Incidental Mutation 'R0325:Sgsm1'
ID |
25710 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Sgsm1
|
Ensembl Gene |
ENSMUSG00000042216 |
Gene Name |
small G protein signaling modulator 1 |
Synonyms |
Rutbc2, D5Bwg1524e, 2410098H20Rik |
MMRRC Submission |
038535-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R0325 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
5 |
Chromosomal Location |
113391086-113458652 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 113436701 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Asparagine
at position 43
(I43N)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000107944
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000048112]
[ENSMUST00000112325]
[ENSMUST00000154248]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000048112
AA Change: I43N
PolyPhen 2
Score 0.985 (Sensitivity: 0.74; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000046544 Gene: ENSMUSG00000042216 AA Change: I43N
Domain | Start | End | E-Value | Type |
RUN
|
127 |
187 |
6.52e-18 |
SMART |
low complexity region
|
401 |
413 |
N/A |
INTRINSIC |
low complexity region
|
454 |
469 |
N/A |
INTRINSIC |
TBC
|
559 |
1053 |
2.88e-29 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000112325
AA Change: I43N
PolyPhen 2
Score 0.990 (Sensitivity: 0.72; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000107944 Gene: ENSMUSG00000042216 AA Change: I43N
Domain | Start | End | E-Value | Type |
RUN
|
127 |
187 |
6.52e-18 |
SMART |
low complexity region
|
401 |
413 |
N/A |
INTRINSIC |
low complexity region
|
454 |
469 |
N/A |
INTRINSIC |
SCOP:d1fkma1
|
539 |
615 |
1e-6 |
SMART |
Blast:TBC
|
559 |
675 |
1e-71 |
BLAST |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000140981
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000145708
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000154248
AA Change: I43N
PolyPhen 2
Score 0.966 (Sensitivity: 0.77; Specificity: 0.95)
|
SMART Domains |
Protein: ENSMUSP00000114932 Gene: ENSMUSG00000042216 AA Change: I43N
Domain | Start | End | E-Value | Type |
RUN
|
127 |
187 |
6.52e-18 |
SMART |
low complexity region
|
401 |
413 |
N/A |
INTRINSIC |
low complexity region
|
509 |
524 |
N/A |
INTRINSIC |
SCOP:d1fkma1
|
594 |
670 |
9e-7 |
SMART |
Blast:TBC
|
614 |
706 |
3e-55 |
BLAST |
|
Coding Region Coverage |
- 1x: 99.0%
- 3x: 98.1%
- 10x: 95.9%
- 20x: 92.0%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 103 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4fm2 |
T |
C |
4: 144,282,081 (GRCm39) |
Y237C |
probably damaging |
Het |
Adcyap1 |
A |
G |
17: 93,510,260 (GRCm39) |
D96G |
probably benign |
Het |
Adgrv1 |
C |
T |
13: 81,688,134 (GRCm39) |
V1749M |
probably damaging |
Het |
Adnp2 |
A |
T |
18: 80,173,868 (GRCm39) |
N180K |
probably benign |
Het |
Ahdc1 |
G |
T |
4: 132,790,030 (GRCm39) |
A424S |
unknown |
Het |
Alpk3 |
G |
A |
7: 80,717,701 (GRCm39) |
R86H |
possibly damaging |
Het |
Atf7ip |
A |
C |
6: 136,537,987 (GRCm39) |
T49P |
possibly damaging |
Het |
Atp7b |
G |
A |
8: 22,518,467 (GRCm39) |
L124F |
probably benign |
Het |
Bub1 |
A |
T |
2: 127,643,314 (GRCm39) |
L1010* |
probably null |
Het |
Cd300c |
C |
A |
11: 114,850,411 (GRCm39) |
E131* |
probably null |
Het |
Cep135 |
A |
G |
5: 76,763,590 (GRCm39) |
K527E |
probably damaging |
Het |
Cfd |
G |
T |
10: 79,727,592 (GRCm39) |
E89* |
probably null |
Het |
Crb1 |
A |
C |
1: 139,168,904 (GRCm39) |
C871W |
probably damaging |
Het |
D6Ertd527e |
A |
T |
6: 87,088,277 (GRCm39) |
S147C |
unknown |
Het |
Ddx60 |
A |
T |
8: 62,436,889 (GRCm39) |
E946D |
probably benign |
Het |
Dmrt1 |
G |
A |
19: 25,523,371 (GRCm39) |
E241K |
probably benign |
Het |
Dnah11 |
C |
G |
12: 117,976,074 (GRCm39) |
V2782L |
probably benign |
Het |
Dzip1 |
T |
C |
14: 119,146,969 (GRCm39) |
I313M |
probably damaging |
Het |
Egln3 |
T |
C |
12: 54,250,298 (GRCm39) |
E17G |
probably benign |
Het |
Eif3d |
A |
G |
15: 77,852,420 (GRCm39) |
V42A |
probably damaging |
Het |
Elapor1 |
A |
G |
3: 108,368,567 (GRCm39) |
L808P |
probably damaging |
Het |
Eogt |
C |
A |
6: 97,090,916 (GRCm39) |
G408W |
probably damaging |
Het |
Fip1l1 |
T |
A |
5: 74,756,503 (GRCm39) |
N498K |
probably damaging |
Het |
Fmn2 |
T |
A |
1: 174,437,520 (GRCm39) |
|
probably null |
Het |
Fndc3b |
T |
C |
3: 27,521,579 (GRCm39) |
E532G |
probably damaging |
Het |
Gabrb3 |
T |
C |
7: 57,415,278 (GRCm39) |
L116P |
probably damaging |
Het |
Galnt6 |
A |
T |
15: 100,591,352 (GRCm39) |
|
probably null |
Het |
Glmp |
G |
A |
3: 88,232,391 (GRCm39) |
M1I |
probably null |
Het |
Gm5478 |
T |
C |
15: 101,552,761 (GRCm39) |
D79G |
probably damaging |
Het |
Gnb1 |
T |
G |
4: 155,636,140 (GRCm39) |
D153E |
probably benign |
Het |
Grik2 |
T |
C |
10: 49,116,821 (GRCm39) |
I86V |
probably damaging |
Het |
Hdac3 |
C |
T |
18: 38,074,005 (GRCm39) |
|
probably null |
Het |
Hdgfl2 |
G |
A |
17: 56,406,181 (GRCm39) |
R523H |
possibly damaging |
Het |
Ifngr1 |
T |
A |
10: 19,473,180 (GRCm39) |
N43K |
probably damaging |
Het |
Iqgap1 |
A |
G |
7: 80,401,678 (GRCm39) |
W476R |
probably benign |
Het |
Jag1 |
A |
G |
2: 136,937,365 (GRCm39) |
|
probably null |
Het |
Kars1 |
T |
C |
8: 112,734,848 (GRCm39) |
D46G |
probably benign |
Het |
Kcnd2 |
A |
G |
6: 21,216,682 (GRCm39) |
I129V |
probably damaging |
Het |
Lama3 |
A |
C |
18: 12,615,183 (GRCm39) |
D1369A |
probably damaging |
Het |
Lars1 |
A |
T |
18: 42,383,967 (GRCm39) |
V76E |
possibly damaging |
Het |
Lgals9 |
T |
C |
11: 78,854,274 (GRCm39) |
I337V |
probably damaging |
Het |
Lrp1b |
T |
C |
2: 40,741,723 (GRCm39) |
D3068G |
probably damaging |
Het |
Med12l |
A |
G |
3: 58,984,480 (GRCm39) |
T462A |
possibly damaging |
Het |
Megf9 |
T |
A |
4: 70,374,178 (GRCm39) |
D286V |
probably damaging |
Het |
Meox1 |
T |
A |
11: 101,770,227 (GRCm39) |
S167C |
probably damaging |
Het |
Mier2 |
C |
T |
10: 79,378,430 (GRCm39) |
|
probably null |
Het |
Mrps2 |
C |
A |
2: 28,359,791 (GRCm39) |
T216K |
probably damaging |
Het |
Mto1 |
A |
T |
9: 78,360,286 (GRCm39) |
D258V |
probably damaging |
Het |
Mug1 |
A |
T |
6: 121,826,801 (GRCm39) |
H208L |
probably benign |
Het |
Myo15b |
T |
A |
11: 115,775,091 (GRCm39) |
I751N |
probably damaging |
Het |
Napg |
C |
T |
18: 63,120,034 (GRCm39) |
R149C |
probably damaging |
Het |
Ndrg4 |
T |
A |
8: 96,437,563 (GRCm39) |
M17K |
probably damaging |
Het |
Nfrkb |
T |
G |
9: 31,325,476 (GRCm39) |
M973R |
probably benign |
Het |
Nxph4 |
C |
T |
10: 127,362,780 (GRCm39) |
R37H |
probably damaging |
Het |
Oas1e |
A |
G |
5: 120,933,460 (GRCm39) |
I35T |
probably damaging |
Het |
Oc90 |
C |
T |
15: 65,769,514 (GRCm39) |
|
probably null |
Het |
Or4b12 |
A |
T |
2: 90,095,880 (GRCm39) |
M298K |
probably null |
Het |
Or52d3 |
A |
T |
7: 104,229,567 (GRCm39) |
D238V |
probably damaging |
Het |
Or8j3 |
G |
A |
2: 86,029,055 (GRCm39) |
L14F |
possibly damaging |
Het |
Or8k30 |
A |
T |
2: 86,339,549 (GRCm39) |
T249S |
probably benign |
Het |
Or9a7 |
A |
T |
6: 40,521,057 (GRCm39) |
N285K |
possibly damaging |
Het |
Papola |
T |
A |
12: 105,773,452 (GRCm39) |
I157N |
probably damaging |
Het |
Pcyox1l |
G |
C |
18: 61,830,964 (GRCm39) |
P303A |
possibly damaging |
Het |
Pkdrej |
T |
C |
15: 85,703,752 (GRCm39) |
N728S |
probably benign |
Het |
Pkp4 |
A |
G |
2: 59,148,873 (GRCm39) |
D542G |
probably damaging |
Het |
Pla2g5 |
C |
T |
4: 138,527,967 (GRCm39) |
D100N |
probably benign |
Het |
Poln |
C |
T |
5: 34,307,108 (GRCm39) |
R31H |
probably benign |
Het |
Ppp3ca |
G |
A |
3: 136,640,900 (GRCm39) |
A484T |
probably benign |
Het |
Prag1 |
A |
G |
8: 36,570,958 (GRCm39) |
T514A |
probably benign |
Het |
Pramel28 |
A |
T |
4: 143,693,310 (GRCm39) |
V56E |
probably damaging |
Het |
Prex2 |
G |
A |
1: 11,270,281 (GRCm39) |
|
probably null |
Het |
Prrc2b |
G |
T |
2: 32,089,103 (GRCm39) |
W403L |
probably damaging |
Het |
Pter |
A |
T |
2: 13,005,748 (GRCm39) |
K307M |
probably damaging |
Het |
Ptpn5 |
G |
A |
7: 46,740,506 (GRCm39) |
S99L |
probably benign |
Het |
Ptpn5 |
A |
C |
7: 46,740,507 (GRCm39) |
S99A |
probably benign |
Het |
Rpap1 |
A |
C |
2: 119,602,321 (GRCm39) |
H674Q |
probably benign |
Het |
Rph3a |
A |
T |
5: 121,081,127 (GRCm39) |
D623E |
probably benign |
Het |
Sdr9c7 |
G |
T |
10: 127,734,588 (GRCm39) |
E25D |
probably benign |
Het |
Septin9 |
T |
G |
11: 117,247,458 (GRCm39) |
V479G |
probably damaging |
Het |
Sgo2a |
A |
G |
1: 58,055,856 (GRCm39) |
D680G |
probably benign |
Het |
Sgo2b |
A |
T |
8: 64,381,410 (GRCm39) |
I474N |
probably benign |
Het |
Shprh |
G |
A |
10: 11,045,853 (GRCm39) |
M891I |
probably benign |
Het |
Skic2 |
A |
T |
17: 35,063,791 (GRCm39) |
Y551N |
possibly damaging |
Het |
Slc12a9 |
A |
G |
5: 137,321,108 (GRCm39) |
M469T |
probably damaging |
Het |
Slc4a2 |
A |
T |
5: 24,640,941 (GRCm39) |
I747F |
probably damaging |
Het |
Slc7a6 |
T |
A |
8: 106,921,149 (GRCm39) |
N373K |
probably damaging |
Het |
Slc7a6os |
T |
C |
8: 106,927,688 (GRCm39) |
D296G |
probably benign |
Het |
Sncaip |
A |
G |
18: 53,038,881 (GRCm39) |
T120A |
probably damaging |
Het |
Sorcs1 |
G |
C |
19: 50,301,480 (GRCm39) |
|
probably null |
Het |
Spata16 |
A |
G |
3: 26,721,605 (GRCm39) |
E42G |
probably damaging |
Het |
Spata31e2 |
G |
T |
1: 26,724,347 (GRCm39) |
Q278K |
possibly damaging |
Het |
Syne2 |
A |
T |
12: 76,009,415 (GRCm39) |
M2440L |
probably benign |
Het |
Taf7l2 |
T |
C |
10: 115,949,474 (GRCm39) |
I17M |
probably damaging |
Het |
Tead2 |
A |
G |
7: 44,875,179 (GRCm39) |
E232G |
probably damaging |
Het |
Tmf1 |
T |
G |
6: 97,153,465 (GRCm39) |
T203P |
possibly damaging |
Het |
Trrap |
C |
A |
5: 144,753,205 (GRCm39) |
H1843Q |
probably benign |
Het |
Unc79 |
C |
A |
12: 103,137,903 (GRCm39) |
Q2314K |
probably damaging |
Het |
Unc80 |
G |
T |
1: 66,550,040 (GRCm39) |
G766V |
probably damaging |
Het |
Vmn1r217 |
A |
G |
13: 23,298,764 (GRCm39) |
L46P |
probably damaging |
Het |
Vmn2r80 |
A |
T |
10: 78,984,773 (GRCm39) |
I42F |
possibly damaging |
Het |
Vwa5a |
T |
C |
9: 38,639,961 (GRCm39) |
V403A |
probably damaging |
Het |
Zfp42 |
T |
C |
8: 43,748,988 (GRCm39) |
E171G |
probably damaging |
Het |
Zfp64 |
A |
T |
2: 168,767,960 (GRCm39) |
S551T |
probably benign |
Het |
|
Other mutations in Sgsm1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00230:Sgsm1
|
APN |
5 |
113,392,930 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00503:Sgsm1
|
APN |
5 |
113,424,008 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01377:Sgsm1
|
APN |
5 |
113,424,048 (GRCm39) |
splice site |
probably benign |
|
IGL01602:Sgsm1
|
APN |
5 |
113,433,531 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01605:Sgsm1
|
APN |
5 |
113,433,531 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01669:Sgsm1
|
APN |
5 |
113,411,356 (GRCm39) |
missense |
probably benign |
|
IGL01920:Sgsm1
|
APN |
5 |
113,421,471 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01951:Sgsm1
|
APN |
5 |
113,434,633 (GRCm39) |
splice site |
probably benign |
|
IGL02387:Sgsm1
|
APN |
5 |
113,400,929 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02690:Sgsm1
|
APN |
5 |
113,434,633 (GRCm39) |
splice site |
probably benign |
|
IGL03177:Sgsm1
|
APN |
5 |
113,398,859 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03186:Sgsm1
|
APN |
5 |
113,432,887 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03398:Sgsm1
|
APN |
5 |
113,403,182 (GRCm39) |
missense |
possibly damaging |
0.67 |
caliente
|
UTSW |
5 |
113,428,328 (GRCm39) |
intron |
probably benign |
|
Chili
|
UTSW |
5 |
113,405,989 (GRCm39) |
intron |
probably benign |
|
pimiento
|
UTSW |
5 |
113,411,123 (GRCm39) |
missense |
probably benign |
0.15 |
R0048:Sgsm1
|
UTSW |
5 |
113,416,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R0058:Sgsm1
|
UTSW |
5 |
113,432,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R0058:Sgsm1
|
UTSW |
5 |
113,432,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R0082:Sgsm1
|
UTSW |
5 |
113,436,702 (GRCm39) |
missense |
probably benign |
0.01 |
R0085:Sgsm1
|
UTSW |
5 |
113,427,136 (GRCm39) |
splice site |
probably benign |
|
R0099:Sgsm1
|
UTSW |
5 |
113,422,226 (GRCm39) |
splice site |
probably benign |
|
R0269:Sgsm1
|
UTSW |
5 |
113,434,795 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0310:Sgsm1
|
UTSW |
5 |
113,411,571 (GRCm39) |
missense |
probably benign |
0.00 |
R0420:Sgsm1
|
UTSW |
5 |
113,411,625 (GRCm39) |
missense |
probably benign |
0.16 |
R0594:Sgsm1
|
UTSW |
5 |
113,458,428 (GRCm39) |
missense |
probably benign |
0.00 |
R0599:Sgsm1
|
UTSW |
5 |
113,392,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R0631:Sgsm1
|
UTSW |
5 |
113,432,989 (GRCm39) |
splice site |
probably benign |
|
R0744:Sgsm1
|
UTSW |
5 |
113,427,050 (GRCm39) |
missense |
probably benign |
0.38 |
R0833:Sgsm1
|
UTSW |
5 |
113,427,050 (GRCm39) |
missense |
probably benign |
0.38 |
R0919:Sgsm1
|
UTSW |
5 |
113,406,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R0944:Sgsm1
|
UTSW |
5 |
113,413,740 (GRCm39) |
missense |
probably benign |
0.40 |
R1169:Sgsm1
|
UTSW |
5 |
113,427,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R1232:Sgsm1
|
UTSW |
5 |
113,421,577 (GRCm39) |
nonsense |
probably null |
|
R1473:Sgsm1
|
UTSW |
5 |
113,411,123 (GRCm39) |
missense |
probably benign |
0.15 |
R1535:Sgsm1
|
UTSW |
5 |
113,411,135 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1796:Sgsm1
|
UTSW |
5 |
113,421,483 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1878:Sgsm1
|
UTSW |
5 |
113,411,381 (GRCm39) |
missense |
probably damaging |
0.97 |
R2084:Sgsm1
|
UTSW |
5 |
113,433,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R3855:Sgsm1
|
UTSW |
5 |
113,411,125 (GRCm39) |
missense |
probably benign |
0.01 |
R3856:Sgsm1
|
UTSW |
5 |
113,411,125 (GRCm39) |
missense |
probably benign |
0.01 |
R4294:Sgsm1
|
UTSW |
5 |
113,433,270 (GRCm39) |
missense |
probably damaging |
1.00 |
R4373:Sgsm1
|
UTSW |
5 |
113,405,989 (GRCm39) |
intron |
probably benign |
|
R4558:Sgsm1
|
UTSW |
5 |
113,405,977 (GRCm39) |
intron |
probably benign |
|
R4610:Sgsm1
|
UTSW |
5 |
113,403,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R4667:Sgsm1
|
UTSW |
5 |
113,407,913 (GRCm39) |
critical splice donor site |
probably null |
|
R4838:Sgsm1
|
UTSW |
5 |
113,430,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R4890:Sgsm1
|
UTSW |
5 |
113,428,328 (GRCm39) |
intron |
probably benign |
|
R4992:Sgsm1
|
UTSW |
5 |
113,430,486 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5366:Sgsm1
|
UTSW |
5 |
113,398,905 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5776:Sgsm1
|
UTSW |
5 |
113,398,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R5813:Sgsm1
|
UTSW |
5 |
113,398,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R6000:Sgsm1
|
UTSW |
5 |
113,434,704 (GRCm39) |
missense |
probably damaging |
1.00 |
R6354:Sgsm1
|
UTSW |
5 |
113,430,522 (GRCm39) |
missense |
probably damaging |
0.99 |
R6440:Sgsm1
|
UTSW |
5 |
113,426,997 (GRCm39) |
critical splice donor site |
probably null |
|
R6831:Sgsm1
|
UTSW |
5 |
113,428,246 (GRCm39) |
missense |
probably damaging |
0.97 |
R7307:Sgsm1
|
UTSW |
5 |
113,421,512 (GRCm39) |
missense |
probably benign |
0.00 |
R7309:Sgsm1
|
UTSW |
5 |
113,416,712 (GRCm39) |
splice site |
probably null |
|
R7387:Sgsm1
|
UTSW |
5 |
113,411,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R7439:Sgsm1
|
UTSW |
5 |
113,422,187 (GRCm39) |
missense |
probably damaging |
0.99 |
R7485:Sgsm1
|
UTSW |
5 |
113,427,501 (GRCm39) |
splice site |
probably null |
|
R7624:Sgsm1
|
UTSW |
5 |
113,422,201 (GRCm39) |
nonsense |
probably null |
|
R7632:Sgsm1
|
UTSW |
5 |
113,423,948 (GRCm39) |
missense |
possibly damaging |
0.54 |
R7669:Sgsm1
|
UTSW |
5 |
113,400,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R7727:Sgsm1
|
UTSW |
5 |
113,422,193 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7732:Sgsm1
|
UTSW |
5 |
113,414,196 (GRCm39) |
missense |
probably benign |
0.26 |
R7961:Sgsm1
|
UTSW |
5 |
113,430,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R8088:Sgsm1
|
UTSW |
5 |
113,403,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R8213:Sgsm1
|
UTSW |
5 |
113,398,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R8278:Sgsm1
|
UTSW |
5 |
113,407,958 (GRCm39) |
missense |
probably damaging |
0.98 |
R8480:Sgsm1
|
UTSW |
5 |
113,411,284 (GRCm39) |
missense |
probably benign |
0.01 |
R8796:Sgsm1
|
UTSW |
5 |
113,411,123 (GRCm39) |
missense |
probably benign |
0.15 |
R8816:Sgsm1
|
UTSW |
5 |
113,435,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R8904:Sgsm1
|
UTSW |
5 |
113,421,495 (GRCm39) |
missense |
probably benign |
0.00 |
R8905:Sgsm1
|
UTSW |
5 |
113,421,495 (GRCm39) |
missense |
probably benign |
0.00 |
R8952:Sgsm1
|
UTSW |
5 |
113,432,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R9046:Sgsm1
|
UTSW |
5 |
113,436,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R9162:Sgsm1
|
UTSW |
5 |
113,430,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R9249:Sgsm1
|
UTSW |
5 |
113,428,201 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9375:Sgsm1
|
UTSW |
5 |
113,422,139 (GRCm39) |
missense |
unknown |
|
R9377:Sgsm1
|
UTSW |
5 |
113,436,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R9461:Sgsm1
|
UTSW |
5 |
113,423,898 (GRCm39) |
critical splice donor site |
probably null |
|
R9662:Sgsm1
|
UTSW |
5 |
113,427,097 (GRCm39) |
missense |
probably benign |
0.03 |
R9722:Sgsm1
|
UTSW |
5 |
113,428,207 (GRCm39) |
missense |
possibly damaging |
0.75 |
R9726:Sgsm1
|
UTSW |
5 |
113,458,418 (GRCm39) |
missense |
probably benign |
|
Z1177:Sgsm1
|
UTSW |
5 |
113,430,576 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- AGTCAGGATAAAGCAAGCCCTCCG -3'
(R):5'- CTTCAGACACTCTGGTGCTGAACTC -3'
Sequencing Primer
(F):5'- AGCCCCCTCACAGTTCTG -3'
(R):5'- TGAACTCACAGTCTCCAGGTG -3'
|
Posted On |
2013-04-16 |