Incidental Mutation 'R2114:Gcn1'
ID |
232916 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Gcn1
|
Ensembl Gene |
ENSMUSG00000041638 |
Gene Name |
GCN1 activator of EIF2AK4 |
Synonyms |
Gcn1l1, G431004K08Rik, GCN1L |
MMRRC Submission |
040118-MU
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.948)
|
Stock # |
R2114 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
5 |
Chromosomal Location |
115703313-115760713 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 115736884 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Methionine to Leucine
at position 1276
(M1276L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000069432
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000064454]
|
AlphaFold |
E9PVA8 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000064454
AA Change: M1276L
PolyPhen 2
Score 0.351 (Sensitivity: 0.90; Specificity: 0.89)
|
SMART Domains |
Protein: ENSMUSP00000069432 Gene: ENSMUSG00000041638 AA Change: M1276L
Domain | Start | End | E-Value | Type |
low complexity region
|
64 |
84 |
N/A |
INTRINSIC |
low complexity region
|
108 |
117 |
N/A |
INTRINSIC |
low complexity region
|
142 |
154 |
N/A |
INTRINSIC |
Pfam:DUF3554
|
357 |
705 |
2e-61 |
PFAM |
coiled coil region
|
806 |
866 |
N/A |
INTRINSIC |
Blast:ARM
|
1028 |
1068 |
6e-11 |
BLAST |
coiled coil region
|
1180 |
1203 |
N/A |
INTRINSIC |
low complexity region
|
1457 |
1466 |
N/A |
INTRINSIC |
low complexity region
|
1501 |
1510 |
N/A |
INTRINSIC |
ARM
|
1527 |
1567 |
3.69e1 |
SMART |
Blast:ARM
|
1602 |
1644 |
1e-5 |
BLAST |
Blast:EZ_HEAT
|
1671 |
1704 |
1e-7 |
BLAST |
low complexity region
|
1926 |
1934 |
N/A |
INTRINSIC |
low complexity region
|
1956 |
1972 |
N/A |
INTRINSIC |
ARM
|
2034 |
2070 |
9.27e1 |
SMART |
low complexity region
|
2326 |
2334 |
N/A |
INTRINSIC |
ARM
|
2416 |
2455 |
2.16e1 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000151030
AA Change: H877L
|
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.6%
- 10x: 97.4%
- 20x: 95.6%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 96 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
a |
A |
G |
2: 154,889,649 (GRCm39) |
R72G |
probably benign |
Het |
Adgrb1 |
T |
A |
15: 74,412,411 (GRCm39) |
|
probably null |
Het |
Akr1b7 |
G |
A |
6: 34,395,929 (GRCm39) |
A144T |
possibly damaging |
Het |
Anapc5 |
C |
T |
5: 122,926,001 (GRCm39) |
V685I |
probably benign |
Het |
Apba3 |
T |
C |
10: 81,108,946 (GRCm39) |
Y570H |
probably damaging |
Het |
Arf5 |
C |
T |
6: 28,424,783 (GRCm39) |
Q71* |
probably null |
Het |
Arl15 |
C |
T |
13: 114,104,196 (GRCm39) |
S111F |
probably damaging |
Het |
Ash1l |
C |
T |
3: 88,890,571 (GRCm39) |
L817F |
probably benign |
Het |
Auh |
G |
A |
13: 52,989,532 (GRCm39) |
P308L |
probably benign |
Het |
Blvra |
G |
T |
2: 126,927,989 (GRCm39) |
E80* |
probably null |
Het |
Bmp10 |
A |
C |
6: 87,411,441 (GRCm39) |
E411D |
probably benign |
Het |
Ccdc148 |
T |
C |
2: 58,892,128 (GRCm39) |
E188G |
probably damaging |
Het |
Ces1a |
A |
G |
8: 93,766,179 (GRCm39) |
L145P |
possibly damaging |
Het |
Chsy3 |
G |
A |
18: 59,312,561 (GRCm39) |
V345I |
probably damaging |
Het |
Ckmt2 |
T |
A |
13: 92,003,964 (GRCm39) |
I345F |
probably benign |
Het |
Col5a2 |
T |
A |
1: 45,415,964 (GRCm39) |
E1394D |
probably damaging |
Het |
Dnah6 |
T |
C |
6: 73,121,018 (GRCm39) |
N1492S |
probably damaging |
Het |
Dock3 |
T |
C |
9: 106,870,743 (GRCm39) |
N557S |
probably benign |
Het |
Edem2 |
G |
A |
2: 155,544,479 (GRCm39) |
R424C |
probably damaging |
Het |
Exoc4 |
T |
A |
6: 33,324,760 (GRCm39) |
N351K |
possibly damaging |
Het |
Eya1 |
A |
T |
1: 14,340,998 (GRCm39) |
F163I |
probably damaging |
Het |
Ezh1 |
A |
C |
11: 101,099,011 (GRCm39) |
S290A |
probably benign |
Het |
Fam83f |
T |
G |
15: 80,576,468 (GRCm39) |
V373G |
possibly damaging |
Het |
Fam83h |
A |
T |
15: 75,874,146 (GRCm39) |
Y1064N |
probably damaging |
Het |
Fat4 |
A |
T |
3: 39,035,633 (GRCm39) |
H3095L |
probably benign |
Het |
Fbxo38 |
A |
C |
18: 62,639,711 (GRCm39) |
I1051S |
possibly damaging |
Het |
Galnt6 |
G |
C |
15: 100,612,122 (GRCm39) |
C173W |
probably damaging |
Het |
Gcc2 |
T |
A |
10: 58,105,362 (GRCm39) |
C99* |
probably null |
Het |
Gm266 |
T |
G |
12: 111,452,116 (GRCm39) |
Q30P |
possibly damaging |
Het |
Gsdma |
A |
T |
11: 98,563,838 (GRCm39) |
E264V |
probably damaging |
Het |
Ift74 |
A |
G |
4: 94,515,496 (GRCm39) |
T138A |
probably benign |
Het |
Ikzf1 |
T |
G |
11: 11,719,473 (GRCm39) |
H480Q |
probably damaging |
Het |
Ints14 |
T |
G |
9: 64,887,077 (GRCm39) |
L336R |
probably damaging |
Het |
Irak1 |
G |
T |
X: 73,066,218 (GRCm39) |
P197Q |
possibly damaging |
Het |
Kcna6 |
A |
G |
6: 126,716,322 (GRCm39) |
V189A |
possibly damaging |
Het |
Kcnh4 |
A |
G |
11: 100,650,421 (GRCm39) |
M4T |
probably damaging |
Het |
Kif4 |
A |
G |
X: 99,709,323 (GRCm39) |
S315G |
probably benign |
Het |
L3mbtl1 |
T |
A |
2: 162,801,990 (GRCm39) |
|
probably null |
Het |
Lrwd1 |
T |
A |
5: 136,159,332 (GRCm39) |
Y431F |
probably damaging |
Het |
Madd |
A |
G |
2: 90,994,367 (GRCm39) |
V884A |
probably damaging |
Het |
Maz |
C |
A |
7: 126,624,677 (GRCm39) |
C281F |
probably damaging |
Het |
Mb |
G |
T |
15: 76,906,759 (GRCm39) |
Q9K |
probably benign |
Het |
Mllt10 |
A |
G |
2: 18,167,380 (GRCm39) |
N435S |
probably benign |
Het |
Mrm3 |
T |
C |
11: 76,135,347 (GRCm39) |
M186T |
possibly damaging |
Het |
Naprt |
T |
C |
15: 75,763,637 (GRCm39) |
Y395C |
probably damaging |
Het |
Nccrp1 |
T |
A |
7: 28,246,334 (GRCm39) |
Q76L |
probably benign |
Het |
Nlgn1 |
T |
A |
3: 26,187,414 (GRCm39) |
N157I |
probably damaging |
Het |
Nmi |
T |
C |
2: 51,838,719 (GRCm39) |
T272A |
probably benign |
Het |
Obscn |
C |
T |
11: 59,022,484 (GRCm39) |
V754M |
probably damaging |
Het |
Pcdhb12 |
A |
G |
18: 37,569,265 (GRCm39) |
E137G |
probably damaging |
Het |
Pdk2 |
A |
G |
11: 94,918,088 (GRCm39) |
Y382H |
probably damaging |
Het |
Phka1 |
C |
T |
X: 101,653,807 (GRCm39) |
R290H |
probably damaging |
Het |
Pick1 |
T |
A |
15: 79,139,781 (GRCm39) |
|
probably benign |
Het |
Pik3r2 |
T |
C |
8: 71,222,029 (GRCm39) |
I585V |
probably benign |
Het |
Pitrm1 |
A |
T |
13: 6,607,809 (GRCm39) |
Y268F |
probably damaging |
Het |
Polr2b |
G |
A |
5: 77,468,817 (GRCm39) |
E198K |
probably damaging |
Het |
Prelid3b |
T |
C |
2: 174,311,243 (GRCm39) |
N9D |
probably damaging |
Het |
Prex2 |
T |
A |
1: 11,256,937 (GRCm39) |
N1216K |
probably damaging |
Het |
Prkab2 |
A |
T |
3: 97,574,711 (GRCm39) |
M236L |
possibly damaging |
Het |
Prkar2b |
T |
A |
12: 32,017,279 (GRCm39) |
N257I |
probably damaging |
Het |
Prkcd |
A |
G |
14: 30,327,808 (GRCm39) |
C208R |
probably damaging |
Het |
Prkch |
T |
A |
12: 73,749,290 (GRCm39) |
S347T |
probably benign |
Het |
Prr12 |
A |
G |
7: 44,695,506 (GRCm39) |
V1320A |
unknown |
Het |
Ptk2 |
A |
G |
15: 73,114,255 (GRCm39) |
V701A |
possibly damaging |
Het |
Ptpra |
G |
T |
2: 130,381,655 (GRCm39) |
R372L |
probably damaging |
Het |
Ptx3 |
T |
A |
3: 66,132,187 (GRCm39) |
I236N |
probably damaging |
Het |
Ralgapa1 |
T |
C |
12: 55,833,134 (GRCm39) |
|
probably null |
Het |
Rgr |
T |
A |
14: 36,760,809 (GRCm39) |
|
probably null |
Het |
Rgs7 |
T |
A |
1: 174,918,639 (GRCm39) |
N235I |
probably damaging |
Het |
Rgsl1 |
T |
A |
1: 153,693,295 (GRCm39) |
M629L |
probably benign |
Het |
Rpgrip1 |
A |
T |
14: 52,387,024 (GRCm39) |
E781V |
probably benign |
Het |
Rrh |
T |
C |
3: 129,604,336 (GRCm39) |
I288M |
probably damaging |
Het |
Rtf1 |
T |
A |
2: 119,535,999 (GRCm39) |
H184Q |
probably benign |
Het |
Rusc1 |
T |
C |
3: 88,999,014 (GRCm39) |
D256G |
probably benign |
Het |
Scap |
T |
C |
9: 110,210,341 (GRCm39) |
Y917H |
probably damaging |
Het |
Scn9a |
T |
C |
2: 66,314,396 (GRCm39) |
E1774G |
probably damaging |
Het |
Sec11c |
A |
T |
18: 65,933,720 (GRCm39) |
T9S |
probably benign |
Het |
Slc24a2 |
C |
T |
4: 86,909,592 (GRCm39) |
V664I |
probably benign |
Het |
Stim2 |
A |
G |
5: 54,261,819 (GRCm39) |
Q237R |
probably damaging |
Het |
Synpo2 |
T |
A |
3: 122,873,537 (GRCm39) |
H1143L |
probably benign |
Het |
Syt4 |
A |
G |
18: 31,573,520 (GRCm39) |
Y332H |
probably damaging |
Het |
Tcf23 |
G |
A |
5: 31,130,919 (GRCm39) |
D186N |
probably benign |
Het |
Tcf3 |
C |
A |
10: 80,246,040 (GRCm39) |
G628W |
probably damaging |
Het |
Tcof1 |
T |
C |
18: 60,965,857 (GRCm39) |
E415G |
possibly damaging |
Het |
Tlr5 |
T |
C |
1: 182,803,194 (GRCm39) |
W833R |
probably damaging |
Het |
Tmem132b |
A |
G |
5: 125,699,615 (GRCm39) |
E92G |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,577,352 (GRCm39) |
S24514T |
probably damaging |
Het |
Txndc16 |
T |
C |
14: 45,382,484 (GRCm39) |
E587G |
probably benign |
Het |
Ubr4 |
A |
T |
4: 139,156,922 (GRCm39) |
K2316* |
probably null |
Het |
Usp20 |
T |
A |
2: 30,906,317 (GRCm39) |
C562S |
probably damaging |
Het |
Vat1 |
A |
T |
11: 101,356,568 (GRCm39) |
V131E |
probably damaging |
Het |
Vgll1 |
A |
C |
X: 56,137,790 (GRCm39) |
K53T |
probably damaging |
Het |
Zfp1005 |
T |
A |
2: 150,109,819 (GRCm39) |
C170S |
unknown |
Het |
Zfp592 |
G |
A |
7: 80,674,544 (GRCm39) |
V503M |
probably damaging |
Het |
Zfp786 |
A |
G |
6: 47,803,931 (GRCm39) |
V37A |
probably damaging |
Het |
Zscan30 |
A |
G |
18: 24,104,173 (GRCm39) |
|
noncoding transcript |
Het |
|
Other mutations in Gcn1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00869:Gcn1
|
APN |
5 |
115,726,202 (GRCm39) |
splice site |
probably benign |
|
IGL00974:Gcn1
|
APN |
5 |
115,751,852 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL01566:Gcn1
|
APN |
5 |
115,749,117 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01843:Gcn1
|
APN |
5 |
115,757,759 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01885:Gcn1
|
APN |
5 |
115,714,174 (GRCm39) |
splice site |
probably null |
|
IGL02081:Gcn1
|
APN |
5 |
115,723,930 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02118:Gcn1
|
APN |
5 |
115,748,938 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02150:Gcn1
|
APN |
5 |
115,747,927 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02190:Gcn1
|
APN |
5 |
115,752,183 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02219:Gcn1
|
APN |
5 |
115,751,826 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL02507:Gcn1
|
APN |
5 |
115,723,940 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02644:Gcn1
|
APN |
5 |
115,713,250 (GRCm39) |
missense |
probably benign |
|
IGL02678:Gcn1
|
APN |
5 |
115,751,814 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02748:Gcn1
|
APN |
5 |
115,748,859 (GRCm39) |
splice site |
probably null |
|
IGL02755:Gcn1
|
APN |
5 |
115,742,065 (GRCm39) |
splice site |
probably null |
|
IGL02896:Gcn1
|
APN |
5 |
115,757,707 (GRCm39) |
splice site |
probably benign |
|
cusp
|
UTSW |
5 |
115,749,119 (GRCm39) |
missense |
probably damaging |
1.00 |
farthing
|
UTSW |
5 |
115,714,167 (GRCm39) |
splice site |
probably benign |
|
IGL03147:Gcn1
|
UTSW |
5 |
115,748,917 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0362:Gcn1
|
UTSW |
5 |
115,714,167 (GRCm39) |
splice site |
probably benign |
|
R0540:Gcn1
|
UTSW |
5 |
115,727,015 (GRCm39) |
missense |
probably benign |
0.00 |
R0569:Gcn1
|
UTSW |
5 |
115,733,118 (GRCm39) |
missense |
probably benign |
0.00 |
R0570:Gcn1
|
UTSW |
5 |
115,730,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R0584:Gcn1
|
UTSW |
5 |
115,733,074 (GRCm39) |
missense |
probably damaging |
1.00 |
R0630:Gcn1
|
UTSW |
5 |
115,719,148 (GRCm39) |
missense |
probably benign |
0.06 |
R0656:Gcn1
|
UTSW |
5 |
115,727,362 (GRCm39) |
missense |
probably benign |
0.27 |
R0801:Gcn1
|
UTSW |
5 |
115,729,065 (GRCm39) |
missense |
probably benign |
0.12 |
R0890:Gcn1
|
UTSW |
5 |
115,717,852 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1400:Gcn1
|
UTSW |
5 |
115,752,220 (GRCm39) |
missense |
probably damaging |
1.00 |
R1485:Gcn1
|
UTSW |
5 |
115,712,676 (GRCm39) |
missense |
probably benign |
|
R1574:Gcn1
|
UTSW |
5 |
115,753,611 (GRCm39) |
missense |
probably benign |
|
R1574:Gcn1
|
UTSW |
5 |
115,753,611 (GRCm39) |
missense |
probably benign |
|
R1673:Gcn1
|
UTSW |
5 |
115,720,356 (GRCm39) |
missense |
probably benign |
|
R1894:Gcn1
|
UTSW |
5 |
115,727,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R2116:Gcn1
|
UTSW |
5 |
115,736,884 (GRCm39) |
missense |
probably benign |
0.35 |
R2117:Gcn1
|
UTSW |
5 |
115,736,884 (GRCm39) |
missense |
probably benign |
0.35 |
R2152:Gcn1
|
UTSW |
5 |
115,747,888 (GRCm39) |
missense |
probably benign |
0.07 |
R2162:Gcn1
|
UTSW |
5 |
115,730,191 (GRCm39) |
missense |
probably benign |
0.18 |
R2216:Gcn1
|
UTSW |
5 |
115,731,720 (GRCm39) |
missense |
probably benign |
|
R2218:Gcn1
|
UTSW |
5 |
115,757,720 (GRCm39) |
missense |
probably benign |
0.04 |
R2278:Gcn1
|
UTSW |
5 |
115,749,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R2280:Gcn1
|
UTSW |
5 |
115,750,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R3719:Gcn1
|
UTSW |
5 |
115,717,876 (GRCm39) |
missense |
probably benign |
0.03 |
R3729:Gcn1
|
UTSW |
5 |
115,721,453 (GRCm39) |
splice site |
probably benign |
|
R3833:Gcn1
|
UTSW |
5 |
115,730,191 (GRCm39) |
missense |
probably benign |
0.18 |
R3932:Gcn1
|
UTSW |
5 |
115,725,893 (GRCm39) |
missense |
probably benign |
0.11 |
R4067:Gcn1
|
UTSW |
5 |
115,737,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R4152:Gcn1
|
UTSW |
5 |
115,751,413 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4179:Gcn1
|
UTSW |
5 |
115,726,109 (GRCm39) |
missense |
probably benign |
0.00 |
R4292:Gcn1
|
UTSW |
5 |
115,714,207 (GRCm39) |
missense |
possibly damaging |
0.49 |
R4350:Gcn1
|
UTSW |
5 |
115,741,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R4493:Gcn1
|
UTSW |
5 |
115,732,203 (GRCm39) |
missense |
probably benign |
|
R4672:Gcn1
|
UTSW |
5 |
115,744,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R4749:Gcn1
|
UTSW |
5 |
115,752,461 (GRCm39) |
missense |
probably benign |
|
R4753:Gcn1
|
UTSW |
5 |
115,754,537 (GRCm39) |
missense |
probably benign |
|
R4826:Gcn1
|
UTSW |
5 |
115,731,752 (GRCm39) |
missense |
probably benign |
|
R4873:Gcn1
|
UTSW |
5 |
115,714,229 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4875:Gcn1
|
UTSW |
5 |
115,714,229 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4932:Gcn1
|
UTSW |
5 |
115,730,203 (GRCm39) |
missense |
probably benign |
0.00 |
R4992:Gcn1
|
UTSW |
5 |
115,737,225 (GRCm39) |
missense |
probably benign |
0.29 |
R5049:Gcn1
|
UTSW |
5 |
115,744,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R5211:Gcn1
|
UTSW |
5 |
115,757,371 (GRCm39) |
missense |
probably benign |
0.04 |
R5226:Gcn1
|
UTSW |
5 |
115,726,126 (GRCm39) |
missense |
probably benign |
0.01 |
R5338:Gcn1
|
UTSW |
5 |
115,721,462 (GRCm39) |
missense |
probably benign |
0.00 |
R5914:Gcn1
|
UTSW |
5 |
115,748,194 (GRCm39) |
synonymous |
silent |
|
R5932:Gcn1
|
UTSW |
5 |
115,730,435 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6422:Gcn1
|
UTSW |
5 |
115,747,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R6435:Gcn1
|
UTSW |
5 |
115,749,081 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6607:Gcn1
|
UTSW |
5 |
115,747,537 (GRCm39) |
missense |
probably damaging |
0.98 |
R6724:Gcn1
|
UTSW |
5 |
115,747,217 (GRCm39) |
splice site |
probably null |
|
R6861:Gcn1
|
UTSW |
5 |
115,749,108 (GRCm39) |
missense |
probably benign |
|
R6875:Gcn1
|
UTSW |
5 |
115,726,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R6910:Gcn1
|
UTSW |
5 |
115,744,597 (GRCm39) |
missense |
probably benign |
0.42 |
R6975:Gcn1
|
UTSW |
5 |
115,751,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R7027:Gcn1
|
UTSW |
5 |
115,754,605 (GRCm39) |
critical splice donor site |
probably null |
|
R7038:Gcn1
|
UTSW |
5 |
115,749,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R7171:Gcn1
|
UTSW |
5 |
115,728,352 (GRCm39) |
missense |
probably benign |
0.02 |
R7276:Gcn1
|
UTSW |
5 |
115,749,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R7456:Gcn1
|
UTSW |
5 |
115,743,005 (GRCm39) |
nonsense |
probably null |
|
R7473:Gcn1
|
UTSW |
5 |
115,719,863 (GRCm39) |
missense |
probably benign |
0.09 |
R7517:Gcn1
|
UTSW |
5 |
115,757,755 (GRCm39) |
missense |
probably benign |
0.01 |
R7714:Gcn1
|
UTSW |
5 |
115,733,359 (GRCm39) |
missense |
probably damaging |
0.97 |
R7752:Gcn1
|
UTSW |
5 |
115,753,627 (GRCm39) |
missense |
probably damaging |
1.00 |
R7812:Gcn1
|
UTSW |
5 |
115,731,751 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7922:Gcn1
|
UTSW |
5 |
115,752,527 (GRCm39) |
missense |
probably benign |
|
R8070:Gcn1
|
UTSW |
5 |
115,727,057 (GRCm39) |
missense |
probably benign |
0.09 |
R8218:Gcn1
|
UTSW |
5 |
115,719,588 (GRCm39) |
missense |
probably benign |
0.00 |
R8329:Gcn1
|
UTSW |
5 |
115,747,921 (GRCm39) |
missense |
probably damaging |
0.99 |
R8413:Gcn1
|
UTSW |
5 |
115,717,698 (GRCm39) |
missense |
probably benign |
0.00 |
R8795:Gcn1
|
UTSW |
5 |
115,752,454 (GRCm39) |
missense |
probably benign |
0.02 |
R8802:Gcn1
|
UTSW |
5 |
115,747,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R8899:Gcn1
|
UTSW |
5 |
115,717,220 (GRCm39) |
missense |
probably benign |
0.04 |
R8946:Gcn1
|
UTSW |
5 |
115,733,404 (GRCm39) |
missense |
probably benign |
0.02 |
R8963:Gcn1
|
UTSW |
5 |
115,727,153 (GRCm39) |
missense |
probably benign |
0.25 |
R9006:Gcn1
|
UTSW |
5 |
115,719,566 (GRCm39) |
missense |
probably benign |
0.22 |
R9163:Gcn1
|
UTSW |
5 |
115,742,944 (GRCm39) |
missense |
probably benign |
|
R9177:Gcn1
|
UTSW |
5 |
115,719,867 (GRCm39) |
missense |
probably benign |
0.35 |
R9187:Gcn1
|
UTSW |
5 |
115,752,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R9411:Gcn1
|
UTSW |
5 |
115,733,098 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9541:Gcn1
|
UTSW |
5 |
115,754,416 (GRCm39) |
missense |
probably benign |
0.00 |
R9574:Gcn1
|
UTSW |
5 |
115,713,341 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9630:Gcn1
|
UTSW |
5 |
115,741,349 (GRCm39) |
missense |
probably damaging |
0.99 |
R9651:Gcn1
|
UTSW |
5 |
115,747,665 (GRCm39) |
critical splice donor site |
probably null |
|
R9761:Gcn1
|
UTSW |
5 |
115,729,064 (GRCm39) |
missense |
probably benign |
0.05 |
R9765:Gcn1
|
UTSW |
5 |
115,735,131 (GRCm39) |
nonsense |
probably null |
|
Z1177:Gcn1
|
UTSW |
5 |
115,752,208 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1191:Gcn1
|
UTSW |
5 |
115,713,352 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
Predicted Primers |
PCR Primer
(F):5'- AATTGTCCTCCTTCCACATGGG -3'
(R):5'- TTGACATTCTCCTGCGAAGGC -3'
Sequencing Primer
(F):5'- CTTCCACATGGGGCGCC -3'
(R):5'- GCAATGCTGCCCGCTTAC -3'
|
Posted On |
2014-09-18 |