Incidental Mutation 'R0164:Tenm4'
ID 24041
Institutional Source Beutler Lab
Gene Symbol Tenm4
Ensembl Gene ENSMUSG00000048078
Gene Name teneurin transmembrane protein 4
Synonyms Doc4, l7Rn3, Ten-m4, ELM2, l(7)-3Rn, Odz4
MMRRC Submission 038440-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R0164 (G1)
Quality Score 188
Status Validated
Chromosome 7
Chromosomal Location 96171246-96911093 bp(+) (GRCm38)
Type of Mutation splice site
DNA Base Change (assembly) T to G at 96729340 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000102784 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000107162] [ENSMUST00000107165] [ENSMUST00000107166]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000107162
SMART Domains Protein: ENSMUSP00000102780
Gene: ENSMUSG00000048078

DomainStartEndE-ValueType
Pfam:Ten_N 10 410 5.6e-195 PFAM
transmembrane domain 411 433 N/A INTRINSIC
EGF_like 637 665 3.43e1 SMART
EGF 668 696 2.29e1 SMART
EGF 701 730 1.88e-1 SMART
EGF 733 762 1.13e1 SMART
EGF 767 797 2.39e1 SMART
EGF 800 828 4.32e-1 SMART
EGF 831 859 6.02e0 SMART
EGF 862 894 9.93e-1 SMART
low complexity region 900 914 N/A INTRINSIC
Pfam:RHS_repeat 2327 2380 5.5e-7 PFAM
Pfam:Tox-GHH 2740 2818 5.2e-34 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000107165
SMART Domains Protein: ENSMUSP00000102783
Gene: ENSMUSG00000048078

DomainStartEndE-ValueType
Pfam:Ten_N 36 402 1.1e-171 PFAM
transmembrane domain 403 425 N/A INTRINSIC
EGF_like 629 657 3.43e1 SMART
EGF 660 688 2.29e1 SMART
EGF 693 722 1.88e-1 SMART
EGF 725 754 1.13e1 SMART
EGF 759 789 2.39e1 SMART
EGF 792 820 4.32e-1 SMART
EGF 823 851 6.02e0 SMART
EGF 863 895 9.93e-1 SMART
low complexity region 901 915 N/A INTRINSIC
Pfam:RHS_repeat 2335 2368 1.6e-7 PFAM
Pfam:Tox-GHH 2749 2826 1.8e-32 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000107166
SMART Domains Protein: ENSMUSP00000102784
Gene: ENSMUSG00000048078

DomainStartEndE-ValueType
Pfam:Ten_N 35 193 1.4e-83 PFAM
Pfam:Ten_N 187 365 5e-78 PFAM
transmembrane domain 366 388 N/A INTRINSIC
EGF_like 592 620 3.43e1 SMART
EGF 623 651 2.29e1 SMART
EGF 656 685 1.88e-1 SMART
EGF 688 717 1.13e1 SMART
EGF 722 752 2.39e1 SMART
EGF 755 783 4.32e-1 SMART
EGF 786 814 6.02e0 SMART
EGF 826 858 9.93e-1 SMART
low complexity region 864 878 N/A INTRINSIC
Pfam:RHS_repeat 2298 2351 3.8e-7 PFAM
Pfam:Tox-GHH 2711 2789 3.9e-34 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000131541
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.4%
  • 10x: 96.7%
  • 20x: 94.0%
Validation Efficiency 98% (85/87)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene plays a role in establishing proper neuronal connectivity during development. Defects in this gene have been associated with hereditary essential tremor-5. [provided by RefSeq, Oct 2016]
PHENOTYPE: Various ENU-induced alleles cause prenatal lethality associated with impaired mesoderm development and lead to pleiotropic phenotypes. The most severe alleles cause failure of gastrulation and somitogenesis while the least severe one allows survival to adulthood with runting of variable penetrance. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 89 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2010315B03Rik T C 9: 124,295,159 (GRCm38) probably benign Het
4732465J04Rik GATCTATCTATCTATCTATCTATCTATCTATCTATCTATC GATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATC 10: 95,794,578 (GRCm38) probably null Het
4930522L14Rik T C 5: 109,736,847 (GRCm38) K382E probably damaging Het
Adck1 A G 12: 88,455,510 (GRCm38) E297G probably damaging Het
Ahrr G A 13: 74,283,024 (GRCm38) probably benign Het
Aldh3a2 C T 11: 61,248,888 (GRCm38) V473I probably benign Het
Arfgef3 A T 10: 18,647,915 (GRCm38) I369K possibly damaging Het
Atl2 A G 17: 79,853,831 (GRCm38) probably benign Het
Atp1b3 T C 9: 96,338,709 (GRCm38) I178V possibly damaging Het
Axdnd1 T C 1: 156,378,386 (GRCm38) E520G possibly damaging Het
Bahcc1 A T 11: 120,285,074 (GRCm38) probably benign Het
BB019430 A T 10: 58,704,271 (GRCm38) noncoding transcript Het
BC028528 A T 3: 95,887,334 (GRCm38) probably benign Het
Btbd1 T A 7: 81,801,003 (GRCm38) Q343L probably benign Het
Catsper1 A G 19: 5,339,475 (GRCm38) T473A possibly damaging Het
Chmp6 G A 11: 119,915,523 (GRCm38) probably null Het
D130040H23Rik T C 8: 69,302,543 (GRCm38) V200A possibly damaging Het
D830013O20Rik C T 12: 73,364,331 (GRCm38) noncoding transcript Het
Dcaf1 T A 9: 106,844,145 (GRCm38) S379T possibly damaging Het
Dcaf4 G A 12: 83,535,988 (GRCm38) probably benign Het
Dhx58 T C 11: 100,695,324 (GRCm38) I624V probably benign Het
Disp3 T C 4: 148,254,251 (GRCm38) E821G probably damaging Het
Dlc1 T A 8: 36,599,440 (GRCm38) E464V probably damaging Het
Dnah10 G A 5: 124,783,834 (GRCm38) V2151I probably damaging Het
Dnah6 C T 6: 73,188,535 (GRCm38) probably benign Het
Dnah8 G A 17: 30,748,665 (GRCm38) G2617D probably benign Het
Dnah9 C A 11: 65,918,804 (GRCm38) E872* probably null Het
Dock9 T C 14: 121,597,665 (GRCm38) Y99C probably damaging Het
Dpy19l3 T A 7: 35,716,646 (GRCm38) I310F probably damaging Het
Fggy A T 4: 95,837,654 (GRCm38) I137F probably damaging Het
Gli2 A G 1: 118,890,283 (GRCm38) probably benign Het
Gm14421 A T 2: 177,056,722 (GRCm38) noncoding transcript Het
Gm5689 T A 18: 42,173,543 (GRCm38) D58E probably damaging Het
Grin2a A G 16: 9,994,821 (GRCm38) probably null Het
Grin2b A G 6: 135,778,648 (GRCm38) probably benign Het
Incenp A G 19: 9,894,879 (GRCm38) S72P probably benign Het
Ipo11 A G 13: 106,910,194 (GRCm38) probably benign Het
Klc3 T A 7: 19,394,926 (GRCm38) N469Y possibly damaging Het
Lrrc42 A G 4: 107,247,505 (GRCm38) S88P probably benign Het
Lrrc49 G A 9: 60,680,600 (GRCm38) T93I probably benign Het
Ltn1 G A 16: 87,405,519 (GRCm38) probably benign Het
Mlycd A T 8: 119,407,641 (GRCm38) Q294L probably damaging Het
Mmrn1 T A 6: 60,975,815 (GRCm38) probably benign Het
Mrpl22 T A 11: 58,171,821 (GRCm38) I19N probably benign Het
Msh3 T A 13: 92,349,209 (GRCm38) K202N probably damaging Het
N4bp2 T C 5: 65,803,573 (GRCm38) probably benign Het
Ncam1 C T 9: 49,568,409 (GRCm38) D90N probably damaging Het
Nckap5 A T 1: 126,024,407 (GRCm38) D1405E possibly damaging Het
Ncoa2 A G 1: 13,186,731 (GRCm38) probably null Het
Ncoa6 TGC TGCGC 2: 155,408,291 (GRCm38) probably null Het
Nlrp1b A T 11: 71,164,099 (GRCm38) W844R probably damaging Het
Nmnat1 G T 4: 149,469,150 (GRCm38) N168K possibly damaging Het
Olfr1446 A G 19: 12,890,445 (GRCm38) L44P probably damaging Het
Ost4 T C 5: 30,907,459 (GRCm38) H26R probably damaging Het
Otog G A 7: 46,304,231 (GRCm38) V2638M probably damaging Het
Otogl A T 10: 107,874,530 (GRCm38) I566N probably damaging Het
Pcyt1a T C 16: 32,470,186 (GRCm38) S282P probably damaging Het
Prkcg G A 7: 3,329,119 (GRCm38) E581K probably damaging Het
Ralgps2 A G 1: 156,887,089 (GRCm38) probably null Het
Rnf157 A G 11: 116,354,810 (GRCm38) probably benign Het
Scmh1 T C 4: 120,529,865 (GRCm38) probably benign Het
Sgo2b T C 8: 63,938,383 (GRCm38) H150R possibly damaging Het
Sh2b3 T G 5: 121,829,037 (GRCm38) T5P probably damaging Het
Skint6 A T 4: 112,991,236 (GRCm38) probably benign Het
Slfn10-ps T C 11: 83,035,302 (GRCm38) noncoding transcript Het
Sspo T A 6: 48,494,194 (GRCm38) probably benign Het
Tcp1 T A 17: 12,922,747 (GRCm38) probably benign Het
Tdp2 A G 13: 24,838,239 (GRCm38) M214V probably damaging Het
Tmem144 G A 3: 79,839,273 (GRCm38) probably benign Het
Tmem204 A G 17: 25,058,350 (GRCm38) I187T probably damaging Het
Tmem208 T G 8: 105,334,694 (GRCm38) D117E probably benign Het
Tnks1bp1 C T 2: 85,059,221 (GRCm38) P631S possibly damaging Het
Tomm70a T C 16: 57,147,821 (GRCm38) V517A probably damaging Het
Ttc7 T C 17: 87,379,895 (GRCm38) V801A probably damaging Het
Txndc5 A T 13: 38,507,953 (GRCm38) C146S probably damaging Het
Ubac2 A G 14: 122,008,917 (GRCm38) probably benign Het
Ube4b G T 4: 149,360,324 (GRCm38) T493K probably damaging Het
Ufl1 A T 4: 25,256,008 (GRCm38) Y504N probably benign Het
Ugt1a6a T C 1: 88,139,270 (GRCm38) V266A possibly damaging Het
Ugt1a6b T A 1: 88,107,467 (GRCm38) C176S probably damaging Het
Ulk3 T A 9: 57,590,686 (GRCm38) I90N probably damaging Het
Unc13c T C 9: 73,694,892 (GRCm38) I1357M probably benign Het
Vmn1r28 G A 6: 58,265,717 (GRCm38) A182T probably benign Het
Vmn2r114 A G 17: 23,309,826 (GRCm38) probably null Het
Vmn2r91 A C 17: 18,106,137 (GRCm38) N228T probably benign Het
Wdr43 T G 17: 71,631,997 (GRCm38) probably benign Het
Wisp1 T C 15: 66,919,210 (GRCm38) L287P probably damaging Het
Zbtb6 G T 2: 37,429,588 (GRCm38) Y109* probably null Het
Zfp980 A G 4: 145,701,997 (GRCm38) D432G probably benign Het
Other mutations in Tenm4
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00228:Tenm4 APN 7 96,868,009 (GRCm38) missense probably benign 0.00
IGL00468:Tenm4 APN 7 96,874,472 (GRCm38) missense probably damaging 0.98
IGL00519:Tenm4 APN 7 96,805,138 (GRCm38) splice site probably benign
IGL00979:Tenm4 APN 7 96,729,391 (GRCm38) missense probably damaging 0.96
IGL01401:Tenm4 APN 7 96,874,267 (GRCm38) missense probably damaging 1.00
IGL01459:Tenm4 APN 7 96,729,385 (GRCm38) missense probably damaging 1.00
IGL01519:Tenm4 APN 7 96,895,177 (GRCm38) missense probably damaging 1.00
IGL01545:Tenm4 APN 7 96,874,303 (GRCm38) missense probably benign 0.00
IGL01579:Tenm4 APN 7 96,863,502 (GRCm38) missense probably benign 0.00
IGL01587:Tenm4 APN 7 96,863,502 (GRCm38) missense probably benign 0.00
IGL01625:Tenm4 APN 7 96,885,358 (GRCm38) missense probably damaging 1.00
IGL01655:Tenm4 APN 7 96,553,724 (GRCm38) missense probably damaging 1.00
IGL01683:Tenm4 APN 7 96,885,404 (GRCm38) missense possibly damaging 0.84
IGL01728:Tenm4 APN 7 96,896,064 (GRCm38) missense probably damaging 1.00
IGL01732:Tenm4 APN 7 96,895,509 (GRCm38) missense probably damaging 1.00
IGL01924:Tenm4 APN 7 96,895,212 (GRCm38) missense probably damaging 1.00
IGL01966:Tenm4 APN 7 96,553,550 (GRCm38) missense probably damaging 1.00
IGL02177:Tenm4 APN 7 96,895,662 (GRCm38) missense probably benign 0.40
IGL02207:Tenm4 APN 7 96,874,116 (GRCm38) missense possibly damaging 0.85
IGL02269:Tenm4 APN 7 96,823,822 (GRCm38) missense probably damaging 1.00
IGL02274:Tenm4 APN 7 96,854,734 (GRCm38) missense probably damaging 1.00
IGL02375:Tenm4 APN 7 96,704,137 (GRCm38) missense possibly damaging 0.52
IGL02415:Tenm4 APN 7 96,874,074 (GRCm38) missense probably damaging 0.98
IGL02472:Tenm4 APN 7 96,774,176 (GRCm38) unclassified probably benign
IGL02656:Tenm4 APN 7 96,885,433 (GRCm38) missense probably damaging 1.00
IGL02678:Tenm4 APN 7 96,896,219 (GRCm38) missense probably damaging 1.00
IGL02829:Tenm4 APN 7 96,894,998 (GRCm38) nonsense probably null
IGL02863:Tenm4 APN 7 96,873,706 (GRCm38) missense probably damaging 1.00
IGL03145:Tenm4 APN 7 96,842,968 (GRCm38) missense probably damaging 0.98
IGL03153:Tenm4 APN 7 96,873,762 (GRCm38) missense probably damaging 1.00
principium UTSW 7 96,797,481 (GRCm38) missense probably damaging 0.98
toccata UTSW 7 96,902,989 (GRCm38) critical splice donor site probably null
P0026:Tenm4 UTSW 7 96,874,527 (GRCm38) missense probably damaging 1.00
R0097:Tenm4 UTSW 7 96,892,926 (GRCm38) missense probably damaging 1.00
R0097:Tenm4 UTSW 7 96,892,926 (GRCm38) missense probably damaging 1.00
R0140:Tenm4 UTSW 7 96,896,052 (GRCm38) missense possibly damaging 0.78
R0277:Tenm4 UTSW 7 96,694,950 (GRCm38) missense possibly damaging 0.54
R0323:Tenm4 UTSW 7 96,694,950 (GRCm38) missense possibly damaging 0.54
R0362:Tenm4 UTSW 7 96,772,035 (GRCm38) nonsense probably null
R0381:Tenm4 UTSW 7 96,905,881 (GRCm38) missense probably damaging 1.00
R0420:Tenm4 UTSW 7 96,873,766 (GRCm38) missense possibly damaging 0.85
R0426:Tenm4 UTSW 7 96,777,851 (GRCm38) missense probably damaging 1.00
R0513:Tenm4 UTSW 7 96,895,623 (GRCm38) missense probably benign 0.35
R0624:Tenm4 UTSW 7 96,774,020 (GRCm38) missense probably damaging 1.00
R0837:Tenm4 UTSW 7 96,896,275 (GRCm38) splice site probably benign
R1037:Tenm4 UTSW 7 96,797,481 (GRCm38) missense probably damaging 0.98
R1172:Tenm4 UTSW 7 96,848,044 (GRCm38) missense probably damaging 1.00
R1422:Tenm4 UTSW 7 96,550,051 (GRCm38) missense probably damaging 0.99
R1427:Tenm4 UTSW 7 96,843,048 (GRCm38) missense probably benign 0.42
R1462:Tenm4 UTSW 7 96,704,153 (GRCm38) missense probably damaging 1.00
R1462:Tenm4 UTSW 7 96,704,153 (GRCm38) missense probably damaging 1.00
R1597:Tenm4 UTSW 7 96,902,989 (GRCm38) critical splice donor site probably null
R1701:Tenm4 UTSW 7 96,902,889 (GRCm38) missense probably damaging 1.00
R1707:Tenm4 UTSW 7 96,888,685 (GRCm38) missense probably damaging 1.00
R1809:Tenm4 UTSW 7 96,873,780 (GRCm38) missense probably benign 0.17
R1812:Tenm4 UTSW 7 96,895,940 (GRCm38) missense probably damaging 1.00
R1895:Tenm4 UTSW 7 96,735,808 (GRCm38) missense probably damaging 1.00
R1933:Tenm4 UTSW 7 96,895,326 (GRCm38) missense probably damaging 1.00
R1946:Tenm4 UTSW 7 96,735,808 (GRCm38) missense probably damaging 1.00
R2108:Tenm4 UTSW 7 96,906,290 (GRCm38) missense probably damaging 1.00
R2151:Tenm4 UTSW 7 96,902,847 (GRCm38) missense probably damaging 1.00
R2247:Tenm4 UTSW 7 96,906,009 (GRCm38) missense probably benign 0.03
R2329:Tenm4 UTSW 7 96,895,862 (GRCm38) missense probably benign 0.00
R2893:Tenm4 UTSW 7 96,894,990 (GRCm38) missense probably damaging 1.00
R2990:Tenm4 UTSW 7 96,893,125 (GRCm38) splice site probably null
R3409:Tenm4 UTSW 7 96,895,160 (GRCm38) missense probably damaging 1.00
R3410:Tenm4 UTSW 7 96,852,530 (GRCm38) missense probably damaging 0.99
R3411:Tenm4 UTSW 7 96,852,530 (GRCm38) missense probably damaging 0.99
R3440:Tenm4 UTSW 7 96,553,516 (GRCm38) missense probably benign 0.00
R3441:Tenm4 UTSW 7 96,553,516 (GRCm38) missense probably benign 0.00
R3719:Tenm4 UTSW 7 96,863,563 (GRCm38) missense possibly damaging 0.92
R3772:Tenm4 UTSW 7 96,694,880 (GRCm38) missense probably damaging 1.00
R3773:Tenm4 UTSW 7 96,694,880 (GRCm38) missense probably damaging 1.00
R4093:Tenm4 UTSW 7 96,895,772 (GRCm38) missense probably damaging 1.00
R4439:Tenm4 UTSW 7 96,895,815 (GRCm38) missense probably benign 0.01
R4441:Tenm4 UTSW 7 96,895,815 (GRCm38) missense probably benign 0.01
R4510:Tenm4 UTSW 7 96,894,863 (GRCm38) missense probably benign
R4511:Tenm4 UTSW 7 96,894,863 (GRCm38) missense probably benign
R4543:Tenm4 UTSW 7 96,895,815 (GRCm38) missense probably benign 0.01
R4645:Tenm4 UTSW 7 96,895,742 (GRCm38) missense probably damaging 1.00
R4701:Tenm4 UTSW 7 96,895,349 (GRCm38) missense probably damaging 1.00
R4707:Tenm4 UTSW 7 96,774,046 (GRCm38) missense probably damaging 0.99
R4714:Tenm4 UTSW 7 96,894,924 (GRCm38) missense probably damaging 1.00
R4742:Tenm4 UTSW 7 96,797,484 (GRCm38) missense probably damaging 0.99
R4784:Tenm4 UTSW 7 96,774,046 (GRCm38) missense probably damaging 0.99
R4785:Tenm4 UTSW 7 96,774,046 (GRCm38) missense probably damaging 0.99
R4801:Tenm4 UTSW 7 96,906,245 (GRCm38) missense probably damaging 0.97
R4802:Tenm4 UTSW 7 96,906,245 (GRCm38) missense probably damaging 0.97
R4880:Tenm4 UTSW 7 96,905,818 (GRCm38) splice site probably null
R5036:Tenm4 UTSW 7 96,852,561 (GRCm38) missense probably damaging 1.00
R5036:Tenm4 UTSW 7 96,694,790 (GRCm38) missense probably damaging 1.00
R5050:Tenm4 UTSW 7 96,895,788 (GRCm38) missense probably damaging 1.00
R5103:Tenm4 UTSW 7 96,842,957 (GRCm38) missense probably damaging 1.00
R5106:Tenm4 UTSW 7 96,843,149 (GRCm38) missense probably damaging 0.99
R5118:Tenm4 UTSW 7 96,893,086 (GRCm38) missense probably damaging 1.00
R5272:Tenm4 UTSW 7 96,874,203 (GRCm38) missense probably damaging 0.98
R5282:Tenm4 UTSW 7 96,837,331 (GRCm38) missense possibly damaging 0.90
R5403:Tenm4 UTSW 7 96,888,827 (GRCm38) missense probably damaging 1.00
R5404:Tenm4 UTSW 7 96,894,680 (GRCm38) missense probably damaging 1.00
R5567:Tenm4 UTSW 7 96,896,209 (GRCm38) nonsense probably null
R5590:Tenm4 UTSW 7 96,797,401 (GRCm38) missense possibly damaging 0.93
R5590:Tenm4 UTSW 7 96,797,400 (GRCm38) missense possibly damaging 0.73
R5597:Tenm4 UTSW 7 96,553,517 (GRCm38) missense probably benign 0.00
R5782:Tenm4 UTSW 7 96,893,039 (GRCm38) missense probably benign 0.00
R5861:Tenm4 UTSW 7 96,843,217 (GRCm38) intron probably benign
R5890:Tenm4 UTSW 7 96,902,860 (GRCm38) missense probably damaging 1.00
R5930:Tenm4 UTSW 7 96,854,719 (GRCm38) missense probably damaging 1.00
R5940:Tenm4 UTSW 7 96,845,895 (GRCm38) missense probably damaging 1.00
R6012:Tenm4 UTSW 7 96,522,433 (GRCm38) intron probably benign
R6060:Tenm4 UTSW 7 96,873,711 (GRCm38) missense probably damaging 1.00
R6104:Tenm4 UTSW 7 96,837,289 (GRCm38) missense probably damaging 0.97
R6283:Tenm4 UTSW 7 96,874,494 (GRCm38) missense probably benign 0.33
R6333:Tenm4 UTSW 7 96,774,124 (GRCm38) missense probably damaging 1.00
R6522:Tenm4 UTSW 7 96,843,044 (GRCm38) missense possibly damaging 0.88
R6616:Tenm4 UTSW 7 96,553,496 (GRCm38) missense probably benign 0.01
R6746:Tenm4 UTSW 7 96,892,860 (GRCm38) missense probably damaging 1.00
R6751:Tenm4 UTSW 7 96,845,712 (GRCm38) missense possibly damaging 0.95
R6806:Tenm4 UTSW 7 96,811,959 (GRCm38) missense possibly damaging 0.95
R6807:Tenm4 UTSW 7 96,895,271 (GRCm38) missense probably damaging 1.00
R6807:Tenm4 UTSW 7 96,553,496 (GRCm38) missense probably benign 0.01
R6809:Tenm4 UTSW 7 96,553,496 (GRCm38) missense probably benign 0.01
R6810:Tenm4 UTSW 7 96,553,496 (GRCm38) missense probably benign 0.01
R6811:Tenm4 UTSW 7 96,553,496 (GRCm38) missense probably benign 0.01
R6853:Tenm4 UTSW 7 96,837,295 (GRCm38) missense possibly damaging 0.94
R6886:Tenm4 UTSW 7 96,797,392 (GRCm38) missense possibly damaging 0.85
R6920:Tenm4 UTSW 7 96,895,550 (GRCm38) missense probably damaging 1.00
R6937:Tenm4 UTSW 7 96,553,496 (GRCm38) missense probably benign 0.01
R6939:Tenm4 UTSW 7 96,553,496 (GRCm38) missense probably benign 0.01
R7011:Tenm4 UTSW 7 96,896,135 (GRCm38) nonsense probably null
R7033:Tenm4 UTSW 7 96,895,223 (GRCm38) nonsense probably null
R7040:Tenm4 UTSW 7 96,553,496 (GRCm38) missense probably benign 0.01
R7083:Tenm4 UTSW 7 96,895,349 (GRCm38) missense probably damaging 1.00
R7238:Tenm4 UTSW 7 96,553,496 (GRCm38) missense probably benign 0.01
R7239:Tenm4 UTSW 7 96,735,813 (GRCm38) missense possibly damaging 0.47
R7239:Tenm4 UTSW 7 96,553,496 (GRCm38) missense probably benign 0.01
R7337:Tenm4 UTSW 7 96,874,126 (GRCm38) missense probably benign 0.44
R7400:Tenm4 UTSW 7 96,694,803 (GRCm38) missense probably damaging 0.97
R7407:Tenm4 UTSW 7 96,773,987 (GRCm38) missense possibly damaging 0.89
R7449:Tenm4 UTSW 7 96,874,213 (GRCm38) missense possibly damaging 0.65
R7473:Tenm4 UTSW 7 96,774,146 (GRCm38) missense probably damaging 1.00
R7477:Tenm4 UTSW 7 96,845,808 (GRCm38) missense probably damaging 0.99
R7489:Tenm4 UTSW 7 96,837,314 (GRCm38) missense possibly damaging 0.90
R7498:Tenm4 UTSW 7 96,848,017 (GRCm38) missense probably damaging 1.00
R7562:Tenm4 UTSW 7 96,888,814 (GRCm38) missense probably damaging 1.00
R7615:Tenm4 UTSW 7 96,845,926 (GRCm38) missense probably damaging 1.00
R7624:Tenm4 UTSW 7 96,895,985 (GRCm38) missense possibly damaging 0.95
R7626:Tenm4 UTSW 7 96,893,014 (GRCm38) missense probably damaging 1.00
R7690:Tenm4 UTSW 7 96,863,533 (GRCm38) missense probably benign 0.00
R7692:Tenm4 UTSW 7 96,895,403 (GRCm38) missense probably damaging 1.00
R7748:Tenm4 UTSW 7 96,894,702 (GRCm38) missense probably damaging 1.00
R7763:Tenm4 UTSW 7 96,895,692 (GRCm38) missense probably benign 0.38
R7792:Tenm4 UTSW 7 96,774,014 (GRCm38) missense possibly damaging 0.54
R7855:Tenm4 UTSW 7 96,873,874 (GRCm38) missense probably damaging 1.00
R7868:Tenm4 UTSW 7 96,906,380 (GRCm38) missense possibly damaging 0.79
R7878:Tenm4 UTSW 7 96,852,357 (GRCm38) missense probably damaging 1.00
R7997:Tenm4 UTSW 7 96,874,305 (GRCm38) missense probably benign 0.44
R8017:Tenm4 UTSW 7 96,704,041 (GRCm38) missense probably damaging 1.00
R8019:Tenm4 UTSW 7 96,704,041 (GRCm38) missense probably damaging 1.00
R8054:Tenm4 UTSW 7 96,729,346 (GRCm38) splice site probably benign
R8061:Tenm4 UTSW 7 96,852,456 (GRCm38) missense probably damaging 1.00
R8108:Tenm4 UTSW 7 96,854,728 (GRCm38) missense probably benign 0.39
R8140:Tenm4 UTSW 7 96,895,176 (GRCm38) missense probably damaging 1.00
R8214:Tenm4 UTSW 7 96,895,407 (GRCm38) missense probably damaging 1.00
R8258:Tenm4 UTSW 7 96,867,991 (GRCm38) missense probably damaging 1.00
R8259:Tenm4 UTSW 7 96,867,991 (GRCm38) missense probably damaging 1.00
R8364:Tenm4 UTSW 7 96,772,106 (GRCm38) critical splice donor site probably null
R8542:Tenm4 UTSW 7 96,811,932 (GRCm38) missense probably damaging 0.99
R8669:Tenm4 UTSW 7 96,905,941 (GRCm38) missense probably benign
R8670:Tenm4 UTSW 7 96,905,941 (GRCm38) missense probably benign
R8683:Tenm4 UTSW 7 96,902,857 (GRCm38) missense probably damaging 0.99
R8691:Tenm4 UTSW 7 96,905,941 (GRCm38) missense probably benign
R8692:Tenm4 UTSW 7 96,905,941 (GRCm38) missense probably benign
R8714:Tenm4 UTSW 7 96,905,941 (GRCm38) missense probably benign
R8716:Tenm4 UTSW 7 96,905,941 (GRCm38) missense probably benign
R8735:Tenm4 UTSW 7 96,905,941 (GRCm38) missense probably benign
R8736:Tenm4 UTSW 7 96,905,941 (GRCm38) missense probably benign
R8737:Tenm4 UTSW 7 96,905,941 (GRCm38) missense probably benign
R8738:Tenm4 UTSW 7 96,905,941 (GRCm38) missense probably benign
R8738:Tenm4 UTSW 7 96,873,840 (GRCm38) missense probably damaging 1.00
R8739:Tenm4 UTSW 7 96,905,941 (GRCm38) missense probably benign
R8776:Tenm4 UTSW 7 96,895,032 (GRCm38) missense probably damaging 1.00
R8776-TAIL:Tenm4 UTSW 7 96,895,032 (GRCm38) missense probably damaging 1.00
R8777:Tenm4 UTSW 7 96,896,037 (GRCm38) missense probably damaging 1.00
R8777-TAIL:Tenm4 UTSW 7 96,896,037 (GRCm38) missense probably damaging 1.00
R8817:Tenm4 UTSW 7 96,874,128 (GRCm38) missense probably benign 0.01
R8851:Tenm4 UTSW 7 96,852,503 (GRCm38) missense probably damaging 1.00
R8913:Tenm4 UTSW 7 96,702,745 (GRCm38) splice site probably benign
R8977:Tenm4 UTSW 7 96,811,970 (GRCm38) missense probably damaging 1.00
R9100:Tenm4 UTSW 7 96,845,854 (GRCm38) missense probably damaging 1.00
R9136:Tenm4 UTSW 7 96,823,918 (GRCm38) missense possibly damaging 0.69
R9163:Tenm4 UTSW 7 96,823,873 (GRCm38) missense probably damaging 1.00
R9188:Tenm4 UTSW 7 96,772,027 (GRCm38) missense probably damaging 1.00
R9195:Tenm4 UTSW 7 96,892,919 (GRCm38) missense probably damaging 1.00
R9217:Tenm4 UTSW 7 96,885,439 (GRCm38) missense probably damaging 1.00
R9344:Tenm4 UTSW 7 96,896,145 (GRCm38) missense probably damaging 1.00
R9414:Tenm4 UTSW 7 96,896,160 (GRCm38) missense probably benign
R9466:Tenm4 UTSW 7 96,550,045 (GRCm38) missense possibly damaging 0.79
R9559:Tenm4 UTSW 7 96,823,849 (GRCm38) missense probably benign
R9626:Tenm4 UTSW 7 96,896,138 (GRCm38) missense probably damaging 1.00
R9673:Tenm4 UTSW 7 96,867,989 (GRCm38) missense probably damaging 1.00
R9676:Tenm4 UTSW 7 96,895,431 (GRCm38) missense probably damaging 1.00
R9678:Tenm4 UTSW 7 96,737,412 (GRCm38) missense possibly damaging 0.94
R9775:Tenm4 UTSW 7 96,906,554 (GRCm38) missense possibly damaging 0.92
R9790:Tenm4 UTSW 7 96,888,839 (GRCm38) missense probably damaging 1.00
R9791:Tenm4 UTSW 7 96,888,839 (GRCm38) missense probably damaging 1.00
R9803:Tenm4 UTSW 7 96,553,478 (GRCm38) missense probably damaging 1.00
X0021:Tenm4 UTSW 7 96,873,909 (GRCm38) nonsense probably null
X0026:Tenm4 UTSW 7 96,868,087 (GRCm38) missense probably damaging 0.98
X0066:Tenm4 UTSW 7 96,894,794 (GRCm38) missense probably damaging 1.00
X0066:Tenm4 UTSW 7 96,848,030 (GRCm38) missense probably damaging 1.00
Z1176:Tenm4 UTSW 7 96,905,914 (GRCm38) missense probably benign 0.00
Z1177:Tenm4 UTSW 7 96,863,585 (GRCm38) missense probably damaging 0.96
Predicted Primers PCR Primer
(F):5'- AAAAGGTCAAGACCTCCTGAAACTGTG -3'
(R):5'- ATGCCCTGAAAGCATCCTCGAAG -3'

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