CALU (calumenin) - Rat Genome Database
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Gene: CALU (calumenin) Homo sapiens
Analyze
Symbol: CALU
Name: calumenin
RGD ID: 733017
HGNC Page HGNC
Description: Exhibits calcium ion binding activity. Predicted to be involved in post-translational protein modification. Localizes to endoplasmic reticulum. Biomarker of colorectal carcinoma.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: crocalbin; crocalbin-like protein; FLJ90608; IEF SSP 9302; multiple EF-hand protein; reticulocalbin
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 Ensembl7128,739,292 - 128,773,400 (+)EnsemblGRCh38hg38GRCh38
GRCh387128,739,359 - 128,773,400 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh377128,379,346 - 128,413,477 (+)NCBIGRCh37GRCh37hg19GRCh37
GRCh377128,379,413 - 128,413,454 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 367128,166,672 - 128,198,764 (+)NCBINCBI36hg18NCBI36
Build 347127,973,386 - 128,005,478NCBI
Celera7123,175,101 - 123,207,285 (+)NCBI
Cytogenetic Map7q32.1NCBI
HuRef7122,740,343 - 122,774,461 (+)NCBIHuRef
CHM1_17128,312,626 - 128,346,717 (+)NCBICHM1_1
CRA_TCAGchr7v27127,762,331 - 127,796,461 (+)NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
1,2-dimethylhydrazine  (ISO)
1,3-dinitrobenzene  (ISO)
1,4-dithiothreitol  (EXP)
1-naphthyl isothiocyanate  (ISO)
17beta-estradiol  (EXP)
17beta-hydroxy-5alpha-androstan-3-one  (EXP)
2,2',4,4'-Tetrabromodiphenyl ether  (EXP)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2,6-dinitrotoluene  (ISO)
4,4'-diaminodiphenylmethane  (ISO)
acrylamide  (ISO)
aldehydo-D-glucose  (EXP)
ammonium chloride  (ISO)
Aroclor 1254  (ISO)
atrazine  (EXP)
Azaspiracid  (EXP)
benzo[a]pyrene  (ISO)
benzo[a]pyrene diol epoxide I  (EXP)
bisphenol A  (ISO)
bleomycin A2  (ISO)
Bromadiolone  (ISO)
cadmium dichloride  (ISO)
caffeine  (EXP)
carbon nanotube  (EXP,ISO)
chloroform  (ISO)
chloropicrin  (EXP)
cobalt dichloride  (EXP)
coumestrol  (EXP)
CU-O LINKAGE  (EXP)
cyclosporin A  (EXP)
D-glucose  (EXP)
dexamethasone  (ISO)
dimethylarsinic acid  (ISO)
dopamine  (ISO)
doxorubicin  (EXP)
elemental selenium  (EXP)
Enterolactone  (EXP)
enzyme inhibitor  (EXP)
erythromycin estolate  (ISO)
ethanol  (ISO)
ethyl methanesulfonate  (EXP)
fenoldopam  (ISO)
folic acid  (ISO)
formaldehyde  (EXP)
fragrance  (EXP)
glafenine  (ISO)
glucose  (EXP)
hyaluronic acid  (ISO)
hydrogen peroxide  (EXP,ISO)
L-1,4-dithiothreitol  (EXP)
lead diacetate  (ISO)
methyl methanesulfonate  (EXP)
methylmercury chloride  (EXP)
nickel atom  (EXP)
nickel subsulfide  (ISO)
paracetamol  (EXP,ISO)
PCB138  (ISO)
perfluorooctanoic acid  (EXP,ISO)
phenol  (EXP)
potassium dichromate  (ISO)
resveratrol  (EXP)
selenium atom  (EXP)
silver atom  (ISO)
silver(0)  (ISO)
sodium fluoride  (ISO)
tert-butyl hydroperoxide  (EXP)
tetrachloromethane  (ISO)
tetracycline  (ISO)
tetrahydropalmatine  (EXP)
thapsigargin  (EXP)
theophylline  (ISO)
thioacetamide  (EXP)
trichostatin A  (EXP)
tunicamycin  (EXP)
valproic acid  (EXP)
vincristine  (EXP)
vitamin E  (EXP)
warfarin  (EXP,ISO)
yohimbine  (ISO)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

References

Additional References at PubMed
PMID:9218460   PMID:9598325   PMID:9675259   PMID:10094503   PMID:10222138   PMID:10631319   PMID:11076863   PMID:11230166   PMID:11827452   PMID:12477932   PMID:12643545   PMID:12665801  
PMID:12690205   PMID:14702039   PMID:15489334   PMID:15489336   PMID:15561718   PMID:16303743   PMID:16344560   PMID:16381901   PMID:16964243   PMID:17048007   PMID:17049586   PMID:17081065  
PMID:17081983   PMID:17110338   PMID:17189218   PMID:17596133   PMID:18029348   PMID:18688696   PMID:19794411   PMID:19913121   PMID:19946888   PMID:19958090   PMID:20020283   PMID:20149073  
PMID:20200517   PMID:20360068   PMID:20499136   PMID:20553802   PMID:20628086   PMID:20673165   PMID:21057703   PMID:21565611   PMID:21873635   PMID:21988832   PMID:22113938   PMID:22188360  
PMID:22190034   PMID:22268729   PMID:22304920   PMID:22514732   PMID:22768251   PMID:22863883   PMID:22939629   PMID:23402259   PMID:23438482   PMID:23443559   PMID:23455924   PMID:23464991  
PMID:23704328   PMID:23752268   PMID:24136234   PMID:24189400   PMID:24244333   PMID:25036637   PMID:25120007   PMID:25416956   PMID:25437307   PMID:25798074   PMID:25823396   PMID:25852190  
PMID:25921289   PMID:25963833   PMID:25963840   PMID:26124285   PMID:26186194   PMID:26344197   PMID:26496610   PMID:26618866   PMID:26638075   PMID:26972000   PMID:27107014   PMID:27377895  
PMID:27432908   PMID:27545878   PMID:27684187   PMID:27705803   PMID:27790916   PMID:27880917   PMID:28189267   PMID:28330616   PMID:28378594   PMID:28514442   PMID:29319298   PMID:29507755  
PMID:29509190   PMID:29513927   PMID:29568061   PMID:29615496   PMID:29777862   PMID:29802200   PMID:30021884   PMID:30196744   PMID:30349055   PMID:30462309   PMID:30619335   PMID:30833792  
PMID:30948266   PMID:31056421   PMID:31536960   PMID:31586073   PMID:31617661   PMID:31753913   PMID:31980649   PMID:32203420   PMID:32469983   PMID:32838362  


Genomics

Comparative Map Data
CALU
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl7128,739,292 - 128,773,400 (+)EnsemblGRCh38hg38GRCh38
GRCh387128,739,359 - 128,773,400 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh377128,379,346 - 128,413,477 (+)NCBIGRCh37GRCh37hg19GRCh37
GRCh377128,379,413 - 128,413,454 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 367128,166,672 - 128,198,764 (+)NCBINCBI36hg18NCBI36
Build 347127,973,386 - 128,005,478NCBI
Celera7123,175,101 - 123,207,285 (+)NCBI
Cytogenetic Map7q32.1NCBI
HuRef7122,740,343 - 122,774,461 (+)NCBIHuRef
CHM1_17128,312,626 - 128,346,717 (+)NCBICHM1_1
CRA_TCAGchr7v27127,762,331 - 127,796,461 (+)NCBI
Calu
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39629,348,105 - 29,376,674 (+)NCBIGRCm39mm39
GRCm38629,348,106 - 29,376,675 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl629,348,069 - 29,377,110 (+)EnsemblGRCm38mm10GRCm38
MGSCv37629,298,119 - 29,326,675 (+)NCBIGRCm37mm9NCBIm37
MGSCv36629,298,155 - 29,326,678 (+)NCBImm8
Celera629,355,300 - 29,383,863 (+)NCBICelera
Cytogenetic Map6A3.3NCBI
Calu
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.2457,949,086 - 57,976,589 (+)NCBI
Rnor_6.0 Ensembl456,625,561 - 56,653,111 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.0456,625,611 - 56,653,112 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.0456,392,772 - 56,420,273 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4456,228,617 - 56,256,118 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.1456,484,215 - 56,512,241 (+)NCBI
Celera453,057,097 - 53,084,601 (+)NCBICelera
Cytogenetic Map4q22NCBI
Calu
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554799,541,568 - 9,572,266 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049554799,541,574 - 9,572,189 (+)NCBIChiLan1.0ChiLan1.0
CALU
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.17133,215,235 - 133,247,541 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl7133,223,269 - 133,247,167 (+)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v07120,691,092 - 120,723,303 (+)NCBIMhudiblu_PPA_v0panPan3
CALU
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1 Ensembl147,872,076 - 7,925,078 (-)EnsemblCanFam3.1canFam3CanFam3.1
CanFam3.1147,869,946 - 7,899,302 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
Calu
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
SpeTri2.0NW_00493647915,665,979 - 15,697,016 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
CALU
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1819,841,718 - 19,884,128 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11819,841,718 - 19,875,804 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21820,911,135 - 20,945,220 (-)NCBISscrofa10.2Sscrofa10.2susScr3
CALU
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12197,338,875 - 97,370,947 (+)NCBI
ChlSab1.1 Ensembl2197,338,913 - 97,373,156 (+)Ensembl
Calu
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046247837,417,505 - 7,448,711 (-)NCBI

Position Markers
STS-M13299  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377128,412,417 - 128,412,640UniSTSGRCh37
Build 367128,199,653 - 128,199,876RGDNCBI36
Celera7123,208,171 - 123,208,394RGD
Cytogenetic Map7q32.1UniSTS
HuRef7122,773,401 - 122,773,624UniSTS
CRA_TCAGchr7v27127,795,401 - 127,795,624UniSTS
GeneMap99-GB4 RH Map7586.37UniSTS
NCBI RH Map71192.6UniSTS
A009L17  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377128,395,013 - 128,395,115UniSTSGRCh37
Build 367128,182,249 - 128,182,351RGDNCBI36
Celera7123,190,768 - 123,190,870RGD
Cytogenetic Map7q32.1UniSTS
HuRef7122,756,000 - 122,756,102UniSTS
CRA_TCAGchr7v27127,777,997 - 127,778,099UniSTS
GeneMap99-GB4 RH Map7586.67UniSTS
NCBI RH Map71192.6UniSTS
RH66822  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377128,412,464 - 128,412,624UniSTSGRCh37
Build 367128,199,700 - 128,199,860RGDNCBI36
Celera7123,208,218 - 123,208,378RGD
Cytogenetic Map7q32.1UniSTS
HuRef7122,773,448 - 122,773,608UniSTS
CRA_TCAGchr7v27127,795,448 - 127,795,608UniSTS
GeneMap99-GB4 RH Map7586.06UniSTS
NCBI RH Map71176.7UniSTS
RH48732  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377128,409,376 - 128,409,537UniSTSGRCh37
Build 367128,196,612 - 128,196,773RGDNCBI36
Celera7123,205,130 - 123,205,291RGD
Cytogenetic Map7q32.1UniSTS
HuRef7122,770,359 - 122,770,520UniSTS
CRA_TCAGchr7v27127,792,360 - 127,792,521UniSTS
GeneMap99-GB4 RH Map7596.51UniSTS
NCBI RH Map71179.1UniSTS
RH64944  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377128,380,356 - 128,380,486UniSTSGRCh37
Build 367128,167,592 - 128,167,722RGDNCBI36
Celera7123,176,111 - 123,176,241RGD
Cytogenetic Map7q32.1UniSTS
HuRef7122,741,353 - 122,741,483UniSTS
CRA_TCAGchr7v27127,763,341 - 127,763,471UniSTS
SHGC-52887  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377128,411,667 - 128,411,824UniSTSGRCh37
Build 367128,198,903 - 128,199,060RGDNCBI36
Celera7123,207,421 - 123,207,578RGD
Cytogenetic Map7q32.1UniSTS
HuRef7122,772,650 - 122,772,807UniSTS
CRA_TCAGchr7v27127,794,651 - 127,794,808UniSTS
STS-H01049  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377128,411,277 - 128,411,417UniSTSGRCh37
Build 367128,198,513 - 128,198,653RGDNCBI36
Celera7123,207,031 - 123,207,171RGD
Cytogenetic Map7q32.1UniSTS
HuRef7122,772,260 - 122,772,400UniSTS
CRA_TCAGchr7v27127,794,261 - 127,794,401UniSTS
GeneMap99-GB4 RH Map7586.67UniSTS
NCBI RH Map71192.6UniSTS
G20679  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377128,411,297 - 128,411,511UniSTSGRCh37
Build 367128,198,533 - 128,198,747RGDNCBI36
Celera7123,207,051 - 123,207,265RGD
Cytogenetic Map7q32.1UniSTS
HuRef7122,772,280 - 122,772,494UniSTS
CRA_TCAGchr7v27127,794,281 - 127,794,495UniSTS
A006B29  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377128,411,297 - 128,411,511UniSTSGRCh37
Build 367128,198,533 - 128,198,747RGDNCBI36
Celera7123,207,051 - 123,207,265RGD
Cytogenetic Map7q32.1UniSTS
HuRef7122,772,280 - 122,772,494UniSTS
CRA_TCAGchr7v27127,794,281 - 127,794,495UniSTS
GeneMap99-GB4 RH Map7586.37UniSTS
NCBI RH Map71192.6UniSTS
UniSTS:464721  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377128,394,316 - 128,394,509UniSTSGRCh37
Build 367128,181,552 - 128,181,745RGDNCBI36
Celera7123,190,071 - 123,190,264RGD
HuRef7122,755,303 - 122,755,496UniSTS
CRA_TCAGchr7v27127,777,300 - 127,777,493UniSTS
UniSTS:464722  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377128,394,583 - 128,394,776UniSTSGRCh37
Build 367128,181,819 - 128,182,012RGDNCBI36
Celera7123,190,338 - 123,190,531RGD
HuRef7122,755,570 - 122,755,763UniSTS
CRA_TCAGchr7v27127,777,567 - 127,777,760UniSTS
A002N36  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377128,410,342 - 128,410,543UniSTSGRCh37
Build 367128,197,578 - 128,197,779RGDNCBI36
Celera7123,206,096 - 123,206,297RGD
Cytogenetic Map7q32.1UniSTS
HuRef7122,771,325 - 122,771,526UniSTS
CRA_TCAGchr7v27127,793,326 - 127,793,527UniSTS
GeneMap99-GB4 RH Map7588.28UniSTS
Whitehead-RH Map7554.8UniSTS
RH12835  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377128,410,391 - 128,410,573UniSTSGRCh37
Build 367128,197,627 - 128,197,809RGDNCBI36
Celera7123,206,145 - 123,206,327RGD
Cytogenetic Map7q32.1UniSTS
HuRef7122,771,374 - 122,771,556UniSTS
CRA_TCAGchr7v27127,793,375 - 127,793,557UniSTS
GeneMap99-GB4 RH Map7586.37UniSTS
NCBI RH Map71192.6UniSTS
RH44842  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377128,411,277 - 128,411,387UniSTSGRCh37
Build 367128,198,513 - 128,198,623RGDNCBI36
Celera7123,207,031 - 123,207,141RGD
Cytogenetic Map7q32.1UniSTS
HuRef7122,772,260 - 122,772,370UniSTS
CRA_TCAGchr7v27127,794,261 - 127,794,371UniSTS
GeneMap99-GB4 RH Map7586.67UniSTS
NCBI RH Map71192.6UniSTS
SHGC-35138  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377128,380,377 - 128,380,526UniSTSGRCh37
Build 367128,167,613 - 128,167,762RGDNCBI36
Celera7123,176,132 - 123,176,281RGD
Cytogenetic Map7q32.1UniSTS
HuRef7122,741,374 - 122,741,523UniSTS
CRA_TCAGchr7v27127,763,362 - 127,763,511UniSTS
Stanford-G3 RH Map76410.0UniSTS
GeneMap99-GB4 RH Map7586.06UniSTS
Whitehead-RH Map7553.3UniSTS
GeneMap99-G3 RH Map76410.0UniSTS
STS-N32527  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377128,411,974 - 128,412,107UniSTSGRCh37
Build 367128,199,210 - 128,199,343RGDNCBI36
Celera7123,207,728 - 123,207,861RGD
Cytogenetic Map7q32.1UniSTS
HuRef7122,772,957 - 122,773,090UniSTS
CRA_TCAGchr7v27127,794,958 - 127,795,091UniSTS
GeneMap99-GB4 RH Map7586.37UniSTS
NCBI RH Map71192.6UniSTS
RH45162  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377128,410,770 - 128,410,981UniSTSGRCh37
Build 367128,198,006 - 128,198,217RGDNCBI36
Celera7123,206,524 - 123,206,735RGD
Cytogenetic Map7q32.1UniSTS
HuRef7122,771,753 - 122,771,964UniSTS
CRA_TCAGchr7v27127,793,754 - 127,793,965UniSTS
GeneMap99-GB4 RH Map7586.47UniSTS
NCBI RH Map71192.6UniSTS
G32645  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377128,395,013 - 128,395,114UniSTSGRCh37
Celera7123,190,768 - 123,190,869UniSTS
Cytogenetic Map7q32.1UniSTS
CRA_TCAGchr7v27127,777,997 - 127,778,098UniSTS
MARC_11525-11526:1001518036:1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377128,398,977 - 128,399,888UniSTSGRCh37
Celera7123,194,732 - 123,195,643UniSTS
HuRef7122,759,964 - 122,760,875UniSTS
CRA_TCAGchr7v27127,781,961 - 127,782,872UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:5877
Count of miRNA genes:799
Interacting mature miRNAs:960
Transcripts:ENST00000249364, ENST00000449187, ENST00000479257, ENST00000493278, ENST00000535011, ENST00000535623, ENST00000538546, ENST00000542996
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.


Expression


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

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High 4 1 41 7 21 3 11 10
Medium 2427 2265 1673 576 1268 418 4313 2147 3139 397 1436 1596 171 1204 2787 4
Low 7 725 52 48 682 47 2 43 571 19 13 7 4 1 1 2 2
Below cutoff 1 1 3

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_033110 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001130674 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001199671 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001199672 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001199673 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001219 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_074086 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017012659 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC024952 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF013759 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF257659 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF345637 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK027460 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK056338 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK074862 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK075089 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK312446 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AW068942 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC013383 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BF438624 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BT006826 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BT020143 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX091230 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH236950 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471070 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR457039 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR541835 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA023987 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA703012 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HM002604 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HM002605 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HM002606 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HM002607 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HM002609 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HM002610 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HM002611 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HM002613 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HM002615 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HM002616 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U67280 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000249364   ⟹   ENSP00000249364
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7128,739,359 - 128,773,400 (+)Ensembl
RefSeq Acc Id: ENST00000449187   ⟹   ENSP00000408838
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7128,739,363 - 128,770,576 (+)Ensembl
RefSeq Acc Id: ENST00000479257   ⟹   ENSP00000420381
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7128,739,404 - 128,769,936 (+)Ensembl
RefSeq Acc Id: ENST00000493278   ⟹   ENSP00000417973
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7128,758,962 - 128,771,807 (+)Ensembl
RefSeq Acc Id: ENST00000535011   ⟹   ENSP00000442110
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7128,739,292 - 128,771,477 (+)Ensembl
RefSeq Acc Id: ENST00000542996   ⟹   ENSP00000438248
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7128,739,292 - 128,771,477 (+)Ensembl
RefSeq Acc Id: NM_001130674   ⟹   NP_001124146
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387128,739,359 - 128,773,400 (+)NCBI
GRCh377128,379,346 - 128,413,477 (+)ENTREZGENE
HuRef7122,740,343 - 122,774,461 (+)ENTREZGENE
CHM1_17128,312,626 - 128,346,717 (+)NCBI
CRA_TCAGchr7v27127,762,331 - 127,796,461 (+)ENTREZGENE
Sequence:
RefSeq Acc Id: NM_001199671   ⟹   NP_001186600
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387128,739,359 - 128,773,400 (+)NCBI
GRCh377128,379,346 - 128,413,477 (+)ENTREZGENE
HuRef7122,740,343 - 122,774,461 (+)ENTREZGENE
CHM1_17128,312,626 - 128,346,717 (+)NCBI
CRA_TCAGchr7v27127,762,331 - 127,796,461 (+)ENTREZGENE
Sequence:
RefSeq Acc Id: NM_001199672   ⟹   NP_001186601
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387128,739,359 - 128,773,400 (+)NCBI
GRCh377128,379,346 - 128,413,477 (+)ENTREZGENE
HuRef7122,740,343 - 122,774,461 (+)ENTREZGENE
CHM1_17128,312,626 - 128,346,717 (+)NCBI
CRA_TCAGchr7v27127,762,331 - 127,796,461 (+)ENTREZGENE
Sequence:
RefSeq Acc Id: NM_001199673   ⟹   NP_001186602
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387128,739,359 - 128,773,400 (+)NCBI
GRCh377128,379,346 - 128,413,477 (+)ENTREZGENE
HuRef7122,740,343 - 122,774,461 (+)ENTREZGENE
CHM1_17128,312,626 - 128,346,717 (+)NCBI
CRA_TCAGchr7v27127,762,331 - 127,796,461 (+)ENTREZGENE
Sequence:
RefSeq Acc Id: NM_001219   ⟹   NP_001210
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387128,739,359 - 128,773,400 (+)NCBI
GRCh377128,379,346 - 128,413,477 (+)ENTREZGENE
Build 367128,166,672 - 128,198,764 (+)NCBI Archive
HuRef7122,740,343 - 122,774,461 (+)ENTREZGENE
CHM1_17128,312,626 - 128,346,717 (+)NCBI
CRA_TCAGchr7v27127,762,331 - 127,796,461 (+)ENTREZGENE
Sequence:
RefSeq Acc Id: NR_074086
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387128,739,359 - 128,773,400 (+)NCBI
HuRef7122,740,343 - 122,774,461 (+)NCBI
CHM1_17128,312,626 - 128,346,717 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017012659   ⟹   XP_016868148
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387128,739,371 - 128,771,852 (+)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001124146 (Get FASTA)   NCBI Sequence Viewer  
  NP_001186600 (Get FASTA)   NCBI Sequence Viewer  
  NP_001186601 (Get FASTA)   NCBI Sequence Viewer  
  NP_001186602 (Get FASTA)   NCBI Sequence Viewer  
  NP_001210 (Get FASTA)   NCBI Sequence Viewer  
  XP_016868148 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAB97725 (Get FASTA)   NCBI Sequence Viewer  
  AAC17216 (Get FASTA)   NCBI Sequence Viewer  
  AAF76141 (Get FASTA)   NCBI Sequence Viewer  
  AAH13383 (Get FASTA)   NCBI Sequence Viewer  
  AAK72908 (Get FASTA)   NCBI Sequence Viewer  
  AAP35472 (Get FASTA)   NCBI Sequence Viewer  
  AAV38945 (Get FASTA)   NCBI Sequence Viewer  
  ADG45004 (Get FASTA)   NCBI Sequence Viewer  
  ADG45005 (Get FASTA)   NCBI Sequence Viewer  
  ADG45006 (Get FASTA)   NCBI Sequence Viewer  
  ADG45007 (Get FASTA)   NCBI Sequence Viewer  
  ADG45009 (Get FASTA)   NCBI Sequence Viewer  
  ADG45010 (Get FASTA)   NCBI Sequence Viewer  
  ADG45011 (Get FASTA)   NCBI Sequence Viewer  
  ADG45013 (Get FASTA)   NCBI Sequence Viewer  
  ADG45015 (Get FASTA)   NCBI Sequence Viewer  
  ADG45016 (Get FASTA)   NCBI Sequence Viewer  
  BAG35353 (Get FASTA)   NCBI Sequence Viewer  
  BAG51328 (Get FASTA)   NCBI Sequence Viewer  
  BAG51681 (Get FASTA)   NCBI Sequence Viewer  
  BAG52017 (Get FASTA)   NCBI Sequence Viewer  
  BAG52065 (Get FASTA)   NCBI Sequence Viewer  
  CAG33320 (Get FASTA)   NCBI Sequence Viewer  
  CAG46634 (Get FASTA)   NCBI Sequence Viewer  
  EAL24113 (Get FASTA)   NCBI Sequence Viewer  
  EAW83674 (Get FASTA)   NCBI Sequence Viewer  
  EAW83675 (Get FASTA)   NCBI Sequence Viewer  
  EAW83676 (Get FASTA)   NCBI Sequence Viewer  
  EAW83677 (Get FASTA)   NCBI Sequence Viewer  
  EAW83678 (Get FASTA)   NCBI Sequence Viewer  
  EAW83679 (Get FASTA)   NCBI Sequence Viewer  
  O43852 (Get FASTA)   NCBI Sequence Viewer  
Reference Sequences
RefSeq Acc Id: NP_001186600   ⟸   NM_001199671
- Peptide Label: isoform c precursor
- UniProtKB: O43852 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001186601   ⟸   NM_001199672
- Peptide Label: isoform d precursor
- UniProtKB: O43852 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001210   ⟸   NM_001219
- Peptide Label: isoform a precursor
- UniProtKB: O43852 (UniProtKB/Swiss-Prot),   B3KQF5 (UniProtKB/TrEMBL),   Q6IAW5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001186602   ⟸   NM_001199673
- Peptide Label: isoform e precursor
- UniProtKB: O43852 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001124146   ⟸   NM_001130674
- Peptide Label: isoform b precursor
- UniProtKB: O43852 (UniProtKB/Swiss-Prot),   A0A024R755 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016868148   ⟸   XM_017012659
- Peptide Label: isoform X1
- UniProtKB: O43852 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000438248   ⟸   ENST00000542996
RefSeq Acc Id: ENSP00000420381   ⟸   ENST00000479257
RefSeq Acc Id: ENSP00000417973   ⟸   ENST00000493278
RefSeq Acc Id: ENSP00000442110   ⟸   ENST00000535011
RefSeq Acc Id: ENSP00000249364   ⟸   ENST00000249364
RefSeq Acc Id: ENSP00000408838   ⟸   ENST00000449187
Protein Domains
EF-hand

Promoters
RGD ID:6805355
Promoter ID:HG_KWN:59632
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_001130674,   NM_001219,   UC003VNR.1
Position:
Human AssemblyChrPosition (strand)Source
Build 367128,166,321 - 128,166,821 (+)MPROMDB
RGD ID:7211875
Promoter ID:EPDNEW_H11684
Type:initiation region
Name:CALU_1
Description:calumenin
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh387128,739,371 - 128,739,431EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 7q32.1-33(chr7:128747478-134018250)x3 copy number gain See cases [RCV000051072] Chr7:128747478..134018250 [GRCh38]
Chr7:128387532..133703003 [GRCh37]
Chr7:128174768..133353543 [NCBI36]
Chr7:7q32.1-33
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 7q31.33-32.3(chr7:126859732-132750936)x1 copy number loss See cases [RCV000054171] Chr7:126859732..132750936 [GRCh38]
Chr7:126499786..132435696 [GRCh37]
Chr7:126287022..132086236 [NCBI36]
Chr7:7q31.33-32.3
pathogenic
NM_001708.2(OPN1SW):c.236G>A (p.Gly79Glu) single nucleotide variant Malignant melanoma [RCV000067625] Chr7:128775555 [GRCh38]
Chr7:128415609 [GRCh37]
Chr7:128202845 [NCBI36]
Chr7:7q32.1
not provided
NM_001219.5(CALU):c.582+133A>G single nucleotide variant warfarin response - Dosage [RCV000211348] Chr7:128759170 [GRCh38]
Chr7:128399224 [GRCh37]
Chr7:7q32.1
drug response
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 7q21.3-36.3(chr7:97419852-158923762)x3 copy number gain See cases [RCV000136717] Chr7:97419852..158923762 [GRCh38]
Chr7:97049164..158716453 [GRCh37]
Chr7:96887100..158409214 [NCBI36]
Chr7:7q21.3-36.3
pathogenic
GRCh38/hg38 7q31.2-33(chr7:117326805-134790689)x1 copy number loss See cases [RCV000138226] Chr7:117326805..134790689 [GRCh38]
Chr7:116966859..134475440 [GRCh37]
Chr7:116754095..134125980 [NCBI36]
Chr7:7q31.2-33
pathogenic
GRCh38/hg38 7q31.32-36.3(chr7:121863759-159335865)x3 copy number gain See cases [RCV000138847] Chr7:121863759..159335865 [GRCh38]
Chr7:121503813..159128555 [GRCh37]
Chr7:121291049..158821316 [NCBI36]
Chr7:7q31.32-36.3
pathogenic
GRCh38/hg38 7q31.2-36.3(chr7:115459015-159325817)x3 copy number gain See cases [RCV000141413] Chr7:115459015..159325817 [GRCh38]
Chr7:115099069..159118507 [GRCh37]
Chr7:114886305..158811268 [NCBI36]
Chr7:7q31.2-36.3
pathogenic
GRCh38/hg38 7q32.1(chr7:127817826-129237503)x3 copy number gain See cases [RCV000142106] Chr7:127817826..129237503 [GRCh38]
Chr7:127457880..128877344 [GRCh37]
Chr7:127245116..128664580 [NCBI36]
Chr7:7q32.1
likely benign|uncertain significance
GRCh38/hg38 7q31.33-33(chr7:124170657-134163594)x1 copy number loss See cases [RCV000142552] Chr7:124170657..134163594 [GRCh38]
Chr7:123810711..133848346 [GRCh37]
Chr7:123597947..133498886 [NCBI36]
Chr7:7q31.33-33
pathogenic
GRCh38/hg38 7q31.32-32.1(chr7:122018122-128907727)x1 copy number loss See cases [RCV000142521] Chr7:122018122..128907727 [GRCh38]
Chr7:121658176..128547780 [GRCh37]
Chr7:121445412..128335016 [NCBI36]
Chr7:7q31.32-32.1
pathogenic
GRCh37/hg19 7q32.1-36.3(chr7:128312450-159119220) copy number gain not provided [RCV000767558] Chr7:128312450..159119220 [GRCh37]
Chr7:7q32.1-36.3
pathogenic
TMEM106B-BRAF fusion deletion Pleomorphic xanthoastrocytoma [RCV000454357] Chr7:12258147..140494267 [GRCh37]
Chr7:7p21.3-q34
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 7q22.1-36.3(chr7:98969247-159119707)x3 copy number gain See cases [RCV000447709] Chr7:98969247..159119707 [GRCh37]
Chr7:7q22.1-36.3
pathogenic
GRCh37/hg19 7q32.1-34(chr7:127295698-139524358)x1 copy number loss See cases [RCV000447722] Chr7:127295698..139524358 [GRCh37]
Chr7:7q32.1-34
pathogenic
GRCh37/hg19 7q32.1-36.3(chr7:128276078-159119707)x3 copy number gain See cases [RCV000447956] Chr7:128276078..159119707 [GRCh37]
Chr7:7q32.1-36.3
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-q36.3(chr7:43361-159119707)x3 copy number gain See cases [RCV000511549] Chr7:43361..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7q22.1-36.3(chr7:98693388-159119707)x3 copy number gain not provided [RCV000682911] Chr7:98693388..159119707 [GRCh37]
Chr7:7q22.1-36.3
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 7p22.3-q36.3(chr7:44935-159126310)x3 copy number gain not provided [RCV000746280] Chr7:44935..159126310 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
NM_001219.5(CALU):c.*3435T>C single nucleotide variant not provided [RCV001038144] Chr7:128772602 [GRCh38]
Chr7:128412656 [GRCh37]
Chr7:7q32.1
uncertain significance
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
NM_001219.5(CALU):c.*3479A>G single nucleotide variant not provided [RCV001064888] Chr7:128772646 [GRCh38]
Chr7:128412700 [GRCh37]
Chr7:7q32.1
uncertain significance
GRCh37/hg19 7q31.32-32.2(chr7:121480906-129389003)x1 copy number loss not provided [RCV000847911] Chr7:121480906..129389003 [GRCh37]
Chr7:7q31.32-32.2
pathogenic
GRCh37/hg19 7q32.1(chr7:127999644-128465294)x3 copy number gain not provided [RCV000846728] Chr7:127999644..128465294 [GRCh37]
Chr7:7q32.1
uncertain significance
GRCh37/hg19 7q32.1(chr7:128412321-128546131)x1 copy number loss not provided [RCV000849406] Chr7:128412321..128546131 [GRCh37]
Chr7:7q32.1
uncertain significance
GRCh37/hg19 7q31.1-36.3(chr7:109251060-159119707)x3 copy number gain not provided [RCV001005994] Chr7:109251060..159119707 [GRCh37]
Chr7:7q31.1-36.3
pathogenic
NM_001219.5(CALU):c.*3404G>A single nucleotide variant not provided [RCV001057462] Chr7:128772571 [GRCh38]
Chr7:128412625 [GRCh37]
Chr7:7q32.1
uncertain significance

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:1458 AgrOrtholog
COSMIC CALU COSMIC
Ensembl Genes ENSG00000128595 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000249364 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000408838 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000417973 ENTREZGENE, UniProtKB/TrEMBL
  ENSP00000420381 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000438248 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000442110 ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000249364 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000449187 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000479257 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000493278 ENTREZGENE, UniProtKB/TrEMBL
  ENST00000535011 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000542996 ENTREZGENE, UniProtKB/Swiss-Prot
GTEx ENSG00000128595 GTEx
HGNC ID HGNC:1458 ENTREZGENE
Human Proteome Map CALU Human Proteome Map
InterPro Calumenin 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
KEGG Report hsa:813 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 813 ENTREZGENE
OMIM 603420 OMIM
PANTHER PTHR10827:SF76 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam EF-hand_5 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EF-hand_7 UniProtKB/TrEMBL
  EF-hand_8 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB CALU RGD, PharmGKB
PROSITE EF_HAND_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EF_HAND_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART EFh UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF47473 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A024R755 ENTREZGENE, UniProtKB/TrEMBL
  B3KQF5 ENTREZGENE, UniProtKB/TrEMBL
  CALU_HUMAN UniProtKB/Swiss-Prot
  H0Y875_HUMAN UniProtKB/TrEMBL
  O43852 ENTREZGENE
  Q6IAW5 ENTREZGENE, UniProtKB/TrEMBL
UniProt Secondary B3KPG9 UniProtKB/Swiss-Prot
  D6QS48 UniProtKB/Swiss-Prot
  D6QS49 UniProtKB/Swiss-Prot
  D6QS50 UniProtKB/Swiss-Prot
  D6QS51 UniProtKB/Swiss-Prot
  D6QS52 UniProtKB/Swiss-Prot
  D6QS53 UniProtKB/Swiss-Prot
  D6QS54 UniProtKB/Swiss-Prot
  D6QS55 UniProtKB/Swiss-Prot
  D6QS56 UniProtKB/Swiss-Prot
  D6QS57 UniProtKB/Swiss-Prot
  D6QS58 UniProtKB/Swiss-Prot
  D6QS59 UniProtKB/Swiss-Prot
  F5H1Q9 UniProtKB/Swiss-Prot
  F5H879 UniProtKB/Swiss-Prot
  O60456 UniProtKB/Swiss-Prot
  Q6FHB9 UniProtKB/Swiss-Prot
  Q96RL3 UniProtKB/Swiss-Prot
  Q9NR43 UniProtKB/Swiss-Prot