Incidental Mutation 'R7516:Crem'
ID |
585937 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Crem
|
Ensembl Gene |
ENSMUSG00000063889 |
Gene Name |
cAMP responsive element modulator |
Synonyms |
ICER |
MMRRC Submission |
045589-MU
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.416)
|
Stock # |
R7516 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
18 |
Chromosomal Location |
3266048-3337748 bp(-) (GRCm39) |
Type of Mutation |
splice site (21 bp from exon) |
DNA Base Change (assembly) |
T to C
at 3299141 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000127353
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000025069]
[ENSMUST00000082141]
[ENSMUST00000122958]
[ENSMUST00000123672]
[ENSMUST00000126578]
[ENSMUST00000129435]
[ENSMUST00000130455]
[ENSMUST00000130599]
[ENSMUST00000131899]
[ENSMUST00000134027]
[ENSMUST00000136961]
[ENSMUST00000137568]
[ENSMUST00000142690]
[ENSMUST00000144496]
[ENSMUST00000146265]
[ENSMUST00000148305]
[ENSMUST00000149803]
[ENSMUST00000150235]
[ENSMUST00000151311]
[ENSMUST00000152108]
[ENSMUST00000152900]
[ENSMUST00000154135]
[ENSMUST00000154470]
[ENSMUST00000154715]
[ENSMUST00000156234]
[ENSMUST00000165086]
|
AlphaFold |
P27699 |
Predicted Effect |
probably null
Transcript: ENSMUST00000025069
|
SMART Domains |
Protein: ENSMUSP00000025069 Gene: ENSMUSG00000063889
Domain | Start | End | E-Value | Type |
low complexity region
|
77 |
88 |
N/A |
INTRINSIC |
Pfam:pKID
|
112 |
153 |
3.1e-20 |
PFAM |
BRLZ
|
285 |
343 |
3.8e-6 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000082141
|
SMART Domains |
Protein: ENSMUSP00000080780 Gene: ENSMUSG00000063889
Domain | Start | End | E-Value | Type |
Pfam:pKID
|
63 |
104 |
2.6e-20 |
PFAM |
BRLZ
|
248 |
306 |
3.8e-6 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000122958
|
SMART Domains |
Protein: ENSMUSP00000121118 Gene: ENSMUSG00000063889
Domain | Start | End | E-Value | Type |
low complexity region
|
24 |
35 |
N/A |
INTRINSIC |
Pfam:pKID
|
59 |
100 |
7.8e-21 |
PFAM |
BRLZ
|
244 |
301 |
2.73e-7 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000123672
|
SMART Domains |
Protein: ENSMUSP00000120557 Gene: ENSMUSG00000063889
Domain | Start | End | E-Value | Type |
Pfam:pKID
|
47 |
88 |
1.5e-20 |
PFAM |
BRLZ
|
157 |
214 |
2.73e-7 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000126578
|
SMART Domains |
Protein: ENSMUSP00000114780 Gene: ENSMUSG00000063889
Domain | Start | End | E-Value | Type |
low complexity region
|
24 |
35 |
N/A |
INTRINSIC |
Pfam:pKID
|
59 |
100 |
7.8e-21 |
PFAM |
BRLZ
|
244 |
302 |
3.8e-6 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000127601
|
SMART Domains |
Protein: ENSMUSP00000118649 Gene: ENSMUSG00000063889
Domain | Start | End | E-Value | Type |
low complexity region
|
63 |
74 |
N/A |
INTRINSIC |
Pfam:pKID
|
98 |
139 |
3.1e-21 |
PFAM |
BRLZ
|
271 |
328 |
2.73e-7 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000129435
|
SMART Domains |
Protein: ENSMUSP00000117438 Gene: ENSMUSG00000063889
Domain | Start | End | E-Value | Type |
Pfam:pKID
|
10 |
51 |
5.6e-21 |
PFAM |
BRLZ
|
183 |
240 |
2.73e-7 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000130455
|
SMART Domains |
Protein: ENSMUSP00000121541 Gene: ENSMUSG00000063889
Domain | Start | End | E-Value | Type |
low complexity region
|
67 |
78 |
N/A |
INTRINSIC |
Pfam:pKID
|
102 |
143 |
2.8e-20 |
PFAM |
BRLZ
|
275 |
333 |
3.8e-6 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000130599
|
SMART Domains |
Protein: ENSMUSP00000115471 Gene: ENSMUSG00000063889
Domain | Start | End | E-Value | Type |
Pfam:pKID
|
47 |
88 |
1.6e-20 |
PFAM |
BRLZ
|
169 |
226 |
2.73e-7 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000131899
|
SMART Domains |
Protein: ENSMUSP00000119353 Gene: ENSMUSG00000063889
Domain | Start | End | E-Value | Type |
low complexity region
|
67 |
78 |
N/A |
INTRINSIC |
Pfam:pKID
|
102 |
143 |
2.2e-20 |
PFAM |
BRLZ
|
224 |
282 |
3.8e-6 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000134027
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000136961
|
SMART Domains |
Protein: ENSMUSP00000115363 Gene: ENSMUSG00000063889
Domain | Start | End | E-Value | Type |
Pfam:pKID
|
35 |
76 |
6.5e-21 |
PFAM |
BRLZ
|
208 |
265 |
2.73e-7 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000137568
|
SMART Domains |
Protein: ENSMUSP00000115336 Gene: ENSMUSG00000063889
Domain | Start | End | E-Value | Type |
Pfam:pKID
|
53 |
94 |
1.5e-20 |
PFAM |
BRLZ
|
163 |
221 |
3.8e-6 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000142690
|
SMART Domains |
Protein: ENSMUSP00000122282 Gene: ENSMUSG00000063889
Domain | Start | End | E-Value | Type |
low complexity region
|
61 |
72 |
N/A |
INTRINSIC |
Pfam:pKID
|
96 |
138 |
4.8e-21 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000144496
|
SMART Domains |
Protein: ENSMUSP00000120349 Gene: ENSMUSG00000063889
Domain | Start | End | E-Value | Type |
Pfam:pKID
|
35 |
76 |
6.9e-21 |
PFAM |
BRLZ
|
220 |
277 |
2.73e-7 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000146265
|
SMART Domains |
Protein: ENSMUSP00000119638 Gene: ENSMUSG00000063889
Domain | Start | End | E-Value | Type |
low complexity region
|
67 |
78 |
N/A |
INTRINSIC |
Pfam:pKID
|
102 |
143 |
2.1e-20 |
PFAM |
BRLZ
|
212 |
269 |
2.73e-7 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000148305
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000149803
|
SMART Domains |
Protein: ENSMUSP00000121210 Gene: ENSMUSG00000063889
Domain | Start | End | E-Value | Type |
Pfam:pKID
|
47 |
89 |
2.6e-21 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000150235
|
SMART Domains |
Protein: ENSMUSP00000121233 Gene: ENSMUSG00000063889
Domain | Start | End | E-Value | Type |
low complexity region
|
77 |
88 |
N/A |
INTRINSIC |
Pfam:pKID
|
112 |
153 |
1.1e-20 |
PFAM |
BRLZ
|
297 |
354 |
2.73e-7 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000151311
|
SMART Domains |
Protein: ENSMUSP00000118267 Gene: ENSMUSG00000063889
Domain | Start | End | E-Value | Type |
Pfam:pKID
|
63 |
104 |
7.5e-21 |
PFAM |
BRLZ
|
236 |
293 |
2.73e-7 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000152108
|
SMART Domains |
Protein: ENSMUSP00000122241 Gene: ENSMUSG00000063889
Domain | Start | End | E-Value | Type |
Pfam:pKID
|
35 |
76 |
4.7e-21 |
PFAM |
BRLZ
|
157 |
214 |
2.73e-7 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000152900
|
SMART Domains |
Protein: ENSMUSP00000123515 Gene: ENSMUSG00000063889
Domain | Start | End | E-Value | Type |
Pfam:pKID
|
53 |
94 |
2.4e-20 |
PFAM |
BRLZ
|
238 |
296 |
3.8e-6 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000154135
|
SMART Domains |
Protein: ENSMUSP00000122051 Gene: ENSMUSG00000063889
Domain | Start | End | E-Value | Type |
Pfam:pKID
|
63 |
104 |
1.9e-20 |
PFAM |
BRLZ
|
185 |
243 |
3.8e-6 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000154470
|
SMART Domains |
Protein: ENSMUSP00000118128 Gene: ENSMUSG00000063889
Domain | Start | End | E-Value | Type |
low complexity region
|
77 |
88 |
N/A |
INTRINSIC |
Pfam:pKID
|
112 |
153 |
2.3e-20 |
PFAM |
BRLZ
|
222 |
280 |
3.8e-6 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000154715
|
SMART Domains |
Protein: ENSMUSP00000122179 Gene: ENSMUSG00000063889
Domain | Start | End | E-Value | Type |
low complexity region
|
49 |
60 |
N/A |
INTRINSIC |
Pfam:pKID
|
84 |
125 |
8.7e-21 |
PFAM |
BRLZ
|
269 |
327 |
3.8e-6 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000156234
|
SMART Domains |
Protein: ENSMUSP00000121388 Gene: ENSMUSG00000063889
Domain | Start | End | E-Value | Type |
low complexity region
|
61 |
72 |
N/A |
INTRINSIC |
Pfam:pKID
|
96 |
137 |
9.1e-21 |
PFAM |
BRLZ
|
281 |
339 |
3.8e-6 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000165086
|
SMART Domains |
Protein: ENSMUSP00000127353 Gene: ENSMUSG00000063889
Domain | Start | End | E-Value | Type |
low complexity region
|
77 |
88 |
N/A |
INTRINSIC |
Pfam:pKID
|
112 |
153 |
2.4e-20 |
PFAM |
BRLZ
|
234 |
292 |
3.8e-6 |
SMART |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.2%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: This gene encodes a basic-leucine zipper domain-containing protein that localizes to gene promoters, where it binds to the cyclic AMP response element (CRE). Different protein isoforms encoded by this gene may function as either activators or repressors of transcription. Activity of this gene is important in multiple developmental processes, including spermatogenesis. Mutation of this gene causes male infertility. Alternative splicing and promoter usage result in multiple transcript variants for this gene. [provided by RefSeq, Oct 2012] PHENOTYPE: Homozygotes for targeted mutations exhibit reduced regenerative capacity after partial hepatectomy and reduced cardiac function. Males are sterile due to a block in spermiogenesis associated with a lack of postmeiotic gene expression. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam28 |
T |
A |
14: 68,868,125 (GRCm39) |
I407F |
probably damaging |
Het |
Agbl1 |
A |
G |
7: 76,075,669 (GRCm39) |
Y437C |
probably damaging |
Het |
Alkbh5 |
T |
C |
11: 60,429,979 (GRCm39) |
V244A |
probably damaging |
Het |
Arap1 |
T |
C |
7: 101,058,538 (GRCm39) |
F1390L |
probably benign |
Het |
Asph |
T |
C |
4: 9,630,940 (GRCm39) |
D136G |
possibly damaging |
Het |
Atp8a2 |
A |
T |
14: 60,094,516 (GRCm39) |
Y841N |
probably damaging |
Het |
Cald1 |
A |
T |
6: 34,686,492 (GRCm39) |
|
probably benign |
Het |
Capn11 |
A |
G |
17: 45,949,766 (GRCm39) |
I400T |
possibly damaging |
Het |
Cdh18 |
T |
A |
15: 23,259,684 (GRCm39) |
|
probably null |
Het |
Ces2h |
T |
A |
8: 105,743,458 (GRCm39) |
L204Q |
probably damaging |
Het |
Chrna3 |
G |
A |
9: 54,922,653 (GRCm39) |
A385V |
probably benign |
Het |
Clca4a |
A |
T |
3: 144,672,009 (GRCm39) |
L311Q |
probably damaging |
Het |
Clip1 |
A |
G |
5: 123,721,448 (GRCm39) |
V1149A |
probably benign |
Het |
Clip3 |
T |
A |
7: 29,998,268 (GRCm39) |
V238D |
possibly damaging |
Het |
Col12a1 |
A |
G |
9: 79,520,192 (GRCm39) |
|
probably null |
Het |
Coro2a |
A |
G |
4: 46,562,992 (GRCm39) |
V54A |
probably benign |
Het |
Dennd5b |
T |
C |
6: 148,969,878 (GRCm39) |
I192V |
probably benign |
Het |
Dst |
A |
G |
1: 34,209,560 (GRCm39) |
N1209S |
probably benign |
Het |
Ero1a |
T |
A |
14: 45,525,480 (GRCm39) |
M385L |
probably benign |
Het |
Fam13a |
A |
T |
6: 58,932,248 (GRCm39) |
V375D |
probably damaging |
Het |
Fgfbp3 |
T |
A |
19: 36,896,324 (GRCm39) |
Y98F |
possibly damaging |
Het |
Frem3 |
T |
C |
8: 81,338,712 (GRCm39) |
V335A |
probably damaging |
Het |
Gm19410 |
T |
A |
8: 36,263,433 (GRCm39) |
D951E |
probably benign |
Het |
Gpatch1 |
T |
C |
7: 35,007,625 (GRCm39) |
D145G |
probably benign |
Het |
H60c |
G |
T |
10: 3,209,746 (GRCm39) |
C180* |
probably null |
Het |
Hmcn1 |
T |
C |
1: 150,498,718 (GRCm39) |
T4054A |
probably benign |
Het |
Hrg |
A |
G |
16: 22,780,048 (GRCm39) |
Y442C |
unknown |
Het |
Hspg2 |
C |
T |
4: 137,269,931 (GRCm39) |
R2327C |
possibly damaging |
Het |
Klhl31 |
G |
T |
9: 77,558,429 (GRCm39) |
A382S |
probably damaging |
Het |
Knl1 |
T |
C |
2: 118,901,179 (GRCm39) |
V960A |
probably damaging |
Het |
Lztr1 |
C |
T |
16: 17,327,525 (GRCm39) |
A76V |
possibly damaging |
Het |
Me3 |
G |
T |
7: 89,497,183 (GRCm39) |
E395* |
probably null |
Het |
Morc2b |
G |
A |
17: 33,356,435 (GRCm39) |
H446Y |
probably benign |
Het |
Mroh7 |
A |
T |
4: 106,548,316 (GRCm39) |
M1054K |
probably benign |
Het |
Ms4a6b |
T |
C |
19: 11,506,907 (GRCm39) |
V232A |
probably benign |
Het |
Nmt2 |
C |
A |
2: 3,313,767 (GRCm39) |
D224E |
probably damaging |
Het |
Nox4 |
C |
A |
7: 86,970,905 (GRCm39) |
R261S |
probably benign |
Het |
Obscn |
T |
A |
11: 59,015,416 (GRCm39) |
K1019* |
probably null |
Het |
Or4a15 |
T |
A |
2: 89,193,719 (GRCm39) |
N18I |
probably benign |
Het |
Or4g7 |
T |
A |
2: 111,309,282 (GRCm39) |
V51D |
probably benign |
Het |
Or5p67 |
G |
A |
7: 107,922,223 (GRCm39) |
S220F |
probably damaging |
Het |
Or8k24 |
C |
T |
2: 86,216,328 (GRCm39) |
V145I |
probably benign |
Het |
Pcdha11 |
A |
T |
18: 37,144,671 (GRCm39) |
N254I |
probably damaging |
Het |
Pck2 |
T |
A |
14: 55,779,913 (GRCm39) |
I54N |
probably benign |
Het |
Pkd1l3 |
T |
A |
8: 110,361,861 (GRCm39) |
W978R |
probably damaging |
Het |
Plxna4 |
T |
C |
6: 32,214,703 (GRCm39) |
T593A |
probably benign |
Het |
Podn |
G |
A |
4: 107,879,321 (GRCm39) |
R266W |
probably damaging |
Het |
Ptpn22 |
A |
G |
3: 103,792,854 (GRCm39) |
D335G |
probably benign |
Het |
Pxn |
A |
G |
5: 115,644,922 (GRCm39) |
D3G |
unknown |
Het |
Rapgefl1 |
T |
G |
11: 98,736,960 (GRCm39) |
V320G |
probably benign |
Het |
Rel |
A |
G |
11: 23,692,785 (GRCm39) |
I416T |
probably benign |
Het |
Sema5b |
A |
G |
16: 35,471,540 (GRCm39) |
N378D |
probably benign |
Het |
Sh3bp4 |
C |
A |
1: 89,073,368 (GRCm39) |
L739M |
probably damaging |
Het |
Skint2 |
A |
T |
4: 112,483,168 (GRCm39) |
D191V |
probably damaging |
Het |
Slc3a1 |
T |
C |
17: 85,371,190 (GRCm39) |
Y581H |
probably damaging |
Het |
Smcr8 |
G |
T |
11: 60,670,814 (GRCm39) |
C654F |
probably benign |
Het |
Spta1 |
A |
C |
1: 174,025,349 (GRCm39) |
Q738P |
probably damaging |
Het |
Sptlc3 |
C |
A |
2: 139,431,438 (GRCm39) |
A320D |
probably benign |
Het |
Thnsl2 |
T |
A |
6: 71,108,990 (GRCm39) |
K274* |
probably null |
Het |
Tmed2 |
T |
A |
5: 124,685,055 (GRCm39) |
I68K |
possibly damaging |
Het |
Tmtc4 |
G |
A |
14: 123,180,735 (GRCm39) |
A326V |
possibly damaging |
Het |
Tnks2 |
T |
A |
19: 36,849,064 (GRCm39) |
S179T |
possibly damaging |
Het |
Trim34b |
G |
T |
7: 103,978,918 (GRCm39) |
C55F |
probably damaging |
Het |
Trpm4 |
T |
A |
7: 44,954,444 (GRCm39) |
E1129V |
probably damaging |
Het |
Tvp23b |
T |
C |
11: 62,782,867 (GRCm39) |
S188P |
possibly damaging |
Het |
Usp1 |
A |
G |
4: 98,822,356 (GRCm39) |
T557A |
probably damaging |
Het |
Vmn2r66 |
C |
T |
7: 84,661,176 (GRCm39) |
C18Y |
possibly damaging |
Het |
Vmn2r85 |
T |
A |
10: 130,254,852 (GRCm39) |
T611S |
probably damaging |
Het |
Vps13c |
T |
C |
9: 67,862,289 (GRCm39) |
S2969P |
possibly damaging |
Het |
Wdr74 |
T |
A |
19: 8,713,554 (GRCm39) |
C62* |
probably null |
Het |
Wfikkn1 |
A |
T |
17: 26,097,020 (GRCm39) |
C435S |
probably damaging |
Het |
Zbtb45 |
A |
T |
7: 12,740,269 (GRCm39) |
F449I |
probably damaging |
Het |
|
Other mutations in Crem |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01085:Crem
|
APN |
18 |
3,299,236 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01532:Crem
|
APN |
18 |
3,276,732 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02500:Crem
|
APN |
18 |
3,273,477 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03280:Crem
|
APN |
18 |
3,273,415 (GRCm39) |
splice site |
probably benign |
|
menthe
|
UTSW |
18 |
3,268,070 (GRCm39) |
missense |
probably damaging |
1.00 |
R0379:Crem
|
UTSW |
18 |
3,299,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R0987:Crem
|
UTSW |
18 |
3,288,060 (GRCm39) |
missense |
probably damaging |
0.98 |
R1829:Crem
|
UTSW |
18 |
3,295,037 (GRCm39) |
splice site |
probably null |
|
R1932:Crem
|
UTSW |
18 |
3,299,284 (GRCm39) |
missense |
probably benign |
0.27 |
R2086:Crem
|
UTSW |
18 |
3,288,098 (GRCm39) |
intron |
probably benign |
|
R2093:Crem
|
UTSW |
18 |
3,299,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R4152:Crem
|
UTSW |
18 |
3,288,055 (GRCm39) |
missense |
probably damaging |
0.99 |
R4568:Crem
|
UTSW |
18 |
3,299,175 (GRCm39) |
missense |
probably damaging |
0.98 |
R4758:Crem
|
UTSW |
18 |
3,327,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R6032:Crem
|
UTSW |
18 |
3,267,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R6032:Crem
|
UTSW |
18 |
3,267,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R6445:Crem
|
UTSW |
18 |
3,309,671 (GRCm39) |
missense |
probably benign |
|
R6525:Crem
|
UTSW |
18 |
3,268,070 (GRCm39) |
missense |
probably damaging |
1.00 |
R6651:Crem
|
UTSW |
18 |
3,325,428 (GRCm39) |
missense |
probably benign |
0.18 |
R7035:Crem
|
UTSW |
18 |
3,327,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R7137:Crem
|
UTSW |
18 |
3,273,459 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7401:Crem
|
UTSW |
18 |
3,295,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R7463:Crem
|
UTSW |
18 |
3,295,094 (GRCm39) |
missense |
probably benign |
0.06 |
R8095:Crem
|
UTSW |
18 |
3,295,106 (GRCm39) |
missense |
probably benign |
0.00 |
R8146:Crem
|
UTSW |
18 |
3,288,007 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8266:Crem
|
UTSW |
18 |
3,309,535 (GRCm39) |
intron |
probably benign |
|
R8308:Crem
|
UTSW |
18 |
3,295,397 (GRCm39) |
missense |
possibly damaging |
0.55 |
R8825:Crem
|
UTSW |
18 |
3,268,061 (GRCm39) |
missense |
probably damaging |
0.99 |
R8899:Crem
|
UTSW |
18 |
3,295,370 (GRCm39) |
missense |
probably damaging |
0.99 |
R8976:Crem
|
UTSW |
18 |
3,268,088 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9681:Crem
|
UTSW |
18 |
3,268,067 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Crem
|
UTSW |
18 |
3,267,730 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- GGAATCCTCCAAGTATTCAAGACGAC -3'
(R):5'- TTTCTGTAGCTGGATCAGGC -3'
Sequencing Primer
(F):5'- ACAGCCGAATGCAGTGC -3'
(R):5'- AGGCACTGGAAGAGGCTCC -3'
|
Posted On |
2019-10-18 |