Incidental Mutation 'IGL02982:Psg29'
ID 406600
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Psg29
Ensembl Gene ENSMUSG00000023159
Gene Name pregnancy-specific beta-1-glycoprotein 29
Synonyms cea17
Accession Numbers
Essential gene? Probably non essential (E-score: 0.052) question?
Stock # IGL02982
Quality Score
Status
Chromosome 7
Chromosomal Location 16937402-16949681 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 16945632 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 401 (T401A)
Ref Sequence ENSEMBL: ENSMUSP00000075320 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000075934]
AlphaFold Q3URN6
Predicted Effect probably damaging
Transcript: ENSMUST00000075934
AA Change: T401A

PolyPhen 2 Score 0.981 (Sensitivity: 0.75; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000075320
Gene: ENSMUSG00000023159
AA Change: T401A

DomainStartEndE-ValueType
IG 40 137 7.77e-1 SMART
IG 156 257 8.72e-4 SMART
IG 276 377 2.44e0 SMART
IGc2 393 457 3.06e-8 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam5 G T 8: 25,294,447 (GRCm39) A384D probably benign Het
Adamts19 T A 18: 59,157,590 (GRCm39) C961S probably damaging Het
Agbl2 G A 2: 90,636,159 (GRCm39) C565Y probably damaging Het
Aox3 G A 1: 58,166,846 (GRCm39) E190K probably benign Het
Arf2 T G 11: 103,872,602 (GRCm39) D74E probably damaging Het
Bptf T G 11: 106,967,500 (GRCm39) D960A probably damaging Het
Ccdc180 G T 4: 45,903,840 (GRCm39) probably benign Het
Ces1a A G 8: 93,771,603 (GRCm39) F65L probably damaging Het
Def8 T C 8: 124,183,278 (GRCm39) probably benign Het
Fat4 T C 3: 38,944,992 (GRCm39) L1295P probably damaging Het
Filip1l A G 16: 57,392,595 (GRCm39) H1061R probably damaging Het
Fut2 C T 7: 45,300,193 (GRCm39) G193E possibly damaging Het
Gldc A G 19: 30,122,545 (GRCm39) probably null Het
Golgb1 A C 16: 36,746,172 (GRCm39) D2917A probably damaging Het
Gpc5 G A 14: 115,607,400 (GRCm39) C334Y probably damaging Het
Gpsm1 T A 2: 26,214,871 (GRCm39) L252Q probably damaging Het
Iars1 C T 13: 49,863,185 (GRCm39) R546C probably benign Het
Kbtbd8 G T 6: 95,103,547 (GRCm39) V399L probably benign Het
Kcnd2 A T 6: 21,217,148 (GRCm39) D284V probably damaging Het
Kcnj6 T C 16: 94,633,376 (GRCm39) K227R possibly damaging Het
Lhx9 A T 1: 138,766,349 (GRCm39) H155Q probably damaging Het
Mcm9 A G 10: 53,501,922 (GRCm39) V221A probably damaging Het
Myo9a A T 9: 59,815,491 (GRCm39) K2237* probably null Het
Ntf3 A T 6: 126,079,340 (GRCm39) D55E probably damaging Het
Or13a28 A T 7: 140,217,865 (GRCm39) I84F probably benign Het
Or4c15b G T 2: 89,113,453 (GRCm39) T29K probably damaging Het
Plek T A 11: 16,931,826 (GRCm39) I342F probably damaging Het
Polrmt A G 10: 79,574,182 (GRCm39) Y853H probably damaging Het
Ptprb A G 10: 116,158,533 (GRCm39) T822A probably benign Het
Ptprq A C 10: 107,422,545 (GRCm39) F1616V probably damaging Het
Rpe65 T A 3: 159,305,998 (GRCm39) V19E probably damaging Het
Scamp2 G A 9: 57,488,832 (GRCm39) A178T probably benign Het
Spata31e5 T C 1: 28,817,135 (GRCm39) H299R probably damaging Het
Spta1 A G 1: 174,014,854 (GRCm39) I445V probably benign Het
Tas2r135 A G 6: 42,383,187 (GRCm39) E242G probably benign Het
Ttc22 T C 4: 106,495,783 (GRCm39) V379A probably damaging Het
Unc5d C T 8: 29,142,881 (GRCm39) G857E probably damaging Het
Usp28 A G 9: 48,929,739 (GRCm39) I43V probably benign Het
Vmn2r68 A T 7: 84,883,649 (GRCm39) M152K probably benign Het
Wrn C T 8: 33,833,094 (GRCm39) G133R probably damaging Het
Zfyve26 G A 12: 79,310,644 (GRCm39) T187M probably damaging Het
Zic2 A G 14: 122,715,979 (GRCm39) E367G probably damaging Het
Other mutations in Psg29
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01020:Psg29 APN 7 16,942,657 (GRCm39) missense probably benign 0.42
IGL01107:Psg29 APN 7 16,938,850 (GRCm39) missense probably benign 0.01
IGL01348:Psg29 APN 7 16,944,598 (GRCm39) missense probably benign 0.09
IGL01353:Psg29 APN 7 16,938,938 (GRCm39) missense possibly damaging 0.54
IGL02546:Psg29 APN 7 16,942,707 (GRCm39) missense probably damaging 1.00
IGL02611:Psg29 APN 7 16,942,716 (GRCm39) missense probably benign 0.15
IGL03072:Psg29 APN 7 16,942,719 (GRCm39) missense probably benign 0.06
macular UTSW 7 16,944,460 (GRCm39) missense probably benign 0.23
papular UTSW 7 16,945,837 (GRCm39) makesense probably null
R1744:Psg29 UTSW 7 16,944,278 (GRCm39) missense probably damaging 1.00
R2272:Psg29 UTSW 7 16,944,621 (GRCm39) missense probably benign 0.19
R3054:Psg29 UTSW 7 16,942,727 (GRCm39) missense probably benign 0.29
R3790:Psg29 UTSW 7 16,938,950 (GRCm39) missense possibly damaging 0.71
R3963:Psg29 UTSW 7 16,942,510 (GRCm39) missense probably benign 0.01
R4464:Psg29 UTSW 7 16,944,575 (GRCm39) missense possibly damaging 0.61
R4740:Psg29 UTSW 7 16,942,458 (GRCm39) missense probably benign 0.00
R4774:Psg29 UTSW 7 16,944,460 (GRCm39) missense probably benign 0.23
R4902:Psg29 UTSW 7 16,945,837 (GRCm39) makesense probably null
R4977:Psg29 UTSW 7 16,942,556 (GRCm39) missense probably damaging 1.00
R5071:Psg29 UTSW 7 16,945,763 (GRCm39) missense probably damaging 1.00
R5072:Psg29 UTSW 7 16,945,763 (GRCm39) missense probably damaging 1.00
R5074:Psg29 UTSW 7 16,945,763 (GRCm39) missense probably damaging 1.00
R5169:Psg29 UTSW 7 16,945,578 (GRCm39) missense probably damaging 1.00
R5415:Psg29 UTSW 7 16,945,561 (GRCm39) splice site probably null
R5729:Psg29 UTSW 7 16,944,459 (GRCm39) missense probably damaging 0.98
R6023:Psg29 UTSW 7 16,944,437 (GRCm39) missense possibly damaging 0.82
R6127:Psg29 UTSW 7 16,945,671 (GRCm39) missense probably benign 0.00
R6900:Psg29 UTSW 7 16,938,857 (GRCm39) nonsense probably null
R7142:Psg29 UTSW 7 16,944,546 (GRCm39) missense probably damaging 1.00
R7297:Psg29 UTSW 7 16,944,616 (GRCm39) nonsense probably null
R7448:Psg29 UTSW 7 16,945,648 (GRCm39) missense possibly damaging 0.90
R7973:Psg29 UTSW 7 16,944,462 (GRCm39) missense probably benign 0.03
R8027:Psg29 UTSW 7 16,942,565 (GRCm39) missense possibly damaging 0.69
R8979:Psg29 UTSW 7 16,937,544 (GRCm39) start gained probably benign
R9744:Psg29 UTSW 7 16,944,495 (GRCm39) missense probably benign 0.01
X0017:Psg29 UTSW 7 16,944,586 (GRCm39) nonsense probably null
Posted On 2016-08-02