Incidental Mutation 'IGL01100:Fat3'
ID 51917
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Fat3
Ensembl Gene ENSMUSG00000074505
Gene Name FAT atypical cadherin 3
Synonyms 9430076A06Rik, D430038H04Rik, LOC382129, LOC234973
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.417) question?
Stock # IGL01100
Quality Score
Status
Chromosome 9
Chromosomal Location 15910189-16501285 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to T at 16375228 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Phenylalanine to Isoleucine at position 1000 (F1000I)
Ref Sequence ENSEMBL: ENSMUSP00000148968 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000082170] [ENSMUST00000217308]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000082170
AA Change: F1000I

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000080808
Gene: ENSMUSG00000074505
AA Change: F1000I

DomainStartEndE-ValueType
signal peptide 1 27 N/A INTRINSIC
CA 65 151 3e-7 SMART
CA 175 259 8.9e-22 SMART
CA 280 368 8.9e-4 SMART
CA 389 465 2.6e-11 SMART
CA 489 571 2e-29 SMART
low complexity region 684 697 N/A INTRINSIC
CA 743 824 1e-24 SMART
low complexity region 830 840 N/A INTRINSIC
CA 848 929 7.6e-26 SMART
CA 953 1034 1.5e-25 SMART
CA 1060 1141 6.6e-32 SMART
CA 1165 1247 1.5e-30 SMART
CA 1273 1349 1.8e-8 SMART
CA 1375 1453 2.9e-12 SMART
CA 1477 1559 3e-22 SMART
CA 1583 1664 3.1e-16 SMART
CA 1688 1762 4.2e-22 SMART
CA 1793 1876 2.5e-26 SMART
CA 1900 1975 1.5e-8 SMART
low complexity region 1983 1994 N/A INTRINSIC
CA 1999 2077 1.4e-18 SMART
CA 2101 2179 6.6e-10 SMART
CA 2203 2280 4.9e-19 SMART
CA 2304 2387 4.3e-29 SMART
CA 2411 2489 4.2e-11 SMART
CA 2513 2593 2.8e-22 SMART
CA 2617 2701 4.3e-10 SMART
CA 2719 2807 2.5e-7 SMART
CA 2831 2917 3.3e-27 SMART
CA 2941 3022 9.4e-23 SMART
CA 3046 3124 2.4e-26 SMART
CA 3148 3229 1.3e-32 SMART
CA 3253 3334 1.3e-29 SMART
CA 3358 3439 4.9e-28 SMART
CA 3463 3544 6.4e-12 SMART
EGF 3793 3828 1.3e-1 SMART
LamG 3852 3989 4.3e-25 SMART
EGF 4019 4053 2.7e-6 SMART
EGF 4058 4091 4.5e-6 SMART
EGF_CA 4093 4129 3.9e-11 SMART
transmembrane domain 4151 4170 N/A INTRINSIC
Predicted Effect probably damaging
Transcript: ENSMUST00000217308
AA Change: F1000I

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: Mice homozgyous for a knock-out allele exhibit abnormal amacrine cell differentiation and migration that result in the formation of two additional plexiform layers and thickened retinal ganglion layer. [provided by MGI curators]
Allele List at MGI

All alleles(3) : Gene trapped(3)

Other mutations in this stock
Total: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca13 T G 11: 9,274,673 (GRCm38) probably null Het
Abca8a C T 11: 110,058,423 (GRCm38) probably null Het
Acad11 A G 9: 104,076,408 (GRCm38) T32A probably damaging Het
Ak7 T A 12: 105,713,574 (GRCm38) N122K probably benign Het
Arrb1 A T 7: 99,587,213 (GRCm38) probably null Het
Csde1 C A 3: 103,040,525 (GRCm38) R132S possibly damaging Het
Emilin1 A G 5: 30,918,404 (GRCm38) H663R probably benign Het
Etaa1 A G 11: 17,952,576 (GRCm38) probably null Het
Foxj2 T C 6: 122,828,391 (GRCm38) L74P probably damaging Het
Gas6 C T 8: 13,475,118 (GRCm38) V289M probably benign Het
Gm10801 A T 2: 98,663,983 (GRCm38) Y135F probably benign Het
Ihh C T 1: 74,946,442 (GRCm38) A295T probably damaging Het
Ip6k2 G T 9: 108,805,744 (GRCm38) S305I probably damaging Het
Kcnk2 A G 1: 189,339,936 (GRCm38) V65A probably damaging Het
Kif26b G A 1: 178,917,244 (GRCm38) C1635Y probably benign Het
Klhdc4 G A 8: 121,821,843 (GRCm38) Q44* probably null Het
Madd C A 2: 91,158,040 (GRCm38) R1216L probably damaging Het
Myo15 T A 11: 60,511,158 (GRCm38) C3076S probably damaging Het
Olfr365 A T 2: 37,201,640 (GRCm38) H133L possibly damaging Het
Olfr670 T A 7: 104,959,995 (GRCm38) I246F probably benign Het
Polq C A 16: 37,061,112 (GRCm38) P934T probably benign Het
Prkaa1 A T 15: 5,174,318 (GRCm38) K227M probably damaging Het
Psap G A 10: 60,299,929 (GRCm38) G388S probably benign Het
Repin1 A G 6: 48,596,905 (GRCm38) E200G probably damaging Het
Samd9l C A 6: 3,375,863 (GRCm38) S466I possibly damaging Het
Slc5a3 A G 16: 92,079,222 (GRCm38) probably benign Het
Smg9 G A 7: 24,416,951 (GRCm38) V314M probably damaging Het
Tktl1 G A X: 74,200,626 (GRCm38) R352H probably benign Het
Ube2z A G 11: 96,063,023 (GRCm38) V123A probably damaging Het
Vmn1r176 A T 7: 23,835,624 (GRCm38) F35I probably benign Het
Zdhhc18 A T 4: 133,612,958 (GRCm38) Y293N probably damaging Het
Other mutations in Fat3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00662:Fat3 APN 9 15,996,427 (GRCm38) missense possibly damaging 0.77
IGL00962:Fat3 APN 9 15,915,519 (GRCm38) missense probably benign 0.14
IGL00966:Fat3 APN 9 15,999,094 (GRCm38) missense possibly damaging 0.69
IGL01104:Fat3 APN 9 16,375,728 (GRCm38) missense possibly damaging 0.92
IGL01104:Fat3 APN 9 15,998,460 (GRCm38) missense probably damaging 1.00
IGL01121:Fat3 APN 9 15,998,401 (GRCm38) missense probably benign 0.00
IGL01407:Fat3 APN 9 16,378,023 (GRCm38) missense probably benign 0.01
IGL01444:Fat3 APN 9 15,998,848 (GRCm38) missense probably damaging 1.00
IGL01634:Fat3 APN 9 15,998,358 (GRCm38) missense probably damaging 1.00
IGL01649:Fat3 APN 9 16,376,719 (GRCm38) missense possibly damaging 0.95
IGL01839:Fat3 APN 9 15,997,872 (GRCm38) missense probably damaging 1.00
IGL01867:Fat3 APN 9 16,377,901 (GRCm38) missense probably benign 0.03
IGL01894:Fat3 APN 9 16,375,849 (GRCm38) missense probably benign
IGL01913:Fat3 APN 9 15,998,790 (GRCm38) missense probably damaging 0.99
IGL02033:Fat3 APN 9 15,915,352 (GRCm38) missense possibly damaging 0.50
IGL02035:Fat3 APN 9 16,377,970 (GRCm38) missense probably benign 0.06
IGL02146:Fat3 APN 9 15,999,582 (GRCm38) missense probably benign
IGL02147:Fat3 APN 9 15,995,985 (GRCm38) missense probably damaging 1.00
IGL02161:Fat3 APN 9 15,997,050 (GRCm38) missense probably benign 0.10
IGL02161:Fat3 APN 9 15,997,051 (GRCm38) nonsense probably null
IGL02164:Fat3 APN 9 16,031,424 (GRCm38) splice site probably benign
IGL02269:Fat3 APN 9 15,915,577 (GRCm38) missense possibly damaging 0.84
IGL02314:Fat3 APN 9 15,969,838 (GRCm38) missense possibly damaging 0.61
IGL02393:Fat3 APN 9 15,988,412 (GRCm38) nonsense probably null
IGL02410:Fat3 APN 9 15,997,845 (GRCm38) missense probably damaging 1.00
IGL02504:Fat3 APN 9 15,959,798 (GRCm38) missense probably damaging 1.00
IGL02572:Fat3 APN 9 15,960,506 (GRCm38) missense probably benign
IGL02623:Fat3 APN 9 15,997,137 (GRCm38) missense probably damaging 1.00
IGL02654:Fat3 APN 9 15,996,975 (GRCm38) missense possibly damaging 0.84
IGL02749:Fat3 APN 9 16,006,711 (GRCm38) missense possibly damaging 0.93
IGL02810:Fat3 APN 9 16,376,850 (GRCm38) missense probably damaging 1.00
IGL02839:Fat3 APN 9 15,919,170 (GRCm38) missense probably damaging 1.00
IGL02890:Fat3 APN 9 15,915,340 (GRCm38) missense probably benign 0.03
IGL02892:Fat3 APN 9 16,377,562 (GRCm38) missense probably damaging 1.00
IGL03090:Fat3 APN 9 16,377,239 (GRCm38) nonsense probably null
IGL03144:Fat3 APN 9 16,375,245 (GRCm38) missense probably damaging 1.00
IGL03199:Fat3 APN 9 16,377,048 (GRCm38) missense possibly damaging 0.83
IGL03365:Fat3 APN 9 15,996,469 (GRCm38) missense probably damaging 1.00
IGL03392:Fat3 APN 9 16,003,862 (GRCm38) missense probably benign
IGL03408:Fat3 APN 9 15,997,957 (GRCm38) nonsense probably null
gagged UTSW 9 15,998,271 (GRCm38) missense probably damaging 1.00
hushed UTSW 9 15,959,869 (GRCm38) missense possibly damaging 0.72
Muffled UTSW 9 15,937,991 (GRCm38) critical splice donor site probably null
muted UTSW 9 15,997,477 (GRCm38) missense possibly damaging 0.93
Softened UTSW 9 16,378,185 (GRCm38) missense probably benign
BB001:Fat3 UTSW 9 15,999,297 (GRCm38) missense probably damaging 1.00
BB002:Fat3 UTSW 9 16,031,360 (GRCm38) missense possibly damaging 0.77
BB011:Fat3 UTSW 9 15,999,297 (GRCm38) missense probably damaging 1.00
BB012:Fat3 UTSW 9 16,031,360 (GRCm38) missense possibly damaging 0.77
F6893:Fat3 UTSW 9 16,006,789 (GRCm38) missense probably damaging 0.99
IGL03050:Fat3 UTSW 9 15,996,600 (GRCm38) missense probably benign 0.04
PIT4142001:Fat3 UTSW 9 15,992,118 (GRCm38) critical splice donor site probably null
PIT4283001:Fat3 UTSW 9 16,006,601 (GRCm38) missense possibly damaging 0.77
PIT4378001:Fat3 UTSW 9 16,376,808 (GRCm38) missense probably benign 0.05
PIT4434001:Fat3 UTSW 9 15,996,316 (GRCm38) missense probably benign 0.00
PIT4468001:Fat3 UTSW 9 15,996,351 (GRCm38) missense probably benign 0.06
R0001:Fat3 UTSW 9 16,377,873 (GRCm38) missense probably damaging 0.99
R0005:Fat3 UTSW 9 15,962,866 (GRCm38) missense probably damaging 1.00
R0005:Fat3 UTSW 9 15,962,866 (GRCm38) missense probably damaging 1.00
R0038:Fat3 UTSW 9 15,915,010 (GRCm38) missense probably damaging 1.00
R0046:Fat3 UTSW 9 15,965,979 (GRCm38) missense possibly damaging 0.65
R0089:Fat3 UTSW 9 15,938,205 (GRCm38) missense probably benign
R0135:Fat3 UTSW 9 16,006,777 (GRCm38) missense probably damaging 1.00
R0255:Fat3 UTSW 9 15,969,706 (GRCm38) splice site probably benign
R0349:Fat3 UTSW 9 16,031,180 (GRCm38) missense probably damaging 1.00
R0361:Fat3 UTSW 9 15,998,403 (GRCm38) missense possibly damaging 0.77
R0382:Fat3 UTSW 9 15,959,756 (GRCm38) missense probably damaging 1.00
R0418:Fat3 UTSW 9 16,246,896 (GRCm38) missense probably damaging 1.00
R0419:Fat3 UTSW 9 15,992,256 (GRCm38) missense probably damaging 1.00
R0437:Fat3 UTSW 9 15,996,932 (GRCm38) missense probably damaging 1.00
R0441:Fat3 UTSW 9 15,945,008 (GRCm38) splice site probably benign
R0480:Fat3 UTSW 9 15,997,729 (GRCm38) missense probably benign 0.00
R0510:Fat3 UTSW 9 15,999,685 (GRCm38) nonsense probably null
R0665:Fat3 UTSW 9 15,997,402 (GRCm38) missense probably benign
R0715:Fat3 UTSW 9 16,375,123 (GRCm38) missense probably benign
R0727:Fat3 UTSW 9 15,996,699 (GRCm38) missense probably damaging 1.00
R0882:Fat3 UTSW 9 16,031,368 (GRCm38) missense possibly damaging 0.84
R0946:Fat3 UTSW 9 15,997,804 (GRCm38) missense possibly damaging 0.95
R1068:Fat3 UTSW 9 15,970,034 (GRCm38) missense probably benign
R1081:Fat3 UTSW 9 16,375,284 (GRCm38) missense possibly damaging 0.62
R1082:Fat3 UTSW 9 16,006,615 (GRCm38) missense probably damaging 1.00
R1148:Fat3 UTSW 9 15,996,774 (GRCm38) missense probably damaging 1.00
R1148:Fat3 UTSW 9 15,996,774 (GRCm38) missense probably damaging 1.00
R1233:Fat3 UTSW 9 15,922,745 (GRCm38) missense probably benign
R1306:Fat3 UTSW 9 16,376,679 (GRCm38) missense probably damaging 1.00
R1311:Fat3 UTSW 9 16,021,410 (GRCm38) missense probably damaging 1.00
R1338:Fat3 UTSW 9 15,925,091 (GRCm38) missense probably benign 0.00
R1395:Fat3 UTSW 9 16,246,916 (GRCm38) missense probably benign 0.00
R1466:Fat3 UTSW 9 16,375,482 (GRCm38) missense probably damaging 0.96
R1466:Fat3 UTSW 9 16,375,482 (GRCm38) missense probably damaging 0.96
R1510:Fat3 UTSW 9 15,960,055 (GRCm38) missense probably damaging 1.00
R1528:Fat3 UTSW 9 15,925,091 (GRCm38) missense probably benign 0.00
R1531:Fat3 UTSW 9 15,997,465 (GRCm38) missense probably damaging 1.00
R1659:Fat3 UTSW 9 15,997,183 (GRCm38) missense possibly damaging 0.91
R1697:Fat3 UTSW 9 15,944,880 (GRCm38) missense probably benign 0.05
R1699:Fat3 UTSW 9 15,938,398 (GRCm38) missense probably damaging 1.00
R1728:Fat3 UTSW 9 15,996,315 (GRCm38) missense possibly damaging 0.65
R1729:Fat3 UTSW 9 15,996,315 (GRCm38) missense possibly damaging 0.65
R1731:Fat3 UTSW 9 15,995,937 (GRCm38) missense probably benign
R1784:Fat3 UTSW 9 15,996,315 (GRCm38) missense possibly damaging 0.65
R1789:Fat3 UTSW 9 16,376,985 (GRCm38) missense probably benign 0.00
R1794:Fat3 UTSW 9 15,997,138 (GRCm38) missense probably benign 0.15
R1794:Fat3 UTSW 9 15,997,136 (GRCm38) nonsense probably null
R1830:Fat3 UTSW 9 15,915,340 (GRCm38) missense probably benign 0.03
R1835:Fat3 UTSW 9 15,998,088 (GRCm38) missense probably damaging 1.00
R1887:Fat3 UTSW 9 15,967,061 (GRCm38) missense probably damaging 1.00
R1898:Fat3 UTSW 9 15,960,130 (GRCm38) missense probably damaging 1.00
R1909:Fat3 UTSW 9 15,998,115 (GRCm38) missense probably benign
R1912:Fat3 UTSW 9 15,969,988 (GRCm38) missense probably damaging 1.00
R1917:Fat3 UTSW 9 15,997,057 (GRCm38) missense possibly damaging 0.55
R1967:Fat3 UTSW 9 15,968,295 (GRCm38) missense probably benign 0.00
R2070:Fat3 UTSW 9 15,999,370 (GRCm38) missense probably benign 0.21
R2100:Fat3 UTSW 9 16,377,430 (GRCm38) missense possibly damaging 0.73
R2104:Fat3 UTSW 9 15,998,517 (GRCm38) missense possibly damaging 0.77
R2113:Fat3 UTSW 9 15,999,786 (GRCm38) missense probably damaging 1.00
R2132:Fat3 UTSW 9 16,246,719 (GRCm38) critical splice donor site probably null
R2136:Fat3 UTSW 9 16,377,051 (GRCm38) missense probably benign 0.01
R2146:Fat3 UTSW 9 15,990,512 (GRCm38) missense probably benign 0.01
R2233:Fat3 UTSW 9 15,998,271 (GRCm38) missense probably damaging 1.00
R2234:Fat3 UTSW 9 15,998,271 (GRCm38) missense probably damaging 1.00
R2273:Fat3 UTSW 9 15,915,262 (GRCm38) missense probably benign
R2285:Fat3 UTSW 9 16,376,173 (GRCm38) missense probably damaging 1.00
R2363:Fat3 UTSW 9 15,998,271 (GRCm38) missense probably damaging 1.00
R2365:Fat3 UTSW 9 15,998,271 (GRCm38) missense probably damaging 1.00
R2367:Fat3 UTSW 9 15,998,271 (GRCm38) missense probably damaging 1.00
R2403:Fat3 UTSW 9 15,969,871 (GRCm38) missense probably damaging 1.00
R2447:Fat3 UTSW 9 15,998,271 (GRCm38) missense probably damaging 1.00
R2496:Fat3 UTSW 9 15,966,103 (GRCm38) missense probably benign 0.01
R2509:Fat3 UTSW 9 15,925,014 (GRCm38) missense possibly damaging 0.82
R2932:Fat3 UTSW 9 16,375,944 (GRCm38) missense probably damaging 1.00
R2986:Fat3 UTSW 9 15,992,128 (GRCm38) missense probably damaging 1.00
R3054:Fat3 UTSW 9 15,960,496 (GRCm38) missense probably benign
R3056:Fat3 UTSW 9 15,960,496 (GRCm38) missense probably benign
R3729:Fat3 UTSW 9 16,247,041 (GRCm38) splice site probably benign
R3745:Fat3 UTSW 9 15,998,271 (GRCm38) missense probably damaging 1.00
R3806:Fat3 UTSW 9 15,998,271 (GRCm38) missense probably damaging 1.00
R3859:Fat3 UTSW 9 15,997,228 (GRCm38) nonsense probably null
R3862:Fat3 UTSW 9 15,998,271 (GRCm38) missense probably damaging 1.00
R3890:Fat3 UTSW 9 15,998,271 (GRCm38) missense probably damaging 1.00
R3892:Fat3 UTSW 9 15,998,271 (GRCm38) missense probably damaging 1.00
R3950:Fat3 UTSW 9 15,998,271 (GRCm38) missense probably damaging 1.00
R3972:Fat3 UTSW 9 15,998,271 (GRCm38) missense probably damaging 1.00
R4004:Fat3 UTSW 9 15,998,271 (GRCm38) missense probably damaging 1.00
R4005:Fat3 UTSW 9 15,998,271 (GRCm38) missense probably damaging 1.00
R4086:Fat3 UTSW 9 15,998,271 (GRCm38) missense probably damaging 1.00
R4111:Fat3 UTSW 9 15,998,271 (GRCm38) missense probably damaging 1.00
R4113:Fat3 UTSW 9 15,998,271 (GRCm38) missense probably damaging 1.00
R4227:Fat3 UTSW 9 16,377,693 (GRCm38) missense probably damaging 1.00
R4352:Fat3 UTSW 9 16,246,778 (GRCm38) missense possibly damaging 0.55
R4394:Fat3 UTSW 9 15,922,792 (GRCm38) missense probably benign 0.11
R4403:Fat3 UTSW 9 15,944,873 (GRCm38) missense probably damaging 1.00
R4433:Fat3 UTSW 9 16,031,152 (GRCm38) missense probably damaging 0.99
R4453:Fat3 UTSW 9 15,998,271 (GRCm38) missense probably damaging 1.00
R4479:Fat3 UTSW 9 15,998,271 (GRCm38) missense probably damaging 1.00
R4480:Fat3 UTSW 9 15,998,271 (GRCm38) missense probably damaging 1.00
R4521:Fat3 UTSW 9 15,922,942 (GRCm38) missense probably null 0.71
R4620:Fat3 UTSW 9 15,996,894 (GRCm38) missense probably damaging 1.00
R4700:Fat3 UTSW 9 16,031,173 (GRCm38) missense probably damaging 1.00
R4721:Fat3 UTSW 9 16,029,966 (GRCm38) missense probably damaging 1.00
R4790:Fat3 UTSW 9 15,998,484 (GRCm38) missense probably damaging 1.00
R4796:Fat3 UTSW 9 15,999,732 (GRCm38) missense probably benign 0.17
R4823:Fat3 UTSW 9 15,996,507 (GRCm38) missense probably benign
R4836:Fat3 UTSW 9 16,377,723 (GRCm38) missense probably damaging 1.00
R4842:Fat3 UTSW 9 15,997,587 (GRCm38) missense probably damaging 1.00
R4849:Fat3 UTSW 9 16,377,948 (GRCm38) missense probably benign 0.03
R4856:Fat3 UTSW 9 16,021,330 (GRCm38) missense probably benign
R4869:Fat3 UTSW 9 16,377,477 (GRCm38) missense probably damaging 0.98
R4886:Fat3 UTSW 9 16,021,330 (GRCm38) missense probably benign
R4899:Fat3 UTSW 9 15,969,799 (GRCm38) missense probably damaging 1.00
R4941:Fat3 UTSW 9 16,375,152 (GRCm38) missense probably damaging 1.00
R4986:Fat3 UTSW 9 15,998,340 (GRCm38) missense probably damaging 1.00
R5058:Fat3 UTSW 9 15,996,858 (GRCm38) missense probably damaging 1.00
R5079:Fat3 UTSW 9 15,999,127 (GRCm38) missense probably benign 0.01
R5080:Fat3 UTSW 9 15,999,338 (GRCm38) missense probably benign 0.35
R5174:Fat3 UTSW 9 15,999,570 (GRCm38) missense probably damaging 1.00
R5183:Fat3 UTSW 9 15,960,313 (GRCm38) missense probably damaging 0.99
R5203:Fat3 UTSW 9 16,378,142 (GRCm38) missense possibly damaging 0.79
R5216:Fat3 UTSW 9 16,377,537 (GRCm38) missense probably damaging 1.00
R5230:Fat3 UTSW 9 15,990,560 (GRCm38) missense possibly damaging 0.51
R5318:Fat3 UTSW 9 16,376,629 (GRCm38) missense probably damaging 1.00
R5377:Fat3 UTSW 9 16,376,443 (GRCm38) missense probably benign 0.05
R5385:Fat3 UTSW 9 15,922,675 (GRCm38) missense possibly damaging 0.82
R5436:Fat3 UTSW 9 15,960,514 (GRCm38) missense probably benign 0.02
R5437:Fat3 UTSW 9 16,085,308 (GRCm38) missense probably damaging 1.00
R5453:Fat3 UTSW 9 15,996,864 (GRCm38) missense probably damaging 1.00
R5460:Fat3 UTSW 9 15,919,167 (GRCm38) missense probably damaging 1.00
R5516:Fat3 UTSW 9 15,998,709 (GRCm38) missense probably damaging 1.00
R5568:Fat3 UTSW 9 16,376,923 (GRCm38) nonsense probably null
R5628:Fat3 UTSW 9 15,966,096 (GRCm38) missense probably damaging 1.00
R5835:Fat3 UTSW 9 16,375,833 (GRCm38) missense probably damaging 1.00
R5845:Fat3 UTSW 9 16,377,210 (GRCm38) missense probably damaging 1.00
R5898:Fat3 UTSW 9 15,938,461 (GRCm38) missense probably benign 0.15
R5941:Fat3 UTSW 9 15,999,501 (GRCm38) missense probably benign 0.07
R5974:Fat3 UTSW 9 16,006,528 (GRCm38) critical splice donor site probably null
R5986:Fat3 UTSW 9 15,998,317 (GRCm38) missense probably benign 0.22
R6015:Fat3 UTSW 9 16,376,050 (GRCm38) missense possibly damaging 0.55
R6031:Fat3 UTSW 9 15,988,492 (GRCm38) missense probably benign 0.02
R6031:Fat3 UTSW 9 15,988,492 (GRCm38) missense probably benign 0.02
R6042:Fat3 UTSW 9 16,377,817 (GRCm38) missense probably benign 0.12
R6051:Fat3 UTSW 9 16,375,455 (GRCm38) missense possibly damaging 0.83
R6052:Fat3 UTSW 9 15,922,679 (GRCm38) missense probably null
R6119:Fat3 UTSW 9 16,376,568 (GRCm38) missense possibly damaging 0.82
R6161:Fat3 UTSW 9 16,377,522 (GRCm38) missense probably damaging 1.00
R6254:Fat3 UTSW 9 15,996,145 (GRCm38) missense probably benign 0.19
R6318:Fat3 UTSW 9 15,916,984 (GRCm38) intron probably benign
R6347:Fat3 UTSW 9 15,998,372 (GRCm38) missense probably damaging 1.00
R6348:Fat3 UTSW 9 15,937,991 (GRCm38) critical splice donor site probably null
R6351:Fat3 UTSW 9 15,938,398 (GRCm38) missense probably damaging 1.00
R6450:Fat3 UTSW 9 15,999,170 (GRCm38) missense possibly damaging 0.51
R6460:Fat3 UTSW 9 15,967,000 (GRCm38) missense probably damaging 1.00
R6524:Fat3 UTSW 9 15,992,256 (GRCm38) missense probably damaging 1.00
R6533:Fat3 UTSW 9 15,998,899 (GRCm38) missense probably benign 0.02
R6565:Fat3 UTSW 9 15,915,327 (GRCm38) missense probably benign
R6576:Fat3 UTSW 9 16,377,210 (GRCm38) missense probably damaging 1.00
R6649:Fat3 UTSW 9 16,376,742 (GRCm38) missense probably damaging 1.00
R6716:Fat3 UTSW 9 15,919,269 (GRCm38) missense probably benign
R6719:Fat3 UTSW 9 15,996,144 (GRCm38) missense probably benign
R6753:Fat3 UTSW 9 15,915,061 (GRCm38) missense possibly damaging 0.82
R6754:Fat3 UTSW 9 15,915,061 (GRCm38) missense possibly damaging 0.82
R6755:Fat3 UTSW 9 15,915,061 (GRCm38) missense possibly damaging 0.82
R6792:Fat3 UTSW 9 16,375,644 (GRCm38) missense probably damaging 1.00
R6802:Fat3 UTSW 9 15,915,061 (GRCm38) missense possibly damaging 0.82
R6803:Fat3 UTSW 9 15,996,787 (GRCm38) missense probably damaging 0.99
R6831:Fat3 UTSW 9 16,376,551 (GRCm38) missense probably damaging 0.98
R6831:Fat3 UTSW 9 15,915,061 (GRCm38) missense possibly damaging 0.82
R6833:Fat3 UTSW 9 15,915,061 (GRCm38) missense possibly damaging 0.82
R6877:Fat3 UTSW 9 15,999,268 (GRCm38) missense probably benign
R6894:Fat3 UTSW 9 15,997,776 (GRCm38) missense probably damaging 1.00
R6915:Fat3 UTSW 9 16,377,748 (GRCm38) missense probably benign 0.37
R6931:Fat3 UTSW 9 15,959,942 (GRCm38) missense possibly damaging 0.89
R6934:Fat3 UTSW 9 16,376,956 (GRCm38) missense probably damaging 0.98
R6940:Fat3 UTSW 9 15,916,800 (GRCm38) splice site probably null
R6959:Fat3 UTSW 9 15,996,885 (GRCm38) missense possibly damaging 0.91
R6969:Fat3 UTSW 9 16,029,916 (GRCm38) missense probably benign 0.29
R6986:Fat3 UTSW 9 16,021,335 (GRCm38) missense probably damaging 1.00
R6993:Fat3 UTSW 9 15,919,221 (GRCm38) missense probably damaging 1.00
R7039:Fat3 UTSW 9 16,376,265 (GRCm38) missense probably damaging 1.00
R7051:Fat3 UTSW 9 16,377,827 (GRCm38) missense probably damaging 1.00
R7089:Fat3 UTSW 9 15,996,918 (GRCm38) missense probably benign 0.01
R7136:Fat3 UTSW 9 16,378,185 (GRCm38) missense probably benign
R7137:Fat3 UTSW 9 15,997,148 (GRCm38) missense probably damaging 1.00
R7154:Fat3 UTSW 9 15,996,864 (GRCm38) missense probably damaging 1.00
R7170:Fat3 UTSW 9 16,006,574 (GRCm38) missense probably damaging 0.99
R7183:Fat3 UTSW 9 15,922,837 (GRCm38) missense possibly damaging 0.81
R7237:Fat3 UTSW 9 16,377,214 (GRCm38) missense probably damaging 1.00
R7288:Fat3 UTSW 9 15,998,592 (GRCm38) missense probably damaging 1.00
R7293:Fat3 UTSW 9 15,915,296 (GRCm38) missense
R7293:Fat3 UTSW 9 15,915,040 (GRCm38) missense
R7381:Fat3 UTSW 9 16,246,987 (GRCm38) missense probably damaging 1.00
R7438:Fat3 UTSW 9 15,988,482 (GRCm38) missense probably benign
R7537:Fat3 UTSW 9 15,938,319 (GRCm38) missense probably damaging 1.00
R7560:Fat3 UTSW 9 15,996,842 (GRCm38) missense probably damaging 1.00
R7585:Fat3 UTSW 9 15,998,262 (GRCm38) missense probably benign 0.03
R7623:Fat3 UTSW 9 15,988,324 (GRCm38) missense probably damaging 1.00
R7624:Fat3 UTSW 9 15,959,869 (GRCm38) missense possibly damaging 0.72
R7684:Fat3 UTSW 9 15,988,268 (GRCm38) critical splice donor site probably null
R7690:Fat3 UTSW 9 15,998,181 (GRCm38) missense probably damaging 1.00
R7804:Fat3 UTSW 9 15,990,592 (GRCm38) missense probably benign 0.01
R7809:Fat3 UTSW 9 16,006,628 (GRCm38) missense probably damaging 1.00
R7924:Fat3 UTSW 9 15,999,297 (GRCm38) missense probably damaging 1.00
R7925:Fat3 UTSW 9 16,031,360 (GRCm38) missense possibly damaging 0.77
R7954:Fat3 UTSW 9 15,998,412 (GRCm38) missense probably damaging 1.00
R8021:Fat3 UTSW 9 15,999,109 (GRCm38) missense probably damaging 0.99
R8118:Fat3 UTSW 9 15,960,104 (GRCm38) missense probably benign
R8141:Fat3 UTSW 9 15,997,066 (GRCm38) missense possibly damaging 0.79
R8163:Fat3 UTSW 9 15,959,759 (GRCm38) missense probably damaging 1.00
R8170:Fat3 UTSW 9 15,947,496 (GRCm38) missense probably damaging 0.97
R8201:Fat3 UTSW 9 15,997,477 (GRCm38) missense possibly damaging 0.93
R8258:Fat3 UTSW 9 15,990,591 (GRCm38) missense possibly damaging 0.79
R8259:Fat3 UTSW 9 15,990,591 (GRCm38) missense possibly damaging 0.79
R8274:Fat3 UTSW 9 16,377,490 (GRCm38) nonsense probably null
R8275:Fat3 UTSW 9 16,246,750 (GRCm38) missense probably damaging 1.00
R8345:Fat3 UTSW 9 15,999,274 (GRCm38) missense probably benign 0.08
R8350:Fat3 UTSW 9 15,915,139 (GRCm38) missense
R8405:Fat3 UTSW 9 15,995,871 (GRCm38) missense probably damaging 1.00
R8421:Fat3 UTSW 9 15,998,184 (GRCm38) missense probably damaging 1.00
R8450:Fat3 UTSW 9 15,915,139 (GRCm38) missense
R8472:Fat3 UTSW 9 16,375,267 (GRCm38) missense possibly damaging 0.90
R8482:Fat3 UTSW 9 16,246,967 (GRCm38) missense probably benign 0.02
R8680:Fat3 UTSW 9 15,997,407 (GRCm38) missense probably damaging 0.99
R8690:Fat3 UTSW 9 15,967,101 (GRCm38) missense probably benign 0.45
R8748:Fat3 UTSW 9 15,922,865 (GRCm38) missense possibly damaging 0.70
R8756:Fat3 UTSW 9 16,376,589 (GRCm38) missense probably damaging 1.00
R8834:Fat3 UTSW 9 16,031,197 (GRCm38) missense probably damaging 1.00
R8848:Fat3 UTSW 9 15,967,102 (GRCm38) missense probably damaging 1.00
R8884:Fat3 UTSW 9 16,029,984 (GRCm38) missense probably damaging 1.00
R8898:Fat3 UTSW 9 15,947,526 (GRCm38) missense probably benign 0.04
R8930:Fat3 UTSW 9 15,999,523 (GRCm38) missense probably benign 0.06
R8932:Fat3 UTSW 9 15,999,523 (GRCm38) missense probably benign 0.06
R8954:Fat3 UTSW 9 16,376,568 (GRCm38) missense probably benign 0.00
R8995:Fat3 UTSW 9 16,375,602 (GRCm38) missense probably damaging 1.00
R9000:Fat3 UTSW 9 16,006,799 (GRCm38) missense probably benign 0.12
R9000:Fat3 UTSW 9 15,960,520 (GRCm38) missense possibly damaging 0.82
R9060:Fat3 UTSW 9 15,999,486 (GRCm38) missense possibly damaging 0.80
R9116:Fat3 UTSW 9 15,998,125 (GRCm38) missense probably benign 0.34
R9136:Fat3 UTSW 9 15,922,442 (GRCm38) missense
R9193:Fat3 UTSW 9 15,998,952 (GRCm38) missense probably benign
R9235:Fat3 UTSW 9 15,922,378 (GRCm38) missense probably null
R9257:Fat3 UTSW 9 15,996,567 (GRCm38) missense probably benign
R9297:Fat3 UTSW 9 15,997,700 (GRCm38) missense probably damaging 1.00
R9307:Fat3 UTSW 9 16,021,423 (GRCm38) missense probably damaging 1.00
R9412:Fat3 UTSW 9 15,997,407 (GRCm38) missense probably damaging 0.99
R9427:Fat3 UTSW 9 16,377,395 (GRCm38) nonsense probably null
R9430:Fat3 UTSW 9 16,376,085 (GRCm38) missense probably damaging 1.00
R9480:Fat3 UTSW 9 16,031,407 (GRCm38) missense probably damaging 1.00
R9497:Fat3 UTSW 9 15,992,208 (GRCm38) missense probably damaging 0.99
R9547:Fat3 UTSW 9 15,999,846 (GRCm38) missense possibly damaging 0.86
R9569:Fat3 UTSW 9 15,919,199 (GRCm38) missense
R9591:Fat3 UTSW 9 16,377,040 (GRCm38) missense probably benign 0.01
R9615:Fat3 UTSW 9 16,378,047 (GRCm38) missense probably benign 0.00
R9649:Fat3 UTSW 9 15,996,758 (GRCm38) missense possibly damaging 0.57
R9671:Fat3 UTSW 9 16,375,575 (GRCm38) missense possibly damaging 0.93
R9750:Fat3 UTSW 9 16,003,861 (GRCm38) missense probably benign 0.00
R9777:Fat3 UTSW 9 15,915,241 (GRCm38) missense probably benign
RF006:Fat3 UTSW 9 15,998,617 (GRCm38) missense probably benign 0.36
X0021:Fat3 UTSW 9 16,029,931 (GRCm38) missense probably null 0.66
X0026:Fat3 UTSW 9 15,996,333 (GRCm38) missense probably benign
X0064:Fat3 UTSW 9 15,919,277 (GRCm38) missense probably benign
Z1176:Fat3 UTSW 9 16,375,617 (GRCm38) missense probably benign
Z1176:Fat3 UTSW 9 16,375,429 (GRCm38) missense probably damaging 1.00
Z1176:Fat3 UTSW 9 15,947,526 (GRCm38) missense probably damaging 0.98
Z1177:Fat3 UTSW 9 15,965,991 (GRCm38) missense possibly damaging 0.68
Z1177:Fat3 UTSW 9 15,947,538 (GRCm38) missense probably damaging 1.00
Z1177:Fat3 UTSW 9 15,923,026 (GRCm38) missense possibly damaging 0.81
Z1177:Fat3 UTSW 9 15,969,835 (GRCm38) missense probably damaging 0.99
Posted On 2013-06-21