Mutagenetix > Incidental Mutation

Incidental Mutation 'R7210:Tnip3'

560994

Institutional Source

Beutler Lab

Gene Symbol

Tnip3

Ensembl Gene

ENSMUSG00000044162

Gene Name

TNFAIP3 interacting protein 3

Synonyms

9030611K07Rik

MMRRC Submission

045239-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7210 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

65567382-65611024 bp(+) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

C to T at 65570495 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Stop codon at position 30 (R30*)

Ref Sequence

ENSEMBL: ENSMUSP00000109874 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000114236] [ENSMUST00000212375] [ENSMUST00000212402]

AlphaFold

A0A1D5RMN0

Predicted Effect

probably null
Transcript: ENSMUST00000114236
AA Change: R30*

SMART Domains

Protein: ENSMUSP00000109874
Gene: ENSMUSG00000044162
AA Change: R30*

Domain	Start	End	E-Value	Type
coiled coil region	20	145	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000212375
AA Change: R101*

Predicted Effect

probably null
Transcript: ENSMUST00000212402
AA Change: R90*

Meta Mutation Damage Score

0.9755

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 98.9%

Validation Efficiency

100% (60/60)

MGI Phenotype

PHENOTYPE: Mice homozygous for a knock-out allele are viable and fertile and do not develop spontaneous inflammatory or autoimmune disease; mutant macrophages exhibit normal responses to IL-10 and LPS. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 59 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcc3	G	A	11: 94,264,767 (GRCm39)	P194S	probably benign	Het
Ackr2	C	T	9: 121,737,943 (GRCm39)	A106V	possibly damaging	Het
Alg3	G	A	16: 20,424,644 (GRCm39)	P112L	unknown	Het
Areg	T	A	5: 91,288,764 (GRCm39)	Y23*	probably null	Het
Aspn	A	G	13: 49,719,967 (GRCm39)	T328A	probably benign	Het
B020011L13Rik	A	T	1: 117,729,241 (GRCm39)	E249D	possibly damaging	Het
Bptf	G	A	11: 106,945,290 (GRCm39)	Q2650*	probably null	Het
Btbd3	A	T	2: 138,125,664 (GRCm39)	R283W	probably damaging	Het
Cep131	T	C	11: 119,955,615 (GRCm39)	H1035R	probably damaging	Het
Cfap57	A	T	4: 118,433,900 (GRCm39)	Y959*	probably null	Het
Cnot1	T	C	8: 96,515,286 (GRCm39)	Y25C	probably damaging	Het
Crebbp	G	A	16: 3,902,121 (GRCm39)	H2373Y	possibly damaging	Het
Ctnna3	T	C	10: 64,086,547 (GRCm39)	L373P	probably damaging	Het
Cyp8b1	T	A	9: 121,744,246 (GRCm39)	D362V	probably damaging	Het
D630003M21Rik	T	A	2: 158,057,932 (GRCm39)		probably null	Het
Dpp6	T	C	5: 27,803,801 (GRCm39)	I249T	probably damaging	Het
Fam149b	T	G	14: 20,428,540 (GRCm39)	I475M	probably damaging	Het
Fat1	A	G	8: 45,476,540 (GRCm39)	Y1862C	probably damaging	Het
Fcrl5	A	T	3: 87,353,719 (GRCm39)	N355Y	possibly damaging	Het
Fgd6	C	T	10: 93,969,954 (GRCm39)	T1201I	probably damaging	Het
Fndc8	A	T	11: 82,788,692 (GRCm39)	D174V	probably damaging	Het
Gatb	A	G	3: 85,481,527 (GRCm39)	H26R	probably benign	Het
Gm37240	T	A	3: 84,405,114 (GRCm39)	T230S	probably benign	Het
Gria4	T	C	9: 4,464,135 (GRCm39)	Q609R	probably damaging	Het
Gse1	C	A	8: 120,957,441 (GRCm39)	T644K	unknown	Het
Ifit1bl1	T	G	19: 34,571,564 (GRCm39)	I298L	probably benign	Het
Il31ra	T	C	13: 112,686,034 (GRCm39)	D85G	possibly damaging	Het
Katnip	T	C	7: 125,471,411 (GRCm39)	V1504A	probably damaging	Het
Lyst	T	C	13: 13,831,568 (GRCm39)	L1664P	probably damaging	Het
Mrpl35	A	G	6: 71,794,722 (GRCm39)	L82S	possibly damaging	Het
Myo7b	G	A	18: 32,140,155 (GRCm39)	R212C	probably damaging	Het
Myom2	T	C	8: 15,154,114 (GRCm39)	V684A	probably damaging	Het
Nbeal1	G	C	1: 60,276,310 (GRCm39)	V684L	probably benign	Het
Nop58	G	T	1: 59,749,539 (GRCm39)		probably null	Het
Nudt13	T	A	14: 20,359,852 (GRCm39)	I193N	possibly damaging	Het
Nyap1	C	A	5: 137,736,244 (GRCm39)	R81L	probably damaging	Het
Or1e28-ps1	T	C	11: 73,615,699 (GRCm39)	I50M	possibly damaging	Het
Oxct2b	A	C	4: 123,010,069 (GRCm39)		probably benign	Het
Pcf11	C	T	7: 92,312,684 (GRCm39)	A230T	probably benign	Het
Phactr4	A	T	4: 132,085,582 (GRCm39)	*695R	probably null	Het
Pkd1	T	C	17: 24,794,840 (GRCm39)	S2176P	probably damaging	Het
Plch2	C	A	4: 155,093,543 (GRCm39)	R133L	probably damaging	Het
Ptprq	G	T	10: 107,521,032 (GRCm39)	N713K	probably damaging	Het
Ptrh2	A	T	11: 86,580,793 (GRCm39)	T137S	probably benign	Het
R3hdm1	A	G	1: 128,138,945 (GRCm39)	Y718C	possibly damaging	Het
Rftn1	T	A	17: 50,301,335 (GRCm39)	R505*	probably null	Het
Rps15a	A	G	7: 117,708,334 (GRCm39)	F128L	probably benign	Het
Slc25a25	A	T	2: 32,310,408 (GRCm39)	M177K	possibly damaging	Het
Smgc	C	A	15: 91,744,492 (GRCm39)	P631Q	probably damaging	Het
Sox2	T	C	3: 34,705,306 (GRCm39)	S248P	probably damaging	Het
Sycp1	T	C	3: 102,760,808 (GRCm39)	K702E	probably damaging	Het
Tes	G	T	6: 17,104,761 (GRCm39)	C414F	probably damaging	Het
Tet1	A	T	10: 62,650,280 (GRCm39)	C14S	probably null	Het
Tle3	C	T	9: 61,319,587 (GRCm39)	P452S	probably damaging	Het
Tmc6	A	C	11: 117,666,670 (GRCm39)	L131R	possibly damaging	Het
Tnrc6b	G	T	15: 80,813,486 (GRCm39)	G1748W	probably damaging	Het
Ugt2b38	T	G	5: 87,558,284 (GRCm39)	D459A	probably damaging	Het
Zdhhc2	A	T	8: 40,920,480 (GRCm39)	R246S	probably damaging	Het
Zscan22	T	A	7: 12,640,748 (GRCm39)	C331S	probably damaging	Het

Other mutations in Tnip3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01736:Tnip3	APN	6	65,573,107 (GRCm39)	splice site	probably benign
IGL02054:Tnip3	APN	6	65,567,595 (GRCm39)	missense	possibly damaging	0.72
IGL02382:Tnip3	APN	6	65,591,779 (GRCm39)	critical splice donor site	probably null
nickle_nip	UTSW	6	65,591,779 (GRCm39)	critical splice donor site	probably null
R0671:Tnip3	UTSW	6	65,574,347 (GRCm39)	missense	probably damaging	1.00
R1344:Tnip3	UTSW	6	65,574,413 (GRCm39)	missense	probably benign	0.44
R1418:Tnip3	UTSW	6	65,574,413 (GRCm39)	missense	probably benign	0.44
R3748:Tnip3	UTSW	6	65,591,747 (GRCm39)	missense	probably damaging	0.99
R3953:Tnip3	UTSW	6	65,574,379 (GRCm39)	missense	possibly damaging	0.48
R3955:Tnip3	UTSW	6	65,574,379 (GRCm39)	missense	possibly damaging	0.48
R5775:Tnip3	UTSW	6	65,591,741 (GRCm39)	missense	probably benign	0.01
R5930:Tnip3	UTSW	6	65,582,937 (GRCm39)	missense	probably damaging	1.00
R6108:Tnip3	UTSW	6	65,502,395 (GRCm39)	splice site	probably null
R6495:Tnip3	UTSW	6	65,582,846 (GRCm39)	missense	probably benign	0.05
R7956:Tnip3	UTSW	6	65,591,779 (GRCm39)	critical splice donor site	probably null
R7983:Tnip3	UTSW	6	65,515,630 (GRCm39)	missense	probably damaging	1.00
R8267:Tnip3	UTSW	6	65,582,826 (GRCm39)	missense	possibly damaging	0.77
R8957:Tnip3	UTSW	6	65,582,843 (GRCm39)	missense	probably benign	0.05
Z1177:Tnip3	UTSW	6	65,591,717 (GRCm39)	missense	possibly damaging	0.90

Predicted Primers

PCR Primer
(F):5'- AGCATATTAGGCTGGCCCATC -3'
(R):5'- AGCAGGGTTATAACTACCACATTC -3'

Sequencing Primer
(F):5'- AGGGCCTTTTACATGCTAAGC -3'
(R):5'- TCAGTTGTCATAGCACAAACATG -3'

Posted On

2019-06-26