Incidental Mutation 'R7395:Greb1'
ID |
573766 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Greb1
|
Ensembl Gene |
ENSMUSG00000036523 |
Gene Name |
gene regulated by estrogen in breast cancer protein |
Synonyms |
5730583K22Rik |
MMRRC Submission |
045477-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R7395 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
12 |
Chromosomal Location |
16720616-16850887 bp(-) (GRCm39) |
Type of Mutation |
critical splice donor site (2 bp from exon) |
DNA Base Change (assembly) |
A to T
at 16759431 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000044454
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000048064]
[ENSMUST00000048064]
[ENSMUST00000048064]
[ENSMUST00000048064]
[ENSMUST00000048064]
[ENSMUST00000159120]
[ENSMUST00000162112]
|
AlphaFold |
Q3UHK3 |
Predicted Effect |
probably null
Transcript: ENSMUST00000048064
|
SMART Domains |
Protein: ENSMUSP00000044454 Gene: ENSMUSG00000036523
Domain | Start | End | E-Value | Type |
Pfam:GREB1
|
1 |
1954 |
N/A |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000048064
|
SMART Domains |
Protein: ENSMUSP00000044454 Gene: ENSMUSG00000036523
Domain | Start | End | E-Value | Type |
Pfam:GREB1
|
1 |
1954 |
N/A |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000048064
|
SMART Domains |
Protein: ENSMUSP00000044454 Gene: ENSMUSG00000036523
Domain | Start | End | E-Value | Type |
Pfam:GREB1
|
1 |
1954 |
N/A |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000048064
|
SMART Domains |
Protein: ENSMUSP00000044454 Gene: ENSMUSG00000036523
Domain | Start | End | E-Value | Type |
Pfam:GREB1
|
1 |
1954 |
N/A |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000048064
|
SMART Domains |
Protein: ENSMUSP00000044454 Gene: ENSMUSG00000036523
Domain | Start | End | E-Value | Type |
Pfam:GREB1
|
1 |
1954 |
N/A |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000159120
|
SMART Domains |
Protein: ENSMUSP00000125339 Gene: ENSMUSG00000036523
Domain | Start | End | E-Value | Type |
low complexity region
|
52 |
71 |
N/A |
INTRINSIC |
low complexity region
|
292 |
303 |
N/A |
INTRINSIC |
low complexity region
|
437 |
453 |
N/A |
INTRINSIC |
low complexity region
|
480 |
503 |
N/A |
INTRINSIC |
low complexity region
|
631 |
643 |
N/A |
INTRINSIC |
low complexity region
|
1100 |
1118 |
N/A |
INTRINSIC |
low complexity region
|
1196 |
1207 |
N/A |
INTRINSIC |
low complexity region
|
1251 |
1265 |
N/A |
INTRINSIC |
low complexity region
|
1596 |
1607 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000160347
|
SMART Domains |
Protein: ENSMUSP00000124897 Gene: ENSMUSG00000036523
Domain | Start | End | E-Value | Type |
Pfam:GREB1
|
1 |
121 |
4.5e-61 |
PFAM |
|
Predicted Effect |
|
SMART Domains |
Protein: ENSMUSP00000124922 Gene: ENSMUSG00000036523 AA Change: S120R
Domain | Start | End | E-Value | Type |
Pfam:GREB1
|
1 |
122 |
1.8e-41 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000162112
|
SMART Domains |
Protein: ENSMUSP00000124348 Gene: ENSMUSG00000036523
Domain | Start | End | E-Value | Type |
low complexity region
|
52 |
71 |
N/A |
INTRINSIC |
low complexity region
|
292 |
303 |
N/A |
INTRINSIC |
low complexity region
|
437 |
453 |
N/A |
INTRINSIC |
low complexity region
|
480 |
503 |
N/A |
INTRINSIC |
low complexity region
|
631 |
643 |
N/A |
INTRINSIC |
low complexity region
|
1128 |
1146 |
N/A |
INTRINSIC |
low complexity region
|
1224 |
1235 |
N/A |
INTRINSIC |
low complexity region
|
1279 |
1293 |
N/A |
INTRINSIC |
low complexity region
|
1624 |
1635 |
N/A |
INTRINSIC |
|
Meta Mutation Damage Score |
0.9492 |
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.8%
|
Validation Efficiency |
99% (92/93) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is an estrogen-responsive gene that is an early response gene in the estrogen receptor-regulated pathway. It is thought to play an important role in hormone-responsive tissues and cancer. Three alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3830403N18Rik |
G |
T |
X: 55,184,140 (GRCm39) |
|
probably null |
Het |
4930433I11Rik |
A |
T |
7: 40,639,102 (GRCm39) |
T13S |
probably damaging |
Het |
Abca13 |
A |
G |
11: 9,241,658 (GRCm39) |
I1174V |
probably benign |
Het |
Acoxl |
G |
A |
2: 127,726,336 (GRCm39) |
V237M |
probably damaging |
Het |
Adam33 |
A |
C |
2: 130,903,089 (GRCm39) |
W52G |
probably benign |
Het |
Adgrv1 |
T |
C |
13: 81,707,467 (GRCm39) |
H1313R |
probably damaging |
Het |
Ap3d1 |
T |
C |
10: 80,566,716 (GRCm39) |
T89A |
probably benign |
Het |
Armc8 |
T |
C |
9: 99,415,185 (GRCm39) |
E165G |
probably damaging |
Het |
Atp6v1c1 |
T |
C |
15: 38,691,949 (GRCm39) |
*383Q |
probably null |
Het |
Atp8b4 |
A |
T |
2: 126,217,614 (GRCm39) |
L634Q |
possibly damaging |
Het |
B3glct |
A |
G |
5: 149,649,069 (GRCm39) |
|
probably null |
Het |
Bhlhe40 |
TG |
TGG |
6: 108,641,818 (GRCm39) |
254 |
probably null |
Het |
Bicd2 |
A |
G |
13: 49,531,706 (GRCm39) |
D316G |
possibly damaging |
Het |
Bop1 |
A |
T |
15: 76,338,041 (GRCm39) |
S610T |
probably damaging |
Het |
Car11 |
T |
A |
7: 45,350,745 (GRCm39) |
Y80* |
probably null |
Het |
Ccdc121rt2 |
A |
T |
5: 112,598,035 (GRCm39) |
E194V |
possibly damaging |
Het |
Ccdc96 |
T |
C |
5: 36,642,609 (GRCm39) |
I205T |
probably benign |
Het |
Ces2a |
A |
G |
8: 105,466,273 (GRCm39) |
E390G |
probably benign |
Het |
Cfap54 |
C |
A |
10: 92,720,565 (GRCm39) |
V2630L |
unknown |
Het |
Chek2 |
G |
T |
5: 111,019,974 (GRCm39) |
|
probably null |
Het |
Cntn3 |
C |
T |
6: 102,314,355 (GRCm39) |
|
probably null |
Het |
Cpne3 |
A |
T |
4: 19,528,239 (GRCm39) |
D339E |
probably damaging |
Het |
Crocc2 |
C |
T |
1: 93,143,829 (GRCm39) |
Q1403* |
probably null |
Het |
Crppa |
A |
T |
12: 36,551,994 (GRCm39) |
I283F |
possibly damaging |
Het |
Csnka2ip |
G |
A |
16: 64,299,803 (GRCm39) |
T187I |
|
Het |
Ctu1 |
A |
G |
7: 43,326,019 (GRCm39) |
H226R |
possibly damaging |
Het |
Cubn |
G |
T |
2: 13,291,875 (GRCm39) |
Q3317K |
probably damaging |
Het |
Cyp17a1 |
A |
G |
19: 46,659,134 (GRCm39) |
L169P |
probably benign |
Het |
Dcc |
T |
A |
18: 71,507,640 (GRCm39) |
K911* |
probably null |
Het |
Dcun1d2 |
G |
A |
8: 13,328,675 (GRCm39) |
R75* |
probably null |
Het |
Defb19 |
A |
T |
2: 152,421,943 (GRCm39) |
|
probably null |
Het |
Dffb |
A |
T |
4: 154,053,570 (GRCm39) |
S257R |
probably damaging |
Het |
Dip2c |
A |
C |
13: 9,664,413 (GRCm39) |
N942T |
probably damaging |
Het |
Dnah3 |
T |
A |
7: 119,565,474 (GRCm39) |
I169F |
|
Het |
Dnah3 |
T |
C |
7: 119,660,183 (GRCm39) |
M830V |
probably benign |
Het |
Dnajc5g |
G |
A |
5: 31,269,009 (GRCm39) |
S130N |
possibly damaging |
Het |
Dscaml1 |
C |
A |
9: 45,613,703 (GRCm39) |
Q939K |
possibly damaging |
Het |
Evpl |
G |
C |
11: 116,117,905 (GRCm39) |
N761K |
possibly damaging |
Het |
Fbxw8 |
A |
T |
5: 118,206,280 (GRCm39) |
I556N |
probably damaging |
Het |
Fry |
G |
T |
5: 150,304,348 (GRCm39) |
M579I |
possibly damaging |
Het |
Ggt7 |
A |
T |
2: 155,337,800 (GRCm39) |
M488K |
probably benign |
Het |
Gnpnat1 |
T |
A |
14: 45,619,038 (GRCm39) |
H107L |
probably benign |
Het |
Golga2 |
C |
A |
2: 32,195,599 (GRCm39) |
P798Q |
possibly damaging |
Het |
Gpr35 |
G |
A |
1: 92,910,929 (GRCm39) |
A214T |
probably damaging |
Het |
Hdac10 |
G |
A |
15: 89,012,487 (GRCm39) |
T32I |
probably benign |
Het |
Hkdc1 |
G |
A |
10: 62,221,478 (GRCm39) |
T860I |
probably damaging |
Het |
Icam5 |
C |
A |
9: 20,946,738 (GRCm39) |
P422Q |
possibly damaging |
Het |
Ist1 |
A |
C |
8: 110,404,159 (GRCm39) |
S238A |
probably benign |
Het |
Lrig2 |
T |
C |
3: 104,404,836 (GRCm39) |
N91D |
probably benign |
Het |
Mapt |
A |
C |
11: 104,218,949 (GRCm39) |
D352A |
probably damaging |
Het |
Micall2 |
G |
A |
5: 139,702,124 (GRCm39) |
P373L |
possibly damaging |
Het |
Mocs1 |
A |
G |
17: 49,761,585 (GRCm39) |
S560G |
possibly damaging |
Het |
Mpo |
A |
G |
11: 87,691,950 (GRCm39) |
D461G |
probably damaging |
Het |
Myo1a |
G |
T |
10: 127,546,309 (GRCm39) |
V271L |
probably damaging |
Het |
Ncoa1 |
G |
A |
12: 4,345,188 (GRCm39) |
P720S |
not run |
Het |
Ncr1 |
T |
A |
7: 4,341,150 (GRCm39) |
I47N |
probably damaging |
Het |
Ndufb6 |
G |
A |
4: 40,277,730 (GRCm39) |
R66C |
probably damaging |
Het |
Obox5 |
A |
T |
7: 15,492,668 (GRCm39) |
S208C |
probably damaging |
Het |
Or10q1 |
T |
C |
19: 13,726,502 (GRCm39) |
S11P |
probably damaging |
Het |
Or2n1d |
A |
T |
17: 38,646,755 (GRCm39) |
K236* |
probably null |
Het |
Or5p75-ps1 |
T |
A |
7: 108,107,611 (GRCm39) |
F116Y |
unknown |
Het |
Or7d9 |
T |
A |
9: 20,197,826 (GRCm39) |
M285K |
probably damaging |
Het |
Padi4 |
A |
C |
4: 140,488,983 (GRCm39) |
V152G |
probably damaging |
Het |
Pdzd7 |
A |
T |
19: 45,025,450 (GRCm39) |
D348E |
probably damaging |
Het |
Pdzph1 |
T |
A |
17: 59,186,154 (GRCm39) |
K1212N |
possibly damaging |
Het |
Piezo2 |
C |
T |
18: 63,160,634 (GRCm39) |
G2341R |
probably damaging |
Het |
Plb1 |
A |
G |
5: 32,511,028 (GRCm39) |
K1298E |
probably benign |
Het |
Prr14l |
A |
G |
5: 32,985,982 (GRCm39) |
L1171P |
probably benign |
Het |
Rab11fip5 |
T |
C |
6: 85,318,850 (GRCm39) |
T680A |
probably benign |
Het |
Rev1 |
A |
T |
1: 38,127,146 (GRCm39) |
N371K |
possibly damaging |
Het |
Rsf1 |
CGGCGGCGG |
CGGCGGCGGGGGCGGCGG |
7: 97,229,133 (GRCm39) |
|
probably benign |
Het |
Ryr2 |
A |
G |
13: 11,799,997 (GRCm39) |
C917R |
probably damaging |
Het |
Sall1 |
A |
T |
8: 89,757,549 (GRCm39) |
S852T |
possibly damaging |
Het |
Serpine2 |
A |
G |
1: 79,779,272 (GRCm39) |
F296L |
probably damaging |
Het |
Slc12a6 |
A |
T |
2: 112,182,887 (GRCm39) |
N754I |
probably damaging |
Het |
Slc39a6 |
A |
T |
18: 24,718,332 (GRCm39) |
L575Q |
probably damaging |
Het |
Smarcc2 |
T |
A |
10: 128,321,475 (GRCm39) |
L890Q |
probably damaging |
Het |
Smg5 |
T |
A |
3: 88,268,378 (GRCm39) |
V1006D |
probably damaging |
Het |
Ssh2 |
T |
C |
11: 77,283,899 (GRCm39) |
V51A |
probably damaging |
Het |
St14 |
T |
C |
9: 31,008,195 (GRCm39) |
K547E |
probably benign |
Het |
Stag1 |
T |
G |
9: 100,678,781 (GRCm39) |
V234G |
probably damaging |
Het |
Stag3 |
A |
T |
5: 138,280,207 (GRCm39) |
Q24L |
probably benign |
Het |
Stra6 |
T |
C |
9: 58,048,380 (GRCm39) |
Y158H |
probably damaging |
Het |
Tcstv1a |
A |
T |
13: 120,355,666 (GRCm39) |
|
probably null |
Het |
Tmem196 |
G |
A |
12: 119,975,002 (GRCm39) |
C62Y |
probably damaging |
Het |
Tmem265 |
T |
A |
7: 127,164,039 (GRCm39) |
F84L |
|
Het |
Tph1 |
C |
T |
7: 46,306,627 (GRCm39) |
|
probably null |
Het |
Ttn |
A |
G |
2: 76,776,834 (GRCm39) |
I1522T |
unknown |
Het |
Ulk4 |
T |
A |
9: 121,084,178 (GRCm39) |
Q129L |
probably benign |
Het |
Usp17la |
T |
A |
7: 104,510,792 (GRCm39) |
S466T |
probably benign |
Het |
Vmn2r31 |
A |
T |
7: 7,387,744 (GRCm39) |
V609E |
probably damaging |
Het |
Vmn2r52 |
C |
T |
7: 9,904,744 (GRCm39) |
C365Y |
probably benign |
Het |
Zbtb4 |
A |
T |
11: 69,666,937 (GRCm39) |
T81S |
possibly damaging |
Het |
Zfp605 |
A |
T |
5: 110,259,885 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Greb1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00155:Greb1
|
APN |
12 |
16,761,962 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01316:Greb1
|
APN |
12 |
16,748,587 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01464:Greb1
|
APN |
12 |
16,764,827 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01474:Greb1
|
APN |
12 |
16,734,502 (GRCm39) |
missense |
probably benign |
|
IGL01522:Greb1
|
APN |
12 |
16,751,202 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01824:Greb1
|
APN |
12 |
16,761,717 (GRCm39) |
nonsense |
probably null |
|
IGL01837:Greb1
|
APN |
12 |
16,734,452 (GRCm39) |
missense |
probably benign |
0.19 |
IGL01991:Greb1
|
APN |
12 |
16,749,682 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01996:Greb1
|
APN |
12 |
16,740,846 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL02213:Greb1
|
APN |
12 |
16,756,233 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02267:Greb1
|
APN |
12 |
16,767,209 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02512:Greb1
|
APN |
12 |
16,742,713 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02583:Greb1
|
APN |
12 |
16,756,296 (GRCm39) |
splice site |
probably benign |
|
IGL02613:Greb1
|
APN |
12 |
16,789,889 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02648:Greb1
|
APN |
12 |
16,758,683 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02679:Greb1
|
APN |
12 |
16,758,724 (GRCm39) |
missense |
probably damaging |
1.00 |
begraben
|
UTSW |
12 |
16,734,374 (GRCm39) |
missense |
possibly damaging |
0.51 |
Eared
|
UTSW |
12 |
16,723,864 (GRCm39) |
missense |
probably damaging |
1.00 |
Humpback
|
UTSW |
12 |
16,751,172 (GRCm39) |
missense |
probably damaging |
1.00 |
pied_billed
|
UTSW |
12 |
16,774,858 (GRCm39) |
missense |
possibly damaging |
0.79 |
rednecked
|
UTSW |
12 |
16,732,153 (GRCm39) |
missense |
probably damaging |
0.99 |
G1patch:Greb1
|
UTSW |
12 |
16,738,568 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03048:Greb1
|
UTSW |
12 |
16,783,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R0083:Greb1
|
UTSW |
12 |
16,746,452 (GRCm39) |
missense |
probably benign |
|
R0100:Greb1
|
UTSW |
12 |
16,730,225 (GRCm39) |
missense |
probably benign |
0.41 |
R0100:Greb1
|
UTSW |
12 |
16,730,225 (GRCm39) |
missense |
probably benign |
0.41 |
R0220:Greb1
|
UTSW |
12 |
16,732,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R0245:Greb1
|
UTSW |
12 |
16,746,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R0540:Greb1
|
UTSW |
12 |
16,732,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R0547:Greb1
|
UTSW |
12 |
16,773,412 (GRCm39) |
missense |
probably benign |
|
R0563:Greb1
|
UTSW |
12 |
16,730,268 (GRCm39) |
missense |
probably benign |
0.23 |
R0607:Greb1
|
UTSW |
12 |
16,732,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R0610:Greb1
|
UTSW |
12 |
16,746,443 (GRCm39) |
missense |
probably benign |
|
R0652:Greb1
|
UTSW |
12 |
16,746,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R0659:Greb1
|
UTSW |
12 |
16,730,213 (GRCm39) |
missense |
probably damaging |
0.99 |
R0945:Greb1
|
UTSW |
12 |
16,723,803 (GRCm39) |
missense |
probably benign |
0.31 |
R1055:Greb1
|
UTSW |
12 |
16,732,252 (GRCm39) |
missense |
probably damaging |
0.98 |
R1445:Greb1
|
UTSW |
12 |
16,757,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R1471:Greb1
|
UTSW |
12 |
16,761,775 (GRCm39) |
missense |
probably damaging |
0.97 |
R1503:Greb1
|
UTSW |
12 |
16,774,820 (GRCm39) |
nonsense |
probably null |
|
R1566:Greb1
|
UTSW |
12 |
16,761,829 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1614:Greb1
|
UTSW |
12 |
16,751,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R1623:Greb1
|
UTSW |
12 |
16,724,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R1751:Greb1
|
UTSW |
12 |
16,773,439 (GRCm39) |
splice site |
probably benign |
|
R1778:Greb1
|
UTSW |
12 |
16,740,895 (GRCm39) |
missense |
probably benign |
|
R1842:Greb1
|
UTSW |
12 |
16,746,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R2040:Greb1
|
UTSW |
12 |
16,752,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R2153:Greb1
|
UTSW |
12 |
16,749,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R2178:Greb1
|
UTSW |
12 |
16,746,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R2194:Greb1
|
UTSW |
12 |
16,740,909 (GRCm39) |
missense |
probably benign |
0.08 |
R2248:Greb1
|
UTSW |
12 |
16,730,379 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2474:Greb1
|
UTSW |
12 |
16,764,954 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2509:Greb1
|
UTSW |
12 |
16,774,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R2860:Greb1
|
UTSW |
12 |
16,761,746 (GRCm39) |
missense |
probably benign |
0.28 |
R2861:Greb1
|
UTSW |
12 |
16,761,746 (GRCm39) |
missense |
probably benign |
0.28 |
R2862:Greb1
|
UTSW |
12 |
16,761,746 (GRCm39) |
missense |
probably benign |
0.28 |
R2866:Greb1
|
UTSW |
12 |
16,749,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R2890:Greb1
|
UTSW |
12 |
16,754,479 (GRCm39) |
missense |
probably damaging |
1.00 |
R3056:Greb1
|
UTSW |
12 |
16,738,592 (GRCm39) |
missense |
probably damaging |
0.96 |
R3863:Greb1
|
UTSW |
12 |
16,752,421 (GRCm39) |
missense |
probably damaging |
1.00 |
R3864:Greb1
|
UTSW |
12 |
16,752,421 (GRCm39) |
missense |
probably damaging |
1.00 |
R3956:Greb1
|
UTSW |
12 |
16,732,300 (GRCm39) |
missense |
probably damaging |
1.00 |
R4493:Greb1
|
UTSW |
12 |
16,748,611 (GRCm39) |
missense |
probably benign |
0.14 |
R4548:Greb1
|
UTSW |
12 |
16,749,676 (GRCm39) |
missense |
probably damaging |
1.00 |
R4683:Greb1
|
UTSW |
12 |
16,761,774 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4739:Greb1
|
UTSW |
12 |
16,746,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R4770:Greb1
|
UTSW |
12 |
16,731,357 (GRCm39) |
missense |
probably benign |
0.03 |
R4838:Greb1
|
UTSW |
12 |
16,734,361 (GRCm39) |
critical splice donor site |
probably null |
|
R4925:Greb1
|
UTSW |
12 |
16,731,472 (GRCm39) |
missense |
probably damaging |
1.00 |
R4982:Greb1
|
UTSW |
12 |
16,774,762 (GRCm39) |
missense |
probably damaging |
0.98 |
R5009:Greb1
|
UTSW |
12 |
16,774,858 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5086:Greb1
|
UTSW |
12 |
16,758,023 (GRCm39) |
intron |
probably benign |
|
R5213:Greb1
|
UTSW |
12 |
16,764,791 (GRCm39) |
nonsense |
probably null |
|
R5310:Greb1
|
UTSW |
12 |
16,766,760 (GRCm39) |
missense |
probably benign |
0.09 |
R5353:Greb1
|
UTSW |
12 |
16,738,567 (GRCm39) |
nonsense |
probably null |
|
R5544:Greb1
|
UTSW |
12 |
16,723,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R5605:Greb1
|
UTSW |
12 |
16,758,727 (GRCm39) |
missense |
probably damaging |
0.96 |
R5708:Greb1
|
UTSW |
12 |
16,723,843 (GRCm39) |
missense |
probably benign |
0.11 |
R5837:Greb1
|
UTSW |
12 |
16,738,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R5890:Greb1
|
UTSW |
12 |
16,783,422 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5938:Greb1
|
UTSW |
12 |
16,767,259 (GRCm39) |
missense |
probably damaging |
1.00 |
R6049:Greb1
|
UTSW |
12 |
16,731,395 (GRCm39) |
missense |
probably damaging |
0.99 |
R6093:Greb1
|
UTSW |
12 |
16,734,487 (GRCm39) |
missense |
probably benign |
|
R6120:Greb1
|
UTSW |
12 |
16,758,622 (GRCm39) |
missense |
probably damaging |
0.99 |
R6175:Greb1
|
UTSW |
12 |
16,724,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R6247:Greb1
|
UTSW |
12 |
16,766,676 (GRCm39) |
missense |
probably damaging |
1.00 |
R6274:Greb1
|
UTSW |
12 |
16,785,152 (GRCm39) |
missense |
probably damaging |
0.97 |
R6376:Greb1
|
UTSW |
12 |
16,749,580 (GRCm39) |
missense |
probably damaging |
0.97 |
R6523:Greb1
|
UTSW |
12 |
16,734,374 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6557:Greb1
|
UTSW |
12 |
16,760,384 (GRCm39) |
missense |
probably benign |
0.00 |
R6602:Greb1
|
UTSW |
12 |
16,759,441 (GRCm39) |
missense |
probably benign |
0.44 |
R6621:Greb1
|
UTSW |
12 |
16,742,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R6645:Greb1
|
UTSW |
12 |
16,748,580 (GRCm39) |
missense |
probably benign |
0.07 |
R6725:Greb1
|
UTSW |
12 |
16,738,568 (GRCm39) |
missense |
probably damaging |
1.00 |
R6750:Greb1
|
UTSW |
12 |
16,738,584 (GRCm39) |
missense |
probably benign |
0.05 |
R6863:Greb1
|
UTSW |
12 |
16,734,421 (GRCm39) |
missense |
probably damaging |
1.00 |
R6914:Greb1
|
UTSW |
12 |
16,757,903 (GRCm39) |
missense |
probably damaging |
0.97 |
R6996:Greb1
|
UTSW |
12 |
16,773,355 (GRCm39) |
missense |
probably benign |
0.00 |
R7083:Greb1
|
UTSW |
12 |
16,773,315 (GRCm39) |
missense |
probably benign |
|
R7147:Greb1
|
UTSW |
12 |
16,783,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R7238:Greb1
|
UTSW |
12 |
16,724,673 (GRCm39) |
missense |
probably damaging |
0.99 |
R7290:Greb1
|
UTSW |
12 |
16,761,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R7358:Greb1
|
UTSW |
12 |
16,774,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R7526:Greb1
|
UTSW |
12 |
16,766,766 (GRCm39) |
missense |
probably benign |
0.00 |
R7530:Greb1
|
UTSW |
12 |
16,767,207 (GRCm39) |
missense |
probably benign |
0.02 |
R7536:Greb1
|
UTSW |
12 |
16,732,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R7643:Greb1
|
UTSW |
12 |
16,761,997 (GRCm39) |
missense |
probably damaging |
0.99 |
R7732:Greb1
|
UTSW |
12 |
16,723,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R7740:Greb1
|
UTSW |
12 |
16,790,122 (GRCm39) |
start gained |
probably benign |
|
R7747:Greb1
|
UTSW |
12 |
16,724,796 (GRCm39) |
missense |
probably benign |
0.01 |
R7760:Greb1
|
UTSW |
12 |
16,773,417 (GRCm39) |
missense |
probably benign |
|
R7937:Greb1
|
UTSW |
12 |
16,766,670 (GRCm39) |
missense |
probably damaging |
0.99 |
R8043:Greb1
|
UTSW |
12 |
16,761,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R8259:Greb1
|
UTSW |
12 |
16,774,925 (GRCm39) |
nonsense |
probably null |
|
R8553:Greb1
|
UTSW |
12 |
16,773,328 (GRCm39) |
missense |
probably benign |
0.00 |
R8559:Greb1
|
UTSW |
12 |
16,746,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R8690:Greb1
|
UTSW |
12 |
16,746,548 (GRCm39) |
missense |
probably benign |
0.03 |
R8830:Greb1
|
UTSW |
12 |
16,738,520 (GRCm39) |
missense |
probably benign |
0.35 |
R8911:Greb1
|
UTSW |
12 |
16,740,903 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8963:Greb1
|
UTSW |
12 |
16,774,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R8986:Greb1
|
UTSW |
12 |
16,734,457 (GRCm39) |
missense |
probably damaging |
0.99 |
R9013:Greb1
|
UTSW |
12 |
16,789,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R9279:Greb1
|
UTSW |
12 |
16,732,153 (GRCm39) |
missense |
probably damaging |
0.99 |
R9360:Greb1
|
UTSW |
12 |
16,790,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R9563:Greb1
|
UTSW |
12 |
16,774,824 (GRCm39) |
missense |
probably benign |
0.06 |
R9616:Greb1
|
UTSW |
12 |
16,790,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R9627:Greb1
|
UTSW |
12 |
16,756,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R9731:Greb1
|
UTSW |
12 |
16,738,598 (GRCm39) |
missense |
probably damaging |
1.00 |
R9761:Greb1
|
UTSW |
12 |
16,751,275 (GRCm39) |
missense |
probably benign |
0.05 |
Z1176:Greb1
|
UTSW |
12 |
16,746,757 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Greb1
|
UTSW |
12 |
16,752,492 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- AACATACCTGAGACGCCTGTG -3'
(R):5'- ACATGACTTCAGGCCAAGAG -3'
Sequencing Primer
(F):5'- TACCTGAGACGCCTGTGCATAC -3'
(R):5'- GTTGAATTTCTCCGAGATGCAAAACC -3'
|
Posted On |
2019-09-13 |