Mutagenetix > Incidental Mutation

Incidental Mutation 'R9554:Fam120b'

720692

Institutional Source

Beutler Lab

Gene Symbol

Fam120b

Ensembl Gene

ENSMUSG00000014763

Gene Name

family with sequence similarity 120, member B

Synonyms

4932442K08Rik, CCPG

MMRRC Submission

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R9554 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

15616464-15653843 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 15626020 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Alanine to Threonine at position 458 (A458T)

Ref Sequence

ENSEMBL: ENSMUSP00000054420 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000055352]

AlphaFold

Q6RI63

Predicted Effect

possibly damaging
Transcript: ENSMUST00000055352
AA Change: A458T

PolyPhen 2 Score 0.954 (Sensitivity: 0.79; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000054420
Gene: ENSMUSG00000014763
AA Change: A458T

Domain	Start	End	E-Value	Type
Blast:XPGN	1	111	7e-46	BLAST
SCOP:d1a77_2	21	185	6e-8	SMART
internal_repeat_1	324	364	9.23e-10	PROSPERO
internal_repeat_1	372	412	9.23e-10	PROSPERO
low complexity region	650	664	N/A	INTRINSIC

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.9%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 58 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca9	T	C	11: 110,029,107 (GRCm39)	E817G	probably benign	Het
Abhd12b	A	G	12: 70,215,988 (GRCm39)	T182A	probably benign	Het
Allc	A	T	12: 28,607,414 (GRCm39)	C279*	probably null	Het
Ang	A	G	14: 51,338,976 (GRCm39)	D39G	probably damaging	Het
Atp8b3	G	A	10: 80,360,197 (GRCm39)	T958M	probably damaging	Het
Ccn4	G	A	15: 66,784,900 (GRCm39)	R191K	probably benign	Het
Ccnyl1	A	G	1: 64,753,750 (GRCm39)	Y187C	probably damaging	Het
Cfhr4	A	T	1: 139,668,169 (GRCm39)	S321R	probably benign	Het
Chd3	A	T	11: 69,251,015 (GRCm39)	W616R	probably damaging	Het
Cyp17a1	C	T	19: 46,657,165 (GRCm39)	R361H	probably damaging	Het
Cyp2t4	G	A	7: 26,854,717 (GRCm39)	V66M	possibly damaging	Het
Dcp1a	A	G	14: 30,201,691 (GRCm39)	Q38R	probably benign	Het
Ddias	T	C	7: 92,507,560 (GRCm39)	N785S	probably benign	Het
Depdc5	A	G	5: 33,122,076 (GRCm39)	N1133S	probably benign	Het
Dhx8	T	A	11: 101,645,614 (GRCm39)	Y877*	probably null	Het
Dlk1	G	A	12: 109,420,889 (GRCm39)	V15I	unknown	Het
Fgd4	G	A	16: 16,308,353 (GRCm39)	T9I	probably benign	Het
Fhip1b	C	A	7: 105,038,915 (GRCm39)	R108L	probably damaging	Het
Gfpt1	C	T	6: 87,062,323 (GRCm39)	R561W	probably damaging	Het
Gm5773	A	G	3: 93,680,340 (GRCm39)	D4G	probably benign	Het
Helz2	T	A	2: 180,882,470 (GRCm39)	T108S	probably damaging	Het
Hivep1	G	A	13: 42,308,251 (GRCm39)	D164N	possibly damaging	Het
Kif15	G	T	9: 122,828,585 (GRCm39)	L902F	probably damaging	Het
Lrp2	T	A	2: 69,261,497 (GRCm39)	R4481S	probably damaging	Het
Mcm3ap	T	C	10: 76,332,310 (GRCm39)	V1209A	probably damaging	Het
Mkrn1	C	T	6: 39,376,838 (GRCm39)	R377H	probably benign	Het
Ms4a4a	G	A	19: 11,367,708 (GRCm39)	M191I	probably benign	Het
Myh11	T	A	16: 14,018,580 (GRCm39)	N1922I		Het
Nbeal1	C	T	1: 60,290,287 (GRCm39)	Q998*	probably null	Het
Neil3	C	A	8: 54,061,770 (GRCm39)	G204C	probably damaging	Het
Nsmce1	T	C	7: 125,066,994 (GRCm39)	E262G	possibly damaging	Het
Oc90	G	A	15: 65,761,437 (GRCm39)	P194S	probably benign	Het
Oplah	A	G	15: 76,193,787 (GRCm39)	S57P	probably benign	Het
Or10u4	A	T	10: 129,802,181 (GRCm39)	F123L	probably benign	Het
Or1x6	T	A	11: 50,939,223 (GRCm39)	Y96*	probably null	Het
Or2aj4	T	A	16: 19,384,722 (GRCm39)	I304F	possibly damaging	Het
Or4a73	C	A	2: 89,420,710 (GRCm39)	V250F	probably damaging	Het
Or4d5	T	A	9: 40,012,160 (GRCm39)	M209L	probably benign	Het
Or51g1	A	T	7: 102,633,774 (GRCm39)	I199N	probably damaging	Het
Or5p70	A	G	7: 107,994,365 (GRCm39)	T13A	probably benign	Het
Or8g28	A	C	9: 39,169,756 (GRCm39)	F71V	possibly damaging	Het
Pdzd8	A	T	19: 59,333,574 (GRCm39)	L149Q	probably damaging	Het
Pid1	A	G	1: 84,137,032 (GRCm39)	V33A	probably benign	Het
Polr3gl	A	G	3: 96,489,037 (GRCm39)	V60A	possibly damaging	Het
Prdm1	A	G	10: 44,317,242 (GRCm39)	V527A	probably benign	Het
Sbf2	T	C	7: 110,040,671 (GRCm39)	I385M	probably damaging	Het
Setbp1	C	T	18: 78,826,599 (GRCm39)	S1338N	probably benign	Het
Sh2b2	T	C	5: 136,253,006 (GRCm39)	T389A	probably benign	Het
Skint9	A	T	4: 112,248,915 (GRCm39)	M171K	probably benign	Het
Slx4	C	A	16: 3,805,820 (GRCm39)	M577I	probably benign	Het
Srcap	T	C	7: 127,151,577 (GRCm39)	S2092P	probably damaging	Het
Traf6	T	A	2: 101,518,953 (GRCm39)	H147Q	probably benign	Het
Ttn	T	A	2: 76,547,693 (GRCm39)	E32159V	possibly damaging	Het
Ubn1	T	C	16: 4,888,492 (GRCm39)	S154P	unknown	Het
Uchl1	T	A	5: 66,833,649 (GRCm39)	M6K	probably damaging	Het
Vmn1r193	A	T	13: 22,403,989 (GRCm39)	M1K	probably null	Het
Zfp429	T	A	13: 67,538,531 (GRCm39)	K304N	probably benign	Het
Zfp607b	T	A	7: 27,402,464 (GRCm39)	S307T	probably damaging	Het

Other mutations in Fam120b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00588:Fam120b	APN	17	15,622,857 (GRCm39)	nonsense	probably null
IGL01874:Fam120b	APN	17	15,623,301 (GRCm39)	nonsense	probably null
IGL02111:Fam120b	APN	17	15,622,847 (GRCm39)	missense	possibly damaging	0.67
IGL02395:Fam120b	APN	17	15,622,777 (GRCm39)	missense	probably damaging	1.00
IGL02901:Fam120b	APN	17	15,627,964 (GRCm39)	splice site	probably benign
IGL03380:Fam120b	APN	17	15,623,396 (GRCm39)	splice site	probably benign
R0139:Fam120b	UTSW	17	15,646,446 (GRCm39)	splice site	probably benign
R0242:Fam120b	UTSW	17	15,643,186 (GRCm39)	missense	probably damaging	1.00
R0242:Fam120b	UTSW	17	15,643,186 (GRCm39)	missense	probably damaging	1.00
R0244:Fam120b	UTSW	17	15,637,899 (GRCm39)	missense	probably damaging	1.00
R0486:Fam120b	UTSW	17	15,646,550 (GRCm39)	splice site	probably benign
R0551:Fam120b	UTSW	17	15,651,905 (GRCm39)	splice site	probably benign
R0584:Fam120b	UTSW	17	15,622,384 (GRCm39)	missense	probably damaging	1.00
R0620:Fam120b	UTSW	17	15,623,189 (GRCm39)	missense	probably benign
R1606:Fam120b	UTSW	17	15,622,073 (GRCm39)	missense	possibly damaging	0.79
R1638:Fam120b	UTSW	17	15,622,759 (GRCm39)	missense	possibly damaging	0.95
R2022:Fam120b	UTSW	17	15,644,638 (GRCm39)	missense	possibly damaging	0.70
R3411:Fam120b	UTSW	17	15,651,897 (GRCm39)	splice site	probably benign
R4422:Fam120b	UTSW	17	15,622,445 (GRCm39)	missense	probably damaging	1.00
R4754:Fam120b	UTSW	17	15,643,224 (GRCm39)	missense	probably damaging	1.00
R4756:Fam120b	UTSW	17	15,622,658 (GRCm39)	missense	probably damaging	1.00
R4883:Fam120b	UTSW	17	15,623,294 (GRCm39)	missense	probably benign
R5400:Fam120b	UTSW	17	15,623,388 (GRCm39)	missense	possibly damaging	0.55
R5418:Fam120b	UTSW	17	15,622,061 (GRCm39)	missense	probably damaging	1.00
R5632:Fam120b	UTSW	17	15,623,344 (GRCm39)	missense	probably benign	0.08
R5878:Fam120b	UTSW	17	15,622,502 (GRCm39)	missense	probably damaging	1.00
R6030:Fam120b	UTSW	17	15,622,172 (GRCm39)	missense	probably damaging	1.00
R6030:Fam120b	UTSW	17	15,622,172 (GRCm39)	missense	probably damaging	1.00
R6846:Fam120b	UTSW	17	15,635,091 (GRCm39)	missense	probably damaging	1.00
R6929:Fam120b	UTSW	17	15,643,290 (GRCm39)	missense	possibly damaging	0.78
R7356:Fam120b	UTSW	17	15,627,958 (GRCm39)	missense	probably benign	0.05
R7616:Fam120b	UTSW	17	15,623,098 (GRCm39)	missense	possibly damaging	0.79
R7848:Fam120b	UTSW	17	15,626,036 (GRCm39)	missense	possibly damaging	0.93
R8386:Fam120b	UTSW	17	15,643,246 (GRCm39)	missense	probably benign	0.01
R8782:Fam120b	UTSW	17	15,622,472 (GRCm39)	missense	probably damaging	0.98
R9364:Fam120b	UTSW	17	15,626,020 (GRCm39)	missense	possibly damaging	0.95

Predicted Primers

PCR Primer
(F):5'- AAGTGAAGGTTTGAACTTGTTAGCC -3'
(R):5'- TCGCTGAATCAGACCAACTG -3'

Sequencing Primer
(F):5'- GGTTTGAACTTGTTAGCCCTAAAAC -3'
(R):5'- TGAATCAGACCAACTGGCCTC -3'

Posted On

2022-08-09