Incidental Mutation 'R9266:Psg28'
ID 702543
Institutional Source Beutler Lab
Gene Symbol Psg28
Ensembl Gene ENSMUSG00000030373
Gene Name pregnancy-specific beta-1-glycoprotein 28
Synonyms
MMRRC Submission
Accession Numbers
Essential gene? Probably non essential (E-score: 0.085) question?
Stock # R9266 (G1)
Quality Score 225.009
Status Not validated
Chromosome 7
Chromosomal Location 18156461-18165966 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to G at 18161752 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Leucine to Phenylalanine at position 250 (L250F)
Ref Sequence ENSEMBL: ENSMUSP00000019291 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000019291]
AlphaFold Q4KL66
Predicted Effect probably benign
Transcript: ENSMUST00000019291
AA Change: L250F

PolyPhen 2 Score 0.007 (Sensitivity: 0.96; Specificity: 0.75)
SMART Domains Protein: ENSMUSP00000019291
Gene: ENSMUSG00000030373
AA Change: L250F

DomainStartEndE-ValueType
IG 40 138 1.84e-2 SMART
IG 157 258 1.67e0 SMART
IG 277 376 1.65e-4 SMART
IGc2 394 458 8.31e-10 SMART
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.0%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 67 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcf1 C A 17: 36,270,178 (GRCm39) E627* probably null Het
Aoc1l2 A G 6: 48,907,171 (GRCm39) N57S probably benign Het
Arhgap42 A G 9: 9,006,386 (GRCm39) V670A probably benign Het
Arhgef16 C A 4: 154,375,922 (GRCm39) R24L probably benign Het
Atad2 A T 15: 57,985,967 (GRCm39) D251E probably benign Het
Atf2 T C 2: 73,649,271 (GRCm39) S447G probably benign Het
Atp8b1 T C 18: 64,704,108 (GRCm39) M337V probably benign Het
Atp8b1 C T 18: 64,710,528 (GRCm39) D170N possibly damaging Het
Azin2 C A 4: 128,856,230 (GRCm39) probably benign Het
Btbd16 C T 7: 130,417,516 (GRCm39) R344C probably damaging Het
Cdh19 A G 1: 110,817,771 (GRCm39) L657P probably damaging Het
Crybg3 A T 16: 59,372,544 (GRCm39) V598E probably damaging Het
Cwc22 A G 2: 77,754,952 (GRCm39) I208T probably benign Het
Cyp4a32 T A 4: 115,468,307 (GRCm39) D292E probably damaging Het
Dnah10 G A 5: 124,845,990 (GRCm39) V1510I probably benign Het
Dpp3 G T 19: 4,964,686 (GRCm39) Y540* probably null Het
Efcab8 G C 2: 153,646,861 (GRCm39) V397L unknown Het
Elf1 A G 14: 79,798,290 (GRCm39) D59G probably benign Het
Epc1 A T 18: 6,449,219 (GRCm39) M476K probably benign Het
Espnl C A 1: 91,272,771 (GRCm39) S710R probably benign Het
Fam171b T C 2: 83,683,926 (GRCm39) W148R probably damaging Het
Fhod1 A G 8: 106,065,531 (GRCm39) L88P unknown Het
Frmd4a A G 2: 4,610,846 (GRCm39) S999G probably damaging Het
Glmp T C 3: 88,233,036 (GRCm39) I58T probably damaging Het
Gm45861 T A 8: 28,074,674 (GRCm39) D1341E unknown Het
Gpr179 A G 11: 97,227,766 (GRCm39) I1463T probably benign Het
Gsdmc2 T C 15: 63,698,088 (GRCm39) E339G probably damaging Het
Insm1 A T 2: 146,064,933 (GRCm39) I250F probably damaging Het
Insm1 G A 2: 146,064,943 (GRCm39) G253D possibly damaging Het
Itih1 A T 14: 30,652,222 (GRCm39) S824T probably damaging Het
Lactb A G 9: 66,878,499 (GRCm39) Y190H possibly damaging Het
Lrba T C 3: 86,198,774 (GRCm39) M197T probably benign Het
Lrrc4c A G 2: 97,459,853 (GRCm39) I160V probably benign Het
Lrrc59 A T 11: 94,532,044 (GRCm39) probably null Het
Ltk A T 2: 119,585,121 (GRCm39) M425K possibly damaging Het
Map9 T C 3: 82,278,594 (GRCm39) V198A possibly damaging Het
Mms22l T C 4: 24,578,878 (GRCm39) Y746H probably damaging Het
Ms4a4b A G 19: 11,432,060 (GRCm39) I60M probably benign Het
Mtif2 T C 11: 29,480,065 (GRCm39) W44R probably benign Het
Nadsyn1 A T 7: 143,369,348 (GRCm39) W128R probably damaging Het
Nrcam G A 12: 44,636,917 (GRCm39) A1117T probably damaging Het
Ntng1 G A 3: 110,050,923 (GRCm39) probably benign Het
Ntng1 A G 3: 110,051,162 (GRCm39) F56L unknown Het
Oas2 A T 5: 120,887,637 (GRCm39) Y68N probably damaging Het
Or4c119 A T 2: 88,986,854 (GRCm39) F222I possibly damaging Het
Or5b101 A C 19: 13,005,648 (GRCm39) L15R probably damaging Het
Or6c6c T C 10: 129,541,547 (GRCm39) S267P probably benign Het
Pals2 T C 6: 50,140,463 (GRCm39) M161T probably benign Het
Paqr8 C T 1: 21,005,863 (GRCm39) T339I probably benign Het
Pcdhga10 A G 18: 37,881,814 (GRCm39) E525G probably benign Het
S100a13 G T 3: 90,423,170 (GRCm39) D54Y unknown Het
Slc16a4 A T 3: 107,199,788 (GRCm39) T12S probably benign Het
Slc9b1 A G 3: 135,054,468 (GRCm39) probably benign Het
Slit3 T C 11: 35,598,808 (GRCm39) S1471P probably damaging Het
Smpdl3a T C 10: 57,678,596 (GRCm39) V133A possibly damaging Het
Snap23 C T 2: 120,414,781 (GRCm39) probably benign Het
Spp2 A G 1: 88,344,975 (GRCm39) M146V probably benign Het
Syf2 C A 4: 134,663,321 (GRCm39) N164K possibly damaging Het
Sync T G 4: 129,187,179 (GRCm39) Y70* probably null Het
Tex56 A G 13: 35,116,569 (GRCm39) K106R possibly damaging Het
Tmigd3 T C 3: 105,824,216 (GRCm39) F62L probably benign Het
Trpa1 C T 1: 14,980,953 (GRCm39) probably null Het
U2surp A T 9: 95,366,468 (GRCm39) I480N probably damaging Het
Usf3 C T 16: 44,040,095 (GRCm39) T1525I probably damaging Het
Vmn2r2 T C 3: 64,024,057 (GRCm39) I841M probably damaging Het
Zfp335 T A 2: 164,738,007 (GRCm39) Q868L probably benign Het
Zscan10 A G 17: 23,828,385 (GRCm39) E309G possibly damaging Het
Other mutations in Psg28
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00673:Psg28 APN 7 18,161,816 (GRCm39) missense probably damaging 1.00
IGL01118:Psg28 APN 7 18,162,017 (GRCm39) missense probably damaging 1.00
IGL01606:Psg28 APN 7 18,164,296 (GRCm39) missense probably benign 0.01
R0276:Psg28 UTSW 7 18,164,321 (GRCm39) missense probably benign 0.00
R0391:Psg28 UTSW 7 18,160,098 (GRCm39) missense probably benign 0.02
R0713:Psg28 UTSW 7 18,156,999 (GRCm39) missense possibly damaging 0.61
R1454:Psg28 UTSW 7 18,161,889 (GRCm39) missense possibly damaging 0.50
R1725:Psg28 UTSW 7 18,161,936 (GRCm39) missense possibly damaging 0.67
R2176:Psg28 UTSW 7 18,161,804 (GRCm39) missense probably damaging 1.00
R3154:Psg28 UTSW 7 18,160,348 (GRCm39) missense possibly damaging 0.91
R4520:Psg28 UTSW 7 18,156,826 (GRCm39) missense probably benign 0.00
R5010:Psg28 UTSW 7 18,161,816 (GRCm39) missense probably damaging 1.00
R5529:Psg28 UTSW 7 18,164,373 (GRCm39) missense probably benign 0.15
R5772:Psg28 UTSW 7 18,164,640 (GRCm39) missense probably damaging 1.00
R6039:Psg28 UTSW 7 18,160,107 (GRCm39) missense possibly damaging 0.82
R6039:Psg28 UTSW 7 18,160,107 (GRCm39) missense possibly damaging 0.82
R6046:Psg28 UTSW 7 18,160,305 (GRCm39) missense probably damaging 1.00
R6275:Psg28 UTSW 7 18,164,365 (GRCm39) missense probably damaging 1.00
R6586:Psg28 UTSW 7 18,164,469 (GRCm39) missense probably damaging 0.99
R6928:Psg28 UTSW 7 18,157,003 (GRCm39) missense possibly damaging 0.80
R7197:Psg28 UTSW 7 18,164,509 (GRCm39) missense probably damaging 1.00
R7237:Psg28 UTSW 7 18,161,769 (GRCm39) missense possibly damaging 0.65
R7859:Psg28 UTSW 7 18,160,149 (GRCm39) missense probably damaging 1.00
R7863:Psg28 UTSW 7 18,162,042 (GRCm39) missense possibly damaging 0.62
R7993:Psg28 UTSW 7 18,160,401 (GRCm39) missense possibly damaging 0.63
R8009:Psg28 UTSW 7 18,156,922 (GRCm39) missense probably damaging 0.96
R8115:Psg28 UTSW 7 18,164,311 (GRCm39) missense probably benign 0.15
R8247:Psg28 UTSW 7 18,156,864 (GRCm39) missense probably benign 0.01
R8984:Psg28 UTSW 7 18,156,981 (GRCm39) missense probably damaging 0.97
R9160:Psg28 UTSW 7 18,164,640 (GRCm39) missense probably damaging 1.00
R9336:Psg28 UTSW 7 18,156,905 (GRCm39) missense possibly damaging 0.67
R9758:Psg28 UTSW 7 18,164,602 (GRCm39) missense probably benign 0.18
R9758:Psg28 UTSW 7 18,156,887 (GRCm39) nonsense probably null
R9782:Psg28 UTSW 7 18,164,331 (GRCm39) missense probably benign 0.00
RF016:Psg28 UTSW 7 18,156,847 (GRCm39) missense probably damaging 0.97
X0020:Psg28 UTSW 7 18,161,864 (GRCm39) missense possibly damaging 0.95
Predicted Primers
Posted On 2022-03-25