Incidental Mutation 'R9051:Col4a2'
ID |
688375 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Col4a2
|
Ensembl Gene |
ENSMUSG00000031503 |
Gene Name |
collagen, type IV, alpha 2 |
Synonyms |
Col4a-2 |
MMRRC Submission |
068877-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R9051 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
8 |
Chromosomal Location |
11362805-11499287 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 11498198 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Phenylalanine to Serine
at position 1669
(F1669S)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000033899
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000033899]
|
AlphaFold |
P08122 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000033899
AA Change: F1669S
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000033899 Gene: ENSMUSG00000031503 AA Change: F1669S
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 |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.9%
- 20x: 99.6%
|
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: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
T |
11: 9,285,232 (GRCm39) |
T3289S |
probably damaging |
Het |
Actr1b |
G |
T |
1: 36,740,534 (GRCm39) |
Q240K |
probably benign |
Het |
Adamts19 |
T |
C |
18: 59,034,048 (GRCm39) |
V341A |
probably damaging |
Het |
Akirin2 |
C |
A |
4: 34,551,148 (GRCm39) |
S35* |
probably null |
Het |
Alg3 |
G |
T |
16: 20,427,765 (GRCm39) |
Q90K |
probably benign |
Het |
Alox12 |
C |
T |
11: 70,138,153 (GRCm39) |
R394H |
possibly damaging |
Het |
Ankrd17 |
A |
C |
5: 90,411,134 (GRCm39) |
M1387R |
probably damaging |
Het |
Anp32b |
T |
G |
4: 46,468,592 (GRCm39) |
F121V |
possibly damaging |
Het |
Atp2b2 |
A |
G |
6: 113,740,566 (GRCm39) |
V815A |
probably damaging |
Het |
Atxn7l1 |
T |
C |
12: 33,417,420 (GRCm39) |
L527S |
probably benign |
Het |
B9d2 |
C |
T |
7: 25,385,462 (GRCm39) |
L91F |
possibly damaging |
Het |
Bcl2l11 |
T |
A |
2: 128,000,221 (GRCm39) |
I188N |
probably damaging |
Het |
Bnc2 |
A |
C |
4: 84,210,138 (GRCm39) |
S744A |
probably benign |
Het |
Casr |
T |
G |
16: 36,330,414 (GRCm39) |
M307L |
probably benign |
Het |
Cd109 |
CATTTATTTATTTATTTATTTATTTATTTATTTAT |
CATTTATTTATTTATTTATTTATTTATTTATTTATTTAT |
9: 78,619,782 (GRCm39) |
|
probably benign |
Het |
Cd109 |
TTATA |
TTATATATA |
9: 78,619,813 (GRCm39) |
|
probably benign |
Het |
Cd22 |
A |
G |
7: 30,575,449 (GRCm39) |
S198P |
probably benign |
Het |
Cd37 |
C |
A |
7: 44,886,622 (GRCm39) |
V99L |
probably benign |
Het |
Cdkn1c |
A |
G |
7: 143,013,964 (GRCm39) |
S161P |
possibly damaging |
Het |
Chi3l1 |
G |
T |
1: 134,111,919 (GRCm39) |
|
probably null |
Het |
Dchs2 |
A |
T |
3: 83,261,493 (GRCm39) |
H2587L |
probably benign |
Het |
Ddx19a |
A |
T |
8: 111,710,228 (GRCm39) |
M124K |
probably benign |
Het |
Dnhd1 |
A |
T |
7: 105,341,933 (GRCm39) |
H1244L |
possibly damaging |
Het |
Dnpep |
G |
A |
1: 75,292,329 (GRCm39) |
P165L |
probably damaging |
Het |
Dpp3 |
T |
C |
19: 4,973,172 (GRCm39) |
R141G |
probably benign |
Het |
Dpysl3 |
T |
C |
18: 43,462,814 (GRCm39) |
D521G |
probably damaging |
Het |
Dusp4 |
T |
A |
8: 35,284,345 (GRCm39) |
M220K |
probably damaging |
Het |
Duxf4 |
G |
A |
10: 58,071,711 (GRCm39) |
P168S |
probably damaging |
Het |
Edc4 |
T |
A |
8: 106,613,833 (GRCm39) |
L391Q |
probably damaging |
Het |
Edrf1 |
A |
C |
7: 133,273,207 (GRCm39) |
I1221L |
probably benign |
Het |
Elavl2 |
A |
G |
4: 91,199,847 (GRCm39) |
L12P |
probably benign |
Het |
Fastkd3 |
T |
A |
13: 68,733,071 (GRCm39) |
V464D |
probably damaging |
Het |
Flt4 |
C |
A |
11: 49,527,598 (GRCm39) |
N920K |
probably benign |
Het |
Gimap3 |
T |
C |
6: 48,742,259 (GRCm39) |
T224A |
probably benign |
Het |
Gm9772 |
T |
A |
17: 22,225,565 (GRCm39) |
K112* |
probably null |
Het |
Gp5 |
C |
A |
16: 30,127,976 (GRCm39) |
V233L |
|
Het |
Gpr25 |
A |
T |
1: 136,188,026 (GRCm39) |
W196R |
probably benign |
Het |
Hs3st4 |
G |
A |
7: 123,582,680 (GRCm39) |
G93S |
probably damaging |
Het |
Igsf10 |
A |
G |
3: 59,236,668 (GRCm39) |
L1171S |
probably benign |
Het |
Itgb7 |
C |
T |
15: 102,126,359 (GRCm39) |
G526S |
possibly damaging |
Het |
Kcnh8 |
G |
A |
17: 53,141,642 (GRCm39) |
C295Y |
probably damaging |
Het |
Klhl8 |
A |
G |
5: 104,015,709 (GRCm39) |
|
probably null |
Het |
Krt1c |
T |
A |
15: 101,726,317 (GRCm39) |
I74F |
unknown |
Het |
Lamp5 |
G |
T |
2: 135,911,054 (GRCm39) |
M262I |
probably benign |
Het |
Lrp5 |
G |
T |
19: 3,680,156 (GRCm39) |
R443S |
possibly damaging |
Het |
Lrrc66 |
G |
T |
5: 73,765,267 (GRCm39) |
A592E |
probably benign |
Het |
Lrrc66 |
C |
T |
5: 73,765,268 (GRCm39) |
A592T |
probably benign |
Het |
Mettl23 |
T |
A |
11: 116,744,865 (GRCm39) |
V93D |
unknown |
Het |
Mier2 |
G |
A |
10: 79,384,274 (GRCm39) |
R166W |
probably damaging |
Het |
Mkrn2os |
G |
A |
6: 115,562,325 (GRCm39) |
R213W |
probably benign |
Het |
Mrps36 |
T |
A |
13: 100,877,715 (GRCm39) |
I22L |
probably damaging |
Het |
Msantd5f4 |
A |
G |
4: 73,557,185 (GRCm39) |
N6S |
possibly damaging |
Het |
Myocd |
T |
C |
11: 65,077,795 (GRCm39) |
R667G |
probably benign |
Het |
Ncapg |
T |
A |
5: 45,853,140 (GRCm39) |
L869M |
probably damaging |
Het |
Ndst3 |
T |
C |
3: 123,465,549 (GRCm39) |
N141S |
probably benign |
Het |
Neu2 |
A |
T |
1: 87,524,965 (GRCm39) |
R317* |
probably null |
Het |
Nf1 |
G |
T |
11: 79,364,168 (GRCm39) |
V1533F |
probably damaging |
Het |
Npy4r |
T |
A |
14: 33,869,083 (GRCm39) |
R68S |
possibly damaging |
Het |
Nr1h5 |
T |
C |
3: 102,853,427 (GRCm39) |
H360R |
probably null |
Het |
Or1x6 |
G |
A |
11: 50,938,938 (GRCm39) |
M1I |
probably null |
Het |
Or4f14c |
T |
C |
2: 111,941,441 (GRCm39) |
D52G |
probably damaging |
Het |
Or9s15 |
T |
C |
1: 92,524,978 (GRCm39) |
S246P |
probably damaging |
Het |
Osmr |
A |
C |
15: 6,882,027 (GRCm39) |
V39G |
probably damaging |
Het |
Plekhm2 |
T |
C |
4: 141,359,732 (GRCm39) |
D345G |
possibly damaging |
Het |
Prkaa2 |
G |
T |
4: 104,906,600 (GRCm39) |
S165* |
probably null |
Het |
Qser1 |
A |
T |
2: 104,593,292 (GRCm39) |
F1575Y |
possibly damaging |
Het |
Rasl11a |
C |
A |
5: 146,782,107 (GRCm39) |
D27E |
probably benign |
Het |
Ret |
A |
T |
6: 118,142,888 (GRCm39) |
Y929* |
probably null |
Het |
Samd9l |
T |
A |
6: 3,373,493 (GRCm39) |
E1256V |
probably benign |
Het |
Scnn1g |
A |
G |
7: 121,341,566 (GRCm39) |
I243V |
possibly damaging |
Het |
Slc6a3 |
C |
T |
13: 73,718,031 (GRCm39) |
R514* |
probably null |
Het |
Sorcs3 |
C |
T |
19: 48,194,809 (GRCm39) |
A64V |
probably benign |
Het |
Sos1 |
G |
T |
17: 80,715,723 (GRCm39) |
N1011K |
probably benign |
Het |
Srbd1 |
C |
A |
17: 86,428,115 (GRCm39) |
A373S |
possibly damaging |
Het |
Tas1r1 |
C |
T |
4: 152,122,833 (GRCm39) |
W4* |
probably null |
Het |
Tcf15 |
C |
T |
2: 151,985,690 (GRCm39) |
R49C |
probably damaging |
Het |
Tex30 |
A |
G |
1: 44,127,136 (GRCm39) |
V124A |
possibly damaging |
Het |
Tgif1 |
T |
C |
17: 71,151,882 (GRCm39) |
D243G |
|
Het |
Tgtp1 |
T |
G |
11: 48,877,916 (GRCm39) |
D263A |
probably damaging |
Het |
Themis3 |
T |
A |
17: 66,862,864 (GRCm39) |
T365S |
probably benign |
Het |
Thoc2l |
C |
A |
5: 104,666,818 (GRCm39) |
P447T |
probably benign |
Het |
Tprg1 |
A |
T |
16: 25,231,662 (GRCm39) |
I213F |
probably damaging |
Het |
Traf4 |
A |
T |
11: 78,052,005 (GRCm39) |
C160S |
probably damaging |
Het |
Trio |
T |
C |
15: 27,732,770 (GRCm39) |
E3037G |
possibly damaging |
Het |
Ttbk2 |
G |
T |
2: 120,575,911 (GRCm39) |
S1022* |
probably null |
Het |
Ttc6 |
T |
C |
12: 57,783,949 (GRCm39) |
Y1803H |
probably damaging |
Het |
Ttn |
A |
C |
2: 76,549,452 (GRCm39) |
Y31742D |
probably benign |
Het |
Ttn |
G |
T |
2: 76,617,595 (GRCm39) |
P16292Q |
probably damaging |
Het |
Ubr5 |
A |
G |
15: 38,002,503 (GRCm39) |
V1510A |
|
Het |
Vac14 |
A |
G |
8: 111,379,869 (GRCm39) |
D389G |
probably benign |
Het |
Vwa8 |
A |
G |
14: 79,324,150 (GRCm39) |
D1151G |
probably benign |
Het |
Zfp608 |
T |
C |
18: 55,032,266 (GRCm39) |
N558S |
probably 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 |
R4716:Col4a2
|
UTSW |
8 |
11,452,224 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|
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'- TCGGGCATGTGACCTCTAAC -3'
(R):5'- ACTTTGGGATCAGCATCTGAG -3'
Sequencing Primer
(F):5'- TGTGACCTCTAACACACTTCATC -3'
(R):5'- TTACATAGTTCCAGGCTAGGCAG -3'
|
Posted On |
2021-11-19 |