Incidental Mutation 'R7726:Men1'
ID |
595529 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Men1
|
Ensembl Gene |
ENSMUSG00000024947 |
Gene Name |
multiple endocrine neoplasia 1 |
Synonyms |
menin |
MMRRC Submission |
045782-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R7726 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
19 |
Chromosomal Location |
6385009-6390921 bp(+) (GRCm39) |
Type of Mutation |
critical splice donor site (1 bp from exon) |
DNA Base Change (assembly) |
G to A
at 6387312 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000109130
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000025897]
[ENSMUST00000056391]
[ENSMUST00000078137]
[ENSMUST00000079327]
[ENSMUST00000113500]
[ENSMUST00000113501]
[ENSMUST00000113502]
[ENSMUST00000113502]
[ENSMUST00000113502]
[ENSMUST00000113503]
[ENSMUST00000113504]
[ENSMUST00000124556]
[ENSMUST00000130382]
[ENSMUST00000142496]
[ENSMUST00000152349]
[ENSMUST00000166909]
[ENSMUST00000170132]
|
AlphaFold |
O88559 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000025897
|
SMART Domains |
Protein: ENSMUSP00000025897 Gene: ENSMUSG00000024948
Domain | Start | End | E-Value | Type |
S_TKc
|
16 |
273 |
2.41e-90 |
SMART |
low complexity region
|
358 |
369 |
N/A |
INTRINSIC |
low complexity region
|
425 |
444 |
N/A |
INTRINSIC |
CNH
|
488 |
801 |
1.31e-128 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000056391
|
SMART Domains |
Protein: ENSMUSP00000058149 Gene: ENSMUSG00000024947
Domain | Start | End | E-Value | Type |
Pfam:Menin
|
1 |
611 |
N/A |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000078137
|
SMART Domains |
Protein: ENSMUSP00000077272 Gene: ENSMUSG00000024947
Domain | Start | End | E-Value | Type |
Pfam:Menin
|
1 |
396 |
2.6e-241 |
PFAM |
Pfam:Menin
|
392 |
556 |
1.5e-62 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000079327
|
SMART Domains |
Protein: ENSMUSP00000078306 Gene: ENSMUSG00000024947
Domain | Start | End | E-Value | Type |
Pfam:Menin
|
1 |
611 |
N/A |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000113500
|
SMART Domains |
Protein: ENSMUSP00000109128 Gene: ENSMUSG00000024947
Domain | Start | End | E-Value | Type |
Pfam:Menin
|
1 |
611 |
N/A |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000113501
|
SMART Domains |
Protein: ENSMUSP00000109129 Gene: ENSMUSG00000024947
Domain | Start | End | E-Value | Type |
Pfam:Menin
|
1 |
183 |
2.6e-104 |
PFAM |
Pfam:Menin
|
184 |
576 |
3.2e-213 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000113502
|
SMART Domains |
Protein: ENSMUSP00000109130 Gene: ENSMUSG00000024947
Domain | Start | End | E-Value | Type |
Pfam:Menin
|
7 |
515 |
1.5e-254 |
PFAM |
Pfam:Menin
|
536 |
615 |
4.9e-26 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000113502
|
SMART Domains |
Protein: ENSMUSP00000109130 Gene: ENSMUSG00000024947
Domain | Start | End | E-Value | Type |
Pfam:Menin
|
7 |
515 |
1.5e-254 |
PFAM |
Pfam:Menin
|
536 |
615 |
4.9e-26 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000113502
|
SMART Domains |
Protein: ENSMUSP00000109130 Gene: ENSMUSG00000024947
Domain | Start | End | E-Value | Type |
Pfam:Menin
|
7 |
515 |
1.5e-254 |
PFAM |
Pfam:Menin
|
536 |
615 |
4.9e-26 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000113503
|
SMART Domains |
Protein: ENSMUSP00000109131 Gene: ENSMUSG00000024947
Domain | Start | End | E-Value | Type |
Pfam:Menin
|
1 |
616 |
N/A |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000113504
|
SMART Domains |
Protein: ENSMUSP00000109132 Gene: ENSMUSG00000024947
Domain | Start | End | E-Value | Type |
Pfam:Menin
|
1 |
611 |
N/A |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000124556
|
SMART Domains |
Protein: ENSMUSP00000121375 Gene: ENSMUSG00000024948
Domain | Start | End | E-Value | Type |
Pfam:Pkinase
|
16 |
56 |
4e-7 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000130382
|
SMART Domains |
Protein: ENSMUSP00000120123 Gene: ENSMUSG00000024948
Domain | Start | End | E-Value | Type |
S_TKc
|
16 |
233 |
3.4e-14 |
SMART |
low complexity region
|
314 |
325 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000142496
|
SMART Domains |
Protein: ENSMUSP00000114243 Gene: ENSMUSG00000024948
Domain | Start | End | E-Value | Type |
Pfam:Pkinase
|
16 |
56 |
4e-7 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000152349
|
SMART Domains |
Protein: ENSMUSP00000115741 Gene: ENSMUSG00000024948
Domain | Start | End | E-Value | Type |
Pfam:Pkinase
|
16 |
57 |
3.7e-7 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000166909
|
SMART Domains |
Protein: ENSMUSP00000133085 Gene: ENSMUSG00000024947
Domain | Start | End | E-Value | Type |
Pfam:Menin
|
1 |
62 |
8.9e-29 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000170132
|
SMART Domains |
Protein: ENSMUSP00000126655 Gene: ENSMUSG00000024947
Domain | Start | End | E-Value | Type |
Pfam:Menin
|
1 |
135 |
1.6e-81 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000170292
|
SMART Domains |
Protein: ENSMUSP00000128607 Gene: ENSMUSG00000024947
Domain | Start | End | E-Value | Type |
Pfam:Menin
|
4 |
106 |
1.2e-28 |
PFAM |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.8%
|
Validation Efficiency |
100% (65/65) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes menin, a putative tumor suppressor associated with a syndrome known as multiple endocrine neoplasia type 1. In vitro studies have shown menin is localized to the nucleus, possesses two functional nuclear localization signals, and inhibits transcriptional activation by JunD, however, the function of this protein is not known. Two messages have been detected on northern blots but the larger message has not been characterized. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2008] PHENOTYPE: Homozygotes for targeted null mutations die at embryonic day 11.5-13.5 with reduced size, edema, open neural tube and defects of the nervous system, heart and liver. Heterozygotes develop tumors of the pancreas, parathyroid, thyroid, adrenal and pituitary. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam34 |
T |
G |
8: 44,104,208 (GRCm39) |
N479T |
probably damaging |
Het |
Add3 |
C |
G |
19: 53,227,892 (GRCm39) |
L526V |
probably damaging |
Het |
Alas1 |
T |
C |
9: 106,124,150 (GRCm39) |
T3A |
probably benign |
Het |
Arap3 |
C |
T |
18: 38,122,520 (GRCm39) |
D579N |
probably damaging |
Het |
Armc6 |
C |
A |
8: 70,675,248 (GRCm39) |
D326Y |
probably damaging |
Het |
Atp6v1e2 |
G |
A |
17: 87,251,813 (GRCm39) |
T195I |
probably damaging |
Het |
Atrnl1 |
A |
G |
19: 57,690,504 (GRCm39) |
E904G |
probably damaging |
Het |
Bhlhe40 |
T |
A |
6: 108,639,559 (GRCm39) |
D112E |
probably benign |
Het |
Brf1 |
T |
G |
12: 112,927,865 (GRCm39) |
K438T |
probably benign |
Het |
Cabs1 |
A |
T |
5: 88,128,145 (GRCm39) |
E265D |
probably damaging |
Het |
Ccdc162 |
T |
A |
10: 41,429,071 (GRCm39) |
M1937L |
probably benign |
Het |
Cd55b |
A |
T |
1: 130,339,230 (GRCm39) |
S299R |
possibly damaging |
Het |
Chordc1 |
A |
G |
9: 18,213,510 (GRCm39) |
*120W |
probably null |
Het |
Col17a1 |
C |
A |
19: 47,643,629 (GRCm39) |
|
probably null |
Het |
Cpne8 |
A |
T |
15: 90,385,621 (GRCm39) |
I469K |
possibly damaging |
Het |
Crtac1 |
G |
T |
19: 42,290,690 (GRCm39) |
S337* |
probably null |
Het |
Cx3cl1 |
T |
C |
8: 95,506,867 (GRCm39) |
S291P |
probably damaging |
Het |
Dhx36 |
G |
T |
3: 62,396,389 (GRCm39) |
Q423K |
probably benign |
Het |
Eif3h |
G |
T |
15: 51,650,219 (GRCm39) |
Q322K |
possibly damaging |
Het |
Ero1b |
A |
G |
13: 12,620,722 (GRCm39) |
*494W |
probably null |
Het |
Exph5 |
G |
A |
9: 53,284,475 (GRCm39) |
V519I |
possibly damaging |
Het |
Fam184a |
C |
A |
10: 53,509,802 (GRCm39) |
E126* |
probably null |
Het |
Fam222b |
A |
G |
11: 78,044,577 (GRCm39) |
D46G |
probably damaging |
Het |
Fbxl6 |
C |
A |
15: 76,420,086 (GRCm39) |
R509L |
probably damaging |
Het |
Fgf14 |
T |
C |
14: 124,373,656 (GRCm39) |
Y86C |
probably damaging |
Het |
Fras1 |
A |
T |
5: 96,860,310 (GRCm39) |
I2119F |
probably benign |
Het |
Gpr37 |
G |
A |
6: 25,669,116 (GRCm39) |
T576I |
possibly damaging |
Het |
Hnrnpul2 |
G |
T |
19: 8,808,644 (GRCm39) |
R702L |
possibly damaging |
Het |
Iqgap1 |
T |
C |
7: 80,407,204 (GRCm39) |
N342S |
probably benign |
Het |
Kcnh6 |
T |
C |
11: 105,908,401 (GRCm39) |
V339A |
probably benign |
Het |
Klk1b9 |
A |
T |
7: 43,627,840 (GRCm39) |
N46I |
possibly damaging |
Het |
Kndc1 |
C |
A |
7: 139,519,751 (GRCm39) |
S1703R |
possibly damaging |
Het |
Lyn |
C |
A |
4: 3,756,428 (GRCm39) |
Y306* |
probably null |
Het |
Manba |
C |
T |
3: 135,223,770 (GRCm39) |
T219M |
probably benign |
Het |
Mastl |
T |
C |
2: 23,030,807 (GRCm39) |
|
probably null |
Het |
Med15 |
T |
G |
16: 17,473,038 (GRCm39) |
M550L |
possibly damaging |
Het |
Msh4 |
C |
T |
3: 153,571,957 (GRCm39) |
|
probably null |
Het |
Myh6 |
G |
T |
14: 55,202,822 (GRCm39) |
D32E |
probably damaging |
Het |
Ntmt2 |
A |
G |
1: 163,530,753 (GRCm39) |
C229R |
probably benign |
Het |
Ntn4 |
A |
G |
10: 93,569,544 (GRCm39) |
D419G |
possibly damaging |
Het |
Nup155 |
C |
T |
15: 8,151,623 (GRCm39) |
P393S |
probably damaging |
Het |
Or2y1d |
T |
A |
11: 49,321,727 (GRCm39) |
C141* |
probably null |
Het |
Or6b2b |
A |
T |
1: 92,419,029 (GRCm39) |
F149L |
probably benign |
Het |
Pakap |
C |
T |
4: 57,709,876 (GRCm39) |
P274S |
probably damaging |
Het |
Papss2 |
A |
T |
19: 32,611,403 (GRCm39) |
|
probably null |
Het |
Pcdhgc3 |
T |
C |
18: 37,939,932 (GRCm39) |
V111A |
possibly damaging |
Het |
Pcnx2 |
C |
T |
8: 126,577,069 (GRCm39) |
V988I |
probably benign |
Het |
Pom121 |
C |
T |
5: 135,407,002 (GRCm39) |
G1178S |
probably damaging |
Het |
Prss33 |
A |
G |
17: 24,053,203 (GRCm39) |
C213R |
probably damaging |
Het |
Scap |
G |
A |
9: 110,207,435 (GRCm39) |
|
probably null |
Het |
Shfl |
T |
C |
9: 20,784,461 (GRCm39) |
Y182H |
possibly damaging |
Het |
Sirpb1c |
T |
A |
3: 15,902,550 (GRCm39) |
I10F |
possibly damaging |
Het |
Slc28a2b |
A |
G |
2: 122,317,214 (GRCm39) |
E25G |
probably damaging |
Het |
Spata31e2 |
C |
A |
1: 26,723,579 (GRCm39) |
A534S |
probably benign |
Het |
Spink5 |
T |
C |
18: 44,096,419 (GRCm39) |
L16P |
probably damaging |
Het |
Sting1 |
C |
T |
18: 35,868,318 (GRCm39) |
A261T |
probably damaging |
Het |
Stk4 |
T |
G |
2: 163,952,146 (GRCm39) |
M1R |
probably null |
Het |
Stub1 |
A |
T |
17: 26,050,106 (GRCm39) |
Y253* |
probably null |
Het |
Tasor |
C |
A |
14: 27,169,454 (GRCm39) |
N338K |
probably damaging |
Het |
Tbce |
A |
G |
13: 14,203,875 (GRCm39) |
V29A |
probably damaging |
Het |
Tchhl1 |
A |
G |
3: 93,379,065 (GRCm39) |
R590G |
probably benign |
Het |
Ubr4 |
C |
T |
4: 139,186,231 (GRCm39) |
P613L |
unknown |
Het |
Vmn2r3 |
G |
T |
3: 64,182,939 (GRCm39) |
C253* |
probably null |
Het |
Wfdc8 |
C |
A |
2: 164,441,906 (GRCm39) |
E215D |
possibly damaging |
Het |
Zfp874b |
T |
C |
13: 67,621,975 (GRCm39) |
D441G |
probably benign |
Het |
Zscan4d |
G |
T |
7: 10,899,169 (GRCm39) |
P36Q |
possibly damaging |
Het |
|
Other mutations in Men1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00158:Men1
|
APN |
19 |
6,387,237 (GRCm39) |
splice site |
probably null |
|
IGL00160:Men1
|
APN |
19 |
6,387,237 (GRCm39) |
splice site |
probably null |
|
IGL00161:Men1
|
APN |
19 |
6,387,237 (GRCm39) |
splice site |
probably null |
|
IGL00229:Men1
|
APN |
19 |
6,387,237 (GRCm39) |
splice site |
probably null |
|
IGL00231:Men1
|
APN |
19 |
6,387,237 (GRCm39) |
splice site |
probably null |
|
IGL00232:Men1
|
APN |
19 |
6,387,237 (GRCm39) |
splice site |
probably null |
|
IGL00434:Men1
|
APN |
19 |
6,387,237 (GRCm39) |
splice site |
probably null |
|
IGL00467:Men1
|
APN |
19 |
6,387,237 (GRCm39) |
splice site |
probably null |
|
IGL00468:Men1
|
APN |
19 |
6,387,237 (GRCm39) |
splice site |
probably null |
|
IGL00470:Men1
|
APN |
19 |
6,387,237 (GRCm39) |
splice site |
probably null |
|
IGL00476:Men1
|
APN |
19 |
6,387,237 (GRCm39) |
splice site |
probably null |
|
IGL02305:Men1
|
APN |
19 |
6,390,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R0468:Men1
|
UTSW |
19 |
6,386,953 (GRCm39) |
missense |
probably null |
0.99 |
R0856:Men1
|
UTSW |
19 |
6,385,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R1384:Men1
|
UTSW |
19 |
6,389,921 (GRCm39) |
missense |
probably benign |
0.12 |
R1870:Men1
|
UTSW |
19 |
6,387,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R1987:Men1
|
UTSW |
19 |
6,388,867 (GRCm39) |
missense |
probably damaging |
0.99 |
R2321:Men1
|
UTSW |
19 |
6,389,868 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4538:Men1
|
UTSW |
19 |
6,386,784 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4763:Men1
|
UTSW |
19 |
6,385,102 (GRCm39) |
critical splice donor site |
probably null |
|
R6147:Men1
|
UTSW |
19 |
6,387,272 (GRCm39) |
missense |
probably damaging |
0.97 |
R7598:Men1
|
UTSW |
19 |
6,389,735 (GRCm39) |
missense |
probably benign |
0.06 |
R7949:Men1
|
UTSW |
19 |
6,388,323 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8283:Men1
|
UTSW |
19 |
6,386,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R8290:Men1
|
UTSW |
19 |
6,388,316 (GRCm39) |
missense |
probably benign |
0.09 |
R8998:Men1
|
UTSW |
19 |
6,389,960 (GRCm39) |
missense |
probably benign |
0.03 |
R8999:Men1
|
UTSW |
19 |
6,389,960 (GRCm39) |
missense |
probably benign |
0.03 |
RF002:Men1
|
UTSW |
19 |
6,390,146 (GRCm39) |
missense |
probably damaging |
0.97 |
|
Predicted Primers |
PCR Primer
(F):5'- ATTTACGTTGCTGTGCCCTAG -3'
(R):5'- GCTTCTAGAGCCAAAGGGAG -3'
Sequencing Primer
(F):5'- AGCAGGCTCAAGGTGGTACATC -3'
(R):5'- TCTAGAGCCAAAGGGAGAGGGG -3'
|
Posted On |
2019-11-12 |