DHRS7C (dehydrogenase/reductase 7C) - Rat Genome Database

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Gene: DHRS7C (dehydrogenase/reductase 7C) Homo sapiens
Analyze
Symbol: DHRS7C
Name: dehydrogenase/reductase 7C
RGD ID: 1602060
HGNC Page HGNC:32423
Description: Predicted to enable NAD-retinol dehydrogenase activity. Predicted to be involved in glucose import; intracellular calcium ion homeostasis; and regulation of release of sequestered calcium ion into cytosol by sarcoplasmic reticulum. Predicted to be located in longitudinal sarcoplasmic reticulum and sarcoplasmic reticulum membrane.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: dehydrogenase/reductase (SDR family) member 7C; dehydrogenase/reductase SDR family member 7C; sarcoplasmic reticulum protein of 35 kDa; SDR32C2; short chain dehydrogenase/reductase family 32C, member 2; short-chain dehydrogenase/reductase family 32C member 2
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
GRCh38179,771,438 - 9,791,592 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl179,771,434 - 9,791,592 (-)EnsemblGRCh38hg38GRCh38
GRCh37179,674,755 - 9,694,909 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36179,615,480 - 9,635,326 (-)NCBINCBI36Build 36hg18NCBI36
Celera179,707,201 - 9,727,047 (-)NCBICelera
Cytogenetic Map17p13.1NCBI
HuRef179,575,182 - 9,595,046 (-)NCBIHuRef
CHM1_1179,684,765 - 9,704,628 (-)NCBICHM1_1
T2T-CHM13v2.0179,679,162 - 9,699,310 (-)NCBIT2T-CHM13v2.0
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
Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:12477932   PMID:19027726   PMID:19490893   PMID:21873635   PMID:22143674  


Genomics

Comparative Map Data
DHRS7C
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38179,771,438 - 9,791,592 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl179,771,434 - 9,791,592 (-)EnsemblGRCh38hg38GRCh38
GRCh37179,674,755 - 9,694,909 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36179,615,480 - 9,635,326 (-)NCBINCBI36Build 36hg18NCBI36
Celera179,707,201 - 9,727,047 (-)NCBICelera
Cytogenetic Map17p13.1NCBI
HuRef179,575,182 - 9,595,046 (-)NCBIHuRef
CHM1_1179,684,765 - 9,704,628 (-)NCBICHM1_1
T2T-CHM13v2.0179,679,162 - 9,699,310 (-)NCBIT2T-CHM13v2.0
Dhrs7c
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391167,689,097 - 67,706,828 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1167,689,013 - 67,706,828 (+)EnsemblGRCm39 Ensembl
GRCm381167,798,271 - 67,816,002 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1167,798,187 - 67,816,002 (+)EnsemblGRCm38mm10GRCm38
MGSCv371167,611,773 - 67,629,504 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361167,614,483 - 67,632,200 (+)NCBIMGSCv36mm8
Celera1174,742,016 - 74,759,751 (+)NCBICelera
Cytogenetic Map11B3NCBI
cM Map1141.13NCBI
Dhrs7c
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81052,994,205 - 53,012,281 (+)NCBIGRCr8
mRatBN7.21052,495,262 - 52,513,338 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1052,495,262 - 52,513,338 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1057,157,229 - 57,175,369 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01056,646,238 - 56,664,378 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01052,151,891 - 52,170,073 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01054,352,270 - 54,370,653 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1054,352,270 - 54,370,653 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01054,098,500 - 54,116,883 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41054,518,094 - 54,536,171 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11054,531,747 - 54,549,796 (+)NCBI
Celera1051,675,569 - 51,693,645 (+)NCBICelera
Cytogenetic Map10q24NCBI
Dhrs7c
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554677,330,188 - 7,342,053 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049554677,330,267 - 7,341,897 (+)NCBIChiLan1.0ChiLan1.0
DHRS7C
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21963,959,016 - 63,979,110 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11768,768,554 - 68,788,662 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01741,864,761 - 41,884,938 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11746,608,656 - 46,628,709 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1746,608,656 - 46,628,709 (+)Ensemblpanpan1.1panPan2
DHRS7C
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1534,224,699 - 34,239,847 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl534,224,700 - 34,239,798 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha534,360,745 - 34,375,901 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0534,328,723 - 34,343,881 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl534,328,725 - 34,343,822 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1534,294,553 - 34,309,712 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0534,252,649 - 34,267,793 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0534,433,105 - 34,448,262 (-)NCBIUU_Cfam_GSD_1.0
Dhrs7c
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440560249,257,918 - 49,277,926 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365952,732,103 - 2,752,131 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365952,732,106 - 2,769,782 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
DHRS7C
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1254,641,178 - 54,661,447 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11254,647,773 - 54,661,442 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21257,405,743 - 57,419,599 (-)NCBISscrofa10.2Sscrofa10.2susScr3
DHRS7C
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1169,111,538 - 9,132,553 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl169,111,957 - 9,132,355 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366605912,209,865 - 12,230,268 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Dhrs7c
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462478612,222,248 - 12,236,301 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462478612,222,735 - 12,236,209 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in DHRS7C
15 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 17p13.1(chr17:7750804-10112969)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052460]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052460]|See cases [RCV000052460] Chr17:7750804..10112969 [GRCh38]
Chr17:7654122..10016286 [GRCh37]
Chr17:7594847..9957011 [NCBI36]
Chr17:17p13.1
pathogenic
NM_001105571.2(DHRS7C):c.474G>A (p.Thr158=) single nucleotide variant Malignant melanoma [RCV000071743] Chr17:9779829 [GRCh38]
Chr17:9683146 [GRCh37]
Chr17:9623871 [NCBI36]
Chr17:17p13.1
not provided
GRCh38/hg38 17p13.2-12(chr17:5732953-12095349)x3 copy number gain See cases [RCV000134851] Chr17:5732953..12095349 [GRCh38]
Chr17:5636273..11998666 [GRCh37]
Chr17:5576997..11939391 [NCBI36]
Chr17:17p13.2-12
pathogenic
GRCh38/hg38 17p13.3-12(chr17:162016-12343901)x3 copy number gain See cases [RCV000138531] Chr17:162016..12343901 [GRCh38]
Chr17:45835..12247218 [GRCh37]
Chr17:11807..12187943 [NCBI36]
Chr17:17p13.3-12
pathogenic
GRCh38/hg38 17p13.3-12(chr17:150732-14764202)x3 copy number gain See cases [RCV000142236] Chr17:150732..14764202 [GRCh38]
Chr17:525..14667519 [GRCh37]
Chr17:525..14608244 [NCBI36]
Chr17:17p13.3-12
pathogenic
GRCh38/hg38 17p13.1-12(chr17:9701182-11983353)x1 copy number loss Ductal breast carcinoma [RCV000207166] Chr17:9701182..11983353 [GRCh38]
Chr17:9604499..11886670 [GRCh37]
Chr17:17p13.1-12
uncertain significance
Single allele complex Ductal breast carcinoma [RCV000207129] Chr17:9586165..16325968 [GRCh37]
Chr17:17p13.1-11.2
uncertain significance
GRCh37/hg19 17p13.1(chr17:7929776-9995862)x3 copy number gain See cases [RCV000447853] Chr17:7929776..9995862 [GRCh37]
Chr17:17p13.1
uncertain significance
GRCh37/hg19 17p13.1(chr17:7431013-9868179)x3 copy number gain See cases [RCV000511388] Chr17:7431013..9868179 [GRCh37]
Chr17:17p13.1
uncertain significance
GRCh37/hg19 17p13.3-12(chr17:525-15027737)x3 copy number gain See cases [RCV000511786] Chr17:525..15027737 [GRCh37]
Chr17:17p13.3-12
pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938) copy number gain See cases [RCV000511439] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3
pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)x3 copy number gain See cases [RCV000512441] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3
pathogenic
GRCh37/hg19 17p13.3-12(chr17:525-11186432)x3 copy number gain not provided [RCV000683866] Chr17:525..11186432 [GRCh37]
Chr17:17p13.3-12
pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:8547-81060040)x3 copy number gain not provided [RCV000739324] Chr17:8547..81060040 [GRCh37]
Chr17:17p13.3-q25.3
pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:7214-81058310)x3 copy number gain not provided [RCV000739320] Chr17:7214..81058310 [GRCh37]
Chr17:17p13.3-q25.3
pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:12344-81057996)x3 copy number gain not provided [RCV000739325] Chr17:12344..81057996 [GRCh37]
Chr17:17p13.3-q25.3
pathogenic
NM_001105571.3(DHRS7C):c.404C>A (p.Ala135Asp) single nucleotide variant Inborn genetic diseases [RCV003272125] Chr17:9779899 [GRCh38]
Chr17:9683216 [GRCh37]
Chr17:17p13.1
uncertain significance
NM_001105571.3(DHRS7C):c.268-12T>C single nucleotide variant not provided [RCV000910605] Chr17:9780047 [GRCh38]
Chr17:9683364 [GRCh37]
Chr17:17p13.1
benign
NM_001105571.3(DHRS7C):c.155-10T>C single nucleotide variant not provided [RCV000961459] Chr17:9781604 [GRCh38]
Chr17:9684921 [GRCh37]
Chr17:17p13.1
benign
GRCh37/hg19 17p13.1(chr17:7929776-9995862) copy number gain not specified [RCV002052588] Chr17:7929776..9995862 [GRCh37]
Chr17:17p13.1
uncertain significance
NM_001105571.3(DHRS7C):c.317T>C (p.Val106Ala) single nucleotide variant Inborn genetic diseases [RCV003258060] Chr17:9779986 [GRCh38]
Chr17:9683303 [GRCh37]
Chr17:17p13.1
uncertain significance
NM_001105571.3(DHRS7C):c.271T>C (p.Phe91Leu) single nucleotide variant Inborn genetic diseases [RCV002865024] Chr17:9780032 [GRCh38]
Chr17:9683349 [GRCh37]
Chr17:17p13.1
uncertain significance
NM_001105571.3(DHRS7C):c.637G>A (p.Asp213Asn) single nucleotide variant Inborn genetic diseases [RCV002670673] Chr17:9772857 [GRCh38]
Chr17:9676174 [GRCh37]
Chr17:17p13.1
uncertain significance
NM_001105571.3(DHRS7C):c.445G>A (p.Ala149Thr) single nucleotide variant Inborn genetic diseases [RCV002934109] Chr17:9779858 [GRCh38]
Chr17:9683175 [GRCh37]
Chr17:17p13.1
uncertain significance
NM_001105571.3(DHRS7C):c.628G>C (p.Glu210Gln) single nucleotide variant Inborn genetic diseases [RCV002831801] Chr17:9772866 [GRCh38]
Chr17:9676183 [GRCh37]
Chr17:17p13.1
uncertain significance
NM_001105571.3(DHRS7C):c.408T>G (p.His136Gln) single nucleotide variant Inborn genetic diseases [RCV002792590] Chr17:9779895 [GRCh38]
Chr17:9683212 [GRCh37]
Chr17:17p13.1
uncertain significance
NM_001105571.3(DHRS7C):c.598G>A (p.Gly200Ser) single nucleotide variant Inborn genetic diseases [RCV002898468] Chr17:9772896 [GRCh38]
Chr17:9676213 [GRCh37]
Chr17:17p13.1
uncertain significance
NM_001105571.3(DHRS7C):c.259C>A (p.Pro87Thr) single nucleotide variant Inborn genetic diseases [RCV002808085] Chr17:9781490 [GRCh38]
Chr17:9684807 [GRCh37]
Chr17:17p13.1
uncertain significance
NM_001105571.3(DHRS7C):c.692C>T (p.Pro231Leu) single nucleotide variant Inborn genetic diseases [RCV003192110] Chr17:9772802 [GRCh38]
Chr17:9676119 [GRCh37]
Chr17:17p13.1
uncertain significance
NM_001105571.3(DHRS7C):c.613C>T (p.Leu205Phe) single nucleotide variant Inborn genetic diseases [RCV003185997] Chr17:9772881 [GRCh38]
Chr17:9676198 [GRCh37]
Chr17:17p13.1
uncertain significance
NM_001105571.3(DHRS7C):c.674G>A (p.Arg225Gln) single nucleotide variant Inborn genetic diseases [RCV003195167] Chr17:9772820 [GRCh38]
Chr17:9676137 [GRCh37]
Chr17:17p13.1
uncertain significance
GRCh38/hg38 17p13.3-12(chr17:165730-11404096)x3 copy number gain Chromosome 17p13.3 duplication syndrome [RCV003327726] Chr17:165730..11404096 [GRCh38]
Chr17:17p13.3-12
pathogenic
NM_001105571.3(DHRS7C):c.73G>A (p.Glu25Lys) single nucleotide variant Inborn genetic diseases [RCV003343356] Chr17:9791212 [GRCh38]
Chr17:9694529 [GRCh37]
Chr17:17p13.1
uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:877
Count of miRNA genes:420
Interacting mature miRNAs:469
Transcripts:ENST00000330255, ENST00000571134, ENST00000571771
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.

Markers in Region
RH79746  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37179,674,754 - 9,674,989UniSTSGRCh37
Build 36179,615,479 - 9,615,714RGDNCBI36
Celera179,707,200 - 9,707,435RGD
Cytogenetic Map17p13.1UniSTS
HuRef179,575,185 - 9,575,420UniSTS


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 pharyngeal arch
High
Medium 1 678 3 10 6 1 724 957 1 2 6 11 724
Low 265 266 111 47 72 9 195 300 608 6 364 33 36 94 146 1 2
Below cutoff 1270 785 609 206 489 146 1454 558 1726 88 429 477 59 792 804

Sequence


RefSeq Acc Id: ENST00000330255   ⟹   ENSP00000327975
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl179,771,434 - 9,791,297 (-)Ensembl
RefSeq Acc Id: ENST00000571134   ⟹   ENSP00000459579
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl179,771,438 - 9,791,592 (-)Ensembl
RefSeq Acc Id: ENST00000571771   ⟹   ENSP00000461902
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl179,771,434 - 9,779,921 (-)Ensembl
RefSeq Acc Id: NM_001105571   ⟹   NP_001099041
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38179,771,438 - 9,791,592 (-)NCBI
GRCh37179,674,751 - 9,694,894 (-)NCBI
Build 36179,615,480 - 9,635,326 (-)NCBI Archive
Celera179,707,201 - 9,727,047 (-)RGD
HuRef179,575,182 - 9,595,046 (-)ENTREZGENE
CHM1_1179,684,765 - 9,704,628 (-)NCBI
T2T-CHM13v2.0179,679,162 - 9,699,310 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001220493   ⟹   NP_001207422
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38179,771,438 - 9,791,592 (-)NCBI
GRCh37179,674,751 - 9,694,894 (-)NCBI
HuRef179,575,182 - 9,595,046 (-)ENTREZGENE
CHM1_1179,684,765 - 9,704,628 (-)NCBI
T2T-CHM13v2.0179,679,162 - 9,699,310 (-)NCBI
Sequence:
RefSeq Acc Id: NP_001099041   ⟸   NM_001105571
- Peptide Label: isoform 2 precursor
- UniProtKB: A6NNS2 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001207422   ⟸   NM_001220493
- Peptide Label: isoform 1 precursor
- UniProtKB: B7ZW74 (UniProtKB/Swiss-Prot),   B9EJH3 (UniProtKB/Swiss-Prot),   A6NNS2 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000459579   ⟸   ENST00000571134
RefSeq Acc Id: ENSP00000461902   ⟸   ENST00000571771
RefSeq Acc Id: ENSP00000327975   ⟸   ENST00000330255

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-A6NNS2-F1-model_v2 AlphaFold A6NNS2 1-312 view protein structure

Promoters
RGD ID:7233983
Promoter ID:EPDNEW_H22738
Type:multiple initiation site
Name:DHRS7C_1
Description:dehydrogenase/reductase 7C
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38179,791,589 - 9,791,649EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:32423 AgrOrtholog
COSMIC DHRS7C COSMIC
Ensembl Genes ENSG00000184544 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000330255 ENTREZGENE
  ENST00000330255.9 UniProtKB/Swiss-Prot
  ENST00000571134 ENTREZGENE
  ENST00000571134.2 UniProtKB/Swiss-Prot
  ENST00000571771.5 UniProtKB/TrEMBL
Gene3D-CATH NAD(P)-binding Rossmann-like Domain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000184544 GTEx
HGNC ID HGNC:32423 ENTREZGENE
Human Proteome Map DHRS7C Human Proteome Map
InterPro NAD(P)-bd_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Sc_DH/Rdtase_CS UniProtKB/Swiss-Prot
  SDR_fam UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:201140 UniProtKB/Swiss-Prot
NCBI Gene 201140 ENTREZGENE
OMIM 616161 OMIM
PANTHER DEHYDROGENASE/REDUCTASE SDR FAMILY MEMBER 7C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR44668 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam adh_short UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA142671977 PharmGKB
PRINTS GDHRDH UniProtKB/Swiss-Prot
  SDRFAMILY UniProtKB/Swiss-Prot
PROSITE ADH_SHORT UniProtKB/Swiss-Prot
Superfamily-SCOP SSF51735 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A6NNS2 ENTREZGENE
  B7ZW74 ENTREZGENE
  B9EJH3 ENTREZGENE
  DRS7C_HUMAN UniProtKB/Swiss-Prot
  I3NI52_HUMAN UniProtKB/TrEMBL
UniProt Secondary B7ZW74 UniProtKB/Swiss-Prot
  B9EJH3 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-05-31 DHRS7C  dehydrogenase/reductase 7C    dehydrogenase/reductase (SDR family) member 7C  Symbol and/or name change 5135510 APPROVED