Incidental Mutation 'R7814:Psg23'
ID 601356
Institutional Source Beutler Lab
Gene Symbol Psg23
Ensembl Gene ENSMUSG00000074359
Gene Name pregnancy-specific beta-1-glycoprotein 23
Synonyms 1620401C02Rik
MMRRC Submission 045869-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R7814 (G1)
Quality Score 225.009
Status Validated
Chromosome 7
Chromosomal Location 18340268-18350426 bp(-) (GRCm39)
Type of Mutation makesense
DNA Base Change (assembly) A to T at 18340839 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Stop codon to Arginine at position 472 (*472R)
Ref Sequence ENSEMBL: ENSMUSP00000056586 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000057810]
AlphaFold Q9D2U0
Predicted Effect probably null
Transcript: ENSMUST00000057810
AA Change: *472R
SMART Domains Protein: ENSMUSP00000056586
Gene: ENSMUSG00000074359
AA Change: *472R

DomainStartEndE-ValueType
IG 39 138 2.03e-4 SMART
IG 159 260 4.16e-1 SMART
IG 276 375 1.25e-4 SMART
IGc2 393 457 4.7e-9 SMART
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.2%
Validation Efficiency 100% (90/90)
MGI Phenotype PHENOTYPE: Mice homozygous for this spontaneous mutation display no phenotypic abnormalities. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 93 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1110065P20Rik C T 4: 124,744,395 (GRCm39) G20R not run Het
Adamts13 A T 2: 26,886,561 (GRCm39) M927L probably benign Het
Akap6 T A 12: 53,187,744 (GRCm39) N1719K probably benign Het
Ank3 G A 10: 69,822,734 (GRCm39) V468M Het
Aox1 A G 1: 58,124,626 (GRCm39) T956A probably benign Het
Ap4m1 T C 5: 138,173,079 (GRCm39) V140A probably benign Het
Apc A G 18: 34,405,592 (GRCm39) T173A probably damaging Het
Bclaf1 A G 10: 20,210,365 (GRCm39) T839A possibly damaging Het
Btn2a2 T A 13: 23,666,976 (GRCm39) I210F possibly damaging Het
Cadps A G 14: 12,376,706 (GRCm38) W1269R probably damaging Het
Capn2 G C 1: 182,319,711 (GRCm39) P159R probably damaging Het
Cblif C A 19: 11,727,551 (GRCm39) P125Q probably benign Het
Ccdc134 T G 15: 82,015,724 (GRCm39) V68G probably damaging Het
Cdh26 A G 2: 178,111,828 (GRCm39) T463A probably damaging Het
Cfap206 C T 4: 34,716,347 (GRCm39) V373I probably benign Het
Clpx T C 9: 65,231,583 (GRCm39) probably null Het
Ctnnd2 A T 15: 31,020,874 (GRCm39) Y1145F probably benign Het
Ctr9 T A 7: 110,633,134 (GRCm39) D127E probably benign Het
Cyp2f2 G A 7: 26,828,678 (GRCm39) V183I probably benign Het
Cyp7b1 G A 3: 18,151,466 (GRCm39) S249L probably benign Het
D630023F18Rik T A 1: 65,155,850 (GRCm39) D125V possibly damaging Het
Dbh A T 2: 27,064,860 (GRCm39) Y357F probably damaging Het
Dbp T A 7: 45,356,414 (GRCm39) L175Q probably benign Het
Dmwd A T 7: 18,814,768 (GRCm39) T473S probably benign Het
Dnah9 T A 11: 65,896,486 (GRCm39) Q2446L probably damaging Het
Dnmbp T C 19: 43,842,615 (GRCm39) K498R probably benign Het
Dop1b T A 16: 93,596,859 (GRCm39) I1924N probably damaging Het
Dsg1a T A 18: 20,471,572 (GRCm39) probably null Het
Dzank1 T C 2: 144,364,484 (GRCm39) T38A probably damaging Het
Egfem1 A G 3: 29,740,940 (GRCm39) H538R probably damaging Het
Entpd1 T C 19: 40,715,891 (GRCm39) C353R probably damaging Het
Ephx2 C A 14: 66,347,678 (GRCm39) C78F probably benign Het
Faf2 A T 13: 54,808,774 (GRCm39) H388L probably benign Het
Fam186a G A 15: 99,842,545 (GRCm39) T1233I possibly damaging Het
Gfra2 C A 14: 71,133,410 (GRCm39) A80E probably damaging Het
Gm17175 T A 14: 51,811,492 (GRCm39) probably benign Het
Gm8180 T C 14: 44,021,103 (GRCm39) D35G possibly damaging Het
Gpr68 C T 12: 100,845,302 (GRCm39) V81M probably damaging Het
Hsd3b6 A G 3: 98,718,259 (GRCm39) L35P probably damaging Het
Hspd1 A C 1: 55,117,803 (GRCm39) V485G possibly damaging Het
Il16 A G 7: 83,319,348 (GRCm39) V381A possibly damaging Het
Il17rd G A 14: 26,822,074 (GRCm39) C600Y probably benign Het
Ins2 C A 7: 142,233,323 (GRCm39) probably benign Het
Iqca1l G T 5: 24,750,420 (GRCm39) Q626K possibly damaging Het
Itsn2 T C 12: 4,708,561 (GRCm39) I872T probably benign Het
Jakmip3 A T 7: 138,620,858 (GRCm39) D219V probably damaging Het
Jph4 T C 14: 55,347,192 (GRCm39) T452A probably damaging Het
Kazn T C 4: 141,937,481 (GRCm39) E12G unknown Het
Kif20b A C 19: 34,928,355 (GRCm39) S1206R possibly damaging Het
Lca5l A G 16: 95,963,757 (GRCm39) probably null Het
Lgals2 A T 15: 78,735,533 (GRCm39) S60R probably benign Het
Lrrc37 T A 11: 103,504,999 (GRCm39) H2323L possibly damaging Het
Map10 A G 8: 126,398,350 (GRCm39) E581G probably benign Het
Map2k7 G T 8: 4,293,744 (GRCm39) R128L probably benign Het
Mapk8 G C 14: 33,132,834 (GRCm39) S34* probably null Het
Mcat A G 15: 83,432,110 (GRCm39) Y253H probably damaging Het
Mmp2 T C 8: 93,576,798 (GRCm39) L607P probably benign Het
Ncor1 A T 11: 62,224,752 (GRCm39) V836E probably damaging Het
Neb A G 2: 52,027,392 (GRCm39) S7113P probably damaging Het
Nphp4 T C 4: 152,608,729 (GRCm39) F446L possibly damaging Het
Nphp4 G T 4: 152,628,860 (GRCm39) D749Y probably damaging Het
Or14j4 T A 17: 37,921,547 (GRCm39) T32S probably benign Het
Or1j10 T C 2: 36,266,821 (GRCm39) I11T possibly damaging Het
Or4c99 A G 2: 88,329,416 (GRCm39) probably benign Het
Or5k8 T C 16: 58,644,365 (GRCm39) K236E probably damaging Het
Osbpl11 A T 16: 33,030,431 (GRCm39) R220* probably null Het
Plrg1 G A 3: 82,964,144 (GRCm39) V26M probably damaging Het
Polr1b C A 2: 128,967,464 (GRCm39) F952L probably damaging Het
Ppfia3 A C 7: 45,001,686 (GRCm39) S560A probably benign Het
Ppp3cc T A 14: 70,462,464 (GRCm39) N391I possibly damaging Het
Prdx6b T C 2: 80,123,304 (GRCm39) S38P possibly damaging Het
Rapgef4 A T 2: 72,053,461 (GRCm39) M587L probably benign Het
Rfx3 T A 19: 27,803,470 (GRCm39) M247L probably benign Het
Rgs7 T A 1: 174,903,635 (GRCm39) H463L probably benign Het
Riiad1 G T 3: 94,373,162 (GRCm39) S106R probably benign Het
Rims4 A C 2: 163,760,548 (GRCm39) I19S probably benign Het
Ros1 A T 10: 51,972,233 (GRCm39) M1648K probably benign Het
Rrn3 T C 16: 13,629,453 (GRCm39) F590L probably benign Het
Samd9l T A 6: 3,374,793 (GRCm39) T823S possibly damaging Het
Sfxn1 C A 13: 54,245,250 (GRCm39) P115Q possibly damaging Het
Slc10a7 T C 8: 79,425,202 (GRCm39) probably null Het
Slc25a16 A T 10: 62,773,199 (GRCm39) M142L probably benign Het
Stat2 CGCTGGAGCCAGCCCCACAAGTCCTGCTGGAGCCAGCCCCACAAGTCCTGCTGGAGCCAGCCCCACAAGTCCTGCTGGAGCCAGCCCCACAAGTCCTGCTGGAGCCAGCCCCACAAGTCCAGCTGGAGCCAGCCCCACAAGTCCTGCTGGAGCTAGCCCCACAAGTCCTGCTGGAGCCAGCCCCACAAGTCCTGCTGGAGCTAGCCCCACAAGTCCAGCTGGAGCCAGC CGCTGGAGCCAGCCCCACAAGTCCTGCTGGAGCCAGCCCCACAAGTCCTGCTGGAGCCAGCCCCACAAGTCCTGCTGGAGCCAGCCCCACAAGTCCAGCTGGAGCCAGCCCCACAAGTCCTGCTGGAGCTAGCCCCACAAGTCCTGCTGGAGCCAGCCCCACAAGTCCTGCTGGAGCTAGCCCCACAAGTCCAGCTGGAGCCAGC 10: 128,126,597 (GRCm39) probably benign Het
Stat5a T G 11: 100,765,853 (GRCm39) L313R probably damaging Het
Strap A G 6: 137,718,976 (GRCm39) E176G possibly damaging Het
Tlr4 T G 4: 66,759,316 (GRCm39) L703R probably damaging Het
Trim36 A T 18: 46,300,691 (GRCm39) V660D possibly damaging Het
Tspoap1 T A 11: 87,666,350 (GRCm39) D980E probably damaging Het
Usp28 T C 9: 48,915,218 (GRCm39) V157A probably benign Het
Vmn2r17 A T 5: 109,575,739 (GRCm39) R203S probably benign Het
Vmn2r66 T C 7: 84,656,472 (GRCm39) I181M probably benign Het
Zan T A 5: 137,461,841 (GRCm39) T1113S unknown Het
Zfp442 C T 2: 150,251,402 (GRCm39) D167N possibly damaging Het
Other mutations in Psg23
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00814:Psg23 APN 7 18,348,608 (GRCm39) nonsense probably null
IGL01309:Psg23 APN 7 18,348,465 (GRCm39) missense probably damaging 1.00
IGL01736:Psg23 APN 7 18,346,122 (GRCm39) missense possibly damaging 0.76
IGL02142:Psg23 APN 7 18,344,345 (GRCm39) missense probably benign 0.01
IGL02728:Psg23 APN 7 18,340,853 (GRCm39) missense probably benign 0.02
IGL03080:Psg23 APN 7 18,340,910 (GRCm39) missense probably damaging 1.00
IGL03130:Psg23 APN 7 18,344,341 (GRCm39) missense probably benign 0.25
R0113:Psg23 UTSW 7 18,345,927 (GRCm39) missense probably benign 0.31
R0137:Psg23 UTSW 7 18,348,558 (GRCm39) missense probably benign 0.00
R0544:Psg23 UTSW 7 18,348,607 (GRCm39) missense probably damaging 1.00
R1368:Psg23 UTSW 7 18,348,645 (GRCm39) missense probably benign 0.13
R1840:Psg23 UTSW 7 18,344,363 (GRCm39) missense possibly damaging 0.67
R1869:Psg23 UTSW 7 18,348,543 (GRCm39) missense probably benign 0.09
R1875:Psg23 UTSW 7 18,344,375 (GRCm39) missense probably benign 0.10
R2041:Psg23 UTSW 7 18,348,703 (GRCm39) missense possibly damaging 0.78
R2096:Psg23 UTSW 7 18,348,668 (GRCm39) missense probably damaging 1.00
R3110:Psg23 UTSW 7 18,344,369 (GRCm39) missense possibly damaging 0.72
R3112:Psg23 UTSW 7 18,344,369 (GRCm39) missense possibly damaging 0.72
R3790:Psg23 UTSW 7 18,346,126 (GRCm39) missense probably benign 0.00
R3892:Psg23 UTSW 7 18,345,966 (GRCm39) missense probably damaging 1.00
R4074:Psg23 UTSW 7 18,341,043 (GRCm39) missense possibly damaging 0.66
R4200:Psg23 UTSW 7 18,345,990 (GRCm39) missense probably damaging 1.00
R4865:Psg23 UTSW 7 18,346,039 (GRCm39) missense probably benign 0.14
R5337:Psg23 UTSW 7 18,345,997 (GRCm39) missense probably benign 0.00
R6016:Psg23 UTSW 7 18,346,112 (GRCm39) missense probably benign 0.00
R6951:Psg23 UTSW 7 18,348,636 (GRCm39) missense probably damaging 1.00
R7033:Psg23 UTSW 7 18,348,669 (GRCm39) missense possibly damaging 0.82
R7212:Psg23 UTSW 7 18,341,064 (GRCm39) missense probably benign 0.00
R7427:Psg23 UTSW 7 18,345,908 (GRCm39) splice site probably null
R7527:Psg23 UTSW 7 18,348,699 (GRCm39) missense probably damaging 1.00
R7864:Psg23 UTSW 7 18,344,435 (GRCm39) missense possibly damaging 0.87
R7897:Psg23 UTSW 7 18,341,108 (GRCm39) missense possibly damaging 0.83
R8155:Psg23 UTSW 7 18,346,179 (GRCm39) missense probably damaging 1.00
R8358:Psg23 UTSW 7 18,348,522 (GRCm39) missense probably benign 0.00
R9032:Psg23 UTSW 7 18,348,660 (GRCm39) missense possibly damaging 0.83
R9085:Psg23 UTSW 7 18,348,660 (GRCm39) missense possibly damaging 0.83
R9365:Psg23 UTSW 7 18,344,393 (GRCm39) missense probably damaging 1.00
R9577:Psg23 UTSW 7 18,346,067 (GRCm39) missense probably benign 0.00
R9688:Psg23 UTSW 7 18,344,547 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TGTTTACCACTTAGAACACAGGATG -3'
(R):5'- ATCCGTTGGCTCTTCAATAAGC -3'

Sequencing Primer
(F):5'- GATGTCAGCGCCATCTTGTGAC -3'
(R):5'- CGTTGGCTCTTCAATAAGCAGAGTC -3'
Posted On 2019-11-26