Mutagenetix > Incidental Mutation

Incidental Mutation 'R0212:Pou6f1'

33573

Institutional Source

Beutler Lab

Gene Symbol

Pou6f1

Ensembl Gene

ENSMUSG00000009739

Gene Name

POU domain, class 6, transcription factor 1

Synonyms

cns-1, 2310038G18Rik, Emb

MMRRC Submission

038463-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.466) question?

Stock #

R0212 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

100473199-100497865 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 100478696 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 129 (V129A)

Ref Sequence

ENSEMBL: ENSMUSP00000145707 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000058274] [ENSMUST00000073837] [ENSMUST00000176271] [ENSMUST00000176300] [ENSMUST00000177202]

AlphaFold

Q07916

Predicted Effect

probably benign
Transcript: ENSMUST00000058274

SMART Domains

Protein: ENSMUSP00000049955
Gene: ENSMUSG00000009739

Domain	Start	End	E-Value	Type
low complexity region	113	132	N/A	INTRINSIC
low complexity region	181	193	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000073837
AA Change: V404A

PolyPhen 2 Score 0.284 (Sensitivity: 0.91; Specificity: 0.88)

SMART Domains

Protein: ENSMUSP00000073504
Gene: ENSMUSG00000009739
AA Change: V404A

Domain	Start	End	E-Value	Type
low complexity region	174	232	N/A	INTRINSIC
POU	414	488	6.32e-44	SMART
HOX	509	571	7.03e-22	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000176140

SMART Domains

Protein: ENSMUSP00000135670
Gene: ENSMUSG00000009739

Domain	Start	End	E-Value	Type
POU	139	213	6.32e-44	SMART
HOX	234	296	7.03e-22	SMART

Predicted Effect

possibly damaging
Transcript: ENSMUST00000176271
AA Change: V129A

PolyPhen 2 Score 0.745 (Sensitivity: 0.85; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000134760
Gene: ENSMUSG00000009739
AA Change: V129A

Domain	Start	End	E-Value	Type
POU	139	213	6.32e-44	SMART
HOX	234	296	7.03e-22	SMART

Predicted Effect

possibly damaging
Transcript: ENSMUST00000176271
AA Change: V129A

PolyPhen 2 Score 0.745 (Sensitivity: 0.85; Specificity: 0.92)

Predicted Effect

probably benign
Transcript: ENSMUST00000176300

Predicted Effect

probably benign
Transcript: ENSMUST00000177202

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000177335

SMART Domains

Protein: ENSMUSP00000135627
Gene: ENSMUSG00000009739

Domain	Start	End	E-Value	Type
POU	28	102	6.32e-44	SMART
HOX	123	185	7.03e-22	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000230790

Coding Region Coverage

1x: 99.3%
3x: 98.6%
10x: 97.1%
20x: 95.1%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 72 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ablim2	G	A	5: 36,006,254 (GRCm39)		probably null	Het
Adat1	T	A	8: 112,713,840 (GRCm39)	D113V	possibly damaging	Het
Arhgap40	T	G	2: 158,392,495 (GRCm39)	L656V	probably damaging	Het
Atg2a	T	C	19: 6,296,584 (GRCm39)	I330T	probably damaging	Het
Cad	A	G	5: 31,235,454 (GRCm39)	D2137G	probably damaging	Het
Cd8a	G	A	6: 71,350,633 (GRCm39)	E33K	probably benign	Het
Cemip	C	A	7: 83,622,398 (GRCm39)	G594C	probably damaging	Het
Chd6	T	A	2: 160,894,767 (GRCm39)	D31V	probably damaging	Het
Cmpk1	A	T	4: 114,822,216 (GRCm39)	M111K	possibly damaging	Het
Crispld2	T	G	8: 120,737,370 (GRCm39)	H40Q	probably benign	Het
Depdc5	A	G	5: 33,069,586 (GRCm39)	T441A	probably benign	Het
Dpm1	T	C	2: 168,069,414 (GRCm39)	N5S	probably benign	Het
Ercc4	A	G	16: 12,941,196 (GRCm39)		probably null	Het
Fam83f	A	T	15: 80,574,779 (GRCm39)	M229L	probably benign	Het
Fgd5	A	T	6: 91,965,189 (GRCm39)	D474V	probably damaging	Het
Fgf21	G	T	7: 45,263,526 (GRCm39)	P184Q	probably benign	Het
Fry	A	T	5: 150,419,862 (GRCm39)	D1008V	probably damaging	Het
Gjd2	T	C	2: 113,841,953 (GRCm39)	T175A	probably benign	Het
Gphn	C	T	12: 78,684,326 (GRCm39)	T577I	probably damaging	Het
Ifi207	A	T	1: 173,563,964 (GRCm39)	N18K	possibly damaging	Het
Ifne	T	C	4: 88,797,972 (GRCm39)	R149G	possibly damaging	Het
Ift80	A	T	3: 68,847,506 (GRCm39)	L330H	probably benign	Het
Inpp4b	A	T	8: 82,497,546 (GRCm39)	H122L	probably benign	Het
Inpp5e	T	C	2: 26,298,352 (GRCm39)		probably null	Het
Ism1	T	C	2: 139,582,177 (GRCm39)	L163S	probably benign	Het
Itga11	T	A	9: 62,653,251 (GRCm39)	V375E	probably benign	Het
Itpr3	T	G	17: 27,308,293 (GRCm39)	F306V	probably damaging	Het
Kif19a	A	T	11: 114,675,736 (GRCm39)	I403F	possibly damaging	Het
Klf12	A	T	14: 100,260,298 (GRCm39)	S144T	probably benign	Het
Lyst	C	T	13: 13,810,570 (GRCm39)	H747Y	possibly damaging	Het
Mccc2	A	G	13: 100,091,163 (GRCm39)	Y445H	probably benign	Het
Mei1	G	A	15: 81,980,132 (GRCm39)		probably null	Het
Metap2	T	A	10: 93,697,242 (GRCm39)	K479N	probably damaging	Het
Mief2	A	T	11: 60,621,493 (GRCm39)	D62V	probably damaging	Het
Mtrf1	A	G	14: 79,656,719 (GRCm39)	D407G	probably benign	Het
Myo3a	A	G	2: 22,296,659 (GRCm39)	R210G	probably damaging	Het
Nkx2-2	T	C	2: 147,026,090 (GRCm39)	H216R	probably damaging	Het
Nos1	A	G	5: 118,048,277 (GRCm39)	E694G	possibly damaging	Het
Nptn	A	T	9: 58,535,164 (GRCm39)	Y103F	probably benign	Het
Nrxn1	A	G	17: 90,670,186 (GRCm39)		probably benign	Het
Numbl	T	C	7: 26,980,184 (GRCm39)	S389P	probably damaging	Het
Or10d5	A	G	9: 39,861,236 (GRCm39)	V277A	probably benign	Het
Or1q1	T	A	2: 36,887,644 (GRCm39)	V274E	possibly damaging	Het
Or1q1	A	T	2: 36,887,335 (GRCm39)	D171V	probably damaging	Het
Or5b105	G	A	19: 13,080,642 (GRCm39)	R3C	possibly damaging	Het
Or5d16	A	G	2: 87,773,435 (GRCm39)	F179S	probably damaging	Het
Or5i1	C	T	2: 87,613,826 (GRCm39)	P314L	unknown	Het
Or8g20	C	A	9: 39,396,384 (GRCm39)	S55I	probably damaging	Het
Osm	T	G	11: 4,188,465 (GRCm39)	S31A	probably benign	Het
Paqr4	T	C	17: 23,957,294 (GRCm39)	M70V	probably benign	Het
Pikfyve	T	A	1: 65,302,064 (GRCm39)	Y1607N	probably benign	Het
Plec	A	C	15: 76,075,505 (GRCm39)	Y402*	probably null	Het
Polq	A	G	16: 36,887,216 (GRCm39)	K1631E	probably damaging	Het
Prm2	A	G	16: 10,609,463 (GRCm39)		probably benign	Het
Prtn3	A	G	10: 79,716,971 (GRCm39)	Y112C	probably damaging	Het
Qrfp	T	A	2: 31,698,797 (GRCm39)	H45L	probably benign	Het
Rps6ka5	A	T	12: 100,519,428 (GRCm39)		probably null	Het
Rspo1	G	A	4: 124,885,190 (GRCm39)	R22Q	probably benign	Het
Slc10a1	A	C	12: 81,014,486 (GRCm39)	L78R	possibly damaging	Het
Slc26a5	A	T	5: 22,028,547 (GRCm39)	Y340*	probably null	Het
Sptbn2	T	C	19: 4,796,970 (GRCm39)		probably null	Het
St3gal6	C	A	16: 58,293,816 (GRCm39)	A238S	probably damaging	Het
St3gal6	G	T	16: 58,293,818 (GRCm39)	A237E	probably damaging	Het
Tmem131l	A	T	3: 83,820,575 (GRCm39)	S1226T	probably benign	Het
Togaram2	C	T	17: 72,031,978 (GRCm39)	L866F	probably damaging	Het
Txndc17	A	G	11: 72,098,558 (GRCm39)	T37A	probably benign	Het
Vmn2r105	C	A	17: 20,428,827 (GRCm39)	V750F	possibly damaging	Het
Vmn2r54	T	A	7: 12,366,424 (GRCm39)	Y170F	probably benign	Het
Wrnip1	T	C	13: 33,005,889 (GRCm39)	V577A	probably benign	Het
Zc3h7b	A	G	15: 81,660,529 (GRCm39)	T226A	probably benign	Het
Zfp948	T	C	17: 21,808,422 (GRCm39)	I538T	probably benign	Het
Zzef1	A	G	11: 72,764,736 (GRCm39)	E1401G	possibly damaging	Het

Other mutations in Pou6f1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00480:Pou6f1	APN	15	100,477,928 (GRCm39)	splice site	probably benign
IGL02451:Pou6f1	APN	15	100,477,821 (GRCm39)	missense	possibly damaging	0.80
IGL02545:Pou6f1	APN	15	100,481,306 (GRCm39)	nonsense	probably null
R0076:Pou6f1	UTSW	15	100,485,717 (GRCm39)	nonsense	probably null
R0076:Pou6f1	UTSW	15	100,485,717 (GRCm39)	nonsense	probably null
R1297:Pou6f1	UTSW	15	100,476,186 (GRCm39)	missense	probably damaging	1.00
R2863:Pou6f1	UTSW	15	100,478,689 (GRCm39)	splice site	probably null
R2905:Pou6f1	UTSW	15	100,483,839 (GRCm39)	missense	probably benign
R3418:Pou6f1	UTSW	15	100,478,805 (GRCm39)	missense	probably benign	0.00
R4161:Pou6f1	UTSW	15	100,478,724 (GRCm39)	missense	probably damaging	0.98
R4793:Pou6f1	UTSW	15	100,476,293 (GRCm39)	missense	probably damaging	1.00
R5617:Pou6f1	UTSW	15	100,483,874 (GRCm39)	missense	possibly damaging	0.95
R5947:Pou6f1	UTSW	15	100,484,001 (GRCm39)	missense	possibly damaging	0.77
R6261:Pou6f1	UTSW	15	100,477,827 (GRCm39)	missense	probably damaging	0.99
R6731:Pou6f1	UTSW	15	100,477,764 (GRCm39)	missense	possibly damaging	0.57
R7696:Pou6f1	UTSW	15	100,481,979 (GRCm39)	missense	probably benign	0.30
R8795:Pou6f1	UTSW	15	100,485,686 (GRCm39)	missense	possibly damaging	0.68
R8941:Pou6f1	UTSW	15	100,489,742 (GRCm39)	missense	probably damaging	0.99
R9114:Pou6f1	UTSW	15	100,478,789 (GRCm39)	missense	probably benign	0.28
R9731:Pou6f1	UTSW	15	100,476,206 (GRCm39)	missense	possibly damaging	0.91
R9737:Pou6f1	UTSW	15	100,481,282 (GRCm39)	missense	probably benign	0.01
X0019:Pou6f1	UTSW	15	100,481,203 (GRCm39)	missense	probably damaging	0.99
Z1177:Pou6f1	UTSW	15	100,481,122 (GRCm39)	missense	possibly damaging	0.82

Predicted Primers

PCR Primer
(F):5'- AGTCAGCCAGAGGCACAGTGTAAC -3'
(R):5'- TCTTCGATGACCACAGGTGGAAATG -3'

Sequencing Primer
(F):5'- agacgcttgccactgaac -3'
(R):5'- TTCACGCAGGGTGTCTGAC -3'

Posted On

2013-05-09