PRSS36 (serine protease 36) - Rat Genome Database

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Gene: PRSS36 (serine protease 36) Homo sapiens
Analyze
Symbol: PRSS36
Name: serine protease 36
RGD ID: 1604524
HGNC Page HGNC:26906
Description: Enables serine-type endopeptidase activity. Predicted to be involved in proteolysis. Located in cytoplasm.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: FLJ90661; polyserase 2; polyserase-2; polyserine protease 2; polyserine protease-2; protease, serine 36; protease, serine, 36
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Alliance Genes
More Info more info ...
Related Pseudogenes: PRSS40A   PRSS40B  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381631,138,926 - 31,150,066 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1631,138,926 - 31,150,083 (-)EnsemblGRCh38hg38GRCh38
GRCh371631,150,247 - 31,161,387 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361631,057,750 - 31,068,888 (-)NCBINCBI36Build 36hg18NCBI36
Celera1629,136,608 - 29,147,773 (+)NCBICelera
Cytogenetic Map16p11.2NCBI
HuRef1628,711,400 - 28,723,215 (-)NCBIHuRef
CHM1_11632,467,970 - 32,479,132 (-)NCBICHM1_1
T2T-CHM13v2.01631,526,407 - 31,537,545 (-)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

Biological Process
proteolysis  (IEA)

Cellular Component

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:8889548   PMID:12477932   PMID:14702039   PMID:15536082   PMID:16341674   PMID:21873635  


Genomics

Comparative Map Data
PRSS36
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381631,138,926 - 31,150,066 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1631,138,926 - 31,150,083 (-)EnsemblGRCh38hg38GRCh38
GRCh371631,150,247 - 31,161,387 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361631,057,750 - 31,068,888 (-)NCBINCBI36Build 36hg18NCBI36
Celera1629,136,608 - 29,147,773 (+)NCBICelera
Cytogenetic Map16p11.2NCBI
HuRef1628,711,400 - 28,723,215 (-)NCBIHuRef
CHM1_11632,467,970 - 32,479,132 (-)NCBICHM1_1
T2T-CHM13v2.01631,526,407 - 31,537,545 (-)NCBIT2T-CHM13v2.0
Prss36
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm397127,531,810 - 127,545,897 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl7127,531,810 - 127,545,897 (-)EnsemblGRCm39 Ensembl
GRCm387127,932,638 - 127,946,725 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl7127,932,638 - 127,946,725 (-)EnsemblGRCm38mm10GRCm38
MGSCv377135,076,152 - 135,090,239 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv367127,723,784 - 127,737,873 (-)NCBIMGSCv36mm8
Celera7127,767,827 - 127,781,907 (-)NCBICelera
Cytogenetic Map7F3NCBI
cM Map769.84NCBI
Prss36
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81191,973,556 - 192,002,231 (-)NCBIGRCr8
mRatBN7.21182,543,085 - 182,561,141 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1182,543,085 - 182,559,280 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1190,893,626 - 190,909,613 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01198,079,717 - 198,095,704 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01190,750,112 - 190,766,179 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01199,379,374 - 199,396,339 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1199,379,374 - 199,395,363 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01206,402,154 - 206,419,120 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41187,217,603 - 187,233,400 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera1180,193,893 - 180,209,989 (-)NCBICelera
Cytogenetic Map1q37NCBI
Prss36
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554937,979,292 - 7,990,673 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554937,979,080 - 7,985,028 (-)NCBIChiLan1.0ChiLan1.0
PRSS36
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21834,344,932 - 34,356,186 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11639,146,331 - 39,157,584 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01623,818,719 - 23,829,983 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11631,507,244 - 31,518,727 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1631,507,455 - 31,518,727 (-)Ensemblpanpan1.1panPan2
PRSS36
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1617,096,996 - 17,107,676 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl617,096,996 - 17,107,420 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha618,672,381 - 18,683,065 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0617,228,763 - 17,238,603 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl617,227,413 - 17,238,612 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1617,028,146 - 17,038,823 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0616,947,167 - 16,957,836 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0617,260,231 - 17,270,035 (+)NCBIUU_Cfam_GSD_1.0
Prss36
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024409344125,393,862 - 125,406,692 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493650113,494,831 - 13,503,977 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493650113,494,628 - 13,504,042 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
PRSS36
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl317,345,892 - 17,354,665 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1317,345,015 - 17,354,688 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2317,517,635 - 17,526,482 (-)NCBISscrofa10.2Sscrofa10.2susScr3
PRSS36
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1527,829,359 - 27,840,677 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl527,827,511 - 27,839,907 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660681,626,683 - 1,637,574 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0

Variants

.
Variants in PRSS36
35 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 16p11.2-11.1(chr16:30691912-36160463)x3 copy number gain See cases [RCV000133811] Chr16:30691912..36160463 [GRCh38]
Chr16:30703233..35147508 [GRCh37]
Chr16:30610734..35005009 [NCBI36]
Chr16:16p11.2-11.1
pathogenic
GRCh38/hg38 16p11.2(chr16:29909613-31438697)x3 copy number gain See cases [RCV000135339] Chr16:29909613..31438697 [GRCh38]
Chr16:29920934..31450018 [GRCh37]
Chr16:29828435..31357519 [NCBI36]
Chr16:16p11.2
pathogenic
GRCh38/hg38 16p12.1-11.2(chr16:27311746-31193406)x3 copy number gain See cases [RCV000140341] Chr16:27311746..31193406 [GRCh38]
Chr16:27323067..31204727 [GRCh37]
Chr16:27230568..31112228 [NCBI36]
Chr16:16p12.1-11.2
pathogenic
GRCh38/hg38 16p12.2-11.2(chr16:23752047-31943755)x3 copy number gain See cases [RCV000141141] Chr16:23752047..31943755 [GRCh38]
Chr16:23763368..31955076 [GRCh37]
Chr16:23670869..31862577 [NCBI36]
Chr16:16p12.2-11.2
pathogenic
GRCh37/hg19 16p11.2(chr16:31123271-31153163)x4 copy number gain Ductal breast carcinoma [RCV000207157] Chr16:31123271..31153163 [GRCh37]
Chr16:16p11.2
uncertain significance
GRCh37/hg19 16p11.2(chr16:31154186-31926800)x3 copy number gain Ductal breast carcinoma [RCV000207245] Chr16:31154186..31926800 [GRCh37]
Chr16:16p11.2
uncertain significance
GRCh37/hg19 16p13.3-11.2(chr16:1279324-31926800)x3 copy number gain Ductal breast carcinoma [RCV000207053] Chr16:1279324..31926800 [GRCh37]
Chr16:16p13.3-11.2
uncertain significance
Single allele deletion Branched-chain keto acid dehydrogenase kinase deficiency [RCV000735205] Chr16:30554158..31536880 [GRCh37]
Chr16:16p11.2
uncertain significance
GRCh37/hg19 16p11.2(chr16:30943854-31171177)x1 copy number loss See cases [RCV000446201] Chr16:30943854..31171177 [GRCh37]
Chr16:16p11.2
uncertain significance
GRCh37/hg19 16p13.3-q24.3(chr16:69193-90274381)x3 copy number gain See cases [RCV000446684] Chr16:69193..90274381 [GRCh37]
Chr16:16p13.3-q24.3
pathogenic
GRCh37/hg19 16p11.2(chr16:30830287-31827011)x4 copy number gain See cases [RCV000447708] Chr16:30830287..31827011 [GRCh37]
Chr16:16p11.2
uncertain significance
GRCh37/hg19 16p11.2(chr16:28826162-29043901)x1 copy number loss See cases [RCV000448084] Chr16:28826162..29043901 [GRCh37]
Chr16:16p11.2
likely pathogenic
GRCh37/hg19 16p11.2(chr16:30952806-31177641)x1 copy number loss See cases [RCV000511906] Chr16:30952806..31177641 [GRCh37]
Chr16:16p11.2
likely pathogenic
GRCh37/hg19 16p13.2-q24.3(chr16:9273328-89548493)x3 copy number gain See cases [RCV000511622] Chr16:9273328..89548493 [GRCh37]
Chr16:16p13.2-q24.3
uncertain significance
maternal UPD(16p) complex Hemimegalencephaly [RCV000494707] Chr16:1280042..33710558 [GRCh37]
Chr16:16p13.3-11.2
pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062)x3 copy number gain See cases [RCV000512138] Chr16:85881..90155062 [GRCh37]
Chr16:16p13.3-q24.3
pathogenic
NM_173502.5(PRSS36):c.2333C>A (p.Ser778Tyr) single nucleotide variant Inborn genetic diseases [RCV003269834] Chr16:31139373 [GRCh38]
Chr16:31150694 [GRCh37]
Chr16:16p11.2
uncertain significance
NM_173502.5(PRSS36):c.640G>A (p.Gly214Ser) single nucleotide variant Inborn genetic diseases [RCV003239344] Chr16:31145869 [GRCh38]
Chr16:31157190 [GRCh37]
Chr16:16p11.2
uncertain significance
GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062) copy number gain See cases [RCV000511296] Chr16:85881..90155062 [GRCh37]
Chr16:16p13.3-q24.3
pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:88165-90163275)x3 copy number gain not provided [RCV000738917] Chr16:88165..90163275 [GRCh37]
Chr16:16p13.3-q24.3
pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:88165-90274695)x3 copy number gain not provided [RCV000738918] Chr16:88165..90274695 [GRCh37]
Chr16:16p13.3-q24.3
pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:61451-90294632)x3 copy number gain not provided [RCV000738915] Chr16:61451..90294632 [GRCh37]
Chr16:16p13.3-q24.3
pathogenic
GRCh37/hg19 16p11.2(chr16:30738551-34194635)x3 copy number gain not provided [RCV000739123] Chr16:30738551..34194635 [GRCh37]
Chr16:16p11.2
benign
GRCh37/hg19 16p11.2(chr16:30851860-31156762)x1 copy number loss not provided [RCV000848082] Chr16:30851860..31156762 [GRCh37]
Chr16:16p11.2
pathogenic
NM_173502.5(PRSS36):c.220G>C (p.Gly74Arg) single nucleotide variant not provided [RCV000889060] Chr16:31149125 [GRCh38]
Chr16:31160446 [GRCh37]
Chr16:16p11.2
benign
GRCh37/hg19 16p13.3-11.2(chr16:5805001-34230001) copy number gain Microcephaly [RCV001252948] Chr16:5805001..34230001 [GRCh37]
Chr16:16p13.3-11.2
pathogenic
GRCh37/hg19 16p11.2(chr16:30350747-31905898)x3 copy number gain not provided [RCV001258619] Chr16:30350747..31905898 [GRCh37]
Chr16:16p11.2
uncertain significance
GRCh37/hg19 16p11.2(chr16:30943854-31171177) copy number loss not specified [RCV002052525] Chr16:30943854..31171177 [GRCh37]
Chr16:16p11.2
likely pathogenic
NM_173502.5(PRSS36):c.170C>A (p.Thr57Asn) single nucleotide variant Inborn genetic diseases [RCV003299314] Chr16:31149175 [GRCh38]
Chr16:31160496 [GRCh37]
Chr16:16p11.2
uncertain significance
NM_173502.5(PRSS36):c.1969C>G (p.Gln657Glu) single nucleotide variant Inborn genetic diseases [RCV003262855] Chr16:31140690 [GRCh38]
Chr16:31152011 [GRCh37]
Chr16:16p11.2
uncertain significance
NM_173502.5(PRSS36):c.1271C>G (p.Ala424Gly) single nucleotide variant Inborn genetic diseases [RCV002905071] Chr16:31142823 [GRCh38]
Chr16:31154144 [GRCh37]
Chr16:16p11.2
uncertain significance
NM_173502.5(PRSS36):c.220G>A (p.Gly74Ser) single nucleotide variant Inborn genetic diseases [RCV002752406] Chr16:31149125 [GRCh38]
Chr16:31160446 [GRCh37]
Chr16:16p11.2
uncertain significance
NM_173502.5(PRSS36):c.2464C>T (p.Pro822Ser) single nucleotide variant Inborn genetic diseases [RCV002773823] Chr16:31139242 [GRCh38]
Chr16:31150563 [GRCh37]
Chr16:16p11.2
uncertain significance
NM_173502.5(PRSS36):c.1450C>T (p.Pro484Ser) single nucleotide variant Inborn genetic diseases [RCV002749215] Chr16:31142552 [GRCh38]
Chr16:31153873 [GRCh37]
Chr16:16p11.2
uncertain significance
NM_173502.5(PRSS36):c.1703G>A (p.Gly568Asp) single nucleotide variant Inborn genetic diseases [RCV002865296] Chr16:31141779 [GRCh38]
Chr16:31153100 [GRCh37]
Chr16:16p11.2
uncertain significance
NM_173502.5(PRSS36):c.2324C>T (p.Thr775Met) single nucleotide variant Inborn genetic diseases [RCV003012649] Chr16:31139382 [GRCh38]
Chr16:31150703 [GRCh37]
Chr16:16p11.2
uncertain significance
NM_173502.5(PRSS36):c.1516T>G (p.Cys506Gly) single nucleotide variant Inborn genetic diseases [RCV002751651] Chr16:31142486 [GRCh38]
Chr16:31153807 [GRCh37]
Chr16:16p11.2
uncertain significance
NM_173502.5(PRSS36):c.1321G>A (p.Gly441Arg) single nucleotide variant Inborn genetic diseases [RCV002739859] Chr16:31142773 [GRCh38]
Chr16:31154094 [GRCh37]
Chr16:16p11.2
uncertain significance
NM_173502.5(PRSS36):c.2063G>A (p.Arg688Gln) single nucleotide variant Inborn genetic diseases [RCV002784970] Chr16:31140596 [GRCh38]
Chr16:31151917 [GRCh37]
Chr16:16p11.2
uncertain significance
NM_173502.5(PRSS36):c.1424T>A (p.Leu475Gln) single nucleotide variant Inborn genetic diseases [RCV002930162] Chr16:31142578 [GRCh38]
Chr16:31153899 [GRCh37]
Chr16:16p11.2
uncertain significance
NM_173502.5(PRSS36):c.176C>T (p.Pro59Leu) single nucleotide variant Inborn genetic diseases [RCV002874034] Chr16:31149169 [GRCh38]
Chr16:31160490 [GRCh37]
Chr16:16p11.2
uncertain significance
NM_173502.5(PRSS36):c.2062C>T (p.Arg688Trp) single nucleotide variant Inborn genetic diseases [RCV002788010] Chr16:31140597 [GRCh38]
Chr16:31151918 [GRCh37]
Chr16:16p11.2
uncertain significance
NM_173502.5(PRSS36):c.2033C>T (p.Pro678Leu) single nucleotide variant Inborn genetic diseases [RCV002788638] Chr16:31140626 [GRCh38]
Chr16:31151947 [GRCh37]
Chr16:16p11.2
uncertain significance
NM_173502.5(PRSS36):c.1958G>C (p.Ser653Thr) single nucleotide variant Inborn genetic diseases [RCV002744684] Chr16:31140701 [GRCh38]
Chr16:31152022 [GRCh37]
Chr16:16p11.2
uncertain significance
NM_173502.5(PRSS36):c.761G>A (p.Arg254His) single nucleotide variant Inborn genetic diseases [RCV002645003] Chr16:31143797 [GRCh38]
Chr16:31155118 [GRCh37]
Chr16:16p11.2
uncertain significance
NM_173502.5(PRSS36):c.655A>G (p.Thr219Ala) single nucleotide variant Inborn genetic diseases [RCV002803678] Chr16:31145854 [GRCh38]
Chr16:31157175 [GRCh37]
Chr16:16p11.2
uncertain significance
NM_173502.5(PRSS36):c.2125G>T (p.Ala709Ser) single nucleotide variant Inborn genetic diseases [RCV002934982] Chr16:31140534 [GRCh38]
Chr16:31151855 [GRCh37]
Chr16:16p11.2
uncertain significance
NM_173502.5(PRSS36):c.2344G>A (p.Val782Met) single nucleotide variant Inborn genetic diseases [RCV002702676] Chr16:31139362 [GRCh38]
Chr16:31150683 [GRCh37]
Chr16:16p11.2
uncertain significance
NM_173502.5(PRSS36):c.1988G>A (p.Arg663His) single nucleotide variant Inborn genetic diseases [RCV002809006] Chr16:31140671 [GRCh38]
Chr16:31151992 [GRCh37]
Chr16:16p11.2
uncertain significance
NM_173502.5(PRSS36):c.1979A>T (p.Gln660Leu) single nucleotide variant Inborn genetic diseases [RCV002836127] Chr16:31140680 [GRCh38]
Chr16:31152001 [GRCh37]
Chr16:16p11.2
uncertain significance
NM_173502.5(PRSS36):c.1403G>A (p.Gly468Asp) single nucleotide variant Inborn genetic diseases [RCV002963938] Chr16:31142599 [GRCh38]
Chr16:31153920 [GRCh37]
Chr16:16p11.2
uncertain significance
NM_173502.5(PRSS36):c.1506G>C (p.Glu502Asp) single nucleotide variant Inborn genetic diseases [RCV002648773] Chr16:31142496 [GRCh38]
Chr16:31153817 [GRCh37]
Chr16:16p11.2
uncertain significance
NM_173502.5(PRSS36):c.59C>A (p.Ala20Asp) single nucleotide variant Inborn genetic diseases [RCV003185557] Chr16:31149710 [GRCh38]
Chr16:31161031 [GRCh37]
Chr16:16p11.2
uncertain significance
NM_173502.5(PRSS36):c.33G>A (p.Met11Ile) single nucleotide variant Inborn genetic diseases [RCV003197239] Chr16:31150003 [GRCh38]
Chr16:31161324 [GRCh37]
Chr16:16p11.2
likely benign
NM_173502.5(PRSS36):c.2369G>C (p.Arg790Pro) single nucleotide variant Inborn genetic diseases [RCV003300882] Chr16:31139337 [GRCh38]
Chr16:31150658 [GRCh37]
Chr16:16p11.2
uncertain significance
NM_173502.5(PRSS36):c.2468C>G (p.Thr823Ser) single nucleotide variant Inborn genetic diseases [RCV003184550] Chr16:31139238 [GRCh38]
Chr16:31150559 [GRCh37]
Chr16:16p11.2
uncertain significance
NM_173502.5(PRSS36):c.33G>C (p.Met11Ile) single nucleotide variant Inborn genetic diseases [RCV003265899] Chr16:31150003 [GRCh38]
Chr16:31161324 [GRCh37]
Chr16:16p11.2
likely benign
NM_173502.5(PRSS36):c.2344G>C (p.Val782Leu) single nucleotide variant Inborn genetic diseases [RCV003262912] Chr16:31139362 [GRCh38]
Chr16:31150683 [GRCh37]
Chr16:16p11.2
uncertain significance
NM_173502.5(PRSS36):c.2264C>G (p.Ala755Gly) single nucleotide variant Inborn genetic diseases [RCV003354535] Chr16:31140319 [GRCh38]
Chr16:31151640 [GRCh37]
Chr16:16p11.2
uncertain significance
NM_173502.5(PRSS36):c.32T>C (p.Met11Thr) single nucleotide variant Inborn genetic diseases [RCV003386161] Chr16:31150004 [GRCh38]
Chr16:31161325 [GRCh37]
Chr16:16p11.2
uncertain significance
NM_173502.5(PRSS36):c.1961C>T (p.Ser654Phe) single nucleotide variant Inborn genetic diseases [RCV003373530] Chr16:31140698 [GRCh38]
Chr16:31152019 [GRCh37]
Chr16:16p11.2
uncertain significance
NM_173502.5(PRSS36):c.118C>T (p.Arg40Cys) single nucleotide variant Inborn genetic diseases [RCV003350037] Chr16:31149227 [GRCh38]
Chr16:31160548 [GRCh37]
Chr16:16p11.2
uncertain significance
NM_173502.5(PRSS36):c.1741C>G (p.Pro581Ala) single nucleotide variant Inborn genetic diseases [RCV003383265] Chr16:31141741 [GRCh38]
Chr16:31153062 [GRCh37]
Chr16:16p11.2
uncertain significance
NM_173502.5(PRSS36):c.2520G>T (p.Pro840=) single nucleotide variant not provided [RCV003411335] Chr16:31139186 [GRCh38]
Chr16:31150507 [GRCh37]
Chr16:16p11.2
likely benign
NM_173502.5(PRSS36):c.1818G>A (p.Glu606=) single nucleotide variant not provided [RCV003426681] Chr16:31141552 [GRCh38]
Chr16:31152873 [GRCh37]
Chr16:16p11.2
likely benign
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:3325
Count of miRNA genes:878
Interacting mature miRNAs:1075
Transcripts:ENST00000268281, ENST00000418068, ENST00000561897, ENST00000562368, ENST00000562390, ENST00000563693, ENST00000569305, ENST00000569614, ENST00000571878
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.


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 12 23 86 5 53 6 85 31 15 97 2
Low 2356 2236 1520 522 1158 362 3633 1561 3038 335 1314 1514 168 1102 2195 3 1
Below cutoff 64 724 118 101 699 102 665 625 589 83 106 77 2 5 590 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001258290 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001258291 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_173502 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011545758 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017022968 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017022969 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017022970 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017022971 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054379683 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054379684 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001751845 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001751846 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001751847 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001751848 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC009088 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI864473 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ627034 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK075142 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK290310 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK297997 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK301409 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AW450407 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC137396 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC144615 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM768465 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ184141 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU598342 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471192 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068262 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CQ783206 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

RefSeq Acc Id: ENST00000268281   ⟹   ENSP00000268281
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1631,138,926 - 31,150,066 (-)Ensembl
RefSeq Acc Id: ENST00000418068   ⟹   ENSP00000407160
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1631,138,982 - 31,150,066 (-)Ensembl
RefSeq Acc Id: ENST00000561897
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1631,149,101 - 31,150,008 (-)Ensembl
RefSeq Acc Id: ENST00000562368
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1631,138,928 - 31,149,534 (-)Ensembl
RefSeq Acc Id: ENST00000562390
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1631,149,272 - 31,150,083 (-)Ensembl
RefSeq Acc Id: ENST00000563693
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1631,141,464 - 31,142,858 (-)Ensembl
RefSeq Acc Id: ENST00000569305   ⟹   ENSP00000454768
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1631,138,994 - 31,150,061 (-)Ensembl
RefSeq Acc Id: ENST00000569614
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1631,148,466 - 31,149,534 (-)Ensembl
RefSeq Acc Id: ENST00000571878   ⟹   ENSP00000460298
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1631,139,067 - 31,140,734 (-)Ensembl
RefSeq Acc Id: NM_001258290   ⟹   NP_001245219
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381631,138,926 - 31,150,066 (-)NCBI
HuRef1628,711,400 - 28,723,215 (-)NCBI
CHM1_11632,467,970 - 32,479,132 (-)NCBI
T2T-CHM13v2.01631,526,407 - 31,537,545 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001258291   ⟹   NP_001245220
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381631,138,926 - 31,150,066 (-)NCBI
GRCh371631,150,244 - 31,161,415 (-)NCBI
HuRef1628,711,400 - 28,723,215 (-)NCBI
CHM1_11632,467,970 - 32,479,132 (-)NCBI
T2T-CHM13v2.01631,526,407 - 31,537,545 (-)NCBI
Sequence:
RefSeq Acc Id: NM_173502   ⟹   NP_775773
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381631,138,926 - 31,150,066 (-)NCBI
GRCh371631,150,244 - 31,161,415 (-)NCBI
Build 361631,057,750 - 31,068,888 (-)NCBI Archive
Celera1629,136,608 - 29,147,773 (+)RGD
HuRef1628,711,400 - 28,723,215 (-)NCBI
CHM1_11632,467,970 - 32,479,132 (-)NCBI
T2T-CHM13v2.01631,526,407 - 31,537,545 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017022968   ⟹   XP_016878457
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381631,138,926 - 31,150,066 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017022971   ⟹   XP_016878460
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381631,138,926 - 31,150,066 (-)NCBI
Sequence:
RefSeq Acc Id: XM_054379683   ⟹   XP_054235658
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01631,526,407 - 31,537,545 (-)NCBI
RefSeq Acc Id: XM_054379684   ⟹   XP_054235659
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01631,526,407 - 31,537,545 (-)NCBI
RefSeq Acc Id: NP_775773   ⟸   NM_173502
- Peptide Label: isoform 1 precursor
- UniProtKB: E7EX56 (UniProtKB/Swiss-Prot),   B7ZMK8 (UniProtKB/Swiss-Prot),   B4DW80 (UniProtKB/Swiss-Prot),   A8K2P5 (UniProtKB/Swiss-Prot),   Q8NBY4 (UniProtKB/Swiss-Prot),   Q5K4E3 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001245219   ⟸   NM_001258290
- Peptide Label: isoform 2 precursor
- UniProtKB: Q5K4E3 (UniProtKB/Swiss-Prot),   B4DNP1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001245220   ⟸   NM_001258291
- Peptide Label: isoform 3 precursor
- UniProtKB: Q5K4E3 (UniProtKB/Swiss-Prot),   B4DNP1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016878460   ⟸   XM_017022971
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_016878457   ⟸   XM_017022968
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: ENSP00000268281   ⟸   ENST00000268281
RefSeq Acc Id: ENSP00000460298   ⟸   ENST00000571878
RefSeq Acc Id: ENSP00000407160   ⟸   ENST00000418068
RefSeq Acc Id: ENSP00000454768   ⟸   ENST00000569305
RefSeq Acc Id: XP_054235659   ⟸   XM_054379684
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054235658   ⟸   XM_054379683
- Peptide Label: isoform X1
Protein Domains
Peptidase S1

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q5K4E3-F1-model_v2 AlphaFold Q5K4E3 1-855 view protein structure

Promoters
RGD ID:6811016
Promoter ID:HG_ACW:30315
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:PRSS36.CAPR07
Position:
Human AssemblyChrPosition (strand)Source
Build 361631,061,241 - 31,061,741 (-)MPROMDB
RGD ID:6793397
Promoter ID:HG_KWN:23606
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3
Transcripts:NM_173502
Position:
Human AssemblyChrPosition (strand)Source
Build 361631,068,696 - 31,069,196 (-)MPROMDB
RGD ID:7232083
Promoter ID:EPDNEW_H21787
Type:initiation region
Name:PRSS36_1
Description:protease, serine 36
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
GRCh381631,150,066 - 31,150,126EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:26906 AgrOrtholog
COSMIC PRSS36 COSMIC
Ensembl Genes ENSG00000178226 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000268281 ENTREZGENE
  ENST00000268281.9 UniProtKB/Swiss-Prot
  ENST00000418068 ENTREZGENE
  ENST00000418068.6 UniProtKB/Swiss-Prot
  ENST00000569305 ENTREZGENE
  ENST00000569305.1 UniProtKB/Swiss-Prot
  ENST00000571878.1 UniProtKB/TrEMBL
Gene3D-CATH 2.40.10.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000178226 GTEx
HGNC ID HGNC:26906 ENTREZGENE
Human Proteome Map PRSS36 Human Proteome Map
InterPro Pept_S1A_polyserase-2 UniProtKB/Swiss-Prot
  Peptidase_S1_PA UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Peptidase_S1_PA_chymotrypsin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Peptidase_S1A UniProtKB/Swiss-Prot
  Trypsin_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TRYPSIN_HIS UniProtKB/Swiss-Prot
  TRYPSIN_SER UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:146547 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 146547 ENTREZGENE
OMIM 610560 OMIM
PANTHER POLYSERASE-2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TRANSMEMBRANE PROTEASE SERINE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Trypsin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA142671123 PharmGKB
PIRSF Polyserase-2 UniProtKB/Swiss-Prot
PRINTS CHYMOTRYPSIN UniProtKB/Swiss-Prot
PROSITE TRYPSIN_DOM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TRYPSIN_HIS UniProtKB/Swiss-Prot
  TRYPSIN_SER UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART Tryp_SPc UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF50494 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A8K2P5 ENTREZGENE
  B4DNP1 ENTREZGENE, UniProtKB/TrEMBL
  B4DW80 ENTREZGENE
  B7ZMK8 ENTREZGENE
  E7EX56 ENTREZGENE
  I3L3A6_HUMAN UniProtKB/TrEMBL
  POLS2_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
  Q8NBY4 ENTREZGENE
UniProt Secondary A8K2P5 UniProtKB/Swiss-Prot
  B4DW80 UniProtKB/Swiss-Prot
  B7ZMK8 UniProtKB/Swiss-Prot
  E7EX56 UniProtKB/Swiss-Prot
  Q8NBY4 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2018-01-23 PRSS36  serine protease 36    protease, serine 36  Symbol and/or name change 5135510 APPROVED
2015-11-24 PRSS36  protease, serine 36    protease, serine, 36  Symbol and/or name change 5135510 APPROVED