Mutagenetix > Incidental Mutation

Incidental Mutation 'R0364:Tshz1'

30252

Institutional Source

Beutler Lab

Gene Symbol

Tshz1

Ensembl Gene

ENSMUSG00000046982

Gene Name

teashirt zinc finger family member 1

Synonyms

Tsh1, teashirt1, D18Bwg1409e, Mtsh1, NY-CO-33, Sdccag33, 5730407I04Rik

MMRRC Submission

038570-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R0364 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

84029752-84105831 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 84034249 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Asparagine at position 53 (I53N)

Ref Sequence

ENSEMBL: ENSMUSP00000089388 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000060303]

AlphaFold

Q5DTH5

Predicted Effect

probably benign
Transcript: ENSMUST00000060303
AA Change: I53N

PolyPhen 2 Score 0.310 (Sensitivity: 0.90; Specificity: 0.89)

SMART Domains

Protein: ENSMUSP00000089388
Gene: ENSMUSG00000046982
AA Change: I53N

Domain	Start	End	E-Value	Type
low complexity region	18	29	N/A	INTRINSIC
low complexity region	89	100	N/A	INTRINSIC
low complexity region	153	195	N/A	INTRINSIC
ZnF_C2H2	246	270	1.86e0	SMART
ZnF_C2H2	307	331	3.83e-2	SMART
ZnF_C2H2	416	440	5.34e0	SMART
low complexity region	497	515	N/A	INTRINSIC
HOX	890	964	4.15e-4	SMART
ZnF_C2H2	976	998	4.34e-1	SMART
ZnF_C2H2	1044	1067	4.47e-3	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000175783

SMART Domains

Protein: ENSMUSP00000135640
Gene: ENSMUSG00000046982

Domain	Start	End	E-Value	Type
ZnF_C2H2	43	67	1.7e-4	SMART
ZnF_C2H2	152	176	2.3e-2	SMART
low complexity region	233	251	N/A	INTRINSIC
HOX	626	700	2.1e-6	SMART
ZnF_C2H2	712	734	1.9e-3	SMART
ZnF_C2H2	780	803	1.8e-5	SMART

Meta Mutation Damage Score

0.0601

Coding Region Coverage

1x: 99.0%
3x: 98.0%
10x: 95.3%
20x: 89.3%

Validation Efficiency

99% (86/87)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a colon cancer antigen that was defined by serological analysis of recombinant cDNA expression libraries. The encoded protein is a member of the teashirt C2H2-type zinc-finger protein family and may be involved in transcriptional regulation of developmental processes. Mutations in this gene may be associated with congenital aural atresia syndrome. [provided by RefSeq, Jan 2012]
PHENOTYPE: Mice homozygous for a null allele die shortly after birth of respiratory distress, have defects in soft palate formation, have altered axial skeleton and have middle ear defects. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 87 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acp7	G	A	7: 28,310,553 (GRCm39)		probably benign	Het
Ano7	A	G	1: 93,316,380 (GRCm39)	D221G	probably benign	Het
Arhgef12	A	T	9: 42,929,697 (GRCm39)	N199K	probably damaging	Het
Arpc2	A	G	1: 74,276,046 (GRCm39)	N26S	probably null	Het
Camta2	G	A	11: 70,574,136 (GRCm39)	T127I	probably damaging	Het
Ccdc13	T	A	9: 121,627,282 (GRCm39)	N665I	probably damaging	Het
Ccdc178	C	T	18: 22,048,119 (GRCm39)	R757H	probably damaging	Het
Cfap52	A	C	11: 67,844,436 (GRCm39)	I93S	possibly damaging	Het
Cmklr1	A	T	5: 113,752,578 (GRCm39)	L141H	probably damaging	Het
Crybb3	T	A	5: 113,223,819 (GRCm39)	I197F	probably damaging	Het
Cryzl1	G	A	16: 91,504,155 (GRCm39)	P97S	probably benign	Het
Cubn	T	C	2: 13,315,318 (GRCm39)		probably benign	Het
Cyp2d37-ps	T	C	15: 82,574,253 (GRCm39)		noncoding transcript	Het
Cyp4a12b	C	A	4: 115,290,117 (GRCm39)	N223K	probably benign	Het
Dennd2a	T	C	6: 39,485,233 (GRCm39)	T349A	probably benign	Het
Dnah12	A	G	14: 26,445,628 (GRCm39)	T730A	probably benign	Het
Dock5	G	A	14: 68,060,129 (GRCm39)		probably benign	Het
Dync2i1	A	G	12: 116,221,097 (GRCm39)		probably benign	Het
Elac2	A	G	11: 64,870,136 (GRCm39)	Y67C	probably damaging	Het
Elmo1	A	T	13: 20,748,663 (GRCm39)	K503*	probably null	Het
Endou	A	T	15: 97,616,854 (GRCm39)		probably benign	Het
Eng	T	C	2: 32,569,149 (GRCm39)	S559P	probably benign	Het
Epc2	T	A	2: 49,427,145 (GRCm39)	V563E	possibly damaging	Het
Fbxw17	T	C	13: 50,586,477 (GRCm39)	S40P	possibly damaging	Het
Flt4	A	T	11: 49,527,818 (GRCm39)	M924L	probably benign	Het
Fyb1	A	G	15: 6,610,272 (GRCm39)	K282E	probably damaging	Het
Gabpa	T	A	16: 84,654,275 (GRCm39)	N317K	possibly damaging	Het
Gli3	G	T	13: 15,899,349 (GRCm39)	G912V	probably benign	Het
Gm10295	C	A	7: 71,000,361 (GRCm39)	C73F	unknown	Het
Gm10382	G	T	5: 125,466,728 (GRCm39)		probably benign	Het
Gp1ba	T	C	11: 70,531,284 (GRCm39)		probably benign	Het
Gpr146	G	A	5: 139,364,933 (GRCm39)		probably benign	Het
Grm5	A	G	7: 87,723,594 (GRCm39)	Y628C	probably damaging	Het
Hexa	A	G	9: 59,471,218 (GRCm39)	N491D	probably benign	Het
Hexd	T	A	11: 121,102,969 (GRCm39)	H62Q	probably benign	Het
Hpx	G	T	7: 105,245,471 (GRCm39)	Q101K	probably benign	Het
Ino80	G	A	2: 119,213,441 (GRCm39)	R1249C	probably damaging	Het
Inpp4b	A	T	8: 82,723,943 (GRCm39)	T492S	probably benign	Het
Iqgap2	A	C	13: 95,867,783 (GRCm39)		probably benign	Het
Islr2	T	C	9: 58,107,027 (GRCm39)	T78A	possibly damaging	Het
Itga9	A	G	9: 118,670,210 (GRCm39)	T177A	probably benign	Het
Itpkc	A	C	7: 26,927,174 (GRCm39)	S247A	possibly damaging	Het
Kirrel1	T	C	3: 86,997,106 (GRCm39)	Y287C	probably damaging	Het
Kiz	T	G	2: 146,784,076 (GRCm39)	S536R	probably benign	Het
Klhl9	T	G	4: 88,638,527 (GRCm39)	K571N	probably benign	Het
Kprp	A	T	3: 92,731,642 (GRCm39)	Y469*	probably null	Het
Ksr1	A	T	11: 78,919,851 (GRCm39)		probably benign	Het
Lrrc37a	C	T	11: 103,391,466 (GRCm39)	V1320I	possibly damaging	Het
Ltf	A	T	9: 110,854,235 (GRCm39)	N350I	probably benign	Het
Msl3l2	G	A	10: 55,991,947 (GRCm39)	R224Q	possibly damaging	Het
Myh6	A	T	14: 55,185,804 (GRCm39)	Y1490*	probably null	Het
Necap1	A	G	6: 122,857,728 (GRCm39)		probably benign	Het
Nf1	A	T	11: 79,332,783 (GRCm39)	K810*	probably null	Het
Nkx6-3	A	G	8: 23,647,722 (GRCm39)	E227G	possibly damaging	Het
Nlrp1a	T	A	11: 71,004,830 (GRCm39)		probably benign	Het
Obscn	G	A	11: 59,019,107 (GRCm39)	A969V	probably benign	Het
Or11a4	T	C	17: 37,536,934 (GRCm39)	L306P	possibly damaging	Het
Or7g32	G	A	9: 19,389,268 (GRCm39)	Q90*	probably null	Het
Or8b40	A	G	9: 38,027,325 (GRCm39)	T78A	probably benign	Het
Or8k33	A	T	2: 86,384,123 (GRCm39)	L115Q	probably damaging	Het
Pcdhb17	C	A	18: 37,618,888 (GRCm39)	A226E	possibly damaging	Het
Phldb1	A	T	9: 44,610,632 (GRCm39)		probably benign	Het
Plekha5	G	A	6: 140,537,473 (GRCm39)	R646K	possibly damaging	Het
Pon2	G	A	6: 5,266,156 (GRCm39)	Q288*	probably null	Het
Prr14	G	A	7: 127,073,751 (GRCm39)	R205H	probably benign	Het
Ptpn13	C	A	5: 103,681,214 (GRCm39)	R805S	probably damaging	Het
Pyroxd2	A	T	19: 42,735,992 (GRCm39)	V62D	probably damaging	Het
Rab37	G	T	11: 115,047,790 (GRCm39)	C44F	probably damaging	Het
Rbm44	T	C	1: 91,080,069 (GRCm39)	S52P	probably benign	Het
Rusf1	C	T	7: 127,889,786 (GRCm39)	R1H	probably damaging	Het
Scn5a	T	C	9: 119,351,665 (GRCm39)	D772G	probably damaging	Het
Slc7a5	A	G	8: 122,611,754 (GRCm39)	F425L	probably benign	Het
Slk	T	A	19: 47,608,628 (GRCm39)	L527*	probably null	Het
Stpg4	T	A	17: 87,697,142 (GRCm39)		probably null	Het
Taar6	C	A	10: 23,861,046 (GRCm39)	V167L	probably benign	Het
Tas2r123	T	A	6: 132,824,644 (GRCm39)	S180R	probably benign	Het
Tmc2	C	T	2: 130,044,023 (GRCm39)	R86W	probably benign	Het
Tmem200c	T	A	17: 69,147,543 (GRCm39)	V42E	probably damaging	Het
Trhde	T	C	10: 114,338,887 (GRCm39)		probably benign	Het
Tshz3	A	G	7: 36,469,958 (GRCm39)	E649G	probably benign	Het
Ttll7	C	A	3: 146,650,936 (GRCm39)	R719S	possibly damaging	Het
Utp4	T	C	8: 107,625,169 (GRCm39)		probably benign	Het
Vmn1r35	A	G	6: 66,655,827 (GRCm39)	I281T	probably damaging	Het
Vps39	T	G	2: 120,176,119 (GRCm39)	K76T	probably damaging	Het
Whamm	A	G	7: 81,243,799 (GRCm39)	T674A	probably benign	Het
Zbtb16	A	G	9: 48,654,876 (GRCm39)		probably benign	Het
Zfp623	T	C	15: 75,820,510 (GRCm39)	S489P	probably benign	Het

Other mutations in Tshz1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01486:Tshz1	APN	18	84,031,634 (GRCm39)	missense	possibly damaging	0.94
IGL02934:Tshz1	APN	18	84,031,215 (GRCm39)	missense	probably damaging	1.00
ANU18:Tshz1	UTSW	18	84,032,786 (GRCm39)	missense	probably damaging	1.00
PIT4810001:Tshz1	UTSW	18	84,031,375 (GRCm39)	missense	possibly damaging	0.85
R0052:Tshz1	UTSW	18	84,033,070 (GRCm39)	missense	possibly damaging	0.76
R0052:Tshz1	UTSW	18	84,033,070 (GRCm39)	missense	possibly damaging	0.76
R0391:Tshz1	UTSW	18	84,034,174 (GRCm39)	missense	possibly damaging	0.93
R0515:Tshz1	UTSW	18	84,034,090 (GRCm39)	missense	probably benign
R0942:Tshz1	UTSW	18	84,031,178 (GRCm39)	missense	probably damaging	0.99
R0943:Tshz1	UTSW	18	84,033,356 (GRCm39)	missense	probably benign	0.04
R1472:Tshz1	UTSW	18	84,031,930 (GRCm39)	missense	possibly damaging	0.93
R1895:Tshz1	UTSW	18	84,031,558 (GRCm39)	missense	probably damaging	1.00
R2022:Tshz1	UTSW	18	84,031,987 (GRCm39)	missense	probably damaging	0.98
R2860:Tshz1	UTSW	18	84,033,105 (GRCm39)	missense	probably damaging	1.00
R2861:Tshz1	UTSW	18	84,033,105 (GRCm39)	missense	probably damaging	1.00
R4027:Tshz1	UTSW	18	84,032,954 (GRCm39)	missense	possibly damaging	0.74
R4028:Tshz1	UTSW	18	84,032,954 (GRCm39)	missense	possibly damaging	0.74
R4030:Tshz1	UTSW	18	84,032,954 (GRCm39)	missense	possibly damaging	0.74
R4031:Tshz1	UTSW	18	84,032,954 (GRCm39)	missense	possibly damaging	0.74
R4119:Tshz1	UTSW	18	84,032,314 (GRCm39)	missense	probably benign	0.00
R4233:Tshz1	UTSW	18	84,034,320 (GRCm39)	missense	probably benign	0.00
R4573:Tshz1	UTSW	18	84,033,207 (GRCm39)	missense	probably damaging	1.00
R4604:Tshz1	UTSW	18	84,031,499 (GRCm39)	missense	probably damaging	1.00
R4960:Tshz1	UTSW	18	84,032,987 (GRCm39)	missense	probably benign	0.08
R5085:Tshz1	UTSW	18	84,032,053 (GRCm39)	missense	probably benign	0.01
R5124:Tshz1	UTSW	18	84,033,592 (GRCm39)	missense	probably damaging	1.00
R5150:Tshz1	UTSW	18	84,031,340 (GRCm39)	nonsense	probably null
R5357:Tshz1	UTSW	18	84,033,205 (GRCm39)	missense	probably damaging	1.00
R5530:Tshz1	UTSW	18	84,031,393 (GRCm39)	missense	probably damaging	1.00
R5718:Tshz1	UTSW	18	84,032,649 (GRCm39)	missense	probably damaging	1.00
R5750:Tshz1	UTSW	18	84,032,086 (GRCm39)	missense	possibly damaging	0.93
R5778:Tshz1	UTSW	18	84,033,805 (GRCm39)	missense	probably damaging	1.00
R6052:Tshz1	UTSW	18	84,032,194 (GRCm39)	missense	probably damaging	1.00
R6279:Tshz1	UTSW	18	84,033,436 (GRCm39)	missense	probably damaging	1.00
R6393:Tshz1	UTSW	18	84,031,345 (GRCm39)	missense	probably damaging	1.00
R6407:Tshz1	UTSW	18	84,034,091 (GRCm39)	missense	possibly damaging	0.55
R6425:Tshz1	UTSW	18	84,033,688 (GRCm39)	missense	probably damaging	0.99
R6998:Tshz1	UTSW	18	84,033,966 (GRCm39)	missense	probably benign	0.00
R7165:Tshz1	UTSW	18	84,034,052 (GRCm39)	missense	probably damaging	1.00
R7233:Tshz1	UTSW	18	84,032,944 (GRCm39)	missense	possibly damaging	0.63
R7330:Tshz1	UTSW	18	84,032,956 (GRCm39)	missense	probably damaging	0.96
R7491:Tshz1	UTSW	18	84,033,766 (GRCm39)	missense	probably damaging	1.00
R7579:Tshz1	UTSW	18	84,032,790 (GRCm39)	nonsense	probably null
R7592:Tshz1	UTSW	18	84,032,173 (GRCm39)	missense	probably damaging	1.00
R7659:Tshz1	UTSW	18	84,034,200 (GRCm39)	missense	probably damaging	0.97
R7702:Tshz1	UTSW	18	84,032,461 (GRCm39)	missense	probably damaging	1.00
R7844:Tshz1	UTSW	18	84,032,296 (GRCm39)	missense	probably benign	0.00
R7908:Tshz1	UTSW	18	84,032,732 (GRCm39)	nonsense	probably null
R7941:Tshz1	UTSW	18	84,033,517 (GRCm39)	missense	possibly damaging	0.91
R7947:Tshz1	UTSW	18	84,033,782 (GRCm39)	missense	probably damaging	1.00
R8435:Tshz1	UTSW	18	84,032,149 (GRCm39)	missense	probably damaging	1.00
R8750:Tshz1	UTSW	18	84,033,162 (GRCm39)	missense	probably damaging	1.00
R8774:Tshz1	UTSW	18	84,033,101 (GRCm39)	missense	possibly damaging	0.96
R8774-TAIL:Tshz1	UTSW	18	84,033,101 (GRCm39)	missense	possibly damaging	0.96
R9029:Tshz1	UTSW	18	84,031,639 (GRCm39)	missense	probably damaging	0.98
R9031:Tshz1	UTSW	18	84,032,987 (GRCm39)	missense	probably benign	0.08
R9573:Tshz1	UTSW	18	84,032,404 (GRCm39)	missense	probably benign	0.45
R9584:Tshz1	UTSW	18	84,033,089 (GRCm39)	missense	probably damaging	1.00
R9596:Tshz1	UTSW	18	84,031,904 (GRCm39)	missense	possibly damaging	0.92
R9701:Tshz1	UTSW	18	84,032,579 (GRCm39)	missense	possibly damaging	0.96

Predicted Primers

PCR Primer
(F):5'- AATGCTAGGCTAGACCAGCAGGAC -3'
(R):5'- GCATGATCGACTCCTCTGACTGTG -3'

Sequencing Primer
(F):5'- AAGTTCGCATACACGGCTTTG -3'
(R):5'- GGGTCATTTTTCTCTCGTAGC -3'

Posted On

2013-04-24