MCHR2 (melanin concentrating hormone receptor 2) - Rat Genome Database

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Gene: MCHR2 (melanin concentrating hormone receptor 2) Homo sapiens
Analyze
Symbol: MCHR2
Name: melanin concentrating hormone receptor 2
RGD ID: 1347761
HGNC Page HGNC:20867
Description: Predicted to enable G protein-coupled peptide receptor activity. Predicted to be involved in neuropeptide signaling pathway. Predicted to be located in plasma membrane.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: G protein-coupled receptor 145; G protein-coupled receptor slt; G-protein coupled receptor 145; GPR145; GPRv17; MCH receptor 2; MCH-2R; MCH-R2; MCH2; MCH2R; MCHR-2; melanin-concentrating hormone 2; melanin-concentrating hormone receptor 2; SLT
RGD Orthologs
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Candidate Gene For: BW142_H BW141_H
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38699,918,519 - 99,994,223 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl699,918,519 - 99,994,247 (-)EnsemblGRCh38hg38GRCh38
GRCh376100,366,395 - 100,442,099 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 366100,474,507 - 100,548,835 (-)NCBINCBI36Build 36hg18NCBI36
Build 346100,475,364 - 100,548,844NCBI
Celera6101,011,840 - 101,086,179 (-)NCBICelera
Cytogenetic Map6q16.2NCBI
HuRef697,807,284 - 97,881,990 (-)NCBIHuRef
CHM1_16100,629,793 - 100,704,123 (-)NCBICHM1_1
T2T-CHM13v2.06101,091,896 - 101,168,099 (-)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

Biological Process

Cellular Component

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:11274220   PMID:11355873   PMID:11404457   PMID:11416225   PMID:11459838   PMID:11478907   PMID:11839762   PMID:12127971   PMID:12477932   PMID:12620396   PMID:14574404   PMID:14702039  
PMID:15229878   PMID:15340116   PMID:15489334   PMID:15941924   PMID:16754659   PMID:17698913   PMID:19502010   PMID:19683862   PMID:19927306   PMID:20099459   PMID:21102462   PMID:21873635  
PMID:22123324   PMID:25231870   PMID:26461262   PMID:27306922   PMID:29066024   PMID:29987050  


Genomics

Comparative Map Data
MCHR2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38699,918,519 - 99,994,223 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl699,918,519 - 99,994,247 (-)EnsemblGRCh38hg38GRCh38
GRCh376100,366,395 - 100,442,099 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 366100,474,507 - 100,548,835 (-)NCBINCBI36Build 36hg18NCBI36
Build 346100,475,364 - 100,548,844NCBI
Celera6101,011,840 - 101,086,179 (-)NCBICelera
Cytogenetic Map6q16.2NCBI
HuRef697,807,284 - 97,881,990 (-)NCBIHuRef
CHM1_16100,629,793 - 100,704,123 (-)NCBICHM1_1
T2T-CHM13v2.06101,091,896 - 101,168,099 (-)NCBIT2T-CHM13v2.0
Mchr2
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0NW_00495541125,737,220 - 25,767,225 (-)NCBIChiLan1.0ChiLan1.0
MCHR2
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v25119,958,638 - 120,034,759 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan16117,840,972 - 117,917,268 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0697,753,053 - 97,829,175 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.16101,635,774 - 101,709,401 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl6101,636,699 - 101,671,226 (-)Ensemblpanpan1.1panPan2
MCHR2
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11258,083,916 - 58,108,328 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1258,083,890 - 58,108,354 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1257,843,430 - 57,867,840 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01258,907,909 - 58,932,320 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1258,906,909 - 58,955,596 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11258,257,905 - 58,282,306 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01258,111,572 - 58,135,981 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01258,351,465 - 58,375,910 (-)NCBIUU_Cfam_GSD_1.0
Mchr2
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494692,978,312 - 93,018,329 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049366511,433,711 - 1,473,832 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049366511,434,100 - 1,473,703 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
MCHR2
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl166,837,600 - 66,877,276 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1166,837,664 - 66,856,947 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2175,563,571 - 75,602,483 (-)NCBISscrofa10.2Sscrofa10.2susScr3
MCHR2
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11373,920,940 - 73,984,381 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1373,955,513 - 73,984,213 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604046,259,642 - 46,312,776 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Mchr2
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046248105,036,578 - 5,051,451 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in MCHR2
18 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 6q16.1-16.3(chr6:97853776-102580597)x1 copy number loss See cases [RCV000052193] Chr6:97853776..102580597 [GRCh38]
Chr6:98301652..103028472 [GRCh37]
Chr6:98408373..103135165 [NCBI36]
Chr6:6q16.1-16.3
pathogenic
GRCh38/hg38 6q16.1-16.3(chr6:98668529-101266950)x1 copy number loss See cases [RCV000052194] Chr6:98668529..101266950 [GRCh38]
Chr6:99116405..101714826 [GRCh37]
Chr6:99223126..101821547 [NCBI36]
Chr6:6q16.1-16.3
pathogenic
NM_001040179.1(MCHR2):c.606G>A (p.Thr202=) single nucleotide variant Malignant melanoma [RCV000067052] Chr6:99934499 [GRCh38]
Chr6:100382375 [GRCh37]
Chr6:100489096 [NCBI36]
Chr6:6q16.2
not provided
NM_001040179.1(MCHR2):c.454C>T (p.Arg152Trp) single nucleotide variant Malignant melanoma [RCV000067053] Chr6:99943082 [GRCh38]
Chr6:100390958 [GRCh37]
Chr6:100497679 [NCBI36]
Chr6:6q16.2
not provided
NM_001040179.1(MCHR2):c.40G>A (p.Glu14Lys) single nucleotide variant Malignant melanoma [RCV000061283] Chr6:99956108 [GRCh38]
Chr6:100403984 [GRCh37]
Chr6:100510705 [NCBI36]
Chr6:6q16.2
not provided
NM_001040179.1(MCHR2):c.708-2006A>G single nucleotide variant Lung cancer [RCV000096366] Chr6:99923261 [GRCh38]
Chr6:100371137 [GRCh37]
Chr6:6q16.2
uncertain significance
GRCh38/hg38 6q16.1-16.3(chr6:97136778-102732059)x3 copy number gain See cases [RCV000139784] Chr6:97136778..102732059 [GRCh38]
Chr6:97584654..103179934 [GRCh37]
Chr6:97691375..103286627 [NCBI36]
Chr6:6q16.1-16.3
likely benign
GRCh38/hg38 6q13-24.1(chr6:74382807-142040500)x3 copy number gain See cases [RCV000139729] Chr6:74382807..142040500 [GRCh38]
Chr6:75092523..142361637 [GRCh37]
Chr6:75149243..142403330 [NCBI36]
Chr6:6q13-24.1
pathogenic
GRCh38/hg38 6q16.1-22.31(chr6:96609994-122161548)x1 copy number loss See cases [RCV000139465] Chr6:96609994..122161548 [GRCh38]
Chr6:97057870..122482694 [GRCh37]
Chr6:97164591..122524393 [NCBI36]
Chr6:6q16.1-22.31
pathogenic
GRCh38/hg38 6q16.2-16.3(chr6:99831123-100194965)x1 copy number loss See cases [RCV000143169] Chr6:99831123..100194965 [GRCh38]
Chr6:100278999..100642841 [GRCh37]
Chr6:100385720..100749562 [NCBI36]
Chr6:6q16.2-16.3
uncertain significance
GRCh38/hg38 6q16.2-16.3(chr6:99830479-100195802)x1 copy number loss See cases [RCV000143588] Chr6:99830479..100195802 [GRCh38]
Chr6:100278355..100643678 [GRCh37]
Chr6:100385076..100750399 [NCBI36]
Chr6:6q16.2-16.3
uncertain significance
GRCh37/hg19 6q15-16.3(chr6:92576950-104658245)x1 copy number loss See cases [RCV000446720] Chr6:92576950..104658245 [GRCh37]
Chr6:6q15-16.3
pathogenic
GRCh37/hg19 6q16.1-16.3(chr6:99283597-100910572)x1 copy number loss See cases [RCV000447651] Chr6:99283597..100910572 [GRCh37]
Chr6:6q16.1-16.3
uncertain significance
GRCh37/hg19 6q14.3-22.31(chr6:85988428-120548687)x1 copy number loss See cases [RCV000445666] Chr6:85988428..120548687 [GRCh37]
Chr6:6q14.3-22.31
pathogenic
GRCh37/hg19 6p25.3-q27(chr6:156975-170919482)x3 copy number gain See cases [RCV000512067] Chr6:156975..170919482 [GRCh37]
Chr6:6p25.3-q27
pathogenic
GRCh37/hg19 6p25.3-q27(chr6:156975-170919482) copy number gain See cases [RCV000510595] Chr6:156975..170919482 [GRCh37]
Chr6:6p25.3-q27
pathogenic
GRCh37/hg19 6q16.2-16.3(chr6:100278355-104929075)x1 copy number loss See cases [RCV000510294] Chr6:100278355..104929075 [GRCh37]
Chr6:6q16.2-16.3
uncertain significance
GRCh37/hg19 6q16.1-21(chr6:97384446-110247755)x1 copy number loss See cases [RCV000510703] Chr6:97384446..110247755 [GRCh37]
Chr6:6q16.1-21
pathogenic
GRCh37/hg19 6q16.2-16.3(chr6:100263899-100793037)x3 copy number gain See cases [RCV000511607] Chr6:100263899..100793037 [GRCh37]
Chr6:6q16.2-16.3
uncertain significance
NM_001040179.2(MCHR2):c.488T>A (p.Ile163Asn) single nucleotide variant Inborn genetic diseases [RCV003258548] Chr6:99943048 [GRCh38]
Chr6:100390924 [GRCh37]
Chr6:6q16.2
uncertain significance
NM_001040179.2(MCHR2):c.485T>C (p.Phe162Ser) single nucleotide variant Inborn genetic diseases [RCV003239421] Chr6:99943051 [GRCh38]
Chr6:100390927 [GRCh37]
Chr6:6q16.2
uncertain significance
NM_001040179.2(MCHR2):c.859G>T (p.Gly287Cys) single nucleotide variant Inborn genetic diseases [RCV003267049] Chr6:99921104 [GRCh38]
Chr6:100368980 [GRCh37]
Chr6:6q16.2
uncertain significance
GRCh37/hg19 6q16.1-21(chr6:94202605-109878834)x1 copy number loss See cases [RCV000512470] Chr6:94202605..109878834 [GRCh37]
Chr6:6q16.1-21
pathogenic
Single allele deletion not provided [RCV000677983] Chr6:99177111..99980698 [GRCh38]
Chr6:99624986..100428573 [GRCh37]
Chr6:6q16.2
uncertain significance
GRCh37/hg19 6q16.1-22.1(chr6:95549951-116684929)x1 copy number loss not provided [RCV000682693] Chr6:95549951..116684929 [GRCh37]
Chr6:6q16.1-22.1
pathogenic
GRCh37/hg19 6p25.3-q27(chr6:60107-171054786)x3 copy number gain not provided [RCV000745400] Chr6:60107..171054786 [GRCh37]
Chr6:6p25.3-q27
pathogenic
GRCh37/hg19 6p25.3-q27(chr6:108666-170980171)x3 copy number gain not provided [RCV000745403] Chr6:108666..170980171 [GRCh37]
Chr6:6p25.3-q27
pathogenic
GRCh37/hg19 6p25.3-q27(chr6:165632-170919470)x3 copy number gain not provided [RCV000745404] Chr6:165632..170919470 [GRCh37]
Chr6:6p25.3-q27
pathogenic
GRCh37/hg19 6q16.2(chr6:100427015-100449301)x3 copy number gain not provided [RCV000745933] Chr6:100427015..100449301 [GRCh37]
Chr6:6q16.2
benign
NM_001040179.2(MCHR2):c.419G>A (p.Arg140Gln) single nucleotide variant Inborn genetic diseases [RCV003245006] Chr6:99943117 [GRCh38]
Chr6:100390993 [GRCh37]
Chr6:6q16.2
uncertain significance
NM_001040179.2(MCHR2):c.537C>T (p.Asp179=) single nucleotide variant not provided [RCV000968095] Chr6:99942999 [GRCh38]
Chr6:100390875 [GRCh37]
Chr6:6q16.2
benign
NM_001040179.2(MCHR2):c.405C>T (p.Leu135=) single nucleotide variant not provided [RCV000915302] Chr6:99943131 [GRCh38]
Chr6:100391007 [GRCh37]
Chr6:6q16.2
likely benign
NM_001040179.2(MCHR2):c.915C>A (p.Leu305=) single nucleotide variant not provided [RCV000913558] Chr6:99921048 [GRCh38]
Chr6:100368924 [GRCh37]
Chr6:6q16.2
benign
GRCh37/hg19 6q16.1-21(chr6:96946110-106497526)x1 copy number loss not provided [RCV002472620] Chr6:96946110..106497526 [GRCh37]
Chr6:6q16.1-21
pathogenic
GRCh37/hg19 6q16.1-21(chr6:96596732-105554568)x1 copy number loss not provided [RCV002472644] Chr6:96596732..105554568 [GRCh37]
Chr6:6q16.1-21
pathogenic
GRCh37/hg19 6q16.1-21(chr6:98949950-114533905)x1 copy number loss Deletion 6q16 q21 [RCV001263224] Chr6:98949950..114533905 [GRCh37]
Chr6:6q16.1-21
pathogenic
NM_001040179.2(MCHR2):c.240G>T (p.Leu80Phe) single nucleotide variant Inborn genetic diseases [RCV003276799] Chr6:99947914 [GRCh38]
Chr6:100395790 [GRCh37]
Chr6:6q16.2
uncertain significance
GRCh37/hg19 6q15-16.3(chr6:92576950-104658245) copy number loss not specified [RCV002053599] Chr6:92576950..104658245 [GRCh37]
Chr6:6q15-16.3
pathogenic
GRCh37/hg19 6q14.3-22.31(chr6:85988428-120548687) copy number loss not specified [RCV002053595] Chr6:85988428..120548687 [GRCh37]
Chr6:6q14.3-22.31
pathogenic
GRCh37/hg19 6q15-22.2(chr6:92054891-118329651) copy number loss not specified [RCV002053598] Chr6:92054891..118329651 [GRCh37]
Chr6:6q15-22.2
pathogenic
GRCh37/hg19 6q16.2-16.3(chr6:100403323-100774188)x3 copy number gain not provided [RCV002474769] Chr6:100403323..100774188 [GRCh37]
Chr6:6q16.2-16.3
uncertain significance
NM_001040179.2(MCHR2):c.434G>A (p.Arg145Lys) single nucleotide variant Inborn genetic diseases [RCV002734178] Chr6:99943102 [GRCh38]
Chr6:100390978 [GRCh37]
Chr6:6q16.2
uncertain significance
NM_001040179.2(MCHR2):c.149T>C (p.Val50Ala) single nucleotide variant Inborn genetic diseases [RCV002907317] Chr6:99955999 [GRCh38]
Chr6:100403875 [GRCh37]
Chr6:6q16.2
uncertain significance
NM_001040179.2(MCHR2):c.272A>C (p.His91Pro) single nucleotide variant Inborn genetic diseases [RCV002818923] Chr6:99947882 [GRCh38]
Chr6:100395758 [GRCh37]
Chr6:6q16.2
uncertain significance
NM_001040179.2(MCHR2):c.59G>T (p.Trp20Leu) single nucleotide variant Inborn genetic diseases [RCV002873761] Chr6:99956089 [GRCh38]
Chr6:100403965 [GRCh37]
Chr6:6q16.2
uncertain significance
NM_001040179.2(MCHR2):c.815T>C (p.Leu272Pro) single nucleotide variant Inborn genetic diseases [RCV002849760] Chr6:99921148 [GRCh38]
Chr6:100369024 [GRCh37]
Chr6:6q16.2
uncertain significance
NM_001040179.2(MCHR2):c.157A>G (p.Ile53Val) single nucleotide variant Inborn genetic diseases [RCV002941088] Chr6:99955991 [GRCh38]
Chr6:100403867 [GRCh37]
Chr6:6q16.2
uncertain significance
NM_001040179.2(MCHR2):c.403C>T (p.Leu135Phe) single nucleotide variant Inborn genetic diseases [RCV003363963] Chr6:99943133 [GRCh38]
Chr6:100391009 [GRCh37]
Chr6:6q16.2
uncertain significance
GRCh37/hg19 6q15-21(chr6:92468126-109410569)x1 copy number loss not provided [RCV003482928] Chr6:92468126..109410569 [GRCh37]
Chr6:6q15-21
pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:475
Count of miRNA genes:373
Interacting mature miRNAs:399
Transcripts:ENST00000281806, ENST00000369212
Prediction methods: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.

Markers in Region
PMC34708P1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376100,395,711 - 100,395,827UniSTSGRCh37
Build 366100,502,432 - 100,502,548RGDNCBI36
Celera6101,039,767 - 101,039,883RGD
Cytogenetic Map6q16UniSTS
HuRef697,835,210 - 97,835,326UniSTS
PMC34708P2  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376100,382,284 - 100,382,393UniSTSGRCh37
Build 366100,489,005 - 100,489,114RGDNCBI36
Celera6101,026,339 - 101,026,448RGD
Cytogenetic Map6q16UniSTS
HuRef697,821,783 - 97,821,892UniSTS


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
High
Medium 45
Low 7 2 7 2 1 771 3 89 16 1 1
Below cutoff 777 194 155 34 170 24 334 250 1065 59 422 212 11 233 176

Sequence


RefSeq Acc Id: ENST00000281806   ⟹   ENSP00000281806
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl699,918,519 - 99,994,223 (-)Ensembl
RefSeq Acc Id: ENST00000369212   ⟹   ENSP00000358214
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl699,920,752 - 99,994,247 (-)Ensembl
RefSeq Acc Id: NM_001040179   ⟹   NP_001035269
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38699,918,519 - 99,994,223 (-)NCBI
GRCh376100,367,786 - 100,442,114 (-)ENTREZGENE
Build 366100,474,507 - 100,548,820 (-)NCBI Archive
HuRef697,807,284 - 97,881,990 (-)ENTREZGENE
CHM1_16100,629,793 - 100,704,108 (-)NCBI
T2T-CHM13v2.06101,091,896 - 101,167,918 (-)NCBI
Sequence:
RefSeq Acc Id: NM_032503   ⟹   NP_115892
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38699,918,519 - 99,994,223 (-)NCBI
GRCh376100,367,786 - 100,442,114 (-)ENTREZGENE
Build 366100,474,507 - 100,548,835 (-)NCBI Archive
HuRef697,807,284 - 97,881,990 (-)ENTREZGENE
CHM1_16100,629,793 - 100,704,123 (-)NCBI
T2T-CHM13v2.06101,091,896 - 101,167,918 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024446571   ⟹   XP_024302339
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38699,918,519 - 99,994,223 (-)NCBI
Sequence:
RefSeq Acc Id: XM_054356560   ⟹   XP_054212535
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.06101,091,896 - 101,168,099 (-)NCBI
RefSeq Acc Id: NP_115892   ⟸   NM_032503
- UniProtKB: Q6Q377 (UniProtKB/Swiss-Prot),   Q5VTV7 (UniProtKB/Swiss-Prot),   E1P5D7 (UniProtKB/Swiss-Prot),   B3KVW4 (UniProtKB/Swiss-Prot),   Q9BXA8 (UniProtKB/Swiss-Prot),   Q969V1 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001035269   ⟸   NM_001040179
- UniProtKB: Q6Q377 (UniProtKB/Swiss-Prot),   Q5VTV7 (UniProtKB/Swiss-Prot),   E1P5D7 (UniProtKB/Swiss-Prot),   B3KVW4 (UniProtKB/Swiss-Prot),   Q9BXA8 (UniProtKB/Swiss-Prot),   Q969V1 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_024302339   ⟸   XM_024446571
- Peptide Label: isoform X1
- UniProtKB: Q969V1 (UniProtKB/Swiss-Prot),   Q6Q377 (UniProtKB/Swiss-Prot),   Q5VTV7 (UniProtKB/Swiss-Prot),   E1P5D7 (UniProtKB/Swiss-Prot),   B3KVW4 (UniProtKB/Swiss-Prot),   Q9BXA8 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000281806   ⟸   ENST00000281806
RefSeq Acc Id: ENSP00000358214   ⟸   ENST00000369212
RefSeq Acc Id: XP_054212535   ⟸   XM_054356560
- Peptide Label: isoform X1
- UniProtKB: Q9BXA8 (UniProtKB/Swiss-Prot),   Q969V1 (UniProtKB/Swiss-Prot),   Q6Q377 (UniProtKB/Swiss-Prot),   Q5VTV7 (UniProtKB/Swiss-Prot),   E1P5D7 (UniProtKB/Swiss-Prot),   B3KVW4 (UniProtKB/Swiss-Prot)

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q969V1-F1-model_v2 AlphaFold Q969V1 1-340 view protein structure

Promoters
RGD ID:7208765
Promoter ID:EPDNEW_H10127
Type:initiation region
Name:MCHR2_1
Description:melanin concentrating hormone receptor 2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38699,994,195 - 99,994,255EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:20867 AgrOrtholog
COSMIC MCHR2 COSMIC
Ensembl Genes ENSG00000152034 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000281806 ENTREZGENE
  ENST00000281806.7 UniProtKB/Swiss-Prot
  ENST00000369212 ENTREZGENE
  ENST00000369212.2 UniProtKB/Swiss-Prot
Gene3D-CATH Rhodopsin 7-helix transmembrane proteins UniProtKB/Swiss-Prot
GTEx ENSG00000152034 GTEx
HGNC ID HGNC:20867 ENTREZGENE
Human Proteome Map MCHR2 Human Proteome Map
InterPro GPCR_Rhodpsn UniProtKB/Swiss-Prot
  GPCR_Rhodpsn_7TM UniProtKB/Swiss-Prot
  MCH2_receptor UniProtKB/Swiss-Prot
  MCH_rcpt UniProtKB/Swiss-Prot
KEGG Report hsa:84539 UniProtKB/Swiss-Prot
NCBI Gene 84539 ENTREZGENE
OMIM 606111 OMIM
PANTHER MELANIN CONCENTRATING HORMONE RECEPTOR 2-RELATED UniProtKB/Swiss-Prot
  NEUROPEPTIDES RECEPTOR UniProtKB/Swiss-Prot
Pfam 7tm_1 UniProtKB/Swiss-Prot
PharmGKB PA134950856 PharmGKB
PRINTS GPCRRHODOPSN UniProtKB/Swiss-Prot
  MCH2RECEPTOR UniProtKB/Swiss-Prot
  MCHRECEPTOR UniProtKB/Swiss-Prot
PROSITE G_PROTEIN_RECEP_F1_1 UniProtKB/Swiss-Prot
  G_PROTEIN_RECEP_F1_2 UniProtKB/Swiss-Prot
Superfamily-SCOP Family A G protein-coupled receptor-like UniProtKB/Swiss-Prot
UniProt B3KVW4 ENTREZGENE
  E1P5D7 ENTREZGENE
  MCHR2_HUMAN UniProtKB/Swiss-Prot
  Q5VTV7 ENTREZGENE
  Q6Q377 ENTREZGENE
  Q969V1 ENTREZGENE
  Q9BXA8 ENTREZGENE
UniProt Secondary B3KVW4 UniProtKB/Swiss-Prot
  E1P5D7 UniProtKB/Swiss-Prot
  Q5VTV7 UniProtKB/Swiss-Prot
  Q6Q377 UniProtKB/Swiss-Prot
  Q9BXA8 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-12-01 MCHR2  melanin concentrating hormone receptor 2    melanin-concentrating hormone receptor 2  Symbol and/or name change 5135510 APPROVED