Incidental Mutation 'IGL00094:Tnxb'
ID 797
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Tnxb
Ensembl Gene ENSMUSG00000033327
Gene Name tenascin XB
Synonyms Tnx, TN-MHC
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL00094
Quality Score
Status
Chromosome 17
Chromosomal Location 34879431-34938789 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 34904603 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glycine to Cysteine at position 1123 (G1123C)
Ref Sequence ENSEMBL: ENSMUSP00000127487 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000087399] [ENSMUST00000168533]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000087399
AA Change: G1246C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000084661
Gene: ENSMUSG00000033327
AA Change: G1246C

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 damaging
Transcript: ENSMUST00000168533
AA Change: G1123C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000127487
Gene: ENSMUSG00000033327
AA Change: G1123C

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
Predicted Effect noncoding transcript
Transcript: ENSMUST00000179962
Coding Region Coverage
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: 61 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aacs T A 5: 125,591,254 (GRCm39) N547K probably benign Het
Abca13 A G 11: 9,247,443 (GRCm39) T2397A probably benign Het
Abcc1 A G 16: 14,288,398 (GRCm39) N1341S probably null Het
Adcy9 T A 16: 4,122,446 (GRCm39) I535L probably benign Het
Akap6 A G 12: 53,187,763 (GRCm39) S1726G possibly damaging Het
Ap3d1 T C 10: 80,577,813 (GRCm39) M5V probably benign Het
Ash1l T A 3: 88,889,019 (GRCm39) N299K probably benign Het
B3gnt2 C T 11: 22,786,151 (GRCm39) V346I probably benign Het
Ceacam14 G A 7: 17,548,062 (GRCm39) V51I probably damaging Het
Cfap69 T C 5: 5,634,682 (GRCm39) D812G probably damaging Het
Cfap97d1 A G 11: 101,881,646 (GRCm39) E114G possibly damaging Het
Chrna9 T C 5: 66,126,600 (GRCm39) V118A probably benign Het
Cpsf7 A G 19: 10,517,151 (GRCm39) R418G probably damaging Het
Csnk1g3 T C 18: 54,052,075 (GRCm39) Y215H probably damaging Het
Dcaf5 A C 12: 80,386,097 (GRCm39) N676K probably benign Het
Dld A T 12: 31,385,576 (GRCm39) M255K probably benign Het
Esr2 A T 12: 76,180,670 (GRCm39) L417H probably damaging Het
Fsip2 T A 2: 82,820,730 (GRCm39) S5488T probably benign Het
Gatb A T 3: 85,509,227 (GRCm39) I130L possibly damaging Het
Gbp9 T C 5: 105,229,130 (GRCm39) K506E probably benign Het
Hkdc1 T C 10: 62,229,568 (GRCm39) N703S probably damaging Het
Itgb3 T A 11: 104,524,410 (GRCm39) V182E probably damaging Het
Itih4 A T 14: 30,617,426 (GRCm39) Y582F probably damaging Het
Lancl2 T A 6: 57,701,522 (GRCm39) probably benign Het
Lgals3 A G 14: 47,622,175 (GRCm39) K197R probably benign Het
Lipe T C 7: 25,082,977 (GRCm39) T767A probably damaging Het
Lrp2 T A 2: 69,338,123 (GRCm39) D1219V probably damaging Het
Lrriq3 T A 3: 154,806,698 (GRCm39) C116S probably benign Het
Mcm5 T G 8: 75,851,573 (GRCm39) probably null Het
Mtpn G T 6: 35,499,711 (GRCm39) T31K probably damaging Het
Mycbp2 A T 14: 103,460,486 (GRCm39) Y1494N probably damaging Het
Nbeal1 G T 1: 60,274,350 (GRCm39) E498* probably null Het
Nos1 T G 5: 118,048,165 (GRCm39) S657A probably damaging Het
Nr3c1 A T 18: 39,561,661 (GRCm39) probably null Het
Or12e7 T A 2: 87,288,271 (GRCm39) V254E probably damaging Het
Or13a17 A T 7: 140,271,349 (GRCm39) H177L probably damaging Het
Or4c127 T A 2: 89,833,365 (GRCm39) I205N possibly damaging Het
Or7g32 T A 9: 19,408,155 (GRCm39) I37N probably damaging Het
Or8g20 T C 9: 39,395,944 (GRCm39) I202V probably benign Het
Or8s8 T G 15: 98,354,299 (GRCm39) V36G possibly damaging Het
Or9i1 A T 19: 13,839,150 (GRCm39) probably benign Het
Osbp2 T G 11: 3,661,848 (GRCm39) S735R probably benign Het
Otop3 A T 11: 115,235,279 (GRCm39) T304S probably benign Het
Pcdhac2 A T 18: 37,278,128 (GRCm39) L369F probably damaging Het
Pick1 T C 15: 79,131,457 (GRCm39) probably benign Het
Prlhr A T 19: 60,456,119 (GRCm39) V149E probably damaging Het
Prss12 G A 3: 123,280,598 (GRCm39) probably benign Het
Rab19 A T 6: 39,365,132 (GRCm39) probably benign Het
Ralgapb T C 2: 158,262,776 (GRCm39) W5R probably damaging Het
Rfx4 T A 10: 84,676,063 (GRCm39) L44Q probably damaging Het
Scube2 T C 7: 109,407,661 (GRCm39) T760A probably damaging Het
Shcbp1 A C 8: 4,804,258 (GRCm39) Y145* probably null Het
Snx31 T A 15: 36,545,761 (GRCm39) probably null Het
Spopl A T 2: 23,427,643 (GRCm39) V163E possibly damaging Het
Sqor T C 2: 122,629,463 (GRCm39) I107T probably damaging Het
Tcte1 T C 17: 45,845,854 (GRCm39) F153L probably damaging Het
Tnfrsf11b T A 15: 54,123,238 (GRCm39) H121L probably damaging Het
Tnip1 G T 11: 54,831,643 (GRCm39) Y10* probably null Het
Wdr62 T C 7: 29,942,948 (GRCm39) E515G probably benign Het
Zfand1 A T 3: 10,413,590 (GRCm39) D32E probably null Het
Zfp112 A C 7: 23,821,668 (GRCm39) T3P probably damaging Het
Other mutations in Tnxb
AlleleSourceChrCoordTypePredicted EffectPPH Score
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
R0326:Tnxb UTSW 17 34,917,153 (GRCm39) missense probably benign 0.32
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
Posted On 2011-07-12