Incidental Mutation 'IGL01833:Prxl2b'
ID 154864
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Prxl2b
Ensembl Gene ENSMUSG00000029059
Gene Name peroxiredoxin like 2B
Synonyms PM/PGFS, Fam213b, 2810405K02Rik
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL01833
Quality Score
Status
Chromosome 4
Chromosomal Location 154980884-154983522 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) G to T at 154981059 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000131753 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000030935] [ENSMUST00000079269] [ENSMUST00000080559] [ENSMUST00000105634] [ENSMUST00000105635] [ENSMUST00000163732] [ENSMUST00000132281]
AlphaFold Q9DB60
Predicted Effect probably benign
Transcript: ENSMUST00000030935
SMART Domains Protein: ENSMUSP00000030935
Gene: ENSMUSG00000029059

DomainStartEndE-ValueType
Pfam:AhpC-TSA_2 53 166 9.9e-25 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000079269
SMART Domains Protein: ENSMUSP00000078252
Gene: ENSMUSG00000058183

DomainStartEndE-ValueType
transmembrane domain 20 42 N/A INTRINSIC
Pfam:Peptidase_M13_N 99 498 1.7e-135 PFAM
Pfam:Peptidase_M13 559 767 1.2e-68 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000080559
SMART Domains Protein: ENSMUSP00000079399
Gene: ENSMUSG00000058183

DomainStartEndE-ValueType
transmembrane domain 20 42 N/A INTRINSIC
Pfam:Peptidase_M13_N 76 512 4.8e-131 PFAM
Pfam:Peptidase_M13 573 779 3.4e-71 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000105634
SMART Domains Protein: ENSMUSP00000101259
Gene: ENSMUSG00000058183

DomainStartEndE-ValueType
transmembrane domain 20 42 N/A INTRINSIC
Pfam:Peptidase_M13_N 76 512 1.4e-105 PFAM
Pfam:Peptidase_M13 573 781 4e-74 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000105635
SMART Domains Protein: ENSMUSP00000101260
Gene: ENSMUSG00000058183

DomainStartEndE-ValueType
transmembrane domain 20 42 N/A INTRINSIC
Pfam:Peptidase_M13_N 76 475 1.6e-135 PFAM
Pfam:Peptidase_M13 536 744 1.2e-68 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000123513
Predicted Effect noncoding transcript
Transcript: ENSMUST00000129623
Predicted Effect probably benign
Transcript: ENSMUST00000163732
SMART Domains Protein: ENSMUSP00000131753
Gene: ENSMUSG00000058183

DomainStartEndE-ValueType
transmembrane domain 20 42 N/A INTRINSIC
Pfam:Peptidase_M13_N 99 498 1.7e-135 PFAM
Pfam:Peptidase_M13 559 765 3.3e-71 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000132281
SMART Domains Protein: ENSMUSP00000116611
Gene: ENSMUSG00000029059

DomainStartEndE-ValueType
Pfam:AhpC-TSA_2 9 114 4.2e-25 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acsbg3 A G 17: 57,188,062 (GRCm39) N190S probably benign Het
Adamts18 T A 8: 114,469,728 (GRCm39) Y658F probably benign Het
Camsap3 T A 8: 3,658,508 (GRCm39) L1151Q probably damaging Het
Casp14 T A 10: 78,551,237 (GRCm39) Y16F probably damaging Het
Clip2 A T 5: 134,526,938 (GRCm39) probably benign Het
Clip4 G A 17: 72,134,785 (GRCm39) probably benign Het
Cyb5r4 G A 9: 86,941,505 (GRCm39) probably null Het
Ep400 A T 5: 110,827,874 (GRCm39) N2329K unknown Het
Fam163a T A 1: 155,955,742 (GRCm39) I17F probably damaging Het
Galnt1 T A 18: 24,400,617 (GRCm39) I241N probably damaging Het
Galnt14 T G 17: 73,811,899 (GRCm39) I441L probably benign Het
Gpr45 T C 1: 43,071,402 (GRCm39) L15P probably benign Het
Hivep1 A T 13: 42,308,464 (GRCm39) K235* probably null Het
Kcnip2 T C 19: 45,782,746 (GRCm39) probably null Het
Kpna3 T C 14: 61,607,894 (GRCm39) N437S possibly damaging Het
Lmtk2 A T 5: 144,112,753 (GRCm39) R1158* probably null Het
Lpo A G 11: 87,698,159 (GRCm39) V612A possibly damaging Het
Myh15 T C 16: 48,934,421 (GRCm39) C663R probably damaging Het
Nacad G A 11: 6,555,700 (GRCm39) R17C unknown Het
Or7a35 A T 10: 78,853,770 (GRCm39) M205L probably benign Het
Pcsk2 A G 2: 143,529,500 (GRCm39) Q99R possibly damaging Het
Pkd1l2 T C 8: 117,787,264 (GRCm39) N593S probably benign Het
Plce1 G A 19: 38,709,425 (GRCm39) S1093N probably damaging Het
Rhpn2 T A 7: 35,075,596 (GRCm39) Y258N probably benign Het
Serpinb9d T C 13: 33,384,688 (GRCm39) Y222H probably damaging Het
Shprh T C 10: 11,066,806 (GRCm39) L1401P probably damaging Het
Slc5a7 A G 17: 54,588,861 (GRCm39) L262P probably damaging Het
Stat2 T G 10: 128,117,045 (GRCm39) F293V probably benign Het
Stpg4 T A 17: 87,702,585 (GRCm39) probably null Het
Styk1 G T 6: 131,279,329 (GRCm39) probably benign Het
Sult2a2 T A 7: 13,468,721 (GRCm39) D62E probably damaging Het
Sytl2 G A 7: 90,045,745 (GRCm39) V632M probably damaging Het
Themis C T 10: 28,658,307 (GRCm39) Q445* probably null Het
Tmem225 A T 9: 40,059,725 (GRCm39) E35V probably damaging Het
Vmn1r48 T A 6: 90,013,265 (GRCm39) T187S probably damaging Het
Xpnpep1 A G 19: 52,988,824 (GRCm39) Y463H probably damaging Het
Other mutations in Prxl2b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03102:Prxl2b APN 4 154,981,058 (GRCm39) unclassified probably benign
R1350:Prxl2b UTSW 4 154,982,585 (GRCm39) missense probably damaging 1.00
R1676:Prxl2b UTSW 4 154,981,520 (GRCm39) missense probably benign 0.05
R1778:Prxl2b UTSW 4 154,981,814 (GRCm39) missense probably damaging 0.98
R2164:Prxl2b UTSW 4 154,982,606 (GRCm39) missense probably damaging 1.00
R4468:Prxl2b UTSW 4 154,981,507 (GRCm39) missense probably benign 0.01
R5007:Prxl2b UTSW 4 154,981,531 (GRCm39) splice site probably null
R5386:Prxl2b UTSW 4 154,983,462 (GRCm39) start codon destroyed probably benign 0.01
R6820:Prxl2b UTSW 4 154,982,623 (GRCm39) missense probably damaging 1.00
R7437:Prxl2b UTSW 4 154,981,053 (GRCm39) missense possibly damaging 0.53
X0063:Prxl2b UTSW 4 154,983,410 (GRCm39) missense probably benign 0.03
Z1176:Prxl2b UTSW 4 154,983,446 (GRCm39) missense probably damaging 1.00
Posted On 2014-02-04