Incidental Mutation 'R7248:Ncor1'
ID 563700
Institutional Source Beutler Lab
Gene Symbol Ncor1
Ensembl Gene ENSMUSG00000018501
Gene Name nuclear receptor co-repressor 1
Synonyms Rxrip13, 5730405M06Rik, A230020K14Rik, N-CoR
MMRRC Submission 045311-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R7248 (G1)
Quality Score 225.009
Status Validated
Chromosome 11
Chromosomal Location 62207132-62348200 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 62275598 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Arginine at position 128 (K128R)
Ref Sequence ENSEMBL: ENSMUSP00000125317 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000018645] [ENSMUST00000101066] [ENSMUST00000101067] [ENSMUST00000127471] [ENSMUST00000151498] [ENSMUST00000155486]
AlphaFold no structure available at present
Predicted Effect possibly damaging
Transcript: ENSMUST00000018645
AA Change: K528R

PolyPhen 2 Score 0.635 (Sensitivity: 0.87; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000018645
Gene: ENSMUSG00000018501
AA Change: K528R

DomainStartEndE-ValueType
low complexity region 51 74 N/A INTRINSIC
Pfam:GPS2_interact 150 239 1.4e-37 PFAM
coiled coil region 302 329 N/A INTRINSIC
low complexity region 349 366 N/A INTRINSIC
SANT 437 485 2.76e-7 SMART
coiled coil region 507 544 N/A INTRINSIC
low complexity region 593 617 N/A INTRINSIC
SANT 624 672 3.29e-14 SMART
low complexity region 710 731 N/A INTRINSIC
low complexity region 771 788 N/A INTRINSIC
low complexity region 888 899 N/A INTRINSIC
low complexity region 987 995 N/A INTRINSIC
low complexity region 1002 1013 N/A INTRINSIC
low complexity region 1036 1049 N/A INTRINSIC
internal_repeat_2 1061 1298 1.62e-6 PROSPERO
internal_repeat_2 1299 1515 1.62e-6 PROSPERO
low complexity region 1516 1527 N/A INTRINSIC
coiled coil region 1712 1749 N/A INTRINSIC
low complexity region 1834 1848 N/A INTRINSIC
low complexity region 1969 1980 N/A INTRINSIC
low complexity region 2036 2055 N/A INTRINSIC
PDB:3N00|B 2064 2084 4e-7 PDB
low complexity region 2086 2101 N/A INTRINSIC
low complexity region 2157 2168 N/A INTRINSIC
PDB:2OVM|B 2267 2290 2e-8 PDB
low complexity region 2311 2324 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000101066
AA Change: K528R

PolyPhen 2 Score 0.635 (Sensitivity: 0.87; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000098627
Gene: ENSMUSG00000018501
AA Change: K528R

DomainStartEndE-ValueType
low complexity region 51 74 N/A INTRINSIC
coiled coil region 176 217 N/A INTRINSIC
coiled coil region 302 329 N/A INTRINSIC
low complexity region 349 366 N/A INTRINSIC
SANT 437 485 2.76e-7 SMART
coiled coil region 507 544 N/A INTRINSIC
low complexity region 593 617 N/A INTRINSIC
SANT 624 672 3.29e-14 SMART
low complexity region 710 731 N/A INTRINSIC
low complexity region 771 788 N/A INTRINSIC
low complexity region 888 899 N/A INTRINSIC
low complexity region 987 995 N/A INTRINSIC
low complexity region 1002 1013 N/A INTRINSIC
low complexity region 1036 1049 N/A INTRINSIC
internal_repeat_2 1061 1298 1.62e-6 PROSPERO
internal_repeat_2 1299 1515 1.62e-6 PROSPERO
low complexity region 1516 1527 N/A INTRINSIC
coiled coil region 1712 1749 N/A INTRINSIC
low complexity region 1834 1848 N/A INTRINSIC
low complexity region 1969 1980 N/A INTRINSIC
low complexity region 2036 2055 N/A INTRINSIC
PDB:3N00|B 2064 2084 4e-7 PDB
low complexity region 2086 2101 N/A INTRINSIC
low complexity region 2157 2168 N/A INTRINSIC
PDB:2OVM|B 2267 2290 2e-8 PDB
low complexity region 2311 2324 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000101067
AA Change: K528R

PolyPhen 2 Score 0.635 (Sensitivity: 0.87; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000098628
Gene: ENSMUSG00000018501
AA Change: K528R

DomainStartEndE-ValueType
low complexity region 51 74 N/A INTRINSIC
coiled coil region 176 217 N/A INTRINSIC
coiled coil region 302 329 N/A INTRINSIC
low complexity region 349 366 N/A INTRINSIC
SANT 437 485 2.76e-7 SMART
coiled coil region 507 544 N/A INTRINSIC
low complexity region 593 617 N/A INTRINSIC
SANT 624 672 3.29e-14 SMART
low complexity region 716 734 N/A INTRINSIC
low complexity region 838 849 N/A INTRINSIC
low complexity region 937 945 N/A INTRINSIC
low complexity region 952 963 N/A INTRINSIC
low complexity region 986 999 N/A INTRINSIC
low complexity region 1448 1459 N/A INTRINSIC
coiled coil region 1645 1682 N/A INTRINSIC
low complexity region 1767 1781 N/A INTRINSIC
low complexity region 1902 1913 N/A INTRINSIC
low complexity region 1969 1988 N/A INTRINSIC
PDB:3N00|B 1997 2017 4e-7 PDB
low complexity region 2019 2034 N/A INTRINSIC
low complexity region 2089 2100 N/A INTRINSIC
PDB:2OVM|B 2199 2222 2e-8 PDB
low complexity region 2243 2256 N/A INTRINSIC
Predicted Effect probably damaging
Transcript: ENSMUST00000127471
AA Change: K529R

PolyPhen 2 Score 0.972 (Sensitivity: 0.77; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000121806
Gene: ENSMUSG00000018501
AA Change: K529R

DomainStartEndE-ValueType
low complexity region 51 74 N/A INTRINSIC
coiled coil region 176 217 N/A INTRINSIC
coiled coil region 302 329 N/A INTRINSIC
low complexity region 349 366 N/A INTRINSIC
SANT 437 485 2.76e-7 SMART
coiled coil region 508 545 N/A INTRINSIC
low complexity region 594 618 N/A INTRINSIC
SANT 625 673 3.29e-14 SMART
low complexity region 711 732 N/A INTRINSIC
low complexity region 756 773 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000151498
AA Change: K128R

PolyPhen 2 Score 0.892 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000125317
Gene: ENSMUSG00000018501
AA Change: K128R

DomainStartEndE-ValueType
SANT 37 85 2.76e-7 SMART
coiled coil region 107 144 N/A INTRINSIC
low complexity region 193 217 N/A INTRINSIC
SANT 224 272 3.29e-14 SMART
low complexity region 316 337 N/A INTRINSIC
low complexity region 361 378 N/A INTRINSIC
low complexity region 478 489 N/A INTRINSIC
low complexity region 577 585 N/A INTRINSIC
low complexity region 592 603 N/A INTRINSIC
low complexity region 684 697 N/A INTRINSIC
internal_repeat_2 700 830 5.77e-7 PROSPERO
internal_repeat_2 855 961 5.77e-7 PROSPERO
Predicted Effect unknown
Transcript: ENSMUST00000155486
AA Change: K537R
SMART Domains Protein: ENSMUSP00000122647
Gene: ENSMUSG00000018501
AA Change: K537R

DomainStartEndE-ValueType
low complexity region 51 74 N/A INTRINSIC
coiled coil region 176 217 N/A INTRINSIC
coiled coil region 311 338 N/A INTRINSIC
low complexity region 358 375 N/A INTRINSIC
SANT 446 494 2.76e-7 SMART
coiled coil region 516 541 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000161288
SMART Domains Protein: ENSMUSP00000124045
Gene: ENSMUSG00000018501

DomainStartEndE-ValueType
SANT 22 70 3.29e-14 SMART
low complexity region 114 135 N/A INTRINSIC
low complexity region 159 176 N/A INTRINSIC
Predicted Effect
SMART Domains Protein: ENSMUSP00000124120
Gene: ENSMUSG00000018501
AA Change: K24R

DomainStartEndE-ValueType
coiled coil region 3 40 N/A INTRINSIC
low complexity region 90 114 N/A INTRINSIC
SANT 121 169 3.29e-14 SMART
low complexity region 207 225 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000162236
SMART Domains Protein: ENSMUSP00000124698
Gene: ENSMUSG00000018501

DomainStartEndE-ValueType
low complexity region 1 14 N/A INTRINSIC
low complexity region 41 65 N/A INTRINSIC
SANT 72 120 3.29e-14 SMART
low complexity region 164 185 N/A INTRINSIC
low complexity region 225 242 N/A INTRINSIC
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.5%
  • 20x: 98.4%
Validation Efficiency 97% (75/77)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein that mediates ligand-independent transcription repression of thyroid-hormone and retinoic-acid receptors by promoting chromatin condensation and preventing access of the transcription machinery. It is part of a complex which also includes histone deacetylases and transcriptional regulators similar to the yeast protein Sin3p. This gene is located between the Charcot-Marie-Tooth and Smith-Magenis syndrome critical regions on chromosome 17. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 17 and 20.[provided by RefSeq, Jun 2010]
PHENOTYPE: Mice homozygous for a targeted mutation in this gene exhibit embryonic lethality with erythrocytic, thymocytic and central nervous system development abnormalities. Mice homozygous for a hypomorphic allele exhibit increased thyroid hormone sensitivity under hypothyroid conditions. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 76 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700006A11Rik A G 3: 124,207,959 (GRCm39) probably null Het
Aldh16a1 A G 7: 44,795,018 (GRCm39) Y484H probably damaging Het
Arhgap26 T C 18: 39,439,907 (GRCm39) probably null Het
Atxn7l1 A G 12: 33,417,194 (GRCm39) T452A probably benign Het
Baz1a C T 12: 54,947,293 (GRCm39) E1119K probably damaging Het
Btaf1 A T 19: 36,922,714 (GRCm39) E39D possibly damaging Het
Bud13 G T 9: 46,194,413 (GRCm39) E29* probably null Het
Ccdc150 C T 1: 54,344,057 (GRCm39) T530I probably benign Het
Chd6 G A 2: 160,803,199 (GRCm39) Q2160* probably null Het
Cluap1 T A 16: 3,737,364 (GRCm39) I172N possibly damaging Het
Cnot2 T C 10: 116,334,278 (GRCm39) N329S probably benign Het
Cog4 A T 8: 111,608,834 (GRCm39) T175S unknown Het
Coq7 C A 7: 118,128,897 (GRCm39) R46L probably benign Het
D630045J12Rik A T 6: 38,145,198 (GRCm39) V1276E probably damaging Het
Dcaf15 A G 8: 84,829,394 (GRCm39) V116A possibly damaging Het
Ddr2 C T 1: 169,822,198 (GRCm39) V417I probably benign Het
Defa25 G A 8: 21,575,216 (GRCm39) C65Y probably damaging Het
Dhx38 T C 8: 110,285,559 (GRCm39) T425A probably benign Het
Diaph1 T C 18: 38,022,829 (GRCm39) T782A probably benign Het
Dnah7b T A 1: 46,181,245 (GRCm39) M1044K possibly damaging Het
Dusp16 G A 6: 134,695,940 (GRCm39) T297M probably benign Het
Esyt2 A G 12: 116,305,858 (GRCm39) N363D probably damaging Het
Fasl C T 1: 161,615,760 (GRCm39) C32Y possibly damaging Het
Flg T C 3: 93,189,041 (GRCm39) V137A probably benign Het
Gm57858 T A 3: 36,080,086 (GRCm39) T224S probably benign Het
Gpr150 G A 13: 76,204,126 (GRCm39) A273V probably benign Het
Grk5 A G 19: 60,879,045 (GRCm39) T10A probably benign Het
Hivep2 A G 10: 14,006,909 (GRCm39) K1169R possibly damaging Het
Ido2 A C 8: 25,030,657 (GRCm39) Y224* probably null Het
Ido2 A G 8: 25,038,839 (GRCm39) I149T probably damaging Het
Iqca1l C T 5: 24,749,269 (GRCm39) S743N probably benign Het
Kctd2 A G 11: 115,312,845 (GRCm39) T126A possibly damaging Het
Khdc4 T C 3: 88,600,886 (GRCm39) S228P probably damaging Het
Kif1a T C 1: 92,969,305 (GRCm39) D1090G probably benign Het
Klrb1a A T 6: 128,586,697 (GRCm39) H222Q possibly damaging Het
Kndc1 A C 7: 139,500,699 (GRCm39) H688P probably damaging Het
Lrriq1 C A 10: 103,059,611 (GRCm39) V141F possibly damaging Het
Malrd1 A G 2: 16,106,722 (GRCm39) I1845V unknown Het
Mob3c G A 4: 115,688,881 (GRCm39) R138H probably benign Het
Mre11a T A 9: 14,723,209 (GRCm39) D394E possibly damaging Het
Myh7b A T 2: 155,464,106 (GRCm39) I536F probably damaging Het
Nacad T A 11: 6,548,589 (GRCm39) K1382* probably null Het
Or10am5 T C 7: 6,517,520 (GRCm39) N303D probably damaging Het
Ostn T A 16: 27,165,719 (GRCm39) probably null Het
Pacs1 G A 19: 5,189,003 (GRCm39) T793I probably damaging Het
Pcdhb2 T C 18: 37,429,547 (GRCm39) S507P probably damaging Het
Pde2a A G 7: 101,152,597 (GRCm39) K393E possibly damaging Het
Pfkl T A 10: 77,825,423 (GRCm39) N656Y probably damaging Het
Phf20 T A 2: 156,135,331 (GRCm39) probably null Het
Plekha6 G T 1: 133,203,586 (GRCm39) E550* probably null Het
Plxna4 A T 6: 32,139,095 (GRCm39) V1691E probably damaging Het
Rag1 A T 2: 101,472,123 (GRCm39) H1006Q probably damaging Het
Rfx4 C T 10: 84,740,919 (GRCm39) P679L probably benign Het
Ripor2 A G 13: 24,878,128 (GRCm39) H301R probably damaging Het
Rrp12 A T 19: 41,871,877 (GRCm39) I469N possibly damaging Het
Serpinb6b A G 13: 33,161,559 (GRCm39) T211A probably benign Het
Sf1 A T 19: 6,426,383 (GRCm39) H547L unknown Het
Slc29a1 T C 17: 45,903,108 (GRCm39) D9G probably damaging Het
Sptan1 T A 2: 29,892,311 (GRCm39) M1075K probably benign Het
Syngap1 A G 17: 27,176,741 (GRCm39) D474G probably damaging Het
Syt16 C T 12: 74,313,483 (GRCm39) R470C probably damaging Het
Timeless A G 10: 128,087,870 (GRCm39) T1148A probably benign Het
Tmem116 A T 5: 121,601,899 (GRCm39) probably null Het
Tmem158 A T 9: 123,089,390 (GRCm39) I74N probably damaging Het
Traf5 T A 1: 191,743,432 (GRCm39) D174V probably benign Het
Trim65 A T 11: 116,018,534 (GRCm39) I247N probably benign Het
Tsfm A T 10: 126,847,500 (GRCm39) V197E probably benign Het
Utrn A G 10: 12,604,562 (GRCm39) C539R possibly damaging Het
Vps13a A T 19: 16,655,406 (GRCm39) F1874Y probably benign Het
Wdr6 A G 9: 108,453,238 (GRCm39) M215T possibly damaging Het
Wdr75 T A 1: 45,856,560 (GRCm39) W528R probably damaging Het
Zc3h7b A G 15: 81,655,988 (GRCm39) D112G possibly damaging Het
Zc3hav1 C T 6: 38,330,911 (GRCm39) D83N probably benign Het
Zfp369 T A 13: 65,443,931 (GRCm39) V358E probably damaging Het
Zfp946 T A 17: 22,672,489 (GRCm39) C29* probably null Het
Zng1 A G 19: 24,898,505 (GRCm39) S318P probably damaging Het
Other mutations in Ncor1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01067:Ncor1 APN 11 62,283,354 (GRCm39) missense probably damaging 1.00
IGL01343:Ncor1 APN 11 62,216,312 (GRCm39) critical splice donor site probably null
IGL01392:Ncor1 APN 11 62,231,420 (GRCm39) missense probably damaging 0.99
IGL01402:Ncor1 APN 11 62,231,300 (GRCm39) missense probably damaging 1.00
IGL01714:Ncor1 APN 11 62,225,410 (GRCm39) missense possibly damaging 0.58
IGL01772:Ncor1 APN 11 62,240,173 (GRCm39) intron probably benign
IGL01889:Ncor1 APN 11 62,225,427 (GRCm39) missense possibly damaging 0.69
IGL02058:Ncor1 APN 11 62,235,463 (GRCm39) missense probably damaging 1.00
IGL02065:Ncor1 APN 11 62,310,435 (GRCm39) missense possibly damaging 0.95
IGL02073:Ncor1 APN 11 62,249,743 (GRCm39) missense probably damaging 0.99
IGL02176:Ncor1 APN 11 62,220,485 (GRCm39) unclassified probably benign
IGL02288:Ncor1 APN 11 62,240,229 (GRCm39) missense probably benign 0.01
IGL02348:Ncor1 APN 11 62,224,485 (GRCm39) splice site probably benign
IGL02608:Ncor1 APN 11 62,264,040 (GRCm39) missense probably benign 0.07
laggard UTSW 11 62,260,130 (GRCm39) missense probably damaging 1.00
Shortstep UTSW 11 62,225,367 (GRCm39) missense probably damaging 1.00
LCD18:Ncor1 UTSW 11 62,419,782 (GRCm38) critical splice acceptor site probably benign
PIT4382001:Ncor1 UTSW 11 62,235,489 (GRCm39) missense probably damaging 0.96
PIT4576001:Ncor1 UTSW 11 62,224,543 (GRCm39) missense probably damaging 0.99
R0026:Ncor1 UTSW 11 62,329,255 (GRCm39) missense probably damaging 1.00
R0038:Ncor1 UTSW 11 62,283,377 (GRCm39) missense probably damaging 0.99
R0038:Ncor1 UTSW 11 62,283,377 (GRCm39) missense probably damaging 0.99
R0103:Ncor1 UTSW 11 62,233,871 (GRCm39) missense possibly damaging 0.85
R0103:Ncor1 UTSW 11 62,233,871 (GRCm39) missense possibly damaging 0.85
R0144:Ncor1 UTSW 11 62,283,421 (GRCm39) missense probably damaging 1.00
R0427:Ncor1 UTSW 11 62,301,746 (GRCm39) missense probably damaging 1.00
R0501:Ncor1 UTSW 11 62,264,148 (GRCm39) missense possibly damaging 0.73
R0544:Ncor1 UTSW 11 62,224,603 (GRCm39) missense probably damaging 1.00
R0544:Ncor1 UTSW 11 62,224,602 (GRCm39) missense probably damaging 1.00
R0563:Ncor1 UTSW 11 62,234,056 (GRCm39) missense probably damaging 0.97
R1074:Ncor1 UTSW 11 62,283,377 (GRCm39) missense probably damaging 0.99
R1266:Ncor1 UTSW 11 62,224,866 (GRCm39) missense probably damaging 0.98
R1444:Ncor1 UTSW 11 62,294,632 (GRCm39) missense probably damaging 1.00
R1452:Ncor1 UTSW 11 62,225,457 (GRCm39) missense probably damaging 1.00
R1534:Ncor1 UTSW 11 62,269,330 (GRCm39) missense possibly damaging 0.92
R1710:Ncor1 UTSW 11 62,313,831 (GRCm39) missense probably damaging 1.00
R1762:Ncor1 UTSW 11 62,275,610 (GRCm39) missense possibly damaging 0.82
R1771:Ncor1 UTSW 11 62,217,938 (GRCm39) missense probably damaging 1.00
R1864:Ncor1 UTSW 11 62,272,245 (GRCm39) missense probably damaging 1.00
R1902:Ncor1 UTSW 11 62,228,984 (GRCm39) missense probably damaging 1.00
R1906:Ncor1 UTSW 11 62,240,211 (GRCm39) missense possibly damaging 0.81
R2009:Ncor1 UTSW 11 62,216,427 (GRCm39) missense probably benign 0.43
R3708:Ncor1 UTSW 11 62,235,513 (GRCm39) missense probably damaging 1.00
R3825:Ncor1 UTSW 11 62,264,183 (GRCm39) missense probably benign 0.00
R3923:Ncor1 UTSW 11 62,216,442 (GRCm39) missense probably damaging 1.00
R3966:Ncor1 UTSW 11 62,235,583 (GRCm39) missense probably damaging 1.00
R4049:Ncor1 UTSW 11 62,220,494 (GRCm39) splice site probably null
R4350:Ncor1 UTSW 11 62,301,644 (GRCm39) critical splice donor site probably null
R4351:Ncor1 UTSW 11 62,301,644 (GRCm39) critical splice donor site probably null
R4359:Ncor1 UTSW 11 62,249,736 (GRCm39) missense probably damaging 1.00
R4712:Ncor1 UTSW 11 62,235,660 (GRCm39) missense probably damaging 1.00
R4723:Ncor1 UTSW 11 62,269,438 (GRCm39) missense probably benign 0.26
R4863:Ncor1 UTSW 11 62,283,464 (GRCm39) missense possibly damaging 0.92
R4875:Ncor1 UTSW 11 62,324,437 (GRCm39) small deletion probably benign
R4956:Ncor1 UTSW 11 62,231,431 (GRCm39) missense probably damaging 1.00
R4993:Ncor1 UTSW 11 62,234,167 (GRCm39) missense probably damaging 1.00
R5079:Ncor1 UTSW 11 62,236,063 (GRCm39) missense possibly damaging 0.92
R5144:Ncor1 UTSW 11 62,240,290 (GRCm39) missense probably damaging 1.00
R5223:Ncor1 UTSW 11 62,229,826 (GRCm39) missense probably damaging 1.00
R5243:Ncor1 UTSW 11 62,229,788 (GRCm39) missense probably damaging 1.00
R5271:Ncor1 UTSW 11 62,231,371 (GRCm39) missense probably damaging 1.00
R5285:Ncor1 UTSW 11 62,283,475 (GRCm39) missense probably damaging 1.00
R5533:Ncor1 UTSW 11 62,233,837 (GRCm39) missense probably benign 0.00
R5580:Ncor1 UTSW 11 62,280,604 (GRCm39) nonsense probably null
R5593:Ncor1 UTSW 11 62,260,130 (GRCm39) missense probably damaging 1.00
R5609:Ncor1 UTSW 11 62,249,679 (GRCm39) splice site probably null
R5632:Ncor1 UTSW 11 62,229,060 (GRCm39) missense possibly damaging 0.85
R5830:Ncor1 UTSW 11 62,235,589 (GRCm39) missense possibly damaging 0.71
R5896:Ncor1 UTSW 11 62,274,016 (GRCm39) missense probably damaging 1.00
R5973:Ncor1 UTSW 11 62,240,136 (GRCm39) splice site probably null
R6013:Ncor1 UTSW 11 62,211,903 (GRCm39) missense probably benign
R6019:Ncor1 UTSW 11 62,263,987 (GRCm39) missense probably benign 0.00
R6032:Ncor1 UTSW 11 62,264,147 (GRCm39) missense possibly damaging 0.54
R6032:Ncor1 UTSW 11 62,264,147 (GRCm39) missense possibly damaging 0.54
R6075:Ncor1 UTSW 11 62,208,675 (GRCm39) missense probably damaging 1.00
R6091:Ncor1 UTSW 11 62,310,443 (GRCm39) missense probably damaging 0.98
R6248:Ncor1 UTSW 11 62,257,808 (GRCm39) missense probably damaging 1.00
R6281:Ncor1 UTSW 11 62,264,371 (GRCm39) missense possibly damaging 0.71
R6351:Ncor1 UTSW 11 62,264,124 (GRCm39) missense probably benign 0.30
R6469:Ncor1 UTSW 11 62,234,128 (GRCm39) missense probably damaging 1.00
R6502:Ncor1 UTSW 11 62,272,240 (GRCm39) nonsense probably null
R6614:Ncor1 UTSW 11 62,221,645 (GRCm39) missense probably benign 0.01
R6650:Ncor1 UTSW 11 62,225,367 (GRCm39) missense probably damaging 1.00
R6765:Ncor1 UTSW 11 62,264,272 (GRCm39) missense probably benign 0.01
R6852:Ncor1 UTSW 11 62,234,071 (GRCm39) missense probably damaging 0.97
R6909:Ncor1 UTSW 11 62,220,312 (GRCm39) missense probably damaging 1.00
R6965:Ncor1 UTSW 11 62,244,059 (GRCm39) critical splice donor site probably null
R7054:Ncor1 UTSW 11 62,275,619 (GRCm39) missense probably null
R7352:Ncor1 UTSW 11 62,224,737 (GRCm39) missense probably damaging 0.99
R7396:Ncor1 UTSW 11 62,234,044 (GRCm39) missense probably damaging 0.99
R7434:Ncor1 UTSW 11 62,274,025 (GRCm39) missense probably damaging 0.99
R7552:Ncor1 UTSW 11 62,264,250 (GRCm39) missense possibly damaging 0.53
R7565:Ncor1 UTSW 11 62,292,091 (GRCm39) missense probably damaging 1.00
R7575:Ncor1 UTSW 11 62,274,082 (GRCm39) missense probably benign 0.21
R7622:Ncor1 UTSW 11 62,208,794 (GRCm39) missense probably benign 0.00
R7664:Ncor1 UTSW 11 62,289,154 (GRCm39) missense probably damaging 1.00
R7814:Ncor1 UTSW 11 62,224,752 (GRCm39) missense probably damaging 0.99
R7963:Ncor1 UTSW 11 62,225,359 (GRCm39) missense probably benign 0.28
R7990:Ncor1 UTSW 11 62,240,321 (GRCm39) critical splice acceptor site probably null
R8302:Ncor1 UTSW 11 62,224,681 (GRCm39) missense probably benign 0.00
R8334:Ncor1 UTSW 11 62,274,070 (GRCm39) missense probably damaging 0.99
R8512:Ncor1 UTSW 11 62,324,437 (GRCm39) small deletion probably benign
R8728:Ncor1 UTSW 11 62,221,685 (GRCm39) missense probably benign 0.04
R8777:Ncor1 UTSW 11 62,324,494 (GRCm39) missense probably damaging 1.00
R8777:Ncor1 UTSW 11 62,324,492 (GRCm39) missense probably benign 0.03
R8777-TAIL:Ncor1 UTSW 11 62,324,494 (GRCm39) missense probably damaging 1.00
R8777-TAIL:Ncor1 UTSW 11 62,324,492 (GRCm39) missense probably benign 0.03
R8821:Ncor1 UTSW 11 62,260,234 (GRCm39) missense probably benign 0.07
R8831:Ncor1 UTSW 11 62,260,234 (GRCm39) missense probably benign 0.07
R8988:Ncor1 UTSW 11 62,233,871 (GRCm39) nonsense probably null
R9111:Ncor1 UTSW 11 62,280,585 (GRCm39) missense possibly damaging 0.95
R9147:Ncor1 UTSW 11 62,224,672 (GRCm39) missense probably damaging 1.00
R9391:Ncor1 UTSW 11 62,216,376 (GRCm39) nonsense probably null
R9467:Ncor1 UTSW 11 62,324,448 (GRCm39) small insertion probably benign
R9467:Ncor1 UTSW 11 62,324,437 (GRCm39) small insertion probably benign
R9510:Ncor1 UTSW 11 62,324,442 (GRCm39) small insertion probably benign
R9511:Ncor1 UTSW 11 62,324,449 (GRCm39) small insertion probably benign
R9560:Ncor1 UTSW 11 62,263,948 (GRCm39) missense possibly damaging 0.96
R9687:Ncor1 UTSW 11 62,260,193 (GRCm39) missense possibly damaging 0.93
X0065:Ncor1 UTSW 11 62,249,817 (GRCm39) missense probably benign 0.23
X0065:Ncor1 UTSW 11 62,245,395 (GRCm39) critical splice donor site probably null
Z1176:Ncor1 UTSW 11 62,329,342 (GRCm39) critical splice acceptor site probably null
Predicted Primers PCR Primer
(F):5'- CATCCCTGCAAAATAAGGTCG -3'
(R):5'- CTCCCCAATAATGTTGTTCCAAG -3'

Sequencing Primer
(F):5'- CCCAGTACTAGATTTAAAGGCCTGTG -3'
(R):5'- TTCTAGCAGCAGATTGCC -3'
Posted On 2019-06-26