Incidental Mutation 'R1686:Tep1'
ID 189375
Institutional Source Beutler Lab
Gene Symbol Tep1
Ensembl Gene ENSMUSG00000006281
Gene Name telomerase associated protein 1
Synonyms Tp1
MMRRC Submission 039719-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R1686 (G1)
Quality Score 225
Status Validated
Chromosome 14
Chromosomal Location 51061516-51108017 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 51074245 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Glycine at position 1880 (E1880G)
Ref Sequence ENSEMBL: ENSMUSP00000006444 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000006444] [ENSMUST00000227526]
AlphaFold P97499
Predicted Effect probably benign
Transcript: ENSMUST00000006444
AA Change: E1880G

PolyPhen 2 Score 0.119 (Sensitivity: 0.93; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000006444
Gene: ENSMUSG00000006281
AA Change: E1880G

DomainStartEndE-ValueType
Pfam:TEP1_N 1 29 2.8e-20 PFAM
Pfam:TEP1_N 31 59 1.4e-20 PFAM
Pfam:TEP1_N 61 89 3.1e-20 PFAM
Pfam:TEP1_N 91 119 3e-20 PFAM
low complexity region 195 207 N/A INTRINSIC
low complexity region 211 229 N/A INTRINSIC
Pfam:TROVE 230 685 3.2e-136 PFAM
Pfam:DUF4062 909 1020 2.4e-22 PFAM
Pfam:NACHT 1171 1346 9.2e-38 PFAM
low complexity region 1393 1405 N/A INTRINSIC
low complexity region 1622 1641 N/A INTRINSIC
WD40 1673 1711 2.98e-1 SMART
WD40 1714 1752 5.33e0 SMART
WD40 1755 1794 1.52e-4 SMART
WD40 1797 1835 3.27e-4 SMART
WD40 1838 1877 3.09e-1 SMART
WD40 1880 1919 2.24e-2 SMART
WD40 1925 1962 4.95e0 SMART
WD40 1968 2003 2.29e1 SMART
WD40 2008 2045 1.72e0 SMART
WD40 2058 2097 3.89e-11 SMART
WD40 2103 2142 3.93e-7 SMART
WD40 2145 2182 4.38e-5 SMART
WD40 2184 2232 1.24e0 SMART
WD40 2235 2273 1.14e-3 SMART
WD40 2275 2315 4.46e-1 SMART
Blast:WD40 2316 2353 4e-12 BLAST
WD40 2546 2583 6.79e-2 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000226430
Predicted Effect noncoding transcript
Transcript: ENSMUST00000227193
Predicted Effect noncoding transcript
Transcript: ENSMUST00000227228
Predicted Effect probably benign
Transcript: ENSMUST00000227526
Meta Mutation Damage Score 0.1406 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.4%
  • 10x: 96.4%
  • 20x: 92.9%
Validation Efficiency 100% (85/85)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene product is a component of the ribonucleoprotein complex responsible for telomerase activity which catalyzes the addition of new telomeres on the chromosome ends. The telomerase-associated proteins are conserved from ciliates to humans. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]
PHENOTYPE: Mice homozygous for a disruption in this gene show no obvious phenotype. No changes are seen in telomerase activity or telomere length. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 79 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700017N19Rik G A 10: 100,448,722 (GRCm39) V400I probably damaging Het
Abcb1b A G 5: 8,848,782 (GRCm39) N14S probably damaging Het
Adamts14 A G 10: 61,034,439 (GRCm39) Y1150H probably benign Het
Adgrg3 A G 8: 95,759,997 (GRCm39) N72S probably benign Het
Akain1 T A 17: 69,746,527 (GRCm39) F3I possibly damaging Het
Akr1c21 T C 13: 4,627,452 (GRCm39) L182P probably damaging Het
Arhgap21 A T 2: 20,886,659 (GRCm39) Y12N probably damaging Het
Aup1 A T 6: 83,032,226 (GRCm39) H131L probably damaging Het
Bag6 A G 17: 35,363,928 (GRCm39) T812A possibly damaging Het
Bmp2k A G 5: 97,211,392 (GRCm39) Y520C unknown Het
Calm4 T G 13: 3,888,302 (GRCm39) V136G probably damaging Het
Catsper2 A G 2: 121,230,523 (GRCm39) probably null Het
Cc2d2a A G 5: 43,896,713 (GRCm39) T1537A possibly damaging Het
Cntn2 A T 1: 132,454,049 (GRCm39) V319D possibly damaging Het
Cux1 G A 5: 136,304,235 (GRCm39) R1314* probably null Het
Cxcl12 A G 6: 117,150,508 (GRCm39) I79V probably damaging Het
Cyp2j6 T C 4: 96,412,014 (GRCm39) D418G probably benign Het
Ddx28 G C 8: 106,737,190 (GRCm39) D289E probably damaging Het
Fabp3 C T 4: 130,206,180 (GRCm39) T57I probably benign Het
Fam135a A C 1: 24,068,887 (GRCm39) S448A probably benign Het
Fbxo33 G T 12: 59,251,626 (GRCm39) N30K possibly damaging Het
Fgf12 A C 16: 28,217,093 (GRCm39) Y21D probably damaging Het
Galntl5 C T 5: 25,415,432 (GRCm39) S288L probably benign Het
Gart G T 16: 91,422,237 (GRCm39) A760D probably damaging Het
Gba2 A T 4: 43,573,869 (GRCm39) probably benign Het
Gm10518 C A 1: 179,631,357 (GRCm39) S139* probably null Het
Gm4781 A T 10: 100,232,837 (GRCm39) noncoding transcript Het
Gm9790 A G 3: 85,823,156 (GRCm39) noncoding transcript Het
Gmps G A 3: 63,893,075 (GRCm39) G127R probably damaging Het
Golim4 A T 3: 75,802,443 (GRCm39) V283E probably benign Het
Gprc5a A T 6: 135,055,918 (GRCm39) I122F possibly damaging Het
Gzmc T C 14: 56,471,341 (GRCm39) K67E probably benign Het
Hapln3 C A 7: 78,771,638 (GRCm39) V84L probably benign Het
Hif3a T A 7: 16,778,789 (GRCm39) N377Y possibly damaging Het
Ifi211 G A 1: 173,726,969 (GRCm39) H392Y probably damaging Het
Iqgap3 T A 3: 88,015,663 (GRCm39) probably benign Het
Itga10 T A 3: 96,559,141 (GRCm39) F410Y probably damaging Het
Jup T C 11: 100,263,260 (GRCm39) Y705C probably damaging Het
Khsrp C T 17: 57,332,597 (GRCm39) A228T probably benign Het
Lmntd2 C T 7: 140,790,998 (GRCm39) G445D probably damaging Het
Lyst T C 13: 13,809,290 (GRCm39) V320A possibly damaging Het
Magel2 T A 7: 62,027,988 (GRCm39) H297Q possibly damaging Het
Mbd6 T C 10: 127,123,286 (GRCm39) E33G probably damaging Het
Mob3b A G 4: 34,985,910 (GRCm39) probably benign Het
Mroh2a T C 1: 88,162,334 (GRCm39) probably null Het
Mroh2a C T 1: 88,158,402 (GRCm39) R150* probably null Het
Mymk A T 2: 26,952,346 (GRCm39) W174R probably damaging Het
Nckap1 C T 2: 80,348,286 (GRCm39) S889N probably benign Het
Nipal3 T C 4: 135,174,599 (GRCm39) Y384C possibly damaging Het
Nt5c3b A G 11: 100,330,920 (GRCm39) probably benign Het
Obox6 T A 7: 15,567,750 (GRCm39) L232F probably damaging Het
Obscn A C 11: 58,997,113 (GRCm39) probably benign Het
Or7g12 T C 9: 18,899,839 (GRCm39) L185P probably damaging Het
Phkb A G 8: 86,748,278 (GRCm39) I706V probably benign Het
Plcb2 A G 2: 118,546,168 (GRCm39) probably benign Het
Plek2 T C 12: 78,941,184 (GRCm39) D216G probably damaging Het
Plxnb2 T C 15: 89,046,665 (GRCm39) Y855C probably damaging Het
Prkcz T C 4: 155,355,713 (GRCm39) T227A probably damaging Het
Psma7 A T 2: 179,679,215 (GRCm39) D184E probably benign Het
Rai14 T A 15: 10,592,282 (GRCm39) L204F probably damaging Het
Ralgapa2 A G 2: 146,199,920 (GRCm39) V1208A probably benign Het
Rapgef6 A G 11: 54,582,458 (GRCm39) R67G possibly damaging Het
Ryr2 C T 13: 11,618,665 (GRCm39) probably benign Het
Satb1 T C 17: 52,047,027 (GRCm39) S763G probably benign Het
Sdk1 A T 5: 142,020,292 (GRCm39) H690L probably benign Het
Sfrp5 A C 19: 42,190,143 (GRCm39) V103G possibly damaging Het
Six6 A G 12: 72,988,451 (GRCm39) E208G probably benign Het
Sspo A T 6: 48,437,334 (GRCm39) H1364L probably benign Het
Stard9 A T 2: 120,529,973 (GRCm39) T2077S probably benign Het
Tacr3 T C 3: 134,535,254 (GRCm39) L74P probably damaging Het
Tgfb3 A T 12: 86,116,517 (GRCm39) probably benign Het
Thap7 G A 16: 17,346,576 (GRCm39) P136S probably damaging Het
Thoc2l T A 5: 104,667,789 (GRCm39) Y770* probably null Het
Tmc2 T C 2: 130,098,036 (GRCm39) V717A possibly damaging Het
Usp43 T A 11: 67,778,593 (GRCm39) S446C probably damaging Het
Vwa3a C T 7: 120,379,371 (GRCm39) S492L probably damaging Het
Wdhd1 T A 14: 47,493,672 (GRCm39) N16I probably damaging Het
Wdr95 A T 5: 149,516,566 (GRCm39) D327V probably damaging Het
Zfp128 T G 7: 12,624,563 (GRCm39) Y310* probably null Het
Other mutations in Tep1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00482:Tep1 APN 14 51,080,641 (GRCm39) missense probably damaging 1.00
IGL00490:Tep1 APN 14 51,070,930 (GRCm39) missense probably damaging 0.97
IGL01114:Tep1 APN 14 51,088,096 (GRCm39) missense probably damaging 0.98
IGL01294:Tep1 APN 14 51,067,114 (GRCm39) splice site probably benign
IGL01902:Tep1 APN 14 51,103,548 (GRCm39) splice site probably benign
IGL01910:Tep1 APN 14 51,081,569 (GRCm39) missense probably benign 0.06
IGL01925:Tep1 APN 14 51,061,955 (GRCm39) unclassified probably benign
IGL01965:Tep1 APN 14 51,100,952 (GRCm39) splice site probably benign
IGL02071:Tep1 APN 14 51,071,506 (GRCm39) missense possibly damaging 0.93
IGL02124:Tep1 APN 14 51,091,581 (GRCm39) unclassified probably benign
IGL02189:Tep1 APN 14 51,064,283 (GRCm39) missense probably benign
IGL02252:Tep1 APN 14 51,067,712 (GRCm39) missense possibly damaging 0.93
IGL02299:Tep1 APN 14 51,078,128 (GRCm39) missense probably damaging 0.99
IGL02343:Tep1 APN 14 51,066,704 (GRCm39) missense probably damaging 0.99
IGL02423:Tep1 APN 14 51,082,077 (GRCm39) missense possibly damaging 0.53
IGL02537:Tep1 APN 14 51,073,570 (GRCm39) missense probably damaging 0.96
IGL02601:Tep1 APN 14 51,070,935 (GRCm39) nonsense probably null
IGL02941:Tep1 APN 14 51,103,494 (GRCm39) missense probably damaging 0.98
IGL02990:Tep1 APN 14 51,105,703 (GRCm39) missense possibly damaging 0.86
IGL03144:Tep1 APN 14 51,081,474 (GRCm39) splice site probably benign
IGL03209:Tep1 APN 14 51,078,160 (GRCm39) splice site probably benign
R0240_Tep1_347 UTSW 14 51,100,486 (GRCm39) splice site probably benign
R0972_Tep1_893 UTSW 14 51,061,753 (GRCm39) unclassified probably benign
R1686_Tep1_375 UTSW 14 51,074,245 (GRCm39) missense probably benign 0.12
R7232_Tep1_671 UTSW 14 51,081,789 (GRCm39) missense unknown
R8009_Tep1_822 UTSW 14 51,061,687 (GRCm39) missense possibly damaging 0.93
PIT4305001:Tep1 UTSW 14 51,066,684 (GRCm39) missense possibly damaging 0.90
PIT4362001:Tep1 UTSW 14 51,103,510 (GRCm39) missense probably benign 0.23
R0058:Tep1 UTSW 14 51,071,522 (GRCm39) missense possibly damaging 0.85
R0060:Tep1 UTSW 14 51,103,486 (GRCm39) missense probably damaging 1.00
R0109:Tep1 UTSW 14 51,089,373 (GRCm39) splice site probably null
R0123:Tep1 UTSW 14 51,067,150 (GRCm39) missense possibly damaging 0.84
R0134:Tep1 UTSW 14 51,067,150 (GRCm39) missense possibly damaging 0.84
R0148:Tep1 UTSW 14 51,062,246 (GRCm39) missense possibly damaging 0.70
R0240:Tep1 UTSW 14 51,100,486 (GRCm39) splice site probably benign
R0243:Tep1 UTSW 14 51,084,444 (GRCm39) missense probably damaging 1.00
R0373:Tep1 UTSW 14 51,074,225 (GRCm39) missense possibly damaging 0.85
R0432:Tep1 UTSW 14 51,104,280 (GRCm39) small deletion probably benign
R0464:Tep1 UTSW 14 51,085,141 (GRCm39) missense probably benign 0.00
R0566:Tep1 UTSW 14 51,082,871 (GRCm39) critical splice donor site probably null
R0691:Tep1 UTSW 14 51,104,301 (GRCm39) nonsense probably null
R0787:Tep1 UTSW 14 51,066,687 (GRCm39) missense possibly damaging 0.85
R0972:Tep1 UTSW 14 51,061,753 (GRCm39) unclassified probably benign
R1263:Tep1 UTSW 14 51,082,970 (GRCm39) missense possibly damaging 0.84
R1300:Tep1 UTSW 14 51,064,512 (GRCm39) critical splice donor site probably null
R1327:Tep1 UTSW 14 51,090,556 (GRCm39) missense probably benign 0.18
R1556:Tep1 UTSW 14 51,090,499 (GRCm39) missense probably benign 0.06
R1584:Tep1 UTSW 14 51,103,494 (GRCm39) missense probably damaging 0.98
R1607:Tep1 UTSW 14 51,062,020 (GRCm39) missense probably null 0.99
R1715:Tep1 UTSW 14 51,092,024 (GRCm39) missense possibly damaging 0.92
R1778:Tep1 UTSW 14 51,067,079 (GRCm39) intron probably benign
R1993:Tep1 UTSW 14 51,061,641 (GRCm39) missense possibly damaging 0.93
R2071:Tep1 UTSW 14 51,091,739 (GRCm39) missense probably benign 0.23
R2104:Tep1 UTSW 14 51,088,037 (GRCm39) splice site probably benign
R2118:Tep1 UTSW 14 51,093,029 (GRCm39) splice site probably null
R2119:Tep1 UTSW 14 51,076,443 (GRCm39) missense probably benign 0.13
R2208:Tep1 UTSW 14 51,104,321 (GRCm39) missense probably benign 0.01
R2241:Tep1 UTSW 14 51,091,667 (GRCm39) missense probably benign 0.01
R2243:Tep1 UTSW 14 51,091,667 (GRCm39) missense probably benign 0.01
R2311:Tep1 UTSW 14 51,071,024 (GRCm39) missense possibly damaging 0.95
R2420:Tep1 UTSW 14 51,071,480 (GRCm39) missense probably benign
R2874:Tep1 UTSW 14 51,088,107 (GRCm39) missense possibly damaging 0.71
R3084:Tep1 UTSW 14 51,064,511 (GRCm39) critical splice donor site probably null
R3086:Tep1 UTSW 14 51,064,511 (GRCm39) critical splice donor site probably null
R3621:Tep1 UTSW 14 51,066,477 (GRCm39) missense probably damaging 0.99
R3815:Tep1 UTSW 14 51,105,772 (GRCm39) missense possibly damaging 0.71
R4124:Tep1 UTSW 14 51,081,191 (GRCm39) missense possibly damaging 0.93
R4125:Tep1 UTSW 14 51,081,191 (GRCm39) missense possibly damaging 0.93
R4127:Tep1 UTSW 14 51,081,191 (GRCm39) missense possibly damaging 0.93
R4134:Tep1 UTSW 14 51,082,317 (GRCm39) missense probably benign
R4152:Tep1 UTSW 14 51,075,051 (GRCm39) missense possibly damaging 0.72
R4153:Tep1 UTSW 14 51,075,051 (GRCm39) missense possibly damaging 0.72
R4191:Tep1 UTSW 14 51,074,263 (GRCm39) missense probably damaging 0.96
R4248:Tep1 UTSW 14 51,100,351 (GRCm39) missense possibly damaging 0.93
R4293:Tep1 UTSW 14 51,084,318 (GRCm39) missense probably benign
R4569:Tep1 UTSW 14 51,062,197 (GRCm39) missense probably benign 0.01
R4704:Tep1 UTSW 14 51,074,530 (GRCm39) missense probably benign 0.06
R4815:Tep1 UTSW 14 51,078,759 (GRCm39) missense probably damaging 0.99
R4978:Tep1 UTSW 14 51,082,891 (GRCm39) missense possibly damaging 0.93
R4989:Tep1 UTSW 14 51,076,457 (GRCm39) missense probably benign
R5022:Tep1 UTSW 14 51,066,456 (GRCm39) missense probably benign 0.27
R5057:Tep1 UTSW 14 51,066,456 (GRCm39) missense probably benign 0.27
R5063:Tep1 UTSW 14 51,088,084 (GRCm39) missense possibly damaging 0.86
R5118:Tep1 UTSW 14 51,093,044 (GRCm39) splice site probably null
R5128:Tep1 UTSW 14 51,081,736 (GRCm39) makesense probably null
R5149:Tep1 UTSW 14 51,074,855 (GRCm39) nonsense probably null
R5171:Tep1 UTSW 14 51,062,259 (GRCm39) missense probably benign 0.01
R5201:Tep1 UTSW 14 51,105,567 (GRCm39) missense probably benign 0.01
R5260:Tep1 UTSW 14 51,076,088 (GRCm39) missense probably benign
R5339:Tep1 UTSW 14 51,082,031 (GRCm39) missense probably damaging 0.99
R5384:Tep1 UTSW 14 51,105,774 (GRCm39) missense probably damaging 0.98
R5385:Tep1 UTSW 14 51,105,774 (GRCm39) missense probably damaging 0.98
R5386:Tep1 UTSW 14 51,105,774 (GRCm39) missense probably damaging 0.98
R5594:Tep1 UTSW 14 51,067,339 (GRCm39) missense possibly damaging 0.86
R5639:Tep1 UTSW 14 51,091,062 (GRCm39) missense possibly damaging 0.85
R5749:Tep1 UTSW 14 51,081,529 (GRCm39) missense possibly damaging 0.59
R5756:Tep1 UTSW 14 51,074,836 (GRCm39) critical splice donor site probably null
R6013:Tep1 UTSW 14 51,098,505 (GRCm39) missense probably damaging 0.97
R6014:Tep1 UTSW 14 51,084,457 (GRCm39) missense probably benign 0.12
R6248:Tep1 UTSW 14 51,067,715 (GRCm39) missense probably damaging 0.98
R6264:Tep1 UTSW 14 51,082,970 (GRCm39) missense probably damaging 0.99
R6363:Tep1 UTSW 14 51,062,005 (GRCm39) missense probably benign 0.04
R6381:Tep1 UTSW 14 51,082,888 (GRCm39) missense probably damaging 0.99
R6462:Tep1 UTSW 14 51,081,836 (GRCm39) missense probably benign
R6942:Tep1 UTSW 14 51,074,194 (GRCm39) missense possibly damaging 0.85
R6951:Tep1 UTSW 14 51,071,370 (GRCm39) critical splice donor site probably null
R6979:Tep1 UTSW 14 51,076,094 (GRCm39) missense possibly damaging 0.93
R6999:Tep1 UTSW 14 51,088,162 (GRCm39) missense possibly damaging 0.86
R7099:Tep1 UTSW 14 51,081,944 (GRCm39) splice site probably null
R7208:Tep1 UTSW 14 51,062,013 (GRCm39) critical splice acceptor site probably null
R7232:Tep1 UTSW 14 51,081,789 (GRCm39) missense unknown
R7249:Tep1 UTSW 14 51,061,732 (GRCm39) missense possibly damaging 0.86
R7325:Tep1 UTSW 14 51,103,495 (GRCm39) missense probably damaging 0.99
R7409:Tep1 UTSW 14 51,104,312 (GRCm39) missense possibly damaging 0.67
R7499:Tep1 UTSW 14 51,091,047 (GRCm39) missense probably damaging 0.99
R7542:Tep1 UTSW 14 51,099,948 (GRCm39) nonsense probably null
R7806:Tep1 UTSW 14 51,074,266 (GRCm39) missense possibly damaging 0.85
R7825:Tep1 UTSW 14 51,081,344 (GRCm39) critical splice acceptor site probably null
R7901:Tep1 UTSW 14 51,064,308 (GRCm39) missense possibly damaging 0.88
R7961:Tep1 UTSW 14 51,061,687 (GRCm39) missense possibly damaging 0.93
R7993:Tep1 UTSW 14 51,067,710 (GRCm39) missense probably benign 0.41
R8009:Tep1 UTSW 14 51,061,687 (GRCm39) missense possibly damaging 0.93
R8085:Tep1 UTSW 14 51,066,753 (GRCm39) missense probably benign 0.11
R8299:Tep1 UTSW 14 51,105,502 (GRCm39) missense probably benign 0.06
R8330:Tep1 UTSW 14 51,085,162 (GRCm39) missense possibly damaging 0.86
R8396:Tep1 UTSW 14 51,074,529 (GRCm39) missense probably benign 0.23
R8475:Tep1 UTSW 14 51,078,712 (GRCm39) missense probably damaging 1.00
R8695:Tep1 UTSW 14 51,082,894 (GRCm39) missense possibly damaging 0.85
R8726:Tep1 UTSW 14 51,085,080 (GRCm39) missense probably damaging 0.98
R8812:Tep1 UTSW 14 51,074,589 (GRCm39) missense probably damaging 0.98
R9152:Tep1 UTSW 14 51,104,162 (GRCm39) missense probably benign 0.14
R9269:Tep1 UTSW 14 51,081,766 (GRCm39) missense probably damaging 0.98
R9299:Tep1 UTSW 14 51,081,988 (GRCm39) splice site probably benign
R9365:Tep1 UTSW 14 51,064,597 (GRCm39) missense probably damaging 1.00
R9398:Tep1 UTSW 14 51,066,429 (GRCm39) missense possibly damaging 0.85
R9408:Tep1 UTSW 14 51,074,637 (GRCm39) missense possibly damaging 0.85
R9445:Tep1 UTSW 14 51,082,967 (GRCm39) missense possibly damaging 0.95
R9487:Tep1 UTSW 14 51,066,687 (GRCm39) missense possibly damaging 0.93
R9555:Tep1 UTSW 14 51,105,888 (GRCm39) missense possibly damaging 0.52
R9597:Tep1 UTSW 14 51,100,465 (GRCm39) missense probably damaging 0.99
R9715:Tep1 UTSW 14 51,081,759 (GRCm39) missense
R9732:Tep1 UTSW 14 51,088,162 (GRCm39) missense probably benign 0.33
R9777:Tep1 UTSW 14 51,076,443 (GRCm39) nonsense probably null
RF007:Tep1 UTSW 14 51,098,402 (GRCm39) missense possibly damaging 0.92
X0024:Tep1 UTSW 14 51,064,576 (GRCm39) missense possibly damaging 0.86
X0060:Tep1 UTSW 14 51,074,221 (GRCm39) missense probably benign 0.25
Z1177:Tep1 UTSW 14 51,085,222 (GRCm39) missense probably damaging 0.99
Predicted Primers PCR Primer
(F):5'- GGCAGCAGGAACCTTCTTTCCAAG -3'
(R):5'- TCCATGTCGTTTTGAGCCCATACTG -3'

Sequencing Primer
(F):5'- ccgcccactcccATGAC -3'
(R):5'- CATACTGAGAACAGGCTCTGTTG -3'
Posted On 2014-05-14