Incidental Mutation 'R7139:Muc21'
ID |
553312 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Muc21
|
Ensembl Gene |
ENSMUSG00000090588 |
Gene Name |
mucin 21 |
Synonyms |
epiglycanin, Gm9573 |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.097)
|
Stock # |
R7139 (G1)
|
Quality Score |
180.468 |
Status
|
Not validated
|
Chromosome |
17 |
Chromosomal Location |
35928815-35937529 bp(-) (GRCm39) |
Type of Mutation |
intron |
DNA Base Change (assembly) |
TCCTGAGGCAGTGCTGGATACAGGGGTGGTTGGGGTGGGTGAAGAGCCTGAGGCAGTGCTGGAT to TCCTGAGGCAGTGCTGGAT
at 35933525 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000134221
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000164502]
[ENSMUST00000174521]
|
AlphaFold |
F7C950 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000164502
|
SMART Domains |
Protein: ENSMUSP00000130987 Gene: ENSMUSG00000090588
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
23 |
N/A |
INTRINSIC |
low complexity region
|
26 |
39 |
N/A |
INTRINSIC |
low complexity region
|
42 |
59 |
N/A |
INTRINSIC |
low complexity region
|
76 |
144 |
N/A |
INTRINSIC |
low complexity region
|
149 |
578 |
N/A |
INTRINSIC |
low complexity region
|
580 |
653 |
N/A |
INTRINSIC |
low complexity region
|
655 |
1179 |
N/A |
INTRINSIC |
low complexity region
|
1183 |
1373 |
N/A |
INTRINSIC |
low complexity region
|
1383 |
1436 |
N/A |
INTRINSIC |
low complexity region
|
1438 |
1479 |
N/A |
INTRINSIC |
Pfam:Epiglycanin_C
|
1518 |
1605 |
3.8e-22 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000174521
|
SMART Domains |
Protein: ENSMUSP00000134221 Gene: ENSMUSG00000090509
Domain | Start | End | E-Value | Type |
Pfam:SFTA2
|
80 |
117 |
9.2e-18 |
PFAM |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.1%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2510039O18Rik |
A |
G |
4: 148,026,295 (GRCm39) |
R272G |
possibly damaging |
Het |
4930512M02Rik |
T |
A |
11: 11,540,078 (GRCm39) |
N179Y |
unknown |
Het |
4930562C15Rik |
A |
T |
16: 4,668,048 (GRCm39) |
M480L |
probably benign |
Het |
Abcd4 |
A |
G |
12: 84,653,072 (GRCm39) |
C377R |
probably benign |
Het |
Adam23 |
C |
A |
1: 63,584,736 (GRCm39) |
D381E |
probably damaging |
Het |
Angpt1 |
T |
A |
15: 42,539,747 (GRCm39) |
Q37H |
probably damaging |
Het |
Apeh |
A |
T |
9: 107,969,345 (GRCm39) |
F260I |
probably damaging |
Het |
Cadps2 |
T |
C |
6: 23,410,888 (GRCm39) |
Y681C |
probably damaging |
Het |
Ccdc162 |
T |
C |
10: 41,542,717 (GRCm39) |
M386V |
possibly damaging |
Het |
Celsr2 |
T |
C |
3: 108,322,675 (GRCm39) |
S46G |
unknown |
Het |
Cfc1 |
T |
C |
1: 34,575,560 (GRCm39) |
L78P |
probably benign |
Het |
Chd7 |
T |
C |
4: 8,865,865 (GRCm39) |
V2724A |
probably benign |
Het |
Clca3a1 |
A |
T |
3: 144,461,063 (GRCm39) |
V196E |
possibly damaging |
Het |
Cma1 |
T |
C |
14: 56,181,273 (GRCm39) |
H44R |
probably damaging |
Het |
Cnot2 |
T |
C |
10: 116,330,924 (GRCm39) |
N394S |
probably benign |
Het |
Cplx3 |
A |
T |
9: 57,522,879 (GRCm39) |
H160Q |
probably benign |
Het |
Cstf3 |
A |
T |
2: 104,483,409 (GRCm39) |
I372F |
possibly damaging |
Het |
Cyb5rl |
A |
C |
4: 106,928,208 (GRCm39) |
I115L |
probably benign |
Het |
D5Ertd579e |
A |
G |
5: 36,771,320 (GRCm39) |
L1025P |
probably damaging |
Het |
Dmtn |
T |
C |
14: 70,854,867 (GRCm39) |
N36S |
probably benign |
Het |
Dnah6 |
A |
G |
6: 73,112,663 (GRCm39) |
V1647A |
probably damaging |
Het |
Dock6 |
T |
C |
9: 21,712,572 (GRCm39) |
Y2063C |
probably damaging |
Het |
Dst |
T |
A |
1: 34,338,888 (GRCm39) |
D5149E |
probably damaging |
Het |
Fancl |
A |
G |
11: 26,353,358 (GRCm39) |
M85V |
probably benign |
Het |
Fgd2 |
T |
A |
17: 29,592,229 (GRCm39) |
F387Y |
probably damaging |
Het |
Fshr |
A |
T |
17: 89,293,589 (GRCm39) |
I363N |
possibly damaging |
Het |
Glce |
G |
T |
9: 61,977,716 (GRCm39) |
S56* |
probably null |
Het |
Gm26727 |
A |
T |
2: 67,263,381 (GRCm39) |
S49T |
unknown |
Het |
Gm36210 |
T |
A |
7: 4,902,277 (GRCm39) |
D131V |
probably damaging |
Het |
Gm5089 |
T |
C |
14: 122,673,403 (GRCm39) |
D106G |
unknown |
Het |
Gm5622 |
G |
T |
14: 51,893,339 (GRCm39) |
E89* |
probably null |
Het |
H2-Eb2 |
C |
T |
17: 34,553,395 (GRCm39) |
R194W |
probably benign |
Het |
Hivep1 |
A |
T |
13: 42,313,430 (GRCm39) |
E1890V |
probably benign |
Het |
Ighv1-53 |
A |
T |
12: 115,122,441 (GRCm39) |
C5* |
probably null |
Het |
Ighv2-5 |
T |
A |
12: 113,649,219 (GRCm39) |
Y78F |
probably benign |
Het |
Il9 |
C |
T |
13: 56,628,426 (GRCm39) |
V88I |
probably benign |
Het |
Kidins220 |
A |
G |
12: 25,044,820 (GRCm39) |
T163A |
probably damaging |
Het |
Lama4 |
G |
T |
10: 38,951,491 (GRCm39) |
D1079Y |
probably damaging |
Het |
Lrrc34 |
T |
C |
3: 30,679,036 (GRCm39) |
I354V |
probably benign |
Het |
Macroh2a2 |
T |
A |
10: 61,593,674 (GRCm39) |
M1L |
unknown |
Het |
Mpeg1 |
A |
T |
19: 12,439,078 (GRCm39) |
T179S |
probably benign |
Het |
Mrgpra2a |
A |
T |
7: 47,076,337 (GRCm39) |
L307H |
probably damaging |
Het |
Mst1 |
G |
A |
9: 107,960,027 (GRCm39) |
R328H |
probably damaging |
Het |
Nav3 |
C |
A |
10: 109,689,338 (GRCm39) |
S313I |
probably benign |
Het |
Nmt2 |
T |
G |
2: 3,285,352 (GRCm39) |
S7A |
probably benign |
Het |
Nsmce1 |
T |
C |
7: 125,068,254 (GRCm39) |
S197G |
probably benign |
Het |
Ociad2 |
A |
G |
5: 73,493,218 (GRCm39) |
V4A |
probably benign |
Het |
Or56a41 |
G |
T |
7: 104,742,005 (GRCm39) |
T7K |
probably benign |
Het |
Osmr |
T |
C |
15: 6,850,569 (GRCm39) |
D679G |
possibly damaging |
Het |
Pappa |
T |
A |
4: 65,107,687 (GRCm39) |
F699L |
probably benign |
Het |
Parp8 |
T |
A |
13: 117,161,802 (GRCm39) |
M40L |
probably benign |
Het |
Pcyox1 |
A |
T |
6: 86,371,519 (GRCm39) |
N122K |
possibly damaging |
Het |
Pkd1l1 |
T |
C |
11: 8,840,737 (GRCm39) |
S1224G |
|
Het |
Pkd1l3 |
T |
A |
8: 110,362,972 (GRCm39) |
S1088T |
probably damaging |
Het |
Prrt1 |
T |
C |
17: 34,850,051 (GRCm39) |
V155A |
probably benign |
Het |
Rbm6 |
A |
C |
9: 107,730,410 (GRCm39) |
D79E |
probably damaging |
Het |
Sec31b |
A |
T |
19: 44,507,375 (GRCm39) |
S819T |
probably benign |
Het |
Slc22a27 |
A |
T |
19: 7,903,912 (GRCm39) |
I75N |
probably damaging |
Het |
Slc25a54 |
G |
A |
3: 109,005,905 (GRCm39) |
G138R |
probably damaging |
Het |
Slc6a12 |
T |
C |
6: 121,342,278 (GRCm39) |
S612P |
probably benign |
Het |
Slc7a2 |
A |
T |
8: 41,368,050 (GRCm39) |
I605F |
probably benign |
Het |
Slit2 |
A |
G |
5: 48,402,025 (GRCm39) |
T805A |
probably benign |
Het |
Strbp |
A |
T |
2: 37,514,514 (GRCm39) |
H308Q |
probably benign |
Het |
Stxbp4 |
G |
A |
11: 90,497,835 (GRCm39) |
Q155* |
probably null |
Het |
Sybu |
A |
T |
15: 44,541,110 (GRCm39) |
N317K |
possibly damaging |
Het |
Taok1 |
G |
A |
11: 77,462,459 (GRCm39) |
S210F |
probably damaging |
Het |
Tapbp |
A |
G |
17: 34,139,022 (GRCm39) |
D72G |
possibly damaging |
Het |
Thbd |
G |
T |
2: 148,248,461 (GRCm39) |
T469K |
probably benign |
Het |
Tia1 |
T |
C |
6: 86,404,670 (GRCm39) |
Y302H |
possibly damaging |
Het |
Tlr4 |
T |
C |
4: 66,758,520 (GRCm39) |
F438L |
probably benign |
Het |
Tmem235 |
C |
T |
11: 117,751,723 (GRCm39) |
S49L |
probably damaging |
Het |
Trip4 |
A |
G |
9: 65,792,503 (GRCm39) |
|
probably benign |
Het |
Trrap |
C |
A |
5: 144,739,988 (GRCm39) |
L1137I |
possibly damaging |
Het |
Vmo1 |
T |
C |
11: 70,404,674 (GRCm39) |
E109G |
probably benign |
Het |
Wdfy4 |
T |
C |
14: 32,873,535 (GRCm39) |
Y258C |
|
Het |
Wdr91 |
T |
G |
6: 34,885,198 (GRCm39) |
N121T |
possibly damaging |
Het |
Zfp39 |
T |
C |
11: 58,781,385 (GRCm39) |
H459R |
probably damaging |
Het |
Zfp936 |
T |
A |
7: 42,839,715 (GRCm39) |
I394K |
possibly damaging |
Het |
Zpr1 |
G |
A |
9: 46,192,357 (GRCm39) |
D423N |
probably damaging |
Het |
|
Other mutations in Muc21 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
BB009:Muc21
|
UTSW |
17 |
35,933,525 (GRCm39) |
intron |
probably benign |
|
FR4304:Muc21
|
UTSW |
17 |
35,933,013 (GRCm39) |
intron |
probably benign |
|
R0334:Muc21
|
UTSW |
17 |
35,933,614 (GRCm39) |
intron |
probably benign |
|
R0946:Muc21
|
UTSW |
17 |
35,929,105 (GRCm39) |
missense |
probably benign |
0.32 |
R1117:Muc21
|
UTSW |
17 |
35,930,920 (GRCm39) |
intron |
probably benign |
|
R1345:Muc21
|
UTSW |
17 |
35,932,489 (GRCm39) |
intron |
probably benign |
|
R1697:Muc21
|
UTSW |
17 |
35,931,540 (GRCm39) |
intron |
probably benign |
|
R1750:Muc21
|
UTSW |
17 |
35,931,940 (GRCm39) |
intron |
probably benign |
|
R1756:Muc21
|
UTSW |
17 |
35,930,131 (GRCm39) |
intron |
probably benign |
|
R1946:Muc21
|
UTSW |
17 |
35,933,416 (GRCm39) |
intron |
probably benign |
|
R1978:Muc21
|
UTSW |
17 |
35,933,857 (GRCm39) |
intron |
probably benign |
|
R1991:Muc21
|
UTSW |
17 |
35,929,600 (GRCm39) |
missense |
probably benign |
0.32 |
R1992:Muc21
|
UTSW |
17 |
35,929,600 (GRCm39) |
missense |
probably benign |
0.32 |
R2063:Muc21
|
UTSW |
17 |
35,932,297 (GRCm39) |
intron |
probably benign |
|
R2356:Muc21
|
UTSW |
17 |
35,932,563 (GRCm39) |
intron |
probably benign |
|
R2866:Muc21
|
UTSW |
17 |
35,930,599 (GRCm39) |
intron |
probably benign |
|
R3826:Muc21
|
UTSW |
17 |
35,932,504 (GRCm39) |
intron |
probably benign |
|
R4020:Muc21
|
UTSW |
17 |
35,930,953 (GRCm39) |
intron |
probably benign |
|
R4474:Muc21
|
UTSW |
17 |
35,931,496 (GRCm39) |
intron |
probably benign |
|
R4677:Muc21
|
UTSW |
17 |
35,930,599 (GRCm39) |
intron |
probably benign |
|
R4786:Muc21
|
UTSW |
17 |
35,930,221 (GRCm39) |
intron |
probably benign |
|
R5071:Muc21
|
UTSW |
17 |
35,931,444 (GRCm39) |
intron |
probably benign |
|
R5173:Muc21
|
UTSW |
17 |
35,931,633 (GRCm39) |
intron |
probably benign |
|
R5283:Muc21
|
UTSW |
17 |
35,932,224 (GRCm39) |
intron |
probably benign |
|
R5446:Muc21
|
UTSW |
17 |
35,933,395 (GRCm39) |
intron |
probably benign |
|
R5542:Muc21
|
UTSW |
17 |
35,933,395 (GRCm39) |
intron |
probably benign |
|
R5716:Muc21
|
UTSW |
17 |
35,931,675 (GRCm39) |
intron |
probably benign |
|
R5913:Muc21
|
UTSW |
17 |
35,934,123 (GRCm39) |
intron |
probably benign |
|
R6011:Muc21
|
UTSW |
17 |
35,933,074 (GRCm39) |
intron |
probably benign |
|
R6198:Muc21
|
UTSW |
17 |
35,931,808 (GRCm39) |
intron |
probably benign |
|
R6394:Muc21
|
UTSW |
17 |
35,931,058 (GRCm39) |
intron |
probably benign |
|
R6786:Muc21
|
UTSW |
17 |
35,934,057 (GRCm39) |
intron |
probably benign |
|
R6940:Muc21
|
UTSW |
17 |
35,934,118 (GRCm39) |
intron |
probably benign |
|
R7082:Muc21
|
UTSW |
17 |
35,932,093 (GRCm39) |
missense |
unknown |
|
R7103:Muc21
|
UTSW |
17 |
35,932,432 (GRCm39) |
missense |
unknown |
|
R7110:Muc21
|
UTSW |
17 |
35,933,510 (GRCm39) |
intron |
probably benign |
|
R7165:Muc21
|
UTSW |
17 |
35,932,870 (GRCm39) |
missense |
unknown |
|
R7200:Muc21
|
UTSW |
17 |
35,933,525 (GRCm39) |
intron |
probably benign |
|
R7204:Muc21
|
UTSW |
17 |
35,932,105 (GRCm39) |
intron |
probably benign |
|
R7289:Muc21
|
UTSW |
17 |
35,929,761 (GRCm39) |
missense |
unknown |
|
R7290:Muc21
|
UTSW |
17 |
35,929,761 (GRCm39) |
missense |
unknown |
|
R7295:Muc21
|
UTSW |
17 |
35,929,761 (GRCm39) |
missense |
unknown |
|
R7319:Muc21
|
UTSW |
17 |
35,932,935 (GRCm39) |
intron |
probably benign |
|
R7462:Muc21
|
UTSW |
17 |
35,931,568 (GRCm39) |
missense |
unknown |
|
R7529:Muc21
|
UTSW |
17 |
35,930,123 (GRCm39) |
missense |
unknown |
|
R7718:Muc21
|
UTSW |
17 |
35,933,728 (GRCm39) |
missense |
unknown |
|
R7762:Muc21
|
UTSW |
17 |
35,932,977 (GRCm39) |
missense |
unknown |
|
R7788:Muc21
|
UTSW |
17 |
35,929,798 (GRCm39) |
missense |
unknown |
|
R7798:Muc21
|
UTSW |
17 |
35,932,146 (GRCm39) |
missense |
unknown |
|
R7831:Muc21
|
UTSW |
17 |
35,929,651 (GRCm39) |
missense |
unknown |
|
R7896:Muc21
|
UTSW |
17 |
35,930,917 (GRCm39) |
missense |
unknown |
|
R7899:Muc21
|
UTSW |
17 |
35,931,493 (GRCm39) |
intron |
probably benign |
|
R7932:Muc21
|
UTSW |
17 |
35,933,525 (GRCm39) |
intron |
probably benign |
|
R8025:Muc21
|
UTSW |
17 |
35,931,879 (GRCm39) |
intron |
probably benign |
|
R8077:Muc21
|
UTSW |
17 |
35,930,628 (GRCm39) |
intron |
probably benign |
|
R8090:Muc21
|
UTSW |
17 |
35,932,617 (GRCm39) |
missense |
unknown |
|
R8169:Muc21
|
UTSW |
17 |
35,932,072 (GRCm39) |
missense |
unknown |
|
R8184:Muc21
|
UTSW |
17 |
35,933,722 (GRCm39) |
missense |
unknown |
|
R8209:Muc21
|
UTSW |
17 |
35,930,599 (GRCm39) |
intron |
probably benign |
|
R8226:Muc21
|
UTSW |
17 |
35,930,599 (GRCm39) |
intron |
probably benign |
|
R8464:Muc21
|
UTSW |
17 |
35,933,098 (GRCm39) |
intron |
probably benign |
|
R8670:Muc21
|
UTSW |
17 |
35,932,540 (GRCm39) |
missense |
unknown |
|
R8783:Muc21
|
UTSW |
17 |
35,930,875 (GRCm39) |
missense |
unknown |
|
R8856:Muc21
|
UTSW |
17 |
35,931,865 (GRCm39) |
missense |
unknown |
|
R9155:Muc21
|
UTSW |
17 |
35,932,131 (GRCm39) |
missense |
unknown |
|
R9214:Muc21
|
UTSW |
17 |
35,931,838 (GRCm39) |
missense |
unknown |
|
R9353:Muc21
|
UTSW |
17 |
35,930,545 (GRCm39) |
missense |
unknown |
|
R9618:Muc21
|
UTSW |
17 |
35,932,935 (GRCm39) |
intron |
probably benign |
|
R9621:Muc21
|
UTSW |
17 |
35,932,720 (GRCm39) |
missense |
unknown |
|
R9679:Muc21
|
UTSW |
17 |
35,930,491 (GRCm39) |
missense |
unknown |
|
RF025:Muc21
|
UTSW |
17 |
35,933,771 (GRCm39) |
intron |
probably benign |
|
Z1176:Muc21
|
UTSW |
17 |
35,932,137 (GRCm39) |
missense |
unknown |
|
Z1177:Muc21
|
UTSW |
17 |
35,931,951 (GRCm39) |
missense |
unknown |
|
Z1177:Muc21
|
UTSW |
17 |
35,931,817 (GRCm39) |
missense |
unknown |
|
|
Predicted Primers |
PCR Primer
(F):5'- ATCCTGAGGCAGTGCTAGATG -3'
(R):5'- CACCACTGTATCCAGCACTG -3'
Sequencing Primer
(F):5'- TGGGTGCTGATCCTGAGGC -3'
(R):5'- ACTGGCTCAGGCTCTACAC -3'
|
Posted On |
2019-05-15 |