Incidental Mutation 'R9142:Gm9736'
ID 694403
Institutional Source Beutler Lab
Gene Symbol Gm9736
Ensembl Gene ENSMUSG00000112380
Gene Name predicted gene 9736
Synonyms
MMRRC Submission 068934-MU
Accession Numbers
Essential gene? Not available question?
Stock # R9142 (G1)
Quality Score 225.009
Status Validated
Chromosome 10
Chromosomal Location 77586355-77587188 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 77586849 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Cysteine to Arginine at position 114 (C114R)
Ref Sequence ENSEMBL: ENSMUSP00000151736 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000092366] [ENSMUST00000219969]
AlphaFold A0A1W2P7N1
Predicted Effect probably benign
Transcript: ENSMUST00000092366
SMART Domains Protein: ENSMUSP00000090020
Gene: ENSMUSG00000069581

DomainStartEndE-ValueType
Blast:TSPN 1 71 8e-40 BLAST
SCOP:d1c4ra_ 2 67 2e-7 SMART
low complexity region 190 200 N/A INTRINSIC
Pfam:EPTP 208 255 2.6e-22 PFAM
Pfam:EPTP 260 307 1.4e-21 PFAM
Pfam:EPTP 312 359 8.9e-14 PFAM
Pfam:EPTP 362 417 6.2e-13 PFAM
Pfam:EPTP 422 469 1.3e-20 PFAM
Predicted Effect unknown
Transcript: ENSMUST00000219969
AA Change: C114R
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency 100% (64/64)
Allele List at MGI
Other mutations in this stock
Total: 68 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adprs C A 4: 126,215,360 (GRCm39) G35V probably damaging Het
Apob A C 12: 8,062,705 (GRCm39) D3729A possibly damaging Het
App G A 16: 84,900,127 (GRCm39) H108Y probably damaging Het
Arap3 G A 18: 38,112,934 (GRCm39) A1092V possibly damaging Het
Arid3a T C 10: 79,787,612 (GRCm39) S550P unknown Het
Armc2 T G 10: 41,851,404 (GRCm39) E259D probably benign Het
Atp13a2 A G 4: 140,729,364 (GRCm39) D566G probably damaging Het
Bnc2 A G 4: 84,474,111 (GRCm39) C12R probably benign Het
Btbd16 C T 7: 130,417,516 (GRCm39) R344C probably damaging Het
Cc2d2b C T 19: 40,753,845 (GRCm39) R123* probably null Het
Cdc37l1 T A 19: 28,989,402 (GRCm39) H286Q possibly damaging Het
Cfap54 A T 10: 92,820,097 (GRCm39) L1239Q possibly damaging Het
Cfap58 T C 19: 47,974,993 (GRCm39) probably null Het
Col6a3 A T 1: 90,706,566 (GRCm39) D2789E unknown Het
Ctnna2 G T 6: 76,879,423 (GRCm39) probably benign Het
Dazl A G 17: 50,590,178 (GRCm39) V271A probably benign Het
Dennd4c A T 4: 86,755,637 (GRCm39) N1610Y probably benign Het
Dusp13b T A 14: 21,792,756 (GRCm39) K56N probably benign Het
Erbb2 T A 11: 98,312,884 (GRCm39) I149N probably damaging Het
Erbb4 A T 1: 68,388,552 (GRCm39) C217S probably damaging Het
Fbxw21 A G 9: 108,985,413 (GRCm39) C122R probably damaging Het
Fktn G A 4: 53,734,854 (GRCm39) G125D probably benign Het
Foxm1 T A 6: 128,344,298 (GRCm39) I182N probably damaging Het
Ggnbp2 T C 11: 84,730,886 (GRCm39) N381S possibly damaging Het
Gja3 T C 14: 57,274,048 (GRCm39) E108G probably benign Het
Gm40460 C A 7: 141,794,499 (GRCm39) G106V unknown Het
Gpbp1 A T 13: 111,563,033 (GRCm39) D492E unknown Het
Gper1 T C 5: 139,412,312 (GRCm39) V219A possibly damaging Het
Gtf2e1 C T 16: 37,356,364 (GRCm39) R56Q probably benign Het
H2ac10 T C 13: 23,718,151 (GRCm39) L24P probably damaging Het
Ide T C 19: 37,307,898 (GRCm39) N38S Het
Kat6a T A 8: 23,430,072 (GRCm39) M1809K unknown Het
Kdm2b A T 5: 123,127,112 (GRCm39) probably benign Het
Kif7 A T 7: 79,356,585 (GRCm39) M702K probably benign Het
Lrrtm4 T A 6: 79,999,426 (GRCm39) N279K probably damaging Het
Mcrip1 G A 11: 120,435,542 (GRCm39) P31L probably damaging Het
Mettl25b A G 3: 87,831,195 (GRCm39) I444T probably benign Het
Nf1 T A 11: 79,362,315 (GRCm39) S1497R probably damaging Het
Nf1 T A 11: 79,366,688 (GRCm39) I1607N probably damaging Het
Nrde2 G T 12: 100,117,518 (GRCm39) T47K probably benign Het
Or5w12 C T 2: 87,502,313 (GRCm39) V133I probably benign Het
Or6b2b T G 1: 92,419,411 (GRCm39) E22A probably benign Het
Or6c1 T C 10: 129,518,285 (GRCm39) T108A probably benign Het
Ppargc1a G A 5: 51,652,146 (GRCm39) T184I possibly damaging Het
Ppp1r15a T C 7: 45,173,920 (GRCm39) D296G probably damaging Het
Prl7c1 C T 13: 27,964,751 (GRCm39) probably benign Het
Prss42 G T 9: 110,628,228 (GRCm39) R124L possibly damaging Het
Psmd1 T G 1: 86,064,817 (GRCm39) Y950D probably damaging Het
Ptprr A T 10: 116,024,119 (GRCm39) L250F possibly damaging Het
Rabgef1 T A 5: 130,237,554 (GRCm39) M208K possibly damaging Het
Rps6ka2 A G 17: 7,437,793 (GRCm39) Y17C probably damaging Het
Scart2 T A 7: 139,877,806 (GRCm39) D929E probably damaging Het
Sec23ip T A 7: 128,363,226 (GRCm39) C463S probably damaging Het
Serpina3n A G 12: 104,379,710 (GRCm39) T368A probably damaging Het
Sez6l C T 5: 112,609,083 (GRCm39) A589T probably benign Het
Smok2b G A 17: 13,453,637 (GRCm39) probably null Het
Spag5 T A 11: 78,192,823 (GRCm39) Y52N possibly damaging Het
Tenm3 G A 8: 48,788,548 (GRCm39) S494L unknown Het
Top3b T C 16: 16,701,299 (GRCm39) Y204H probably damaging Het
Trim43b C T 9: 88,973,452 (GRCm39) V94M possibly damaging Het
Trps1 T G 15: 50,524,658 (GRCm39) I1091L probably damaging Het
Ttk G A 9: 83,725,741 (GRCm39) R221Q probably damaging Het
Ttn A C 2: 76,549,466 (GRCm39) M31737R probably damaging Het
Uso1 T A 5: 92,335,125 (GRCm39) L495* probably null Het
Usp19 A G 9: 108,372,284 (GRCm39) D447G possibly damaging Het
Zdhhc2 A G 8: 40,920,563 (GRCm39) E274G probably damaging Het
Zfp106 T A 2: 120,350,935 (GRCm39) Y1595F probably damaging Het
Zfp932 A T 5: 110,157,520 (GRCm39) H406L probably damaging Het
Other mutations in Gm9736
AlleleSourceChrCoordTypePredicted EffectPPH Score
R7101:Gm9736 UTSW 10 77,587,167 (GRCm39) missense unknown
R8422:Gm9736 UTSW 10 77,586,714 (GRCm39) missense unknown
R9349:Gm9736 UTSW 10 77,586,393 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- TTGACAGCATGAGGACTGG -3'
(R):5'- CATGTCTGTCTGCTCTGACG -3'

Sequencing Primer
(F):5'- CATGAGGACTGGCAGCTAGAC -3'
(R):5'- ATGACTGCCCAGAGAGCTG -3'
Posted On 2022-01-20