Incidental Mutation 'R6248:Ncor1'
ID 505619
Institutional Source Beutler Lab
Gene Symbol Ncor1
Ensembl Gene ENSMUSG00000018501
Gene Name nuclear receptor co-repressor 1
Synonyms Rxrip13, 5730405M06Rik, A230020K14Rik, N-CoR
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R6248 (G1)
Quality Score 225.009
Status Validated
Chromosome 11
Chromosomal Location 62207132-62348200 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 62257808 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Proline to Serine at position 329 (P329S)
Ref Sequence ENSEMBL: ENSMUSP00000122654 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000018645] [ENSMUST00000101066] [ENSMUST00000101067] [ENSMUST00000151498] [ENSMUST00000155712]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000018645
AA Change: P1013S

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000018645
Gene: ENSMUSG00000018501
AA Change: P1013S

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 probably damaging
Transcript: ENSMUST00000101066
AA Change: P1013S

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000098627
Gene: ENSMUSG00000018501
AA Change: P1013S

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 probably damaging
Transcript: ENSMUST00000101067
AA Change: P963S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000098628
Gene: ENSMUSG00000018501
AA Change: P963S

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 noncoding transcript
Transcript: ENSMUST00000101068
Predicted Effect probably damaging
Transcript: ENSMUST00000151498
AA Change: P603S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000125317
Gene: ENSMUSG00000018501
AA Change: P603S

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 probably damaging
Transcript: ENSMUST00000155712
AA Change: P329S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000122654
Gene: ENSMUSG00000018501
AA Change: P329S

DomainStartEndE-ValueType
low complexity region 26 47 N/A INTRINSIC
low complexity region 87 104 N/A INTRINSIC
low complexity region 204 215 N/A INTRINSIC
low complexity region 303 311 N/A INTRINSIC
low complexity region 318 329 N/A INTRINSIC
low complexity region 352 365 N/A INTRINSIC
low complexity region 785 796 N/A INTRINSIC
coiled coil region 982 1019 N/A INTRINSIC
low complexity region 1104 1118 N/A INTRINSIC
low complexity region 1239 1250 N/A INTRINSIC
low complexity region 1306 1325 N/A INTRINSIC
PDB:3N00|B 1334 1354 3e-7 PDB
low complexity region 1356 1371 N/A INTRINSIC
low complexity region 1427 1438 N/A INTRINSIC
PDB:2OVM|B 1537 1560 2e-8 PDB
low complexity region 1581 1594 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000161116
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.0%
  • 20x: 94.2%
Validation Efficiency 100% (92/92)
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: 93 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930523C07Rik T C 1: 159,902,978 (GRCm39) S83P possibly damaging Het
Actr10 A T 12: 70,999,733 (GRCm39) E176D probably benign Het
Adcy3 G A 12: 4,258,662 (GRCm39) probably null Het
AI429214 T A 8: 37,461,278 (GRCm39) I142N probably damaging Het
Alox12 A G 11: 70,143,936 (GRCm39) L148S probably damaging Het
Ank3 A G 10: 69,809,680 (GRCm39) I1147V probably benign Het
Apoc2 C T 7: 19,407,493 (GRCm39) V12I probably benign Het
Arap3 T C 18: 38,124,407 (GRCm39) S311G probably benign Het
Arih2 G T 9: 108,488,841 (GRCm39) H292Q probably damaging Het
Cdc14a A T 3: 116,101,843 (GRCm39) D312E probably benign Het
Cdh12 T G 15: 21,237,800 (GRCm39) W12G possibly damaging Het
Cisd2 A T 3: 135,114,616 (GRCm39) N118K probably damaging Het
Cntnap5b A G 1: 99,999,827 (GRCm39) Q195R probably benign Het
Cyp2r1 A G 7: 114,161,966 (GRCm39) probably null Het
Cyp4f37 A G 17: 32,848,864 (GRCm39) D244G possibly damaging Het
Dab1 C T 4: 104,588,948 (GRCm39) A524V probably benign Het
Dido1 T A 2: 180,302,048 (GRCm39) H1952L probably damaging Het
Dnah10 T A 5: 124,871,283 (GRCm39) probably null Het
Dnal4 T A 15: 79,646,714 (GRCm39) M56L probably damaging Het
Emilin2 A G 17: 71,581,112 (GRCm39) V538A probably benign Het
Eps8l2 A G 7: 140,922,015 (GRCm39) D31G probably damaging Het
Erp44 A T 4: 48,219,479 (GRCm39) L112* probably null Het
Etl4 C T 2: 20,813,900 (GRCm39) T1907I possibly damaging Het
Exoc3 A G 13: 74,330,400 (GRCm39) F510L probably benign Het
Fam114a2 G T 11: 57,383,942 (GRCm39) T324K possibly damaging Het
Fer1l4 G A 2: 155,888,091 (GRCm39) R465C probably damaging Het
Frmd4b A C 6: 97,436,173 (GRCm39) S2R probably benign Het
Fscn1 A T 5: 142,946,778 (GRCm39) D192V possibly damaging Het
Gm3486 T A 14: 41,206,472 (GRCm39) *200C probably null Het
Gusb A T 5: 130,029,366 (GRCm39) H138Q probably benign Het
Hdac9 A T 12: 34,578,293 (GRCm39) M4K possibly damaging Het
Hhipl1 G T 12: 108,284,964 (GRCm39) R439L probably benign Het
Hoxd9 A G 2: 74,528,980 (GRCm39) E194G probably benign Het
Itgb1 A G 8: 129,448,902 (GRCm39) S503G possibly damaging Het
Kcnt2 T A 1: 140,437,216 (GRCm39) C500S probably damaging Het
Kdm7a G A 6: 39,123,983 (GRCm39) S727L possibly damaging Het
Klhdc4 A G 8: 122,540,507 (GRCm39) F92L probably damaging Het
Klrb1a A G 6: 128,596,137 (GRCm39) V62A probably damaging Het
Krit1 A G 5: 3,863,032 (GRCm39) probably null Het
Krt40 A G 11: 99,432,566 (GRCm39) I150T possibly damaging Het
Larp4b A G 13: 9,208,738 (GRCm39) T464A probably benign Het
Lrrc52 T G 1: 167,293,964 (GRCm39) D107A probably damaging Het
Mapkap1 G T 2: 34,408,692 (GRCm39) V35F probably damaging Het
Mccc1 A G 3: 36,044,313 (GRCm39) V171A probably damaging Het
Metap1d A T 2: 71,346,104 (GRCm39) R222* probably null Het
Mrgpre G A 7: 143,334,603 (GRCm39) A300V probably benign Het
Mterf1b C A 5: 4,246,606 (GRCm39) N82K probably benign Het
Myh9 C T 15: 77,669,422 (GRCm39) W533* probably null Het
Myom2 A G 8: 15,148,472 (GRCm39) probably null Het
Nr2f1 T C 13: 78,344,611 (GRCm39) probably benign Het
Or10x1 T G 1: 174,197,236 (GRCm39) V251G probably benign Het
Or11a4 T A 17: 37,536,451 (GRCm39) L145* probably null Het
Or2a57 C T 6: 43,212,838 (GRCm39) Q99* probably null Het
Or2w6 A T 13: 21,843,244 (GRCm39) I83N possibly damaging Het
Or52p2 T C 7: 102,237,237 (GRCm39) T238A probably benign Het
Or6c210 A G 10: 129,496,532 (GRCm39) I286V probably benign Het
Or6z1 A T 7: 6,504,675 (GRCm39) C183* probably null Het
Pcdha11 T C 18: 37,138,950 (GRCm39) L193P probably benign Het
Pcdhb20 T A 18: 37,639,285 (GRCm39) F604I probably damaging Het
Pde1a T C 2: 79,708,545 (GRCm39) H291R probably damaging Het
Pfkm G A 15: 98,024,260 (GRCm39) V423M probably damaging Het
Pira1 C A 7: 3,739,337 (GRCm39) E510D probably benign Het
Pkd2l1 G T 19: 44,146,108 (GRCm39) Q149K probably benign Het
Pkhd1l1 T A 15: 44,392,955 (GRCm39) N1763K probably benign Het
Pla2g4a G A 1: 149,748,338 (GRCm39) T282I probably damaging Het
Prpf39 A C 12: 65,089,528 (GRCm39) N89H probably damaging Het
Rad54l2 A G 9: 106,587,537 (GRCm39) F743L probably damaging Het
Raver2 A G 4: 100,991,320 (GRCm39) probably null Het
Ric8b T C 10: 84,783,709 (GRCm39) L189P probably damaging Het
Sccpdh T C 1: 179,495,957 (GRCm39) F13L probably benign Het
Scd2 T C 19: 44,291,448 (GRCm39) F296L probably damaging Het
Scg2 G T 1: 79,414,023 (GRCm39) D233E probably benign Het
Sema5b C A 16: 35,448,377 (GRCm39) probably null Het
Skint5 A T 4: 113,636,286 (GRCm39) V644E unknown Het
Slc44a5 G T 3: 153,969,678 (GRCm39) V612F possibly damaging Het
Snd1 C T 6: 28,520,234 (GRCm39) R107* probably null Het
Sun5 G T 2: 153,702,589 (GRCm39) T189K probably damaging Het
Tap1 A T 17: 34,412,151 (GRCm39) E452V probably damaging Het
Tcam1 A G 11: 106,173,652 (GRCm39) N32S probably benign Het
Tep1 T C 14: 51,067,715 (GRCm39) E2167G probably damaging Het
Tm9sf1 C T 14: 55,873,827 (GRCm39) R557H probably damaging Het
Tmem175 T C 5: 108,793,821 (GRCm39) V317A probably damaging Het
Tsga13 A G 6: 30,874,139 (GRCm39) V231A probably benign Het
Tspan12 A G 6: 21,799,970 (GRCm39) S126P probably damaging Het
Uvrag G T 7: 98,637,398 (GRCm39) D143E probably damaging Het
Vmn1r230 T A 17: 21,067,036 (GRCm39) M75K possibly damaging Het
Vmn2r120 A T 17: 57,852,287 (GRCm39) F10I probably benign Het
Vmn2r57 T C 7: 41,049,284 (GRCm39) T822A probably benign Het
Vmn2r67 T C 7: 84,799,768 (GRCm39) Y490C probably damaging Het
Zc3h7b T A 15: 81,667,386 (GRCm39) W644R probably damaging Het
Zeb1 A G 18: 5,766,962 (GRCm39) D491G probably damaging Het
Zfp709 TCGACG TCG 8: 72,644,552 (GRCm39) probably benign Het
Zfp831 A T 2: 174,486,308 (GRCm39) T328S possibly 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
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
R7248:Ncor1 UTSW 11 62,275,598 (GRCm39) missense possibly damaging 0.89
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'- ACAGGAACAGGTGACTTGTTTC -3'
(R):5'- GGTTTCTTGCACTCCATGTAATATACC -3'

Sequencing Primer
(F):5'- GGAACAGGTGACTTGTTTCAAAAAC -3'
(R):5'- CCAATTGGAACGCCCGTAAGTG -3'
Posted On 2018-02-28