Incidental Mutation 'R5579:Ncoa6'
ID |
438244 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Ncoa6
|
Ensembl Gene |
ENSMUSG00000038369 |
Gene Name |
nuclear receptor coactivator 6 |
Synonyms |
ASC-2, RAP250, NRC, AIB3, ASC2, PRIP |
MMRRC Submission |
043267-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R5579 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
2 |
Chromosomal Location |
155232585-155315741 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 155248597 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Leucine to Serine
at position 1569
(L1569S)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000105295
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000043126]
[ENSMUST00000109670]
[ENSMUST00000123293]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000043126
AA Change: L1569S
PolyPhen 2
Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000045386 Gene: ENSMUSG00000038369 AA Change: L1569S
Domain | Start | End | E-Value | Type |
Pfam:Nucleic_acid_bd
|
47 |
190 |
3.3e-55 |
PFAM |
coiled coil region
|
256 |
296 |
N/A |
INTRINSIC |
low complexity region
|
375 |
383 |
N/A |
INTRINSIC |
internal_repeat_1
|
450 |
597 |
3.31e-5 |
PROSPERO |
low complexity region
|
615 |
630 |
N/A |
INTRINSIC |
internal_repeat_1
|
636 |
793 |
3.31e-5 |
PROSPERO |
low complexity region
|
844 |
860 |
N/A |
INTRINSIC |
low complexity region
|
909 |
931 |
N/A |
INTRINSIC |
low complexity region
|
986 |
998 |
N/A |
INTRINSIC |
low complexity region
|
1002 |
1046 |
N/A |
INTRINSIC |
low complexity region
|
1126 |
1139 |
N/A |
INTRINSIC |
low complexity region
|
1258 |
1273 |
N/A |
INTRINSIC |
low complexity region
|
1328 |
1351 |
N/A |
INTRINSIC |
low complexity region
|
1543 |
1564 |
N/A |
INTRINSIC |
low complexity region
|
1578 |
1599 |
N/A |
INTRINSIC |
low complexity region
|
1607 |
1618 |
N/A |
INTRINSIC |
low complexity region
|
1808 |
1825 |
N/A |
INTRINSIC |
low complexity region
|
1894 |
1908 |
N/A |
INTRINSIC |
low complexity region
|
2043 |
2053 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000109670
AA Change: L1569S
PolyPhen 2
Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000105295 Gene: ENSMUSG00000038369 AA Change: L1569S
Domain | Start | End | E-Value | Type |
Pfam:Nucleic_acid_bd
|
45 |
195 |
3.6e-60 |
PFAM |
coiled coil region
|
256 |
296 |
N/A |
INTRINSIC |
low complexity region
|
375 |
383 |
N/A |
INTRINSIC |
internal_repeat_1
|
450 |
597 |
3.31e-5 |
PROSPERO |
low complexity region
|
615 |
630 |
N/A |
INTRINSIC |
internal_repeat_1
|
636 |
793 |
3.31e-5 |
PROSPERO |
low complexity region
|
844 |
860 |
N/A |
INTRINSIC |
low complexity region
|
909 |
931 |
N/A |
INTRINSIC |
low complexity region
|
986 |
998 |
N/A |
INTRINSIC |
low complexity region
|
1002 |
1046 |
N/A |
INTRINSIC |
low complexity region
|
1126 |
1139 |
N/A |
INTRINSIC |
low complexity region
|
1258 |
1273 |
N/A |
INTRINSIC |
low complexity region
|
1328 |
1351 |
N/A |
INTRINSIC |
low complexity region
|
1543 |
1564 |
N/A |
INTRINSIC |
low complexity region
|
1578 |
1599 |
N/A |
INTRINSIC |
low complexity region
|
1607 |
1618 |
N/A |
INTRINSIC |
low complexity region
|
1808 |
1825 |
N/A |
INTRINSIC |
low complexity region
|
1894 |
1908 |
N/A |
INTRINSIC |
low complexity region
|
2043 |
2053 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000123293
|
SMART Domains |
Protein: ENSMUSP00000118113 Gene: ENSMUSG00000038369
Domain | Start | End | E-Value | Type |
Pfam:Nucleic_acid_bd
|
45 |
195 |
2.4e-60 |
PFAM |
coiled coil region
|
256 |
296 |
N/A |
INTRINSIC |
low complexity region
|
375 |
383 |
N/A |
INTRINSIC |
low complexity region
|
564 |
573 |
N/A |
INTRINSIC |
low complexity region
|
615 |
630 |
N/A |
INTRINSIC |
low complexity region
|
844 |
860 |
N/A |
INTRINSIC |
low complexity region
|
909 |
931 |
N/A |
INTRINSIC |
low complexity region
|
986 |
998 |
N/A |
INTRINSIC |
low complexity region
|
1002 |
1046 |
N/A |
INTRINSIC |
low complexity region
|
1126 |
1139 |
N/A |
INTRINSIC |
low complexity region
|
1258 |
1273 |
N/A |
INTRINSIC |
low complexity region
|
1328 |
1351 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000146942
|
Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.8%
- 10x: 98.9%
- 20x: 97.0%
|
Validation Efficiency |
|
MGI Phenotype |
PHENOTYPE: Homozygotes for targeted null mutations exhibit retarded embryonic growth and defects of the placenta, heart, liver, and nervous system. Mutants die around midgestation. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 114 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca3 |
G |
T |
17: 24,595,703 (GRCm39) |
C352F |
probably damaging |
Het |
Abce1 |
A |
T |
8: 80,427,215 (GRCm39) |
I237N |
possibly damaging |
Het |
Acrbp |
A |
G |
6: 125,038,062 (GRCm39) |
D421G |
probably benign |
Het |
Adam8 |
T |
A |
7: 139,568,897 (GRCm39) |
Y201F |
probably benign |
Het |
Adgrf1 |
T |
A |
17: 43,621,955 (GRCm39) |
C731S |
probably damaging |
Het |
Akap8l |
A |
T |
17: 32,540,916 (GRCm39) |
I529N |
probably damaging |
Het |
Akap9 |
G |
A |
5: 4,114,714 (GRCm39) |
G114D |
possibly damaging |
Het |
Alox12b |
T |
A |
11: 69,053,758 (GRCm39) |
D158E |
probably benign |
Het |
Ankrd11 |
A |
G |
8: 123,610,970 (GRCm39) |
S2639P |
probably damaging |
Het |
Ankrd42 |
T |
C |
7: 92,239,390 (GRCm39) |
Y466C |
possibly damaging |
Het |
Apobr |
T |
C |
7: 126,186,847 (GRCm39) |
I786T |
probably benign |
Het |
Arhgef12 |
C |
T |
9: 42,921,489 (GRCm39) |
G329R |
probably benign |
Het |
Btnl1 |
T |
C |
17: 34,600,526 (GRCm39) |
|
probably null |
Het |
Ccdc174 |
A |
G |
6: 91,858,331 (GRCm39) |
|
probably null |
Het |
Ccdc183 |
T |
C |
2: 25,505,434 (GRCm39) |
D177G |
possibly damaging |
Het |
Cd14 |
A |
G |
18: 36,859,288 (GRCm39) |
Y56H |
probably benign |
Het |
Cep162 |
G |
A |
9: 87,085,724 (GRCm39) |
A1200V |
probably benign |
Het |
Clic3 |
T |
C |
2: 25,348,319 (GRCm39) |
L128P |
probably damaging |
Het |
Cntnap5b |
A |
T |
1: 100,311,120 (GRCm39) |
R538* |
probably null |
Het |
Cntnap5b |
A |
T |
1: 100,311,124 (GRCm39) |
Q539L |
probably benign |
Het |
Coq7 |
A |
T |
7: 118,116,558 (GRCm39) |
N214K |
unknown |
Het |
Cramp1 |
G |
A |
17: 25,192,087 (GRCm39) |
H1018Y |
possibly damaging |
Het |
Crtac1 |
T |
A |
19: 42,293,245 (GRCm39) |
D288V |
probably damaging |
Het |
Dab2ip |
C |
T |
2: 35,605,339 (GRCm39) |
R132* |
probably null |
Het |
Dis3l |
C |
A |
9: 64,238,117 (GRCm39) |
C125F |
probably benign |
Het |
Dnmt1 |
A |
T |
9: 20,831,501 (GRCm39) |
V543D |
probably damaging |
Het |
Dock9 |
A |
T |
14: 121,837,107 (GRCm39) |
L67Q |
probably damaging |
Het |
Ehbp1 |
A |
T |
11: 22,087,846 (GRCm39) |
S413T |
probably damaging |
Het |
Endov |
A |
G |
11: 119,395,923 (GRCm39) |
I158V |
probably benign |
Het |
Epb41l4b |
A |
G |
4: 57,064,802 (GRCm39) |
V469A |
possibly damaging |
Het |
Etf1 |
G |
A |
18: 35,046,654 (GRCm39) |
P119S |
probably damaging |
Het |
Fam135a |
A |
G |
1: 24,068,808 (GRCm39) |
L491P |
possibly damaging |
Het |
Fancd2 |
A |
T |
6: 113,537,012 (GRCm39) |
|
probably null |
Het |
Fank1 |
T |
A |
7: 133,471,058 (GRCm39) |
|
probably null |
Het |
Fbh1 |
A |
G |
2: 11,753,804 (GRCm39) |
I846T |
probably damaging |
Het |
Gas2l3 |
T |
C |
10: 89,249,928 (GRCm39) |
T397A |
probably benign |
Het |
Gga1 |
T |
C |
15: 78,777,388 (GRCm39) |
V513A |
probably damaging |
Het |
Ggt1 |
T |
C |
10: 75,421,782 (GRCm39) |
V543A |
probably damaging |
Het |
Gm11596 |
A |
T |
11: 99,683,717 (GRCm39) |
C134* |
probably null |
Het |
Gnal |
C |
T |
18: 67,221,842 (GRCm39) |
R82C |
unknown |
Het |
Hat1 |
T |
C |
2: 71,240,582 (GRCm39) |
V92A |
possibly damaging |
Het |
Icosl |
C |
T |
10: 77,909,597 (GRCm39) |
R181C |
probably damaging |
Het |
Ift46 |
A |
G |
9: 44,698,160 (GRCm39) |
M208V |
possibly damaging |
Het |
Ighv1-26 |
T |
C |
12: 114,752,219 (GRCm39) |
K42E |
possibly damaging |
Het |
Ipo5 |
A |
G |
14: 121,176,025 (GRCm39) |
K617E |
probably benign |
Het |
Irx5 |
A |
G |
8: 93,086,541 (GRCm39) |
D208G |
probably benign |
Het |
Itgal |
T |
G |
7: 126,906,101 (GRCm39) |
V397G |
probably benign |
Het |
Itpr2 |
G |
A |
6: 146,074,864 (GRCm39) |
R2297* |
probably null |
Het |
Itpr3 |
A |
G |
17: 27,332,493 (GRCm39) |
D1779G |
probably damaging |
Het |
Khdc4 |
T |
C |
3: 88,607,582 (GRCm39) |
S345P |
probably benign |
Het |
Krt4 |
T |
A |
15: 101,829,669 (GRCm39) |
E286D |
probably benign |
Het |
Loxl4 |
C |
T |
19: 42,592,729 (GRCm39) |
G317E |
probably damaging |
Het |
Mapk6 |
T |
G |
9: 75,295,344 (GRCm39) |
H718P |
possibly damaging |
Het |
Mark2 |
A |
C |
19: 7,260,181 (GRCm39) |
V14G |
probably damaging |
Het |
Mbd5 |
A |
G |
2: 49,162,826 (GRCm39) |
T1103A |
possibly damaging |
Het |
Mcph1 |
A |
G |
8: 18,682,309 (GRCm39) |
E482G |
probably benign |
Het |
Mme |
G |
A |
3: 63,256,066 (GRCm39) |
E509K |
probably damaging |
Het |
Mrgbp |
A |
G |
2: 180,227,276 (GRCm39) |
T204A |
probably damaging |
Het |
Mycbp2 |
A |
T |
14: 103,528,769 (GRCm39) |
F430I |
probably damaging |
Het |
Myo6 |
A |
G |
9: 80,125,002 (GRCm39) |
D27G |
probably damaging |
Het |
Ndc1 |
T |
A |
4: 107,237,901 (GRCm39) |
F235Y |
possibly damaging |
Het |
Nmur2 |
A |
T |
11: 55,923,835 (GRCm39) |
S240T |
probably benign |
Het |
Or14c44 |
T |
A |
7: 86,061,934 (GRCm39) |
Y121* |
probably null |
Het |
Or52ae7 |
G |
A |
7: 103,120,121 (GRCm39) |
V292M |
probably damaging |
Het |
Or5d46 |
A |
T |
2: 88,170,757 (GRCm39) |
I283F |
possibly damaging |
Het |
Osbpl1a |
G |
T |
18: 12,974,249 (GRCm39) |
A62E |
probably damaging |
Het |
Osbpl1a |
A |
C |
18: 13,025,319 (GRCm39) |
S333A |
probably benign |
Het |
Otud4 |
C |
T |
8: 80,390,737 (GRCm39) |
T417I |
probably benign |
Het |
Pagr1a |
T |
C |
7: 126,614,614 (GRCm39) |
E197G |
probably damaging |
Het |
Pcdh18 |
T |
C |
3: 49,699,426 (GRCm39) |
Q1012R |
probably damaging |
Het |
Pcdhgb5 |
A |
C |
18: 37,864,690 (GRCm39) |
I162L |
probably benign |
Het |
Pdpr |
T |
A |
8: 111,850,448 (GRCm39) |
Y462N |
probably damaging |
Het |
Pkhd1 |
A |
T |
1: 20,593,366 (GRCm39) |
H1582Q |
probably damaging |
Het |
Polr1b |
A |
G |
2: 128,952,028 (GRCm39) |
K352R |
probably damaging |
Het |
Poteg |
G |
A |
8: 27,938,065 (GRCm39) |
V12M |
probably damaging |
Het |
Pou2f1 |
A |
C |
1: 165,742,731 (GRCm39) |
V54G |
probably damaging |
Het |
Ppme1 |
A |
G |
7: 99,994,182 (GRCm39) |
L177P |
probably damaging |
Het |
Prkce |
A |
G |
17: 86,927,376 (GRCm39) |
D550G |
probably damaging |
Het |
Prrc2c |
A |
G |
1: 162,508,327 (GRCm39) |
|
probably null |
Het |
Ptpn22 |
A |
G |
3: 103,789,455 (GRCm39) |
|
probably null |
Het |
Rabif |
G |
A |
1: 134,433,943 (GRCm39) |
V86M |
probably damaging |
Het |
Rbm25 |
T |
A |
12: 83,715,281 (GRCm39) |
M484K |
probably benign |
Het |
Rcn2 |
G |
A |
9: 55,964,713 (GRCm39) |
A224T |
probably benign |
Het |
Rexo5 |
T |
A |
7: 119,433,626 (GRCm39) |
|
probably null |
Het |
Rnase1 |
A |
T |
14: 51,383,219 (GRCm39) |
I45N |
probably benign |
Het |
Rnmt |
T |
A |
18: 68,439,186 (GRCm39) |
D98E |
possibly damaging |
Het |
Rprd2 |
A |
G |
3: 95,692,371 (GRCm39) |
F188L |
probably damaging |
Het |
Scube2 |
G |
A |
7: 109,409,944 (GRCm39) |
T643M |
probably damaging |
Het |
Skic3 |
T |
C |
13: 76,333,319 (GRCm39) |
W25R |
probably damaging |
Het |
Slc7a15 |
T |
C |
12: 8,589,344 (GRCm39) |
I68V |
probably benign |
Het |
Slco1a5 |
A |
T |
6: 142,187,851 (GRCm39) |
V496D |
possibly damaging |
Het |
Slitrk6 |
T |
G |
14: 110,988,649 (GRCm39) |
S353R |
possibly damaging |
Het |
Smpd5 |
T |
A |
15: 76,179,325 (GRCm39) |
I53K |
possibly damaging |
Het |
Tas2r108 |
T |
C |
6: 40,471,021 (GRCm39) |
S166P |
probably benign |
Het |
Tcstv7a |
T |
A |
13: 120,289,951 (GRCm39) |
M82L |
probably benign |
Het |
Tecpr1 |
C |
A |
5: 144,151,162 (GRCm39) |
V245L |
possibly damaging |
Het |
Tenm3 |
G |
T |
8: 48,689,799 (GRCm39) |
N1929K |
probably damaging |
Het |
Tigd5 |
T |
G |
15: 75,782,874 (GRCm39) |
F412C |
probably damaging |
Het |
Timm17a |
A |
T |
1: 135,233,926 (GRCm39) |
S74T |
possibly damaging |
Het |
Tle1 |
A |
T |
4: 72,058,045 (GRCm39) |
L60Q |
probably damaging |
Het |
Tmem132d |
T |
C |
5: 127,873,064 (GRCm39) |
E515G |
possibly damaging |
Het |
Tmem65 |
T |
C |
15: 58,666,246 (GRCm39) |
N115S |
probably benign |
Het |
Trmt5 |
C |
A |
12: 73,328,426 (GRCm39) |
R259L |
possibly damaging |
Het |
Trmt9b |
T |
C |
8: 36,979,195 (GRCm39) |
V266A |
probably benign |
Het |
Vmn2r50 |
A |
T |
7: 9,784,016 (GRCm39) |
W153R |
probably benign |
Het |
Vwa3a |
T |
G |
7: 120,367,396 (GRCm39) |
S184A |
probably benign |
Het |
Zbtb25 |
A |
G |
12: 76,395,938 (GRCm39) |
L428P |
possibly damaging |
Het |
Zbtb49 |
C |
T |
5: 38,358,160 (GRCm39) |
D698N |
probably damaging |
Het |
Zbtb8os |
T |
G |
4: 129,234,528 (GRCm39) |
D35E |
probably damaging |
Het |
Zfp316 |
T |
C |
5: 143,250,246 (GRCm39) |
T56A |
unknown |
Het |
Zfp334 |
A |
T |
2: 165,222,407 (GRCm39) |
C545* |
probably null |
Het |
Zmiz1 |
C |
A |
14: 25,645,280 (GRCm39) |
S247R |
probably damaging |
Het |
Zscan18 |
A |
G |
7: 12,509,308 (GRCm39) |
|
probably benign |
Het |
Zzef1 |
T |
C |
11: 72,791,463 (GRCm39) |
V2189A |
probably damaging |
Het |
|
Other mutations in Ncoa6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00484:Ncoa6
|
APN |
2 |
155,248,128 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00849:Ncoa6
|
APN |
2 |
155,263,608 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL00933:Ncoa6
|
APN |
2 |
155,257,317 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00981:Ncoa6
|
APN |
2 |
155,248,099 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01420:Ncoa6
|
APN |
2 |
155,249,507 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02160:Ncoa6
|
APN |
2 |
155,263,003 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL03049:Ncoa6
|
APN |
2 |
155,260,934 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03194:Ncoa6
|
APN |
2 |
155,257,788 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03269:Ncoa6
|
APN |
2 |
155,248,409 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03299:Ncoa6
|
APN |
2 |
155,249,207 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03306:Ncoa6
|
APN |
2 |
155,247,427 (GRCm39) |
missense |
probably benign |
0.30 |
alcoa
|
UTSW |
2 |
155,244,584 (GRCm39) |
unclassified |
probably benign |
|
Aluminum
|
UTSW |
2 |
155,241,613 (GRCm39) |
critical splice acceptor site |
probably null |
|
balboa
|
UTSW |
2 |
155,248,869 (GRCm39) |
missense |
probably benign |
0.05 |
mauna_loa
|
UTSW |
2 |
155,257,147 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4466001:Ncoa6
|
UTSW |
2 |
155,247,577 (GRCm39) |
missense |
probably benign |
|
R0011:Ncoa6
|
UTSW |
2 |
155,250,211 (GRCm39) |
frame shift |
probably null |
|
R0014:Ncoa6
|
UTSW |
2 |
155,279,963 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0079:Ncoa6
|
UTSW |
2 |
155,250,211 (GRCm39) |
frame shift |
probably null |
|
R0080:Ncoa6
|
UTSW |
2 |
155,250,211 (GRCm39) |
frame shift |
probably null |
|
R0081:Ncoa6
|
UTSW |
2 |
155,250,211 (GRCm39) |
frame shift |
probably null |
|
R0164:Ncoa6
|
UTSW |
2 |
155,250,211 (GRCm39) |
frame shift |
probably null |
|
R0166:Ncoa6
|
UTSW |
2 |
155,250,211 (GRCm39) |
frame shift |
probably null |
|
R0172:Ncoa6
|
UTSW |
2 |
155,250,211 (GRCm39) |
frame shift |
probably null |
|
R0173:Ncoa6
|
UTSW |
2 |
155,250,211 (GRCm39) |
frame shift |
probably null |
|
R0245:Ncoa6
|
UTSW |
2 |
155,233,131 (GRCm39) |
missense |
probably benign |
0.00 |
R0284:Ncoa6
|
UTSW |
2 |
155,250,211 (GRCm39) |
frame shift |
probably null |
|
R0285:Ncoa6
|
UTSW |
2 |
155,257,621 (GRCm39) |
missense |
probably damaging |
0.96 |
R0285:Ncoa6
|
UTSW |
2 |
155,250,211 (GRCm39) |
frame shift |
probably null |
|
R0288:Ncoa6
|
UTSW |
2 |
155,250,211 (GRCm39) |
frame shift |
probably null |
|
R0539:Ncoa6
|
UTSW |
2 |
155,257,617 (GRCm39) |
missense |
probably benign |
0.08 |
R0652:Ncoa6
|
UTSW |
2 |
155,233,131 (GRCm39) |
missense |
probably benign |
0.00 |
R0781:Ncoa6
|
UTSW |
2 |
155,253,440 (GRCm39) |
splice site |
probably benign |
|
R1053:Ncoa6
|
UTSW |
2 |
155,275,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R1110:Ncoa6
|
UTSW |
2 |
155,253,440 (GRCm39) |
splice site |
probably benign |
|
R1420:Ncoa6
|
UTSW |
2 |
155,263,073 (GRCm39) |
nonsense |
probably null |
|
R1521:Ncoa6
|
UTSW |
2 |
155,257,142 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1541:Ncoa6
|
UTSW |
2 |
155,257,224 (GRCm39) |
missense |
probably benign |
0.35 |
R1677:Ncoa6
|
UTSW |
2 |
155,244,584 (GRCm39) |
unclassified |
probably benign |
|
R1858:Ncoa6
|
UTSW |
2 |
155,263,559 (GRCm39) |
missense |
probably benign |
0.13 |
R1954:Ncoa6
|
UTSW |
2 |
155,248,741 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1955:Ncoa6
|
UTSW |
2 |
155,248,741 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2040:Ncoa6
|
UTSW |
2 |
155,248,000 (GRCm39) |
missense |
probably damaging |
0.98 |
R2087:Ncoa6
|
UTSW |
2 |
155,248,079 (GRCm39) |
nonsense |
probably null |
|
R2159:Ncoa6
|
UTSW |
2 |
155,249,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R2278:Ncoa6
|
UTSW |
2 |
155,249,570 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2696:Ncoa6
|
UTSW |
2 |
155,279,935 (GRCm39) |
missense |
probably benign |
0.45 |
R2891:Ncoa6
|
UTSW |
2 |
155,279,881 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3618:Ncoa6
|
UTSW |
2 |
155,249,709 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3747:Ncoa6
|
UTSW |
2 |
155,253,561 (GRCm39) |
missense |
probably benign |
0.01 |
R3778:Ncoa6
|
UTSW |
2 |
155,263,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R3784:Ncoa6
|
UTSW |
2 |
155,249,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R3802:Ncoa6
|
UTSW |
2 |
155,247,484 (GRCm39) |
missense |
probably benign |
|
R3820:Ncoa6
|
UTSW |
2 |
155,248,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R3821:Ncoa6
|
UTSW |
2 |
155,248,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R3822:Ncoa6
|
UTSW |
2 |
155,248,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R3870:Ncoa6
|
UTSW |
2 |
155,257,477 (GRCm39) |
splice site |
probably null |
|
R4037:Ncoa6
|
UTSW |
2 |
155,249,290 (GRCm39) |
missense |
probably damaging |
0.98 |
R4488:Ncoa6
|
UTSW |
2 |
155,249,396 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4719:Ncoa6
|
UTSW |
2 |
155,233,081 (GRCm39) |
unclassified |
probably benign |
|
R4732:Ncoa6
|
UTSW |
2 |
155,263,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R4733:Ncoa6
|
UTSW |
2 |
155,263,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R4829:Ncoa6
|
UTSW |
2 |
155,257,147 (GRCm39) |
missense |
probably damaging |
0.99 |
R4835:Ncoa6
|
UTSW |
2 |
155,249,053 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4883:Ncoa6
|
UTSW |
2 |
155,248,687 (GRCm39) |
missense |
probably benign |
0.29 |
R4967:Ncoa6
|
UTSW |
2 |
155,263,252 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5021:Ncoa6
|
UTSW |
2 |
155,248,869 (GRCm39) |
missense |
probably benign |
0.05 |
R5234:Ncoa6
|
UTSW |
2 |
155,279,933 (GRCm39) |
missense |
probably benign |
0.01 |
R5356:Ncoa6
|
UTSW |
2 |
155,263,112 (GRCm39) |
missense |
probably damaging |
0.99 |
R5358:Ncoa6
|
UTSW |
2 |
155,248,907 (GRCm39) |
missense |
probably damaging |
0.97 |
R5375:Ncoa6
|
UTSW |
2 |
155,275,915 (GRCm39) |
missense |
probably benign |
0.16 |
R5412:Ncoa6
|
UTSW |
2 |
155,249,701 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5618:Ncoa6
|
UTSW |
2 |
155,279,817 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5641:Ncoa6
|
UTSW |
2 |
155,263,756 (GRCm39) |
missense |
probably benign |
0.22 |
R5757:Ncoa6
|
UTSW |
2 |
155,253,528 (GRCm39) |
missense |
probably damaging |
1.00 |
R5761:Ncoa6
|
UTSW |
2 |
155,250,061 (GRCm39) |
missense |
probably benign |
0.11 |
R5778:Ncoa6
|
UTSW |
2 |
155,248,688 (GRCm39) |
missense |
probably benign |
0.01 |
R5852:Ncoa6
|
UTSW |
2 |
155,247,419 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5940:Ncoa6
|
UTSW |
2 |
155,257,785 (GRCm39) |
missense |
probably damaging |
0.98 |
R6155:Ncoa6
|
UTSW |
2 |
155,249,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R6374:Ncoa6
|
UTSW |
2 |
155,263,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R6389:Ncoa6
|
UTSW |
2 |
155,237,736 (GRCm39) |
missense |
probably damaging |
0.98 |
R6669:Ncoa6
|
UTSW |
2 |
155,241,613 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7097:Ncoa6
|
UTSW |
2 |
155,279,983 (GRCm39) |
missense |
probably benign |
0.01 |
R7385:Ncoa6
|
UTSW |
2 |
155,249,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R7963:Ncoa6
|
UTSW |
2 |
155,247,916 (GRCm39) |
missense |
probably benign |
0.30 |
R8356:Ncoa6
|
UTSW |
2 |
155,248,172 (GRCm39) |
missense |
possibly damaging |
0.59 |
R8698:Ncoa6
|
UTSW |
2 |
155,257,041 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8859:Ncoa6
|
UTSW |
2 |
155,248,388 (GRCm39) |
missense |
possibly damaging |
0.63 |
R8870:Ncoa6
|
UTSW |
2 |
155,263,078 (GRCm39) |
missense |
probably damaging |
0.99 |
R9041:Ncoa6
|
UTSW |
2 |
155,257,450 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9062:Ncoa6
|
UTSW |
2 |
155,263,348 (GRCm39) |
missense |
probably benign |
0.42 |
R9088:Ncoa6
|
UTSW |
2 |
155,249,726 (GRCm39) |
missense |
probably damaging |
0.98 |
R9225:Ncoa6
|
UTSW |
2 |
155,249,441 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9445:Ncoa6
|
UTSW |
2 |
155,250,063 (GRCm39) |
missense |
probably benign |
0.01 |
R9497:Ncoa6
|
UTSW |
2 |
155,248,238 (GRCm39) |
missense |
probably damaging |
0.97 |
R9514:Ncoa6
|
UTSW |
2 |
155,248,133 (GRCm39) |
missense |
probably benign |
0.19 |
R9656:Ncoa6
|
UTSW |
2 |
155,274,846 (GRCm39) |
missense |
probably damaging |
1.00 |
R9720:Ncoa6
|
UTSW |
2 |
155,250,304 (GRCm39) |
missense |
probably damaging |
0.98 |
R9732:Ncoa6
|
UTSW |
2 |
155,244,636 (GRCm39) |
missense |
probably damaging |
0.99 |
RF033:Ncoa6
|
UTSW |
2 |
155,263,651 (GRCm39) |
small deletion |
probably benign |
|
RF040:Ncoa6
|
UTSW |
2 |
155,263,651 (GRCm39) |
small deletion |
probably benign |
|
RF048:Ncoa6
|
UTSW |
2 |
155,263,632 (GRCm39) |
small deletion |
probably benign |
|
X0017:Ncoa6
|
UTSW |
2 |
155,248,460 (GRCm39) |
missense |
probably benign |
0.05 |
Z1176:Ncoa6
|
UTSW |
2 |
155,263,222 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Ncoa6
|
UTSW |
2 |
155,263,138 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Ncoa6
|
UTSW |
2 |
155,248,062 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
Predicted Primers |
PCR Primer
(F):5'- ACTGTTGACATCAATGCAGACTG -3'
(R):5'- TTCTTGACAACTCTGGAGCTCC -3'
Sequencing Primer
(F):5'- CAGACTGCAAGTGAGTTGGC -3'
(R):5'- GACAACTCTGGAGCTCCTAATGTG -3'
|
Posted On |
2016-10-26 |