Mutagenetix > Incidental Mutation

Incidental Mutation 'R6167:Fam168b'

490177

Institutional Source

Beutler Lab

Gene Symbol

Fam168b

Ensembl Gene

ENSMUSG00000037503

Gene Name

family with sequence similarity 168, member B

Synonyms

MMRRC Submission

044313-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.094) question?

Stock #

R6167 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

34852307-34882094 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 34858684 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Alanine to Valine at position 166 (A166V)

Ref Sequence

ENSEMBL: ENSMUSP00000140573 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000047534] [ENSMUST00000167518] [ENSMUST00000170092] [ENSMUST00000185231] [ENSMUST00000185469] [ENSMUST00000191307]

AlphaFold

Q80XQ8

Predicted Effect

probably damaging
Transcript: ENSMUST00000047534
AA Change: A154V

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000042212
Gene: ENSMUSG00000037503
AA Change: A154V

Domain	Start	End	E-Value	Type
Pfam:TCRP1	1	194	1e-108	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000167518
AA Change: A166V

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000131720
Gene: ENSMUSG00000037503
AA Change: A166V

Domain	Start	End	E-Value	Type
Pfam:TCRP1	1	62	3.3e-26	PFAM
Pfam:TCRP1	54	206	1.1e-89	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000170092
AA Change: A161V

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

SMART Domains

Protein: ENSMUSP00000128676
Gene: ENSMUSG00000037503
AA Change: A161V

Domain	Start	End	E-Value	Type
Pfam:TCRP1	1	201	8.8e-108	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000185231

SMART Domains

Protein: ENSMUSP00000139456
Gene: ENSMUSG00000037503

Domain	Start	End	E-Value	Type
Pfam:TCRP1	1	90	7.5e-19	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000185279

Predicted Effect

probably benign
Transcript: ENSMUST00000185469

SMART Domains

Protein: ENSMUSP00000141150
Gene: ENSMUSG00000037503

Domain	Start	End	E-Value	Type
Pfam:TCRP1	1	66	3.6e-21	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000191307
AA Change: A166V

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000140573
Gene: ENSMUSG00000037503
AA Change: A166V

Domain	Start	End	E-Value	Type
Pfam:TCRP1	1	206	2.8e-108	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000192924

Meta Mutation Damage Score

0.4360

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 98.1%
20x: 94.8%

Validation Efficiency

98% (50/51)

Allele List at MGI

Other mutations in this stock

Total: 55 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca5	T	A	11: 110,182,931 (GRCm39)	E1042V	probably benign	Het
Ahnak2	T	C	12: 112,747,750 (GRCm39)	E1035G	probably benign	Het
Aip	T	G	19: 4,165,188 (GRCm39)	D227A	probably benign	Het
Ankrd13d	T	C	19: 4,323,081 (GRCm39)	H283R	probably damaging	Het
Aox4	C	T	1: 58,303,094 (GRCm39)	T1175I	probably damaging	Het
Atn1	T	C	6: 124,723,700 (GRCm39)		probably benign	Het
Camkk2	A	G	5: 122,902,187 (GRCm39)	S41P	probably damaging	Het
Ceacam16	G	A	7: 19,595,182 (GRCm39)		probably benign	Het
Dcaf15	T	C	8: 84,824,626 (GRCm39)	N524D	possibly damaging	Het
Dcaf7	A	T	11: 105,928,077 (GRCm39)	Y43F	probably damaging	Het
Epha3	T	C	16: 63,433,287 (GRCm39)	I453V	probably benign	Het
Etv1	A	T	12: 38,915,640 (GRCm39)	T413S	possibly damaging	Het
Evx2	A	C	2: 74,489,606 (GRCm39)	L53R	probably damaging	Het
Fancm	A	T	12: 65,141,669 (GRCm39)	Y430F	probably benign	Het
Fyb2	A	G	4: 104,802,661 (GRCm39)	T188A	possibly damaging	Het
Gabbr1	T	C	17: 37,374,271 (GRCm39)	I538T	probably damaging	Het
Glyctk	T	A	9: 106,033,691 (GRCm39)	T208S	possibly damaging	Het
Golga7	T	C	8: 23,735,904 (GRCm39)	D114G	probably damaging	Het
Grip1	T	C	10: 119,733,702 (GRCm39)		probably null	Het
Gtf2f1	G	T	17: 57,311,161 (GRCm39)	S351R	probably damaging	Het
Hook2	T	C	8: 85,721,642 (GRCm39)	L300P	probably damaging	Het
Hsf4	A	G	8: 105,997,481 (GRCm39)	S45G	probably damaging	Het
Iars1	T	A	13: 49,876,190 (GRCm39)	M825K	probably damaging	Het
Kcnj2	A	G	11: 110,963,315 (GRCm39)	I236V	probably benign	Het
Large2	G	A	2: 92,197,433 (GRCm39)	T354I	probably benign	Het
Mak	C	A	13: 41,206,828 (GRCm39)	V101F	probably benign	Het
Mylk2	A	G	2: 152,757,673 (GRCm39)		probably null	Het
Myo18b	A	T	5: 113,020,373 (GRCm39)		probably null	Het
Neb	T	A	2: 52,037,249 (GRCm39)	H2955L	probably benign	Het
Neurl1a	G	C	19: 47,228,367 (GRCm39)	G71A	probably damaging	Het
Ogfrl1	A	T	1: 23,415,309 (GRCm39)	L142Q	probably damaging	Het
Or11g27	C	A	14: 50,771,612 (GRCm39)	H248N	probably damaging	Het
Or1e27-ps1	A	G	11: 73,556,160 (GRCm39)	T242A	probably damaging	Het
P3h4	C	A	11: 100,302,671 (GRCm39)	A322S	probably damaging	Het
Piwil2	A	C	14: 70,660,342 (GRCm39)		probably null	Het
Pkd2l2	A	G	18: 34,561,297 (GRCm39)	D435G	probably damaging	Het
Plekha6	A	G	1: 133,207,145 (GRCm39)	N567S	probably null	Het
Prss54	G	A	8: 96,286,173 (GRCm39)	P300L	possibly damaging	Het
Pxdn	G	A	12: 30,024,000 (GRCm39)	R67Q	probably damaging	Het
Rapgef3	C	A	15: 97,665,292 (GRCm39)		probably benign	Het
Sec24b	C	T	3: 129,782,550 (GRCm39)	G1147S	possibly damaging	Het
Sh2b3	A	T	5: 121,966,418 (GRCm39)		probably null	Het
Sh3glb1	A	T	3: 144,397,664 (GRCm39)	D358E	probably damaging	Het
Shmt2	C	T	10: 127,353,731 (GRCm39)	R478H	probably benign	Het
Slc1a6	A	G	10: 78,637,671 (GRCm39)	E399G	probably benign	Het
Slc22a23	T	A	13: 34,528,542 (GRCm39)	Y80F	probably damaging	Het
Slc25a19	A	G	11: 115,506,377 (GRCm39)	V272A	probably benign	Het
Stk32a	A	T	18: 43,446,474 (GRCm39)	D308V	probably damaging	Het
Tenm3	T	C	8: 48,707,657 (GRCm39)	I1698V	possibly damaging	Het
Thoc5	G	A	11: 4,865,497 (GRCm39)	V359M	probably benign	Het
Tmpo	C	T	10: 90,998,800 (GRCm39)	R329H	probably benign	Het
Trim8	T	C	19: 46,503,626 (GRCm39)	S393P	probably benign	Het
Vill	A	T	9: 118,895,932 (GRCm39)	Y103F	probably damaging	Het
Zfp948	T	G	17: 21,807,911 (GRCm39)	F368V	probably benign	Het
Zpld1	C	T	16: 55,053,962 (GRCm39)	E277K	probably damaging	Het

Other mutations in Fam168b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00340:Fam168b	APN	1	34,875,883 (GRCm39)	start codon destroyed	probably null	0.58
R0207:Fam168b	UTSW	1	34,858,769 (GRCm39)	missense	probably damaging	0.98
R2008:Fam168b	UTSW	1	34,858,946 (GRCm39)	critical splice donor site	probably null
R4020:Fam168b	UTSW	1	34,867,860 (GRCm39)	missense	possibly damaging	0.71
R4617:Fam168b	UTSW	1	34,859,063 (GRCm39)	missense	possibly damaging	0.90
R5154:Fam168b	UTSW	1	34,857,180 (GRCm39)	missense	possibly damaging	0.83
R6600:Fam168b	UTSW	1	34,875,822 (GRCm39)	missense	probably damaging	1.00
R6602:Fam168b	UTSW	1	34,875,822 (GRCm39)	missense	probably damaging	1.00
R6603:Fam168b	UTSW	1	34,875,822 (GRCm39)	missense	probably damaging	1.00
R6627:Fam168b	UTSW	1	34,875,822 (GRCm39)	missense	probably damaging	1.00
R6628:Fam168b	UTSW	1	34,875,822 (GRCm39)	missense	probably damaging	1.00
R6644:Fam168b	UTSW	1	34,875,822 (GRCm39)	missense	probably damaging	1.00
R6692:Fam168b	UTSW	1	34,875,822 (GRCm39)	missense	probably damaging	1.00
R6705:Fam168b	UTSW	1	34,867,864 (GRCm39)	missense	probably damaging	0.98
R6985:Fam168b	UTSW	1	34,858,789 (GRCm39)	missense	probably damaging	1.00
R7387:Fam168b	UTSW	1	34,858,789 (GRCm39)	missense	probably damaging	1.00
R8992:Fam168b	UTSW	1	34,858,862 (GRCm39)	missense	probably benign	0.00
Z1177:Fam168b	UTSW	1	34,858,963 (GRCm39)	nonsense	probably null

Predicted Primers

PCR Primer
(F):5'- GCAGGTACTCAGTTAAGTTCCAC -3'
(R):5'- TTTTCCCCACAGCAAGGCAC -3'

Sequencing Primer
(F):5'- TTCCACAGTGAAGAGGCCACTTG -3'
(R):5'- CGTACTACACACAACCTCTGTATG -3'

Posted On

2017-10-10