Incidental Mutation 'R0413:Plb1'
ID |
36778 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Plb1
|
Ensembl Gene |
ENSMUSG00000029134 |
Gene Name |
phospholipase B1 |
Synonyms |
4632413E21Rik, 4930433E17Rik, 4930539A06Rik |
MMRRC Submission |
038615-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.057)
|
Stock # |
R0413 (G1)
|
Quality Score |
172 |
Status
|
Validated
|
Chromosome |
5 |
Chromosomal Location |
32390035-32521700 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 32512706 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Phenylalanine to Leucine
at position 1355
(F1355L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000144040
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000101376]
[ENSMUST00000202220]
|
AlphaFold |
Q3TTY0 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000101376
AA Change: F1355L
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000098927 Gene: ENSMUSG00000029134 AA Change: F1355L
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
27 |
N/A |
INTRINSIC |
low complexity region
|
57 |
69 |
N/A |
INTRINSIC |
Pfam:Lipase_GDSL
|
398 |
672 |
4e-20 |
PFAM |
Pfam:Lipase_GDSL
|
745 |
1019 |
1.7e-17 |
PFAM |
Pfam:Lipase_GDSL
|
1101 |
1367 |
4.6e-15 |
PFAM |
transmembrane domain
|
1420 |
1442 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000202220
AA Change: F1355L
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000144040 Gene: ENSMUSG00000029134 AA Change: F1355L
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
27 |
N/A |
INTRINSIC |
low complexity region
|
57 |
69 |
N/A |
INTRINSIC |
Pfam:Lipase_GDSL
|
398 |
672 |
4e-20 |
PFAM |
Pfam:Lipase_GDSL
|
745 |
1019 |
1.7e-17 |
PFAM |
Pfam:Lipase_GDSL
|
1101 |
1367 |
4.6e-15 |
PFAM |
transmembrane domain
|
1420 |
1442 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000202453
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000202687
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000202688
|
Meta Mutation Damage Score |
0.3189 |
Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.6%
- 10x: 97.0%
- 20x: 94.9%
|
Validation Efficiency |
99% (99/100) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a membrane-associated phospholipase that displays lysophospholipase and phospholipase A2 activities through removal of sn-1 and sn-2 fatty acids of glycerophospholipids. In addition, it displays lipase and retinyl ester hydrolase activities. The encoded protein is highly conserved and is composed of a large, glycosylated extracellular domain composed of four tandem homologous domains, followed by a hydrophobic segment that anchors the enzyme to the membrane and a short C-terminal cytoplasmic tail. This gene has been identified as a candidate rheumatoid arthritis risk gene. [provided by RefSeq, Jul 2016]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb11 |
A |
G |
2: 69,158,355 (GRCm39) |
|
probably benign |
Het |
Adh1 |
C |
T |
3: 137,986,193 (GRCm39) |
T60I |
probably benign |
Het |
Agtpbp1 |
T |
A |
13: 59,661,966 (GRCm39) |
I282F |
probably damaging |
Het |
Arih2 |
G |
T |
9: 108,493,916 (GRCm39) |
Q166K |
probably damaging |
Het |
Cacna1s |
A |
G |
1: 136,025,947 (GRCm39) |
T1031A |
probably benign |
Het |
Ccdc102a |
C |
A |
8: 95,629,914 (GRCm39) |
E542D |
probably benign |
Het |
Cdk1 |
T |
C |
10: 69,180,929 (GRCm39) |
I94V |
probably benign |
Het |
Cep290 |
C |
T |
10: 100,359,176 (GRCm39) |
Q969* |
probably null |
Het |
Cilp2 |
A |
G |
8: 70,335,643 (GRCm39) |
S452P |
probably benign |
Het |
Col12a1 |
T |
C |
9: 79,606,642 (GRCm39) |
T594A |
probably damaging |
Het |
Cpox |
A |
G |
16: 58,491,232 (GRCm39) |
T148A |
possibly damaging |
Het |
Csf3r |
A |
G |
4: 125,933,460 (GRCm39) |
|
probably benign |
Het |
Csmd1 |
A |
T |
8: 16,760,530 (GRCm39) |
C202S |
probably damaging |
Het |
Dlgap4 |
T |
C |
2: 156,604,746 (GRCm39) |
S261P |
probably damaging |
Het |
Dnah9 |
T |
A |
11: 65,998,961 (GRCm39) |
Y1029F |
probably damaging |
Het |
Dok5 |
T |
C |
2: 170,671,880 (GRCm39) |
|
probably benign |
Het |
Dusp11 |
A |
T |
6: 85,929,352 (GRCm39) |
|
probably benign |
Het |
Edar |
T |
C |
10: 58,465,262 (GRCm39) |
N34D |
probably benign |
Het |
Efcab7 |
C |
T |
4: 99,766,943 (GRCm39) |
T56I |
probably damaging |
Het |
Entpd1 |
G |
A |
19: 40,699,729 (GRCm39) |
V47I |
probably benign |
Het |
Ephx4 |
A |
G |
5: 107,551,601 (GRCm39) |
N62S |
probably benign |
Het |
Etaa1 |
A |
T |
11: 17,896,350 (GRCm39) |
L589* |
probably null |
Het |
Fam135b |
T |
A |
15: 71,335,670 (GRCm39) |
N508I |
probably benign |
Het |
Fam193a |
T |
C |
5: 34,623,552 (GRCm39) |
V27A |
possibly damaging |
Het |
Fmnl1 |
A |
G |
11: 103,084,889 (GRCm39) |
|
probably benign |
Het |
Fstl1 |
A |
C |
16: 37,641,516 (GRCm39) |
|
probably null |
Het |
Gbp4 |
G |
A |
5: 105,268,972 (GRCm39) |
R394C |
possibly damaging |
Het |
Gemin4 |
T |
C |
11: 76,102,148 (GRCm39) |
Y871C |
probably benign |
Het |
Get1 |
T |
G |
16: 95,954,217 (GRCm39) |
S105R |
probably benign |
Het |
Gm7247 |
T |
C |
14: 51,760,929 (GRCm39) |
V166A |
probably benign |
Het |
Gpcpd1 |
A |
T |
2: 132,406,543 (GRCm39) |
|
probably benign |
Het |
Gpnmb |
A |
G |
6: 49,019,737 (GRCm39) |
D36G |
probably benign |
Het |
Ido2 |
C |
T |
8: 25,048,159 (GRCm39) |
|
probably null |
Het |
Igfn1 |
G |
A |
1: 135,895,334 (GRCm39) |
T1744I |
probably benign |
Het |
Inf2 |
T |
G |
12: 112,568,110 (GRCm39) |
F221V |
probably damaging |
Het |
Itga10 |
T |
A |
3: 96,556,375 (GRCm39) |
I170N |
probably damaging |
Het |
Lrp6 |
A |
T |
6: 134,484,587 (GRCm39) |
D345E |
probably damaging |
Het |
Macf1 |
A |
T |
4: 123,366,062 (GRCm39) |
S2900T |
probably benign |
Het |
Med13 |
C |
A |
11: 86,190,033 (GRCm39) |
|
probably benign |
Het |
Morc3 |
T |
C |
16: 93,667,362 (GRCm39) |
V507A |
probably damaging |
Het |
Myadm |
AC |
ACC |
7: 3,345,276 (GRCm39) |
|
probably null |
Het |
Myl6 |
C |
T |
10: 128,328,091 (GRCm39) |
|
probably benign |
Het |
Mylk |
T |
C |
16: 34,742,314 (GRCm39) |
V942A |
probably benign |
Het |
Myorg |
G |
T |
4: 41,498,585 (GRCm39) |
H348Q |
probably benign |
Het |
Ncdn |
G |
T |
4: 126,644,327 (GRCm39) |
T165K |
possibly damaging |
Het |
Ncf1 |
T |
C |
5: 134,251,656 (GRCm39) |
|
probably benign |
Het |
Neb |
T |
C |
2: 52,180,751 (GRCm39) |
|
probably benign |
Het |
Nid1 |
T |
A |
13: 13,656,681 (GRCm39) |
I604N |
probably benign |
Het |
Nsrp1 |
T |
C |
11: 76,936,997 (GRCm39) |
R400G |
probably benign |
Het |
Nup43 |
T |
G |
10: 7,546,791 (GRCm39) |
I137S |
probably benign |
Het |
Nynrin |
A |
G |
14: 56,109,648 (GRCm39) |
N1585S |
possibly damaging |
Het |
Obscn |
T |
A |
11: 58,893,823 (GRCm39) |
Y6748F |
probably benign |
Het |
Omg |
A |
G |
11: 79,393,661 (GRCm39) |
S66P |
possibly damaging |
Het |
Or13a27 |
A |
T |
7: 139,925,108 (GRCm39) |
S265T |
possibly damaging |
Het |
Or2y1d |
T |
C |
11: 49,322,212 (GRCm39) |
V303A |
possibly damaging |
Het |
Or4c15 |
A |
G |
2: 88,759,906 (GRCm39) |
V251A |
probably benign |
Het |
Or51b6b |
A |
T |
7: 103,309,957 (GRCm39) |
F167I |
possibly damaging |
Het |
Or52z1 |
A |
G |
7: 103,437,362 (GRCm39) |
Y41H |
probably damaging |
Het |
Or5ak22 |
T |
C |
2: 85,230,019 (GRCm39) |
N286S |
probably damaging |
Het |
Or8g27 |
A |
G |
9: 39,129,566 (GRCm39) |
I304M |
probably benign |
Het |
Or8k24 |
G |
A |
2: 86,216,058 (GRCm39) |
R235C |
probably benign |
Het |
Ormdl1 |
C |
T |
1: 53,347,978 (GRCm39) |
|
probably benign |
Het |
Ovch2 |
T |
A |
7: 107,381,243 (GRCm39) |
I552L |
probably benign |
Het |
Pcare |
T |
G |
17: 72,059,212 (GRCm39) |
D155A |
probably benign |
Het |
Pcsk9 |
G |
T |
4: 106,311,538 (GRCm39) |
T231N |
probably damaging |
Het |
Pgpep1 |
T |
C |
8: 71,110,100 (GRCm39) |
N22S |
probably damaging |
Het |
Plcg1 |
G |
T |
2: 160,603,349 (GRCm39) |
L1173F |
probably damaging |
Het |
Plch2 |
A |
T |
4: 155,091,373 (GRCm39) |
|
probably null |
Het |
Ppp1r3g |
T |
A |
13: 36,153,331 (GRCm39) |
F250L |
probably damaging |
Het |
Prkcg |
A |
G |
7: 3,368,095 (GRCm39) |
I381V |
probably benign |
Het |
Pum2 |
C |
T |
12: 8,763,464 (GRCm39) |
A207V |
probably benign |
Het |
Rabac1 |
T |
C |
7: 24,669,607 (GRCm39) |
E166G |
probably damaging |
Het |
Rad21l |
G |
A |
2: 151,493,851 (GRCm39) |
S450L |
probably benign |
Het |
Rangap1 |
ACACTCA |
ACA |
15: 81,600,876 (GRCm39) |
|
probably null |
Het |
Reg3b |
G |
T |
6: 78,348,824 (GRCm39) |
C40F |
probably damaging |
Het |
Rfx2 |
A |
G |
17: 57,091,418 (GRCm39) |
|
probably benign |
Het |
Rrp15 |
G |
A |
1: 186,481,346 (GRCm39) |
|
probably benign |
Het |
Schip1 |
G |
T |
3: 68,401,946 (GRCm39) |
G36C |
probably damaging |
Het |
Sec61a2 |
A |
T |
2: 5,881,165 (GRCm39) |
|
probably benign |
Het |
Sema5a |
A |
G |
15: 32,669,590 (GRCm39) |
K705E |
probably damaging |
Het |
Setx |
A |
G |
2: 29,029,290 (GRCm39) |
Y186C |
probably damaging |
Het |
Slc22a23 |
T |
C |
13: 34,367,115 (GRCm39) |
E631G |
probably damaging |
Het |
Slc5a5 |
T |
C |
8: 71,344,319 (GRCm39) |
T134A |
possibly damaging |
Het |
Stx7 |
T |
C |
10: 24,057,492 (GRCm39) |
S173P |
probably damaging |
Het |
Sybu |
T |
C |
15: 44,536,668 (GRCm39) |
T353A |
probably damaging |
Het |
Syde2 |
T |
A |
3: 145,712,887 (GRCm39) |
N1008K |
probably damaging |
Het |
Tiam1 |
T |
C |
16: 89,606,253 (GRCm39) |
|
probably benign |
Het |
Timm10b |
G |
A |
7: 105,327,537 (GRCm39) |
E61K |
probably benign |
Het |
Tm2d1 |
A |
G |
4: 98,253,810 (GRCm39) |
I121T |
probably damaging |
Het |
Trim75 |
T |
C |
8: 65,435,892 (GRCm39) |
E186G |
probably benign |
Het |
Tti1 |
T |
C |
2: 157,837,396 (GRCm39) |
K895E |
probably benign |
Het |
Vmn1r43 |
A |
G |
6: 89,846,830 (GRCm39) |
S219P |
probably damaging |
Het |
Vmn2r73 |
A |
T |
7: 85,521,087 (GRCm39) |
S294T |
possibly damaging |
Het |
Vmn2r94 |
A |
T |
17: 18,464,080 (GRCm39) |
F737I |
probably damaging |
Het |
Vsx2 |
A |
T |
12: 84,616,777 (GRCm39) |
T21S |
probably benign |
Het |
Zfp462 |
G |
T |
4: 55,010,534 (GRCm39) |
R833S |
probably damaging |
Het |
Zfpl1 |
G |
A |
19: 6,132,482 (GRCm39) |
P143L |
probably damaging |
Het |
|
Other mutations in Plb1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00096:Plb1
|
APN |
5 |
32,503,080 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00542:Plb1
|
APN |
5 |
32,427,178 (GRCm39) |
missense |
probably benign |
0.02 |
IGL00835:Plb1
|
APN |
5 |
32,521,516 (GRCm39) |
missense |
unknown |
|
IGL00954:Plb1
|
APN |
5 |
32,455,858 (GRCm39) |
splice site |
probably benign |
|
IGL01350:Plb1
|
APN |
5 |
32,474,408 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01527:Plb1
|
APN |
5 |
32,474,467 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01599:Plb1
|
APN |
5 |
32,499,888 (GRCm39) |
splice site |
probably benign |
|
IGL01690:Plb1
|
APN |
5 |
32,471,041 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01813:Plb1
|
APN |
5 |
32,486,429 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01826:Plb1
|
APN |
5 |
32,438,489 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02263:Plb1
|
APN |
5 |
32,478,692 (GRCm39) |
splice site |
probably benign |
|
IGL02314:Plb1
|
APN |
5 |
32,438,492 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02649:Plb1
|
APN |
5 |
32,519,912 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02701:Plb1
|
APN |
5 |
32,521,541 (GRCm39) |
missense |
unknown |
|
IGL02704:Plb1
|
APN |
5 |
32,511,011 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03170:Plb1
|
APN |
5 |
32,442,246 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03182:Plb1
|
APN |
5 |
32,502,259 (GRCm39) |
splice site |
probably benign |
|
IGL03326:Plb1
|
APN |
5 |
32,488,671 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03046:Plb1
|
UTSW |
5 |
32,485,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R0013:Plb1
|
UTSW |
5 |
32,506,959 (GRCm39) |
splice site |
probably benign |
|
R0013:Plb1
|
UTSW |
5 |
32,506,959 (GRCm39) |
splice site |
probably benign |
|
R0034:Plb1
|
UTSW |
5 |
32,430,457 (GRCm39) |
missense |
probably benign |
0.16 |
R0034:Plb1
|
UTSW |
5 |
32,430,457 (GRCm39) |
missense |
probably benign |
0.16 |
R0330:Plb1
|
UTSW |
5 |
32,512,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R0721:Plb1
|
UTSW |
5 |
32,521,539 (GRCm39) |
missense |
unknown |
|
R0735:Plb1
|
UTSW |
5 |
32,442,264 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1423:Plb1
|
UTSW |
5 |
32,450,601 (GRCm39) |
missense |
probably benign |
|
R1428:Plb1
|
UTSW |
5 |
32,422,256 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1469:Plb1
|
UTSW |
5 |
32,512,170 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1469:Plb1
|
UTSW |
5 |
32,512,170 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1694:Plb1
|
UTSW |
5 |
32,474,621 (GRCm39) |
missense |
probably null |
0.01 |
R1801:Plb1
|
UTSW |
5 |
32,450,587 (GRCm39) |
missense |
probably damaging |
1.00 |
R1804:Plb1
|
UTSW |
5 |
32,511,041 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1900:Plb1
|
UTSW |
5 |
32,444,191 (GRCm39) |
missense |
probably benign |
0.44 |
R1903:Plb1
|
UTSW |
5 |
32,448,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R2101:Plb1
|
UTSW |
5 |
32,507,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R2153:Plb1
|
UTSW |
5 |
32,471,433 (GRCm39) |
missense |
probably damaging |
1.00 |
R2207:Plb1
|
UTSW |
5 |
32,473,984 (GRCm39) |
missense |
possibly damaging |
0.50 |
R2270:Plb1
|
UTSW |
5 |
32,450,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R2271:Plb1
|
UTSW |
5 |
32,450,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R2311:Plb1
|
UTSW |
5 |
32,427,162 (GRCm39) |
missense |
probably benign |
0.01 |
R2850:Plb1
|
UTSW |
5 |
32,450,568 (GRCm39) |
missense |
probably benign |
|
R3103:Plb1
|
UTSW |
5 |
32,485,373 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4444:Plb1
|
UTSW |
5 |
32,487,909 (GRCm39) |
missense |
probably benign |
0.06 |
R4559:Plb1
|
UTSW |
5 |
32,490,175 (GRCm39) |
missense |
probably damaging |
0.99 |
R4577:Plb1
|
UTSW |
5 |
32,404,901 (GRCm39) |
nonsense |
probably null |
|
R4578:Plb1
|
UTSW |
5 |
32,404,901 (GRCm39) |
nonsense |
probably null |
|
R4739:Plb1
|
UTSW |
5 |
32,507,023 (GRCm39) |
splice site |
probably null |
|
R4747:Plb1
|
UTSW |
5 |
32,507,003 (GRCm39) |
missense |
probably benign |
0.08 |
R4806:Plb1
|
UTSW |
5 |
32,447,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R5406:Plb1
|
UTSW |
5 |
32,499,259 (GRCm39) |
missense |
probably damaging |
1.00 |
R5567:Plb1
|
UTSW |
5 |
32,521,543 (GRCm39) |
missense |
unknown |
|
R5574:Plb1
|
UTSW |
5 |
32,487,291 (GRCm39) |
missense |
probably benign |
0.13 |
R5588:Plb1
|
UTSW |
5 |
32,487,293 (GRCm39) |
critical splice donor site |
probably null |
|
R5619:Plb1
|
UTSW |
5 |
32,490,841 (GRCm39) |
missense |
probably damaging |
0.99 |
R5769:Plb1
|
UTSW |
5 |
32,474,866 (GRCm39) |
missense |
probably benign |
0.05 |
R6366:Plb1
|
UTSW |
5 |
32,471,429 (GRCm39) |
missense |
possibly damaging |
0.59 |
R6700:Plb1
|
UTSW |
5 |
32,490,808 (GRCm39) |
missense |
probably damaging |
0.99 |
R7162:Plb1
|
UTSW |
5 |
32,507,007 (GRCm39) |
missense |
probably benign |
0.30 |
R7379:Plb1
|
UTSW |
5 |
32,502,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R7395:Plb1
|
UTSW |
5 |
32,511,028 (GRCm39) |
missense |
probably benign |
0.30 |
R7426:Plb1
|
UTSW |
5 |
32,478,591 (GRCm39) |
splice site |
probably null |
|
R7643:Plb1
|
UTSW |
5 |
32,404,901 (GRCm39) |
nonsense |
probably null |
|
R7657:Plb1
|
UTSW |
5 |
32,487,211 (GRCm39) |
missense |
probably damaging |
0.98 |
R7780:Plb1
|
UTSW |
5 |
32,483,610 (GRCm39) |
splice site |
probably null |
|
R8040:Plb1
|
UTSW |
5 |
32,430,413 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8212:Plb1
|
UTSW |
5 |
32,422,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R8312:Plb1
|
UTSW |
5 |
32,485,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R8560:Plb1
|
UTSW |
5 |
32,460,023 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8770:Plb1
|
UTSW |
5 |
32,404,853 (GRCm39) |
missense |
unknown |
|
R8857:Plb1
|
UTSW |
5 |
32,521,556 (GRCm39) |
missense |
unknown |
|
R9029:Plb1
|
UTSW |
5 |
32,439,079 (GRCm39) |
missense |
probably damaging |
0.99 |
R9110:Plb1
|
UTSW |
5 |
32,521,402 (GRCm39) |
missense |
probably benign |
0.00 |
R9765:Plb1
|
UTSW |
5 |
32,512,731 (GRCm39) |
missense |
probably damaging |
1.00 |
X0018:Plb1
|
UTSW |
5 |
32,443,227 (GRCm39) |
missense |
probably benign |
0.01 |
X0019:Plb1
|
UTSW |
5 |
32,511,041 (GRCm39) |
missense |
probably damaging |
0.99 |
X0027:Plb1
|
UTSW |
5 |
32,427,702 (GRCm39) |
missense |
probably benign |
|
X0028:Plb1
|
UTSW |
5 |
32,460,019 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Plb1
|
UTSW |
5 |
32,468,261 (GRCm39) |
missense |
probably benign |
|
Z1088:Plb1
|
UTSW |
5 |
32,468,191 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Plb1
|
UTSW |
5 |
32,442,241 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
Predicted Primers |
PCR Primer
(F):5'- GCAATAGTGACCAAGTGTCCCTCC -3'
(R):5'- GCACATACACCAGGGTCAACAGTG -3'
Sequencing Primer
(F):5'- GTCATTTTCAGGACAGTGTTGAAC -3'
(R):5'- TGAGCCAATACCCTTAGGGT -3'
|
Posted On |
2013-05-09 |