PPP1R14D (protein phosphatase 1 regulatory inhibitor subunit 14D) - Rat Genome Database

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Gene: PPP1R14D (protein phosphatase 1 regulatory inhibitor subunit 14D) Homo sapiens
Analyze
Symbol: PPP1R14D
Name: protein phosphatase 1 regulatory inhibitor subunit 14D
RGD ID: 1350290
HGNC Page HGNC:14953
Description: Enables protein serine/threonine phosphatase inhibitor activity. Predicted to be located in cytoplasm and membrane.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: CPI17-like; FLJ20251; gastrointestinal and brain-specific PP1-inhibitory protein 1; GBPI-1; GBPI1; gut and brain phosphatase inhibitor 1; MGC119014; MGC119016; PKC-dependent PP1 inhibitory protein; protein phosphatase 1 regulatory subunit 14D
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
GRCh381540,815,451 - 40,828,708 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1540,815,451 - 40,828,709 (-)EnsemblGRCh38hg38GRCh38
GRCh371541,107,649 - 41,120,906 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361538,894,943 - 38,908,199 (-)NCBINCBI36Build 36hg18NCBI36
Build 341538,894,942 - 38,908,199NCBI
Celera1517,875,542 - 17,888,808 (-)NCBICelera
Cytogenetic Map15q15.1NCBI
HuRef1517,956,085 - 17,969,351 (-)NCBIHuRef
CHM1_11541,227,964 - 41,238,849 (-)NCBICHM1_1
T2T-CHM13v2.01538,621,477 - 38,634,737 (-)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

Cellular Component
cytoplasm  (IEA)
membrane  (IEA)

Molecular Function

References

References - curated
# 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
Additional References at PubMed
PMID:11948623   PMID:12477932   PMID:12974676   PMID:14702039   PMID:15489334   PMID:18854154   PMID:21873635   PMID:28330616   PMID:33961781   PMID:36263632  


Genomics

Comparative Map Data
PPP1R14D
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381540,815,451 - 40,828,708 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1540,815,451 - 40,828,709 (-)EnsemblGRCh38hg38GRCh38
GRCh371541,107,649 - 41,120,906 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361538,894,943 - 38,908,199 (-)NCBINCBI36Build 36hg18NCBI36
Build 341538,894,942 - 38,908,199NCBI
Celera1517,875,542 - 17,888,808 (-)NCBICelera
Cytogenetic Map15q15.1NCBI
HuRef1517,956,085 - 17,969,351 (-)NCBIHuRef
CHM1_11541,227,964 - 41,238,849 (-)NCBICHM1_1
T2T-CHM13v2.01538,621,477 - 38,634,737 (-)NCBIT2T-CHM13v2.0
Ppp1r14d
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm392119,048,600 - 119,060,557 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl2119,048,600 - 119,060,387 (-)EnsemblGRCm39 Ensembl
GRCm382119,218,119 - 119,230,076 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl2119,218,119 - 119,229,906 (-)EnsemblGRCm38mm10GRCm38
MGSCv372119,043,859 - 119,055,601 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv362118,909,564 - 118,921,293 (-)NCBIMGSCv36mm8
Celera2120,368,274 - 120,380,400 (-)NCBICelera
Cytogenetic Map2E5NCBI
cM Map259.97NCBI
Ppp1r14d
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr83126,658,886 - 126,673,132 (-)NCBIGRCr8
mRatBN7.23106,205,043 - 106,219,290 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl3106,205,046 - 106,219,649 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx3109,878,149 - 109,892,078 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.03118,473,692 - 118,487,623 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.03116,134,069 - 116,147,998 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.03111,022,920 - 111,037,166 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl3111,022,923 - 111,037,425 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.03117,573,555 - 117,587,801 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.43105,731,271 - 105,745,517 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.13105,627,699 - 105,641,945 (-)NCBI
Celera3105,118,282 - 105,132,528 (-)NCBICelera
Cytogenetic Map3q35NCBI
Ppp1r14d
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554167,681,138 - 7,693,644 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554167,681,138 - 7,693,644 (-)NCBIChiLan1.0ChiLan1.0
PPP1R14D
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21630,055,369 - 30,076,580 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11534,206,805 - 34,228,010 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01519,756,077 - 19,786,920 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11538,007,632 - 38,022,094 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1538,007,632 - 38,022,094 (-)Ensemblpanpan1.1panPan2
PPP1R14D
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1307,953,714 - 7,966,061 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl307,953,844 - 7,965,966 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha308,008,246 - 8,020,731 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0308,082,013 - 8,094,478 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl308,082,256 - 8,094,353 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1308,004,675 - 8,017,165 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0308,112,246 - 8,124,724 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0308,241,538 - 8,254,030 (-)NCBIUU_Cfam_GSD_1.0
Ppp1r14d
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440864086,360,296 - 86,382,575 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049364714,208,762 - 4,230,526 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049364714,208,747 - 4,230,526 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
PPP1R14D
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1130,485,346 - 130,509,559 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11130,473,397 - 130,509,561 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21145,631,423 - 145,667,763 (+)NCBISscrofa10.2Sscrofa10.2susScr3
PPP1R14D
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12642,163,604 - 42,186,624 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2642,164,577 - 42,185,523 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604898,795,392 - 98,818,352 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Ppp1r14d
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248048,064,744 - 8,075,437 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248048,063,592 - 8,087,120 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in PPP1R14D
7 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_001130143.1(PPP1R14D):c.208C>T (p.Leu70=) single nucleotide variant Malignant melanoma [RCV000070749] Chr15:40828434 [GRCh38]
Chr15:41120632 [GRCh37]
Chr15:38907924 [NCBI36]
Chr15:15q15.1		 not provided
NM_001077268.1(ZFYVE19):c.1338-34C>T single nucleotide variant Malignant melanoma [RCV000062857] Chr15:40814114 [GRCh38]
Chr15:41106312 [GRCh37]
Chr15:38893604 [NCBI36]
Chr15:15q15.1		 not provided
GRCh37/hg19 15q11.2-26.3(chr15:20733395-102511616)x4 copy number gain See cases [RCV000447765] Chr15:20733395..102511616 [GRCh37]
Chr15:15q11.2-26.3		 pathogenic
GRCh37/hg19 15q11.2-26.3(chr15:22770422-102429112)x3 copy number gain See cases [RCV000510717] Chr15:22770422..102429112 [GRCh37]
Chr15:15q11.2-26.3		 pathogenic
GRCh37/hg19 15q11.2-26.3(chr15:22770422-102429112) copy number gain See cases [RCV000512019] Chr15:22770422..102429112 [GRCh37]
Chr15:15q11.2-26.3		 pathogenic
GRCh37/hg19 15q14-15.1 chr15:34638237..42057083 complex variant complex Spindle cell sarcoma [RCV000714282] Chr15:34640169..42054561 [GRCh37]
Chr15:15q14-15.1		 pathogenic
Single allele duplication not provided [RCV000677926] Chr15:31115047..102354857 [GRCh37]
Chr15:15q13.2-26.3		 pathogenic
GRCh37/hg19 15q11.1-26.3(chr15:20071673-102461162)x3 copy number gain not provided [RCV000751156] Chr15:20071673..102461162 [GRCh37]
Chr15:15q11.1-26.3		 pathogenic
GRCh37/hg19 15q11.1-26.3(chr15:20016811-102493540)x3 copy number gain not provided [RCV000751155] Chr15:20016811..102493540 [GRCh37]
Chr15:15q11.1-26.3		 pathogenic
NM_017726.8(PPP1R14D):c.63G>C (p.Lys21Asn) single nucleotide variant not specified [RCV004302459] Chr15:40828579 [GRCh38]
Chr15:41120777 [GRCh37]
Chr15:15q15.1		 uncertain significance
GRCh37/hg19 15q15.1(chr15:40464942-41196807)x4 copy number gain not provided [RCV001259208] Chr15:40464942..41196807 [GRCh37]
Chr15:15q15.1		 uncertain significance
NC_000015.9:g.(?_32964879)_(91358519_?)dup duplication Bloom syndrome [RCV001343104]|Familial colorectal cancer [RCV001325176] Chr15:32964879..91358519 [GRCh37]
Chr15:15q13.3-26.1		 uncertain significance
NC_000015.9:g.(?_40987528)_(41230232_?)dup duplication not provided [RCV003113134] Chr15:40987528..41230232 [GRCh37]
Chr15:15q15.1		 uncertain significance
NM_017726.8(PPP1R14D):c.*10A>C single nucleotide variant not specified [RCV004090211] Chr15:40815686 [GRCh38]
Chr15:41107884 [GRCh37]
Chr15:15q15.1		 uncertain significance
NM_017726.8(PPP1R14D):c.134C>G (p.Ser45Cys) single nucleotide variant not specified [RCV004108113] Chr15:40828508 [GRCh38]
Chr15:41120706 [GRCh37]
Chr15:15q15.1		 uncertain significance
NM_017726.8(PPP1R14D):c.203G>T (p.Arg68Leu) single nucleotide variant not specified [RCV004319503] Chr15:40828439 [GRCh38]
Chr15:41120637 [GRCh37]
Chr15:15q15.1		 uncertain significance
NM_017726.8(PPP1R14D):c.190G>T (p.Gly64Cys) single nucleotide variant not specified [RCV004307990] Chr15:40828452 [GRCh38]
Chr15:41120650 [GRCh37]
Chr15:15q15.1		 uncertain significance
NM_017726.8(PPP1R14D):c.231T>A (p.Asp77Glu) single nucleotide variant not specified [RCV004323417] Chr15:40828411 [GRCh38]
Chr15:41120609 [GRCh37]
Chr15:15q15.1		 uncertain significance
GRCh37/hg19 15q15.1(chr15:40892419-41125118)x3 copy number gain not specified [RCV003987091] Chr15:40892419..41125118 [GRCh37]
Chr15:15q15.1		 uncertain significance
GRCh37/hg19 15q11.2-21.2(chr15:22770421-50347130)x3 copy number gain not specified [RCV003987108] Chr15:22770421..50347130 [GRCh37]
Chr15:15q11.2-21.2		 pathogenic
NM_017726.8(PPP1R14D):c.361C>T (p.Arg121Cys) single nucleotide variant not specified [RCV004507331] Chr15:40815973 [GRCh38]
Chr15:41108171 [GRCh37]
Chr15:15q15.1		 likely benign
NM_017726.8(PPP1R14D):c.143T>C (p.Ile48Thr) single nucleotide variant not specified [RCV004507328] Chr15:40828499 [GRCh38]
Chr15:41120697 [GRCh37]
Chr15:15q15.1		 uncertain significance
NM_017726.8(PPP1R14D):c.304G>T (p.Asp102Tyr) single nucleotide variant not specified [RCV004507329] Chr15:40816205 [GRCh38]
Chr15:41108403 [GRCh37]
Chr15:15q15.1		 uncertain significance
NM_017726.8(PPP1R14D):c.321G>A (p.Glu107=) single nucleotide variant not specified [RCV004507330] Chr15:40816188 [GRCh38]
Chr15:41108386 [GRCh37]
Chr15:15q15.1		 likely benign
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:429
Count of miRNA genes:304
Interacting mature miRNAs:334
Transcripts:ENST00000299174, ENST00000427255
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
PPP1R14D_2784  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371541,107,584 - 41,107,982UniSTSGRCh37
Build 361538,894,876 - 38,895,274RGDNCBI36
Celera1517,875,483 - 17,875,881RGD
HuRef1517,956,026 - 17,956,424UniSTS


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 527 13 10 119 13 38 30 30
Low 422 4 674 171 198 60 704 12 274 279 472 778 113 7 392
Below cutoff 835 779 687 275 538 228 1710 675 2001 66 687 603 53 549 975 4

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000299174   ⟹   ENSP00000299174
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1540,815,451 - 40,828,708 (-)Ensembl
RefSeq Acc Id: ENST00000427255   ⟹   ENSP00000398342
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1540,815,571 - 40,828,709 (-)Ensembl
RefSeq Acc Id: NM_001130143   ⟹   NP_001123615
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381540,815,451 - 40,828,708 (-)NCBI
GRCh371541,107,643 - 41,121,283 (-)NCBI
Celera1517,875,542 - 17,888,808 (-)RGD
HuRef1517,956,085 - 17,969,351 (-)ENTREZGENE
CHM1_11541,227,964 - 41,238,849 (-)NCBI
T2T-CHM13v2.01538,621,477 - 38,634,737 (-)NCBI
Sequence:
RefSeq Acc Id: NM_017726   ⟹   NP_060196
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381540,815,451 - 40,828,708 (-)NCBI
GRCh371541,107,643 - 41,121,283 (-)NCBI
Build 361538,894,943 - 38,908,199 (-)NCBI Archive
Celera1517,875,542 - 17,888,808 (-)RGD
HuRef1517,956,085 - 17,969,351 (-)ENTREZGENE
CHM1_11541,227,964 - 41,238,849 (-)NCBI
T2T-CHM13v2.01538,621,477 - 38,634,737 (-)NCBI
Sequence:
Reference Protein Sequences
RefSeq Acc Id: NP_060196   ⟸   NM_017726
- Peptide Label: isoform 1
- UniProtKB: Q4V773 (UniProtKB/Swiss-Prot),   Q9NXH3 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001123615   ⟸   NM_001130143
- Peptide Label: isoform 2
- UniProtKB: E9PAT1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000398342   ⟸   ENST00000427255
RefSeq Acc Id: ENSP00000299174   ⟸   ENST00000299174

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9NXH3-F1-model_v2 AlphaFold Q9NXH3 1-145 view protein structure

Promoters
RGD ID:7229135
Promoter ID:EPDNEW_H20314
Type:initiation region
Name:PPP1R14D_2
Description:protein phosphatase 1 regulatory inhibitor subunit 14D
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H20315  EPDNEW_H20317  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381540,828,708 - 40,828,768EPDNEW
RGD ID:7229139
Promoter ID:EPDNEW_H20315
Type:multiple initiation site
Name:PPP1R14D_3
Description:protein phosphatase 1 regulatory inhibitor subunit 14D
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H20314  EPDNEW_H20317  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381540,829,391 - 40,829,451EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:14953 AgrOrtholog
COSMIC PPP1R14D COSMIC
Ensembl Genes ENSG00000166143 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000299174 ENTREZGENE
  ENST00000299174.10 UniProtKB/Swiss-Prot
  ENST00000427255 ENTREZGENE
  ENST00000427255.2 UniProtKB/TrEMBL
Gene3D-CATH 1.10.150.220 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000166143 GTEx
HGNC ID HGNC:14953 ENTREZGENE
Human Proteome Map PPP1R14D Human Proteome Map
InterPro CPI-17 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  CPI-17_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:54866 UniProtKB/Swiss-Prot
NCBI Gene 54866 ENTREZGENE
OMIM 613256 OMIM
PANTHER PROTEIN PHOSPHATASE 1 REGULATORY SUBUNIT 14D UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR16188 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam PP1_inhibitor UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA33631 PharmGKB
Superfamily-SCOP SSF81790 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt E9PAT1 ENTREZGENE, UniProtKB/TrEMBL
  PP14D_HUMAN UniProtKB/Swiss-Prot
  Q4V755_HUMAN UniProtKB/TrEMBL
  Q4V773 ENTREZGENE
  Q9NXH3 ENTREZGENE
UniProt Secondary Q4V773 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-11-24 PPP1R14D  protein phosphatase 1 regulatory inhibitor subunit 14D    protein phosphatase 1, regulatory (inhibitor) subunit 14D  Symbol and/or name change 5135510 APPROVED