Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01404:Tfg'

278414

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Tfg

Ensembl Gene

ENSMUSG00000022757

Gene Name

Trk-fused gene

Synonyms

Accession Numbers

Essential gene?

Probably essential (E-score: 0.944) question?

Stock #

IGL01404

Quality Score

Status

Chromosome

Chromosomal Location

56510695-56537813 bp(-) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

C to A at 56514856 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000119884 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000065515] [ENSMUST00000096012] [ENSMUST00000156522]

AlphaFold

Q9Z1A1

Predicted Effect

probably benign
Transcript: ENSMUST00000065515

SMART Domains

Protein: ENSMUSP00000067867
Gene: ENSMUSG00000022757

Domain	Start	End	E-Value	Type
PB1	10	91	5.97e-19	SMART
coiled coil region	97	124	N/A	INTRINSIC
low complexity region	208	236	N/A	INTRINSIC
low complexity region	241	269	N/A	INTRINSIC
low complexity region	272	295	N/A	INTRINSIC
low complexity region	304	334	N/A	INTRINSIC
low complexity region	361	373	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000096012

SMART Domains

Protein: ENSMUSP00000093711
Gene: ENSMUSG00000035258

Domain	Start	End	E-Value	Type
signal peptide	1	21	N/A	INTRINSIC
FN3	114	203	3.08e-2	SMART
low complexity region	433	446	N/A	INTRINSIC
low complexity region	634	647	N/A	INTRINSIC
low complexity region	651	664	N/A	INTRINSIC
FN3	841	924	6.29e-8	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000127994

SMART Domains

Protein: ENSMUSP00000121564
Gene: ENSMUSG00000022757

Domain	Start	End	E-Value	Type
Blast:PB1	2	30	6e-11	BLAST
coiled coil region	35	62	N/A	INTRINSIC
low complexity region	147	175	N/A	INTRINSIC
low complexity region	180	208	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000156522

SMART Domains

Protein: ENSMUSP00000119884
Gene: ENSMUSG00000022757

Domain	Start	End	E-Value	Type
low complexity region	82	139	N/A	INTRINSIC
low complexity region	142	165	N/A	INTRINSIC
low complexity region	174	202	N/A	INTRINSIC

Coding Region Coverage

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] There are several documented fusion oncoproteins encoded partially by this gene. This gene also participates in several oncogenic rearrangements resulting in anaplastic lymphoma and mixoid chondrosarcoma, and may play a role in the NF-kappaB pathway. Multiple transcript variants have been found for this gene. [provided by RefSeq, Sep 2010]

Allele List at MGI

Other mutations in this stock

Total: 63 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2700049A03Rik	T	A	12: 71,211,152 (GRCm39)		probably null	Het
4921524L21Rik	T	C	18: 6,638,653 (GRCm39)	S351P	possibly damaging	Het
Ablim3	A	G	18: 62,004,754 (GRCm39)	Y12H	probably damaging	Het
Adam2	C	T	14: 66,314,659 (GRCm39)		probably null	Het
Adgre4	A	T	17: 56,104,639 (GRCm39)	N235I	possibly damaging	Het
Aldh3b1	A	C	19: 3,971,205 (GRCm39)	V153G	probably benign	Het
B430306N03Rik	A	G	17: 48,628,101 (GRCm39)	Y177C	probably damaging	Het
Cast	A	T	13: 74,886,406 (GRCm39)	Y249*	probably null	Het
Cfap43	T	C	19: 47,784,105 (GRCm39)	D476G	probably benign	Het
Cpa4	T	C	6: 30,581,701 (GRCm39)	I216T	possibly damaging	Het
Cpeb3	T	C	19: 37,065,948 (GRCm39)	D407G	probably benign	Het
Ctnnal1	T	C	4: 56,829,590 (GRCm39)	D413G	probably damaging	Het
Cyb5a	A	G	18: 84,895,985 (GRCm39)	S84G	probably benign	Het
Dpy19l4	C	A	4: 11,273,006 (GRCm39)		probably null	Het
Erbin	A	T	13: 103,975,972 (GRCm39)	S641T	probably damaging	Het
Espn	T	A	4: 152,222,901 (GRCm39)	T326S	probably benign	Het
Extl1	T	C	4: 134,086,514 (GRCm39)	M514V	probably benign	Het
Fancc	G	A	13: 63,509,452 (GRCm39)	L134F	probably damaging	Het
Fis1	C	T	5: 136,994,828 (GRCm39)	A90V	probably benign	Het
Gdi2	A	G	13: 3,614,611 (GRCm39)	T319A	probably benign	Het
Gjc3	A	G	5: 137,956,120 (GRCm39)	F55S	probably damaging	Het
Gm10762	C	T	2: 128,809,005 (GRCm39)		probably benign	Het
Got1	A	G	19: 43,493,048 (GRCm39)	I291T	possibly damaging	Het
Gpr179	C	A	11: 97,229,012 (GRCm39)	G1048*	probably null	Het
Ino80	T	A	2: 119,287,199 (GRCm39)	D56V	possibly damaging	Het
Kcp	C	A	6: 29,496,638 (GRCm39)	C624F	probably damaging	Het
Kctd1	T	A	18: 15,102,610 (GRCm39)	Q857L	probably damaging	Het
Lins1	G	A	7: 66,363,676 (GRCm39)	V524I	probably damaging	Het
Lrp1	A	T	10: 127,430,901 (GRCm39)	Y383N	probably damaging	Het
Mgam	A	C	6: 40,621,879 (GRCm39)	K84Q	probably benign	Het
Mib2	T	A	4: 155,739,393 (GRCm39)	E862V	probably damaging	Het
Myh1	G	T	11: 67,112,977 (GRCm39)	R1827L	possibly damaging	Het
Myh10	T	C	11: 68,642,866 (GRCm39)		probably null	Het
Myo1e	A	G	9: 70,245,048 (GRCm39)	Y382C	probably benign	Het
Nktr	G	A	9: 121,570,218 (GRCm39)		probably null	Het
Nlrc4	A	G	17: 74,752,706 (GRCm39)	I559T	probably damaging	Het
Nod2	A	T	8: 89,390,364 (GRCm39)	M224L	probably benign	Het
Or4d5	A	G	9: 40,012,558 (GRCm39)	I76T	probably benign	Het
Or52n4	A	T	7: 104,293,687 (GRCm39)	Y295*	probably null	Het
Or5k8	G	A	16: 58,644,958 (GRCm39)	T38I	probably damaging	Het
Pex7	G	T	10: 19,770,557 (GRCm39)		probably benign	Het
Ptprb	A	T	10: 116,175,341 (GRCm39)	D1112V	probably benign	Het
Rubcn	G	A	16: 32,647,666 (GRCm39)	T636M	probably damaging	Het
Scn5a	A	C	9: 119,315,536 (GRCm39)	L1724R	probably damaging	Het
Sec14l2	T	C	11: 4,066,710 (GRCm39)	D34G	possibly damaging	Het
Serpina3k	A	G	12: 104,306,882 (GRCm39)	D38G	probably benign	Het
Sh3bgr	A	C	16: 96,007,690 (GRCm39)	K18N	probably damaging	Het
Sh3bp5l	A	T	11: 58,236,886 (GRCm39)	H281L	probably benign	Het
Slc28a2	T	G	2: 122,282,538 (GRCm39)	I287M	probably damaging	Het
Slc2a1	T	A	4: 118,989,435 (GRCm39)	M45K	possibly damaging	Het
Syt11	A	G	3: 88,669,523 (GRCm39)	I123T	probably benign	Het
Tmem177	T	C	1: 119,837,791 (GRCm39)	D296G	probably damaging	Het
Trabd2b	A	G	4: 114,457,153 (GRCm39)	I357V	probably benign	Het
Trp63	C	A	16: 25,639,135 (GRCm39)		probably benign	Het
Ugt1a8	T	C	1: 88,015,617 (GRCm39)	L10P	probably benign	Het
Vmn2r103	A	G	17: 20,032,696 (GRCm39)	I823M	probably damaging	Het
Vmn2r45	T	C	7: 8,484,467 (GRCm39)	N446S	probably damaging	Het
Vps13c	A	T	9: 67,820,486 (GRCm39)		probably null	Het
Vwa3b	C	T	1: 37,193,117 (GRCm39)	T11I	probably benign	Het
Vwf	A	C	6: 125,654,933 (GRCm39)	Q2543P	probably damaging	Het
Yap1	G	A	9: 7,934,742 (GRCm39)		probably benign	Het
Zfp282	A	C	6: 47,874,770 (GRCm39)	D325A	probably damaging	Het
Zfyve9	T	G	4: 108,539,348 (GRCm39)	Y975S	probably damaging	Het

Other mutations in Tfg

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01402:Tfg	APN	16	56,514,856 (GRCm39)	splice site	probably benign
IGL01548:Tfg	APN	16	56,521,465 (GRCm39)	missense	probably damaging	1.00
trafalgar	UTSW	16	56,532,997 (GRCm39)	missense	possibly damaging	0.90
R0003:Tfg	UTSW	16	56,511,351 (GRCm39)	missense	possibly damaging	0.96
R0003:Tfg	UTSW	16	56,511,351 (GRCm39)	missense	possibly damaging	0.96
R0036:Tfg	UTSW	16	56,511,358 (GRCm39)	missense	probably benign	0.18
R1730:Tfg	UTSW	16	56,533,152 (GRCm39)	missense	probably damaging	1.00
R2025:Tfg	UTSW	16	56,525,988 (GRCm39)	missense	possibly damaging	0.65
R4629:Tfg	UTSW	16	56,533,039 (GRCm39)	missense	probably damaging	1.00
R4676:Tfg	UTSW	16	56,514,854 (GRCm39)	splice site	probably null
R4879:Tfg	UTSW	16	56,521,520 (GRCm39)	missense	probably damaging	1.00
R4916:Tfg	UTSW	16	56,514,759 (GRCm39)	splice site	probably null
R5237:Tfg	UTSW	16	56,533,071 (GRCm39)	missense	possibly damaging	0.80
R5568:Tfg	UTSW	16	56,521,450 (GRCm39)	missense	probably benign	0.14
R5698:Tfg	UTSW	16	56,521,467 (GRCm39)	missense	probably damaging	0.98
R5887:Tfg	UTSW	16	56,514,779 (GRCm39)	nonsense	probably null
R7213:Tfg	UTSW	16	56,521,516 (GRCm39)	missense	probably benign	0.03
R7392:Tfg	UTSW	16	56,532,972 (GRCm39)	critical splice donor site	probably null
R7514:Tfg	UTSW	16	56,525,972 (GRCm39)	critical splice donor site	probably null
R7632:Tfg	UTSW	16	56,532,997 (GRCm39)	missense	possibly damaging	0.90
R8304:Tfg	UTSW	16	56,521,581 (GRCm39)	missense	possibly damaging	0.87
R9254:Tfg	UTSW	16	56,526,050 (GRCm39)	missense	probably damaging	1.00
R9432:Tfg	UTSW	16	56,524,868 (GRCm39)	nonsense	probably null

Posted On

2015-04-16