Incidental Mutation 'R9579:Gm5225'
ID 722480
Institutional Source Beutler Lab
Gene Symbol Gm5225
Ensembl Gene ENSMUSG00000095266
Gene Name predicted gene 5225
Synonyms
MMRRC Submission
Accession Numbers
Essential gene? Not available question?
Stock # R9579 (G1)
Quality Score 225.009
Status Not validated
Chromosome 17
Chromosomal Location 24242748-24243255 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to C at 24242897 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Histidine to Proline at position 22 (H22P)
Ref Sequence ENSEMBL: ENSMUSP00000137349 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000178572]
AlphaFold no structure available at present
Predicted Effect possibly damaging
Transcript: ENSMUST00000178572
AA Change: H22P

PolyPhen 2 Score 0.883 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000137349
Gene: ENSMUSG00000095266
AA Change: H22P

DomainStartEndE-ValueType
Pfam:AhpC-TSA 1 86 2.7e-8 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.7%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 41 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam19 C A 11: 46,009,262 (GRCm39) H229N probably benign Het
Ak9 C A 10: 41,213,576 (GRCm39) H260Q Het
Akap3 G A 6: 126,850,974 (GRCm39) V831I probably damaging Het
Arhgap45 T C 10: 79,853,843 (GRCm39) F119S probably benign Het
Best3 A G 10: 116,829,100 (GRCm39) T127A probably damaging Het
Ccdc7a G A 8: 129,774,134 (GRCm39) Q134* probably null Het
Ceacam5 C A 7: 17,479,561 (GRCm39) S226Y probably damaging Het
Creb3l1 C T 2: 91,822,231 (GRCm39) probably null Het
Cul4a G A 8: 13,186,147 (GRCm39) E450K probably damaging Het
Cyb5a A T 18: 84,891,273 (GRCm39) R89S probably benign Het
Dnah2 A G 11: 69,368,041 (GRCm39) L1766P probably damaging Het
Gbp4 T C 5: 105,270,947 (GRCm39) E228G probably damaging Het
Ghr A G 15: 3,349,612 (GRCm39) I522T probably benign Het
Herc2 T A 7: 55,758,500 (GRCm39) C796S probably damaging Het
Hmgxb4 G T 8: 75,756,638 (GRCm39) A588S probably damaging Het
Lats2 G A 14: 57,937,191 (GRCm39) P433S probably damaging Het
Lrfn1 C T 7: 28,166,769 (GRCm39) T721I probably damaging Het
Matcap1 A T 8: 106,012,379 (GRCm39) S23T probably benign Het
Mpzl3 G A 9: 44,973,350 (GRCm39) V30I probably benign Het
Or2r3 A T 6: 42,448,574 (GRCm39) C179* probably null Het
Pcdh15 A G 10: 74,457,117 (GRCm39) Y1298C possibly damaging Het
Plcd4 C A 1: 74,596,948 (GRCm39) H397N probably benign Het
Pnn G A 12: 59,117,030 (GRCm39) A201T possibly damaging Het
Ptprd C G 4: 75,872,315 (GRCm39) A1134P possibly damaging Het
Rabl3 T C 16: 37,362,230 (GRCm39) V23A probably damaging Het
Rnf157 T C 11: 116,240,822 (GRCm39) N423S probably benign Het
Rtn1 T C 12: 72,270,289 (GRCm39) D601G probably damaging Het
Rxfp1 A G 3: 79,557,946 (GRCm39) Y511H probably damaging Het
Sema5b T C 16: 35,467,582 (GRCm39) M282T probably benign Het
Slco5a1 G T 1: 12,949,383 (GRCm39) S669* probably null Het
Sphkap C G 1: 83,255,295 (GRCm39) G818A probably damaging Het
Stk26 C T X: 49,930,618 (GRCm39) probably benign Het
Syne3 T C 12: 104,942,107 (GRCm39) S12G probably damaging Het
Tmem150a C A 6: 72,334,070 (GRCm39) Q51K probably benign Het
Ttn C T 2: 76,550,196 (GRCm39) D31662N probably damaging Het
Ttn C T 2: 76,578,602 (GRCm39) G24097D probably damaging Het
Tubb4b T C 2: 25,114,139 (GRCm39) T55A probably benign Het
Vcan A T 13: 89,837,713 (GRCm39) D2610E possibly damaging Het
Xkr5 T C 8: 18,983,785 (GRCm39) T586A probably benign Het
Zfp260 T C 7: 29,805,108 (GRCm39) F336S Het
Zic1 A G 9: 91,246,790 (GRCm39) F94S probably damaging Het
Other mutations in Gm5225
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0116:Gm5225 UTSW 17 24,243,032 (GRCm39) missense probably benign 0.02
Predicted Primers PCR Primer
(F):5'- GAAGTCTGGTTGCCCACATG -3'
(R):5'- GTCCCACAGGTAGGTCATTGAC -3'

Sequencing Primer
(F):5'- TGGTTGCCCACATGTCCCG -3'
(R):5'- CATTGACTGTCATTGGCGAAGGAC -3'
Posted On 2022-08-09