Mutagenetix > Incidental Mutation

Incidental Mutation 'R8350:Fam81a'

645477

Institutional Source

Beutler Lab

Gene Symbol

Fam81a

Ensembl Gene

ENSMUSG00000032224

Gene Name

family with sequence similarity 81, member A

Synonyms

6430514L14Rik

MMRRC Submission

067868-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.056) question?

Stock #

R8350 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

69996586-70049840 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 70032300 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Serine at position 64 (N64S)

Ref Sequence

ENSEMBL: ENSMUSP00000034749 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000034749] [ENSMUST00000123206] [ENSMUST00000141775]

AlphaFold

Q3UXZ6

Predicted Effect

probably damaging
Transcript: ENSMUST00000034749
AA Change: N64S

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000034749
Gene: ENSMUSG00000032224
AA Change: N64S

Domain	Start	End	E-Value	Type
coiled coil region	75	106	N/A	INTRINSIC
coiled coil region	158	187	N/A	INTRINSIC
low complexity region	349	358	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000123206
AA Change: N64S

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

Predicted Effect

probably damaging
Transcript: ENSMUST00000141775
AA Change: N64S

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.1%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 55 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700123K08Rik	G	A	5: 138,561,188 (GRCm39)	T158M	probably benign	Het
Akirin2	T	A	4: 34,551,082 (GRCm39)	F13Y	probably damaging	Het
Arhgef2	G	A	3: 88,553,527 (GRCm39)	R886H	probably damaging	Het
Armc12	T	A	17: 28,751,031 (GRCm39)	D82E	probably damaging	Het
Atg2a	T	C	19: 6,296,841 (GRCm39)	S382P	probably benign	Het
Bola1	G	A	3: 96,104,573 (GRCm39)	A7V	probably benign	Het
Cep170	A	G	1: 176,564,445 (GRCm39)	L271S		Het
Cers3	T	C	7: 66,414,090 (GRCm39)	F92S	possibly damaging	Het
Chmp4c	A	T	3: 10,450,746 (GRCm39)	M109L	possibly damaging	Het
Cnmd	T	A	14: 79,882,821 (GRCm39)	K202*	probably null	Het
Cnp	T	C	11: 100,467,267 (GRCm39)	I70T	probably damaging	Het
Col27a1	C	A	4: 63,248,134 (GRCm39)	T1721K	unknown	Het
Crtac1	G	A	19: 42,297,625 (GRCm39)	R242W	probably damaging	Het
Cry2	T	C	2: 92,244,286 (GRCm39)	R296G	probably benign	Het
Cyp2t4	A	G	7: 26,856,806 (GRCm39)	D282G	possibly damaging	Het
Dip2a	G	T	10: 76,100,690 (GRCm39)	T1495N	probably damaging	Het
Dmbt1	T	C	7: 130,687,147 (GRCm39)		probably null	Het
Dmp1	A	T	5: 104,360,765 (GRCm39)	K480N	probably damaging	Het
Dnah17	A	G	11: 117,977,873 (GRCm39)	S1820P	probably damaging	Het
Dnah6	A	G	6: 73,172,798 (GRCm39)	V220A	probably benign	Het
Eif4a3l1	C	T	6: 136,306,241 (GRCm39)	T234I	possibly damaging	Het
Epha3	T	C	16: 63,472,853 (GRCm39)	D344G	possibly damaging	Het
Esyt2	C	A	12: 116,327,102 (GRCm39)	Q557K	probably damaging	Het
Fam72a	A	T	1: 131,461,663 (GRCm39)	D116V	probably damaging	Het
Fat3	T	A	9: 15,826,435 (GRCm39)	T358S		Het
Frat2	A	T	19: 41,836,223 (GRCm39)	I43N	probably damaging	Het
Fryl	A	T	5: 73,226,073 (GRCm39)	D1863E	probably benign	Het
Gm43302	A	T	5: 105,422,573 (GRCm39)		probably null	Het
Grid2ip	A	G	5: 143,363,273 (GRCm39)	Y422C	probably damaging	Het
Hap1	T	G	11: 100,240,107 (GRCm39)	D563A	probably damaging	Het
Hbb-bs	T	C	7: 103,475,951 (GRCm39)	D122G	probably benign	Het
Hs3st3b1	G	C	11: 63,780,390 (GRCm39)	P246A	probably benign	Het
Hsd17b4	T	G	18: 50,297,734 (GRCm39)	L341R	probably benign	Het
Kbtbd11	G	A	8: 15,078,603 (GRCm39)	V401M	probably damaging	Het
Lss	T	A	10: 76,371,429 (GRCm39)	L120Q	probably damaging	Het
Mdc1	T	G	17: 36,159,191 (GRCm39)	S524A	probably benign	Het
Myoz3	T	C	18: 60,712,074 (GRCm39)	Y168C	probably damaging	Het
Nceh1	C	A	3: 27,293,813 (GRCm39)	D190E	probably damaging	Het
Neb	T	C	2: 52,096,194 (GRCm39)	R5039G	probably benign	Het
Nup50	T	A	15: 84,819,476 (GRCm39)	V250E	probably benign	Het
Pcnx3	T	A	19: 5,723,254 (GRCm39)	N1314Y	probably damaging	Het
Pdzk1	A	G	3: 96,759,024 (GRCm39)	N143S	probably benign	Het
Rnf223	T	G	4: 156,217,120 (GRCm39)	L165R	probably damaging	Het
Sbf1	A	T	15: 89,183,712 (GRCm39)	F1267Y	probably damaging	Het
Scrn3	T	G	2: 73,160,113 (GRCm39)	I252R	possibly damaging	Het
Sdr39u1	T	C	14: 56,135,363 (GRCm39)	I193M	probably damaging	Het
Sh2d7	A	G	9: 54,448,191 (GRCm39)	R71G	probably benign	Het
Slc12a9	C	A	5: 137,313,737 (GRCm39)	V741L	probably benign	Het
Syk	T	C	13: 52,774,935 (GRCm39)	L225P	probably damaging	Het
Tbx1	A	T	16: 18,400,795 (GRCm39)	V463E	unknown	Het
Tmem67	C	T	4: 12,087,891 (GRCm39)	R19H	probably benign	Het
Ttn	T	A	2: 76,609,108 (GRCm39)	I17666F	possibly damaging	Het
Vcpip1	A	G	1: 9,794,831 (GRCm39)	V1180A	probably benign	Het
Wdr27	T	C	17: 15,152,787 (GRCm39)	T107A	probably benign	Het
Zfp106	T	C	2: 120,366,099 (GRCm39)	R58G		Het

Other mutations in Fam81a

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01636:Fam81a	APN	9	70,006,434 (GRCm39)	nonsense	probably null
IGL02010:Fam81a	APN	9	70,006,419 (GRCm39)	missense	probably benign	0.04
IGL02891:Fam81a	APN	9	70,017,558 (GRCm39)	missense	probably damaging	1.00
R0100:Fam81a	UTSW	9	70,010,091 (GRCm39)	splice site	probably benign
R0497:Fam81a	UTSW	9	70,003,401 (GRCm39)	missense	possibly damaging	0.47
R0621:Fam81a	UTSW	9	70,000,929 (GRCm39)	missense	probably benign	0.35
R1075:Fam81a	UTSW	9	70,017,556 (GRCm39)	nonsense	probably null
R1524:Fam81a	UTSW	9	70,032,390 (GRCm39)	missense	probably damaging	1.00
R4970:Fam81a	UTSW	9	70,000,872 (GRCm39)	nonsense	probably null
R5138:Fam81a	UTSW	9	70,006,457 (GRCm39)	missense	probably benign	0.01
R5209:Fam81a	UTSW	9	70,032,442 (GRCm39)	missense	probably benign	0.06
R6139:Fam81a	UTSW	9	70,010,100 (GRCm39)	critical splice donor site	probably null
R6378:Fam81a	UTSW	9	70,017,628 (GRCm39)	missense	probably damaging	1.00
R7145:Fam81a	UTSW	9	70,017,560 (GRCm39)	missense	probably damaging	1.00
R8030:Fam81a	UTSW	9	70,010,191 (GRCm39)	missense	probably benign	0.11
R8450:Fam81a	UTSW	9	70,032,300 (GRCm39)	missense	probably damaging	1.00
R8781:Fam81a	UTSW	9	70,032,381 (GRCm39)	missense	probably damaging	1.00
R9021:Fam81a	UTSW	9	70,017,538 (GRCm39)	critical splice donor site	probably null

Predicted Primers

PCR Primer
(F):5'- AAGCATGCATACAGGACTGTG -3'
(R):5'- ATGTGACTCCCTTCTGCAGG -3'

Sequencing Primer
(F):5'- TGACAGCTGGGACTCAGACTTG -3'
(R):5'- CTTCTGCAGGCGAGTGAAGAC -3'

Posted On

2020-09-02