Incidental Mutation 'R5288:Fat2'
ID 424520
Institutional Source Beutler Lab
Gene Symbol Fat2
Ensembl Gene ENSMUSG00000055333
Gene Name FAT atypical cadherin 2
Synonyms LOC245827, mKIAA0811, EMI2, Fath2
MMRRC Submission 042842-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R5288 (G1)
Quality Score 225
Status Not validated
Chromosome 11
Chromosomal Location 55141435-55227390 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 55158482 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Isoleucine at position 3412 (T3412I)
Ref Sequence ENSEMBL: ENSMUSP00000104492 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000068853] [ENSMUST00000108864]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000068853
AA Change: T3412I

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000067556
Gene: ENSMUSG00000055333
AA Change: T3412I

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
CA 55 146 3.65e-4 SMART
CA 170 254 3.99e-10 SMART
low complexity region 337 348 N/A INTRINSIC
CA 384 456 5.11e-8 SMART
CA 480 562 2.71e-21 SMART
CA 586 664 1.12e-2 SMART
CA 737 818 1.69e-22 SMART
CA 842 923 9.59e-22 SMART
CA 947 1028 7.39e-14 SMART
CA 1054 1135 3.74e-24 SMART
CA 1159 1240 1.84e-23 SMART
CA 1266 1342 8.9e-8 SMART
CA 1368 1446 7.4e-5 SMART
CA 1470 1553 1.98e-14 SMART
CA 1577 1658 6.84e-18 SMART
CA 1682 1756 2.76e-13 SMART
CA 1787 1870 1.49e-18 SMART
CA 1894 1966 1.11e-1 SMART
CA 1990 2068 2.4e-13 SMART
CA 2092 2171 3.42e-18 SMART
CA 2190 2270 1.9e-16 SMART
CA 2294 2377 1.49e-27 SMART
CA 2401 2479 8.31e-8 SMART
CA 2503 2583 6.48e-19 SMART
CA 2607 2690 1.53e-6 SMART
CA 2714 2797 3e-14 SMART
CA 2821 2906 5.85e-26 SMART
CA 2930 3011 4.58e-19 SMART
CA 3035 3113 2.1e-27 SMART
CA 3137 3218 9.67e-18 SMART
CA 3243 3321 1.92e-12 SMART
CA 3345 3426 4.04e-29 SMART
CA 3450 3531 1.79e-12 SMART
CA 3555 3629 9.3e-2 SMART
LamG 3794 3923 1.77e-28 SMART
EGF 3952 3986 6.5e-5 SMART
EGF 3991 4024 1.6e-4 SMART
transmembrane domain 4051 4073 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000108864
AA Change: T3412I

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000104492
Gene: ENSMUSG00000055333
AA Change: T3412I

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
CA 55 146 3.65e-4 SMART
CA 170 254 3.99e-10 SMART
low complexity region 337 348 N/A INTRINSIC
CA 384 456 5.11e-8 SMART
CA 480 562 2.71e-21 SMART
CA 586 664 1.12e-2 SMART
CA 737 818 1.69e-22 SMART
CA 842 923 9.59e-22 SMART
CA 947 1028 7.39e-14 SMART
CA 1054 1135 3.74e-24 SMART
CA 1159 1240 1.84e-23 SMART
CA 1266 1342 8.9e-8 SMART
CA 1368 1446 7.4e-5 SMART
CA 1470 1553 1.98e-14 SMART
CA 1577 1658 6.84e-18 SMART
CA 1682 1756 2.76e-13 SMART
CA 1787 1870 1.49e-18 SMART
CA 1894 1966 1.11e-1 SMART
CA 1990 2068 2.4e-13 SMART
CA 2092 2171 3.42e-18 SMART
CA 2190 2270 1.9e-16 SMART
CA 2294 2377 1.49e-27 SMART
CA 2401 2479 8.31e-8 SMART
CA 2503 2583 6.48e-19 SMART
CA 2607 2690 1.53e-6 SMART
CA 2714 2797 3e-14 SMART
CA 2821 2906 5.85e-26 SMART
CA 2930 3011 4.58e-19 SMART
CA 3035 3113 2.1e-27 SMART
CA 3137 3218 9.67e-18 SMART
CA 3243 3321 1.92e-12 SMART
CA 3345 3426 4.04e-29 SMART
CA 3450 3531 1.79e-12 SMART
CA 3555 3629 9.3e-2 SMART
LamG 3794 3923 1.77e-28 SMART
EGF 3952 3986 6.5e-5 SMART
EGF 3991 4024 1.6e-4 SMART
transmembrane domain 4051 4073 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 97.1%
  • 20x: 94.7%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is the second identified human homolog of the Drosophila fat gene, which encodes a tumor suppressor essential for controlling cell proliferation during Drosophila development. The gene product is a member of the cadherin superfamily, a group of integral membrane proteins characterized by the presence of cadherin-type repeats. In addition to containing 34 tandem cadherin-type repeats, the gene product has two epidermal growth factor (EGF)-like repeats and one laminin G domain. This protein most likely functions as a cell adhesion molecule, controlling cell proliferation and playing an important role in cerebellum development. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a knock-out allele are healthy, fertile and overtly normal, with no apparent defects in the development of red blood cells or platelets. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 113 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc12 A T 8: 87,293,168 (GRCm39) Y7N probably damaging Het
Adcy1 A C 11: 7,111,351 (GRCm39) I881L probably benign Het
Aftph T C 11: 20,676,994 (GRCm39) D205G probably damaging Het
Aldh7a1 T A 18: 56,667,325 (GRCm39) N316Y possibly damaging Het
Ankrd36 A G 11: 5,639,340 (GRCm39) probably benign Het
Ccdc88a T G 11: 29,448,416 (GRCm39) N1465K possibly damaging Het
Ccpg1 G A 9: 72,920,326 (GRCm39) S647N probably benign Het
Cep70 T A 9: 99,163,128 (GRCm39) L325Q probably damaging Het
Cfap46 A G 7: 139,193,423 (GRCm39) probably null Het
Cftr C T 6: 18,226,128 (GRCm39) Q359* probably null Het
Chrne A T 11: 70,505,913 (GRCm39) N457K possibly damaging Het
Cntn2 A G 1: 132,451,415 (GRCm39) I438T probably benign Het
Cntn4 T C 6: 106,158,765 (GRCm39) L10P possibly damaging Het
Copg1 G T 6: 87,867,189 (GRCm39) M87I possibly damaging Het
Cyfip1 A T 7: 55,574,883 (GRCm39) M1045L possibly damaging Het
Cyp2c29 C T 19: 39,318,816 (GRCm39) P432L probably damaging Het
Dcaf11 T A 14: 55,800,833 (GRCm39) D96E probably damaging Het
Dmxl2 A G 9: 54,286,041 (GRCm39) S2715P probably benign Het
Dnhd1 G A 7: 105,363,644 (GRCm39) E4069K possibly damaging Het
Dpy19l4 T A 4: 11,289,721 (GRCm39) N330I probably damaging Het
Dpy19l4 G T 4: 11,304,014 (GRCm39) A132D probably damaging Het
Duox2 A G 2: 122,125,617 (GRCm39) V330A probably benign Het
Dusp11 T C 6: 85,924,587 (GRCm39) *322W probably null Het
Dusp8 T A 7: 141,643,730 (GRCm39) Q61L possibly damaging Het
Eml3 G A 19: 8,916,638 (GRCm39) G720S probably damaging Het
F11 A G 8: 45,699,833 (GRCm39) S418P probably damaging Het
Fam91a1 G A 15: 58,320,243 (GRCm39) S645N probably benign Het
Fbxo38 A G 18: 62,674,042 (GRCm39) M13T probably benign Het
Fbxo48 G T 11: 16,904,329 (GRCm39) L160F possibly damaging Het
Gm10134 T A 2: 28,396,372 (GRCm39) probably benign Het
Gm11787 T C 4: 3,511,795 (GRCm39) noncoding transcript Het
Gpatch8 A T 11: 102,399,053 (GRCm39) probably null Het
Gucy2g G A 19: 55,203,548 (GRCm39) A750V probably damaging Het
Hephl1 T C 9: 14,988,150 (GRCm39) T653A possibly damaging Het
Herc3 T A 6: 58,851,263 (GRCm39) M504K probably damaging Het
Hmcn2 A G 2: 31,350,333 (GRCm39) T5077A probably benign Het
Ifitm3 T C 7: 140,590,554 (GRCm39) N2S probably benign Het
Ighe T C 12: 113,235,092 (GRCm39) H356R probably benign Het
Ighv10-3 T A 12: 114,487,125 (GRCm39) M99L probably benign Het
Izumo4 C A 10: 80,538,639 (GRCm39) C30* probably null Het
Jag1 A T 2: 136,937,464 (GRCm39) H303Q possibly damaging Het
Kif24 T C 4: 41,395,373 (GRCm39) E500G probably benign Het
Kng1 A T 16: 22,897,842 (GRCm39) D414V probably damaging Het
Loxhd1 A C 18: 77,451,308 (GRCm39) D410A probably damaging Het
Ltn1 T C 16: 87,212,899 (GRCm39) K554R possibly damaging Het
Ly75 A G 2: 60,133,985 (GRCm39) C1547R probably damaging Het
Ms4a6d A T 19: 11,564,500 (GRCm39) S124T possibly damaging Het
Mtcl3 A G 10: 29,072,766 (GRCm39) D686G probably benign Het
Mtfr2 A G 10: 20,233,448 (GRCm39) D339G probably damaging Het
Myh10 T A 11: 68,692,434 (GRCm39) L1369Q probably damaging Het
Myh11 A T 16: 14,025,872 (GRCm39) V1366D possibly damaging Het
Nadsyn1 A G 7: 143,357,023 (GRCm39) V491A possibly damaging Het
Nav3 T C 10: 109,688,966 (GRCm39) N437S probably benign Het
Ncf1 A G 5: 134,250,659 (GRCm39) L373P probably damaging Het
Neb A T 2: 52,079,873 (GRCm39) I85N probably damaging Het
Nktr A G 9: 121,577,659 (GRCm39) K576E probably benign Het
Nmur2 T A 11: 55,931,040 (GRCm39) I224F probably damaging Het
Oas3 A G 5: 120,895,055 (GRCm39) F978S probably damaging Het
Or10ag53 C T 2: 87,082,827 (GRCm39) P182L probably benign Het
Or10ak9 T C 4: 118,726,772 (GRCm39) S264P probably damaging Het
Or2r3 T A 6: 42,448,186 (GRCm39) I309F probably benign Het
Or2t48 A T 11: 58,420,308 (GRCm39) M168K probably damaging Het
Or5p60 T C 7: 107,724,375 (GRCm39) T32A probably benign Het
Pcyox1 A T 6: 86,369,336 (GRCm39) probably null Het
Pdcd7 G A 9: 65,265,974 (GRCm39) W477* probably null Het
Pitpnm1 T C 19: 4,153,435 (GRCm39) F197S probably damaging Het
Plce1 C A 19: 38,748,535 (GRCm39) N1755K probably damaging Het
Pnpla7 C A 2: 24,931,031 (GRCm39) P882Q probably damaging Het
Pold2 A G 11: 5,826,760 (GRCm39) L58P probably damaging Het
Pomt1 C G 2: 32,134,311 (GRCm39) Y277* probably null Het
Pou4f2 A G 8: 79,162,958 (GRCm39) Y26H unknown Het
Pphln1-ps1 T G 16: 13,495,622 (GRCm39) N240K probably benign Het
Ppm1e A T 11: 87,249,377 (GRCm39) L118Q possibly damaging Het
Pramel34 C T 5: 93,785,607 (GRCm39) M224I possibly damaging Het
Prdx2 T A 8: 85,698,302 (GRCm39) Y164* probably null Het
Prkra T G 2: 76,469,622 (GRCm39) T146P probably damaging Het
Prpf8 A G 11: 75,386,625 (GRCm39) D1038G probably damaging Het
Rab4a A T 8: 124,554,113 (GRCm39) I16L probably benign Het
Rai2 A G X: 160,561,636 (GRCm39) N363S probably benign Het
Ranbp17 A T 11: 33,169,241 (GRCm39) V991D possibly damaging Het
Rimbp2 G A 5: 128,865,656 (GRCm39) T557M probably benign Het
Rmi1 G A 13: 58,557,280 (GRCm39) G510R probably damaging Het
Sdad1 A G 5: 92,434,684 (GRCm39) *687Q probably null Het
Sema6d T C 2: 124,506,166 (GRCm39) L720P probably damaging Het
Setx T G 2: 29,024,045 (GRCm39) probably null Het
Sgsm3 T C 15: 80,892,200 (GRCm39) V256A probably benign Het
Slc28a2b C A 2: 122,353,259 (GRCm39) L480I probably benign Het
Sppl2c T A 11: 104,078,127 (GRCm39) I309K possibly damaging Het
Stard9 A G 2: 120,531,111 (GRCm39) E2456G probably damaging Het
Strn3 C G 12: 51,694,803 (GRCm39) R320P probably damaging Het
Supv3l1 A T 10: 62,266,375 (GRCm39) N600K possibly damaging Het
Syne2 T A 12: 76,146,112 (GRCm39) S6377T possibly damaging Het
Tas2r123 A T 6: 132,824,190 (GRCm39) H29L probably benign Het
Tbl3 C T 17: 24,924,944 (GRCm39) V52M possibly damaging Het
Tbp A G 17: 15,727,609 (GRCm39) I145V probably benign Het
Tcf20 A T 15: 82,739,910 (GRCm39) S514T possibly damaging Het
Tgm4 A G 9: 122,885,559 (GRCm39) Y367C probably damaging Het
Tle1 C T 4: 72,060,081 (GRCm39) V258M probably damaging Het
Tln1 C T 4: 43,540,661 (GRCm39) V1447I probably benign Het
Tnfrsf11b C T 15: 54,141,622 (GRCm39) A8T probably benign Het
Trim80 A T 11: 115,338,843 (GRCm39) T558S probably benign Het
Trmt6 C A 2: 132,650,703 (GRCm39) A302S probably benign Het
Tsen15 C T 1: 152,259,131 (GRCm39) V76I probably damaging Het
Ttc17 A T 2: 94,133,985 (GRCm39) W1067R probably damaging Het
Ucn3 A T 13: 3,991,474 (GRCm39) F59L probably benign Het
Ulk3 T A 9: 57,498,023 (GRCm39) I108N possibly damaging Het
Vmn2r94 A C 17: 18,464,728 (GRCm39) Y521D probably damaging Het
Vps45 T C 3: 95,965,086 (GRCm39) M1V probably null Het
Vta1 C A 10: 14,581,143 (GRCm39) L21F probably damaging Het
Zdhhc21 C T 4: 82,765,929 (GRCm39) G2D probably damaging Het
Zfp169 A T 13: 48,643,751 (GRCm39) C459S possibly damaging Het
Zfp90 C T 8: 107,152,000 (GRCm39) T571M probably damaging Het
Zswim8 A T 14: 20,768,939 (GRCm39) N1119I possibly damaging Het
Other mutations in Fat2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00720:Fat2 APN 11 55,202,070 (GRCm39) missense probably benign
IGL00897:Fat2 APN 11 55,180,078 (GRCm39) missense probably damaging 0.99
IGL01161:Fat2 APN 11 55,175,017 (GRCm39) missense probably benign
IGL01306:Fat2 APN 11 55,201,698 (GRCm39) missense probably benign 0.28
IGL01393:Fat2 APN 11 55,160,135 (GRCm39) missense probably benign 0.00
IGL01529:Fat2 APN 11 55,172,982 (GRCm39) missense probably damaging 1.00
IGL01530:Fat2 APN 11 55,174,213 (GRCm39) missense probably benign 0.42
IGL01555:Fat2 APN 11 55,169,756 (GRCm39) missense probably damaging 0.99
IGL01758:Fat2 APN 11 55,187,035 (GRCm39) missense probably damaging 1.00
IGL01768:Fat2 APN 11 55,153,394 (GRCm39) missense probably damaging 1.00
IGL01939:Fat2 APN 11 55,174,806 (GRCm39) missense probably benign 0.01
IGL01941:Fat2 APN 11 55,202,831 (GRCm39) missense probably benign 0.01
IGL01967:Fat2 APN 11 55,202,649 (GRCm39) missense probably damaging 1.00
IGL01978:Fat2 APN 11 55,160,972 (GRCm39) missense probably benign 0.34
IGL01998:Fat2 APN 11 55,187,021 (GRCm39) missense probably benign 0.00
IGL02001:Fat2 APN 11 55,203,071 (GRCm39) start codon destroyed probably null 0.89
IGL02004:Fat2 APN 11 55,173,666 (GRCm39) missense probably damaging 1.00
IGL02103:Fat2 APN 11 55,180,122 (GRCm39) missense probably damaging 0.96
IGL02131:Fat2 APN 11 55,199,868 (GRCm39) missense probably damaging 1.00
IGL02155:Fat2 APN 11 55,153,245 (GRCm39) missense probably benign 0.00
IGL02223:Fat2 APN 11 55,163,955 (GRCm39) missense probably benign 0.01
IGL02231:Fat2 APN 11 55,171,918 (GRCm39) missense probably damaging 0.98
IGL02312:Fat2 APN 11 55,161,085 (GRCm39) missense probably damaging 1.00
IGL02476:Fat2 APN 11 55,201,950 (GRCm39) missense probably damaging 1.00
IGL02539:Fat2 APN 11 55,172,619 (GRCm39) missense probably damaging 1.00
IGL02553:Fat2 APN 11 55,202,109 (GRCm39) missense probably damaging 1.00
IGL02645:Fat2 APN 11 55,173,654 (GRCm39) missense probably damaging 1.00
IGL02664:Fat2 APN 11 55,201,922 (GRCm39) missense probably damaging 1.00
IGL02708:Fat2 APN 11 55,173,211 (GRCm39) missense probably damaging 0.99
IGL02883:Fat2 APN 11 55,147,444 (GRCm39) missense probably benign 0.16
IGL02894:Fat2 APN 11 55,147,479 (GRCm39) missense probably damaging 1.00
IGL02975:Fat2 APN 11 55,161,020 (GRCm39) missense probably benign 0.00
IGL03085:Fat2 APN 11 55,174,072 (GRCm39) missense probably benign 0.09
IGL03106:Fat2 APN 11 55,202,727 (GRCm39) missense probably benign 0.45
IGL03132:Fat2 APN 11 55,144,746 (GRCm39) missense probably benign 0.25
IGL03133:Fat2 APN 11 55,176,869 (GRCm39) missense probably benign 0.01
IGL03194:Fat2 APN 11 55,201,821 (GRCm39) missense probably benign 0.02
IGL03266:Fat2 APN 11 55,174,855 (GRCm39) missense possibly damaging 0.62
IGL03290:Fat2 APN 11 55,147,045 (GRCm39) missense probably benign 0.33
IGL03291:Fat2 APN 11 55,153,421 (GRCm39) missense probably benign
IGL03325:Fat2 APN 11 55,173,168 (GRCm39) missense probably damaging 1.00
IGL03345:Fat2 APN 11 55,173,187 (GRCm39) missense probably damaging 1.00
IGL03371:Fat2 APN 11 55,201,990 (GRCm39) missense probably benign 0.10
ANU23:Fat2 UTSW 11 55,201,698 (GRCm39) missense probably benign 0.28
BB001:Fat2 UTSW 11 55,153,613 (GRCm39) missense probably benign 0.03
BB011:Fat2 UTSW 11 55,153,613 (GRCm39) missense probably benign 0.03
P0040:Fat2 UTSW 11 55,173,039 (GRCm39) missense possibly damaging 0.89
PIT4504001:Fat2 UTSW 11 55,146,936 (GRCm39) missense possibly damaging 0.68
R0008:Fat2 UTSW 11 55,202,075 (GRCm39) missense probably damaging 1.00
R0008:Fat2 UTSW 11 55,202,075 (GRCm39) missense probably damaging 1.00
R0012:Fat2 UTSW 11 55,153,697 (GRCm39) missense probably benign 0.16
R0012:Fat2 UTSW 11 55,153,697 (GRCm39) missense probably benign 0.16
R0048:Fat2 UTSW 11 55,200,865 (GRCm39) missense probably benign 0.00
R0048:Fat2 UTSW 11 55,200,865 (GRCm39) missense probably benign 0.00
R0098:Fat2 UTSW 11 55,189,431 (GRCm39) missense probably damaging 0.98
R0124:Fat2 UTSW 11 55,174,504 (GRCm39) missense probably damaging 0.98
R0127:Fat2 UTSW 11 55,180,112 (GRCm39) missense probably benign 0.01
R0130:Fat2 UTSW 11 55,142,944 (GRCm39) missense probably benign 0.26
R0131:Fat2 UTSW 11 55,164,037 (GRCm39) missense probably benign
R0158:Fat2 UTSW 11 55,187,011 (GRCm39) missense probably benign 0.00
R0184:Fat2 UTSW 11 55,187,114 (GRCm39) missense probably damaging 1.00
R0367:Fat2 UTSW 11 55,182,919 (GRCm39) splice site probably benign
R0384:Fat2 UTSW 11 55,160,291 (GRCm39) missense possibly damaging 0.81
R0390:Fat2 UTSW 11 55,201,603 (GRCm39) missense probably damaging 0.99
R0403:Fat2 UTSW 11 55,161,175 (GRCm39) missense probably benign 0.42
R0416:Fat2 UTSW 11 55,174,960 (GRCm39) missense possibly damaging 0.94
R0437:Fat2 UTSW 11 55,173,625 (GRCm39) missense probably benign 0.02
R0463:Fat2 UTSW 11 55,153,655 (GRCm39) missense probably damaging 1.00
R0497:Fat2 UTSW 11 55,174,228 (GRCm39) missense probably benign 0.03
R0617:Fat2 UTSW 11 55,202,669 (GRCm39) missense possibly damaging 0.60
R0622:Fat2 UTSW 11 55,173,954 (GRCm39) missense probably damaging 1.00
R0675:Fat2 UTSW 11 55,200,035 (GRCm39) missense probably damaging 0.97
R0811:Fat2 UTSW 11 55,144,459 (GRCm39) missense possibly damaging 0.75
R0812:Fat2 UTSW 11 55,144,459 (GRCm39) missense possibly damaging 0.75
R0869:Fat2 UTSW 11 55,202,601 (GRCm39) missense probably benign 0.08
R0870:Fat2 UTSW 11 55,202,601 (GRCm39) missense probably benign 0.08
R0899:Fat2 UTSW 11 55,147,051 (GRCm39) missense probably damaging 1.00
R1278:Fat2 UTSW 11 55,159,005 (GRCm39) missense probably damaging 1.00
R1383:Fat2 UTSW 11 55,201,599 (GRCm39) missense probably benign
R1428:Fat2 UTSW 11 55,186,913 (GRCm39) missense probably damaging 1.00
R1438:Fat2 UTSW 11 55,178,637 (GRCm39) missense probably damaging 1.00
R1495:Fat2 UTSW 11 55,153,499 (GRCm39) missense probably benign
R1506:Fat2 UTSW 11 55,175,090 (GRCm39) missense probably benign
R1547:Fat2 UTSW 11 55,143,081 (GRCm39) missense probably benign 0.01
R1554:Fat2 UTSW 11 55,144,490 (GRCm39) missense probably benign 0.01
R1562:Fat2 UTSW 11 55,200,800 (GRCm39) missense probably damaging 1.00
R1588:Fat2 UTSW 11 55,174,230 (GRCm39) missense probably damaging 1.00
R1592:Fat2 UTSW 11 55,182,696 (GRCm39) splice site probably null
R1601:Fat2 UTSW 11 55,172,836 (GRCm39) missense probably benign 0.01
R1610:Fat2 UTSW 11 55,169,750 (GRCm39) missense probably damaging 1.00
R1634:Fat2 UTSW 11 55,175,545 (GRCm39) missense probably benign
R1634:Fat2 UTSW 11 55,158,510 (GRCm39) missense probably damaging 1.00
R1644:Fat2 UTSW 11 55,187,007 (GRCm39) missense possibly damaging 0.94
R1644:Fat2 UTSW 11 55,178,609 (GRCm39) missense possibly damaging 0.91
R1691:Fat2 UTSW 11 55,202,678 (GRCm39) missense probably damaging 0.99
R1734:Fat2 UTSW 11 55,172,197 (GRCm39) missense probably benign 0.00
R1748:Fat2 UTSW 11 55,147,473 (GRCm39) missense probably damaging 0.97
R1771:Fat2 UTSW 11 55,201,691 (GRCm39) missense probably benign 0.01
R1800:Fat2 UTSW 11 55,174,718 (GRCm39) missense probably damaging 1.00
R1807:Fat2 UTSW 11 55,180,085 (GRCm39) missense probably damaging 1.00
R1823:Fat2 UTSW 11 55,147,606 (GRCm39) missense probably benign 0.29
R1848:Fat2 UTSW 11 55,202,384 (GRCm39) missense probably damaging 1.00
R1866:Fat2 UTSW 11 55,182,840 (GRCm39) missense probably benign 0.00
R1899:Fat2 UTSW 11 55,153,004 (GRCm39) missense probably benign
R1954:Fat2 UTSW 11 55,201,910 (GRCm39) missense probably benign 0.06
R2010:Fat2 UTSW 11 55,144,653 (GRCm39) missense probably damaging 0.99
R2011:Fat2 UTSW 11 55,173,583 (GRCm39) missense probably damaging 1.00
R2057:Fat2 UTSW 11 55,172,686 (GRCm39) missense possibly damaging 0.60
R2081:Fat2 UTSW 11 55,200,503 (GRCm39) missense possibly damaging 0.94
R2106:Fat2 UTSW 11 55,147,390 (GRCm39) missense probably benign 0.00
R2165:Fat2 UTSW 11 55,194,542 (GRCm39) missense probably benign 0.00
R2176:Fat2 UTSW 11 55,158,401 (GRCm39) critical splice donor site probably null
R2284:Fat2 UTSW 11 55,173,186 (GRCm39) missense probably damaging 1.00
R2338:Fat2 UTSW 11 55,202,727 (GRCm39) missense possibly damaging 0.93
R2340:Fat2 UTSW 11 55,160,922 (GRCm39) missense possibly damaging 0.90
R2427:Fat2 UTSW 11 55,201,638 (GRCm39) missense probably benign 0.15
R2444:Fat2 UTSW 11 55,172,799 (GRCm39) missense probably damaging 1.00
R2858:Fat2 UTSW 11 55,174,599 (GRCm39) missense possibly damaging 0.94
R2882:Fat2 UTSW 11 55,202,131 (GRCm39) missense probably damaging 0.96
R3029:Fat2 UTSW 11 55,175,535 (GRCm39) missense probably damaging 1.00
R3085:Fat2 UTSW 11 55,142,997 (GRCm39) missense possibly damaging 0.79
R3121:Fat2 UTSW 11 55,202,622 (GRCm39) missense probably damaging 1.00
R3418:Fat2 UTSW 11 55,169,824 (GRCm39) missense probably benign 0.01
R3500:Fat2 UTSW 11 55,151,342 (GRCm39) missense probably damaging 0.99
R3607:Fat2 UTSW 11 55,172,511 (GRCm39) missense probably damaging 1.00
R3611:Fat2 UTSW 11 55,202,895 (GRCm39) missense probably benign
R3620:Fat2 UTSW 11 55,147,521 (GRCm39) missense probably damaging 0.97
R3688:Fat2 UTSW 11 55,171,927 (GRCm39) missense probably damaging 0.99
R3704:Fat2 UTSW 11 55,200,476 (GRCm39) missense probably damaging 1.00
R3784:Fat2 UTSW 11 55,147,012 (GRCm39) missense probably benign
R3889:Fat2 UTSW 11 55,172,589 (GRCm39) missense probably damaging 1.00
R3951:Fat2 UTSW 11 55,187,208 (GRCm39) missense probably benign 0.00
R4211:Fat2 UTSW 11 55,174,810 (GRCm39) missense probably damaging 1.00
R4249:Fat2 UTSW 11 55,175,127 (GRCm39) missense probably damaging 0.98
R4406:Fat2 UTSW 11 55,153,094 (GRCm39) missense probably benign 0.00
R4433:Fat2 UTSW 11 55,200,466 (GRCm39) missense possibly damaging 0.91
R4436:Fat2 UTSW 11 55,187,024 (GRCm39) missense probably damaging 1.00
R4498:Fat2 UTSW 11 55,160,923 (GRCm39) missense possibly damaging 0.90
R4560:Fat2 UTSW 11 55,156,777 (GRCm39) missense possibly damaging 0.89
R4594:Fat2 UTSW 11 55,175,578 (GRCm39) missense possibly damaging 0.78
R4663:Fat2 UTSW 11 55,187,039 (GRCm39) nonsense probably null
R4669:Fat2 UTSW 11 55,202,441 (GRCm39) missense probably benign 0.01
R4696:Fat2 UTSW 11 55,175,841 (GRCm39) missense probably benign 0.00
R4734:Fat2 UTSW 11 55,202,294 (GRCm39) missense probably benign 0.01
R4749:Fat2 UTSW 11 55,202,294 (GRCm39) missense probably benign 0.01
R4765:Fat2 UTSW 11 55,172,013 (GRCm39) missense probably damaging 1.00
R4803:Fat2 UTSW 11 55,175,886 (GRCm39) missense probably benign 0.03
R4805:Fat2 UTSW 11 55,174,805 (GRCm39) missense probably benign 0.01
R4822:Fat2 UTSW 11 55,202,144 (GRCm39) missense probably benign 0.02
R4840:Fat2 UTSW 11 55,169,844 (GRCm39) missense probably benign 0.21
R4849:Fat2 UTSW 11 55,201,463 (GRCm39) missense probably damaging 1.00
R4943:Fat2 UTSW 11 55,169,859 (GRCm39) missense probably benign 0.00
R4993:Fat2 UTSW 11 55,173,918 (GRCm39) missense probably damaging 0.99
R5097:Fat2 UTSW 11 55,201,530 (GRCm39) missense probably damaging 1.00
R5104:Fat2 UTSW 11 55,169,814 (GRCm39) missense possibly damaging 0.93
R5115:Fat2 UTSW 11 55,187,159 (GRCm39) missense probably damaging 1.00
R5213:Fat2 UTSW 11 55,144,658 (GRCm39) missense probably benign 0.00
R5254:Fat2 UTSW 11 55,172,001 (GRCm39) missense probably damaging 1.00
R5269:Fat2 UTSW 11 55,178,704 (GRCm39) missense probably benign 0.00
R5355:Fat2 UTSW 11 55,172,992 (GRCm39) missense probably damaging 1.00
R5375:Fat2 UTSW 11 55,153,646 (GRCm39) missense probably benign 0.00
R5379:Fat2 UTSW 11 55,194,767 (GRCm39) missense probably damaging 0.99
R5411:Fat2 UTSW 11 55,143,052 (GRCm39) missense probably benign 0.23
R5416:Fat2 UTSW 11 55,194,514 (GRCm39) missense possibly damaging 0.77
R5480:Fat2 UTSW 11 55,200,912 (GRCm39) missense probably damaging 0.99
R5486:Fat2 UTSW 11 55,144,507 (GRCm39) missense probably benign 0.00
R5526:Fat2 UTSW 11 55,160,187 (GRCm39) missense possibly damaging 0.90
R5532:Fat2 UTSW 11 55,153,163 (GRCm39) missense probably damaging 1.00
R5583:Fat2 UTSW 11 55,144,715 (GRCm39) missense probably benign 0.00
R5588:Fat2 UTSW 11 55,173,103 (GRCm39) missense probably damaging 1.00
R5598:Fat2 UTSW 11 55,171,956 (GRCm39) missense probably damaging 1.00
R5636:Fat2 UTSW 11 55,173,307 (GRCm39) missense probably damaging 1.00
R5653:Fat2 UTSW 11 55,201,142 (GRCm39) missense probably damaging 1.00
R5657:Fat2 UTSW 11 55,201,507 (GRCm39) nonsense probably null
R5660:Fat2 UTSW 11 55,175,002 (GRCm39) missense probably benign 0.00
R5752:Fat2 UTSW 11 55,180,063 (GRCm39) missense possibly damaging 0.48
R5757:Fat2 UTSW 11 55,143,172 (GRCm39) missense probably damaging 1.00
R5792:Fat2 UTSW 11 55,153,151 (GRCm39) missense possibly damaging 0.77
R5872:Fat2 UTSW 11 55,161,208 (GRCm39) missense probably damaging 1.00
R5933:Fat2 UTSW 11 55,174,877 (GRCm39) missense probably damaging 1.00
R6030:Fat2 UTSW 11 55,201,129 (GRCm39) nonsense probably null
R6030:Fat2 UTSW 11 55,201,129 (GRCm39) nonsense probably null
R6032:Fat2 UTSW 11 55,144,760 (GRCm39) missense probably damaging 1.00
R6032:Fat2 UTSW 11 55,144,760 (GRCm39) missense probably damaging 1.00
R6221:Fat2 UTSW 11 55,186,898 (GRCm39) critical splice donor site probably null
R6253:Fat2 UTSW 11 55,187,097 (GRCm39) missense probably damaging 1.00
R6257:Fat2 UTSW 11 55,153,407 (GRCm39) missense probably benign
R6307:Fat2 UTSW 11 55,172,106 (GRCm39) missense possibly damaging 0.63
R6450:Fat2 UTSW 11 55,180,136 (GRCm39) missense probably damaging 0.97
R6453:Fat2 UTSW 11 55,173,042 (GRCm39) missense probably benign 0.29
R6455:Fat2 UTSW 11 55,161,283 (GRCm39) missense probably damaging 0.96
R6483:Fat2 UTSW 11 55,187,171 (GRCm39) missense probably damaging 1.00
R6504:Fat2 UTSW 11 55,153,223 (GRCm39) missense probably benign 0.00
R6520:Fat2 UTSW 11 55,175,814 (GRCm39) missense probably damaging 0.99
R6525:Fat2 UTSW 11 55,174,626 (GRCm39) missense probably damaging 1.00
R6617:Fat2 UTSW 11 55,186,931 (GRCm39) missense probably benign 0.01
R6652:Fat2 UTSW 11 55,143,088 (GRCm39) missense probably benign
R6679:Fat2 UTSW 11 55,200,131 (GRCm39) missense probably damaging 1.00
R6680:Fat2 UTSW 11 55,201,684 (GRCm39) nonsense probably null
R6762:Fat2 UTSW 11 55,144,308 (GRCm39) splice site probably null
R6810:Fat2 UTSW 11 55,173,067 (GRCm39) missense possibly damaging 0.88
R6818:Fat2 UTSW 11 55,200,167 (GRCm39) missense probably benign 0.31
R6919:Fat2 UTSW 11 55,173,597 (GRCm39) missense possibly damaging 0.68
R6939:Fat2 UTSW 11 55,143,300 (GRCm39) nonsense probably null
R6941:Fat2 UTSW 11 55,152,914 (GRCm39) missense probably benign
R7023:Fat2 UTSW 11 55,201,328 (GRCm39) missense probably benign 0.00
R7027:Fat2 UTSW 11 55,160,259 (GRCm39) missense probably benign 0.03
R7027:Fat2 UTSW 11 55,172,677 (GRCm39) nonsense probably null
R7095:Fat2 UTSW 11 55,202,157 (GRCm39) missense probably damaging 1.00
R7102:Fat2 UTSW 11 55,174,260 (GRCm39) missense probably damaging 1.00
R7116:Fat2 UTSW 11 55,173,162 (GRCm39) missense probably damaging 1.00
R7117:Fat2 UTSW 11 55,172,088 (GRCm39) missense probably damaging 1.00
R7167:Fat2 UTSW 11 55,175,827 (GRCm39) missense possibly damaging 0.48
R7213:Fat2 UTSW 11 55,171,871 (GRCm39) nonsense probably null
R7246:Fat2 UTSW 11 55,187,208 (GRCm39) missense probably benign 0.00
R7252:Fat2 UTSW 11 55,202,088 (GRCm39) missense probably damaging 0.98
R7266:Fat2 UTSW 11 55,175,856 (GRCm39) missense probably damaging 0.99
R7316:Fat2 UTSW 11 55,176,893 (GRCm39) missense probably damaging 1.00
R7326:Fat2 UTSW 11 55,173,130 (GRCm39) missense probably damaging 0.99
R7355:Fat2 UTSW 11 55,147,377 (GRCm39) missense probably benign 0.00
R7431:Fat2 UTSW 11 55,199,927 (GRCm39) missense probably damaging 1.00
R7459:Fat2 UTSW 11 55,194,745 (GRCm39) missense probably damaging 1.00
R7460:Fat2 UTSW 11 55,169,789 (GRCm39) missense probably damaging 1.00
R7466:Fat2 UTSW 11 55,201,258 (GRCm39) missense probably damaging 1.00
R7475:Fat2 UTSW 11 55,194,479 (GRCm39) missense probably benign 0.31
R7678:Fat2 UTSW 11 55,173,156 (GRCm39) missense probably damaging 0.99
R7689:Fat2 UTSW 11 55,200,666 (GRCm39) missense probably damaging 1.00
R7704:Fat2 UTSW 11 55,175,173 (GRCm39) missense probably benign 0.03
R7710:Fat2 UTSW 11 55,201,589 (GRCm39) missense probably benign 0.35
R7724:Fat2 UTSW 11 55,175,622 (GRCm39) missense probably damaging 1.00
R7731:Fat2 UTSW 11 55,201,532 (GRCm39) missense probably damaging 1.00
R7739:Fat2 UTSW 11 55,171,957 (GRCm39) nonsense probably null
R7757:Fat2 UTSW 11 55,202,247 (GRCm39) missense probably benign 0.00
R7876:Fat2 UTSW 11 55,202,046 (GRCm39) missense probably benign 0.01
R7883:Fat2 UTSW 11 55,144,190 (GRCm39) splice site probably null
R7924:Fat2 UTSW 11 55,153,613 (GRCm39) missense probably benign 0.03
R7936:Fat2 UTSW 11 55,200,993 (GRCm39) missense probably benign
R7936:Fat2 UTSW 11 55,201,986 (GRCm39) nonsense probably null
R7938:Fat2 UTSW 11 55,163,922 (GRCm39) missense probably damaging 1.00
R7947:Fat2 UTSW 11 55,178,560 (GRCm39) missense probably damaging 1.00
R8049:Fat2 UTSW 11 55,202,892 (GRCm39) missense probably benign 0.13
R8094:Fat2 UTSW 11 55,186,965 (GRCm39) missense probably benign 0.06
R8157:Fat2 UTSW 11 55,142,910 (GRCm39) missense possibly damaging 0.90
R8170:Fat2 UTSW 11 55,161,281 (GRCm39) missense probably damaging 1.00
R8172:Fat2 UTSW 11 55,178,638 (GRCm39) missense probably damaging 1.00
R8182:Fat2 UTSW 11 55,175,223 (GRCm39) missense possibly damaging 0.51
R8188:Fat2 UTSW 11 55,163,997 (GRCm39) missense probably damaging 0.98
R8204:Fat2 UTSW 11 55,175,436 (GRCm39) missense probably benign 0.02
R8211:Fat2 UTSW 11 55,203,035 (GRCm39) missense possibly damaging 0.92
R8255:Fat2 UTSW 11 55,161,101 (GRCm39) missense probably benign 0.19
R8263:Fat2 UTSW 11 55,174,962 (GRCm39) missense probably benign
R8269:Fat2 UTSW 11 55,173,535 (GRCm39) missense possibly damaging 0.48
R8443:Fat2 UTSW 11 55,202,535 (GRCm39) missense probably damaging 1.00
R8465:Fat2 UTSW 11 55,147,530 (GRCm39) missense possibly damaging 0.61
R8480:Fat2 UTSW 11 55,173,794 (GRCm39) missense possibly damaging 0.61
R8511:Fat2 UTSW 11 55,200,063 (GRCm39) missense probably damaging 0.99
R8680:Fat2 UTSW 11 55,144,692 (GRCm39) missense probably benign
R8704:Fat2 UTSW 11 55,172,137 (GRCm39) missense probably damaging 1.00
R8711:Fat2 UTSW 11 55,159,129 (GRCm39) missense probably benign 0.22
R8724:Fat2 UTSW 11 55,173,786 (GRCm39) missense probably damaging 1.00
R8788:Fat2 UTSW 11 55,171,929 (GRCm39) missense possibly damaging 0.90
R8802:Fat2 UTSW 11 55,173,750 (GRCm39) missense possibly damaging 0.95
R8902:Fat2 UTSW 11 55,200,896 (GRCm39) missense probably damaging 1.00
R8940:Fat2 UTSW 11 55,147,636 (GRCm39) missense possibly damaging 0.48
R8956:Fat2 UTSW 11 55,173,729 (GRCm39) missense probably damaging 1.00
R9035:Fat2 UTSW 11 55,194,547 (GRCm39) missense probably damaging 0.99
R9100:Fat2 UTSW 11 55,153,347 (GRCm39) missense probably damaging 1.00
R9132:Fat2 UTSW 11 55,189,436 (GRCm39) missense possibly damaging 0.88
R9173:Fat2 UTSW 11 55,169,763 (GRCm39) missense probably damaging 1.00
R9241:Fat2 UTSW 11 55,147,566 (GRCm39) missense probably benign 0.00
R9253:Fat2 UTSW 11 55,201,397 (GRCm39) missense probably damaging 1.00
R9280:Fat2 UTSW 11 55,201,523 (GRCm39) missense probably benign 0.36
R9351:Fat2 UTSW 11 55,172,127 (GRCm39) missense probably damaging 1.00
R9369:Fat2 UTSW 11 55,201,514 (GRCm39) missense possibly damaging 0.67
R9404:Fat2 UTSW 11 55,144,348 (GRCm39) critical splice donor site probably null
R9431:Fat2 UTSW 11 55,142,838 (GRCm39) missense probably damaging 1.00
R9484:Fat2 UTSW 11 55,200,752 (GRCm39) missense probably damaging 0.99
R9509:Fat2 UTSW 11 55,200,713 (GRCm39) missense possibly damaging 0.51
R9514:Fat2 UTSW 11 55,175,808 (GRCm39) missense probably damaging 0.98
R9606:Fat2 UTSW 11 55,180,093 (GRCm39) missense probably damaging 1.00
R9630:Fat2 UTSW 11 55,147,605 (GRCm39) missense probably benign 0.29
R9727:Fat2 UTSW 11 55,159,137 (GRCm39) missense probably damaging 1.00
R9736:Fat2 UTSW 11 55,194,751 (GRCm39) missense probably damaging 1.00
X0010:Fat2 UTSW 11 55,143,086 (GRCm39) missense probably benign 0.00
X0011:Fat2 UTSW 11 55,201,257 (GRCm39) missense probably damaging 0.98
X0018:Fat2 UTSW 11 55,187,036 (GRCm39) missense probably damaging 1.00
X0028:Fat2 UTSW 11 55,200,240 (GRCm39) missense possibly damaging 0.84
X0067:Fat2 UTSW 11 55,174,060 (GRCm39) missense possibly damaging 0.48
Z1176:Fat2 UTSW 11 55,175,817 (GRCm39) missense probably damaging 1.00
Z1176:Fat2 UTSW 11 55,173,621 (GRCm39) missense probably damaging 1.00
Z1176:Fat2 UTSW 11 55,200,947 (GRCm39) missense probably damaging 0.96
Z1176:Fat2 UTSW 11 55,194,526 (GRCm39) missense probably damaging 1.00
Z1177:Fat2 UTSW 11 55,169,792 (GRCm39) nonsense probably null
Z1186:Fat2 UTSW 11 55,200,625 (GRCm39) missense probably benign
Z1186:Fat2 UTSW 11 55,199,796 (GRCm39) frame shift probably null
Z1187:Fat2 UTSW 11 55,200,625 (GRCm39) missense probably benign
Z1187:Fat2 UTSW 11 55,199,796 (GRCm39) frame shift probably null
Z1188:Fat2 UTSW 11 55,200,625 (GRCm39) missense probably benign
Z1188:Fat2 UTSW 11 55,199,796 (GRCm39) frame shift probably null
Z1189:Fat2 UTSW 11 55,200,625 (GRCm39) missense probably benign
Z1189:Fat2 UTSW 11 55,199,796 (GRCm39) frame shift probably null
Z1190:Fat2 UTSW 11 55,200,625 (GRCm39) missense probably benign
Z1190:Fat2 UTSW 11 55,199,796 (GRCm39) frame shift probably null
Z1191:Fat2 UTSW 11 55,200,625 (GRCm39) missense probably benign
Z1191:Fat2 UTSW 11 55,199,796 (GRCm39) frame shift probably null
Z1192:Fat2 UTSW 11 55,200,625 (GRCm39) missense probably benign
Z1192:Fat2 UTSW 11 55,199,796 (GRCm39) frame shift probably null
Predicted Primers PCR Primer
(F):5'- TTGCCTTTAGGGACAGCTGG -3'
(R):5'- TCCCAAGGCCTCATATCATAGTAAG -3'

Sequencing Primer
(F):5'- CCTTTAGGGACAGCTGGTTGGG -3'
(R):5'- AGAAGCTGGGTTGCAATCCTCTC -3'
Posted On 2016-08-04