RAMP1 (receptor activity modifying protein 1) - Rat Genome Database

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Gene: RAMP1 (receptor activity modifying protein 1) Homo sapiens
Analyze
Symbol: RAMP1
Name: receptor activity modifying protein 1
RGD ID: 735949
HGNC Page HGNC
Description: Enables amylin receptor activity; calcitonin gene-related peptide binding activity; and calcitonin gene-related peptide receptor activity. Involved in several processes, including G protein-coupled receptor signaling pathway; positive regulation of protein glycosylation; and protein localization to plasma membrane. Located in cell surface. Part of CGRP receptor complex and amylin receptor complex 1. Colocalizes with plasma membrane.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: calcitonin receptor-like receptor activity modifying protein 1; calcitonin-receptor-like receptor activity-modifying protein 1; CRLR activity-modifying protein 1; receptor (calcitonin) activity modifying protein 1; receptor (G protein-coupled) activity modifying protein 1; receptor activity-modifying protein 1
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl2237,858,893 - 237,912,106 (+)EnsemblGRCh38hg38GRCh38
GRCh382237,858,555 - 237,912,114 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh372238,768,266 - 238,820,748 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 362238,432,926 - 238,485,495 (+)NCBINCBI36hg18NCBI36
Build 342238,550,286 - 238,602,746NCBI
Celera2232,481,221 - 232,533,800 (+)NCBI
Cytogenetic Map2q37.3NCBI
HuRef2230,560,137 - 230,612,778 (+)NCBIHuRef
CHM1_12238,773,978 - 238,826,564 (+)NCBICHM1_1
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
(S)-nicotine  (ISO)
1,1-dichloroethene  (ISO)
1,2-dichloroethane  (ISO)
1,2-dimethylhydrazine  (ISO)
1-nitropyrene  (EXP)
17alpha-ethynylestradiol  (ISO)
17beta-estradiol  (EXP,ISO)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
3-isobutyl-1-methyl-7H-xanthine  (EXP)
4,4'-diaminodiphenylmethane  (ISO)
4,4'-sulfonyldiphenol  (EXP)
4-hydroxyphenyl retinamide  (ISO)
5-fluorouracil  (EXP)
6-propyl-2-thiouracil  (ISO)
acetamide  (ISO)
aflatoxin B1  (EXP)
aflatoxin B2  (EXP)
ammonium chloride  (ISO)
amphetamine  (ISO)
arsane  (EXP,ISO)
arsenic atom  (EXP,ISO)
atrazine  (EXP)
benzo[a]pyrene  (EXP,ISO)
benzo[e]pyrene  (EXP)
bis(2-ethylhexyl) phthalate  (EXP)
bisphenol A  (EXP,ISO)
cadmium atom  (EXP)
cadmium dichloride  (EXP)
calciol  (ISO)
calcitriol  (EXP)
carbon nanotube  (ISO)
chlordecone  (ISO)
chlorpyrifos  (ISO)
choline  (ISO)
clofibrate  (ISO)
copper atom  (EXP)
copper(0)  (EXP)
Cuprizon  (ISO)
curcumin  (EXP)
cyclophosphamide  (EXP)
cytarabine  (EXP)
deoxynivalenol  (EXP)
dexamethasone  (EXP)
dextran sulfate  (ISO)
dibutyl phthalate  (ISO)
dimethylarsinic acid  (ISO)
diuron  (ISO)
dorsomorphin  (EXP)
doxorubicin  (EXP)
endosulfan  (ISO)
folic acid  (ISO)
fonofos  (EXP)
gentamycin  (ISO)
glyphosate  (ISO)
indometacin  (EXP)
irinotecan  (ISO)
isoprenaline  (ISO)
ketamine  (ISO)
L-methionine  (ISO)
menadione  (EXP)
methapyrilene  (EXP)
methotrexate  (EXP)
N-benzyloxycarbonyl-L-leucyl-L-leucyl-L-leucinal  (ISO)
N-nitrosodiethylamine  (ISO)
N-nitrosodimethylamine  (ISO)
nickel sulfate  (EXP)
nicotine  (ISO)
nitric oxide  (ISO)
nitrofen  (ISO)
paclitaxel  (EXP)
parathion  (EXP)
phenethyl caffeate  (ISO)
phenylephrine  (ISO)
phenylmercury acetate  (EXP)
pirinixic acid  (EXP)
progesterone  (ISO)
quercetin  (EXP)
SB 431542  (EXP)
sodium arsenate  (ISO)
sodium atom  (ISO)
sunitinib  (EXP)
T-2 toxin  (EXP)
tacrolimus hydrate  (ISO)
tamoxifen  (ISO)
temozolomide  (EXP)
terbufos  (EXP)
Tesaglitazar  (ISO)
testosterone  (EXP)
tetrachloromethane  (ISO)
thapsigargin  (EXP)
titanium dioxide  (ISO)
tremolite asbestos  (ISO)
triclosan  (EXP)
triphenyl phosphate  (ISO)
tungsten  (ISO)
tunicamycin  (EXP)
valproic acid  (EXP,ISO)

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
1. GOA_HUMAN data from the GO Consortium
2. RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:8889548   PMID:9620797   PMID:10354609   PMID:10385705   PMID:10882736   PMID:11060459   PMID:11535606   PMID:11693189   PMID:11733510   PMID:11754963   PMID:11804624   PMID:11847213  
PMID:11937264   PMID:11973435   PMID:12036966   PMID:12093471   PMID:12234182   PMID:12419522   PMID:12446722   PMID:12477932   PMID:12565884   PMID:12574158   PMID:12684503   PMID:14722252  
PMID:15245870   PMID:15300632   PMID:15489334   PMID:15613468   PMID:16293613   PMID:16912219   PMID:17310067   PMID:17493758   PMID:17785463   PMID:18039931   PMID:18198792   PMID:18240029  
PMID:18240900   PMID:18593822   PMID:18725456   PMID:19710695   PMID:20100989   PMID:20188075   PMID:20596610   PMID:20826335   PMID:20933260   PMID:21873635   PMID:22208649   PMID:22484227  
PMID:22500019   PMID:22949393   PMID:23237777   PMID:23251661   PMID:23867798   PMID:24104479   PMID:24454825   PMID:25881990   PMID:25982113   PMID:26501962   PMID:28181496   PMID:28611215  
PMID:28691801   PMID:29297736   PMID:30209400   PMID:31150417   PMID:32296183   PMID:33602864  


Genomics

Comparative Map Data
RAMP1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl2237,858,893 - 237,912,106 (+)EnsemblGRCh38hg38GRCh38
GRCh382237,858,555 - 237,912,114 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh372238,768,266 - 238,820,748 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 362238,432,926 - 238,485,495 (+)NCBINCBI36hg18NCBI36
Build 342238,550,286 - 238,602,746NCBI
Celera2232,481,221 - 232,533,800 (+)NCBI
Cytogenetic Map2q37.3NCBI
HuRef2230,560,137 - 230,612,778 (+)NCBIHuRef
CHM1_12238,773,978 - 238,826,564 (+)NCBICHM1_1
Ramp1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39191,107,544 - 91,152,918 (+)NCBIGRCm39mm39
GRCm39 Ensembl191,107,544 - 91,152,918 (+)Ensembl
GRCm38191,179,822 - 91,225,196 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl191,179,822 - 91,225,196 (+)EnsemblGRCm38mm10GRCm38
MGSCv37193,076,399 - 93,121,773 (+)NCBIGRCm37mm9NCBIm37
MGSCv36193,010,447 - 93,054,085 (+)NCBImm8
Celera194,117,772 - 94,162,742 (+)NCBICelera
Cytogenetic Map1DNCBI
cM Map146.08NCBI
Ramp1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.2991,765,481 - 91,816,152 (+)NCBImRatBN7.2
mRatBN7.2 Ensembl991,781,285 - 91,816,151 (+)Ensembl
Rnor_6.0998,313,632 - 98,364,206 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl998,313,632 - 98,364,205 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0997,995,669 - 98,041,719 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4990,402,493 - 90,450,038 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.1990,607,261 - 90,654,807 (+)NCBI
Celera989,308,226 - 89,359,459 (+)NCBICelera
Cytogenetic Map9q36NCBI
Ramp1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0NW_0049555422,530,349 - 2,564,072 (-)NCBIChiLan1.0ChiLan1.0
RAMP1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.12B243,942,771 - 243,995,221 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl2B243,942,771 - 243,995,221 (+)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v02B125,092,164 - 125,144,032 (+)NCBIMhudiblu_PPA_v0panPan3
RAMP1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12548,431,136 - 48,466,070 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2548,437,919 - 48,466,070 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2548,924,771 - 48,962,496 (+)NCBI
ROS_Cfam_1.02548,813,868 - 48,851,604 (+)NCBI
UMICH_Zoey_3.12548,689,424 - 48,727,160 (+)NCBI
UNSW_CanFamBas_1.02548,477,911 - 48,515,642 (+)NCBI
UU_Cfam_GSD_1.02548,710,077 - 48,748,033 (+)NCBI
Ramp1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024405303190,399,529 - 190,436,574 (+)NCBI
SpeTri2.0NW_004936525503,119 - 540,159 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
RAMP1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl15137,490,087 - 137,535,555 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.115137,490,440 - 137,535,555 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.215151,914,286 - 151,944,914 (+)NCBISscrofa10.2Sscrofa10.2susScr3
RAMP1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.110123,873,597 - 123,931,215 (+)NCBIChlSab1.1chlSab2
ChlSab1.1 Ensembl10123,873,351 - 123,931,248 (+)EnsemblChlSab1.1chlSab2
Vero_WHO_p1.0NW_02366604075,479,406 - 75,535,761 (-)NCBIVero_WHO_p1.0
Ramp1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046248473,169,339 - 3,202,393 (+)NCBIHetGla_female_1.0hetGla2

Position Markers
WI-15143  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372238,820,581 - 238,820,730UniSTSGRCh37
Build 362238,485,320 - 238,485,469RGDNCBI36
Celera2232,533,625 - 232,533,774RGD
Cytogenetic Map2q36-q37.1UniSTS
HuRef2230,612,603 - 230,612,752UniSTS
GeneMap99-GB4 RH Map2741.45UniSTS
Whitehead-RH Map21073.8UniSTS
RAMP1__3761  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372238,820,239 - 238,820,766UniSTSGRCh37
Build 362238,484,978 - 238,485,505RGDNCBI36
Celera2232,533,283 - 232,533,810RGD
HuRef2230,612,261 - 230,612,788UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1451
Count of miRNA genes:428
Interacting mature miRNAs:467
Transcripts:ENST00000254661, ENST00000403885, ENST00000404910, ENST00000409726
Prediction methods:Microtar, Miranda, Rnahybrid
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 visual system adipose tissue appendage entire extraembryonic component
High 3 23 2 59
Medium 2203 2196 875 427 435 403 2901 2131 3566 123 947 920 36 542 2435 1
Low 200 703 828 186 1130 53 1393 50 148 230 410 621 136 659 353 3
Below cutoff 19 64 13 3 206 3 42 10 11 45 29 39 3 1 2 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001308353 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_005855 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017003152 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017003153 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017003154 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017003155 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017003156 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC012076 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC016776 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI017108 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ001014 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY265457 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC000548 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BI548986 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM126103 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM978161 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX327017 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471063 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR542032 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR542044 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF510799 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000254661   ⟹   ENSP00000254661
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2237,859,623 - 237,912,106 (+)Ensembl
RefSeq Acc Id: ENST00000403885   ⟹   ENSP00000386046
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2237,859,976 - 237,912,010 (+)Ensembl
RefSeq Acc Id: ENST00000404910   ⟹   ENSP00000384688
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2237,858,893 - 237,912,010 (+)Ensembl
RefSeq Acc Id: ENST00000409726   ⟹   ENSP00000386720
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl2237,859,623 - 237,911,956 (+)Ensembl
RefSeq Acc Id: NM_001308353   ⟹   NP_001295282
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382237,859,623 - 237,912,106 (+)NCBI
CHM1_12238,773,978 - 238,826,567 (+)NCBI
Sequence:
RefSeq Acc Id: NM_005855   ⟹   NP_005846
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382237,859,623 - 237,912,106 (+)NCBI
GRCh372238,768,187 - 238,820,756 (+)ENTREZGENE
Build 362238,432,926 - 238,485,495 (+)NCBI Archive
HuRef2230,560,137 - 230,612,778 (+)ENTREZGENE
CHM1_12238,773,978 - 238,826,567 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017003152   ⟹   XP_016858641
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382237,859,904 - 237,912,114 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017003153   ⟹   XP_016858642
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382237,858,555 - 237,912,114 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017003154   ⟹   XP_016858643
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382237,874,515 - 237,912,114 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017003155   ⟹   XP_016858644
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382237,859,616 - 237,878,772 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017003156   ⟹   XP_016858645
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382237,859,932 - 237,912,114 (+)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_005846   ⟸   NM_005855
- Peptide Label: isoform 1 precursor
- UniProtKB: O60894 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001295282   ⟸   NM_001308353
- Peptide Label: isoform 2
- UniProtKB: E9PC20 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016858642   ⟸   XM_017003153
- Peptide Label: isoform X1
- UniProtKB: E9PC20 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016858644   ⟸   XM_017003155
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_016858641   ⟸   XM_017003152
- Peptide Label: isoform X1
- UniProtKB: E9PC20 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016858645   ⟸   XM_017003156
- Peptide Label: isoform X1
- UniProtKB: E9PC20 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016858643   ⟸   XM_017003154
- Peptide Label: isoform X1
- UniProtKB: E9PC20 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000254661   ⟸   ENST00000254661
RefSeq Acc Id: ENSP00000386046   ⟸   ENST00000403885
RefSeq Acc Id: ENSP00000384688   ⟸   ENST00000404910
RefSeq Acc Id: ENSP00000386720   ⟸   ENST00000409726

Promoters
RGD ID:6863228
Promoter ID:EPDNEW_H4779
Type:initiation region
Name:RAMP1_2
Description:receptor activity modifying protein 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H4780  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh382237,858,880 - 237,858,940EPDNEW
RGD ID:6863230
Promoter ID:EPDNEW_H4780
Type:initiation region
Name:RAMP1_1
Description:receptor activity modifying protein 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H4779  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh382237,859,623 - 237,859,683EPDNEW
RGD ID:6798048
Promoter ID:HG_KWN:37991
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell
Transcripts:ENST00000403885,   ENST00000404910,   ENST00000409726,   OTTHUMT00000257166
Position:
Human AssemblyChrPosition (strand)Source
Build 362238,431,676 - 238,432,176 (+)MPROMDB

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 2q37.1-37.3(chr2:231770279-242126245)x1 copy number loss See cases [RCV000050304] Chr2:231770279..242126245 [GRCh38]
Chr2:232634989..243059659 [GRCh37]
Chr2:232343233..242717069 [NCBI36]
Chr2:2q37.1-37.3
pathogenic
GRCh38/hg38 2q37.3(chr2:236555233-242126245)x1 copy number loss See cases [RCV000051120] Chr2:236555233..242126245 [GRCh38]
Chr2:237463876..243059659 [GRCh37]
Chr2:237128615..242717069 [NCBI36]
Chr2:2q37.3
pathogenic
GRCh38/hg38 2q37.3(chr2:237643996-242126245)x1 copy number loss See cases [RCV000051133] Chr2:237643996..242126245 [GRCh38]
Chr2:238552639..243059659 [GRCh37]
Chr2:238217378..242717069 [NCBI36]
Chr2:2q37.3
pathogenic
GRCh38/hg38 2q37.1-37.3(chr2:234345842-242126245)x1 copy number loss See cases [RCV000051163] Chr2:234345842..242126245 [GRCh38]
Chr2:235254486..243059659 [GRCh37]
Chr2:234919225..242717069 [NCBI36]
Chr2:2q37.1-37.3
pathogenic
GRCh38/hg38 2q37.2-37.3(chr2:235741079-242032456)x1 copy number loss See cases [RCV000052673] Chr2:235741079..242032456 [GRCh38]
Chr2:236649723..242974607 [GRCh37]
Chr2:236314462..242623280 [NCBI36]
Chr2:2q37.2-37.3
pathogenic
GRCh38/hg38 2q37.3(chr2:236775572-242065349)x1 copy number loss See cases [RCV000052674] Chr2:236775572..242065349 [GRCh38]
Chr2:237684215..243007500 [GRCh37]
Chr2:237348954..242656173 [NCBI36]
Chr2:2q37.3
pathogenic
GRCh38/hg38 2q37.3(chr2:237526184-241996090)x1 copy number loss See cases [RCV000052675] Chr2:237526184..241996090 [GRCh38]
Chr2:238434827..242938241 [GRCh37]
Chr2:238099566..242586914 [NCBI36]
Chr2:2q37.3
pathogenic
GRCh38/hg38 2q37.3(chr2:237643996-242065208)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052700]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052700]|See cases [RCV000052700] Chr2:237643996..242065208 [GRCh38]
Chr2:238552639..243007359 [GRCh37]
Chr2:238217378..242656032 [NCBI36]
Chr2:2q37.3
pathogenic
GRCh38/hg38 2q37.3(chr2:237643996-238287366)x3 copy number gain See cases [RCV000052730] Chr2:237643996..238287366 [GRCh38]
Chr2:238552639..239196007 [GRCh37]
Chr2:238217378..238860746 [NCBI36]
Chr2:2q37.3
uncertain significance
GRCh38/hg38 2q37.1-37.3(chr2:234172536-242086301)x1 copy number loss See cases [RCV000052669] Chr2:234172536..242086301 [GRCh38]
Chr2:235081180..243028452 [GRCh37]
Chr2:234745919..242677125 [NCBI36]
Chr2:2q37.1-37.3
pathogenic
GRCh38/hg38 2q37.1-37.3(chr2:234668159-242126245)x1 copy number loss See cases [RCV000052670] Chr2:234668159..242126245 [GRCh38]
Chr2:235576803..243059659 [GRCh37]
Chr2:235241542..242717069 [NCBI36]
Chr2:2q37.1-37.3
pathogenic
GRCh38/hg38 2q37.2-37.3(chr2:234906462-242065208)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052671]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052671]|See cases [RCV000052671] Chr2:234906462..242065208 [GRCh38]
Chr2:235815106..243007359 [GRCh37]
Chr2:235479845..242656032 [NCBI36]
Chr2:2q37.2-37.3
pathogenic
GRCh38/hg38 2q37.2-37.3(chr2:235268768-242065208)x1 copy number loss See cases [RCV000052672] Chr2:235268768..242065208 [GRCh38]
Chr2:236177412..243007359 [GRCh37]
Chr2:235842151..242656032 [NCBI36]
Chr2:2q37.2-37.3
pathogenic
GRCh38/hg38 2q37.1-37.3(chr2:231375505-242065208)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052639]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052639]|See cases [RCV000052639] Chr2:231375505..242065208 [GRCh38]
Chr2:232240216..243007359 [GRCh37]
Chr2:231948460..242656032 [NCBI36]
Chr2:2q37.1-37.3
pathogenic
GRCh38/hg38 2q37.1-37.3(chr2:232857728-242065349)x1 copy number loss See cases [RCV000052640] Chr2:232857728..242065349 [GRCh38]
Chr2:233722438..243007500 [GRCh37]
Chr2:233430682..242656173 [NCBI36]
Chr2:2q37.1-37.3
pathogenic
GRCh38/hg38 2q37.1-37.3(chr2:233420162-242086301)x1 copy number loss See cases [RCV000052641] Chr2:233420162..242086301 [GRCh38]
Chr2:233995840..243028452 [GRCh37]
Chr2:233704084..242677125 [NCBI36]
Chr2:2q37.1-37.3
pathogenic
GRCh38/hg38 2q37.1-37.3(chr2:233453611-242099155)x1 copy number loss See cases [RCV000052642] Chr2:233453611..242099155 [GRCh38]
Chr2:234362257..243041306 [GRCh37]
Chr2:234026996..242689979 [NCBI36]
Chr2:2q37.1-37.3
pathogenic
GRCh38/hg38 2q37.1-37.3(chr2:234225537-241565907)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052975]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052975]|See cases [RCV000052975] Chr2:234225537..241565907 [GRCh38]
Chr2:235134181..242505322 [GRCh37]
Chr2:234798920..242153995 [NCBI36]
Chr2:2q37.1-37.3
pathogenic
GRCh38/hg38 2q37.2-37.3(chr2:235268768-242126245)x3 copy number gain See cases [RCV000052976] Chr2:235268768..242126245 [GRCh38]
Chr2:236177412..243059659 [GRCh37]
Chr2:235842151..242717069 [NCBI36]
Chr2:2q37.2-37.3
pathogenic
GRCh38/hg38 2q37.2-37.3(chr2:235563664-242086301)x3 copy number gain See cases [RCV000052977] Chr2:235563664..242086301 [GRCh38]
Chr2:236472308..243028452 [GRCh37]
Chr2:236137047..242677125 [NCBI36]
Chr2:2q37.2-37.3
pathogenic
GRCh38/hg38 2q37.3(chr2:237813997-240410487)x3 copy number gain See cases [RCV000052978] Chr2:237813997..240410487 [GRCh38]
Chr2:238722640..241349904 [GRCh37]
Chr2:238387379..240998577 [NCBI36]
Chr2:2q37.3
pathogenic
GRCh38/hg38 2q32.2-37.3(chr2:188818195-242065208)x3 copy number gain See cases [RCV000052958] Chr2:188818195..242065208 [GRCh38]
Chr2:189682921..243007359 [GRCh37]
Chr2:189391166..242656032 [NCBI36]
Chr2:2q32.2-37.3
pathogenic
GRCh38/hg38 2q32.2-37.3(chr2:190310736-241892770)x3 copy number gain See cases [RCV000052959] Chr2:190310736..241892770 [GRCh38]
Chr2:191175462..242834921 [GRCh37]
Chr2:190883707..242483594 [NCBI36]
Chr2:2q32.2-37.3
pathogenic
GRCh38/hg38 2q32.3-37.3(chr2:193122313-241074980)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052960]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052960]|See cases [RCV000052960] Chr2:193122313..241074980 [GRCh38]
Chr2:193987039..242014395 [GRCh37]
Chr2:193695284..241663068 [NCBI36]
Chr2:2q32.3-37.3
pathogenic
GRCh38/hg38 2q36.1-37.3(chr2:223992431-242126245)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052972]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052972]|See cases [RCV000052972] Chr2:223992431..242126245 [GRCh38]
Chr2:224857148..243059659 [GRCh37]
Chr2:224565392..242717069 [NCBI36]
Chr2:2q36.1-37.3
pathogenic
GRCh38/hg38 2q36.3-37.3(chr2:227803148-242086301)x3 copy number gain See cases [RCV000052973] Chr2:227803148..242086301 [GRCh38]
Chr2:228667864..243028452 [GRCh37]
Chr2:228376108..242677125 [NCBI36]
Chr2:2q36.3-37.3
pathogenic
Single allele deletion Intellectual disability [RCV001293367] Chr2:237201756..243048760 [GRCh37]
Chr2:2q37.2-37.3
pathogenic
GRCh38/hg38 2q36.3-37.3(chr2:228723579-241404867)x3 copy number gain See cases [RCV000134169] Chr2:228723579..241404867 [GRCh38]
Chr2:229588295..242344282 [GRCh37]
Chr2:229296539..241992955 [NCBI36]
Chr2:2q36.3-37.3
pathogenic
GRCh38/hg38 2q37.3(chr2:237034476-242065208)x1 copy number loss See cases [RCV000135864] Chr2:237034476..242065208 [GRCh38]
Chr2:237943119..243007359 [GRCh37]
Chr2:237607858..242656032 [NCBI36]
Chr2:2q37.3
pathogenic
GRCh38/hg38 2q37.3(chr2:236966763-242065208)x1 copy number loss See cases [RCV000135570] Chr2:236966763..242065208 [GRCh38]
Chr2:237875406..243007359 [GRCh37]
Chr2:237540145..242656032 [NCBI36]
Chr2:2q37.3
pathogenic
GRCh38/hg38 2q37.3(chr2:237232204-242065208)x1 copy number loss See cases [RCV000136566] Chr2:237232204..242065208 [GRCh38]
Chr2:238140847..243007359 [GRCh37]
Chr2:237805586..242656032 [NCBI36]
Chr2:2q37.3
pathogenic
GRCh38/hg38 2q34-37.3(chr2:210579676-242126245)x3 copy number gain See cases [RCV000135934] Chr2:210579676..242126245 [GRCh38]
Chr2:211444400..243059659 [GRCh37]
Chr2:211152645..242717069 [NCBI36]
Chr2:2q34-37.3
pathogenic
GRCh38/hg38 2q37.2-37.3(chr2:235028429-242066108)x1 copy number loss See cases [RCV000136968] Chr2:235028429..242066108 [GRCh38]
Chr2:235937073..243008259 [GRCh37]
Chr2:235601812..242656932 [NCBI36]
Chr2:2q37.2-37.3
pathogenic
GRCh38/hg38 2q37.2-37.3(chr2:234835780-242065208)x1 copy number loss See cases [RCV000137069] Chr2:234835780..242065208 [GRCh38]
Chr2:235744424..243007359 [GRCh37]
Chr2:235409163..242656032 [NCBI36]
Chr2:2q37.2-37.3
pathogenic
GRCh38/hg38 2q37.2-37.3(chr2:235603604-241771051)x1 copy number loss See cases [RCV000136648] Chr2:235603604..241771051 [GRCh38]
Chr2:236512248..242710466 [GRCh37]
Chr2:236176987..242359139 [NCBI36]
Chr2:2q37.2-37.3
pathogenic|uncertain significance
GRCh38/hg38 2q37.1-37.3(chr2:234058757-239443690)x1 copy number loss See cases [RCV000137411] Chr2:234058757..239443690 [GRCh38]
Chr2:234967401..240365384 [GRCh37]
Chr2:234632140..240030321 [NCBI36]
Chr2:2q37.1-37.3
pathogenic
GRCh38/hg38 2q37.2-37.3(chr2:235757098-239443690)x1 copy number loss See cases [RCV000137830] Chr2:235757098..239443690 [GRCh38]
Chr2:236665742..240365384 [GRCh37]
Chr2:236330481..240030321 [NCBI36]
Chr2:2q37.2-37.3
pathogenic|uncertain significance
GRCh38/hg38 2q37.3(chr2:237902870-242126251)x1 copy number loss See cases [RCV000139808] Chr2:237902870..242126251 [GRCh38]
Chr2:238811512..243059659 [GRCh37]
Chr2:238476251..242717075 [NCBI36]
Chr2:2q37.3
pathogenic
GRCh38/hg38 2q37.3(chr2:236775762-242126251)x1 copy number loss See cases [RCV000139527] Chr2:236775762..242126251 [GRCh38]
Chr2:237684405..243059659 [GRCh37]
Chr2:237349144..242717075 [NCBI36]
Chr2:2q37.3
pathogenic
GRCh38/hg38 2q37.3(chr2:236413722-242126251)x1 copy number loss See cases [RCV000139805] Chr2:236413722..242126251 [GRCh38]
Chr2:237322365..243059659 [GRCh37]
Chr2:236987104..242717075 [NCBI36]
Chr2:2q37.3
pathogenic
GRCh38/hg38 2q37.2-37.3(chr2:235846916-241841232)x1 copy number loss See cases [RCV000141661] Chr2:235846916..241841232 [GRCh38]
Chr2:236755560..242783384 [GRCh37]
Chr2:236420299..242432057 [NCBI36]
Chr2:2q37.2-37.3
pathogenic
GRCh38/hg38 2q37.1-37.3(chr2:234159653-241841232)x1 copy number loss See cases [RCV000142291] Chr2:234159653..241841232 [GRCh38]
Chr2:235068297..242783384 [GRCh37]
Chr2:234733036..242432057 [NCBI36]
Chr2:2q37.1-37.3
pathogenic
GRCh38/hg38 2q32.2-37.3(chr2:189436149-241841232)x3 copy number gain See cases [RCV000142307] Chr2:189436149..241841232 [GRCh38]
Chr2:190300875..242783384 [GRCh37]
Chr2:190009120..242432057 [NCBI36]
Chr2:2q32.2-37.3
pathogenic
GRCh38/hg38 2q35-37.3(chr2:218101759-242126245)x3 copy number gain See cases [RCV000143216] Chr2:218101759..242126245 [GRCh38]
Chr2:218966482..243059659 [GRCh37]
Chr2:218674727..242717069 [NCBI36]
Chr2:2q35-37.3
pathogenic
GRCh38/hg38 2q37.1-37.3(chr2:231770279-242126245)x1 copy number loss See cases [RCV000148260] Chr2:231770279..242126245 [GRCh38]
Chr2:232634989..243059659 [GRCh37]
Chr2:232343233..242717069 [NCBI36]
Chr2:2q37.1-37.3
pathogenic
GRCh37/hg19 2q37.3(chr2:237816758-242783384)x1 copy number loss See cases [RCV000449023] Chr2:237816758..242783384 [GRCh37]
Chr2:2q37.3
pathogenic
GRCh37/hg19 2q37.1-37.3(chr2:233784243-243040217)x1 copy number loss See cases [RCV000446034] Chr2:233784243..243040217 [GRCh37]
Chr2:2q37.1-37.3
pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:14238-243048760)x3 copy number gain not provided [RCV000752802] Chr2:14238..243048760 [GRCh37]
Chr2:2p25.3-q37.3
pathogenic
GRCh37/hg19 2q37.3(chr2:237938270-242783384)x1 copy number loss See cases [RCV000446532] Chr2:237938270..242783384 [GRCh37]
Chr2:2q37.3
pathogenic
GRCh37/hg19 2q37.1-37.3(chr2:234495262-242783384)x1 copy number loss See cases [RCV000446061] Chr2:234495262..242783384 [GRCh37]
Chr2:2q37.1-37.3
pathogenic
GRCh37/hg19 2q37.2-37.3(chr2:236285213-242783384)x1 copy number loss See cases [RCV000445750] Chr2:236285213..242783384 [GRCh37]
Chr2:2q37.2-37.3
pathogenic
GRCh37/hg19 2q37.3(chr2:238072533-242783384)x1 copy number loss See cases [RCV000447929] Chr2:238072533..242783384 [GRCh37]
Chr2:2q37.3
pathogenic
GRCh37/hg19 2q37.2-37.3(chr2:236911223-242783384)x1 copy number loss See cases [RCV000447965] Chr2:236911223..242783384 [GRCh37]
Chr2:2q37.2-37.3
pathogenic
GRCh37/hg19 2q37.2-37.3(chr2:236577291-242783384)x1 copy number loss See cases [RCV000448691] Chr2:236577291..242783384 [GRCh37]
Chr2:2q37.2-37.3
pathogenic
GRCh37/hg19 2q37.1-37.3(chr2:234495262-242783384)x1 copy number loss See cases [RCV000512077] Chr2:234495262..242783384 [GRCh37]
Chr2:2q37.1-37.3
pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384) copy number gain See cases [RCV000512056] Chr2:12771..242783384 [GRCh37]
Chr2:2p25.3-q37.3
pathogenic
GRCh37/hg19 2q34-37.3(chr2:213518431-242783384)x3 copy number gain See cases [RCV000512009] Chr2:213518431..242783384 [GRCh37]
Chr2:2q34-37.3
pathogenic
GRCh37/hg19 2q37.1-37.3(chr2:235539337-242783384)x1 copy number loss See cases [RCV000511491] Chr2:235539337..242783384 [GRCh37]
Chr2:2q37.1-37.3
pathogenic
GRCh37/hg19 2q36.1-37.3(chr2:222077224-239394441)x3 copy number gain See cases [RCV000511816] Chr2:222077224..239394441 [GRCh37]
Chr2:2q36.1-37.3
pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)x3 copy number gain See cases [RCV000511212] Chr2:12771..242783384 [GRCh37]
Chr2:2p25.3-q37.3
pathogenic
GRCh37/hg19 2q37.3(chr2:237545100-242783384)x1 copy number loss See cases [RCV000512231] Chr2:237545100..242783384 [GRCh37]
Chr2:2q37.3
pathogenic
GRCh37/hg19 2q37.3(chr2:237480048-241611309)x1 copy number loss not provided [RCV000682151] Chr2:237480048..241611309 [GRCh37]
Chr2:2q37.3
pathogenic
GRCh37/hg19 2q35-37.3(chr2:219225872-242016876)x3 copy number gain not provided [RCV000682170] Chr2:219225872..242016876 [GRCh37]
Chr2:2q35-37.3
pathogenic
GRCh37/hg19 2q37.2-37.3(chr2:235790256-242783384)x1 copy number loss not provided [RCV000682160] Chr2:235790256..242783384 [GRCh37]
Chr2:2q37.2-37.3
pathogenic
GRCh37/hg19 2q37.1-37.3(chr2:234716425-242783384)x3 copy number gain not provided [RCV000682161] Chr2:234716425..242783384 [GRCh37]
Chr2:2q37.1-37.3
pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:15672-243101834)x3 copy number gain not provided [RCV000752804] Chr2:15672..243101834 [GRCh37]
Chr2:2p25.3-q37.3
pathogenic
GRCh37/hg19 2q37.3(chr2:238245132-239052675)x3 copy number gain not provided [RCV000754757] Chr2:238245132..239052675 [GRCh37]
Chr2:2q37.3
uncertain significance
GRCh37/hg19 2q37.3(chr2:238037759-243101834)x1 copy number loss not provided [RCV000740979] Chr2:238037759..243101834 [GRCh37]
Chr2:2q37.3
pathogenic
NM_005855.4(RAMP1):c.402G>A (p.Thr134=) single nucleotide variant not provided [RCV000972644] Chr2:237911738 [GRCh38]
Chr2:238820380 [GRCh37]
Chr2:2q37.3
benign
GRCh37/hg19 2q34-37.3(chr2:210779657-239879183)x3 copy number gain See cases [RCV000790568] Chr2:210779657..239879183 [GRCh37]
Chr2:2q34-37.3
pathogenic
GRCh37/hg19 2q37.2-37.3(chr2:237028693-242708080) copy number loss Chromosome 2q37 deletion syndrome [RCV000767787] Chr2:237028693..242708080 [GRCh37]
Chr2:2q37.2-37.3
pathogenic
GRCh37/hg19 2q37.3(chr2:238795602-242918203) copy number loss Chromosome 2q37 deletion syndrome [RCV000767788] Chr2:238795602..242918203 [GRCh37]
Chr2:2q37.3
likely pathogenic
GRCh37/hg19 2q36.3-37.3(chr2:230814690-242783384)x3 copy number gain not provided [RCV001007519] Chr2:230814690..242783384 [GRCh37]
Chr2:2q36.3-37.3
pathogenic
GRCh37/hg19 2q37.2-37.3(chr2:237265271-242783384)x3 copy number gain not provided [RCV001005380] Chr2:237265271..242783384 [GRCh37]
Chr2:2q37.2-37.3
pathogenic
GRCh37/hg19 2q37.1-37.3(chr2:234090049-239494702)x1 copy number loss not provided [RCV001007520] Chr2:234090049..239494702 [GRCh37]
Chr2:2q37.1-37.3
pathogenic
GRCh37/hg19 2q37.2-37.3(chr2:236172348-241611309)x1 copy number loss not provided [RCV001007525] Chr2:236172348..241611309 [GRCh37]
Chr2:2q37.2-37.3
pathogenic
NM_005855.4(RAMP1):c.390C>A (p.Thr130=) single nucleotide variant not provided [RCV000909063] Chr2:237911726 [GRCh38]
Chr2:238820368 [GRCh37]
Chr2:2q37.3
benign
GRCh37/hg19 2q37.1-37.3(chr2:234791927-242783384)x1 copy number loss not provided [RCV001007522] Chr2:234791927..242783384 [GRCh37]
Chr2:2q37.1-37.3
pathogenic
GRCh37/hg19 2q37.3(chr2:238509115-239053313)x3 copy number gain not provided [RCV001259194] Chr2:238509115..239053313 [GRCh37]
Chr2:2q37.3
uncertain significance
GRCh37/hg19 2q31.2-37.3(chr2:178397959-243007457)x3 copy number gain See cases [RCV001263052] Chr2:178397959..243007457 [GRCh37]
Chr2:2q31.2-37.3
pathogenic
GRCh37/hg19 2q37.1-37.3(chr2:233110452-243028452)x1 copy number loss Chromosome 2q37 deletion syndrome [RCV001263221] Chr2:233110452..243028452 [GRCh37]
Chr2:2q37.1-37.3
pathogenic

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:9843 AgrOrtholog
COSMIC RAMP1 COSMIC
Ensembl Genes ENSG00000132329 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000254661 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000384688 ENTREZGENE, UniProtKB/TrEMBL
  ENSP00000386046 ENTREZGENE, UniProtKB/TrEMBL
  ENSP00000386720 ENTREZGENE, UniProtKB/TrEMBL
Ensembl Transcript ENST00000254661 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000403885 ENTREZGENE, UniProtKB/TrEMBL
  ENST00000404910 ENTREZGENE, UniProtKB/TrEMBL
  ENST00000409726 ENTREZGENE, UniProtKB/TrEMBL
Gene3D-CATH 1.10.150.510 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000132329 GTEx
HGNC ID HGNC:9843 ENTREZGENE
Human Proteome Map RAMP1 Human Proteome Map
InterPro RAMP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RAMP_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:10267 UniProtKB/Swiss-Prot
NCBI Gene 10267 ENTREZGENE
OMIM 605153 OMIM
PANTHER PTHR14076 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam RAMP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA34202 PharmGKB
UniProt E9PC20 ENTREZGENE, UniProtKB/TrEMBL
  O60894 ENTREZGENE
  Q53SN3_HUMAN UniProtKB/TrEMBL
  Q53T50_HUMAN UniProtKB/TrEMBL
  RAMP1_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary Q6FGS5 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-04-12 RAMP1  receptor activity modifying protein 1    receptor (G protein-coupled) activity modifying protein 1  Symbol and/or name change 5135510 APPROVED
2011-08-16 RAMP1  receptor (G protein-coupled) activity modifying protein 1  RAMP1  receptor (G protein-coupled) activity modifying protein 1  Symbol and/or name change 5135510 APPROVED