Incidental Mutation 'R4716:Col4a2'
ID |
354037 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Col4a2
|
Ensembl Gene |
ENSMUSG00000031503 |
Gene Name |
collagen, type IV, alpha 2 |
Synonyms |
Col4a-2 |
MMRRC Submission |
041983-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R4716 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
8 |
Chromosomal Location |
11362805-11499287 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 11452224 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Aspartic acid to Glycine
at position 180
(D180G)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000033899
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000033899]
|
AlphaFold |
P08122 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000033899
AA Change: D180G
PolyPhen 2
Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000033899 Gene: ENSMUSG00000031503 AA Change: D180G
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
28 |
N/A |
INTRINSIC |
Pfam:Collagen
|
56 |
119 |
1.2e-10 |
PFAM |
Pfam:Collagen
|
112 |
174 |
3.9e-8 |
PFAM |
low complexity region
|
193 |
229 |
N/A |
INTRINSIC |
Pfam:Collagen
|
289 |
348 |
1.3e-10 |
PFAM |
low complexity region
|
370 |
389 |
N/A |
INTRINSIC |
low complexity region
|
427 |
445 |
N/A |
INTRINSIC |
Pfam:Collagen
|
488 |
546 |
2e-10 |
PFAM |
Pfam:Collagen
|
590 |
655 |
4.5e-9 |
PFAM |
low complexity region
|
665 |
673 |
N/A |
INTRINSIC |
Pfam:Collagen
|
674 |
731 |
3.5e-10 |
PFAM |
Pfam:Collagen
|
714 |
775 |
4.3e-10 |
PFAM |
Pfam:Collagen
|
773 |
831 |
1.5e-10 |
PFAM |
Pfam:Collagen
|
861 |
935 |
8.1e-10 |
PFAM |
Pfam:Collagen
|
915 |
976 |
1.1e-9 |
PFAM |
Pfam:Collagen
|
978 |
1038 |
2.6e-8 |
PFAM |
Pfam:Collagen
|
1027 |
1091 |
1.7e-10 |
PFAM |
Pfam:Collagen
|
1094 |
1155 |
5.5e-11 |
PFAM |
Pfam:Collagen
|
1147 |
1211 |
1e-10 |
PFAM |
Pfam:Collagen
|
1271 |
1340 |
2.1e-8 |
PFAM |
Pfam:Collagen
|
1330 |
1392 |
7.1e-10 |
PFAM |
C4
|
1484 |
1591 |
7.85e-59 |
SMART |
C4
|
1592 |
1706 |
7.65e-71 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000145295
|
SMART Domains |
Protein: ENSMUSP00000114737 Gene: ENSMUSG00000031503
Domain | Start | End | E-Value | Type |
Pfam:Collagen
|
6 |
55 |
9.7e-8 |
PFAM |
Pfam:Collagen
|
81 |
140 |
4.4e-12 |
PFAM |
Pfam:Collagen
|
145 |
210 |
2.7e-8 |
PFAM |
Pfam:Collagen
|
184 |
239 |
2.9e-8 |
PFAM |
low complexity region
|
280 |
293 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000148654
|
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.1%
- 20x: 94.9%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: This gene encodes the alpha-2 subunit of the type IV collagens, an essential component of basement membranes. The encoded protein forms a triple helical heterotrimer comprised of alpha-1 and alpha-2 subunits that assembles into a type IV collagen network. Canstatin, a peptide derived fom the C-terminus of the collagen chain, is a matrikine that has been shown to inhibit angiogenesis. Homozygous knockout mice for this gene exhibit impaired basement membrane integrity and embryonic lethality. This gene shares a bi-directional promoter with a related gene on chromosome 8. [provided by RefSeq, Nov 2015] PHENOTYPE: ENU-induced missense mutations of this gene result in a variable phenotype affecting the eye, brain and vascular stability in heterozygotes, and fetal or postnatal survival in homozygotes. [provided by MGI curators]
|
Allele List at MGI |
All alleles(10) : Targeted, knock-out(1) Gene trapped(6) Chemically induced(3) |
Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abi3bp |
C |
T |
16: 56,471,088 (GRCm39) |
R578* |
probably null |
Het |
Adam8 |
T |
A |
7: 139,563,851 (GRCm39) |
D717V |
probably benign |
Het |
Aknad1 |
T |
C |
3: 108,682,417 (GRCm39) |
|
probably null |
Het |
Alk |
A |
T |
17: 72,512,937 (GRCm39) |
W341R |
probably damaging |
Het |
Ankdd1b |
G |
A |
13: 96,591,091 (GRCm39) |
Q101* |
probably null |
Het |
Anpep |
A |
C |
7: 79,476,380 (GRCm39) |
S829A |
probably benign |
Het |
Armh3 |
A |
G |
19: 45,948,781 (GRCm39) |
S233P |
probably damaging |
Het |
Ate1 |
A |
T |
7: 130,115,511 (GRCm39) |
C72S |
probably damaging |
Het |
Atp6v0a4 |
G |
A |
6: 38,037,999 (GRCm39) |
L533F |
probably damaging |
Het |
Bach1 |
T |
C |
16: 87,512,267 (GRCm39) |
|
probably benign |
Het |
Baz2b |
T |
C |
2: 59,799,599 (GRCm39) |
D240G |
probably benign |
Het |
Cdc14b |
C |
T |
13: 64,357,014 (GRCm39) |
S21N |
probably damaging |
Het |
Cdh3 |
A |
G |
8: 107,270,520 (GRCm39) |
I466V |
probably benign |
Het |
Cog1 |
A |
G |
11: 113,547,923 (GRCm39) |
E137G |
probably damaging |
Het |
Cyp2c40 |
A |
T |
19: 39,791,105 (GRCm39) |
|
probably null |
Het |
Dclk2 |
C |
T |
3: 86,827,188 (GRCm39) |
R97H |
probably damaging |
Het |
Ddx52 |
T |
C |
11: 83,846,031 (GRCm39) |
|
probably null |
Het |
Dhx58 |
C |
T |
11: 100,587,797 (GRCm39) |
|
probably null |
Het |
Dmp1 |
T |
A |
5: 104,360,427 (GRCm39) |
S368T |
probably damaging |
Het |
Dnah17 |
C |
A |
11: 117,964,474 (GRCm39) |
V2435L |
probably benign |
Het |
Dnajc7 |
A |
G |
11: 100,510,402 (GRCm39) |
V10A |
probably benign |
Het |
Dscam |
G |
T |
16: 96,420,771 (GRCm39) |
T1705K |
possibly damaging |
Het |
Dscaml1 |
G |
A |
9: 45,361,890 (GRCm39) |
V217M |
probably damaging |
Het |
Dync2h1 |
A |
G |
9: 7,142,648 (GRCm39) |
|
probably null |
Het |
F5 |
A |
G |
1: 164,021,488 (GRCm39) |
D1321G |
probably damaging |
Het |
Fam174a |
C |
T |
1: 95,241,770 (GRCm39) |
P77S |
probably benign |
Het |
Fars2 |
G |
A |
13: 36,389,051 (GRCm39) |
R180H |
probably damaging |
Het |
Fnbp1 |
T |
C |
2: 30,945,532 (GRCm39) |
T154A |
probably benign |
Het |
Fsip2 |
T |
A |
2: 82,805,203 (GRCm39) |
N507K |
probably damaging |
Het |
Glg1 |
G |
T |
8: 111,887,407 (GRCm39) |
Y449* |
probably null |
Het |
Gm15130 |
A |
T |
2: 110,964,560 (GRCm39) |
Y187* |
probably null |
Het |
Gm973 |
A |
T |
1: 59,591,713 (GRCm39) |
K366* |
probably null |
Het |
H2bc11 |
T |
A |
13: 22,227,533 (GRCm39) |
V45E |
possibly damaging |
Het |
Hao1 |
A |
G |
2: 134,347,540 (GRCm39) |
I255T |
probably damaging |
Het |
Herc6 |
T |
A |
6: 57,575,423 (GRCm39) |
V148E |
probably damaging |
Het |
Insm2 |
T |
A |
12: 55,647,677 (GRCm39) |
C474S |
possibly damaging |
Het |
Itch |
T |
C |
2: 155,052,502 (GRCm39) |
|
probably null |
Het |
Itga2 |
A |
G |
13: 114,993,909 (GRCm39) |
V748A |
probably damaging |
Het |
Itga9 |
T |
A |
9: 118,510,826 (GRCm39) |
S452T |
probably damaging |
Het |
Kdm4b |
C |
A |
17: 56,693,178 (GRCm39) |
D338E |
probably benign |
Het |
Krt40 |
G |
A |
11: 99,431,045 (GRCm39) |
R155C |
probably damaging |
Het |
Krtap16-1 |
A |
G |
11: 99,876,000 (GRCm39) |
V468A |
probably damaging |
Het |
Lactb2 |
G |
A |
1: 13,708,619 (GRCm39) |
P143L |
probably damaging |
Het |
Lrba |
C |
A |
3: 86,550,021 (GRCm39) |
T2330K |
probably damaging |
Het |
Lrp2bp |
A |
T |
8: 46,466,208 (GRCm39) |
I106F |
probably benign |
Het |
Luzp2 |
A |
G |
7: 54,485,710 (GRCm39) |
K2E |
probably damaging |
Het |
Lypd6 |
T |
C |
2: 50,078,855 (GRCm39) |
|
probably null |
Het |
Maml1 |
A |
T |
11: 50,148,694 (GRCm39) |
D1015E |
probably benign |
Het |
Mdfi |
T |
G |
17: 48,131,906 (GRCm39) |
D106A |
possibly damaging |
Het |
Olfm3 |
T |
C |
3: 114,874,755 (GRCm39) |
M17T |
probably benign |
Het |
Or2n1d |
A |
C |
17: 38,646,731 (GRCm39) |
I228L |
possibly damaging |
Het |
Or2o1 |
A |
G |
11: 49,051,717 (GRCm39) |
Y292C |
probably damaging |
Het |
Or8c16 |
T |
A |
9: 38,130,714 (GRCm39) |
N198K |
probably damaging |
Het |
Or8g30 |
A |
G |
9: 39,230,725 (GRCm39) |
F62L |
probably benign |
Het |
Otud7b |
T |
G |
3: 96,058,227 (GRCm39) |
L261V |
probably damaging |
Het |
P2ry1 |
A |
G |
3: 60,910,893 (GRCm39) |
N11D |
probably damaging |
Het |
Pate2 |
T |
C |
9: 35,596,978 (GRCm39) |
|
probably benign |
Het |
Pcdhb16 |
A |
T |
18: 37,612,458 (GRCm39) |
T473S |
probably benign |
Het |
Per1 |
A |
G |
11: 68,992,057 (GRCm39) |
E137G |
probably damaging |
Het |
Phf11d |
T |
C |
14: 59,590,791 (GRCm39) |
T189A |
probably benign |
Het |
Pik3r5 |
C |
A |
11: 68,386,030 (GRCm39) |
S738R |
possibly damaging |
Het |
Pikfyve |
A |
G |
1: 65,285,635 (GRCm39) |
Y913C |
possibly damaging |
Het |
Pkd1 |
T |
G |
17: 24,795,107 (GRCm39) |
S2265A |
probably damaging |
Het |
Pkhd1l1 |
C |
A |
15: 44,419,428 (GRCm39) |
N2964K |
probably damaging |
Het |
Plch1 |
T |
G |
3: 63,688,967 (GRCm39) |
D79A |
probably damaging |
Het |
Pnliprp1 |
A |
C |
19: 58,728,901 (GRCm39) |
T363P |
possibly damaging |
Het |
Ppp1r10 |
T |
A |
17: 36,240,352 (GRCm39) |
D547E |
probably benign |
Het |
Prkdc |
T |
A |
16: 15,628,701 (GRCm39) |
I3482K |
probably benign |
Het |
Ptpn4 |
A |
G |
1: 119,649,598 (GRCm39) |
Y333H |
probably damaging |
Het |
Ptpru |
T |
A |
4: 131,548,279 (GRCm39) |
M73L |
probably benign |
Het |
Rrp12 |
A |
G |
19: 41,865,867 (GRCm39) |
Y698H |
probably damaging |
Het |
Scaf8 |
T |
C |
17: 3,227,398 (GRCm39) |
F338L |
unknown |
Het |
Slc17a1 |
G |
T |
13: 24,064,576 (GRCm39) |
V347L |
probably benign |
Het |
Slc1a2 |
T |
A |
2: 102,578,883 (GRCm39) |
V263E |
probably damaging |
Het |
Slc29a4 |
T |
C |
5: 142,704,327 (GRCm39) |
V327A |
probably benign |
Het |
Slc6a3 |
A |
C |
13: 73,705,195 (GRCm39) |
I229L |
probably benign |
Het |
Sos2 |
T |
C |
12: 69,654,145 (GRCm39) |
I703V |
probably benign |
Het |
Srpk1 |
T |
C |
17: 28,840,982 (GRCm39) |
T15A |
probably benign |
Het |
St6gal2 |
A |
T |
17: 55,817,367 (GRCm39) |
Q510L |
probably benign |
Het |
Stk24 |
T |
C |
14: 121,532,130 (GRCm39) |
D289G |
possibly damaging |
Het |
Taf2 |
T |
G |
15: 54,929,364 (GRCm39) |
K64T |
probably benign |
Het |
Tbx3 |
A |
G |
5: 119,813,735 (GRCm39) |
E257G |
possibly damaging |
Het |
Tmem102 |
A |
T |
11: 69,695,022 (GRCm39) |
F317I |
probably damaging |
Het |
Trav10 |
A |
G |
14: 53,743,497 (GRCm39) |
S33G |
possibly damaging |
Het |
Ttn |
T |
A |
2: 76,745,408 (GRCm39) |
I5214F |
probably damaging |
Het |
Ube2f |
T |
A |
1: 91,182,002 (GRCm39) |
L2Q |
probably damaging |
Het |
Ube4b |
A |
G |
4: 149,429,069 (GRCm39) |
F857L |
probably damaging |
Het |
Vmn2r18 |
T |
A |
5: 151,485,602 (GRCm39) |
I631F |
possibly damaging |
Het |
Zfp280d |
T |
A |
9: 72,219,947 (GRCm39) |
S241T |
possibly damaging |
Het |
Zfp638 |
T |
A |
6: 83,956,544 (GRCm39) |
L1717* |
probably null |
Het |
Zfp719 |
A |
G |
7: 43,240,535 (GRCm39) |
N708D |
possibly damaging |
Het |
|
Other mutations in Col4a2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00088:Col4a2
|
APN |
8 |
11,493,685 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00485:Col4a2
|
APN |
8 |
11,489,012 (GRCm39) |
missense |
probably benign |
|
IGL00909:Col4a2
|
APN |
8 |
11,498,167 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01574:Col4a2
|
APN |
8 |
11,489,306 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01914:Col4a2
|
APN |
8 |
11,464,754 (GRCm39) |
missense |
possibly damaging |
0.57 |
IGL02147:Col4a2
|
APN |
8 |
11,458,140 (GRCm39) |
missense |
probably benign |
0.28 |
IGL02205:Col4a2
|
APN |
8 |
11,481,305 (GRCm39) |
nonsense |
probably null |
|
IGL02423:Col4a2
|
APN |
8 |
11,483,800 (GRCm39) |
missense |
probably benign |
|
IGL03131:Col4a2
|
APN |
8 |
11,475,979 (GRCm39) |
missense |
probably benign |
|
band
|
UTSW |
8 |
11,498,225 (GRCm39) |
missense |
probably benign |
0.00 |
Binder
|
UTSW |
8 |
11,466,070 (GRCm39) |
missense |
probably damaging |
1.00 |
G4846:Col4a2
|
UTSW |
8 |
11,458,872 (GRCm39) |
splice site |
probably benign |
|
IGL03054:Col4a2
|
UTSW |
8 |
11,498,270 (GRCm39) |
missense |
probably damaging |
0.96 |
R0087:Col4a2
|
UTSW |
8 |
11,491,296 (GRCm39) |
missense |
probably benign |
|
R0124:Col4a2
|
UTSW |
8 |
11,458,871 (GRCm39) |
splice site |
probably benign |
|
R0603:Col4a2
|
UTSW |
8 |
11,464,779 (GRCm39) |
missense |
probably benign |
|
R0646:Col4a2
|
UTSW |
8 |
11,481,252 (GRCm39) |
missense |
probably benign |
0.17 |
R0970:Col4a2
|
UTSW |
8 |
11,465,438 (GRCm39) |
missense |
probably benign |
0.00 |
R1738:Col4a2
|
UTSW |
8 |
11,496,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R1746:Col4a2
|
UTSW |
8 |
11,496,020 (GRCm39) |
missense |
probably benign |
0.35 |
R1826:Col4a2
|
UTSW |
8 |
11,363,509 (GRCm39) |
critical splice donor site |
probably null |
|
R1834:Col4a2
|
UTSW |
8 |
11,452,997 (GRCm39) |
missense |
probably benign |
0.10 |
R2016:Col4a2
|
UTSW |
8 |
11,495,086 (GRCm39) |
missense |
probably benign |
0.04 |
R2017:Col4a2
|
UTSW |
8 |
11,495,086 (GRCm39) |
missense |
probably benign |
0.04 |
R2124:Col4a2
|
UTSW |
8 |
11,466,070 (GRCm39) |
missense |
probably damaging |
1.00 |
R2137:Col4a2
|
UTSW |
8 |
11,483,749 (GRCm39) |
missense |
probably benign |
|
R2207:Col4a2
|
UTSW |
8 |
11,493,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R3156:Col4a2
|
UTSW |
8 |
11,363,414 (GRCm39) |
unclassified |
probably benign |
|
R4169:Col4a2
|
UTSW |
8 |
11,479,391 (GRCm39) |
missense |
probably benign |
0.22 |
R4679:Col4a2
|
UTSW |
8 |
11,481,337 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4705:Col4a2
|
UTSW |
8 |
11,363,504 (GRCm39) |
missense |
possibly damaging |
0.52 |
R4710:Col4a2
|
UTSW |
8 |
11,459,462 (GRCm39) |
missense |
probably benign |
0.22 |
R4730:Col4a2
|
UTSW |
8 |
11,487,590 (GRCm39) |
missense |
probably benign |
|
R4732:Col4a2
|
UTSW |
8 |
11,496,197 (GRCm39) |
missense |
probably benign |
0.02 |
R4732:Col4a2
|
UTSW |
8 |
11,464,779 (GRCm39) |
missense |
probably benign |
|
R4733:Col4a2
|
UTSW |
8 |
11,496,197 (GRCm39) |
missense |
probably benign |
0.02 |
R4733:Col4a2
|
UTSW |
8 |
11,464,779 (GRCm39) |
missense |
probably benign |
|
R4834:Col4a2
|
UTSW |
8 |
11,456,836 (GRCm39) |
nonsense |
probably null |
|
R4835:Col4a2
|
UTSW |
8 |
11,473,570 (GRCm39) |
nonsense |
probably null |
|
R4953:Col4a2
|
UTSW |
8 |
11,479,505 (GRCm39) |
missense |
probably benign |
0.02 |
R5078:Col4a2
|
UTSW |
8 |
11,493,936 (GRCm39) |
missense |
probably benign |
|
R5204:Col4a2
|
UTSW |
8 |
11,448,651 (GRCm39) |
splice site |
probably null |
|
R5221:Col4a2
|
UTSW |
8 |
11,498,225 (GRCm39) |
missense |
probably benign |
0.00 |
R5355:Col4a2
|
UTSW |
8 |
11,495,984 (GRCm39) |
missense |
probably damaging |
0.96 |
R5478:Col4a2
|
UTSW |
8 |
11,448,697 (GRCm39) |
missense |
probably benign |
0.21 |
R5492:Col4a2
|
UTSW |
8 |
11,488,608 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5646:Col4a2
|
UTSW |
8 |
11,491,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R5857:Col4a2
|
UTSW |
8 |
11,475,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R5948:Col4a2
|
UTSW |
8 |
11,470,600 (GRCm39) |
missense |
probably benign |
0.21 |
R6329:Col4a2
|
UTSW |
8 |
11,496,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R6496:Col4a2
|
UTSW |
8 |
11,452,994 (GRCm39) |
missense |
probably damaging |
1.00 |
R6496:Col4a2
|
UTSW |
8 |
11,452,993 (GRCm39) |
nonsense |
probably null |
|
R6531:Col4a2
|
UTSW |
8 |
11,458,135 (GRCm39) |
missense |
probably benign |
0.00 |
R7185:Col4a2
|
UTSW |
8 |
11,449,739 (GRCm39) |
missense |
probably damaging |
0.99 |
R7196:Col4a2
|
UTSW |
8 |
11,448,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R7266:Col4a2
|
UTSW |
8 |
11,475,542 (GRCm39) |
critical splice donor site |
probably null |
|
R7308:Col4a2
|
UTSW |
8 |
11,456,856 (GRCm39) |
critical splice donor site |
probably null |
|
R7341:Col4a2
|
UTSW |
8 |
11,448,678 (GRCm39) |
missense |
probably damaging |
0.97 |
R7394:Col4a2
|
UTSW |
8 |
11,496,184 (GRCm39) |
missense |
probably benign |
0.00 |
R7434:Col4a2
|
UTSW |
8 |
11,471,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R7606:Col4a2
|
UTSW |
8 |
11,493,571 (GRCm39) |
missense |
probably benign |
0.00 |
R7646:Col4a2
|
UTSW |
8 |
11,495,086 (GRCm39) |
missense |
probably benign |
0.04 |
R7712:Col4a2
|
UTSW |
8 |
11,475,376 (GRCm39) |
missense |
probably benign |
|
R7752:Col4a2
|
UTSW |
8 |
11,479,358 (GRCm39) |
missense |
probably benign |
0.38 |
R7844:Col4a2
|
UTSW |
8 |
11,475,453 (GRCm39) |
nonsense |
probably null |
|
R7901:Col4a2
|
UTSW |
8 |
11,479,358 (GRCm39) |
missense |
probably benign |
0.38 |
R8186:Col4a2
|
UTSW |
8 |
11,475,542 (GRCm39) |
critical splice donor site |
probably null |
|
R8331:Col4a2
|
UTSW |
8 |
11,463,985 (GRCm39) |
nonsense |
probably null |
|
R8389:Col4a2
|
UTSW |
8 |
11,498,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R8547:Col4a2
|
UTSW |
8 |
11,479,305 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8927:Col4a2
|
UTSW |
8 |
11,475,543 (GRCm39) |
splice site |
probably null |
|
R9051:Col4a2
|
UTSW |
8 |
11,498,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R9088:Col4a2
|
UTSW |
8 |
11,493,227 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9221:Col4a2
|
UTSW |
8 |
11,491,943 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9323:Col4a2
|
UTSW |
8 |
11,493,413 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9337:Col4a2
|
UTSW |
8 |
11,479,346 (GRCm39) |
missense |
probably benign |
0.00 |
R9377:Col4a2
|
UTSW |
8 |
11,483,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R9697:Col4a2
|
UTSW |
8 |
11,487,628 (GRCm39) |
missense |
probably benign |
0.34 |
R9701:Col4a2
|
UTSW |
8 |
11,493,104 (GRCm39) |
missense |
probably benign |
0.00 |
R9729:Col4a2
|
UTSW |
8 |
11,496,157 (GRCm39) |
missense |
probably benign |
0.08 |
R9802:Col4a2
|
UTSW |
8 |
11,493,104 (GRCm39) |
missense |
probably benign |
0.00 |
|
Predicted Primers |
PCR Primer
(F):5'- GGTGCCTATGTAACCCATGG -3'
(R):5'- CCTGGCAGACTGAGGTATTTGG -3'
Sequencing Primer
(F):5'- GCCATCTGTGGTCATCAT -3'
(R):5'- TTTGGTCTGAGACACTGAGAAC -3'
|
Posted On |
2015-10-21 |