Incidental Mutation 'R1648:Shc2'
ID 174039
Institutional Source Beutler Lab
Gene Symbol Shc2
Ensembl Gene ENSMUSG00000020312
Gene Name SHC (Src homology 2 domain containing) transforming protein 2
Synonyms ShcB, Sli
MMRRC Submission 039684-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R1648 (G1)
Quality Score 225
Status Validated
Chromosome 10
Chromosomal Location 79453885-79473752 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 79461945 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Leucine at position 367 (M367L)
Ref Sequence ENSEMBL: ENSMUSP00000020564 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000020564]
AlphaFold Q8BMC3
Predicted Effect probably benign
Transcript: ENSMUST00000020564
AA Change: M367L

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000020564
Gene: ENSMUSG00000020312
AA Change: M367L

DomainStartEndE-ValueType
PTB 1 154 4.43e-24 SMART
low complexity region 172 178 N/A INTRINSIC
SH2 341 420 5.81e-29 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000163867
AA Change: M367L

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000129491
Gene: ENSMUSG00000020312
AA Change: M367L

DomainStartEndE-ValueType
low complexity region 4 16 N/A INTRINSIC
low complexity region 67 85 N/A INTRINSIC
PTB 126 289 7.41e-35 SMART
low complexity region 307 313 N/A INTRINSIC
SH2 476 555 5.81e-29 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000166450
Predicted Effect noncoding transcript
Transcript: ENSMUST00000168116
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.2%
  • 10x: 95.9%
  • 20x: 91.4%
Validation Efficiency 95% (73/77)
MGI Phenotype PHENOTYPE: Mice homozygous for disruptions in this gene display sensory nerve defects related to nociception. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 71 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1110002E22Rik A G 3: 137,775,181 (GRCm39) N1457D probably benign Het
Adgb A G 10: 10,271,115 (GRCm39) F817L probably damaging Het
Akap6 A T 12: 53,188,789 (GRCm39) K2068* probably null Het
Alms1 T C 6: 85,655,384 (GRCm39) L3310P probably damaging Het
Ankrd27 T A 7: 35,303,278 (GRCm39) D219E probably benign Het
Atp10a T C 7: 58,434,575 (GRCm39) V283A probably damaging Het
Atp11a C T 8: 12,897,495 (GRCm39) S270L probably damaging Het
Casp3 T C 8: 47,091,109 (GRCm39) S254P probably benign Het
Cep104 G A 4: 154,063,553 (GRCm39) probably null Het
Cep170b C T 12: 112,702,806 (GRCm39) T423I probably damaging Het
Cfap58 A G 19: 47,943,844 (GRCm39) E348G probably benign Het
Chd6 A G 2: 160,883,978 (GRCm39) L89S probably damaging Het
Cyp2a22 T C 7: 26,631,793 (GRCm39) S488G probably damaging Het
D130040H23Rik C A 8: 69,755,633 (GRCm39) H363Q probably benign Het
Dcaf7 T A 11: 105,942,628 (GRCm39) F192I probably damaging Het
Ddx20 T C 3: 105,586,504 (GRCm39) I614V probably benign Het
Ehbp1 G A 11: 22,046,000 (GRCm39) T558I probably damaging Het
Eif2ak3 T A 6: 70,860,615 (GRCm39) V397D possibly damaging Het
Eif2b5 T C 16: 20,321,335 (GRCm39) V296A possibly damaging Het
Esr1 A G 10: 4,951,260 (GRCm39) E546G possibly damaging Het
Fras1 T A 5: 96,874,472 (GRCm39) probably null Het
G930045G22Rik T C 6: 50,823,698 (GRCm39) noncoding transcript Het
Gemin5 A T 11: 58,038,805 (GRCm39) L568* probably null Het
Gm22697+Rbm27 AGGTCCAGGCCCAGGCCCTGGTCCTGGCCCTGGCCCTGGTCCCGGCCCAGGCCC AGGTCCCGGCCCAGGCCC 18: 42,434,948 (GRCm39) probably benign Het
Gpr155 T C 2: 73,194,508 (GRCm39) probably null Het
Has1 A G 17: 18,070,247 (GRCm39) Y225H probably damaging Het
Hk3 A G 13: 55,162,274 (GRCm39) F110S probably damaging Het
Iars1 A G 13: 49,876,478 (GRCm39) K848E possibly damaging Het
Kif17 A G 4: 137,997,206 (GRCm39) Y43C probably damaging Het
Kif20b A T 19: 34,914,190 (GRCm39) T355S possibly damaging Het
Kif21a T C 15: 90,878,570 (GRCm39) T237A probably damaging Het
Klc1 T C 12: 111,743,321 (GRCm39) L216P probably damaging Het
Krt7 A C 15: 101,310,448 (GRCm39) S32R probably damaging Het
Lama3 A G 18: 12,665,256 (GRCm39) D2330G possibly damaging Het
Limch1 T A 5: 67,156,599 (GRCm39) S511R probably damaging Het
Luzp2 T A 7: 54,914,018 (GRCm39) probably null Het
Macc1 T C 12: 119,410,156 (GRCm39) M308T probably benign Het
Mroh9 T G 1: 162,873,625 (GRCm39) E510A probably damaging Het
Myo1h G T 5: 114,474,336 (GRCm39) L458F probably damaging Het
Neto1 A T 18: 86,518,179 (GRCm39) Y528F probably damaging Het
Nlrp9b T A 7: 19,760,469 (GRCm39) C187S possibly damaging Het
Nup160 T C 2: 90,540,432 (GRCm39) Y854H probably damaging Het
Odc1 T C 12: 17,598,538 (GRCm39) probably benign Het
Or10a3n A G 7: 108,492,972 (GRCm39) I214T probably damaging Het
Or51a10 A G 7: 103,699,376 (GRCm39) Y62H probably damaging Het
Or5an10 T A 19: 12,276,023 (GRCm39) I158L probably benign Het
Plcb2 A T 2: 118,554,261 (GRCm39) M64K possibly damaging Het
Plcxd3 A T 15: 4,405,291 (GRCm39) I33F probably benign Het
Postn A G 3: 54,283,522 (GRCm39) T534A probably damaging Het
Prkd2 T A 7: 16,591,732 (GRCm39) F588I possibly damaging Het
Prrg4 C A 2: 104,663,088 (GRCm39) A173S probably benign Het
Rinl C T 7: 28,497,057 (GRCm39) A519V probably damaging Het
Rpgrip1l A C 8: 91,979,517 (GRCm39) V975G probably damaging Het
Rps6ka4 C A 19: 6,816,730 (GRCm39) V118L probably benign Het
Rtkn T C 6: 83,112,975 (GRCm39) S16P probably damaging Het
Sbspon C A 1: 15,953,983 (GRCm39) R99L probably damaging Het
Sdf4 G A 4: 156,083,886 (GRCm39) A119T probably damaging Het
Sgpp1 T A 12: 75,762,990 (GRCm39) H397L possibly damaging Het
Slc26a5 T A 5: 22,018,974 (GRCm39) K590* probably null Het
Slc39a12 T C 2: 14,456,803 (GRCm39) V597A probably benign Het
Smcp A T 3: 92,491,788 (GRCm39) C20S unknown Het
Tdrd6 A C 17: 43,938,000 (GRCm39) V1016G possibly damaging Het
Tmem132c T A 5: 127,540,120 (GRCm39) probably benign Het
Tmem170b A T 13: 41,759,738 (GRCm39) Q16L probably null Het
Tmem30a A G 9: 79,700,311 (GRCm39) F61S probably damaging Het
Tnfsf13b T C 8: 10,081,534 (GRCm39) M232T probably damaging Het
Trip11 T A 12: 101,850,651 (GRCm39) K853* probably null Het
Tusc3 C A 8: 39,513,721 (GRCm39) S64* probably null Het
Vmn2r111 A T 17: 22,788,042 (GRCm39) D436E probably benign Het
Zfp607a T C 7: 27,578,493 (GRCm39) V521A probably benign Het
Zfp704 A T 3: 9,536,099 (GRCm39) S140R probably damaging Het
Other mutations in Shc2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00341:Shc2 APN 10 79,456,903 (GRCm39) missense probably damaging 1.00
IGL01586:Shc2 APN 10 79,458,138 (GRCm39) missense probably damaging 0.99
IGL01965:Shc2 APN 10 79,463,023 (GRCm39) splice site probably benign
IGL02149:Shc2 APN 10 79,458,102 (GRCm39) missense probably damaging 1.00
IGL02252:Shc2 APN 10 79,462,204 (GRCm39) missense probably benign 0.00
shrine UTSW 10 79,465,751 (GRCm39) missense probably damaging 0.99
R0538:Shc2 UTSW 10 79,465,974 (GRCm39) splice site probably benign
R0630:Shc2 UTSW 10 79,461,975 (GRCm39) splice site probably null
R0894:Shc2 UTSW 10 79,465,751 (GRCm39) missense probably damaging 0.99
R1166:Shc2 UTSW 10 79,456,946 (GRCm39) missense probably damaging 1.00
R1339:Shc2 UTSW 10 79,462,250 (GRCm39) missense probably benign 0.00
R1465:Shc2 UTSW 10 79,467,136 (GRCm39) missense probably damaging 1.00
R1465:Shc2 UTSW 10 79,467,136 (GRCm39) missense probably damaging 1.00
R1647:Shc2 UTSW 10 79,461,945 (GRCm39) missense probably benign
R1959:Shc2 UTSW 10 79,462,625 (GRCm39) splice site probably null
R3800:Shc2 UTSW 10 79,462,707 (GRCm39) missense probably benign 0.40
R4603:Shc2 UTSW 10 79,459,690 (GRCm39) missense probably benign 0.03
R4635:Shc2 UTSW 10 79,462,120 (GRCm39) missense probably benign 0.35
R4656:Shc2 UTSW 10 79,457,003 (GRCm39) missense probably damaging 1.00
R4715:Shc2 UTSW 10 79,458,213 (GRCm39) missense probably benign 0.01
R4841:Shc2 UTSW 10 79,458,295 (GRCm39) missense probably damaging 0.98
R4842:Shc2 UTSW 10 79,458,295 (GRCm39) missense probably damaging 0.98
R5057:Shc2 UTSW 10 79,459,706 (GRCm39) missense probably benign 0.01
R5394:Shc2 UTSW 10 79,465,933 (GRCm39) missense probably damaging 1.00
R6153:Shc2 UTSW 10 79,465,752 (GRCm39) missense possibly damaging 0.90
R6160:Shc2 UTSW 10 79,462,853 (GRCm39) critical splice donor site probably null
R6178:Shc2 UTSW 10 79,465,954 (GRCm39) missense probably damaging 1.00
R8773:Shc2 UTSW 10 79,456,924 (GRCm39) missense probably damaging 1.00
R8824:Shc2 UTSW 10 79,473,536 (GRCm39) missense probably benign
R8841:Shc2 UTSW 10 79,458,150 (GRCm39) missense probably damaging 1.00
R9081:Shc2 UTSW 10 79,462,762 (GRCm39) critical splice acceptor site probably null
Predicted Primers PCR Primer
(F):5'- ACACACAGTGCTTCACTGGGAAC -3'
(R):5'- GCTCTAACGTACATGCCTTGCTCTG -3'

Sequencing Primer
(F):5'- AACAGGGTGGAGCCTGC -3'
(R):5'- AGATGATGACGCTGCTGC -3'
Posted On 2014-04-24