Incidental Mutation 'R0671:Ncor2'
ID 216147
Institutional Source Beutler Lab
Gene Symbol Ncor2
Ensembl Gene ENSMUSG00000029478
Gene Name nuclear receptor co-repressor 2
Synonyms SMRTe, SMRT
MMRRC Submission 038856-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R0671 (G1)
Quality Score 80
Status Validated
Chromosome 5
Chromosomal Location 125094217-125256283 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 125126451 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Alanine to Threonine at position 136 (A136T)
Ref Sequence ENSEMBL: ENSMUSP00000121588 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000055256] [ENSMUST00000086083] [ENSMUST00000111393] [ENSMUST00000111394] [ENSMUST00000111398] [ENSMUST00000111402] [ENSMUST00000134404] [ENSMUST00000199561]
AlphaFold Q9WU42
Predicted Effect unknown
Transcript: ENSMUST00000055256
AA Change: A722T
SMART Domains Protein: ENSMUSP00000055954
Gene: ENSMUSG00000029478
AA Change: A722T

DomainStartEndE-ValueType
low complexity region 147 154 N/A INTRINSIC
coiled coil region 167 207 N/A INTRINSIC
SANT 428 476 4.42e-6 SMART
coiled coil region 494 550 N/A INTRINSIC
SANT 607 655 1.43e-14 SMART
low complexity region 668 686 N/A INTRINSIC
low complexity region 699 726 N/A INTRINSIC
low complexity region 768 813 N/A INTRINSIC
low complexity region 822 828 N/A INTRINSIC
low complexity region 848 860 N/A INTRINSIC
low complexity region 867 874 N/A INTRINSIC
low complexity region 905 919 N/A INTRINSIC
low complexity region 935 944 N/A INTRINSIC
low complexity region 989 1000 N/A INTRINSIC
low complexity region 1011 1025 N/A INTRINSIC
low complexity region 1027 1043 N/A INTRINSIC
low complexity region 1086 1096 N/A INTRINSIC
low complexity region 1100 1116 N/A INTRINSIC
low complexity region 1366 1380 N/A INTRINSIC
low complexity region 1481 1497 N/A INTRINSIC
low complexity region 1616 1622 N/A INTRINSIC
low complexity region 1709 1726 N/A INTRINSIC
low complexity region 1737 1754 N/A INTRINSIC
low complexity region 1764 1776 N/A INTRINSIC
low complexity region 1800 1807 N/A INTRINSIC
low complexity region 1921 1939 N/A INTRINSIC
low complexity region 1959 1975 N/A INTRINSIC
low complexity region 2062 2076 N/A INTRINSIC
PDB:2GPV|I 2293 2314 8e-8 PDB
low complexity region 2324 2336 N/A INTRINSIC
low complexity region 2433 2453 N/A INTRINSIC
Predicted Effect unknown
Transcript: ENSMUST00000086083
AA Change: A722T
SMART Domains Protein: ENSMUSP00000083250
Gene: ENSMUSG00000029478
AA Change: A722T

DomainStartEndE-ValueType
low complexity region 147 154 N/A INTRINSIC
coiled coil region 167 207 N/A INTRINSIC
SANT 428 476 4.42e-6 SMART
coiled coil region 494 550 N/A INTRINSIC
SANT 607 655 1.43e-14 SMART
low complexity region 668 686 N/A INTRINSIC
low complexity region 699 726 N/A INTRINSIC
low complexity region 768 813 N/A INTRINSIC
low complexity region 822 828 N/A INTRINSIC
low complexity region 848 860 N/A INTRINSIC
low complexity region 867 874 N/A INTRINSIC
low complexity region 905 919 N/A INTRINSIC
low complexity region 935 944 N/A INTRINSIC
low complexity region 988 999 N/A INTRINSIC
low complexity region 1010 1024 N/A INTRINSIC
low complexity region 1026 1042 N/A INTRINSIC
low complexity region 1085 1095 N/A INTRINSIC
low complexity region 1099 1115 N/A INTRINSIC
low complexity region 1364 1378 N/A INTRINSIC
low complexity region 1479 1495 N/A INTRINSIC
low complexity region 1614 1620 N/A INTRINSIC
low complexity region 1707 1724 N/A INTRINSIC
low complexity region 1735 1752 N/A INTRINSIC
low complexity region 1762 1774 N/A INTRINSIC
low complexity region 1798 1805 N/A INTRINSIC
low complexity region 1916 1934 N/A INTRINSIC
low complexity region 1954 1970 N/A INTRINSIC
low complexity region 2057 2071 N/A INTRINSIC
PDB:2GPV|I 2288 2309 8e-8 PDB
low complexity region 2319 2331 N/A INTRINSIC
low complexity region 2428 2448 N/A INTRINSIC
Predicted Effect unknown
Transcript: ENSMUST00000111393
AA Change: A547T
SMART Domains Protein: ENSMUSP00000107024
Gene: ENSMUSG00000029478
AA Change: A547T

DomainStartEndE-ValueType
coiled coil region 1 32 N/A INTRINSIC
SANT 253 301 4.42e-6 SMART
coiled coil region 319 375 N/A INTRINSIC
SANT 432 480 1.43e-14 SMART
low complexity region 493 511 N/A INTRINSIC
low complexity region 524 551 N/A INTRINSIC
low complexity region 593 638 N/A INTRINSIC
low complexity region 647 653 N/A INTRINSIC
low complexity region 673 685 N/A INTRINSIC
low complexity region 692 699 N/A INTRINSIC
low complexity region 730 744 N/A INTRINSIC
low complexity region 760 769 N/A INTRINSIC
low complexity region 813 824 N/A INTRINSIC
low complexity region 835 849 N/A INTRINSIC
low complexity region 851 867 N/A INTRINSIC
low complexity region 910 920 N/A INTRINSIC
low complexity region 924 940 N/A INTRINSIC
low complexity region 1225 1239 N/A INTRINSIC
low complexity region 1340 1356 N/A INTRINSIC
low complexity region 1475 1481 N/A INTRINSIC
low complexity region 1568 1585 N/A INTRINSIC
low complexity region 1596 1613 N/A INTRINSIC
low complexity region 1623 1635 N/A INTRINSIC
low complexity region 1659 1666 N/A INTRINSIC
low complexity region 1780 1798 N/A INTRINSIC
low complexity region 1818 1834 N/A INTRINSIC
low complexity region 1921 1935 N/A INTRINSIC
PDB:2GPV|I 2152 2173 7e-8 PDB
low complexity region 2183 2195 N/A INTRINSIC
low complexity region 2292 2312 N/A INTRINSIC
Predicted Effect unknown
Transcript: ENSMUST00000111394
AA Change: A503T
SMART Domains Protein: ENSMUSP00000107025
Gene: ENSMUSG00000029478
AA Change: A503T

DomainStartEndE-ValueType
SANT 209 257 4.42e-6 SMART
coiled coil region 275 331 N/A INTRINSIC
SANT 388 436 1.43e-14 SMART
low complexity region 449 467 N/A INTRINSIC
low complexity region 480 507 N/A INTRINSIC
low complexity region 549 594 N/A INTRINSIC
low complexity region 603 609 N/A INTRINSIC
low complexity region 629 641 N/A INTRINSIC
low complexity region 648 655 N/A INTRINSIC
low complexity region 686 700 N/A INTRINSIC
low complexity region 716 725 N/A INTRINSIC
low complexity region 769 780 N/A INTRINSIC
low complexity region 791 805 N/A INTRINSIC
low complexity region 807 823 N/A INTRINSIC
low complexity region 866 876 N/A INTRINSIC
low complexity region 880 896 N/A INTRINSIC
low complexity region 1146 1160 N/A INTRINSIC
low complexity region 1261 1277 N/A INTRINSIC
low complexity region 1396 1402 N/A INTRINSIC
low complexity region 1489 1506 N/A INTRINSIC
low complexity region 1517 1534 N/A INTRINSIC
low complexity region 1544 1556 N/A INTRINSIC
low complexity region 1580 1587 N/A INTRINSIC
low complexity region 1701 1719 N/A INTRINSIC
low complexity region 1739 1755 N/A INTRINSIC
low complexity region 1842 1856 N/A INTRINSIC
PDB:2GPV|I 2073 2094 7e-8 PDB
low complexity region 2104 2116 N/A INTRINSIC
low complexity region 2213 2233 N/A INTRINSIC
Predicted Effect unknown
Transcript: ENSMUST00000111398
AA Change: A722T
SMART Domains Protein: ENSMUSP00000107029
Gene: ENSMUSG00000029478
AA Change: A722T

DomainStartEndE-ValueType
low complexity region 147 154 N/A INTRINSIC
coiled coil region 167 207 N/A INTRINSIC
SANT 428 476 4.42e-6 SMART
coiled coil region 494 550 N/A INTRINSIC
SANT 607 655 1.43e-14 SMART
low complexity region 668 686 N/A INTRINSIC
low complexity region 699 726 N/A INTRINSIC
low complexity region 768 813 N/A INTRINSIC
low complexity region 822 828 N/A INTRINSIC
low complexity region 848 860 N/A INTRINSIC
low complexity region 867 874 N/A INTRINSIC
low complexity region 905 919 N/A INTRINSIC
low complexity region 935 944 N/A INTRINSIC
low complexity region 988 999 N/A INTRINSIC
low complexity region 1010 1024 N/A INTRINSIC
low complexity region 1026 1042 N/A INTRINSIC
low complexity region 1085 1095 N/A INTRINSIC
low complexity region 1099 1115 N/A INTRINSIC
low complexity region 1365 1379 N/A INTRINSIC
low complexity region 1480 1496 N/A INTRINSIC
low complexity region 1615 1621 N/A INTRINSIC
low complexity region 1708 1725 N/A INTRINSIC
low complexity region 1736 1753 N/A INTRINSIC
low complexity region 1763 1775 N/A INTRINSIC
low complexity region 1799 1806 N/A INTRINSIC
low complexity region 1920 1938 N/A INTRINSIC
low complexity region 1958 1974 N/A INTRINSIC
low complexity region 2061 2075 N/A INTRINSIC
PDB:2GPV|I 2292 2313 8e-8 PDB
low complexity region 2323 2335 N/A INTRINSIC
low complexity region 2432 2452 N/A INTRINSIC
Predicted Effect unknown
Transcript: ENSMUST00000111402
AA Change: A722T
SMART Domains Protein: ENSMUSP00000107033
Gene: ENSMUSG00000029478
AA Change: A722T

DomainStartEndE-ValueType
Pfam:GPS2_interact 141 229 4.9e-41 PFAM
SANT 428 476 4.42e-6 SMART
coiled coil region 494 550 N/A INTRINSIC
SANT 607 655 1.43e-14 SMART
low complexity region 668 686 N/A INTRINSIC
low complexity region 699 726 N/A INTRINSIC
low complexity region 768 813 N/A INTRINSIC
low complexity region 822 828 N/A INTRINSIC
low complexity region 848 860 N/A INTRINSIC
low complexity region 867 874 N/A INTRINSIC
low complexity region 905 919 N/A INTRINSIC
low complexity region 935 944 N/A INTRINSIC
low complexity region 988 999 N/A INTRINSIC
low complexity region 1010 1024 N/A INTRINSIC
low complexity region 1026 1042 N/A INTRINSIC
low complexity region 1085 1095 N/A INTRINSIC
low complexity region 1099 1115 N/A INTRINSIC
low complexity region 1400 1414 N/A INTRINSIC
low complexity region 1515 1531 N/A INTRINSIC
low complexity region 1650 1656 N/A INTRINSIC
low complexity region 1743 1760 N/A INTRINSIC
low complexity region 1771 1788 N/A INTRINSIC
low complexity region 1798 1810 N/A INTRINSIC
low complexity region 1834 1841 N/A INTRINSIC
low complexity region 1955 1973 N/A INTRINSIC
low complexity region 1993 2009 N/A INTRINSIC
low complexity region 2096 2110 N/A INTRINSIC
PDB:2GPV|I 2327 2348 8e-8 PDB
low complexity region 2358 2370 N/A INTRINSIC
low complexity region 2467 2487 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000149968
Predicted Effect probably benign
Transcript: ENSMUST00000134404
AA Change: A136T

PolyPhen 2 Score 0.134 (Sensitivity: 0.92; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000121588
Gene: ENSMUSG00000029478
AA Change: A136T

DomainStartEndE-ValueType
SANT 2 49 1.94e-2 SMART
low complexity region 84 100 N/A INTRINSIC
low complexity region 113 140 N/A INTRINSIC
low complexity region 182 227 N/A INTRINSIC
low complexity region 236 242 N/A INTRINSIC
low complexity region 262 274 N/A INTRINSIC
low complexity region 281 288 N/A INTRINSIC
low complexity region 319 333 N/A INTRINSIC
low complexity region 349 358 N/A INTRINSIC
low complexity region 402 413 N/A INTRINSIC
low complexity region 424 438 N/A INTRINSIC
low complexity region 440 456 N/A INTRINSIC
low complexity region 499 509 N/A INTRINSIC
low complexity region 513 529 N/A INTRINSIC
low complexity region 813 827 N/A INTRINSIC
low complexity region 928 944 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000199561
SMART Domains Protein: ENSMUSP00000142862
Gene: ENSMUSG00000029478

DomainStartEndE-ValueType
SANT 2 49 1.2e-4 SMART
low complexity region 62 80 N/A INTRINSIC
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.4%
  • 3x: 98.9%
  • 10x: 97.7%
  • 20x: 96.1%
Validation Efficiency 99% (125/126)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a nuclear receptor co-repressor that mediates transcriptional silencing of certain target genes. The encoded protein is a member of a family of thyroid hormone- and retinoic acid receptor-associated co-repressors. This protein acts as part of a multisubunit complex which includes histone deacetylases to modify chromatin structure that prevents basal transcriptional activity of target genes. Aberrant expression of this gene is associated with certain cancers. Alternate splicing results in multiple transcript variants encoding different isoforms.[provided by RefSeq, Apr 2011]
PHENOTYPE: Mice homozygous for a null allele die before E16.5 of heart defects and exhibit neural defects. [provided by MGI curators]
Allele List at MGI

All alleles(145) : Targeted(2) Gene trapped(143)

Other mutations in this stock
Total: 115 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700067K01Rik T C 8: 84,729,637 (GRCm39) probably benign Het
A530064D06Rik G A 17: 48,473,824 (GRCm39) T31I probably benign Het
Abca17 A G 17: 24,500,223 (GRCm39) F1323L probably benign Het
Abcf3 T A 16: 20,369,237 (GRCm39) N206K probably damaging Het
Adam10 A G 9: 70,673,223 (GRCm39) probably benign Het
Adamtsl3 A T 7: 82,172,390 (GRCm39) Q451L probably damaging Het
Adgrl3 T A 5: 81,708,752 (GRCm39) I413N probably benign Het
Asb18 G T 1: 89,920,893 (GRCm39) A128E probably damaging Het
Atf7ip2 T C 16: 10,059,743 (GRCm39) S428P possibly damaging Het
Atp8b5 G T 4: 43,291,672 (GRCm39) C15F possibly damaging Het
Bahcc1 A G 11: 120,178,146 (GRCm39) E2235G probably damaging Het
Blnk G T 19: 40,926,111 (GRCm39) S330* probably null Het
Bpnt1 T G 1: 185,088,808 (GRCm39) N319K probably benign Het
Brip1 G A 11: 86,043,493 (GRCm39) T357I possibly damaging Het
Cadm1 T A 9: 47,725,104 (GRCm39) D288E probably benign Het
Calcoco2 A G 11: 95,998,354 (GRCm39) V23A probably damaging Het
Cand2 G A 6: 115,780,766 (GRCm39) E1217K probably damaging Het
Ccdc154 G T 17: 25,386,259 (GRCm39) probably benign Het
Cdk12 T C 11: 98,120,935 (GRCm39) probably benign Het
Clec4a3 A G 6: 122,930,993 (GRCm39) probably null Het
Cpne2 T A 8: 95,274,970 (GRCm39) probably benign Het
Cyfip1 T C 7: 55,573,710 (GRCm39) probably null Het
Cyp26c1 A G 19: 37,675,009 (GRCm39) H110R probably damaging Het
Cyp2j13 A G 4: 95,959,932 (GRCm39) Y75H probably damaging Het
Defb43 T A 14: 63,249,287 (GRCm39) V10D probably damaging Het
Dhx36 G A 3: 62,401,162 (GRCm39) S368L possibly damaging Het
Dock6 G A 9: 21,715,923 (GRCm39) probably benign Het
Elp2 T C 18: 24,745,499 (GRCm39) probably benign Het
Emilin3 A G 2: 160,750,249 (GRCm39) L453P probably damaging Het
Eml6 A T 11: 29,755,065 (GRCm39) D903E probably benign Het
Ep300 T C 15: 81,500,335 (GRCm39) probably benign Het
Ep400 G A 5: 110,836,062 (GRCm39) T1899M unknown Het
Fancg A G 4: 43,002,998 (GRCm39) S620P probably benign Het
Fbxo42 G A 4: 140,922,550 (GRCm39) V239M probably damaging Het
Fermt2 T C 14: 45,706,776 (GRCm39) D340G probably benign Het
Filip1 A T 9: 79,726,672 (GRCm39) V649E probably damaging Het
Fut8 G A 12: 77,521,791 (GRCm39) E477K probably damaging Het
Gbp3 G A 3: 142,271,151 (GRCm39) G185D probably benign Het
Gclc G T 9: 77,694,080 (GRCm39) D345Y probably damaging Het
Gfus A G 15: 75,800,807 (GRCm39) V27A possibly damaging Het
Gkn2 A G 6: 87,352,800 (GRCm39) D43G possibly damaging Het
Gnptab A G 10: 88,279,166 (GRCm39) probably benign Het
Greb1l C T 18: 10,474,303 (GRCm39) T206I probably damaging Het
Grk4 A G 5: 34,905,611 (GRCm39) N452S probably benign Het
Hcn2 G C 10: 79,570,066 (GRCm39) probably null Het
Hpn T C 7: 30,808,585 (GRCm39) K76E possibly damaging Het
Hspg2 A G 4: 137,280,591 (GRCm39) D3268G probably damaging Het
Immt A T 6: 71,848,541 (GRCm39) Q467L possibly damaging Het
Kalrn T C 16: 33,936,778 (GRCm39) S1636G probably benign Het
Kcnh8 T A 17: 53,285,141 (GRCm39) L1037* probably null Het
Klhl33 T C 14: 51,129,851 (GRCm39) T548A probably damaging Het
Klri2 T C 6: 129,717,171 (GRCm39) I71V probably benign Het
Kmt2c A T 5: 25,609,363 (GRCm39) C254S probably damaging Het
Lama3 T C 18: 12,610,647 (GRCm39) I1170T possibly damaging Het
Med12l A G 3: 59,172,350 (GRCm39) Q1702R probably damaging Het
Mga A T 2: 119,750,391 (GRCm39) probably null Het
Mis18a A T 16: 90,517,561 (GRCm39) I172K possibly damaging Het
Mrgpre T C 7: 143,335,254 (GRCm39) D83G probably benign Het
Mroh2a C A 1: 88,170,142 (GRCm39) A685D possibly damaging Het
Mrpl39 T C 16: 84,531,282 (GRCm39) probably benign Het
Mrrf C T 2: 36,043,710 (GRCm39) A149V probably benign Het
Mycbp2 A T 14: 103,432,024 (GRCm39) M2338K possibly damaging Het
Myo18b T C 5: 112,840,632 (GRCm39) Q2387R probably benign Het
N4bp2 T C 5: 65,964,780 (GRCm39) I943T probably damaging Het
Ncapd3 T A 9: 26,998,773 (GRCm39) N1254K probably benign Het
Ncoa1 A T 12: 4,299,758 (GRCm39) probably null Het
Opa1 T C 16: 29,421,025 (GRCm39) probably benign Het
Or13a25 A G 7: 140,247,590 (GRCm39) D123G probably damaging Het
Or5p59 C A 7: 107,703,363 (GRCm39) Y282* probably null Het
Or8b39 T A 9: 37,996,423 (GRCm39) M97K possibly damaging Het
Or9e1 T A 11: 58,732,681 (GRCm39) I247N possibly damaging Het
Pcdhb4 T C 18: 37,440,795 (GRCm39) M35T probably benign Het
Per3 T C 4: 151,113,288 (GRCm39) I347V probably benign Het
Pex13 G A 11: 23,615,831 (GRCm39) P5L possibly damaging Het
Phkb T A 8: 86,602,322 (GRCm39) W38R probably damaging Het
Plekhf1 A T 7: 37,920,826 (GRCm39) D247E probably benign Het
Plxnb2 A G 15: 89,042,184 (GRCm39) S1607P probably benign Het
Plxnc1 T A 10: 94,635,194 (GRCm39) H1344L possibly damaging Het
Potefam1 A C 2: 111,034,482 (GRCm39) V350G possibly damaging Het
Ptk7 T G 17: 46,901,238 (GRCm39) N196H possibly damaging Het
Rab27a G T 9: 72,982,715 (GRCm39) D7Y probably damaging Het
Rars2 T A 4: 34,630,505 (GRCm39) C82* probably null Het
Rccd1 A T 7: 79,969,965 (GRCm39) probably benign Het
Riiad1 T C 3: 94,379,546 (GRCm39) I56V possibly damaging Het
Rnase4 A G 14: 51,342,507 (GRCm39) E77G probably damaging Het
Rnf126 A T 10: 79,597,441 (GRCm39) I157N possibly damaging Het
Rnf207 T C 4: 152,391,925 (GRCm39) R623G probably benign Het
Rpusd1 T G 17: 25,947,498 (GRCm39) F62V possibly damaging Het
Rxfp1 T C 3: 79,570,600 (GRCm39) probably null Het
Scfd1 A T 12: 51,459,411 (GRCm39) Q324L probably benign Het
Skint3 G T 4: 112,112,974 (GRCm39) E195* probably null Het
Slc7a10 A T 7: 34,896,758 (GRCm39) T165S probably benign Het
Smagp A G 15: 100,519,733 (GRCm39) I97T probably damaging Het
Sostdc1 A G 12: 36,367,340 (GRCm39) H172R probably damaging Het
Spast A G 17: 74,646,446 (GRCm39) probably benign Het
Sspo G T 6: 48,467,325 (GRCm39) probably benign Het
Ston2 C T 12: 91,707,240 (GRCm39) probably null Het
Tas2r103 T G 6: 133,013,313 (GRCm39) E251A probably benign Het
Tbc1d2b A T 9: 90,104,558 (GRCm39) probably benign Het
Telo2 G A 17: 25,332,139 (GRCm39) P143L probably benign Het
Tgfbi A T 13: 56,786,539 (GRCm39) Y674F probably null Het
Tha1 T A 11: 117,763,983 (GRCm39) probably benign Het
Timp4 T A 6: 115,226,814 (GRCm39) S110C probably damaging Het
Tlr6 T C 5: 65,111,935 (GRCm39) K324R probably benign Het
Tnip3 A G 6: 65,574,347 (GRCm39) E137G probably damaging Het
Top6bl A G 19: 4,676,216 (GRCm39) S639P probably damaging Het
Trak1 T C 9: 121,278,021 (GRCm39) probably null Het
Trim47 A G 11: 115,999,178 (GRCm39) S233P probably benign Het
Tspoap1 A T 11: 87,653,635 (GRCm39) E155V probably damaging Het
Uggt1 A T 1: 36,194,209 (GRCm39) L1343Q probably damaging Het
Utp14b T C 1: 78,642,452 (GRCm39) S117P probably benign Het
Vmn1r124 A T 7: 20,994,436 (GRCm39) V36D probably damaging Het
Wdr27 T C 17: 15,148,658 (GRCm39) T112A probably benign Het
Wdr90 T C 17: 26,065,367 (GRCm39) T1630A probably benign Het
Zfp352 A G 4: 90,112,156 (GRCm39) T99A probably benign Het
Other mutations in Ncor2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00330:Ncor2 APN 5 125,119,807 (GRCm39) critical splice donor site probably null
IGL00519:Ncor2 APN 5 125,161,988 (GRCm39) missense unknown
IGL00900:Ncor2 APN 5 125,102,848 (GRCm39) missense probably damaging 1.00
IGL00950:Ncor2 APN 5 125,163,954 (GRCm39) missense unknown
IGL01320:Ncor2 APN 5 125,186,991 (GRCm39) missense probably benign 0.00
IGL01382:Ncor2 APN 5 125,132,837 (GRCm39) missense probably damaging 0.96
IGL01573:Ncor2 APN 5 125,162,090 (GRCm39) missense unknown
IGL01721:Ncor2 APN 5 125,128,001 (GRCm39) missense probably damaging 1.00
IGL01875:Ncor2 APN 5 125,142,934 (GRCm39) missense unknown
IGL02090:Ncor2 APN 5 125,111,467 (GRCm39) missense probably damaging 0.99
IGL02192:Ncor2 APN 5 125,101,301 (GRCm39) missense probably damaging 1.00
IGL02396:Ncor2 APN 5 125,114,978 (GRCm39) missense probably damaging 1.00
IGL02934:Ncor2 APN 5 125,102,621 (GRCm39) missense probably benign 0.33
IGL02997:Ncor2 APN 5 125,196,634 (GRCm39) intron probably benign
R0019:Ncor2 UTSW 5 125,196,545 (GRCm39) critical splice donor site probably null
R0331:Ncor2 UTSW 5 125,161,981 (GRCm39) missense unknown
R0333:Ncor2 UTSW 5 125,111,408 (GRCm39) splice site probably benign
R0403:Ncor2 UTSW 5 125,110,401 (GRCm39) missense possibly damaging 0.73
R0557:Ncor2 UTSW 5 125,183,369 (GRCm39) nonsense probably null
R0562:Ncor2 UTSW 5 125,162,093 (GRCm39) missense unknown
R0699:Ncor2 UTSW 5 125,106,176 (GRCm39) unclassified probably benign
R0865:Ncor2 UTSW 5 125,116,046 (GRCm39) missense probably benign 0.17
R1183:Ncor2 UTSW 5 125,100,585 (GRCm39) missense possibly damaging 0.65
R1325:Ncor2 UTSW 5 125,195,844 (GRCm39) intron probably benign
R1344:Ncor2 UTSW 5 125,102,510 (GRCm39) missense probably damaging 1.00
R1433:Ncor2 UTSW 5 125,187,039 (GRCm39) intron probably benign
R1481:Ncor2 UTSW 5 125,104,202 (GRCm39) nonsense probably null
R1539:Ncor2 UTSW 5 125,187,003 (GRCm39) missense probably benign 0.07
R1558:Ncor2 UTSW 5 125,110,610 (GRCm39) missense probably damaging 1.00
R1585:Ncor2 UTSW 5 125,162,062 (GRCm39) missense unknown
R1611:Ncor2 UTSW 5 125,187,084 (GRCm39) intron probably benign
R1764:Ncor2 UTSW 5 125,105,679 (GRCm39) missense possibly damaging 0.91
R1789:Ncor2 UTSW 5 125,096,954 (GRCm39) missense probably damaging 1.00
R1809:Ncor2 UTSW 5 125,195,857 (GRCm39) intron probably benign
R1901:Ncor2 UTSW 5 125,102,489 (GRCm39) missense probably benign 0.39
R1946:Ncor2 UTSW 5 125,111,476 (GRCm39) missense probably damaging 1.00
R1970:Ncor2 UTSW 5 125,115,982 (GRCm39) missense probably damaging 0.99
R2048:Ncor2 UTSW 5 125,161,996 (GRCm39) missense unknown
R2137:Ncor2 UTSW 5 125,107,776 (GRCm39) missense probably damaging 1.00
R2270:Ncor2 UTSW 5 125,115,019 (GRCm39) missense probably benign 0.33
R2380:Ncor2 UTSW 5 125,113,144 (GRCm39) missense possibly damaging 0.89
R2570:Ncor2 UTSW 5 125,105,864 (GRCm39) critical splice acceptor site probably null
R2918:Ncor2 UTSW 5 125,102,824 (GRCm39) missense probably damaging 0.99
R2921:Ncor2 UTSW 5 125,132,855 (GRCm39) missense probably damaging 1.00
R2922:Ncor2 UTSW 5 125,132,855 (GRCm39) missense probably damaging 1.00
R2923:Ncor2 UTSW 5 125,132,855 (GRCm39) missense probably damaging 1.00
R3116:Ncor2 UTSW 5 125,101,230 (GRCm39) missense probably damaging 1.00
R3768:Ncor2 UTSW 5 125,105,751 (GRCm39) missense probably damaging 1.00
R3826:Ncor2 UTSW 5 125,195,756 (GRCm39) intron probably benign
R3829:Ncor2 UTSW 5 125,195,756 (GRCm39) intron probably benign
R3830:Ncor2 UTSW 5 125,195,756 (GRCm39) intron probably benign
R3951:Ncor2 UTSW 5 125,109,320 (GRCm39) missense possibly damaging 0.94
R4175:Ncor2 UTSW 5 125,128,020 (GRCm39) missense probably damaging 0.99
R4360:Ncor2 UTSW 5 125,106,036 (GRCm39) missense probably damaging 1.00
R4470:Ncor2 UTSW 5 125,179,705 (GRCm39) critical splice donor site probably null
R4490:Ncor2 UTSW 5 125,113,879 (GRCm39) splice site probably null
R4573:Ncor2 UTSW 5 125,132,889 (GRCm39) missense probably damaging 0.99
R4611:Ncor2 UTSW 5 125,107,923 (GRCm39) missense probably damaging 1.00
R4799:Ncor2 UTSW 5 125,114,124 (GRCm39) critical splice donor site probably null
R4851:Ncor2 UTSW 5 125,110,431 (GRCm39) missense possibly damaging 0.93
R4853:Ncor2 UTSW 5 125,158,247 (GRCm39) missense unknown
R4853:Ncor2 UTSW 5 125,102,169 (GRCm39) missense probably damaging 0.99
R4896:Ncor2 UTSW 5 125,126,404 (GRCm39) critical splice donor site probably null
R4997:Ncor2 UTSW 5 125,111,074 (GRCm39) missense probably damaging 0.99
R5057:Ncor2 UTSW 5 125,125,130 (GRCm39) missense possibly damaging 0.86
R5253:Ncor2 UTSW 5 125,103,994 (GRCm39) missense probably benign 0.44
R5461:Ncor2 UTSW 5 125,104,177 (GRCm39) missense probably damaging 1.00
R5585:Ncor2 UTSW 5 125,144,975 (GRCm39) nonsense probably null
R5638:Ncor2 UTSW 5 125,125,364 (GRCm39) missense probably benign 0.33
R5879:Ncor2 UTSW 5 125,103,839 (GRCm39) unclassified probably benign
R5967:Ncor2 UTSW 5 125,146,048 (GRCm39) missense unknown
R5999:Ncor2 UTSW 5 125,110,505 (GRCm39) missense probably damaging 1.00
R6020:Ncor2 UTSW 5 125,097,075 (GRCm39) missense probably benign 0.14
R6109:Ncor2 UTSW 5 125,132,910 (GRCm39) missense probably damaging 1.00
R6423:Ncor2 UTSW 5 125,164,966 (GRCm39) missense unknown
R6462:Ncor2 UTSW 5 125,101,236 (GRCm39) missense probably damaging 1.00
R6478:Ncor2 UTSW 5 125,187,069 (GRCm39) intron probably benign
R7074:Ncor2 UTSW 5 125,126,430 (GRCm39) nonsense probably null
R7179:Ncor2 UTSW 5 125,132,847 (GRCm39) missense unknown
R7261:Ncor2 UTSW 5 125,187,143 (GRCm39) splice site probably null
R7263:Ncor2 UTSW 5 125,109,196 (GRCm39) missense
R7273:Ncor2 UTSW 5 125,100,687 (GRCm39) missense
R7282:Ncor2 UTSW 5 125,097,104 (GRCm39) missense
R7570:Ncor2 UTSW 5 125,107,153 (GRCm39) missense
R7725:Ncor2 UTSW 5 125,100,630 (GRCm39) missense
R7747:Ncor2 UTSW 5 125,104,102 (GRCm39) missense
R7748:Ncor2 UTSW 5 125,187,031 (GRCm39) missense unknown
R7825:Ncor2 UTSW 5 125,114,141 (GRCm39) missense possibly damaging 0.53
R8008:Ncor2 UTSW 5 125,144,983 (GRCm39) missense unknown
R8126:Ncor2 UTSW 5 125,183,268 (GRCm39) missense unknown
R8137:Ncor2 UTSW 5 125,114,957 (GRCm39) missense
R8706:Ncor2 UTSW 5 125,145,010 (GRCm39) missense unknown
R8751:Ncor2 UTSW 5 125,115,964 (GRCm39) missense
R8819:Ncor2 UTSW 5 125,106,291 (GRCm39) missense
R8820:Ncor2 UTSW 5 125,106,291 (GRCm39) missense
R8824:Ncor2 UTSW 5 125,195,821 (GRCm39) missense
R8867:Ncor2 UTSW 5 125,179,739 (GRCm39) missense unknown
R8919:Ncor2 UTSW 5 125,106,253 (GRCm39) missense
R8922:Ncor2 UTSW 5 125,163,939 (GRCm39) missense unknown
R9076:Ncor2 UTSW 5 125,111,086 (GRCm39) missense
R9249:Ncor2 UTSW 5 125,186,988 (GRCm39) missense unknown
R9276:Ncor2 UTSW 5 125,113,150 (GRCm39) missense
R9362:Ncor2 UTSW 5 125,095,265 (GRCm39) missense
R9667:Ncor2 UTSW 5 125,125,545 (GRCm39) missense unknown
R9684:Ncor2 UTSW 5 125,102,139 (GRCm39) missense
Z1088:Ncor2 UTSW 5 125,163,904 (GRCm39) critical splice donor site probably null
Z1088:Ncor2 UTSW 5 125,144,852 (GRCm39) missense unknown
Z1177:Ncor2 UTSW 5 125,113,913 (GRCm39) missense
Z1177:Ncor2 UTSW 5 125,125,058 (GRCm39) missense probably damaging 0.98
Predicted Primers PCR Primer
(F):5'- ACAGTTGCATCGGGGAATAGACAC -3'
(R):5'- CTGACTGATAAGGCTGGAAGGCAC -3'

Sequencing Primer
(F):5'- CATCGGGGAATAGACACTTTGTAG -3'
(R):5'- TGACCCTGGACATACCTTGAC -3'
Posted On 2014-07-25