Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02869:Foxp1'

362511

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Foxp1

Ensembl Gene

ENSMUSG00000030067

Gene Name

forkhead box P1

Synonyms

3110052D19Rik, 4932443N09Rik

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

IGL02869

Quality Score

Status

Chromosome

Chromosomal Location

98902299-99499682 bp(-) (GRCm39)

Type of Mutation

utr 3 prime

DNA Base Change (assembly)

C to A at 98907044 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000135809 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000074346] [ENSMUST00000113322] [ENSMUST00000113324] [ENSMUST00000113326] [ENSMUST00000113328] [ENSMUST00000113329] [ENSMUST00000177437] [ENSMUST00000176565] [ENSMUST00000177229] [ENSMUST00000177230] [ENSMUST00000177307] [ENSMUST00000176632] [ENSMUST00000176850]

AlphaFold

P58462

Predicted Effect

probably benign
Transcript: ENSMUST00000074346

SMART Domains

Protein: ENSMUSP00000073953
Gene: ENSMUSG00000030067

Domain	Start	End	E-Value	Type
coiled coil region	62	113	N/A	INTRINSIC
low complexity region	140	191	N/A	INTRINSIC
low complexity region	200	233	N/A	INTRINSIC
low complexity region	236	250	N/A	INTRINSIC
low complexity region	264	275	N/A	INTRINSIC
low complexity region	317	330	N/A	INTRINSIC
ZnF_C2H2	334	359	8.67e-1	SMART
low complexity region	371	383	N/A	INTRINSIC
low complexity region	432	446	N/A	INTRINSIC
FH	491	572	2.07e-39	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000113322

SMART Domains

Protein: ENSMUSP00000108948
Gene: ENSMUSG00000030067

Domain	Start	End	E-Value	Type
coiled coil region	62	113	N/A	INTRINSIC
low complexity region	140	191	N/A	INTRINSIC
low complexity region	200	233	N/A	INTRINSIC
low complexity region	236	250	N/A	INTRINSIC
low complexity region	264	275	N/A	INTRINSIC
low complexity region	317	330	N/A	INTRINSIC
ZnF_C2H2	334	359	8.67e-1	SMART
low complexity region	371	383	N/A	INTRINSIC
low complexity region	432	446	N/A	INTRINSIC
FH	491	572	2.07e-39	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000113324

SMART Domains

Protein: ENSMUSP00000108950
Gene: ENSMUSG00000030067

Domain	Start	End	E-Value	Type
coiled coil region	62	113	N/A	INTRINSIC
low complexity region	140	192	N/A	INTRINSIC
low complexity region	201	234	N/A	INTRINSIC
low complexity region	237	251	N/A	INTRINSIC
low complexity region	265	276	N/A	INTRINSIC
low complexity region	318	331	N/A	INTRINSIC
ZnF_C2H2	335	360	8.67e-1	SMART
low complexity region	372	384	N/A	INTRINSIC
low complexity region	433	447	N/A	INTRINSIC
FH	492	573	2.07e-39	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000113326

SMART Domains

Protein: ENSMUSP00000108952
Gene: ENSMUSG00000030067

Domain	Start	End	E-Value	Type
low complexity region	108	159	N/A	INTRINSIC
low complexity region	168	201	N/A	INTRINSIC
low complexity region	204	218	N/A	INTRINSIC
low complexity region	232	243	N/A	INTRINSIC
low complexity region	285	298	N/A	INTRINSIC
ZnF_C2H2	302	327	8.67e-1	SMART
low complexity region	339	351	N/A	INTRINSIC
low complexity region	400	414	N/A	INTRINSIC
FH	459	540	2.07e-39	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000113328

SMART Domains

Protein: ENSMUSP00000108954
Gene: ENSMUSG00000030067

Domain	Start	End	E-Value	Type
coiled coil region	62	113	N/A	INTRINSIC
low complexity region	140	191	N/A	INTRINSIC
low complexity region	200	234	N/A	INTRINSIC
low complexity region	237	251	N/A	INTRINSIC
low complexity region	265	276	N/A	INTRINSIC
low complexity region	318	331	N/A	INTRINSIC
ZnF_C2H2	335	360	8.67e-1	SMART
low complexity region	372	384	N/A	INTRINSIC
low complexity region	433	447	N/A	INTRINSIC
FH	492	573	2.07e-39	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000113329

SMART Domains

Protein: ENSMUSP00000108955
Gene: ENSMUSG00000030067

Domain	Start	End	E-Value	Type
coiled coil region	62	113	N/A	INTRINSIC
low complexity region	140	191	N/A	INTRINSIC
low complexity region	200	233	N/A	INTRINSIC
low complexity region	236	250	N/A	INTRINSIC
low complexity region	264	275	N/A	INTRINSIC
low complexity region	317	330	N/A	INTRINSIC
ZnF_C2H2	334	359	8.67e-1	SMART
low complexity region	371	383	N/A	INTRINSIC
low complexity region	432	446	N/A	INTRINSIC
FH	491	579	1.76e-10	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000175880

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000177410

Predicted Effect

probably benign
Transcript: ENSMUST00000177437

SMART Domains

Protein: ENSMUSP00000135809
Gene: ENSMUSG00000030067

Domain	Start	End	E-Value	Type
low complexity region	10	61	N/A	INTRINSIC
low complexity region	70	104	N/A	INTRINSIC
low complexity region	107	121	N/A	INTRINSIC
low complexity region	135	146	N/A	INTRINSIC
low complexity region	188	201	N/A	INTRINSIC
ZnF_C2H2	205	230	8.67e-1	SMART
low complexity region	242	254	N/A	INTRINSIC
low complexity region	303	317	N/A	INTRINSIC
FH	362	443	2.07e-39	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000176565

SMART Domains

Protein: ENSMUSP00000135181
Gene: ENSMUSG00000030067

Domain	Start	End	E-Value	Type
coiled coil region	62	113	N/A	INTRINSIC
low complexity region	140	191	N/A	INTRINSIC
low complexity region	200	234	N/A	INTRINSIC
low complexity region	237	251	N/A	INTRINSIC
low complexity region	265	276	N/A	INTRINSIC
low complexity region	318	331	N/A	INTRINSIC
ZnF_C2H2	335	360	8.67e-1	SMART
low complexity region	372	384	N/A	INTRINSIC
low complexity region	433	447	N/A	INTRINSIC
FH	491	572	2.07e-39	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000177229

SMART Domains

Protein: ENSMUSP00000134817
Gene: ENSMUSG00000030067

Domain	Start	End	E-Value	Type
low complexity region	10	62	N/A	INTRINSIC
low complexity region	71	105	N/A	INTRINSIC
low complexity region	108	122	N/A	INTRINSIC
low complexity region	136	147	N/A	INTRINSIC
low complexity region	189	202	N/A	INTRINSIC
ZnF_C2H2	206	231	8.67e-1	SMART
low complexity region	243	255	N/A	INTRINSIC
low complexity region	304	318	N/A	INTRINSIC
FH	363	444	2.07e-39	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000177230

SMART Domains

Protein: ENSMUSP00000135098
Gene: ENSMUSG00000030067

Domain	Start	End	E-Value	Type
low complexity region	108	160	N/A	INTRINSIC
low complexity region	169	203	N/A	INTRINSIC
low complexity region	206	220	N/A	INTRINSIC
low complexity region	234	245	N/A	INTRINSIC
low complexity region	287	300	N/A	INTRINSIC
ZnF_C2H2	304	329	8.67e-1	SMART
low complexity region	341	353	N/A	INTRINSIC
low complexity region	402	416	N/A	INTRINSIC
FH	461	542	2.07e-39	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000177307

SMART Domains

Protein: ENSMUSP00000135764
Gene: ENSMUSG00000030067

Domain	Start	End	E-Value	Type
coiled coil region	62	113	N/A	INTRINSIC
low complexity region	140	192	N/A	INTRINSIC
low complexity region	201	235	N/A	INTRINSIC
low complexity region	238	252	N/A	INTRINSIC
low complexity region	266	277	N/A	INTRINSIC
low complexity region	319	332	N/A	INTRINSIC
ZnF_C2H2	336	361	8.67e-1	SMART
low complexity region	373	385	N/A	INTRINSIC
low complexity region	434	448	N/A	INTRINSIC
FH	492	573	2.07e-39	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000176632

SMART Domains

Protein: ENSMUSP00000135635
Gene: ENSMUSG00000030067

Domain	Start	End	E-Value	Type
low complexity region	108	159	N/A	INTRINSIC
low complexity region	168	202	N/A	INTRINSIC
low complexity region	205	219	N/A	INTRINSIC
low complexity region	233	244	N/A	INTRINSIC
low complexity region	286	299	N/A	INTRINSIC
ZnF_C2H2	303	328	8.67e-1	SMART
low complexity region	340	352	N/A	INTRINSIC
low complexity region	401	415	N/A	INTRINSIC
FH	460	541	2.07e-39	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000176850

SMART Domains

Protein: ENSMUSP00000135041
Gene: ENSMUSG00000030067

Domain	Start	End	E-Value	Type
low complexity region	108	160	N/A	INTRINSIC
low complexity region	169	203	N/A	INTRINSIC
low complexity region	206	220	N/A	INTRINSIC
low complexity region	234	245	N/A	INTRINSIC
low complexity region	287	300	N/A	INTRINSIC
ZnF_C2H2	304	329	8.67e-1	SMART
low complexity region	341	353	N/A	INTRINSIC
low complexity region	402	416	N/A	INTRINSIC
FH	461	542	2.07e-39	SMART

Coding Region Coverage

Validation Efficiency

MGI Phenotype

PHENOTYPE: Homozygous null mice display embryonic lethality with abnormal outflow tract septation, ventricular septal defects, abnormal cardiac valve morphology, decreased and irregular heart rate, thin ventricular compact zone, and edema. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 95 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930562C15Rik	T	A	16: 4,685,323 (GRCm39)	S1142T	possibly damaging	Het
Aadacl4fm5	T	C	4: 144,512,938 (GRCm39)	I54V	probably benign	Het
Actr3b	T	G	5: 26,037,433 (GRCm39)	V215G	probably damaging	Het
Adam9	C	T	8: 25,460,634 (GRCm39)	V617M	probably damaging	Het
Adgrl2	G	T	3: 148,596,241 (GRCm39)	P32T	probably damaging	Het
Afg2a	G	T	3: 37,518,694 (GRCm39)	G743W	probably damaging	Het
Ago3	A	T	4: 126,261,580 (GRCm39)		probably benign	Het
Allc	A	C	12: 28,623,206 (GRCm39)	I20M	probably benign	Het
Asic3	G	A	5: 24,621,972 (GRCm39)	W361*	probably null	Het
Atf7ip	A	G	6: 136,583,577 (GRCm39)	K1203E	probably damaging	Het
Babam2	C	A	5: 32,162,116 (GRCm39)	H272Q	possibly damaging	Het
Baz2b	G	A	2: 59,807,872 (GRCm39)	T129I	probably benign	Het
C130073F10Rik	A	T	4: 101,747,590 (GRCm39)	Y146*	probably null	Het
Cd247	A	G	1: 165,684,986 (GRCm39)	E74G	probably damaging	Het
Cdh17	A	T	4: 11,814,908 (GRCm39)	Q778L	probably benign	Het
Ceacam1	T	C	7: 25,175,966 (GRCm39)	D76G	probably benign	Het
Cela3a	T	C	4: 137,131,145 (GRCm39)	K198E	probably benign	Het
Cemip2	T	A	19: 21,789,241 (GRCm39)	D558E	probably damaging	Het
Ces2a	T	A	8: 105,465,691 (GRCm39)	D281E	probably damaging	Het
Cetn2	A	T	X: 71,958,527 (GRCm39)	D116E	probably damaging	Het
Cracd	A	G	5: 77,006,890 (GRCm39)	K1084E	unknown	Het
Ctu2	G	T	8: 123,205,530 (GRCm39)		probably null	Het
Cybb	T	C	X: 9,308,828 (GRCm39)	N469D	probably benign	Het
Cygb	C	T	11: 116,540,749 (GRCm39)	R79Q	probably damaging	Het
Cyp2d10	C	T	15: 82,288,069 (GRCm39)	V186M	possibly damaging	Het
Defb29	T	A	2: 152,380,942 (GRCm39)		probably null	Het
Depdc7	T	G	2: 104,560,694 (GRCm39)	Q100P	probably damaging	Het
Dhx30	A	C	9: 109,926,251 (GRCm39)	I91R	probably damaging	Het
Dnm1l	T	A	16: 16,159,288 (GRCm39)	K105*	probably null	Het
Eddm13	T	C	7: 6,272,898 (GRCm39)		probably benign	Het
Efhc1	T	C	1: 21,037,567 (GRCm39)	I248T	probably damaging	Het
Elapor1	A	G	3: 108,380,182 (GRCm39)	I309T	probably benign	Het
Entpd2	A	G	2: 25,288,120 (GRCm39)	T115A	probably damaging	Het
Epb42	G	T	2: 120,856,227 (GRCm39)	A439E	probably benign	Het
Esm1	T	G	13: 113,346,618 (GRCm39)	L81R	probably damaging	Het
F8	T	C	X: 74,330,987 (GRCm39)	S968G	probably benign	Het
Fam234b	T	G	6: 135,202,201 (GRCm39)	Y308D	probably damaging	Het
Fbxo46	T	G	7: 18,871,139 (GRCm39)	V586G	probably damaging	Het
Gm10754	A	T	10: 97,518,136 (GRCm39)		probably benign	Het
Gm12695	A	C	4: 96,650,370 (GRCm39)		probably benign	Het
Gm5468	T	C	15: 25,414,726 (GRCm39)		probably benign	Het
Grhl1	T	C	12: 24,631,490 (GRCm39)	S66P	probably damaging	Het
Gstt3	A	T	10: 75,612,576 (GRCm39)		probably null	Het
Gtf2i	A	G	5: 134,308,281 (GRCm39)		probably benign	Het
Gzmk	C	A	13: 113,308,560 (GRCm39)	G175C	probably damaging	Het
Helz2	T	C	2: 180,872,939 (GRCm39)		probably benign	Het
Ift20	T	C	11: 78,430,780 (GRCm39)		probably benign	Het
Intu	A	G	3: 40,642,216 (GRCm39)	D491G	probably damaging	Het
Itch	G	T	2: 155,015,853 (GRCm39)		probably null	Het
Itgb5	A	G	16: 33,665,362 (GRCm39)	N26S	possibly damaging	Het
Lama2	A	T	10: 26,891,534 (GRCm39)	S2526R	probably damaging	Het
Lat2	A	G	5: 134,637,027 (GRCm39)	I40T	probably damaging	Het
Lipa	T	A	19: 34,471,397 (GRCm39)	M393L	probably benign	Het
Lipa	G	T	19: 34,471,371 (GRCm39)		probably benign	Het
Lpcat1	T	A	13: 73,632,417 (GRCm39)	L10H	probably damaging	Het
Lpcat3	T	C	6: 124,679,970 (GRCm39)	Y348H	possibly damaging	Het
Lrp1b	A	T	2: 40,591,842 (GRCm39)	N50K	unknown	Het
Lrrk2	T	A	15: 91,634,480 (GRCm39)	Y1415N	probably damaging	Het
Lsamp	A	T	16: 41,965,078 (GRCm39)	T312S	probably benign	Het
Man2a2	T	C	7: 80,013,689 (GRCm39)	E454G	probably benign	Het
Mcm3	T	C	1: 20,879,063 (GRCm39)	K570R	probably damaging	Het
Mctp2	C	A	7: 71,878,219 (GRCm39)		probably null	Het
Msantd2	T	G	9: 37,434,796 (GRCm39)	C345W	probably damaging	Het
Musk	T	C	4: 58,354,078 (GRCm39)	I362T	probably benign	Het
Myh15	A	T	16: 48,965,767 (GRCm39)	N1224I	probably benign	Het
Myo18a	A	G	11: 77,755,612 (GRCm39)	Y1983C	probably damaging	Het
Myo18a	C	T	11: 77,720,699 (GRCm39)		probably benign	Het
Myrfl	G	T	10: 116,664,909 (GRCm39)	Q374K	probably damaging	Het
Ndrg1	T	A	15: 66,818,346 (GRCm39)	Q87H	probably benign	Het
Nol9	G	A	4: 152,131,030 (GRCm39)	C351Y	probably damaging	Het
Nr5a1	A	G	2: 38,598,141 (GRCm39)	S219P	probably benign	Het
Or8b43	T	C	9: 38,360,489 (GRCm39)	F107S	possibly damaging	Het
Or8g28	A	T	9: 39,169,520 (GRCm39)	Y149*	probably null	Het
Pcdhb19	A	G	18: 37,631,690 (GRCm39)	D495G	probably damaging	Het
Pfkm	A	G	15: 98,026,123 (GRCm39)	M573V	probably damaging	Het
Plec	A	T	15: 76,065,516 (GRCm39)	L1586Q	probably damaging	Het
Prelp	C	A	1: 133,843,005 (GRCm39)	E47*	probably null	Het
Rbm33	T	A	5: 28,615,753 (GRCm39)	I32N	probably damaging	Het
Rgs12	A	T	5: 35,183,227 (GRCm39)	D310V	probably damaging	Het
Ripor2	A	C	13: 24,880,512 (GRCm39)	H404P	possibly damaging	Het
Sh3d21	T	C	4: 126,056,034 (GRCm39)	E124G	probably benign	Het
Shroom2	C	T	X: 151,442,549 (GRCm39)	S872N	probably benign	Het
Slc44a5	A	G	3: 153,956,651 (GRCm39)	Y301C	probably damaging	Het
Smap1	A	T	1: 23,930,995 (GRCm39)	H66Q	possibly damaging	Het
Smyd1	G	T	6: 71,198,007 (GRCm39)		probably benign	Het
Sptbn4	T	A	7: 27,093,573 (GRCm39)		probably benign	Het
Srsf3-ps	T	A	11: 98,516,146 (GRCm39)	R76*	probably null	Het
Stag3	A	G	5: 138,280,955 (GRCm39)	K49R	probably damaging	Het
Stim1	C	A	7: 101,917,758 (GRCm39)	A46E	unknown	Het
Stxbp2	A	T	8: 3,691,971 (GRCm39)	I538F	probably benign	Het
Tbc1d19	A	G	5: 53,992,559 (GRCm39)	T114A	probably benign	Het
Tln2	G	A	9: 67,128,807 (GRCm39)		probably benign	Het
Trmt10a	T	A	3: 137,857,945 (GRCm39)		probably null	Het
Vwde	G	A	6: 13,187,136 (GRCm39)	H784Y	probably damaging	Het
Zfp773	T	C	7: 7,137,232 (GRCm39)	T121A	probably benign	Het

Other mutations in Foxp1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02191:Foxp1	APN	6	98,922,561 (GRCm39)	missense	probably damaging	0.99
IGL02330:Foxp1	APN	6	98,922,373 (GRCm39)	missense	probably damaging	1.00
IGL02968:Foxp1	APN	6	99,052,822 (GRCm39)	missense	probably damaging	1.00
Foxy	UTSW	6	98,992,471 (GRCm39)	nonsense	probably null
Moxie	UTSW	6	98,992,475 (GRCm39)	critical splice acceptor site	probably null
Roxie	UTSW	6	98,918,595 (GRCm39)	missense	unknown
R0037:Foxp1	UTSW	6	99,139,930 (GRCm39)	missense	probably damaging	1.00
R0063:Foxp1	UTSW	6	98,921,684 (GRCm39)	splice site	probably benign
R0063:Foxp1	UTSW	6	98,921,684 (GRCm39)	splice site	probably benign
R0427:Foxp1	UTSW	6	98,907,164 (GRCm39)	missense	probably damaging	1.00
R0601:Foxp1	UTSW	6	98,907,083 (GRCm39)	missense	probably damaging	1.00
R1356:Foxp1	UTSW	6	98,993,637 (GRCm39)	splice site	probably benign
R1468:Foxp1	UTSW	6	98,955,181 (GRCm39)	missense	possibly damaging	0.62
R1468:Foxp1	UTSW	6	98,955,181 (GRCm39)	missense	possibly damaging	0.62
R1548:Foxp1	UTSW	6	98,922,381 (GRCm39)	missense	probably damaging	1.00
R1696:Foxp1	UTSW	6	98,922,663 (GRCm39)	missense	probably benign	0.18
R1933:Foxp1	UTSW	6	99,052,926 (GRCm39)	small deletion	probably benign
R2152:Foxp1	UTSW	6	98,993,502 (GRCm39)	missense	probably damaging	0.99
R2338:Foxp1	UTSW	6	98,980,254 (GRCm39)	missense	possibly damaging	0.61
R3896:Foxp1	UTSW	6	99,052,897 (GRCm39)	missense	probably benign	0.33
R5006:Foxp1	UTSW	6	99,139,819 (GRCm39)	missense	probably damaging	0.98
R5143:Foxp1	UTSW	6	98,922,493 (GRCm39)	critical splice donor site	probably null
R5428:Foxp1	UTSW	6	98,993,592 (GRCm39)	missense	probably damaging	1.00
R5765:Foxp1	UTSW	6	98,992,423 (GRCm39)	missense	probably damaging	0.99
R5816:Foxp1	UTSW	6	99,052,926 (GRCm39)	small deletion	probably benign
R6172:Foxp1	UTSW	6	98,992,475 (GRCm39)	critical splice acceptor site	probably null
R6172:Foxp1	UTSW	6	98,992,471 (GRCm39)	nonsense	probably null
R6173:Foxp1	UTSW	6	98,992,475 (GRCm39)	critical splice acceptor site	probably null
R6173:Foxp1	UTSW	6	98,992,471 (GRCm39)	nonsense	probably null
R6175:Foxp1	UTSW	6	98,943,037 (GRCm39)	missense	probably damaging	1.00
R6776:Foxp1	UTSW	6	99,052,926 (GRCm39)	small deletion	probably benign
R6782:Foxp1	UTSW	6	98,907,106 (GRCm39)	missense	probably damaging	1.00
R7229:Foxp1	UTSW	6	98,912,373 (GRCm39)	missense	unknown
R7559:Foxp1	UTSW	6	98,922,521 (GRCm39)	missense	unknown
R7715:Foxp1	UTSW	6	98,922,621 (GRCm39)	missense	unknown
R8007:Foxp1	UTSW	6	98,918,595 (GRCm39)	missense	unknown
R8099:Foxp1	UTSW	6	98,922,510 (GRCm39)	missense	unknown
R8317:Foxp1	UTSW	6	99,052,866 (GRCm39)	small deletion	probably benign
R8408:Foxp1	UTSW	6	98,922,543 (GRCm39)	missense	unknown
R8704:Foxp1	UTSW	6	98,993,507 (GRCm39)	missense	unknown
R8705:Foxp1	UTSW	6	98,993,507 (GRCm39)	missense	unknown
R9014:Foxp1	UTSW	6	99,052,866 (GRCm39)	small deletion	probably benign
R9147:Foxp1	UTSW	6	99,052,866 (GRCm39)	small deletion	probably benign
R9399:Foxp1	UTSW	6	99,052,866 (GRCm39)	small deletion	probably benign
R9604:Foxp1	UTSW	6	99,052,926 (GRCm39)	small deletion	probably benign
X0066:Foxp1	UTSW	6	99,052,976 (GRCm39)	nonsense	probably null
Z1177:Foxp1	UTSW	6	98,955,122 (GRCm39)	missense	unknown

Posted On

2015-12-18