CST11 (cystatin 11) - Rat Genome Database

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Gene: CST11 (cystatin 11) Homo sapiens
Analyze
Symbol: CST11
Name: cystatin 11
RGD ID: 735574
HGNC Page HGNC:15959
Description: Predicted to enable cysteine-type endopeptidase inhibitor activity. Involved in defense response to Gram-negative bacterium. Located in several cellular components, including nucleus; sperm flagellum; and sperm head.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: CST8L; CTES2; cystatin-11; cystatin-related epididymal-specific protein; dJ322G13.6; SC13; SC13delta
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
GRCh382023,450,412 - 23,452,876 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2023,450,403 - 23,452,876 (-)EnsemblGRCh38hg38GRCh38
GRCh372023,431,049 - 23,433,513 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 362023,379,041 - 23,381,482 (-)NCBINCBI36Build 36hg18NCBI36
Build 342023,379,040 - 23,381,482NCBI
Celera2023,504,421 - 23,506,862 (-)NCBICelera
Cytogenetic Map20p11.21NCBI
HuRef2023,392,703 - 23,395,144 (-)NCBIHuRef
CHM1_12023,431,037 - 23,433,478 (-)NCBICHM1_1
T2T-CHM13v2.02023,509,944 - 23,512,411 (-)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
cytoplasm  (IBA,IEA,IMP)
extracellular region  (IEA)
nucleus  (IBA,IEA,IMP)
sperm flagellum  (IBA,IDA,IEA)
sperm head  (IBA,IDA,IEA)

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:3202964   PMID:7690606   PMID:7896273   PMID:8179826   PMID:9007972   PMID:11780052   PMID:12072414   PMID:12477932   PMID:15489334   PMID:19081178   PMID:20565543   PMID:21873635  
PMID:29676528   PMID:33961781  


Genomics

Comparative Map Data
CST11
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382023,450,412 - 23,452,876 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2023,450,403 - 23,452,876 (-)EnsemblGRCh38hg38GRCh38
GRCh372023,431,049 - 23,433,513 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 362023,379,041 - 23,381,482 (-)NCBINCBI36Build 36hg18NCBI36
Build 342023,379,040 - 23,381,482NCBI
Celera2023,504,421 - 23,506,862 (-)NCBICelera
Cytogenetic Map20p11.21NCBI
HuRef2023,392,703 - 23,395,144 (-)NCBIHuRef
CHM1_12023,431,037 - 23,433,478 (-)NCBICHM1_1
T2T-CHM13v2.02023,509,944 - 23,512,411 (-)NCBIT2T-CHM13v2.0
Cst11
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm392148,610,538 - 148,613,417 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl2148,610,529 - 148,613,417 (-)EnsemblGRCm39 Ensembl
GRCm382148,768,618 - 148,771,497 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl2148,768,609 - 148,771,497 (-)EnsemblGRCm38mm10GRCm38
MGSCv372148,594,354 - 148,597,233 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv362148,460,059 - 148,462,938 (-)NCBIMGSCv36mm8
Celera2150,030,906 - 150,034,699 (-)NCBICelera
Cytogenetic Map2G3NCBI
cM Map273.54NCBI
Cst11
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr83156,664,551 - 156,667,275 (-)NCBIGRCr8
mRatBN7.23136,211,414 - 136,214,138 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl3136,211,414 - 136,214,138 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx3140,163,405 - 140,165,998 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.03148,747,551 - 148,750,144 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.03146,437,032 - 146,439,756 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.03143,096,056 - 143,098,780 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl3143,096,056 - 143,098,780 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.03149,504,896 - 149,507,620 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.43137,524,412 - 137,527,136 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.13137,429,984 - 137,432,709 (-)NCBI
Celera3135,052,841 - 135,055,541 (-)NCBICelera
Cytogenetic Map3q41NCBI
Cst11
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0NW_00495541530,445,556 - 30,453,439 (-)NCBIChiLan1.0ChiLan1.0
CST11
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22124,317,163 - 24,319,887 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan12024,313,996 - 24,316,720 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v02023,385,639 - 23,388,363 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.12023,736,631 - 23,739,084 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl2023,736,631 - 23,739,084 (-)Ensemblpanpan1.1panPan2
CST11
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.124181,410 - 184,213 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl24180,692 - 184,323 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha24203,332 - 205,991 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.024573,867 - 576,594 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl24573,905 - 576,594 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.124176,259 - 178,909 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.024275,596 - 278,262 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.024559,406 - 562,092 (+)NCBIUU_Cfam_GSD_1.0
Cst11
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024408640148,695,442 - 148,699,181 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049366202,115,924 - 2,119,639 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049366202,115,927 - 2,119,683 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
CST11
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1730,414,051 - 30,417,127 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11730,415,161 - 30,416,984 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21734,503,160 - 34,505,987 (-)NCBISscrofa10.2Sscrofa10.2susScr3
CST11
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Vero_WHO_p1.0NW_0236660787,271,760 - 7,274,744 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Cst11
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462474123,104,474 - 23,106,333 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in CST11
9 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 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 20p11.22-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
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
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_130794.2(CST11):c.198G>T (p.Arg66Ser) single nucleotide variant not specified [RCV004318455] Chr20:23452614 [GRCh38]
Chr20:23433251 [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
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 20p11.21(chr20:23419312-23568490)x1 copy number loss not provided [RCV000741153] Chr20:23419312..23568490 [GRCh37]
Chr20:20p11.21		 benign
GRCh37/hg19 20p11.21(chr20:23427399-23801509)x3 copy number gain not provided [RCV000741154] Chr20:23427399..23801509 [GRCh37]
Chr20:20p11.21		 benign
GRCh37/hg19 20p13-q13.33(chr20:63244-62912463)x3 copy number gain not provided [RCV000741057] Chr20:63244..62912463 [GRCh37]
Chr20:20p13-q13.33		 pathogenic
NM_130794.2(CST11):c.199A>T (p.Ile67Phe) single nucleotide variant not specified [RCV004288080] Chr20:23452613 [GRCh38]
Chr20:23433250 [GRCh37]
Chr20:20p11.21		 uncertain significance
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 20p11.21(chr20:23413239-23569271)x1 copy number loss not provided [RCV001258734] Chr20:23413239..23569271 [GRCh37]
Chr20:20p11.21		 likely benign
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
NM_130794.2(CST11):c.8C>G (p.Ala3Gly) single nucleotide variant not specified [RCV004200309] Chr20:23452804 [GRCh38]
Chr20:23433441 [GRCh37]
Chr20:20p11.21		 uncertain significance
GRCh37/hg19 20p11.21(chr20:23142478-24824349)x3 copy number gain not provided [RCV002474920] Chr20:23142478..24824349 [GRCh37]
Chr20:20p11.21		 uncertain significance
NM_130794.2(CST11):c.100G>A (p.Val34Ile) single nucleotide variant not specified [RCV004192252] Chr20:23452712 [GRCh38]
Chr20:23433349 [GRCh37]
Chr20:20p11.21		 uncertain significance
NM_130794.2(CST11):c.73C>A (p.Gln25Lys) single nucleotide variant not specified [RCV004132329] Chr20:23452739 [GRCh38]
Chr20:23433376 [GRCh37]
Chr20:20p11.21		 uncertain significance
NM_130794.2(CST11):c.157G>A (p.Asp53Asn) single nucleotide variant not specified [RCV004250545] Chr20:23452655 [GRCh38]
Chr20:23433292 [GRCh37]
Chr20:20p11.21		 uncertain significance
NM_130794.2(CST11):c.412G>T (p.Asp138Tyr) single nucleotide variant not specified [RCV004264390] Chr20:23450511 [GRCh38]
Chr20:23431148 [GRCh37]
Chr20:20p11.21		 uncertain significance
GRCh38/hg38 20p13-11.21(chr20:87153-23635465)x3 copy number gain Renal agenesis [RCV003327640] Chr20:87153..23635465 [GRCh38]
Chr20:20p13-11.21		 pathogenic
NM_130794.2(CST11):c.277A>G (p.Thr93Ala) single nucleotide variant not specified [RCV004365111] Chr20:23451872 [GRCh38]
Chr20:23432509 [GRCh37]
Chr20:20p11.21		 uncertain significance
NM_130794.2(CST11):c.278C>A (p.Thr93Asn) single nucleotide variant not specified [RCV004372712] Chr20:23451871 [GRCh38]
Chr20:23432508 [GRCh37]
Chr20:20p11.21		 uncertain significance
NM_130794.2(CST11):c.61G>C (p.Ala21Pro) single nucleotide variant not specified [RCV004372713] Chr20:23452751 [GRCh38]
Chr20:23433388 [GRCh37]
Chr20:20p11.21		 uncertain significance
NC_000020.10:g.16400000_24400000del deletion Hyperinsulinemic hypoglycemia, familial, 1 [RCV003992661] Chr20:16400000..24400000 [GRCh37]
Chr20:20p12.1-11.21		 pathogenic
GRCh37/hg19 20p13-11.21(chr20:68351-23860313)x3 copy number gain not provided [RCV003885495] Chr20:68351..23860313 [GRCh37]
Chr20:20p13-11.21		 pathogenic
NM_130794.2(CST11):c.110T>C (p.Val37Ala) single nucleotide variant not specified [RCV004372711] Chr20:23452702 [GRCh38]
Chr20:23433339 [GRCh37]
Chr20:20p11.21		 uncertain significance
NC_000020.10:g.20158646_24080787del deletion Hyperinsulinemic hypoglycemia, familial, 1 [RCV003992658] Chr20:20158646..24080787 [GRCh37]
Chr20:20p11.23-11.21		 pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:205
Count of miRNA genes:103
Interacting mature miRNAs:104
Transcripts:ENST00000377007, ENST00000377009
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.

Markers in Region
RH103509  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372023,431,094 - 23,431,227UniSTSGRCh37
Build 362023,379,094 - 23,379,227RGDNCBI36
Celera2023,504,474 - 23,504,607RGD
Cytogenetic Map20p11.21UniSTS
HuRef2023,392,756 - 23,392,889UniSTS
GeneMap99-GB4 RH Map20119.38UniSTS


Expression


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

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system adipose tissue appendage entire extraembryonic component
High
Medium 8 3
Low 130 3 2 4 24 1 104 2 1 13 273 12 3 15 9
Below cutoff 470 79 147 61 86 31 734 136 283 95 380 108 31 206 323 2

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000377007   ⟹   ENSP00000366206
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2023,450,403 - 23,452,857 (-)Ensembl
RefSeq Acc Id: ENST00000377009   ⟹   ENSP00000366208
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2023,450,412 - 23,452,876 (-)Ensembl
RefSeq Acc Id: NM_080830   ⟹   NP_543020
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382023,450,412 - 23,452,876 (-)NCBI
GRCh372023,431,041 - 23,433,482 (-)RGD
Build 362023,379,041 - 23,381,482 (-)NCBI Archive
Celera2023,504,421 - 23,506,862 (-)RGD
HuRef2023,392,703 - 23,395,144 (-)RGD
CHM1_12023,431,037 - 23,433,478 (-)NCBI
T2T-CHM13v2.02023,509,944 - 23,512,411 (-)NCBI
Sequence:
RefSeq Acc Id: NM_130794   ⟹   NP_570612
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382023,450,412 - 23,452,876 (-)NCBI
GRCh372023,431,041 - 23,433,482 (-)RGD
Build 362023,379,041 - 23,381,482 (-)NCBI Archive
Celera2023,504,421 - 23,506,862 (-)RGD
HuRef2023,392,703 - 23,395,144 (-)RGD
CHM1_12023,431,037 - 23,433,478 (-)NCBI
T2T-CHM13v2.02023,509,944 - 23,512,411 (-)NCBI
Sequence:
Reference Protein Sequences
RefSeq Acc Id: NP_543020   ⟸   NM_080830
- Peptide Label: isoform 2 precursor
- UniProtKB: Q9H112 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_570612   ⟸   NM_130794
- Peptide Label: isoform 1 precursor
- UniProtKB: Q8WXU6 (UniProtKB/Swiss-Prot),   Q8WXU5 (UniProtKB/Swiss-Prot),   Q0VAF3 (UniProtKB/Swiss-Prot),   Q0VAF2 (UniProtKB/Swiss-Prot),   Q9H113 (UniProtKB/Swiss-Prot),   Q9H112 (UniProtKB/Swiss-Prot),   A0A384P5Z6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000366206   ⟸   ENST00000377007
RefSeq Acc Id: ENSP00000366208   ⟸   ENST00000377009
Protein Domains
Cystatin

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9H112-F1-model_v2 AlphaFold Q9H112 1-138 view protein structure


Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:15959 AgrOrtholog
COSMIC CST11 COSMIC
Ensembl Genes ENSG00000125831 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000377007 ENTREZGENE
  ENST00000377007.3 UniProtKB/Swiss-Prot
  ENST00000377009 ENTREZGENE
  ENST00000377009.8 UniProtKB/Swiss-Prot
Gene3D-CATH 3.10.450.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000125831 GTEx
HGNC ID HGNC:15959 ENTREZGENE
Human Proteome Map CST11 Human Proteome Map
InterPro CST11 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Cystatin_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Cystatin_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:140880 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 140880 ENTREZGENE
OMIM 609731 OMIM
PANTHER CYSTATIN-11 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR47886 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Cystatin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA26974 PharmGKB
SMART SM00043 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF54403 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A384P5Z6 ENTREZGENE, UniProtKB/TrEMBL
  CST11_HUMAN UniProtKB/Swiss-Prot
  Q0VAF2 ENTREZGENE
  Q0VAF3 ENTREZGENE
  Q8WXU5 ENTREZGENE
  Q8WXU6 ENTREZGENE
  Q9H112 ENTREZGENE
  Q9H113 ENTREZGENE
UniProt Secondary Q0VAF2 UniProtKB/Swiss-Prot
  Q0VAF3 UniProtKB/Swiss-Prot
  Q8WXU5 UniProtKB/Swiss-Prot
  Q8WXU6 UniProtKB/Swiss-Prot
  Q9H113 UniProtKB/Swiss-Prot