Incidental Mutation 'R4414:Ktn1'
ID 328078
Institutional Source Beutler Lab
Gene Symbol Ktn1
Ensembl Gene ENSMUSG00000021843
Gene Name kinectin 1
Synonyms
MMRRC Submission 041694-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R4414 (G1)
Quality Score 225
Status Validated
Chromosome 14
Chromosomal Location 47886551-47974021 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) G to A at 47962387 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tryptophan to Stop codon at position 1117 (W1117*)
Ref Sequence ENSEMBL: ENSMUSP00000139946 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000022391] [ENSMUST00000185343] [ENSMUST00000185940] [ENSMUST00000186627] [ENSMUST00000186761] [ENSMUST00000187039] [ENSMUST00000189101] [ENSMUST00000187262] [ENSMUST00000187839] [ENSMUST00000188330] [ENSMUST00000188553] [ENSMUST00000189533] [ENSMUST00000190182] [ENSMUST00000190252] [ENSMUST00000190535] [ENSMUST00000189986] [ENSMUST00000190999] [ENSMUST00000191018] [ENSMUST00000191446] [ENSMUST00000191511]
AlphaFold no structure available at present
Predicted Effect probably null
Transcript: ENSMUST00000022391
AA Change: W1140*
SMART Domains Protein: ENSMUSP00000022391
Gene: ENSMUSG00000021843
AA Change: W1140*

DomainStartEndE-ValueType
transmembrane domain 7 29 N/A INTRINSIC
coiled coil region 40 66 N/A INTRINSIC
low complexity region 108 127 N/A INTRINSIC
low complexity region 150 173 N/A INTRINSIC
low complexity region 203 221 N/A INTRINSIC
coiled coil region 329 372 N/A INTRINSIC
coiled coil region 402 727 N/A INTRINSIC
coiled coil region 764 1028 N/A INTRINSIC
coiled coil region 1089 1267 N/A INTRINSIC
coiled coil region 1302 1326 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000185343
AA Change: W1117*
SMART Domains Protein: ENSMUSP00000140186
Gene: ENSMUSG00000021843
AA Change: W1117*

DomainStartEndE-ValueType
signal peptide 1 39 N/A INTRINSIC
coiled coil region 40 66 N/A INTRINSIC
low complexity region 108 127 N/A INTRINSIC
low complexity region 150 173 N/A INTRINSIC
low complexity region 203 221 N/A INTRINSIC
coiled coil region 329 372 N/A INTRINSIC
coiled coil region 402 727 N/A INTRINSIC
coiled coil region 764 792 N/A INTRINSIC
low complexity region 816 825 N/A INTRINSIC
coiled coil region 836 1005 N/A INTRINSIC
coiled coil region 1066 1192 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000185940
AA Change: W1088*
SMART Domains Protein: ENSMUSP00000139625
Gene: ENSMUSG00000021843
AA Change: W1088*

DomainStartEndE-ValueType
signal peptide 1 39 N/A INTRINSIC
coiled coil region 40 66 N/A INTRINSIC
low complexity region 108 127 N/A INTRINSIC
low complexity region 150 173 N/A INTRINSIC
low complexity region 203 221 N/A INTRINSIC
coiled coil region 329 372 N/A INTRINSIC
coiled coil region 402 727 N/A INTRINSIC
coiled coil region 764 792 N/A INTRINSIC
low complexity region 816 825 N/A INTRINSIC
coiled coil region 836 993 N/A INTRINSIC
coiled coil region 1037 1163 N/A INTRINSIC
coiled coil region 1198 1222 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000186627
AA Change: W1088*
SMART Domains Protein: ENSMUSP00000140873
Gene: ENSMUSG00000021843
AA Change: W1088*

DomainStartEndE-ValueType
signal peptide 1 39 N/A INTRINSIC
coiled coil region 40 66 N/A INTRINSIC
low complexity region 108 127 N/A INTRINSIC
low complexity region 150 173 N/A INTRINSIC
low complexity region 203 221 N/A INTRINSIC
coiled coil region 329 372 N/A INTRINSIC
coiled coil region 402 727 N/A INTRINSIC
coiled coil region 764 792 N/A INTRINSIC
low complexity region 816 825 N/A INTRINSIC
coiled coil region 836 993 N/A INTRINSIC
coiled coil region 1037 1191 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000186761
AA Change: W1111*
SMART Domains Protein: ENSMUSP00000139521
Gene: ENSMUSG00000021843
AA Change: W1111*

DomainStartEndE-ValueType
signal peptide 1 39 N/A INTRINSIC
coiled coil region 40 66 N/A INTRINSIC
low complexity region 108 127 N/A INTRINSIC
low complexity region 150 173 N/A INTRINSIC
low complexity region 203 221 N/A INTRINSIC
coiled coil region 329 372 N/A INTRINSIC
coiled coil region 402 727 N/A INTRINSIC
coiled coil region 764 1016 N/A INTRINSIC
coiled coil region 1060 1210 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000187039
AA Change: W1088*
SMART Domains Protein: ENSMUSP00000140202
Gene: ENSMUSG00000021843
AA Change: W1088*

DomainStartEndE-ValueType
signal peptide 1 39 N/A INTRINSIC
coiled coil region 40 66 N/A INTRINSIC
low complexity region 108 127 N/A INTRINSIC
low complexity region 150 173 N/A INTRINSIC
low complexity region 203 221 N/A INTRINSIC
coiled coil region 329 372 N/A INTRINSIC
coiled coil region 402 727 N/A INTRINSIC
coiled coil region 764 792 N/A INTRINSIC
low complexity region 816 825 N/A INTRINSIC
coiled coil region 836 993 N/A INTRINSIC
coiled coil region 1037 1163 N/A INTRINSIC
coiled coil region 1198 1222 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000188263
Predicted Effect probably null
Transcript: ENSMUST00000189101
AA Change: W1088*
SMART Domains Protein: ENSMUSP00000140178
Gene: ENSMUSG00000021843
AA Change: W1088*

DomainStartEndE-ValueType
signal peptide 1 39 N/A INTRINSIC
coiled coil region 40 66 N/A INTRINSIC
low complexity region 108 127 N/A INTRINSIC
low complexity region 150 173 N/A INTRINSIC
low complexity region 203 221 N/A INTRINSIC
coiled coil region 329 372 N/A INTRINSIC
coiled coil region 402 727 N/A INTRINSIC
coiled coil region 764 792 N/A INTRINSIC
low complexity region 816 825 N/A INTRINSIC
coiled coil region 836 993 N/A INTRINSIC
coiled coil region 1037 1163 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000187262
AA Change: W1140*
SMART Domains Protein: ENSMUSP00000140206
Gene: ENSMUSG00000021843
AA Change: W1140*

DomainStartEndE-ValueType
signal peptide 1 39 N/A INTRINSIC
coiled coil region 40 66 N/A INTRINSIC
low complexity region 108 127 N/A INTRINSIC
low complexity region 150 173 N/A INTRINSIC
low complexity region 203 221 N/A INTRINSIC
coiled coil region 329 372 N/A INTRINSIC
coiled coil region 402 727 N/A INTRINSIC
coiled coil region 764 1028 N/A INTRINSIC
coiled coil region 1089 1215 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000187839
AA Change: W1140*
SMART Domains Protein: ENSMUSP00000140324
Gene: ENSMUSG00000021843
AA Change: W1140*

DomainStartEndE-ValueType
transmembrane domain 7 29 N/A INTRINSIC
coiled coil region 40 66 N/A INTRINSIC
low complexity region 108 127 N/A INTRINSIC
low complexity region 150 173 N/A INTRINSIC
low complexity region 203 221 N/A INTRINSIC
coiled coil region 329 372 N/A INTRINSIC
coiled coil region 402 727 N/A INTRINSIC
coiled coil region 764 1028 N/A INTRINSIC
coiled coil region 1089 1267 N/A INTRINSIC
coiled coil region 1302 1326 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000188330
AA Change: W1088*
SMART Domains Protein: ENSMUSP00000140845
Gene: ENSMUSG00000021843
AA Change: W1088*

DomainStartEndE-ValueType
signal peptide 1 39 N/A INTRINSIC
coiled coil region 40 66 N/A INTRINSIC
low complexity region 108 127 N/A INTRINSIC
low complexity region 150 173 N/A INTRINSIC
low complexity region 203 221 N/A INTRINSIC
coiled coil region 329 372 N/A INTRINSIC
coiled coil region 402 727 N/A INTRINSIC
coiled coil region 764 792 N/A INTRINSIC
low complexity region 816 825 N/A INTRINSIC
coiled coil region 836 993 N/A INTRINSIC
coiled coil region 1037 1187 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000188553
AA Change: W1117*
SMART Domains Protein: ENSMUSP00000140865
Gene: ENSMUSG00000021843
AA Change: W1117*

DomainStartEndE-ValueType
signal peptide 1 39 N/A INTRINSIC
coiled coil region 40 66 N/A INTRINSIC
low complexity region 108 127 N/A INTRINSIC
low complexity region 150 173 N/A INTRINSIC
low complexity region 203 221 N/A INTRINSIC
coiled coil region 329 372 N/A INTRINSIC
coiled coil region 402 727 N/A INTRINSIC
coiled coil region 764 792 N/A INTRINSIC
low complexity region 816 825 N/A INTRINSIC
coiled coil region 836 1005 N/A INTRINSIC
coiled coil region 1066 1216 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000189533
AA Change: W1088*
SMART Domains Protein: ENSMUSP00000140142
Gene: ENSMUSG00000021843
AA Change: W1088*

DomainStartEndE-ValueType
signal peptide 1 39 N/A INTRINSIC
coiled coil region 40 66 N/A INTRINSIC
low complexity region 108 127 N/A INTRINSIC
low complexity region 150 173 N/A INTRINSIC
low complexity region 203 221 N/A INTRINSIC
coiled coil region 329 372 N/A INTRINSIC
coiled coil region 402 727 N/A INTRINSIC
coiled coil region 764 792 N/A INTRINSIC
low complexity region 816 825 N/A INTRINSIC
coiled coil region 836 993 N/A INTRINSIC
coiled coil region 1037 1187 N/A INTRINSIC
coiled coil region 1222 1246 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000190182
AA Change: W1111*
SMART Domains Protein: ENSMUSP00000140301
Gene: ENSMUSG00000021843
AA Change: W1111*

DomainStartEndE-ValueType
signal peptide 1 39 N/A INTRINSIC
coiled coil region 40 66 N/A INTRINSIC
low complexity region 108 127 N/A INTRINSIC
low complexity region 150 173 N/A INTRINSIC
low complexity region 203 221 N/A INTRINSIC
coiled coil region 329 372 N/A INTRINSIC
coiled coil region 402 727 N/A INTRINSIC
coiled coil region 764 1016 N/A INTRINSIC
coiled coil region 1060 1238 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000190252
AA Change: W1111*
SMART Domains Protein: ENSMUSP00000140011
Gene: ENSMUSG00000021843
AA Change: W1111*

DomainStartEndE-ValueType
signal peptide 1 39 N/A INTRINSIC
coiled coil region 40 66 N/A INTRINSIC
low complexity region 108 127 N/A INTRINSIC
low complexity region 150 173 N/A INTRINSIC
low complexity region 203 221 N/A INTRINSIC
coiled coil region 329 372 N/A INTRINSIC
coiled coil region 402 727 N/A INTRINSIC
coiled coil region 764 1016 N/A INTRINSIC
coiled coil region 1060 1210 N/A INTRINSIC
coiled coil region 1245 1269 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000190535
AA Change: W1117*
SMART Domains Protein: ENSMUSP00000139952
Gene: ENSMUSG00000021843
AA Change: W1117*

DomainStartEndE-ValueType
signal peptide 1 39 N/A INTRINSIC
coiled coil region 40 66 N/A INTRINSIC
low complexity region 108 127 N/A INTRINSIC
low complexity region 150 173 N/A INTRINSIC
low complexity region 203 221 N/A INTRINSIC
coiled coil region 329 372 N/A INTRINSIC
coiled coil region 402 727 N/A INTRINSIC
coiled coil region 764 792 N/A INTRINSIC
low complexity region 816 825 N/A INTRINSIC
coiled coil region 836 1005 N/A INTRINSIC
coiled coil region 1066 1244 N/A INTRINSIC
coiled coil region 1279 1303 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000188049
Predicted Effect probably benign
Transcript: ENSMUST00000189986
SMART Domains Protein: ENSMUSP00000139970
Gene: ENSMUSG00000021843

DomainStartEndE-ValueType
Pfam:Rib_recp_KP_reg 29 172 2.1e-7 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000190999
AA Change: W1088*
SMART Domains Protein: ENSMUSP00000139673
Gene: ENSMUSG00000021843
AA Change: W1088*

DomainStartEndE-ValueType
signal peptide 1 39 N/A INTRINSIC
coiled coil region 40 66 N/A INTRINSIC
low complexity region 108 127 N/A INTRINSIC
low complexity region 150 173 N/A INTRINSIC
low complexity region 203 221 N/A INTRINSIC
coiled coil region 329 372 N/A INTRINSIC
coiled coil region 402 727 N/A INTRINSIC
coiled coil region 764 792 N/A INTRINSIC
low complexity region 816 825 N/A INTRINSIC
coiled coil region 836 993 N/A INTRINSIC
coiled coil region 1037 1215 N/A INTRINSIC
coiled coil region 1250 1274 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000191018
AA Change: W1117*
SMART Domains Protein: ENSMUSP00000139585
Gene: ENSMUSG00000021843
AA Change: W1117*

DomainStartEndE-ValueType
signal peptide 1 39 N/A INTRINSIC
coiled coil region 40 66 N/A INTRINSIC
low complexity region 108 127 N/A INTRINSIC
low complexity region 150 173 N/A INTRINSIC
low complexity region 203 221 N/A INTRINSIC
coiled coil region 329 372 N/A INTRINSIC
coiled coil region 402 727 N/A INTRINSIC
coiled coil region 764 792 N/A INTRINSIC
low complexity region 816 825 N/A INTRINSIC
coiled coil region 836 1005 N/A INTRINSIC
coiled coil region 1066 1220 N/A INTRINSIC
coiled coil region 1255 1279 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000191446
AA Change: W1140*
SMART Domains Protein: ENSMUSP00000140748
Gene: ENSMUSG00000021843
AA Change: W1140*

DomainStartEndE-ValueType
signal peptide 1 39 N/A INTRINSIC
coiled coil region 40 66 N/A INTRINSIC
low complexity region 108 127 N/A INTRINSIC
low complexity region 150 173 N/A INTRINSIC
low complexity region 203 221 N/A INTRINSIC
coiled coil region 329 372 N/A INTRINSIC
coiled coil region 402 727 N/A INTRINSIC
coiled coil region 764 1028 N/A INTRINSIC
coiled coil region 1089 1215 N/A INTRINSIC
coiled coil region 1250 1274 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000191511
AA Change: W1117*
SMART Domains Protein: ENSMUSP00000139946
Gene: ENSMUSG00000021843
AA Change: W1117*

DomainStartEndE-ValueType
signal peptide 1 39 N/A INTRINSIC
coiled coil region 40 66 N/A INTRINSIC
low complexity region 108 127 N/A INTRINSIC
low complexity region 150 173 N/A INTRINSIC
low complexity region 203 221 N/A INTRINSIC
coiled coil region 329 372 N/A INTRINSIC
coiled coil region 402 727 N/A INTRINSIC
coiled coil region 764 792 N/A INTRINSIC
low complexity region 816 825 N/A INTRINSIC
coiled coil region 836 1005 N/A INTRINSIC
coiled coil region 1066 1192 N/A INTRINSIC
coiled coil region 1227 1251 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000190857
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.6%
  • 10x: 97.2%
  • 20x: 95.0%
Validation Efficiency 100% (50/50)
MGI Phenotype PHENOTYPE: Mice homozygous for a targeted null mutation or a floxed allele exhibit no discernable phenotype; mice are viable and fertile up to one year of age. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 47 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930503E14Rik T A 14: 44,406,690 (GRCm39) M120L probably benign Het
Aco2 A G 15: 81,773,584 (GRCm39) probably null Het
Acss1 A G 2: 150,501,823 (GRCm39) S115P possibly damaging Het
Ank2 A T 3: 127,019,411 (GRCm39) probably null Het
AU041133 C T 10: 81,987,316 (GRCm39) T323M probably damaging Het
Bdp1 T C 13: 100,167,369 (GRCm39) D2215G probably damaging Het
Bod1l G A 5: 41,977,870 (GRCm39) T1148I probably benign Het
Celsr1 C T 15: 85,847,334 (GRCm39) V1468I probably benign Het
Celsr1 A G 15: 85,812,200 (GRCm39) V2065A probably damaging Het
Cep89 A G 7: 35,115,822 (GRCm39) probably benign Het
Cfap58 A G 19: 47,941,480 (GRCm39) K283E possibly damaging Het
Cog5 C T 12: 31,710,853 (GRCm39) Q78* probably null Het
Col20a1 C T 2: 180,643,043 (GRCm39) R796C possibly damaging Het
Dnah7b A T 1: 46,165,840 (GRCm39) T502S probably benign Het
Dnm1l A G 16: 16,160,559 (GRCm39) probably null Het
Dse A T 10: 34,028,632 (GRCm39) F819L probably benign Het
Eloa G T 4: 135,738,553 (GRCm39) L136I possibly damaging Het
Eloa T A 4: 135,738,576 (GRCm39) H128L probably benign Het
Fbxl6 T C 15: 76,421,924 (GRCm39) E205G possibly damaging Het
Golim4 T G 3: 75,802,347 (GRCm39) N287T probably benign Het
Gpx8 T A 13: 113,179,682 (GRCm39) K206N possibly damaging Het
Iqgap3 G T 3: 88,004,293 (GRCm39) V460F probably benign Het
Kcne4 A T 1: 78,795,651 (GRCm39) M100L probably benign Het
Kmt2a A T 9: 44,721,077 (GRCm39) probably benign Het
Lad1 A G 1: 135,756,484 (GRCm39) D364G probably benign Het
Lmln T G 16: 32,930,220 (GRCm39) I559S probably benign Het
Mapk4 A T 18: 74,063,609 (GRCm39) F538I possibly damaging Het
Mlxipl A G 5: 135,166,253 (GRCm39) probably benign Het
Mmrn1 T C 6: 60,921,570 (GRCm39) L9P probably damaging Het
Mnat1 G A 12: 73,228,601 (GRCm39) R155H probably damaging Het
Mtmr11 T C 3: 96,075,207 (GRCm39) probably benign Het
Naaladl1 T C 19: 6,165,581 (GRCm39) L745P probably damaging Het
Obsl1 A T 1: 75,467,546 (GRCm39) D1409E probably benign Het
Oit3 T C 10: 59,263,925 (GRCm39) Y403C probably damaging Het
Pla2g4e A T 2: 120,013,194 (GRCm39) H375Q probably benign Het
Prodh2 G A 7: 30,205,877 (GRCm39) V238M probably damaging Het
Rdh14 G A 12: 10,441,231 (GRCm39) probably null Het
Rho G A 6: 115,912,191 (GRCm39) V76I probably benign Het
Rock1 A T 18: 10,080,514 (GRCm39) M1010K probably damaging Het
Ros1 A G 10: 52,038,800 (GRCm39) probably null Het
Sim1 A T 10: 50,857,708 (GRCm39) D486V probably benign Het
Spmip6 T C 4: 41,505,574 (GRCm39) T183A possibly damaging Het
Src A G 2: 157,306,573 (GRCm39) D192G probably damaging Het
Stox1 T C 10: 62,495,348 (GRCm39) N975S probably benign Het
Tmem145 A G 7: 25,006,554 (GRCm39) Y54C probably damaging Het
Try4 C T 6: 41,281,905 (GRCm39) P164S possibly damaging Het
Vegfc A T 8: 54,634,130 (GRCm39) N270Y probably benign Het
Other mutations in Ktn1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01017:Ktn1 APN 14 47,946,335 (GRCm39) missense probably benign 0.30
IGL01109:Ktn1 APN 14 47,952,178 (GRCm39) missense probably damaging 1.00
IGL02300:Ktn1 APN 14 47,927,517 (GRCm39) missense probably damaging 1.00
IGL02339:Ktn1 APN 14 47,920,835 (GRCm39) splice site probably benign
IGL02525:Ktn1 APN 14 47,962,200 (GRCm39) critical splice donor site probably null
IGL02565:Ktn1 APN 14 47,910,391 (GRCm39) splice site probably benign
IGL02678:Ktn1 APN 14 47,971,610 (GRCm39) critical splice acceptor site probably null
IGL03181:Ktn1 APN 14 47,970,741 (GRCm39) missense probably benign 0.19
IGL03393:Ktn1 APN 14 47,928,391 (GRCm39) missense probably damaging 1.00
PIT4520001:Ktn1 UTSW 14 47,923,774 (GRCm39) missense probably damaging 0.96
R0035:Ktn1 UTSW 14 47,967,836 (GRCm39) missense probably benign 0.07
R0035:Ktn1 UTSW 14 47,967,836 (GRCm39) missense probably benign 0.07
R0270:Ktn1 UTSW 14 47,952,119 (GRCm39) missense probably benign 0.00
R0370:Ktn1 UTSW 14 47,901,532 (GRCm39) missense probably benign 0.00
R0371:Ktn1 UTSW 14 47,961,460 (GRCm39) nonsense probably null
R0530:Ktn1 UTSW 14 47,970,700 (GRCm39) missense probably benign 0.14
R0531:Ktn1 UTSW 14 47,901,398 (GRCm39) missense probably damaging 0.98
R0611:Ktn1 UTSW 14 47,932,073 (GRCm39) missense probably benign
R0836:Ktn1 UTSW 14 47,938,519 (GRCm39) splice site probably null
R1076:Ktn1 UTSW 14 47,932,095 (GRCm39) missense probably damaging 0.99
R1522:Ktn1 UTSW 14 47,904,873 (GRCm39) missense probably damaging 1.00
R1554:Ktn1 UTSW 14 47,932,964 (GRCm39) missense probably damaging 1.00
R1992:Ktn1 UTSW 14 47,932,978 (GRCm39) missense probably damaging 1.00
R2040:Ktn1 UTSW 14 47,938,069 (GRCm39) splice site probably benign
R2080:Ktn1 UTSW 14 47,963,417 (GRCm39) missense probably damaging 1.00
R2110:Ktn1 UTSW 14 47,931,345 (GRCm39) missense possibly damaging 0.47
R2144:Ktn1 UTSW 14 47,952,109 (GRCm39) missense probably damaging 1.00
R3730:Ktn1 UTSW 14 47,938,606 (GRCm39) missense probably damaging 1.00
R3780:Ktn1 UTSW 14 47,943,860 (GRCm39) splice site probably benign
R3782:Ktn1 UTSW 14 47,943,860 (GRCm39) splice site probably benign
R4610:Ktn1 UTSW 14 47,963,636 (GRCm39) intron probably benign
R4784:Ktn1 UTSW 14 47,930,953 (GRCm39) critical splice donor site probably null
R4838:Ktn1 UTSW 14 47,963,413 (GRCm39) nonsense probably null
R4909:Ktn1 UTSW 14 47,943,917 (GRCm39) missense probably damaging 0.99
R4976:Ktn1 UTSW 14 47,907,756 (GRCm39) critical splice donor site probably null
R5110:Ktn1 UTSW 14 47,941,744 (GRCm39) splice site probably benign
R5257:Ktn1 UTSW 14 47,904,820 (GRCm39) missense probably benign 0.05
R5469:Ktn1 UTSW 14 47,928,377 (GRCm39) missense probably damaging 1.00
R5600:Ktn1 UTSW 14 47,927,490 (GRCm39) missense probably damaging 1.00
R5607:Ktn1 UTSW 14 47,971,554 (GRCm39) intron probably benign
R5608:Ktn1 UTSW 14 47,971,554 (GRCm39) intron probably benign
R5920:Ktn1 UTSW 14 47,961,481 (GRCm39) nonsense probably null
R6045:Ktn1 UTSW 14 47,914,253 (GRCm39) missense probably damaging 1.00
R6139:Ktn1 UTSW 14 47,963,672 (GRCm39) splice site probably null
R6282:Ktn1 UTSW 14 47,901,428 (GRCm39) missense probably damaging 1.00
R6654:Ktn1 UTSW 14 47,927,457 (GRCm39) missense probably damaging 1.00
R6957:Ktn1 UTSW 14 47,904,810 (GRCm39) nonsense probably null
R6959:Ktn1 UTSW 14 47,957,713 (GRCm39) missense probably damaging 1.00
R7170:Ktn1 UTSW 14 47,943,867 (GRCm39) missense probably damaging 1.00
R7206:Ktn1 UTSW 14 47,932,985 (GRCm39) missense probably damaging 0.97
R7442:Ktn1 UTSW 14 47,952,097 (GRCm39) missense probably benign 0.01
R7462:Ktn1 UTSW 14 47,932,089 (GRCm39) missense probably null 1.00
R7513:Ktn1 UTSW 14 47,901,541 (GRCm39) missense possibly damaging 0.77
R7743:Ktn1 UTSW 14 47,907,750 (GRCm39) missense probably damaging 1.00
R8010:Ktn1 UTSW 14 47,943,230 (GRCm39) missense possibly damaging 0.60
R8062:Ktn1 UTSW 14 47,962,429 (GRCm39) critical splice donor site probably null
R8244:Ktn1 UTSW 14 47,912,280 (GRCm39) missense probably null 1.00
R8387:Ktn1 UTSW 14 47,944,744 (GRCm39) splice site probably null
R8724:Ktn1 UTSW 14 47,931,335 (GRCm39) missense probably benign 0.00
R8725:Ktn1 UTSW 14 47,907,757 (GRCm39) critical splice donor site probably benign
R8962:Ktn1 UTSW 14 47,901,248 (GRCm39) missense probably damaging 1.00
R9001:Ktn1 UTSW 14 47,910,409 (GRCm39) missense probably damaging 0.99
R9072:Ktn1 UTSW 14 47,941,694 (GRCm39) missense probably benign 0.25
R9324:Ktn1 UTSW 14 47,948,353 (GRCm39) missense probably benign 0.02
R9423:Ktn1 UTSW 14 47,912,318 (GRCm39) missense probably benign 0.00
R9479:Ktn1 UTSW 14 47,962,174 (GRCm39) missense probably damaging 0.98
R9674:Ktn1 UTSW 14 47,922,213 (GRCm39) missense possibly damaging 0.77
R9718:Ktn1 UTSW 14 47,910,508 (GRCm39) missense probably damaging 0.98
Z1177:Ktn1 UTSW 14 47,929,895 (GRCm39) critical splice acceptor site probably null
Predicted Primers PCR Primer
(F):5'- GTCGGTCCTTGCAGAAACAG -3'
(R):5'- GACTTTCAAATGGGTCAACATCAAG -3'

Sequencing Primer
(F):5'- TCCTTGCAGAAACAGTAGGATATGGC -3'
(R):5'- GTCAACATCAAGACCACCTCAG -3'
Posted On 2015-07-07