Incidental Mutation 'R9649:Stab2'
ID 726972
Institutional Source Beutler Lab
Gene Symbol Stab2
Ensembl Gene ENSMUSG00000035459
Gene Name stabilin 2
Synonyms FEEL-2, STAB-2
MMRRC Submission
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R9649 (G1)
Quality Score 205.468
Status Not validated
Chromosome 10
Chromosomal Location 86677062-86843889 bp(-) (GRCm39)
Type of Mutation frame shift
DNA Base Change (assembly) ACC to AC at 86692561 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000048309 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000035288]
AlphaFold Q8R4U0
Predicted Effect probably null
Transcript: ENSMUST00000035288
SMART Domains Protein: ENSMUSP00000048309
Gene: ENSMUSG00000035459

DomainStartEndE-ValueType
signal peptide 1 27 N/A INTRINSIC
EGF 119 156 1.85e0 SMART
EGF 167 201 2.43e1 SMART
EGF 206 244 1.43e-1 SMART
EGF 248 284 3.82e-2 SMART
EGF 333 370 2.02e-1 SMART
FAS1 414 515 1.06e-8 SMART
FAS1 561 662 3.54e-19 SMART
EGF 746 783 6.76e-3 SMART
EGF 836 873 1.31e0 SMART
EGF 877 917 2.99e-4 SMART
EGF 921 960 3.51e-1 SMART
EGF 964 1002 1.99e0 SMART
FAS1 1038 1138 1.73e-13 SMART
FAS1 1181 1276 1.83e-12 SMART
EGF 1354 1391 6.92e0 SMART
EGF 1401 1435 1.11e1 SMART
EGF 1442 1477 3.01e0 SMART
EGF 1481 1519 1.64e-1 SMART
EGF 1523 1561 1.14e0 SMART
EGF 1565 1603 5.62e0 SMART
FAS1 1638 1734 2.23e-25 SMART
FAS1 1785 1891 6.92e-22 SMART
EGF 1966 2006 1.95e1 SMART
EGF_like 1977 2017 2.46e-1 SMART
EGF 2016 2050 1.14e0 SMART
EGF 2058 2089 1.56e1 SMART
EGF 2093 2130 1.36e1 SMART
EGF 2134 2173 2.13e0 SMART
LINK 2204 2298 2.08e-29 SMART
FAS1 2363 2455 3.19e-12 SMART
transmembrane domain 2467 2489 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000219341
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a large, transmembrane receptor protein which may function in angiogenesis, lymphocyte homing, cell adhesion, or receptor scavenging. The protein contains 7 fasciclin, 15 epidermal growth factor (EGF)-like, and 2 laminin-type EGF-like domains as well as a C-type lectin-like hyaluronan-binding Link module. The protein is primarily expressed on sinusoidal endothelial cells of liver, spleen, and lymph node. The receptor has been shown to bind and endocytose ligands such as hyaluronan, low density lipoprotein, Gram-positive and Gram-negative bacteria, and advanced glycosylation end products. Supporting its possible role as a scavenger receptor, the protein has been shown to cycle between the plasma membrane and lysosomes. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for knock-out alleles exhibit no gross abnormaities. Mice homozygous for one null allele display elevated serum hyaluronic acid levels and decreased metastasis. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 103 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700010B08Rik A T 2: 173,561,706 (GRCm39) H5L unknown Het
Aatk A G 11: 119,901,733 (GRCm39) S888P probably damaging Het
Ahnak A T 19: 8,985,786 (GRCm39) K2357* probably null Het
Arl9 T A 5: 77,155,139 (GRCm39) L90Q probably damaging Het
Atosa A G 9: 74,924,349 (GRCm39) D864G possibly damaging Het
Atxn2 T C 5: 121,949,055 (GRCm39) V1144A probably damaging Het
Batf3 C T 1: 190,830,623 (GRCm39) probably benign Het
Bltp3b C A 10: 89,626,593 (GRCm39) T429K probably benign Het
Brpf3 G A 17: 29,037,597 (GRCm39) E822K probably benign Het
Cabin1 T A 10: 75,575,239 (GRCm39) Q602L probably damaging Het
Cadps T C 14: 12,597,418 (GRCm38) E424G probably damaging Het
Camta1 A G 4: 151,216,004 (GRCm39) L972P possibly damaging Het
Ccdc159 A G 9: 21,840,672 (GRCm39) N80D possibly damaging Het
Cdh1 A C 8: 107,388,604 (GRCm39) E553D possibly damaging Het
Cdk14 T A 5: 5,423,477 (GRCm39) E35V probably benign Het
Cfap70 A G 14: 20,450,546 (GRCm39) L995P probably damaging Het
Col18a1 T A 10: 76,916,673 (GRCm39) E334V unknown Het
Colec12 T A 18: 9,877,000 (GRCm39) I741K unknown Het
Crot A G 5: 9,024,170 (GRCm39) V342A probably benign Het
Ctnnal1 A G 4: 56,865,036 (GRCm39) S27P possibly damaging Het
Cyp2j9 A G 4: 96,460,193 (GRCm39) S437P probably damaging Het
Dennd4c A T 4: 86,743,160 (GRCm39) T1001S probably benign Het
Dffa G A 4: 149,202,276 (GRCm39) V227I probably benign Het
Dnaaf5 T A 5: 139,159,909 (GRCm39) H602Q probably benign Het
Efcab7 G T 4: 99,761,902 (GRCm39) K397N probably damaging Het
Egfl6 C T X: 165,319,235 (GRCm39) V379I probably benign Het
Fadd G A 7: 144,134,384 (GRCm39) T167I probably benign Het
Fam184b T C 5: 45,796,484 (GRCm39) D33G probably damaging Het
Fam237b C T 5: 5,625,549 (GRCm39) Q82* probably null Het
Fam83h G A 15: 75,877,976 (GRCm39) R141W probably damaging Het
Fanci G A 7: 79,076,954 (GRCm39) R564Q probably damaging Het
Fat3 A T 9: 15,908,054 (GRCm39) D2649E possibly damaging Het
Fcrl1 A G 3: 87,291,918 (GRCm39) T46A possibly damaging Het
Fig4 C T 10: 41,143,763 (GRCm39) G232D probably benign Het
Frem3 A T 8: 81,341,145 (GRCm39) H1146L probably damaging Het
Fyttd1 T A 16: 32,715,472 (GRCm39) F133L probably benign Het
Gata2 A G 6: 88,179,505 (GRCm39) N326D probably damaging Het
Gm7298 A T 6: 121,764,491 (GRCm39) T1457S probably damaging Het
Hdac1-ps A T 17: 78,799,075 (GRCm39) Y22F probably benign Het
Heatr5b C T 17: 79,141,524 (GRCm39) probably null Het
Hfm1 T A 5: 107,066,329 (GRCm39) D33V possibly damaging Het
Hmcn2 G A 2: 31,292,450 (GRCm39) A2447T possibly damaging Het
Hs3st3b1 A G 11: 63,812,331 (GRCm39) F128S probably benign Het
Hs3st6 G T 17: 24,972,226 (GRCm39) R56L possibly damaging Het
Hsd17b3 C T 13: 64,212,171 (GRCm39) M168I probably damaging Het
Ighv1-34 G T 12: 114,814,885 (GRCm39) D92E possibly damaging Het
Itgb4 A T 11: 115,885,171 (GRCm39) I1018F possibly damaging Het
Itih3 T C 14: 30,637,605 (GRCm39) D518G possibly damaging Het
Kcnma1 C T 14: 23,501,666 (GRCm39) probably null Het
Klhl11 A T 11: 100,363,506 (GRCm39) S17T probably benign Het
Lilra6 T C 7: 3,917,521 (GRCm39) E158G possibly damaging Het
Loxl1 A G 9: 58,220,037 (GRCm39) W45R probably damaging Het
Lratd1 T C 12: 14,200,190 (GRCm39) N179S probably benign Het
Lrfn1 G T 7: 28,166,255 (GRCm39) V550F probably damaging Het
Lrp1 T C 10: 127,409,368 (GRCm39) K1584E probably benign Het
Lrp4 C G 2: 91,338,914 (GRCm39) P1782A possibly damaging Het
Map3k1 A G 13: 111,885,478 (GRCm39) S1480P probably damaging Het
Mark4 G T 7: 19,160,015 (GRCm39) N748K probably benign Het
Mrpl38 G A 11: 116,025,900 (GRCm39) T142M probably damaging Het
Mrpl41 T C 2: 24,864,481 (GRCm39) T64A probably benign Het
Mrps2 G A 2: 28,359,764 (GRCm39) R207K possibly damaging Het
Myo5a A T 9: 75,099,726 (GRCm39) E96D Het
Nbas A T 12: 13,633,417 (GRCm39) E2274V probably damaging Het
Or4x13 T C 2: 90,231,338 (GRCm39) F111S probably damaging Het
Or51a8 T C 7: 102,549,652 (GRCm39) I26T probably benign Het
Or51ac3 T C 7: 103,213,850 (GRCm39) D212G probably damaging Het
Or5m10b T C 2: 85,699,278 (GRCm39) L114P possibly damaging Het
Or5m10b T A 2: 85,699,819 (GRCm39) N294K probably damaging Het
Or6c35 T A 10: 129,169,368 (GRCm39) I206N possibly damaging Het
Pcdhga12 T A 18: 37,900,288 (GRCm39) D373E probably damaging Het
Pgd A C 4: 149,235,596 (GRCm39) F395V probably damaging Het
Pi16 A G 17: 29,538,363 (GRCm39) M59V possibly damaging Het
Pik3r5 A T 11: 68,381,720 (GRCm39) T255S probably benign Het
Plch2 A T 4: 155,068,516 (GRCm39) V1370E probably benign Het
Plec A G 15: 76,067,153 (GRCm39) I1309T unknown Het
Ppp2r3d A T 9: 124,440,831 (GRCm38) S22R Het
Pramel26 A G 4: 143,542,609 (GRCm39) C4R probably damaging Het
Ptk2b C A 14: 66,413,154 (GRCm39) E342* probably null Het
Ptpn23 T C 9: 110,215,226 (GRCm39) probably null Het
Rfx8 A C 1: 39,722,850 (GRCm39) S256A probably damaging Het
Rnf115 C T 3: 96,665,337 (GRCm39) T69I probably damaging Het
Rnf213 A G 11: 119,370,457 (GRCm39) Y4753C Het
S100a10 A C 3: 93,471,590 (GRCm39) D58A possibly damaging Het
Serpina12 T C 12: 104,004,317 (GRCm39) K105R probably benign Het
Slc20a2 G A 8: 23,028,900 (GRCm39) G124S probably damaging Het
Stard9 C A 2: 120,526,635 (GRCm39) T964N probably benign Het
Stxbp5 T A 10: 9,774,938 (GRCm39) I72F probably damaging Het
Sumf2 T A 5: 129,891,482 (GRCm39) M282K possibly damaging Het
Tle7 T C 8: 110,837,580 (GRCm39) F375L probably damaging Het
Tmem135 G C 7: 88,797,186 (GRCm39) L357V probably benign Het
Tmem185b G T 1: 119,454,613 (GRCm39) V125L probably benign Het
Tmtc1 A G 6: 148,144,714 (GRCm39) M887T probably damaging Het
Tnfaip8 C T 18: 50,223,512 (GRCm39) Q83* probably null Het
Tnks A G 8: 35,306,089 (GRCm39) V1162A probably damaging Het
Tomm70a T A 16: 56,961,072 (GRCm39) Y342N possibly damaging Het
Tpo T A 12: 30,125,875 (GRCm39) D828V probably damaging Het
Ugt8a A T 3: 125,708,338 (GRCm39) N257K probably damaging Het
Unc13d AATGCCTCCCATGCC AATGCCTCCCATGCCTCCCATGCC 11: 115,958,998 (GRCm39) probably benign Het
Vim T A 2: 13,579,703 (GRCm39) M154K probably damaging Het
Virma G T 4: 11,486,045 (GRCm39) M1I probably null Het
Zfp715 A T 7: 42,950,653 (GRCm39) M100K probably benign Het
Zfp748 A T 13: 67,690,647 (GRCm39) C204* probably null Het
Zmynd8 A T 2: 165,680,772 (GRCm39) D236E probably damaging Het
Other mutations in Stab2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00091:Stab2 APN 10 86,705,070 (GRCm39) splice site probably null
IGL00809:Stab2 APN 10 86,684,038 (GRCm39) splice site probably benign
IGL00911:Stab2 APN 10 86,805,617 (GRCm39) missense probably damaging 1.00
IGL01347:Stab2 APN 10 86,737,567 (GRCm39) splice site probably null
IGL01411:Stab2 APN 10 86,815,872 (GRCm39) splice site probably benign
IGL01503:Stab2 APN 10 86,776,477 (GRCm39) splice site probably benign
IGL01599:Stab2 APN 10 86,758,759 (GRCm39) missense probably damaging 1.00
IGL01635:Stab2 APN 10 86,816,992 (GRCm39) missense probably benign 0.04
IGL01640:Stab2 APN 10 86,790,035 (GRCm39) missense probably benign 0.09
IGL01671:Stab2 APN 10 86,805,141 (GRCm39) missense possibly damaging 0.80
IGL02023:Stab2 APN 10 86,707,695 (GRCm39) missense possibly damaging 0.67
IGL02075:Stab2 APN 10 86,803,514 (GRCm39) missense possibly damaging 0.71
IGL02174:Stab2 APN 10 86,695,606 (GRCm39) splice site probably null
IGL02600:Stab2 APN 10 86,790,123 (GRCm39) missense probably damaging 1.00
IGL02666:Stab2 APN 10 86,686,766 (GRCm39) missense possibly damaging 0.67
IGL02668:Stab2 APN 10 86,682,027 (GRCm39) splice site probably benign
IGL02709:Stab2 APN 10 86,682,029 (GRCm39) splice site probably benign
IGL02728:Stab2 APN 10 86,692,420 (GRCm39) missense possibly damaging 0.95
IGL02803:Stab2 APN 10 86,786,133 (GRCm39) splice site probably benign
IGL02938:Stab2 APN 10 86,707,785 (GRCm39) missense possibly damaging 0.77
IGL03033:Stab2 APN 10 86,832,667 (GRCm39) critical splice donor site probably null
IGL03238:Stab2 APN 10 86,690,985 (GRCm39) missense probably damaging 1.00
IGL03402:Stab2 APN 10 86,805,165 (GRCm39) missense probably benign 0.03
prospector UTSW 10 86,737,431 (GRCm39) splice site probably null
songbird UTSW 10 86,694,016 (GRCm39) missense probably damaging 1.00
3-1:Stab2 UTSW 10 86,705,041 (GRCm39) missense probably damaging 0.96
F6893:Stab2 UTSW 10 86,691,035 (GRCm39) missense probably damaging 1.00
K7371:Stab2 UTSW 10 86,779,153 (GRCm39) critical splice donor site probably null
PIT4142001:Stab2 UTSW 10 86,703,039 (GRCm39) missense possibly damaging 0.94
PIT4362001:Stab2 UTSW 10 86,697,299 (GRCm39) nonsense probably null
R0015:Stab2 UTSW 10 86,679,481 (GRCm39) missense probably benign
R0254:Stab2 UTSW 10 86,733,824 (GRCm39) missense probably benign
R0310:Stab2 UTSW 10 86,803,477 (GRCm39) splice site probably benign
R0333:Stab2 UTSW 10 86,677,491 (GRCm39) missense probably benign
R0391:Stab2 UTSW 10 86,783,008 (GRCm39) missense probably benign 0.27
R0400:Stab2 UTSW 10 86,708,474 (GRCm39) missense probably damaging 1.00
R0433:Stab2 UTSW 10 86,679,355 (GRCm39) splice site probably benign
R0440:Stab2 UTSW 10 86,785,792 (GRCm39) missense probably benign 0.23
R0743:Stab2 UTSW 10 86,723,759 (GRCm39) missense probably damaging 1.00
R0847:Stab2 UTSW 10 86,805,735 (GRCm39) missense probably benign 0.00
R0883:Stab2 UTSW 10 86,760,314 (GRCm39) splice site probably benign
R1078:Stab2 UTSW 10 86,742,997 (GRCm39) splice site probably null
R1118:Stab2 UTSW 10 86,721,582 (GRCm39) splice site probably null
R1119:Stab2 UTSW 10 86,695,619 (GRCm39) missense possibly damaging 0.51
R1179:Stab2 UTSW 10 86,786,165 (GRCm39) missense probably damaging 0.98
R1440:Stab2 UTSW 10 86,697,231 (GRCm39) splice site probably null
R1550:Stab2 UTSW 10 86,714,790 (GRCm39) missense probably benign 0.01
R1616:Stab2 UTSW 10 86,721,582 (GRCm39) splice site probably null
R1728:Stab2 UTSW 10 86,773,903 (GRCm39) missense probably benign 0.41
R1768:Stab2 UTSW 10 86,838,872 (GRCm39) missense probably damaging 1.00
R1772:Stab2 UTSW 10 86,790,098 (GRCm39) missense probably benign 0.06
R1776:Stab2 UTSW 10 86,793,680 (GRCm39) missense possibly damaging 0.92
R1784:Stab2 UTSW 10 86,773,903 (GRCm39) missense probably benign 0.41
R1892:Stab2 UTSW 10 86,773,913 (GRCm39) missense probably damaging 0.99
R1957:Stab2 UTSW 10 86,697,334 (GRCm39) missense probably benign 0.13
R1972:Stab2 UTSW 10 86,796,180 (GRCm39) missense probably damaging 0.99
R1975:Stab2 UTSW 10 86,732,360 (GRCm39) critical splice donor site probably null
R1976:Stab2 UTSW 10 86,732,360 (GRCm39) critical splice donor site probably null
R1996:Stab2 UTSW 10 86,838,895 (GRCm39) missense probably damaging 1.00
R2085:Stab2 UTSW 10 86,790,023 (GRCm39) missense probably damaging 1.00
R2149:Stab2 UTSW 10 86,700,904 (GRCm39) nonsense probably null
R2169:Stab2 UTSW 10 86,723,726 (GRCm39) missense probably damaging 1.00
R2201:Stab2 UTSW 10 86,776,503 (GRCm39) missense probably benign 0.22
R2296:Stab2 UTSW 10 86,790,338 (GRCm39) critical splice acceptor site probably null
R2297:Stab2 UTSW 10 86,790,338 (GRCm39) critical splice acceptor site probably null
R2298:Stab2 UTSW 10 86,790,338 (GRCm39) critical splice acceptor site probably null
R2326:Stab2 UTSW 10 86,790,338 (GRCm39) critical splice acceptor site probably null
R2434:Stab2 UTSW 10 86,805,183 (GRCm39) missense possibly damaging 0.78
R2519:Stab2 UTSW 10 86,770,704 (GRCm39) splice site probably benign
R2696:Stab2 UTSW 10 86,697,363 (GRCm39) missense probably benign 0.45
R2883:Stab2 UTSW 10 86,803,550 (GRCm39) missense possibly damaging 0.92
R2923:Stab2 UTSW 10 86,697,325 (GRCm39) missense probably damaging 1.00
R3711:Stab2 UTSW 10 86,702,572 (GRCm39) missense probably damaging 1.00
R3787:Stab2 UTSW 10 86,805,141 (GRCm39) missense possibly damaging 0.50
R3834:Stab2 UTSW 10 86,785,776 (GRCm39) missense possibly damaging 0.87
R3970:Stab2 UTSW 10 86,714,750 (GRCm39) missense probably damaging 0.97
R3979:Stab2 UTSW 10 86,699,320 (GRCm39) missense possibly damaging 0.56
R4003:Stab2 UTSW 10 86,693,988 (GRCm39) missense probably damaging 1.00
R4088:Stab2 UTSW 10 86,758,049 (GRCm39) missense probably damaging 1.00
R4151:Stab2 UTSW 10 86,838,847 (GRCm39) missense probably benign 0.12
R4190:Stab2 UTSW 10 86,714,808 (GRCm39) missense probably damaging 0.98
R4556:Stab2 UTSW 10 86,803,543 (GRCm39) missense possibly damaging 0.95
R4773:Stab2 UTSW 10 86,743,235 (GRCm39) nonsense probably null
R4825:Stab2 UTSW 10 86,783,011 (GRCm39) missense probably benign 0.08
R4865:Stab2 UTSW 10 86,679,364 (GRCm39) splice site probably null
R4871:Stab2 UTSW 10 86,778,099 (GRCm39) missense probably damaging 0.99
R4943:Stab2 UTSW 10 86,790,026 (GRCm39) missense probably damaging 0.99
R4981:Stab2 UTSW 10 86,796,087 (GRCm39) missense probably benign
R4994:Stab2 UTSW 10 86,785,771 (GRCm39) missense probably benign
R4999:Stab2 UTSW 10 86,773,773 (GRCm39) missense probably damaging 0.97
R5061:Stab2 UTSW 10 86,743,249 (GRCm39) missense probably damaging 1.00
R5072:Stab2 UTSW 10 86,699,422 (GRCm39) missense probably benign 0.23
R5073:Stab2 UTSW 10 86,699,422 (GRCm39) missense probably benign 0.23
R5074:Stab2 UTSW 10 86,699,422 (GRCm39) missense probably benign 0.23
R5134:Stab2 UTSW 10 86,707,674 (GRCm39) splice site probably null
R5213:Stab2 UTSW 10 86,743,061 (GRCm39) missense probably damaging 0.99
R5508:Stab2 UTSW 10 86,796,143 (GRCm39) missense probably benign 0.01
R5530:Stab2 UTSW 10 86,783,026 (GRCm39) missense probably benign 0.04
R5540:Stab2 UTSW 10 86,683,989 (GRCm39) missense probably benign 0.30
R5839:Stab2 UTSW 10 86,708,555 (GRCm39) missense probably damaging 0.97
R5949:Stab2 UTSW 10 86,805,713 (GRCm39) missense possibly damaging 0.87
R6015:Stab2 UTSW 10 86,773,906 (GRCm39) missense probably damaging 0.99
R6019:Stab2 UTSW 10 86,838,886 (GRCm39) missense probably benign 0.00
R6116:Stab2 UTSW 10 86,743,054 (GRCm39) missense probably damaging 1.00
R6131:Stab2 UTSW 10 86,719,642 (GRCm39) splice site probably null
R6209:Stab2 UTSW 10 86,758,867 (GRCm39) missense possibly damaging 0.94
R6243:Stab2 UTSW 10 86,743,025 (GRCm39) missense probably damaging 1.00
R6433:Stab2 UTSW 10 86,737,431 (GRCm39) splice site probably null
R6787:Stab2 UTSW 10 86,754,948 (GRCm39) missense probably benign 0.07
R6841:Stab2 UTSW 10 86,778,054 (GRCm39) missense probably damaging 1.00
R6873:Stab2 UTSW 10 86,697,230 (GRCm39) critical splice donor site probably null
R7025:Stab2 UTSW 10 86,686,701 (GRCm39) missense probably damaging 1.00
R7043:Stab2 UTSW 10 86,706,110 (GRCm39) missense probably damaging 0.99
R7047:Stab2 UTSW 10 86,694,016 (GRCm39) missense probably damaging 1.00
R7107:Stab2 UTSW 10 86,741,456 (GRCm39) missense possibly damaging 0.96
R7214:Stab2 UTSW 10 86,735,705 (GRCm39) missense probably damaging 0.99
R7271:Stab2 UTSW 10 86,838,972 (GRCm39) splice site probably null
R7291:Stab2 UTSW 10 86,782,084 (GRCm39) missense probably damaging 0.96
R7336:Stab2 UTSW 10 86,805,049 (GRCm39) nonsense probably null
R7432:Stab2 UTSW 10 86,721,547 (GRCm39) missense probably damaging 0.99
R7580:Stab2 UTSW 10 86,705,028 (GRCm39) missense probably benign 0.00
R7622:Stab2 UTSW 10 86,709,766 (GRCm39) missense possibly damaging 0.65
R7629:Stab2 UTSW 10 86,719,646 (GRCm39) critical splice donor site probably null
R7658:Stab2 UTSW 10 86,816,999 (GRCm39) missense probably benign 0.12
R7798:Stab2 UTSW 10 86,793,776 (GRCm39) missense probably damaging 0.98
R7835:Stab2 UTSW 10 86,708,483 (GRCm39) missense probably benign 0.06
R7845:Stab2 UTSW 10 86,832,758 (GRCm39) missense probably benign 0.09
R7863:Stab2 UTSW 10 86,808,745 (GRCm39) missense probably benign 0.30
R7885:Stab2 UTSW 10 86,714,776 (GRCm39) missense probably benign 0.03
R7904:Stab2 UTSW 10 86,790,056 (GRCm39) nonsense probably null
R7947:Stab2 UTSW 10 86,681,897 (GRCm39) missense probably benign 0.31
R7963:Stab2 UTSW 10 86,683,887 (GRCm39) critical splice donor site probably null
R8014:Stab2 UTSW 10 86,686,767 (GRCm39) missense possibly damaging 0.78
R8021:Stab2 UTSW 10 86,741,403 (GRCm39) missense possibly damaging 0.69
R8024:Stab2 UTSW 10 86,681,916 (GRCm39) missense probably benign 0.34
R8097:Stab2 UTSW 10 86,704,959 (GRCm39) missense possibly damaging 0.86
R8281:Stab2 UTSW 10 86,709,728 (GRCm39) missense probably damaging 0.98
R8462:Stab2 UTSW 10 86,803,598 (GRCm39) missense possibly damaging 0.79
R8670:Stab2 UTSW 10 86,776,587 (GRCm39) missense probably damaging 1.00
R8692:Stab2 UTSW 10 86,808,794 (GRCm39) missense probably damaging 0.99
R8744:Stab2 UTSW 10 86,805,213 (GRCm39) missense probably benign 0.32
R8745:Stab2 UTSW 10 86,805,213 (GRCm39) missense probably benign 0.32
R8782:Stab2 UTSW 10 86,735,685 (GRCm39) missense probably benign 0.00
R8875:Stab2 UTSW 10 86,832,728 (GRCm39) missense probably damaging 1.00
R8978:Stab2 UTSW 10 86,785,782 (GRCm39) missense possibly damaging 0.64
R9141:Stab2 UTSW 10 86,704,911 (GRCm39) missense probably damaging 1.00
R9248:Stab2 UTSW 10 86,727,481 (GRCm39) missense probably damaging 0.98
R9326:Stab2 UTSW 10 86,791,010 (GRCm39) missense probably damaging 1.00
R9426:Stab2 UTSW 10 86,704,911 (GRCm39) missense probably damaging 1.00
R9568:Stab2 UTSW 10 86,699,420 (GRCm39) missense probably damaging 1.00
R9627:Stab2 UTSW 10 86,793,704 (GRCm39) missense probably damaging 0.98
R9635:Stab2 UTSW 10 86,686,651 (GRCm39) nonsense probably null
R9648:Stab2 UTSW 10 86,692,561 (GRCm39) frame shift probably null
R9650:Stab2 UTSW 10 86,692,561 (GRCm39) frame shift probably null
R9726:Stab2 UTSW 10 86,790,095 (GRCm39) missense probably benign 0.00
R9756:Stab2 UTSW 10 86,803,553 (GRCm39) missense possibly damaging 0.50
R9786:Stab2 UTSW 10 86,757,997 (GRCm39) missense probably benign 0.03
RF061:Stab2 UTSW 10 86,702,622 (GRCm39) critical splice acceptor site probably benign
X0023:Stab2 UTSW 10 86,758,062 (GRCm39) critical splice acceptor site probably null
X0025:Stab2 UTSW 10 86,723,680 (GRCm39) missense probably damaging 1.00
Z1176:Stab2 UTSW 10 86,785,778 (GRCm39) missense probably damaging 0.99
Z1177:Stab2 UTSW 10 86,732,460 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GAGGACACTAGGCCTAACATG -3'
(R):5'- TACAAGCTAGTAGAGAGCCAAC -3'

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