Mutagenetix > Incidental Mutation

Incidental Mutation 'R7868:Fsip1'

607894

Institutional Source

Beutler Lab

Gene Symbol

Fsip1

Ensembl Gene

ENSMUSG00000027344

Gene Name

fibrous sheath-interacting protein 1

Synonyms

4933432K11Rik, 1700012M13Rik

MMRRC Submission

045920-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.054) question?

Stock #

R7868 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

117960905-118087447 bp(-) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

G to A at 117966967 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glutamine to Stop codon at position 453 (Q453*)

Ref Sequence

ENSEMBL: ENSMUSP00000155242 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000231133]

AlphaFold

Q9D3V5

Predicted Effect

probably null
Transcript: ENSMUST00000231133
AA Change: Q453*

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.0%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 62 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4933415A04Rik	GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	11: 43,478,257 (GRCm39)		probably null	Het
Acacb	A	G	5: 114,386,288 (GRCm39)	E2274G	probably benign	Het
Adam7	A	G	14: 68,770,090 (GRCm39)	I21T	possibly damaging	Het
Aldh3b3	C	T	19: 4,018,492 (GRCm39)	R57*	probably null	Het
Arhgap22	T	C	14: 33,086,473 (GRCm39)		probably benign	Het
B4galt5	G	T	2: 167,143,340 (GRCm39)	Y361*	probably null	Het
BC005537	C	T	13: 24,987,382 (GRCm39)	R7W	possibly damaging	Het
Bsn	G	T	9: 107,992,098 (GRCm39)	A1218D	possibly damaging	Het
Ccdc141	T	C	2: 76,938,756 (GRCm39)	D283G	probably damaging	Het
Ccdc33	T	A	9: 57,976,374 (GRCm39)	I547F	probably benign	Het
Chdh	A	G	14: 29,753,288 (GRCm39)	N66D	probably benign	Het
Ckap2l	T	A	2: 129,127,209 (GRCm39)	Q323L	probably damaging	Het
Cpvl	T	A	6: 53,951,745 (GRCm39)	I13F	possibly damaging	Het
Creb3l2	G	A	6: 37,312,804 (GRCm39)	P410L	probably damaging	Het
Dna2	T	C	10: 62,805,643 (GRCm39)	V960A	probably benign	Het
Dop1a	G	A	9: 86,384,037 (GRCm39)		probably null	Het
Dpysl5	A	T	5: 30,902,760 (GRCm39)	D64V	probably damaging	Het
Dysf	A	G	6: 84,091,081 (GRCm39)	Q1041R	probably benign	Het
Efcab7	T	C	4: 99,746,154 (GRCm39)	V242A	probably benign	Het
Ehbp1	G	A	11: 22,096,542 (GRCm39)	R341*	probably null	Het
Eif1ad8	G	T	12: 87,563,388 (GRCm39)		probably benign	Het
Fbxo32	A	T	15: 58,077,986 (GRCm39)	W8R	probably damaging	Het
Fpgs	T	C	2: 32,573,472 (GRCm39)	N455D	probably damaging	Het
Gm8257	T	A	14: 44,894,754 (GRCm39)	E12V	probably damaging	Het
Kdm3a	A	T	6: 71,572,473 (GRCm39)	D1029E	probably benign	Het
Lipo4	T	G	19: 33,488,968 (GRCm39)	Q205P	possibly damaging	Het
Lpar6	A	T	14: 73,476,435 (GRCm39)	N132I	probably damaging	Het
Lrp1b	C	T	2: 41,339,246 (GRCm39)	G866S		Het
Man2c1	T	C	9: 57,045,270 (GRCm39)	F460L	probably damaging	Het
Map3k7cl	T	C	16: 87,378,100 (GRCm39)	V72A	probably damaging	Het
Map4k1	A	T	7: 28,699,387 (GRCm39)		probably null	Het
Matn1	A	G	4: 130,682,311 (GRCm39)	E496G	probably damaging	Het
Mfsd2a	A	T	4: 122,850,648 (GRCm39)	V76E	possibly damaging	Het
Mmut	C	T	17: 41,257,934 (GRCm39)	R367C	probably damaging	Het
Mtpap	A	G	18: 4,380,673 (GRCm39)	E117G	probably damaging	Het
Muc17	T	A	5: 137,175,625 (GRCm39)	N15I		Het
Ndufa10	A	G	1: 92,388,169 (GRCm39)	Y275H	probably damaging	Het
Nlrc4	A	T	17: 74,755,047 (GRCm39)	H56Q	possibly damaging	Het
Nrde2	G	A	12: 100,097,446 (GRCm39)	R785C	possibly damaging	Het
Nsun4	C	A	4: 115,891,329 (GRCm39)	C350F	probably benign	Het
Or10x1	A	G	1: 174,196,551 (GRCm39)	T23A	probably benign	Het
Or51f23b	A	G	7: 102,402,812 (GRCm39)	L108P	possibly damaging	Het
Or8g2	T	A	9: 39,821,282 (GRCm39)	F61Y	probably benign	Het
Or9s14	G	A	1: 92,536,237 (GRCm39)	G226D	possibly damaging	Het
Pdcd7	T	A	9: 65,254,261 (GRCm39)	C280S	probably damaging	Het
Peak1	G	T	9: 56,167,754 (GRCm39)	T58K	probably damaging	Het
Phactr2	T	C	10: 13,108,353 (GRCm39)	E573G	probably damaging	Het
Pramel27	A	G	4: 143,578,154 (GRCm39)	H138R	possibly damaging	Het
Ptprz1	G	A	6: 23,000,963 (GRCm39)	A1018T	not run	Het
Ralgapa1	G	T	12: 55,659,423 (GRCm39)	D2032E	probably benign	Het
Rapgef4	T	A	2: 72,031,481 (GRCm39)	N488K	probably benign	Het
Slc1a2	A	G	2: 102,591,530 (GRCm39)	D420G	probably benign	Het
Smyd5	T	A	6: 85,421,297 (GRCm39)	L337Q	probably damaging	Het
Tenm4	G	A	7: 96,555,587 (GRCm39)	R2764H	possibly damaging	Het
Tex35	A	T	1: 156,926,908 (GRCm39)	Y195*	probably null	Het
Tln2	T	C	9: 67,255,508 (GRCm39)	K690E	probably damaging	Het
Trpc4	A	G	3: 54,209,707 (GRCm39)	T691A	probably benign	Het
Tsr1	T	A	11: 74,791,158 (GRCm39)	F246I	possibly damaging	Het
Ttn	ATATCTCTCCAGAGCCTCCCCTGGAGGAGTGGAGTATCTCTCCAGAGCCTCCCCTGGAGGAGTGGAGTATCTCTCCAGAGCCTCCCCTG	ATATCTCTCCAGAGCCTCCCCTGGAGGAGTGGAGTATCTCTCCAGAGCCTCCCCTG	2: 76,746,150 (GRCm39)		probably benign	Het
Ubr4	A	T	4: 139,187,344 (GRCm39)	Y669F	unknown	Het
Uox	A	C	3: 146,316,029 (GRCm39)	D12A	probably benign	Het
Wdr17	A	G	8: 55,149,302 (GRCm39)		probably null	Het

Other mutations in Fsip1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00819:Fsip1	APN	2	118,080,393 (GRCm39)	missense	possibly damaging	0.63
IGL01676:Fsip1	APN	2	118,070,865 (GRCm39)	splice site	probably benign
IGL02039:Fsip1	APN	2	118,070,895 (GRCm39)	missense	probably damaging	1.00
IGL02337:Fsip1	APN	2	118,082,195 (GRCm39)	nonsense	probably null
IGL02668:Fsip1	APN	2	118,082,206 (GRCm39)	missense	probably benign	0.02
IGL03101:Fsip1	APN	2	118,072,144 (GRCm39)	missense	probably damaging	1.00
IGL03155:Fsip1	APN	2	118,082,220 (GRCm39)	missense	probably benign	0.06
R0045:Fsip1	UTSW	2	118,078,773 (GRCm39)	splice site	probably null
R0045:Fsip1	UTSW	2	118,078,773 (GRCm39)	splice site	probably null
R1225:Fsip1	UTSW	2	118,078,831 (GRCm39)	missense	probably damaging	0.98
R1824:Fsip1	UTSW	2	118,063,389 (GRCm39)	missense	probably damaging	0.98
R2048:Fsip1	UTSW	2	118,072,197 (GRCm39)	missense	probably damaging	0.97
R2229:Fsip1	UTSW	2	118,052,925 (GRCm39)	missense	probably benign	0.00
R3026:Fsip1	UTSW	2	118,080,384 (GRCm39)	missense	probably benign	0.06
R3746:Fsip1	UTSW	2	118,063,531 (GRCm39)	missense	probably damaging	0.98
R6275:Fsip1	UTSW	2	118,035,583 (GRCm39)	missense	probably benign	0.06
R6395:Fsip1	UTSW	2	118,067,406 (GRCm39)	missense	probably damaging	0.99
R6923:Fsip1	UTSW	2	118,080,394 (GRCm39)	missense	probably benign	0.01
R7942:Fsip1	UTSW	2	117,967,092 (GRCm39)	missense	probably benign	0.19
R8237:Fsip1	UTSW	2	118,063,483 (GRCm39)	missense	probably damaging	0.99
R8245:Fsip1	UTSW	2	118,075,359 (GRCm39)	missense	unknown
R8345:Fsip1	UTSW	2	118,070,952 (GRCm39)	missense	probably damaging	1.00
R8376:Fsip1	UTSW	2	118,063,519 (GRCm39)	missense	possibly damaging	0.79
R8765:Fsip1	UTSW	2	118,082,154 (GRCm39)	missense	possibly damaging	0.67
R9734:Fsip1	UTSW	2	118,070,916 (GRCm39)	missense	probably benign
Z1176:Fsip1	UTSW	2	117,966,964 (GRCm39)	missense	possibly damaging	0.89

Predicted Primers

PCR Primer
(F):5'- TCTACTTCGAGGAGCAGAGC -3'
(R):5'- TCTGCTATATTCATGGAAGCTTACC -3'

Sequencing Primer
(F):5'- AGCAGAGCCTCGGGTTTG -3'
(R):5'- TTCATGGAAGCTTACCTAGAGAAGAC -3'

Posted On

2019-12-20