Incidental Mutation 'R0268:Itsn2'
ID |
35092 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Itsn2
|
Ensembl Gene |
ENSMUSG00000020640 |
Gene Name |
intersectin 2 |
Synonyms |
Sh3d1B, Sh3p18, Ese2, Eh domain, SH3 domain regulator of endocytosis 2 |
MMRRC Submission |
038494-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R0268 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
12 |
Chromosomal Location |
4642792-4763952 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 4750333 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Arginine to Glutamine
at position 1199
(R1199Q)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000151900
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000062580]
[ENSMUST00000219007]
[ENSMUST00000220311]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably benign
Transcript: ENSMUST00000062580
AA Change: R1199Q
PolyPhen 2
Score 0.115 (Sensitivity: 0.93; Specificity: 0.86)
|
SMART Domains |
Protein: ENSMUSP00000052758 Gene: ENSMUSG00000020640 AA Change: R1199Q
Domain | Start | End | E-Value | Type |
EH
|
15 |
109 |
8.44e-41 |
SMART |
EFh
|
58 |
86 |
7.18e-3 |
SMART |
low complexity region
|
156 |
169 |
N/A |
INTRINSIC |
low complexity region
|
215 |
231 |
N/A |
INTRINSIC |
EH
|
238 |
333 |
4.06e-43 |
SMART |
EFh
|
282 |
310 |
6.16e-2 |
SMART |
coiled coil region
|
366 |
462 |
N/A |
INTRINSIC |
coiled coil region
|
516 |
556 |
N/A |
INTRINSIC |
coiled coil region
|
580 |
715 |
N/A |
INTRINSIC |
SH3
|
721 |
778 |
2.65e-21 |
SMART |
low complexity region
|
791 |
811 |
N/A |
INTRINSIC |
SH3
|
855 |
909 |
8.83e-18 |
SMART |
SH3
|
945 |
999 |
9.1e-20 |
SMART |
SH3
|
1017 |
1077 |
1.55e-13 |
SMART |
SH3
|
1091 |
1146 |
7.22e-23 |
SMART |
RhoGEF
|
1174 |
1355 |
1.93e-56 |
SMART |
PH
|
1396 |
1507 |
1.16e-9 |
SMART |
C2
|
1531 |
1628 |
3.96e-19 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000218923
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000219007
AA Change: R1199Q
PolyPhen 2
Score 0.115 (Sensitivity: 0.93; Specificity: 0.86)
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000219182
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000219308
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000219832
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000220311
AA Change: R1226Q
PolyPhen 2
Score 0.046 (Sensitivity: 0.94; Specificity: 0.83)
|
Meta Mutation Damage Score |
0.0898 |
Coding Region Coverage |
- 1x: 98.7%
- 3x: 97.7%
- 10x: 95.9%
- 20x: 93.0%
|
Validation Efficiency |
98% (93/95) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a cytoplasmic protein which contains SH3 domains. This protein is a member of a family of proteins involved in clathrin-mediated endocytosis. Intersectin 2 is thought to regulate the formation of clathrin-coated vesicles and also may function in the induction of T cell antigen receptor (TCR) endocytosis. [provided by RefSeq, Jan 2017] PHENOTYPE: Mice homozygous for a knock-out allele exhibit normal brain morphology and function and behavior. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930432E11Rik |
T |
A |
7: 29,274,027 (GRCm39) |
|
noncoding transcript |
Het |
Aadacl4 |
A |
T |
4: 144,349,565 (GRCm39) |
H274L |
probably benign |
Het |
Aldh1a7 |
T |
A |
19: 20,686,866 (GRCm39) |
|
probably null |
Het |
Ap3m1 |
A |
C |
14: 21,087,170 (GRCm39) |
|
probably benign |
Het |
Atp5f1a |
C |
A |
18: 77,867,895 (GRCm39) |
N356K |
probably damaging |
Het |
AU021092 |
A |
T |
16: 5,040,031 (GRCm39) |
M31K |
possibly damaging |
Het |
Avpr1a |
T |
C |
10: 122,285,614 (GRCm39) |
V302A |
probably damaging |
Het |
Bicral |
A |
G |
17: 47,124,978 (GRCm39) |
|
probably benign |
Het |
Btbd9 |
C |
T |
17: 30,493,916 (GRCm39) |
D492N |
possibly damaging |
Het |
Casp8ap2 |
A |
T |
4: 32,644,079 (GRCm39) |
I1051F |
probably damaging |
Het |
Cd209e |
T |
C |
8: 3,899,125 (GRCm39) |
I196V |
probably benign |
Het |
Cdc42bpa |
G |
T |
1: 179,983,347 (GRCm39) |
|
probably benign |
Het |
Cdcp3 |
A |
G |
7: 130,839,905 (GRCm39) |
D609G |
probably damaging |
Het |
Clec16a |
T |
A |
16: 10,462,692 (GRCm39) |
L670* |
probably null |
Het |
Cmtm2b |
A |
G |
8: 105,049,066 (GRCm39) |
E27G |
probably damaging |
Het |
Col4a1 |
T |
A |
8: 11,317,588 (GRCm39) |
|
probably benign |
Het |
Cyp26b1 |
A |
T |
6: 84,551,554 (GRCm39) |
F221I |
probably damaging |
Het |
D430041D05Rik |
G |
C |
2: 103,998,295 (GRCm39) |
P1836R |
probably damaging |
Het |
Dennd6b |
T |
C |
15: 89,080,432 (GRCm39) |
Q56R |
probably benign |
Het |
Dip2c |
G |
A |
13: 9,687,186 (GRCm39) |
R1270H |
probably damaging |
Het |
Dlg1 |
T |
C |
16: 31,503,011 (GRCm39) |
C73R |
probably benign |
Het |
Dnah8 |
A |
G |
17: 30,988,681 (GRCm39) |
D3217G |
probably damaging |
Het |
Dtx1 |
T |
C |
5: 120,819,356 (GRCm39) |
E614G |
probably damaging |
Het |
Dut |
C |
A |
2: 125,099,011 (GRCm39) |
A166E |
probably damaging |
Het |
Ebf1 |
C |
A |
11: 44,534,240 (GRCm39) |
D166E |
probably damaging |
Het |
Egln2 |
A |
T |
7: 26,864,672 (GRCm39) |
D84E |
possibly damaging |
Het |
Exosc7 |
T |
A |
9: 122,948,025 (GRCm39) |
S65T |
probably benign |
Het |
Fam83e |
G |
A |
7: 45,376,334 (GRCm39) |
R349Q |
probably benign |
Het |
Fbxl17 |
G |
A |
17: 63,692,062 (GRCm39) |
|
probably benign |
Het |
Fras1 |
A |
G |
5: 96,884,868 (GRCm39) |
N2582S |
probably damaging |
Het |
Fubp1 |
T |
C |
3: 151,925,350 (GRCm39) |
V164A |
probably damaging |
Het |
Gfral |
A |
T |
9: 76,104,383 (GRCm39) |
C210S |
probably damaging |
Het |
Gls |
GGCTGCTGCTGCTGCTGCTGCTGCTGCTG |
GGCTGCTGCTGCTGCTGCTGCTGCTG |
1: 52,271,853 (GRCm39) |
|
probably benign |
Het |
Hcn4 |
A |
C |
9: 58,767,445 (GRCm39) |
E1002A |
unknown |
Het |
Hcrtr2 |
A |
G |
9: 76,135,470 (GRCm39) |
V449A |
probably benign |
Het |
Hectd1 |
T |
C |
12: 51,815,891 (GRCm39) |
S1394G |
possibly damaging |
Het |
Hectd1 |
C |
A |
12: 51,815,890 (GRCm39) |
S1394I |
probably damaging |
Het |
Hecw2 |
A |
G |
1: 53,965,857 (GRCm39) |
|
probably benign |
Het |
Herc3 |
A |
G |
6: 58,845,613 (GRCm39) |
|
probably benign |
Het |
Ipo4 |
T |
C |
14: 55,863,399 (GRCm39) |
Q1073R |
possibly damaging |
Het |
Kcnj3 |
C |
A |
2: 55,484,971 (GRCm39) |
Y356* |
probably null |
Het |
Klb |
T |
A |
5: 65,506,180 (GRCm39) |
D142E |
probably benign |
Het |
Klhl35 |
T |
A |
7: 99,120,958 (GRCm39) |
S409T |
probably benign |
Het |
Krt16 |
T |
A |
11: 100,137,351 (GRCm39) |
|
probably benign |
Het |
Krt82 |
C |
A |
15: 101,450,148 (GRCm39) |
R516L |
probably benign |
Het |
Lce3a |
A |
T |
3: 92,833,038 (GRCm39) |
C21S |
unknown |
Het |
Lims2 |
A |
G |
18: 32,077,573 (GRCm39) |
E103G |
probably benign |
Het |
Map2 |
A |
T |
1: 66,419,881 (GRCm39) |
K71* |
probably null |
Het |
Mthfr |
C |
G |
4: 148,139,885 (GRCm39) |
S618W |
probably damaging |
Het |
Mycbp2 |
T |
A |
14: 103,551,761 (GRCm39) |
R157* |
probably null |
Het |
Nat10 |
C |
A |
2: 103,558,262 (GRCm39) |
|
probably benign |
Het |
Obscn |
G |
A |
11: 58,958,098 (GRCm39) |
T3810M |
possibly damaging |
Het |
Or13a19 |
G |
A |
7: 139,903,068 (GRCm39) |
S152N |
possibly damaging |
Het |
Or1x6 |
T |
A |
11: 50,939,768 (GRCm39) |
M278K |
probably damaging |
Het |
Or5d35 |
A |
T |
2: 87,855,812 (GRCm39) |
I249F |
probably damaging |
Het |
Or5g29 |
A |
G |
2: 85,421,645 (GRCm39) |
T254A |
possibly damaging |
Het |
Or6c209 |
A |
T |
10: 129,483,045 (GRCm39) |
D16V |
possibly damaging |
Het |
Or7a38 |
C |
T |
10: 78,753,439 (GRCm39) |
T255I |
probably damaging |
Het |
Park7 |
A |
G |
4: 150,992,806 (GRCm39) |
V20A |
possibly damaging |
Het |
Pgm2 |
T |
A |
5: 64,263,151 (GRCm39) |
V266E |
probably damaging |
Het |
Phip |
G |
A |
9: 82,753,341 (GRCm39) |
T1801I |
probably damaging |
Het |
Pkhd1l1 |
C |
A |
15: 44,460,407 (GRCm39) |
H4205Q |
probably benign |
Het |
Ppp1r12a |
T |
A |
10: 108,109,242 (GRCm39) |
|
probably benign |
Het |
Pramel26 |
A |
T |
4: 143,537,338 (GRCm39) |
I331N |
probably damaging |
Het |
Ptprq |
A |
T |
10: 107,541,409 (GRCm39) |
D372E |
probably benign |
Het |
Ptprr |
G |
A |
10: 116,088,868 (GRCm39) |
V340I |
possibly damaging |
Het |
Qki |
A |
G |
17: 10,428,575 (GRCm39) |
|
probably benign |
Het |
Qpct |
T |
A |
17: 79,385,081 (GRCm39) |
D240E |
probably benign |
Het |
Ren1 |
A |
G |
1: 133,283,349 (GRCm39) |
T162A |
possibly damaging |
Het |
Rif1 |
T |
C |
2: 51,980,298 (GRCm39) |
|
probably null |
Het |
Sart3 |
A |
G |
5: 113,890,460 (GRCm39) |
V461A |
probably damaging |
Het |
Saxo4 |
A |
G |
19: 10,454,449 (GRCm39) |
V329A |
possibly damaging |
Het |
Scgb1b24 |
G |
A |
7: 33,443,278 (GRCm39) |
G19R |
probably null |
Het |
Spen |
A |
T |
4: 141,204,868 (GRCm39) |
I1253N |
unknown |
Het |
Sspo |
C |
A |
6: 48,442,489 (GRCm39) |
H1995N |
probably benign |
Het |
Tfap2c |
A |
G |
2: 172,393,423 (GRCm39) |
T113A |
probably benign |
Het |
Togaram2 |
T |
C |
17: 72,004,993 (GRCm39) |
|
probably null |
Het |
Trim65 |
T |
A |
11: 116,017,470 (GRCm39) |
|
probably benign |
Het |
Trpm3 |
T |
A |
19: 22,874,885 (GRCm39) |
|
probably null |
Het |
Ubxn7 |
T |
C |
16: 32,178,864 (GRCm39) |
I87T |
probably benign |
Het |
Vav1 |
T |
C |
17: 57,603,090 (GRCm39) |
F81L |
probably damaging |
Het |
Vmn2r102 |
A |
G |
17: 19,898,112 (GRCm39) |
T376A |
probably benign |
Het |
Vmn2r105 |
A |
T |
17: 20,428,938 (GRCm39) |
C713S |
probably benign |
Het |
Zbtb45 |
C |
T |
7: 12,742,254 (GRCm39) |
M1I |
probably null |
Het |
Zfp229 |
A |
T |
17: 21,964,822 (GRCm39) |
M351L |
probably benign |
Het |
Zfp932 |
T |
C |
5: 110,156,929 (GRCm39) |
I176T |
probably benign |
Het |
Zswim1 |
G |
A |
2: 164,668,046 (GRCm39) |
E433K |
probably damaging |
Het |
|
Other mutations in Itsn2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00341:Itsn2
|
APN |
12 |
4,708,027 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL00647:Itsn2
|
APN |
12 |
4,663,311 (GRCm39) |
splice site |
probably benign |
|
IGL00933:Itsn2
|
APN |
12 |
4,757,540 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01686:Itsn2
|
APN |
12 |
4,686,693 (GRCm39) |
splice site |
probably benign |
|
IGL01873:Itsn2
|
APN |
12 |
4,682,366 (GRCm39) |
splice site |
probably benign |
|
IGL02200:Itsn2
|
APN |
12 |
4,686,632 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02280:Itsn2
|
APN |
12 |
4,758,961 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02388:Itsn2
|
APN |
12 |
4,679,557 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02938:Itsn2
|
APN |
12 |
4,747,216 (GRCm39) |
missense |
probably damaging |
0.98 |
Gopher
|
UTSW |
12 |
4,756,983 (GRCm39) |
nonsense |
probably null |
|
inversus
|
UTSW |
12 |
4,689,670 (GRCm39) |
nonsense |
probably null |
|
Liberator
|
UTSW |
12 |
4,716,176 (GRCm39) |
nonsense |
probably null |
|
rolled
|
UTSW |
12 |
4,684,792 (GRCm39) |
nonsense |
probably null |
|
Stratofortress
|
UTSW |
12 |
4,674,927 (GRCm39) |
missense |
probably damaging |
1.00 |
Underground
|
UTSW |
12 |
4,751,276 (GRCm39) |
missense |
probably damaging |
1.00 |
Vole
|
UTSW |
12 |
4,723,420 (GRCm39) |
nonsense |
probably null |
|
R0101:Itsn2
|
UTSW |
12 |
4,683,058 (GRCm39) |
unclassified |
probably benign |
|
R0584:Itsn2
|
UTSW |
12 |
4,747,180 (GRCm39) |
missense |
probably benign |
|
R0604:Itsn2
|
UTSW |
12 |
4,708,189 (GRCm39) |
missense |
probably benign |
0.01 |
R0639:Itsn2
|
UTSW |
12 |
4,762,556 (GRCm39) |
missense |
probably damaging |
0.99 |
R0738:Itsn2
|
UTSW |
12 |
4,685,681 (GRCm39) |
missense |
probably benign |
0.17 |
R1132:Itsn2
|
UTSW |
12 |
4,708,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R1163:Itsn2
|
UTSW |
12 |
4,762,009 (GRCm39) |
missense |
probably benign |
0.30 |
R1169:Itsn2
|
UTSW |
12 |
4,689,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R1258:Itsn2
|
UTSW |
12 |
4,723,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R1297:Itsn2
|
UTSW |
12 |
4,750,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R1423:Itsn2
|
UTSW |
12 |
4,723,572 (GRCm39) |
missense |
probably damaging |
0.97 |
R1572:Itsn2
|
UTSW |
12 |
4,700,044 (GRCm39) |
missense |
probably benign |
0.03 |
R1601:Itsn2
|
UTSW |
12 |
4,708,452 (GRCm39) |
missense |
probably benign |
0.01 |
R1628:Itsn2
|
UTSW |
12 |
4,679,652 (GRCm39) |
missense |
probably benign |
|
R1650:Itsn2
|
UTSW |
12 |
4,687,767 (GRCm39) |
missense |
probably damaging |
0.97 |
R1752:Itsn2
|
UTSW |
12 |
4,761,950 (GRCm39) |
splice site |
probably null |
|
R1758:Itsn2
|
UTSW |
12 |
4,708,160 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1942:Itsn2
|
UTSW |
12 |
4,689,670 (GRCm39) |
nonsense |
probably null |
|
R1976:Itsn2
|
UTSW |
12 |
4,722,733 (GRCm39) |
splice site |
probably benign |
|
R2000:Itsn2
|
UTSW |
12 |
4,716,176 (GRCm39) |
nonsense |
probably null |
|
R2060:Itsn2
|
UTSW |
12 |
4,677,879 (GRCm39) |
missense |
probably damaging |
1.00 |
R2119:Itsn2
|
UTSW |
12 |
4,757,025 (GRCm39) |
missense |
probably benign |
0.32 |
R2168:Itsn2
|
UTSW |
12 |
4,683,044 (GRCm39) |
unclassified |
probably benign |
|
R2394:Itsn2
|
UTSW |
12 |
4,757,005 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2860:Itsn2
|
UTSW |
12 |
4,750,315 (GRCm39) |
splice site |
probably benign |
|
R2861:Itsn2
|
UTSW |
12 |
4,750,315 (GRCm39) |
splice site |
probably benign |
|
R2900:Itsn2
|
UTSW |
12 |
4,680,713 (GRCm39) |
unclassified |
probably benign |
|
R2991:Itsn2
|
UTSW |
12 |
4,708,474 (GRCm39) |
missense |
probably benign |
0.01 |
R3087:Itsn2
|
UTSW |
12 |
4,716,303 (GRCm39) |
missense |
probably damaging |
1.00 |
R3881:Itsn2
|
UTSW |
12 |
4,684,546 (GRCm39) |
unclassified |
probably benign |
|
R4022:Itsn2
|
UTSW |
12 |
4,674,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R4332:Itsn2
|
UTSW |
12 |
4,762,611 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4657:Itsn2
|
UTSW |
12 |
4,763,197 (GRCm39) |
makesense |
probably null |
|
R4727:Itsn2
|
UTSW |
12 |
4,757,660 (GRCm39) |
missense |
probably damaging |
0.99 |
R4745:Itsn2
|
UTSW |
12 |
4,711,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R4770:Itsn2
|
UTSW |
12 |
4,677,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R4905:Itsn2
|
UTSW |
12 |
4,684,583 (GRCm39) |
unclassified |
probably benign |
|
R5269:Itsn2
|
UTSW |
12 |
4,683,553 (GRCm39) |
unclassified |
probably benign |
|
R5314:Itsn2
|
UTSW |
12 |
4,677,960 (GRCm39) |
missense |
probably benign |
0.09 |
R5345:Itsn2
|
UTSW |
12 |
4,722,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R5399:Itsn2
|
UTSW |
12 |
4,703,535 (GRCm39) |
missense |
probably benign |
0.22 |
R5566:Itsn2
|
UTSW |
12 |
4,676,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R5725:Itsn2
|
UTSW |
12 |
4,680,767 (GRCm39) |
unclassified |
probably benign |
|
R5773:Itsn2
|
UTSW |
12 |
4,757,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R6116:Itsn2
|
UTSW |
12 |
4,679,939 (GRCm39) |
unclassified |
probably benign |
|
R6254:Itsn2
|
UTSW |
12 |
4,674,982 (GRCm39) |
splice site |
probably null |
|
R6325:Itsn2
|
UTSW |
12 |
4,756,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R6361:Itsn2
|
UTSW |
12 |
4,679,655 (GRCm39) |
missense |
probably benign |
0.18 |
R6456:Itsn2
|
UTSW |
12 |
4,679,923 (GRCm39) |
unclassified |
probably benign |
|
R6494:Itsn2
|
UTSW |
12 |
4,684,792 (GRCm39) |
nonsense |
probably null |
|
R6854:Itsn2
|
UTSW |
12 |
4,702,382 (GRCm39) |
missense |
probably benign |
0.37 |
R6941:Itsn2
|
UTSW |
12 |
4,679,641 (GRCm39) |
missense |
probably benign |
0.05 |
R6961:Itsn2
|
UTSW |
12 |
4,723,420 (GRCm39) |
nonsense |
probably null |
|
R7326:Itsn2
|
UTSW |
12 |
4,682,985 (GRCm39) |
missense |
unknown |
|
R7387:Itsn2
|
UTSW |
12 |
4,689,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R7465:Itsn2
|
UTSW |
12 |
4,756,983 (GRCm39) |
nonsense |
probably null |
|
R7471:Itsn2
|
UTSW |
12 |
4,758,198 (GRCm39) |
missense |
probably benign |
0.43 |
R7814:Itsn2
|
UTSW |
12 |
4,708,561 (GRCm39) |
missense |
probably benign |
0.14 |
R7854:Itsn2
|
UTSW |
12 |
4,751,276 (GRCm39) |
missense |
probably damaging |
1.00 |
R7879:Itsn2
|
UTSW |
12 |
4,751,265 (GRCm39) |
missense |
probably benign |
0.16 |
R7990:Itsn2
|
UTSW |
12 |
4,685,629 (GRCm39) |
missense |
unknown |
|
R8009:Itsn2
|
UTSW |
12 |
4,714,553 (GRCm39) |
missense |
probably benign |
0.12 |
R8115:Itsn2
|
UTSW |
12 |
4,723,602 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8143:Itsn2
|
UTSW |
12 |
4,683,003 (GRCm39) |
missense |
unknown |
|
R8248:Itsn2
|
UTSW |
12 |
4,712,052 (GRCm39) |
missense |
probably benign |
0.00 |
R8735:Itsn2
|
UTSW |
12 |
4,721,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R8748:Itsn2
|
UTSW |
12 |
4,751,337 (GRCm39) |
missense |
probably benign |
0.36 |
R9018:Itsn2
|
UTSW |
12 |
4,708,091 (GRCm39) |
missense |
possibly damaging |
0.57 |
R9386:Itsn2
|
UTSW |
12 |
4,679,730 (GRCm39) |
missense |
unknown |
|
R9681:Itsn2
|
UTSW |
12 |
4,683,499 (GRCm39) |
missense |
unknown |
|
Z1088:Itsn2
|
UTSW |
12 |
4,762,472 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- ATGATCAATTCCACAGCTCTCTGCC -3'
(R):5'- AAGTTGTCTTGCTGAGCAGCCC -3'
Sequencing Primer
(F):5'- gagacaggaagatagcccag -3'
(R):5'- CGTGTTGGACATGATGAGCT -3'
|
Posted On |
2013-05-09 |