Incidental Mutation 'R1464:Dscam'
ID |
200999 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Dscam
|
Ensembl Gene |
ENSMUSG00000050272 |
Gene Name |
DS cell adhesion molecule |
Synonyms |
4932410A21Rik, Down syndrome cell adhesion molecule |
MMRRC Submission |
039518-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R1464 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
16 |
Chromosomal Location |
96392040-96971952 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 96602453 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Histidine to Leucine
at position 663
(H663L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000056040
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000056102]
|
AlphaFold |
Q9ERC8 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000056102
AA Change: H663L
PolyPhen 2
Score 0.942 (Sensitivity: 0.80; Specificity: 0.94)
|
SMART Domains |
Protein: ENSMUSP00000056040 Gene: ENSMUSG00000050272 AA Change: H663L
Domain | Start | End | E-Value | Type |
IG_like
|
37 |
109 |
1.47e0 |
SMART |
IG
|
130 |
218 |
8.33e-1 |
SMART |
IGc2
|
237 |
300 |
8.7e-13 |
SMART |
IGc2
|
326 |
392 |
1.24e-8 |
SMART |
IGc2
|
419 |
491 |
1.1e-9 |
SMART |
IGc2
|
516 |
582 |
1.99e-7 |
SMART |
IGc2
|
608 |
676 |
1.84e-11 |
SMART |
IGc2
|
702 |
773 |
6.01e-16 |
SMART |
IG
|
794 |
883 |
1.73e-7 |
SMART |
FN3
|
885 |
969 |
7.34e-9 |
SMART |
FN3
|
985 |
1073 |
4.06e-11 |
SMART |
FN3
|
1088 |
1174 |
7.23e-8 |
SMART |
FN3
|
1189 |
1270 |
2.6e-9 |
SMART |
IGc2
|
1301 |
1366 |
2.05e-9 |
SMART |
FN3
|
1380 |
1460 |
7.17e-12 |
SMART |
FN3
|
1477 |
1557 |
4.35e1 |
SMART |
transmembrane domain
|
1595 |
1617 |
N/A |
INTRINSIC |
low complexity region
|
1799 |
1809 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 97.4%
- 3x: 96.8%
- 10x: 95.0%
- 20x: 91.7%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is a member of the immunoglobulin superfamily of cell adhesion molecules (Ig-CAMs), and is involved in human central and peripheral nervous system development. This gene is a candidate for Down syndrome and congenital heart disease (DSCHD). A gene encoding a similar Ig-CAM protein is located on chromosome 11. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Oct 2012] PHENOTYPE: Mice homozygous for a null allele exhibit background-sensitive perinatal lethality associated with respiratory distress, altered C4 ventral root and pre-inspiratory neuron signaling, and abnormal response to hypercapnia. [provided by MGI curators]
|
Allele List at MGI |
All alleles(9) : Targeted(6) Gene trapped(1) Spontaneous(2)
|
Other mutations in this stock |
Total: 113 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6030469F06Rik |
A |
G |
12: 31,234,914 (GRCm39) |
|
noncoding transcript |
Het |
Abca2 |
T |
G |
2: 25,337,846 (GRCm39) |
|
probably benign |
Het |
Adamts8 |
T |
A |
9: 30,862,673 (GRCm39) |
W86R |
probably benign |
Het |
Adh1 |
A |
G |
3: 137,994,508 (GRCm39) |
|
probably null |
Het |
Adipor2 |
A |
T |
6: 119,338,804 (GRCm39) |
W150R |
probably damaging |
Het |
Aff4 |
T |
A |
11: 53,263,351 (GRCm39) |
S124T |
probably damaging |
Het |
Ahnak |
G |
T |
19: 8,982,260 (GRCm39) |
K1181N |
probably damaging |
Het |
Ak2 |
C |
A |
4: 128,896,152 (GRCm39) |
|
probably benign |
Het |
Alkbh5 |
A |
G |
11: 60,429,873 (GRCm39) |
I209V |
probably benign |
Het |
Ankrd11 |
T |
C |
8: 123,619,463 (GRCm39) |
E1442G |
probably damaging |
Het |
Apba2 |
T |
A |
7: 64,345,297 (GRCm39) |
D162E |
probably benign |
Het |
Asic3 |
G |
A |
5: 24,618,819 (GRCm39) |
G37E |
probably damaging |
Het |
AU040320 |
A |
T |
4: 126,685,824 (GRCm39) |
K133N |
possibly damaging |
Het |
C1qtnf7 |
A |
G |
5: 43,766,481 (GRCm39) |
S34G |
probably benign |
Het |
Carf |
A |
G |
1: 60,165,065 (GRCm39) |
|
probably benign |
Het |
Ccdc148 |
T |
A |
2: 58,796,374 (GRCm39) |
R463* |
probably null |
Het |
Ccdc148 |
T |
C |
2: 58,824,455 (GRCm39) |
R329G |
probably damaging |
Het |
Ccdc185 |
A |
G |
1: 182,576,263 (GRCm39) |
I142T |
probably benign |
Het |
Cd274 |
T |
C |
19: 29,359,992 (GRCm39) |
|
probably benign |
Het |
Chrna10 |
G |
A |
7: 101,763,454 (GRCm39) |
P114S |
probably damaging |
Het |
Chst10 |
A |
G |
1: 38,904,772 (GRCm39) |
I311T |
probably damaging |
Het |
Cpne9 |
T |
C |
6: 113,271,698 (GRCm39) |
Y353H |
probably damaging |
Het |
Cubn |
G |
T |
2: 13,330,099 (GRCm39) |
A2594E |
possibly damaging |
Het |
Cyp3a13 |
T |
C |
5: 137,903,827 (GRCm39) |
N277S |
possibly damaging |
Het |
Dctn4 |
A |
G |
18: 60,671,478 (GRCm39) |
T117A |
probably damaging |
Het |
Ddah1 |
A |
T |
3: 145,559,029 (GRCm39) |
K96* |
probably null |
Het |
Ddx5 |
A |
C |
11: 106,675,711 (GRCm39) |
D326E |
probably benign |
Het |
Dlg2 |
T |
C |
7: 91,617,406 (GRCm39) |
S323P |
probably damaging |
Het |
Dnaaf1 |
C |
T |
8: 120,306,049 (GRCm39) |
H109Y |
probably damaging |
Het |
Dnah8 |
C |
A |
17: 30,914,147 (GRCm39) |
R1098S |
possibly damaging |
Het |
Dnajc13 |
T |
C |
9: 104,091,366 (GRCm39) |
T642A |
probably benign |
Het |
Dnajc18 |
A |
G |
18: 35,813,900 (GRCm39) |
S290P |
possibly damaging |
Het |
Eefsec |
C |
T |
6: 88,353,182 (GRCm39) |
|
probably benign |
Het |
Emc1 |
A |
G |
4: 139,098,248 (GRCm39) |
N740S |
probably damaging |
Het |
Enpp2 |
C |
T |
15: 54,727,208 (GRCm39) |
G541D |
probably damaging |
Het |
Fam234b |
C |
T |
6: 135,205,490 (GRCm39) |
T485I |
probably benign |
Het |
Fbxl13 |
A |
T |
5: 21,688,989 (GRCm39) |
I773K |
probably benign |
Het |
Fmo4 |
A |
G |
1: 162,621,924 (GRCm39) |
F429S |
possibly damaging |
Het |
Fndc3b |
A |
G |
3: 27,494,334 (GRCm39) |
|
probably benign |
Het |
Frem1 |
T |
C |
4: 82,930,116 (GRCm39) |
S277G |
probably damaging |
Het |
Gaa |
A |
G |
11: 119,163,810 (GRCm39) |
I221V |
probably benign |
Het |
Gnptab |
A |
G |
10: 88,281,616 (GRCm39) |
|
probably benign |
Het |
Gphn |
T |
A |
12: 78,659,738 (GRCm39) |
|
probably benign |
Het |
Helz2 |
T |
C |
2: 180,881,447 (GRCm39) |
E345G |
probably damaging |
Het |
Ifna4 |
G |
T |
4: 88,760,237 (GRCm39) |
R47I |
probably damaging |
Het |
Igsf21 |
C |
A |
4: 139,761,836 (GRCm39) |
A281S |
probably benign |
Het |
Ikzf3 |
T |
A |
11: 98,407,731 (GRCm39) |
I37L |
probably benign |
Het |
Inpp5d |
A |
T |
1: 87,625,827 (GRCm39) |
|
probably benign |
Het |
Jag1 |
T |
C |
2: 136,957,568 (GRCm39) |
E48G |
probably damaging |
Het |
Jarid2 |
G |
T |
13: 45,001,857 (GRCm39) |
V57F |
probably damaging |
Het |
Kcnj4 |
A |
G |
15: 79,369,605 (GRCm39) |
L125P |
probably damaging |
Het |
Kif21b |
A |
G |
1: 136,083,891 (GRCm39) |
K713E |
possibly damaging |
Het |
Layn |
T |
A |
9: 50,968,886 (GRCm39) |
S286C |
probably damaging |
Het |
Lepr |
T |
A |
4: 101,592,878 (GRCm39) |
D164E |
probably benign |
Het |
Macroh2a1 |
A |
T |
13: 56,230,949 (GRCm39) |
S310T |
probably damaging |
Het |
Map3k1 |
T |
C |
13: 111,892,405 (GRCm39) |
H950R |
possibly damaging |
Het |
Map4k5 |
C |
A |
12: 69,852,124 (GRCm39) |
V801L |
possibly damaging |
Het |
Mapkbp1 |
T |
A |
2: 119,851,742 (GRCm39) |
S895T |
probably benign |
Het |
Mthfr |
T |
A |
4: 148,138,029 (GRCm39) |
|
probably benign |
Het |
Naca |
T |
A |
10: 127,884,157 (GRCm39) |
M2157K |
probably damaging |
Het |
Nav2 |
T |
C |
7: 49,011,952 (GRCm39) |
I61T |
probably damaging |
Het |
Nkx2-5 |
C |
A |
17: 27,058,253 (GRCm39) |
A234S |
probably benign |
Het |
Nol8 |
G |
A |
13: 49,830,264 (GRCm39) |
S1116N |
probably benign |
Het |
Nphp3 |
T |
C |
9: 103,909,078 (GRCm39) |
|
probably benign |
Het |
Nppa |
T |
C |
4: 148,085,304 (GRCm39) |
S5P |
probably benign |
Het |
Nup210 |
A |
G |
6: 91,030,551 (GRCm39) |
V123A |
possibly damaging |
Het |
Or13a21 |
G |
T |
7: 139,999,286 (GRCm39) |
N133K |
probably benign |
Het |
Osbpl11 |
A |
G |
16: 33,049,455 (GRCm39) |
K604R |
probably damaging |
Het |
Osbpl1a |
C |
T |
18: 13,047,615 (GRCm39) |
S113N |
probably benign |
Het |
P2rx4 |
C |
A |
5: 122,852,602 (GRCm39) |
P92Q |
probably damaging |
Het |
Pde9a |
A |
T |
17: 31,692,136 (GRCm39) |
Q148L |
probably benign |
Het |
Phf21b |
T |
A |
15: 84,689,160 (GRCm39) |
H122L |
probably damaging |
Het |
Pik3ca |
T |
A |
3: 32,515,990 (GRCm39) |
F977I |
probably damaging |
Het |
Pkd1l3 |
A |
G |
8: 110,363,059 (GRCm39) |
|
probably benign |
Het |
Potefam1 |
A |
G |
2: 111,055,748 (GRCm39) |
|
probably null |
Het |
Pp2d1 |
T |
G |
17: 53,823,015 (GRCm39) |
K17T |
possibly damaging |
Het |
Ppp4r2 |
A |
G |
6: 100,843,527 (GRCm39) |
E415G |
probably damaging |
Het |
Pramel19 |
T |
A |
4: 101,798,503 (GRCm39) |
L158Q |
probably damaging |
Het |
Prkg1 |
A |
G |
19: 30,556,270 (GRCm39) |
S559P |
probably damaging |
Het |
Prss45 |
A |
T |
9: 110,670,019 (GRCm39) |
Y276F |
possibly damaging |
Het |
Ptk7 |
G |
T |
17: 46,883,517 (GRCm39) |
N849K |
probably damaging |
Het |
Rnf121 |
A |
G |
7: 101,680,782 (GRCm39) |
I125T |
possibly damaging |
Het |
Rnf17 |
A |
G |
14: 56,699,368 (GRCm39) |
N502S |
probably damaging |
Het |
Sap25 |
T |
A |
5: 137,640,622 (GRCm39) |
Y167* |
probably null |
Het |
Sdk2 |
G |
A |
11: 113,720,906 (GRCm39) |
T1341I |
possibly damaging |
Het |
Sgcb |
A |
G |
5: 73,792,896 (GRCm39) |
V302A |
probably benign |
Het |
Skor1 |
T |
A |
9: 63,047,393 (GRCm39) |
M865L |
possibly damaging |
Het |
Slc25a45 |
T |
C |
19: 5,929,928 (GRCm39) |
|
probably benign |
Het |
Slc2a3 |
A |
G |
6: 122,714,269 (GRCm39) |
|
probably benign |
Het |
Slc35g1 |
C |
A |
19: 38,391,665 (GRCm39) |
L316I |
probably benign |
Het |
Slco1a8 |
C |
T |
6: 141,938,243 (GRCm39) |
W225* |
probably null |
Het |
Spint4 |
T |
A |
2: 164,540,568 (GRCm39) |
L33H |
probably damaging |
Het |
Sptlc3 |
A |
T |
2: 139,389,154 (GRCm39) |
D178V |
probably benign |
Het |
Stoml1 |
A |
G |
9: 58,167,709 (GRCm39) |
|
probably benign |
Het |
Tbc1d2 |
T |
A |
4: 46,606,491 (GRCm39) |
Y818F |
possibly damaging |
Het |
Tbc1d24 |
A |
T |
17: 24,400,197 (GRCm39) |
|
probably null |
Het |
Teddm2 |
C |
T |
1: 153,726,277 (GRCm39) |
W146* |
probably null |
Het |
Ttn |
T |
A |
2: 76,589,338 (GRCm39) |
D12948V |
probably damaging |
Het |
Txndc8 |
T |
C |
4: 58,000,274 (GRCm39) |
T102A |
probably damaging |
Het |
Uxs1 |
G |
A |
1: 43,804,076 (GRCm39) |
Q280* |
probably null |
Het |
Vmn1r167 |
T |
C |
7: 23,204,681 (GRCm39) |
T112A |
possibly damaging |
Het |
Vmn1r195 |
A |
T |
13: 22,463,348 (GRCm39) |
I273L |
probably benign |
Het |
Vmn1r28 |
T |
A |
6: 58,242,217 (GRCm39) |
M20K |
probably benign |
Het |
Vmn1r53 |
G |
A |
6: 90,200,914 (GRCm39) |
L137F |
probably benign |
Het |
Vmn2r105 |
G |
A |
17: 20,449,004 (GRCm39) |
|
probably benign |
Het |
Vps13b |
C |
T |
15: 35,709,630 (GRCm39) |
A1859V |
probably benign |
Het |
Vwa5b2 |
A |
G |
16: 20,415,019 (GRCm39) |
H347R |
probably benign |
Het |
Wnk2 |
G |
A |
13: 49,235,451 (GRCm39) |
P655S |
probably damaging |
Het |
Zan |
T |
G |
5: 137,418,191 (GRCm39) |
D2969A |
unknown |
Het |
Zbtb24 |
A |
G |
10: 41,331,075 (GRCm39) |
H334R |
probably damaging |
Het |
Zfp108 |
A |
G |
7: 23,959,973 (GRCm39) |
D188G |
probably benign |
Het |
Zfp784 |
A |
T |
7: 5,038,800 (GRCm39) |
C253S |
possibly damaging |
Het |
Zfr |
T |
G |
15: 12,146,458 (GRCm39) |
C336W |
probably damaging |
Het |
|
Other mutations in Dscam |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00515:Dscam
|
APN |
16 |
96,409,265 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL00841:Dscam
|
APN |
16 |
96,621,077 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01289:Dscam
|
APN |
16 |
96,445,082 (GRCm39) |
nonsense |
probably null |
|
IGL01358:Dscam
|
APN |
16 |
96,411,543 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL01431:Dscam
|
APN |
16 |
96,453,278 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01444:Dscam
|
APN |
16 |
96,474,909 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01767:Dscam
|
APN |
16 |
96,456,136 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01866:Dscam
|
APN |
16 |
96,486,550 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02020:Dscam
|
APN |
16 |
96,517,269 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02023:Dscam
|
APN |
16 |
96,602,397 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02057:Dscam
|
APN |
16 |
96,517,273 (GRCm39) |
nonsense |
probably null |
|
IGL02389:Dscam
|
APN |
16 |
96,442,097 (GRCm39) |
missense |
probably benign |
0.27 |
IGL02409:Dscam
|
APN |
16 |
96,621,088 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL02694:Dscam
|
APN |
16 |
96,394,476 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02899:Dscam
|
APN |
16 |
96,510,447 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02956:Dscam
|
APN |
16 |
96,602,472 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03035:Dscam
|
APN |
16 |
96,621,170 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03191:Dscam
|
APN |
16 |
96,621,969 (GRCm39) |
missense |
probably benign |
0.36 |
growler
|
UTSW |
16 |
96,622,197 (GRCm39) |
missense |
probably damaging |
0.99 |
Twostep
|
UTSW |
16 |
96,626,982 (GRCm39) |
splice site |
probably null |
|
F6893:Dscam
|
UTSW |
16 |
96,857,660 (GRCm39) |
missense |
possibly damaging |
0.78 |
K3955:Dscam
|
UTSW |
16 |
96,474,887 (GRCm39) |
missense |
probably benign |
0.00 |
R0024:Dscam
|
UTSW |
16 |
96,394,585 (GRCm39) |
nonsense |
probably null |
|
R0057:Dscam
|
UTSW |
16 |
96,474,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R0057:Dscam
|
UTSW |
16 |
96,474,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R0117:Dscam
|
UTSW |
16 |
96,474,878 (GRCm39) |
missense |
probably benign |
0.33 |
R0211:Dscam
|
UTSW |
16 |
96,517,279 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0280:Dscam
|
UTSW |
16 |
96,840,206 (GRCm39) |
missense |
possibly damaging |
0.62 |
R0355:Dscam
|
UTSW |
16 |
96,456,105 (GRCm39) |
missense |
probably benign |
0.00 |
R0380:Dscam
|
UTSW |
16 |
96,857,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R0445:Dscam
|
UTSW |
16 |
96,573,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R0492:Dscam
|
UTSW |
16 |
96,626,982 (GRCm39) |
splice site |
probably null |
|
R0534:Dscam
|
UTSW |
16 |
96,453,372 (GRCm39) |
missense |
possibly damaging |
0.67 |
R0593:Dscam
|
UTSW |
16 |
96,573,608 (GRCm39) |
missense |
probably benign |
0.19 |
R0707:Dscam
|
UTSW |
16 |
96,626,982 (GRCm39) |
splice site |
probably null |
|
R0738:Dscam
|
UTSW |
16 |
96,620,981 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1017:Dscam
|
UTSW |
16 |
96,634,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R1377:Dscam
|
UTSW |
16 |
96,573,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R1440:Dscam
|
UTSW |
16 |
96,621,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R1442:Dscam
|
UTSW |
16 |
96,409,274 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1464:Dscam
|
UTSW |
16 |
96,602,453 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1478:Dscam
|
UTSW |
16 |
96,592,110 (GRCm39) |
missense |
probably benign |
0.15 |
R1530:Dscam
|
UTSW |
16 |
96,621,074 (GRCm39) |
missense |
probably damaging |
1.00 |
R1731:Dscam
|
UTSW |
16 |
96,621,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R1765:Dscam
|
UTSW |
16 |
96,486,579 (GRCm39) |
missense |
probably benign |
0.00 |
R1824:Dscam
|
UTSW |
16 |
96,626,781 (GRCm39) |
missense |
probably benign |
0.00 |
R1933:Dscam
|
UTSW |
16 |
96,394,414 (GRCm39) |
missense |
probably benign |
0.00 |
R2005:Dscam
|
UTSW |
16 |
96,840,120 (GRCm39) |
missense |
probably benign |
0.02 |
R2006:Dscam
|
UTSW |
16 |
96,621,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R2101:Dscam
|
UTSW |
16 |
96,411,549 (GRCm39) |
missense |
probably benign |
0.00 |
R2177:Dscam
|
UTSW |
16 |
96,411,524 (GRCm39) |
missense |
probably damaging |
0.98 |
R2342:Dscam
|
UTSW |
16 |
96,420,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R2851:Dscam
|
UTSW |
16 |
96,423,915 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2929:Dscam
|
UTSW |
16 |
96,486,612 (GRCm39) |
missense |
possibly damaging |
0.76 |
R3055:Dscam
|
UTSW |
16 |
96,602,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R3157:Dscam
|
UTSW |
16 |
96,479,710 (GRCm39) |
missense |
probably benign |
0.16 |
R3159:Dscam
|
UTSW |
16 |
96,479,710 (GRCm39) |
missense |
probably benign |
0.16 |
R3944:Dscam
|
UTSW |
16 |
96,622,197 (GRCm39) |
missense |
probably damaging |
0.99 |
R4080:Dscam
|
UTSW |
16 |
96,484,972 (GRCm39) |
missense |
probably benign |
0.01 |
R4285:Dscam
|
UTSW |
16 |
96,510,309 (GRCm39) |
critical splice donor site |
probably null |
|
R4384:Dscam
|
UTSW |
16 |
96,510,416 (GRCm39) |
missense |
probably damaging |
0.99 |
R4460:Dscam
|
UTSW |
16 |
96,411,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R4575:Dscam
|
UTSW |
16 |
96,626,823 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4594:Dscam
|
UTSW |
16 |
96,519,196 (GRCm39) |
missense |
possibly damaging |
0.78 |
R4643:Dscam
|
UTSW |
16 |
96,486,501 (GRCm39) |
missense |
probably damaging |
0.96 |
R4698:Dscam
|
UTSW |
16 |
96,411,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R4716:Dscam
|
UTSW |
16 |
96,420,771 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4743:Dscam
|
UTSW |
16 |
96,631,256 (GRCm39) |
missense |
probably benign |
0.00 |
R4766:Dscam
|
UTSW |
16 |
96,445,188 (GRCm39) |
missense |
probably benign |
0.02 |
R4899:Dscam
|
UTSW |
16 |
96,485,018 (GRCm39) |
missense |
probably benign |
0.01 |
R4987:Dscam
|
UTSW |
16 |
96,498,721 (GRCm39) |
missense |
probably benign |
0.00 |
R4990:Dscam
|
UTSW |
16 |
96,626,715 (GRCm39) |
missense |
probably benign |
0.12 |
R5123:Dscam
|
UTSW |
16 |
96,573,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R5130:Dscam
|
UTSW |
16 |
96,620,979 (GRCm39) |
missense |
probably benign |
0.00 |
R5328:Dscam
|
UTSW |
16 |
96,474,878 (GRCm39) |
missense |
probably benign |
0.33 |
R5666:Dscam
|
UTSW |
16 |
96,519,364 (GRCm39) |
missense |
probably benign |
0.23 |
R5670:Dscam
|
UTSW |
16 |
96,519,364 (GRCm39) |
missense |
probably benign |
0.23 |
R5678:Dscam
|
UTSW |
16 |
96,592,100 (GRCm39) |
missense |
probably benign |
0.16 |
R5827:Dscam
|
UTSW |
16 |
96,451,191 (GRCm39) |
critical splice donor site |
probably null |
|
R5907:Dscam
|
UTSW |
16 |
96,622,120 (GRCm39) |
missense |
probably damaging |
0.97 |
R6032:Dscam
|
UTSW |
16 |
96,451,191 (GRCm39) |
critical splice donor site |
probably null |
|
R6032:Dscam
|
UTSW |
16 |
96,451,191 (GRCm39) |
critical splice donor site |
probably null |
|
R6103:Dscam
|
UTSW |
16 |
96,626,781 (GRCm39) |
missense |
probably benign |
|
R6240:Dscam
|
UTSW |
16 |
96,420,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R6257:Dscam
|
UTSW |
16 |
96,474,914 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6361:Dscam
|
UTSW |
16 |
96,424,011 (GRCm39) |
missense |
probably benign |
0.08 |
R6405:Dscam
|
UTSW |
16 |
96,479,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R6444:Dscam
|
UTSW |
16 |
96,420,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R6560:Dscam
|
UTSW |
16 |
96,626,935 (GRCm39) |
missense |
probably benign |
0.00 |
R6598:Dscam
|
UTSW |
16 |
96,620,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R6622:Dscam
|
UTSW |
16 |
96,446,273 (GRCm39) |
missense |
probably benign |
0.06 |
R6792:Dscam
|
UTSW |
16 |
96,449,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R6792:Dscam
|
UTSW |
16 |
96,394,455 (GRCm39) |
missense |
probably damaging |
0.96 |
R6827:Dscam
|
UTSW |
16 |
96,840,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R6868:Dscam
|
UTSW |
16 |
96,631,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R6898:Dscam
|
UTSW |
16 |
96,631,100 (GRCm39) |
missense |
probably benign |
0.02 |
R6903:Dscam
|
UTSW |
16 |
96,621,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R7051:Dscam
|
UTSW |
16 |
96,620,986 (GRCm39) |
missense |
probably benign |
0.01 |
R7146:Dscam
|
UTSW |
16 |
96,631,117 (GRCm39) |
nonsense |
probably null |
|
R7180:Dscam
|
UTSW |
16 |
96,626,764 (GRCm39) |
missense |
probably damaging |
0.97 |
R7209:Dscam
|
UTSW |
16 |
96,451,544 (GRCm39) |
splice site |
probably null |
|
R7247:Dscam
|
UTSW |
16 |
96,622,008 (GRCm39) |
missense |
probably damaging |
0.99 |
R7269:Dscam
|
UTSW |
16 |
96,479,601 (GRCm39) |
missense |
probably benign |
0.00 |
R7301:Dscam
|
UTSW |
16 |
96,857,732 (GRCm39) |
missense |
probably benign |
0.01 |
R7328:Dscam
|
UTSW |
16 |
96,446,235 (GRCm39) |
nonsense |
probably null |
|
R7368:Dscam
|
UTSW |
16 |
96,445,131 (GRCm39) |
missense |
probably benign |
0.00 |
R7425:Dscam
|
UTSW |
16 |
96,430,598 (GRCm39) |
missense |
probably damaging |
1.00 |
R7474:Dscam
|
UTSW |
16 |
96,621,089 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7536:Dscam
|
UTSW |
16 |
96,442,226 (GRCm39) |
splice site |
probably null |
|
R7624:Dscam
|
UTSW |
16 |
96,411,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R7766:Dscam
|
UTSW |
16 |
96,592,101 (GRCm39) |
missense |
probably benign |
0.31 |
R7817:Dscam
|
UTSW |
16 |
96,442,064 (GRCm39) |
missense |
probably benign |
|
R7843:Dscam
|
UTSW |
16 |
96,626,830 (GRCm39) |
missense |
probably damaging |
0.99 |
R7911:Dscam
|
UTSW |
16 |
96,445,122 (GRCm39) |
missense |
probably benign |
0.01 |
R8108:Dscam
|
UTSW |
16 |
96,445,079 (GRCm39) |
missense |
probably benign |
0.01 |
R8128:Dscam
|
UTSW |
16 |
96,602,374 (GRCm39) |
splice site |
probably null |
|
R8770:Dscam
|
UTSW |
16 |
96,456,106 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8876:Dscam
|
UTSW |
16 |
96,420,828 (GRCm39) |
missense |
probably damaging |
0.96 |
R9005:Dscam
|
UTSW |
16 |
96,602,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R9009:Dscam
|
UTSW |
16 |
96,840,116 (GRCm39) |
missense |
probably benign |
0.10 |
R9168:Dscam
|
UTSW |
16 |
96,420,768 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9176:Dscam
|
UTSW |
16 |
96,486,553 (GRCm39) |
missense |
probably benign |
0.37 |
R9244:Dscam
|
UTSW |
16 |
96,486,429 (GRCm39) |
missense |
possibly damaging |
0.62 |
R9339:Dscam
|
UTSW |
16 |
96,517,263 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9374:Dscam
|
UTSW |
16 |
96,857,857 (GRCm39) |
missense |
probably benign |
0.19 |
R9385:Dscam
|
UTSW |
16 |
96,840,203 (GRCm39) |
missense |
probably benign |
|
R9674:Dscam
|
UTSW |
16 |
96,442,036 (GRCm39) |
missense |
probably benign |
0.03 |
X0025:Dscam
|
UTSW |
16 |
96,510,361 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Dscam
|
UTSW |
16 |
96,573,761 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Dscam
|
UTSW |
16 |
96,409,389 (GRCm39) |
missense |
probably damaging |
0.98 |
|
Predicted Primers |
PCR Primer
(F):5'- CGTGTTCAGCAGAAGACCTATTTCACC -3'
(R):5'- TTCCCAAGATTCTCCATCGGGCAG -3'
Sequencing Primer
(F):5'- ATTTGTTTCAGAGTTTAGAGGAATGC -3'
(R):5'- GGGCAGCGGGTTTTCATC -3'
|
Posted On |
2014-05-23 |