Mutagenetix > Incidental Mutation

Incidental Mutation 'R1996:Apol6'

225780

Institutional Source

Beutler Lab

Gene Symbol

Apol6

Ensembl Gene

ENSMUSG00000033576

Gene Name

apolipoprotein L 6

Synonyms

2310076O14Rik

MMRRC Submission

040006-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.053) question?

Stock #

R1996 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

76929195-76941308 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 76934956 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Asparagine at position 75 (I75N)

Ref Sequence

ENSEMBL: ENSMUSP00000121308 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000127957] [ENSMUST00000129468] [ENSMUST00000142405] [ENSMUST00000149569] [ENSMUST00000152949] [ENSMUST00000166179] [ENSMUST00000229423]

AlphaFold

B7ZC55

Predicted Effect

probably benign
Transcript: ENSMUST00000127957
AA Change: I75N

PolyPhen 2 Score 0.281 (Sensitivity: 0.91; Specificity: 0.88)

SMART Domains

Protein: ENSMUSP00000118257
Gene: ENSMUSG00000033576
AA Change: I75N

Domain	Start	End	E-Value	Type
Pfam:ApoL	15	290	4.1e-76	PFAM
transmembrane domain	294	311	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000129468

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000139304

Predicted Effect

unknown
Transcript: ENSMUST00000142405
AA Change: S57T

SMART Domains

Protein: ENSMUSP00000117135
Gene: ENSMUSG00000033576
AA Change: S57T

Domain	Start	End	E-Value	Type
low complexity region	22	43	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000148197

Predicted Effect

probably benign
Transcript: ENSMUST00000149569
AA Change: I75N

PolyPhen 2 Score 0.281 (Sensitivity: 0.91; Specificity: 0.88)

SMART Domains

Protein: ENSMUSP00000120866
Gene: ENSMUSG00000033576
AA Change: I75N

Domain	Start	End	E-Value	Type
Pfam:ApoL	10	290	7e-98	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000152949
AA Change: I75N

PolyPhen 2 Score 0.281 (Sensitivity: 0.91; Specificity: 0.88)

SMART Domains

Protein: ENSMUSP00000121308
Gene: ENSMUSG00000033576
AA Change: I75N

Domain	Start	End	E-Value	Type
Pfam:ApoL	10	263	2.7e-87	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000166179

SMART Domains

Protein: ENSMUSP00000128399
Gene: ENSMUSG00000018893

Domain	Start	End	E-Value	Type
Pfam:Globin	7	113	1.1e-22	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000229423

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.2%
20x: 95.0%

Validation Efficiency

99% (84/85)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is a member of the apolipoprotein L gene family. The encoded protein is found in the cytoplasm, where it may affect the movement of lipids or allow the binding of lipids to organelles. [provided by RefSeq, Jul 2008]

Allele List at MGI

Other mutations in this stock

Total: 81 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A2m	T	A	6: 121,646,556 (GRCm39)	W1069R	probably damaging	Het
Aaas	C	T	15: 102,248,494 (GRCm39)	V241I	probably benign	Het
Abca3	A	G	17: 24,606,506 (GRCm39)	E787G	probably damaging	Het
Abi3bp	A	T	16: 56,491,720 (GRCm39)	E582D	possibly damaging	Het
Adam21	A	G	12: 81,606,376 (GRCm39)	M462T	possibly damaging	Het
Alox12e	T	C	11: 70,207,034 (GRCm39)	T591A	probably benign	Het
Ankmy2	T	C	12: 36,243,796 (GRCm39)	M337T	probably benign	Het
Antxrl	A	G	14: 33,797,786 (GRCm39)	N587S	probably benign	Het
Atad2b	A	T	12: 5,040,883 (GRCm39)	H184L	probably benign	Het
Atf6b	A	T	17: 34,871,961 (GRCm39)		probably null	Het
B3gnt4	G	A	5: 123,649,402 (GRCm39)	V256I	probably damaging	Het
BC034090	C	T	1: 155,097,340 (GRCm39)		probably benign	Het
Bend4	C	A	5: 67,557,527 (GRCm39)	V430F	probably damaging	Het
Camkv	A	G	9: 107,824,320 (GRCm39)	D244G	probably damaging	Het
Caps2	T	A	10: 112,039,908 (GRCm39)	L450Q	probably damaging	Het
Ccr1	T	A	9: 123,763,551 (GRCm39)	K326N	probably benign	Het
Cep135	T	C	5: 76,780,113 (GRCm39)	I815T	probably benign	Het
Chchd4	A	G	6: 91,442,116 (GRCm39)	Y101H	probably damaging	Het
Copb1	G	C	7: 113,831,438 (GRCm39)	A570G	probably benign	Het
Cpsf2	C	A	12: 101,964,867 (GRCm39)	T505K	probably benign	Het
Cwf19l2	A	G	9: 3,417,947 (GRCm39)	R136G	probably benign	Het
Daxx	A	G	17: 34,132,585 (GRCm39)	T572A	possibly damaging	Het
Etaa1	C	A	11: 17,902,671 (GRCm39)	D89Y	probably damaging	Het
Ezhip	GTCATCATCATCATC	GTCATCATCATCATCATC	X: 5,994,645 (GRCm39)		probably benign	Het
Fchsd2	T	C	7: 100,927,660 (GRCm39)	F701L	probably benign	Het
Fstl5	A	T	3: 76,615,141 (GRCm39)	H734L	probably benign	Het
Gabbr1	T	A	17: 37,380,112 (GRCm39)	W584R	probably damaging	Het
Galc	T	C	12: 98,218,285 (GRCm39)	D189G	probably damaging	Het
Gm9979	T	C	13: 40,859,228 (GRCm39)		noncoding transcript	Het
Grin2b	T	C	6: 136,021,209 (GRCm39)	S31G	possibly damaging	Het
Gtf2ird1	T	C	5: 134,405,740 (GRCm39)		probably benign	Het
Hoxc4	T	C	15: 102,944,183 (GRCm39)	I187T	probably damaging	Het
Hsd3b6	A	T	3: 98,713,597 (GRCm39)	I234N	probably damaging	Het
Ifit3b	T	C	19: 34,588,877 (GRCm39)	C18R	probably damaging	Het
Igdcc4	T	A	9: 65,029,101 (GRCm39)	V246E	probably damaging	Het
Il1rap	A	T	16: 26,541,243 (GRCm39)	T495S	probably benign	Het
Kctd19	T	C	8: 106,121,932 (GRCm39)	E205G	probably null	Het
Kif21a	A	T	15: 90,878,574 (GRCm39)	C235*	probably null	Het
Krt16	A	T	11: 100,139,614 (GRCm39)	S35T	unknown	Het
Lamc2	T	C	1: 153,030,216 (GRCm39)	D142G	possibly damaging	Het
Larp4	G	T	15: 99,882,844 (GRCm39)	W22L	probably damaging	Het
Ldlrad1	C	T	4: 107,072,158 (GRCm39)	R127*	probably null	Het
Mamdc2	G	A	19: 23,341,289 (GRCm39)	Q229*	probably null	Het
Mbtd1	CT	CTT	11: 93,823,222 (GRCm39)		probably null	Het
Msln	T	A	17: 25,973,193 (GRCm39)	M1L	possibly damaging	Het
Mtch2	T	C	2: 90,677,665 (GRCm39)	V8A	possibly damaging	Het
Nav3	A	T	10: 109,689,262 (GRCm39)	N338K	probably damaging	Het
Or10x4	T	C	1: 174,218,983 (GRCm39)	M116T	probably damaging	Het
Or51a39	A	G	7: 102,362,999 (GRCm39)	L207P	probably damaging	Het
Or6c5	C	A	10: 129,074,298 (GRCm39)	N93K	possibly damaging	Het
Otof	A	G	5: 30,578,381 (GRCm39)	V89A	probably benign	Het
Phka2	T	C	X: 159,324,411 (GRCm39)	I255T	probably benign	Het
Pias2	T	C	18: 77,216,759 (GRCm39)		probably null	Het
Pja2	T	A	17: 64,594,639 (GRCm39)		probably null	Het
Plxnb2	C	T	15: 89,042,971 (GRCm39)	V1473I	probably benign	Het
Pnpt1	T	A	11: 29,091,679 (GRCm39)	D363E	probably benign	Het
Prdm5	A	G	6: 65,913,072 (GRCm39)	Y207C	probably damaging	Het
Rexo5	T	A	7: 119,423,080 (GRCm39)	V304E	probably damaging	Het
Robo1	G	T	16: 72,767,067 (GRCm39)	R413L	probably benign	Het
Rsf1	G	A	7: 97,313,839 (GRCm39)	E864K	probably damaging	Het
Scap	C	T	9: 110,202,039 (GRCm39)		probably benign	Het
Scn8a	T	A	15: 100,922,260 (GRCm39)	M1311K	probably damaging	Het
Slc28a2	A	T	2: 122,286,043 (GRCm39)	I460F	probably damaging	Het
Smco1	A	G	16: 32,092,730 (GRCm39)	R134G	probably benign	Het
Spopfm1	A	T	3: 94,173,018 (GRCm39)	M9L	probably benign	Het
Sspo	A	G	6: 48,452,424 (GRCm39)	E2651G	possibly damaging	Het
Stab2	T	C	10: 86,838,895 (GRCm39)	N57S	probably damaging	Het
Tenm3	C	A	8: 48,681,703 (GRCm39)	Q2642H	probably damaging	Het
Thsd7b	G	T	1: 129,686,188 (GRCm39)	E577*	probably null	Het
Tlr3	A	G	8: 45,850,734 (GRCm39)	V721A	probably benign	Het
Tnik	A	G	3: 28,719,829 (GRCm39)	I1226V	probably damaging	Het
Traf3	A	G	12: 111,227,095 (GRCm39)	K328E	probably benign	Het
Tyw1	T	A	5: 130,291,652 (GRCm39)		probably benign	Het
Vmn1r213	T	G	13: 23,196,473 (GRCm39)	V352G	probably benign	Het
Vmn2r111	T	C	17: 22,767,062 (GRCm39)	I812V	probably benign	Het
Vmn2r26	A	G	6: 124,038,144 (GRCm39)	N573S	probably damaging	Het
Vmn2r45	G	A	7: 8,475,024 (GRCm39)	T668I	probably damaging	Het
Zbtb20	T	A	16: 43,430,443 (GRCm39)	V318E	probably damaging	Het
Zc2hc1c	A	G	12: 85,343,434 (GRCm39)	R524G	probably benign	Het
Zc3h18	C	G	8: 123,134,126 (GRCm39)		probably benign	Het
Zfp618	T	C	4: 63,049,452 (GRCm39)		probably null	Het

Other mutations in Apol6

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01598:Apol6	APN	15	76,934,916 (GRCm39)	missense	probably damaging	1.00
IGL01788:Apol6	APN	15	76,935,216 (GRCm39)	missense	possibly damaging	0.81
FR4304:Apol6	UTSW	15	76,935,636 (GRCm39)	frame shift	probably null
FR4449:Apol6	UTSW	15	76,935,643 (GRCm39)	nonsense	probably null
FR4548:Apol6	UTSW	15	76,935,645 (GRCm39)	frame shift	probably null
FR4589:Apol6	UTSW	15	76,935,638 (GRCm39)	frame shift	probably null
FR4737:Apol6	UTSW	15	76,935,642 (GRCm39)	frame shift	probably null
R0350:Apol6	UTSW	15	76,935,147 (GRCm39)	nonsense	probably null
R1167:Apol6	UTSW	15	76,931,308 (GRCm39)	nonsense	probably null
R1906:Apol6	UTSW	15	76,935,060 (GRCm39)	missense	probably damaging	0.99
R2097:Apol6	UTSW	15	76,931,333 (GRCm39)	critical splice donor site	probably null
R5611:Apol6	UTSW	15	76,935,240 (GRCm39)	splice site	probably null
R5980:Apol6	UTSW	15	76,935,219 (GRCm39)	missense	possibly damaging	0.66
R6191:Apol6	UTSW	15	76,940,098 (GRCm39)	missense	probably benign	0.00
R6300:Apol6	UTSW	15	76,935,471 (GRCm39)	missense	probably benign	0.01
R6519:Apol6	UTSW	15	76,935,476 (GRCm39)	nonsense	probably null
R7569:Apol6	UTSW	15	76,934,898 (GRCm39)	unclassified	probably benign
R8072:Apol6	UTSW	15	76,935,303 (GRCm39)	missense	probably benign	0.03
R9010:Apol6	UTSW	15	76,935,697 (GRCm39)	missense	unknown

Predicted Primers

PCR Primer
(F):5'- TTGAAGCCAAGTGTTTGTTTCCC -3'
(R):5'- CGCTGTTAGGCATGATGCTG -3'

Sequencing Primer
(F):5'- GTTTCCCTCACCCACAGG -3'
(R):5'- CATGATGCTGTTGACCTGAGCAAG -3'

Posted On

2014-08-25