Incidental Mutation 'R9709:Sis'
ID 729947
Institutional Source Beutler Lab
Gene Symbol Sis
Ensembl Gene ENSMUSG00000027790
Gene Name sucrase isomaltase
Synonyms 2010204N08Rik, Si-s, sucrase-isomaltase
MMRRC Submission
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R9709 (G1)
Quality Score 148.008
Status Not validated
Chromosome 3
Chromosomal Location 72795890-72875196 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 72799074 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Phenylalanine at position 1726 (Y1726F)
Ref Sequence ENSEMBL: ENSMUSP00000129116 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094190] [ENSMUST00000167334]
AlphaFold F8VQM5
Predicted Effect possibly damaging
Transcript: ENSMUST00000094190
AA Change: Y1726F

PolyPhen 2 Score 0.473 (Sensitivity: 0.89; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000091742
Gene: ENSMUSG00000027790
AA Change: Y1726F

DomainStartEndE-ValueType
transmembrane domain 13 32 N/A INTRINSIC
PD 51 103 1.92e-12 SMART
Pfam:NtCtMGAM_N 115 224 1.2e-35 PFAM
Pfam:Gal_mutarotas_2 225 294 4.8e-9 PFAM
Pfam:Glyco_hydro_31 314 787 2.1e-142 PFAM
PD 917 972 6.69e-12 SMART
Pfam:NtCtMGAM_N 985 1098 6e-33 PFAM
Blast:ANK 1138 1168 1e-5 BLAST
Pfam:Glyco_hydro_31 1186 1682 8.4e-137 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000167334
AA Change: Y1726F

PolyPhen 2 Score 0.473 (Sensitivity: 0.89; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000129116
Gene: ENSMUSG00000027790
AA Change: Y1726F

DomainStartEndE-ValueType
transmembrane domain 13 32 N/A INTRINSIC
PD 51 103 1.92e-12 SMART
Pfam:NtCtMGAM_N 115 224 1.2e-35 PFAM
Pfam:Gal_mutarotas_2 225 294 4.8e-9 PFAM
Pfam:Glyco_hydro_31 314 787 2.1e-142 PFAM
PD 917 972 6.69e-12 SMART
Pfam:NtCtMGAM_N 985 1098 6e-33 PFAM
Blast:ANK 1138 1168 1e-5 BLAST
Pfam:Glyco_hydro_31 1186 1682 8.4e-137 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.5%
  • 20x: 98.3%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a sucrase-isomaltase enzyme that is expressed in the intestinal brush border. The encoded protein is synthesized as a precursor protein that is cleaved by pancreatic proteases into two enzymatic subunits sucrase and isomaltase. These two subunits heterodimerize to form the sucrose-isomaltase complex. This complex is essential for the digestion of dietary carbohydrates including starch, sucrose and isomaltose. Mutations in this gene are the cause of congenital sucrase-isomaltase deficiency.[provided by RefSeq, Apr 2010]
Allele List at MGI
Other mutations in this stock
Total: 100 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1810062G17Rik T C 3: 36,530,356 (GRCm39) S25P unknown Het
4921539E11Rik A G 4: 103,092,678 (GRCm39) I268T unknown Het
4930507D05Rik T A 10: 62,285,581 (GRCm39) C102S unknown Het
Abca14 T A 7: 119,888,739 (GRCm39) Y1228* probably null Het
Abca17 T C 17: 24,517,934 (GRCm39) I792V probably benign Het
Abca6 C A 11: 110,102,589 (GRCm39) L878F probably benign Het
Adk C A 14: 21,126,386 (GRCm39) T4N probably benign Het
Ankrd40cl G A 11: 94,175,560 (GRCm39) S65N probably benign Het
Atg2b A T 12: 105,611,140 (GRCm39) F1264I probably damaging Het
Atl3 T G 19: 7,507,921 (GRCm39) S358A probably benign Het
Atp8a2 T A 14: 60,271,187 (GRCm39) Y248F probably damaging Het
Bcas3 T C 11: 85,474,749 (GRCm39) V785A probably damaging Het
Cckar C T 5: 53,860,201 (GRCm39) probably null Het
Cdc42se2 A G 11: 54,614,417 (GRCm39) F47L probably benign Het
Cfap58 T C 19: 47,963,992 (GRCm39) L540P probably damaging Het
Copg1 A G 6: 87,868,957 (GRCm39) E117G probably benign Het
Cstpp1 T C 2: 91,112,099 (GRCm39) Q250R probably benign Het
Cul2 C T 18: 3,431,560 (GRCm39) T655M probably damaging Het
Ddi2 T C 4: 141,412,429 (GRCm39) Q161R probably benign Het
Dffb T C 4: 154,059,121 (GRCm39) Y52C probably damaging Het
Dll1 T C 17: 15,591,198 (GRCm39) Q249R probably benign Het
Dnmt3a T A 12: 3,957,701 (GRCm39) I894N probably damaging Het
Fshr G A 17: 89,293,265 (GRCm39) T471I probably damaging Het
Gabpb1 C T 2: 126,500,488 (GRCm39) V4I probably benign Het
Gbp9 T C 5: 105,231,542 (GRCm39) Q348R probably damaging Het
Gm21149 G A 5: 15,677,110 (GRCm39) S248F unknown Het
Gpr152 C A 19: 4,192,640 (GRCm39) H60Q probably benign Het
Hdac9 A G 12: 34,362,602 (GRCm39) S612P probably benign Het
Hhipl2 A G 1: 183,199,747 (GRCm39) D102G possibly damaging Het
Hspa9 A G 18: 35,073,294 (GRCm39) V530A possibly damaging Het
Igfbp7 T C 5: 77,549,384 (GRCm39) N173S unknown Het
Ighv1-75 A G 12: 115,797,791 (GRCm39) S44P possibly damaging Het
Iqgap3 C A 3: 88,016,176 (GRCm39) F986L probably damaging Het
Itgax G T 7: 127,735,500 (GRCm39) G523W probably damaging Het
Itih3 A G 14: 30,637,587 (GRCm39) probably null Het
Kcnb2 T C 1: 15,780,523 (GRCm39) I465T probably benign Het
Kmt2b A G 7: 30,279,228 (GRCm39) V1478A probably damaging Het
Ky A T 9: 102,419,411 (GRCm39) I473F probably damaging Het
Lbr A G 1: 181,666,034 (GRCm39) V25A probably damaging Het
Ldlr A G 9: 21,657,135 (GRCm39) T751A probably benign Het
Lrrtm4 A G 6: 80,786,154 (GRCm39) E587G probably damaging Het
Lvrn A C 18: 47,006,847 (GRCm39) probably null Het
Mast2 A T 4: 116,173,044 (GRCm39) C594S probably damaging Het
Mast4 A G 13: 102,910,711 (GRCm39) V644A probably damaging Het
Mcm5 T C 8: 75,842,604 (GRCm39) Y293H probably damaging Het
Mthfd2 A T 6: 83,283,665 (GRCm39) V339E possibly damaging Het
Muc4 A T 16: 32,590,644 (GRCm39) I881F Het
Myo7a A G 7: 97,743,536 (GRCm39) S372P possibly damaging Het
Nbea T A 3: 55,693,879 (GRCm39) K2180* probably null Het
Neb T C 2: 52,101,507 (GRCm39) D4621G probably damaging Het
Nefh C T 11: 4,890,042 (GRCm39) S859N probably benign Het
Nek2 T A 1: 191,563,289 (GRCm39) H384Q possibly damaging Het
Nfkb2 A G 19: 46,298,782 (GRCm39) E645G probably benign Het
Nin G T 12: 70,149,468 (GRCm39) P47Q Het
Nit1 C A 1: 171,171,307 (GRCm39) K178N probably benign Het
Nrap C A 19: 56,317,452 (GRCm39) K1433N probably damaging Het
Nrap T C 19: 56,317,453 (GRCm39) K1433R probably benign Het
Nup85 A G 11: 115,457,463 (GRCm39) Y55C possibly damaging Het
Or2a14 G T 6: 43,130,469 (GRCm39) V77F possibly damaging Het
Pde1b A G 15: 103,411,985 (GRCm39) K29E probably benign Het
Pheta2 G T 15: 82,227,537 (GRCm39) D19Y probably damaging Het
Pheta2 C G 15: 82,227,535 (GRCm39) A18G probably damaging Het
Pik3cg A T 12: 32,226,687 (GRCm39) Y1067N probably benign Het
Pkd1l1 C T 11: 8,799,016 (GRCm39) G2249S probably damaging Het
Plppr4 T A 3: 117,121,976 (GRCm39) T201S possibly damaging Het
Polr1e A G 4: 45,018,678 (GRCm39) T3A probably benign Het
Polr1has A T 17: 37,275,249 (GRCm39) R7S probably benign Het
Pou6f2 G T 13: 18,414,389 (GRCm39) Q129K unknown Het
Ppil4 T A 10: 7,675,341 (GRCm39) D163E probably benign Het
Pradc1 A G 6: 85,424,952 (GRCm39) F82L probably benign Het
Psd3 T C 8: 68,194,414 (GRCm39) K784R probably null Het
Ptgs1 C A 2: 36,141,204 (GRCm39) S550R probably damaging Het
Pxylp1 A G 9: 96,711,030 (GRCm39) L153P probably damaging Het
Rgs10 A C 7: 127,975,729 (GRCm39) F146C probably damaging Het
Rimbp2 G A 5: 128,874,875 (GRCm39) P239S probably damaging Het
Rp1 A G 1: 4,112,255 (GRCm39) Y1199H unknown Het
Rrp12 A T 19: 41,857,231 (GRCm39) M1181K probably benign Het
Rundc3b T C 5: 8,570,982 (GRCm39) N279S probably benign Het
Sbf2 G T 7: 110,027,514 (GRCm39) P494Q probably damaging Het
Scnn1b A G 7: 121,509,693 (GRCm39) T281A probably benign Het
Scube2 A T 7: 109,430,971 (GRCm39) N409K probably damaging Het
Serpina3m A C 12: 104,359,008 (GRCm39) D340A probably damaging Het
Sez6 G A 11: 77,865,121 (GRCm39) E623K possibly damaging Het
Sgpp2 T C 1: 78,367,200 (GRCm39) I111T probably benign Het
Shprh C T 10: 11,038,574 (GRCm39) T443I possibly damaging Het
Slc17a9 T C 2: 180,374,321 (GRCm39) L129P probably damaging Het
Slc1a5 T A 7: 16,527,729 (GRCm39) F342I probably benign Het
Slc4a4 T A 5: 89,188,205 (GRCm39) probably null Het
Slco3a1 T C 7: 73,952,957 (GRCm39) E534G possibly damaging Het
Smok2b A T 17: 13,454,052 (GRCm39) I71F possibly damaging Het
Tmbim7 A T 5: 3,711,809 (GRCm39) H18L probably damaging Het
Tmem151a A T 19: 5,131,876 (GRCm39) Y443* probably null Het
Tnks1bp1 T G 2: 84,902,125 (GRCm39) S1674A probably benign Het
Trappc11 T A 8: 47,946,348 (GRCm39) I1095F probably damaging Het
Trim11 A G 11: 58,872,864 (GRCm39) R183G possibly damaging Het
Trim29 A G 9: 43,231,797 (GRCm39) D348G probably benign Het
Ttc28 A T 5: 111,433,637 (GRCm39) S2224C probably damaging Het
Vps13d C T 4: 144,875,915 (GRCm39) V1537M Het
Zfp1005 T A 2: 150,110,305 (GRCm39) C332S possibly damaging Het
Zfp184 A G 13: 22,143,665 (GRCm39) D457G possibly damaging Het
Other mutations in Sis
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00582:Sis APN 3 72,853,969 (GRCm39) missense probably benign
IGL00715:Sis APN 3 72,841,457 (GRCm39) missense probably damaging 1.00
IGL00721:Sis APN 3 72,850,912 (GRCm39) missense probably damaging 1.00
IGL00766:Sis APN 3 72,814,570 (GRCm39) splice site probably benign
IGL00783:Sis APN 3 72,853,965 (GRCm39) missense probably benign
IGL00805:Sis APN 3 72,841,532 (GRCm39) missense probably benign 0.05
IGL00932:Sis APN 3 72,848,289 (GRCm39) splice site probably benign
IGL01020:Sis APN 3 72,874,171 (GRCm39) missense probably damaging 1.00
IGL01024:Sis APN 3 72,819,209 (GRCm39) missense probably damaging 1.00
IGL01286:Sis APN 3 72,848,358 (GRCm39) missense probably damaging 1.00
IGL01457:Sis APN 3 72,868,354 (GRCm39) missense probably benign
IGL01514:Sis APN 3 72,843,253 (GRCm39) splice site probably benign
IGL01986:Sis APN 3 72,852,545 (GRCm39) missense probably damaging 1.00
IGL02110:Sis APN 3 72,836,032 (GRCm39) nonsense probably null
IGL02132:Sis APN 3 72,854,804 (GRCm39) missense probably benign 0.00
IGL02152:Sis APN 3 72,796,319 (GRCm39) utr 3 prime probably benign
IGL02200:Sis APN 3 72,850,937 (GRCm39) missense probably damaging 0.99
IGL02244:Sis APN 3 72,863,523 (GRCm39) missense probably benign 0.19
IGL02307:Sis APN 3 72,819,167 (GRCm39) splice site probably benign
IGL02374:Sis APN 3 72,832,789 (GRCm39) missense probably benign 0.03
IGL02437:Sis APN 3 72,826,947 (GRCm39) critical splice acceptor site probably null
IGL02571:Sis APN 3 72,863,637 (GRCm39) splice site probably benign
IGL02601:Sis APN 3 72,820,543 (GRCm39) missense probably benign 0.44
IGL03063:Sis APN 3 72,835,630 (GRCm39) missense probably benign
IGL03382:Sis APN 3 72,836,052 (GRCm39) missense probably benign 0.00
IGL03397:Sis APN 3 72,843,212 (GRCm39) missense probably benign 0.44
PIT1430001:Sis UTSW 3 72,830,162 (GRCm39) missense probably damaging 0.97
R0013:Sis UTSW 3 72,817,809 (GRCm39) missense possibly damaging 0.65
R0013:Sis UTSW 3 72,817,809 (GRCm39) missense possibly damaging 0.65
R0046:Sis UTSW 3 72,839,427 (GRCm39) missense probably benign 0.01
R0094:Sis UTSW 3 72,828,770 (GRCm39) missense probably damaging 1.00
R0096:Sis UTSW 3 72,835,600 (GRCm39) missense probably damaging 1.00
R0505:Sis UTSW 3 72,867,629 (GRCm39) missense probably benign 0.29
R0544:Sis UTSW 3 72,858,975 (GRCm39) missense probably damaging 1.00
R0551:Sis UTSW 3 72,832,740 (GRCm39) missense possibly damaging 0.79
R0617:Sis UTSW 3 72,872,938 (GRCm39) missense probably damaging 1.00
R0698:Sis UTSW 3 72,817,831 (GRCm39) missense probably damaging 1.00
R0701:Sis UTSW 3 72,848,378 (GRCm39) missense probably damaging 1.00
R0704:Sis UTSW 3 72,857,155 (GRCm39) missense possibly damaging 0.63
R0706:Sis UTSW 3 72,859,864 (GRCm39) missense probably damaging 1.00
R0710:Sis UTSW 3 72,859,864 (GRCm39) missense probably damaging 1.00
R0752:Sis UTSW 3 72,859,864 (GRCm39) missense probably damaging 1.00
R0753:Sis UTSW 3 72,859,864 (GRCm39) missense probably damaging 1.00
R0754:Sis UTSW 3 72,859,864 (GRCm39) missense probably damaging 1.00
R0767:Sis UTSW 3 72,859,864 (GRCm39) missense probably damaging 1.00
R0769:Sis UTSW 3 72,859,864 (GRCm39) missense probably damaging 1.00
R0772:Sis UTSW 3 72,859,864 (GRCm39) missense probably damaging 1.00
R0774:Sis UTSW 3 72,859,864 (GRCm39) missense probably damaging 1.00
R0776:Sis UTSW 3 72,859,864 (GRCm39) missense probably damaging 1.00
R0818:Sis UTSW 3 72,859,864 (GRCm39) missense probably damaging 1.00
R0819:Sis UTSW 3 72,859,864 (GRCm39) missense probably damaging 1.00
R0885:Sis UTSW 3 72,819,282 (GRCm39) nonsense probably null
R1076:Sis UTSW 3 72,841,431 (GRCm39) missense probably damaging 0.97
R1140:Sis UTSW 3 72,858,949 (GRCm39) missense probably damaging 0.98
R1175:Sis UTSW 3 72,865,437 (GRCm39) splice site probably benign
R1301:Sis UTSW 3 72,853,915 (GRCm39) missense possibly damaging 0.76
R1437:Sis UTSW 3 72,841,475 (GRCm39) missense probably damaging 1.00
R1466:Sis UTSW 3 72,839,393 (GRCm39) missense possibly damaging 0.60
R1466:Sis UTSW 3 72,839,393 (GRCm39) missense possibly damaging 0.60
R1472:Sis UTSW 3 72,796,360 (GRCm39) missense probably benign 0.12
R1584:Sis UTSW 3 72,839,393 (GRCm39) missense possibly damaging 0.60
R1707:Sis UTSW 3 72,816,420 (GRCm39) splice site probably benign
R1715:Sis UTSW 3 72,796,343 (GRCm39) missense possibly damaging 0.47
R1719:Sis UTSW 3 72,872,937 (GRCm39) missense probably damaging 1.00
R1728:Sis UTSW 3 72,872,978 (GRCm39) nonsense probably null
R1784:Sis UTSW 3 72,872,978 (GRCm39) nonsense probably null
R1820:Sis UTSW 3 72,828,475 (GRCm39) missense probably damaging 1.00
R1972:Sis UTSW 3 72,828,337 (GRCm39) missense probably damaging 1.00
R1973:Sis UTSW 3 72,828,337 (GRCm39) missense probably damaging 1.00
R2054:Sis UTSW 3 72,820,570 (GRCm39) missense probably benign 0.01
R2233:Sis UTSW 3 72,820,527 (GRCm39) missense probably benign 0.03
R2235:Sis UTSW 3 72,820,527 (GRCm39) missense probably benign 0.03
R2276:Sis UTSW 3 72,821,934 (GRCm39) nonsense probably null
R2435:Sis UTSW 3 72,819,237 (GRCm39) missense probably benign 0.01
R2885:Sis UTSW 3 72,816,506 (GRCm39) missense probably benign 0.01
R2966:Sis UTSW 3 72,796,343 (GRCm39) missense probably benign 0.30
R3708:Sis UTSW 3 72,850,856 (GRCm39) missense probably benign 0.02
R3790:Sis UTSW 3 72,828,747 (GRCm39) missense probably damaging 1.00
R3807:Sis UTSW 3 72,832,929 (GRCm39) missense probably benign 0.01
R3858:Sis UTSW 3 72,835,985 (GRCm39) missense probably damaging 0.99
R3974:Sis UTSW 3 72,850,968 (GRCm39) missense probably damaging 0.96
R3975:Sis UTSW 3 72,850,968 (GRCm39) missense probably damaging 0.96
R4037:Sis UTSW 3 72,835,935 (GRCm39) missense probably benign
R4080:Sis UTSW 3 72,828,517 (GRCm39) missense probably damaging 1.00
R4204:Sis UTSW 3 72,868,415 (GRCm39) missense probably benign
R4394:Sis UTSW 3 72,863,482 (GRCm39) missense probably damaging 1.00
R4470:Sis UTSW 3 72,835,492 (GRCm39) splice site probably null
R4573:Sis UTSW 3 72,835,570 (GRCm39) missense possibly damaging 0.94
R4868:Sis UTSW 3 72,850,881 (GRCm39) missense probably benign 0.09
R5023:Sis UTSW 3 72,841,455 (GRCm39) missense probably benign 0.05
R5264:Sis UTSW 3 72,857,089 (GRCm39) missense probably damaging 0.98
R5414:Sis UTSW 3 72,859,826 (GRCm39) missense probably benign
R5462:Sis UTSW 3 72,857,171 (GRCm39) missense probably damaging 0.96
R5523:Sis UTSW 3 72,798,754 (GRCm39) missense probably benign 0.00
R5584:Sis UTSW 3 72,817,748 (GRCm39) missense probably damaging 1.00
R5587:Sis UTSW 3 72,821,909 (GRCm39) missense possibly damaging 0.94
R5725:Sis UTSW 3 72,872,931 (GRCm39) missense probably damaging 1.00
R5769:Sis UTSW 3 72,835,568 (GRCm39) missense probably damaging 0.98
R5790:Sis UTSW 3 72,835,507 (GRCm39) missense probably benign
R5864:Sis UTSW 3 72,857,151 (GRCm39) missense probably damaging 1.00
R5902:Sis UTSW 3 72,867,589 (GRCm39) critical splice donor site probably null
R5925:Sis UTSW 3 72,828,713 (GRCm39) splice site probably null
R6018:Sis UTSW 3 72,820,525 (GRCm39) missense possibly damaging 0.95
R6029:Sis UTSW 3 72,835,641 (GRCm39) missense probably benign 0.30
R6124:Sis UTSW 3 72,860,544 (GRCm39) missense possibly damaging 0.69
R6171:Sis UTSW 3 72,868,360 (GRCm39) missense possibly damaging 0.75
R6182:Sis UTSW 3 72,811,626 (GRCm39) missense probably benign 0.05
R6295:Sis UTSW 3 72,874,103 (GRCm39) missense probably damaging 0.99
R6416:Sis UTSW 3 72,819,187 (GRCm39) missense probably damaging 1.00
R6431:Sis UTSW 3 72,865,507 (GRCm39) missense probably benign 0.00
R6472:Sis UTSW 3 72,846,067 (GRCm39) nonsense probably null
R6517:Sis UTSW 3 72,814,475 (GRCm39) missense probably damaging 1.00
R6701:Sis UTSW 3 72,856,860 (GRCm39) missense probably damaging 1.00
R6796:Sis UTSW 3 72,872,951 (GRCm39) missense probably benign 0.06
R6853:Sis UTSW 3 72,798,759 (GRCm39) missense possibly damaging 0.93
R6906:Sis UTSW 3 72,826,818 (GRCm39) missense probably damaging 1.00
R7058:Sis UTSW 3 72,810,940 (GRCm39) missense probably damaging 0.98
R7357:Sis UTSW 3 72,832,404 (GRCm39) missense probably damaging 1.00
R7381:Sis UTSW 3 72,820,625 (GRCm39) splice site probably null
R7439:Sis UTSW 3 72,816,374 (GRCm39) missense possibly damaging 0.81
R7742:Sis UTSW 3 72,832,431 (GRCm39) missense probably benign 0.19
R7813:Sis UTSW 3 72,832,801 (GRCm39) missense probably benign 0.01
R7883:Sis UTSW 3 72,828,329 (GRCm39) missense possibly damaging 0.78
R7899:Sis UTSW 3 72,844,584 (GRCm39) missense probably damaging 1.00
R7915:Sis UTSW 3 72,828,471 (GRCm39) missense probably damaging 0.99
R7985:Sis UTSW 3 72,844,294 (GRCm39) splice site probably null
R8020:Sis UTSW 3 72,816,298 (GRCm39) critical splice donor site probably null
R8023:Sis UTSW 3 72,859,813 (GRCm39) missense probably damaging 0.97
R8029:Sis UTSW 3 72,828,475 (GRCm39) missense probably damaging 1.00
R8053:Sis UTSW 3 72,856,901 (GRCm39) nonsense probably null
R8062:Sis UTSW 3 72,828,321 (GRCm39) nonsense probably null
R8074:Sis UTSW 3 72,824,531 (GRCm39) missense probably damaging 1.00
R8085:Sis UTSW 3 72,814,462 (GRCm39) missense probably damaging 1.00
R8137:Sis UTSW 3 72,796,378 (GRCm39) missense probably benign 0.22
R8349:Sis UTSW 3 72,810,984 (GRCm39) missense probably damaging 1.00
R8354:Sis UTSW 3 72,854,834 (GRCm39) missense possibly damaging 0.84
R8366:Sis UTSW 3 72,865,566 (GRCm39) missense probably damaging 1.00
R8449:Sis UTSW 3 72,810,984 (GRCm39) missense probably damaging 1.00
R8454:Sis UTSW 3 72,854,834 (GRCm39) missense possibly damaging 0.84
R8474:Sis UTSW 3 72,836,730 (GRCm39) missense probably damaging 1.00
R8515:Sis UTSW 3 72,836,742 (GRCm39) missense probably benign 0.00
R8680:Sis UTSW 3 72,867,628 (GRCm39) missense probably damaging 1.00
R8703:Sis UTSW 3 72,867,657 (GRCm39) missense probably damaging 1.00
R9098:Sis UTSW 3 72,844,578 (GRCm39) missense possibly damaging 0.66
R9466:Sis UTSW 3 72,872,910 (GRCm39) critical splice donor site probably null
R9574:Sis UTSW 3 72,828,490 (GRCm39) missense probably benign 0.05
R9630:Sis UTSW 3 72,828,722 (GRCm39) missense probably benign 0.11
R9680:Sis UTSW 3 72,863,621 (GRCm39) missense probably benign 0.12
R9731:Sis UTSW 3 72,835,543 (GRCm39) missense probably benign 0.01
X0009:Sis UTSW 3 72,796,355 (GRCm39) missense probably damaging 0.99
X0024:Sis UTSW 3 72,836,003 (GRCm39) missense probably benign
X0060:Sis UTSW 3 72,828,239 (GRCm39) intron probably benign
Z1176:Sis UTSW 3 72,850,890 (GRCm39) missense probably benign 0.25
Z1176:Sis UTSW 3 72,811,606 (GRCm39) missense probably benign 0.05
Z1177:Sis UTSW 3 72,850,902 (GRCm39) missense probably damaging 1.00
Z1177:Sis UTSW 3 72,817,807 (GRCm39) missense probably damaging 1.00
Z1177:Sis UTSW 3 72,816,505 (GRCm39) missense possibly damaging 0.88
Predicted Primers PCR Primer
(F):5'- GCTGTGATCTAACATGAATCTCATTGG -3'
(R):5'- TCTAGTGGCAAATTTCCTCACTG -3'

Sequencing Primer
(F):5'- TCGGGAGTAAAACTCCAC -3'
(R):5'- TCCTCACTGTATAATGAGAATAGCC -3'
Posted On 2022-10-06