,423 - 14,384,570RGDNCBI36
Celera714,396,765 - 14,396,912RGD
Cytogenetic Map7p21.2UniSTS
HuRef714,299,547 - 14,299,694UniSTS
CRA_TCAGchr7v2714,468,559 - 14,468,706UniSTS
D8S2279  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.1-p12UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map8p23UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map13q14.1-q14.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17p13.1-p12UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q23.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5q14.2UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map1p35.2UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map17q21.2-q21.3UniSTS
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Cytogenetic Map22q12-q13UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map1q24.3UniSTS
Cytogenetic Map9q33.1UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map2p16.2UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map4q21UniSTS
Cytogenetic Map13q12.2UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map1q23UniSTS
Cytogenetic Map11q12-q13UniSTS
Cytogenetic Map11q13.3UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map11q12.1UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map8p21UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map10q26.1UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q33-q34UniSTS
Cytogenetic Map5q11.2-q13.2UniSTS
Cytogenetic Map13q32UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map5q22UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic MapXq13.3UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map3p26.3UniSTS
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map12q24.23UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic MapXp22.31UniSTS
Cytogenetic MapXp21.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3q24UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map14q11.2-q12UniSTS
Cytogenetic Map3p24UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map8q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map11cen-q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map1p35-p34UniSTS
Cytogenetic Map4p13-p12UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map9q31-q34UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q12.12UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1pUniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map2qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map5q14.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map9p21.1UniSTS
Cytogenetic Map9q34.2-q34.3UniSTS
EST-CFZ97756  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37714,842,397 - 14,843,800UniSTSGRCh37
Celera714,820,697 - 14,822,100UniSTS
HuRef714,726,173 - 14,727,576UniSTS
CRA_TCAGchr7v2714,893,913 - 14,895,316UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:7046
Count of miRNA genes:1121
Interacting mature miRNAs:1395
Transcripts:ENST00000258767, ENST00000399322, ENST00000402815, ENST00000403951, ENST00000403963, ENST00000406247, ENST00000407950, ENST00000437998, ENST00000444700, ENST00000463981, ENST00000464065, ENST00000467449, ENST00000471732, ENST00000477401, ENST00000493142
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.


Expression


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

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system adipose tissue appendage entire extraembryonic component
High
Medium 49 2 1 1 46 639 3 8 25
Low 1542 68 302 13 68 15 592 865 2636 82 260 97 2 61 444
Below cutoff 766 2380 1253 466 854 308 3612 1252 457 252 1073 1375 167 1137 2278 4

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_029494 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001350705 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001350706 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001350707 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001350708 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001350709 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001350711 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001350712 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001350714 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001350715 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001350716 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001350717 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001350718 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001350719 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001350720 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001350721 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001350722 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001350723 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001350724 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_145695 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011515154 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011790 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011791 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017011792 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001744571 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB018261 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC005039 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC005248 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC006045 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC006150 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC011229 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC073258 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC105459 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK124856 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK295668 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK304719 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AX032742 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AX032745 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC105005 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC143632 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC143633 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH236948 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471073 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA321150 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000399322   ⟹   ENSP00000382260
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl714,145,049 - 14,841,450 (-)Ensembl
RefSeq Acc Id: ENST00000402815   ⟹   ENSP00000384909
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl714,145,049 - 14,902,751 (-)Ensembl
RefSeq Acc Id: ENST00000403951   ⟹   ENSP00000385780
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl714,145,049 - 14,903,361 (-)Ensembl
RefSeq Acc Id: ENST00000403963
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl714,209,072 - 14,902,999 (-)Ensembl
RefSeq Acc Id: ENST00000406247   ⟹   ENSP00000386066
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl714,175,973 - 14,841,347 (-)Ensembl
RefSeq Acc Id: ENST00000407950   ⟹   ENSP00000385031
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl714,148,309 - 14,902,842 (-)Ensembl
RefSeq Acc Id: ENST00000437998   ⟹   ENSP00000405569
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl714,736,138 - 14,974,777 (-)Ensembl
RefSeq Acc Id: ENST00000463981
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl714,736,174 - 14,903,366 (-)Ensembl
RefSeq Acc Id: ENST00000464065
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl714,694,077 - 14,718,880 (-)Ensembl
RefSeq Acc Id: ENST00000467449
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl714,736,138 - 14,902,908 (-)Ensembl
RefSeq Acc Id: ENST00000471732
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl714,580,903 - 14,736,169 (-)Ensembl
RefSeq Acc Id: ENST00000477401
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl714,621,141 - 14,902,842 (-)Ensembl
RefSeq Acc Id: ENST00000493142
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl714,149,157 - 14,269,201 (-)Ensembl
RefSeq Acc Id: NM_001350705   ⟹   NP_001337634
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38714,145,049 - 14,903,656 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001350706   ⟹   NP_001337635
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38714,145,049 - 14,902,751 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001350707   ⟹   NP_001337636
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38714,145,049 - 14,974,858 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001350708   ⟹   NP_001337637
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38714,145,049 - 14,903,656 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001350709   ⟹   NP_001337638
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38714,145,049 - 14,902,751 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001350711   ⟹   NP_001337640
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38714,145,049 - 14,974,858 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001350712   ⟹   NP_001337641
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38714,145,049 - 14,903,656 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001350714   ⟹   NP_001337643
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38714,145,049 - 14,902,751 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001350715   ⟹   NP_001337644
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38714,145,049 - 14,903,656 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001350716   ⟹   NP_001337645
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38714,145,049 - 14,902,751 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001350717   ⟹   NP_001337646
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38714,145,049 - 14,974,858 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001350718   ⟹   NP_001337647
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38714,145,049 - 14,903,656 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001350719   ⟹   NP_001337648
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38714,145,049 - 14,902,751 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001350720   ⟹   NP_001337649
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38714,145,049 - 14,903,656 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001350721   ⟹   NP_001337650
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38714,145,049 - 14,902,751 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001350722   ⟹   NP_001337651
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38714,145,049 - 14,974,858 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001350723   ⟹   NP_001337652
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38714,145,049 - 14,902,751 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001350724   ⟹   NP_001337653
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38714,145,049 - 14,902,751 (-)NCBI
Sequence:
RefSeq Acc Id: NM_145695   ⟹   NP_663733
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38714,175,973 - 14,841,450 (-)NCBI
GRCh37714,184,674 - 14,943,281 (-)NCBI
Build 36714,182,123 - 14,847,413 (-)NCBI Archive
Celera714,163,789 - 14,859,377 (-)RGD
HuRef714,066,966 - 14,764,852 (-)RGD
CHM1_1714,215,329 - 14,880,671 (-)NCBI
CRA_TCAGchr7v2714,235,562 - 14,932,596 (-)ENTREZGENE
Sequence:
RefSeq Acc Id: XM_011515154   ⟹   XP_011513456
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38714,147,619 - 14,974,777 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017011790   ⟹   XP_016867279
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38714,335,841 - 14,902,956 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017011791   ⟹   XP_016867280
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38714,421,393 - 14,902,955 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017011792   ⟹   XP_016867281
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38714,467,708 - 14,902,955 (-)NCBI
Sequence:
RefSeq Acc Id: XR_001744571
RefSeq Status:
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38714,583,052 - 14,902,957 (-)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001337634 (Get FASTA)   NCBI Sequence Viewer  
  NP_001337635 (Get FASTA)   NCBI Sequence Viewer  
  NP_001337636 (Get FASTA)   NCBI Sequence Viewer  
  NP_001337637 (Get FASTA)   NCBI Sequence Viewer  
  NP_001337638 (Get FASTA)   NCBI Sequence Viewer  
  NP_001337640 (Get FASTA)   NCBI Sequence Viewer  
  NP_001337641 (Get FASTA)   NCBI Sequence Viewer  
  NP_001337643 (Get FASTA)   NCBI Sequence Viewer  
  NP_001337644 (Get FASTA)   NCBI Sequence Viewer  
  NP_001337645 (Get FASTA)   NCBI Sequence Viewer  
  NP_001337646 (Get FASTA)   NCBI Sequence Viewer  
  NP_001337647 (Get FASTA)   NCBI Sequence Viewer  
  NP_001337648 (Get FASTA)   NCBI Sequence Viewer  
  NP_001337649 (Get FASTA)   NCBI Sequence Viewer  
  NP_001337650 (Get FASTA)   NCBI Sequence Viewer  
  NP_001337651 (Get FASTA)   NCBI Sequence Viewer  
  NP_001337652 (Get FASTA)   NCBI Sequence Viewer  
  NP_001337653 (Get FASTA)   NCBI Sequence Viewer  
  NP_663733 (Get FASTA)   NCBI Sequence Viewer  
  XP_011513456 (Get FASTA)   NCBI Sequence Viewer  
  XP_016867279 (Get FASTA)   NCBI Sequence Viewer  
  XP_016867280 (Get FASTA)   NCBI Sequence Viewer  
  XP_016867281 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAC25525 (Get FASTA)   NCBI Sequence Viewer  
  AAI05006 (Get FASTA)   NCBI Sequence Viewer  
  AAI43633 (Get FASTA)   NCBI Sequence Viewer  
  AAP21868 (Get FASTA)   NCBI Sequence Viewer  
  AAP22362 (Get FASTA)   NCBI Sequence Viewer  
  AAS07495 (Get FASTA)   NCBI Sequence Viewer  
  AAS07533 (Get FASTA)   NCBI Sequence Viewer  
  BAA34438 (Get FASTA)   NCBI Sequence Viewer  
  BAH12149 (Get FASTA)   NCBI Sequence Viewer  
  BAH14245 (Get FASTA)   NCBI Sequence Viewer  
  CAC09945 (Get FASTA)   NCBI Sequence Viewer  
  CAC09946 (Get FASTA)   NCBI Sequence Viewer  
  EAL24292 (Get FASTA)   NCBI Sequence Viewer  
  EAL24293 (Get FASTA)   NCBI Sequence Viewer  
  EAW93663 (Get FASTA)   NCBI Sequence Viewer  
  EAW93664 (Get FASTA)   NCBI Sequence Viewer  
  Q9Y6T7 (Get FASTA)   NCBI Sequence Viewer  
Reference Sequences
RefSeq Acc Id: NP_663733   ⟸   NM_145695
- Peptide Label: isoform 2
- UniProtKB: Q9Y6T7 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_011513456   ⟸   XM_011515154
- Peptide Label: isoform X1
- UniProtKB: Q9Y6T7 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_016867279   ⟸   XM_017011790
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_016867280   ⟸   XM_017011791
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: XP_016867281   ⟸   XM_017011792
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: NP_001337651   ⟸   NM_001350722
- Peptide Label: isoform 8
- Sequence:
RefSeq Acc Id: NP_001337640   ⟸   NM_001350711
- Peptide Label: isoform 4
- Sequence:
RefSeq Acc Id: NP_001337646   ⟸   NM_001350717
- Peptide Label: isoform 6
- Sequence:
RefSeq Acc Id: NP_001337636   ⟸   NM_001350707
- Peptide Label: isoform 3
- Sequence:
RefSeq Acc Id: NP_001337649   ⟸   NM_001350720
- Peptide Label: isoform 7
- Sequence:
RefSeq Acc Id: NP_001337641   ⟸   NM_001350712
- Peptide Label: isoform 4
- Sequence:
RefSeq Acc Id: NP_001337644   ⟸   NM_001350715
- Peptide Label: isoform 5
- Sequence:
RefSeq Acc Id: NP_001337647   ⟸   NM_001350718
- Peptide Label: isoform 6
- Sequence:
RefSeq Acc Id: NP_001337637   ⟸   NM_001350708
- Peptide Label: isoform 3
- Sequence:
RefSeq Acc Id: NP_001337634   ⟸   NM_001350705
- Peptide Label: isoform 1
- Sequence:
RefSeq Acc Id: NP_001337653   ⟸   NM_001350724
- Peptide Label: isoform 9
- Sequence:
RefSeq Acc Id: NP_001337652   ⟸   NM_001350723
- Peptide Label: isoform 8
- Sequence:
RefSeq Acc Id: NP_001337650   ⟸   NM_001350721
- Peptide Label: isoform 7
- Sequence:
RefSeq Acc Id: NP_001337643   ⟸   NM_001350714
- Peptide Label: isoform 4
- Sequence:
RefSeq Acc Id: NP_001337645   ⟸   NM_001350716
- Peptide Label: isoform 5
- Sequence:
RefSeq Acc Id: NP_001337648   ⟸   NM_001350719
- Peptide Label: isoform 6
- Sequence:
RefSeq Acc Id: NP_001337638   ⟸   NM_001350709
- Peptide Label: isoform 3
- Sequence:
RefSeq Acc Id: NP_001337635   ⟸   NM_001350706
- Peptide Label: isoform 1
- Sequence:
RefSeq Acc Id: ENSP00000405569   ⟸   ENST00000437998
RefSeq Acc Id: ENSP00000382260   ⟸   ENST00000399322
RefSeq Acc Id: ENSP00000384909   ⟸   ENST00000402815
RefSeq Acc Id: ENSP00000385780   ⟸   ENST00000403951
RefSeq Acc Id: ENSP00000386066   ⟸   ENST00000406247
RefSeq Acc Id: ENSP00000385031   ⟸   ENST00000407950
Promoters
RGD ID:7209969
Promoter ID:EPDNEW_H10730
Type:initiation region
Name:DGKB_1
Description:diacylglycerol kinase beta
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H10731  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38714,974,854 - 14,974,914EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_004080.2(DGKB):c.2125+52844A>C single nucleotide variant Lung cancer [RCV000105701] Chr7:14285671 [GRCh38]
Chr7:14325296 [GRCh37]
Chr7:7p21.2
uncertain significance
NM_004080.2(DGKB):c.2125+4351A>C single nucleotide variant Lung cancer [RCV000105703] Chr7:14334164 [GRCh38]
Chr7:14373789 [GRCh37]
Chr7:7p21.2
uncertain significance
NM_004080.2(DGKB):c.1839-61829A>G single nucleotide variant Lung cancer [RCV000105707] Chr7:14407220 [GRCh38]
Chr7:14446845 [GRCh37]
Chr7:7p21.2
uncertain significance
NM_004080.2(DGKB):c.1838+15584G>T single nucleotide variant Lung cancer [RCV000105721] Chr7:14462577 [GRCh38]
Chr7:14502202 [GRCh37]
Chr7:7p21.2
uncertain significance
NM_004080.2(DGKB):c.1774-12296T>A single nucleotide variant Lung cancer [RCV000105733] Chr7:14490521 [GRCh38]
Chr7:14530146 [GRCh37]
Chr7:7p21.2
uncertain significance
NM_004080.2(DGKB):c.1774-12790C>G single nucleotide variant Lung cancer [RCV000105734] Chr7:14491015 [GRCh38]
Chr7:14530640 [GRCh37]
Chr7:7p21.2
uncertain significance
NM_004080.2(DGKB):c.1773+29328A>T single nucleotide variant Lung cancer [RCV000105747] Chr7:14544884 [GRCh38]
Chr7:14584509 [GRCh37]
Chr7:7p21.2
uncertain significance
NM_004080.2(DGKB):c.1287+3668G>T single nucleotide variant Lung cancer [RCV000105767] Chr7:14617710 [GRCh38]
Chr7:14657335 [GRCh37]
Chr7:7p21.2
uncertain significance
NM_004080.2(DGKB):c.323-949G>T single nucleotide variant Lung cancer [RCV000105801] Chr7:14719634 [GRCh38]
Chr7:14759259 [GRCh37]
Chr7:7p21.2
uncertain significance
NM_004080.2(DGKB):c.71-16744T>C single nucleotide variant Lung cancer [RCV000105808] Chr7:14774475 [GRCh38]
Chr7:14814100 [GRCh37]
Chr7:7p21.2
uncertain significance
NM_004080.2(DGKB):c.70+35988G>C single nucleotide variant Lung cancer [RCV000105810] Chr7:14805206 [GRCh38]
Chr7:14844831 [GRCh37]
Chr7:7p21.2
uncertain significance
NM_004080.2(DGKB):c.70+21283G>C single nucleotide variant Lung cancer [RCV000105811] Chr7:14819911 [GRCh38]
Chr7:14859536 [GRCh37]
Chr7:7p21.2
uncertain significance
GRCh38/hg38 7p22.3-14.1(chr7:54185-41875885)x3 copy number gain See cases [RCV000051159] Chr7:54185..41875885 [GRCh38]
Chr7:54185..41915483 [GRCh37]
Chr7:149268..41882008 [NCBI36]
Chr7:7p22.3-14.1
pathogenic
GRCh38/hg38 7p22.3-q36.3(chr7:53985-159282531)x1 copy number loss See cases [RCV000052250] Chr7:53985..159282531 [GRCh38]
Chr7:53985..159075220 [GRCh37]
Chr7:149068..158767981 [NCBI36]
Chr7:7p22.3-q36.3
pathogenic
GRCh38/hg38 7p21.3-15.3(chr7:8274775-21988311)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052280]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052280]|See cases [RCV000052280] Chr7:8274775..21988311 [GRCh38]
Chr7:8314405..22027929 [GRCh37]
Chr7:8280930..21994454 [NCBI36]
Chr7:7p21.3-15.3
pathogenic
GRCh38/hg38 7p21.3-21.1(chr7:9975653-19356878)x1 copy number loss See cases [RCV000052281] Chr7:9975653..19356878 [GRCh38]
Chr7:10015280..19396501 [GRCh37]
Chr7:9981805..19363026 [NCBI36]
Chr7:7p21.3-21.1
pathogenic
GRCh38/hg38 7p22.3-15.3(chr7:53985-24361531)x3 copy number gain See cases [RCV000053528] Chr7:53985..24361531 [GRCh38]
Chr7:53985..24401150 [GRCh37]
Chr7:149068..24367675 [NCBI36]
Chr7:7p22.3-15.3
pathogenic
GRCh38/hg38 7p22.3-14.2(chr7:54185-37089712)x3 copy number gain See cases [RCV000053530] Chr7:54185..37089712 [GRCh38]
Chr7:54185..37129317 [GRCh37]
Chr7:149268..37095842 [NCBI36]
Chr7:7p22.3-14.2
pathogenic
NM_004080.2(DGKB):c.1195G>A (p.Glu399Lys) single nucleotide variant Malignant melanoma [RCV000067741] Chr7:14621470 [GRCh38]
Chr7:14661095 [GRCh37]
Chr7:14627620 [NCBI36]
Chr7:7p21.2
not provided
GRCh38/hg38 7p22.3-q36.3(chr7:54185-159282390)x1 copy number loss See cases [RCV000135401] Chr7:54185..159282390 [GRCh38]
Chr7:54185..159075079 [GRCh37]
Chr7:149268..158767840 [NCBI36]
Chr7:7p22.3-q36.3
pathogenic
GRCh38/hg38 7p22.3-15.2(chr7:54185-26827634)x3 copy number gain See cases [RCV000136557] Chr7:54185..26827634 [GRCh38]
Chr7:54185..26867253 [GRCh37]
Chr7:149268..26833778 [NCBI36]
Chr7:7p22.3-15.2
pathogenic
GRCh38/hg38 7p21.2-21.1(chr7:13966197-18321354)x1 copy number loss See cases [RCV000136932] Chr7:13966197..18321354 [GRCh38]
Chr7:14005822..18360977 [GRCh37]
Chr7:13972347..18327502 [NCBI36]
Chr7:7p21.2-21.1
pathogenic
GRCh38/hg38 7p22.1-15.2(chr7:5682209-27230311)x3 copy number gain See cases [RCV000136649] Chr7:5682209..27230311 [GRCh38]
Chr7:5721840..27269930 [GRCh37]
Chr7:5688366..27236455 [NCBI36]
Chr7:7p22.1-15.2
pathogenic
GRCh38/hg38 7p21.3-21.2(chr7:13262814-15234164)x3 copy number gain See cases [RCV000136672] Chr7:13262814..15234164 [GRCh38]
Chr7:13302439..15273789 [GRCh37]
Chr7:13268964..15240314 [NCBI36]
Chr7:7p21.3-21.2
uncertain significance
GRCh38/hg38 7p22.3-15.3(chr7:45130-25221165)x3 copy number gain See cases [RCV000137824] Chr7:45130..25221165 [GRCh38]
Chr7:45130..25260784 [GRCh37]
Chr7:140213..25227309 [NCBI36]
Chr7:7p22.3-15.3
pathogenic
GRCh38/hg38 7p21.2(chr7:14404259-14584643)x1 copy number loss See cases [RCV000138391] Chr7:14404259..14584643 [GRCh38]
Chr7:14443884..14624268 [GRCh37]
Chr7:14410409..14590793 [NCBI36]
Chr7:7p21.2
likely benign
GRCh38/hg38 7p21.2(chr7:14691154-14721276)x3 copy number gain See cases [RCV000140268] Chr7:14691154..14721276 [GRCh38]
Chr7:14730779..14760901 [GRCh37]
Chr7:14697304..14727426 [NCBI36]
Chr7:7p21.2
likely benign
GRCh38/hg38 7p22.3-15.2(chr7:1698124-27207295)x3 copy number gain See cases [RCV000143060] Chr7:1698124..27207295 [GRCh38]
Chr7:1737760..27246914 [GRCh37]
Chr7:1704286..27213439 [NCBI36]
Chr7:7p22.3-15.2
pathogenic
GRCh38/hg38 7p21.3-21.2(chr7:11122492-16479303)x1 copy number loss See cases [RCV000142652] Chr7:11122492..16479303 [GRCh38]
Chr7:11162119..16518928 [GRCh37]
Chr7:11128644..16485453 [NCBI36]
Chr7:7p21.3-21.2
pathogenic
GRCh38/hg38 7p21.3-15.2(chr7:10610069-25760560)x1 copy number loss See cases [RCV000142708] Chr7:10610069..25760560 [GRCh38]
Chr7:10649696..25800180 [GRCh37]
Chr7:10616221..25766705 [NCBI36]
Chr7:7p21.3-15.2
pathogenic
GRCh38/hg38 7p21.2(chr7:14844332-15574557)x3 copy number gain See cases [RCV000143528] Chr7:14844332..15574557 [GRCh38]
Chr7:14883957..15614182 [GRCh37]
Chr7:14850482..15580707 [NCBI36]
Chr7:7p21.2
uncertain significance
GRCh38/hg38 7p22.3-15.2(chr7:43360-27196404)x3 copy number gain See cases [RCV000143586] Chr7:43360..27196404 [GRCh38]
Chr7:43360..27236023 [GRCh37]
Chr7:138443..27202548 [NCBI36]
Chr7:7p22.3-15.2
pathogenic
NC_000007.14:g.14919995A>G single nucleotide variant Lung cancer [RCV000105818] Chr7:14919995 [GRCh38]
Chr7:14959620 [GRCh37]
Chr7:7p21.2
uncertain significance
NC_000007.14:g.14928251T>C single nucleotide variant Lung cancer [RCV000105819] Chr7:14928251 [GRCh38]
Chr7:14967876 [GRCh37]
Chr7:7p21.2
uncertain significance
GRCh38/hg38 7p21.2-21.1(chr7:14904894-16925094)x1 copy number loss See cases [RCV000133737] Chr7:14904894..16925094 [GRCh38]
Chr7:14944519..16964718 [GRCh37]
Chr7:14911044..16931243 [NCBI36]
Chr7:7p21.2-21.1
pathogenic
GRCh38/hg38 7p21.2-21.1(chr7:14959516-19467349)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052288]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052288]|See cases [RCV000052288] Chr7:14959516..19467349 [GRCh38]
Chr7:14999141..19506972 [GRCh37]
Chr7:14965666..19473497 [NCBI36]
Chr7:7p21.2-21.1
pathogenic
GRCh37/hg19 7p21.2(chr7:14326482-14443860)x1 copy number loss See cases [RCV000449014] Chr7:14326482..14443860 [GRCh37]
Chr7:7p21.2
likely benign
GRCh37/hg19 7p22.3-21.1(chr7:43360-17656861)x3 copy number gain See cases [RCV000449347] Chr7:43360..17656861 [GRCh37]
Chr7:7p22.3-21.1
pathogenic
TMEM106B-BRAF fusion deletion Pleomorphic xanthoastrocytoma [RCV000454357] Chr7:12258147..140494267 [GRCh37]
Chr7:7p21.3-q34
pathogenic
GRCh37/hg19 7p21.3-14.2(chr7:11562624-36395416)x3 copy number gain See cases [RCV000446478] Chr7:11562624..36395416 [GRCh37]
Chr7:7p21.3-14.2
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43360-159119707)x1 copy number loss See cases [RCV000446044] Chr7:43360..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7p21.3-12.1(chr7:11048840-52863626)x3 copy number gain See cases [RCV000512091] Chr7:11048840..52863626 [GRCh37]
Chr7:7p21.3-12.1
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707) copy number gain See cases [RCV000510686] Chr7:43361..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7p22.3-15.3(chr7:43360-23674928)x3 copy number gain See cases [RCV000510652] Chr7:43360..23674928 [GRCh37]
Chr7:7p22.3-15.3
pathogenic
GRCh37/hg19 7p22.3-14.3(chr7:704573-29257946)x3 copy number gain See cases [RCV000510275] Chr7:704573..29257946 [GRCh37]
Chr7:7p22.3-14.3
pathogenic
GRCh37/hg19 7p21.2-21.1(chr7:14675063-18907030)x1 copy number loss See cases [RCV000511411] Chr7:14675063..18907030 [GRCh37]
Chr7:7p21.2-21.1
likely pathogenic
GRCh37/hg19 7p21.3-21.1(chr7:7660104-18400293)x3 copy number gain See cases [RCV000511575] Chr7:7660104..18400293 [GRCh37]
Chr7:7p21.3-21.1
uncertain significance
GRCh37/hg19 7p22.3-21.2(chr7:43360-14664158)x3 copy number gain See cases [RCV000511772] Chr7:43360..14664158 [GRCh37]
Chr7:7p22.3-21.2
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707)x3 copy number gain See cases [RCV000511549] Chr7:43361..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7p21.2(chr7:14834976-15051923)x1 copy number loss See cases [RCV000510793] Chr7:14834976..15051923 [GRCh37]
Chr7:7p21.2
uncertain significance
GRCh37/hg19 7p21.2(chr7:14477106-15458630)x3 copy number gain not provided [RCV000682878] Chr7:14477106..15458630 [GRCh37]
Chr7:7p21.2
likely benign
GRCh37/hg19 7p21.2(chr7:14584596-16342834)x3 copy number gain not provided [RCV000682890] Chr7:14584596..16342834 [GRCh37]
Chr7:7p21.2
uncertain significance
GRCh37/hg19 7p21.2-15.3(chr7:14544155-21719929)x3 copy number gain not provided [RCV000682908] Chr7:14544155..21719929 [GRCh37]
Chr7:7p21.2-15.3
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:44935-159126310)x3 copy number gain not provided [RCV000746280] Chr7:44935..159126310 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:10704-159122532)x3 copy number gain not provided [RCV000746278] Chr7:10704..159122532 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7p21.2(chr7:14143121-14250269)x1 copy number loss not provided [RCV000746503] Chr7:14143121..14250269 [GRCh37]
Chr7:7p21.2
benign
GRCh37/hg19 7p21.2(chr7:14226741-14294598)x1 copy number loss not provided [RCV000746504] Chr7:14226741..14294598 [GRCh37]
Chr7:7p21.2
benign
GRCh37/hg19 7p21.2(chr7:14554546-14600360)x1 copy number loss not provided [RCV000746505] Chr7:14554546..14600360 [GRCh37]
Chr7:7p21.2
benign
GRCh37/hg19 7p21.2(chr7:14866959-14896580)x1 copy number loss not provided [RCV000746506] Chr7:14866959..14896580 [GRCh37]
Chr7:7p21.2
benign
GRCh37/hg19 7p22.3-q36.3(chr7:10365-159119707)x3 copy number gain not provided [RCV000848126] Chr7:10365..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7p21.2-21.1(chr7:13886653-20267202)x1 copy number loss not provided [RCV001005911] Chr7:13886653..20267202 [GRCh37]
Chr7:7p21.2-21.1
pathogenic
GRCh37/hg19 7p22.3-21.1(chr7:43376-19520619)x3 copy number gain not provided [RCV000848100] Chr7:43376..19520619 [GRCh37]
Chr7:7p22.3-21.1
pathogenic
GRCh37/hg19 7p21.2(chr7:14618816-15070803)x3 copy number gain not provided [RCV000849208] Chr7:14618816..15070803 [GRCh37]
Chr7:7p21.2
uncertain significance
GRCh37/hg19 7p21.2(chr7:14661752-14736539)x1 copy number loss not provided [RCV001005914] Chr7:14661752..14736539 [GRCh37]
Chr7:7p21.2
uncertain significance
GRCh37/hg19 7p21.2(chr7:14350338-15586378)x3 copy number gain not provided [RCV000846253] Chr7:14350338..15586378 [GRCh37]
Chr7:7p21.2
uncertain significance
GRCh37/hg19 7p21.2(chr7:14045578-14259983)x3 copy number gain not provided [RCV001005913] Chr7:14045578..14259983 [GRCh37]
Chr7:7p21.2
likely benign
GRCh37/hg19 7p21.2-21.1(chr7:14470668-20385165)x1 copy number loss Saethre-Chotzen syndrome [RCV001263216] Chr7:14470668..20385165 [GRCh37]
Chr7:7p21.2-21.1
pathogenic
GRCh37/hg19 7p21.2(chr7:14300277-14397548)x1 copy number loss not provided [RCV001259419] Chr7:14300277..14397548 [GRCh37]
Chr7:7p21.2
likely benign
GRCh37/hg19 7p21.2(chr7:13998001-15227144)x3 copy number gain See cases [RCV001526490] Chr7:13998001..15227144 [GRCh37]
Chr7:7p21.2
uncertain significance

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:2850 AgrOrtholog
COSMIC DGKB COSMIC
Ensembl Genes ENSG00000136267 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000382260 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000384909 ENTREZGENE, UniProtKB/TrEMBL
  ENSP00000385031 ENTREZGENE, UniProtKB/TrEMBL
  ENSP00000385780 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000386066 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000405569 UniProtKB/TrEMBL
Ensembl Transcript ENST00000399322 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000402815 ENTREZGENE, UniProtKB/TrEMBL
  ENST00000403951 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000406247 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000407950 ENTREZGENE, UniProtKB/TrEMBL
  ENST00000437998 UniProtKB/TrEMBL
Gene3D-CATH 1.10.238.110 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  3.40.50.10330 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000136267 GTEx
HGNC ID HGNC:2850 ENTREZGENE
Human Proteome Map DGKB Human Proteome Map
InterPro ATP-NAD_kinase_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DAG_kinase_typeI_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DGK UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DGK_typeI_N_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Diacylglycerol_kin_accessory UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Diacylglycerol_kinase_cat_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EF-hand-dom_pair UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EF_Hand_1_Ca_BS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EF_hand_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  NAD/diacylglycerol_kinase_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PE/DAG-bd UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:1607 UniProtKB/Swiss-Prot
NCBI Gene 1607 ENTREZGENE
OMIM 604070 OMIM
PANTHER PTHR11255 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam C1_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DAG_kinase_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DAGK_acc UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DAGK_cat UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EF-hand_7 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA27311 PharmGKB
PROSITE DAGK UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EF_HAND_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EF_HAND_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZF_DAG_PE_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZF_DAG_PE_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART DAGKa UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DAGKc UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EFh UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SM00109 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF111331 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF47473 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt B5MBY2_HUMAN UniProtKB/TrEMBL
  B5MCD5_HUMAN UniProtKB/TrEMBL
  B7ZL83_HUMAN UniProtKB/TrEMBL
  C9JA18_HUMAN UniProtKB/TrEMBL
  DGKB_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
UniProt Secondary A4D116 UniProtKB/Swiss-Prot
  A4D117 UniProtKB/Swiss-Prot
  A8MXU2 UniProtKB/Swiss-Prot
  B5MDK1 UniProtKB/TrEMBL
  O75241 UniProtKB/Swiss-Prot
  Q2M377 UniProtKB/Swiss-Prot
  Q75MF9 UniProtKB/Swiss-Prot
  Q75MU7 UniProtKB/Swiss-Prot
  Q86UI5 UniProtKB/Swiss-Prot
  Q86UM9 UniProtKB/Swiss-Prot
  Q9UQ29 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-01-05 DGKB  diacylglycerol kinase beta  DGKB  diacylglycerol kinase, beta 90kDa  Symbol and/or name change 5135510 APPROVED