Mutagenetix > Incidental Mutation

Incidental Mutation 'R3802:Tektl1'

274365

Institutional Source

Beutler Lab

Gene Symbol

Tektl1

Ensembl Gene

ENSMUSG00000078442

Gene Name

tektin like 1

Synonyms

Ccdc105, 4931413A09Rik

MMRRC Submission

040761-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.072) question?

Stock #

R3802 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

78582760-78588899 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to C at 78584314 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Cysteine at position 367 (F367C)

Ref Sequence

ENSEMBL: ENSMUSP00000101022 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000105383]

AlphaFold

Q9D4K7

Predicted Effect

probably damaging
Transcript: ENSMUST00000105383
AA Change: F367C

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000101022
Gene: ENSMUSG00000078442
AA Change: F367C

Domain	Start	End	E-Value	Type
Pfam:Tektin	115	470	1.6e-19	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000209307

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000210562

Meta Mutation Damage Score

0.6467

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.6%
20x: 96.1%

Validation Efficiency

100% (47/47)

Allele List at MGI

Other mutations in this stock

Total: 47 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
AAdacl4fm3	A	T	4: 144,430,074 (GRCm39)	L305Q	possibly damaging	Het
Abcc2	C	A	19: 43,810,065 (GRCm39)	N874K	probably benign	Het
Axl	A	T	7: 25,487,902 (GRCm39)	M1K	probably null	Het
Btaf1	A	T	19: 36,963,948 (GRCm39)	T840S	probably benign	Het
Btaf1	A	T	19: 36,966,373 (GRCm39)	H1047L	probably benign	Het
Capn13	G	A	17: 73,646,396 (GRCm39)	P339L	probably benign	Het
Ccdc39	A	T	3: 33,874,044 (GRCm39)	M596K	probably damaging	Het
Cfap20dc	G	T	14: 8,510,931 (GRCm38)	D494E	probably benign	Het
Cfap58	G	T	19: 47,941,498 (GRCm39)	D289Y	possibly damaging	Het
Cnn2	A	G	10: 79,829,329 (GRCm39)	D153G	probably benign	Het
Cstdc2	T	C	2: 148,692,616 (GRCm39)	H62R	probably benign	Het
Cubn	T	C	2: 13,365,164 (GRCm39)	I1625V	probably benign	Het
Gprc5b	C	T	7: 118,582,943 (GRCm39)	D309N	possibly damaging	Het
Grm8	T	G	6: 28,125,635 (GRCm39)	N164H	possibly damaging	Het
Gstm3	G	A	3: 107,871,551 (GRCm39)	T210I	probably benign	Het
Hhipl1	A	G	12: 108,278,566 (GRCm39)	E298G	probably benign	Het
Hivep2	A	G	10: 14,024,705 (GRCm39)	D2173G	possibly damaging	Het
Hsd17b8	A	T	17: 34,245,441 (GRCm39)	V231E	probably damaging	Het
Jarid2	T	A	13: 45,056,307 (GRCm39)	N365K	probably benign	Het
Kank4	A	G	4: 98,668,370 (GRCm39)	S26P	probably damaging	Het
Kpnb1	A	T	11: 97,056,955 (GRCm39)	V638E	possibly damaging	Het
Lipo3	C	T	19: 33,762,257 (GRCm39)	C80Y	probably damaging	Het
Mga	T	A	2: 119,777,820 (GRCm39)	N1788K	probably damaging	Het
Mslnl	G	A	17: 25,961,908 (GRCm39)	V128M	probably damaging	Het
Mtmr10	A	G	7: 63,970,376 (GRCm39)	Y373C	probably benign	Het
Ncoa6	C	T	2: 155,247,484 (GRCm39)	G1940D	probably benign	Het
Nelfe	T	A	17: 35,072,877 (GRCm39)	F166L	possibly damaging	Het
Nfatc3	A	G	8: 106,806,277 (GRCm39)	Y374C	probably damaging	Het
Nhlrc3	A	G	3: 53,366,052 (GRCm39)	V147A	possibly damaging	Het
Or51f1d	A	G	7: 102,701,372 (GRCm39)	Y289C	probably benign	Het
Or8g33	G	A	9: 39,337,582 (GRCm39)	P262S	probably damaging	Het
Pak3	G	A	X: 142,492,727 (GRCm39)	V87I	probably damaging	Het
Papolg	A	T	11: 23,826,449 (GRCm39)	I235N	probably damaging	Het
Pdgfrl	T	C	8: 41,438,594 (GRCm39)	S177P	probably damaging	Het
Phf8	T	C	X: 150,355,572 (GRCm39)	S512P	possibly damaging	Het
Plaa	T	C	4: 94,458,125 (GRCm39)	D615G	probably damaging	Het
Prpf4b	T	C	13: 35,067,665 (GRCm39)		probably benign	Het
Sgk1	T	C	10: 21,873,311 (GRCm39)	V259A	probably damaging	Het
Skint4	G	T	4: 111,975,378 (GRCm39)	V113L	probably damaging	Het
Smco1	A	G	16: 32,092,716 (GRCm39)	Y129C	probably benign	Het
Tas2r106	C	A	6: 131,655,329 (GRCm39)	S174I	probably benign	Het
Tsn	A	T	1: 118,233,026 (GRCm39)	F93I	probably damaging	Het
Vav2	T	C	2: 27,157,235 (GRCm39)		probably benign	Het
Vmn2r63	A	T	7: 42,552,829 (GRCm39)	M809K	probably damaging	Het
Zfp260	G	A	7: 29,804,504 (GRCm39)	E135K	probably benign	Het
Zfp808	T	A	13: 62,319,897 (GRCm39)	H375Q	probably damaging	Het
Zkscan2	A	T	7: 123,094,365 (GRCm39)		probably benign	Het

Other mutations in Tektl1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00858:Tektl1	APN	10	78,586,403 (GRCm39)	missense	probably damaging	1.00
IGL01632:Tektl1	APN	10	78,584,536 (GRCm39)	missense	probably benign	0.01
IGL02473:Tektl1	APN	10	78,586,428 (GRCm39)	missense	probably benign	0.05
IGL02606:Tektl1	APN	10	78,584,300 (GRCm39)	missense	probably benign	0.01
IGL03356:Tektl1	APN	10	78,582,966 (GRCm39)	missense	possibly damaging	0.52
R0096:Tektl1	UTSW	10	78,584,539 (GRCm39)	missense	probably benign	0.01
R0096:Tektl1	UTSW	10	78,584,539 (GRCm39)	missense	probably benign	0.01
R0666:Tektl1	UTSW	10	78,586,381 (GRCm39)	missense	probably benign	0.04
R1756:Tektl1	UTSW	10	78,583,031 (GRCm39)	missense	probably damaging	0.96
R1757:Tektl1	UTSW	10	78,583,058 (GRCm39)	missense	probably benign	0.02
R1765:Tektl1	UTSW	10	78,584,502 (GRCm39)	missense	probably benign	0.21
R1956:Tektl1	UTSW	10	78,586,373 (GRCm39)	critical splice donor site	probably null
R2305:Tektl1	UTSW	10	78,584,336 (GRCm39)	missense	probably damaging	1.00
R3845:Tektl1	UTSW	10	78,584,532 (GRCm39)	missense	probably benign
R4023:Tektl1	UTSW	10	78,588,727 (GRCm39)	missense	probably benign	0.03
R4808:Tektl1	UTSW	10	78,588,698 (GRCm39)	missense	probably benign	0.02
R4812:Tektl1	UTSW	10	78,585,050 (GRCm39)	missense	probably benign	0.01
R5391:Tektl1	UTSW	10	78,588,688 (GRCm39)	nonsense	probably null
R5434:Tektl1	UTSW	10	78,584,484 (GRCm39)	nonsense	probably null
R6382:Tektl1	UTSW	10	78,588,675 (GRCm39)	missense	possibly damaging	0.90
R6743:Tektl1	UTSW	10	78,588,726 (GRCm39)	missense	probably benign	0.01
R6749:Tektl1	UTSW	10	78,588,672 (GRCm39)	missense	possibly damaging	0.95
R7177:Tektl1	UTSW	10	78,588,324 (GRCm39)	missense	probably damaging	1.00
R8158:Tektl1	UTSW	10	78,584,509 (GRCm39)	missense	probably benign	0.01
R8504:Tektl1	UTSW	10	78,586,463 (GRCm39)	missense	probably damaging	1.00
R8504:Tektl1	UTSW	10	78,585,038 (GRCm39)	missense	probably benign	0.00
R8558:Tektl1	UTSW	10	78,583,035 (GRCm39)	missense	probably damaging	1.00
R8806:Tektl1	UTSW	10	78,588,306 (GRCm39)	missense	probably damaging	1.00
R8925:Tektl1	UTSW	10	78,588,258 (GRCm39)	missense	probably damaging	1.00
R8927:Tektl1	UTSW	10	78,588,258 (GRCm39)	missense	probably damaging	1.00
R9285:Tektl1	UTSW	10	78,588,234 (GRCm39)	splice site	probably benign
R9407:Tektl1	UTSW	10	78,583,128 (GRCm39)	missense	probably damaging	0.99
X0057:Tektl1	UTSW	10	78,586,375 (GRCm39)	missense	probably null	1.00

Predicted Primers

PCR Primer
(F):5'- CGAACCAAGGGTCTGTTCAG -3'
(R):5'- AGATAAGCAACCGTGTATGCTC -3'

Sequencing Primer
(F):5'- GAACCAAGGGTCTGTTCAGTTTCTC -3'
(R):5'- CACAGAAGATGCGTGAGACCTTG -3'

Posted On

2015-04-02