Incidental Mutation 'R7060:Pdcd11'
| ID |
548233 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Pdcd11
|
| Ensembl Gene |
ENSMUSG00000025047 |
| Gene Name |
programmed cell death 11 |
| Synonyms |
ALG-4, 1110021I22Rik |
| MMRRC Submission |
045157-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.967)
|
| Stock # |
R7060 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
19 |
| Chromosomal Location |
47079183-47119585 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 47099418 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Isoleucine
at position 839
(T839I)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000072008
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000072141]
[ENSMUST00000140512]
|
| AlphaFold |
Q6NS46 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000072141
AA Change: T839I
PolyPhen 2
Score 0.300 (Sensitivity: 0.90; Specificity: 0.89)
|
| SMART Domains |
Protein: ENSMUSP00000072008
Gene: ENSMUSG00000025047
AA Change: T839I
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
53 |
76 |
N/A |
INTRINSIC |
|
S1
|
81 |
171 |
1.05e-7 |
SMART |
|
S1
|
185 |
258 |
2.32e-9 |
SMART |
|
S1
|
279 |
346 |
1.44e-5 |
SMART |
|
S1
|
363 |
436 |
8.55e-8 |
SMART |
|
S1
|
451 |
522 |
3.89e-20 |
SMART |
|
S1
|
540 |
611 |
1.14e-17 |
SMART |
|
S1
|
634 |
707 |
2.76e-2 |
SMART |
|
S1
|
727 |
798 |
2.02e-18 |
SMART |
|
low complexity region
|
813 |
823 |
N/A |
INTRINSIC |
|
S1
|
844 |
911 |
6.13e0 |
SMART |
|
Blast:S1
|
923 |
993 |
8e-39 |
BLAST |
|
low complexity region
|
1018 |
1032 |
N/A |
INTRINSIC |
|
S1
|
1045 |
1120 |
1.3e-7 |
SMART |
|
S1
|
1158 |
1233 |
6.09e-4 |
SMART |
|
S1
|
1239 |
1309 |
4.14e-6 |
SMART |
|
S1
|
1333 |
1407 |
1.57e-6 |
SMART |
|
low complexity region
|
1433 |
1473 |
N/A |
INTRINSIC |
|
coiled coil region
|
1557 |
1588 |
N/A |
INTRINSIC |
|
HAT
|
1591 |
1622 |
6.53e2 |
SMART |
|
HAT
|
1624 |
1661 |
4.12e1 |
SMART |
|
HAT
|
1663 |
1694 |
3.49e2 |
SMART |
|
HAT
|
1696 |
1728 |
3.18e-1 |
SMART |
|
HAT
|
1730 |
1764 |
2.25e2 |
SMART |
|
HAT
|
1766 |
1798 |
8.52e-2 |
SMART |
|
HAT
|
1800 |
1835 |
1.33e1 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000140512
|
| SMART Domains |
Protein: ENSMUSP00000121661
Gene: ENSMUSG00000033033
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Ca_hom_mod
|
6 |
258 |
2.9e-93 |
PFAM |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.0%
|
| Validation Efficiency |
96% (78/81) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] PDCD11 is a NF-kappa-B (NFKB1; 164011)-binding protein that colocalizes with U3 RNA (MIM 180710) in the nucleolus and is required for rRNA maturation and generation of 18S rRNA (Sweet et al., 2003 [PubMed 14624448]; Sweet et al., 2008 [PubMed 17654514]).[supplied by OMIM, Oct 2008]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 79 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abcg4 |
T |
A |
9: 44,186,425 (GRCm39) |
T535S |
probably benign |
Het |
| Adamts19 |
A |
T |
18: 58,970,712 (GRCm39) |
R99* |
probably null |
Het |
| Alg6 |
C |
T |
4: 99,650,198 (GRCm39) |
L473F |
possibly damaging |
Het |
| Ankar |
A |
T |
1: 72,695,272 (GRCm39) |
N893K |
probably benign |
Het |
| Ankrd54 |
G |
A |
15: 78,939,739 (GRCm39) |
A183V |
possibly damaging |
Het |
| Anpep |
G |
T |
7: 79,491,542 (GRCm39) |
T153K |
probably benign |
Het |
| Arap1 |
A |
G |
7: 101,058,564 (GRCm39) |
|
probably null |
Het |
| Aspg |
A |
T |
12: 112,089,387 (GRCm39) |
T392S |
probably benign |
Het |
| B230307C23Rik |
A |
C |
16: 97,811,331 (GRCm39) |
R68S |
probably benign |
Het |
| Bdp1 |
G |
C |
13: 100,196,002 (GRCm39) |
N1253K |
probably damaging |
Het |
| Ccrl2 |
G |
A |
9: 110,884,682 (GRCm39) |
S272F |
probably damaging |
Het |
| Cdon |
T |
C |
9: 35,398,205 (GRCm39) |
L974P |
probably damaging |
Het |
| Celsr1 |
C |
A |
15: 85,916,856 (GRCm39) |
E372D |
probably benign |
Het |
| Cers1 |
A |
T |
8: 70,768,555 (GRCm39) |
M16L |
possibly damaging |
Het |
| Col2a1 |
G |
T |
15: 97,874,022 (GRCm39) |
Q1387K |
unknown |
Het |
| Ddx39b |
G |
A |
17: 35,471,726 (GRCm39) |
V291M |
probably damaging |
Het |
| Dppa2 |
T |
A |
16: 48,136,076 (GRCm39) |
S143T |
probably benign |
Het |
| Dpy19l1 |
A |
T |
9: 24,334,419 (GRCm39) |
M583K |
possibly damaging |
Het |
| Eno3 |
A |
T |
11: 70,552,245 (GRCm39) |
D299V |
possibly damaging |
Het |
| Epha8 |
C |
T |
4: 136,658,469 (GRCm39) |
V969M |
probably damaging |
Het |
| Fcgbp |
A |
T |
7: 27,791,358 (GRCm39) |
H873L |
probably benign |
Het |
| Fhad1 |
CGG |
CG |
4: 141,645,602 (GRCm39) |
|
probably null |
Het |
| Fntb |
A |
C |
12: 76,934,649 (GRCm39) |
N173T |
possibly damaging |
Het |
| Gins2 |
T |
A |
8: 121,308,880 (GRCm39) |
M125L |
probably benign |
Het |
| Gys1 |
G |
A |
7: 45,089,437 (GRCm39) |
A199T |
probably damaging |
Het |
| Herpud1 |
C |
A |
8: 95,117,391 (GRCm39) |
H116N |
probably benign |
Het |
| Hoga1 |
C |
A |
19: 42,048,685 (GRCm39) |
Y134* |
probably null |
Het |
| Il10ra |
A |
G |
9: 45,167,522 (GRCm39) |
I343T |
probably benign |
Het |
| Inava |
T |
C |
1: 136,147,935 (GRCm39) |
K339R |
possibly damaging |
Het |
| Inpp5j |
C |
T |
11: 3,450,133 (GRCm39) |
|
probably null |
Het |
| Itpkb |
T |
C |
1: 180,160,695 (GRCm39) |
S274P |
probably damaging |
Het |
| Kalrn |
C |
T |
16: 34,177,418 (GRCm39) |
C249Y |
probably damaging |
Het |
| Klhl35 |
G |
C |
7: 99,117,665 (GRCm39) |
A70P |
possibly damaging |
Het |
| Lhx1 |
A |
G |
11: 84,411,108 (GRCm39) |
|
probably null |
Het |
| Lmbrd1 |
T |
C |
1: 24,732,047 (GRCm39) |
V88A |
probably benign |
Het |
| Macc1 |
T |
G |
12: 119,411,190 (GRCm39) |
L653V |
probably damaging |
Het |
| Madd |
T |
C |
2: 91,007,452 (GRCm39) |
D220G |
probably damaging |
Het |
| Mllt10 |
T |
A |
2: 18,164,371 (GRCm39) |
H300Q |
possibly damaging |
Het |
| Mlxipl |
G |
A |
5: 135,161,169 (GRCm39) |
A363T |
possibly damaging |
Het |
| Mus81 |
G |
T |
19: 5,537,821 (GRCm39) |
D78E |
probably benign |
Het |
| Mxd1 |
A |
T |
6: 86,630,141 (GRCm39) |
L26M |
probably damaging |
Het |
| Nhsl1 |
C |
T |
10: 18,402,251 (GRCm39) |
T1159M |
probably damaging |
Het |
| Nos1ap |
A |
G |
1: 170,165,694 (GRCm39) |
S190P |
possibly damaging |
Het |
| Nwd1 |
A |
C |
8: 73,393,322 (GRCm39) |
D195A |
probably damaging |
Het |
| Or12d13 |
G |
T |
17: 37,647,352 (GRCm39) |
T257N |
probably benign |
Het |
| Or6k4 |
A |
T |
1: 173,964,376 (GRCm39) |
D22V |
probably benign |
Het |
| Or8c14-ps1 |
G |
A |
9: 38,101,392 (GRCm39) |
V124I |
probably damaging |
Het |
| Or8k24 |
T |
A |
2: 86,216,569 (GRCm39) |
R64S |
possibly damaging |
Het |
| Otof |
T |
C |
5: 30,545,700 (GRCm39) |
D500G |
possibly damaging |
Het |
| Pcgf5 |
T |
A |
19: 36,420,339 (GRCm39) |
Y190* |
probably null |
Het |
| Ppard |
G |
C |
17: 28,517,886 (GRCm39) |
S318T |
probably benign |
Het |
| Ppfia2 |
A |
G |
10: 106,597,970 (GRCm39) |
K178E |
probably damaging |
Het |
| Ppm1n |
G |
T |
7: 19,013,187 (GRCm39) |
R255S |
probably damaging |
Het |
| Ppp1r21 |
A |
G |
17: 88,887,972 (GRCm39) |
Y693C |
probably damaging |
Het |
| Ppp2r5d |
A |
T |
17: 46,998,279 (GRCm39) |
V169E |
possibly damaging |
Het |
| Prc1 |
A |
T |
7: 79,954,121 (GRCm39) |
T53S |
probably benign |
Het |
| Pwp2 |
A |
C |
10: 78,009,084 (GRCm39) |
|
probably null |
Het |
| Rab5c |
G |
A |
11: 100,610,789 (GRCm39) |
R40C |
probably damaging |
Het |
| Ring1 |
A |
G |
17: 34,242,364 (GRCm39) |
C48R |
probably damaging |
Het |
| Rpap1 |
T |
C |
2: 119,604,043 (GRCm39) |
D496G |
probably damaging |
Het |
| Rspo4 |
C |
A |
2: 151,714,998 (GRCm39) |
Q212K |
unknown |
Het |
| Samd9l |
T |
A |
6: 3,372,716 (GRCm39) |
D1515V |
probably damaging |
Het |
| Serinc3 |
T |
C |
2: 163,478,879 (GRCm39) |
T83A |
probably benign |
Het |
| Setd5 |
A |
C |
6: 113,094,343 (GRCm39) |
D420A |
probably damaging |
Het |
| Sidt2 |
T |
C |
9: 45,864,544 (GRCm39) |
T62A |
possibly damaging |
Het |
| Smarcal1 |
T |
C |
1: 72,652,101 (GRCm39) |
V621A |
probably damaging |
Het |
| Srcin1 |
A |
G |
11: 97,464,711 (GRCm39) |
L12P |
probably damaging |
Het |
| Stx18 |
G |
A |
5: 38,278,599 (GRCm39) |
D165N |
possibly damaging |
Het |
| Sumf2 |
A |
G |
5: 129,883,341 (GRCm39) |
K139E |
possibly damaging |
Het |
| Tdo2 |
A |
T |
3: 81,876,866 (GRCm39) |
I102N |
probably damaging |
Het |
| Tdp1 |
T |
A |
12: 99,877,947 (GRCm39) |
S410T |
probably benign |
Het |
| Tmem94 |
A |
T |
11: 115,683,764 (GRCm39) |
I726F |
probably damaging |
Het |
| Ttc21a |
A |
G |
9: 119,795,742 (GRCm39) |
E1192G |
probably damaging |
Het |
| Ttc8 |
T |
C |
12: 98,909,726 (GRCm39) |
I52T |
probably benign |
Het |
| Vmn2r99 |
A |
T |
17: 19,614,826 (GRCm39) |
R849* |
probably null |
Het |
| Wwc1 |
T |
C |
11: 35,806,003 (GRCm39) |
K77E |
possibly damaging |
Het |
| Xirp2 |
A |
T |
2: 67,345,952 (GRCm39) |
E2731V |
probably damaging |
Het |
| Zfp1006 |
A |
C |
8: 129,945,613 (GRCm39) |
I404R |
probably benign |
Het |
| Zfp423 |
G |
A |
8: 88,509,507 (GRCm39) |
T258I |
probably damaging |
Het |
|
| Other mutations in Pdcd11 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00646:Pdcd11
|
APN |
19 |
47,105,767 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
IGL00656:Pdcd11
|
APN |
19 |
47,086,609 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00754:Pdcd11
|
APN |
19 |
47,092,221 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
IGL00907:Pdcd11
|
APN |
19 |
47,096,003 (GRCm39) |
missense |
probably benign |
0.16 |
|
IGL00987:Pdcd11
|
APN |
19 |
47,102,989 (GRCm39) |
intron |
probably benign |
|
|
IGL01346:Pdcd11
|
APN |
19 |
47,098,053 (GRCm39) |
missense |
probably benign |
0.03 |
|
IGL01529:Pdcd11
|
APN |
19 |
47,098,068 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL01670:Pdcd11
|
APN |
19 |
47,094,743 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL01917:Pdcd11
|
APN |
19 |
47,089,604 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
IGL02096:Pdcd11
|
APN |
19 |
47,094,860 (GRCm39) |
missense |
probably benign |
0.10 |
|
IGL02300:Pdcd11
|
APN |
19 |
47,115,381 (GRCm39) |
missense |
probably benign |
|
|
IGL02515:Pdcd11
|
APN |
19 |
47,113,516 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02886:Pdcd11
|
APN |
19 |
47,102,064 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
IGL03158:Pdcd11
|
APN |
19 |
47,116,500 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R0100:Pdcd11
|
UTSW |
19 |
47,091,105 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0100:Pdcd11
|
UTSW |
19 |
47,091,105 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0128:Pdcd11
|
UTSW |
19 |
47,108,301 (GRCm39) |
missense |
probably benign |
0.15 |
|
R0139:Pdcd11
|
UTSW |
19 |
47,099,398 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R0227:Pdcd11
|
UTSW |
19 |
47,101,876 (GRCm39) |
intron |
probably benign |
|
|
R0316:Pdcd11
|
UTSW |
19 |
47,101,611 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R0480:Pdcd11
|
UTSW |
19 |
47,113,476 (GRCm39) |
intron |
probably benign |
|
|
R0577:Pdcd11
|
UTSW |
19 |
47,087,271 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0725:Pdcd11
|
UTSW |
19 |
47,115,730 (GRCm39) |
missense |
probably benign |
0.17 |
|
R1344:Pdcd11
|
UTSW |
19 |
47,118,516 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1418:Pdcd11
|
UTSW |
19 |
47,118,516 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1856:Pdcd11
|
UTSW |
19 |
47,086,626 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2146:Pdcd11
|
UTSW |
19 |
47,093,191 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2147:Pdcd11
|
UTSW |
19 |
47,093,191 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2447:Pdcd11
|
UTSW |
19 |
47,102,995 (GRCm39) |
missense |
probably benign |
0.01 |
|
R2916:Pdcd11
|
UTSW |
19 |
47,101,876 (GRCm39) |
intron |
probably benign |
|
|
R3177:Pdcd11
|
UTSW |
19 |
47,101,703 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3277:Pdcd11
|
UTSW |
19 |
47,101,703 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3712:Pdcd11
|
UTSW |
19 |
47,115,684 (GRCm39) |
intron |
probably benign |
|
|
R4495:Pdcd11
|
UTSW |
19 |
47,099,445 (GRCm39) |
missense |
probably benign |
|
|
R4697:Pdcd11
|
UTSW |
19 |
47,114,786 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R4941:Pdcd11
|
UTSW |
19 |
47,108,325 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4953:Pdcd11
|
UTSW |
19 |
47,116,404 (GRCm39) |
missense |
probably benign |
0.04 |
|
R5048:Pdcd11
|
UTSW |
19 |
47,095,554 (GRCm39) |
missense |
probably benign |
|
|
R5049:Pdcd11
|
UTSW |
19 |
47,095,554 (GRCm39) |
missense |
probably benign |
|
|
R5103:Pdcd11
|
UTSW |
19 |
47,112,893 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5107:Pdcd11
|
UTSW |
19 |
47,094,893 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5139:Pdcd11
|
UTSW |
19 |
47,095,554 (GRCm39) |
missense |
probably benign |
|
|
R5261:Pdcd11
|
UTSW |
19 |
47,101,976 (GRCm39) |
missense |
probably benign |
|
|
R5302:Pdcd11
|
UTSW |
19 |
47,096,083 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5592:Pdcd11
|
UTSW |
19 |
47,091,164 (GRCm39) |
missense |
probably benign |
|
|
R5769:Pdcd11
|
UTSW |
19 |
47,091,076 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R5791:Pdcd11
|
UTSW |
19 |
47,099,430 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R5809:Pdcd11
|
UTSW |
19 |
47,082,247 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5899:Pdcd11
|
UTSW |
19 |
47,093,198 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R5901:Pdcd11
|
UTSW |
19 |
47,116,771 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
R5947:Pdcd11
|
UTSW |
19 |
47,117,702 (GRCm39) |
missense |
probably benign |
0.20 |
|
R6177:Pdcd11
|
UTSW |
19 |
47,108,722 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6489:Pdcd11
|
UTSW |
19 |
47,098,191 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6575:Pdcd11
|
UTSW |
19 |
47,098,117 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6578:Pdcd11
|
UTSW |
19 |
47,099,520 (GRCm39) |
missense |
probably benign |
0.11 |
|
R7009:Pdcd11
|
UTSW |
19 |
47,101,581 (GRCm39) |
missense |
probably benign |
0.17 |
|
R7015:Pdcd11
|
UTSW |
19 |
47,086,665 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7260:Pdcd11
|
UTSW |
19 |
47,117,673 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R7392:Pdcd11
|
UTSW |
19 |
47,116,436 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7601:Pdcd11
|
UTSW |
19 |
47,094,808 (GRCm39) |
missense |
not run |
|
|
R7759:Pdcd11
|
UTSW |
19 |
47,101,637 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R7760:Pdcd11
|
UTSW |
19 |
47,101,637 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R7785:Pdcd11
|
UTSW |
19 |
47,093,125 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7793:Pdcd11
|
UTSW |
19 |
47,094,871 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7810:Pdcd11
|
UTSW |
19 |
47,086,659 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R7863:Pdcd11
|
UTSW |
19 |
47,085,403 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7950:Pdcd11
|
UTSW |
19 |
47,101,876 (GRCm39) |
intron |
probably benign |
|
|
R8062:Pdcd11
|
UTSW |
19 |
47,119,152 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R8184:Pdcd11
|
UTSW |
19 |
47,101,791 (GRCm39) |
nonsense |
probably null |
|
|
R8278:Pdcd11
|
UTSW |
19 |
47,094,736 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8404:Pdcd11
|
UTSW |
19 |
47,093,231 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8508:Pdcd11
|
UTSW |
19 |
47,108,245 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8525:Pdcd11
|
UTSW |
19 |
47,081,337 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
R8787:Pdcd11
|
UTSW |
19 |
47,097,019 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9019:Pdcd11
|
UTSW |
19 |
47,101,658 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9534:Pdcd11
|
UTSW |
19 |
47,108,718 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9660:Pdcd11
|
UTSW |
19 |
47,082,191 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R9712:Pdcd11
|
UTSW |
19 |
47,117,741 (GRCm39) |
missense |
probably damaging |
0.98 |
|
RF010:Pdcd11
|
UTSW |
19 |
47,101,890 (GRCm39) |
frame shift |
probably null |
|
|
RF027:Pdcd11
|
UTSW |
19 |
47,101,888 (GRCm39) |
frame shift |
probably null |
|
|
RF039:Pdcd11
|
UTSW |
19 |
47,101,894 (GRCm39) |
frame shift |
probably null |
|
|
RF061:Pdcd11
|
UTSW |
19 |
47,101,884 (GRCm39) |
frame shift |
probably null |
|
|
X0065:Pdcd11
|
UTSW |
19 |
47,085,335 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- GTGTGTGACTCAGTACATGAACC -3'
(R):5'- AAATTCTGTATCCAGCAGAGGAGG -3'
Sequencing Primer
(F):5'- TGTGACTCAGTACATGAACCACCAC -3'
(R):5'- GAGAAGCACAGGGTCTCACC -3'
|
| Posted On |
2019-05-13 |
Incidental Mutation