Incidental Mutation 'R1682:Rp1l1'
| ID |
189280 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Rp1l1
|
| Ensembl Gene |
ENSMUSG00000046049 |
| Gene Name |
retinitis pigmentosa 1 homolog like 1 |
| Synonyms |
Dcdc4, Rp1hl1 |
| MMRRC Submission |
039718-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.073)
|
| Stock # |
R1682 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
14 |
| Chromosomal Location |
64229880-64270955 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 64266417 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Serine to Threonine
at position 668
(S668T)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000055449
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000058229]
|
| AlphaFold |
Q8CGM2 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000058229
AA Change: S668T
PolyPhen 2
Score 0.984 (Sensitivity: 0.74; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000055449
Gene: ENSMUSG00000046049
AA Change: S668T
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
11 |
21 |
N/A |
INTRINSIC |
|
DCX
|
37 |
121 |
1.58e-13 |
SMART |
|
DCX
|
155 |
239 |
1e-15 |
SMART |
|
low complexity region
|
709 |
728 |
N/A |
INTRINSIC |
|
low complexity region
|
870 |
884 |
N/A |
INTRINSIC |
|
low complexity region
|
1159 |
1177 |
N/A |
INTRINSIC |
|
low complexity region
|
1228 |
1239 |
N/A |
INTRINSIC |
|
low complexity region
|
1612 |
1618 |
N/A |
INTRINSIC |
|
low complexity region
|
1642 |
1652 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000224314
|
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.4%
- 10x: 96.6%
- 20x: 93.5%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: This gene encodes a member of the doublecortin family. This protein is a retinal-specific protein. It contains two N-terminal doublecortin domains, which can assemble and stabilize axonemal microtubules, but lacks the C-terminal repetitive regions including the 16aa repeat found in human RP1L1. This protein and the RP1 protein, another retinal-specific protein, play essential and synergistic roles in affecting photosensitivity and outer segment morphogenesis of rod photoreceptors. [provided by RefSeq, Sep 2010]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit retinal photoreceptor abnormalities, including scattered outer segment disorganization, reduced electroretinogram amplitudes, and progressive retinal rod cell degeneration. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 88 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acaca |
A |
G |
11: 84,283,043 (GRCm39) |
D2203G |
probably benign |
Het |
| Acin1 |
A |
G |
14: 54,901,175 (GRCm39) |
S629P |
probably damaging |
Het |
| Agbl2 |
T |
A |
2: 90,614,434 (GRCm39) |
I22N |
probably benign |
Het |
| Ank1 |
A |
G |
8: 23,599,343 (GRCm39) |
E796G |
probably damaging |
Het |
| Ankrd13d |
A |
G |
19: 4,332,961 (GRCm39) |
L13P |
probably damaging |
Het |
| Ankrd36 |
T |
C |
11: 5,557,143 (GRCm39) |
S364P |
possibly damaging |
Het |
| Ap2a1 |
T |
C |
7: 44,565,362 (GRCm39) |
T126A |
probably benign |
Het |
| Apob |
A |
G |
12: 8,062,365 (GRCm39) |
I3616V |
probably benign |
Het |
| Arl5a |
A |
T |
2: 52,306,214 (GRCm39) |
N39K |
probably benign |
Het |
| Baiap2 |
G |
A |
11: 119,888,366 (GRCm39) |
R334H |
probably damaging |
Het |
| Bbox1 |
T |
A |
2: 110,122,893 (GRCm39) |
N132I |
possibly damaging |
Het |
| Bcl11b |
A |
G |
12: 107,882,908 (GRCm39) |
L469P |
probably damaging |
Het |
| Brca1 |
A |
G |
11: 101,416,391 (GRCm39) |
I581T |
probably damaging |
Het |
| Cacng2 |
T |
C |
15: 78,002,997 (GRCm39) |
Y32C |
probably damaging |
Het |
| Capn9 |
G |
T |
8: 125,338,304 (GRCm39) |
|
probably null |
Het |
| Cdh18 |
A |
G |
15: 23,400,671 (GRCm39) |
T290A |
probably benign |
Het |
| Cdk5rap2 |
C |
T |
4: 70,220,387 (GRCm39) |
V593I |
possibly damaging |
Het |
| Cep128 |
G |
C |
12: 91,197,596 (GRCm39) |
D91E |
probably damaging |
Het |
| Cep295 |
T |
C |
9: 15,245,217 (GRCm39) |
M1080V |
probably benign |
Het |
| Coq8b |
T |
A |
7: 26,939,549 (GRCm39) |
M193K |
probably benign |
Het |
| Csn1s2b |
A |
G |
5: 87,970,162 (GRCm39) |
Y131C |
probably damaging |
Het |
| D130043K22Rik |
T |
C |
13: 25,066,539 (GRCm39) |
S779P |
probably damaging |
Het |
| Dgat1 |
C |
T |
15: 76,387,219 (GRCm39) |
C356Y |
probably benign |
Het |
| Dipk1c |
A |
T |
18: 84,754,988 (GRCm39) |
I155F |
possibly damaging |
Het |
| Dnah12 |
A |
T |
14: 26,500,840 (GRCm39) |
T1543S |
possibly damaging |
Het |
| Dock3 |
T |
C |
9: 106,851,040 (GRCm39) |
S821G |
probably damaging |
Het |
| Dock4 |
G |
A |
12: 40,775,779 (GRCm39) |
C574Y |
probably damaging |
Het |
| Dr1 |
T |
C |
5: 108,417,604 (GRCm39) |
I50T |
probably damaging |
Het |
| Dzip3 |
A |
T |
16: 48,778,780 (GRCm39) |
|
probably null |
Het |
| Eln |
C |
A |
5: 134,732,636 (GRCm39) |
*861L |
probably null |
Het |
| Eml6 |
T |
A |
11: 29,709,065 (GRCm39) |
H24L |
probably benign |
Het |
| Eps8l3 |
A |
C |
3: 107,798,622 (GRCm39) |
T503P |
possibly damaging |
Het |
| Fgf1 |
C |
A |
18: 38,974,985 (GRCm39) |
D155Y |
possibly damaging |
Het |
| Fkbp15 |
A |
T |
4: 62,242,431 (GRCm39) |
M507K |
probably damaging |
Het |
| Flnb |
A |
T |
14: 7,913,121 (GRCm38) |
R1463S |
probably benign |
Het |
| Fras1 |
C |
T |
5: 96,793,732 (GRCm39) |
T1018I |
probably benign |
Het |
| Gm10803 |
T |
A |
2: 93,394,533 (GRCm39) |
C102S |
probably damaging |
Het |
| Gpatch1 |
C |
A |
7: 35,002,812 (GRCm39) |
V233L |
possibly damaging |
Het |
| Gramd1a |
T |
C |
7: 30,842,325 (GRCm39) |
|
probably null |
Het |
| Gsk3a |
T |
C |
7: 24,935,133 (GRCm39) |
T106A |
possibly damaging |
Het |
| Hap1 |
A |
G |
11: 100,240,302 (GRCm39) |
V136A |
possibly damaging |
Het |
| Helq |
A |
T |
5: 100,940,679 (GRCm39) |
S307T |
probably benign |
Het |
| Herc2 |
T |
A |
7: 55,738,148 (GRCm39) |
S264T |
possibly damaging |
Het |
| Htr4 |
A |
G |
18: 62,561,137 (GRCm39) |
M133V |
possibly damaging |
Het |
| Iqca1 |
C |
A |
1: 90,070,453 (GRCm39) |
G133V |
probably null |
Het |
| Jakmip2 |
A |
G |
18: 43,714,896 (GRCm39) |
|
probably null |
Het |
| Ldhd |
T |
A |
8: 112,354,745 (GRCm39) |
S358C |
possibly damaging |
Het |
| Lrp1 |
A |
T |
10: 127,410,201 (GRCm39) |
V1515E |
probably damaging |
Het |
| Ltbp3 |
A |
G |
19: 5,801,782 (GRCm39) |
D700G |
probably benign |
Het |
| Magel2 |
T |
G |
7: 62,029,983 (GRCm39) |
S962R |
unknown |
Het |
| Map2 |
A |
C |
1: 66,454,781 (GRCm39) |
|
probably null |
Het |
| Map3k1 |
T |
A |
13: 111,893,684 (GRCm39) |
E704V |
probably damaging |
Het |
| Mrpl39 |
A |
T |
16: 84,527,347 (GRCm39) |
V180D |
probably damaging |
Het |
| Myef2 |
T |
C |
2: 124,939,978 (GRCm39) |
M383V |
probably damaging |
Het |
| Myh3 |
A |
G |
11: 66,979,891 (GRCm39) |
Y610C |
probably damaging |
Het |
| Or10ak7 |
A |
G |
4: 118,791,778 (GRCm39) |
L89P |
probably damaging |
Het |
| Or51h1 |
T |
C |
7: 102,308,904 (GRCm39) |
V292A |
probably damaging |
Het |
| Or8g54 |
T |
A |
9: 39,706,954 (GRCm39) |
Y94* |
probably null |
Het |
| Oxtr |
C |
T |
6: 112,454,138 (GRCm39) |
R42Q |
probably benign |
Het |
| Pabpc1 |
T |
A |
15: 36,605,785 (GRCm39) |
N135I |
possibly damaging |
Het |
| Pcsk6 |
T |
A |
7: 65,559,976 (GRCm39) |
H100Q |
probably damaging |
Het |
| Pdss1 |
A |
G |
2: 22,805,531 (GRCm39) |
K270E |
probably damaging |
Het |
| Pigx |
A |
T |
16: 31,906,268 (GRCm39) |
S18T |
possibly damaging |
Het |
| Plbd2 |
T |
A |
5: 120,623,849 (GRCm39) |
T558S |
probably damaging |
Het |
| Plppr1 |
A |
T |
4: 49,325,617 (GRCm39) |
|
probably null |
Het |
| Plppr2 |
T |
A |
9: 21,855,717 (GRCm39) |
V230E |
possibly damaging |
Het |
| Pola2 |
A |
G |
19: 6,003,091 (GRCm39) |
|
probably null |
Het |
| Ppp2r3d |
A |
G |
9: 101,089,505 (GRCm39) |
S273P |
probably benign |
Het |
| Prkdc |
A |
G |
16: 15,494,853 (GRCm39) |
E741G |
probably benign |
Het |
| Prom2 |
C |
A |
2: 127,382,082 (GRCm39) |
V111L |
possibly damaging |
Het |
| Rapgef4 |
A |
G |
2: 72,056,912 (GRCm39) |
D557G |
possibly damaging |
Het |
| Rgs10 |
T |
C |
7: 127,975,694 (GRCm39) |
T158A |
probably benign |
Het |
| Rnf123 |
A |
C |
9: 107,954,597 (GRCm39) |
Y40D |
probably benign |
Het |
| Rnf14 |
A |
G |
18: 38,441,242 (GRCm39) |
T211A |
probably benign |
Het |
| Sema6d |
T |
A |
2: 124,507,069 (GRCm39) |
L946Q |
probably benign |
Het |
| Sgcd |
T |
G |
11: 47,085,869 (GRCm39) |
K94Q |
probably benign |
Het |
| Skor2 |
A |
T |
18: 76,947,211 (GRCm39) |
D311V |
unknown |
Het |
| Slc34a1 |
A |
T |
13: 23,996,623 (GRCm39) |
I43F |
probably damaging |
Het |
| Spdye4c |
C |
A |
2: 128,434,542 (GRCm39) |
P40T |
probably damaging |
Het |
| Srp72 |
C |
A |
5: 77,135,717 (GRCm39) |
Q216K |
possibly damaging |
Het |
| Tmem62 |
C |
T |
2: 120,837,538 (GRCm39) |
T485I |
probably benign |
Het |
| Tmem94 |
G |
T |
11: 115,681,056 (GRCm39) |
V432L |
probably damaging |
Het |
| Trio |
T |
C |
15: 27,744,232 (GRCm39) |
|
probably null |
Het |
| Uggt2 |
A |
T |
14: 119,292,055 (GRCm39) |
D581E |
probably benign |
Het |
| Unc5d |
T |
A |
8: 29,249,109 (GRCm39) |
S319C |
probably damaging |
Het |
| Vmn1r211 |
T |
C |
13: 23,035,813 (GRCm39) |
I285V |
probably damaging |
Het |
| Vmn2r68 |
A |
G |
7: 84,882,574 (GRCm39) |
Y393H |
possibly damaging |
Het |
| Vmn2r99 |
A |
C |
17: 19,598,207 (GRCm39) |
N77T |
probably damaging |
Het |
|
| Other mutations in Rp1l1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00494:Rp1l1
|
APN |
14 |
64,266,174 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02063:Rp1l1
|
APN |
14 |
64,266,985 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02132:Rp1l1
|
APN |
14 |
64,266,259 (GRCm39) |
missense |
probably benign |
|
|
IGL02430:Rp1l1
|
APN |
14 |
64,266,735 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02977:Rp1l1
|
APN |
14 |
64,265,599 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL03213:Rp1l1
|
APN |
14 |
64,265,864 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL03346:Rp1l1
|
APN |
14 |
64,266,889 (GRCm39) |
missense |
probably benign |
|
|
R0085:Rp1l1
|
UTSW |
14 |
64,259,744 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0347:Rp1l1
|
UTSW |
14 |
64,268,253 (GRCm39) |
nonsense |
probably null |
|
|
R0362:Rp1l1
|
UTSW |
14 |
64,268,515 (GRCm39) |
nonsense |
probably null |
|
|
R0369:Rp1l1
|
UTSW |
14 |
64,266,837 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R0538:Rp1l1
|
UTSW |
14 |
64,259,541 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0544:Rp1l1
|
UTSW |
14 |
64,269,515 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0780:Rp1l1
|
UTSW |
14 |
64,267,800 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R0944:Rp1l1
|
UTSW |
14 |
64,269,681 (GRCm39) |
missense |
probably benign |
0.05 |
|
R1051:Rp1l1
|
UTSW |
14 |
64,269,984 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1126:Rp1l1
|
UTSW |
14 |
64,267,918 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1450:Rp1l1
|
UTSW |
14 |
64,265,599 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1483:Rp1l1
|
UTSW |
14 |
64,266,496 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
R1508:Rp1l1
|
UTSW |
14 |
64,268,341 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R1553:Rp1l1
|
UTSW |
14 |
64,269,343 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1651:Rp1l1
|
UTSW |
14 |
64,268,442 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R1809:Rp1l1
|
UTSW |
14 |
64,265,415 (GRCm39) |
missense |
probably benign |
0.18 |
|
R1885:Rp1l1
|
UTSW |
14 |
64,265,839 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1887:Rp1l1
|
UTSW |
14 |
64,265,839 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1898:Rp1l1
|
UTSW |
14 |
64,269,039 (GRCm39) |
missense |
probably benign |
0.04 |
|
R1924:Rp1l1
|
UTSW |
14 |
64,268,992 (GRCm39) |
missense |
probably benign |
|
|
R1939:Rp1l1
|
UTSW |
14 |
64,267,042 (GRCm39) |
missense |
probably benign |
|
|
R1941:Rp1l1
|
UTSW |
14 |
64,259,701 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2129:Rp1l1
|
UTSW |
14 |
64,266,415 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R2363:Rp1l1
|
UTSW |
14 |
64,267,447 (GRCm39) |
missense |
possibly damaging |
0.55 |
|
R3894:Rp1l1
|
UTSW |
14 |
64,266,756 (GRCm39) |
missense |
probably benign |
|
|
R3974:Rp1l1
|
UTSW |
14 |
64,267,758 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3975:Rp1l1
|
UTSW |
14 |
64,267,758 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3976:Rp1l1
|
UTSW |
14 |
64,267,758 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4072:Rp1l1
|
UTSW |
14 |
64,265,581 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4672:Rp1l1
|
UTSW |
14 |
64,268,719 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4673:Rp1l1
|
UTSW |
14 |
64,268,719 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4749:Rp1l1
|
UTSW |
14 |
64,267,249 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4755:Rp1l1
|
UTSW |
14 |
64,267,519 (GRCm39) |
missense |
probably benign |
0.34 |
|
R4877:Rp1l1
|
UTSW |
14 |
64,263,620 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4930:Rp1l1
|
UTSW |
14 |
64,269,655 (GRCm39) |
missense |
probably benign |
|
|
R5039:Rp1l1
|
UTSW |
14 |
64,268,805 (GRCm39) |
missense |
probably benign |
0.21 |
|
R5106:Rp1l1
|
UTSW |
14 |
64,265,395 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5184:Rp1l1
|
UTSW |
14 |
64,267,629 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5215:Rp1l1
|
UTSW |
14 |
64,267,462 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5409:Rp1l1
|
UTSW |
14 |
64,268,070 (GRCm39) |
missense |
probably benign |
0.02 |
|
R5575:Rp1l1
|
UTSW |
14 |
64,268,433 (GRCm39) |
missense |
probably benign |
0.23 |
|
R5696:Rp1l1
|
UTSW |
14 |
64,267,195 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5739:Rp1l1
|
UTSW |
14 |
64,269,619 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5878:Rp1l1
|
UTSW |
14 |
64,266,355 (GRCm39) |
missense |
probably benign |
0.09 |
|
R6133:Rp1l1
|
UTSW |
14 |
64,267,545 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6134:Rp1l1
|
UTSW |
14 |
64,267,545 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6135:Rp1l1
|
UTSW |
14 |
64,267,545 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6428:Rp1l1
|
UTSW |
14 |
64,269,838 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R6594:Rp1l1
|
UTSW |
14 |
64,269,126 (GRCm39) |
nonsense |
probably null |
|
|
R6736:Rp1l1
|
UTSW |
14 |
64,267,173 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R6800:Rp1l1
|
UTSW |
14 |
64,268,599 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R6848:Rp1l1
|
UTSW |
14 |
64,265,667 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R6878:Rp1l1
|
UTSW |
14 |
64,269,301 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6922:Rp1l1
|
UTSW |
14 |
64,267,834 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R6980:Rp1l1
|
UTSW |
14 |
64,266,169 (GRCm39) |
missense |
probably benign |
0.02 |
|
R7053:Rp1l1
|
UTSW |
14 |
64,268,958 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R7151:Rp1l1
|
UTSW |
14 |
64,266,475 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R7291:Rp1l1
|
UTSW |
14 |
64,269,747 (GRCm39) |
missense |
probably benign |
0.10 |
|
R7335:Rp1l1
|
UTSW |
14 |
64,269,447 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7344:Rp1l1
|
UTSW |
14 |
64,267,069 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7470:Rp1l1
|
UTSW |
14 |
64,266,015 (GRCm39) |
missense |
probably benign |
|
|
R7570:Rp1l1
|
UTSW |
14 |
64,269,023 (GRCm39) |
nonsense |
probably null |
|
|
R7585:Rp1l1
|
UTSW |
14 |
64,267,588 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R7591:Rp1l1
|
UTSW |
14 |
64,263,558 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7667:Rp1l1
|
UTSW |
14 |
64,267,252 (GRCm39) |
missense |
probably benign |
0.04 |
|
R7862:Rp1l1
|
UTSW |
14 |
64,265,476 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7935:Rp1l1
|
UTSW |
14 |
64,268,674 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8256:Rp1l1
|
UTSW |
14 |
64,265,602 (GRCm39) |
missense |
probably benign |
0.18 |
|
R8403:Rp1l1
|
UTSW |
14 |
64,266,258 (GRCm39) |
missense |
probably benign |
0.21 |
|
R8709:Rp1l1
|
UTSW |
14 |
64,269,295 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8817:Rp1l1
|
UTSW |
14 |
64,268,085 (GRCm39) |
missense |
probably benign |
|
|
R8971:Rp1l1
|
UTSW |
14 |
64,259,445 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9380:Rp1l1
|
UTSW |
14 |
64,266,475 (GRCm39) |
missense |
probably benign |
0.29 |
|
R9438:Rp1l1
|
UTSW |
14 |
64,265,574 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R9501:Rp1l1
|
UTSW |
14 |
64,266,039 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9652:Rp1l1
|
UTSW |
14 |
64,269,714 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9683:Rp1l1
|
UTSW |
14 |
64,269,126 (GRCm39) |
missense |
probably damaging |
0.97 |
|
X0057:Rp1l1
|
UTSW |
14 |
64,267,489 (GRCm39) |
missense |
probably benign |
0.14 |
|
X0063:Rp1l1
|
UTSW |
14 |
64,266,672 (GRCm39) |
missense |
probably damaging |
0.98 |
|
Z1088:Rp1l1
|
UTSW |
14 |
64,267,827 (GRCm39) |
missense |
probably benign |
0.01 |
|
Z1088:Rp1l1
|
UTSW |
14 |
64,266,207 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
Z1176:Rp1l1
|
UTSW |
14 |
64,266,593 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1177:Rp1l1
|
UTSW |
14 |
64,269,746 (GRCm39) |
missense |
probably damaging |
0.99 |
|
| Predicted Primers |
PCR Primer
(F):5'- CCAAGGGTGACAACCCCTGTATTTC -3'
(R):5'- CCAGCACTGGGTGAATTTGAAGGAG -3'
Sequencing Primer
(F):5'- TCACATGGGTCTTCAGACAG -3'
(R):5'- AATTTGAAGGAGATTGTGGTGC -3'
|
| Posted On |
2014-05-14 |
Incidental Mutation