Imported Annotations - CTD | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
muscular dystrophy | EXP | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:22906800 |


![]() |
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) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
muscular dystrophy | EXP | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:22906800 |
|
|
|
|
|
|
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 | 8889548 11804574 14622217 16429581 16489065 19368807 20147288 20471375 22750213 22754043 23545415 26482433 26712693 26742039 27533450 28753106 30602570 |
PRIMA1 (Homo sapiens - human) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Prima1 (Mus musculus - house mouse) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Prima1 (Rattus norvegicus - Norway rat) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Prima1 (Chinchilla lanigera - long-tailed chinchilla) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
PRIMA1 (Pan paniscus - bonobo/pygmy chimpanzee) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
PRIMA1 (Canis lupus familiaris - dog) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Prima1 (Ictidomys tridecemlineatus - thirteen-lined ground squirrel) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
PRIMA1 (Sus scrofa - pig) |
|
SHGC-144590 |
|
||||||||||||||||||||||||||||||||||||||||
SHGC-52824 |
|
||||||||||||||||||||||||||||||||||||||||
SHGC-112367 |
|
||||||||||||||||||||||||||||||||||||||||
G09284 |
|
||||||||||||||||||||||||||||||||||||||||
PRIMA1__5578 |
|
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 | NG_009069 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
NM_178013 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_011536456 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_024449482 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_002957532 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_002957533 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
GenBank Nucleotide | AL132642 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
AL157858 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AX573535 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AY225516 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AY225517 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BU726715 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CH471061 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
RefSeq Acc Id: | NM_178013 ⟹ NP_821092 | ||||||||||||||||||||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||||||||||||
Position: |
|
||||||||||||||||||||||||||||||||||
Sequence: |
CGCCAGGCAAGTTCGCCCCAGGAGCGGGCGCCGCTGGCCGAGATGCTCCTCCGGGACTTGGTGChide sequence |
RefSeq Acc Id: | XM_011536456 ⟹ XP_011534758 | |||||||||
RefSeq Status: | ||||||||||
Type: | CODING | |||||||||
Position: |
|
|||||||||
Sequence: |
GGATTATTTATTTCGCCTCCACCCACGGCTTTGCTGCCCCAGCGGGAGCTCCCTGCCGGCGCCThide sequence |
RefSeq Acc Id: | XM_024449482 ⟹ XP_024305250 | |||||||||
RefSeq Status: | ||||||||||
Type: | CODING | |||||||||
Position: |
|
|||||||||
Sequence: |
GAAACAGAGCTGCCGCGGGGGGAACGCGGACCTCTTTTCCCCGAGCCCAGGGTCGGCTGGGGCChide sequence |
RefSeq Acc Id: | XR_002957532 | |||||||||
RefSeq Status: | ||||||||||
Type: | NON-CODING | |||||||||
Position: |
|
|||||||||
Sequence: |
GAAACAGAGCTGCCGCGGGGGGAACGCGGACCTCTTTTCCCCGAGCCCAGGGTCGGCTGGGGCChide sequence |
RefSeq Acc Id: | XR_002957533 | |||||||||
RefSeq Status: | ||||||||||
Type: | NON-CODING | |||||||||
Position: |
|
|||||||||
Sequence: |
GAAACAGAGCTGCCGCGGGGGGAACGCGGACCTCTTTTCCCCGAGCCCAGGGTCGGCTGGGGCChide sequence |
Protein RefSeqs | NP_821092 | (Get FASTA) | NCBI Sequence Viewer |
XP_011534758 | (Get FASTA) | NCBI Sequence Viewer | |
XP_024305250 | (Get FASTA) | NCBI Sequence Viewer | |
GenBank Protein | AAO74853 | (Get FASTA) | NCBI Sequence Viewer |
AAO74854 | (Get FASTA) | NCBI Sequence Viewer | |
CAD59989 | (Get FASTA) | NCBI Sequence Viewer | |
EAW81532 | (Get FASTA) | NCBI Sequence Viewer | |
EAW81533 | (Get FASTA) | NCBI Sequence Viewer | |
EAW81534 | (Get FASTA) | NCBI Sequence Viewer | |
Q86XR5 | (Get FASTA) | NCBI Sequence Viewer |
RefSeq Acc Id: | NP_821092 ⟸ NM_178013 |
- Peptide Label: | precursor |
- UniProtKB: | Q86XR5 (UniProtKB/Swiss-Prot), A0A024R6J9 (UniProtKB/TrEMBL) |
- Sequence: |
MLLRDLVLRRGCCWSSLLLHCALHPLWGFVQVTHGEPQKSCSKVTDSCRHVCQCRPPPPLPPPPhide sequence |
RefSeq Acc Id: | XP_011534758 ⟸ XM_011536456 |
- Peptide Label: | isoform X1 |
- UniProtKB: | Q86XR5 (UniProtKB/Swiss-Prot), A0A024R6J9 (UniProtKB/TrEMBL) |
- Sequence: |
MLLRDLVLRRGCCWSSLLLHCALHPLWGFVQVTHGEPQKSCSKVTDSCRHVCQCRPPPPLPPPPhide sequence |
RefSeq Acc Id: | XP_024305250 ⟸ XM_024449482 |
- Peptide Label: | isoform X2 |
- Sequence: |
MLLRDLVLRRGCCWSSLLLHCALHPLWGFVQVTHGEPQKSCSKVTDSCRHVCQCRPPPPLPPPPhide sequence |
RGD ID: | 7228471 | |||||||||
Promoter ID: | EPDNEW_H19981 | |||||||||
Type: | initiation region | |||||||||
Name: | PRIMA1_2 | |||||||||
Description: | proline rich membrane anchor 1 | |||||||||
SO ACC ID: | SO:0000170 | |||||||||
Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | |||||||||
Experiment Methods: | Single-end sequencing. | |||||||||
Position: |
|
RGD ID: | 7228473 | |||||||||
Promoter ID: | EPDNEW_H19982 | |||||||||
Type: | multiple initiation site | |||||||||
Name: | PRIMA1_1 | |||||||||
Description: | proline rich membrane anchor 1 | |||||||||
SO ACC ID: | SO:0000170 | |||||||||
Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | |||||||||
Experiment Methods: | Single-end sequencing. | |||||||||
Position: |
|
RGD ID: | 7228475 | |||||||||
Promoter ID: | EPDNEW_H19983 | |||||||||
Type: | initiation region | |||||||||
Name: | PRIMA1_3 | |||||||||
Description: | proline rich membrane anchor 1 | |||||||||
SO ACC ID: | SO:0000170 | |||||||||
Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | |||||||||
Experiment Methods: | Single-end sequencing.; Paired-end sequencing. | |||||||||
Position: |
|
Name | Type | Condition(s) | Position(s) | Clinical significance |
NM_178013.4(PRIMA1):c.402G>A (p.Glu134=) | single nucleotide variant | Nocturnal frontal lobe epilepsy [RCV000555225] | Chr14:93721504 [GRCh38] Chr14:94187850 [GRCh37] Chr14:14q32.12 |
benign |
NM_178013.4(PRIMA1):c.91C>G (p.Gln31Glu) | single nucleotide variant | Nocturnal frontal lobe epilepsy [RCV000525771] | Chr14:93787628 [GRCh38] Chr14:94253974 [GRCh37] Chr14:14q32.12 |
uncertain significance |
NM_178013.3(PRIMA1):c.230-11352A>G | single nucleotide variant | Lung cancer [RCV000099236] | Chr14:93748722 [GRCh38] Chr14:94215068 [GRCh37] Chr14:14q32.12 |
uncertain significance |
GRCh38/hg38 14q32.11-32.13(chr14:90255156-95274696)x1 | copy number loss | Coarse facial features [RCV000051551]|See cases [RCV000051551] | Chr14:90255156..95274696 [GRCh38] Chr14:90721500..95741033 [GRCh37] Chr14:89791253..94810786 [NCBI36] Chr14:14q32.11-32.13 |
pathogenic |
GRCh38/hg38 14q31.2-32.33(chr14:83912345-106855405)x3 | copy number gain | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052294]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052294]|See cases [RCV000052294] | Chr14:83912345..106855405 [GRCh38] Chr14:84378689..107263620 [GRCh37] Chr14:83448442..106334665 [NCBI36] Chr14:14q31.2-32.33 |
pathogenic |
GRCh38/hg38 14q24.2-32.2(chr14:72787506-99596719)x3 | copy number gain | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052293]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052293]|See cases [RCV000052293] | Chr14:72787506..99596719 [GRCh38] Chr14:73254214..100063056 [GRCh37] Chr14:72323967..99132809 [NCBI36] Chr14:14q24.2-32.2 |
pathogenic |
GRCh38/hg38 14q31.3-32.33(chr14:86094030-106832642)x3 | copy number gain | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052295]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052295]|See cases [RCV000052295] | Chr14:86094030..106832642 [GRCh38] Chr14:86560374..107240869 [GRCh37] Chr14:85630127..106311914 [NCBI36] Chr14:14q31.3-32.33 |
pathogenic |
GRCh38/hg38 14q32.12-32.33(chr14:91455861-106832642)x3 | copy number gain | Laryngeal cleft [RCV000052296]|See cases [RCV000052296] | Chr14:91455861..106832642 [GRCh38] Chr14:91922205..107240869 [GRCh37] Chr14:90991958..106311914 [NCBI36] Chr14:14q32.12-32.33 |
pathogenic |
NM_178013.3(PRIMA1):c.379G>A (p.Glu127Lys) | single nucleotide variant | Malignant melanoma [RCV000062821] | Chr14:93721527 [GRCh38] Chr14:94187873 [GRCh37] Chr14:93257626 [NCBI36] Chr14:14q32.12 |
not provided |
GRCh38/hg38 14q24.3-32.33(chr14:73655772-106879298)x3 | copy number gain | See cases [RCV000134000] | Chr14:73655772..106879298 [GRCh38] Chr14:74122475..107287505 [GRCh37] Chr14:73192228..106358550 [NCBI36] Chr14:14q24.3-32.33 |
pathogenic |
GRCh38/hg38 14q11.2-32.33(chr14:20151149-106855263)x3 | copy number gain | See cases [RCV000135543] | Chr14:20151149..106855263 [GRCh38] Chr14:20619308..107263478 [GRCh37] Chr14:19689148..106334523 [NCBI36] Chr14:14q11.2-32.33 |
pathogenic |
GRCh38/hg38 14q32.12-32.33(chr14:92540983-104863658)x3 | copy number gain | See cases [RCV000135896] | Chr14:92540983..104863658 [GRCh38] Chr14:93007328..105329995 [GRCh37] Chr14:92077081..104401040 [NCBI36] Chr14:14q32.12-32.33 |
pathogenic |
GRCh38/hg38 14q24.3-32.33(chr14:77222795-106879298)x3 | copy number gain | See cases [RCV000138230] | Chr14:77222795..106879298 [GRCh38] Chr14:77689138..107287505 [GRCh37] Chr14:76758891..106358550 [NCBI36] Chr14:14q24.3-32.33 |
pathogenic |
GRCh38/hg38 14q11.2-32.33(chr14:20043514-106877229)x3 | copy number gain | See cases [RCV000143373] | Chr14:20043514..106877229 [GRCh38] Chr14:20511673..107285437 [GRCh37] Chr14:19581513..106356482 [NCBI36] Chr14:14q11.2-32.33 |
pathogenic |
NM_178013.4(PRIMA1):c.222C>T (p.Ser74=) | single nucleotide variant | Nocturnal frontal lobe epilepsy [RCV000542492] | Chr14:93779183 [GRCh38] Chr14:94245529 [GRCh37] Chr14:14q32.12 |
benign |
GRCh37/hg19 14q11.2-32.33(chr14:19794561-107234280)x3 | copy number gain | See cases [RCV000446256] | Chr14:19794561..107234280 [GRCh37] Chr14:14q11.2-32.33 |
pathogenic |
GRCh37/hg19 14q23.2-32.33(chr14:62493932-107285437)x3 | copy number gain | See cases [RCV000448557] | Chr14:62493932..107285437 [GRCh37] Chr14:14q23.2-32.33 |
pathogenic |
GRCh37/hg19 14q11.2-32.33(chr14:20511673-107285437) | copy number gain | See cases [RCV000512041] | Chr14:20511673..107285437 [GRCh37] Chr14:14q11.2-32.33 |
pathogenic |
GRCh37/hg19 14q32.12-32.13(chr14:93498930-96059698)x3 | copy number gain | See cases [RCV000511246] | Chr14:93498930..96059698 [GRCh37] Chr14:14q32.12-32.13 |
uncertain significance |
NM_178013.4(PRIMA1):c.164G>A (p.Arg55Gln) | single nucleotide variant | Nocturnal frontal lobe epilepsy [RCV000653468] | Chr14:93779241 [GRCh38] Chr14:94245587 [GRCh37] Chr14:14q32.12 |
uncertain significance |
NM_178013.4(PRIMA1):c.16T>G (p.Leu6Val) | single nucleotide variant | Nocturnal frontal lobe epilepsy [RCV000653469] | Chr14:93787703 [GRCh38] Chr14:94254049 [GRCh37] Chr14:14q32.12 |
uncertain significance |
NM_178013.4(PRIMA1):c.378C>T (p.Asp126=) | single nucleotide variant | Nocturnal frontal lobe epilepsy [RCV000653470] | Chr14:93721528 [GRCh38] Chr14:94187874 [GRCh37] Chr14:14q32.12 |
likely benign |
NM_178013.4(PRIMA1):c.332T>C (p.Val111Ala) | single nucleotide variant | Nocturnal frontal lobe epilepsy [RCV000653467] | Chr14:93737268 [GRCh38] Chr14:94203614 [GRCh37] Chr14:14q32.12 |
uncertain significance |
GRCh37/hg19 14q24.2-32.33(chr14:73750741-107285437)x3 | copy number gain | See cases [RCV000512497] | Chr14:73750741..107285437 [GRCh37] Chr14:14q24.2-32.33 |
pathogenic |
NM_178013.4(PRIMA1):c.87C>A (p.Phe29Leu) | single nucleotide variant | Nocturnal frontal lobe epilepsy [RCV000685106] | Chr14:93787632 [GRCh38] Chr14:94253978 [GRCh37] Chr14:14q32.12 |
uncertain significance |
GRCh37/hg19 14q31.2-32.2(chr14:84783137-96908198)x1 | copy number loss | not provided [RCV000683625] | Chr14:84783137..96908198 [GRCh37] Chr14:14q31.2-32.2 |
pathogenic |
NM_178013.4(PRIMA1):c.228A>T (p.Pro76=) | single nucleotide variant | Nocturnal frontal lobe epilepsy [RCV000705397] | Chr14:93779177 [GRCh38] Chr14:94245523 [GRCh37] Chr14:14q32.12 |
uncertain significance |
NM_178013.4(PRIMA1):c.102T>C (p.His34=) | single nucleotide variant | not provided [RCV000712855] | Chr14:93779303 [GRCh38] Chr14:94245649 [GRCh37] Chr14:14q32.12 |
benign |
NM_178013.4(PRIMA1):c.420G>A (p.Ser140=) | single nucleotide variant | not provided [RCV000712856] | Chr14:93721486 [GRCh38] Chr14:94187832 [GRCh37] Chr14:14q32.12 |
benign |
NM_178013.4(PRIMA1):c.99G>A (p.Thr33=) | single nucleotide variant | not provided [RCV000712857] | Chr14:93779306 [GRCh38] Chr14:94245652 [GRCh37] Chr14:14q32.12 |
benign |
NM_178013.4(PRIMA1):c.99G>C (p.Thr33=) | single nucleotide variant | not provided [RCV000712858] | Chr14:93779306 [GRCh38] Chr14:94245652 [GRCh37] Chr14:14q32.12 |
likely benign |
NM_178013.4(PRIMA1):c.102_103inv (p.Gly35Ser) | inversion | Nocturnal frontal lobe epilepsy [RCV000693148] | Chr14:93779302..93779303 [GRCh38] Chr14:94245648..94245649 [GRCh37] Chr14:14q32.12 |
uncertain significance |
GRCh37/hg19 14q11.1-32.33(chr14:19000422-107289053)x3 | copy number gain | not provided [RCV000738412] | Chr14:19000422..107289053 [GRCh37] Chr14:14q11.1-32.33 |
pathogenic |
GRCh37/hg19 14q11.2-32.33(chr14:19280733-107287663)x3 | copy number gain | not provided [RCV000738413] | Chr14:19280733..107287663 [GRCh37] Chr14:14q11.2-32.33 |
pathogenic |
GRCh37/hg19 14q11.2-32.33(chr14:19327823-107287663)x3 | copy number gain | not provided [RCV000738414] | Chr14:19327823..107287663 [GRCh37] Chr14:14q11.2-32.33 |
pathogenic |
NM_178013.4(PRIMA1):c.116A>C (p.Lys39Thr) | single nucleotide variant | Nocturnal frontal lobe epilepsy [RCV000796752] | Chr14:93779289 [GRCh38] Chr14:94245635 [GRCh37] Chr14:14q32.12 |
uncertain significance |
NM_178013.4(PRIMA1):c.295G>A (p.Val99Ile) | single nucleotide variant | Nocturnal frontal lobe epilepsy [RCV000803074] | Chr14:93737305 [GRCh38] Chr14:94203651 [GRCh37] Chr14:14q32.12 |
uncertain significance |
GRCh37/hg19 14q32.12-32.33(chr14:91969028-107285437)x3 | copy number gain | not provided [RCV000848687] | Chr14:91969028..107285437 [GRCh37] Chr14:14q32.12-32.33 |
pathogenic |
NM_178013.4(PRIMA1):c.292G>A (p.Ala98Thr) | single nucleotide variant | Nocturnal frontal lobe epilepsy [RCV000810879] | Chr14:93737308 [GRCh38] Chr14:94203654 [GRCh37] Chr14:14q32.12 |
uncertain significance |
Database | Acc Id | Source(s) |
AGR Gene | HGNC:18319 | AgrOrtholog |
COSMIC | PRIMA1 | COSMIC |
Ensembl Genes | ENSG00000175785 | ENTREZGENE, UniProtKB/Swiss-Prot |
ENSG00000274089 | UniProtKB/Swiss-Prot | |
Ensembl Protein | ENSP00000320948 | UniProtKB/Swiss-Prot |
ENSP00000376848 | ENTREZGENE, UniProtKB/Swiss-Prot | |
ENSP00000376851 | UniProtKB/Swiss-Prot | |
ENSP00000434370 | ENTREZGENE, UniProtKB/Swiss-Prot | |
ENSP00000479082 | UniProtKB/Swiss-Prot | |
ENSP00000479855 | UniProtKB/Swiss-Prot | |
ENSP00000486875 | UniProtKB/Swiss-Prot | |
ENSP00000486953 | UniProtKB/Swiss-Prot | |
Ensembl Transcript | ENST00000316227 | UniProtKB/Swiss-Prot |
ENST00000393140 | ENTREZGENE, UniProtKB/Swiss-Prot | |
ENST00000393143 | UniProtKB/Swiss-Prot | |
ENST00000477603 | ENTREZGENE, UniProtKB/Swiss-Prot | |
ENST00000611347 | UniProtKB/Swiss-Prot | |
ENST00000617019 | UniProtKB/Swiss-Prot | |
ENST00000627063 | UniProtKB/Swiss-Prot | |
ENST00000629961 | UniProtKB/Swiss-Prot | |
GTEx | ENSG00000175785 | GTEx |
ENSG00000274089 | GTEx | |
HGNC ID | HGNC:18319 | ENTREZGENE |
Human Proteome Map | PRIMA1 | Human Proteome Map |
KEGG Report | hsa:145270 | UniProtKB/Swiss-Prot |
NCBI Gene | 145270 | ENTREZGENE |
OMIM | 613851 | OMIM |
PharmGKB | PA38315 | PharmGKB |
UniGene | Hs.432401 | ENTREZGENE |
UniProt | A0A024R6J9 | ENTREZGENE, UniProtKB/TrEMBL |
PRIMA_HUMAN | UniProtKB/Swiss-Prot, ENTREZGENE | |
UniProt Secondary | Q86XR6 | UniProtKB/Swiss-Prot |
![]() |
More on PRIMA1 | |
![]() |
Alliance Gene |
![]() |
NCBI Gene |
![]() |
Ensembl Gene |
![]() |
JBrowse: hg19 hg38 |
![]() |
HGNC Report |
![]() |
NCBI Genome Data Viewer |
CRRD Object Information | |
CRRD ID: | 1315672 |
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.