Incidental Mutation 'R7155:Rims1'
ID |
557183 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Rims1
|
Ensembl Gene |
ENSMUSG00000041670 |
Gene Name |
regulating synaptic membrane exocytosis 1 |
Synonyms |
RIM1alpha, C030033M19Rik, RIM1, RIM1a |
MMRRC Submission |
045226-MU
|
Accession Numbers |
|
Essential gene? |
Possibly essential
(E-score: 0.675)
|
Stock # |
R7155 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
1 |
Chromosomal Location |
22356475-22845203 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to G
at 22503174 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Leucine to Phenylalanine
at position 670
(L670F)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000095420
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000081544]
[ENSMUST00000097809]
[ENSMUST00000097810]
[ENSMUST00000097811]
[ENSMUST00000115273]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000081544
AA Change: L670F
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000080259 Gene: ENSMUSG00000041670 AA Change: L670F
Domain | Start | End | E-Value | Type |
low complexity region
|
5 |
18 |
N/A |
INTRINSIC |
coiled coil region
|
30 |
52 |
N/A |
INTRINSIC |
Pfam:FYVE_2
|
102 |
205 |
2.6e-9 |
PFAM |
low complexity region
|
283 |
293 |
N/A |
INTRINSIC |
low complexity region
|
329 |
345 |
N/A |
INTRINSIC |
low complexity region
|
381 |
394 |
N/A |
INTRINSIC |
PDZ
|
449 |
528 |
1.44e-15 |
SMART |
low complexity region
|
535 |
551 |
N/A |
INTRINSIC |
C2
|
593 |
703 |
7.55e-1 |
SMART |
low complexity region
|
710 |
721 |
N/A |
INTRINSIC |
low complexity region
|
899 |
934 |
N/A |
INTRINSIC |
low complexity region
|
1011 |
1025 |
N/A |
INTRINSIC |
C2
|
1120 |
1223 |
7.45e-15 |
SMART |
low complexity region
|
1245 |
1253 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000097809
AA Change: L670F
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000095418 Gene: ENSMUSG00000041670 AA Change: L670F
Domain | Start | End | E-Value | Type |
low complexity region
|
5 |
18 |
N/A |
INTRINSIC |
coiled coil region
|
30 |
52 |
N/A |
INTRINSIC |
Pfam:FYVE_2
|
102 |
205 |
1e-9 |
PFAM |
low complexity region
|
283 |
293 |
N/A |
INTRINSIC |
low complexity region
|
329 |
345 |
N/A |
INTRINSIC |
low complexity region
|
381 |
394 |
N/A |
INTRINSIC |
PDZ
|
449 |
528 |
1.44e-15 |
SMART |
low complexity region
|
535 |
551 |
N/A |
INTRINSIC |
C2
|
593 |
703 |
7.55e-1 |
SMART |
low complexity region
|
710 |
721 |
N/A |
INTRINSIC |
low complexity region
|
862 |
874 |
N/A |
INTRINSIC |
low complexity region
|
974 |
1009 |
N/A |
INTRINSIC |
low complexity region
|
1086 |
1100 |
N/A |
INTRINSIC |
C2
|
1195 |
1298 |
7.45e-15 |
SMART |
low complexity region
|
1320 |
1328 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000097810
AA Change: L670F
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000095419 Gene: ENSMUSG00000041670 AA Change: L670F
Domain | Start | End | E-Value | Type |
low complexity region
|
5 |
18 |
N/A |
INTRINSIC |
coiled coil region
|
30 |
52 |
N/A |
INTRINSIC |
PDB:2CJS|C
|
131 |
193 |
2e-32 |
PDB |
low complexity region
|
283 |
293 |
N/A |
INTRINSIC |
low complexity region
|
329 |
345 |
N/A |
INTRINSIC |
low complexity region
|
381 |
394 |
N/A |
INTRINSIC |
PDZ
|
449 |
528 |
1.44e-15 |
SMART |
low complexity region
|
535 |
551 |
N/A |
INTRINSIC |
C2
|
593 |
703 |
7.55e-1 |
SMART |
low complexity region
|
710 |
721 |
N/A |
INTRINSIC |
low complexity region
|
862 |
874 |
N/A |
INTRINSIC |
low complexity region
|
916 |
929 |
N/A |
INTRINSIC |
low complexity region
|
1035 |
1070 |
N/A |
INTRINSIC |
low complexity region
|
1147 |
1161 |
N/A |
INTRINSIC |
C2
|
1256 |
1359 |
7.45e-15 |
SMART |
low complexity region
|
1381 |
1389 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000097811
AA Change: L670F
PolyPhen 2
Score 0.992 (Sensitivity: 0.70; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000095420 Gene: ENSMUSG00000041670 AA Change: L670F
Domain | Start | End | E-Value | Type |
low complexity region
|
5 |
18 |
N/A |
INTRINSIC |
coiled coil region
|
30 |
52 |
N/A |
INTRINSIC |
Pfam:FYVE_2
|
102 |
205 |
1.6e-9 |
PFAM |
low complexity region
|
283 |
293 |
N/A |
INTRINSIC |
low complexity region
|
329 |
345 |
N/A |
INTRINSIC |
low complexity region
|
381 |
394 |
N/A |
INTRINSIC |
PDZ
|
449 |
528 |
1.44e-15 |
SMART |
low complexity region
|
535 |
551 |
N/A |
INTRINSIC |
C2
|
593 |
703 |
7.55e-1 |
SMART |
low complexity region
|
710 |
721 |
N/A |
INTRINSIC |
low complexity region
|
867 |
881 |
N/A |
INTRINSIC |
low complexity region
|
944 |
957 |
N/A |
INTRINSIC |
low complexity region
|
1063 |
1098 |
N/A |
INTRINSIC |
low complexity region
|
1175 |
1189 |
N/A |
INTRINSIC |
C2
|
1284 |
1387 |
7.45e-15 |
SMART |
low complexity region
|
1409 |
1417 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000115273
AA Change: L670F
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000110928 Gene: ENSMUSG00000041670 AA Change: L670F
Domain | Start | End | E-Value | Type |
low complexity region
|
5 |
18 |
N/A |
INTRINSIC |
coiled coil region
|
30 |
52 |
N/A |
INTRINSIC |
Pfam:FYVE_2
|
102 |
205 |
2.8e-9 |
PFAM |
low complexity region
|
283 |
293 |
N/A |
INTRINSIC |
low complexity region
|
329 |
345 |
N/A |
INTRINSIC |
low complexity region
|
381 |
394 |
N/A |
INTRINSIC |
PDZ
|
449 |
528 |
1.44e-15 |
SMART |
low complexity region
|
535 |
551 |
N/A |
INTRINSIC |
C2
|
593 |
703 |
7.55e-1 |
SMART |
low complexity region
|
710 |
721 |
N/A |
INTRINSIC |
low complexity region
|
950 |
985 |
N/A |
INTRINSIC |
low complexity region
|
1062 |
1076 |
N/A |
INTRINSIC |
C2
|
1171 |
1274 |
7.45e-15 |
SMART |
low complexity region
|
1296 |
1304 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000185942
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 98.8%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a RAS gene superfamily member that regulates synaptic vesicle exocytosis. This gene also plays a role in the regulation of voltage-gated calcium channels during neurotransmitter and insulin release. Mutations have suggested a role cognition and have been identified as the cause of cone-rod dystrophy type 7. Multiple transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Mar 2012] PHENOTYPE: Mice homozygous for disruptions in this gene display defects in maternal care and abnormalities in synaptic transmission in the central nervous system. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921509C19Rik |
A |
G |
2: 151,315,489 (GRCm39) |
L63P |
possibly damaging |
Het |
Abca13 |
A |
T |
11: 9,479,010 (GRCm39) |
Y4286F |
probably benign |
Het |
Aldh5a1 |
A |
C |
13: 25,095,572 (GRCm39) |
V515G |
possibly damaging |
Het |
Ankrd42 |
T |
C |
7: 92,241,141 (GRCm39) |
E406G |
possibly damaging |
Het |
Arfgef2 |
T |
A |
2: 166,707,733 (GRCm39) |
M1043K |
probably benign |
Het |
Arhgef11 |
T |
A |
3: 87,616,879 (GRCm39) |
Y383* |
probably null |
Het |
Aste1 |
C |
T |
9: 105,282,335 (GRCm39) |
P614L |
probably damaging |
Het |
B3galt5 |
T |
A |
16: 96,117,005 (GRCm39) |
S213T |
probably damaging |
Het |
Bak1 |
A |
G |
17: 27,241,434 (GRCm39) |
L108P |
possibly damaging |
Het |
Bcl6 |
G |
A |
16: 23,784,976 (GRCm39) |
R675* |
probably null |
Het |
Bdp1 |
T |
G |
13: 100,197,659 (GRCm39) |
T909P |
possibly damaging |
Het |
Cacna1i |
A |
G |
15: 80,279,439 (GRCm39) |
H2060R |
probably benign |
Het |
Cdhr3 |
G |
T |
12: 33,111,772 (GRCm39) |
P246Q |
probably damaging |
Het |
Colgalt1 |
T |
C |
8: 72,076,354 (GRCm39) |
S602P |
probably damaging |
Het |
Csde1 |
T |
C |
3: 102,947,269 (GRCm39) |
S74P |
probably damaging |
Het |
Cyp51 |
A |
T |
5: 4,137,846 (GRCm39) |
C366S |
possibly damaging |
Het |
Dcaf7 |
A |
G |
11: 105,928,016 (GRCm39) |
N23D |
probably damaging |
Het |
Ddx10 |
G |
A |
9: 53,028,588 (GRCm39) |
A772V |
probably benign |
Het |
Ddx4 |
A |
G |
13: 112,750,319 (GRCm39) |
F404S |
probably benign |
Het |
Dlg4 |
T |
A |
11: 69,908,042 (GRCm39) |
M1K |
probably null |
Het |
Dnajc6 |
T |
C |
4: 101,470,142 (GRCm39) |
V293A |
probably damaging |
Het |
Etl4 |
G |
T |
2: 20,811,742 (GRCm39) |
R1643L |
probably damaging |
Het |
F13b |
G |
A |
1: 139,435,895 (GRCm39) |
E234K |
probably damaging |
Het |
Fam171a1 |
T |
C |
2: 3,226,766 (GRCm39) |
I633T |
probably benign |
Het |
Frem3 |
A |
G |
8: 81,342,668 (GRCm39) |
I1654V |
probably benign |
Het |
Galr2 |
A |
G |
11: 116,174,408 (GRCm39) |
E346G |
possibly damaging |
Het |
Gck |
G |
A |
11: 5,899,705 (GRCm39) |
|
probably benign |
Het |
Gen1 |
G |
T |
12: 11,291,833 (GRCm39) |
T717K |
probably benign |
Het |
Gpatch8 |
TTCCTCCTCCTCCTCTTCCTCCTCCTC |
TTCCTCCTCCTCCTCCTCTTCCTCCTCCTC |
11: 102,371,014 (GRCm39) |
|
probably benign |
Het |
Hat1 |
A |
G |
2: 71,251,595 (GRCm39) |
T215A |
possibly damaging |
Het |
Hmbox1 |
A |
T |
14: 65,134,486 (GRCm39) |
M38K |
probably damaging |
Het |
Ifi47 |
A |
G |
11: 48,987,369 (GRCm39) |
K379E |
probably benign |
Het |
Ift81 |
T |
C |
5: 122,707,062 (GRCm39) |
Y460C |
probably damaging |
Het |
Jarid2 |
T |
A |
13: 45,055,938 (GRCm39) |
S381R |
probably damaging |
Het |
Kmt2b |
A |
T |
7: 30,279,388 (GRCm39) |
V1458E |
probably damaging |
Het |
Kpna4 |
G |
T |
3: 68,997,266 (GRCm39) |
P336Q |
probably damaging |
Het |
Krt84 |
T |
C |
15: 101,440,689 (GRCm39) |
R168G |
probably damaging |
Het |
Lhx8 |
T |
A |
3: 154,030,221 (GRCm39) |
Y137F |
possibly damaging |
Het |
Lin7b |
T |
C |
7: 45,019,651 (GRCm39) |
E19G |
probably damaging |
Het |
Lrmda |
A |
T |
14: 22,634,608 (GRCm39) |
R131S |
probably damaging |
Het |
Lrrc75b |
C |
T |
10: 75,389,512 (GRCm39) |
A280T |
possibly damaging |
Het |
Megf11 |
G |
A |
9: 64,555,233 (GRCm39) |
R268K |
probably null |
Het |
Mgat4e |
G |
T |
1: 134,469,697 (GRCm39) |
Q116K |
probably damaging |
Het |
Mlkl |
A |
G |
8: 112,046,035 (GRCm39) |
L325P |
probably damaging |
Het |
Mup2 |
A |
G |
4: 60,137,641 (GRCm39) |
L134P |
probably damaging |
Het |
Myo19 |
A |
G |
11: 84,791,412 (GRCm39) |
E489G |
probably damaging |
Het |
Ncbp3 |
C |
A |
11: 72,938,835 (GRCm39) |
P37Q |
probably damaging |
Het |
Nf2 |
A |
G |
11: 4,749,964 (GRCm39) |
V236A |
probably damaging |
Het |
Nlrp1a |
A |
T |
11: 71,014,905 (GRCm39) |
M115K |
possibly damaging |
Het |
Nsf |
T |
A |
11: 103,719,356 (GRCm39) |
K649* |
probably null |
Het |
Olfml2b |
A |
T |
1: 170,494,354 (GRCm39) |
I313L |
probably benign |
Het |
Or2ak4 |
T |
A |
11: 58,649,109 (GRCm39) |
I206N |
probably damaging |
Het |
Or52u1 |
T |
A |
7: 104,237,764 (GRCm39) |
V251D |
possibly damaging |
Het |
Papln |
T |
A |
12: 83,823,295 (GRCm39) |
L444Q |
probably damaging |
Het |
Phc3 |
T |
C |
3: 30,968,346 (GRCm39) |
I897V |
probably benign |
Het |
Plcg1 |
T |
C |
2: 160,596,300 (GRCm39) |
L632P |
probably damaging |
Het |
Pramel21 |
A |
T |
4: 143,342,735 (GRCm39) |
I281F |
probably benign |
Het |
Prkg1 |
T |
C |
19: 31,279,701 (GRCm39) |
T178A |
probably damaging |
Het |
Ptges |
T |
A |
2: 30,782,816 (GRCm39) |
T79S |
probably benign |
Het |
Rab26 |
T |
C |
17: 24,751,263 (GRCm39) |
T81A |
probably damaging |
Het |
Rai14 |
T |
A |
15: 10,595,089 (GRCm39) |
I145L |
possibly damaging |
Het |
Rasgrf1 |
A |
G |
9: 89,884,414 (GRCm39) |
T960A |
possibly damaging |
Het |
Rfx1 |
A |
T |
8: 84,821,455 (GRCm39) |
I755F |
probably damaging |
Het |
Rtkn |
G |
A |
6: 83,126,692 (GRCm39) |
C297Y |
probably damaging |
Het |
Sec23a |
A |
T |
12: 59,036,229 (GRCm39) |
N378K |
probably benign |
Het |
Slc1a2 |
T |
C |
2: 102,597,340 (GRCm39) |
M449T |
probably damaging |
Het |
Slc22a3 |
G |
A |
17: 12,652,518 (GRCm39) |
L369F |
possibly damaging |
Het |
Slc34a1 |
A |
G |
13: 24,006,390 (GRCm39) |
E472G |
probably benign |
Het |
Slc49a4 |
G |
T |
16: 35,555,947 (GRCm39) |
T171K |
probably benign |
Het |
Smad6 |
G |
T |
9: 63,929,069 (GRCm39) |
D82E |
unknown |
Het |
Smgc |
A |
T |
15: 91,736,811 (GRCm39) |
I463F |
possibly damaging |
Het |
Strada |
C |
A |
11: 106,061,865 (GRCm39) |
G166C |
probably damaging |
Het |
Tcaf3 |
A |
G |
6: 42,570,825 (GRCm39) |
V309A |
probably benign |
Het |
Tet2 |
C |
T |
3: 133,175,352 (GRCm39) |
E1332K |
possibly damaging |
Het |
Tfcp2l1 |
A |
G |
1: 118,596,362 (GRCm39) |
N366D |
probably damaging |
Het |
Tll2 |
G |
A |
19: 41,105,723 (GRCm39) |
P369L |
possibly damaging |
Het |
Tox4 |
T |
C |
14: 52,529,554 (GRCm39) |
V505A |
probably benign |
Het |
Trbv4 |
A |
G |
6: 41,036,787 (GRCm39) |
D104G |
probably damaging |
Het |
Ugdh |
T |
C |
5: 65,574,380 (GRCm39) |
E416G |
probably damaging |
Het |
Usp47 |
T |
A |
7: 111,686,220 (GRCm39) |
C613S |
probably damaging |
Het |
Vmn1r11 |
T |
A |
6: 57,115,147 (GRCm39) |
N270K |
probably benign |
Het |
Wsb2 |
T |
A |
5: 117,509,160 (GRCm39) |
L147Q |
probably damaging |
Het |
Xrn1 |
G |
A |
9: 95,861,198 (GRCm39) |
A453T |
possibly damaging |
Het |
Zan |
A |
G |
5: 137,460,106 (GRCm39) |
S1262P |
unknown |
Het |
Zswim4 |
A |
G |
8: 84,946,556 (GRCm39) |
L700P |
probably damaging |
Het |
|
Other mutations in Rims1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00227:Rims1
|
APN |
1 |
22,507,323 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00535:Rims1
|
APN |
1 |
22,503,172 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01021:Rims1
|
APN |
1 |
22,525,701 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01106:Rims1
|
APN |
1 |
22,449,671 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01128:Rims1
|
APN |
1 |
22,573,256 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01548:Rims1
|
APN |
1 |
22,577,683 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01688:Rims1
|
APN |
1 |
22,467,764 (GRCm39) |
missense |
probably benign |
0.22 |
IGL02089:Rims1
|
APN |
1 |
22,669,556 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL02245:Rims1
|
APN |
1 |
22,416,712 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02355:Rims1
|
APN |
1 |
22,522,288 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02362:Rims1
|
APN |
1 |
22,522,288 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02682:Rims1
|
APN |
1 |
22,358,708 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03006:Rims1
|
APN |
1 |
22,367,178 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03054:Rims1
|
UTSW |
1 |
22,360,333 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4504001:Rims1
|
UTSW |
1 |
22,467,684 (GRCm39) |
missense |
|
|
R0031:Rims1
|
UTSW |
1 |
22,367,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R0118:Rims1
|
UTSW |
1 |
22,416,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R0390:Rims1
|
UTSW |
1 |
22,635,607 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0483:Rims1
|
UTSW |
1 |
22,507,263 (GRCm39) |
splice site |
probably benign |
|
R0744:Rims1
|
UTSW |
1 |
22,497,709 (GRCm39) |
splice site |
probably null |
|
R0836:Rims1
|
UTSW |
1 |
22,497,709 (GRCm39) |
splice site |
probably null |
|
R1218:Rims1
|
UTSW |
1 |
22,522,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R1228:Rims1
|
UTSW |
1 |
22,511,837 (GRCm39) |
missense |
probably null |
1.00 |
R1374:Rims1
|
UTSW |
1 |
22,367,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R1474:Rims1
|
UTSW |
1 |
22,577,362 (GRCm39) |
splice site |
probably benign |
|
R1652:Rims1
|
UTSW |
1 |
22,363,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R1712:Rims1
|
UTSW |
1 |
22,367,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R1730:Rims1
|
UTSW |
1 |
22,416,753 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1783:Rims1
|
UTSW |
1 |
22,416,753 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1861:Rims1
|
UTSW |
1 |
22,635,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R1899:Rims1
|
UTSW |
1 |
22,498,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R1937:Rims1
|
UTSW |
1 |
22,358,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R2010:Rims1
|
UTSW |
1 |
22,367,220 (GRCm39) |
missense |
probably damaging |
1.00 |
R2049:Rims1
|
UTSW |
1 |
22,635,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R2124:Rims1
|
UTSW |
1 |
22,474,732 (GRCm39) |
nonsense |
probably null |
|
R2860:Rims1
|
UTSW |
1 |
22,503,227 (GRCm39) |
missense |
probably benign |
0.01 |
R2861:Rims1
|
UTSW |
1 |
22,503,227 (GRCm39) |
missense |
probably benign |
0.01 |
R2914:Rims1
|
UTSW |
1 |
22,844,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R3740:Rims1
|
UTSW |
1 |
22,443,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R3741:Rims1
|
UTSW |
1 |
22,443,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R3773:Rims1
|
UTSW |
1 |
22,492,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R3874:Rims1
|
UTSW |
1 |
22,498,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R3901:Rims1
|
UTSW |
1 |
22,572,578 (GRCm39) |
missense |
probably benign |
0.00 |
R3964:Rims1
|
UTSW |
1 |
22,497,709 (GRCm39) |
splice site |
probably null |
|
R4037:Rims1
|
UTSW |
1 |
22,514,793 (GRCm39) |
missense |
probably damaging |
0.96 |
R4039:Rims1
|
UTSW |
1 |
22,514,793 (GRCm39) |
missense |
probably damaging |
0.96 |
R4056:Rims1
|
UTSW |
1 |
22,363,163 (GRCm39) |
splice site |
probably benign |
|
R4062:Rims1
|
UTSW |
1 |
22,572,664 (GRCm39) |
missense |
probably benign |
0.00 |
R4552:Rims1
|
UTSW |
1 |
22,443,718 (GRCm39) |
missense |
probably damaging |
0.99 |
R4658:Rims1
|
UTSW |
1 |
22,497,793 (GRCm39) |
missense |
probably damaging |
0.98 |
R4688:Rims1
|
UTSW |
1 |
22,518,528 (GRCm39) |
nonsense |
probably null |
|
R4696:Rims1
|
UTSW |
1 |
22,358,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R4720:Rims1
|
UTSW |
1 |
22,497,731 (GRCm39) |
missense |
probably damaging |
1.00 |
R4764:Rims1
|
UTSW |
1 |
22,518,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R4780:Rims1
|
UTSW |
1 |
22,361,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R4931:Rims1
|
UTSW |
1 |
22,573,028 (GRCm39) |
missense |
probably benign |
0.26 |
R5137:Rims1
|
UTSW |
1 |
22,358,844 (GRCm39) |
nonsense |
probably null |
|
R5153:Rims1
|
UTSW |
1 |
22,522,328 (GRCm39) |
nonsense |
probably null |
|
R5305:Rims1
|
UTSW |
1 |
22,635,623 (GRCm39) |
missense |
probably damaging |
0.99 |
R5354:Rims1
|
UTSW |
1 |
22,577,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R5386:Rims1
|
UTSW |
1 |
22,482,469 (GRCm39) |
missense |
probably damaging |
0.99 |
R5485:Rims1
|
UTSW |
1 |
22,522,289 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5643:Rims1
|
UTSW |
1 |
22,577,590 (GRCm39) |
missense |
probably damaging |
1.00 |
R5929:Rims1
|
UTSW |
1 |
22,507,322 (GRCm39) |
missense |
probably damaging |
1.00 |
R5988:Rims1
|
UTSW |
1 |
22,635,544 (GRCm39) |
missense |
probably damaging |
1.00 |
R6160:Rims1
|
UTSW |
1 |
22,503,235 (GRCm39) |
missense |
probably damaging |
0.98 |
R6579:Rims1
|
UTSW |
1 |
22,496,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R6790:Rims1
|
UTSW |
1 |
22,507,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R7048:Rims1
|
UTSW |
1 |
22,511,901 (GRCm39) |
missense |
probably damaging |
1.00 |
R7100:Rims1
|
UTSW |
1 |
22,416,697 (GRCm39) |
missense |
probably benign |
0.27 |
R7171:Rims1
|
UTSW |
1 |
22,498,740 (GRCm39) |
missense |
|
|
R7448:Rims1
|
UTSW |
1 |
22,474,699 (GRCm39) |
missense |
|
|
R7505:Rims1
|
UTSW |
1 |
22,573,077 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7567:Rims1
|
UTSW |
1 |
22,507,291 (GRCm39) |
missense |
probably damaging |
0.99 |
R7639:Rims1
|
UTSW |
1 |
22,844,750 (GRCm39) |
missense |
probably benign |
0.02 |
R7955:Rims1
|
UTSW |
1 |
22,507,322 (GRCm39) |
missense |
probably damaging |
1.00 |
R8005:Rims1
|
UTSW |
1 |
22,482,437 (GRCm39) |
missense |
|
|
R8071:Rims1
|
UTSW |
1 |
22,358,760 (GRCm39) |
nonsense |
probably null |
|
R8465:Rims1
|
UTSW |
1 |
22,498,731 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8517:Rims1
|
UTSW |
1 |
22,522,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R8703:Rims1
|
UTSW |
1 |
22,496,137 (GRCm39) |
missense |
|
|
R8726:Rims1
|
UTSW |
1 |
22,633,181 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9090:Rims1
|
UTSW |
1 |
22,498,773 (GRCm39) |
missense |
|
|
R9179:Rims1
|
UTSW |
1 |
22,482,490 (GRCm39) |
missense |
probably damaging |
0.99 |
R9271:Rims1
|
UTSW |
1 |
22,498,773 (GRCm39) |
missense |
|
|
R9291:Rims1
|
UTSW |
1 |
22,467,746 (GRCm39) |
missense |
|
|
R9394:Rims1
|
UTSW |
1 |
22,511,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R9578:Rims1
|
UTSW |
1 |
22,523,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R9614:Rims1
|
UTSW |
1 |
22,491,969 (GRCm39) |
nonsense |
probably null |
|
R9726:Rims1
|
UTSW |
1 |
22,669,493 (GRCm39) |
missense |
probably null |
0.21 |
Z1088:Rims1
|
UTSW |
1 |
22,358,810 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Rims1
|
UTSW |
1 |
22,523,752 (GRCm39) |
nonsense |
probably null |
|
Z1177:Rims1
|
UTSW |
1 |
22,511,858 (GRCm39) |
missense |
probably benign |
0.44 |
Z1177:Rims1
|
UTSW |
1 |
22,507,322 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Rims1
|
UTSW |
1 |
22,367,163 (GRCm39) |
missense |
possibly damaging |
0.93 |
Z1177:Rims1
|
UTSW |
1 |
22,511,885 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1186:Rims1
|
UTSW |
1 |
22,449,706 (GRCm39) |
missense |
|
|
|
Predicted Primers |
PCR Primer
(F):5'- GTGGAACCATGCCTTTCACC -3'
(R):5'- TGAGCTTATCCTCTTCCATACAGG -3'
Sequencing Primer
(F):5'- TTTCACCACGCACCTGGAG -3'
(R):5'- AGGTACTTCACTATCTGCTTTCAGAG -3'
|
Posted On |
2019-06-26 |