SCGN (secretagogin, EF-hand calcium binding protein) - Rat Genome Database

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Gene: SCGN (secretagogin, EF-hand calcium binding protein) Homo sapiens
Analyze
Symbol: SCGN
Name: secretagogin, EF-hand calcium binding protein
RGD ID: 1347901
HGNC Page HGNC:16941
Description: Predicted to enable calcium ion binding activity. Predicted to be located in cytoplasm. Predicted to be active in several cellular components, including cytosol; dendrite; and terminal bouton.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: calbindin-like; CALBL; DJ501N12.8; SECRET; secretagogin; SEGN; setagin
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
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
GRCh38625,652,215 - 25,701,783 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl625,652,201 - 25,701,783 (+)EnsemblGRCh38hg38GRCh38
GRCh37625,652,443 - 25,702,011 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36625,760,408 - 25,809,990 (+)NCBINCBI36Build 36hg18NCBI36
Build 34625,760,407 - 25,809,985NCBI
Celera626,879,633 - 26,929,216 (+)NCBICelera
Cytogenetic Map6p22.2NCBI
HuRef625,595,416 - 25,644,987 (+)NCBIHuRef
CHM1_1625,654,627 - 25,704,213 (+)NCBICHM1_1
T2T-CHM13v2.0625,518,025 - 25,567,550 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


1 to 20 of 53 rows

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
SCGNHuman17alpha-ethynylestradiol multiple interactionsISOScgn (Mus musculus)6480464[Tetrachlorodibenzodioxin co-treated with Ethinyl Estradiol] results in increased expression of SCGN mRNACTDPMID:17942748
SCGNHuman2,3,7,8-tetrachlorodibenzodioxine multiple interactionsISOScgn (Mus musculus)6480464[Tetrachlorodibenzodioxin co-treated with Ethinyl Estradiol] results in increased expression of SCGN mRNACTDPMID:17942748
SCGNHuman2,3,7,8-tetrachlorodibenzodioxine multiple interactionsEXP 6480464[Endosulfan co-treated with Tetrachlorodibenzodioxin] results in decreased expression of SCGN mRNACTDPMID:26159488
SCGNHuman2,3,7,8-tetrachlorodibenzodioxine decreases expressionEXP 6480464Tetrachlorodibenzodioxin results in decreased expression of SCGN mRNACTDPMID:20106945 and PMID:21632981
SCGNHuman3-isobutyl-1-methyl-7H-xanthine multiple interactionsEXP 6480464[INS protein co-treated with Dexamethasone co-treated with 1-Methyl-3-isobutylxanthine co-treated with Indomethacin co-treated with bisphenol S] results in increased expression of SCGN mRNACTDPMID:28628672
SCGNHuman4,4'-sulfonyldiphenol multiple interactionsEXP 6480464[INS protein co-treated with Dexamethasone co-treated with 1-Methyl-3-isobutylxanthine co-treated with Indomethacin co-treated with bisphenol S] results in increased expression of SCGN mRNACTDPMID:28628672
SCGNHuman6-propyl-2-thiouracil increases expressionISOScgn (Rattus norvegicus)6480464Propylthiouracil results in increased expression of SCGN mRNACTDPMID:24780913
SCGNHuman6-propyl-2-thiouracil decreases expressionISOScgn (Rattus norvegicus)6480464Propylthiouracil results in decreased expression of SCGN mRNACTDPMID:30047161
SCGNHumanacrylamide increases expressionISOScgn (Rattus norvegicus)6480464Acrylamide results in increased expression of SCGN mRNACTDPMID:28959563
SCGNHumanaflatoxin B1 affects expressionEXP 6480464Aflatoxin B1 affects the expression of SCGN proteinCTDPMID:20106945
SCGNHumanaflatoxin B1 decreases methylationEXP 6480464Aflatoxin B1 results in decreased methylation of SCGN geneCTDPMID:27153756
SCGNHumanaflatoxin B1 decreases expressionEXP 6480464Aflatoxin B1 results in decreased expression of SCGN mRNACTDPMID:22100608 and PMID:32234424
SCGNHumanaflatoxin M1 decreases expressionEXP 6480464Aflatoxin M1 results in decreased expression of SCGN mRNACTDPMID:30928695
SCGNHumanall-trans-retinoic acid increases expressionEXP 6480464Tretinoin results in increased expression of SCGN mRNACTDPMID:23724009
SCGNHumanamitrole decreases expressionISOScgn (Rattus norvegicus)6480464Amitrole results in decreased expression of SCGN mRNACTDPMID:30047161
SCGNHumanarsane affects methylationEXP 6480464Arsenic affects the methylation of SCGN geneCTDPMID:25304211
SCGNHumanarsenic atom affects methylationEXP 6480464Arsenic affects the methylation of SCGN geneCTDPMID:25304211
SCGNHumanbenzo[a]pyrene increases expressionEXP 6480464Benzo(a)pyrene results in increased expression of SCGN mRNACTDPMID:21632981
SCGNHumanbenzo[a]pyrene decreases expressionEXP 6480464Benzo(a)pyrene results in decreased expression of SCGN mRNACTDPMID:32234424
SCGNHumanbenzo[a]pyrene increases methylationEXP 6480464Benzo(a)pyrene results in increased methylation of SCGN exon and Benzo(a)pyrene results in increased methylation of SCGN promoterCTDPMID:27901495

1 to 20 of 53 rows

Cellular Component
1 to 13 of 13 rows

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
SCGNHumancytoplasm located_inNAS 150520179 PMID:10811645UniProtPMID:10811645
SCGNHumancytoplasm located_inIEAUniProtKB-KW:KW-0963150520179 UniProtGO_REF:0000043
SCGNHumancytoplasm located_inIEAUniProtKB-SubCell:SL-0086150520179 UniProtGO_REF:0000044
SCGNHumancytoplasmic vesicle located_inIEAUniProtKB-KW:KW-0968150520179 UniProtGO_REF:0000043
SCGNHumancytosol is_active_inIBAMGI:88248 more ...150520179 GO_CentralGO_REF:0000033
SCGNHumandendrite is_active_inIBAMGI:88248 more ...150520179 GO_CentralGO_REF:0000033
SCGNHumanextracellular region located_inIEAUniProtKB-KW:KW-0964150520179 UniProtGO_REF:0000043
SCGNHumanextracellular region located_inIEAUniProtKB-SubCell:SL-0243150520179 UniProtGO_REF:0000044
SCGNHumanmembrane located_inIEAUniProtKB-KW:KW-0472150520179 UniProtGO_REF:0000043
SCGNHumannucleus is_active_inIBAMGI:88248 more ...150520179 GO_CentralGO_REF:0000033
SCGNHumansynapse is_active_inIBAFB:FBgn0004580 more ...150520179 GO_CentralGO_REF:0000033
SCGNHumanterminal bouton is_active_inIBAFB:FBgn0004580 and PANTHER:PTN000463232150520179 GO_CentralGO_REF:0000033
SCGNHumantransport vesicle membrane located_inIEAUniProtKB-SubCell:SL-0245150520179 UniProtGO_REF:0000044
1 to 13 of 13 rows

Molecular Function

  


#
Reference Title
Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
PMID:10811645   PMID:11709487   PMID:12477932   PMID:14574404   PMID:14702039   PMID:15237930   PMID:15489334   PMID:15766553   PMID:16189514   PMID:17083620   PMID:19084217   PMID:19503597  
PMID:20529129   PMID:21288557   PMID:21528130   PMID:21873635   PMID:21976236   PMID:22474393   PMID:22921511   PMID:23102406   PMID:25226615   PMID:26186194   PMID:28223495   PMID:28325894  
PMID:28492151   PMID:28514442   PMID:28637794   PMID:29499408   PMID:29702679   PMID:31512254   PMID:31663849   PMID:32296183   PMID:33961781   PMID:36588101  



SCGN
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38625,652,215 - 25,701,783 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl625,652,201 - 25,701,783 (+)EnsemblGRCh38hg38GRCh38
GRCh37625,652,443 - 25,702,011 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36625,760,408 - 25,809,990 (+)NCBINCBI36Build 36hg18NCBI36
Build 34625,760,407 - 25,809,985NCBI
Celera626,879,633 - 26,929,216 (+)NCBICelera
Cytogenetic Map6p22.2NCBI
HuRef625,595,416 - 25,644,987 (+)NCBIHuRef
CHM1_1625,654,627 - 25,704,213 (+)NCBICHM1_1
T2T-CHM13v2.0625,518,025 - 25,567,550 (+)NCBIT2T-CHM13v2.0
Scgn
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391324,137,439 - 24,175,310 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1324,137,439 - 24,175,197 (-)EnsemblGRCm39 Ensembl
GRCm381323,953,456 - 23,991,327 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1323,953,456 - 23,991,214 (-)EnsemblGRCm38mm10GRCm38
MGSCv371324,045,325 - 24,083,083 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361323,960,921 - 23,998,679 (-)NCBIMGSCv36mm8
Celera1324,185,142 - 24,222,913 (-)NCBICelera
Cytogenetic Map13A3.1NCBI
cM Map1310.01NCBI
Scgn
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81741,534,558 - 41,576,525 (+)NCBIGRCr8
mRatBN7.21741,106,681 - 41,148,656 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1741,106,467 - 41,148,667 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1741,174,261 - 41,215,631 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01742,778,305 - 42,819,675 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01741,062,609 - 41,103,976 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01743,357,888 - 43,399,321 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1743,357,888 - 43,399,321 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01745,214,579 - 45,256,809 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41748,225,075 - 48,266,508 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11748,227,915 - 48,269,349 (+)NCBI
Celera1740,739,598 - 40,779,916 (+)NCBICelera
Cytogenetic Map17p11NCBI
Scgn
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554831,392,770 - 1,429,594 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554831,392,772 - 1,429,563 (-)NCBIChiLan1.0ChiLan1.0
SCGN
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2540,299,097 - 40,367,239 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1636,300,454 - 36,350,030 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0625,486,599 - 25,571,272 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1625,812,650 - 25,862,236 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl625,812,443 - 25,862,227 (+)Ensemblpanpan1.1panPan2
SCGN
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.13523,602,244 - 23,638,108 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl3523,602,343 - 23,638,055 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha3523,531,684 - 23,540,559 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.03523,717,908 - 23,753,767 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl3523,717,868 - 23,753,765 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.13523,527,247 - 23,563,304 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.03523,577,972 - 23,614,023 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.03525,015,623 - 25,051,501 (+)NCBIUU_Cfam_GSD_1.0
Scgn
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_0244049461,929,640 - 1,965,364 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049366711,655,978 - 1,693,175 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049366711,656,179 - 1,696,580 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
SCGN
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl720,389,493 - 20,432,978 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1720,389,156 - 20,432,985 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2721,689,440 - 21,732,931 (+)NCBISscrofa10.2Sscrofa10.2susScr3
SCGN
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11746,554,759 - 46,605,282 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1746,565,302 - 46,604,710 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604425,585,367 - 25,635,700 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Scgn
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247561,368,434 - 1,407,885 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247561,368,330 - 1,407,914 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

.

.
Variants in SCGN
35 total Variants

Predicted Target Of
Summary Value
Count of predictions:495
Count of miRNA genes:362
Interacting mature miRNAs:382
Transcripts:ENST00000334979, ENST00000377961
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.


1 to 10 of 34 rows
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD ID
Symbol
Name
LOD
P Value
Trait
Sub Trait
Chr
Start
Stop
Species
597117141GWAS1213215_Hmathematical ability QTL GWAS1213215 (human)5e-09mathematical ability62569070825690709Human
597191952GWAS1288026_Hsystemic lupus erythematosus QTL GWAS1288026 (human)1e-08systemic lupus erythematosus62568405125684052Human
597061790GWAS1157864_Hlung carcinoma QTL GWAS1157864 (human)0.0000001lung carcinoma62568437825684379Human
1298458BW9_HBody weight QTL 9 (human)2.70.0002Body fat amount6691196032911960Human
597103390GWAS1199464_Hplatelet crit QTL GWAS1199464 (human)1e-09platelet quantity (VT:0003179)plateletcrit (CMO:0001349)62567616925676170Human
597175698GWAS1271772_Hnon-alcoholic fatty liver disease, type 2 diabetes mellitus QTL GWAS1271772 (human)4e-09non-alcoholic fatty liver disease, type 2 diabetes mellitus62567304525673046Human
597208087GWAS1304161_Hvitamin D measurement QTL GWAS1304161 (human)4e-11vitamin D measurement62566264525662646Human
597204744GWAS1300818_Hupper aerodigestive tract neoplasm QTL GWAS1300818 (human)6e-11upper aerodigestive tract neoplasm62568437825684379Human
597224009GWAS1320083_HBMI-adjusted waist circumference QTL GWAS1320083 (human)2e-08body size trait (VT:0100005)62568305225683053Human
1358854MULTSCL4_HMultiple sclerosis susceptibility QTL 4 (human)Multiple sclerosis susceptibility6691196032911960Human

1 to 10 of 34 rows
RH99089  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37625,701,700 - 25,701,840UniSTSGRCh37
Build 36625,809,679 - 25,809,819RGDNCBI36
Celera626,928,904 - 26,929,044RGD
Cytogenetic Map6p22.3-p22.1UniSTS
HuRef625,644,675 - 25,644,815UniSTS
GeneMap99-GB4 RH Map6104.59UniSTS
SCGN_9148  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37625,701,504 - 25,702,087UniSTSGRCh37
Build 36625,809,483 - 25,810,066RGDNCBI36
Celera626,928,708 - 26,929,292RGD
HuRef625,644,479 - 25,645,063UniSTS
D6S1468  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37625,650,714 - 25,650,841UniSTSGRCh37
Build 36625,758,693 - 25,758,820RGDNCBI36
Celera626,877,918 - 26,878,045RGD
Cytogenetic Map6p22.3-p22.1UniSTS
HuRef625,593,701 - 25,593,828UniSTS
AL021842  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37625,654,747 - 25,654,878UniSTSGRCh37
Build 36625,762,726 - 25,762,857RGDNCBI36
Celera626,881,951 - 26,882,082RGD
Cytogenetic Map6p22.3-p22.1UniSTS
HuRef625,597,734 - 25,597,865UniSTS




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
1187 2310 1757 2006 4155 1661 1940 4 595 796 449 1649 5254 4978 13 3342 1 724 1381 1227 148 1



Ensembl Acc Id: ENST00000334979   ⟹   ENSP00000333933
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl625,652,404 - 25,701,335 (+)Ensembl
Ensembl Acc Id: ENST00000377961   ⟹   ENSP00000367197
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl625,652,215 - 25,701,783 (+)Ensembl
Ensembl Acc Id: ENST00000612225   ⟹   ENSP00000484392
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl625,652,201 - 25,701,774 (+)Ensembl
RefSeq Acc Id: NM_006998   ⟹   NP_008929
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38625,652,215 - 25,701,783 (+)NCBI
GRCh37625,652,429 - 25,702,011 (+)ENTREZGENE
Build 36625,760,408 - 25,809,990 (+)NCBI Archive
HuRef625,595,416 - 25,644,987 (+)ENTREZGENE
CHM1_1625,654,627 - 25,704,213 (+)NCBI
T2T-CHM13v2.0625,518,025 - 25,567,550 (+)NCBI
Sequence:
RefSeq Acc Id: XM_054354044   ⟹   XP_054210019
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0625,527,119 - 25,567,550 (+)NCBI
1 to 12 of 12 rows
Protein RefSeqs NP_008929 (Get FASTA)   NCBI Sequence Viewer  
  XP_054210019 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH00336 (Get FASTA)   NCBI Sequence Viewer  
  AAH03036 (Get FASTA)   NCBI Sequence Viewer  
  AAL16052 (Get FASTA)   NCBI Sequence Viewer  
  BAF82166 (Get FASTA)   NCBI Sequence Viewer  
  CAA76365 (Get FASTA)   NCBI Sequence Viewer  
  EAW55487 (Get FASTA)   NCBI Sequence Viewer  
  EAW55488 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000367197
  ENSP00000367197.2
GenBank Protein O76038 (Get FASTA)   NCBI Sequence Viewer  
1 to 12 of 12 rows
RefSeq Acc Id: NP_008929   ⟸   NM_006998
- UniProtKB: Q96QV7 (UniProtKB/Swiss-Prot),   Q5VV44 (UniProtKB/Swiss-Prot),   A8K0B2 (UniProtKB/Swiss-Prot),   Q9UJF6 (UniProtKB/Swiss-Prot),   O76038 (UniProtKB/Swiss-Prot),   A0A994J4C2 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSP00000333933   ⟸   ENST00000334979
Ensembl Acc Id: ENSP00000484392   ⟸   ENST00000612225
Ensembl Acc Id: ENSP00000367197   ⟸   ENST00000377961
RefSeq Acc Id: XP_054210019   ⟸   XM_054354044
- Peptide Label: isoform X1
EF-hand

Name Modeler Protein Id AA Range Protein Structure
AF-O76038-F1-model_v2 AlphaFold O76038 1-276 view protein structure

RGD ID:6872224
Promoter ID:EPDNEW_H9277
Type:initiation region
Name:SCGN_1
Description:secretagogin, EF-hand calcium binding protein
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
GRCh38625,652,225 - 25,652,285EPDNEW


1 to 37 of 37 rows
Database
Acc Id
Source(s)
COSMIC SCGN COSMIC
Ensembl Genes ENSG00000079689 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000377961 ENTREZGENE
  ENST00000377961.3 UniProtKB/Swiss-Prot
Gene3D-CATH EF-hand UniProtKB/Swiss-Prot
GTEx ENSG00000079689 GTEx
HGNC ID HGNC:16941 ENTREZGENE
Human Proteome Map SCGN Human Proteome Map
InterPro Calbindin_Ca-bind UniProtKB/Swiss-Prot
  EF-hand-dom_pair UniProtKB/Swiss-Prot
  EF_Hand_1_Ca_BS UniProtKB/Swiss-Prot
  EF_hand_dom UniProtKB/Swiss-Prot
  EFh_SCGN UniProtKB/Swiss-Prot
KEGG Report hsa:10590 UniProtKB/Swiss-Prot
NCBI Gene 10590 ENTREZGENE
OMIM 609202 OMIM
PANTHER CALBINDIN UniProtKB/Swiss-Prot
  SECRETAGOGIN UniProtKB/Swiss-Prot
Pfam EF-hand_5 UniProtKB/Swiss-Prot
  EF-hand_7 UniProtKB/Swiss-Prot
PharmGKB PA38428 PharmGKB
PROSITE EF_HAND_1 UniProtKB/Swiss-Prot
  EF_HAND_2 UniProtKB/Swiss-Prot
SMART EFh UniProtKB/Swiss-Prot
Superfamily-SCOP SSF47473 UniProtKB/Swiss-Prot
UniProt A0A994J4C2 ENTREZGENE, UniProtKB/TrEMBL
  A8K0B2 ENTREZGENE
  O76038 ENTREZGENE
  Q5VV44 ENTREZGENE
  Q96P10_HUMAN UniProtKB/TrEMBL
  Q96QV7 ENTREZGENE
  Q9UJF6 ENTREZGENE
  SEGN_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary A8K0B2 UniProtKB/Swiss-Prot
  Q5VV44 UniProtKB/Swiss-Prot
  Q96QV7 UniProtKB/Swiss-Prot
  Q9UJF6 UniProtKB/Swiss-Prot
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