Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02971:Fam83f'

365830

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Fam83f

Ensembl Gene

ENSMUSG00000022408

Gene Name

family with sequence similarity 83, member F

Synonyms

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.051) question?

Stock #

IGL02971

Quality Score

Status

Chromosome

Chromosomal Location

80556048-80584626 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 80556350 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 78 (V78A)

Ref Sequence

ENSEMBL: ENSMUSP00000023044 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000023044]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000023044
AA Change: V78A

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000023044
Gene: ENSMUSG00000022408
AA Change: V78A

Domain	Start	End	E-Value	Type
Pfam:DUF1669	15	291	1.5e-111	PFAM
Pfam:PLDc_2	148	286	6.4e-12	PFAM
low complexity region	346	360	N/A	INTRINSIC
low complexity region	447	458	N/A	INTRINSIC

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 45 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A930018P22Rik	C	T	2: 103,953,564 (GRCm39)	T130I	probably benign	Het
Ahi1	T	C	10: 20,876,450 (GRCm39)	L787P	possibly damaging	Het
Atf3	A	G	1: 190,909,640 (GRCm39)	S10P	probably benign	Het
Cdr2l	A	G	11: 115,281,726 (GRCm39)	N77S	probably damaging	Het
Cnp	A	G	11: 100,467,525 (GRCm39)	D156G	probably benign	Het
Cntn3	A	T	6: 102,145,894 (GRCm39)	D982E	probably damaging	Het
Col22a1	A	G	15: 71,878,587 (GRCm39)	L190S	probably damaging	Het
Csmd3	C	T	15: 47,777,325 (GRCm39)		probably benign	Het
Dnah5	A	G	15: 28,384,607 (GRCm39)	D3117G	probably damaging	Het
Dock5	T	C	14: 67,994,558 (GRCm39)	E1834G	probably null	Het
Eea1	A	G	10: 95,877,389 (GRCm39)	T1368A	probably benign	Het
Fcgbp	G	A	7: 27,800,898 (GRCm39)	V1315I	probably damaging	Het
Fsd2	A	T	7: 81,198,671 (GRCm39)	Y364*	probably null	Het
Gm21976	G	A	13: 98,439,057 (GRCm39)	G16R	probably null	Het
Guca2b	A	G	4: 119,514,885 (GRCm39)	S59P	probably damaging	Het
Hars2	A	G	18: 36,919,231 (GRCm39)	E123G	probably damaging	Het
Hdac2	A	T	10: 36,876,370 (GRCm39)	K462*	probably null	Het
Huwe1	T	A	X: 150,710,622 (GRCm39)		probably benign	Het
Iqgap3	T	A	3: 87,997,611 (GRCm39)	N262K	probably benign	Het
Kat6b	A	G	14: 21,719,826 (GRCm39)	S1502G	probably damaging	Het
Mapkapk3	A	T	9: 107,134,279 (GRCm39)	D328E	probably benign	Het
Naca	C	T	10: 127,877,437 (GRCm39)		probably benign	Het
Npffr1	T	C	10: 61,449,918 (GRCm39)	V64A	probably damaging	Het
Oga	A	G	19: 45,750,682 (GRCm39)	F671S	probably damaging	Het
Or2t49	A	G	11: 58,393,211 (GRCm39)	L57P	probably damaging	Het
Or8b3b	T	A	9: 38,584,564 (GRCm39)	M72L	probably damaging	Het
Pcca	A	G	14: 123,126,945 (GRCm39)	D718G	probably damaging	Het
Pde6a	A	C	18: 61,397,326 (GRCm39)	D670A	probably damaging	Het
Pramel7	T	A	2: 87,320,417 (GRCm39)	E292V	probably benign	Het
Prmt9	A	C	8: 78,291,698 (GRCm39)	M357L	probably benign	Het
Ptgfr	A	T	3: 151,540,963 (GRCm39)	S182T	probably benign	Het
Rtraf	A	T	14: 19,866,260 (GRCm39)	M152K	possibly damaging	Het
Satb1	T	C	17: 52,049,717 (GRCm39)	D579G	possibly damaging	Het
Serpinb6a	A	G	13: 34,115,453 (GRCm39)		probably null	Het
Slc5a9	T	C	4: 111,747,497 (GRCm39)	I297V	possibly damaging	Het
Slf1	T	A	13: 77,195,223 (GRCm39)		probably benign	Het
St8sia2	C	T	7: 73,616,559 (GRCm39)	V139M	probably damaging	Het
Tas2r114	T	C	6: 131,666,243 (GRCm39)	M262V	probably benign	Het
Tmem147	A	G	7: 30,428,847 (GRCm39)		probably benign	Het
Tmem220	A	G	11: 66,924,933 (GRCm39)		probably null	Het
Uspl1	A	G	5: 149,125,156 (GRCm39)	N35S	possibly damaging	Het
Vmn1r170	A	T	7: 23,305,759 (GRCm39)	I54F	possibly damaging	Het
Vmn2r121	T	G	X: 123,037,591 (GRCm39)	I810L	probably damaging	Het
Wbp2nl	A	T	15: 82,189,945 (GRCm39)	T46S	possibly damaging	Het
Zfp955b	T	A	17: 33,519,940 (GRCm39)	M57K	probably benign	Het

Other mutations in Fam83f

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R0212:Fam83f	UTSW	15	80,574,779 (GRCm39)	missense	probably benign	0.00
R0347:Fam83f	UTSW	15	80,556,458 (GRCm39)	missense	probably damaging	1.00
R0976:Fam83f	UTSW	15	80,576,285 (GRCm39)	missense	probably damaging	1.00
R1724:Fam83f	UTSW	15	80,576,468 (GRCm39)	missense	possibly damaging	0.65
R1725:Fam83f	UTSW	15	80,576,468 (GRCm39)	missense	possibly damaging	0.65
R1741:Fam83f	UTSW	15	80,576,468 (GRCm39)	missense	possibly damaging	0.65
R1796:Fam83f	UTSW	15	80,574,283 (GRCm39)	missense	possibly damaging	0.80
R1870:Fam83f	UTSW	15	80,574,113 (GRCm39)	splice site	probably benign
R1899:Fam83f	UTSW	15	80,576,281 (GRCm39)	missense	probably damaging	1.00
R2022:Fam83f	UTSW	15	80,576,468 (GRCm39)	missense	possibly damaging	0.65
R2114:Fam83f	UTSW	15	80,576,468 (GRCm39)	missense	possibly damaging	0.65
R2115:Fam83f	UTSW	15	80,576,468 (GRCm39)	missense	possibly damaging	0.65
R4090:Fam83f	UTSW	15	80,576,393 (GRCm39)	missense	possibly damaging	0.85
R4865:Fam83f	UTSW	15	80,576,650 (GRCm39)	missense	probably damaging	1.00
R4893:Fam83f	UTSW	15	80,576,156 (GRCm39)	missense	probably damaging	1.00
R5206:Fam83f	UTSW	15	80,576,255 (GRCm39)	missense	possibly damaging	0.86
R5739:Fam83f	UTSW	15	80,576,206 (GRCm39)	missense	probably damaging	1.00
R6468:Fam83f	UTSW	15	80,576,312 (GRCm39)	missense	possibly damaging	0.77
R7838:Fam83f	UTSW	15	80,576,704 (GRCm39)	missense	possibly damaging	0.94
R8070:Fam83f	UTSW	15	80,556,281 (GRCm39)	missense	probably damaging	1.00
R8082:Fam83f	UTSW	15	80,574,119 (GRCm39)	missense	probably damaging	0.98
R9071:Fam83f	UTSW	15	80,576,206 (GRCm39)	missense	probably damaging	1.00
R9711:Fam83f	UTSW	15	80,574,819 (GRCm39)	missense	probably damaging	1.00

Posted On

2015-12-18