Mutagenetix > Incidental Mutation

Incidental Mutation 'R7841:Faxc'

606286

Institutional Source

Beutler Lab

Gene Symbol

Faxc

Ensembl Gene

ENSMUSG00000028246

Gene Name

failed axon connections homolog

Synonyms

6230409E13Rik

MMRRC Submission

045895-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.169) question?

Stock #

R7841 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

21931329-21996839 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 21958584 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Histidine to Arginine at position 247 (H247R)

Ref Sequence

ENSEMBL: ENSMUSP00000029908 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000029908]

AlphaFold

Q3UMF9

Predicted Effect

probably benign
Transcript: ENSMUST00000029908
AA Change: H247R

PolyPhen 2 Score 0.116 (Sensitivity: 0.93; Specificity: 0.86)

SMART Domains

Protein: ENSMUSP00000029908
Gene: ENSMUSG00000028246
AA Change: H247R

Domain	Start	End	E-Value	Type
low complexity region	66	82	N/A	INTRINSIC
SCOP:d1k0ma2	93	172	1e-3	SMART
Pfam:GST_C_3	197	328	1.5e-34	PFAM

Coding Region Coverage

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

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 76 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700016H13Rik	T	C	5: 103,802,806 (GRCm39)	K16R	possibly damaging	Het
2810408A11Rik	A	G	11: 69,790,112 (GRCm39)	F210L	probably benign	Het
Adam6a	G	T	12: 113,509,078 (GRCm39)	D484Y	probably damaging	Het
B9d1	A	G	11: 61,397,192 (GRCm39)	Y29C	possibly damaging	Het
Cald1	T	C	6: 34,722,696 (GRCm39)	F115L	unknown	Het
Ccnd1	A	T	7: 144,491,718 (GRCm39)	M107K	probably damaging	Het
Ccnh	G	A	13: 85,337,712 (GRCm39)	A20T	probably benign	Het
Cep162	T	C	9: 87,126,369 (GRCm39)	D181G	probably benign	Het
Cep44	AACGC	A	8: 56,994,018 (GRCm39)		probably null	Het
Ces2b	A	G	8: 105,561,692 (GRCm39)	D262G	probably benign	Het
Cic	A	G	7: 24,985,192 (GRCm39)	Y1146C	probably damaging	Het
Cmtm1	G	A	8: 105,036,108 (GRCm39)	R174C	possibly damaging	Het
Cobl	G	T	11: 12,203,324 (GRCm39)	P1126H	probably damaging	Het
Col14a1	T	A	15: 55,245,876 (GRCm39)	M460K	unknown	Het
Cst11	G	A	2: 148,613,227 (GRCm39)	R33W	possibly damaging	Het
Cyp19a1	A	T	9: 54,079,089 (GRCm39)	V340E	probably benign	Het
Dbt	A	T	3: 116,339,746 (GRCm39)	Q378L	possibly damaging	Het
Dchs1	A	G	7: 105,412,180 (GRCm39)	V1312A	probably benign	Het
Eif3l	T	C	15: 78,973,779 (GRCm39)	M398T	probably benign	Het
Fbxl17	T	C	17: 63,794,820 (GRCm39)	R421G	probably damaging	Het
Fbxo3	T	A	2: 103,890,337 (GRCm39)	D450E	unknown	Het
Fmn1	T	C	2: 113,359,810 (GRCm39)		probably null	Het
Foxs1	T	A	2: 152,774,907 (GRCm39)	M49L	possibly damaging	Het
Gucy1a2	A	G	9: 3,634,766 (GRCm39)	E270G	probably benign	Het
Helz2	T	C	2: 180,874,695 (GRCm39)	D1933G	probably damaging	Het
Hspa4	G	A	11: 53,157,887 (GRCm39)	A572V	possibly damaging	Het
Ica1	T	A	6: 8,737,072 (GRCm39)	D174V	probably damaging	Het
Igfbp6	A	T	15: 102,056,352 (GRCm39)	Q137L	possibly damaging	Het
Il1r2	T	C	1: 40,144,628 (GRCm39)	L105P	probably damaging	Het
Iqca1	A	T	1: 89,987,337 (GRCm39)	C72S		Het
Itgbl1	T	C	14: 124,209,645 (GRCm39)		probably null	Het
Ivl	T	A	3: 92,479,699 (GRCm39)	Q122L	possibly damaging	Het
Kdsr	T	C	1: 106,671,415 (GRCm39)	E198G	probably damaging	Het
Lama2	T	C	10: 27,031,529 (GRCm39)	T1510A	probably benign	Het
Lrrc37a	A	T	11: 103,391,931 (GRCm39)	Y1165N	probably benign	Het
Mycbp2	A	G	14: 103,384,267 (GRCm39)		probably null	Het
Myh3	A	G	11: 66,989,518 (GRCm39)	E1546G	probably damaging	Het
Nacad	A	T	11: 6,551,031 (GRCm39)	V720E	probably benign	Het
Napa	A	G	7: 15,849,559 (GRCm39)	D257G	possibly damaging	Het
Nif3l1	T	C	1: 58,487,042 (GRCm39)	V76A	probably damaging	Het
Nkapd1	A	C	9: 50,521,716 (GRCm39)	S68R	probably damaging	Het
Nphp4	G	A	4: 152,581,140 (GRCm39)	S108N	probably benign	Het
Npr1	A	T	3: 90,362,175 (GRCm39)	L990H	probably damaging	Het
Nup205	A	G	6: 35,224,372 (GRCm39)	R322G	unknown	Het
Or4a79	C	A	2: 89,552,309 (GRCm39)	A49S	probably benign	Het
Or4q3	G	T	14: 50,583,285 (GRCm39)	Q174K	probably benign	Het
Or52n2c	T	A	7: 104,574,066 (GRCm39)	I302F	possibly damaging	Het
Or8c14-ps1	T	G	9: 38,101,777 (GRCm39)	M252R	unknown	Het
Or8c19-ps1	T	A	9: 38,220,817 (GRCm39)	V242E	unknown	Het
Ovch2	G	T	7: 107,393,298 (GRCm39)	Q192K	probably benign	Het
Pcca	T	A	14: 122,800,384 (GRCm39)	D91E	probably benign	Het
Pole2	T	C	12: 69,251,032 (GRCm39)	T444A	probably damaging	Het
Ppip5k1	T	C	2: 121,173,276 (GRCm39)	K466E	probably benign	Het
Prr35	A	T	17: 26,167,458 (GRCm39)	Y26*	probably null	Het
Ptgfrn	A	T	3: 100,968,126 (GRCm39)	I489N	probably damaging	Het
Rassf1	A	G	9: 107,438,744 (GRCm39)	*341W	probably null	Het
Ret	G	A	6: 118,132,321 (GRCm39)	P1040S	probably damaging	Het
Rictor	C	T	15: 6,801,635 (GRCm39)	S441L	probably benign	Het
Rsf1	A	AAGGCGACGG	7: 97,229,111 (GRCm39)		probably null	Het
Slc6a17	A	T	3: 107,384,214 (GRCm39)	Y377N	possibly damaging	Het
Snrnp200	C	A	2: 127,078,754 (GRCm39)	D1806E	probably benign	Het
Synj2	G	A	17: 6,094,419 (GRCm39)	R1215H	unknown	Het
Tbc1d5	TTGCTGCTGGTGTTGCTGCTGCTGCTGCTG	TTGCTGCTG	17: 51,106,950 (GRCm39)		probably benign	Het
Top2a	A	T	11: 98,913,176 (GRCm39)	D85E	probably damaging	Het
Tram1l1	A	T	3: 124,115,353 (GRCm39)	Q171L	probably damaging	Het
Tram1l1	G	T	3: 124,115,354 (GRCm39)	Q171H	probably damaging	Het
Tspyl4	A	G	10: 34,174,267 (GRCm39)	H253R	probably damaging	Het
Ttn	T	C	2: 76,662,490 (GRCm39)	I23V		Het
Ubr5	T	C	15: 37,981,150 (GRCm39)	N2376D		Het
Ugt2b37	T	C	5: 87,398,489 (GRCm39)	N316D	probably benign	Het
Usp31	A	C	7: 121,247,679 (GRCm39)	S1255A	probably benign	Het
Usp31	A	T	7: 121,276,535 (GRCm39)	V334E	probably damaging	Het
Vmn2r108	A	G	17: 20,690,305 (GRCm39)		probably null	Het
Vmn2r87	T	A	10: 130,333,095 (GRCm39)	T52S	probably benign	Het
Vrk2	C	A	11: 26,421,457 (GRCm39)	L500F	probably damaging	Het
Zan	T	A	5: 137,435,064 (GRCm39)	I2110F	unknown	Het

Other mutations in Faxc

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00391:Faxc	APN	4	21,948,725 (GRCm39)	missense	probably damaging	1.00
IGL00418:Faxc	APN	4	21,958,490 (GRCm39)	missense	possibly damaging	0.55
IGL01714:Faxc	APN	4	21,936,688 (GRCm39)	missense	probably damaging	1.00
IGL02193:Faxc	APN	4	21,993,486 (GRCm39)	missense	possibly damaging	0.69
IGL02290:Faxc	APN	4	21,993,390 (GRCm39)	missense	possibly damaging	0.73
IGL03271:Faxc	APN	4	21,948,757 (GRCm39)	missense	possibly damaging	0.74
R0131:Faxc	UTSW	4	21,936,659 (GRCm39)	missense	probably damaging	1.00
R0409:Faxc	UTSW	4	21,948,751 (GRCm39)	missense	probably benign	0.00
R0615:Faxc	UTSW	4	21,958,608 (GRCm39)	missense	probably benign	0.01
R1973:Faxc	UTSW	4	21,993,405 (GRCm39)	missense	probably benign	0.35
R2027:Faxc	UTSW	4	21,958,439 (GRCm39)	splice site	probably benign
R2181:Faxc	UTSW	4	21,931,591 (GRCm39)	missense	probably benign	0.02
R4243:Faxc	UTSW	4	21,982,491 (GRCm39)	missense	probably benign	0.01
R4845:Faxc	UTSW	4	21,993,358 (GRCm39)	missense	probably damaging	1.00
R5260:Faxc	UTSW	4	21,948,744 (GRCm39)	missense	probably damaging	1.00
R5306:Faxc	UTSW	4	21,931,557 (GRCm39)	utr 5 prime	probably benign
R6187:Faxc	UTSW	4	21,958,445 (GRCm39)	missense	possibly damaging	0.52
R6237:Faxc	UTSW	4	21,993,376 (GRCm39)	missense	possibly damaging	0.95
R6721:Faxc	UTSW	4	21,982,672 (GRCm39)	splice site	probably null
R6825:Faxc	UTSW	4	21,931,672 (GRCm39)	missense	probably benign	0.00
R8351:Faxc	UTSW	4	21,932,046 (GRCm39)	splice site	probably null
R8491:Faxc	UTSW	4	21,993,319 (GRCm39)	missense	probably damaging	0.97
R8905:Faxc	UTSW	4	21,982,398 (GRCm39)	missense	probably damaging	1.00
R9715:Faxc	UTSW	4	21,993,307 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TCTGATGCAGAGCAGTAACCTG -3'
(R):5'- ACTAGGGGCCTTGTTTAAATGG -3'

Sequencing Primer
(F):5'- GATGCAGAGCAGTAACCTGTTTCC -3'
(R):5'- TGCAACCTACATATGGGAGC -3'

Posted On

2019-12-20