Incidental Mutation 'R7332:Mas1'
ID 569325
Institutional Source Beutler Lab
Gene Symbol Mas1
Ensembl Gene ENSMUSG00000068037
Gene Name MAS1 oncogene
Synonyms Mas receptor, Mas-1, MasR
MMRRC Submission 045425-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R7332 (G1)
Quality Score 225.009
Status Validated
Chromosome 17
Chromosomal Location 13059966-13087030 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 13061106 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 106 (T106A)
Ref Sequence ENSEMBL: ENSMUSP00000086409 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000089015] [ENSMUST00000159223] [ENSMUST00000159865] [ENSMUST00000161747] [ENSMUST00000162119] [ENSMUST00000162333] [ENSMUST00000162389] [ENSMUST00000165020] [ENSMUST00000167152]
AlphaFold P30554
Predicted Effect probably benign
Transcript: ENSMUST00000089015
AA Change: T106A

PolyPhen 2 Score 0.174 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000086409
Gene: ENSMUSG00000068037
AA Change: T106A

DomainStartEndE-ValueType
Pfam:7TM_GPCR_Srx 39 227 3.6e-7 PFAM
Pfam:7tm_1 48 279 3.1e-23 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000159223
SMART Domains Protein: ENSMUSP00000124295
Gene: ENSMUSG00000068037

DomainStartEndE-ValueType
transmembrane domain 36 58 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000159865
Predicted Effect probably benign
Transcript: ENSMUST00000161747
AA Change: T106A

PolyPhen 2 Score 0.174 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000123902
Gene: ENSMUSG00000068037
AA Change: T106A

DomainStartEndE-ValueType
Pfam:7TM_GPCR_Srx 39 227 3.6e-7 PFAM
Pfam:7tm_1 48 279 3.1e-23 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000162119
AA Change: T106A

PolyPhen 2 Score 0.174 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000124952
Gene: ENSMUSG00000068037
AA Change: T106A

DomainStartEndE-ValueType
SCOP:d1l9ha_ 31 92 1e-5 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000162333
AA Change: T106A

PolyPhen 2 Score 0.174 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000125108
Gene: ENSMUSG00000068037
AA Change: T106A

DomainStartEndE-ValueType
Pfam:7TM_GPCR_Srx 39 226 2.6e-7 PFAM
Pfam:7tm_1 48 279 5.7e-16 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000162389
SMART Domains Protein: ENSMUSP00000124879
Gene: ENSMUSG00000068037

DomainStartEndE-ValueType
SCOP:d1l9ha_ 31 76 1e-4 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000165020
AA Change: T106A

PolyPhen 2 Score 0.174 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000132300
Gene: ENSMUSG00000068037
AA Change: T106A

DomainStartEndE-ValueType
Pfam:7TM_GPCR_Srx 39 227 3.6e-7 PFAM
Pfam:7tm_1 48 279 3.1e-23 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000167152
AA Change: T106A

PolyPhen 2 Score 0.174 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000131341
Gene: ENSMUSG00000068037
AA Change: T106A

DomainStartEndE-ValueType
Pfam:7TM_GPCR_Srx 39 227 3.6e-7 PFAM
Pfam:7tm_1 48 279 3.1e-23 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency 100% (68/68)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a class I seven-transmembrane G-protein-coupled receptor. The encoded protein is a receptor for angiotensin-(1-7) and preferentially couples to the Gq protein, activating the phospholipase C signaling pathway. The encoded protein may play a role in multiple processes including hypotension, smooth muscle relaxation and cardioprotection by mediating the effects of angiotensin-(1-7). [provided by RefSeq, May 2012]
PHENOTYPE: Mice homozygous for disruptions in this gene show enhanced long term potentiation and higher levels of anxiety. They are otherwise normal and fertile. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 67 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Afap1l2 A G 19: 56,906,553 (GRCm39) S449P probably damaging Het
Atp6v0c A C 17: 24,388,198 (GRCm39) S21A probably benign Het
Cacna1e T C 1: 154,601,547 (GRCm39) Y40C possibly damaging Het
Cdadc1 A G 14: 59,813,213 (GRCm39) I398T possibly damaging Het
Cfap44 T A 16: 44,250,191 (GRCm39) D756E probably damaging Het
Clcnkb A T 4: 141,141,243 (GRCm39) L104Q probably null Het
Clk1 G A 1: 58,451,853 (GRCm39) H421Y probably benign Het
Cmpk2 A T 12: 26,528,061 (GRCm39) D426V probably damaging Het
Cmya5 A G 13: 93,229,061 (GRCm39) L2009S possibly damaging Het
Col5a2 C G 1: 45,419,325 (GRCm39) D1252H probably damaging Het
Coro1b A G 19: 4,199,356 (GRCm39) K5R probably benign Het
Csmd2 A G 4: 128,313,360 (GRCm39) T1346A Het
Csrp1 G T 1: 135,667,149 (GRCm39) W4L probably benign Het
Cyp3a25 A G 5: 145,929,817 (GRCm39) I184T probably damaging Het
Egfl7 C A 2: 26,480,725 (GRCm39) R128S probably benign Het
Fggy A T 4: 95,511,719 (GRCm39) N157I probably damaging Het
Gldc A T 19: 30,093,926 (GRCm39) L697Q probably damaging Het
Gm4952 T A 19: 12,604,373 (GRCm39) Y262N probably damaging Het
Gsap T A 5: 21,495,119 (GRCm39) M821K probably benign Het
Hps1 T C 19: 42,766,351 (GRCm39) probably null Het
Hsbp1l1 T C 18: 80,280,038 (GRCm39) probably benign Het
Igfbp7 G A 5: 77,499,803 (GRCm39) T220I probably damaging Het
Ints3 T C 3: 90,322,819 (GRCm39) Q137R probably damaging Het
Kcna6 A G 6: 126,716,292 (GRCm39) F199S possibly damaging Het
Kirrel1 T C 3: 86,995,705 (GRCm39) I410V probably benign Het
Llgl2 T C 11: 115,739,125 (GRCm39) V332A probably damaging Het
Lrrc27 A G 7: 138,822,661 (GRCm39) I517M probably damaging Het
Mast4 T A 13: 102,887,932 (GRCm39) Y1159F possibly damaging Het
Mmp2 A G 8: 93,576,780 (GRCm39) D601G probably damaging Het
Mycbp2 T A 14: 103,434,793 (GRCm39) I2217F probably damaging Het
Mycbp2 A G 14: 103,393,889 (GRCm39) S2891P probably damaging Het
Naip6 A G 13: 100,437,209 (GRCm39) V438A possibly damaging Het
Or4g17 A G 2: 111,209,738 (GRCm39) H131R not run Het
Pdf T C 8: 107,775,173 (GRCm39) R20G probably benign Het
Pfdn2 T C 1: 171,184,162 (GRCm39) L47P probably damaging Het
Pik3c2g C A 6: 139,841,981 (GRCm39) N795K Het
Ppip5k1 A T 2: 121,142,450 (GRCm39) V1333D probably damaging Het
Pramel51 T C 12: 88,143,187 (GRCm39) T339A possibly damaging Het
Prss44 A T 9: 110,644,530 (GRCm39) I213F probably damaging Het
Rbm47 A G 5: 66,183,557 (GRCm39) Y349H probably damaging Het
Rcl1 A T 19: 29,108,096 (GRCm39) T253S probably benign Het
Rdh1 A G 10: 127,595,754 (GRCm39) probably benign Het
Scn7a C T 2: 66,522,898 (GRCm39) W935* probably null Het
Sec24b T C 3: 129,835,042 (GRCm39) N52S probably benign Het
Serpinb5 A T 1: 106,800,091 (GRCm39) I94L probably benign Het
Setx T C 2: 29,036,638 (GRCm39) V1041A probably benign Het
Slco3a1 G A 7: 73,968,232 (GRCm39) A496V possibly damaging Het
Spag5 T A 11: 78,204,205 (GRCm39) L486* probably null Het
Spink5 T C 18: 44,115,317 (GRCm39) I183T probably damaging Het
Srd5a1 T C 13: 69,759,173 (GRCm39) Y65C probably benign Het
Ssh2 T A 11: 77,344,349 (GRCm39) I778N possibly damaging Het
Sstr1 C T 12: 58,260,172 (GRCm39) S265L probably damaging Het
Syne2 T A 12: 76,014,529 (GRCm39) probably null Het
Tctn1 A T 5: 122,399,547 (GRCm39) D92E probably damaging Het
Tiam2 A G 17: 3,503,644 (GRCm39) I940M probably damaging Het
Tmeff2 T C 1: 51,018,599 (GRCm39) W194R unknown Het
Tomm20 T C 8: 127,663,903 (GRCm39) T94A probably benign Het
Ucn2 A G 9: 108,815,532 (GRCm39) N98S probably benign Het
V1rd19 A T 7: 23,702,743 (GRCm39) I70L probably benign Het
Vmn1r18 A G 6: 57,367,503 (GRCm39) L17P probably benign Het
Vmn2r61 A G 7: 41,909,534 (GRCm39) T20A probably benign Het
Wdr59 G A 8: 112,220,986 (GRCm39) T182I Het
Zfp40 A T 17: 23,395,155 (GRCm39) C477* probably null Het
Zfp68 A G 5: 138,604,830 (GRCm39) S498P possibly damaging Het
Zfp729b T C 13: 67,757,755 (GRCm39) probably null Het
Zfp846 T G 9: 20,505,521 (GRCm39) N460K probably benign Het
Zim1 T C 7: 6,680,352 (GRCm39) Y437C probably damaging Het
Other mutations in Mas1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00230:Mas1 APN 17 13,060,877 (GRCm39) missense probably benign 0.00
IGL00583:Mas1 APN 17 13,060,852 (GRCm39) missense possibly damaging 0.69
IGL01805:Mas1 APN 17 13,061,117 (GRCm39) missense probably damaging 1.00
IGL03263:Mas1 APN 17 13,060,451 (GRCm39) missense possibly damaging 0.83
R0732:Mas1 UTSW 17 13,060,634 (GRCm39) missense probably benign 0.17
R1768:Mas1 UTSW 17 13,060,586 (GRCm39) missense probably damaging 1.00
R1872:Mas1 UTSW 17 13,061,078 (GRCm39) missense probably damaging 1.00
R1967:Mas1 UTSW 17 13,060,923 (GRCm39) missense probably benign 0.00
R2032:Mas1 UTSW 17 13,061,457 (GRCm39) splice site probably benign
R3851:Mas1 UTSW 17 13,060,880 (GRCm39) missense probably benign 0.01
R4120:Mas1 UTSW 17 13,061,233 (GRCm39) missense probably damaging 1.00
R7113:Mas1 UTSW 17 13,061,324 (GRCm39) missense probably benign 0.00
R7297:Mas1 UTSW 17 13,060,745 (GRCm39) missense probably damaging 1.00
R7787:Mas1 UTSW 17 13,061,374 (GRCm39) missense possibly damaging 0.94
R9072:Mas1 UTSW 17 13,060,839 (GRCm39) missense possibly damaging 0.66
R9622:Mas1 UTSW 17 13,060,898 (GRCm39) missense probably benign
Predicted Primers PCR Primer
(F):5'- GACATACTCCATGGTGGTCAC -3'
(R):5'- CTGGGTCATCATGAGCATCTCC -3'

Sequencing Primer
(F):5'- TGGTCACCAAGCACGAAAG -3'
(R):5'- CTTTGTGGAGAATGGGATCCTCCTC -3'
Posted On 2019-09-13