Incidental Mutation 'IGL01314:Mug2'
ID 73774
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Mug2
Ensembl Gene ENSMUSG00000030131
Gene Name murinoglobulin 2
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.054) question?
Stock # IGL01314
Quality Score
Status
Chromosome 6
Chromosomal Location 122006761-122085965 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to C at 122081279 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Phenylalanine to Leucine at position 1267 (F1267L)
Ref Sequence ENSEMBL: ENSMUSP00000080469 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000081777]
AlphaFold P28666
Predicted Effect possibly damaging
Transcript: ENSMUST00000081777
AA Change: F1267L

PolyPhen 2 Score 0.621 (Sensitivity: 0.87; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000080469
Gene: ENSMUSG00000030131
AA Change: F1267L

DomainStartEndE-ValueType
Pfam:A2M_N 128 221 3.5e-21 PFAM
A2M_N_2 449 599 1.05e-42 SMART
low complexity region 711 728 N/A INTRINSIC
A2M 740 830 7.16e-36 SMART
Pfam:Thiol-ester_cl 963 992 1e-18 PFAM
low complexity region 994 1005 N/A INTRINSIC
Pfam:A2M_comp 1012 1097 5.8e-34 PFAM
Pfam:A2M_comp 1093 1243 3e-47 PFAM
A2M_recep 1353 1440 1.85e-38 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamts12 C T 15: 11,071,853 (GRCm38) A161V probably benign Het
Bptf A T 11: 107,054,853 (GRCm38) V2520E probably damaging Het
C87436 T C 6: 86,457,855 (GRCm38) F395S probably damaging Het
Capn1 T C 19: 5,989,984 (GRCm38) probably benign Het
Ceacam5 T A 7: 17,747,256 (GRCm38) Y309* probably null Het
Clasp2 A G 9: 113,906,127 (GRCm38) D1011G possibly damaging Het
Csmd3 A G 15: 47,849,755 (GRCm38) Y1608H probably damaging Het
Dcaf1 T C 9: 106,834,191 (GRCm38) I77T probably benign Het
Dcdc2a T C 13: 25,102,604 (GRCm38) L170P probably damaging Het
Ddx28 A G 8: 106,010,580 (GRCm38) F282S probably damaging Het
Egf A G 3: 129,686,260 (GRCm38) I497T probably benign Het
Emsy A G 7: 98,593,455 (GRCm38) V1159A probably benign Het
Hk3 C A 13: 55,007,063 (GRCm38) probably benign Het
Htt A G 5: 34,878,856 (GRCm38) D2049G probably benign Het
Inpp5d C A 1: 87,683,750 (GRCm38) S45* probably null Het
Irf8 A G 8: 120,753,380 (GRCm38) Y119C probably damaging Het
Klk1b4 T C 7: 44,211,176 (GRCm38) probably null Het
Macf1 A G 4: 123,486,720 (GRCm38) S1273P probably damaging Het
Man2c1 A T 9: 57,141,819 (GRCm38) H867L probably benign Het
Mgat4e T C 1: 134,541,449 (GRCm38) T286A probably damaging Het
Necab1 T A 4: 15,005,079 (GRCm38) E128D probably damaging Het
Or10ak9 G A 4: 118,869,131 (GRCm38) V117I probably benign Het
Pds5a A G 5: 65,615,294 (GRCm38) V1322A probably benign Het
Poc1b C T 10: 99,129,641 (GRCm38) T144I probably damaging Het
Prcc T A 3: 87,870,080 (GRCm38) N196Y probably damaging Het
Psma5 G A 3: 108,279,795 (GRCm38) V237M possibly damaging Het
Rap1gds1 A G 3: 139,050,561 (GRCm38) L11P probably damaging Het
Rapgef3 A G 15: 97,748,223 (GRCm38) F132S probably damaging Het
Rgs13 T G 1: 144,171,441 (GRCm38) D14A probably benign Het
Rlig1 A C 10: 100,573,611 (GRCm38) D313E probably damaging Het
Stxbp4 A G 11: 90,621,649 (GRCm38) probably benign Het
Tcerg1 C A 18: 42,573,309 (GRCm38) A1017D probably damaging Het
Tent5c T C 3: 100,473,174 (GRCm38) K89E probably benign Het
Tmem79 T C 3: 88,332,576 (GRCm38) I276V possibly damaging Het
Tmem94 C A 11: 115,790,009 (GRCm38) H113N probably damaging Het
Vil1 G A 1: 74,428,238 (GRCm38) D715N probably damaging Het
Vmn2r96 A G 17: 18,582,964 (GRCm38) T187A probably benign Het
Zfhx4 T A 3: 5,413,094 (GRCm38) S3590T probably damaging Het
Other mutations in Mug2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00708:Mug2 APN 6 122,047,487 (GRCm38) missense possibly damaging 0.83
IGL00957:Mug2 APN 6 122,040,654 (GRCm38) missense probably damaging 0.99
IGL01338:Mug2 APN 6 122,049,628 (GRCm38) splice site probably benign
IGL01477:Mug2 APN 6 122,081,684 (GRCm38) splice site probably benign
IGL01926:Mug2 APN 6 122,036,104 (GRCm38) splice site probably benign
IGL02019:Mug2 APN 6 122,047,435 (GRCm38) missense probably benign 0.02
IGL02305:Mug2 APN 6 122,036,056 (GRCm38) missense probably benign
IGL02310:Mug2 APN 6 122,059,123 (GRCm38) splice site probably benign
IGL02484:Mug2 APN 6 122,072,753 (GRCm38) missense probably damaging 1.00
IGL02516:Mug2 APN 6 122,070,843 (GRCm38) missense probably damaging 1.00
IGL02531:Mug2 APN 6 122,072,771 (GRCm38) missense probably damaging 1.00
IGL02666:Mug2 APN 6 122,081,326 (GRCm38) missense probably damaging 1.00
IGL02936:Mug2 APN 6 122,081,387 (GRCm38) critical splice donor site probably null
R0114:Mug2 UTSW 6 122,040,648 (GRCm38) missense probably damaging 1.00
R0119:Mug2 UTSW 6 122,036,063 (GRCm38) missense probably benign 0.00
R0123:Mug2 UTSW 6 122,074,714 (GRCm38) missense possibly damaging 0.89
R0144:Mug2 UTSW 6 122,071,011 (GRCm38) splice site probably benign
R0225:Mug2 UTSW 6 122,074,714 (GRCm38) missense possibly damaging 0.89
R0514:Mug2 UTSW 6 122,081,599 (GRCm38) missense probably damaging 1.00
R0763:Mug2 UTSW 6 122,075,294 (GRCm38) missense probably benign
R0959:Mug2 UTSW 6 122,085,495 (GRCm38) missense probably benign 0.33
R1104:Mug2 UTSW 6 122,059,055 (GRCm38) missense probably benign
R1239:Mug2 UTSW 6 122,081,678 (GRCm38) splice site probably benign
R1318:Mug2 UTSW 6 122,077,402 (GRCm38) missense probably damaging 1.00
R1460:Mug2 UTSW 6 122,040,533 (GRCm38) splice site probably benign
R1706:Mug2 UTSW 6 122,036,232 (GRCm38) splice site probably benign
R1761:Mug2 UTSW 6 122,074,705 (GRCm38) missense probably benign 0.20
R1901:Mug2 UTSW 6 122,071,842 (GRCm38) missense probably benign 0.02
R1913:Mug2 UTSW 6 122,070,870 (GRCm38) missense probably damaging 1.00
R1943:Mug2 UTSW 6 122,079,639 (GRCm38) missense probably benign
R2054:Mug2 UTSW 6 122,077,492 (GRCm38) missense probably damaging 1.00
R2060:Mug2 UTSW 6 122,079,612 (GRCm38) missense probably benign
R2420:Mug2 UTSW 6 122,083,460 (GRCm38) missense probably damaging 1.00
R2432:Mug2 UTSW 6 122,084,376 (GRCm38) missense possibly damaging 0.93
R2916:Mug2 UTSW 6 122,074,724 (GRCm38) splice site probably null
R2918:Mug2 UTSW 6 122,074,724 (GRCm38) splice site probably null
R3423:Mug2 UTSW 6 122,047,506 (GRCm38) splice site probably benign
R3834:Mug2 UTSW 6 122,049,787 (GRCm38) critical splice donor site probably null
R3902:Mug2 UTSW 6 122,075,567 (GRCm38) missense probably damaging 1.00
R3941:Mug2 UTSW 6 122,063,563 (GRCm38) missense probably benign
R4227:Mug2 UTSW 6 122,040,732 (GRCm38) missense probably benign 0.10
R4284:Mug2 UTSW 6 122,063,673 (GRCm38) missense probably benign 0.00
R4287:Mug2 UTSW 6 122,063,673 (GRCm38) missense probably benign 0.00
R4377:Mug2 UTSW 6 122,071,007 (GRCm38) critical splice donor site probably null
R4419:Mug2 UTSW 6 122,079,630 (GRCm38) missense probably damaging 1.00
R4498:Mug2 UTSW 6 122,082,752 (GRCm38) missense probably damaging 0.99
R4566:Mug2 UTSW 6 122,079,638 (GRCm38) missense probably benign 0.00
R4690:Mug2 UTSW 6 122,036,296 (GRCm38) missense probably benign
R4732:Mug2 UTSW 6 122,071,872 (GRCm38) missense probably damaging 0.99
R4733:Mug2 UTSW 6 122,071,872 (GRCm38) missense probably damaging 0.99
R4741:Mug2 UTSW 6 122,079,613 (GRCm38) missense probably benign
R4888:Mug2 UTSW 6 122,081,195 (GRCm38) missense probably damaging 1.00
R5199:Mug2 UTSW 6 122,040,660 (GRCm38) missense probably benign
R5347:Mug2 UTSW 6 122,081,592 (GRCm38) missense probably damaging 1.00
R5457:Mug2 UTSW 6 122,049,729 (GRCm38) nonsense probably null
R5495:Mug2 UTSW 6 122,079,650 (GRCm38) missense probably damaging 0.96
R5509:Mug2 UTSW 6 122,084,381 (GRCm38) missense possibly damaging 0.84
R6006:Mug2 UTSW 6 122,083,500 (GRCm38) missense probably null 0.98
R6180:Mug2 UTSW 6 122,079,606 (GRCm38) missense probably benign 0.01
R6184:Mug2 UTSW 6 122,037,046 (GRCm38) missense probably benign
R6199:Mug2 UTSW 6 122,047,439 (GRCm38) missense probably benign 0.05
R6262:Mug2 UTSW 6 122,075,255 (GRCm38) missense probably damaging 1.00
R6416:Mug2 UTSW 6 122,082,754 (GRCm38) missense probably damaging 1.00
R6548:Mug2 UTSW 6 122,047,442 (GRCm38) missense probably damaging 1.00
R6703:Mug2 UTSW 6 122,078,694 (GRCm38) missense probably benign 0.25
R7106:Mug2 UTSW 6 122,082,721 (GRCm38) missense probably damaging 1.00
R7131:Mug2 UTSW 6 122,075,247 (GRCm38) missense probably damaging 1.00
R7372:Mug2 UTSW 6 122,083,466 (GRCm38) missense possibly damaging 0.88
R7379:Mug2 UTSW 6 122,047,487 (GRCm38) missense possibly damaging 0.83
R7419:Mug2 UTSW 6 122,040,570 (GRCm38) missense possibly damaging 0.86
R7423:Mug2 UTSW 6 122,079,726 (GRCm38) missense probably benign 0.00
R7581:Mug2 UTSW 6 122,063,711 (GRCm38) missense probably damaging 1.00
R7582:Mug2 UTSW 6 122,079,644 (GRCm38) missense probably damaging 0.99
R7672:Mug2 UTSW 6 122,040,719 (GRCm38) missense probably benign 0.37
R7713:Mug2 UTSW 6 122,078,795 (GRCm38) missense possibly damaging 0.83
R7759:Mug2 UTSW 6 122,081,358 (GRCm38) missense probably damaging 1.00
R7834:Mug2 UTSW 6 122,036,282 (GRCm38) missense probably benign
R7850:Mug2 UTSW 6 122,075,211 (GRCm38) missense probably damaging 1.00
R8029:Mug2 UTSW 6 122,081,545 (GRCm38) critical splice acceptor site probably null
R8127:Mug2 UTSW 6 122,075,608 (GRCm38) missense probably benign 0.01
R8335:Mug2 UTSW 6 122,040,584 (GRCm38) missense probably benign
R8348:Mug2 UTSW 6 122,072,233 (GRCm38) nonsense probably null
R8557:Mug2 UTSW 6 122,063,701 (GRCm38) missense probably damaging 0.99
R8798:Mug2 UTSW 6 122,081,610 (GRCm38) missense probably damaging 1.00
R8823:Mug2 UTSW 6 122,063,689 (GRCm38) missense possibly damaging 0.89
R9029:Mug2 UTSW 6 122,084,369 (GRCm38) missense probably damaging 1.00
R9153:Mug2 UTSW 6 122,040,668 (GRCm38) missense possibly damaging 0.71
R9185:Mug2 UTSW 6 122,077,483 (GRCm38) missense probably benign 0.06
R9186:Mug2 UTSW 6 122,075,289 (GRCm38) missense probably damaging 0.99
R9418:Mug2 UTSW 6 122,040,741 (GRCm38) missense probably benign 0.00
R9464:Mug2 UTSW 6 122,051,731 (GRCm38) missense probably benign 0.01
R9622:Mug2 UTSW 6 122,051,792 (GRCm38) missense probably benign 0.29
Z1177:Mug2 UTSW 6 122,037,121 (GRCm38) missense probably damaging 1.00
Posted On 2013-10-07