Mutagenetix > Incidental Mutation

Incidental Mutation 'R1978:Phyhipl'

222036

Institutional Source

Beutler Lab

Gene Symbol

Phyhipl

Ensembl Gene

ENSMUSG00000037747

Gene Name

phytanoyl-CoA hydroxylase interacting protein-like

Synonyms

4921522K17Rik, PHY2

MMRRC Submission

039991-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.081) question?

Stock #

R1978 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

70393516-70435121 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to C at 70395591 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Methionine to Arginine at position 205 (M205R)

Ref Sequence

ENSEMBL: ENSMUSP00000045807 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000046513] [ENSMUST00000062883] [ENSMUST00000105436] [ENSMUST00000162251] [ENSMUST00000173042]

AlphaFold

Q8BGT8

Predicted Effect

possibly damaging
Transcript: ENSMUST00000046513
AA Change: M205R

PolyPhen 2 Score 0.938 (Sensitivity: 0.80; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000045807
Gene: ENSMUSG00000037747
AA Change: M205R

Domain	Start	End	E-Value	Type
FN3	49	142	6.16e-2	SMART
Blast:FN3	188	262	2e-45	BLAST

Predicted Effect

probably benign
Transcript: ENSMUST00000062883

SMART Domains

Protein: ENSMUSP00000051375
Gene: ENSMUSG00000043259

Domain	Start	End	E-Value	Type
low complexity region	200	222	N/A	INTRINSIC
low complexity region	274	294	N/A	INTRINSIC
coiled coil region	304	372	N/A	INTRINSIC
coiled coil region	529	557	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000105436

SMART Domains

Protein: ENSMUSP00000101076
Gene: ENSMUSG00000043259

Domain	Start	End	E-Value	Type
low complexity region	118	140	N/A	INTRINSIC
low complexity region	192	212	N/A	INTRINSIC
coiled coil region	222	290	N/A	INTRINSIC
coiled coil region	447	475	N/A	INTRINSIC

Predicted Effect

unknown
Transcript: ENSMUST00000162144
AA Change: M192R

SMART Domains

Protein: ENSMUSP00000124828
Gene: ENSMUSG00000037747
AA Change: M192R

Domain	Start	End	E-Value	Type
FN3	37	130	6.16e-2	SMART
Blast:FN3	176	212	1e-15	BLAST

Predicted Effect

probably benign
Transcript: ENSMUST00000162251
AA Change: M160R

PolyPhen 2 Score 0.330 (Sensitivity: 0.90; Specificity: 0.89)

SMART Domains

Protein: ENSMUSP00000125179
Gene: ENSMUSG00000037747
AA Change: M160R

Domain	Start	End	E-Value	Type
FN3	4	97	6.16e-2	SMART
Blast:FN3	143	217	9e-46	BLAST

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000162470

Predicted Effect

probably benign
Transcript: ENSMUST00000173042

SMART Domains

Protein: ENSMUSP00000134648
Gene: ENSMUSG00000043259

Domain	Start	End	E-Value	Type
low complexity region	200	222	N/A	INTRINSIC
low complexity region	274	294	N/A	INTRINSIC
coiled coil region	304	372	N/A	INTRINSIC
coiled coil region	528	556	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000219514

Coding Region Coverage

1x: 99.1%
3x: 98.4%
10x: 96.7%
20x: 93.9%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 74 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
0610040J01Rik	T	A	5: 64,055,880 (GRCm39)	C205*	probably null	Het
4921539E11Rik	T	A	4: 103,127,961 (GRCm39)	T55S	possibly damaging	Het
Akap12	A	G	10: 4,263,855 (GRCm39)	D88G	probably benign	Het
Ankrd53	C	A	6: 83,740,185 (GRCm39)	F84L	probably damaging	Het
Apol7b	A	C	15: 77,307,539 (GRCm39)	F319V	probably damaging	Het
Bsn	A	G	9: 107,991,748 (GRCm39)	S1335P	probably benign	Het
Cep192	T	C	18: 67,936,228 (GRCm39)		probably null	Het
Cfap57	A	G	4: 118,450,329 (GRCm39)	S598P	probably benign	Het
Commd8	T	C	5: 72,322,842 (GRCm39)	H25R	probably damaging	Het
Crisp4	T	C	1: 18,198,889 (GRCm39)	I143V	probably benign	Het
Cyp4a12b	A	T	4: 115,295,342 (GRCm39)	T483S	probably benign	Het
Dbx2	C	T	15: 95,530,234 (GRCm39)	M244I	probably damaging	Het
Dnah6	T	G	6: 73,098,953 (GRCm39)	H1982P	possibly damaging	Het
Fam220a	C	A	5: 143,548,882 (GRCm39)	P98Q	probably damaging	Het
Ggnbp1	A	G	17: 27,248,517 (GRCm39)	K29E	possibly damaging	Het
Gm14569	A	C	X: 35,695,781 (GRCm39)	M976R	probably benign	Het
Hck	G	T	2: 152,971,776 (GRCm39)	W112C	probably damaging	Het
Heatr5a	A	T	12: 51,986,441 (GRCm39)	S591T	possibly damaging	Het
Hhat	A	G	1: 192,399,415 (GRCm39)	S242P	probably benign	Het
Hnrnpll	A	G	17: 80,351,947 (GRCm39)	S333P	probably benign	Het
Hoxc6	T	C	15: 102,918,439 (GRCm39)		probably null	Het
Inpp5j	G	A	11: 3,452,150 (GRCm39)	P367S	probably damaging	Het
Lamc2	A	G	1: 153,009,343 (GRCm39)		probably null	Het
Loxhd1	T	A	18: 77,409,338 (GRCm39)	I194N	possibly damaging	Het
Miga1	CCAGGGCAG	CCAG	3: 152,040,941 (GRCm39)		probably null	Het
Mkln1	C	T	6: 31,467,465 (GRCm39)	Q60*	probably null	Het
Muc21	T	A	17: 35,933,857 (GRCm39)		probably benign	Het
Mybph	C	A	1: 134,124,734 (GRCm39)	H185N	probably benign	Het
Myo1g	T	C	11: 6,470,829 (GRCm39)	D9G	possibly damaging	Het
Myo6	A	T	9: 80,136,207 (GRCm39)	D110V	probably damaging	Het
Ncoa7	A	G	10: 30,567,295 (GRCm39)	V412A	probably benign	Het
Neb	T	C	2: 52,177,357 (GRCm39)	K1328R	probably damaging	Het
Olfm5	T	A	7: 103,813,948 (GRCm39)	Q22L	unknown	Het
Or10ak7	A	T	4: 118,791,381 (GRCm39)	Y221*	probably null	Het
Or4d11	T	C	19: 12,013,705 (GRCm39)	T134A	probably benign	Het
Or5j1	C	T	2: 86,879,179 (GRCm39)	V134M	possibly damaging	Het
Or6b3	C	A	1: 92,439,499 (GRCm39)	G84C	probably damaging	Het
Or6p1	T	A	1: 174,258,657 (GRCm39)	I221N	probably damaging	Het
Or7a39	A	G	10: 78,715,114 (GRCm39)	Y36C	probably damaging	Het
P3h1	A	T	4: 119,105,173 (GRCm39)	Q717L	probably null	Het
Pclo	T	C	5: 14,763,809 (GRCm39)	I4094T	unknown	Het
Pfdn6	G	A	17: 34,158,051 (GRCm39)	R73W	probably benign	Het
Pitpnm1	C	T	19: 4,157,973 (GRCm39)		probably null	Het
Plcg1	A	G	2: 160,594,498 (GRCm39)		probably null	Het
Pnldc1	A	G	17: 13,125,392 (GRCm39)	S81P	possibly damaging	Het
Pno1	T	C	11: 17,154,519 (GRCm39)	I221V	possibly damaging	Het
Porcn	A	G	X: 8,070,540 (GRCm39)	V75A	probably damaging	Het
Prkcg	T	A	7: 3,353,862 (GRCm39)	C69S	probably damaging	Het
Rbbp6	G	T	7: 122,598,711 (GRCm39)		probably benign	Het
Resf1	T	A	6: 149,227,930 (GRCm39)	N325K	probably benign	Het
Rif1	GCCACCA	GCCA	2: 52,000,336 (GRCm39)		probably benign	Het
Scly	A	G	1: 91,247,891 (GRCm39)	D413G	probably damaging	Het
Scn11a	G	A	9: 119,609,861 (GRCm39)	R996*	probably null	Het
Skic3	T	C	13: 76,282,934 (GRCm39)	V752A	probably benign	Het
Slc6a13	A	T	6: 121,309,332 (GRCm39)	D281V	probably damaging	Het
Slfn5	T	C	11: 82,847,442 (GRCm39)	V109A	probably benign	Het
Smyd1	A	T	6: 71,289,703 (GRCm39)		probably null	Het
Snx29	T	A	16: 11,185,588 (GRCm39)	M57K	probably benign	Het
Stag1	T	G	9: 100,770,139 (GRCm39)	I603S	probably benign	Het
Svep1	C	A	4: 58,097,292 (GRCm39)	C1417F	possibly damaging	Het
Tbc1d23	T	C	16: 57,009,714 (GRCm39)	I392V	probably benign	Het
Tchh	T	C	3: 93,354,106 (GRCm39)	L1182P	unknown	Het
Tle3	T	A	9: 61,301,915 (GRCm39)	V108E	probably damaging	Het
Tmem144	T	C	3: 79,732,707 (GRCm39)		probably null	Het
Tpr	T	G	1: 150,295,658 (GRCm39)	L894V	possibly damaging	Het
Trappc9	A	T	15: 72,871,874 (GRCm39)	V472E	probably damaging	Het
Trim38	T	C	13: 23,975,081 (GRCm39)	V340A	probably damaging	Het
Ttn	A	T	2: 76,641,587 (GRCm39)	L5176Q	possibly damaging	Het
Vmn1r12	T	A	6: 57,136,494 (GRCm39)	I197N	possibly damaging	Het
Vmn1r26	T	C	6: 57,986,111 (GRCm39)	Y26C	possibly damaging	Het
Vwa3a	A	G	7: 120,358,177 (GRCm39)	I83V	probably null	Het
Xirp1	C	T	9: 119,847,657 (GRCm39)	E409K	probably benign	Het
Zc3h14	T	G	12: 98,730,181 (GRCm39)	I46R	probably damaging	Het
Zfp976	A	G	7: 42,263,265 (GRCm39)	C191R	probably damaging	Het

Other mutations in Phyhipl

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02140:Phyhipl	APN	10	70,406,660 (GRCm39)	missense	probably damaging	1.00
IGL03374:Phyhipl	APN	10	70,401,109 (GRCm39)	missense	possibly damaging	0.47
PIT4366001:Phyhipl	UTSW	10	70,404,788 (GRCm39)	missense	probably benign
R0512:Phyhipl	UTSW	10	70,404,748 (GRCm39)	missense	probably damaging	0.99
R0688:Phyhipl	UTSW	10	70,395,085 (GRCm39)	missense	probably damaging	1.00
R1136:Phyhipl	UTSW	10	70,404,902 (GRCm39)	missense	probably damaging	1.00
R1465:Phyhipl	UTSW	10	70,406,798 (GRCm39)	missense	probably damaging	1.00
R1465:Phyhipl	UTSW	10	70,406,798 (GRCm39)	missense	probably damaging	1.00
R1802:Phyhipl	UTSW	10	70,434,855 (GRCm39)	missense	probably benign
R4077:Phyhipl	UTSW	10	70,404,903 (GRCm39)	missense	probably damaging	1.00
R4960:Phyhipl	UTSW	10	70,404,815 (GRCm39)	missense	probably benign	0.40
R4976:Phyhipl	UTSW	10	70,404,904 (GRCm39)	missense	probably damaging	1.00
R5119:Phyhipl	UTSW	10	70,404,904 (GRCm39)	missense	probably damaging	1.00
R5739:Phyhipl	UTSW	10	70,395,399 (GRCm39)	missense	possibly damaging	0.92
R6303:Phyhipl	UTSW	10	70,395,387 (GRCm39)	splice site	probably null
R6304:Phyhipl	UTSW	10	70,395,387 (GRCm39)	splice site	probably null
R6649:Phyhipl	UTSW	10	70,404,843 (GRCm39)	missense	probably damaging	1.00
R9150:Phyhipl	UTSW	10	70,404,887 (GRCm39)	missense	probably damaging	1.00
R9237:Phyhipl	UTSW	10	70,406,720 (GRCm39)	missense	possibly damaging	0.82
R9293:Phyhipl	UTSW	10	70,401,116 (GRCm39)	missense	probably damaging	0.97
R9461:Phyhipl	UTSW	10	70,395,243 (GRCm39)	missense	possibly damaging	0.95
R9595:Phyhipl	UTSW	10	70,395,512 (GRCm39)	nonsense	probably null
X0022:Phyhipl	UTSW	10	70,404,791 (GRCm39)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- CGTGTACATACAGTAGAAGTCCCC -3'
(R):5'- GGGTCCAATCCATGATTAGTGTC -3'

Sequencing Primer
(F):5'- CCCCAAAGTATAAGTTAGTATTGGGG -3'
(R):5'- GTCCAATCCATGATTAGTGTCAAAAG -3'

Posted On

2014-08-25