Incidental Mutation 'IGL02829:Tenm4'
ID 361349
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Tenm4
Ensembl Gene ENSMUSG00000048078
Gene Name teneurin transmembrane protein 4
Synonyms Doc4, l7Rn3, Ten-m4, ELM2, l(7)-3Rn, Odz4
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # IGL02829
Quality Score
Status
Chromosome 7
Chromosomal Location 96171246-96911093 bp(+) (GRCm38)
Type of Mutation nonsense
DNA Base Change (assembly) C to T at 96894998 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Glutamine to Stop codon at position 2074 (Q2074*)
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 null
Transcript: ENSMUST00000107162
AA Change: Q2103*
SMART Domains Protein: ENSMUSP00000102780
Gene: ENSMUSG00000048078
AA Change: Q2103*

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 null
Transcript: ENSMUST00000107165
AA Change: Q2111*
SMART Domains Protein: ENSMUSP00000102783
Gene: ENSMUSG00000048078
AA Change: Q2111*

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 null
Transcript: ENSMUST00000107166
AA Change: Q2074*
SMART Domains Protein: ENSMUSP00000102784
Gene: ENSMUSG00000048078
AA Change: Q2074*

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
Coding Region Coverage
Validation Efficiency
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: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Bbs9 A G 9: 22,579,484 (GRCm38) T303A probably damaging Het
Bet1 T A 6: 4,086,795 (GRCm38) M1L probably benign Het
Bicc1 A C 10: 70,958,880 (GRCm38) V149G probably damaging Het
Braf C A 6: 39,627,728 (GRCm38) L655F possibly damaging Het
Cd101 A G 3: 101,018,565 (GRCm38) probably benign Het
Cobll1 T C 2: 65,126,045 (GRCm38) K290E probably damaging Het
Col6a5 A T 9: 105,934,307 (GRCm38) I671K unknown Het
D130052B06Rik A C 11: 33,623,864 (GRCm38) T154P probably benign Het
Dglucy A C 12: 100,871,404 (GRCm38) H602P probably damaging Het
Fbxo34 A G 14: 47,529,689 (GRCm38) I220V probably benign Het
Gm42878 A G 5: 121,537,203 (GRCm38) V101A probably damaging Het
Gsdmc4 A G 15: 63,892,648 (GRCm38) L381P probably benign Het
Ifi208 C A 1: 173,682,840 (GRCm38) P187H probably damaging Het
Lrrc37a A T 11: 103,491,174 (GRCm38) C2473S unknown Het
Miip T A 4: 147,863,061 (GRCm38) N214I probably benign Het
Mrc2 A G 11: 105,336,707 (GRCm38) T589A possibly damaging Het
Mtss1 A G 15: 59,058,428 (GRCm38) probably benign Het
Mypn T C 10: 63,192,586 (GRCm38) R233G probably benign Het
Naip6 A T 13: 100,300,765 (GRCm38) C417S probably benign Het
Olfr1084 T A 2: 86,639,255 (GRCm38) Y151F possibly damaging Het
Olfr1216 A C 2: 89,013,677 (GRCm38) L129W probably damaging Het
Olfr275 C T 4: 52,826,027 (GRCm38) P210L probably damaging Het
Pcsk1 T C 13: 75,126,836 (GRCm38) Y515H probably damaging Het
Pla2g2e T A 4: 138,880,436 (GRCm38) Y42* probably null Het
Polh A T 17: 46,172,902 (GRCm38) L479Q possibly damaging Het
Prr36 T A 8: 4,215,278 (GRCm38) R157S possibly damaging Het
Reck T A 4: 43,891,014 (GRCm38) C51S probably damaging Het
Rev3l A G 10: 39,825,240 (GRCm38) D1911G probably damaging Het
Scgb1b27 A T 7: 34,021,748 (GRCm38) probably null Het
Sema4g G A 19: 44,992,749 (GRCm38) R47Q possibly damaging Het
Serinc1 A T 10: 57,523,965 (GRCm38) Y158* probably null Het
Slc15a2 C A 16: 36,757,193 (GRCm38) G435C possibly damaging Het
Tbc1d17 C A 7: 44,848,872 (GRCm38) probably benign Het
Tns3 A G 11: 8,519,564 (GRCm38) C244R probably damaging Het
Vmn2r2 A T 3: 64,118,751 (GRCm38) probably benign Het
Vmn2r44 T A 7: 8,377,880 (GRCm38) Q338L possibly damaging Het
Wdr70 C T 15: 7,976,982 (GRCm38) D363N possibly damaging Het
Yipf7 A T 5: 69,541,091 (GRCm38) S24R 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
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
R0164:Tenm4 UTSW 7 96,729,340 (GRCm38) splice site probably benign
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
Posted On 2015-12-18