Mutagenetix > Incidental Mutation

Incidental Mutation 'R6597:Tekt3'

524956

Institutional Source

Beutler Lab

Gene Symbol

Tekt3

Ensembl Gene

ENSMUSG00000042189

Gene Name

tektin 3

Synonyms

4933407G07Rik

MMRRC Submission

044721-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R6597 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

62952485-62985786 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 62972085 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 247 (D247G)

Ref Sequence

ENSEMBL: ENSMUSP00000042063 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000035732]

AlphaFold

Q6X6Z7

Predicted Effect

probably benign
Transcript: ENSMUST00000035732
AA Change: D247G

PolyPhen 2 Score 0.188 (Sensitivity: 0.92; Specificity: 0.87)

SMART Domains

Protein: ENSMUSP00000042063
Gene: ENSMUSG00000042189
AA Change: D247G

Domain	Start	End	E-Value	Type
Pfam:Tektin	99	481	5.6e-149	PFAM

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 98.0%
20x: 94.2%

Validation Efficiency

100% (50/50)

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. The exact function of this gene is not known. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a null allele exhibit defective sperm motility. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 53 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A2m	A	G	6: 121,625,080 (GRCm39)	Y486C	probably damaging	Het
Asb17	A	T	3: 153,550,321 (GRCm39)	T118S	probably damaging	Het
Atl2	T	A	17: 80,160,195 (GRCm39)	D293V	possibly damaging	Het
Bbs1	T	A	19: 4,949,334 (GRCm39)	M242L	probably benign	Het
Btg1	T	A	10: 96,454,182 (GRCm39)	S65T	probably damaging	Het
Cfap54	T	C	10: 92,834,902 (GRCm39)	D1101G	possibly damaging	Het
Cmpk2	G	T	12: 26,524,144 (GRCm39)	V314L	possibly damaging	Het
Fbxl8	A	C	8: 105,995,523 (GRCm39)	D345A	probably benign	Het
Gys2	T	A	6: 142,402,035 (GRCm39)	H268L	probably benign	Het
Hecw1	T	A	13: 14,491,403 (GRCm39)	R117*	probably null	Het
Hoxd10	G	A	2: 74,522,984 (GRCm39)	A221T	probably benign	Het
Hspa13	A	T	16: 75,562,085 (GRCm39)	L38Q	probably damaging	Het
Inava	G	T	1: 136,153,927 (GRCm39)	A87E	probably damaging	Het
Ipo11	A	G	13: 107,002,371 (GRCm39)		probably null	Het
Itgb8	A	G	12: 119,137,133 (GRCm39)	V390A	possibly damaging	Het
Kalrn	T	A	16: 34,003,117 (GRCm39)	I1370F	probably damaging	Het
Macf1	T	C	4: 123,276,485 (GRCm39)	N6086S	probably damaging	Het
Ms4a13	T	C	19: 11,170,303 (GRCm39)	T14A	probably benign	Het
Or11g26	T	A	14: 50,753,008 (GRCm39)	C116S	probably benign	Het
Or55b10	A	T	7: 102,143,628 (GRCm39)	I118N	probably damaging	Het
Or5ac22	C	T	16: 59,135,713 (GRCm39)	R19H	probably benign	Het
Or5d37	A	G	2: 87,923,413 (GRCm39)	F289S	probably damaging	Het
Or8b47	A	T	9: 38,435,300 (GRCm39)	I91F	probably benign	Het
Or9q1	T	A	19: 13,805,821 (GRCm39)		probably benign	Het
Patl2	T	A	2: 122,016,645 (GRCm39)		probably benign	Het
Pcdhga7	T	C	18: 37,850,059 (GRCm39)	S689P	probably benign	Het
Pitpnc1	G	T	11: 107,117,058 (GRCm39)	Y227*	probably null	Het
Pla2g2e	T	C	4: 138,607,984 (GRCm39)	V22A	unknown	Het
Ppil1	C	A	17: 29,480,852 (GRCm39)	V24F	probably benign	Het
Prl3b1	G	A	13: 27,431,957 (GRCm39)		probably null	Het
Rabgef1	G	A	5: 130,219,885 (GRCm39)		probably null	Het
Rhot2	A	T	17: 26,059,886 (GRCm39)	W341R	probably damaging	Het
Rps6kc1	A	T	1: 190,482,381 (GRCm39)	W286R	probably benign	Het
Rrs1	A	G	1: 9,616,601 (GRCm39)	T285A	probably damaging	Het
Shc3	T	A	13: 51,597,009 (GRCm39)	D338V	possibly damaging	Het
Siglech	A	T	7: 55,418,211 (GRCm39)	M60L	probably benign	Het
Slc12a6	G	T	2: 112,183,280 (GRCm39)	V756F	probably damaging	Het
Slc43a2	G	A	11: 75,462,681 (GRCm39)	G507D	probably damaging	Het
Slf1	A	G	13: 77,197,248 (GRCm39)	S789P	probably benign	Het
Spata31d1d	C	A	13: 59,873,871 (GRCm39)	M1221I	probably benign	Het
Srgap1	T	C	10: 121,628,276 (GRCm39)	N899D	probably benign	Het
Stag1	G	A	9: 100,769,473 (GRCm39)	M529I	probably benign	Het
Tmppe	A	T	9: 114,234,312 (GRCm39)	M204L	probably benign	Het
Tpsg1	G	A	17: 25,588,271 (GRCm39)		probably benign	Het
Ttn	A	G	2: 76,628,315 (GRCm39)	V6288A	probably benign	Het
Ttn	A	T	2: 76,723,444 (GRCm39)		probably benign	Het
Twsg1	C	A	17: 66,244,799 (GRCm39)	V73F	probably damaging	Het
Vmn2r102	A	G	17: 19,914,450 (GRCm39)	T672A	probably damaging	Het
Vps36	A	G	8: 22,692,320 (GRCm39)	I66V	probably benign	Het
Xrcc4	A	T	13: 90,149,048 (GRCm39)	D157E	probably benign	Het
Zbbx	T	A	3: 75,043,761 (GRCm39)	Q162L	probably damaging	Het
Zfp560	T	A	9: 20,259,297 (GRCm39)	I522L	probably benign	Het
Zscan20	T	C	4: 128,479,539 (GRCm39)	N984S	probably damaging	Het

Other mutations in Tekt3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00505:Tekt3	APN	11	62,961,064 (GRCm39)	missense	probably benign	0.19
IGL00851:Tekt3	APN	11	62,961,226 (GRCm39)	missense	probably benign	0.01
IGL01469:Tekt3	APN	11	62,964,294 (GRCm39)	missense	probably damaging	1.00
IGL02123:Tekt3	APN	11	62,974,766 (GRCm39)	missense	probably benign	0.05
R1517:Tekt3	UTSW	11	62,961,316 (GRCm39)	missense	probably damaging	1.00
R1616:Tekt3	UTSW	11	62,978,024 (GRCm39)	splice site	probably null
R1750:Tekt3	UTSW	11	62,960,867 (GRCm39)	missense	probably damaging	0.96
R2087:Tekt3	UTSW	11	62,985,523 (GRCm39)	missense	possibly damaging	0.95
R2174:Tekt3	UTSW	11	62,985,514 (GRCm39)	missense	possibly damaging	0.90
R2249:Tekt3	UTSW	11	62,974,778 (GRCm39)	missense	probably benign
R4835:Tekt3	UTSW	11	62,972,085 (GRCm39)	missense	probably benign	0.19
R5198:Tekt3	UTSW	11	62,961,134 (GRCm39)	missense	probably damaging	1.00
R5452:Tekt3	UTSW	11	62,985,619 (GRCm39)	missense	probably damaging	0.99
R5518:Tekt3	UTSW	11	62,974,768 (GRCm39)	missense	probably benign	0.00
R5946:Tekt3	UTSW	11	62,985,573 (GRCm39)	missense	probably damaging	0.98
R6150:Tekt3	UTSW	11	62,985,483 (GRCm39)	missense	possibly damaging	0.95
R6191:Tekt3	UTSW	11	62,968,999 (GRCm39)	missense	probably damaging	0.98
R6547:Tekt3	UTSW	11	62,961,304 (GRCm39)	missense	possibly damaging	0.50
R7259:Tekt3	UTSW	11	62,974,592 (GRCm39)	missense	possibly damaging	0.79
R7578:Tekt3	UTSW	11	62,985,486 (GRCm39)	missense	probably damaging	0.99
R7878:Tekt3	UTSW	11	62,961,277 (GRCm39)	nonsense	probably null
R8056:Tekt3	UTSW	11	62,974,785 (GRCm39)	critical splice donor site	probably null
R8082:Tekt3	UTSW	11	62,961,056 (GRCm39)	missense	probably benign	0.00
R8104:Tekt3	UTSW	11	62,968,945 (GRCm39)	missense	probably benign	0.33
R8865:Tekt3	UTSW	11	62,961,058 (GRCm39)	missense	probably benign
R8917:Tekt3	UTSW	11	62,978,052 (GRCm39)	missense	probably damaging	0.98
R9013:Tekt3	UTSW	11	62,974,684 (GRCm39)	missense	probably damaging	1.00
R9039:Tekt3	UTSW	11	62,972,169 (GRCm39)	missense	possibly damaging	0.59

Predicted Primers

PCR Primer
(F):5'- TCCTCAGGCCTCACATGTATG -3'
(R):5'- GGCTGTTCCATGATAGTTGTAGAATAC -3'

Sequencing Primer
(F):5'- TGTATGGCCATCTCCACAAATG -3'
(R):5'- GCCTACGTGCTGCATCATTATGAAAG -3'

Posted On

2018-06-22