Incidental Mutation 'R1809:Rp1l1'
| ID |
203736 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Rp1l1
|
| Ensembl Gene |
ENSMUSG00000046049 |
| Gene Name |
retinitis pigmentosa 1 homolog like 1 |
| Synonyms |
Dcdc4, Rp1hl1 |
| MMRRC Submission |
039838-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.078)
|
| Stock # |
R1809 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
14 |
| Chromosomal Location |
64229880-64270955 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 64265415 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Methionine to Leucine
at position 334
(M334L)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000055449
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000058229]
|
| AlphaFold |
Q8CGM2 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000058229
AA Change: M334L
PolyPhen 2
Score 0.183 (Sensitivity: 0.92; Specificity: 0.87)
|
| SMART Domains |
Protein: ENSMUSP00000055449
Gene: ENSMUSG00000046049
AA Change: M334L
| 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
|
| Meta Mutation Damage Score |
0.0979 |
| Coding Region Coverage |
- 1x: 97.5%
- 3x: 96.8%
- 10x: 94.9%
- 20x: 91.2%
|
| Validation Efficiency |
96% (107/111) |
| 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: 104 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Ablim2 |
A |
G |
5: 36,000,614 (GRCm39) |
|
probably benign |
Het |
| Adamts20 |
C |
T |
15: 94,238,968 (GRCm39) |
S750N |
probably damaging |
Het |
| Adh6a |
G |
A |
3: 138,036,722 (GRCm39) |
R370H |
possibly damaging |
Het |
| Akr1b7 |
A |
G |
6: 34,396,046 (GRCm39) |
N183D |
probably damaging |
Het |
| Aktip |
A |
T |
8: 91,856,348 (GRCm39) |
I43N |
probably damaging |
Het |
| Ankrd26 |
A |
T |
6: 118,502,883 (GRCm39) |
|
probably benign |
Het |
| Ano9 |
G |
A |
7: 140,688,717 (GRCm39) |
T144I |
possibly damaging |
Het |
| Anpep |
G |
T |
7: 79,491,571 (GRCm39) |
D143E |
probably benign |
Het |
| Aox1 |
C |
A |
1: 58,333,484 (GRCm39) |
Q234K |
probably benign |
Het |
| Ap1g1 |
C |
G |
8: 110,559,814 (GRCm39) |
|
probably benign |
Het |
| Arhgef4 |
G |
A |
1: 34,849,636 (GRCm39) |
|
probably null |
Het |
| Arsj |
A |
G |
3: 126,231,944 (GRCm39) |
Y230C |
possibly damaging |
Het |
| Asmt |
C |
T |
X: 169,109,480 (GRCm39) |
|
probably benign |
Het |
| Astl |
A |
T |
2: 127,187,405 (GRCm39) |
K72N |
probably damaging |
Het |
| Atp2b2 |
G |
A |
6: 113,780,704 (GRCm39) |
|
probably benign |
Het |
| Baiap2l1 |
A |
C |
5: 144,261,365 (GRCm39) |
|
probably null |
Het |
| C7 |
A |
T |
15: 5,063,821 (GRCm39) |
N193K |
probably damaging |
Het |
| Cacna2d4 |
G |
T |
6: 119,247,785 (GRCm39) |
R362L |
probably damaging |
Het |
| Cct4 |
T |
A |
11: 22,947,615 (GRCm39) |
D189E |
probably benign |
Het |
| Cd300lg |
G |
A |
11: 101,933,938 (GRCm39) |
G62S |
probably benign |
Het |
| Cdk14 |
T |
A |
5: 5,060,901 (GRCm39) |
M307L |
probably damaging |
Het |
| Cfi |
G |
A |
3: 129,666,768 (GRCm39) |
|
probably null |
Het |
| Clec2g |
G |
T |
6: 128,957,273 (GRCm39) |
|
probably null |
Het |
| Cntnap2 |
T |
C |
6: 46,965,609 (GRCm39) |
S807P |
probably damaging |
Het |
| Col6a3 |
T |
A |
1: 90,755,671 (GRCm39) |
H206L |
probably damaging |
Het |
| Ct55 |
A |
G |
X: 52,735,716 (GRCm39) |
E99G |
probably benign |
Het |
| Cyp2c23 |
A |
T |
19: 44,009,997 (GRCm39) |
|
probably benign |
Het |
| Degs1l |
T |
C |
1: 180,887,252 (GRCm39) |
I279T |
probably damaging |
Het |
| Dlec1 |
T |
C |
9: 118,965,767 (GRCm39) |
V1058A |
probably benign |
Het |
| Dpp9 |
A |
G |
17: 56,506,038 (GRCm39) |
Y454H |
probably damaging |
Het |
| Drosha |
G |
A |
15: 12,890,198 (GRCm39) |
G920R |
probably null |
Het |
| Duox2 |
A |
G |
2: 122,114,378 (GRCm39) |
S1142P |
possibly damaging |
Het |
| Fam13a |
C |
T |
6: 58,942,045 (GRCm39) |
|
probably null |
Het |
| Filip1l |
A |
G |
16: 57,327,023 (GRCm39) |
R18G |
probably benign |
Het |
| Foxa1 |
A |
G |
12: 57,589,527 (GRCm39) |
V231A |
probably damaging |
Het |
| Gm4787 |
A |
T |
12: 81,425,303 (GRCm39) |
M285K |
possibly damaging |
Het |
| Gm5084 |
T |
A |
13: 60,360,320 (GRCm39) |
|
noncoding transcript |
Het |
| Gm6788 |
G |
A |
19: 28,740,586 (GRCm39) |
|
noncoding transcript |
Het |
| Gm9922 |
G |
T |
14: 101,966,841 (GRCm39) |
|
probably benign |
Het |
| Gtf3c4 |
A |
T |
2: 28,723,988 (GRCm39) |
Y440* |
probably null |
Het |
| Helq |
A |
G |
5: 100,921,820 (GRCm39) |
S795P |
probably damaging |
Het |
| Helz |
T |
A |
11: 107,489,997 (GRCm39) |
S151T |
possibly damaging |
Het |
| Irgm1 |
T |
C |
11: 48,757,440 (GRCm39) |
T124A |
probably benign |
Het |
| Itgam |
C |
T |
7: 127,670,109 (GRCm39) |
P134S |
possibly damaging |
Het |
| Kdm6a |
T |
C |
X: 18,102,923 (GRCm39) |
Y217H |
probably benign |
Het |
| Kif6 |
T |
C |
17: 50,208,812 (GRCm39) |
L744P |
probably benign |
Het |
| Kmt2c |
C |
T |
5: 25,489,190 (GRCm39) |
R1203H |
probably damaging |
Het |
| Ksr2 |
A |
G |
5: 117,693,535 (GRCm39) |
T328A |
probably damaging |
Het |
| Lig1 |
T |
C |
7: 13,034,281 (GRCm39) |
|
probably benign |
Het |
| Lpar3 |
G |
A |
3: 145,946,303 (GRCm39) |
|
probably benign |
Het |
| Lrrk2 |
T |
C |
15: 91,584,095 (GRCm39) |
F285S |
possibly damaging |
Het |
| Marchf7 |
A |
G |
2: 60,062,637 (GRCm39) |
D148G |
probably benign |
Het |
| Mcee |
T |
C |
7: 64,050,049 (GRCm39) |
L60S |
probably damaging |
Het |
| Mob2 |
A |
G |
7: 141,570,111 (GRCm39) |
I81T |
probably damaging |
Het |
| Mphosph8 |
T |
A |
14: 56,909,909 (GRCm39) |
D87E |
probably damaging |
Het |
| Msantd5f9 |
A |
G |
4: 73,835,754 (GRCm39) |
F237L |
probably benign |
Het |
| Myo1g |
T |
C |
11: 6,462,283 (GRCm39) |
T560A |
probably benign |
Het |
| Nagk |
C |
T |
6: 83,774,169 (GRCm39) |
T42I |
probably benign |
Het |
| Naip1 |
G |
T |
13: 100,562,747 (GRCm39) |
T806K |
probably benign |
Het |
| Ncor2 |
A |
G |
5: 125,195,857 (GRCm39) |
|
probably benign |
Het |
| Ocln |
G |
T |
13: 100,647,967 (GRCm39) |
Y401* |
probably null |
Het |
| Odad2 |
T |
A |
18: 7,211,630 (GRCm39) |
Y748F |
probably benign |
Het |
| Oma1 |
T |
A |
4: 103,182,374 (GRCm39) |
N292K |
probably damaging |
Het |
| Or8b55 |
G |
A |
9: 38,727,443 (GRCm39) |
V215I |
probably benign |
Het |
| Ovch2 |
T |
A |
7: 107,389,412 (GRCm39) |
|
probably null |
Het |
| Pcdhb16 |
T |
C |
18: 37,611,441 (GRCm39) |
F134L |
probably damaging |
Het |
| Pipox |
A |
T |
11: 77,772,360 (GRCm39) |
Y337N |
probably benign |
Het |
| Polr3b |
A |
G |
10: 84,528,865 (GRCm39) |
D763G |
probably damaging |
Het |
| Pygo1 |
T |
A |
9: 72,852,078 (GRCm39) |
N88K |
probably damaging |
Het |
| Rab3gap1 |
T |
C |
1: 127,862,251 (GRCm39) |
M674T |
probably damaging |
Het |
| Rbm25 |
T |
C |
12: 83,719,501 (GRCm39) |
|
probably benign |
Het |
| Rbm26 |
C |
T |
14: 105,354,542 (GRCm39) |
|
probably benign |
Het |
| Rbms2 |
G |
A |
10: 127,974,055 (GRCm39) |
T187I |
possibly damaging |
Het |
| Rnase11 |
T |
A |
14: 51,287,184 (GRCm39) |
R123S |
probably benign |
Het |
| Rngtt |
A |
G |
4: 33,443,614 (GRCm39) |
N485D |
probably benign |
Het |
| Rps9 |
T |
A |
7: 3,707,726 (GRCm39) |
L56Q |
probably damaging |
Het |
| Saysd1 |
C |
A |
14: 20,133,170 (GRCm39) |
|
probably benign |
Het |
| Sema4d |
C |
T |
13: 51,867,727 (GRCm39) |
|
probably null |
Het |
| Shisa5 |
A |
T |
9: 108,869,998 (GRCm39) |
D34V |
probably damaging |
Het |
| Skil |
A |
G |
3: 31,171,655 (GRCm39) |
D547G |
probably damaging |
Het |
| Slc2a5 |
T |
A |
4: 150,227,514 (GRCm39) |
F444L |
probably damaging |
Het |
| Slc9b2 |
T |
G |
3: 135,022,892 (GRCm39) |
C10G |
possibly damaging |
Het |
| Sorcs2 |
G |
T |
5: 36,386,564 (GRCm39) |
|
probably benign |
Het |
| Stk17b |
T |
G |
1: 53,805,140 (GRCm39) |
K140N |
possibly damaging |
Het |
| Stradb |
T |
A |
1: 59,033,549 (GRCm39) |
L404Q |
possibly damaging |
Het |
| Synj2 |
T |
C |
17: 6,076,826 (GRCm39) |
M432T |
possibly damaging |
Het |
| Tanc1 |
G |
T |
2: 59,630,441 (GRCm39) |
R800L |
probably damaging |
Het |
| Tenm4 |
A |
G |
7: 96,522,987 (GRCm39) |
M1473V |
probably benign |
Het |
| Tesc |
A |
G |
5: 118,199,667 (GRCm39) |
I190V |
probably benign |
Het |
| Tex15 |
T |
C |
8: 34,064,262 (GRCm39) |
F1231L |
probably benign |
Het |
| Thrsp |
T |
C |
7: 97,066,332 (GRCm39) |
I127V |
probably benign |
Het |
| Tlr6 |
A |
T |
5: 65,111,055 (GRCm39) |
C617* |
probably null |
Het |
| Trank1 |
A |
T |
9: 111,221,893 (GRCm39) |
I2877F |
probably benign |
Het |
| Tut4 |
T |
A |
4: 108,406,552 (GRCm39) |
H1373Q |
probably damaging |
Het |
| Ucp1 |
T |
C |
8: 84,024,496 (GRCm39) |
S274P |
probably damaging |
Het |
| Ucp2 |
T |
A |
7: 100,147,606 (GRCm39) |
V195E |
probably damaging |
Het |
| Vars2 |
T |
C |
17: 35,973,108 (GRCm39) |
T394A |
probably damaging |
Het |
| Vmn1r1 |
A |
G |
1: 181,985,371 (GRCm39) |
V98A |
possibly damaging |
Het |
| Vmn1r225 |
A |
G |
17: 20,722,918 (GRCm39) |
I120V |
probably benign |
Het |
| Vmn2r102 |
A |
T |
17: 19,897,881 (GRCm39) |
M299L |
probably benign |
Het |
| Vmn2r25 |
A |
G |
6: 123,802,337 (GRCm39) |
V522A |
probably benign |
Het |
| Vmn2r70 |
T |
C |
7: 85,215,130 (GRCm39) |
I135V |
probably benign |
Het |
| Vwf |
T |
C |
6: 125,567,138 (GRCm39) |
|
probably benign |
Het |
| Zfp446 |
T |
C |
7: 12,713,048 (GRCm39) |
F29L |
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 |
|
R1682:Rp1l1
|
UTSW |
14 |
64,266,417 (GRCm39) |
missense |
probably damaging |
0.98 |
|
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'- AGTAGCTCACTGCCTTGTTC -3'
(R):5'- TAAGATGCCCCAAGGGTAGC -3'
Sequencing Primer
(F):5'- TGTCATACACTCGAGGGGCAG -3'
(R):5'- GGTAGCCCTCCTGTCTGCAAC -3'
|
| Posted On |
2014-06-23 |
Incidental Mutation