Incidental Mutation 'R5618:Tmprss11d'
| ID |
439629 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Tmprss11d
|
| Ensembl Gene |
ENSMUSG00000061259 |
| Gene Name |
transmembrane protease, serine 11d |
| Synonyms |
AsP |
| MMRRC Submission |
043277-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.065)
|
| Stock # |
R5618 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
5 |
| Chromosomal Location |
86450713-86521246 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 86454154 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Methionine to Lysine
at position 217
(M217K)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000113079
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000031175]
[ENSMUST00000122377]
|
| AlphaFold |
Q8VHK8 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000031175
AA Change: M355K
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000031175
Gene: ENSMUSG00000061259
AA Change: M355K
| Domain | Start | End | E-Value | Type |
|---|
|
transmembrane domain
|
13 |
35 |
N/A |
INTRINSIC |
|
SEA
|
41 |
164 |
4.92e-2 |
SMART |
|
Tryp_SPc
|
185 |
411 |
1.29e-86 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000122377
AA Change: M217K
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000113079
Gene: ENSMUSG00000061259
AA Change: M217K
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
22 |
N/A |
INTRINSIC |
|
Tryp_SPc
|
47 |
273 |
1.29e-86 |
SMART |
|
| Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.6%
- 10x: 97.2%
- 20x: 95.2%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a trypsin-like serine protease released from the submucosal serous glands onto mucous membrane. It is a type II integral membrane protein and has 29-38% identity in the sequence of the catalytic region with human hepsin, enteropeptidase, acrosin, and mast cell tryptase. The noncatalytic region has little similarity to other known proteins. This protein may play some biological role in the host defense system on the mucous membrane independently of or in cooperation with other substances in airway mucous or bronchial secretions. [provided by RefSeq, Jul 2008]
PHENOTYPE: Aged female mice homozygous for a knock-in allele exhibit increased lymphoma incidence. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 51 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700028K03Rik |
G |
A |
5: 107,696,065 (GRCm39) |
W167* |
probably null |
Het |
| Acvr1 |
C |
T |
2: 58,352,955 (GRCm39) |
R335Q |
probably damaging |
Het |
| Atg7 |
A |
G |
6: 114,650,660 (GRCm39) |
D67G |
probably damaging |
Het |
| Avil |
T |
C |
10: 126,846,446 (GRCm39) |
F417S |
possibly damaging |
Het |
| AW551984 |
A |
T |
9: 39,502,000 (GRCm39) |
L702Q |
probably damaging |
Het |
| Bcl7a |
A |
T |
5: 123,499,265 (GRCm39) |
N95Y |
probably damaging |
Het |
| Cblb |
A |
G |
16: 51,973,031 (GRCm39) |
D454G |
possibly damaging |
Het |
| Cc2d2a |
A |
T |
5: 43,887,249 (GRCm39) |
Q1226H |
probably benign |
Het |
| Cct5 |
A |
G |
15: 31,598,161 (GRCm39) |
S13P |
possibly damaging |
Het |
| Clca3a1 |
C |
T |
3: 144,710,738 (GRCm39) |
E822K |
probably benign |
Het |
| Csgalnact2 |
A |
T |
6: 118,103,277 (GRCm39) |
D228E |
probably damaging |
Het |
| Defb12 |
A |
T |
8: 19,164,814 (GRCm39) |
M8K |
possibly damaging |
Het |
| Dipk1b |
T |
C |
2: 26,524,887 (GRCm39) |
S96P |
probably damaging |
Het |
| Dysf |
A |
G |
6: 84,083,806 (GRCm39) |
D736G |
probably benign |
Het |
| Exog |
G |
T |
9: 119,291,817 (GRCm39) |
D365Y |
probably damaging |
Het |
| Fam222b |
T |
G |
11: 78,045,066 (GRCm39) |
V81G |
probably benign |
Het |
| Fbl |
A |
G |
7: 27,878,411 (GRCm39) |
E301G |
probably damaging |
Het |
| Fez1 |
A |
T |
9: 36,755,228 (GRCm39) |
N76Y |
probably damaging |
Het |
| Gnb4 |
C |
T |
3: 32,645,356 (GRCm39) |
V112I |
probably benign |
Het |
| H2-Q4 |
T |
A |
17: 35,598,901 (GRCm39) |
F57Y |
probably damaging |
Het |
| Ift88 |
T |
C |
14: 57,718,965 (GRCm39) |
I650T |
possibly damaging |
Het |
| Kif1b |
A |
T |
4: 149,354,346 (GRCm39) |
D231E |
possibly damaging |
Het |
| Lig4 |
A |
T |
8: 10,022,021 (GRCm39) |
D586E |
probably benign |
Het |
| Mlc1 |
C |
A |
15: 88,858,769 (GRCm39) |
L126F |
probably damaging |
Het |
| Muc4 |
A |
G |
16: 32,754,253 (GRCm38) |
T1376A |
probably benign |
Het |
| Ncoa6 |
A |
T |
2: 155,279,817 (GRCm39) |
D66E |
possibly damaging |
Het |
| Or6ae1 |
A |
G |
7: 139,742,185 (GRCm39) |
V226A |
probably damaging |
Het |
| Or8b44 |
C |
T |
9: 38,410,036 (GRCm39) |
Q24* |
probably null |
Het |
| Pard6a |
T |
C |
8: 106,429,546 (GRCm39) |
V168A |
probably damaging |
Het |
| Pmpcb |
A |
G |
5: 21,947,786 (GRCm39) |
N163S |
possibly damaging |
Het |
| Pramel27 |
A |
T |
4: 143,577,263 (GRCm39) |
E15V |
possibly damaging |
Het |
| Prdm2 |
C |
T |
4: 142,860,107 (GRCm39) |
C1061Y |
probably benign |
Het |
| Prkdc |
A |
G |
16: 15,627,476 (GRCm39) |
Y3378C |
probably damaging |
Het |
| Sema6a |
A |
T |
18: 47,415,015 (GRCm39) |
V425E |
probably damaging |
Het |
| Sema7a |
A |
T |
9: 57,867,566 (GRCm39) |
E439D |
possibly damaging |
Het |
| Serpinf1 |
T |
A |
11: 75,301,010 (GRCm39) |
T402S |
possibly damaging |
Het |
| Sf3a2 |
T |
C |
10: 80,640,410 (GRCm39) |
|
probably benign |
Het |
| Skic3 |
T |
A |
13: 76,321,545 (GRCm39) |
S1346T |
probably benign |
Het |
| Smchd1 |
A |
T |
17: 71,762,722 (GRCm39) |
D172E |
probably damaging |
Het |
| Spag5 |
T |
G |
11: 78,194,906 (GRCm39) |
I71S |
probably benign |
Het |
| Spata31d1d |
G |
A |
13: 59,874,214 (GRCm39) |
A1107V |
probably benign |
Het |
| Svep1 |
A |
C |
4: 58,070,537 (GRCm39) |
S2416R |
probably benign |
Het |
| Tbc1d9 |
A |
G |
8: 83,969,221 (GRCm39) |
Y503C |
probably damaging |
Het |
| Tlr9 |
A |
T |
9: 106,101,938 (GRCm39) |
I410F |
possibly damaging |
Het |
| Tmem87a |
C |
A |
2: 120,199,787 (GRCm39) |
L452F |
probably benign |
Het |
| Uqcc4 |
G |
A |
17: 25,403,963 (GRCm39) |
S101N |
probably damaging |
Het |
| Vmn2r80 |
T |
C |
10: 78,984,755 (GRCm39) |
Y36H |
probably benign |
Het |
| Vmn2r87 |
A |
T |
10: 130,315,817 (GRCm39) |
F83Y |
probably damaging |
Het |
| Vmp1 |
C |
T |
11: 86,554,388 (GRCm39) |
R75H |
probably benign |
Het |
| Wapl |
T |
A |
14: 34,413,863 (GRCm39) |
Y242N |
possibly damaging |
Het |
| Zfp473 |
T |
A |
7: 44,391,156 (GRCm39) |
D6V |
probably benign |
Het |
|
| Other mutations in Tmprss11d |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02393:Tmprss11d
|
APN |
5 |
86,451,471 (GRCm39) |
makesense |
probably null |
|
|
IGL02519:Tmprss11d
|
APN |
5 |
86,454,164 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02666:Tmprss11d
|
APN |
5 |
86,479,052 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02974:Tmprss11d
|
APN |
5 |
86,454,235 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03305:Tmprss11d
|
APN |
5 |
86,474,279 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0440:Tmprss11d
|
UTSW |
5 |
86,486,671 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R1261:Tmprss11d
|
UTSW |
5 |
86,457,239 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
R1544:Tmprss11d
|
UTSW |
5 |
86,486,658 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2018:Tmprss11d
|
UTSW |
5 |
86,487,413 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R2036:Tmprss11d
|
UTSW |
5 |
86,457,128 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R2267:Tmprss11d
|
UTSW |
5 |
86,521,208 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4063:Tmprss11d
|
UTSW |
5 |
86,457,177 (GRCm39) |
missense |
probably benign |
0.04 |
|
R4087:Tmprss11d
|
UTSW |
5 |
86,457,138 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4665:Tmprss11d
|
UTSW |
5 |
86,457,260 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4666:Tmprss11d
|
UTSW |
5 |
86,457,260 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4784:Tmprss11d
|
UTSW |
5 |
86,454,140 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4785:Tmprss11d
|
UTSW |
5 |
86,454,140 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5077:Tmprss11d
|
UTSW |
5 |
86,457,122 (GRCm39) |
critical splice donor site |
probably null |
|
|
R5201:Tmprss11d
|
UTSW |
5 |
86,457,214 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R5350:Tmprss11d
|
UTSW |
5 |
86,486,746 (GRCm39) |
missense |
probably benign |
0.08 |
|
R5523:Tmprss11d
|
UTSW |
5 |
86,486,729 (GRCm39) |
missense |
probably benign |
0.05 |
|
R5643:Tmprss11d
|
UTSW |
5 |
86,474,388 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5834:Tmprss11d
|
UTSW |
5 |
86,454,169 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6422:Tmprss11d
|
UTSW |
5 |
86,457,284 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6706:Tmprss11d
|
UTSW |
5 |
86,478,962 (GRCm39) |
missense |
probably benign |
0.03 |
|
R6735:Tmprss11d
|
UTSW |
5 |
86,457,159 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6778:Tmprss11d
|
UTSW |
5 |
86,457,209 (GRCm39) |
missense |
probably benign |
0.34 |
|
R7013:Tmprss11d
|
UTSW |
5 |
86,474,432 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7273:Tmprss11d
|
UTSW |
5 |
86,485,098 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7488:Tmprss11d
|
UTSW |
5 |
86,474,309 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7627:Tmprss11d
|
UTSW |
5 |
86,457,365 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R7742:Tmprss11d
|
UTSW |
5 |
86,451,493 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7937:Tmprss11d
|
UTSW |
5 |
86,457,349 (GRCm39) |
missense |
probably benign |
0.06 |
|
R8419:Tmprss11d
|
UTSW |
5 |
86,457,165 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8794:Tmprss11d
|
UTSW |
5 |
86,486,680 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- TGGTTTGACTATCCTATAGCAATTAAC -3'
(R):5'- TTCTCAAATTTGGCATAGAGTCATTGA -3'
Sequencing Primer
(F):5'- GCAATTAACAATTGGTATTTTTGTGC -3'
(R):5'- ACTCATAATTTCTGAGGTCTGGTTTC -3'
|
| Posted On |
2016-11-08 |
Incidental Mutation