Mutagenetix > Incidental Mutation

Incidental Mutation 'R5096:Fam114a1'

388037

Institutional Source

Beutler Lab

Gene Symbol

Fam114a1

Ensembl Gene

ENSMUSG00000029185

Gene Name

family with sequence similarity 114, member A1

Synonyms

1190001N04Rik, 9130005N14Rik

MMRRC Submission

042685-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R5096 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

65127459-65199217 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 65137234 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Methionine to Lysine at position 59 (M59K)

Ref Sequence

ENSEMBL: ENSMUSP00000119284 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000031080] [ENSMUST00000139366]

AlphaFold

Q9D281

Predicted Effect

probably benign
Transcript: ENSMUST00000031080
AA Change: M59K

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

SMART Domains

Protein: ENSMUSP00000031080
Gene: ENSMUSG00000029185
AA Change: M59K

Domain	Start	End	E-Value	Type
Pfam:DUF719	125	300	5e-65	PFAM
low complexity region	355	365	N/A	INTRINSIC
low complexity region	413	432	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000139366
AA Change: M59K

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

SMART Domains

Protein: ENSMUSP00000119284
Gene: ENSMUSG00000029185
AA Change: M59K

Domain	Start	End	E-Value	Type
Pfam:DUF719	121	177	7e-16	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000197119

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.1%
3x: 98.3%
10x: 96.1%
20x: 91.6%

Validation Efficiency

95% (61/64)

Allele List at MGI

Other mutations in this stock

Total: 49 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acin1	A	T	14: 54,916,679 (GRCm39)		probably benign	Het
Adar	T	A	3: 89,654,598 (GRCm39)	*728C	probably null	Het
Ap3b1	A	G	13: 94,616,357 (GRCm39)	R753G	unknown	Het
Atp9b	C	T	18: 80,805,399 (GRCm39)	V720I	probably benign	Het
AY358078	A	C	14: 52,063,575 (GRCm39)	D407A	probably benign	Het
Ccdc185	A	G	1: 182,576,354 (GRCm39)	S112P	possibly damaging	Het
Cir1	A	G	2: 73,134,105 (GRCm39)	S155P	probably damaging	Het
Colq	C	T	14: 31,274,911 (GRCm39)	E76K	possibly damaging	Het
Cthrc1	T	A	15: 38,947,815 (GRCm39)	I104N	probably damaging	Het
D930020B18Rik	A	T	10: 121,503,709 (GRCm39)	I92L	probably benign	Het
Eif3i	C	T	4: 129,494,237 (GRCm39)	E21K	probably damaging	Het
Fam163b	A	G	2: 27,002,761 (GRCm39)	S79P	probably benign	Het
Fam181b	T	G	7: 92,730,452 (GRCm39)		probably benign	Het
Fsip2	G	A	2: 82,821,460 (GRCm39)	S5731N	probably benign	Het
Fzd9	C	T	5: 135,278,713 (GRCm39)	V391I	probably damaging	Het
Gbp5	A	G	3: 142,207,122 (GRCm39)	D97G	probably damaging	Het
Gm10715	T	C	9: 3,038,157 (GRCm39)		probably benign	Het
Grhl1	A	T	12: 24,653,049 (GRCm39)	K418M	probably damaging	Het
H2-Q4	T	A	17: 35,598,689 (GRCm39)		probably benign	Het
Hmcn1	C	A	1: 150,486,420 (GRCm39)	A4329S	probably damaging	Het
Hspa8	T	C	9: 40,714,197 (GRCm39)		probably benign	Het
Ica1l	T	C	1: 60,067,313 (GRCm39)	T26A	possibly damaging	Het
Ifi209	T	A	1: 173,472,300 (GRCm39)	N380K	probably benign	Het
Inpp5e	G	T	2: 26,289,537 (GRCm39)	N482K	probably damaging	Het
Iqsec3	C	T	6: 121,363,657 (GRCm39)	V866M	probably damaging	Het
Kbtbd2	A	G	6: 56,756,260 (GRCm39)	V492A	probably benign	Het
Kcnb2	A	G	1: 15,781,068 (GRCm39)	R647G	probably benign	Het
Lcmt1	T	G	7: 123,000,691 (GRCm39)	V75G	probably damaging	Het
Lrp4	A	G	2: 91,316,137 (GRCm39)	I752V	possibly damaging	Het
Mmp17	C	A	5: 129,682,627 (GRCm39)	P422Q	probably damaging	Het
Myo3a	A	T	2: 22,464,254 (GRCm39)	H165L	probably benign	Het
Nos3	C	T	5: 24,576,955 (GRCm39)	T494I	probably damaging	Het
Or1ak2	T	C	2: 36,827,815 (GRCm39)	V228A	possibly damaging	Het
Or4p22	C	T	2: 88,317,646 (GRCm39)	T190I	possibly damaging	Het
Or51q1c	T	C	7: 103,652,667 (GRCm39)	Y68H	probably benign	Het
Or8u8	A	G	2: 86,012,276 (GRCm39)	Y60H	probably damaging	Het
Pkn2	A	C	3: 142,545,092 (GRCm39)	V27G	probably damaging	Het
Scube2	T	C	7: 109,398,451 (GRCm39)		probably benign	Het
Skint7	A	G	4: 111,839,152 (GRCm39)	I149V	probably damaging	Het
Smc4	T	A	3: 68,928,612 (GRCm39)	I412K	probably damaging	Het
Snx19	T	A	9: 30,340,082 (GRCm39)	C407S	probably benign	Het
Speer3	C	G	5: 13,846,394 (GRCm39)	A238G	possibly damaging	Het
Sytl2	T	A	7: 90,025,290 (GRCm39)	I426N	possibly damaging	Het
Tbce	A	T	13: 14,203,990 (GRCm39)		probably benign	Het
Tdpoz2	T	C	3: 93,559,819 (GRCm39)	E51G	possibly damaging	Het
Tmem221	A	G	8: 72,011,353 (GRCm39)	L34P	probably damaging	Het
Tmem92	T	C	11: 94,669,862 (GRCm39)	T90A	probably benign	Het
Tpr	A	G	1: 150,321,953 (GRCm39)	D42G	probably damaging	Het
Wt1	A	G	2: 104,973,470 (GRCm39)	T237A	probably damaging	Het

Other mutations in Fam114a1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00674:Fam114a1	APN	5	65,137,347 (GRCm39)	missense	probably benign	0.31
IGL01013:Fam114a1	APN	5	65,188,738 (GRCm39)	critical splice donor site	probably null
IGL02032:Fam114a1	APN	5	65,172,714 (GRCm39)	missense	probably benign	0.11
IGL02117:Fam114a1	APN	5	65,187,465 (GRCm39)	missense	probably benign	0.08
IGL02388:Fam114a1	APN	5	65,166,323 (GRCm39)	unclassified	probably benign
IGL02563:Fam114a1	APN	5	65,163,491 (GRCm39)	splice site	probably null
IGL02803:Fam114a1	APN	5	65,163,135 (GRCm39)	splice site	probably benign
R1183:Fam114a1	UTSW	5	65,191,731 (GRCm39)	missense	probably damaging	1.00
R2073:Fam114a1	UTSW	5	65,153,247 (GRCm39)	critical splice donor site	probably null
R2086:Fam114a1	UTSW	5	65,137,402 (GRCm39)	missense	probably benign	0.39
R3834:Fam114a1	UTSW	5	65,163,416 (GRCm39)	missense	possibly damaging	0.65
R4519:Fam114a1	UTSW	5	65,163,225 (GRCm39)	missense	probably benign
R4749:Fam114a1	UTSW	5	65,166,409 (GRCm39)	missense	probably damaging	1.00
R4937:Fam114a1	UTSW	5	65,137,070 (GRCm39)	missense	probably damaging	0.97
R5038:Fam114a1	UTSW	5	65,166,388 (GRCm39)	missense	probably damaging	1.00
R5368:Fam114a1	UTSW	5	65,163,452 (GRCm39)	missense	possibly damaging	0.52
R5460:Fam114a1	UTSW	5	65,185,776 (GRCm39)	missense	probably damaging	0.99
R5734:Fam114a1	UTSW	5	65,166,389 (GRCm39)	missense	probably damaging	1.00
R6242:Fam114a1	UTSW	5	65,188,695 (GRCm39)	missense	probably damaging	0.98
R6950:Fam114a1	UTSW	5	65,137,322 (GRCm39)	missense	possibly damaging	0.88
R7460:Fam114a1	UTSW	5	65,196,050 (GRCm39)	missense	possibly damaging	0.51
R7570:Fam114a1	UTSW	5	65,187,402 (GRCm39)	splice site	probably null
R8913:Fam114a1	UTSW	5	65,185,821 (GRCm39)	missense	possibly damaging	0.77
R9095:Fam114a1	UTSW	5	65,188,733 (GRCm39)	missense	probably benign	0.08
R9171:Fam114a1	UTSW	5	65,191,713 (GRCm39)	critical splice acceptor site	probably null
R9203:Fam114a1	UTSW	5	65,137,300 (GRCm39)	missense	probably damaging	1.00
R9318:Fam114a1	UTSW	5	65,153,227 (GRCm39)	missense	possibly damaging	0.77
R9640:Fam114a1	UTSW	5	65,166,394 (GRCm39)	missense	probably damaging	0.99
R9656:Fam114a1	UTSW	5	65,163,246 (GRCm39)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- ATGCTCGTGACACCATAGC -3'
(R):5'- CTTAGCAACAGTGGCCAAAGAC -3'

Sequencing Primer
(F):5'- GCTCGTGACACCATAGCCAATG -3'
(R):5'- ACCAGGGTGTCTTCAGTT -3'

Posted On

2016-06-06