Incidental Mutation 'IGL03265:4932438A13Rik'
ID 415036
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 4932438A13Rik
Ensembl Gene ENSMUSG00000037270
Gene Name RIKEN cDNA 4932438A13 gene
Synonyms Tweek, FSA
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # IGL03265
Quality Score
Status
Chromosome 3
Chromosomal Location 36863104-37053033 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to A at 37047991 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glutamic Acid at position 4777 (D4777E)
Ref Sequence ENSEMBL: ENSMUSP00000117808 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000057272] [ENSMUST00000138950] [ENSMUST00000152564]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000057272
AA Change: D4777E

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
SMART Domains Protein: ENSMUSP00000060199
Gene: ENSMUSG00000037270
AA Change: D4777E

DomainStartEndE-ValueType
transmembrane domain 25 47 N/A INTRINSIC
low complexity region 701 716 N/A INTRINSIC
low complexity region 767 779 N/A INTRINSIC
low complexity region 1127 1138 N/A INTRINSIC
low complexity region 1154 1166 N/A INTRINSIC
low complexity region 1226 1240 N/A INTRINSIC
low complexity region 1381 1402 N/A INTRINSIC
low complexity region 1541 1547 N/A INTRINSIC
low complexity region 1593 1607 N/A INTRINSIC
low complexity region 1810 1821 N/A INTRINSIC
low complexity region 1981 1995 N/A INTRINSIC
low complexity region 2182 2191 N/A INTRINSIC
low complexity region 2336 2349 N/A INTRINSIC
low complexity region 2614 2657 N/A INTRINSIC
low complexity region 3468 3480 N/A INTRINSIC
low complexity region 3717 3742 N/A INTRINSIC
low complexity region 3816 3837 N/A INTRINSIC
low complexity region 3919 3929 N/A INTRINSIC
low complexity region 3941 3948 N/A INTRINSIC
low complexity region 4024 4038 N/A INTRINSIC
low complexity region 4041 4049 N/A INTRINSIC
low complexity region 4117 4149 N/A INTRINSIC
low complexity region 4172 4185 N/A INTRINSIC
low complexity region 4359 4380 N/A INTRINSIC
FSA_C 4386 4990 N/A SMART
low complexity region 4993 5004 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000126099
Predicted Effect probably benign
Transcript: ENSMUST00000138950
AA Change: D1279E

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000118092
Gene: ENSMUSG00000037270
AA Change: D1279E

DomainStartEndE-ValueType
low complexity region 254 279 N/A INTRINSIC
low complexity region 353 374 N/A INTRINSIC
low complexity region 526 540 N/A INTRINSIC
low complexity region 543 551 N/A INTRINSIC
low complexity region 619 651 N/A INTRINSIC
low complexity region 674 687 N/A INTRINSIC
low complexity region 861 882 N/A INTRINSIC
FSA_C 888 1492 N/A SMART
low complexity region 1495 1506 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000139667
Predicted Effect unknown
Transcript: ENSMUST00000141740
AA Change: D1357E
SMART Domains Protein: ENSMUSP00000117814
Gene: ENSMUSG00000037270
AA Change: D1357E

DomainStartEndE-ValueType
low complexity region 28 40 N/A INTRINSIC
low complexity region 298 323 N/A INTRINSIC
low complexity region 397 418 N/A INTRINSIC
low complexity region 500 510 N/A INTRINSIC
low complexity region 522 529 N/A INTRINSIC
low complexity region 605 619 N/A INTRINSIC
low complexity region 622 630 N/A INTRINSIC
low complexity region 698 730 N/A INTRINSIC
low complexity region 753 766 N/A INTRINSIC
low complexity region 940 961 N/A INTRINSIC
FSA_C 967 1571 N/A SMART
low complexity region 1574 1585 N/A INTRINSIC
Predicted Effect unknown
Transcript: ENSMUST00000146948
AA Change: D1482E
SMART Domains Protein: ENSMUSP00000121356
Gene: ENSMUSG00000037270
AA Change: D1482E

DomainStartEndE-ValueType
low complexity region 121 133 N/A INTRINSIC
low complexity region 167 177 N/A INTRINSIC
low complexity region 458 483 N/A INTRINSIC
low complexity region 557 578 N/A INTRINSIC
low complexity region 730 744 N/A INTRINSIC
low complexity region 747 755 N/A INTRINSIC
low complexity region 823 855 N/A INTRINSIC
low complexity region 878 891 N/A INTRINSIC
low complexity region 1065 1086 N/A INTRINSIC
FSA_C 1092 1696 N/A SMART
low complexity region 1699 1710 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000152564
AA Change: D4777E

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
SMART Domains Protein: ENSMUSP00000117808
Gene: ENSMUSG00000037270
AA Change: D4777E

DomainStartEndE-ValueType
transmembrane domain 25 47 N/A INTRINSIC
low complexity region 701 716 N/A INTRINSIC
low complexity region 767 779 N/A INTRINSIC
low complexity region 1127 1138 N/A INTRINSIC
low complexity region 1154 1166 N/A INTRINSIC
low complexity region 1226 1240 N/A INTRINSIC
low complexity region 1381 1402 N/A INTRINSIC
low complexity region 1541 1547 N/A INTRINSIC
low complexity region 1593 1607 N/A INTRINSIC
low complexity region 1810 1821 N/A INTRINSIC
low complexity region 1981 1995 N/A INTRINSIC
low complexity region 2182 2191 N/A INTRINSIC
low complexity region 2336 2349 N/A INTRINSIC
low complexity region 2614 2657 N/A INTRINSIC
low complexity region 3468 3480 N/A INTRINSIC
low complexity region 3717 3742 N/A INTRINSIC
low complexity region 3816 3837 N/A INTRINSIC
low complexity region 3919 3929 N/A INTRINSIC
low complexity region 3941 3948 N/A INTRINSIC
low complexity region 4024 4038 N/A INTRINSIC
low complexity region 4041 4049 N/A INTRINSIC
low complexity region 4117 4149 N/A INTRINSIC
low complexity region 4172 4185 N/A INTRINSIC
low complexity region 4359 4380 N/A INTRINSIC
FSA_C 4386 4990 N/A SMART
low complexity region 4993 5004 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000196036
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is located on the long arm of chromosome 4 in a region that is associated with susceptibility to celiac disease. The encoded protein is similar to a Chinese hamster protein that is associated with spermatocyte and adipocyte differentiation. The C-terminus of the protein is also similar to a Caenorhabditis elegans protein that plays a role in lipid storage. In mammals, this protein is thought to function in the regulation of epithelial growth and differentiation, and in tumor development. [provided by RefSeq, Oct 2009]
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca8a C A 11: 110,053,103 (GRCm38) M1113I probably benign Het
Acvr1b A G 15: 101,203,078 (GRCm38) R374G probably damaging Het
Akr1a1 A G 4: 116,637,817 (GRCm38) M286T probably benign Het
Anapc1 T C 2: 128,627,197 (GRCm38) S1575G probably damaging Het
Apba2 A G 7: 64,695,323 (GRCm38) D87G probably damaging Het
Arhgap21 A G 2: 20,849,628 (GRCm38) F1641S probably benign Het
Atad2b T A 12: 5,024,628 (GRCm38) H1062Q probably benign Het
Bivm A G 1: 44,141,845 (GRCm38) R396G probably damaging Het
Bmi1 T A 2: 18,681,861 (GRCm38) M17K possibly damaging Het
Bptf T C 11: 107,054,628 (GRCm38) N2480S probably benign Het
Cacna2d3 T C 14: 28,952,286 (GRCm38) E944G probably damaging Het
Ces2a C T 8: 104,737,443 (GRCm38) H236Y possibly damaging Het
Dnah7a T C 1: 53,528,848 (GRCm38) D1863G probably benign Het
Dnajc17 C A 2: 119,185,718 (GRCm38) E91D probably benign Het
Dus2 C A 8: 106,033,791 (GRCm38) probably benign Het
Epha6 T C 16: 60,060,231 (GRCm38) probably benign Het
Erap1 A T 13: 74,664,127 (GRCm38) T354S probably damaging Het
Fbxo11 T C 17: 87,992,831 (GRCm38) H851R probably damaging Het
Gm20532 G A 2: 26,632,684 (GRCm38) C90Y unknown Het
Gpr21 T C 2: 37,518,074 (GRCm38) Y211H probably damaging Het
Hectd4 A G 5: 121,259,939 (GRCm38) probably benign Het
Hephl1 G A 9: 15,060,959 (GRCm38) T895I probably benign Het
Hey1 T C 3: 8,664,914 (GRCm38) Y161C probably benign Het
Kdr A G 5: 75,960,773 (GRCm38) Y526H probably damaging Het
Lpp A G 16: 24,761,987 (GRCm38) Y151C probably damaging Het
Macc1 A G 12: 119,446,976 (GRCm38) N493S probably benign Het
Olfr1022 T A 2: 85,869,150 (GRCm38) M186K possibly damaging Het
Olfr1101 T A 2: 86,989,080 (GRCm38) Y32F probably damaging Het
Olfr315 T C 11: 58,778,871 (GRCm38) V248A probably damaging Het
Olfr605 C A 7: 103,442,448 (GRCm38) R225L probably benign Het
Olfr786 A T 10: 129,436,925 (GRCm38) T38S possibly damaging Het
Pcdhb21 A G 18: 37,515,153 (GRCm38) D445G probably damaging Het
Prkra T C 2: 76,640,270 (GRCm38) N123D probably benign Het
Slc25a33 A C 4: 149,762,436 (GRCm38) L56R probably damaging Het
Usp36 A G 11: 118,264,809 (GRCm38) V714A possibly damaging Het
Vmn1r174 T A 7: 23,754,473 (GRCm38) L188* probably null Het
Vmn2r12 A G 5: 109,092,070 (GRCm38) V209A probably benign Het
Zfp809 A G 9: 22,243,043 (GRCm38) Y352C probably benign Het
Other mutations in 4932438A13Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00428:4932438A13Rik APN 3 37,011,727 (GRCm38) missense probably benign 0.00
IGL00434:4932438A13Rik APN 3 36,987,299 (GRCm38) missense probably damaging 0.98
IGL00640:4932438A13Rik APN 3 36,908,218 (GRCm38) missense probably damaging 1.00
IGL00693:4932438A13Rik APN 3 37,052,547 (GRCm38) utr 3 prime probably benign
IGL00721:4932438A13Rik APN 3 37,030,751 (GRCm38) splice site probably null
IGL00756:4932438A13Rik APN 3 36,908,218 (GRCm38) missense probably damaging 1.00
IGL00896:4932438A13Rik APN 3 37,039,462 (GRCm38) missense probably benign
IGL00902:4932438A13Rik APN 3 37,041,345 (GRCm38) missense probably damaging 1.00
IGL00980:4932438A13Rik APN 3 37,000,041 (GRCm38) missense probably damaging 1.00
IGL01019:4932438A13Rik APN 3 37,006,984 (GRCm38) critical splice acceptor site probably null
IGL01025:4932438A13Rik APN 3 37,046,280 (GRCm38) missense possibly damaging 0.89
IGL01306:4932438A13Rik APN 3 37,005,013 (GRCm38) splice site probably benign
IGL01370:4932438A13Rik APN 3 36,947,755 (GRCm38) missense probably benign 0.07
IGL01377:4932438A13Rik APN 3 36,973,452 (GRCm38) critical splice donor site probably null
IGL01401:4932438A13Rik APN 3 36,942,292 (GRCm38) missense probably benign
IGL01419:4932438A13Rik APN 3 37,048,121 (GRCm38) missense probably damaging 1.00
IGL01432:4932438A13Rik APN 3 37,003,759 (GRCm38) missense possibly damaging 0.87
IGL01433:4932438A13Rik APN 3 36,887,770 (GRCm38) missense probably damaging 1.00
IGL01452:4932438A13Rik APN 3 36,996,308 (GRCm38) unclassified probably benign
IGL01520:4932438A13Rik APN 3 36,973,260 (GRCm38) nonsense probably null
IGL01524:4932438A13Rik APN 3 36,942,382 (GRCm38) missense possibly damaging 0.90
IGL01628:4932438A13Rik APN 3 37,008,485 (GRCm38) missense probably damaging 1.00
IGL01638:4932438A13Rik APN 3 36,974,311 (GRCm38) missense probably damaging 1.00
IGL01650:4932438A13Rik APN 3 36,992,673 (GRCm38) splice site probably benign
IGL01717:4932438A13Rik APN 3 37,034,736 (GRCm38) missense probably benign
IGL01767:4932438A13Rik APN 3 37,041,363 (GRCm38) missense probably benign 0.29
IGL01813:4932438A13Rik APN 3 36,928,520 (GRCm38) missense possibly damaging 0.90
IGL01998:4932438A13Rik APN 3 36,957,016 (GRCm38) missense possibly damaging 0.49
IGL02172:4932438A13Rik APN 3 37,004,873 (GRCm38) missense probably damaging 0.99
IGL02197:4932438A13Rik APN 3 36,906,735 (GRCm38) missense probably damaging 1.00
IGL02248:4932438A13Rik APN 3 36,969,290 (GRCm38) critical splice donor site probably null
IGL02273:4932438A13Rik APN 3 36,921,437 (GRCm38) splice site probably benign
IGL02403:4932438A13Rik APN 3 37,030,664 (GRCm38) missense probably benign
IGL02492:4932438A13Rik APN 3 37,048,113 (GRCm38) missense probably benign 0.04
IGL02517:4932438A13Rik APN 3 36,958,868 (GRCm38) missense probably damaging 1.00
IGL02519:4932438A13Rik APN 3 36,895,315 (GRCm38) missense probably damaging 1.00
IGL02586:4932438A13Rik APN 3 37,044,608 (GRCm38) nonsense probably null
IGL02620:4932438A13Rik APN 3 37,035,945 (GRCm38) missense possibly damaging 0.95
IGL02621:4932438A13Rik APN 3 37,041,484 (GRCm38) splice site probably benign
IGL02670:4932438A13Rik APN 3 36,967,305 (GRCm38) nonsense probably null
IGL02806:4932438A13Rik APN 3 36,946,494 (GRCm38) missense possibly damaging 0.95
IGL02985:4932438A13Rik APN 3 36,958,757 (GRCm38) missense probably damaging 0.99
IGL03004:4932438A13Rik APN 3 36,965,677 (GRCm38) splice site probably benign
IGL03037:4932438A13Rik APN 3 36,969,207 (GRCm38) missense probably benign 0.23
IGL03037:4932438A13Rik APN 3 36,969,208 (GRCm38) missense probably damaging 1.00
IGL03062:4932438A13Rik APN 3 37,038,517 (GRCm38) splice site probably benign
IGL03137:4932438A13Rik APN 3 37,034,602 (GRCm38) missense probably damaging 0.98
IGL03150:4932438A13Rik APN 3 36,948,066 (GRCm38) missense probably damaging 1.00
IGL03204:4932438A13Rik APN 3 37,050,934 (GRCm38) splice site probably benign
IGL03207:4932438A13Rik APN 3 36,949,996 (GRCm38) missense possibly damaging 0.73
IGL03256:4932438A13Rik APN 3 36,906,683 (GRCm38) splice site probably benign
IGL03264:4932438A13Rik APN 3 37,002,635 (GRCm38) missense probably damaging 1.00
IGL03303:4932438A13Rik APN 3 36,870,077 (GRCm38) missense possibly damaging 0.90
admonished UTSW 3 36,948,304 (GRCm38) missense probably damaging 1.00
alerted UTSW 3 37,033,265 (GRCm38) missense possibly damaging 0.85
informed UTSW 3 36,965,849 (GRCm38) missense probably damaging 1.00
resolved UTSW 3 36,921,221 (GRCm38) missense possibly damaging 0.60
tipped UTSW 3 36,988,085 (GRCm38) missense possibly damaging 0.81
warned UTSW 3 36,965,621 (GRCm38) missense probably damaging 1.00
FR4340:4932438A13Rik UTSW 3 37,050,752 (GRCm38) critical splice acceptor site probably benign
FR4737:4932438A13Rik UTSW 3 37,050,754 (GRCm38) critical splice acceptor site probably benign
PIT4515001:4932438A13Rik UTSW 3 36,974,236 (GRCm38) missense probably damaging 1.00
R0035:4932438A13Rik UTSW 3 36,987,598 (GRCm38) nonsense probably null
R0047:4932438A13Rik UTSW 3 36,908,192 (GRCm38) missense possibly damaging 0.83
R0047:4932438A13Rik UTSW 3 36,908,192 (GRCm38) missense possibly damaging 0.83
R0068:4932438A13Rik UTSW 3 36,952,221 (GRCm38) missense probably benign 0.28
R0068:4932438A13Rik UTSW 3 36,952,221 (GRCm38) missense probably benign 0.28
R0092:4932438A13Rik UTSW 3 37,028,159 (GRCm38) missense probably benign 0.41
R0233:4932438A13Rik UTSW 3 36,948,563 (GRCm38) nonsense probably null
R0233:4932438A13Rik UTSW 3 36,948,563 (GRCm38) nonsense probably null
R0256:4932438A13Rik UTSW 3 36,917,773 (GRCm38) missense probably benign 0.01
R0277:4932438A13Rik UTSW 3 36,943,182 (GRCm38) nonsense probably null
R0321:4932438A13Rik UTSW 3 36,906,788 (GRCm38) splice site probably null
R0323:4932438A13Rik UTSW 3 36,943,182 (GRCm38) nonsense probably null
R0335:4932438A13Rik UTSW 3 36,969,152 (GRCm38) missense probably damaging 1.00
R0375:4932438A13Rik UTSW 3 37,046,252 (GRCm38) missense probably damaging 0.99
R0437:4932438A13Rik UTSW 3 36,989,804 (GRCm38) missense possibly damaging 0.81
R0445:4932438A13Rik UTSW 3 37,000,065 (GRCm38) missense probably damaging 0.99
R0496:4932438A13Rik UTSW 3 36,987,635 (GRCm38) missense probably damaging 1.00
R0531:4932438A13Rik UTSW 3 37,036,825 (GRCm38) missense probably damaging 1.00
R0543:4932438A13Rik UTSW 3 36,996,458 (GRCm38) missense probably benign 0.22
R0545:4932438A13Rik UTSW 3 36,987,690 (GRCm38) splice site probably benign
R0674:4932438A13Rik UTSW 3 37,044,626 (GRCm38) missense possibly damaging 0.86
R0745:4932438A13Rik UTSW 3 36,928,463 (GRCm38) missense probably damaging 1.00
R0755:4932438A13Rik UTSW 3 36,946,364 (GRCm38) missense probably damaging 1.00
R0785:4932438A13Rik UTSW 3 36,959,334 (GRCm38) splice site probably benign
R1056:4932438A13Rik UTSW 3 37,044,680 (GRCm38) missense probably benign 0.44
R1056:4932438A13Rik UTSW 3 36,983,453 (GRCm38) missense possibly damaging 0.69
R1080:4932438A13Rik UTSW 3 36,988,255 (GRCm38) missense probably damaging 1.00
R1103:4932438A13Rik UTSW 3 36,996,523 (GRCm38) missense probably benign
R1119:4932438A13Rik UTSW 3 36,987,045 (GRCm38) missense probably damaging 1.00
R1170:4932438A13Rik UTSW 3 37,044,631 (GRCm38) missense probably damaging 0.98
R1183:4932438A13Rik UTSW 3 36,895,303 (GRCm38) missense possibly damaging 0.51
R1186:4932438A13Rik UTSW 3 36,996,312 (GRCm38) unclassified probably benign
R1201:4932438A13Rik UTSW 3 36,948,375 (GRCm38) missense probably benign
R1219:4932438A13Rik UTSW 3 36,946,470 (GRCm38) nonsense probably null
R1270:4932438A13Rik UTSW 3 36,952,184 (GRCm38) missense probably damaging 1.00
R1273:4932438A13Rik UTSW 3 36,987,210 (GRCm38) missense probably damaging 1.00
R1338:4932438A13Rik UTSW 3 37,052,535 (GRCm38) missense unknown
R1364:4932438A13Rik UTSW 3 36,987,030 (GRCm38) missense probably damaging 1.00
R1437:4932438A13Rik UTSW 3 36,942,429 (GRCm38) missense possibly damaging 0.65
R1447:4932438A13Rik UTSW 3 36,965,586 (GRCm38) missense probably damaging 0.98
R1467:4932438A13Rik UTSW 3 37,035,945 (GRCm38) missense probably damaging 0.99
R1467:4932438A13Rik UTSW 3 37,035,945 (GRCm38) missense probably damaging 0.99
R1470:4932438A13Rik UTSW 3 36,998,331 (GRCm38) missense probably benign 0.31
R1470:4932438A13Rik UTSW 3 36,998,331 (GRCm38) missense probably benign 0.31
R1481:4932438A13Rik UTSW 3 37,008,434 (GRCm38) missense probably damaging 0.99
R1528:4932438A13Rik UTSW 3 37,052,535 (GRCm38) missense unknown
R1533:4932438A13Rik UTSW 3 37,041,375 (GRCm38) missense probably damaging 1.00
R1546:4932438A13Rik UTSW 3 36,870,056 (GRCm38) missense possibly damaging 0.64
R1606:4932438A13Rik UTSW 3 36,942,399 (GRCm38) missense probably damaging 1.00
R1638:4932438A13Rik UTSW 3 37,035,812 (GRCm38) nonsense probably null
R1772:4932438A13Rik UTSW 3 36,959,432 (GRCm38) missense probably damaging 1.00
R1896:4932438A13Rik UTSW 3 36,908,231 (GRCm38) nonsense probably null
R1919:4932438A13Rik UTSW 3 37,006,983 (GRCm38) critical splice acceptor site probably null
R1983:4932438A13Rik UTSW 3 36,887,865 (GRCm38) missense probably null 1.00
R1987:4932438A13Rik UTSW 3 36,953,985 (GRCm38) critical splice donor site probably null
R1992:4932438A13Rik UTSW 3 37,000,032 (GRCm38) missense probably benign 0.32
R1999:4932438A13Rik UTSW 3 36,908,211 (GRCm38) missense probably damaging 1.00
R2004:4932438A13Rik UTSW 3 36,895,378 (GRCm38) missense possibly damaging 0.77
R2010:4932438A13Rik UTSW 3 36,928,551 (GRCm38) missense probably benign 0.09
R2027:4932438A13Rik UTSW 3 37,047,961 (GRCm38) splice site probably benign
R2039:4932438A13Rik UTSW 3 37,003,878 (GRCm38) missense possibly damaging 0.66
R2054:4932438A13Rik UTSW 3 36,947,853 (GRCm38) missense probably benign 0.01
R2089:4932438A13Rik UTSW 3 36,988,256 (GRCm38) missense probably damaging 1.00
R2091:4932438A13Rik UTSW 3 36,988,256 (GRCm38) missense probably damaging 1.00
R2091:4932438A13Rik UTSW 3 36,988,256 (GRCm38) missense probably damaging 1.00
R2091:4932438A13Rik UTSW 3 36,953,970 (GRCm38) missense probably damaging 1.00
R2220:4932438A13Rik UTSW 3 36,875,530 (GRCm38) critical splice donor site probably null
R2374:4932438A13Rik UTSW 3 36,885,396 (GRCm38) missense probably benign 0.00
R2437:4932438A13Rik UTSW 3 36,958,685 (GRCm38) splice site probably null
R2860:4932438A13Rik UTSW 3 36,965,849 (GRCm38) missense probably damaging 1.00
R2861:4932438A13Rik UTSW 3 36,965,849 (GRCm38) missense probably damaging 1.00
R2909:4932438A13Rik UTSW 3 36,947,953 (GRCm38) missense probably damaging 1.00
R2925:4932438A13Rik UTSW 3 37,007,122 (GRCm38) missense probably damaging 0.99
R2940:4932438A13Rik UTSW 3 36,958,805 (GRCm38) missense probably damaging 1.00
R3015:4932438A13Rik UTSW 3 36,875,462 (GRCm38) missense probably damaging 1.00
R3086:4932438A13Rik UTSW 3 37,011,703 (GRCm38) missense possibly damaging 0.56
R3159:4932438A13Rik UTSW 3 36,959,415 (GRCm38) missense probably benign 0.17
R3440:4932438A13Rik UTSW 3 37,041,912 (GRCm38) nonsense probably null
R3703:4932438A13Rik UTSW 3 36,987,581 (GRCm38) missense probably damaging 1.00
R3705:4932438A13Rik UTSW 3 36,987,581 (GRCm38) missense probably damaging 1.00
R3795:4932438A13Rik UTSW 3 37,030,565 (GRCm38) missense probably benign 0.30
R3820:4932438A13Rik UTSW 3 37,040,434 (GRCm38) missense probably damaging 1.00
R3862:4932438A13Rik UTSW 3 36,885,398 (GRCm38) missense possibly damaging 0.73
R3944:4932438A13Rik UTSW 3 37,030,061 (GRCm38) missense possibly damaging 0.90
R4020:4932438A13Rik UTSW 3 37,012,575 (GRCm38) intron probably benign
R4091:4932438A13Rik UTSW 3 37,030,589 (GRCm38) missense probably benign 0.00
R4159:4932438A13Rik UTSW 3 36,931,083 (GRCm38) missense probably benign 0.00
R4231:4932438A13Rik UTSW 3 36,920,236 (GRCm38) missense probably benign 0.10
R4368:4932438A13Rik UTSW 3 36,988,147 (GRCm38) nonsense probably null
R4413:4932438A13Rik UTSW 3 36,958,681 (GRCm38) splice site probably null
R4475:4932438A13Rik UTSW 3 37,040,395 (GRCm38) missense probably damaging 1.00
R4488:4932438A13Rik UTSW 3 37,003,933 (GRCm38) missense probably null 0.93
R4489:4932438A13Rik UTSW 3 37,003,933 (GRCm38) missense probably null 0.93
R4516:4932438A13Rik UTSW 3 36,895,311 (GRCm38) missense possibly damaging 0.90
R4580:4932438A13Rik UTSW 3 37,030,025 (GRCm38) missense probably benign 0.02
R4672:4932438A13Rik UTSW 3 36,889,990 (GRCm38) makesense probably null
R4705:4932438A13Rik UTSW 3 37,041,889 (GRCm38) missense probably benign 0.03
R4735:4932438A13Rik UTSW 3 37,004,967 (GRCm38) missense possibly damaging 0.84
R4741:4932438A13Rik UTSW 3 36,942,375 (GRCm38) missense probably damaging 0.99
R4754:4932438A13Rik UTSW 3 37,022,466 (GRCm38) nonsense probably null
R4778:4932438A13Rik UTSW 3 36,937,065 (GRCm38) missense possibly damaging 0.90
R4833:4932438A13Rik UTSW 3 36,964,968 (GRCm38) missense probably damaging 0.96
R4896:4932438A13Rik UTSW 3 36,965,937 (GRCm38) missense probably damaging 1.00
R4910:4932438A13Rik UTSW 3 36,998,199 (GRCm38) missense probably damaging 1.00
R4922:4932438A13Rik UTSW 3 36,987,165 (GRCm38) missense probably damaging 1.00
R4941:4932438A13Rik UTSW 3 36,919,901 (GRCm38) missense probably benign 0.41
R4941:4932438A13Rik UTSW 3 36,917,702 (GRCm38) missense probably damaging 1.00
R4980:4932438A13Rik UTSW 3 36,943,312 (GRCm38) missense probably damaging 1.00
R5030:4932438A13Rik UTSW 3 36,943,399 (GRCm38) intron probably benign
R5049:4932438A13Rik UTSW 3 37,041,390 (GRCm38) missense probably damaging 1.00
R5049:4932438A13Rik UTSW 3 37,040,506 (GRCm38) intron probably benign
R5089:4932438A13Rik UTSW 3 36,987,502 (GRCm38) missense probably benign 0.02
R5092:4932438A13Rik UTSW 3 37,000,085 (GRCm38) missense probably benign 0.14
R5122:4932438A13Rik UTSW 3 37,034,757 (GRCm38) splice site probably null
R5210:4932438A13Rik UTSW 3 37,033,265 (GRCm38) missense possibly damaging 0.85
R5246:4932438A13Rik UTSW 3 37,048,050 (GRCm38) missense probably damaging 1.00
R5289:4932438A13Rik UTSW 3 37,000,109 (GRCm38) missense probably damaging 0.97
R5348:4932438A13Rik UTSW 3 37,048,146 (GRCm38) missense probably damaging 1.00
R5394:4932438A13Rik UTSW 3 36,917,668 (GRCm38) missense probably damaging 1.00
R5434:4932438A13Rik UTSW 3 36,875,516 (GRCm38) missense probably damaging 1.00
R5667:4932438A13Rik UTSW 3 36,917,677 (GRCm38) missense probably benign 0.00
R5686:4932438A13Rik UTSW 3 36,917,660 (GRCm38) missense probably benign 0.00
R5701:4932438A13Rik UTSW 3 36,921,360 (GRCm38) missense probably benign 0.10
R5778:4932438A13Rik UTSW 3 36,958,714 (GRCm38) missense probably damaging 1.00
R5787:4932438A13Rik UTSW 3 36,992,733 (GRCm38) splice site probably null
R5800:4932438A13Rik UTSW 3 37,052,443 (GRCm38) missense probably damaging 1.00
R5819:4932438A13Rik UTSW 3 37,048,600 (GRCm38) missense probably benign 0.12
R5820:4932438A13Rik UTSW 3 37,039,526 (GRCm38) missense probably benign 0.00
R5952:4932438A13Rik UTSW 3 36,965,621 (GRCm38) missense probably damaging 1.00
R5975:4932438A13Rik UTSW 3 36,969,221 (GRCm38) missense possibly damaging 0.64
R5996:4932438A13Rik UTSW 3 36,931,116 (GRCm38) missense probably benign 0.07
R6192:4932438A13Rik UTSW 3 36,988,169 (GRCm38) missense probably benign 0.00
R6225:4932438A13Rik UTSW 3 36,948,304 (GRCm38) missense probably damaging 1.00
R6234:4932438A13Rik UTSW 3 36,983,471 (GRCm38) missense probably benign 0.00
R6244:4932438A13Rik UTSW 3 36,956,999 (GRCm38) missense probably benign
R6263:4932438A13Rik UTSW 3 36,931,111 (GRCm38) missense probably benign 0.06
R6351:4932438A13Rik UTSW 3 36,908,228 (GRCm38) missense probably damaging 1.00
R6380:4932438A13Rik UTSW 3 37,033,307 (GRCm38) missense probably benign 0.19
R6468:4932438A13Rik UTSW 3 37,008,443 (GRCm38) missense probably damaging 1.00
R6759:4932438A13Rik UTSW 3 36,988,085 (GRCm38) missense possibly damaging 0.81
R6792:4932438A13Rik UTSW 3 37,011,566 (GRCm38) critical splice acceptor site probably null
R6809:4932438A13Rik UTSW 3 36,874,282 (GRCm38) missense probably damaging 0.98
R6841:4932438A13Rik UTSW 3 37,021,481 (GRCm38) missense probably damaging 1.00
R6959:4932438A13Rik UTSW 3 36,967,189 (GRCm38) missense probably damaging 1.00
R7102:4932438A13Rik UTSW 3 36,940,798 (GRCm38) missense probably damaging 0.99
R7188:4932438A13Rik UTSW 3 36,950,013 (GRCm38) missense probably benign 0.06
R7212:4932438A13Rik UTSW 3 37,048,009 (GRCm38) missense
R7425:4932438A13Rik UTSW 3 36,983,394 (GRCm38) missense probably benign 0.02
R7425:4932438A13Rik UTSW 3 36,948,341 (GRCm38) missense probably benign
R7451:4932438A13Rik UTSW 3 37,022,807 (GRCm38) splice site probably null
R7604:4932438A13Rik UTSW 3 36,949,843 (GRCm38) splice site probably null
R7622:4932438A13Rik UTSW 3 36,948,413 (GRCm38) nonsense probably null
R7671:4932438A13Rik UTSW 3 36,943,231 (GRCm38) missense probably damaging 0.99
R7699:4932438A13Rik UTSW 3 36,974,172 (GRCm38) missense possibly damaging 0.67
R7699:4932438A13Rik UTSW 3 37,026,154 (GRCm38) missense probably benign 0.00
R7700:4932438A13Rik UTSW 3 36,974,172 (GRCm38) missense possibly damaging 0.67
R7700:4932438A13Rik UTSW 3 37,026,154 (GRCm38) missense probably benign 0.00
R7748:4932438A13Rik UTSW 3 36,959,335 (GRCm38) critical splice acceptor site probably null
R7767:4932438A13Rik UTSW 3 36,920,287 (GRCm38) critical splice donor site probably null
R7787:4932438A13Rik UTSW 3 36,885,408 (GRCm38) missense probably damaging 1.00
R7830:4932438A13Rik UTSW 3 36,964,932 (GRCm38) frame shift probably null
R7849:4932438A13Rik UTSW 3 37,026,328 (GRCm38) missense
R7912:4932438A13Rik UTSW 3 37,007,069 (GRCm38) missense probably damaging 0.99
R7914:4932438A13Rik UTSW 3 36,946,283 (GRCm38) missense probably benign 0.13
R7945:4932438A13Rik UTSW 3 36,965,893 (GRCm38) missense probably benign 0.03
R8039:4932438A13Rik UTSW 3 36,943,214 (GRCm38) missense probably benign 0.12
R8101:4932438A13Rik UTSW 3 37,008,502 (GRCm38) missense probably damaging 1.00
R8143:4932438A13Rik UTSW 3 36,946,508 (GRCm38) critical splice donor site probably null
R8145:4932438A13Rik UTSW 3 36,998,267 (GRCm38) missense probably damaging 1.00
R8171:4932438A13Rik UTSW 3 36,975,713 (GRCm38) missense probably benign 0.00
R8210:4932438A13Rik UTSW 3 37,012,881 (GRCm38) missense
R8250:4932438A13Rik UTSW 3 36,917,662 (GRCm38) missense probably damaging 0.99
R8369:4932438A13Rik UTSW 3 37,011,603 (GRCm38) missense
R8478:4932438A13Rik UTSW 3 37,033,277 (GRCm38) missense possibly damaging 0.74
R8558:4932438A13Rik UTSW 3 37,048,601 (GRCm38) missense
R8688:4932438A13Rik UTSW 3 37,035,917 (GRCm38) missense
R8724:4932438A13Rik UTSW 3 36,890,893 (GRCm38) missense probably damaging 0.99
R8818:4932438A13Rik UTSW 3 36,996,548 (GRCm38) missense possibly damaging 0.60
R8869:4932438A13Rik UTSW 3 36,958,858 (GRCm38) missense probably damaging 0.99
R8887:4932438A13Rik UTSW 3 37,033,354 (GRCm38) missense possibly damaging 0.95
R8899:4932438A13Rik UTSW 3 36,988,280 (GRCm38) missense probably damaging 1.00
R8907:4932438A13Rik UTSW 3 36,948,146 (GRCm38) nonsense probably null
R8960:4932438A13Rik UTSW 3 37,012,983 (GRCm38) missense probably damaging 1.00
R8990:4932438A13Rik UTSW 3 36,921,221 (GRCm38) missense possibly damaging 0.60
R9021:4932438A13Rik UTSW 3 36,998,344 (GRCm38) missense probably benign 0.00
R9048:4932438A13Rik UTSW 3 37,011,777 (GRCm38) missense
R9100:4932438A13Rik UTSW 3 37,044,758 (GRCm38) missense
R9166:4932438A13Rik UTSW 3 36,987,367 (GRCm38) missense probably damaging 1.00
R9176:4932438A13Rik UTSW 3 36,956,703 (GRCm38) missense possibly damaging 0.82
R9202:4932438A13Rik UTSW 3 36,890,821 (GRCm38) missense probably benign
R9303:4932438A13Rik UTSW 3 37,044,820 (GRCm38) missense
R9305:4932438A13Rik UTSW 3 37,044,820 (GRCm38) missense
R9332:4932438A13Rik UTSW 3 37,050,840 (GRCm38) missense
R9362:4932438A13Rik UTSW 3 36,957,013 (GRCm38) missense probably benign
R9493:4932438A13Rik UTSW 3 37,011,736 (GRCm38) missense
R9534:4932438A13Rik UTSW 3 36,998,270 (GRCm38) missense probably benign 0.01
R9569:4932438A13Rik UTSW 3 37,012,621 (GRCm38) missense
R9593:4932438A13Rik UTSW 3 36,947,941 (GRCm38) missense probably damaging 1.00
R9600:4932438A13Rik UTSW 3 37,041,416 (GRCm38) nonsense probably null
R9733:4932438A13Rik UTSW 3 37,048,583 (GRCm38) missense
R9751:4932438A13Rik UTSW 3 37,011,740 (GRCm38) missense
RF013:4932438A13Rik UTSW 3 37,050,757 (GRCm38) critical splice acceptor site probably benign
RF015:4932438A13Rik UTSW 3 37,050,748 (GRCm38) critical splice acceptor site probably benign
RF021:4932438A13Rik UTSW 3 37,050,748 (GRCm38) critical splice acceptor site probably benign
RF023:4932438A13Rik UTSW 3 37,050,760 (GRCm38) critical splice acceptor site probably benign
RF034:4932438A13Rik UTSW 3 37,050,760 (GRCm38) critical splice acceptor site probably benign
RF035:4932438A13Rik UTSW 3 37,050,758 (GRCm38) critical splice acceptor site probably benign
RF055:4932438A13Rik UTSW 3 37,050,757 (GRCm38) critical splice acceptor site probably benign
X0050:4932438A13Rik UTSW 3 36,957,128 (GRCm38) missense probably damaging 1.00
Z1088:4932438A13Rik UTSW 3 36,987,567 (GRCm38) missense probably damaging 1.00
Z1177:4932438A13Rik UTSW 3 36,983,440 (GRCm38) missense possibly damaging 0.88
Z1177:4932438A13Rik UTSW 3 36,919,950 (GRCm38) missense probably benign
Z1177:4932438A13Rik UTSW 3 37,036,707 (GRCm38) missense
Posted On 2016-08-02