Incidental Mutation 'R4836:Cntln'
| ID |
373226 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Cntln
|
| Ensembl Gene |
ENSMUSG00000038070 |
| Gene Name |
centlein, centrosomal protein |
| Synonyms |
D530005L17Rik, B430108F07Rik |
| MMRRC Submission |
042451-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.340)
|
| Stock # |
R4836 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
4 |
| Chromosomal Location |
84802546-85050158 bp(+) (GRCm39) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
T to A
at 84967957 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Stop codon
at position 725
(Y725*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000130491
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000047023]
[ENSMUST00000169371]
|
| AlphaFold |
A2AM05 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000047023
AA Change: Y725*
|
| SMART Domains |
Protein: ENSMUSP00000044138
Gene: ENSMUSG00000038070
AA Change: Y725*
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
4 |
24 |
N/A |
INTRINSIC |
|
low complexity region
|
58 |
86 |
N/A |
INTRINSIC |
|
coiled coil region
|
96 |
126 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
198 |
219 |
1.25e-5 |
PROSPERO |
|
low complexity region
|
242 |
251 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
321 |
342 |
1.25e-5 |
PROSPERO |
|
low complexity region
|
346 |
358 |
N/A |
INTRINSIC |
|
coiled coil region
|
404 |
433 |
N/A |
INTRINSIC |
|
low complexity region
|
434 |
446 |
N/A |
INTRINSIC |
|
coiled coil region
|
458 |
481 |
N/A |
INTRINSIC |
|
coiled coil region
|
516 |
584 |
N/A |
INTRINSIC |
|
coiled coil region
|
606 |
648 |
N/A |
INTRINSIC |
|
coiled coil region
|
674 |
780 |
N/A |
INTRINSIC |
|
low complexity region
|
815 |
829 |
N/A |
INTRINSIC |
|
coiled coil region
|
973 |
1114 |
N/A |
INTRINSIC |
|
low complexity region
|
1206 |
1217 |
N/A |
INTRINSIC |
|
Blast:HisKA
|
1270 |
1326 |
1e-24 |
BLAST |
|
low complexity region
|
1327 |
1348 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000169371
AA Change: Y725*
|
| SMART Domains |
Protein: ENSMUSP00000130491
Gene: ENSMUSG00000038070
AA Change: Y725*
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
4 |
24 |
N/A |
INTRINSIC |
|
low complexity region
|
58 |
86 |
N/A |
INTRINSIC |
|
coiled coil region
|
96 |
126 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
198 |
219 |
1.24e-5 |
PROSPERO |
|
low complexity region
|
242 |
251 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
321 |
342 |
1.24e-5 |
PROSPERO |
|
low complexity region
|
346 |
358 |
N/A |
INTRINSIC |
|
coiled coil region
|
404 |
433 |
N/A |
INTRINSIC |
|
low complexity region
|
434 |
446 |
N/A |
INTRINSIC |
|
coiled coil region
|
458 |
481 |
N/A |
INTRINSIC |
|
coiled coil region
|
516 |
584 |
N/A |
INTRINSIC |
|
coiled coil region
|
606 |
648 |
N/A |
INTRINSIC |
|
coiled coil region
|
674 |
780 |
N/A |
INTRINSIC |
|
low complexity region
|
815 |
829 |
N/A |
INTRINSIC |
|
coiled coil region
|
972 |
1113 |
N/A |
INTRINSIC |
|
low complexity region
|
1205 |
1216 |
N/A |
INTRINSIC |
|
Blast:HisKA
|
1269 |
1325 |
1e-24 |
BLAST |
|
low complexity region
|
1326 |
1347 |
N/A |
INTRINSIC |
|
| Meta Mutation Damage Score |
0.9755 |
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.4%
- 10x: 96.6%
- 20x: 93.2%
|
| Validation Efficiency |
98% (87/89) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 78 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acox1 |
A |
T |
11: 116,066,152 (GRCm39) |
S453T |
probably benign |
Het |
| Ahnak2 |
A |
T |
12: 112,740,550 (GRCm39) |
V368D |
probably damaging |
Het |
| Ankrd53 |
A |
T |
6: 83,745,134 (GRCm39) |
Y448F |
probably damaging |
Het |
| Arhgef15 |
A |
T |
11: 68,840,751 (GRCm39) |
|
probably benign |
Het |
| Atg2b |
T |
C |
12: 105,613,073 (GRCm39) |
N1166S |
probably benign |
Het |
| Atl3 |
C |
T |
19: 7,486,910 (GRCm39) |
R77* |
probably null |
Het |
| Bend6 |
T |
C |
1: 33,922,654 (GRCm39) |
|
probably benign |
Het |
| Ccnt1 |
C |
A |
15: 98,465,444 (GRCm39) |
R25L |
probably damaging |
Het |
| Cct4 |
A |
G |
11: 22,952,898 (GRCm39) |
T525A |
probably benign |
Het |
| Cep350 |
T |
C |
1: 155,804,579 (GRCm39) |
I835V |
probably damaging |
Het |
| Cimap2 |
T |
A |
4: 106,467,724 (GRCm39) |
|
probably null |
Het |
| Clcn1 |
G |
T |
6: 42,286,898 (GRCm39) |
V652L |
probably damaging |
Het |
| Cog5 |
T |
C |
12: 31,969,732 (GRCm39) |
F21L |
probably benign |
Het |
| D6Ertd527e |
GGCAGCAGCAGCA |
GGCAGCAGCAGCAGCA |
6: 87,088,406 (GRCm39) |
|
probably benign |
Het |
| Dnm2 |
A |
T |
9: 21,402,626 (GRCm39) |
|
probably benign |
Het |
| Dnmt1 |
C |
T |
9: 20,819,854 (GRCm39) |
V1430I |
probably damaging |
Het |
| Dpep1 |
A |
G |
8: 123,927,106 (GRCm39) |
D285G |
probably damaging |
Het |
| Eef2kmt |
C |
T |
16: 5,066,867 (GRCm39) |
V129M |
probably damaging |
Het |
| Epha3 |
A |
T |
16: 63,403,920 (GRCm39) |
M726K |
probably damaging |
Het |
| Fat3 |
A |
G |
9: 16,289,019 (GRCm39) |
L168P |
probably damaging |
Het |
| Frem3 |
T |
A |
8: 81,390,026 (GRCm39) |
F1759Y |
probably damaging |
Het |
| Fubp3 |
T |
A |
2: 31,498,153 (GRCm39) |
S56R |
possibly damaging |
Het |
| Gm1965 |
T |
C |
6: 89,122,392 (GRCm39) |
|
noncoding transcript |
Het |
| Gm5592 |
C |
T |
7: 40,864,958 (GRCm39) |
|
probably benign |
Het |
| H1f9 |
T |
A |
11: 94,858,843 (GRCm39) |
L46* |
probably null |
Het |
| Irs1 |
TGGGGTGGACATCGAACTGAAGGAG |
TG |
1: 82,265,453 (GRCm39) |
913 |
probably null |
Het |
| Isl1 |
A |
G |
13: 116,439,619 (GRCm39) |
M243T |
probably benign |
Het |
| Itpr1 |
A |
T |
6: 108,366,498 (GRCm39) |
I142F |
probably damaging |
Het |
| Jak1 |
T |
C |
4: 101,012,263 (GRCm39) |
T1069A |
probably damaging |
Het |
| Jmjd1c |
T |
C |
10: 67,069,225 (GRCm39) |
V1848A |
probably benign |
Het |
| Kdm5a |
T |
C |
6: 120,389,363 (GRCm39) |
V930A |
probably damaging |
Het |
| Kdm5b |
C |
A |
1: 134,521,053 (GRCm39) |
|
probably null |
Het |
| Lilra5 |
T |
C |
7: 4,241,713 (GRCm39) |
F171L |
possibly damaging |
Het |
| Map1b |
A |
G |
13: 99,567,562 (GRCm39) |
S1720P |
unknown |
Het |
| Mcpt1 |
A |
T |
14: 56,257,017 (GRCm39) |
Q185L |
probably damaging |
Het |
| Mmp20 |
T |
A |
9: 7,644,027 (GRCm39) |
D238E |
possibly damaging |
Het |
| Mov10l1 |
A |
T |
15: 88,904,472 (GRCm39) |
I784F |
possibly damaging |
Het |
| Mroh2b |
C |
T |
15: 4,933,752 (GRCm39) |
P101S |
probably damaging |
Het |
| Myh3 |
G |
T |
11: 66,987,765 (GRCm39) |
A1413S |
probably benign |
Het |
| Naa80 |
A |
T |
9: 107,460,738 (GRCm39) |
Y211F |
probably damaging |
Het |
| Npdc1 |
G |
A |
2: 25,298,957 (GRCm39) |
D284N |
probably damaging |
Het |
| Or12j4 |
A |
G |
7: 140,046,989 (GRCm39) |
R292G |
probably damaging |
Het |
| Or2t48 |
A |
C |
11: 58,420,308 (GRCm39) |
M168R |
probably damaging |
Het |
| Or4a66 |
A |
G |
2: 88,531,544 (GRCm39) |
I43T |
probably damaging |
Het |
| Or5g9 |
A |
G |
2: 85,551,793 (GRCm39) |
I15V |
probably benign |
Het |
| Or8k22 |
A |
T |
2: 86,163,571 (GRCm39) |
M43K |
probably benign |
Het |
| Or8k23 |
G |
A |
2: 86,186,094 (GRCm39) |
L211F |
probably benign |
Het |
| Palld |
T |
A |
8: 62,140,415 (GRCm39) |
T531S |
probably benign |
Het |
| Parp4 |
A |
G |
14: 56,823,195 (GRCm39) |
E105G |
probably benign |
Het |
| Phf11a |
A |
T |
14: 59,525,028 (GRCm39) |
S59T |
probably damaging |
Het |
| Ppp1r12b |
G |
T |
1: 134,883,471 (GRCm39) |
A17E |
probably benign |
Het |
| Rad50 |
A |
T |
11: 53,541,480 (GRCm39) |
I1252N |
probably damaging |
Het |
| Ramp3 |
A |
G |
11: 6,624,761 (GRCm39) |
|
probably null |
Het |
| Rrbp1 |
G |
A |
2: 143,830,337 (GRCm39) |
T610I |
possibly damaging |
Het |
| Scart2 |
T |
C |
7: 139,879,021 (GRCm39) |
I1051T |
probably benign |
Het |
| Semp2l2a |
C |
T |
8: 13,888,007 (GRCm39) |
S28N |
probably benign |
Het |
| Slc4a10 |
A |
G |
2: 62,098,531 (GRCm39) |
Y555C |
probably damaging |
Het |
| Slc5a2 |
A |
G |
7: 127,866,677 (GRCm39) |
|
probably null |
Het |
| Smoc1 |
T |
A |
12: 81,226,322 (GRCm39) |
D371E |
probably damaging |
Het |
| Stmn1 |
T |
A |
4: 134,197,495 (GRCm39) |
|
probably benign |
Het |
| Sulf1 |
C |
T |
1: 12,912,910 (GRCm39) |
L715F |
probably benign |
Het |
| Surf1 |
T |
C |
2: 26,804,255 (GRCm39) |
T180A |
possibly damaging |
Het |
| Syne2 |
A |
G |
12: 76,026,593 (GRCm39) |
I3474V |
probably damaging |
Het |
| Tchh |
A |
T |
3: 93,352,455 (GRCm39) |
R632W |
unknown |
Het |
| Tchh |
A |
T |
3: 93,354,895 (GRCm39) |
D1445V |
unknown |
Het |
| Tctn1 |
A |
T |
5: 122,383,568 (GRCm39) |
M505K |
probably benign |
Het |
| Tdrkh |
T |
A |
3: 94,332,897 (GRCm39) |
I150N |
probably damaging |
Het |
| Tespa1 |
C |
T |
10: 130,198,028 (GRCm39) |
T350I |
probably benign |
Het |
| Thbs1 |
A |
G |
2: 117,945,499 (GRCm39) |
Y326C |
possibly damaging |
Het |
| Tmem208 |
C |
T |
8: 106,055,296 (GRCm39) |
S119F |
probably damaging |
Het |
| Tmprss6 |
G |
C |
15: 78,329,588 (GRCm39) |
A91G |
probably damaging |
Het |
| Trp53bp2 |
C |
T |
1: 182,259,147 (GRCm39) |
R67W |
probably damaging |
Het |
| Ttn |
A |
G |
2: 76,541,541 (GRCm39) |
I25488T |
possibly damaging |
Het |
| Txnl4a |
A |
G |
18: 80,265,468 (GRCm39) |
E111G |
probably damaging |
Het |
| Unc13b |
T |
G |
4: 43,237,137 (GRCm39) |
I3402M |
probably damaging |
Het |
| Vmn1r188 |
A |
C |
13: 22,272,291 (GRCm39) |
I82L |
probably benign |
Het |
| Zfp65 |
A |
G |
13: 67,856,994 (GRCm39) |
V95A |
probably benign |
Het |
| Zfp985 |
T |
A |
4: 147,668,612 (GRCm39) |
S493R |
probably damaging |
Het |
|
| Other mutations in Cntln |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00639:Cntln
|
APN |
4 |
84,924,671 (GRCm39) |
missense |
probably benign |
0.25 |
|
IGL00743:Cntln
|
APN |
4 |
84,897,652 (GRCm39) |
missense |
probably benign |
0.06 |
|
IGL01014:Cntln
|
APN |
4 |
84,968,145 (GRCm39) |
missense |
probably benign |
0.25 |
|
IGL02217:Cntln
|
APN |
4 |
85,018,495 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02323:Cntln
|
APN |
4 |
84,968,026 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02353:Cntln
|
APN |
4 |
84,968,087 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL02360:Cntln
|
APN |
4 |
84,968,087 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL02616:Cntln
|
APN |
4 |
85,033,689 (GRCm39) |
critical splice donor site |
probably null |
|
|
PIT4696001:Cntln
|
UTSW |
4 |
84,892,237 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0110:Cntln
|
UTSW |
4 |
85,014,994 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0324:Cntln
|
UTSW |
4 |
85,010,932 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0349:Cntln
|
UTSW |
4 |
84,914,722 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0519:Cntln
|
UTSW |
4 |
84,923,290 (GRCm39) |
splice site |
probably benign |
|
|
R0529:Cntln
|
UTSW |
4 |
84,986,062 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0582:Cntln
|
UTSW |
4 |
84,802,978 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1077:Cntln
|
UTSW |
4 |
84,914,716 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1345:Cntln
|
UTSW |
4 |
84,892,228 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1457:Cntln
|
UTSW |
4 |
85,015,076 (GRCm39) |
missense |
probably benign |
0.33 |
|
R1571:Cntln
|
UTSW |
4 |
84,865,823 (GRCm39) |
nonsense |
probably null |
|
|
R1622:Cntln
|
UTSW |
4 |
84,981,418 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1681:Cntln
|
UTSW |
4 |
84,865,872 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1777:Cntln
|
UTSW |
4 |
85,048,916 (GRCm39) |
missense |
probably benign |
0.23 |
|
R1808:Cntln
|
UTSW |
4 |
85,015,000 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1882:Cntln
|
UTSW |
4 |
85,019,072 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2056:Cntln
|
UTSW |
4 |
84,967,911 (GRCm39) |
missense |
probably benign |
|
|
R2965:Cntln
|
UTSW |
4 |
84,892,264 (GRCm39) |
critical splice donor site |
probably null |
|
|
R2968:Cntln
|
UTSW |
4 |
84,875,504 (GRCm39) |
missense |
probably benign |
0.27 |
|
R3104:Cntln
|
UTSW |
4 |
84,875,406 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R3106:Cntln
|
UTSW |
4 |
84,875,406 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R3121:Cntln
|
UTSW |
4 |
84,923,289 (GRCm39) |
splice site |
probably benign |
|
|
R3617:Cntln
|
UTSW |
4 |
84,923,214 (GRCm39) |
nonsense |
probably null |
|
|
R4009:Cntln
|
UTSW |
4 |
84,981,452 (GRCm39) |
missense |
probably benign |
0.45 |
|
R4036:Cntln
|
UTSW |
4 |
84,924,725 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4548:Cntln
|
UTSW |
4 |
85,015,079 (GRCm39) |
missense |
probably benign |
0.27 |
|
R4592:Cntln
|
UTSW |
4 |
84,889,419 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4666:Cntln
|
UTSW |
4 |
84,889,453 (GRCm39) |
missense |
probably benign |
0.13 |
|
R4826:Cntln
|
UTSW |
4 |
84,923,281 (GRCm39) |
missense |
probably benign |
0.03 |
|
R4856:Cntln
|
UTSW |
4 |
84,889,466 (GRCm39) |
missense |
probably benign |
0.35 |
|
R4886:Cntln
|
UTSW |
4 |
84,889,466 (GRCm39) |
missense |
probably benign |
0.35 |
|
R4995:Cntln
|
UTSW |
4 |
84,968,120 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5090:Cntln
|
UTSW |
4 |
84,865,830 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5202:Cntln
|
UTSW |
4 |
84,889,466 (GRCm39) |
missense |
probably benign |
0.35 |
|
R5905:Cntln
|
UTSW |
4 |
84,889,410 (GRCm39) |
missense |
probably benign |
0.03 |
|
R5953:Cntln
|
UTSW |
4 |
84,968,156 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R6028:Cntln
|
UTSW |
4 |
84,889,410 (GRCm39) |
missense |
probably benign |
0.03 |
|
R6298:Cntln
|
UTSW |
4 |
85,014,998 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6351:Cntln
|
UTSW |
4 |
85,033,591 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6371:Cntln
|
UTSW |
4 |
84,802,816 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6481:Cntln
|
UTSW |
4 |
84,985,747 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6864:Cntln
|
UTSW |
4 |
85,015,029 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6874:Cntln
|
UTSW |
4 |
84,985,996 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6919:Cntln
|
UTSW |
4 |
85,033,605 (GRCm39) |
missense |
probably benign |
0.04 |
|
R7071:Cntln
|
UTSW |
4 |
85,018,622 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7113:Cntln
|
UTSW |
4 |
84,968,064 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7152:Cntln
|
UTSW |
4 |
84,802,937 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R7253:Cntln
|
UTSW |
4 |
85,036,710 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7289:Cntln
|
UTSW |
4 |
84,964,540 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R7440:Cntln
|
UTSW |
4 |
84,981,453 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R7670:Cntln
|
UTSW |
4 |
84,897,577 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R7707:Cntln
|
UTSW |
4 |
84,802,853 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7895:Cntln
|
UTSW |
4 |
84,981,561 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R8176:Cntln
|
UTSW |
4 |
84,806,926 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8247:Cntln
|
UTSW |
4 |
85,019,017 (GRCm39) |
missense |
probably benign |
0.39 |
|
R8264:Cntln
|
UTSW |
4 |
85,016,648 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8293:Cntln
|
UTSW |
4 |
84,952,075 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8536:Cntln
|
UTSW |
4 |
84,875,286 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8844:Cntln
|
UTSW |
4 |
84,892,234 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8924:Cntln
|
UTSW |
4 |
84,806,936 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8955:Cntln
|
UTSW |
4 |
84,986,110 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R8960:Cntln
|
UTSW |
4 |
85,018,961 (GRCm39) |
missense |
possibly damaging |
0.59 |
|
R8979:Cntln
|
UTSW |
4 |
85,048,910 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9255:Cntln
|
UTSW |
4 |
85,019,103 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R9314:Cntln
|
UTSW |
4 |
84,924,719 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9353:Cntln
|
UTSW |
4 |
84,802,597 (GRCm39) |
unclassified |
probably benign |
|
|
R9361:Cntln
|
UTSW |
4 |
84,968,151 (GRCm39) |
missense |
probably benign |
0.23 |
|
R9376:Cntln
|
UTSW |
4 |
84,875,258 (GRCm39) |
missense |
probably benign |
0.24 |
|
R9382:Cntln
|
UTSW |
4 |
84,968,318 (GRCm39) |
missense |
probably benign |
0.13 |
|
R9471:Cntln
|
UTSW |
4 |
84,968,019 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R9478:Cntln
|
UTSW |
4 |
84,897,630 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9527:Cntln
|
UTSW |
4 |
84,892,120 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9788:Cntln
|
UTSW |
4 |
84,968,093 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9793:Cntln
|
UTSW |
4 |
84,985,798 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- TGTGTCCTTGTGCTAAATGGAAC -3'
(R):5'- ATCTGTGGTGGCCATCTCAG -3'
Sequencing Primer
(F):5'- CCTTGTGCTAAATGGAACTTTCATC -3'
(R):5'- GGTGGCCATCTCAGATTTAGC -3'
|
| Posted On |
2016-03-01 |
Incidental Mutation