Incidental Mutation 'R7102:Fat2'
ID 550933
Institutional Source Beutler Lab
Gene Symbol Fat2
Ensembl Gene ENSMUSG00000055333
Gene Name FAT atypical cadherin 2
Synonyms LOC245827, mKIAA0811, EMI2, Fath2
MMRRC Submission 045194-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R7102 (G1)
Quality Score 225.009
Status Not validated
Chromosome 11
Chromosomal Location 55141435-55227390 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 55174260 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Proline to Leucine at position 2151 (P2151L)
Ref Sequence ENSEMBL: ENSMUSP00000067556 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000068853] [ENSMUST00000108864]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000068853
AA Change: P2151L

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000067556
Gene: ENSMUSG00000055333
AA Change: P2151L

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 damaging
Transcript: ENSMUST00000108864
AA Change: P2151L

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000104492
Gene: ENSMUSG00000055333
AA Change: P2151L

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: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.0%
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: 98 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca13 A T 11: 9,285,215 (GRCm39) H3283L probably damaging Het
Abcb1a T G 5: 8,744,072 (GRCm39) S233A probably benign Het
Actr10 T C 12: 70,999,805 (GRCm39) probably null Het
Acvr2b C T 9: 119,261,619 (GRCm39) A380V probably damaging Het
Adcy5 A G 16: 35,119,995 (GRCm39) E1168G probably damaging Het
Akap12 C T 10: 4,303,226 (GRCm39) T117I probably damaging Het
Alox5 T A 6: 116,390,429 (GRCm39) Y516F probably benign Het
Amigo2 T C 15: 97,143,741 (GRCm39) N227S probably damaging Het
Anpep C A 7: 79,486,061 (GRCm39) V554L probably benign Het
Ap5b1 T A 19: 5,620,215 (GRCm39) V545E possibly damaging Het
Bbs9 C T 9: 22,490,849 (GRCm39) L326F probably damaging Het
Bltp1 T G 3: 36,994,947 (GRCm39) Y990D probably damaging Het
Cadps C T 14: 12,603,738 (GRCm38) G361R probably damaging Het
Ccdc57 C A 11: 120,812,557 (GRCm39) E66* probably null Het
Ccr6 G A 17: 8,475,019 (GRCm39) V75I probably benign Het
Cdk6 T C 5: 3,570,709 (GRCm39) F300S probably damaging Het
Cenpb A C 2: 131,020,799 (GRCm39) V333G probably damaging Het
Clca4a T C 3: 144,667,670 (GRCm39) I434V probably benign Het
Coro2b T A 9: 62,328,667 (GRCm39) D447V possibly damaging Het
Cpeb3 T C 19: 37,152,119 (GRCm39) S86G probably benign Het
Cry2 C A 2: 92,243,438 (GRCm39) A468S probably damaging Het
Csf2rb2 T C 15: 78,181,272 (GRCm39) Y40C probably damaging Het
Ddx49 T A 8: 70,753,726 (GRCm39) T48S probably damaging Het
Dennd10 T A 19: 60,821,034 (GRCm39) M272K probably damaging Het
Dip2c A G 13: 9,654,572 (GRCm39) T727A probably benign Het
Dnai3 A T 3: 145,761,459 (GRCm39) S632R possibly damaging Het
Ebf4 A T 2: 130,151,651 (GRCm39) I183F probably benign Het
Elavl3 G T 9: 21,930,025 (GRCm39) P293Q possibly damaging Het
Esyt1 A T 10: 128,352,105 (GRCm39) L768Q probably damaging Het
Fgfbp3 G T 19: 36,896,606 (GRCm39) A4E possibly damaging Het
Flg T A 3: 93,200,335 (GRCm39) V277D unknown Het
Fndc3b T C 3: 27,524,383 (GRCm39) D459G possibly damaging Het
Fras1 A G 5: 96,718,900 (GRCm39) Q438R probably benign Het
Glipr1l2 A T 10: 111,928,330 (GRCm39) probably null Het
Gm7347 T A 5: 26,262,382 (GRCm39) probably null Het
Grm6 G A 11: 50,753,804 (GRCm39) V703I possibly damaging Het
Gtf2h1 T A 7: 46,468,550 (GRCm39) V496E probably benign Het
Ifna12 A G 4: 88,521,388 (GRCm39) L53P probably damaging Het
Invs T A 4: 48,407,674 (GRCm39) S550T probably benign Het
Irak2 G T 6: 113,663,810 (GRCm39) C453F probably damaging Het
Itih2 G T 2: 10,110,574 (GRCm39) Q506K probably benign Het
Kidins220 T C 12: 25,107,662 (GRCm39) I1614T probably benign Het
Krtap5-3 T A 7: 141,755,992 (GRCm39) C276* probably null Het
Lama3 T A 18: 12,685,870 (GRCm39) M1128K possibly damaging Het
Lhfpl4 C T 6: 113,171,106 (GRCm39) A27T possibly damaging Het
Lyplal1 A G 1: 185,832,524 (GRCm39) V77A probably damaging Het
Malrd1 A T 2: 16,147,114 (GRCm39) E1985D unknown Het
Mlx A C 11: 100,979,802 (GRCm39) Q161P probably benign Het
Mroh2b T A 15: 4,977,485 (GRCm39) M1279K probably benign Het
Myh7b A G 2: 155,464,119 (GRCm39) E540G probably damaging Het
Neb T A 2: 52,194,067 (GRCm39) D653V probably damaging Het
Nek10 T A 14: 14,828,517 (GRCm38) L113Q probably damaging Het
Nlrp4c T A 7: 6,068,708 (GRCm39) L203* probably null Het
Nscme3l T A 19: 5,553,623 (GRCm39) T53S probably benign Het
Ntpcr T A 8: 126,456,794 (GRCm39) C5S unknown Het
Nwd1 A G 8: 73,421,957 (GRCm39) D1001G probably damaging Het
Or12j5 T A 7: 140,084,229 (GRCm39) T48S probably benign Het
Or14a256 C T 7: 86,265,475 (GRCm39) C126Y probably benign Het
Or4p22 T A 2: 88,317,492 (GRCm39) C139S probably damaging Het
Or6c208 A C 10: 129,224,036 (GRCm39) D178A probably damaging Het
Osbpl3 T A 6: 50,297,115 (GRCm39) S564C probably damaging Het
Pax6 C A 2: 105,522,604 (GRCm39) P264T probably damaging Het
Plppr4 T C 3: 117,116,832 (GRCm39) R342G probably damaging Het
Prg4 C T 1: 150,328,005 (GRCm39) C220Y probably damaging Het
Prune2 T A 19: 17,098,577 (GRCm39) D1360E probably benign Het
Ranbp2 T A 10: 58,299,772 (GRCm39) S469T probably damaging Het
Rbfox1 A T 16: 7,187,698 (GRCm39) K43N probably benign Het
Rgs22 T C 15: 36,122,459 (GRCm39) D25G probably damaging Het
Rnf113a2 G A 12: 84,464,545 (GRCm39) G146S probably damaging Het
Sbpl T A 17: 24,173,608 (GRCm39) K55* probably null Het
Scel G A 14: 103,781,268 (GRCm39) W138* probably null Het
Scgb2b19 T C 7: 32,979,711 (GRCm39) I12V probably null Het
Scn9a T A 2: 66,379,359 (GRCm39) M358L probably damaging Het
Sdk2 C A 11: 113,733,516 (GRCm39) E924* probably null Het
Sipa1l3 T C 7: 29,048,012 (GRCm39) Q1292R possibly damaging Het
Skint4 G A 4: 111,975,298 (GRCm39) G86D probably damaging Het
Slc28a3 C T 13: 58,736,028 (GRCm39) V57I probably benign Het
Slc9a4 T C 1: 40,662,559 (GRCm39) S609P probably damaging Het
Slc9a4 C T 1: 40,619,799 (GRCm39) P42S probably benign Het
Slitrk1 T A 14: 109,150,061 (GRCm39) T217S probably benign Het
Spindoc C T 19: 7,335,807 (GRCm39) R327H probably benign Het
Stk36 T C 1: 74,661,382 (GRCm39) S470P probably benign Het
Sypl1 C T 12: 33,024,254 (GRCm39) P196L probably benign Het
Tekt4 T A 17: 25,693,718 (GRCm39) I285N probably damaging Het
Tgm5 T A 2: 120,876,979 (GRCm39) I686F possibly damaging Het
Thsd4 C A 9: 59,883,587 (GRCm39) R933L probably damaging Het
Treml1 T A 17: 48,673,700 (GRCm39) I237N probably damaging Het
Txndc16 T C 14: 45,442,839 (GRCm39) I119V probably benign Het
Ubr3 C A 2: 69,728,166 (GRCm39) N176K probably damaging Het
Vit A G 17: 78,932,426 (GRCm39) Y511C probably damaging Het
Vwa5b2 G A 16: 20,422,984 (GRCm39) G994D probably benign Het
Wnk1 T C 6: 119,925,268 (GRCm39) T1648A unknown Het
Ythdf1 G A 2: 180,553,315 (GRCm39) T300I probably damaging Het
Zan A G 5: 137,452,462 (GRCm39) probably null Het
Zbbx A G 3: 75,019,401 (GRCm39) L103P probably benign Het
Zfp105 A G 9: 122,758,869 (GRCm39) D180G probably damaging Het
Zfp114 T A 7: 23,880,083 (GRCm39) L144Q possibly damaging Het
Zfp128 T C 7: 12,624,399 (GRCm39) C256R probably 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
R5288:Fat2 UTSW 11 55,158,482 (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
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'- TAGTCCAGAGGTCCTGTCAC -3'
(R):5'- ACTGATAAGGATTTGGGAGCC -3'

Sequencing Primer
(F):5'- CGTGAGGACTCCAGTTTTAAAGTC -3'
(R):5'- GCCAATGGGACTGTCACATATG -3'
Posted On 2019-05-15