Incidental Mutation 'R3155:Glrp1'
ID 263442
Institutional Source Beutler Lab
Gene Symbol Glrp1
Ensembl Gene ENSMUSG00000062310
Gene Name glutamine repeat protein 1
Synonyms GRP-1
MMRRC Submission 040606-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.080) question?
Stock # R3155 (G1)
Quality Score 124
Status Not validated
Chromosome 1
Chromosomal Location 88427593-88437788 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to A at 88430976 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamine to Histidine at position 131 (Q131H)
Ref Sequence ENSEMBL: ENSMUSP00000063883 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000067625]
AlphaFold E9Q9S8
Predicted Effect unknown
Transcript: ENSMUST00000067625
AA Change: Q131H
SMART Domains Protein: ENSMUSP00000063883
Gene: ENSMUSG00000062310
AA Change: Q131H

DomainStartEndE-ValueType
coiled coil region 26 58 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.4%
  • 20x: 95.5%
Validation Efficiency 100% (39/39)
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4933407L21Rik T C 1: 85,859,104 (GRCm39) probably benign Het
Aco1 T C 4: 40,182,915 (GRCm39) V487A probably damaging Het
Adh1 A G 3: 137,986,250 (GRCm39) E79G probably damaging Het
Aebp1 A G 11: 5,821,425 (GRCm39) N608S probably benign Het
Ahctf1 G A 1: 179,583,148 (GRCm39) R43C probably damaging Het
Ahnak A T 19: 8,987,541 (GRCm39) I2942L possibly damaging Het
Anxa9 A T 3: 95,209,716 (GRCm39) D134E probably benign Het
Ccdc14 A G 16: 34,544,222 (GRCm39) D860G probably damaging Het
Cdhr3 T A 12: 33,099,152 (GRCm39) I480F possibly damaging Het
Cldn34a C T X: 151,346,840 (GRCm39) H171Y probably benign Het
Cyp2d9 T A 15: 82,336,843 (GRCm39) probably null Het
Dmbt1 T A 7: 130,651,887 (GRCm39) Y376* probably null Het
Fancm T C 12: 65,163,195 (GRCm39) I1453T probably benign Het
Fbxw11 A G 11: 32,689,244 (GRCm39) I456V possibly damaging Het
Fut2 A T 7: 45,300,091 (GRCm39) L227Q probably damaging Het
Gbp5 T C 3: 142,208,888 (GRCm39) probably null Het
Gm6871 T C 7: 41,223,079 (GRCm39) N3S probably benign Het
H2-Eb1 C A 17: 34,533,348 (GRCm39) T190K probably damaging Het
Kdr T A 5: 76,129,065 (GRCm39) I194F probably benign Het
Klhdc7a A G 4: 139,694,500 (GRCm39) V149A probably benign Het
Lrit3 A G 3: 129,585,044 (GRCm39) F238S probably benign Het
Map10 A T 8: 126,398,313 (GRCm39) I569F possibly damaging Het
Myh6 A G 14: 55,182,125 (GRCm39) I1761T probably damaging Het
Npc1l1 A C 11: 6,171,840 (GRCm39) D874E probably benign Het
Or4k15c T C 14: 50,321,982 (GRCm39) D52G probably benign Het
Or8c17 T A 9: 38,179,836 (GRCm39) M1K probably null Het
Pawr A G 10: 108,245,370 (GRCm39) T193A probably benign Het
Ppp2r3d T C 9: 101,089,559 (GRCm39) K255E possibly damaging Het
Rbp3 A T 14: 33,679,071 (GRCm39) K1006N probably damaging Het
Rif1 GCCACCA GCCA 2: 52,000,336 (GRCm39) probably benign Het
Rin2 A G 2: 145,702,771 (GRCm39) K489R probably benign Het
Rlf A G 4: 121,006,529 (GRCm39) V817A probably damaging Het
Rusc1 T C 3: 88,999,038 (GRCm39) D248G probably benign Het
Slc15a4 A G 5: 127,681,600 (GRCm39) probably null Het
Stk4 T A 2: 163,993,663 (GRCm39) M98K probably benign Het
Taf15 T A 11: 83,393,599 (GRCm39) H307Q probably benign Het
Urgcp A T 11: 5,666,327 (GRCm39) F670L probably damaging Het
Vmn2r76 T C 7: 85,874,959 (GRCm39) T673A probably damaging Het
Zfp324 G A 7: 12,702,817 (GRCm39) M60I probably damaging Het
Other mutations in Glrp1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02890:Glrp1 APN 1 88,437,510 (GRCm39) splice site probably null
IGL02997:Glrp1 APN 1 88,437,507 (GRCm39) splice site probably benign
R1824:Glrp1 UTSW 1 88,437,511 (GRCm39) critical splice donor site probably null
R2852:Glrp1 UTSW 1 88,430,997 (GRCm39) small insertion probably benign
R3156:Glrp1 UTSW 1 88,430,976 (GRCm39) missense unknown
R4371:Glrp1 UTSW 1 88,430,997 (GRCm39) small insertion probably benign
R4471:Glrp1 UTSW 1 88,431,196 (GRCm39) missense unknown
R5183:Glrp1 UTSW 1 88,437,574 (GRCm39) missense unknown
R5206:Glrp1 UTSW 1 88,430,997 (GRCm39) small deletion probably benign
R5396:Glrp1 UTSW 1 88,431,066 (GRCm39) small deletion probably benign
R6223:Glrp1 UTSW 1 88,431,164 (GRCm39) nonsense probably null
R7019:Glrp1 UTSW 1 88,430,890 (GRCm39) missense unknown
R7209:Glrp1 UTSW 1 88,431,004 (GRCm39) missense unknown
R8514:Glrp1 UTSW 1 88,431,042 (GRCm39) small deletion probably benign
Z1177:Glrp1 UTSW 1 88,437,524 (GRCm39) missense not run
Predicted Primers PCR Primer
(F):5'- GTGGATTTTAAGTGTGGAACCC -3'
(R):5'- TGCCAAGGCTTAGCAGAAAG -3'

Sequencing Primer
(F):5'- AAGTGTGGAACCCATGTCTATG -3'
(R):5'- TGGGGATCTTAGACTAATACCCAG -3'
Posted On 2015-02-05