Incidental Mutation 'R2091:Skint6'
ID |
500544 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Skint6
|
Ensembl Gene |
ENSMUSG00000087194 |
Gene Name |
selection and upkeep of intraepithelial T cells 6 |
Synonyms |
OTTMUSG00000008519 |
MMRRC Submission |
040096-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.063)
|
Stock # |
R2091 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
4 |
Chromosomal Location |
112661813-113144170 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 112703881 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Asparagine to Serine
at position 998
(N998S)
|
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: N998S
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000121870 Gene: ENSMUSG00000087194 AA Change: N998S
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: N998S
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000132312 Gene: ENSMUSG00000087194 AA Change: N998S
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: 99.2%
- 3x: 98.6%
- 10x: 97.3%
- 20x: 95.5%
|
Validation Efficiency |
96% (55/57) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 100 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921504E06Rik |
G |
C |
2: 19,522,357 (GRCm39) |
N247K |
probably damaging |
Het |
4930402F06Rik |
T |
C |
2: 35,266,079 (GRCm39) |
K197R |
probably benign |
Het |
AA986860 |
T |
C |
1: 130,670,906 (GRCm39) |
L376P |
probably benign |
Het |
Adamts10 |
T |
C |
17: 33,770,166 (GRCm39) |
|
probably null |
Het |
Adamts7 |
T |
C |
9: 90,070,493 (GRCm39) |
|
probably null |
Het |
Adgrl1 |
T |
C |
8: 84,661,093 (GRCm39) |
I862T |
probably damaging |
Het |
Agbl1 |
G |
A |
7: 76,239,248 (GRCm39) |
V583M |
probably damaging |
Het |
Apba2 |
T |
A |
7: 64,345,341 (GRCm39) |
V177D |
probably benign |
Het |
Arfgap2 |
A |
G |
2: 91,100,586 (GRCm39) |
K297R |
probably benign |
Het |
Armh3 |
A |
T |
19: 45,941,119 (GRCm39) |
L300Q |
probably damaging |
Het |
Atg14 |
A |
T |
14: 47,780,352 (GRCm39) |
I474N |
probably damaging |
Het |
Atp2b4 |
C |
A |
1: 133,642,968 (GRCm39) |
V1046F |
probably benign |
Het |
Best1 |
A |
G |
19: 9,969,443 (GRCm39) |
V205A |
probably benign |
Het |
Bicdl1 |
A |
G |
5: 115,862,638 (GRCm39) |
S206P |
probably damaging |
Het |
Bltp1 |
T |
C |
3: 37,008,119 (GRCm39) |
V1725A |
probably damaging |
Het |
Bltp1 |
C |
T |
3: 37,042,405 (GRCm39) |
T2797I |
probably damaging |
Het |
Cacna1h |
C |
T |
17: 25,651,850 (GRCm39) |
C98Y |
possibly damaging |
Het |
Calhm3 |
T |
A |
19: 47,140,430 (GRCm39) |
D221V |
probably damaging |
Het |
Ccdc93 |
T |
A |
1: 121,411,071 (GRCm39) |
|
probably null |
Het |
Cd248 |
A |
T |
19: 5,120,074 (GRCm39) |
I641F |
possibly damaging |
Het |
Chrnb3 |
C |
T |
8: 27,884,262 (GRCm39) |
T333M |
probably damaging |
Het |
Cyb5rl |
A |
G |
4: 106,928,203 (GRCm39) |
H113R |
probably damaging |
Het |
Dab1 |
C |
T |
4: 104,588,948 (GRCm39) |
A524V |
probably benign |
Het |
Ddx59 |
T |
A |
1: 136,344,447 (GRCm39) |
D39E |
probably benign |
Het |
Defa5 |
A |
G |
8: 21,787,513 (GRCm39) |
D20G |
probably damaging |
Het |
Dido1 |
A |
T |
2: 180,303,677 (GRCm39) |
V1409E |
probably benign |
Het |
Dlc1 |
A |
T |
8: 37,404,763 (GRCm39) |
V342E |
probably benign |
Het |
Dsc2 |
G |
A |
18: 20,166,351 (GRCm39) |
T760I |
possibly damaging |
Het |
Dync1h1 |
A |
G |
12: 110,616,022 (GRCm39) |
I3057V |
probably benign |
Het |
Etnk2 |
T |
G |
1: 133,304,791 (GRCm39) |
|
probably null |
Het |
Fbp2 |
G |
T |
13: 63,006,021 (GRCm39) |
L31I |
probably damaging |
Het |
Gbp7 |
A |
T |
3: 142,240,383 (GRCm39) |
I34F |
probably damaging |
Het |
Gcfc2 |
A |
G |
6: 81,920,460 (GRCm39) |
E415G |
probably damaging |
Het |
Glp1r |
T |
C |
17: 31,144,523 (GRCm39) |
L232P |
probably damaging |
Het |
Gm10822 |
A |
G |
2: 73,729,619 (GRCm39) |
|
noncoding transcript |
Het |
Gm42669 |
G |
A |
5: 107,655,776 (GRCm39) |
V1192M |
probably benign |
Het |
Gpr37 |
A |
G |
6: 25,689,062 (GRCm39) |
S12P |
possibly damaging |
Het |
Gpt |
A |
G |
15: 76,582,176 (GRCm39) |
E211G |
possibly damaging |
Het |
Grxcr1 |
T |
C |
5: 68,267,755 (GRCm39) |
I168T |
probably damaging |
Het |
Hat1 |
T |
C |
2: 71,264,378 (GRCm39) |
V272A |
probably benign |
Het |
Igkv8-30 |
A |
C |
6: 70,094,070 (GRCm39) |
C114G |
probably damaging |
Het |
Kcne4 |
T |
C |
1: 78,795,624 (GRCm39) |
S91P |
probably benign |
Het |
Kif5b |
G |
A |
18: 6,213,248 (GRCm39) |
Q715* |
probably null |
Het |
Lamb1 |
T |
A |
12: 31,337,428 (GRCm39) |
N386K |
probably damaging |
Het |
Lcmt2 |
T |
C |
2: 120,969,097 (GRCm39) |
N662S |
probably damaging |
Het |
Lnx1 |
G |
T |
5: 74,780,727 (GRCm39) |
H324N |
probably benign |
Het |
Lrrc4 |
T |
G |
6: 28,830,586 (GRCm39) |
D343A |
probably benign |
Het |
Mars1 |
A |
G |
10: 127,135,154 (GRCm39) |
S646P |
probably damaging |
Het |
Mboat7 |
T |
C |
7: 3,687,010 (GRCm39) |
|
probably benign |
Het |
Mlip |
C |
T |
9: 77,072,145 (GRCm39) |
V341I |
possibly damaging |
Het |
Mterf1b |
A |
T |
5: 4,247,057 (GRCm39) |
T233S |
possibly damaging |
Het |
Myo3a |
A |
T |
2: 22,338,488 (GRCm39) |
H442L |
probably damaging |
Het |
Myrf |
A |
T |
19: 10,201,964 (GRCm39) |
V171D |
possibly damaging |
Het |
Nbas |
G |
A |
12: 13,411,046 (GRCm39) |
D897N |
probably benign |
Het |
Nfx1 |
T |
C |
4: 40,977,004 (GRCm39) |
V226A |
probably benign |
Het |
Nlrp4a |
T |
C |
7: 26,149,578 (GRCm39) |
L395P |
probably damaging |
Het |
Nrros |
C |
T |
16: 31,962,975 (GRCm39) |
W311* |
probably null |
Het |
Nsun6 |
A |
G |
2: 15,044,542 (GRCm39) |
|
probably null |
Het |
Ntrk2 |
A |
G |
13: 59,007,115 (GRCm39) |
H239R |
possibly damaging |
Het |
Or10g9 |
T |
C |
9: 39,912,500 (GRCm39) |
T8A |
probably benign |
Het |
Or4k51 |
A |
T |
2: 111,584,731 (GRCm39) |
M46L |
probably benign |
Het |
Or5aq7 |
T |
C |
2: 86,938,606 (GRCm39) |
N42D |
probably damaging |
Het |
Or5p70 |
A |
G |
7: 107,995,068 (GRCm39) |
H247R |
probably damaging |
Het |
Pate4 |
C |
A |
9: 35,519,553 (GRCm39) |
A46S |
possibly damaging |
Het |
Pcdhb18 |
T |
C |
18: 37,623,653 (GRCm39) |
S328P |
probably damaging |
Het |
Pdk4 |
A |
G |
6: 5,494,857 (GRCm39) |
|
probably benign |
Het |
Pigm |
T |
C |
1: 172,205,100 (GRCm39) |
Y279H |
probably damaging |
Het |
Plaat3 |
A |
G |
19: 7,556,474 (GRCm39) |
I92V |
probably damaging |
Het |
Plxdc2 |
A |
G |
2: 16,718,494 (GRCm39) |
I379M |
probably damaging |
Het |
Ppp1r35 |
A |
G |
5: 137,778,156 (GRCm39) |
N217S |
possibly damaging |
Het |
Prex1 |
G |
A |
2: 166,411,285 (GRCm39) |
T1438I |
possibly damaging |
Het |
Ptger4 |
T |
A |
15: 5,272,326 (GRCm39) |
I98F |
possibly damaging |
Het |
Rasl11a |
T |
A |
5: 146,783,927 (GRCm39) |
I124N |
probably damaging |
Het |
Rest |
A |
G |
5: 77,429,126 (GRCm39) |
K515R |
possibly damaging |
Het |
Ryr1 |
A |
G |
7: 28,785,474 (GRCm39) |
L1746P |
probably damaging |
Het |
Ryr2 |
G |
T |
13: 11,960,863 (GRCm39) |
T25K |
probably benign |
Het |
Sacs |
A |
T |
14: 61,429,368 (GRCm39) |
I476L |
possibly damaging |
Het |
Serpina3g |
A |
T |
12: 104,205,417 (GRCm39) |
D52V |
probably damaging |
Het |
Skp2 |
C |
A |
15: 9,113,786 (GRCm39) |
G376C |
probably damaging |
Het |
Slc10a4 |
G |
A |
5: 73,174,482 (GRCm39) |
|
probably benign |
Het |
Slc24a2 |
G |
T |
4: 86,929,883 (GRCm39) |
P538T |
probably damaging |
Het |
Sntg1 |
T |
A |
1: 8,665,763 (GRCm39) |
T184S |
probably benign |
Het |
Ssbp1 |
A |
G |
6: 40,453,433 (GRCm39) |
Y73C |
probably null |
Het |
St18 |
G |
A |
1: 6,898,195 (GRCm39) |
V666M |
probably benign |
Het |
Suclg1 |
A |
G |
6: 73,241,259 (GRCm39) |
K193R |
probably benign |
Het |
Tcp11l1 |
T |
C |
2: 104,514,484 (GRCm39) |
I428V |
possibly damaging |
Het |
Th |
T |
A |
7: 142,449,280 (GRCm39) |
D275V |
probably damaging |
Het |
Tnrc18 |
A |
C |
5: 142,759,396 (GRCm39) |
S813R |
unknown |
Het |
Tnrc6a |
T |
C |
7: 122,771,343 (GRCm39) |
|
probably null |
Het |
Trap1 |
A |
C |
16: 3,863,903 (GRCm39) |
Y472* |
probably null |
Het |
Trdv1 |
C |
A |
14: 54,119,626 (GRCm39) |
Q96K |
probably benign |
Het |
Trpm8 |
T |
C |
1: 88,271,048 (GRCm39) |
I446T |
probably damaging |
Het |
Tti2 |
T |
C |
8: 31,644,294 (GRCm39) |
L297P |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,565,355 (GRCm39) |
G26545R |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,587,488 (GRCm39) |
D13208G |
probably damaging |
Het |
Tubb3 |
A |
G |
8: 124,148,417 (GRCm39) |
|
probably null |
Het |
Umodl1 |
A |
G |
17: 31,190,893 (GRCm39) |
M247V |
probably benign |
Het |
Wrn |
T |
A |
8: 33,757,853 (GRCm39) |
H812L |
probably benign |
Het |
Zfp174 |
A |
G |
16: 3,672,506 (GRCm39) |
R352G |
possibly damaging |
Het |
Zfp955a |
T |
A |
17: 33,461,731 (GRCm39) |
K134* |
probably null |
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 |
|
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 |
R5436:Skint6
|
UTSW |
4 |
112,953,788 (GRCm39) |
missense |
probably benign |
0.08 |
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 |
|
Posted On |
2017-12-01 |