Incidental Mutation 'R1858:Ncoa6'
ID |
206291 |
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 |
039882-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R1858 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
2 |
Chromosomal Location |
155232585-155315741 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to T
at 155263559 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Glutamine to Lysine
at position 292
(Q292K)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000118113
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000043126]
[ENSMUST00000109669]
[ENSMUST00000109670]
[ENSMUST00000123293]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably benign
Transcript: ENSMUST00000043126
AA Change: Q292K
PolyPhen 2
Score 0.134 (Sensitivity: 0.92; Specificity: 0.86)
|
SMART Domains |
Protein: ENSMUSP00000045386 Gene: ENSMUSG00000038369 AA Change: Q292K
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 benign
Transcript: ENSMUST00000109669
AA Change: Q292K
PolyPhen 2
Score 0.108 (Sensitivity: 0.93; Specificity: 0.86)
|
SMART Domains |
Protein: ENSMUSP00000105294 Gene: ENSMUSG00000038369 AA Change: Q292K
Domain | Start | End | E-Value | Type |
Pfam:Nucleic_acid_bd
|
45 |
195 |
2.6e-61 |
PFAM |
SCOP:d1lsha3
|
239 |
321 |
5e-3 |
SMART |
low complexity region
|
375 |
383 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000109670
AA Change: Q292K
PolyPhen 2
Score 0.134 (Sensitivity: 0.92; Specificity: 0.86)
|
SMART Domains |
Protein: ENSMUSP00000105295 Gene: ENSMUSG00000038369 AA Change: Q292K
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
AA Change: Q292K
PolyPhen 2
Score 0.134 (Sensitivity: 0.92; Specificity: 0.86)
|
SMART Domains |
Protein: ENSMUSP00000118113 Gene: ENSMUSG00000038369 AA Change: Q292K
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: ENSMUST00000141928
|
Meta Mutation Damage Score |
0.1188 |
Coding Region Coverage |
- 1x: 97.4%
- 3x: 96.7%
- 10x: 94.8%
- 20x: 91.0%
|
Validation Efficiency |
97% (112/116) |
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: 110 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A830018L16Rik |
C |
A |
1: 12,045,177 (GRCm39) |
A443E |
unknown |
Het |
Acacb |
A |
T |
5: 114,334,770 (GRCm39) |
Y613F |
probably benign |
Het |
Adam23 |
A |
C |
1: 63,596,615 (GRCm39) |
I566L |
probably benign |
Het |
Adar |
G |
T |
3: 89,646,589 (GRCm39) |
R338L |
probably benign |
Het |
Akap14 |
C |
T |
X: 36,420,779 (GRCm39) |
A476T |
probably damaging |
Het |
Amotl1 |
T |
A |
9: 14,486,697 (GRCm39) |
Q399L |
probably benign |
Het |
Ankrd16 |
T |
G |
2: 11,783,407 (GRCm39) |
L3R |
probably benign |
Het |
Arfgap1 |
G |
C |
2: 180,615,881 (GRCm39) |
G187R |
probably damaging |
Het |
Arhgap19 |
A |
T |
19: 41,767,592 (GRCm39) |
V399D |
probably benign |
Het |
Arl4d |
A |
G |
11: 101,557,578 (GRCm39) |
T35A |
probably damaging |
Het |
Atr |
T |
A |
9: 95,747,150 (GRCm39) |
I144N |
probably damaging |
Het |
Bptf |
A |
G |
11: 106,964,127 (GRCm39) |
M1574T |
probably benign |
Het |
Cacna1h |
T |
A |
17: 25,599,781 (GRCm39) |
D1684V |
probably damaging |
Het |
Celsr1 |
C |
A |
15: 85,916,960 (GRCm39) |
V338F |
probably damaging |
Het |
Cep164 |
T |
C |
9: 45,734,938 (GRCm39) |
|
probably benign |
Het |
Clock |
C |
A |
5: 76,388,756 (GRCm39) |
G390C |
possibly damaging |
Het |
Col6a6 |
A |
G |
9: 105,658,301 (GRCm39) |
F637S |
probably damaging |
Het |
Crebrf |
T |
A |
17: 26,961,937 (GRCm39) |
Y345N |
probably benign |
Het |
Cstdc3 |
A |
T |
16: 36,128,449 (GRCm39) |
I15F |
probably damaging |
Het |
Cul1 |
A |
G |
6: 47,502,458 (GRCm39) |
|
probably null |
Het |
Cyb5r4 |
C |
T |
9: 86,923,332 (GRCm39) |
S185L |
probably benign |
Het |
Cyp3a57 |
T |
C |
5: 145,318,059 (GRCm39) |
Y347H |
probably damaging |
Het |
Dgkq |
G |
T |
5: 108,801,597 (GRCm39) |
T487K |
probably benign |
Het |
Dmkn |
T |
C |
7: 30,463,990 (GRCm39) |
V143A |
probably benign |
Het |
Dmp1 |
A |
T |
5: 104,355,496 (GRCm39) |
E32V |
possibly damaging |
Het |
Dsc3 |
T |
C |
18: 20,098,773 (GRCm39) |
D802G |
probably damaging |
Het |
Dse |
T |
C |
10: 34,029,225 (GRCm39) |
T622A |
probably benign |
Het |
Duxf4 |
A |
G |
10: 58,071,602 (GRCm39) |
V204A |
probably benign |
Het |
Dyrk1b |
A |
T |
7: 27,882,071 (GRCm39) |
|
probably null |
Het |
Ehd2 |
T |
C |
7: 15,686,113 (GRCm39) |
T320A |
probably benign |
Het |
Eif3a |
A |
C |
19: 60,770,635 (GRCm39) |
L71V |
probably damaging |
Het |
Eif4e1b |
A |
G |
13: 54,935,091 (GRCm39) |
|
probably null |
Het |
Fam131b |
A |
G |
6: 42,295,914 (GRCm39) |
F161L |
probably damaging |
Het |
Fam171b |
A |
T |
2: 83,683,725 (GRCm39) |
M81L |
probably benign |
Het |
Gal3st4 |
T |
C |
5: 138,269,050 (GRCm39) |
|
probably null |
Het |
Gdf11 |
A |
T |
10: 128,722,315 (GRCm39) |
V180E |
probably damaging |
Het |
Grin3a |
T |
A |
4: 49,792,437 (GRCm39) |
Y432F |
probably benign |
Het |
Hif1a |
C |
A |
12: 73,990,929 (GRCm39) |
H708N |
probably benign |
Het |
Hmcn2 |
G |
T |
2: 31,305,295 (GRCm39) |
|
probably null |
Het |
Hs3st6 |
T |
A |
17: 24,976,973 (GRCm39) |
M151K |
possibly damaging |
Het |
Hyal2 |
T |
A |
9: 107,449,537 (GRCm39) |
L431Q |
probably benign |
Het |
Hyal6 |
A |
T |
6: 24,740,857 (GRCm39) |
T337S |
probably benign |
Het |
Igsf5 |
A |
T |
16: 96,187,829 (GRCm39) |
|
probably null |
Het |
Kif13a |
G |
A |
13: 47,018,314 (GRCm39) |
|
probably benign |
Het |
Krtap19-3 |
G |
A |
16: 88,674,878 (GRCm39) |
|
probably benign |
Het |
Lgalsl |
T |
C |
11: 20,779,420 (GRCm39) |
D75G |
probably benign |
Het |
Lrrc56 |
A |
G |
7: 140,787,421 (GRCm39) |
M353V |
probably benign |
Het |
Ltbp2 |
T |
A |
12: 84,877,555 (GRCm39) |
K337* |
probably null |
Het |
Mdn1 |
C |
T |
4: 32,730,881 (GRCm39) |
H2917Y |
probably benign |
Het |
Medag |
A |
G |
5: 149,353,259 (GRCm39) |
I151M |
probably damaging |
Het |
Meiob |
T |
C |
17: 25,042,544 (GRCm39) |
V124A |
probably damaging |
Het |
Mmp3 |
A |
G |
9: 7,451,799 (GRCm39) |
H379R |
probably benign |
Het |
Mpg |
A |
G |
11: 32,181,957 (GRCm39) |
|
probably null |
Het |
Ndufaf6 |
G |
T |
4: 11,053,474 (GRCm39) |
H277Q |
probably benign |
Het |
Nlrp4c |
A |
G |
7: 6,087,655 (GRCm39) |
I763V |
probably benign |
Het |
Nlrp5 |
A |
T |
7: 23,117,586 (GRCm39) |
I437F |
probably damaging |
Het |
Noc2l |
G |
A |
4: 156,329,727 (GRCm39) |
R435Q |
probably damaging |
Het |
Nova2 |
T |
C |
7: 18,692,326 (GRCm39) |
I485T |
probably damaging |
Het |
Nrxn2 |
G |
A |
19: 6,538,825 (GRCm39) |
V794I |
probably benign |
Het |
Nup210l |
A |
G |
3: 90,061,806 (GRCm39) |
T662A |
probably damaging |
Het |
Or2ad1 |
A |
T |
13: 21,326,564 (GRCm39) |
I221N |
probably damaging |
Het |
Or2b28 |
A |
G |
13: 21,531,346 (GRCm39) |
M83V |
possibly damaging |
Het |
Or2p2 |
A |
T |
13: 21,256,641 (GRCm39) |
F277I |
probably damaging |
Het |
Or51aa2 |
G |
A |
7: 103,187,859 (GRCm39) |
T194I |
probably damaging |
Het |
Or51e2 |
A |
C |
7: 102,391,571 (GRCm39) |
I213S |
probably damaging |
Het |
Or51l14 |
G |
A |
7: 103,101,332 (GRCm39) |
V263I |
probably benign |
Het |
Or9g8 |
T |
C |
2: 85,607,582 (GRCm39) |
L218P |
probably damaging |
Het |
Pelp1 |
G |
A |
11: 70,285,568 (GRCm39) |
P767S |
probably damaging |
Het |
Pfdn1 |
C |
A |
18: 36,584,153 (GRCm39) |
M60I |
probably benign |
Het |
Plaat1 |
G |
A |
16: 29,036,470 (GRCm39) |
G36D |
probably damaging |
Het |
Plcxd3 |
T |
A |
15: 4,546,093 (GRCm39) |
|
probably benign |
Het |
Plekhg1 |
C |
A |
10: 3,895,917 (GRCm39) |
D436E |
possibly damaging |
Het |
Ppfibp1 |
G |
A |
6: 146,892,090 (GRCm39) |
V117I |
probably benign |
Het |
Prss44 |
A |
G |
9: 110,643,177 (GRCm39) |
K24R |
probably benign |
Het |
Ptger1 |
G |
T |
8: 84,395,107 (GRCm39) |
G195W |
probably benign |
Het |
Ptgs1 |
A |
C |
2: 36,132,782 (GRCm39) |
D260A |
probably benign |
Het |
Ptprd |
T |
A |
4: 75,865,384 (GRCm39) |
T1198S |
probably damaging |
Het |
Qsox2 |
A |
G |
2: 26,104,074 (GRCm39) |
S319P |
probably damaging |
Het |
Rab35 |
A |
G |
5: 115,778,147 (GRCm39) |
I38V |
probably damaging |
Het |
Rapgef4 |
A |
G |
2: 71,861,408 (GRCm39) |
I33V |
possibly damaging |
Het |
Rbbp8nl |
C |
T |
2: 179,924,006 (GRCm39) |
|
probably benign |
Het |
Riok1 |
A |
T |
13: 38,242,694 (GRCm39) |
K473* |
probably null |
Het |
Rtca |
C |
T |
3: 116,287,764 (GRCm39) |
G288S |
probably benign |
Het |
Sag |
A |
T |
1: 87,742,570 (GRCm39) |
D114V |
probably benign |
Het |
Sdk2 |
C |
T |
11: 113,729,472 (GRCm39) |
|
silent |
Het |
Sec61g |
A |
G |
11: 16,456,371 (GRCm39) |
|
probably null |
Het |
Sf3a3 |
A |
T |
4: 124,623,288 (GRCm39) |
I440F |
probably damaging |
Het |
Sgta |
T |
C |
10: 80,884,695 (GRCm39) |
K205E |
possibly damaging |
Het |
Slc36a4 |
A |
G |
9: 15,632,006 (GRCm39) |
T61A |
probably damaging |
Het |
Slc5a4a |
T |
C |
10: 76,002,569 (GRCm39) |
S242P |
probably benign |
Het |
Srgap3 |
A |
T |
6: 112,748,479 (GRCm39) |
L391Q |
probably damaging |
Het |
Stard13 |
T |
C |
5: 151,018,903 (GRCm39) |
Y60C |
probably damaging |
Het |
Styxl2 |
T |
C |
1: 165,928,415 (GRCm39) |
Y399C |
possibly damaging |
Het |
Syt12 |
G |
T |
19: 4,497,825 (GRCm39) |
H386N |
probably damaging |
Het |
Thyn1 |
T |
A |
9: 26,915,070 (GRCm39) |
M74K |
probably benign |
Het |
Tmem130 |
C |
A |
5: 144,689,093 (GRCm39) |
|
probably null |
Het |
Trim71 |
A |
G |
9: 114,392,016 (GRCm39) |
V57A |
possibly damaging |
Het |
Twf1 |
T |
C |
15: 94,483,428 (GRCm39) |
|
probably benign |
Het |
Tyro3 |
T |
A |
2: 119,632,176 (GRCm39) |
I81N |
possibly damaging |
Het |
Unc13a |
A |
T |
8: 72,105,043 (GRCm39) |
C740S |
probably damaging |
Het |
Vmn1r15 |
A |
T |
6: 57,235,616 (GRCm39) |
K161N |
probably benign |
Het |
Vmn1r16 |
A |
T |
6: 57,299,884 (GRCm39) |
I246N |
probably damaging |
Het |
Vmn1r42 |
A |
G |
6: 89,821,597 (GRCm39) |
I324T |
probably benign |
Het |
Vmn2r35 |
T |
C |
7: 7,819,805 (GRCm39) |
Y155C |
possibly damaging |
Het |
Wif1 |
T |
A |
10: 120,919,788 (GRCm39) |
|
probably null |
Het |
Wscd2 |
G |
A |
5: 113,689,231 (GRCm39) |
R79Q |
possibly damaging |
Het |
Zan |
G |
T |
5: 137,404,139 (GRCm39) |
|
probably benign |
Het |
Zfp9 |
G |
T |
6: 118,442,021 (GRCm39) |
H214N |
probably benign |
Het |
Zfp985 |
A |
T |
4: 147,667,315 (GRCm39) |
Y61F |
probably benign |
Het |
Zscan30 |
A |
G |
18: 24,104,524 (GRCm39) |
|
noncoding transcript |
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 |
|
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 |
R5579:Ncoa6
|
UTSW |
2 |
155,248,597 (GRCm39) |
missense |
probably damaging |
1.00 |
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'- CTTGCATTGGGCTAGGCAAG -3'
(R):5'- CAACAGAGTCATCCCTCAGG -3'
Sequencing Primer
(F):5'- AAGGGAGCCTTCTTCCACC -3'
(R):5'- AGGATCTTTACCTCCAGCGC -3'
|
Posted On |
2014-06-23 |