Mutagenetix > Incidental Mutation

Incidental Mutation 'R2422:Tlk1'

249346

Institutional Source

Beutler Lab

Gene Symbol

Tlk1

Ensembl Gene

ENSMUSG00000041997

Gene Name

tousled-like kinase 1

Synonyms

4930545J15Rik

MMRRC Submission

040384-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R2422 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

70712407-70825728 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 70770005 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Glutamic Acid to Glycine at position 110 (E110G)

Ref Sequence

ENSEMBL: ENSMUSP00000035961 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000038584]

AlphaFold

Q8C0V0

Predicted Effect

probably damaging
Transcript: ENSMUST00000038584
AA Change: E110G

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000035961
Gene: ENSMUSG00000041997
AA Change: E110G

Domain	Start	End	E-Value	Type
low complexity region	20	33	N/A	INTRINSIC
low complexity region	68	85	N/A	INTRINSIC
low complexity region	170	192	N/A	INTRINSIC
coiled coil region	248	277	N/A	INTRINSIC
coiled coil region	403	441	N/A	INTRINSIC
S_TKc	456	734	4.41e-75	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000124629

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000132542

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000133734

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000135128

Meta Mutation Damage Score

0.1007

Coding Region Coverage

1x: 99.1%
3x: 98.5%
10x: 97.1%
20x: 94.5%

Validation Efficiency

99% (77/78)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a serine/threonine kinase that may be involved in the regulation of chromatin assembly. The encoded protein is only active when it is phosphorylated, and this phosphorylation is cell cycle-dependent, with the maximal activity of this protein coming during S phase. The catalytic activity of this protein is diminished by DNA damage and by blockage of DNA replication. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2011]

Allele List at MGI

Other mutations in this stock

Total: 77 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2010300C02Rik	C	A	1: 37,613,475	V1084L	probably benign	Het
4933409G03Rik	A	T	2: 68,591,520	N47I	probably benign	Het
Actr5	T	C	2: 158,636,081	F457S	probably damaging	Het
Adamts3	A	G	5: 89,683,175	S1007P	probably damaging	Het
Adck2	C	T	6: 39,583,998	A440V	possibly damaging	Het
Birc6	T	A	17: 74,660,614	L301Q	probably damaging	Het
Ccdc18	A	C	5: 108,228,588	E1298D	probably damaging	Het
Ccdc77	A	G	6: 120,339,159	C186R	probably benign	Het
Cdk12	T	G	11: 98,219,074	S640R	probably benign	Het
Cdv3	T	C	9: 103,365,118		probably benign	Het
Celf2	G	A	2: 6,553,889	T364I	probably damaging	Het
Cmtr2	C	A	8: 110,222,781	S574R	probably benign	Het
Col14a1	T	C	15: 55,449,922	L56P	unknown	Het
Dctn1	C	T	6: 83,199,800	L1241F	possibly damaging	Het
Depdc5	T	C	5: 32,991,035	F1505S	probably damaging	Het
Dhcr24	G	T	4: 106,561,094		probably benign	Het
Dnajc21	A	G	15: 10,461,935	S127P	probably benign	Het
Entpd7	A	T	19: 43,728,088	Y507F	possibly damaging	Het
Fbp1	T	C	13: 62,871,306	K24E	probably benign	Het
Galr1	A	T	18: 82,405,923	N76K	probably damaging	Het
Glrb	A	G	3: 80,860,235	I226T	probably damaging	Het
Gm17421	T	A	12: 113,369,487		noncoding transcript	Het
Gm4950	T	A	18: 51,865,784	Q33L	probably benign	Het
Gm5415	C	T	1: 32,545,861	A323T	possibly damaging	Het
Gm6583	A	T	5: 112,355,118	V240D	probably damaging	Het
Gnat2	A	T	3: 108,095,539	M88L	probably damaging	Het
Gpr183	A	G	14: 121,954,177	Y311H	probably damaging	Het
H2-M10.5	A	G	17: 36,774,999	I308V	probably benign	Het
Hipk3	C	T	2: 104,471,485	G121R	probably benign	Het
Hjurp	A	G	1: 88,266,561		probably benign	Het
Homez	C	A	14: 54,857,574	V226F	probably benign	Het
Inf2	C	A	12: 112,610,824	A1034D	unknown	Het
Kcnc4	G	T	3: 107,445,547	P572T	probably benign	Het
Kmt2d	T	C	15: 98,862,266	E1037G	unknown	Het
Krt78	T	C	15: 101,947,264	E704G	probably damaging	Het
Lama1	A	T	17: 67,750,553	M541L	probably benign	Het
Lmbrd2	C	T	15: 9,194,765	T618M	possibly damaging	Het
Ly6g6e	G	A	17: 35,078,146	R121Q	probably benign	Het
Mettl22	T	C	16: 8,487,361	F293L	probably damaging	Het
Mib1	T	C	18: 10,751,906	S263P	probably damaging	Het
Ndufaf1	T	C	2: 119,655,737	E298G	probably damaging	Het
Nek1	T	C	8: 61,019,901	V152A	probably damaging	Het
Nlrp4d	T	A	7: 10,362,945	D876V	probably benign	Het
Olfr178	T	C	16: 58,889,965	E85G	probably benign	Het
Olfr235	A	T	19: 12,268,919	T230S	probably damaging	Het
Olfr740	T	C	14: 50,453,436	L128P	probably damaging	Het
Olfr975	A	G	9: 39,950,528	L81P	possibly damaging	Het
Pcdha11	G	T	18: 37,007,272	L651F	probably damaging	Het
Plekhg1	G	A	10: 3,958,048	M988I	probably benign	Het
Plxnb1	G	A	9: 109,108,438	R1169H	probably benign	Het
Ppp4r3a	A	G	12: 101,042,653		probably benign	Het
Pum2	A	T	12: 8,748,931	Q930L	possibly damaging	Het
Rbp4	T	C	19: 38,124,344	E67G	probably damaging	Het
Rgs9	C	A	11: 109,225,777		probably null	Het
Sipa1	A	T	19: 5,652,112	D923E	possibly damaging	Het
Smc1a	A	G	X: 152,047,975		probably benign	Het
Snx33	C	A	9: 56,918,538	M546I	probably benign	Het
Spag17	T	A	3: 100,027,619	W714R	probably benign	Het
Spata2	C	T	2: 167,484,206	R231Q	probably damaging	Het
Stard9	C	T	2: 120,700,284	R2341C	probably benign	Het
Tas2r116	A	T	6: 132,855,594	I53F	possibly damaging	Het
Tmem102	T	A	11: 69,804,537	E203V	probably benign	Het
Top2b	T	G	14: 16,409,189	I777M	probably damaging	Het
Ttc23l	CT	CTTGGATT	15: 10,537,562		probably benign	Het
Ttc23l	G	A	15: 10,537,566	S206L	probably benign	Het
Tyw5	A	G	1: 57,396,748	I82T	possibly damaging	Het
Uba6	A	G	5: 86,132,616		probably null	Het
Ugcg	C	T	4: 59,207,798	P46S	probably benign	Het
Unc13c	T	C	9: 73,931,547	Y674C	probably damaging	Het
Vmn2r105	T	A	17: 20,227,835	R242S	probably benign	Het
Vmn2r12	A	G	5: 109,086,532	Y605H	probably benign	Het
Wdr77	A	T	3: 105,960,021	K62*	probably null	Het
Zfhx4	C	A	3: 5,390,405	A1153E	probably benign	Het
Zfp266	C	A	9: 20,499,262	V540L	possibly damaging	Het
Zfp638	C	A	6: 83,966,439		probably benign	Het
Zfp644	A	G	5: 106,637,244	M479T	possibly damaging	Het
Zfp951	G	A	5: 104,815,277	T141I	probably benign	Het

Other mutations in Tlk1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00673:Tlk1	APN	2	70745516	missense	probably damaging	1.00
IGL01087:Tlk1	APN	2	70752316	missense	possibly damaging	0.64
IGL01514:Tlk1	APN	2	70752266	missense	probably benign	0.00
IGL02976:Tlk1	APN	2	70721591	nonsense	probably null
IGL03024:Tlk1	APN	2	70746036	nonsense	probably null
Aku-aku	UTSW	2	70738445	missense	probably damaging	0.98
Heyerdahl	UTSW	2	70738426	nonsense	probably null
K3955:Tlk1	UTSW	2	70721701	missense	possibly damaging	0.85
R0107:Tlk1	UTSW	2	70713989	makesense	probably null
R0226:Tlk1	UTSW	2	70714169	unclassified	probably benign
R0332:Tlk1	UTSW	2	70745565	splice site	probably null
R0601:Tlk1	UTSW	2	70714158	missense	probably benign	0.44
R1739:Tlk1	UTSW	2	70721077	missense	probably damaging	1.00
R2080:Tlk1	UTSW	2	70738445	missense	probably damaging	0.98
R3843:Tlk1	UTSW	2	70749327	missense	probably benign	0.05
R3970:Tlk1	UTSW	2	70716652	missense	probably damaging	1.00
R4191:Tlk1	UTSW	2	70725547	missense	probably damaging	1.00
R4867:Tlk1	UTSW	2	70721571	nonsense	probably null
R5022:Tlk1	UTSW	2	70742065	missense	probably benign	0.10
R5275:Tlk1	UTSW	2	70752205	intron	probably benign
R5469:Tlk1	UTSW	2	70721668	missense	probably benign	0.15
R6531:Tlk1	UTSW	2	70742083	missense	probably benign	0.00
R6592:Tlk1	UTSW	2	70714153	missense	probably damaging	1.00
R6797:Tlk1	UTSW	2	70738426	nonsense	probably null
R7030:Tlk1	UTSW	2	70721928	missense	probably damaging	1.00
R7705:Tlk1	UTSW	2	70786672	splice site	probably null
R7970:Tlk1	UTSW	2	70752300	missense	possibly damaging	0.64
R8284:Tlk1	UTSW	2	70714021	missense	probably benign
R8765:Tlk1	UTSW	2	70752237	missense	probably benign	0.20
R9004:Tlk1	UTSW	2	70721946	missense	probably damaging	1.00
R9059:Tlk1	UTSW	2	70786933	missense	possibly damaging	0.65
R9114:Tlk1	UTSW	2	70742158	missense	probably benign	0.20
R9408:Tlk1	UTSW	2	70786875	critical splice donor site	probably null
R9464:Tlk1	UTSW	2	70713997	missense	probably benign	0.00
R9622:Tlk1	UTSW	2	70786937	missense	probably damaging	1.00
R9768:Tlk1	UTSW	2	70770056	missense	probably damaging	0.99
R9776:Tlk1	UTSW	2	70725564	missense	probably damaging	1.00
X0028:Tlk1	UTSW	2	70746031	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TGTGCTTCATTAAGGCCACCC -3'
(R):5'- GCATTGAGAACATGTTACCTTGC -3'

Sequencing Primer
(F):5'- TTCATTAAGGCCACCCCCACTC -3'
(R):5'- GAGAACATGTTACCTTGCTTACTTAG -3'

Posted On

2014-11-12