Incidental Mutation 'R5436:Skint6'
ID |
428324 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Skint6
|
Ensembl Gene |
ENSMUSG00000087194 |
Gene Name |
selection and upkeep of intraepithelial T cells 6 |
Synonyms |
OTTMUSG00000008519 |
MMRRC Submission |
043001-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.063)
|
Stock # |
R5436 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
4 |
Chromosomal Location |
112661813-113144170 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to G
at 112953788 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Leucine
at position 459
(I459L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000132312
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000138966]
[ENSMUST00000171224]
|
AlphaFold |
A7XUZ6 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000138966
AA Change: I459L
PolyPhen 2
Score 0.083 (Sensitivity: 0.93; Specificity: 0.85)
|
SMART Domains |
Protein: ENSMUSP00000121870 Gene: ENSMUSG00000087194 AA Change: I459L
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
24 |
N/A |
INTRINSIC |
IGv
|
44 |
125 |
2.32e-8 |
SMART |
internal_repeat_1
|
219 |
594 |
1.11e-41 |
PROSPERO |
low complexity region
|
601 |
610 |
N/A |
INTRINSIC |
low complexity region
|
678 |
690 |
N/A |
INTRINSIC |
internal_repeat_1
|
701 |
1076 |
1.11e-41 |
PROSPERO |
transmembrane domain
|
1087 |
1104 |
N/A |
INTRINSIC |
transmembrane domain
|
1164 |
1186 |
N/A |
INTRINSIC |
transmembrane domain
|
1206 |
1228 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000171224
AA Change: I459L
PolyPhen 2
Score 0.083 (Sensitivity: 0.93; Specificity: 0.85)
|
SMART Domains |
Protein: ENSMUSP00000132312 Gene: ENSMUSG00000087194 AA Change: I459L
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
24 |
N/A |
INTRINSIC |
IGv
|
44 |
125 |
2.32e-8 |
SMART |
internal_repeat_1
|
219 |
594 |
1.11e-41 |
PROSPERO |
low complexity region
|
601 |
610 |
N/A |
INTRINSIC |
low complexity region
|
678 |
690 |
N/A |
INTRINSIC |
internal_repeat_1
|
701 |
1076 |
1.11e-41 |
PROSPERO |
transmembrane domain
|
1087 |
1104 |
N/A |
INTRINSIC |
transmembrane domain
|
1164 |
1186 |
N/A |
INTRINSIC |
transmembrane domain
|
1206 |
1228 |
N/A |
INTRINSIC |
|
Meta Mutation Damage Score |
0.0898 |
Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.6%
- 10x: 97.3%
- 20x: 95.4%
|
Validation Efficiency |
99% (106/107) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 100 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930449A18Rik |
T |
C |
3: 59,754,114 (GRCm39) |
|
noncoding transcript |
Het |
Abca9 |
G |
A |
11: 110,025,062 (GRCm39) |
L994F |
probably damaging |
Het |
Abl2 |
A |
T |
1: 156,457,450 (GRCm39) |
S239C |
probably damaging |
Het |
Acsl5 |
T |
A |
19: 55,267,997 (GRCm39) |
|
probably null |
Het |
Aff1 |
C |
T |
5: 103,931,736 (GRCm39) |
T126I |
probably damaging |
Het |
Amtn |
T |
C |
5: 88,529,485 (GRCm39) |
L107P |
probably damaging |
Het |
Ankrd45 |
A |
G |
1: 160,986,682 (GRCm39) |
|
probably benign |
Het |
Arl6ip5 |
G |
A |
6: 97,187,887 (GRCm39) |
V36I |
probably damaging |
Het |
Ascc3 |
T |
A |
10: 50,535,079 (GRCm39) |
D657E |
probably damaging |
Het |
Ascl1 |
T |
A |
10: 87,328,808 (GRCm39) |
Q48L |
unknown |
Het |
Asic4 |
T |
A |
1: 75,427,963 (GRCm39) |
V163E |
probably benign |
Het |
Atm |
A |
T |
9: 53,371,104 (GRCm39) |
M2245K |
probably benign |
Het |
Barx2 |
T |
G |
9: 31,824,285 (GRCm39) |
T35P |
probably damaging |
Het |
Bdh1 |
C |
T |
16: 31,275,475 (GRCm39) |
R235C |
probably damaging |
Het |
C8b |
T |
A |
4: 104,657,546 (GRCm39) |
Y404* |
probably null |
Het |
Car5a |
A |
G |
8: 122,643,981 (GRCm39) |
|
probably benign |
Het |
Ccdc13 |
T |
C |
9: 121,628,109 (GRCm39) |
I169M |
probably benign |
Het |
Cd163 |
A |
T |
6: 124,304,923 (GRCm39) |
D1100V |
probably benign |
Het |
Cimap2 |
A |
T |
4: 106,467,690 (GRCm39) |
H315Q |
probably benign |
Het |
Cntfr |
T |
C |
4: 41,663,322 (GRCm39) |
N162D |
probably damaging |
Het |
Cops3 |
T |
G |
11: 59,715,171 (GRCm39) |
D289A |
probably damaging |
Het |
Crbn |
A |
T |
6: 106,772,861 (GRCm39) |
S42R |
probably damaging |
Het |
Cth |
T |
A |
3: 157,600,463 (GRCm39) |
H397L |
probably benign |
Het |
Dact2 |
A |
G |
17: 14,416,010 (GRCm39) |
L730P |
probably damaging |
Het |
Dhx37 |
C |
T |
5: 125,506,867 (GRCm39) |
G210R |
probably benign |
Het |
Dnaaf9 |
C |
A |
2: 130,606,419 (GRCm39) |
K415N |
probably benign |
Het |
Dnah1 |
T |
C |
14: 31,038,704 (GRCm39) |
I126V |
probably benign |
Het |
Dnttip2 |
T |
C |
3: 122,072,418 (GRCm39) |
I566T |
probably damaging |
Het |
Ehbp1l1 |
G |
T |
19: 5,766,276 (GRCm39) |
R412S |
possibly damaging |
Het |
Fam110b |
A |
C |
4: 5,799,104 (GRCm39) |
Q174P |
probably benign |
Het |
Fam149a |
A |
T |
8: 45,801,508 (GRCm39) |
S457T |
probably benign |
Het |
Fat3 |
A |
C |
9: 15,871,810 (GRCm39) |
V3527G |
probably benign |
Het |
Fat4 |
A |
G |
3: 38,945,495 (GRCm39) |
M1463V |
probably benign |
Het |
Gak |
T |
A |
5: 108,740,218 (GRCm39) |
I566F |
possibly damaging |
Het |
Gdf10 |
T |
A |
14: 33,654,213 (GRCm39) |
I240N |
probably damaging |
Het |
Gprc6a |
T |
A |
10: 51,502,798 (GRCm39) |
H355L |
probably benign |
Het |
Gxylt1 |
T |
C |
15: 93,145,780 (GRCm39) |
K338R |
probably damaging |
Het |
Hexim2 |
A |
T |
11: 103,029,095 (GRCm39) |
E49V |
probably null |
Het |
Hfm1 |
T |
C |
5: 107,040,638 (GRCm39) |
D709G |
possibly damaging |
Het |
Ighv1-49 |
T |
C |
12: 115,019,081 (GRCm39) |
K19R |
probably damaging |
Het |
Il17a |
T |
A |
1: 20,803,870 (GRCm39) |
Y88* |
probably null |
Het |
Iqsec1 |
A |
T |
6: 90,822,343 (GRCm39) |
|
probably benign |
Het |
Itih2 |
T |
C |
2: 10,110,007 (GRCm39) |
D582G |
probably benign |
Het |
Klc3 |
T |
C |
7: 19,131,884 (GRCm39) |
|
probably null |
Het |
Larp4 |
T |
A |
15: 99,883,995 (GRCm39) |
N78K |
probably damaging |
Het |
Larp4b |
A |
G |
13: 9,218,936 (GRCm39) |
D526G |
possibly damaging |
Het |
Limch1 |
T |
C |
5: 67,131,909 (GRCm39) |
V133A |
possibly damaging |
Het |
Lmbr1l |
G |
A |
15: 98,802,672 (GRCm39) |
R426C |
probably damaging |
Het |
Lox |
T |
A |
18: 52,662,175 (GRCm39) |
D76V |
probably benign |
Het |
Lrrc8d |
T |
A |
5: 105,960,418 (GRCm39) |
I276N |
probably damaging |
Het |
Ltbr |
G |
A |
6: 125,289,757 (GRCm39) |
R146W |
probably damaging |
Het |
Marchf10 |
A |
T |
11: 105,292,991 (GRCm39) |
Y139N |
possibly damaging |
Het |
Mrc1 |
T |
G |
2: 14,271,326 (GRCm39) |
I410S |
probably damaging |
Het |
Mrto4 |
A |
T |
4: 139,075,276 (GRCm39) |
C176S |
probably damaging |
Het |
Mtch1 |
G |
T |
17: 29,566,564 (GRCm39) |
D66E |
probably benign |
Het |
Nbas |
T |
G |
12: 13,424,812 (GRCm39) |
L1017R |
probably damaging |
Het |
Nherf4 |
A |
G |
9: 44,159,652 (GRCm39) |
V448A |
possibly damaging |
Het |
Nim1k |
A |
G |
13: 120,189,065 (GRCm39) |
|
probably benign |
Het |
Nlrp6 |
T |
A |
7: 140,502,630 (GRCm39) |
Y245* |
probably null |
Het |
Or11g7 |
T |
G |
14: 50,691,184 (GRCm39) |
V225G |
probably damaging |
Het |
Or2t43 |
T |
A |
11: 58,457,763 (GRCm39) |
H136L |
probably benign |
Het |
Or4c3 |
T |
A |
2: 89,852,009 (GRCm39) |
M134L |
probably benign |
Het |
Or51q1 |
A |
T |
7: 103,628,473 (GRCm39) |
I25F |
probably benign |
Het |
Or5h24 |
C |
T |
16: 58,919,182 (GRCm39) |
V58I |
unknown |
Het |
Or8b1 |
A |
C |
9: 38,399,835 (GRCm39) |
D170A |
probably benign |
Het |
Pcare |
A |
T |
17: 72,057,837 (GRCm39) |
S613R |
probably damaging |
Het |
Pcnx1 |
G |
T |
12: 81,907,180 (GRCm39) |
G12V |
probably damaging |
Het |
Pkp1 |
T |
A |
1: 135,846,656 (GRCm39) |
K32M |
probably damaging |
Het |
Poc5 |
T |
C |
13: 96,533,321 (GRCm39) |
W150R |
probably damaging |
Het |
Ppp1r16b |
T |
A |
2: 158,599,253 (GRCm39) |
|
probably benign |
Het |
Prune2 |
T |
A |
19: 16,998,007 (GRCm39) |
M248K |
probably damaging |
Het |
Rb1 |
A |
T |
14: 73,450,580 (GRCm39) |
|
probably null |
Het |
Rhod |
A |
G |
19: 4,476,615 (GRCm39) |
C169R |
probably benign |
Het |
Rif1 |
T |
C |
2: 52,010,983 (GRCm39) |
|
probably benign |
Het |
Rnpc3 |
G |
A |
3: 113,418,648 (GRCm39) |
A100V |
probably damaging |
Het |
Rsf1 |
GCGGC |
GCGGCGGCGTCGGC |
7: 97,229,138 (GRCm39) |
|
probably benign |
Het |
Scnn1a |
A |
T |
6: 125,319,985 (GRCm39) |
D528V |
possibly damaging |
Het |
Sdhaf3 |
C |
A |
6: 7,038,855 (GRCm39) |
T59K |
probably benign |
Het |
Sec31a |
C |
A |
5: 100,511,698 (GRCm39) |
A330S |
probably damaging |
Het |
Sgk3 |
A |
G |
1: 9,952,097 (GRCm39) |
D241G |
probably damaging |
Het |
Slco1a5 |
A |
T |
6: 142,200,118 (GRCm39) |
V222E |
probably damaging |
Het |
Slit3 |
T |
A |
11: 35,598,738 (GRCm39) |
N1447K |
probably benign |
Het |
Sorbs2 |
A |
G |
8: 46,249,038 (GRCm39) |
H628R |
probably damaging |
Het |
St6galnac2 |
A |
G |
11: 116,575,353 (GRCm39) |
|
probably benign |
Het |
Tbc1d31 |
T |
C |
15: 57,816,267 (GRCm39) |
V667A |
probably benign |
Het |
Tbx20 |
A |
T |
9: 24,681,016 (GRCm39) |
Y159N |
probably damaging |
Het |
Tmprss11b |
T |
A |
5: 86,810,092 (GRCm39) |
Q296L |
probably benign |
Het |
Ttc6 |
T |
A |
12: 57,721,380 (GRCm39) |
|
probably null |
Het |
Ttn |
T |
A |
2: 76,701,243 (GRCm39) |
|
probably benign |
Het |
Tubgcp4 |
T |
A |
2: 121,018,617 (GRCm39) |
L340H |
probably damaging |
Het |
Tubgcp4 |
T |
A |
2: 121,024,663 (GRCm39) |
F613I |
probably benign |
Het |
Urb1 |
T |
C |
16: 90,589,650 (GRCm39) |
Y377C |
probably damaging |
Het |
Utp15 |
G |
A |
13: 98,397,354 (GRCm39) |
|
probably null |
Het |
Vstm2b |
A |
G |
7: 40,550,707 (GRCm39) |
|
probably null |
Het |
Vwde |
A |
T |
6: 13,190,627 (GRCm39) |
V488D |
probably damaging |
Het |
Wee1 |
TCCCC |
TCCC |
7: 109,723,776 (GRCm39) |
|
probably null |
Het |
Zfp276 |
A |
T |
8: 123,992,021 (GRCm39) |
|
probably benign |
Het |
Zfp318 |
T |
A |
17: 46,723,975 (GRCm39) |
S1993T |
possibly damaging |
Het |
Zfp959 |
T |
C |
17: 56,204,626 (GRCm39) |
L218P |
probably benign |
Het |
Zxdc |
A |
G |
6: 90,347,542 (GRCm39) |
D301G |
probably damaging |
Het |
|
Other mutations in Skint6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01123:Skint6
|
APN |
4 |
112,661,879 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL01296:Skint6
|
APN |
4 |
113,093,637 (GRCm39) |
missense |
probably benign |
0.37 |
IGL01343:Skint6
|
APN |
4 |
113,140,823 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01543:Skint6
|
APN |
4 |
112,757,160 (GRCm39) |
missense |
probably benign |
0.18 |
IGL01633:Skint6
|
APN |
4 |
113,095,246 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01818:Skint6
|
APN |
4 |
112,805,766 (GRCm39) |
missense |
probably benign |
0.18 |
IGL02124:Skint6
|
APN |
4 |
112,944,993 (GRCm39) |
missense |
probably benign |
|
IGL02517:Skint6
|
APN |
4 |
112,805,737 (GRCm39) |
splice site |
probably benign |
|
IGL02647:Skint6
|
APN |
4 |
112,985,088 (GRCm39) |
splice site |
probably benign |
|
IGL02887:Skint6
|
APN |
4 |
113,095,381 (GRCm39) |
nonsense |
probably null |
|
IGL03026:Skint6
|
APN |
4 |
112,848,441 (GRCm39) |
splice site |
probably null |
|
IGL03030:Skint6
|
APN |
4 |
112,870,153 (GRCm39) |
missense |
probably benign |
0.03 |
meissner
|
UTSW |
4 |
112,661,891 (GRCm39) |
missense |
possibly damaging |
0.86 |
Tegmentum
|
UTSW |
4 |
112,700,019 (GRCm39) |
splice site |
probably null |
|
PIT4576001:Skint6
|
UTSW |
4 |
112,910,564 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0058:Skint6
|
UTSW |
4 |
112,904,012 (GRCm39) |
splice site |
probably benign |
|
R0058:Skint6
|
UTSW |
4 |
112,904,012 (GRCm39) |
splice site |
probably benign |
|
R0099:Skint6
|
UTSW |
4 |
112,668,698 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0158:Skint6
|
UTSW |
4 |
113,042,011 (GRCm39) |
splice site |
probably benign |
|
R0164:Skint6
|
UTSW |
4 |
112,848,433 (GRCm39) |
splice site |
probably benign |
|
R0312:Skint6
|
UTSW |
4 |
112,666,297 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0591:Skint6
|
UTSW |
4 |
112,715,366 (GRCm39) |
splice site |
probably benign |
|
R0762:Skint6
|
UTSW |
4 |
112,722,848 (GRCm39) |
splice site |
probably benign |
|
R0941:Skint6
|
UTSW |
4 |
113,095,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R1023:Skint6
|
UTSW |
4 |
113,095,300 (GRCm39) |
missense |
probably benign |
0.20 |
R1132:Skint6
|
UTSW |
4 |
112,755,296 (GRCm39) |
critical splice donor site |
probably null |
|
R1228:Skint6
|
UTSW |
4 |
112,711,649 (GRCm39) |
missense |
probably benign |
|
R1338:Skint6
|
UTSW |
4 |
112,870,158 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1432:Skint6
|
UTSW |
4 |
112,726,721 (GRCm39) |
splice site |
probably benign |
|
R1512:Skint6
|
UTSW |
4 |
113,095,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R1577:Skint6
|
UTSW |
4 |
113,005,720 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1733:Skint6
|
UTSW |
4 |
113,034,234 (GRCm39) |
splice site |
probably benign |
|
R1762:Skint6
|
UTSW |
4 |
113,093,678 (GRCm39) |
missense |
probably damaging |
0.98 |
R1891:Skint6
|
UTSW |
4 |
112,703,893 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1908:Skint6
|
UTSW |
4 |
112,749,187 (GRCm39) |
missense |
probably benign |
|
R2069:Skint6
|
UTSW |
4 |
113,095,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R2089:Skint6
|
UTSW |
4 |
112,703,881 (GRCm39) |
missense |
probably benign |
|
R2091:Skint6
|
UTSW |
4 |
112,703,881 (GRCm39) |
missense |
probably benign |
|
R2091:Skint6
|
UTSW |
4 |
112,703,881 (GRCm39) |
missense |
probably benign |
|
R2144:Skint6
|
UTSW |
4 |
113,093,457 (GRCm39) |
missense |
possibly damaging |
0.84 |
R2166:Skint6
|
UTSW |
4 |
112,711,649 (GRCm39) |
missense |
probably benign |
0.01 |
R2192:Skint6
|
UTSW |
4 |
112,722,909 (GRCm39) |
nonsense |
probably null |
|
R2267:Skint6
|
UTSW |
4 |
112,700,019 (GRCm39) |
splice site |
probably null |
|
R2312:Skint6
|
UTSW |
4 |
113,095,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R2324:Skint6
|
UTSW |
4 |
112,729,654 (GRCm39) |
splice site |
probably null |
|
R2342:Skint6
|
UTSW |
4 |
113,034,180 (GRCm39) |
missense |
probably benign |
0.00 |
R3028:Skint6
|
UTSW |
4 |
113,093,690 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3704:Skint6
|
UTSW |
4 |
112,993,669 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3752:Skint6
|
UTSW |
4 |
112,700,096 (GRCm39) |
splice site |
probably benign |
|
R3760:Skint6
|
UTSW |
4 |
112,794,655 (GRCm39) |
missense |
possibly damaging |
0.53 |
R3827:Skint6
|
UTSW |
4 |
112,794,634 (GRCm39) |
missense |
probably benign |
|
R4377:Skint6
|
UTSW |
4 |
113,093,715 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4406:Skint6
|
UTSW |
4 |
113,013,683 (GRCm39) |
missense |
probably benign |
0.01 |
R4611:Skint6
|
UTSW |
4 |
112,931,273 (GRCm39) |
missense |
probably benign |
|
R4780:Skint6
|
UTSW |
4 |
113,093,594 (GRCm39) |
missense |
probably damaging |
0.98 |
R4788:Skint6
|
UTSW |
4 |
113,095,533 (GRCm39) |
missense |
possibly damaging |
0.54 |
R4818:Skint6
|
UTSW |
4 |
112,812,589 (GRCm39) |
intron |
probably benign |
|
R4900:Skint6
|
UTSW |
4 |
112,924,667 (GRCm39) |
missense |
probably benign |
0.03 |
R4972:Skint6
|
UTSW |
4 |
112,692,265 (GRCm39) |
missense |
probably benign |
|
R5008:Skint6
|
UTSW |
4 |
112,848,452 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5016:Skint6
|
UTSW |
4 |
113,028,730 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5085:Skint6
|
UTSW |
4 |
113,093,465 (GRCm39) |
missense |
probably damaging |
0.99 |
R5165:Skint6
|
UTSW |
4 |
112,722,865 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5221:Skint6
|
UTSW |
4 |
112,752,121 (GRCm39) |
splice site |
probably null |
|
R5310:Skint6
|
UTSW |
4 |
113,041,965 (GRCm39) |
nonsense |
probably null |
|
R5423:Skint6
|
UTSW |
4 |
112,707,937 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5447:Skint6
|
UTSW |
4 |
112,963,106 (GRCm39) |
missense |
probably benign |
0.34 |
R5564:Skint6
|
UTSW |
4 |
112,846,162 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5629:Skint6
|
UTSW |
4 |
112,870,176 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5936:Skint6
|
UTSW |
4 |
112,953,790 (GRCm39) |
missense |
probably benign |
0.33 |
R5993:Skint6
|
UTSW |
4 |
112,666,276 (GRCm39) |
missense |
probably benign |
0.02 |
R6027:Skint6
|
UTSW |
4 |
112,953,761 (GRCm39) |
splice site |
probably null |
|
R6174:Skint6
|
UTSW |
4 |
112,696,510 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6497:Skint6
|
UTSW |
4 |
113,093,595 (GRCm39) |
missense |
probably damaging |
0.98 |
R6552:Skint6
|
UTSW |
4 |
112,924,687 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6645:Skint6
|
UTSW |
4 |
112,749,235 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6810:Skint6
|
UTSW |
4 |
112,805,577 (GRCm39) |
splice site |
probably null |
|
R7003:Skint6
|
UTSW |
4 |
112,963,109 (GRCm39) |
missense |
probably benign |
0.01 |
R7211:Skint6
|
UTSW |
4 |
113,095,566 (GRCm39) |
missense |
probably benign |
0.09 |
R7269:Skint6
|
UTSW |
4 |
112,711,686 (GRCm39) |
splice site |
probably null |
|
R7398:Skint6
|
UTSW |
4 |
112,755,335 (GRCm39) |
missense |
probably benign |
0.00 |
R7438:Skint6
|
UTSW |
4 |
113,095,425 (GRCm39) |
missense |
probably damaging |
1.00 |
R7461:Skint6
|
UTSW |
4 |
113,034,243 (GRCm39) |
splice site |
probably null |
|
R7536:Skint6
|
UTSW |
4 |
112,668,744 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7613:Skint6
|
UTSW |
4 |
113,034,243 (GRCm39) |
splice site |
probably null |
|
R7956:Skint6
|
UTSW |
4 |
112,703,894 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8118:Skint6
|
UTSW |
4 |
113,013,691 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8118:Skint6
|
UTSW |
4 |
112,722,872 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8197:Skint6
|
UTSW |
4 |
112,752,040 (GRCm39) |
splice site |
probably null |
|
R8218:Skint6
|
UTSW |
4 |
112,696,471 (GRCm39) |
splice site |
probably null |
|
R8344:Skint6
|
UTSW |
4 |
113,093,642 (GRCm39) |
missense |
probably damaging |
1.00 |
R8518:Skint6
|
UTSW |
4 |
113,095,465 (GRCm39) |
missense |
possibly damaging |
0.58 |
R8776:Skint6
|
UTSW |
4 |
112,661,885 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8776-TAIL:Skint6
|
UTSW |
4 |
112,661,885 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8794:Skint6
|
UTSW |
4 |
113,049,869 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8796:Skint6
|
UTSW |
4 |
112,661,891 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8812:Skint6
|
UTSW |
4 |
112,846,149 (GRCm39) |
missense |
probably benign |
0.00 |
R8866:Skint6
|
UTSW |
4 |
112,711,650 (GRCm39) |
missense |
probably benign |
|
R8881:Skint6
|
UTSW |
4 |
112,672,716 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8949:Skint6
|
UTSW |
4 |
112,931,296 (GRCm39) |
missense |
probably benign |
0.04 |
R8967:Skint6
|
UTSW |
4 |
112,729,701 (GRCm39) |
nonsense |
probably null |
|
R9005:Skint6
|
UTSW |
4 |
113,095,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R9007:Skint6
|
UTSW |
4 |
113,095,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R9053:Skint6
|
UTSW |
4 |
113,095,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R9055:Skint6
|
UTSW |
4 |
113,095,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R9144:Skint6
|
UTSW |
4 |
112,985,102 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9149:Skint6
|
UTSW |
4 |
113,034,173 (GRCm39) |
missense |
probably damaging |
0.98 |
R9297:Skint6
|
UTSW |
4 |
112,668,717 (GRCm39) |
missense |
probably benign |
0.00 |
R9388:Skint6
|
UTSW |
4 |
113,049,838 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9407:Skint6
|
UTSW |
4 |
113,034,224 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9475:Skint6
|
UTSW |
4 |
112,664,037 (GRCm39) |
critical splice donor site |
probably null |
|
R9515:Skint6
|
UTSW |
4 |
112,715,375 (GRCm39) |
missense |
probably benign |
|
R9572:Skint6
|
UTSW |
4 |
112,985,128 (GRCm39) |
missense |
probably benign |
|
R9689:Skint6
|
UTSW |
4 |
113,093,546 (GRCm39) |
missense |
probably damaging |
0.99 |
R9744:Skint6
|
UTSW |
4 |
112,666,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R9785:Skint6
|
UTSW |
4 |
112,740,884 (GRCm39) |
missense |
possibly damaging |
0.86 |
Z1176:Skint6
|
UTSW |
4 |
113,095,491 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1176:Skint6
|
UTSW |
4 |
112,749,211 (GRCm39) |
missense |
possibly damaging |
0.53 |
Z1176:Skint6
|
UTSW |
4 |
113,095,492 (GRCm39) |
missense |
possibly damaging |
0.83 |
Z1177:Skint6
|
UTSW |
4 |
112,963,158 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1177:Skint6
|
UTSW |
4 |
112,664,125 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
Predicted Primers |
PCR Primer
(F):5'- TCAGGGTCCCTTCAGCAAAATC -3'
(R):5'- TGTTTGCTAGGAAAGAATTTGCAG -3'
Sequencing Primer
(F):5'- ATGGCAGTCTCTAGATGGTCAATCC -3'
(R):5'- GCAAACAGTACTGCTCTAG -3'
|
Posted On |
2016-09-01 |