Mutagenetix > Incidental Mutation

Incidental Mutation 'R4616:Fam90a1a'

351048

Institutional Source

Beutler Lab

Gene Symbol

Fam90a1a

Ensembl Gene

ENSMUSG00000079112

Gene Name

family with sequence similarity 90, member A1A

Synonyms

C86695

MMRRC Submission

041827-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.070) question?

Stock #

R4616 (G1)

Quality Score

216

Status

Validated

Chromosome

Chromosomal Location

21958714-21964303 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

C to A at 21963846 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Glutamine to Lysine at position 406 (Q406K)

Ref Sequence

ENSEMBL: ENSMUSP00000106369 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000110741]

AlphaFold

A2A4E2

Predicted Effect

possibly damaging
Transcript: ENSMUST00000110741
AA Change: Q406K

PolyPhen 2 Score 0.483 (Sensitivity: 0.89; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000106369
Gene: ENSMUSG00000079112
AA Change: Q406K

Domain	Start	End	E-Value	Type
ZnF_C2HC	39	57	2.08e-1	SMART
low complexity region	379	384	N/A	INTRINSIC
low complexity region	388	401	N/A	INTRINSIC

Meta Mutation Damage Score

0.1795

Coding Region Coverage

1x: 99.4%
3x: 98.7%
10x: 97.4%
20x: 95.6%

Validation Efficiency

100% (64/64)

Allele List at MGI

Other mutations in this stock

Total: 60 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2010111I01Rik	G	A	13: 63,298,751	E123K	probably damaging	Het
4931417E11Rik	A	G	6: 73,469,269	V99A	probably benign	Het
Acod1	C	T	14: 103,055,345	T435M	probably benign	Het
Adgrf5	T	C	17: 43,452,440	F1078L	probably benign	Het
Adh6a	A	T	3: 138,324,947	N110I	probably damaging	Het
Aldh16a1	T	C	7: 45,148,788		probably benign	Het
Arhgef17	A	G	7: 100,882,485	F1302S	probably damaging	Het
Bcl2a1a	C	T	9: 88,957,453	R135W	probably damaging	Het
Bpifa6	T	C	2: 153,982,988	S28P	possibly damaging	Het
C9	A	G	15: 6,491,463	D51G	probably damaging	Het
Cfb	T	A	17: 34,859,068	H962L	probably benign	Het
Chn2	G	A	6: 54,290,403	M292I	probably damaging	Het
Clec16a	T	A	16: 10,644,883		probably null	Het
Cyp1a1	T	C	9: 57,701,756	S307P	probably benign	Het
Dsg3	T	C	18: 20,531,559	V538A	probably benign	Het
Erbb3	G	A	10: 128,572,770	Q815*	probably null	Het
Frmd3	T	C	4: 74,187,872	V585A	probably benign	Het
Gm7102	C	T	19: 61,175,926	G24R	unknown	Het
Gm8214	T	C	1: 183,681,897		noncoding transcript	Het
Gpld1	G	A	13: 24,984,816	G771D	probably damaging	Het
Gpr20	T	C	15: 73,695,736	N268S	probably benign	Het
Gria2	A	T	3: 80,706,897	I612N	probably damaging	Het
Ifit1bl1	T	C	19: 34,594,610	E149G	probably damaging	Het
Ighv1-82	T	C	12: 115,952,660	T77A	probably benign	Het
Ighv2-9	G	T	12: 113,879,219	T76K	probably damaging	Het
Igkv6-13	A	T	6: 70,458,035	M1K	probably null	Het
Igkv8-21	A	T	6: 70,315,157	S34T	probably benign	Het
Itpr1	A	G	6: 108,481,223	N1985D	probably damaging	Het
Lama3	T	C	18: 12,504,397		probably null	Het
Lamc2	T	C	1: 153,166,169	Y73C	probably damaging	Het
Maff	A	G	15: 79,357,698	D105G	probably damaging	Het
Mep1a	C	T	17: 43,486,241	V312M	possibly damaging	Het
Mfap4	C	A	11: 61,485,509		probably benign	Het
Mrgbp	A	T	2: 180,585,314		silent	Het
Mtmr4	T	C	11: 87,610,935	L548S	probably damaging	Het
Myo7b	T	C	18: 32,003,487		probably null	Het
Myo9a	T	C	9: 59,821,649	I596T	probably damaging	Het
Olfr38	G	T	6: 42,762,418	R122L	probably benign	Het
Olfr594	C	T	7: 103,220,422	R235*	probably null	Het
Pcsk5	T	G	19: 17,560,750	Q904H	probably benign	Het
Pdzrn3	G	T	6: 101,152,009	H565Q	probably damaging	Het
Phkg2	C	T	7: 127,577,620	R61W	probably damaging	Het
Pkd2l1	C	A	19: 44,154,134	A490S	probably damaging	Het
Pomgnt1	T	A	4: 116,154,890	I337N	probably damaging	Het
Psmd3	T	C	11: 98,682,926	V66A	probably benign	Het
Ptger3	T	C	3: 157,567,294	S93P	probably damaging	Het
Rbm27	T	A	18: 42,301,775	D301E	probably damaging	Het
Rdh16	A	T	10: 127,801,513		probably null	Het
Slc35a5	A	T	16: 45,144,292	F193I	probably benign	Het
Slc4a4	A	G	5: 89,038,561	K167R	probably damaging	Het
Sort1	A	T	3: 108,355,541	T772S	possibly damaging	Het
Sptbn5	T	A	2: 120,048,757		noncoding transcript	Het
Stard5	G	T	7: 83,633,281		probably benign	Het
Tbc1d22a	A	G	15: 86,235,685	T61A	probably damaging	Het
Tox2	T	C	2: 163,320,647	L479P	probably damaging	Het
Usp53	A	T	3: 122,959,120	M80K	probably damaging	Het
Vmn1r209	A	T	13: 22,805,965	L185Q	probably damaging	Het
Vmn2r59	A	G	7: 42,012,438	I651T	probably benign	Het
Vsig1	G	T	X: 140,926,386	A95S	probably benign	Het
Zfhx4	T	C	3: 5,413,067	S3556P	possibly damaging	Het

Other mutations in Fam90a1a

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02084:Fam90a1a	APN	8	21959297	missense	probably benign	0.00
R0442:Fam90a1a	UTSW	8	21963058	missense	probably benign	0.00
R1708:Fam90a1a	UTSW	8	21961448	missense	probably damaging	0.96
R1733:Fam90a1a	UTSW	8	21963369	nonsense	probably null
R1783:Fam90a1a	UTSW	8	21963463	missense	probably benign
R1818:Fam90a1a	UTSW	8	21963771	missense	possibly damaging	0.68
R1818:Fam90a1a	UTSW	8	21963772	missense	probably damaging	0.98
R1998:Fam90a1a	UTSW	8	21963697	missense	probably benign
R2256:Fam90a1a	UTSW	8	21963517	missense	possibly damaging	0.96
R2257:Fam90a1a	UTSW	8	21963517	missense	possibly damaging	0.96
R3747:Fam90a1a	UTSW	8	21963205	nonsense	probably null
R3976:Fam90a1a	UTSW	8	21961416	missense	probably damaging	0.99
R4667:Fam90a1a	UTSW	8	21963346	missense	possibly damaging	0.53
R5749:Fam90a1a	UTSW	8	21963041	missense	possibly damaging	0.92
R6462:Fam90a1a	UTSW	8	21959282	missense	probably benign	0.00
R6807:Fam90a1a	UTSW	8	21963352	missense	probably benign	0.33
R7214:Fam90a1a	UTSW	8	21963625	missense	probably benign	0.01
R8038:Fam90a1a	UTSW	8	21963439	missense	possibly damaging	0.96
R8924:Fam90a1a	UTSW	8	21961413	missense	probably benign
R9267:Fam90a1a	UTSW	8	21963075	missense	probably benign	0.00
R9323:Fam90a1a	UTSW	8	21963624	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- ATAGAGTTCCACAGGGCATCCG -3'
(R):5'- GTGCTCATTTGGAAGTACCCTG -3'

Sequencing Primer
(F):5'- ATCCGCTGGCCGTGTTG -3'
(R):5'- GCTCATTTGGAAGTACCCTGACATG -3'

Posted On

2015-10-08