Incidental Mutation 'R3785:Tekt1'
ID |
272223 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Tekt1
|
Ensembl Gene |
ENSMUSG00000020799 |
Gene Name |
tektin 1 |
Synonyms |
MT14 |
MMRRC Submission |
040752-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.190)
|
Stock # |
R3785 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
11 |
Chromosomal Location |
72235548-72253268 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 72235720 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Threonine
at position 376
(I376T)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000104143
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000021155]
[ENSMUST00000108502]
[ENSMUST00000108503]
|
AlphaFold |
Q9DAJ2 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000021155
AA Change: I376T
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000021155 Gene: ENSMUSG00000020799 AA Change: I376T
Domain | Start | End | E-Value | Type |
Pfam:Tektin
|
16 |
398 |
1.3e-150 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000108502
AA Change: I376T
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000104142 Gene: ENSMUSG00000020799 AA Change: I376T
Domain | Start | End | E-Value | Type |
Pfam:Tektin
|
16 |
399 |
5.5e-152 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000108503
AA Change: I376T
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000104143 Gene: ENSMUSG00000020799 AA Change: I376T
Domain | Start | End | E-Value | Type |
Pfam:Tektin
|
16 |
399 |
5.5e-152 |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000158122
|
Meta Mutation Damage Score |
0.5797 |
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.5%
- 10x: 97.2%
- 20x: 94.8%
|
Validation Efficiency |
95% (38/40) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene product belongs to the tektin family of proteins. Tektins comprise a family of filament-forming proteins that are coassembled with tubulins to form ciliary and flagellar microtubules. This gene is predominantly expressed in the testis and in mouse, tektin 1 mRNA was localized to the spermatocytes and round spermatids in the seminiferous tubules, indicating that it may play a role in spermatogenesis. [provided by RefSeq, Jul 2008]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700012B07Rik |
G |
T |
11: 109,684,980 (GRCm39) |
C172* |
probably null |
Het |
A2ml1 |
C |
T |
6: 128,521,887 (GRCm39) |
|
probably null |
Het |
Aak1 |
T |
C |
6: 86,942,560 (GRCm39) |
F701S |
unknown |
Het |
Arid2 |
T |
A |
15: 96,270,439 (GRCm39) |
D1517E |
possibly damaging |
Het |
Cyp2r1 |
C |
T |
7: 114,153,931 (GRCm39) |
V88I |
possibly damaging |
Het |
Dennd3 |
T |
C |
15: 73,419,426 (GRCm39) |
V739A |
possibly damaging |
Het |
Dnah11 |
G |
T |
12: 117,981,337 (GRCm39) |
Q2610K |
probably damaging |
Het |
Gm5698 |
T |
C |
1: 31,016,560 (GRCm39) |
T164A |
probably benign |
Het |
Gpt2 |
G |
T |
8: 86,252,202 (GRCm39) |
V506L |
probably benign |
Het |
Gpx6 |
A |
G |
13: 21,497,956 (GRCm39) |
T76A |
probably benign |
Het |
Htra3 |
A |
T |
5: 35,828,472 (GRCm39) |
L136H |
probably benign |
Het |
Ifitm10 |
G |
A |
7: 141,882,335 (GRCm39) |
T145I |
possibly damaging |
Het |
Inpp5k |
T |
C |
11: 75,538,512 (GRCm39) |
L461P |
probably damaging |
Het |
Kcnd3 |
C |
A |
3: 105,575,541 (GRCm39) |
T555K |
possibly damaging |
Het |
Kif13b |
C |
T |
14: 65,037,849 (GRCm39) |
T1505I |
probably benign |
Het |
Mcf2l |
G |
T |
8: 12,930,099 (GRCm39) |
G40C |
probably damaging |
Het |
Mettl3 |
A |
T |
14: 52,537,363 (GRCm39) |
I102N |
probably benign |
Het |
Muc5b |
C |
T |
7: 141,418,853 (GRCm39) |
T3933I |
possibly damaging |
Het |
Mus81 |
G |
A |
19: 5,535,389 (GRCm39) |
|
probably benign |
Het |
Myo15a |
A |
T |
11: 60,368,398 (GRCm39) |
Y386F |
probably damaging |
Het |
Mypn |
C |
A |
10: 63,028,961 (GRCm39) |
R34L |
probably benign |
Het |
Neurod1 |
T |
A |
2: 79,284,939 (GRCm39) |
N148I |
probably damaging |
Het |
Or4f56 |
T |
C |
2: 111,703,831 (GRCm39) |
Y123C |
probably damaging |
Het |
Or8g32 |
T |
C |
9: 39,305,678 (GRCm39) |
V197A |
probably benign |
Het |
Or9g3 |
G |
A |
2: 85,589,797 (GRCm39) |
P308S |
probably benign |
Het |
Pmepa1 |
G |
A |
2: 173,069,926 (GRCm39) |
R210W |
probably damaging |
Het |
Ptch1 |
T |
G |
13: 63,672,773 (GRCm39) |
E944A |
probably benign |
Het |
Rnf5 |
A |
G |
17: 34,820,906 (GRCm39) |
|
probably null |
Het |
Sacs |
C |
A |
14: 61,421,410 (GRCm39) |
Q116K |
probably damaging |
Het |
Sall4 |
A |
G |
2: 168,598,043 (GRCm39) |
S266P |
probably damaging |
Het |
Senp6 |
T |
G |
9: 79,999,568 (GRCm39) |
I74S |
probably benign |
Het |
Slc13a4 |
T |
A |
6: 35,264,827 (GRCm39) |
T131S |
probably damaging |
Het |
Slc9a4 |
C |
A |
1: 40,623,130 (GRCm39) |
P123Q |
probably damaging |
Het |
Stxbp4 |
T |
A |
11: 90,426,441 (GRCm39) |
|
probably null |
Het |
Swt1 |
T |
C |
1: 151,255,155 (GRCm39) |
D814G |
probably benign |
Het |
Synrg |
T |
C |
11: 83,892,746 (GRCm39) |
F613S |
probably damaging |
Het |
Ttbk2 |
A |
T |
2: 120,604,296 (GRCm39) |
|
probably benign |
Het |
Txnl4b |
C |
T |
8: 110,299,409 (GRCm39) |
A123V |
probably damaging |
Het |
Wap |
G |
A |
11: 6,588,550 (GRCm39) |
Q25* |
probably null |
Het |
Zfp26 |
A |
T |
9: 20,349,098 (GRCm39) |
C489S |
probably damaging |
Het |
Zfp804b |
G |
A |
5: 6,820,153 (GRCm39) |
T934M |
possibly damaging |
Het |
|
Other mutations in Tekt1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
PIT4544001:Tekt1
|
UTSW |
11 |
72,245,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R0463:Tekt1
|
UTSW |
11 |
72,242,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R0531:Tekt1
|
UTSW |
11 |
72,236,420 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1190:Tekt1
|
UTSW |
11 |
72,246,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R1908:Tekt1
|
UTSW |
11 |
72,242,761 (GRCm39) |
missense |
probably benign |
0.41 |
R3783:Tekt1
|
UTSW |
11 |
72,235,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R3784:Tekt1
|
UTSW |
11 |
72,235,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R3787:Tekt1
|
UTSW |
11 |
72,235,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R3831:Tekt1
|
UTSW |
11 |
72,245,645 (GRCm39) |
missense |
probably benign |
0.03 |
R3832:Tekt1
|
UTSW |
11 |
72,245,645 (GRCm39) |
missense |
probably benign |
0.03 |
R3833:Tekt1
|
UTSW |
11 |
72,245,645 (GRCm39) |
missense |
probably benign |
0.03 |
R3916:Tekt1
|
UTSW |
11 |
72,236,574 (GRCm39) |
missense |
possibly damaging |
0.83 |
R3917:Tekt1
|
UTSW |
11 |
72,236,574 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5645:Tekt1
|
UTSW |
11 |
72,242,663 (GRCm39) |
missense |
probably benign |
0.02 |
R7740:Tekt1
|
UTSW |
11 |
72,250,544 (GRCm39) |
missense |
probably benign |
0.03 |
R8472:Tekt1
|
UTSW |
11 |
72,242,850 (GRCm39) |
missense |
possibly damaging |
0.61 |
Z1176:Tekt1
|
UTSW |
11 |
72,236,524 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1186:Tekt1
|
UTSW |
11 |
72,250,597 (GRCm39) |
missense |
probably benign |
|
Z1187:Tekt1
|
UTSW |
11 |
72,250,597 (GRCm39) |
missense |
probably benign |
|
Z1188:Tekt1
|
UTSW |
11 |
72,250,597 (GRCm39) |
missense |
probably benign |
|
Z1189:Tekt1
|
UTSW |
11 |
72,250,597 (GRCm39) |
missense |
probably benign |
|
Z1190:Tekt1
|
UTSW |
11 |
72,250,597 (GRCm39) |
missense |
probably benign |
|
Z1191:Tekt1
|
UTSW |
11 |
72,250,597 (GRCm39) |
missense |
probably benign |
|
Z1192:Tekt1
|
UTSW |
11 |
72,250,597 (GRCm39) |
missense |
probably benign |
|
|
Predicted Primers |
PCR Primer
(F):5'- ACCTGAAATGAGAGCTCTGTG -3'
(R):5'- CACTGCCTAGAGAAGCAAGG -3'
Sequencing Primer
(F):5'- GTGCTAACTCTTGTCTTACGATGCAG -3'
(R):5'- TGTGATTATCCCTCACGC -3'
|
Posted On |
2015-03-25 |