CST5 (cystatin D) - Rat Genome Database

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Gene: CST5 (cystatin D) Homo sapiens
Analyze
Symbol: CST5
Name: cystatin D
RGD ID: 1322184
HGNC Page HGNC:2477
Description: Enables cysteine-type endopeptidase inhibitor activity. Predicted to be involved in several processes, including bone mineralization; calcium ion homeostasis; and endochondral bone morphogenesis. Predicted to act upstream of or within cell maturation and chondrocyte differentiation. Located in extracellular region.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: cystatin 5; cystatin-5; cystatin-D; cysteine-proteinase inhibitor; MGC71922
RGD Orthologs
Mouse
Rat
Bonobo
Green Monkey
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
GRCh382023,875,934 - 23,879,748 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2023,875,934 - 23,879,748 (-)EnsemblGRCh38hg38GRCh38
GRCh372023,856,571 - 23,860,385 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 362023,804,572 - 23,808,380 (-)NCBINCBI36Build 36hg18NCBI36
Build 342023,804,792 - 23,808,371NCBI
Celera2023,929,951 - 23,933,759 (-)NCBICelera
Cytogenetic Map20p11.21NCBI
HuRef2023,813,604 - 23,817,412 (-)NCBIHuRef
CHM1_12023,856,749 - 23,860,557 (-)NCBICHM1_1
T2T-CHM13v2.02023,935,655 - 23,939,469 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:1939105   PMID:3202964   PMID:7690606   PMID:7896273   PMID:8083219   PMID:8179826   PMID:8340398   PMID:8422752   PMID:8444475   PMID:9007972   PMID:11780052   PMID:11879580  
PMID:12477932   PMID:15489334   PMID:15728581   PMID:17207965   PMID:18615156   PMID:19199708   PMID:19662683   PMID:20223287   PMID:20379614   PMID:21873635   PMID:23376485   PMID:26158294  
PMID:26364852   PMID:28514442   PMID:28694499   PMID:33961781   PMID:35509820  


Genomics

Comparative Map Data
CST5
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382023,875,934 - 23,879,748 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2023,875,934 - 23,879,748 (-)EnsemblGRCh38hg38GRCh38
GRCh372023,856,571 - 23,860,385 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 362023,804,572 - 23,808,380 (-)NCBINCBI36Build 36hg18NCBI36
Build 342023,804,792 - 23,808,371NCBI
Celera2023,929,951 - 23,933,759 (-)NCBICelera
Cytogenetic Map20p11.21NCBI
HuRef2023,813,604 - 23,817,412 (-)NCBIHuRef
CHM1_12023,856,749 - 23,860,557 (-)NCBICHM1_1
T2T-CHM13v2.02023,935,655 - 23,939,469 (-)NCBIT2T-CHM13v2.0
Cst5
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm392149,247,242 - 149,252,217 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl2149,246,977 - 149,252,213 (+)EnsemblGRCm39 Ensembl
GRCm382149,405,249 - 149,410,278 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl2149,405,057 - 149,410,293 (+)EnsemblGRCm38mm10GRCm38
MGSCv372149,230,985 - 149,236,014 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv362149,096,690 - 149,101,719 (+)NCBIMGSCv36mm8
Celera2150,661,381 - 150,663,520 (+)NCBICelera
Cytogenetic Map2G3NCBI
cM Map273.8NCBI
Cst5
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr83158,033,791 - 158,038,345 (+)NCBIGRCr8
mRatBN7.23137,573,194 - 137,577,754 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl3137,573,194 - 137,577,754 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx3141,505,992 - 141,510,482 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.03150,089,686 - 150,094,176 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.03147,806,172 - 147,810,725 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.03144,569,502 - 144,574,112 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl3144,569,502 - 144,574,112 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.03150,943,493 - 150,948,103 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.43138,967,434 - 138,972,106 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.13138,873,315 - 139,339,652 (+)NCBI
Celera3136,259,691 - 136,264,235 (+)NCBICelera
Cytogenetic Map3q41NCBI
CST5
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22124,756,245 - 24,760,063 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan12024,753,078 - 24,756,896 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v02023,824,663 - 23,828,483 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.12024,178,197 - 24,182,009 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl2024,178,197 - 24,182,016 (-)Ensemblpanpan1.1panPan2
CST5
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1253,015,431 - 53,020,125 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl253,015,687 - 53,019,336 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366605092,820,941 - 92,824,956 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0

Variants

.
Variants in CST5
21 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 20p13-11.21(chr20:89939-25697564)x3 copy number gain See cases [RCV000051227] Chr20:89939..25697564 [GRCh38]
Chr20:70580..25678200 [GRCh37]
Chr20:18580..25626200 [NCBI36]
Chr20:20p13-11.21		 pathogenic
GRCh38/hg38 20p11.22-q11.1(chr20:22061586-30285812)x3 copy number gain See cases [RCV000053000] Chr20:22061586..30285812 [GRCh38]
Chr20:22042224..29520488 [GRCh37]
Chr20:21990224..28134149 [NCBI36]
Chr20:20p11.22-q11.1		 pathogenic
GRCh38/hg38 20p11.21(chr20:23455796-24880833)x3 copy number gain See cases [RCV000053001] Chr20:23455796..24880833 [GRCh38]
Chr20:23436433..24861469 [GRCh37]
Chr20:23384433..24809469 [NCBI36]
Chr20:20p11.21		 pathogenic
GRCh38/hg38 20p12.2-q12(chr20:9811433-39316956)x3 copy number gain See cases [RCV000052999] Chr20:9811433..39316956 [GRCh38]
Chr20:9792081..37945599 [GRCh37]
Chr20:9740081..37379013 [NCBI36]
Chr20:20p12.2-q12		 pathogenic
GRCh38/hg38 20p11.21(chr20:23455996-24050737)x3 copy number gain See cases [RCV000133802] Chr20:23455996..24050737 [GRCh38]
Chr20:23436633..24031374 [GRCh37]
Chr20:23384633..23979374 [NCBI36]
Chr20:20p11.21		 uncertain significance
GRCh38/hg38 20p13-q11.1(chr20:80106-30227427)x3 copy number gain See cases [RCV000133996] Chr20:80106..30227427 [GRCh38]
Chr20:60747..29462103 [GRCh37]
Chr20:8747..28075764 [NCBI36]
Chr20:20p13-q11.1		 pathogenic
GRCh38/hg38 20p13-q13.33(chr20:99557-64277321)x3 copy number gain See cases [RCV000135859] Chr20:99557..64277321 [GRCh38]
Chr20:80198..62908674 [GRCh37]
Chr20:28198..62379118 [NCBI36]
Chr20:20p13-q13.33		 pathogenic
GRCh38/hg38 20p13-11.1(chr20:80927-26324843)x3 copy number gain See cases [RCV000142017] Chr20:80927..26324843 [GRCh38]
Chr20:61568..26305479 [GRCh37]
Chr20:9568..26253479 [NCBI36]
Chr20:20p13-11.1		 pathogenic
GRCh37/hg19 20p13-11.1(chr20:80198-26075841)x3 copy number gain See cases [RCV000239954] Chr20:80198..26075841 [GRCh37]
Chr20:20p13-11.1		 pathogenic
GRCh37/hg19 20p12.1-q11.21(chr20:17705775-31600738)x3 copy number gain See cases [RCV000240436] Chr20:17705775..31600738 [GRCh37]
Chr20:20p12.1-q11.21		 pathogenic
GRCh37/hg19 20p13-q11.21(chr20:80198-26208081)x3 copy number gain not provided [RCV000487461] Chr20:80198..26208081 [GRCh37]
Chr20:20p13-q11.21		 pathogenic
GRCh37/hg19 20p11.23-11.1(chr20:18500917-25847320)x1 copy number loss See cases [RCV000510621] Chr20:18500917..25847320 [GRCh37]
Chr20:20p11.23-11.1		 pathogenic
GRCh37/hg19 20p13-q13.33(chr20:61569-62915555)x3 copy number gain See cases [RCV000510832] Chr20:61569..62915555 [GRCh37]
Chr20:20p13-q13.33		 pathogenic
NM_001900.5(CST5):c.247A>C (p.Asn83His) single nucleotide variant Inborn genetic diseases [RCV003262944] Chr20:23877603 [GRCh38]
Chr20:23858240 [GRCh37]
Chr20:20p11.21		 uncertain significance
GRCh37/hg19 20p13-q13.33(chr20:61569-62915555) copy number gain See cases [RCV000512450] Chr20:61569..62915555 [GRCh37]
Chr20:20p13-q13.33		 pathogenic
GRCh37/hg19 20p11.22-11.21(chr20:21680345-24383453)x1 copy number loss See cases [RCV000663385] Chr20:21680345..24383453 [GRCh37]
Chr20:20p11.22-11.21		 likely pathogenic
Single allele duplication not provided [RCV000677978] Chr20:17705775..31600738 [GRCh37]
Chr20:20p12.1-q11.21		 pathogenic
GRCh37/hg19 20p13-q13.33(chr20:63244-62948788)x3 copy number gain not provided [RCV000741058] Chr20:63244..62948788 [GRCh37]
Chr20:20p13-q13.33		 pathogenic
GRCh37/hg19 20p13-q13.33(chr20:63244-62961294)x3 copy number gain not provided [RCV000741059] Chr20:63244..62961294 [GRCh37]
Chr20:20p13-q13.33		 pathogenic
GRCh37/hg19 20p13-q13.33(chr20:63244-62912463)x3 copy number gain not provided [RCV000741057] Chr20:63244..62912463 [GRCh37]
Chr20:20p13-q13.33		 pathogenic
GRCh37/hg19 20p13-11.1(chr20:61568-26305479)x3 copy number gain not provided [RCV001007068] Chr20:61568..26305479 [GRCh37]
Chr20:20p13-11.1		 pathogenic
GRCh37/hg19 20p11.23-q11.21(chr20:19750804-30479077)x3 copy number gain not provided [RCV001258738] Chr20:19750804..30479077 [GRCh37]
Chr20:20p11.23-q11.21		 likely pathogenic
GRCh37/hg19 20p11.23-q11.22(chr20:18665879-33903216)x3 copy number gain not provided [RCV001829151] Chr20:18665879..33903216 [GRCh37]
Chr20:20p11.23-q11.22		 likely pathogenic
GRCh37/hg19 20p11.21(chr20:23142478-24824349)x3 copy number gain not provided [RCV002474920] Chr20:23142478..24824349 [GRCh37]
Chr20:20p11.21		 uncertain significance
NM_001900.5(CST5):c.239G>T (p.Gly80Val) single nucleotide variant Inborn genetic diseases [RCV002836916] Chr20:23877611 [GRCh38]
Chr20:23858248 [GRCh37]
Chr20:20p11.21		 uncertain significance
NM_001900.5(CST5):c.224A>T (p.Tyr75Phe) single nucleotide variant Inborn genetic diseases [RCV002683426] Chr20:23879453 [GRCh38]
Chr20:23860090 [GRCh37]
Chr20:20p11.21		 uncertain significance
NM_001900.5(CST5):c.101T>C (p.Ile34Thr) single nucleotide variant Inborn genetic diseases [RCV002945266] Chr20:23879576 [GRCh38]
Chr20:23860213 [GRCh37]
Chr20:20p11.21		 uncertain significance
NM_001900.5(CST5):c.287C>T (p.Thr96Ile) single nucleotide variant Inborn genetic diseases [RCV002860258] Chr20:23877563 [GRCh38]
Chr20:23858200 [GRCh37]
Chr20:20p11.21		 uncertain significance
NM_001900.5(CST5):c.384G>C (p.Trp128Cys) single nucleotide variant Inborn genetic diseases [RCV002773348] Chr20:23876233 [GRCh38]
Chr20:23856870 [GRCh37]
Chr20:20p11.21		 uncertain significance
NM_001900.5(CST5):c.137G>A (p.Cys46Tyr) single nucleotide variant Inborn genetic diseases [RCV002693187] Chr20:23879540 [GRCh38]
Chr20:23860177 [GRCh37]
Chr20:20p11.21		 uncertain significance
NM_001900.5(CST5):c.418C>T (p.Arg140Trp) single nucleotide variant Inborn genetic diseases [RCV002930769] Chr20:23876199 [GRCh38]
Chr20:23856836 [GRCh37]
Chr20:20p11.21		 uncertain significance
NM_001900.5(CST5):c.107C>T (p.Ala36Val) single nucleotide variant Inborn genetic diseases [RCV002789013] Chr20:23879570 [GRCh38]
Chr20:23860207 [GRCh37]
Chr20:20p11.21		 uncertain significance
NM_001900.5(CST5):c.161A>C (p.Glu54Ala) single nucleotide variant Inborn genetic diseases [RCV002825984] Chr20:23879516 [GRCh38]
Chr20:23860153 [GRCh37]
Chr20:20p11.21		 uncertain significance
NM_001900.5(CST5):c.202C>A (p.Pro68Thr) single nucleotide variant Inborn genetic diseases [RCV002827839] Chr20:23879475 [GRCh38]
Chr20:23860112 [GRCh37]
Chr20:20p11.21		 uncertain significance
NM_001900.5(CST5):c.137G>T (p.Cys46Phe) single nucleotide variant Inborn genetic diseases [RCV002747143] Chr20:23879540 [GRCh38]
Chr20:23860177 [GRCh37]
Chr20:20p11.21		 uncertain significance
NM_001900.5(CST5):c.338T>C (p.Leu113Pro) single nucleotide variant Inborn genetic diseases [RCV002649120] Chr20:23877512 [GRCh38]
Chr20:23858149 [GRCh37]
Chr20:20p11.21		 uncertain significance
NM_001900.5(CST5):c.91G>A (p.Ala31Thr) single nucleotide variant Inborn genetic diseases [RCV003199480] Chr20:23879586 [GRCh38]
Chr20:23860223 [GRCh37]
Chr20:20p11.21		 uncertain significance
NM_001900.5(CST5):c.67G>A (p.Ala23Thr) single nucleotide variant Inborn genetic diseases [RCV003195670] Chr20:23879610 [GRCh38]
Chr20:23860247 [GRCh37]
Chr20:20p11.21		 uncertain significance
NM_001900.5(CST5):c.351G>C (p.Glu117Asp) single nucleotide variant Inborn genetic diseases [RCV003372532] Chr20:23876266 [GRCh38]
Chr20:23856903 [GRCh37]
Chr20:20p11.21		 uncertain significance
NM_001900.5(CST5):c.172G>A (p.Val58Ile) single nucleotide variant Inborn genetic diseases [RCV003375036] Chr20:23879505 [GRCh38]
Chr20:23860142 [GRCh37]
Chr20:20p11.21		 uncertain significance
GRCh37/hg19 20p13-11.21(chr20:68351-23860313)x3 copy number gain not provided [RCV003885495] Chr20:68351..23860313 [GRCh37]
Chr20:20p13-11.21		 pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:315
Count of miRNA genes:277
Interacting mature miRNAs:288
Transcripts:ENST00000304710
Prediction methods:Miranda, Rnahybrid
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
GDB:196500  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372023,860,084 - 23,860,314UniSTSGRCh37
Build 362023,808,084 - 23,808,314RGDNCBI36
Celera2023,933,463 - 23,933,693RGD
Cytogenetic Map20p11.21UniSTS
HuRef2023,817,116 - 23,817,346UniSTS
SHGC-11944  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372023,614,340 - 23,614,436UniSTSGRCh37
GRCh372023,856,617 - 23,856,713UniSTSGRCh37
Build 362023,562,340 - 23,562,436RGDNCBI36
Celera2023,687,607 - 23,687,703RGD
Celera2023,929,996 - 23,930,092UniSTS
Cytogenetic Map20p11.21UniSTS
HuRef2023,813,649 - 23,813,745UniSTS
HuRef2023,574,809 - 23,574,905UniSTS
TNG Radiation Hybrid Map2012719.0UniSTS
Stanford-G3 RH Map201188.0UniSTS
GeneMap99-G3 RH Map201221.0UniSTS
RH66796  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372023,856,867 - 23,858,227UniSTSGRCh37
Celera2023,930,246 - 23,931,606UniSTS
Cytogenetic Map20p11.21UniSTS
HuRef2023,813,899 - 23,815,259UniSTS
GeneMap99-GB4 RH Map20123.03UniSTS
NCBI RH Map20188.2UniSTS


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 2 2
Medium 113 10 4 3 1 108 7 29 12
Low 566 2 194 25 19 25 36 513 11 121 143 570 4 2 3 1
Below cutoff 588 397 473 150 212 121 693 280 877 140 395 304 35 256 395 2

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000304710   ⟹   ENSP00000307132
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2023,875,934 - 23,879,748 (-)Ensembl
RefSeq Acc Id: NM_001900   ⟹   NP_001891
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382023,875,934 - 23,879,748 (-)NCBI
GRCh372023,856,572 - 23,860,380 (-)ENTREZGENE
Build 362023,804,572 - 23,808,371 (-)NCBI Archive
HuRef2023,813,604 - 23,817,412 (-)ENTREZGENE
CHM1_12023,856,749 - 23,860,557 (-)NCBI
T2T-CHM13v2.02023,935,655 - 23,939,469 (-)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001891 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH62678 (Get FASTA)   NCBI Sequence Viewer  
  AAH69514 (Get FASTA)   NCBI Sequence Viewer  
  CAA42590 (Get FASTA)   NCBI Sequence Viewer  
  CAA49838 (Get FASTA)   NCBI Sequence Viewer  
  EAX10132 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000307132
  ENSP00000307132.4
GenBank Protein P28325 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_001891   ⟸   NM_001900
- Peptide Label: precursor
- UniProtKB: Q5JRF5 (UniProtKB/Swiss-Prot),   Q9UCA0 (UniProtKB/Swiss-Prot),   P28325 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000307132   ⟸   ENST00000304710

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-P28325-F1-model_v2 AlphaFold P28325 1-142 view protein structure

Promoters
RGD ID:13206551
Promoter ID:EPDNEW_H26856
Type:multiple initiation site
Name:CST5_1
Description:cystatin D
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
GRCh382023,879,748 - 23,879,808EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:2477 AgrOrtholog
COSMIC CST5 COSMIC
Ensembl Genes ENSG00000170367 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000304710 ENTREZGENE
  ENST00000304710.5 UniProtKB/Swiss-Prot
Gene3D-CATH 3.10.450.10 UniProtKB/Swiss-Prot
GTEx ENSG00000170367 GTEx
HGNC ID HGNC:2477 ENTREZGENE
Human Proteome Map CST5 Human Proteome Map
InterPro Cystatin_dom UniProtKB/Swiss-Prot
  Cystatin_sf UniProtKB/Swiss-Prot
  Prot_inh_cystat_CS UniProtKB/Swiss-Prot
KEGG Report hsa:1473 UniProtKB/Swiss-Prot
NCBI Gene 1473 ENTREZGENE
OMIM 123858 OMIM
PANTHER CYSTATIN UniProtKB/Swiss-Prot
  CYSTATIN-D UniProtKB/Swiss-Prot
Pfam Cystatin UniProtKB/Swiss-Prot
PharmGKB PA26978 PharmGKB
PROSITE CYSTATIN UniProtKB/Swiss-Prot
SMART SM00043 UniProtKB/Swiss-Prot
Superfamily-SCOP SSF54403 UniProtKB/Swiss-Prot
UniProt CYTD_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
  Q5JRF5 ENTREZGENE
  Q9UCA0 ENTREZGENE
UniProt Secondary Q5JRF5 UniProtKB/Swiss-Prot
  Q9UCA0 UniProtKB/Swiss-Prot