Incidental Mutation 'R0326:Tnxb'
ID 25924
Institutional Source Beutler Lab
Gene Symbol Tnxb
Ensembl Gene ENSMUSG00000033327
Gene Name tenascin XB
Synonyms Tnx, TN-MHC
MMRRC Submission 038536-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R0326 (G1)
Quality Score 225
Status Not validated
Chromosome 17
Chromosomal Location 34879431-34938789 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 34917153 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Glycine at position 2183 (S2183G)
Ref Sequence ENSEMBL: ENSMUSP00000084661 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000087399] [ENSMUST00000168533]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000087399
AA Change: S2183G

PolyPhen 2 Score 0.317 (Sensitivity: 0.90; Specificity: 0.89)
SMART Domains Protein: ENSMUSP00000084661
Gene: ENSMUSG00000033327
AA Change: S2183G

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
low complexity region 33 44 N/A INTRINSIC
low complexity region 69 89 N/A INTRINSIC
low complexity region 92 103 N/A INTRINSIC
EGF 173 201 1.59e1 SMART
EGF 204 232 7.41e0 SMART
EGF 235 263 2.64e1 SMART
EGF 266 294 2.64e1 SMART
EGF 297 325 9.13e0 SMART
EGF 328 356 2.07e1 SMART
EGF_like 359 387 3.16e1 SMART
EGF_like 390 418 4.64e1 SMART
EGF_like 421 449 3.29e1 SMART
EGF_like 452 480 7.09e1 SMART
EGF 483 511 1.15e1 SMART
EGF 514 542 1.91e1 SMART
EGF_like 545 573 4.11e1 SMART
EGF 576 604 7.95e0 SMART
EGF 607 635 1.23e1 SMART
EGF_like 638 666 4.93e1 SMART
EGF_like 674 702 5.24e1 SMART
EGF 705 733 2.29e1 SMART
FN3 736 816 4.12e-3 SMART
FN3 827 904 1.21e-9 SMART
FN3 1047 1126 3.97e-5 SMART
FN3 1142 1223 3.62e-8 SMART
low complexity region 1230 1241 N/A INTRINSIC
FN3 1242 1320 2.31e-6 SMART
FN3 1351 1431 8.77e-7 SMART
FN3 1460 1539 3.01e-5 SMART
FN3 1556 1636 2.76e-4 SMART
FN3 1657 1736 5.78e-7 SMART
FN3 1752 1832 4.7e-7 SMART
FN3 1851 1929 1.95e-4 SMART
FN3 1955 2034 4.56e-5 SMART
FN3 2066 2145 2.23e-8 SMART
FN3 2164 2244 7.75e-8 SMART
FN3 2279 2358 8.5e-5 SMART
FN3 2387 2467 2.94e-8 SMART
FN3 2501 2580 1.7e-4 SMART
low complexity region 2588 2598 N/A INTRINSIC
FN3 2607 2687 6.75e-8 SMART
FN3 2716 2795 7.4e-5 SMART
FN3 2822 2902 1.35e-7 SMART
FN3 2931 3010 5.61e-5 SMART
FN3 3026 3106 6.01e-5 SMART
FN3 3120 3199 6.45e-5 SMART
FN3 3214 3293 9.54e-8 SMART
FN3 3316 3396 2.81e-5 SMART
FN3 3416 3502 1.98e-5 SMART
FN3 3518 3596 5.65e-10 SMART
FN3 3607 3682 7.63e-7 SMART
FN3 3695 3770 6.54e-6 SMART
FBG 3787 3997 8.88e-125 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000168533
SMART Domains Protein: ENSMUSP00000127487
Gene: ENSMUSG00000033327

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
low complexity region 33 44 N/A INTRINSIC
low complexity region 69 89 N/A INTRINSIC
low complexity region 92 103 N/A INTRINSIC
EGF 173 201 1.59e1 SMART
EGF 204 232 7.41e0 SMART
EGF 235 263 2.64e1 SMART
EGF 266 294 2.64e1 SMART
EGF 297 325 9.13e0 SMART
EGF 328 356 2.07e1 SMART
EGF_like 359 387 3.16e1 SMART
EGF_like 390 418 4.64e1 SMART
EGF_like 421 449 3.29e1 SMART
EGF_like 452 480 7.09e1 SMART
EGF 483 511 1.15e1 SMART
EGF 514 542 1.91e1 SMART
EGF_like 545 573 4.11e1 SMART
EGF 576 604 7.95e0 SMART
EGF 607 635 1.23e1 SMART
EGF_like 638 666 4.93e1 SMART
EGF_like 674 702 5.24e1 SMART
EGF 705 733 2.29e1 SMART
FN3 736 816 4.12e-3 SMART
FN3 827 904 1.21e-9 SMART
FN3 924 1003 3.97e-5 SMART
FN3 1019 1100 3.62e-8 SMART
low complexity region 1107 1118 N/A INTRINSIC
FN3 1119 1197 2.31e-6 SMART
FN3 1228 1308 8.77e-7 SMART
FN3 1337 1416 3.01e-5 SMART
FN3 1433 1513 2.76e-4 SMART
FN3 1534 1613 5.78e-7 SMART
FN3 1629 1709 4.7e-7 SMART
FN3 1728 1806 1.95e-4 SMART
FN3 1832 1911 4.56e-5 SMART
FN3 1943 2022 2.23e-8 SMART
FN3 2051 2130 5.61e-5 SMART
FN3 2146 2226 6.01e-5 SMART
FN3 2240 2319 6.45e-5 SMART
FN3 2334 2413 9.54e-8 SMART
FN3 2436 2516 2.81e-5 SMART
FN3 2536 2622 1.98e-5 SMART
FN3 2638 2716 5.65e-10 SMART
FN3 2727 2802 7.63e-7 SMART
FN3 2815 2890 6.54e-6 SMART
FBG 2907 3117 8.88e-125 SMART
Coding Region Coverage
  • 1x: 99.0%
  • 3x: 98.0%
  • 10x: 95.8%
  • 20x: 91.8%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the tenascin family of extracellular matrix glycoproteins. The tenascins have anti-adhesive effects, as opposed to fibronectin which is adhesive. This protein is thought to function in matrix maturation during wound healing, and its deficiency has been associated with the connective tissue disorder Ehlers-Danlos syndrome. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. It is one of four genes in this cluster which have been duplicated. The duplicated copy of this gene is incomplete and is a pseudogene which is transcribed but does not encode a protein. The structure of this gene is unusual in that it overlaps the CREBL1 and CYP21A2 genes at its 5' and 3' ends, respectively. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygous null mice have stretchy skin, similar to patients with human Ehlers-Danlos syndrome. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 99 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
AA986860 C T 1: 130,670,635 (GRCm39) P286S possibly damaging Het
Aagab T A 9: 63,526,444 (GRCm39) S156T probably damaging Het
Abca14 T G 7: 119,823,642 (GRCm39) Y390D probably damaging Het
Abcc2 T A 19: 43,814,386 (GRCm39) I1122N possibly damaging Het
Adamts16 T C 13: 70,927,730 (GRCm39) E503G possibly damaging Het
Adamts9 A T 6: 92,835,038 (GRCm39) C697* probably null Het
Adgrv1 T C 13: 81,623,112 (GRCm39) D3837G possibly damaging Het
Ahcyl T A 16: 45,974,246 (GRCm39) D377V probably benign Het
Aire T A 10: 77,878,433 (GRCm39) R128S probably damaging Het
Alkbh2 A C 5: 114,262,011 (GRCm39) *240E probably null Het
Als2 T C 1: 59,219,742 (GRCm39) Y1191C probably damaging Het
Anapc5 A T 5: 122,952,667 (GRCm39) V186E probably benign Het
Apob C T 12: 8,040,307 (GRCm39) A548V probably damaging Het
B3galt4 A T 17: 34,169,722 (GRCm39) V172E probably damaging Het
Bbs7 A C 3: 36,646,525 (GRCm39) C432G possibly damaging Het
Cacna2d3 T A 14: 28,767,601 (GRCm39) E758V probably damaging Het
Cactin T G 10: 81,158,496 (GRCm39) L154R probably benign Het
Ccdc88a A C 11: 29,411,021 (GRCm39) R502S probably benign Het
Ccnf A T 17: 24,450,784 (GRCm39) I398N possibly damaging Het
Chd1 A T 17: 15,988,828 (GRCm39) D1527V probably damaging Het
Chd1 A T 17: 15,988,830 (GRCm39) M1528L probably benign Het
Chrac1 G A 15: 72,964,675 (GRCm39) probably null Het
Cln3 T G 7: 126,182,217 (GRCm39) M1L probably damaging Het
Cnot6 T C 11: 49,568,263 (GRCm39) Y442C probably damaging Het
Col19a1 A T 1: 24,324,132 (GRCm39) probably null Het
Col1a2 T C 6: 4,537,838 (GRCm39) F1116L unknown Het
Col1a2 G A 6: 4,518,822 (GRCm39) probably benign Het
Cops4 T G 5: 100,676,408 (GRCm39) V53G probably damaging Het
Crnkl1 A G 2: 145,761,875 (GRCm39) S561P probably benign Het
Ctnnb1 C A 9: 120,780,778 (GRCm39) Q99K probably benign Het
Cxcr5 T C 9: 44,424,578 (GRCm39) S360G probably benign Het
Dab2 G A 15: 6,447,797 (GRCm39) V60M probably damaging Het
Ddx3y A T Y: 1,263,321 (GRCm39) Y648* probably null Het
Dennd2a T A 6: 39,474,044 (GRCm39) D430V probably damaging Het
Dsp G T 13: 38,376,846 (GRCm39) E1544* probably null Het
Efcab7 A T 4: 99,719,631 (GRCm39) M38L possibly damaging Het
Fto A G 8: 92,136,155 (GRCm39) N141S probably damaging Het
Gabrp A G 11: 33,504,362 (GRCm39) F318L probably damaging Het
Gmeb1 A C 4: 131,969,663 (GRCm39) C103W probably damaging Het
Heatr9 T C 11: 83,405,365 (GRCm39) D365G probably damaging Het
Hif3a G A 7: 16,778,325 (GRCm39) R436W probably benign Het
Hint2 A G 4: 43,654,378 (GRCm39) V145A probably damaging Het
Hmcn2 T A 2: 31,313,237 (GRCm39) L3482* probably null Het
Hsd3b1 A T 3: 98,760,590 (GRCm39) Y134N probably damaging Het
Impg2 T A 16: 56,080,848 (GRCm39) V775E probably damaging Het
Ipo5 A G 14: 121,159,635 (GRCm39) I154M probably benign Het
Itgad T A 7: 127,797,550 (GRCm39) F893Y probably benign Het
Itprid1 A T 6: 55,875,228 (GRCm39) M393L possibly damaging Het
Kdm4a T C 4: 118,018,903 (GRCm39) R438G probably benign Het
Klk1b11 T A 7: 43,425,943 (GRCm39) M1K probably null Het
Lama5 A T 2: 179,824,219 (GRCm39) V2602D possibly damaging Het
Lrch3 T C 16: 32,799,870 (GRCm39) S35P probably damaging Het
Mfn2 A G 4: 147,967,745 (GRCm39) L441P probably damaging Het
Mgat4c A T 10: 102,224,565 (GRCm39) I260F probably damaging Het
Mon1b T A 8: 114,364,375 (GRCm39) S51T probably benign Het
Myh11 T C 16: 14,036,744 (GRCm39) D993G probably benign Het
Myo1a A G 10: 127,552,166 (GRCm39) N762D probably benign Het
Nacc2 A T 2: 25,950,345 (GRCm39) Y464N probably damaging Het
Nckap1 A G 2: 80,383,714 (GRCm39) I150T probably benign Het
Ndufv2 G T 17: 66,387,816 (GRCm39) P119T probably damaging Het
Noc4l G A 5: 110,800,241 (GRCm39) R95* probably null Het
Ntng1 A T 3: 110,042,819 (GRCm39) Y2* probably null Het
Oog4 T C 4: 143,165,773 (GRCm39) N53D probably benign Het
Or10ak11 A T 4: 118,687,022 (GRCm39) V205D possibly damaging Het
Or4d11 C T 19: 12,013,525 (GRCm39) V194I probably benign Het
Or6c6c A G 10: 129,541,638 (GRCm39) E297G possibly damaging Het
Or9i1b C T 19: 13,896,873 (GRCm39) T163I probably benign Het
Phkg2 T G 7: 127,173,075 (GRCm39) L11R probably damaging Het
Pogz A G 3: 94,777,424 (GRCm39) D368G probably damaging Het
Prex2 T A 1: 11,355,289 (GRCm39) L1530Q probably damaging Het
Prmt1 C T 7: 44,628,878 (GRCm39) E144K probably damaging Het
Prss8 T A 7: 127,526,348 (GRCm39) I121F probably benign Het
Psmd13 T C 7: 140,477,624 (GRCm39) L314P probably damaging Het
Ptch2 G A 4: 116,966,081 (GRCm39) G467D probably damaging Het
Rbm20 C A 19: 53,852,596 (GRCm39) P1192Q probably damaging Het
Rpl19 T A 11: 97,919,200 (GRCm39) D45E probably benign Het
Rsph10b C T 5: 143,903,946 (GRCm39) A219V probably damaging Het
Rtraf C T 14: 19,864,600 (GRCm39) probably null Het
Scaf1 T A 7: 44,658,175 (GRCm39) T235S probably damaging Het
Shank1 T A 7: 43,968,594 (GRCm39) C296S unknown Het
Slc39a7 A T 17: 34,247,924 (GRCm39) V426D probably damaging Het
Slc41a2 A T 10: 83,119,610 (GRCm39) V384D probably damaging Het
Slco1c1 T C 6: 141,505,499 (GRCm39) L475P probably benign Het
Slco6d1 A C 1: 98,418,359 (GRCm39) K515T probably benign Het
Sos2 T C 12: 69,682,459 (GRCm39) E253G probably damaging Het
Sp6 G T 11: 96,912,361 (GRCm39) D25Y possibly damaging Het
Syt11 A C 3: 88,669,855 (GRCm39) D12E possibly damaging Het
Taf2 A G 15: 54,910,856 (GRCm39) L606P probably damaging Het
Tbc1d5 A G 17: 51,273,764 (GRCm39) Y116H probably damaging Het
Tnfrsf8 A G 4: 145,015,029 (GRCm39) I243T possibly damaging Het
Trim66 T C 7: 109,059,379 (GRCm39) Y853C probably benign Het
Ttn T A 2: 76,567,839 (GRCm39) T27685S probably damaging Het
Ttn T C 2: 76,573,466 (GRCm39) E25809G probably damaging Het
Uvssa G A 5: 33,566,191 (GRCm39) G445S probably benign Het
Zfp326 T C 5: 106,058,141 (GRCm39) S427P probably damaging Het
Zfp592 A G 7: 80,674,637 (GRCm39) T534A possibly damaging Het
Zfp672 A G 11: 58,207,173 (GRCm39) S383P possibly damaging Het
Zfp799 A G 17: 33,039,700 (GRCm39) S188P possibly damaging Het
Zyg11b A C 4: 108,129,450 (GRCm39) V54G possibly damaging Het
Other mutations in Tnxb
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00094:Tnxb APN 17 34,904,603 (GRCm39) missense probably damaging 1.00
IGL00424:Tnxb APN 17 34,933,666 (GRCm39) missense probably damaging 1.00
IGL00486:Tnxb APN 17 34,911,356 (GRCm39) missense probably damaging 1.00
IGL00952:Tnxb APN 17 34,932,102 (GRCm39) missense probably damaging 1.00
IGL00974:Tnxb APN 17 34,937,707 (GRCm39) critical splice donor site probably null
IGL01017:Tnxb APN 17 34,912,782 (GRCm39) missense probably damaging 0.98
IGL01082:Tnxb APN 17 34,933,584 (GRCm39) missense probably damaging 0.97
IGL01397:Tnxb APN 17 34,933,647 (GRCm39) missense probably damaging 0.99
IGL01473:Tnxb APN 17 34,904,675 (GRCm39) missense probably damaging 0.99
IGL01642:Tnxb APN 17 34,937,488 (GRCm39) missense probably damaging 1.00
IGL01774:Tnxb APN 17 34,907,813 (GRCm39) missense probably damaging 1.00
IGL01971:Tnxb APN 17 34,891,271 (GRCm39) missense probably damaging 1.00
IGL02016:Tnxb APN 17 34,891,249 (GRCm39) missense probably damaging 0.98
IGL02160:Tnxb APN 17 34,933,719 (GRCm39) missense probably benign 0.01
IGL02473:Tnxb APN 17 34,936,736 (GRCm39) missense probably damaging 1.00
IGL02666:Tnxb APN 17 34,903,913 (GRCm39) missense probably benign 0.20
IGL02831:Tnxb APN 17 34,922,545 (GRCm39) missense possibly damaging 0.93
IGL02838:Tnxb APN 17 34,908,606 (GRCm39) missense possibly damaging 0.74
IGL02965:Tnxb APN 17 34,928,628 (GRCm39) missense possibly damaging 0.93
IGL03155:Tnxb APN 17 34,932,569 (GRCm39) missense probably damaging 1.00
IGL03194:Tnxb APN 17 34,914,921 (GRCm39) nonsense probably null
IGL03215:Tnxb APN 17 34,911,499 (GRCm39) missense possibly damaging 0.66
IGL03256:Tnxb APN 17 34,907,694 (GRCm39) missense probably damaging 1.00
BB008:Tnxb UTSW 17 34,907,672 (GRCm39) missense probably damaging 1.00
BB018:Tnxb UTSW 17 34,907,672 (GRCm39) missense probably damaging 1.00
E0370:Tnxb UTSW 17 34,897,917 (GRCm39) missense probably damaging 1.00
R0006:Tnxb UTSW 17 34,901,266 (GRCm39) missense probably benign 0.07
R0049:Tnxb UTSW 17 34,928,542 (GRCm39) missense possibly damaging 0.93
R0050:Tnxb UTSW 17 34,892,299 (GRCm39) missense probably damaging 1.00
R0233:Tnxb UTSW 17 34,918,007 (GRCm39) missense probably benign 0.32
R0233:Tnxb UTSW 17 34,918,007 (GRCm39) missense probably benign 0.32
R0311:Tnxb UTSW 17 34,935,958 (GRCm39) missense probably damaging 0.97
R0387:Tnxb UTSW 17 34,902,548 (GRCm39) missense probably benign 0.30
R0396:Tnxb UTSW 17 34,890,707 (GRCm39) missense probably damaging 1.00
R0511:Tnxb UTSW 17 34,937,219 (GRCm39) missense probably damaging 0.96
R0540:Tnxb UTSW 17 34,890,892 (GRCm39) missense probably damaging 1.00
R0563:Tnxb UTSW 17 34,935,921 (GRCm39) missense probably benign 0.05
R0575:Tnxb UTSW 17 34,936,180 (GRCm39) missense possibly damaging 0.91
R0586:Tnxb UTSW 17 34,891,118 (GRCm39) missense probably damaging 1.00
R0607:Tnxb UTSW 17 34,890,892 (GRCm39) missense probably damaging 1.00
R0622:Tnxb UTSW 17 34,937,703 (GRCm39) missense probably damaging 1.00
R0624:Tnxb UTSW 17 34,902,522 (GRCm39) missense probably damaging 1.00
R0709:Tnxb UTSW 17 34,908,328 (GRCm39) missense probably damaging 1.00
R0898:Tnxb UTSW 17 34,889,719 (GRCm39) missense probably damaging 1.00
R0970:Tnxb UTSW 17 34,917,917 (GRCm39) missense possibly damaging 0.85
R0972:Tnxb UTSW 17 34,904,117 (GRCm39) missense probably damaging 1.00
R1118:Tnxb UTSW 17 34,904,017 (GRCm39) missense probably damaging 1.00
R1119:Tnxb UTSW 17 34,904,017 (GRCm39) missense probably damaging 1.00
R1226:Tnxb UTSW 17 34,907,903 (GRCm39) missense probably damaging 1.00
R1296:Tnxb UTSW 17 34,890,551 (GRCm39) missense probably damaging 1.00
R1297:Tnxb UTSW 17 34,929,140 (GRCm39) missense probably damaging 0.96
R1349:Tnxb UTSW 17 34,929,267 (GRCm39) missense possibly damaging 0.67
R1356:Tnxb UTSW 17 34,914,446 (GRCm39) missense possibly damaging 0.53
R1372:Tnxb UTSW 17 34,929,267 (GRCm39) missense possibly damaging 0.67
R1521:Tnxb UTSW 17 34,930,477 (GRCm39) missense probably damaging 1.00
R1522:Tnxb UTSW 17 34,937,612 (GRCm39) missense probably damaging 1.00
R1532:Tnxb UTSW 17 34,929,804 (GRCm39) missense probably damaging 1.00
R1735:Tnxb UTSW 17 34,936,944 (GRCm39) missense probably damaging 1.00
R1778:Tnxb UTSW 17 34,902,548 (GRCm39) missense probably benign 0.30
R1802:Tnxb UTSW 17 34,922,863 (GRCm39) missense probably damaging 0.98
R1824:Tnxb UTSW 17 34,911,307 (GRCm39) nonsense probably null
R1838:Tnxb UTSW 17 34,897,884 (GRCm39) missense probably damaging 0.96
R1863:Tnxb UTSW 17 34,889,848 (GRCm39) missense probably damaging 1.00
R1865:Tnxb UTSW 17 34,922,431 (GRCm39) nonsense probably null
R1867:Tnxb UTSW 17 34,890,821 (GRCm39) missense probably damaging 1.00
R1883:Tnxb UTSW 17 34,908,539 (GRCm39) missense probably benign 0.01
R1884:Tnxb UTSW 17 34,908,539 (GRCm39) missense probably benign 0.01
R1889:Tnxb UTSW 17 34,914,799 (GRCm39) missense probably damaging 0.97
R1969:Tnxb UTSW 17 34,898,055 (GRCm39) missense probably benign 0.20
R1989:Tnxb UTSW 17 34,912,859 (GRCm39) missense probably damaging 1.00
R1989:Tnxb UTSW 17 34,902,351 (GRCm39) missense probably benign 0.08
R1991:Tnxb UTSW 17 34,901,225 (GRCm39) missense probably damaging 1.00
R1991:Tnxb UTSW 17 34,890,878 (GRCm39) missense probably damaging 1.00
R1992:Tnxb UTSW 17 34,890,878 (GRCm39) missense probably damaging 1.00
R2001:Tnxb UTSW 17 34,911,553 (GRCm39) missense possibly damaging 0.82
R2018:Tnxb UTSW 17 34,890,724 (GRCm39) missense probably benign 0.04
R2030:Tnxb UTSW 17 34,937,443 (GRCm39) missense probably damaging 1.00
R2037:Tnxb UTSW 17 34,918,179 (GRCm39) missense probably damaging 1.00
R2103:Tnxb UTSW 17 34,901,225 (GRCm39) missense probably damaging 1.00
R2116:Tnxb UTSW 17 34,891,201 (GRCm39) missense probably damaging 1.00
R2206:Tnxb UTSW 17 34,928,391 (GRCm39) missense possibly damaging 0.86
R2207:Tnxb UTSW 17 34,928,391 (GRCm39) missense possibly damaging 0.86
R2215:Tnxb UTSW 17 34,923,114 (GRCm39) missense possibly damaging 0.93
R2413:Tnxb UTSW 17 34,937,252 (GRCm39) missense probably damaging 0.99
R2680:Tnxb UTSW 17 34,922,594 (GRCm39) missense possibly damaging 0.51
R2910:Tnxb UTSW 17 34,891,424 (GRCm39) missense probably damaging 1.00
R2984:Tnxb UTSW 17 34,897,636 (GRCm39) nonsense probably null
R3120:Tnxb UTSW 17 34,911,329 (GRCm39) missense possibly damaging 0.86
R3429:Tnxb UTSW 17 34,922,561 (GRCm39) missense probably damaging 0.98
R3429:Tnxb UTSW 17 34,891,605 (GRCm39) nonsense probably null
R3552:Tnxb UTSW 17 34,937,695 (GRCm39) missense probably damaging 1.00
R3698:Tnxb UTSW 17 34,909,407 (GRCm39) critical splice donor site probably null
R3720:Tnxb UTSW 17 34,931,938 (GRCm39) missense possibly damaging 0.95
R3841:Tnxb UTSW 17 34,917,897 (GRCm39) missense possibly damaging 0.72
R3848:Tnxb UTSW 17 34,909,369 (GRCm39) missense possibly damaging 0.82
R3886:Tnxb UTSW 17 34,937,885 (GRCm39) missense probably damaging 1.00
R4074:Tnxb UTSW 17 34,890,845 (GRCm39) missense probably benign 0.22
R4159:Tnxb UTSW 17 34,930,491 (GRCm39) missense probably damaging 0.99
R4160:Tnxb UTSW 17 34,930,491 (GRCm39) missense probably damaging 0.99
R4161:Tnxb UTSW 17 34,930,491 (GRCm39) missense probably damaging 0.99
R4181:Tnxb UTSW 17 34,928,428 (GRCm39) missense possibly damaging 0.93
R4210:Tnxb UTSW 17 34,929,951 (GRCm39) missense possibly damaging 0.84
R4275:Tnxb UTSW 17 34,917,205 (GRCm39) missense probably damaging 0.98
R4329:Tnxb UTSW 17 34,912,838 (GRCm39) missense probably damaging 1.00
R4394:Tnxb UTSW 17 34,897,636 (GRCm39) nonsense probably null
R4395:Tnxb UTSW 17 34,897,636 (GRCm39) nonsense probably null
R4397:Tnxb UTSW 17 34,897,636 (GRCm39) nonsense probably null
R4540:Tnxb UTSW 17 34,922,309 (GRCm39) missense possibly damaging 0.86
R4673:Tnxb UTSW 17 34,891,514 (GRCm39) missense probably damaging 0.99
R4719:Tnxb UTSW 17 34,908,394 (GRCm39) missense probably damaging 1.00
R4725:Tnxb UTSW 17 34,918,041 (GRCm39) missense probably damaging 0.99
R4753:Tnxb UTSW 17 34,914,909 (GRCm39) missense possibly damaging 0.71
R4777:Tnxb UTSW 17 34,890,917 (GRCm39) missense probably damaging 1.00
R4837:Tnxb UTSW 17 34,936,981 (GRCm39) missense probably damaging 0.98
R4898:Tnxb UTSW 17 34,914,566 (GRCm39) missense possibly damaging 0.95
R4938:Tnxb UTSW 17 34,932,606 (GRCm39) missense probably damaging 1.00
R5044:Tnxb UTSW 17 34,936,457 (GRCm39) missense probably damaging 1.00
R5100:Tnxb UTSW 17 34,929,902 (GRCm39) missense probably damaging 0.99
R5223:Tnxb UTSW 17 34,923,052 (GRCm39) missense possibly damaging 0.51
R5269:Tnxb UTSW 17 34,922,582 (GRCm39) missense possibly damaging 0.95
R5333:Tnxb UTSW 17 34,909,205 (GRCm39) missense probably damaging 1.00
R5454:Tnxb UTSW 17 34,928,599 (GRCm39) missense possibly damaging 0.71
R5470:Tnxb UTSW 17 34,935,947 (GRCm39) missense probably null 1.00
R5475:Tnxb UTSW 17 34,908,567 (GRCm39) missense probably damaging 1.00
R5574:Tnxb UTSW 17 34,929,998 (GRCm39) missense probably benign
R5596:Tnxb UTSW 17 34,907,778 (GRCm39) missense probably damaging 1.00
R5599:Tnxb UTSW 17 34,909,179 (GRCm39) missense probably benign 0.22
R5599:Tnxb UTSW 17 34,909,176 (GRCm39) missense probably damaging 1.00
R5615:Tnxb UTSW 17 34,902,392 (GRCm39) missense probably damaging 1.00
R5620:Tnxb UTSW 17 34,936,504 (GRCm39) nonsense probably null
R5625:Tnxb UTSW 17 34,904,185 (GRCm39) missense probably benign 0.30
R5734:Tnxb UTSW 17 34,917,884 (GRCm39) missense possibly damaging 0.53
R5896:Tnxb UTSW 17 34,891,126 (GRCm39) missense probably damaging 1.00
R5961:Tnxb UTSW 17 34,937,609 (GRCm39) missense probably damaging 1.00
R5974:Tnxb UTSW 17 34,904,681 (GRCm39) missense probably damaging 1.00
R6091:Tnxb UTSW 17 34,929,338 (GRCm39) missense probably damaging 0.98
R6134:Tnxb UTSW 17 34,890,986 (GRCm39) missense probably damaging 0.96
R6325:Tnxb UTSW 17 34,911,398 (GRCm39) missense probably damaging 1.00
R6358:Tnxb UTSW 17 34,897,968 (GRCm39) missense probably damaging 0.98
R6362:Tnxb UTSW 17 34,913,362 (GRCm39) missense probably damaging 1.00
R6432:Tnxb UTSW 17 34,936,891 (GRCm39) missense probably damaging 1.00
R6461:Tnxb UTSW 17 34,890,872 (GRCm39) missense probably damaging 1.00
R6467:Tnxb UTSW 17 34,912,898 (GRCm39) missense probably damaging 1.00
R6476:Tnxb UTSW 17 34,909,166 (GRCm39) missense probably damaging 0.98
R6477:Tnxb UTSW 17 34,938,513 (GRCm39) missense probably damaging 1.00
R6631:Tnxb UTSW 17 34,937,222 (GRCm39) missense probably damaging 1.00
R6774:Tnxb UTSW 17 34,928,606 (GRCm39) nonsense probably null
R6787:Tnxb UTSW 17 34,929,710 (GRCm39) missense probably benign 0.02
R6805:Tnxb UTSW 17 34,917,127 (GRCm39) missense possibly damaging 0.93
R6860:Tnxb UTSW 17 34,932,131 (GRCm39) missense probably damaging 0.99
R6883:Tnxb UTSW 17 34,937,493 (GRCm39) missense probably damaging 1.00
R7049:Tnxb UTSW 17 34,936,242 (GRCm39) critical splice donor site probably null
R7107:Tnxb UTSW 17 34,890,314 (GRCm39) missense unknown
R7172:Tnxb UTSW 17 34,914,994 (GRCm39) missense probably damaging 1.00
R7206:Tnxb UTSW 17 34,923,075 (GRCm39) missense possibly damaging 0.71
R7219:Tnxb UTSW 17 34,898,039 (GRCm39) missense probably benign 0.08
R7237:Tnxb UTSW 17 34,901,170 (GRCm39) missense possibly damaging 0.82
R7257:Tnxb UTSW 17 34,935,475 (GRCm39) missense probably benign 0.44
R7269:Tnxb UTSW 17 34,914,428 (GRCm39) missense probably damaging 1.00
R7302:Tnxb UTSW 17 34,897,875 (GRCm39) missense probably benign 0.41
R7372:Tnxb UTSW 17 34,936,228 (GRCm39) missense possibly damaging 0.72
R7384:Tnxb UTSW 17 34,937,492 (GRCm39) missense probably damaging 1.00
R7447:Tnxb UTSW 17 34,937,444 (GRCm39) missense probably damaging 1.00
R7449:Tnxb UTSW 17 34,922,335 (GRCm39) missense possibly damaging 0.93
R7480:Tnxb UTSW 17 34,934,747 (GRCm39) missense probably damaging 0.96
R7506:Tnxb UTSW 17 34,934,665 (GRCm39) missense possibly damaging 0.89
R7586:Tnxb UTSW 17 34,935,382 (GRCm39) missense probably damaging 0.98
R7688:Tnxb UTSW 17 34,890,880 (GRCm39) missense probably benign 0.23
R7690:Tnxb UTSW 17 34,908,501 (GRCm39) missense probably damaging 1.00
R7690:Tnxb UTSW 17 34,908,494 (GRCm39) missense probably benign 0.03
R7732:Tnxb UTSW 17 34,913,254 (GRCm39) missense probably damaging 1.00
R7735:Tnxb UTSW 17 34,890,398 (GRCm39) missense unknown
R7760:Tnxb UTSW 17 34,931,911 (GRCm39) missense probably damaging 0.96
R7874:Tnxb UTSW 17 34,930,417 (GRCm39) missense probably damaging 1.00
R7909:Tnxb UTSW 17 34,911,428 (GRCm39) missense probably benign 0.02
R7922:Tnxb UTSW 17 34,933,577 (GRCm39) missense probably damaging 1.00
R7931:Tnxb UTSW 17 34,907,672 (GRCm39) missense probably damaging 1.00
R7949:Tnxb UTSW 17 34,936,103 (GRCm39) missense probably damaging 1.00
R7953:Tnxb UTSW 17 34,929,077 (GRCm39) missense probably benign 0.03
R7953:Tnxb UTSW 17 34,928,509 (GRCm39) missense possibly damaging 0.86
R7977:Tnxb UTSW 17 34,929,194 (GRCm39) missense possibly damaging 0.92
R7985:Tnxb UTSW 17 34,935,984 (GRCm39) critical splice donor site probably null
R7987:Tnxb UTSW 17 34,929,194 (GRCm39) missense possibly damaging 0.92
R8040:Tnxb UTSW 17 34,935,532 (GRCm39) missense probably damaging 1.00
R8053:Tnxb UTSW 17 34,923,153 (GRCm39) missense probably damaging 0.98
R8074:Tnxb UTSW 17 34,922,955 (GRCm39) missense probably benign 0.32
R8089:Tnxb UTSW 17 34,891,763 (GRCm39) missense unknown
R8169:Tnxb UTSW 17 34,918,181 (GRCm39) missense possibly damaging 0.96
R8348:Tnxb UTSW 17 34,929,102 (GRCm39) missense possibly damaging 0.92
R8352:Tnxb UTSW 17 34,908,381 (GRCm39) missense probably damaging 1.00
R8362:Tnxb UTSW 17 34,931,946 (GRCm39) missense probably damaging 0.99
R8452:Tnxb UTSW 17 34,908,381 (GRCm39) missense probably damaging 1.00
R8527:Tnxb UTSW 17 34,907,634 (GRCm39) missense probably damaging 1.00
R8754:Tnxb UTSW 17 34,934,882 (GRCm39) missense probably damaging 1.00
R8813:Tnxb UTSW 17 34,938,136 (GRCm39) missense probably damaging 1.00
R8936:Tnxb UTSW 17 34,904,646 (GRCm39) missense probably damaging 1.00
R8986:Tnxb UTSW 17 34,897,646 (GRCm39) missense possibly damaging 0.66
R9001:Tnxb UTSW 17 34,922,410 (GRCm39) missense probably benign 0.32
R9215:Tnxb UTSW 17 34,891,564 (GRCm39) missense unknown
R9226:Tnxb UTSW 17 34,904,766 (GRCm39) missense probably damaging 1.00
R9276:Tnxb UTSW 17 34,929,134 (GRCm39) missense possibly damaging 0.60
R9279:Tnxb UTSW 17 34,898,088 (GRCm39) missense possibly damaging 0.46
R9363:Tnxb UTSW 17 34,917,294 (GRCm39) missense possibly damaging 0.93
R9367:Tnxb UTSW 17 34,931,993 (GRCm39) missense probably damaging 1.00
R9494:Tnxb UTSW 17 34,904,796 (GRCm39) missense probably damaging 1.00
R9606:Tnxb UTSW 17 34,914,578 (GRCm39) missense possibly damaging 0.82
R9650:Tnxb UTSW 17 34,930,629 (GRCm39) missense probably damaging 0.99
R9677:Tnxb UTSW 17 34,917,878 (GRCm39) missense possibly damaging 0.93
R9690:Tnxb UTSW 17 34,936,171 (GRCm39) missense probably damaging 1.00
R9761:Tnxb UTSW 17 34,903,987 (GRCm39) missense probably benign 0.32
X0004:Tnxb UTSW 17 34,922,389 (GRCm39) missense possibly damaging 0.71
X0010:Tnxb UTSW 17 34,890,908 (GRCm39) missense probably damaging 1.00
X0019:Tnxb UTSW 17 34,913,163 (GRCm39) missense possibly damaging 0.51
X0063:Tnxb UTSW 17 34,922,482 (GRCm39) missense probably damaging 0.98
X0064:Tnxb UTSW 17 34,913,006 (GRCm39) missense probably damaging 1.00
Z1177:Tnxb UTSW 17 34,937,700 (GRCm39) missense probably damaging 0.99
Z1177:Tnxb UTSW 17 34,902,305 (GRCm39) missense probably damaging 1.00
Z1177:Tnxb UTSW 17 34,890,740 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- AGCGTTGGGACTTGGAAATTCCTTC -3'
(R):5'- AGCTACCAGGGGACTTGGATTCTAC -3'

Sequencing Primer
(F):5'- GGGACTTGGAAATTCCTTCCATAAAC -3'
(R):5'- GGAAGTAGGCCACATACTTGTCC -3'
Posted On 2013-04-16