Mutagenetix > Incidental Mutation

Incidental Mutation 'R0391:Tshz1'

31739

Institutional Source

Beutler Lab

Gene Symbol

Tshz1

Ensembl Gene

ENSMUSG00000046982

Gene Name

teashirt zinc finger family member 1

Synonyms

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

MMRRC Submission

038597-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R0391 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

84011627-84086404 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 84016049 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Serine at position 78 (F78S)

Ref Sequence

ENSEMBL: ENSMUSP00000089388 (fasta)

Gene Model

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

AlphaFold

Q5DTH5

Predicted Effect

possibly damaging
Transcript: ENSMUST00000060303
AA Change: F78S

PolyPhen 2 Score 0.931 (Sensitivity: 0.81; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000089388
Gene: ENSMUSG00000046982
AA Change: F78S

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

0.0939

Coding Region Coverage

1x: 99.1%
3x: 98.2%
10x: 95.9%
20x: 91.8%

Validation Efficiency

97% (97/100)

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: 97 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
9530002B09Rik	T	A	4: 122,701,177 (GRCm38)		probably benign	Het
Abcc2	G	A	19: 43,821,605 (GRCm38)		probably benign	Het
Abcc8	C	G	7: 46,122,173 (GRCm38)	G838A	probably damaging	Het
Akr1c21	G	A	13: 4,581,200 (GRCm38)	A245T	probably damaging	Het
Anapc15-ps	T	C	10: 95,673,277 (GRCm38)	E47G	probably damaging	Het
Apoa1	A	G	9: 46,229,842 (GRCm38)	T79A	probably benign	Het
Atp6v1b1	A	G	6: 83,756,921 (GRCm38)	H378R	possibly damaging	Het
C4b	A	G	17: 34,735,614 (GRCm38)		probably benign	Het
Catsperd	A	T	17: 56,662,821 (GRCm38)	E638D	probably benign	Het
Cckar	C	T	5: 53,706,253 (GRCm38)		probably null	Het
Cfap100	C	T	6: 90,405,339 (GRCm38)		probably benign	Het
Chd1	G	T	17: 15,749,894 (GRCm38)	G970C	probably damaging	Het
Col14a1	A	G	15: 55,446,259 (GRCm38)		probably benign	Het
Col17a1	C	T	19: 47,663,824 (GRCm38)	V698M	probably damaging	Het
Cpeb1	T	C	7: 81,361,725 (GRCm38)	D156G	possibly damaging	Het
Cryl1	A	G	14: 57,303,775 (GRCm38)	Y151H	possibly damaging	Het
Csmd3	C	A	15: 47,657,573 (GRCm38)	V1881L	probably damaging	Het
Ctnnal1	C	T	4: 56,847,921 (GRCm38)	A73T	probably damaging	Het
Cyp2c37	T	C	19: 39,994,506 (GRCm38)	S180P	probably damaging	Het
Cyp2c54	T	C	19: 40,072,169 (GRCm38)	T123A	possibly damaging	Het
Dennd6b	T	C	15: 89,187,214 (GRCm38)	D304G	probably damaging	Het
Dnmt3l	T	C	10: 78,051,916 (GRCm38)		probably benign	Het
Eci1	G	A	17: 24,433,260 (GRCm38)		probably null	Het
Efhc1	A	G	1: 20,960,188 (GRCm38)	Y115C	probably damaging	Het
Ern1	T	A	11: 106,407,178 (GRCm38)	K706*	probably null	Het
Fam129c	T	A	8: 71,602,499 (GRCm38)		probably benign	Het
Ghrl	T	C	6: 113,719,338 (GRCm38)	E31G	probably damaging	Het
Gpr108	A	C	17: 57,243,101 (GRCm38)	V179G	probably benign	Het
Henmt1	A	G	3: 108,958,535 (GRCm38)		probably benign	Het
Ift172	A	G	5: 31,286,667 (GRCm38)	V69A	probably damaging	Het
Il17ra	T	C	6: 120,476,979 (GRCm38)		probably benign	Het
Il17rb	T	C	14: 30,004,347 (GRCm38)	N95D	probably benign	Het
Il17rb	G	T	14: 30,006,155 (GRCm38)		probably null	Het
Iqub	G	A	6: 24,446,155 (GRCm38)	L757F	probably benign	Het
Itpr1	T	C	6: 108,378,167 (GRCm38)	V473A	probably benign	Het
Itpr2	T	G	6: 146,229,773 (GRCm38)	N1978H	probably damaging	Het
Klk1b26	T	A	7: 44,012,727 (GRCm38)	F3Y	probably damaging	Het
Lars	A	G	18: 42,251,363 (GRCm38)	V50A	probably benign	Het
Lax1	G	T	1: 133,680,066 (GRCm38)	H312Q	probably benign	Het
Lctl	T	C	9: 64,122,314 (GRCm38)		probably benign	Het
Lrp2	G	A	2: 69,460,337 (GRCm38)		probably benign	Het
Lrp2	T	A	2: 69,456,858 (GRCm38)	D3745V	probably damaging	Het
Lvrn	A	T	18: 46,850,466 (GRCm38)	H92L	probably benign	Het
March1	A	G	8: 66,418,973 (GRCm38)	T385A	probably damaging	Het
Marf1	C	T	16: 14,142,534 (GRCm38)	A549T	probably damaging	Het
Mbd5	T	C	2: 49,272,416 (GRCm38)	V970A	possibly damaging	Het
Mccc1	A	G	3: 35,963,570 (GRCm38)		probably benign	Het
Mpp4	A	T	1: 59,143,829 (GRCm38)		probably benign	Het
Mrnip	G	A	11: 50,199,920 (GRCm38)	A304T	probably damaging	Het
Muc5b	T	C	7: 141,865,082 (GRCm38)	S3922P	possibly damaging	Het
Myh3	T	A	11: 67,096,507 (GRCm38)		probably benign	Het
Nbea	A	T	3: 56,037,277 (GRCm38)	H555Q	probably damaging	Het
Nlrp9c	A	T	7: 26,371,476 (GRCm38)		probably benign	Het
Nmur1	A	T	1: 86,387,678 (GRCm38)	V178E	probably damaging	Het
Nod2	T	G	8: 88,663,778 (GRCm38)	S238A	probably benign	Het
Ogfod1	A	T	8: 94,063,023 (GRCm38)	T451S	probably damaging	Het
Olfr145	G	A	9: 37,897,842 (GRCm38)	G146D	probably benign	Het
Olfr23	T	C	11: 73,941,109 (GRCm38)	F288L	probably damaging	Het
Olfr372	C	T	8: 72,058,400 (GRCm38)	T240M	probably damaging	Het
Olfr716	T	A	7: 107,148,187 (GRCm38)	Y290*	probably null	Het
Pcdh20	T	C	14: 88,468,668 (GRCm38)	I399V	probably benign	Het
Pdlim1	G	T	19: 40,243,573 (GRCm38)	H120Q	probably damaging	Het
Plg	T	C	17: 12,419,081 (GRCm38)	V798A	probably damaging	Het
Polr2c	A	G	8: 94,857,775 (GRCm38)	I39V	possibly damaging	Het
Ppfia2	C	A	10: 106,830,714 (GRCm38)		probably benign	Het
Ppp1r3a	A	T	6: 14,719,697 (GRCm38)	I406N	probably benign	Het
Psg28	A	T	7: 18,426,173 (GRCm38)	M366K	probably benign	Het
Rad54b	T	C	4: 11,601,702 (GRCm38)	I419T	probably damaging	Het
Rnf43	A	G	11: 87,731,282 (GRCm38)	Q403R	possibly damaging	Het
Sema6a	G	A	18: 47,290,045 (GRCm38)		probably null	Het
Slc28a3	A	G	13: 58,569,415 (GRCm38)		probably benign	Het
Smad2	A	T	18: 76,289,037 (GRCm38)		probably null	Het
Smad4	G	A	18: 73,658,649 (GRCm38)	P274S	probably benign	Het
Smchd1	A	T	17: 71,403,154 (GRCm38)	V906D	probably damaging	Het
Soat2	C	A	15: 102,158,753 (GRCm38)	R320S	possibly damaging	Het
Spata33	C	T	8: 123,221,887 (GRCm38)	A57V	probably damaging	Het
Stab1	A	G	14: 31,143,418 (GRCm38)	L1814P	probably benign	Het
Stab2	T	C	10: 86,947,144 (GRCm38)	K680R	probably benign	Het
Stil	A	G	4: 115,041,172 (GRCm38)		probably null	Het
Sympk	T	A	7: 19,046,849 (GRCm38)	L759H	probably benign	Het
Tet1	A	T	10: 62,814,546 (GRCm38)		probably null	Het
Tfpi2	A	T	6: 3,965,460 (GRCm38)	N117K	probably benign	Het
Tle3	A	G	9: 61,416,661 (GRCm38)	Y766C	probably damaging	Het
Trpt1	C	A	19: 6,997,930 (GRCm38)		probably null	Het
Ttc1	T	C	11: 43,738,808 (GRCm38)	D177G	probably damaging	Het
Ttc13	T	A	8: 124,674,401 (GRCm38)	Y741F	probably damaging	Het
Ulk3	C	T	9: 57,594,832 (GRCm38)	S462L	probably benign	Het
Utrn	C	T	10: 12,525,333 (GRCm38)		probably benign	Het
V1rd19	A	C	7: 24,003,585 (GRCm38)	T159P	probably damaging	Het
Vars	T	C	17: 35,011,486 (GRCm38)	V515A	possibly damaging	Het
Vmn1r85	A	G	7: 13,084,588 (GRCm38)	Y210H	probably benign	Het
Vmn2r89	A	G	14: 51,455,978 (GRCm38)	T262A	probably damaging	Het
Vps53	G	A	11: 76,121,579 (GRCm38)	T209I	probably benign	Het
Wdfy2	T	C	14: 62,925,133 (GRCm38)	F95L	possibly damaging	Het
Wwp1	G	T	4: 19,627,911 (GRCm38)	S694Y	probably damaging	Het
Zbtb8b	T	A	4: 129,432,670 (GRCm38)	D201V	probably damaging	Het
Zmym5	A	C	14: 56,804,451 (GRCm38)	N123K	possibly damaging	Het

Other mutations in Tshz1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01486:Tshz1	APN	18	84,013,509 (GRCm38)	missense	possibly damaging	0.94
IGL02934:Tshz1	APN	18	84,013,090 (GRCm38)	missense	probably damaging	1.00
ANU18:Tshz1	UTSW	18	84,014,661 (GRCm38)	missense	probably damaging	1.00
PIT4810001:Tshz1	UTSW	18	84,013,250 (GRCm38)	missense	possibly damaging	0.85
R0052:Tshz1	UTSW	18	84,014,945 (GRCm38)	missense	possibly damaging	0.76
R0052:Tshz1	UTSW	18	84,014,945 (GRCm38)	missense	possibly damaging	0.76
R0364:Tshz1	UTSW	18	84,016,124 (GRCm38)	missense	probably benign	0.31
R0515:Tshz1	UTSW	18	84,015,965 (GRCm38)	missense	probably benign
R0942:Tshz1	UTSW	18	84,013,053 (GRCm38)	missense	probably damaging	0.99
R0943:Tshz1	UTSW	18	84,015,231 (GRCm38)	missense	probably benign	0.04
R1472:Tshz1	UTSW	18	84,013,805 (GRCm38)	missense	possibly damaging	0.93
R1895:Tshz1	UTSW	18	84,013,433 (GRCm38)	missense	probably damaging	1.00
R2022:Tshz1	UTSW	18	84,013,862 (GRCm38)	missense	probably damaging	0.98
R2860:Tshz1	UTSW	18	84,014,980 (GRCm38)	missense	probably damaging	1.00
R2861:Tshz1	UTSW	18	84,014,980 (GRCm38)	missense	probably damaging	1.00
R4027:Tshz1	UTSW	18	84,014,829 (GRCm38)	missense	possibly damaging	0.74
R4028:Tshz1	UTSW	18	84,014,829 (GRCm38)	missense	possibly damaging	0.74
R4030:Tshz1	UTSW	18	84,014,829 (GRCm38)	missense	possibly damaging	0.74
R4031:Tshz1	UTSW	18	84,014,829 (GRCm38)	missense	possibly damaging	0.74
R4119:Tshz1	UTSW	18	84,014,189 (GRCm38)	missense	probably benign	0.00
R4233:Tshz1	UTSW	18	84,016,195 (GRCm38)	missense	probably benign	0.00
R4573:Tshz1	UTSW	18	84,015,082 (GRCm38)	missense	probably damaging	1.00
R4604:Tshz1	UTSW	18	84,013,374 (GRCm38)	missense	probably damaging	1.00
R4960:Tshz1	UTSW	18	84,014,862 (GRCm38)	missense	probably benign	0.08
R5085:Tshz1	UTSW	18	84,013,928 (GRCm38)	missense	probably benign	0.01
R5124:Tshz1	UTSW	18	84,015,467 (GRCm38)	missense	probably damaging	1.00
R5150:Tshz1	UTSW	18	84,013,215 (GRCm38)	nonsense	probably null
R5357:Tshz1	UTSW	18	84,015,080 (GRCm38)	missense	probably damaging	1.00
R5530:Tshz1	UTSW	18	84,013,268 (GRCm38)	missense	probably damaging	1.00
R5718:Tshz1	UTSW	18	84,014,524 (GRCm38)	missense	probably damaging	1.00
R5750:Tshz1	UTSW	18	84,013,961 (GRCm38)	missense	possibly damaging	0.93
R5778:Tshz1	UTSW	18	84,015,680 (GRCm38)	missense	probably damaging	1.00
R6052:Tshz1	UTSW	18	84,014,069 (GRCm38)	missense	probably damaging	1.00
R6279:Tshz1	UTSW	18	84,015,311 (GRCm38)	missense	probably damaging	1.00
R6393:Tshz1	UTSW	18	84,013,220 (GRCm38)	missense	probably damaging	1.00
R6407:Tshz1	UTSW	18	84,015,966 (GRCm38)	missense	possibly damaging	0.55
R6425:Tshz1	UTSW	18	84,015,563 (GRCm38)	missense	probably damaging	0.99
R6998:Tshz1	UTSW	18	84,015,841 (GRCm38)	missense	probably benign	0.00
R7165:Tshz1	UTSW	18	84,015,927 (GRCm38)	missense	probably damaging	1.00
R7233:Tshz1	UTSW	18	84,014,819 (GRCm38)	missense	possibly damaging	0.63
R7330:Tshz1	UTSW	18	84,014,831 (GRCm38)	missense	probably damaging	0.96
R7491:Tshz1	UTSW	18	84,015,641 (GRCm38)	missense	probably damaging	1.00
R7579:Tshz1	UTSW	18	84,014,665 (GRCm38)	nonsense	probably null
R7592:Tshz1	UTSW	18	84,014,048 (GRCm38)	missense	probably damaging	1.00
R7659:Tshz1	UTSW	18	84,016,075 (GRCm38)	missense	probably damaging	0.97
R7702:Tshz1	UTSW	18	84,014,336 (GRCm38)	missense	probably damaging	1.00
R7844:Tshz1	UTSW	18	84,014,171 (GRCm38)	missense	probably benign	0.00
R7908:Tshz1	UTSW	18	84,014,607 (GRCm38)	nonsense	probably null
R7941:Tshz1	UTSW	18	84,015,392 (GRCm38)	missense	possibly damaging	0.91
R7947:Tshz1	UTSW	18	84,015,657 (GRCm38)	missense	probably damaging	1.00
R8435:Tshz1	UTSW	18	84,014,024 (GRCm38)	missense	probably damaging	1.00
R8750:Tshz1	UTSW	18	84,015,037 (GRCm38)	missense	probably damaging	1.00
R8774:Tshz1	UTSW	18	84,014,976 (GRCm38)	missense	possibly damaging	0.96
R8774-TAIL:Tshz1	UTSW	18	84,014,976 (GRCm38)	missense	possibly damaging	0.96
R9029:Tshz1	UTSW	18	84,013,514 (GRCm38)	missense	probably damaging	0.98
R9031:Tshz1	UTSW	18	84,014,862 (GRCm38)	missense	probably benign	0.08
R9573:Tshz1	UTSW	18	84,014,279 (GRCm38)	missense	probably benign	0.45
R9584:Tshz1	UTSW	18	84,014,964 (GRCm38)	missense	probably damaging	1.00
R9596:Tshz1	UTSW	18	84,013,779 (GRCm38)	missense	possibly damaging	0.92
R9701:Tshz1	UTSW	18	84,014,454 (GRCm38)	missense	possibly damaging	0.96

Predicted Primers

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

Sequencing Primer
(F):5'- CTCTGAGAATAAGTTCGCATACACG -3'
(R):5'- TAGCTTACGTTCCCGAGGAAG -3'

Posted On

2013-04-24