Incidental Mutation 'R8493:Notch1'
| ID |
658095 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Notch1
|
| Ensembl Gene |
ENSMUSG00000026923 |
| Gene Name |
notch 1 |
| Synonyms |
9930111A19Rik, Motch A, Tan1, Mis6, lin-12, N1 |
| MMRRC Submission |
067935-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R8493 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
2 |
| Chromosomal Location |
26347914-26393834 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 26362251 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Alanine
at position 27
(V27A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000115258
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000028288]
[ENSMUST00000132820]
|
| AlphaFold |
Q01705 |
| Predicted Effect |
silent
Transcript: ENSMUST00000028288
|
| SMART Domains |
Protein: ENSMUSP00000028288
Gene: ENSMUSG00000026923
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
18 |
N/A |
INTRINSIC |
|
EGF
|
23 |
58 |
1.63e1 |
SMART |
|
EGF
|
62 |
99 |
4.29e-5 |
SMART |
|
EGF
|
105 |
139 |
6.25e-7 |
SMART |
|
EGF_CA
|
140 |
176 |
1.02e-6 |
SMART |
|
EGF_CA
|
178 |
216 |
4.21e-13 |
SMART |
|
EGF
|
221 |
255 |
6.7e-7 |
SMART |
|
EGF_CA
|
257 |
293 |
6.8e-8 |
SMART |
|
EGF_CA
|
295 |
333 |
1.16e-10 |
SMART |
|
EGF_CA
|
335 |
371 |
3.17e-8 |
SMART |
|
EGF
|
375 |
410 |
5.32e-1 |
SMART |
|
EGF_CA
|
412 |
450 |
4.59e-14 |
SMART |
|
EGF_CA
|
452 |
488 |
1.02e-11 |
SMART |
|
EGF_CA
|
490 |
526 |
4.81e-8 |
SMART |
|
EGF_CA
|
528 |
564 |
3.19e-13 |
SMART |
|
EGF_CA
|
566 |
601 |
1.91e-11 |
SMART |
|
EGF_CA
|
603 |
639 |
1.78e-11 |
SMART |
|
EGF_CA
|
641 |
676 |
9.62e-8 |
SMART |
|
EGF_CA
|
678 |
714 |
2.38e-12 |
SMART |
|
EGF_CA
|
716 |
751 |
5.23e-9 |
SMART |
|
EGF_CA
|
753 |
789 |
6.25e-7 |
SMART |
|
EGF_CA
|
791 |
827 |
1.1e-11 |
SMART |
|
EGF
|
832 |
867 |
2.03e-6 |
SMART |
|
EGF_CA
|
869 |
905 |
5.73e-15 |
SMART |
|
EGF_CA
|
907 |
943 |
4.56e-9 |
SMART |
|
EGF_CA
|
945 |
981 |
1.64e-10 |
SMART |
|
EGF_CA
|
983 |
1019 |
5.83e-7 |
SMART |
|
EGF_CA
|
1021 |
1057 |
1.05e-13 |
SMART |
|
EGF
|
1062 |
1095 |
8.12e-6 |
SMART |
|
EGF
|
1100 |
1143 |
5.66e-5 |
SMART |
|
EGF_CA
|
1145 |
1181 |
1.1e-11 |
SMART |
|
EGF_CA
|
1183 |
1219 |
3.87e-12 |
SMART |
|
EGF_CA
|
1221 |
1265 |
2.89e-11 |
SMART |
|
EGF_CA
|
1267 |
1305 |
1.2e-8 |
SMART |
|
EGF
|
1310 |
1346 |
5.74e-6 |
SMART |
|
EGF
|
1351 |
1384 |
4.1e-2 |
SMART |
|
EGF
|
1390 |
1426 |
2.66e-1 |
SMART |
|
NL
|
1442 |
1480 |
4.08e-16 |
SMART |
|
NL
|
1483 |
1522 |
1.08e-15 |
SMART |
|
NL
|
1523 |
1562 |
7.39e-14 |
SMART |
|
NOD
|
1566 |
1622 |
1.81e-32 |
SMART |
|
NODP
|
1660 |
1722 |
3.27e-30 |
SMART |
|
low complexity region
|
1729 |
1746 |
N/A |
INTRINSIC |
|
ANK
|
1870 |
1912 |
1.07e2 |
SMART |
|
ANK
|
1917 |
1946 |
4.82e-3 |
SMART |
|
ANK
|
1950 |
1980 |
6.71e-2 |
SMART |
|
ANK
|
1984 |
2013 |
1.23e0 |
SMART |
|
ANK
|
2017 |
2046 |
9.13e-4 |
SMART |
|
ANK
|
2050 |
2079 |
2.97e-3 |
SMART |
|
low complexity region
|
2205 |
2222 |
N/A |
INTRINSIC |
|
low complexity region
|
2364 |
2395 |
N/A |
INTRINSIC |
|
DUF3454
|
2453 |
2517 |
2.01e-30 |
SMART |
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000132820
AA Change: V27A
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.8%
- 20x: 99.3%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the NOTCH family of proteins. Members of this Type I transmembrane protein family share structural characteristics including an extracellular domain consisting of multiple epidermal growth factor-like (EGF) repeats, and an intracellular domain consisting of multiple different domain types. Notch signaling is an evolutionarily conserved intercellular signaling pathway that regulates interactions between physically adjacent cells through binding of Notch family receptors to their cognate ligands. The encoded preproprotein is proteolytically processed in the trans-Golgi network to generate two polypeptide chains that heterodimerize to form the mature cell-surface receptor. This receptor plays a role in the development of numerous cell and tissue types. Mutations in this gene are associated with aortic valve disease, Adams-Oliver syndrome, T-cell acute lymphoblastic leukemia, chronic lymphocytic leukemia, and head and neck squamous cell carcinoma. [provided by RefSeq, Jan 2016]
PHENOTYPE: Homozygotes for null alleles exhibit defects in embryonic development resulting in lethality at some point in organogenesis. Lethal phenotype may be affected by genetic background. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 78 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930562C15Rik |
A |
T |
16: 4,653,453 (GRCm39) |
M1L |
unknown |
Het |
| Abca13 |
T |
A |
11: 9,460,668 (GRCm39) |
I4226N |
probably damaging |
Het |
| Ankrd10 |
C |
A |
8: 11,678,518 (GRCm39) |
E125* |
probably null |
Het |
| Apob |
A |
T |
12: 8,059,009 (GRCm39) |
D2497V |
possibly damaging |
Het |
| Arap1 |
G |
A |
7: 101,035,725 (GRCm39) |
W87* |
probably null |
Het |
| Arhgef37 |
C |
T |
18: 61,640,277 (GRCm39) |
V261I |
probably benign |
Het |
| Arl4a |
A |
C |
12: 40,086,472 (GRCm39) |
C92G |
probably benign |
Het |
| Arrdc2 |
C |
T |
8: 71,289,501 (GRCm39) |
|
probably null |
Het |
| Atg16l1 |
A |
C |
1: 87,706,704 (GRCm39) |
T355P |
probably damaging |
Het |
| Card14 |
T |
G |
11: 119,224,435 (GRCm39) |
|
probably null |
Het |
| Cd109 |
G |
A |
9: 78,564,801 (GRCm39) |
V249I |
probably benign |
Het |
| Cdhr4 |
A |
G |
9: 107,873,453 (GRCm39) |
D395G |
probably damaging |
Het |
| Celsr1 |
C |
A |
15: 85,822,207 (GRCm39) |
M1703I |
possibly damaging |
Het |
| Cfap157 |
A |
G |
2: 32,669,752 (GRCm39) |
I277T |
probably benign |
Het |
| Chst4 |
A |
G |
8: 110,757,095 (GRCm39) |
V173A |
probably damaging |
Het |
| Clca4b |
T |
C |
3: 144,617,911 (GRCm39) |
N731D |
probably benign |
Het |
| Col11a2 |
A |
G |
17: 34,278,936 (GRCm39) |
E1122G |
possibly damaging |
Het |
| Csf1r |
C |
G |
18: 61,247,954 (GRCm39) |
P341A |
probably damaging |
Het |
| Dclk3 |
A |
G |
9: 111,297,215 (GRCm39) |
E253G |
probably benign |
Het |
| Dnah2 |
T |
A |
11: 69,343,804 (GRCm39) |
D2829V |
probably damaging |
Het |
| Dnah7a |
T |
C |
1: 53,512,067 (GRCm39) |
N2998S |
probably damaging |
Het |
| Ehbp1 |
C |
T |
11: 22,235,842 (GRCm39) |
|
probably benign |
Het |
| Eprs1 |
A |
T |
1: 185,139,371 (GRCm39) |
K919* |
probably null |
Het |
| Esp16 |
A |
T |
17: 39,850,821 (GRCm39) |
K67* |
probably null |
Het |
| Fam169a |
G |
T |
13: 97,259,367 (GRCm39) |
E474D |
probably benign |
Het |
| Fam83h |
C |
T |
15: 75,874,502 (GRCm39) |
R945H |
probably benign |
Het |
| Flnb |
T |
A |
14: 7,869,822 (GRCm38) |
V195E |
probably damaging |
Het |
| Gm3159 |
T |
C |
14: 4,398,567 (GRCm38) |
I86T |
probably damaging |
Het |
| Gm4744 |
G |
A |
6: 40,926,281 (GRCm39) |
S103F |
|
Het |
| Gvin2 |
A |
G |
7: 105,548,088 (GRCm39) |
S1655P |
probably benign |
Het |
| Ift122 |
T |
A |
6: 115,887,292 (GRCm39) |
I713N |
probably benign |
Het |
| Ilkap |
A |
G |
1: 91,306,266 (GRCm39) |
I105T |
probably damaging |
Het |
| Isl1 |
G |
T |
13: 116,441,835 (GRCm39) |
H133N |
possibly damaging |
Het |
| Jade1 |
T |
A |
3: 41,559,113 (GRCm39) |
L398Q |
possibly damaging |
Het |
| Kcnh7 |
C |
T |
2: 62,681,003 (GRCm39) |
V195M |
probably benign |
Het |
| Kif3a |
A |
T |
11: 53,489,627 (GRCm39) |
K669* |
probably null |
Het |
| L3mbtl4 |
G |
A |
17: 68,937,239 (GRCm39) |
R420H |
probably damaging |
Het |
| Mrgprb1 |
A |
T |
7: 48,097,321 (GRCm39) |
I197N |
probably damaging |
Het |
| Mthfd1 |
A |
G |
12: 76,340,929 (GRCm39) |
T263A |
probably damaging |
Het |
| Mtmr7 |
G |
A |
8: 41,059,927 (GRCm39) |
A62V |
possibly damaging |
Het |
| Naxe |
A |
G |
3: 87,965,757 (GRCm39) |
|
probably benign |
Het |
| Ndufs2 |
T |
C |
1: 171,068,677 (GRCm39) |
T51A |
probably benign |
Het |
| Nlrc5 |
T |
A |
8: 95,249,848 (GRCm39) |
L1824Q |
probably damaging |
Het |
| Nucks1 |
A |
T |
1: 131,857,473 (GRCm39) |
M169L |
probably benign |
Het |
| Or10ag53 |
T |
A |
2: 87,083,215 (GRCm39) |
D311E |
probably benign |
Het |
| Or13p4 |
C |
T |
4: 118,547,229 (GRCm39) |
S140N |
probably benign |
Het |
| Or4a80 |
T |
A |
2: 89,582,599 (GRCm39) |
Y191F |
probably benign |
Het |
| Or4k45 |
T |
A |
2: 111,395,324 (GRCm39) |
H155L |
probably damaging |
Het |
| Or51aa2 |
A |
T |
7: 103,187,479 (GRCm39) |
S321T |
probably benign |
Het |
| Or52n20 |
G |
T |
7: 104,320,022 (GRCm39) |
V38L |
probably benign |
Het |
| Or5w10 |
T |
A |
2: 87,375,114 (GRCm39) |
Y258F |
probably damaging |
Het |
| Pcnt |
C |
T |
10: 76,239,457 (GRCm39) |
|
probably null |
Het |
| Pdcd7 |
T |
C |
9: 65,254,039 (GRCm39) |
S206P |
probably benign |
Het |
| Pdia4 |
A |
T |
6: 47,773,575 (GRCm39) |
Y591* |
probably null |
Het |
| Pgap6 |
G |
T |
17: 26,340,931 (GRCm39) |
R678L |
probably damaging |
Het |
| Plxna4 |
C |
T |
6: 32,192,647 (GRCm39) |
M771I |
probably benign |
Het |
| Pramel47 |
C |
T |
5: 95,488,092 (GRCm39) |
H9Y |
possibly damaging |
Het |
| Ptpn13 |
A |
G |
5: 103,712,031 (GRCm39) |
Y1643C |
probably damaging |
Het |
| Ptpn13 |
A |
G |
5: 103,717,671 (GRCm39) |
I1906V |
probably benign |
Het |
| Rab33b |
T |
A |
3: 51,391,795 (GRCm39) |
S15T |
probably benign |
Het |
| Rasip1 |
A |
T |
7: 45,284,467 (GRCm39) |
M644L |
possibly damaging |
Het |
| Rnf4 |
G |
A |
5: 34,506,035 (GRCm39) |
C55Y |
probably damaging |
Het |
| Sel1l |
A |
T |
12: 91,780,735 (GRCm39) |
Y585* |
probably null |
Het |
| Slc40a1 |
A |
T |
1: 45,950,576 (GRCm39) |
F292Y |
probably damaging |
Het |
| Smarca4 |
G |
A |
9: 21,570,144 (GRCm39) |
D716N |
probably damaging |
Het |
| Sp7 |
T |
A |
15: 102,266,837 (GRCm39) |
H323L |
possibly damaging |
Het |
| Speer1m |
T |
C |
5: 11,971,489 (GRCm39) |
L147P |
probably damaging |
Het |
| Sprtn |
A |
G |
8: 125,629,933 (GRCm39) |
S409G |
probably benign |
Het |
| St3gal2 |
T |
G |
8: 111,688,853 (GRCm39) |
L131R |
probably damaging |
Het |
| Tctn1 |
A |
G |
5: 122,399,552 (GRCm39) |
C91R |
probably damaging |
Het |
| Tgm1 |
A |
T |
14: 55,937,754 (GRCm39) |
V785E |
probably damaging |
Het |
| Topaz1 |
G |
T |
9: 122,579,573 (GRCm39) |
V828L |
probably benign |
Het |
| Triobp |
C |
T |
15: 78,878,326 (GRCm39) |
H1750Y |
possibly damaging |
Het |
| Ttc27 |
G |
A |
17: 75,050,047 (GRCm39) |
|
probably null |
Het |
| Usp2 |
G |
A |
9: 43,987,350 (GRCm39) |
G216D |
possibly damaging |
Het |
| Vmn2r99 |
A |
G |
17: 19,614,020 (GRCm39) |
D580G |
probably benign |
Het |
| Wbp1l |
G |
A |
19: 46,640,988 (GRCm39) |
R106H |
possibly damaging |
Het |
| Zmym2 |
G |
T |
14: 57,151,606 (GRCm39) |
C497F |
probably damaging |
Het |
|
| Other mutations in Notch1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00164:Notch1
|
APN |
2 |
26,350,058 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL01343:Notch1
|
APN |
2 |
26,362,917 (GRCm39) |
missense |
probably benign |
0.25 |
|
IGL02066:Notch1
|
APN |
2 |
26,350,408 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
IGL02158:Notch1
|
APN |
2 |
26,350,351 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02541:Notch1
|
APN |
2 |
26,358,515 (GRCm39) |
missense |
probably benign |
0.12 |
|
IGL03280:Notch1
|
APN |
2 |
26,367,886 (GRCm39) |
intron |
probably benign |
|
|
IGL03338:Notch1
|
APN |
2 |
26,349,971 (GRCm39) |
missense |
probably benign |
|
|
Antero
|
UTSW |
2 |
26,366,126 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
march
|
UTSW |
2 |
26,359,911 (GRCm39) |
missense |
probably damaging |
0.98 |
|
PIT4494001:Notch1
|
UTSW |
2 |
26,356,485 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0013:Notch1
|
UTSW |
2 |
26,363,830 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R0025:Notch1
|
UTSW |
2 |
26,360,943 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0129:Notch1
|
UTSW |
2 |
26,350,470 (GRCm39) |
missense |
probably benign |
0.06 |
|
R0285:Notch1
|
UTSW |
2 |
26,350,873 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R0531:Notch1
|
UTSW |
2 |
26,356,584 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0747:Notch1
|
UTSW |
2 |
26,362,152 (GRCm39) |
missense |
unknown |
|
|
R1440:Notch1
|
UTSW |
2 |
26,370,976 (GRCm39) |
intron |
probably benign |
|
|
R1502:Notch1
|
UTSW |
2 |
26,374,335 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R1539:Notch1
|
UTSW |
2 |
26,362,125 (GRCm39) |
nonsense |
probably null |
|
|
R1623:Notch1
|
UTSW |
2 |
26,368,624 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R1844:Notch1
|
UTSW |
2 |
26,350,446 (GRCm39) |
missense |
probably benign |
0.12 |
|
R1863:Notch1
|
UTSW |
2 |
26,359,962 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1874:Notch1
|
UTSW |
2 |
26,371,591 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R1926:Notch1
|
UTSW |
2 |
26,371,669 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2156:Notch1
|
UTSW |
2 |
26,350,873 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R2196:Notch1
|
UTSW |
2 |
26,353,816 (GRCm39) |
nonsense |
probably null |
|
|
R2209:Notch1
|
UTSW |
2 |
26,350,019 (GRCm39) |
missense |
probably benign |
|
|
R2382:Notch1
|
UTSW |
2 |
26,363,793 (GRCm39) |
missense |
probably benign |
0.40 |
|
R2508:Notch1
|
UTSW |
2 |
26,355,485 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R2873:Notch1
|
UTSW |
2 |
26,350,247 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R2874:Notch1
|
UTSW |
2 |
26,350,247 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R3798:Notch1
|
UTSW |
2 |
26,368,630 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4019:Notch1
|
UTSW |
2 |
26,371,154 (GRCm39) |
missense |
probably benign |
0.03 |
|
R4305:Notch1
|
UTSW |
2 |
26,367,936 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4334:Notch1
|
UTSW |
2 |
26,350,048 (GRCm39) |
missense |
probably benign |
0.22 |
|
R4504:Notch1
|
UTSW |
2 |
26,362,189 (GRCm39) |
missense |
probably benign |
0.16 |
|
R4624:Notch1
|
UTSW |
2 |
26,368,093 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R4659:Notch1
|
UTSW |
2 |
26,360,901 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4703:Notch1
|
UTSW |
2 |
26,361,170 (GRCm39) |
missense |
probably benign |
|
|
R4869:Notch1
|
UTSW |
2 |
26,361,191 (GRCm39) |
missense |
probably benign |
0.21 |
|
R4938:Notch1
|
UTSW |
2 |
26,364,136 (GRCm39) |
nonsense |
probably null |
|
|
R4989:Notch1
|
UTSW |
2 |
26,371,193 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5010:Notch1
|
UTSW |
2 |
26,366,126 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
R5283:Notch1
|
UTSW |
2 |
26,358,638 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5303:Notch1
|
UTSW |
2 |
26,368,631 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5635:Notch1
|
UTSW |
2 |
26,366,173 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5755:Notch1
|
UTSW |
2 |
26,363,704 (GRCm39) |
missense |
probably benign |
0.12 |
|
R5926:Notch1
|
UTSW |
2 |
26,366,116 (GRCm39) |
missense |
probably benign |
0.35 |
|
R5947:Notch1
|
UTSW |
2 |
26,352,540 (GRCm39) |
intron |
probably benign |
|
|
R6053:Notch1
|
UTSW |
2 |
26,362,924 (GRCm39) |
missense |
probably benign |
0.06 |
|
R6161:Notch1
|
UTSW |
2 |
26,358,743 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6162:Notch1
|
UTSW |
2 |
26,352,207 (GRCm39) |
missense |
probably benign |
|
|
R6174:Notch1
|
UTSW |
2 |
26,375,454 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R6199:Notch1
|
UTSW |
2 |
26,359,911 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6209:Notch1
|
UTSW |
2 |
26,362,817 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6251:Notch1
|
UTSW |
2 |
26,364,182 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R6493:Notch1
|
UTSW |
2 |
26,362,110 (GRCm39) |
missense |
unknown |
|
|
R6723:Notch1
|
UTSW |
2 |
26,368,118 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6736:Notch1
|
UTSW |
2 |
26,350,298 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7020:Notch1
|
UTSW |
2 |
26,371,586 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R7058:Notch1
|
UTSW |
2 |
26,353,830 (GRCm39) |
missense |
probably benign |
0.05 |
|
R7154:Notch1
|
UTSW |
2 |
26,349,950 (GRCm39) |
missense |
probably benign |
|
|
R7291:Notch1
|
UTSW |
2 |
26,366,387 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7379:Notch1
|
UTSW |
2 |
26,369,479 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7560:Notch1
|
UTSW |
2 |
26,350,177 (GRCm39) |
missense |
probably benign |
0.43 |
|
R7610:Notch1
|
UTSW |
2 |
26,368,191 (GRCm39) |
missense |
probably benign |
0.13 |
|
R7833:Notch1
|
UTSW |
2 |
26,349,545 (GRCm39) |
makesense |
probably null |
|
|
R7988:Notch1
|
UTSW |
2 |
26,361,013 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8514:Notch1
|
UTSW |
2 |
26,362,181 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8523:Notch1
|
UTSW |
2 |
26,354,917 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R8677:Notch1
|
UTSW |
2 |
26,359,936 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8696:Notch1
|
UTSW |
2 |
26,368,004 (GRCm39) |
critical splice acceptor site |
probably benign |
|
|
R8833:Notch1
|
UTSW |
2 |
26,371,615 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8964:Notch1
|
UTSW |
2 |
26,371,062 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R9091:Notch1
|
UTSW |
2 |
26,369,895 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9144:Notch1
|
UTSW |
2 |
26,349,587 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9145:Notch1
|
UTSW |
2 |
26,349,587 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9151:Notch1
|
UTSW |
2 |
26,367,939 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9270:Notch1
|
UTSW |
2 |
26,369,895 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9463:Notch1
|
UTSW |
2 |
26,359,845 (GRCm39) |
missense |
probably benign |
0.20 |
|
R9546:Notch1
|
UTSW |
2 |
26,371,127 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R9674:Notch1
|
UTSW |
2 |
26,361,308 (GRCm39) |
missense |
probably damaging |
0.98 |
|
X0018:Notch1
|
UTSW |
2 |
26,352,239 (GRCm39) |
nonsense |
probably null |
|
|
X0066:Notch1
|
UTSW |
2 |
26,360,347 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
Z1088:Notch1
|
UTSW |
2 |
26,367,127 (GRCm39) |
missense |
probably damaging |
0.99 |
|
Z1177:Notch1
|
UTSW |
2 |
26,350,321 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
| Predicted Primers |
PCR Primer
(F):5'- ACCAATGATGACACCAGGG -3'
(R):5'- CAACCACCACGTGTCTATATGC -3'
Sequencing Primer
(F):5'- ATGATGACACCAGGGAGCCTC -3'
(R):5'- GCTATAAAATCTCTGCTCGTGATTTG -3'
|
| Posted On |
2021-01-18 |
Incidental Mutation