Mutagenetix > Incidental Mutation

Incidental Mutation 'R5946:Trip10'

472204

Institutional Source

Beutler Lab

Gene Symbol

Trip10

Ensembl Gene

ENSMUSG00000019487

Gene Name

thyroid hormone receptor interactor 10

Synonyms

Cip4

Accession Numbers

Essential gene?

Probably essential (E-score: 0.753) question?

Stock #

R5946 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

57556455-57570665 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to G at 57557963 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Glycine at position 50 (V50G)

Ref Sequence

ENSEMBL: ENSMUSP00000153467 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000005975] [ENSMUST00000019631] [ENSMUST00000224152] [ENSMUST00000224885] [ENSMUST00000224947] [ENSMUST00000225664]

AlphaFold

Q8CJ53

Predicted Effect

probably benign
Transcript: ENSMUST00000005975

SMART Domains

Protein: ENSMUSP00000005975
Gene: ENSMUSG00000005823

Domain	Start	End	E-Value	Type
low complexity region	61	75	N/A	INTRINSIC
low complexity region	86	103	N/A	INTRINSIC
Pfam:Lung_7-TM_R	240	529	2.3e-98	PFAM
low complexity region	535	547	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000019631
AA Change: V50G

PolyPhen 2 Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000019631
Gene: ENSMUSG00000019487
AA Change: V50G

Domain	Start	End	E-Value	Type
FCH	1	94	9.95e-29	SMART
coiled coil region	117	197	N/A	INTRINSIC
low complexity region	310	318	N/A	INTRINSIC
PDB:2KE4\|A	332	425	3e-35	PDB
low complexity region	433	455	N/A	INTRINSIC
low complexity region	458	467	N/A	INTRINSIC
SH3	489	546	2.44e-11	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000224152
AA Change: V50G

PolyPhen 2 Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000224586

Predicted Effect

probably damaging
Transcript: ENSMUST00000224885
AA Change: V50G

PolyPhen 2 Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)

Predicted Effect

probably damaging
Transcript: ENSMUST00000224947
AA Change: V50G

PolyPhen 2 Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000225523

Predicted Effect

probably benign
Transcript: ENSMUST00000225664

Coding Region Coverage

1x: 99.9%
3x: 99.5%
10x: 97.6%
20x: 92.4%

Validation Efficiency

MGI Phenotype

PHENOTYPE: Mice homozygous for a knock-out allele exhibit increased insulin-stimulated glucose uptake in adipocytes and decreased circulating glucose levels. Mice homozygous for another knock-out allele exhibit impaired integrin-dependent T-cell trafficking. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 58 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcc9	A	G	6: 142,571,678 (GRCm39)	F1137S	probably damaging	Het
Actr6	G	T	10: 89,564,054 (GRCm39)	Q73K	probably benign	Het
Adamtsl3	G	A	7: 82,225,265 (GRCm39)	G358D	probably damaging	Het
Aggf1	A	G	13: 95,508,084 (GRCm39)	V94A	probably damaging	Het
Arpc3	A	G	5: 122,541,459 (GRCm39)	Y57C	probably damaging	Het
Asb2	A	G	12: 103,287,814 (GRCm39)	Y630H	probably benign	Het
Atp1a1	A	T	3: 101,497,090 (GRCm39)	N405K	probably benign	Het
C6	G	T	15: 4,837,996 (GRCm39)	D869Y	possibly damaging	Het
Cds2	A	G	2: 132,139,168 (GRCm39)	Y137C	probably damaging	Het
Ceacam12	A	T	7: 17,803,131 (GRCm39)	E179V	probably damaging	Het
Chgb	T	A	2: 132,634,516 (GRCm39)	Y153N	probably benign	Het
Cit	T	A	5: 116,135,593 (GRCm39)	L1831Q	probably damaging	Het
Cpne8	C	A	15: 90,373,191 (GRCm39)	*578L	probably null	Het
Cspg5	A	G	9: 110,080,151 (GRCm39)	T440A	probably damaging	Het
Dnah7a	A	C	1: 53,598,467 (GRCm39)	V1393G	probably damaging	Het
Dnajb8	A	G	6: 88,199,575 (GRCm39)	D37G	probably benign	Het
Dst	A	G	1: 34,213,273 (GRCm39)	I1063M	probably benign	Het
Efs	T	G	14: 55,156,951 (GRCm39)		probably null	Het
Gpatch1	A	G	7: 34,991,257 (GRCm39)	S596P	probably damaging	Het
Hbs1l	C	A	10: 21,217,655 (GRCm39)	H190Q	probably benign	Het
Ighm	A	G	12: 113,386,329 (GRCm39)	V7A	unknown	Het
Ivd	A	T	2: 118,707,370 (GRCm39)	I295F	possibly damaging	Het
Kcnq5	A	C	1: 21,575,931 (GRCm39)	S258A	probably damaging	Het
Mad1l1	G	T	5: 140,247,334 (GRCm39)	P331Q	probably damaging	Het
Mcf2l	G	T	8: 13,063,922 (GRCm39)	G1045C	probably damaging	Het
Mcoln1	T	A	8: 3,558,701 (GRCm39)	I233N	probably damaging	Het
Mmp13	T	C	9: 7,276,580 (GRCm39)	L225P	probably damaging	Het
Muc5ac	G	A	7: 141,371,644 (GRCm39)	C2615Y	possibly damaging	Het
Myh7b	T	C	2: 155,463,315 (GRCm39)	F516L	probably damaging	Het
Obsl1	A	T	1: 75,467,851 (GRCm39)	S1347R	probably damaging	Het
Ogn	A	G	13: 49,771,761 (GRCm39)	N207S	probably benign	Het
Or2h15	C	A	17: 38,441,598 (GRCm39)	A162S	probably benign	Het
Or8b12	T	A	9: 37,658,330 (GRCm39)	L300Q	probably damaging	Het
Pcdha2	G	T	18: 37,074,159 (GRCm39)	V597L	probably damaging	Het
Pcnt	T	A	10: 76,217,897 (GRCm39)	Y2126F	possibly damaging	Het
Pgbd5	A	T	8: 125,101,056 (GRCm39)	M400K	possibly damaging	Het
Pklr	A	T	3: 89,043,503 (GRCm39)	E5V	probably benign	Het
Pkp4	T	A	2: 59,135,411 (GRCm39)	D94E	probably benign	Het
Ppan	C	T	9: 20,800,969 (GRCm39)	Q111*	probably null	Het
Prkcb	A	G	7: 122,143,926 (GRCm39)	N330S	probably benign	Het
Prl4a1	T	A	13: 28,202,499 (GRCm39)	W25R	probably damaging	Het
Rars2	T	A	4: 34,656,855 (GRCm39)	H501Q	possibly damaging	Het
Ryr2	T	C	13: 11,741,839 (GRCm39)	D2114G	probably damaging	Het
Serinc2	G	T	4: 130,149,314 (GRCm39)	T351K	possibly damaging	Het
Slc22a12	A	G	19: 6,587,881 (GRCm39)	F358L	probably damaging	Het
Sorcs2	A	C	5: 36,186,427 (GRCm39)	V905G	probably damaging	Het
Tekt3	G	C	11: 62,985,573 (GRCm39)	A460P	probably damaging	Het
Tm4sf1	T	G	3: 57,200,289 (GRCm39)	I109L	possibly damaging	Het
Tmc5	A	T	7: 118,269,948 (GRCm39)	E899D	probably damaging	Het
Tmem268	C	T	4: 63,486,746 (GRCm39)	P90S	probably damaging	Het
Trim38	A	G	13: 23,966,717 (GRCm39)	M55V	probably benign	Het
Usp25	T	A	16: 76,911,942 (GRCm39)	C990*	probably null	Het
Uts2	A	G	4: 151,083,506 (GRCm39)	D39G	probably benign	Het
Vezf1	T	A	11: 87,964,560 (GRCm39)	C49*	probably null	Het
Wee2	T	A	6: 40,440,146 (GRCm39)	N431K	probably null	Het
Yeats2	C	A	16: 20,026,513 (GRCm39)	Y796*	probably null	Het
Zfp592	G	A	7: 80,687,645 (GRCm39)	G890D	possibly damaging	Het
Zfp647	G	A	15: 76,796,285 (GRCm39)	P125L	probably damaging	Het

Other mutations in Trip10

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01071:Trip10	APN	17	57,561,332 (GRCm39)	missense	possibly damaging	0.91
IGL01639:Trip10	APN	17	57,561,165 (GRCm39)	unclassified	probably benign
IGL01758:Trip10	APN	17	57,568,409 (GRCm39)	missense	possibly damaging	0.51
IGL02184:Trip10	APN	17	57,564,272 (GRCm39)	missense	probably damaging	1.00
IGL02554:Trip10	APN	17	57,570,135 (GRCm39)	missense	probably damaging	0.99
IGL02641:Trip10	APN	17	57,569,411 (GRCm39)	missense	probably benign	0.06
R0092:Trip10	UTSW	17	57,557,798 (GRCm39)	missense	possibly damaging	0.46
R0139:Trip10	UTSW	17	57,568,633 (GRCm39)	splice site	probably null
R0179:Trip10	UTSW	17	57,569,349 (GRCm39)	splice site	probably benign
R1173:Trip10	UTSW	17	57,560,363 (GRCm39)	missense	probably damaging	0.98
R1416:Trip10	UTSW	17	57,557,800 (GRCm39)	missense	probably damaging	1.00
R2223:Trip10	UTSW	17	57,570,039 (GRCm39)	missense	possibly damaging	0.70
R2259:Trip10	UTSW	17	57,562,135 (GRCm39)	missense	probably benign	0.00
R3950:Trip10	UTSW	17	57,560,411 (GRCm39)	critical splice donor site	probably null
R4420:Trip10	UTSW	17	57,562,448 (GRCm39)	missense	probably benign	0.05
R4643:Trip10	UTSW	17	57,568,658 (GRCm39)	nonsense	probably null
R4940:Trip10	UTSW	17	57,570,017 (GRCm39)	missense	possibly damaging	0.65
R5189:Trip10	UTSW	17	57,568,288 (GRCm39)	critical splice acceptor site	probably null
R5595:Trip10	UTSW	17	57,569,460 (GRCm39)	missense	probably damaging	1.00
R6613:Trip10	UTSW	17	57,562,197 (GRCm39)	splice site	probably null
R6738:Trip10	UTSW	17	57,563,899 (GRCm39)	missense	probably benign
R6948:Trip10	UTSW	17	57,569,448 (GRCm39)	missense	probably damaging	1.00
R6994:Trip10	UTSW	17	57,562,331 (GRCm39)	missense	probably damaging	1.00
R7489:Trip10	UTSW	17	57,557,966 (GRCm39)	missense	probably damaging	1.00
R7729:Trip10	UTSW	17	57,569,442 (GRCm39)	missense	probably damaging	1.00
R7750:Trip10	UTSW	17	57,568,667 (GRCm39)	missense	possibly damaging	0.58
R8260:Trip10	UTSW	17	57,564,314 (GRCm39)	missense	probably benign
R8781:Trip10	UTSW	17	57,562,313 (GRCm39)	missense	probably benign	0.01
R9005:Trip10	UTSW	17	57,569,416 (GRCm39)	missense	probably damaging	0.99
R9108:Trip10	UTSW	17	57,560,519 (GRCm39)	missense	probably damaging	1.00
RF024:Trip10	UTSW	17	57,562,045 (GRCm39)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- GATCAGTTTGAGGTGCTGGAAC -3'
(R):5'- GCGAGTAAATTCCACCTTAGGAC -3'

Sequencing Primer
(F):5'- TGAGGTGCTGGAACGCCAC -3'
(R):5'- CTTAGGACATCCAGACTAACAGGAG -3'

Posted On

2017-03-31