Incidental Mutation 'R7779:Jak3'
ID |
599087 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Jak3
|
Ensembl Gene |
ENSMUSG00000031805 |
Gene Name |
Janus kinase 3 |
Synonyms |
|
MMRRC Submission |
045835-MU
|
Accession Numbers |
|
Essential gene? |
Possibly essential
(E-score: 0.702)
|
Stock # |
R7779 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
8 |
Chromosomal Location |
72129027-72143221 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to T
at 72139932 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Arginine to Leucine
at position 1045
(R1045L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000060073
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000034260]
[ENSMUST00000034261]
[ENSMUST00000051995]
[ENSMUST00000110012]
[ENSMUST00000110013]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably benign
Transcript: ENSMUST00000034260
|
SMART Domains |
Protein: ENSMUSP00000034260 Gene: ENSMUSG00000031803
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
28 |
N/A |
INTRINSIC |
Pfam:Galactosyl_T
|
121 |
314 |
5.9e-44 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000034261
|
SMART Domains |
Protein: ENSMUSP00000034261 Gene: ENSMUSG00000079019
Domain | Start | End | E-Value | Type |
low complexity region
|
3 |
16 |
N/A |
INTRINSIC |
IlGF
|
26 |
120 |
2.46e-10 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000051995
AA Change: R1045L
PolyPhen 2
Score 0.008 (Sensitivity: 0.96; Specificity: 0.76)
|
SMART Domains |
Protein: ENSMUSP00000060073 Gene: ENSMUSG00000031805 AA Change: R1045L
Domain | Start | End | E-Value | Type |
B41
|
20 |
254 |
2.2e-42 |
SMART |
SH2
|
370 |
460 |
5.57e-8 |
SMART |
low complexity region
|
488 |
503 |
N/A |
INTRINSIC |
STYKc
|
517 |
773 |
3.58e-12 |
SMART |
TyrKc
|
818 |
1091 |
4.59e-105 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000110012
AA Change: R1045L
PolyPhen 2
Score 0.008 (Sensitivity: 0.96; Specificity: 0.76)
|
SMART Domains |
Protein: ENSMUSP00000105639 Gene: ENSMUSG00000031805 AA Change: R1045L
Domain | Start | End | E-Value | Type |
B41
|
20 |
254 |
2.2e-42 |
SMART |
SH2
|
370 |
460 |
5.57e-8 |
SMART |
low complexity region
|
488 |
503 |
N/A |
INTRINSIC |
STYKc
|
517 |
773 |
3.58e-12 |
SMART |
TyrKc
|
818 |
1091 |
4.59e-105 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000110013
AA Change: R1045L
PolyPhen 2
Score 0.008 (Sensitivity: 0.96; Specificity: 0.76)
|
SMART Domains |
Protein: ENSMUSP00000105640 Gene: ENSMUSG00000031805 AA Change: R1045L
Domain | Start | End | E-Value | Type |
B41
|
20 |
254 |
2.2e-42 |
SMART |
SH2
|
370 |
460 |
5.57e-8 |
SMART |
low complexity region
|
488 |
503 |
N/A |
INTRINSIC |
STYKc
|
517 |
773 |
3.58e-12 |
SMART |
TyrKc
|
818 |
1091 |
4.59e-105 |
SMART |
|
Meta Mutation Damage Score |
0.0980 |
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.2%
|
Validation Efficiency |
98% (92/94) |
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 member of the Janus kinase (JAK) family of tyrosine kinases involved in cytokine receptor-mediated intracellular signal transduction. It is predominantly expressed in immune cells and transduces a signal in response to its activation via tyrosine phosphorylation by interleukin receptors. Mutations in this gene are associated with autosomal SCID (severe combined immunodeficiency disease). [provided by RefSeq, Jul 2008] PHENOTYPE: Mice homozygous for a knock-out allele exhibit impaired B cell development, small thymi and T cell proliferate. Point mutation homozygotes develop autoimmune inflammatory bowel disease, decreased susceptibility to malaria infection and/or increased susceptibility to bacterial infection. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9330159F19Rik |
T |
A |
10: 29,101,316 (GRCm39) |
V563E |
probably damaging |
Het |
Adra1d |
A |
G |
2: 131,403,805 (GRCm39) |
V95A |
probably damaging |
Het |
Ak7 |
A |
C |
12: 105,708,609 (GRCm39) |
I355L |
probably benign |
Het |
Ank1 |
G |
A |
8: 23,586,763 (GRCm39) |
|
probably null |
Het |
Apol7c |
A |
T |
15: 77,409,946 (GRCm39) |
H333Q |
probably damaging |
Het |
Arfgef3 |
T |
C |
10: 18,470,771 (GRCm39) |
M1665V |
probably damaging |
Het |
Arid5b |
A |
G |
10: 67,932,606 (GRCm39) |
Y1099H |
probably damaging |
Het |
Atp8b1 |
A |
G |
18: 64,674,453 (GRCm39) |
S943P |
probably damaging |
Het |
BC005537 |
C |
T |
13: 24,987,382 (GRCm39) |
R7W |
possibly damaging |
Het |
Bcl2l2 |
C |
T |
14: 55,121,836 (GRCm39) |
|
probably benign |
Het |
Bco1 |
A |
G |
8: 117,844,135 (GRCm39) |
Y283C |
probably damaging |
Het |
Brd4 |
A |
T |
17: 32,431,910 (GRCm39) |
D652E |
probably benign |
Het |
Cacna1s |
G |
A |
1: 136,046,767 (GRCm39) |
A1799T |
probably damaging |
Het |
Camsap3 |
A |
G |
8: 3,647,887 (GRCm39) |
Y65C |
probably damaging |
Het |
Capn1 |
T |
C |
19: 6,044,116 (GRCm39) |
K535E |
probably benign |
Het |
Cbl |
A |
G |
9: 44,070,393 (GRCm39) |
S480P |
probably benign |
Het |
Cfap99 |
A |
C |
5: 34,469,008 (GRCm39) |
N294T |
probably benign |
Het |
Defa24 |
A |
C |
8: 22,225,355 (GRCm39) |
S82R |
probably benign |
Het |
Dnai2 |
T |
C |
11: 114,645,235 (GRCm39) |
F557L |
possibly damaging |
Het |
Dnhd1 |
T |
A |
7: 105,327,122 (GRCm39) |
H690Q |
probably benign |
Het |
Dock2 |
A |
G |
11: 34,605,282 (GRCm39) |
V279A |
probably benign |
Het |
Dst |
T |
A |
1: 34,233,678 (GRCm39) |
V3462E |
probably damaging |
Het |
E2f3 |
T |
G |
13: 30,102,598 (GRCm39) |
H221P |
probably damaging |
Het |
Eif2b4 |
A |
T |
5: 31,347,998 (GRCm39) |
I238N |
probably damaging |
Het |
Eno4 |
T |
C |
19: 58,956,975 (GRCm39) |
S530P |
probably benign |
Het |
Epb42 |
T |
G |
2: 120,864,916 (GRCm39) |
K58N |
probably benign |
Het |
Etl4 |
C |
T |
2: 20,714,288 (GRCm39) |
T129I |
probably damaging |
Het |
Extl1 |
A |
G |
4: 134,085,014 (GRCm39) |
F652S |
probably damaging |
Het |
Extl1 |
T |
C |
4: 134,087,908 (GRCm39) |
K449E |
probably benign |
Het |
F13b |
T |
A |
1: 139,444,124 (GRCm39) |
V486E |
probably benign |
Het |
Fbln2 |
T |
A |
6: 91,210,176 (GRCm39) |
L40Q |
probably damaging |
Het |
Glp2r |
C |
T |
11: 67,600,609 (GRCm39) |
W413* |
probably null |
Het |
Grin2b |
A |
T |
6: 135,755,792 (GRCm39) |
Y507* |
probably null |
Het |
H2-M11 |
G |
T |
17: 36,859,698 (GRCm39) |
L230F |
probably benign |
Het |
Il36a |
T |
C |
2: 24,106,613 (GRCm39) |
Y66H |
probably damaging |
Het |
Itpr1 |
A |
G |
6: 108,500,309 (GRCm39) |
E2634G |
possibly damaging |
Het |
Itpr3 |
A |
T |
17: 27,315,037 (GRCm39) |
Y728F |
probably damaging |
Het |
Jak1 |
C |
T |
4: 101,017,339 (GRCm39) |
E764K |
probably benign |
Het |
Jam2 |
T |
C |
16: 84,606,271 (GRCm39) |
I95T |
probably damaging |
Het |
Kdf1 |
T |
C |
4: 133,255,796 (GRCm39) |
V171A |
probably damaging |
Het |
Lactbl1 |
A |
T |
4: 136,358,307 (GRCm39) |
K93* |
probably null |
Het |
Lcn6 |
T |
C |
2: 25,570,805 (GRCm39) |
V131A |
probably benign |
Het |
Lpar5 |
T |
A |
6: 125,059,207 (GRCm39) |
D309E |
probably damaging |
Het |
Lrfn4 |
T |
C |
19: 4,663,715 (GRCm39) |
E273G |
probably damaging |
Het |
Lta4h |
C |
T |
10: 93,310,811 (GRCm39) |
T447I |
probably benign |
Het |
Lyst |
A |
G |
13: 13,809,128 (GRCm39) |
E266G |
probably damaging |
Het |
Mab21l1 |
A |
T |
3: 55,690,796 (GRCm39) |
I128F |
possibly damaging |
Het |
Mrgprb4 |
T |
G |
7: 47,848,895 (GRCm39) |
N11T |
probably benign |
Het |
Mroh6 |
G |
A |
15: 75,760,505 (GRCm39) |
T23I |
possibly damaging |
Het |
Myo1f |
T |
C |
17: 33,797,247 (GRCm39) |
I143T |
probably benign |
Het |
Myof |
C |
T |
19: 37,927,838 (GRCm39) |
D1092N |
probably damaging |
Het |
Ncan |
G |
T |
8: 70,567,661 (GRCm39) |
D150E |
probably damaging |
Het |
Or1d2 |
T |
A |
11: 74,255,771 (GRCm39) |
I92N |
probably damaging |
Het |
Or2y1f |
T |
A |
11: 49,185,048 (GRCm39) |
L300Q |
probably damaging |
Het |
Or6c88 |
A |
T |
10: 129,407,180 (GRCm39) |
I219F |
probably damaging |
Het |
Pcm1 |
A |
G |
8: 41,782,061 (GRCm39) |
Y1948C |
probably damaging |
Het |
Pcsk6 |
A |
T |
7: 65,675,152 (GRCm39) |
T669S |
probably benign |
Het |
Pdlim5 |
A |
C |
3: 141,948,447 (GRCm39) |
N613K |
probably benign |
Het |
Pdzk1 |
T |
A |
3: 96,764,589 (GRCm39) |
V291D |
probably damaging |
Het |
Plbd2 |
T |
C |
5: 120,625,743 (GRCm39) |
Q408R |
probably damaging |
Het |
Ppp1r37 |
C |
A |
7: 19,266,712 (GRCm39) |
A392S |
possibly damaging |
Het |
Proser2 |
T |
A |
2: 6,107,878 (GRCm39) |
|
probably null |
Het |
Psmd12 |
T |
C |
11: 107,388,405 (GRCm39) |
V406A |
probably benign |
Het |
Rab3gap2 |
T |
C |
1: 184,991,641 (GRCm39) |
V709A |
probably damaging |
Het |
Radil |
T |
C |
5: 142,473,320 (GRCm39) |
E787G |
probably benign |
Het |
Rai14 |
A |
C |
15: 10,593,112 (GRCm39) |
D177E |
probably damaging |
Het |
Rbms2 |
G |
A |
10: 127,979,315 (GRCm39) |
T166I |
probably damaging |
Het |
Rrh |
C |
T |
3: 129,608,969 (GRCm39) |
C115Y |
probably benign |
Het |
Slc1a6 |
C |
T |
10: 78,631,789 (GRCm39) |
T205I |
probably damaging |
Het |
Sost |
T |
C |
11: 101,857,675 (GRCm39) |
E42G |
possibly damaging |
Het |
Spcs3 |
T |
A |
8: 54,982,805 (GRCm39) |
I46F |
possibly damaging |
Het |
Spg11 |
A |
G |
2: 121,901,420 (GRCm39) |
S1507P |
probably damaging |
Het |
Sprtn |
C |
T |
8: 125,624,982 (GRCm39) |
P29L |
possibly damaging |
Het |
Sptan1 |
C |
T |
2: 29,911,319 (GRCm39) |
T1886I |
probably damaging |
Het |
Strn4 |
T |
C |
7: 16,565,417 (GRCm39) |
F394S |
probably damaging |
Het |
Syt14 |
A |
T |
1: 192,666,751 (GRCm39) |
M51K |
unknown |
Het |
Terb2 |
A |
G |
2: 122,016,975 (GRCm39) |
K32R |
probably benign |
Het |
Tex15 |
G |
A |
8: 34,065,309 (GRCm39) |
G1580R |
probably damaging |
Het |
Thumpd3 |
T |
C |
6: 113,036,950 (GRCm39) |
V283A |
probably damaging |
Het |
Tm7sf2 |
T |
C |
19: 6,112,947 (GRCm39) |
Y418C |
possibly damaging |
Het |
Trim24 |
T |
G |
6: 37,896,332 (GRCm39) |
F263C |
probably damaging |
Het |
Trim24 |
T |
A |
6: 37,896,333 (GRCm39) |
F263L |
probably damaging |
Het |
Trip11 |
A |
G |
12: 101,849,796 (GRCm39) |
S1423P |
probably damaging |
Het |
Vps13c |
G |
A |
9: 67,788,704 (GRCm39) |
V326M |
probably damaging |
Het |
Vps37c |
T |
C |
19: 10,689,988 (GRCm39) |
V150A |
probably damaging |
Het |
Wdr90 |
C |
T |
17: 26,065,300 (GRCm39) |
R1652Q |
probably damaging |
Het |
Wfdc9 |
A |
G |
2: 164,492,516 (GRCm39) |
V37A |
probably damaging |
Het |
Yif1b |
T |
A |
7: 28,945,328 (GRCm39) |
M227K |
probably damaging |
Het |
Zbtb18 |
T |
C |
1: 177,274,505 (GRCm39) |
|
probably benign |
Het |
Zfp318 |
A |
G |
17: 46,710,820 (GRCm39) |
T848A |
probably benign |
Het |
Zfp808 |
T |
A |
13: 62,320,571 (GRCm39) |
I600K |
possibly damaging |
Het |
Zmym1 |
C |
A |
4: 126,948,038 (GRCm39) |
S111I |
probably benign |
Het |
Zmym2 |
A |
G |
14: 57,165,740 (GRCm39) |
T688A |
probably damaging |
Het |
|
Other mutations in Jak3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00226:Jak3
|
APN |
8 |
72,134,341 (GRCm39) |
splice site |
probably benign |
|
IGL00720:Jak3
|
APN |
8 |
72,136,681 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00966:Jak3
|
APN |
8 |
72,131,656 (GRCm39) |
missense |
probably benign |
0.24 |
IGL01147:Jak3
|
APN |
8 |
72,136,047 (GRCm39) |
missense |
probably benign |
|
IGL01308:Jak3
|
APN |
8 |
72,137,810 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01328:Jak3
|
APN |
8 |
72,132,264 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01386:Jak3
|
APN |
8 |
72,136,933 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01515:Jak3
|
APN |
8 |
72,133,206 (GRCm39) |
splice site |
probably null |
|
IGL01870:Jak3
|
APN |
8 |
72,133,434 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02132:Jak3
|
APN |
8 |
72,131,124 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02413:Jak3
|
APN |
8 |
72,138,763 (GRCm39) |
splice site |
probably null |
|
IGL02752:Jak3
|
APN |
8 |
72,135,595 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL03089:Jak3
|
APN |
8 |
72,138,727 (GRCm39) |
missense |
probably benign |
0.15 |
IGL03177:Jak3
|
APN |
8 |
72,135,014 (GRCm39) |
missense |
probably damaging |
1.00 |
barbed
|
UTSW |
8 |
72,131,425 (GRCm39) |
missense |
possibly damaging |
0.88 |
beanstalk
|
UTSW |
8 |
72,139,932 (GRCm39) |
missense |
probably benign |
0.01 |
Bonis
|
UTSW |
8 |
72,131,898 (GRCm39) |
missense |
probably benign |
0.05 |
citron
|
UTSW |
8 |
72,139,620 (GRCm39) |
splice site |
probably benign |
|
corrupt
|
UTSW |
8 |
72,136,696 (GRCm39) |
missense |
probably damaging |
1.00 |
daniels
|
UTSW |
8 |
72,134,299 (GRCm39) |
missense |
possibly damaging |
0.48 |
Deposuit
|
UTSW |
8 |
72,138,048 (GRCm39) |
missense |
probably damaging |
1.00 |
distortion
|
UTSW |
8 |
72,136,622 (GRCm39) |
missense |
probably damaging |
1.00 |
Downcast
|
UTSW |
8 |
72,138,155 (GRCm39) |
missense |
probably benign |
0.07 |
fake_news
|
UTSW |
8 |
72,138,601 (GRCm39) |
missense |
probably damaging |
1.00 |
Implevit
|
UTSW |
8 |
72,131,417 (GRCm39) |
missense |
probably benign |
|
mount_tai
|
UTSW |
8 |
72,136,021 (GRCm39) |
missense |
probably damaging |
1.00 |
potentes
|
UTSW |
8 |
72,138,702 (GRCm39) |
missense |
probably damaging |
0.99 |
Riot
|
UTSW |
8 |
72,134,960 (GRCm39) |
missense |
probably damaging |
1.00 |
thistle
|
UTSW |
8 |
72,138,027 (GRCm39) |
critical splice acceptor site |
probably null |
|
thistle2
|
UTSW |
8 |
72,138,189 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4403001:Jak3
|
UTSW |
8 |
72,136,993 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4515001:Jak3
|
UTSW |
8 |
72,132,286 (GRCm39) |
missense |
probably benign |
0.21 |
R0013:Jak3
|
UTSW |
8 |
72,136,971 (GRCm39) |
missense |
probably damaging |
0.98 |
R0496:Jak3
|
UTSW |
8 |
72,135,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R0522:Jak3
|
UTSW |
8 |
72,134,918 (GRCm39) |
splice site |
probably benign |
|
R0531:Jak3
|
UTSW |
8 |
72,139,620 (GRCm39) |
splice site |
probably benign |
|
R0538:Jak3
|
UTSW |
8 |
72,138,126 (GRCm39) |
missense |
probably benign |
|
R0612:Jak3
|
UTSW |
8 |
72,136,021 (GRCm39) |
missense |
probably damaging |
1.00 |
R0744:Jak3
|
UTSW |
8 |
72,136,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R0833:Jak3
|
UTSW |
8 |
72,136,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R0836:Jak3
|
UTSW |
8 |
72,136,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R1183:Jak3
|
UTSW |
8 |
72,137,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R1420:Jak3
|
UTSW |
8 |
72,134,182 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1793:Jak3
|
UTSW |
8 |
72,138,590 (GRCm39) |
splice site |
probably benign |
|
R1967:Jak3
|
UTSW |
8 |
72,134,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R1983:Jak3
|
UTSW |
8 |
72,140,780 (GRCm39) |
missense |
probably benign |
|
R1983:Jak3
|
UTSW |
8 |
72,131,019 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2058:Jak3
|
UTSW |
8 |
72,138,027 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2060:Jak3
|
UTSW |
8 |
72,136,059 (GRCm39) |
nonsense |
probably null |
|
R2060:Jak3
|
UTSW |
8 |
72,133,358 (GRCm39) |
nonsense |
probably null |
|
R3705:Jak3
|
UTSW |
8 |
72,134,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R3734:Jak3
|
UTSW |
8 |
72,129,225 (GRCm39) |
unclassified |
probably benign |
|
R4231:Jak3
|
UTSW |
8 |
72,138,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R4596:Jak3
|
UTSW |
8 |
72,137,275 (GRCm39) |
missense |
probably damaging |
0.99 |
R4844:Jak3
|
UTSW |
8 |
72,134,299 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4897:Jak3
|
UTSW |
8 |
72,138,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R5038:Jak3
|
UTSW |
8 |
72,138,702 (GRCm39) |
missense |
probably damaging |
0.99 |
R5469:Jak3
|
UTSW |
8 |
72,131,417 (GRCm39) |
missense |
probably benign |
|
R5538:Jak3
|
UTSW |
8 |
72,131,417 (GRCm39) |
missense |
probably benign |
|
R5718:Jak3
|
UTSW |
8 |
72,136,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R5799:Jak3
|
UTSW |
8 |
72,131,344 (GRCm39) |
missense |
probably damaging |
1.00 |
R5909:Jak3
|
UTSW |
8 |
72,136,875 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5959:Jak3
|
UTSW |
8 |
72,134,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R6260:Jak3
|
UTSW |
8 |
72,131,954 (GRCm39) |
missense |
probably benign |
0.00 |
R6798:Jak3
|
UTSW |
8 |
72,133,615 (GRCm39) |
missense |
probably damaging |
0.99 |
R7013:Jak3
|
UTSW |
8 |
72,131,425 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7070:Jak3
|
UTSW |
8 |
72,137,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R7122:Jak3
|
UTSW |
8 |
72,138,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R7166:Jak3
|
UTSW |
8 |
72,134,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R7225:Jak3
|
UTSW |
8 |
72,138,155 (GRCm39) |
missense |
probably benign |
0.07 |
R7440:Jak3
|
UTSW |
8 |
72,133,362 (GRCm39) |
missense |
probably benign |
0.02 |
R7489:Jak3
|
UTSW |
8 |
72,136,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R7773:Jak3
|
UTSW |
8 |
72,131,686 (GRCm39) |
missense |
probably benign |
|
R8511:Jak3
|
UTSW |
8 |
72,138,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R8808:Jak3
|
UTSW |
8 |
72,138,164 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8859:Jak3
|
UTSW |
8 |
72,131,160 (GRCm39) |
missense |
probably benign |
0.37 |
R9079:Jak3
|
UTSW |
8 |
72,131,898 (GRCm39) |
missense |
probably benign |
0.05 |
R9320:Jak3
|
UTSW |
8 |
72,134,265 (GRCm39) |
missense |
probably benign |
0.03 |
R9389:Jak3
|
UTSW |
8 |
72,136,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R9664:Jak3
|
UTSW |
8 |
72,131,366 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Jak3
|
UTSW |
8 |
72,133,327 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
Predicted Primers |
PCR Primer
(F):5'- GACCTCCAGATCATCTCCTGAC -3'
(R):5'- CACATTTCTGAAGCCCTTGAAGC -3'
Sequencing Primer
(F):5'- CCAGATCATCTCCTGACCTCAG -3'
(R):5'- TCTGAAGCCCTTGAAGCTGAGC -3'
|
Posted On |
2019-11-26 |