Mutagenetix > Incidental Mutation

Incidental Mutation 'R2146:Ttc7'

233870

Institutional Source

Beutler Lab

Gene Symbol

Ttc7

Ensembl Gene

ENSMUSG00000036918

Gene Name

tetratricopeptide repeat domain 7

Synonyms

fsn, 1700007L07Rik, 1110035E02Rik, hea

MMRRC Submission

040149-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.854) question?

Stock #

R2146 (G1)

Quality Score

218

Status

Validated

Chromosome

Chromosomal Location

87590328-87689197 bp(+) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

T to C at 87654135 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000114181 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000041110] [ENSMUST00000125875] [ENSMUST00000144204] [ENSMUST00000154255]

AlphaFold

Q8BGB2

Predicted Effect

probably benign
Transcript: ENSMUST00000041110

SMART Domains

Protein: ENSMUSP00000040771
Gene: ENSMUSG00000036918

Domain	Start	End	E-Value	Type
low complexity region	40	56	N/A	INTRINSIC
low complexity region	68	76	N/A	INTRINSIC
Pfam:TPR_9	387	458	8.7e-4	PFAM
Blast:TPR	488	532	7e-20	BLAST
Blast:TPR	534	566	3e-7	BLAST
TPR	567	600	1.11e1	SMART
low complexity region	666	684	N/A	INTRINSIC
TPR	711	744	7.89e1	SMART
TPR	745	778	3.87e-2	SMART
TPR	779	812	9.99e1	SMART
TPR	813	846	1.39e-3	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000125875

SMART Domains

Protein: ENSMUSP00000115351
Gene: ENSMUSG00000036918

Domain	Start	End	E-Value	Type
low complexity region	40	56	N/A	INTRINSIC
low complexity region	68	76	N/A	INTRINSIC
Pfam:TPR_9	387	458	1.2e-3	PFAM
Blast:TPR	488	532	7e-20	BLAST
Blast:TPR	534	566	3e-7	BLAST
TPR	567	600	1.11e1	SMART
low complexity region	666	684	N/A	INTRINSIC
TPR	711	744	7.89e1	SMART
TPR	745	778	3.87e-2	SMART
low complexity region	787	801	N/A	INTRINSIC
low complexity region	806	818	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000144204

SMART Domains

Protein: ENSMUSP00000122563
Gene: ENSMUSG00000036918

Domain	Start	End	E-Value	Type
low complexity region	40	56	N/A	INTRINSIC
low complexity region	68	76	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000154255

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.4%
20x: 95.4%

Validation Efficiency

99% (84/85)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein containing tetratricopeptide repeats. Mutations in this gene disrupt intestinal development and can cause early onset inflammatory bowel disease and intestinal atresia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]
PHENOTYPE: Homozygotes for a spontaneous mutation exhibit reduced growth, sparse hair, thickened, scaly skin, increased numbers of splenic B cells, macrophages, and erythroid cells, elevated IgE, glomerulonephritis, and forestomach papillomas. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 85 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700013D24Rik	A	T	6: 124,324,803 (GRCm39)		probably null	Het
9530002B09Rik	T	A	4: 122,583,198 (GRCm39)	C13*	probably null	Het
Abca12	C	A	1: 71,302,647 (GRCm39)	V2191L	probably benign	Het
Adamts18	G	C	8: 114,571,635 (GRCm39)	A116G	possibly damaging	Het
Anxa2	TCCC	TCC	9: 69,397,036 (GRCm39)		probably null	Het
Arfgef1	C	T	1: 10,270,103 (GRCm39)	A349T	probably benign	Het
Arhgap6	A	G	X: 167,579,496 (GRCm39)	T94A	probably benign	Het
Arhgef5	T	C	6: 43,260,252 (GRCm39)	S1413P	probably damaging	Het
Atg4c	C	A	4: 99,109,463 (GRCm39)	N143K	possibly damaging	Het
C1qtnf12	A	G	4: 156,050,922 (GRCm39)	N297S	probably benign	Het
Cadps2	G	T	6: 23,838,998 (GRCm39)		probably benign	Het
Ccdc185	G	T	1: 182,575,085 (GRCm39)	H535N	possibly damaging	Het
Ccdc57	A	G	11: 120,776,051 (GRCm39)		probably benign	Het
Cd163	A	G	6: 124,286,167 (GRCm39)	H239R	probably damaging	Het
Ceacam2	G	T	7: 25,227,368 (GRCm39)	C166*	probably null	Het
Ces5a	T	A	8: 94,261,327 (GRCm39)	E33D	probably benign	Het
Chl1	T	C	6: 103,692,362 (GRCm39)		probably null	Het
Chsy3	G	A	18: 59,309,544 (GRCm39)	V266I	probably benign	Het
Cpa5	G	T	6: 30,626,821 (GRCm39)	R251L	probably damaging	Het
Cps1	A	C	1: 67,191,538 (GRCm39)		probably benign	Het
Csmd3	CCTTTGCGCTT	CCTT	15: 47,604,632 (GRCm39)		probably null	Het
Cstf1	T	C	2: 172,217,683 (GRCm39)	Y99H	probably damaging	Het
Cyp2j11	G	A	4: 96,204,595 (GRCm39)	T317I	probably damaging	Het
Dcaf8l	T	C	X: 88,449,883 (GRCm39)	D82G	possibly damaging	Het
Dennd3	C	T	15: 73,395,345 (GRCm39)	T146M	probably damaging	Het
Dennd3	A	T	15: 73,426,909 (GRCm39)	H762L	probably benign	Het
Dnah2	T	C	11: 69,406,587 (GRCm39)	M552V	probably benign	Het
Dnajc22	T	C	15: 99,002,264 (GRCm39)	V303A	probably benign	Het
Dtx2	T	G	5: 136,059,464 (GRCm39)	L458R	probably benign	Het
Fat3	A	T	9: 15,901,808 (GRCm39)	F3072L	probably benign	Het
Fgf5	T	C	5: 98,423,409 (GRCm39)	*265R	probably null	Het
Fndc11	A	G	2: 180,863,918 (GRCm39)	E241G	probably damaging	Het
Glb1	T	C	9: 114,279,716 (GRCm39)	Y375H	probably damaging	Het
Gm4922	T	G	10: 18,659,264 (GRCm39)	Q486P	probably benign	Het
Gm5786	A	T	12: 59,128,084 (GRCm39)		noncoding transcript	Het
Hepacam2	A	T	6: 3,463,378 (GRCm39)		probably benign	Het
Ints9	G	A	14: 65,223,792 (GRCm39)	G89R	possibly damaging	Het
Iqcm	T	A	8: 76,615,241 (GRCm39)	W441R	probably damaging	Het
Itga10	T	C	3: 96,558,808 (GRCm39)	L382P	possibly damaging	Het
Itga10	G	T	3: 96,561,039 (GRCm39)	G635W	probably damaging	Het
Kbtbd2	A	G	6: 56,756,075 (GRCm39)	Y554H	probably damaging	Het
Kif1b	T	C	4: 149,268,766 (GRCm39)	K1649R	probably damaging	Het
L1cam	A	T	X: 72,904,747 (GRCm39)	F536Y	probably damaging	Het
Magee1	A	T	X: 104,166,564 (GRCm39)	D783V	probably damaging	Het
Marveld3	A	T	8: 110,686,434 (GRCm39)	V144E	probably benign	Het
Mcam	T	C	9: 44,047,932 (GRCm39)	V59A	probably damaging	Het
Mdga2	C	T	12: 66,915,515 (GRCm39)	E47K	probably damaging	Het
Metrn	T	A	17: 26,015,601 (GRCm39)	E38V	probably damaging	Het
Mfrp	T	C	9: 44,015,015 (GRCm39)	L314P	probably benign	Het
Mgat4f	T	A	1: 134,318,251 (GRCm39)	M341K	probably damaging	Het
Mideas	G	T	12: 84,219,809 (GRCm39)	P382T	probably damaging	Het
Mospd2	A	G	X: 163,739,473 (GRCm39)		probably null	Het
Mycbp2	G	A	14: 103,393,358 (GRCm39)	H3068Y	probably damaging	Het
Myh6	C	T	14: 55,191,228 (GRCm39)	R871H	probably damaging	Het
Nup214	C	T	2: 31,924,478 (GRCm39)	S1669F	probably damaging	Het
Or13c7b	A	G	4: 43,821,178 (GRCm39)	F61S	probably damaging	Het
Or5b111	T	C	19: 13,291,485 (GRCm39)	T55A	probably benign	Het
Or8i2	T	A	2: 86,852,009 (GRCm39)	N293I	probably damaging	Het
Parvb	A	G	15: 84,116,369 (GRCm39)	K33E	possibly damaging	Het
Pdcd11	A	G	19: 47,093,191 (GRCm39)	M490V	probably benign	Het
Pkd2	A	C	5: 104,603,456 (GRCm39)		probably benign	Het
Reps1	T	A	10: 17,969,061 (GRCm39)	D206E	probably benign	Het
Rimkla	T	A	4: 119,331,779 (GRCm39)	M140L	possibly damaging	Het
Rnf13	T	G	3: 57,709,907 (GRCm39)	I150S	probably null	Het
Rxfp4	C	T	3: 88,560,200 (GRCm39)	A84T	probably damaging	Het
Serpinb8	T	A	1: 107,533,657 (GRCm39)	D237E	probably benign	Het
Sgo2b	T	G	8: 64,381,057 (GRCm39)	T592P	probably benign	Het
Slc35d1	A	T	4: 103,062,349 (GRCm39)	I228N	probably damaging	Het
Slc39a1	T	G	3: 90,156,757 (GRCm39)	H104Q	probably benign	Het
Slc6a6	T	C	6: 91,712,161 (GRCm39)	V230A	probably benign	Het
Slc9a3	A	G	13: 74,269,722 (GRCm39)	E30G	probably benign	Het
Slc9c1	A	G	16: 45,413,827 (GRCm39)	Y985C	probably benign	Het
Supt6	A	G	11: 78,121,758 (GRCm39)	F298S	probably damaging	Het
Tada2a	T	C	11: 83,970,455 (GRCm39)	D432G	probably damaging	Het
Thoc2l	T	C	5: 104,666,857 (GRCm39)	F460L	probably benign	Het
Tmem131	C	A	1: 36,851,690 (GRCm39)	V938L	probably benign	Het
Tnpo3	A	G	6: 29,589,035 (GRCm39)	V105A	probably benign	Het
Ttn	T	C	2: 76,727,532 (GRCm39)		probably benign	Het
Usp16	T	C	16: 87,270,075 (GRCm39)		probably null	Het
Usp36	A	G	11: 118,159,491 (GRCm39)	L486S	probably benign	Het
Uty	T	C	Y: 1,239,816 (GRCm39)	I72V	probably benign	Het
Vps51	A	G	19: 6,118,164 (GRCm39)	V777A	probably benign	Het
Zfp160	A	G	17: 21,247,244 (GRCm39)	K598R	probably benign	Het
Zfp39	T	C	11: 58,781,158 (GRCm39)	N535D	probably benign	Het
Zfp804a	A	G	2: 82,089,008 (GRCm39)	T946A	probably benign	Het

Other mutations in Ttc7

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00341:Ttc7	APN	17	87,670,992 (GRCm39)	missense	possibly damaging	0.66
IGL00980:Ttc7	APN	17	87,628,874 (GRCm39)	missense	possibly damaging	0.82
IGL01638:Ttc7	APN	17	87,666,540 (GRCm39)	critical splice acceptor site	probably null
IGL01896:Ttc7	APN	17	87,666,552 (GRCm39)	missense	probably damaging	0.99
IGL02643:Ttc7	APN	17	87,648,327 (GRCm39)	missense	possibly damaging	0.85
R0164:Ttc7	UTSW	17	87,687,323 (GRCm39)	missense	probably damaging	1.00
R0164:Ttc7	UTSW	17	87,687,323 (GRCm39)	missense	probably damaging	1.00
R0310:Ttc7	UTSW	17	87,669,292 (GRCm39)	missense	probably benign	0.00
R0412:Ttc7	UTSW	17	87,637,472 (GRCm39)	missense	probably benign	0.20
R0520:Ttc7	UTSW	17	87,666,579 (GRCm39)	missense	possibly damaging	0.93
R1216:Ttc7	UTSW	17	87,654,006 (GRCm39)	missense	possibly damaging	0.85
R1262:Ttc7	UTSW	17	87,648,364 (GRCm39)	missense	probably benign	0.09
R1337:Ttc7	UTSW	17	87,597,724 (GRCm39)	missense	probably damaging	1.00
R1537:Ttc7	UTSW	17	87,629,891 (GRCm39)	missense	possibly damaging	0.88
R1586:Ttc7	UTSW	17	87,669,373 (GRCm39)	critical splice donor site	probably null
R1678:Ttc7	UTSW	17	87,669,329 (GRCm39)	missense	probably damaging	1.00
R1747:Ttc7	UTSW	17	87,614,443 (GRCm39)	missense	possibly damaging	0.87
R3878:Ttc7	UTSW	17	87,678,166 (GRCm39)	intron	probably benign
R3934:Ttc7	UTSW	17	87,678,166 (GRCm39)	intron	probably benign
R4007:Ttc7	UTSW	17	87,597,679 (GRCm39)	missense	possibly damaging	0.69
R4256:Ttc7	UTSW	17	87,628,829 (GRCm39)	critical splice acceptor site	probably null
R4671:Ttc7	UTSW	17	87,654,048 (GRCm39)	missense	probably damaging	1.00
R4676:Ttc7	UTSW	17	87,678,163 (GRCm39)	intron	probably benign
R4677:Ttc7	UTSW	17	87,678,163 (GRCm39)	intron	probably benign
R4784:Ttc7	UTSW	17	87,648,325 (GRCm39)	missense	probably benign	0.03
R4833:Ttc7	UTSW	17	87,641,749 (GRCm39)	missense	probably damaging	1.00
R4927:Ttc7	UTSW	17	87,654,133 (GRCm39)	splice site	probably null
R4940:Ttc7	UTSW	17	87,614,386 (GRCm39)	missense	probably benign	0.02
R5183:Ttc7	UTSW	17	87,600,306 (GRCm39)	missense	probably damaging	1.00
R5634:Ttc7	UTSW	17	87,649,515 (GRCm39)	missense	probably benign
R5710:Ttc7	UTSW	17	87,597,674 (GRCm39)	missense	probably damaging	1.00
R5867:Ttc7	UTSW	17	87,629,900 (GRCm39)	missense	possibly damaging	0.49
R6437:Ttc7	UTSW	17	87,637,534 (GRCm39)	missense	probably damaging	1.00
R6982:Ttc7	UTSW	17	87,614,437 (GRCm39)	missense	probably damaging	1.00
R7299:Ttc7	UTSW	17	87,653,970 (GRCm39)	missense	possibly damaging	0.68
R7849:Ttc7	UTSW	17	87,600,374 (GRCm39)	missense	probably null	0.00
R8098:Ttc7	UTSW	17	87,641,756 (GRCm39)	missense	probably benign	0.21
R8471:Ttc7	UTSW	17	87,601,454 (GRCm39)	missense	probably benign	0.24
R8889:Ttc7	UTSW	17	87,637,520 (GRCm39)	missense	probably damaging	1.00
R8892:Ttc7	UTSW	17	87,637,520 (GRCm39)	missense	probably damaging	1.00
R9225:Ttc7	UTSW	17	87,637,502 (GRCm39)	missense	probably damaging	1.00
R9427:Ttc7	UTSW	17	87,678,147 (GRCm39)	intron	probably benign
R9436:Ttc7	UTSW	17	87,600,320 (GRCm39)	missense	possibly damaging	0.94

Predicted Primers

PCR Primer
(F):5'- TAAGGTCCCTAAACTGGCGGTC -3'
(R):5'- AACAGTTCTCCCCTCTGAGC -3'

Sequencing Primer
(F):5'- AAACTGGCGGTCTCTCCC -3'
(R):5'- TGAGCCCACAGCCTCTATG -3'

Posted On

2014-10-01