Incidental Mutation 'R7341:Rgsl1'
| ID |
569818 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Rgsl1
|
| Ensembl Gene |
ENSMUSG00000042641 |
| Gene Name |
regulator of G-protein signaling like 1 |
| Synonyms |
4930415K13Rik, Rgsl2 |
| MMRRC Submission |
045431-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R7341 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
1 |
| Chromosomal Location |
153655127-153719888 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 153669591 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Threonine
at position 265
(I265T)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000139215
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000124558]
[ENSMUST00000141249]
[ENSMUST00000185164]
|
| AlphaFold |
A0A5F8MPV0 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000124558
AA Change: I945T
PolyPhen 2
Score 0.013 (Sensitivity: 0.96; Specificity: 0.78)
|
| SMART Domains |
Protein: ENSMUSP00000135642
Gene: ENSMUSG00000042641
AA Change: I945T
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
122 |
136 |
N/A |
INTRINSIC |
|
low complexity region
|
242 |
254 |
N/A |
INTRINSIC |
|
low complexity region
|
316 |
325 |
N/A |
INTRINSIC |
|
Pfam:RGS
|
644 |
754 |
7.1e-12 |
PFAM |
|
transmembrane domain
|
956 |
973 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000141249
AA Change: I265T
PolyPhen 2
Score 0.013 (Sensitivity: 0.96; Specificity: 0.78)
|
| SMART Domains |
Protein: ENSMUSP00000139215
Gene: ENSMUSG00000042641
AA Change: I265T
| Domain | Start | End | E-Value | Type |
|---|
|
Blast:RGS
|
3 |
300 |
3e-30 |
BLAST |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000184095
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000185164
|
| SMART Domains |
Protein: ENSMUSP00000139340
Gene: ENSMUSG00000042641
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
157 |
171 |
N/A |
INTRINSIC |
|
low complexity region
|
277 |
289 |
N/A |
INTRINSIC |
|
low complexity region
|
351 |
360 |
N/A |
INTRINSIC |
|
Pfam:RGS
|
679 |
789 |
4.1e-11 |
PFAM |
|
| Meta Mutation Damage Score |
0.0846 |
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.8%
- 20x: 99.3%
|
| Validation Efficiency |
100% (92/92) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 90 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abcb11 |
C |
T |
2: 69,130,211 (GRCm39) |
D282N |
probably damaging |
Het |
| Adam3 |
T |
A |
8: 25,177,996 (GRCm39) |
N639I |
possibly damaging |
Het |
| Adamtsl3 |
T |
A |
7: 82,206,082 (GRCm39) |
C756S |
probably damaging |
Het |
| Arhgap31 |
C |
T |
16: 38,532,876 (GRCm39) |
|
probably null |
Het |
| Ascl4 |
G |
A |
10: 85,764,529 (GRCm39) |
A59T |
possibly damaging |
Het |
| Ash1l |
T |
A |
3: 88,889,066 (GRCm39) |
I315N |
possibly damaging |
Het |
| Atp6v0d2 |
T |
C |
4: 19,887,330 (GRCm39) |
D206G |
possibly damaging |
Het |
| Baz1b |
T |
A |
5: 135,251,970 (GRCm39) |
L923I |
probably damaging |
Het |
| Birc6 |
T |
A |
17: 74,919,069 (GRCm39) |
N1966K |
probably damaging |
Het |
| Bod1l |
T |
C |
5: 41,946,200 (GRCm39) |
N3025S |
probably benign |
Het |
| Bub1b |
C |
A |
2: 118,467,267 (GRCm39) |
H863Q |
possibly damaging |
Het |
| C1rb |
T |
A |
6: 124,554,411 (GRCm39) |
Y397* |
probably null |
Het |
| Ccdc180 |
A |
G |
4: 45,898,644 (GRCm39) |
E164G |
possibly damaging |
Het |
| Ccdc9 |
C |
T |
7: 16,014,552 (GRCm39) |
V230M |
probably damaging |
Het |
| Cchcr1 |
C |
A |
17: 35,837,610 (GRCm39) |
N437K |
probably benign |
Het |
| Cdhr2 |
T |
A |
13: 54,867,305 (GRCm39) |
L408Q |
probably damaging |
Het |
| Cep89 |
G |
A |
7: 35,129,353 (GRCm39) |
R630H |
probably damaging |
Het |
| Chd1 |
T |
C |
17: 15,990,499 (GRCm39) |
S1684P |
probably damaging |
Het |
| CN725425 |
A |
G |
15: 91,126,873 (GRCm39) |
Y221C |
possibly damaging |
Het |
| Col4a2 |
T |
C |
8: 11,448,678 (GRCm39) |
V66A |
probably damaging |
Het |
| Cpd |
C |
A |
11: 76,737,779 (GRCm39) |
R5L |
unknown |
Het |
| Cpeb4 |
C |
T |
11: 31,868,807 (GRCm39) |
T422I |
possibly damaging |
Het |
| Cspg4b |
G |
T |
13: 113,454,706 (GRCm39) |
G251C |
|
Het |
| Cyp1a1 |
G |
T |
9: 57,608,107 (GRCm39) |
R245L |
probably damaging |
Het |
| Cyp4f39 |
A |
G |
17: 32,705,928 (GRCm39) |
T340A |
probably damaging |
Het |
| Cyp4v3 |
A |
T |
8: 45,774,787 (GRCm39) |
F122L |
probably benign |
Het |
| Drc1 |
T |
A |
5: 30,521,812 (GRCm39) |
L728Q |
probably damaging |
Het |
| Dsel |
C |
T |
1: 111,789,303 (GRCm39) |
G411S |
probably damaging |
Het |
| Ecpas |
A |
T |
4: 58,809,415 (GRCm39) |
V1653D |
possibly damaging |
Het |
| Ermp1 |
T |
A |
19: 29,623,654 (GRCm39) |
H112L |
probably benign |
Het |
| Exoc8 |
T |
C |
8: 125,623,320 (GRCm39) |
D349G |
probably damaging |
Het |
| Fam151a |
T |
A |
4: 106,592,707 (GRCm39) |
M63K |
probably benign |
Het |
| Fmo9 |
C |
A |
1: 166,504,115 (GRCm39) |
G149V |
probably damaging |
Het |
| Fndc8 |
A |
G |
11: 82,789,603 (GRCm39) |
T254A |
possibly damaging |
Het |
| Foxi3 |
G |
A |
6: 70,937,862 (GRCm39) |
V365I |
probably benign |
Het |
| Frem2 |
C |
T |
3: 53,561,916 (GRCm39) |
G864S |
probably damaging |
Het |
| Fstl5 |
T |
A |
3: 76,389,704 (GRCm39) |
|
probably null |
Het |
| Garnl3 |
T |
A |
2: 32,924,141 (GRCm39) |
E247V |
probably damaging |
Het |
| Gdi1 |
G |
A |
X: 73,350,461 (GRCm39) |
R55H |
probably benign |
Het |
| Gorasp1 |
T |
A |
9: 119,766,600 (GRCm39) |
|
probably benign |
Het |
| Hcar2 |
T |
C |
5: 124,002,541 (GRCm39) |
N321D |
possibly damaging |
Het |
| Hoxb6 |
G |
T |
11: 96,190,395 (GRCm39) |
M131I |
probably damaging |
Het |
| Kif13a |
A |
G |
13: 46,980,221 (GRCm39) |
V177A |
probably damaging |
Het |
| Limch1 |
C |
T |
5: 67,191,545 (GRCm39) |
T794I |
probably benign |
Het |
| Lmbrd2 |
A |
G |
15: 9,165,906 (GRCm39) |
Y260C |
possibly damaging |
Het |
| Lmo7 |
A |
G |
14: 102,122,948 (GRCm39) |
N379S |
probably benign |
Het |
| Lrp6 |
G |
T |
6: 134,427,781 (GRCm39) |
P1604T |
probably damaging |
Het |
| Lrrc14 |
A |
T |
15: 76,598,711 (GRCm39) |
E449V |
probably damaging |
Het |
| Lrrc8c |
T |
C |
5: 105,755,133 (GRCm39) |
Y303H |
probably damaging |
Het |
| Mecr |
T |
G |
4: 131,570,986 (GRCm39) |
V58G |
probably null |
Het |
| Med12l |
T |
A |
3: 58,949,824 (GRCm39) |
D193E |
possibly damaging |
Het |
| Moap1 |
T |
C |
12: 102,709,438 (GRCm39) |
E37G |
probably damaging |
Het |
| Mrgprb2 |
T |
A |
7: 48,202,644 (GRCm39) |
Y27F |
probably benign |
Het |
| Ms4a6d |
G |
A |
19: 11,567,437 (GRCm39) |
Q155* |
probably null |
Het |
| Ndufs5 |
A |
T |
4: 123,609,744 (GRCm39) |
C43* |
probably null |
Het |
| Oaz2 |
A |
T |
9: 65,596,183 (GRCm39) |
D83V |
|
Het |
| Or2t29 |
A |
T |
11: 58,433,533 (GRCm39) |
Y269* |
probably null |
Het |
| Or5ac22 |
T |
A |
16: 59,135,512 (GRCm39) |
N86I |
possibly damaging |
Het |
| Palm |
A |
G |
10: 79,652,697 (GRCm39) |
T191A |
probably damaging |
Het |
| Pclo |
C |
A |
5: 14,725,850 (GRCm39) |
D1569E |
unknown |
Het |
| Ppid |
T |
A |
3: 79,507,604 (GRCm39) |
D264E |
probably benign |
Het |
| Ppp1r3a |
A |
G |
6: 14,718,749 (GRCm39) |
S722P |
probably damaging |
Het |
| Ranbp2 |
A |
G |
10: 58,321,619 (GRCm39) |
S2639G |
possibly damaging |
Het |
| Rbak |
T |
C |
5: 143,161,827 (GRCm39) |
T68A |
probably benign |
Het |
| Rbm15b |
C |
T |
9: 106,762,246 (GRCm39) |
G641R |
probably benign |
Het |
| Rmdn1 |
T |
A |
4: 19,586,837 (GRCm39) |
Y98* |
probably null |
Het |
| Sfxn3 |
T |
G |
19: 45,037,701 (GRCm39) |
N52K |
probably benign |
Het |
| Slc17a3 |
G |
T |
13: 24,030,867 (GRCm39) |
G182* |
probably null |
Het |
| Slc29a3 |
A |
T |
10: 60,586,437 (GRCm39) |
Y10N |
probably benign |
Het |
| Slc43a1 |
T |
C |
2: 84,693,278 (GRCm39) |
Y577H |
probably damaging |
Het |
| Smarcd3 |
T |
A |
5: 24,800,435 (GRCm39) |
I210F |
possibly damaging |
Het |
| Snapc4 |
A |
T |
2: 26,259,273 (GRCm39) |
S626T |
probably benign |
Het |
| Sp5 |
T |
A |
2: 70,307,041 (GRCm39) |
L242* |
probably null |
Het |
| Spata25 |
C |
G |
2: 164,669,582 (GRCm39) |
G143A |
probably damaging |
Het |
| Spata6 |
T |
A |
4: 111,625,935 (GRCm39) |
Y101* |
probably null |
Het |
| Tdp2 |
T |
G |
13: 25,016,059 (GRCm39) |
S89A |
probably benign |
Het |
| Tlr6 |
T |
C |
5: 65,110,972 (GRCm39) |
E645G |
probably benign |
Het |
| Tmem209 |
T |
C |
6: 30,494,794 (GRCm39) |
I355V |
probably benign |
Het |
| Trappc8 |
A |
T |
18: 20,985,704 (GRCm39) |
Y646N |
probably damaging |
Het |
| Tspoap1 |
A |
G |
11: 87,657,205 (GRCm39) |
N399S |
probably damaging |
Het |
| Ube4b |
A |
G |
4: 149,427,458 (GRCm39) |
Y897H |
probably damaging |
Het |
| Urb1 |
CACTTAC |
CAC |
16: 90,569,461 (GRCm39) |
|
probably benign |
Het |
| Usp9y |
A |
T |
Y: 1,315,759 (GRCm39) |
|
probably null |
Het |
| Vmn2r1 |
T |
C |
3: 64,012,877 (GRCm39) |
*913Q |
probably null |
Het |
| Vmn2r12 |
T |
A |
5: 109,234,113 (GRCm39) |
T700S |
possibly damaging |
Het |
| Vmn2r12 |
C |
T |
5: 109,239,811 (GRCm39) |
A251T |
possibly damaging |
Het |
| Wdr70 |
A |
C |
15: 7,953,725 (GRCm39) |
F389V |
possibly damaging |
Het |
| Wdr91 |
A |
T |
6: 34,868,395 (GRCm39) |
M442K |
possibly damaging |
Het |
| Ydjc |
T |
C |
16: 16,968,762 (GRCm39) |
C234R |
probably benign |
Het |
| Zfp87 |
A |
G |
13: 74,520,467 (GRCm39) |
Y204H |
possibly damaging |
Het |
|
| Other mutations in Rgsl1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01372:Rgsl1
|
APN |
1 |
153,701,887 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02253:Rgsl1
|
APN |
1 |
153,669,513 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02345:Rgsl1
|
APN |
1 |
153,679,755 (GRCm39) |
splice site |
probably null |
|
|
IGL02409:Rgsl1
|
APN |
1 |
153,701,989 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
IGL02587:Rgsl1
|
APN |
1 |
153,675,684 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02652:Rgsl1
|
APN |
1 |
153,701,236 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02797:Rgsl1
|
APN |
1 |
153,683,454 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03032:Rgsl1
|
APN |
1 |
153,701,948 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
IGL03082:Rgsl1
|
APN |
1 |
153,675,693 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
IGL03123:Rgsl1
|
APN |
1 |
153,701,687 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03213:Rgsl1
|
APN |
1 |
153,701,587 (GRCm39) |
missense |
probably benign |
0.12 |
|
IGL03410:Rgsl1
|
APN |
1 |
153,669,501 (GRCm39) |
missense |
probably null |
0.82 |
|
Bam
|
UTSW |
1 |
153,669,898 (GRCm39) |
missense |
probably benign |
0.00 |
|
Candygram
|
UTSW |
1 |
153,697,245 (GRCm39) |
nonsense |
probably null |
|
|
wham
|
UTSW |
1 |
153,678,038 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL03050:Rgsl1
|
UTSW |
1 |
153,701,422 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
PIT4519001:Rgsl1
|
UTSW |
1 |
153,701,716 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
R0149:Rgsl1
|
UTSW |
1 |
153,669,510 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0536:Rgsl1
|
UTSW |
1 |
153,701,927 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0633:Rgsl1
|
UTSW |
1 |
153,719,853 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R0726:Rgsl1
|
UTSW |
1 |
153,678,074 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0839:Rgsl1
|
UTSW |
1 |
153,677,980 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1240:Rgsl1
|
UTSW |
1 |
153,660,937 (GRCm39) |
missense |
probably benign |
0.18 |
|
R1355:Rgsl1
|
UTSW |
1 |
153,683,507 (GRCm39) |
start codon destroyed |
probably null |
0.23 |
|
R1491:Rgsl1
|
UTSW |
1 |
153,701,672 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R1688:Rgsl1
|
UTSW |
1 |
153,680,422 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1694:Rgsl1
|
UTSW |
1 |
153,680,422 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1842:Rgsl1
|
UTSW |
1 |
153,675,543 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2008:Rgsl1
|
UTSW |
1 |
153,701,651 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R2114:Rgsl1
|
UTSW |
1 |
153,693,295 (GRCm39) |
missense |
probably benign |
|
|
R2116:Rgsl1
|
UTSW |
1 |
153,693,295 (GRCm39) |
missense |
probably benign |
|
|
R2176:Rgsl1
|
UTSW |
1 |
153,701,014 (GRCm39) |
splice site |
probably benign |
|
|
R2229:Rgsl1
|
UTSW |
1 |
153,698,104 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R2895:Rgsl1
|
UTSW |
1 |
153,703,294 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3923:Rgsl1
|
UTSW |
1 |
153,679,876 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R4001:Rgsl1
|
UTSW |
1 |
153,693,330 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4434:Rgsl1
|
UTSW |
1 |
153,678,087 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
R4489:Rgsl1
|
UTSW |
1 |
153,703,282 (GRCm39) |
missense |
probably benign |
0.27 |
|
R4649:Rgsl1
|
UTSW |
1 |
153,693,328 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4925:Rgsl1
|
UTSW |
1 |
153,688,023 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4928:Rgsl1
|
UTSW |
1 |
153,669,514 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5045:Rgsl1
|
UTSW |
1 |
153,697,268 (GRCm39) |
nonsense |
probably null |
|
|
R5304:Rgsl1
|
UTSW |
1 |
153,703,238 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R5331:Rgsl1
|
UTSW |
1 |
153,678,038 (GRCm39) |
missense |
probably benign |
0.02 |
|
R5373:Rgsl1
|
UTSW |
1 |
153,666,053 (GRCm39) |
missense |
probably benign |
0.33 |
|
R5374:Rgsl1
|
UTSW |
1 |
153,666,053 (GRCm39) |
missense |
probably benign |
0.33 |
|
R5566:Rgsl1
|
UTSW |
1 |
153,669,520 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5649:Rgsl1
|
UTSW |
1 |
153,701,639 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R6062:Rgsl1
|
UTSW |
1 |
153,675,618 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R6142:Rgsl1
|
UTSW |
1 |
153,687,984 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6158:Rgsl1
|
UTSW |
1 |
153,679,767 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R6184:Rgsl1
|
UTSW |
1 |
153,703,194 (GRCm39) |
missense |
probably benign |
0.08 |
|
R6273:Rgsl1
|
UTSW |
1 |
153,703,211 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
R6384:Rgsl1
|
UTSW |
1 |
153,703,291 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R6419:Rgsl1
|
UTSW |
1 |
153,698,117 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6568:Rgsl1
|
UTSW |
1 |
153,697,292 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R6660:Rgsl1
|
UTSW |
1 |
153,701,512 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
R6745:Rgsl1
|
UTSW |
1 |
153,698,063 (GRCm39) |
missense |
probably benign |
0.18 |
|
R6892:Rgsl1
|
UTSW |
1 |
153,697,245 (GRCm39) |
nonsense |
probably null |
|
|
R6974:Rgsl1
|
UTSW |
1 |
153,675,568 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7172:Rgsl1
|
UTSW |
1 |
153,701,966 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R7200:Rgsl1
|
UTSW |
1 |
153,660,945 (GRCm39) |
missense |
probably benign |
0.33 |
|
R7275:Rgsl1
|
UTSW |
1 |
153,679,876 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R7313:Rgsl1
|
UTSW |
1 |
153,683,622 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R7448:Rgsl1
|
UTSW |
1 |
153,719,847 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7662:Rgsl1
|
UTSW |
1 |
153,701,225 (GRCm39) |
missense |
probably benign |
|
|
R7703:Rgsl1
|
UTSW |
1 |
153,669,610 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R7846:Rgsl1
|
UTSW |
1 |
153,701,783 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R8408:Rgsl1
|
UTSW |
1 |
153,701,435 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
R8860:Rgsl1
|
UTSW |
1 |
153,697,100 (GRCm39) |
nonsense |
probably null |
|
|
R8894:Rgsl1
|
UTSW |
1 |
153,698,119 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R9043:Rgsl1
|
UTSW |
1 |
153,717,567 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R9187:Rgsl1
|
UTSW |
1 |
153,669,613 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R9280:Rgsl1
|
UTSW |
1 |
153,669,898 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9326:Rgsl1
|
UTSW |
1 |
153,679,768 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9388:Rgsl1
|
UTSW |
1 |
153,693,355 (GRCm39) |
missense |
probably benign |
|
|
R9479:Rgsl1
|
UTSW |
1 |
153,657,445 (GRCm39) |
missense |
unknown |
|
|
X0020:Rgsl1
|
UTSW |
1 |
153,701,131 (GRCm39) |
missense |
probably benign |
0.33 |
|
X0065:Rgsl1
|
UTSW |
1 |
153,679,779 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
Z1177:Rgsl1
|
UTSW |
1 |
153,701,734 (GRCm39) |
missense |
not run |
|
|
Z1177:Rgsl1
|
UTSW |
1 |
153,693,356 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
| Predicted Primers |
PCR Primer
(F):5'- GCCTGTTAGTTCCTCACAGG -3'
(R):5'- ACCCTAAAATCGAATCACTGGG -3'
Sequencing Primer
(F):5'- TCCTCACAGGATTGGAAATGATG -3'
(R):5'- TCATAAGCTCCGGGTCACAGAG -3'
|
| Posted On |
2019-09-13 |
Incidental Mutation