Incidental Mutation 'R4838:Greb1'
ID |
374441 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Greb1
|
Ensembl Gene |
ENSMUSG00000036523 |
Gene Name |
gene regulated by estrogen in breast cancer protein |
Synonyms |
5730583K22Rik |
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R4838 (G1)
|
Quality Score |
225 |
Status
|
Not 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 16734361 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000124348
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000048064]
[ENSMUST00000048064]
[ENSMUST00000048064]
[ENSMUST00000048064]
[ENSMUST00000159120]
[ENSMUST00000159120]
[ENSMUST00000159120]
[ENSMUST00000159120]
[ENSMUST00000162112]
[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: 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 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 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 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 |
noncoding transcript
Transcript: ENSMUST00000160755
|
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 |
|
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 |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000223113
|
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 96.9%
- 20x: 94.0%
|
Validation Efficiency |
|
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: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca15 |
T |
C |
7: 119,944,523 (GRCm39) |
V386A |
probably benign |
Het |
Adk |
G |
A |
14: 21,419,154 (GRCm39) |
A247T |
probably damaging |
Het |
Ankrd27 |
T |
A |
7: 35,291,231 (GRCm39) |
L9Q |
possibly damaging |
Het |
Atad2 |
A |
G |
15: 57,966,679 (GRCm39) |
L638P |
probably damaging |
Het |
Atf7ip |
T |
A |
6: 136,573,489 (GRCm39) |
D1009E |
probably benign |
Het |
Bend7 |
A |
T |
2: 4,749,133 (GRCm39) |
K83N |
probably damaging |
Het |
Bicc1 |
C |
T |
10: 70,781,146 (GRCm39) |
D562N |
possibly damaging |
Het |
Calcrl |
T |
A |
2: 84,181,549 (GRCm39) |
N200Y |
probably damaging |
Het |
Ccdc125 |
C |
A |
13: 100,814,453 (GRCm39) |
A11E |
possibly damaging |
Het |
Cd5l |
A |
G |
3: 87,273,258 (GRCm39) |
T76A |
probably benign |
Het |
Cdhr5 |
A |
T |
7: 140,853,644 (GRCm39) |
I2N |
probably damaging |
Het |
Cdk10 |
C |
T |
8: 123,957,353 (GRCm39) |
A230V |
probably damaging |
Het |
Cep128 |
T |
C |
12: 90,966,319 (GRCm39) |
|
probably benign |
Het |
Cep131 |
T |
C |
11: 119,966,982 (GRCm39) |
N186D |
probably damaging |
Het |
Cfhr4 |
T |
A |
1: 139,661,181 (GRCm39) |
D556V |
probably damaging |
Het |
Cog7 |
G |
T |
7: 121,570,604 (GRCm39) |
P168Q |
probably damaging |
Het |
Col28a1 |
T |
A |
6: 8,014,559 (GRCm39) |
M949L |
probably benign |
Het |
Coq8b |
T |
A |
7: 26,950,016 (GRCm39) |
M365K |
probably damaging |
Het |
Cpa1 |
A |
G |
6: 30,639,515 (GRCm39) |
E18G |
possibly damaging |
Het |
Csmd2 |
A |
G |
4: 128,411,542 (GRCm39) |
H2520R |
probably benign |
Het |
Cyp2c69 |
T |
C |
19: 39,866,038 (GRCm39) |
N185S |
probably benign |
Het |
Dpm1 |
G |
A |
2: 168,052,456 (GRCm39) |
T260I |
probably damaging |
Het |
Dtx3 |
A |
T |
10: 127,027,176 (GRCm39) |
|
probably null |
Het |
Eepd1 |
T |
C |
9: 25,500,756 (GRCm39) |
V401A |
possibly damaging |
Het |
Ehhadh |
A |
G |
16: 21,581,952 (GRCm39) |
S347P |
possibly damaging |
Het |
Elp3 |
A |
G |
14: 65,785,313 (GRCm39) |
|
probably null |
Het |
Enam |
C |
T |
5: 88,640,967 (GRCm39) |
Q210* |
probably null |
Het |
Epha1 |
C |
T |
6: 42,340,750 (GRCm39) |
R607H |
probably benign |
Het |
Erich6 |
A |
G |
3: 58,544,251 (GRCm39) |
I112T |
probably benign |
Het |
F830045P16Rik |
A |
G |
2: 129,302,470 (GRCm39) |
V374A |
possibly damaging |
Het |
Fam171a2 |
C |
A |
11: 102,329,511 (GRCm39) |
R416L |
possibly damaging |
Het |
Fbn1 |
T |
C |
2: 125,214,319 (GRCm39) |
N764S |
probably benign |
Het |
Fip1l1 |
C |
T |
5: 74,752,600 (GRCm39) |
T469I |
probably damaging |
Het |
Flad1 |
G |
A |
3: 89,313,217 (GRCm39) |
R342C |
probably damaging |
Het |
Fzd3 |
A |
G |
14: 65,477,269 (GRCm39) |
V95A |
probably benign |
Het |
Garem1 |
T |
C |
18: 21,280,950 (GRCm39) |
T469A |
probably benign |
Het |
Gm17093 |
A |
G |
14: 44,755,805 (GRCm39) |
Y24C |
unknown |
Het |
Grap2 |
T |
C |
15: 80,522,762 (GRCm39) |
V96A |
possibly damaging |
Het |
Grid2ip |
A |
T |
5: 143,374,530 (GRCm39) |
K913* |
probably null |
Het |
Gzmk |
T |
C |
13: 113,309,555 (GRCm39) |
D126G |
probably damaging |
Het |
Hibch |
A |
G |
1: 52,924,337 (GRCm39) |
I171V |
possibly damaging |
Het |
Hipk2 |
G |
T |
6: 38,795,339 (GRCm39) |
T310K |
possibly damaging |
Het |
Hk3 |
T |
C |
13: 55,154,231 (GRCm39) |
Y815C |
probably damaging |
Het |
Hps5 |
A |
T |
7: 46,437,778 (GRCm39) |
V99E |
probably damaging |
Het |
Hspg2 |
A |
G |
4: 137,268,977 (GRCm39) |
H2203R |
possibly damaging |
Het |
Il12rb2 |
A |
G |
6: 67,286,121 (GRCm39) |
V108A |
probably damaging |
Het |
Il6st |
C |
T |
13: 112,627,044 (GRCm39) |
R279* |
probably null |
Het |
Kdm2a |
A |
C |
19: 4,375,054 (GRCm39) |
S692R |
probably benign |
Het |
Kif13a |
T |
C |
13: 46,980,224 (GRCm39) |
K176R |
probably damaging |
Het |
Kif5b |
T |
C |
18: 6,216,869 (GRCm39) |
K485E |
probably damaging |
Het |
Ktn1 |
C |
T |
14: 47,963,413 (GRCm39) |
R1111* |
probably null |
Het |
Lrrc23 |
A |
T |
6: 124,755,152 (GRCm39) |
N128K |
probably benign |
Het |
Mad1l1 |
G |
A |
5: 140,286,017 (GRCm39) |
Q293* |
probably null |
Het |
Man1b1 |
A |
T |
2: 25,235,487 (GRCm39) |
I338F |
possibly damaging |
Het |
Marchf1 |
G |
T |
8: 66,921,015 (GRCm39) |
V225L |
probably damaging |
Het |
Matcap2 |
A |
T |
9: 22,335,673 (GRCm39) |
D97V |
probably damaging |
Het |
Mrpl3 |
A |
G |
9: 104,934,231 (GRCm39) |
D118G |
probably damaging |
Het |
Nomo1 |
A |
T |
7: 45,733,139 (GRCm39) |
Q1209L |
unknown |
Het |
Nrcam |
A |
G |
12: 44,620,802 (GRCm39) |
E949G |
probably damaging |
Het |
Olfm5 |
T |
G |
7: 103,803,572 (GRCm39) |
N297T |
probably damaging |
Het |
Or51h7 |
T |
A |
7: 102,591,453 (GRCm39) |
L110F |
probably damaging |
Het |
Pcdh7 |
A |
T |
5: 57,878,146 (GRCm39) |
N567I |
probably damaging |
Het |
Pkn1 |
A |
G |
8: 84,404,595 (GRCm39) |
L495P |
probably damaging |
Het |
Pkp1 |
T |
C |
1: 135,810,326 (GRCm39) |
S415G |
probably damaging |
Het |
Pou2f1 |
T |
A |
1: 165,744,492 (GRCm39) |
Q53L |
probably null |
Het |
Pramel26 |
G |
A |
4: 143,537,375 (GRCm39) |
Q319* |
probably null |
Het |
Prkce |
A |
G |
17: 86,937,511 (GRCm39) |
K648R |
probably benign |
Het |
Ptprh |
G |
A |
7: 4,576,429 (GRCm39) |
T277I |
possibly damaging |
Het |
Rpl31 |
C |
T |
1: 39,410,048 (GRCm39) |
R83C |
probably benign |
Het |
Rpusd3 |
G |
A |
6: 113,393,837 (GRCm39) |
Q194* |
probably null |
Het |
Sgsm1 |
T |
A |
5: 113,430,492 (GRCm39) |
N298Y |
probably damaging |
Het |
She |
G |
A |
3: 89,758,946 (GRCm39) |
G355D |
probably benign |
Het |
Shld2 |
A |
G |
14: 33,990,582 (GRCm39) |
V108A |
probably benign |
Het |
Snx11 |
C |
T |
11: 96,665,284 (GRCm39) |
E9K |
possibly damaging |
Het |
Soat1 |
C |
A |
1: 156,260,507 (GRCm39) |
A444S |
probably benign |
Het |
Sox6 |
T |
C |
7: 115,085,897 (GRCm39) |
Y690C |
probably damaging |
Het |
Spata13 |
T |
A |
14: 60,970,628 (GRCm39) |
F10I |
probably benign |
Het |
St18 |
C |
A |
1: 6,873,129 (GRCm39) |
T288K |
probably benign |
Het |
Tifa |
C |
T |
3: 127,590,235 (GRCm39) |
S2F |
probably damaging |
Het |
Tmem232 |
A |
T |
17: 65,737,883 (GRCm39) |
S392R |
probably benign |
Het |
Tmtc3 |
T |
C |
10: 100,302,082 (GRCm39) |
N289S |
probably damaging |
Het |
Tpo |
A |
G |
12: 30,142,633 (GRCm39) |
F697S |
probably damaging |
Het |
Trp53 |
A |
G |
11: 69,478,456 (GRCm39) |
T122A |
probably damaging |
Het |
Trps1 |
A |
C |
15: 50,690,712 (GRCm39) |
I10S |
probably benign |
Het |
Tubgcp5 |
C |
T |
7: 55,443,933 (GRCm39) |
|
probably benign |
Het |
Unc13c |
T |
G |
9: 73,839,354 (GRCm39) |
Y499S |
possibly damaging |
Het |
Unc45a |
C |
A |
7: 79,982,783 (GRCm39) |
D381Y |
probably damaging |
Het |
Upf1 |
G |
C |
8: 70,792,018 (GRCm39) |
H402Q |
probably benign |
Het |
Uroc1 |
A |
T |
6: 90,326,174 (GRCm39) |
I510F |
possibly damaging |
Het |
Usp15 |
A |
G |
10: 122,963,662 (GRCm39) |
F589L |
probably damaging |
Het |
Vmn2r76 |
T |
C |
7: 85,874,733 (GRCm39) |
Y748C |
probably damaging |
Het |
Wwp1 |
T |
C |
4: 19,662,143 (GRCm39) |
N151D |
probably benign |
Het |
Zbtb40 |
A |
T |
4: 136,728,527 (GRCm39) |
S439T |
probably benign |
Het |
Zbtb6 |
A |
T |
2: 37,318,728 (GRCm39) |
L400* |
probably null |
Het |
Zfp125 |
C |
T |
12: 20,949,961 (GRCm39) |
|
noncoding transcript |
Het |
Zmynd8 |
A |
C |
2: 165,681,954 (GRCm39) |
Y183* |
probably null |
Het |
Zpld2 |
A |
G |
4: 133,920,410 (GRCm39) |
V585A |
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 |
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 |
R7395:Greb1
|
UTSW |
12 |
16,759,431 (GRCm39) |
critical splice donor site |
probably null |
|
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'- CTTACAGCAACTGTTACGGC -3'
(R):5'- ACTGTGACGCTAAGCTCTG -3'
Sequencing Primer
(F):5'- GATCTCATGTAGCCCAGATTGGAC -3'
(R):5'- GTGCTCTCCCCTCGCAC -3'
|
Posted On |
2016-03-16 |