Incidental Mutation 'R3880:Trip13'
ID |
312795 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Trip13
|
Ensembl Gene |
ENSMUSG00000021569 |
Gene Name |
thyroid hormone receptor interactor 13 |
Synonyms |
D13Ertd328e, 2410002G23Rik |
MMRRC Submission |
040794-MU
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.926)
|
Stock # |
R3880 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
13 |
Chromosomal Location |
74060577-74085855 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 74066597 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Tyrosine to Cysteine
at position 318
(Y318C)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000022053
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000022053]
[ENSMUST00000222156]
|
AlphaFold |
Q3UA06 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000022053
AA Change: Y318C
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000022053 Gene: ENSMUSG00000021569 AA Change: Y318C
Domain | Start | End | E-Value | Type |
AAA
|
171 |
323 |
1.13e-10 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000222156
|
Meta Mutation Damage Score |
0.9173 |
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.5%
- 10x: 97.1%
- 20x: 94.5%
|
Validation Efficiency |
92% (35/38) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein that interacts with thyroid hormone receptors, also known as hormone-dependent transcription factors. The gene product interacts specifically with the ligand binding domain. This gene is one of several that may play a role in early-stage non-small cell lung cancer. [provided by RefSeq, Oct 2009] PHENOTYPE: Mice homozygous for a gene trapped allele exhibit postnatal lethality, infertility, reduced gonad size, tail defects and meiotic arrest of sperm and oocytes associated with unrepaired double strand breaks. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc9 |
A |
G |
6: 142,584,959 (GRCm39) |
W872R |
probably damaging |
Het |
Abcg3 |
T |
C |
5: 105,086,046 (GRCm39) |
|
probably benign |
Het |
Adgrv1 |
T |
A |
13: 81,583,824 (GRCm39) |
Q4627L |
probably benign |
Het |
Armc2 |
T |
C |
10: 41,839,721 (GRCm39) |
I415V |
possibly damaging |
Het |
Atp1b1 |
C |
T |
1: 164,270,874 (GRCm39) |
R35H |
probably benign |
Het |
Bcas3 |
A |
G |
11: 85,261,948 (GRCm39) |
M107V |
probably benign |
Het |
Ccdc43 |
T |
C |
11: 102,583,029 (GRCm39) |
|
probably null |
Het |
Dtx4 |
A |
C |
19: 12,463,820 (GRCm39) |
S321A |
probably benign |
Het |
Enox1 |
A |
T |
14: 77,848,826 (GRCm39) |
H379L |
possibly damaging |
Het |
Evx1 |
A |
T |
6: 52,290,846 (GRCm39) |
D6V |
probably damaging |
Het |
Fubp1 |
T |
A |
3: 151,926,133 (GRCm39) |
V286E |
probably damaging |
Het |
Itgav |
T |
C |
2: 83,598,645 (GRCm39) |
V234A |
probably damaging |
Het |
Khdc3 |
T |
C |
9: 73,010,872 (GRCm39) |
S241P |
possibly damaging |
Het |
Lipc |
T |
A |
9: 70,727,800 (GRCm39) |
I16F |
probably damaging |
Het |
Mael |
T |
C |
1: 166,064,437 (GRCm39) |
|
probably benign |
Het |
Myo7b |
T |
G |
18: 32,102,567 (GRCm39) |
E1487A |
probably damaging |
Het |
Or52a33 |
T |
G |
7: 103,288,831 (GRCm39) |
K172T |
probably benign |
Het |
Osgin1 |
A |
G |
8: 120,168,191 (GRCm39) |
H6R |
probably benign |
Het |
Otog |
C |
T |
7: 45,937,445 (GRCm39) |
T1718I |
possibly damaging |
Het |
Otogl |
T |
C |
10: 107,663,565 (GRCm39) |
E1002G |
probably damaging |
Het |
Pkd1l1 |
T |
C |
11: 8,911,983 (GRCm39) |
N241S |
unknown |
Het |
Psmd9 |
C |
T |
5: 123,372,653 (GRCm39) |
|
probably benign |
Het |
Secisbp2l |
C |
T |
2: 125,582,657 (GRCm39) |
G933D |
possibly damaging |
Het |
Slc6a2 |
C |
A |
8: 93,716,846 (GRCm39) |
N337K |
probably damaging |
Het |
Snx19 |
A |
T |
9: 30,373,688 (GRCm39) |
Q917L |
probably damaging |
Het |
Srsf3 |
T |
C |
17: 29,255,257 (GRCm39) |
V14A |
probably damaging |
Het |
Sspo |
G |
A |
6: 48,471,874 (GRCm39) |
V4729I |
probably benign |
Het |
Syngap1 |
T |
A |
17: 27,172,038 (GRCm39) |
I82N |
probably damaging |
Het |
Telo2 |
A |
T |
17: 25,325,807 (GRCm39) |
M407K |
probably damaging |
Het |
Thsd7b |
G |
A |
1: 129,523,107 (GRCm39) |
G47D |
probably damaging |
Het |
Tradd |
A |
T |
8: 105,987,287 (GRCm39) |
N6K |
possibly damaging |
Het |
Trim30a |
C |
A |
7: 104,060,396 (GRCm39) |
C460F |
probably benign |
Het |
Ubfd1 |
T |
A |
7: 121,667,999 (GRCm39) |
|
probably benign |
Het |
Uggt1 |
A |
G |
1: 36,215,885 (GRCm39) |
|
probably benign |
Het |
Wdr7 |
T |
A |
18: 63,857,226 (GRCm39) |
C101S |
possibly damaging |
Het |
Zfp345 |
T |
C |
2: 150,314,075 (GRCm39) |
I487M |
possibly damaging |
Het |
|
Other mutations in Trip13 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03094:Trip13
|
APN |
13 |
74,081,075 (GRCm39) |
missense |
probably benign |
0.00 |
E0370:Trip13
|
UTSW |
13 |
74,068,558 (GRCm39) |
splice site |
probably benign |
|
R0153:Trip13
|
UTSW |
13 |
74,068,183 (GRCm39) |
missense |
possibly damaging |
0.52 |
R1945:Trip13
|
UTSW |
13 |
74,076,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R4206:Trip13
|
UTSW |
13 |
74,081,009 (GRCm39) |
missense |
probably benign |
0.00 |
R5758:Trip13
|
UTSW |
13 |
74,085,614 (GRCm39) |
missense |
probably benign |
0.00 |
R6278:Trip13
|
UTSW |
13 |
74,061,439 (GRCm39) |
missense |
probably benign |
0.00 |
R6298:Trip13
|
UTSW |
13 |
74,084,378 (GRCm39) |
nonsense |
probably null |
|
R7106:Trip13
|
UTSW |
13 |
74,062,651 (GRCm39) |
missense |
probably benign |
0.04 |
R7159:Trip13
|
UTSW |
13 |
74,068,130 (GRCm39) |
missense |
probably benign |
0.04 |
R7544:Trip13
|
UTSW |
13 |
74,081,021 (GRCm39) |
missense |
probably benign |
0.00 |
R8035:Trip13
|
UTSW |
13 |
74,061,373 (GRCm39) |
missense |
probably benign |
|
R8488:Trip13
|
UTSW |
13 |
74,081,032 (GRCm39) |
missense |
probably benign |
|
R8720:Trip13
|
UTSW |
13 |
74,063,590 (GRCm39) |
missense |
probably benign |
|
R8881:Trip13
|
UTSW |
13 |
74,077,795 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8915:Trip13
|
UTSW |
13 |
74,081,085 (GRCm39) |
missense |
probably benign |
|
R9555:Trip13
|
UTSW |
13 |
74,084,252 (GRCm39) |
missense |
probably benign |
0.02 |
|
Predicted Primers |
PCR Primer
(F):5'- GGCGTCTATAATAAAATGCCTATGAG -3'
(R):5'- GAACTGAGTCTTTAAAGCACCTTG -3'
Sequencing Primer
(F):5'- GAACTAGAGTACATTAAGCTATGCC -3'
(R):5'- TCTCTTGACCTCGGTGGAAAGAAC -3'
|
Posted On |
2015-04-30 |