Incidental Mutation 'R5585:Ncor2'
ID 438653
Institutional Source Beutler Lab
Gene Symbol Ncor2
Ensembl Gene ENSMUSG00000029478
Gene Name nuclear receptor co-repressor 2
Synonyms SMRTe, SMRT
MMRRC Submission 043139-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R5585 (G1)
Quality Score 225
Status Not validated
Chromosome 5
Chromosomal Location 125094217-125256283 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) C to A at 125144975 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Stop codon at position 556 (E556*)
Ref Sequence ENSEMBL: ENSMUSP00000107033 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000055256] [ENSMUST00000086083] [ENSMUST00000111393] [ENSMUST00000111394] [ENSMUST00000111398] [ENSMUST00000111402]
AlphaFold Q9WU42
Predicted Effect probably null
Transcript: ENSMUST00000055256
AA Change: E556*
SMART Domains Protein: ENSMUSP00000055954
Gene: ENSMUSG00000029478
AA Change: E556*

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 probably null
Transcript: ENSMUST00000086083
AA Change: E556*
SMART Domains Protein: ENSMUSP00000083250
Gene: ENSMUSG00000029478
AA Change: E556*

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 probably null
Transcript: ENSMUST00000111393
AA Change: E381*
SMART Domains Protein: ENSMUSP00000107024
Gene: ENSMUSG00000029478
AA Change: E381*

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 probably null
Transcript: ENSMUST00000111394
AA Change: E337*
SMART Domains Protein: ENSMUSP00000107025
Gene: ENSMUSG00000029478
AA Change: E337*

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 probably null
Transcript: ENSMUST00000111398
AA Change: E556*
SMART Domains Protein: ENSMUSP00000107029
Gene: ENSMUSG00000029478
AA Change: E556*

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 probably null
Transcript: ENSMUST00000111402
AA Change: E556*
SMART Domains Protein: ENSMUSP00000107033
Gene: ENSMUSG00000029478
AA Change: E556*

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
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.6%
  • 20x: 96.3%
Validation Efficiency
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: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1600014C23Rik A T 17: 46,044,670 (GRCm39) I17N unknown Het
4932414N04Rik A G 2: 68,571,770 (GRCm39) T549A probably benign Het
9330159F19Rik C A 10: 29,101,271 (GRCm39) S548Y possibly damaging Het
Aanat A G 11: 116,487,799 (GRCm39) Y166C probably damaging Het
Adra2a G T 19: 54,034,670 (GRCm39) A9S probably benign Het
Ap4m1 A G 5: 138,170,502 (GRCm39) Y17C probably damaging Het
Arhgap33 T G 7: 30,223,260 (GRCm39) M891L probably benign Het
Calm5 A G 13: 3,904,372 (GRCm39) D22G possibly damaging Het
Ccdc15 C T 9: 37,188,699 (GRCm39) R795H probably benign Het
Cngb1 T A 8: 95,989,767 (GRCm39) I323F probably damaging Het
Cyp26b1 A G 6: 84,554,171 (GRCm39) F74L probably damaging Het
Dpagt1 G A 9: 44,240,439 (GRCm39) probably null Het
Ercc8 C T 13: 108,312,123 (GRCm39) P196S probably damaging Het
Gm10985 A C 3: 53,752,674 (GRCm39) Y19S probably damaging Het
Hfm1 G A 5: 107,059,305 (GRCm39) S239L probably benign Het
Hgf A G 5: 16,769,799 (GRCm39) D91G possibly damaging Het
Lefty2 T A 1: 180,720,828 (GRCm39) V27D possibly damaging Het
Lrp2 G A 2: 69,294,968 (GRCm39) T3450I possibly damaging Het
Lrrc38 A G 4: 143,076,961 (GRCm39) I75V probably damaging Het
Nedd9 A G 13: 41,469,950 (GRCm39) L401P probably damaging Het
Nfatc4 T C 14: 56,064,212 (GRCm39) L163P probably damaging Het
Nln T C 13: 104,161,569 (GRCm39) N667S possibly damaging Het
Or5w20 A G 2: 87,727,019 (GRCm39) T159A possibly damaging Het
Pnpla8 T C 12: 44,329,847 (GRCm39) I133T probably benign Het
Psma1 C T 7: 113,873,302 (GRCm39) G12S probably damaging Het
Psmd3 G A 11: 98,573,707 (GRCm39) G51D possibly damaging Het
Ptprb A G 10: 116,216,759 (GRCm39) Q1959R probably damaging Het
Rhbdf1 A G 11: 32,160,222 (GRCm39) probably null Het
Rnf167 T C 11: 70,540,308 (GRCm39) V110A probably damaging Het
Rrp9 C T 9: 106,362,525 (GRCm39) S470F probably benign Het
Rtn3 G A 19: 7,435,560 (GRCm39) P125L probably benign Het
Scube1 C T 15: 83,561,124 (GRCm39) C156Y probably damaging Het
Tgm2 A T 2: 157,973,375 (GRCm39) Y245* probably null Het
Timeless T C 10: 128,076,112 (GRCm39) I68T probably damaging Het
Ttn A G 2: 76,645,054 (GRCm39) S12934P probably damaging Het
Vwa5b2 T A 16: 20,413,428 (GRCm39) Y214* probably null Het
Yars2 T A 16: 16,122,484 (GRCm39) N7K probably damaging Het
Zfp142 G A 1: 74,617,404 (GRCm39) Q150* probably null Het
Zfp995 C T 17: 22,106,339 (GRCm39) 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
R0671:Ncor2 UTSW 5 125,126,451 (GRCm39) missense probably benign 0.13
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
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'- TCAGCTAGGGGCAGTTTACTCC -3'
(R):5'- AGCACCCTTTTAGCCAGCTG -3'

Sequencing Primer
(F):5'- AGGGGCAGTTTACTCCAACTTCAC -3'
(R):5'- GCAGCTCTTTCCTCTCTGCAG -3'
Posted On 2016-10-26