Imported Annotations - CTD | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Prostatic Neoplasms | EXP | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:17013881 |


![]() |
Create Name: | |
Description: |
![]() |
Save what matters to you |
{{ loginError }} |
Sign in with your RGD account |
Create New Account | Recover Password |
Analyze GeneStrainQTL List |
![]() Gene Annotator (Functional Annotation) unavailable |
![]() Gene Annotator (Annotation Distribution) unavailable |
![]() Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable |
Gene Annotator (Functional Annotation) |
Gene Annotator (Annotation Distribution) |
Variant Visualizer (Genomic Variants) |
![]() InterViewer (Protein-Protein Interactions) unavailable |
![]() Gviewer (Genome Viewer) unavailable |
![]() Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable |
InterViewer (Protein-Protein Interactions) |
GViewer (Genome Viewer) |
Variant Visualizer (Damaging Variants) |
![]() Gene Annotator (Annotation Comparison) unavailable |
![]() OLGA (Gene List Generator) unavailable |
![]() |
Gene Annotator (Annotation Comparison) |
OLGA (Gene List Generator) |
Excel (Download) |
![]() MOET (Multi-Ontology Enrichement) unavailable |
![]() GOLF (Gene-Ortholog Location Finder) unavailable |
|
MOET (Multi-Ontology Enrichement) |
GOLF (Gene-Ortholog Location Finder) |
Imported Annotations - CTD | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Prostatic Neoplasms | EXP | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:17013881 |
|
|
|
|
|
|
|
|
|
|
|
|
1. | GOA_HUMAN data from the GO Consortium |
2. | RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations |
3. | RGD automated import pipeline for gene-chemical interactions |
PubMed | 9628581 11847130 11921445 12477932 12975309 14517240 15164053 15308636 15489334 15652484 16303743 16467190 16677073 17353931 17805346 18178549 18508857 18552768 19199708 19322201 19615732 19913121 19995400 20562859 20628086 22190034 22863883 23245351 23551011 23685074 23979138 24366813 24711643 24804790 25097228 25192599 25512553 25544563 25921289 25963833 26344197 26496610 26972000 27432908 27462432 27642162 28366632 28514442 28515276 28581483 29229926 29540532 30723194 |
ERP44 (Homo sapiens - human) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Erp44 (Mus musculus - house mouse) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Erp44 (Rattus norvegicus - Norway rat) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Erp44 (Chinchilla lanigera - long-tailed chinchilla) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
ERP44 (Pan paniscus - bonobo/pygmy chimpanzee) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
ERP44 (Canis lupus familiaris - dog) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Erp44 (Ictidomys tridecemlineatus - thirteen-lined ground squirrel) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
ERP44 (Sus scrofa - pig) |
|
A004T01 |
|
|||||||||||||||||||||||||||||||||||||||||||||
STS-R74235 |
|
|||||||||||||||||||||||||||||||||||||||||||||
A007D04 |
|
|||||||||||||||||||||||||||||||||||||||||||||
SHGC-57144 |
|
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. |
RefSeq Transcripts | NM_015051 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
GenBank Nucleotide | AB011145 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
AJ344330 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK075024 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AL137072 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AL358937 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AL360084 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AY359048 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC005374 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BQ881761 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BX648519 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CH471105 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CQ783816 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
GQ891369 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
GQ900902 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
RefSeq Acc Id: | NM_015051 ⟹ NP_055866 | |||||||||||||||||||||||||||||
RefSeq Status: | VALIDATED | |||||||||||||||||||||||||||||
Type: | CODING | |||||||||||||||||||||||||||||
Position: |
|
|||||||||||||||||||||||||||||
Sequence: |
GGGCAGGACCCGGAAGTGAGGGTGTGAGAGGCCTCTCTGGAAGTTGTCCCGGGTGTTCGCCGCThide sequence |
Protein RefSeqs | NP_055866 | (Get FASTA) | NCBI Sequence Viewer |
GenBank Protein | AAH05374 | (Get FASTA) | NCBI Sequence Viewer |
AAQ89407 | (Get FASTA) | NCBI Sequence Viewer | |
ADO22231 | (Get FASTA) | NCBI Sequence Viewer | |
ADO22419 | (Get FASTA) | NCBI Sequence Viewer | |
BAA25499 | (Get FASTA) | NCBI Sequence Viewer | |
BAG52054 | (Get FASTA) | NCBI Sequence Viewer | |
CAC87611 | (Get FASTA) | NCBI Sequence Viewer | |
CAF86876 | (Get FASTA) | NCBI Sequence Viewer | |
EAW58922 | (Get FASTA) | NCBI Sequence Viewer | |
EAW58923 | (Get FASTA) | NCBI Sequence Viewer | |
Q9BS26 | (Get FASTA) | NCBI Sequence Viewer |
RefSeq Acc Id: | NP_055866 ⟸ NM_015051 |
- Peptide Label: | precursor |
- UniProtKB: | Q9BS26 (UniProtKB/Swiss-Prot) |
- Sequence: |
MHPAVFLSLPDLRCSLLLLVTWVFTPVTTEITSLDTENIDEILNNADVALVNFYADWCRFSQMLhide sequence |
RGD ID: | 7215667 | |||||||||
Promoter ID: | EPDNEW_H13580 | |||||||||
Type: | initiation region | |||||||||
Name: | ERP44_1 | |||||||||
Description: | endoplasmic reticulum protein 44 | |||||||||
SO ACC ID: | SO:0000170 | |||||||||
Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | |||||||||
Experiment Methods: | Single-end sequencing. | |||||||||
Position: |
|
RGD ID: | 6807819 | |||||||||
Promoter ID: | HG_KWN:64324 | |||||||||
Type: | CpG-Island | |||||||||
SO ACC ID: | SO:0000170 | |||||||||
Source: | MPROMDB | |||||||||
Tissues & Cell Lines: | CD4+TCell, CD4+TCell_12Hour, CD4+TCell_2Hour, HeLa_S3, Jurkat, K562, Lymphoblastoid, NB4 | |||||||||
Transcripts: | NM_014425, NM_183245, OTTHUMT00000053402, OTTHUMT00000053405, OTTHUMT00000053406, OTTHUMT00000053408, OTTHUMT00000053409, UC004BAQ.1, UC004BAR.1, UC010MSY.1, UC010MSZ.1, UC010MTA.1, UC010MTB.1 | |||||||||
Position: |
|
Name | Type | Condition(s) | Position(s) | Clinical significance |
GRCh38/hg38 9q22.33-33.1(chr9:99138048-115011033)x1 | copy number loss | Abnormal facial shape [RCV000050315]|See cases [RCV000050315] | Chr9:99138048..115011033 [GRCh38] Chr9:101900330..117773312 [GRCh37] Chr9:100940151..116813133 [NCBI36] Chr9:9q22.33-33.1 |
pathogenic |
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3 | copy number gain | Global developmental delay [RCV000050347]|Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000050348]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000050348]|See cases [RCV000050348] | Chr9:193412..138179445 [GRCh38] Chr9:204193..141073897 [GRCh37] Chr9:194193..140193718 [NCBI36] Chr9:9p24.3-q34.3 |
pathogenic |
GRCh38/hg38 9q22.33-31.1(chr9:99465640-100281736)x1 | copy number loss | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051063]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051063]|See cases [RCV000051063] | Chr9:99465640..100281736 [GRCh38] Chr9:102227922..103044018 [GRCh37] Chr9:101267743..102083839 [NCBI36] Chr9:9q22.33-31.1 |
uncertain significance |
GRCh38/hg38 9q22.33-33.1(chr9:99349916-115767475)x1 | copy number loss | Chiari malformation type II [RCV000052921]|See cases [RCV000052921] | Chr9:99349916..115767475 [GRCh38] Chr9:102112198..118529754 [GRCh37] Chr9:101152019..117569575 [NCBI36] Chr9:9q22.33-33.1 |
pathogenic |
GRCh38/hg38 9q22.33-31.1(chr9:99465640-100394582)x1 | copy number loss | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052885]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052885]|See cases [RCV000052885] | Chr9:99465640..100394582 [GRCh38] Chr9:102227922..103156864 [GRCh37] Chr9:101267743..102196685 [NCBI36] Chr9:9q22.33-31.1 |
uncertain significance |
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138124532)x3 | copy number gain | Intrauterine growth retardation [RCV000053745]|See cases [RCV000053745] | Chr9:193412..138124532 [GRCh38] Chr9:204193..141018984 [GRCh37] Chr9:194193..140138805 [NCBI36] Chr9:9p24.3-q34.3 |
pathogenic |
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138114463)x3 | copy number gain | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053746]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053746]|See cases [RCV000053746] | Chr9:193412..138114463 [GRCh38] Chr9:214367..141008915 [GRCh37] Chr9:204367..140128736 [NCBI36] Chr9:9p24.3-q34.3 |
pathogenic |
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3 | copy number gain | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053748]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053748]|See cases [RCV000053748] | Chr9:193412..138179445 [GRCh38] Chr9:266045..141073897 [GRCh37] Chr9:256045..140193718 [NCBI36] Chr9:9p24.3-q34.3 |
pathogenic |
GRCh38/hg38 9q22.32-31.2(chr9:94184266-106730550)x3 | copy number gain | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053774]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053774]|See cases [RCV000053774] | Chr9:94184266..106730550 [GRCh38] Chr9:96946548..109492831 [GRCh37] Chr9:95986369..108532652 [NCBI36] Chr9:9q22.32-31.2 |
pathogenic |
GRCh38/hg38 9q22.1-32(chr9:88522292-113687796)x3 | copy number gain | Global developmental delay [RCV000053752]|See cases [RCV000053752] | Chr9:88522292..113687796 [GRCh38] Chr9:91137207..116450076 [GRCh37] Chr9:90327027..115489897 [NCBI36] Chr9:9q22.1-32 |
pathogenic |
NM_015051.2(ERP44):c.1016+1203A>C | single nucleotide variant | Lung cancer [RCV000107943] | Chr9:100005303 [GRCh38] Chr9:102767585 [GRCh37] Chr9:9q31.1 |
uncertain significance |
NM_015051.2(ERP44):c.471+573T>A | single nucleotide variant | Lung cancer [RCV000107944] | Chr9:100021469 [GRCh38] Chr9:102783751 [GRCh37] Chr9:9q31.1 |
uncertain significance |
GRCh38/hg38 9p24.3-q34.3(chr9:204193-138179445) | copy number gain | See cases [RCV000133791] | Chr9:204193..138179445 [GRCh38] Chr9:204193..141073897 [GRCh37] Chr9:194193..140193718 [NCBI36] Chr9:9p24.3-q34.3 |
pathogenic |
GRCh38/hg38 9q22.32-31.3(chr9:95061030-108695569)x1 | copy number loss | See cases [RCV000134375] | Chr9:95061030..108695569 [GRCh38] Chr9:97823312..111457849 [GRCh37] Chr9:96863133..110497670 [NCBI36] Chr9:9q22.32-31.3 |
pathogenic |
GRCh38/hg38 9q21.11-31.2(chr9:68420430-106579493)x3 | copy number gain | See cases [RCV000136788] | Chr9:68420430..106579493 [GRCh38] Chr9:71130848..109341774 [GRCh37] Chr9:70225166..108381595 [NCBI36] Chr9:9q21.11-31.2 |
pathogenic |
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138124524)x3 | copy number gain | See cases [RCV000138783] | Chr9:193412..138124524 [GRCh38] Chr9:204090..141018976 [GRCh37] Chr9:194090..140138797 [NCBI36] Chr9:9p24.3-q34.3 |
pathogenic |
GRCh38/hg38 9q22.33-31.3(chr9:99024205-109947890)x1 | copy number loss | See cases [RCV000138281] | Chr9:99024205..109947890 [GRCh38] Chr9:101786487..112710170 [GRCh37] Chr9:100826308..111749991 [NCBI36] Chr9:9q22.33-31.3 |
pathogenic|likely pathogenic |
GRCh38/hg38 9p11.2-q34.3(chr9:193412-138159073)x3 | copy number gain | See cases [RCV000139207] | Chr9:193412..138159073 [GRCh38] Chr9:68420641..141053525 [GRCh37] Chr9:67910461..140173346 [NCBI36] Chr9:9p11.2-q34.3 |
pathogenic |
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138159073)x3 | copy number gain | See cases [RCV000138962] | Chr9:193412..138159073 [GRCh38] Chr9:204104..141053525 [GRCh37] Chr9:194104..140173346 [NCBI36] Chr9:9p24.3-q34.3 |
pathogenic|conflicting data from submitters |
GRCh38/hg38 9q21.12-31.3(chr9:69627642-111454304)x3 | copy number gain | See cases [RCV000139789] | Chr9:69627642..111454304 [GRCh38] Chr9:72242558..114216584 [GRCh37] Chr9:71432378..113256405 [NCBI36] Chr9:9q21.12-31.3 |
pathogenic |
GRCh38/hg38 9p24.3-q34.3(chr9:203861-138125937)x3 | copy number gain | See cases [RCV000141876] | Chr9:203861..138125937 [GRCh38] Chr9:203861..141020389 [GRCh37] Chr9:193861..140140210 [NCBI36] Chr9:9p24.3-q34.3 |
pathogenic |
GRCh38/hg38 9p24.3-q34.3(chr9:203862-138125937)x3 | copy number gain | See cases [RCV000143476] | Chr9:203862..138125937 [GRCh38] Chr9:203862..141020389 [GRCh37] Chr9:193862..140140210 [NCBI36] Chr9:9p24.3-q34.3 |
pathogenic |
GRCh38/hg38 9q22.33-33.1(chr9:99138048-115011033)x1 | copy number loss | See cases [RCV000148264] | Chr9:99138048..115011033 [GRCh38] Chr9:101900330..117773312 [GRCh37] Chr9:100940151..116813133 [NCBI36] Chr9:9q22.33-33.1 |
pathogenic |
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3 | copy number gain | See cases [RCV000148113] | Chr9:193412..138179445 [GRCh38] Chr9:204193..141073897 [GRCh37] Chr9:194193..140193718 [NCBI36] Chr9:9p24.3-q34.3 |
pathogenic |
GRCh37/hg19 9p24.3-q34.3(chr9:163131-141122114)x3 | copy number gain | See cases [RCV000240081] | Chr9:163131..141122114 [GRCh37] Chr9:9p24.3-q34.3 |
pathogenic |
GRCh37/hg19 9p24.3-q34.3(chr9:62525-141006407) | copy number gain | See cases [RCV000449375] | Chr9:62525..141006407 [GRCh37] Chr9:9p24.3-q34.3 |
pathogenic |
Single allele | deletion | Infantile nephronophthisis [RCV000454326] | Chr9:102860399..102967421 [GRCh37] Chr9:9q31.1 |
likely pathogenic |
GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020389)x3 | copy number gain | See cases [RCV000447207] | Chr9:203861..141020389 [GRCh37] Chr9:9p24.3-q34.3 |
pathogenic |
NC_000009.11:g.(?_102339410)_(109549354_?)del | deletion | Schizophrenia [RCV000416788] | Chr9:102339410..109549354 [GRCh37] Chr9:101379231..108589175 [NCBI36] Chr9:9q22.33-31.2 |
likely pathogenic |
GRCh37/hg19 9p24.3-q34.3(chr9:203864-141020389)x3 | copy number gain | See cases [RCV000448978] | Chr9:203864..141020389 [GRCh37] Chr9:9p24.3-q34.3 |
pathogenic |
GRCh37/hg19 9q22.32-31.1(chr9:97553176-102919383)x3 | copy number gain | See cases [RCV000510672] | Chr9:97553176..102919383 [GRCh37] Chr9:9q22.32-31.1 |
likely pathogenic |
GRCh37/hg19 9q21.11-34.3(chr9:71069743-140999928) | copy number gain | Global developmental delay [RCV000626548]|Seizures [RCV000626548] | Chr9:71069743..140999928 [GRCh37] Chr9:9q21.11-34.3 |
likely pathogenic |
GRCh37/hg19 9p24.3-q34.3(chr9:203862-141020389) | copy number gain | See cases [RCV000512392] | Chr9:203862..141020389 [GRCh37] Chr9:9p24.3-q34.3 |
pathogenic |
GRCh37/hg19 9q31.1(chr9:102777978-102826067)x0 | copy number loss | not provided [RCV000748547] | Chr9:102777978..102826067 [GRCh37] Chr9:9q31.1 |
benign |
GRCh37/hg19 9p24.3-q34.3(chr9:10590-141122247)x3 | copy number gain | not provided [RCV000748055] | Chr9:10590..141122247 [GRCh37] Chr9:9p24.3-q34.3 |
pathogenic |
GRCh37/hg19 9p24.3-q34.3(chr9:10590-141107672)x3 | copy number gain | not provided [RCV000748053] | Chr9:10590..141107672 [GRCh37] Chr9:9p24.3-q34.3 |
pathogenic |
GRCh37/hg19 9p24.3-q34.3(chr9:46587-141066491)x3 | copy number gain | not provided [RCV000748063] | Chr9:46587..141066491 [GRCh37] Chr9:9p24.3-q34.3 |
pathogenic |
GRCh37/hg19 9p24.3-q34.3(chr9:10590-141114095)x2 | copy number gain | not provided [RCV000748054] | Chr9:10590..141114095 [GRCh37] Chr9:9p24.3-q34.3 |
pathogenic |
GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020388)x3 | copy number gain | not provided [RCV000845900] | Chr9:203861..141020388 [GRCh37] Chr9:9p24.3-q34.3 |
pathogenic |
GRCh37/hg19 9q31.1(chr9:102756663-103038495)x3 | copy number gain | not provided [RCV000847015] | Chr9:102756663..103038495 [GRCh37] Chr9:9q31.1 |
uncertain significance |
GRCh37/hg19 9q21.11-34.3(chr9:71416475-141020389)x3 | copy number gain | not provided [RCV000847808] | Chr9:71416475..141020389 [GRCh37] Chr9:9q21.11-34.3 |
pathogenic |
Database | Acc Id | Source(s) |
AGR Gene | HGNC:18311 | AgrOrtholog |
COSMIC | ERP44 | COSMIC |
Ensembl Genes | ENSG00000023318 | ENTREZGENE, UniProtKB/Swiss-Prot |
Ensembl Protein | ENSP00000262455 | ENTREZGENE, UniProtKB/Swiss-Prot |
Ensembl Transcript | ENST00000262455 | ENTREZGENE, UniProtKB/Swiss-Prot |
Gene3D-CATH | 3.40.30.10 | UniProtKB/Swiss-Prot |
GTEx | ENSG00000023318 | GTEx |
HGNC ID | HGNC:18311 | ENTREZGENE |
Human Proteome Map | ERP44 | Human Proteome Map |
InterPro | ERp44_PDI_b | UniProtKB/Swiss-Prot |
ERp44_PDI_b' | UniProtKB/Swiss-Prot | |
Thioredoxin-like_sf | UniProtKB/Swiss-Prot | |
Thioredoxin_domain | UniProtKB/Swiss-Prot | |
KEGG Report | hsa:23071 | UniProtKB/Swiss-Prot |
NCBI Gene | 23071 | ENTREZGENE |
OMIM | 609170 | OMIM |
Pfam | Thioredoxin | UniProtKB/Swiss-Prot |
PharmGKB | PA164719295 | PharmGKB |
PROSITE | ER_TARGET | UniProtKB/Swiss-Prot |
THIOREDOXIN_2 | UniProtKB/Swiss-Prot | |
Superfamily-SCOP | SSF52833 | UniProtKB/Swiss-Prot |
UniGene | Hs.154023 | ENTREZGENE |
UniProt | A0A384MEE7_HUMAN | UniProtKB/TrEMBL |
ERP44_HUMAN | UniProtKB/Swiss-Prot | |
L8EAR9_HUMAN | UniProtKB/TrEMBL | |
Q9BS26 | ENTREZGENE | |
UniProt Secondary | O60319 | UniProtKB/Swiss-Prot |
Q4VXC1 | UniProtKB/Swiss-Prot | |
Q5VWZ7 | UniProtKB/Swiss-Prot | |
Q6UW14 | UniProtKB/Swiss-Prot | |
Q8WX67 | UniProtKB/Swiss-Prot |
![]() |
More on ERP44 | |
![]() |
Alliance Gene |
![]() |
NCBI Gene |
![]() |
Ensembl Gene |
![]() |
JBrowse: hg19 hg38 |
![]() |
HGNC Report |
![]() |
NCBI Genome Data Viewer |
CRRD Object Information | |
CRRD ID: | 1319370 |
Created: | 2005-01-12 |
Species: | Homo sapiens |
Last Modified: | 2019-11-26 |
Status: | ACTIVE |
![]() |
![]() |
![]() |
![]() |
RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.