Incidental Mutation 'IGL02648:Psg26'
ID 302008
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Psg26
Ensembl Gene ENSMUSG00000070799
Gene Name pregnancy-specific beta-1-glycoprotein 26
Synonyms EG574429, cea14
Accession Numbers
Essential gene? Probably non essential (E-score: 0.048) question?
Stock # IGL02648
Quality Score
Status
Chromosome 7
Chromosomal Location 18208507-18218102 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 18216691 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Aspartic acid at position 49 (E49D)
Ref Sequence ENSEMBL: ENSMUSP00000092392 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094798]
AlphaFold Q4KL65
Predicted Effect probably benign
Transcript: ENSMUST00000094798
AA Change: E49D

PolyPhen 2 Score 0.053 (Sensitivity: 0.94; Specificity: 0.84)
SMART Domains Protein: ENSMUSP00000092392
Gene: ENSMUSG00000070799
AA Change: E49D

DomainStartEndE-ValueType
IG 40 141 4.93e-3 SMART
IG 160 261 2.39e-1 SMART
IG 280 379 6.07e-3 SMART
IGc2 397 461 5.48e-10 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aadacl4 A T 4: 144,344,392 (GRCm39) probably null Het
Acp4 A G 7: 43,904,414 (GRCm39) probably benign Het
Adgrv1 A T 13: 81,659,738 (GRCm39) M1997K probably benign Het
Arhgdib T C 6: 136,910,647 (GRCm39) D38G probably damaging Het
Bbox1 T G 2: 110,135,871 (GRCm39) D36A probably damaging Het
Cacna1c T C 6: 118,734,457 (GRCm39) K104R probably damaging Het
Cacna1i G A 15: 80,182,839 (GRCm39) C75Y probably damaging Het
Ccdc14 T C 16: 34,517,528 (GRCm39) L70S probably damaging Het
Ccdc88a T G 11: 29,451,051 (GRCm39) V1580G probably benign Het
Cdadc1 C A 14: 59,823,812 (GRCm39) D227Y probably damaging Het
Chd3 T C 11: 69,242,976 (GRCm39) Y1415C probably damaging Het
Cngb3 A G 4: 19,428,489 (GRCm39) N493S probably benign Het
Dock10 T A 1: 80,551,840 (GRCm39) Y665F probably damaging Het
Gm10549 C A 18: 33,597,303 (GRCm39) probably benign Het
Greb1 C T 12: 16,758,683 (GRCm39) V678M probably damaging Het
Gucy2c G A 6: 136,706,211 (GRCm39) R497* probably null Het
Itgad T C 7: 127,782,546 (GRCm39) probably benign Het
Lgr4 C A 2: 109,842,718 (GRCm39) T877K probably damaging Het
Lrig3 A G 10: 125,802,463 (GRCm39) D40G probably benign Het
Myo3b T C 2: 69,935,716 (GRCm39) probably benign Het
Neb A G 2: 52,161,093 (GRCm39) Y2193H possibly damaging Het
Or4b1 T A 2: 89,979,697 (GRCm39) I218F possibly damaging Het
Or8b3b T C 9: 38,584,312 (GRCm39) M143V probably benign Het
Pard6b A G 2: 167,940,847 (GRCm39) Q278R probably benign Het
Pate10 A T 9: 35,652,405 (GRCm39) M21L probably benign Het
Pkd2l1 T C 19: 44,143,975 (GRCm39) Y366C possibly damaging Het
Prl2c1 A G 13: 28,041,542 (GRCm39) D188G probably benign Het
Prl3a1 G T 13: 27,454,218 (GRCm39) M65I probably benign Het
Rapgef3 G A 15: 97,656,273 (GRCm39) R38W probably damaging Het
Rrn3 T C 16: 13,629,453 (GRCm39) F590L probably benign Het
Serpina12 T C 12: 104,004,267 (GRCm39) K122E probably benign Het
Slc39a6 T C 18: 24,715,424 (GRCm39) I699V probably damaging Het
Tmem259 G A 10: 79,813,651 (GRCm39) P443S probably damaging Het
Vmn1r75 T A 7: 11,615,091 (GRCm39) F274L probably benign Het
Other mutations in Psg26
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01010:Psg26 APN 7 18,212,255 (GRCm39) missense possibly damaging 0.83
IGL01383:Psg26 APN 7 18,214,179 (GRCm39) missense possibly damaging 0.90
IGL01453:Psg26 APN 7 18,213,999 (GRCm39) missense possibly damaging 0.91
IGL01603:Psg26 APN 7 18,209,028 (GRCm39) missense probably damaging 0.98
IGL02201:Psg26 APN 7 18,214,071 (GRCm39) missense probably benign 0.04
IGL02468:Psg26 APN 7 18,212,387 (GRCm39) missense probably damaging 0.96
IGL02812:Psg26 APN 7 18,209,080 (GRCm39) missense probably benign 0.00
R0226:Psg26 UTSW 7 18,217,883 (GRCm39) missense possibly damaging 0.81
R0352:Psg26 UTSW 7 18,209,181 (GRCm39) missense probably benign 0.00
R0369:Psg26 UTSW 7 18,216,481 (GRCm39) nonsense probably null
R0718:Psg26 UTSW 7 18,212,212 (GRCm39) missense probably benign 0.18
R0718:Psg26 UTSW 7 18,209,160 (GRCm39) missense probably benign 0.23
R1710:Psg26 UTSW 7 18,213,966 (GRCm39) missense probably damaging 0.99
R1899:Psg26 UTSW 7 18,212,350 (GRCm39) missense probably benign 0.01
R1958:Psg26 UTSW 7 18,212,264 (GRCm39) missense probably benign 0.04
R2102:Psg26 UTSW 7 18,209,067 (GRCm39) missense probably damaging 1.00
R3766:Psg26 UTSW 7 18,208,996 (GRCm39) missense probably benign
R4544:Psg26 UTSW 7 18,212,464 (GRCm39) missense probably damaging 1.00
R4977:Psg26 UTSW 7 18,209,235 (GRCm39) missense probably benign 0.11
R5000:Psg26 UTSW 7 18,214,057 (GRCm39) missense possibly damaging 0.95
R5376:Psg26 UTSW 7 18,214,030 (GRCm39) missense probably benign
R5416:Psg26 UTSW 7 18,216,525 (GRCm39) missense probably benign
R5435:Psg26 UTSW 7 18,212,398 (GRCm39) missense possibly damaging 0.60
R6000:Psg26 UTSW 7 18,216,617 (GRCm39) nonsense probably null
R6285:Psg26 UTSW 7 18,216,753 (GRCm39) missense probably benign
R7062:Psg26 UTSW 7 18,216,521 (GRCm39) missense probably damaging 1.00
R7083:Psg26 UTSW 7 18,213,934 (GRCm39) nonsense probably null
R7513:Psg26 UTSW 7 18,209,225 (GRCm39) missense probably benign 0.03
R7817:Psg26 UTSW 7 18,216,572 (GRCm39) missense not run
R7857:Psg26 UTSW 7 18,212,215 (GRCm39) missense possibly damaging 0.71
R7905:Psg26 UTSW 7 18,209,242 (GRCm39) missense probably benign 0.00
R8047:Psg26 UTSW 7 18,212,474 (GRCm39) missense possibly damaging 0.50
R8789:Psg26 UTSW 7 18,216,494 (GRCm39) missense probably damaging 1.00
R8877:Psg26 UTSW 7 18,217,865 (GRCm39) missense probably benign 0.01
R9012:Psg26 UTSW 7 18,216,596 (GRCm39) missense probably benign 0.19
R9203:Psg26 UTSW 7 18,212,382 (GRCm39) missense probably damaging 0.98
R9327:Psg26 UTSW 7 18,216,480 (GRCm39) missense probably damaging 1.00
R9547:Psg26 UTSW 7 18,214,087 (GRCm39) missense probably benign 0.00
Z1177:Psg26 UTSW 7 18,214,216 (GRCm39) missense probably benign 0.02
Posted On 2015-04-16