Incidental Mutation 'R4865:Grp'
ID 374878
Institutional Source Beutler Lab
Gene Symbol Grp
Ensembl Gene ENSMUSG00000024517
Gene Name gastrin releasing peptide
Synonyms BLP
MMRRC Submission 042475-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R4865 (G1)
Quality Score 225
Status Validated
Chromosome 18
Chromosomal Location 66005891-66019667 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 66013041 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Valine at position 69 (D69V)
Ref Sequence ENSEMBL: ENSMUSP00000133437 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000025395] [ENSMUST00000173530] [ENSMUST00000173985]
AlphaFold Q8R1I2
Predicted Effect probably damaging
Transcript: ENSMUST00000025395
AA Change: D69V

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000025395
Gene: ENSMUSG00000024517
AA Change: D69V

DomainStartEndE-ValueType
signal peptide 1 23 N/A INTRINSIC
Pfam:Bombesin 43 56 9.1e-10 PFAM
low complexity region 82 95 N/A INTRINSIC
low complexity region 98 112 N/A INTRINSIC
Predicted Effect probably damaging
Transcript: ENSMUST00000173530
AA Change: D69V

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000139014
Gene: ENSMUSG00000024517
AA Change: D69V

DomainStartEndE-ValueType
signal peptide 1 23 N/A INTRINSIC
Pfam:Bombesin 43 56 1.2e-11 PFAM
low complexity region 82 95 N/A INTRINSIC
low complexity region 98 112 N/A INTRINSIC
Predicted Effect probably damaging
Transcript: ENSMUST00000173985
AA Change: D69V

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000133437
Gene: ENSMUSG00000024517
AA Change: D69V

DomainStartEndE-ValueType
signal peptide 1 23 N/A INTRINSIC
Pfam:Bombesin 43 56 3.5e-11 PFAM
low complexity region 82 95 N/A INTRINSIC
low complexity region 98 112 N/A INTRINSIC
Meta Mutation Damage Score 0.6467 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 97.0%
  • 20x: 94.4%
Validation Efficiency 98% (86/88)
MGI Phenotype FUNCTION: This gene encodes a neuropeptide hormone that affects various biological processes such as neuroendocrine regulation, gastrointestinal secretion, nociception, cell proliferation and inflammation. The encoded protein undergoes proteolytic processing to generate multiple mature peptides with biological activity. [provided by RefSeq, Aug 2015]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit attenuated scratching response to chloroquine, SLIGRL and BAM8-22. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 79 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ablim3 C T 18: 61,938,157 (GRCm39) V639M probably damaging Het
Adgrf4 A G 17: 42,978,156 (GRCm39) S396P probably damaging Het
Aldh3b2 T A 19: 4,028,469 (GRCm39) I123N probably damaging Het
Aldh5a1 A G 13: 25,095,567 (GRCm39) Y517H probably damaging Het
Aph1c A C 9: 66,735,120 (GRCm39) I77S probably damaging Het
Armc8 A G 9: 99,408,942 (GRCm39) probably null Het
Atp13a5 G A 16: 29,066,912 (GRCm39) P1020L probably damaging Het
BC024139 A T 15: 76,010,266 (GRCm39) M80K possibly damaging Het
Cdk5rap1 C T 2: 154,212,876 (GRCm39) probably null Het
Cenpn A G 8: 117,661,512 (GRCm39) I204V probably damaging Het
Ces4a A T 8: 105,873,790 (GRCm39) M420L probably benign Het
Chdh T A 14: 29,755,681 (GRCm39) D322E probably benign Het
Clcn6 A T 4: 148,104,223 (GRCm39) I223N probably damaging Het
Clec4b1 A G 6: 123,045,428 (GRCm39) K50E possibly damaging Het
Creg1 T A 1: 165,597,432 (GRCm39) C135* probably null Het
Cyp4f13 C T 17: 33,144,678 (GRCm39) R411Q probably damaging Het
Dnah7b T C 1: 46,234,234 (GRCm39) F1426L probably damaging Het
Dock9 A T 14: 121,780,917 (GRCm39) *1917R probably null Het
Dync1h1 T G 12: 110,606,235 (GRCm39) L2435R possibly damaging Het
Eif3l C A 15: 78,965,849 (GRCm39) Y166* probably null Het
Emilin1 T A 5: 31,075,128 (GRCm39) N456K possibly damaging Het
Fam83f C T 15: 80,576,650 (GRCm39) R434C probably damaging Het
Fbxw9 A G 8: 85,786,785 (GRCm39) D10G possibly damaging Het
Flt1 C A 5: 147,620,749 (GRCm39) A132S probably benign Het
Fsip2 T G 2: 82,821,295 (GRCm39) V5676G possibly damaging Het
Gas2l3 CACTCGTCATACT CACT 10: 89,266,820 (GRCm39) probably benign Het
Gm11596 A G 11: 99,684,064 (GRCm39) probably benign Het
Gm6522 T C 3: 106,183,286 (GRCm39) noncoding transcript Het
Gm6728 A G 6: 136,464,072 (GRCm39) noncoding transcript Het
Gria4 T A 9: 4,464,295 (GRCm39) I556F possibly damaging Het
Gucy1a1 G T 3: 82,026,469 (GRCm39) probably benign Het
Haus5 A T 7: 30,357,980 (GRCm39) L376Q probably damaging Het
Ifne A T 4: 88,797,942 (GRCm39) Y159N probably damaging Het
Ift80 A G 3: 68,898,092 (GRCm39) V81A probably benign Het
Inpp5b T C 4: 124,645,288 (GRCm39) V192A probably benign Het
Kcnh4 A G 11: 100,640,569 (GRCm39) S486P probably damaging Het
Kif5b A G 18: 6,222,912 (GRCm39) probably benign Het
Macf1 T A 4: 123,327,096 (GRCm39) E4800D probably damaging Het
Mblac2 C T 13: 81,860,095 (GRCm39) Q150* probably null Het
Mc1r A T 8: 124,134,255 (GRCm39) T3S probably benign Het
Med17 G A 9: 15,176,668 (GRCm39) Q70* probably null Het
Myocd A T 11: 65,069,856 (GRCm39) probably null Het
Nphp3 T C 9: 103,909,169 (GRCm39) L793P probably benign Het
Or1ad1 A G 11: 50,876,370 (GRCm39) T281A probably damaging Het
Or2m13 A T 16: 19,226,051 (GRCm39) F238L probably damaging Het
Or4a68 T G 2: 89,270,003 (GRCm39) T207P possibly damaging Het
Or5an10 T C 19: 12,275,944 (GRCm39) D184G probably damaging Het
Or5ap2 T A 2: 85,680,060 (GRCm39) M88K probably damaging Het
Or8c13 T A 9: 38,091,196 (GRCm39) T308S possibly damaging Het
Piezo1 A T 8: 123,213,660 (GRCm39) L1745Q probably damaging Het
Prdm10 T A 9: 31,258,376 (GRCm39) H600Q probably damaging Het
Psapl1 C A 5: 36,362,211 (GRCm39) L268M probably damaging Het
Psg23 T C 7: 18,346,039 (GRCm39) I219V probably benign Het
Rexo5 A T 7: 119,400,553 (GRCm39) R113* probably null Het
Rgs22 A T 15: 36,100,358 (GRCm39) I243N probably damaging Het
Rhbdf1 G A 11: 32,164,517 (GRCm39) T183I probably damaging Het
Rhobtb1 T C 10: 69,106,554 (GRCm39) M373T probably benign Het
Ros1 G T 10: 52,048,966 (GRCm39) A88E probably damaging Het
Sdr16c6 A G 4: 4,058,834 (GRCm39) F251L probably benign Het
Skil A G 3: 31,167,562 (GRCm39) Y398C probably damaging Het
Slc22a3 A T 17: 12,683,419 (GRCm39) M148K probably benign Het
Slco4c1 G A 1: 96,768,953 (GRCm39) P303L probably damaging Het
Sntn A T 14: 13,679,103 (GRCm38) K92N probably benign Het
Spry4 A T 18: 38,722,876 (GRCm39) S296T probably benign Het
St8sia1 A G 6: 142,774,796 (GRCm39) F261S probably damaging Het
Stab2 C T 10: 86,679,364 (GRCm39) probably null Het
Stk24 A T 14: 121,530,866 (GRCm39) C363* probably null Het
Tank G A 2: 61,408,979 (GRCm39) probably benign Het
Tmem67 T C 4: 12,070,262 (GRCm39) N387S probably benign Het
Treml1 A T 17: 48,673,885 (GRCm39) I304L probably benign Het
Trim13 A G 14: 61,842,966 (GRCm39) I328V probably benign Het
Upk2 A G 9: 44,365,382 (GRCm39) V62A probably damaging Het
Urb2 A T 8: 124,756,374 (GRCm39) K694* probably null Het
Vmn2r17 C A 5: 109,574,985 (GRCm39) N97K probably damaging Het
Vmn2r57 A T 7: 41,049,892 (GRCm39) V619D probably damaging Het
Vmn2r92 G A 17: 18,387,634 (GRCm39) R213Q probably benign Het
Wnt6 G A 1: 74,821,788 (GRCm39) C123Y probably damaging Het
Zfp292 A G 4: 34,819,563 (GRCm39) I253T probably damaging Het
Zfp52 C T 17: 21,781,505 (GRCm39) S451L probably damaging Het
Other mutations in Grp
AlleleSourceChrCoordTypePredicted EffectPPH Score
PIT4362001:Grp UTSW 18 66,019,297 (GRCm39) missense probably benign 0.18
R0584:Grp UTSW 18 66,006,766 (GRCm39) missense possibly damaging 0.79
R1144:Grp UTSW 18 66,013,041 (GRCm39) missense probably damaging 0.99
R5085:Grp UTSW 18 66,013,230 (GRCm39) missense probably benign
R6084:Grp UTSW 18 66,013,008 (GRCm39) missense probably damaging 0.99
R6198:Grp UTSW 18 66,013,057 (GRCm39) missense possibly damaging 0.96
R6325:Grp UTSW 18 66,006,824 (GRCm39) critical splice donor site probably null
Predicted Primers PCR Primer
(F):5'- AGCAGAGCCCATGTGTTGTG -3'
(R):5'- AACGTCGTTAAAGTAGCTGCCG -3'

Sequencing Primer
(F):5'- CATGTGTTGTGTATAGCCCAAC -3'
(R):5'- GTTAAAGTAGCTGCCGTCCTCG -3'
Posted On 2016-03-17