Mutagenetix > Incidental Mutation

Incidental Mutation 'R5999:Zfhx2'

480741

Institutional Source

Beutler Lab

Gene Symbol

Zfhx2

Ensembl Gene

ENSMUSG00000040721

Gene Name

zinc finger homeobox 2

Synonyms

zfh-5

MMRRC Submission

044178-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.295) question?

Stock #

R5999 (G1)

Quality Score

218.009

Status

Validated

Chromosome

Chromosomal Location

55297719-55329781 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 55311462 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Proline at position 411 (S411P)

Ref Sequence

ENSEMBL: ENSMUSP00000045156 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000036328] [ENSMUST00000183822] [ENSMUST00000185121]

AlphaFold

Q2MHN3

Predicted Effect

probably benign
Transcript: ENSMUST00000036328
AA Change: S411P

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000045156
Gene: ENSMUSG00000040721
AA Change: S411P

Domain	Start	End	E-Value	Type
low complexity region	22	42	N/A	INTRINSIC
ZnF_C2H2	230	252	1.43e1	SMART
low complexity region	333	345	N/A	INTRINSIC
low complexity region	428	439	N/A	INTRINSIC
ZnF_C2H2	446	469	8.94e-3	SMART
ZnF_U1	498	532	6.98e-1	SMART
ZnF_C2H2	501	525	3.21e-4	SMART
ZnF_U1	560	594	1.36e0	SMART
ZnF_C2H2	563	587	3.29e-1	SMART
low complexity region	597	623	N/A	INTRINSIC
ZnF_C2H2	752	776	6.4e0	SMART
ZnF_C2H2	815	839	2.02e-1	SMART
ZnF_U1	861	895	1.78e1	SMART
ZnF_C2H2	864	888	5.34e-1	SMART
ZnF_C2H2	974	997	1.51e1	SMART
ZnF_C2H2	1003	1026	1.51e0	SMART
low complexity region	1087	1103	N/A	INTRINSIC
low complexity region	1106	1126	N/A	INTRINSIC
ZnF_U1	1182	1216	3.42e0	SMART
ZnF_C2H2	1185	1209	8.22e-2	SMART
ZnF_U1	1239	1273	3.73e0	SMART
ZnF_C2H2	1242	1266	6.67e-2	SMART
low complexity region	1277	1304	N/A	INTRINSIC
low complexity region	1314	1326	N/A	INTRINSIC
low complexity region	1332	1346	N/A	INTRINSIC
low complexity region	1349	1359	N/A	INTRINSIC
low complexity region	1379	1400	N/A	INTRINSIC
low complexity region	1457	1465	N/A	INTRINSIC
ZnF_C2H2	1474	1497	5.34e0	SMART
low complexity region	1522	1531	N/A	INTRINSIC
low complexity region	1542	1554	N/A	INTRINSIC
low complexity region	1562	1583	N/A	INTRINSIC
HOX	1589	1651	1.97e-16	SMART
low complexity region	1656	1665	N/A	INTRINSIC
coiled coil region	1693	1723	N/A	INTRINSIC
ZnF_C2H2	1761	1783	2.53e-2	SMART
low complexity region	1837	1847	N/A	INTRINSIC
HOX	1851	1913	2.34e-18	SMART
low complexity region	1984	1995	N/A	INTRINSIC
low complexity region	2001	2051	N/A	INTRINSIC
HOX	2058	2120	1.52e-17	SMART
ZnF_U1	2136	2170	1.09e1	SMART
ZnF_C2H2	2139	2163	5.4e1	SMART
low complexity region	2328	2354	N/A	INTRINSIC
low complexity region	2385	2426	N/A	INTRINSIC
ZnF_U1	2482	2516	8.31e-1	SMART
ZnF_C2H2	2485	2509	9.46e0	SMART
low complexity region	2523	2538	N/A	INTRINSIC
low complexity region	2553	2562	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000176665

SMART Domains

Protein: ENSMUSP00000134955
Gene: ENSMUSG00000040721

Domain	Start	End	E-Value	Type
ZnF_C2H2	13	37	5.34e-1	SMART
ZnF_C2H2	133	156	1.51e1	SMART
ZnF_C2H2	162	185	1.51e0	SMART
low complexity region	246	262	N/A	INTRINSIC
low complexity region	265	285	N/A	INTRINSIC
ZnF_C2H2	344	368	8.22e-2	SMART
ZnF_C2H2	401	425	6.67e-2	SMART
low complexity region	436	463	N/A	INTRINSIC
low complexity region	473	485	N/A	INTRINSIC
low complexity region	491	505	N/A	INTRINSIC
low complexity region	508	518	N/A	INTRINSIC
low complexity region	538	559	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000176872

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000183750

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000183822

SMART Domains

Protein: ENSMUSP00000140371
Gene: ENSMUSG00000045691

Domain	Start	End	E-Value	Type
PDB:2JMU\|A	5	64	3e-23	PDB

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000183993

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000185121

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000185430

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.9%
3x: 99.4%
10x: 97.2%
20x: 90.9%

Validation Efficiency

98% (55/56)

Allele List at MGI

Other mutations in this stock

Total: 57 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acot5	A	G	12: 84,122,328 (GRCm39)	D304G	probably benign	Het
Acyp2	C	T	11: 30,456,354 (GRCm39)	E98K	possibly damaging	Het
Akap9	A	G	5: 4,093,925 (GRCm39)	N2149S	probably damaging	Het
Akp3	T	A	1: 87,055,263 (GRCm39)	Y437N	probably damaging	Het
Anks1b	C	T	10: 90,194,910 (GRCm39)	T530I	probably damaging	Het
Bltp2	T	C	11: 78,176,294 (GRCm39)	F1799L	probably damaging	Het
Bnc2	C	T	4: 84,474,137 (GRCm39)	R3H	probably benign	Het
Cald1	A	T	6: 34,723,273 (GRCm39)		probably benign	Het
Capn9	A	G	8: 125,315,817 (GRCm39)	T87A	probably damaging	Het
Ccdc88c	A	G	12: 100,934,613 (GRCm39)	L175P	probably damaging	Het
Cd226	T	C	18: 89,225,343 (GRCm39)	V80A	probably damaging	Het
Cd44	A	T	2: 102,675,742 (GRCm39)	N310K	probably benign	Het
Cenpc1	T	A	5: 86,160,122 (GRCm39)	K905N	probably damaging	Het
Cept1	A	T	3: 106,440,759 (GRCm39)	D133E	probably damaging	Het
Cltc	T	C	11: 86,594,955 (GRCm39)	H1381R	possibly damaging	Het
Col4a4	T	A	1: 82,470,340 (GRCm39)	T730S	unknown	Het
Col6a4	A	T	9: 105,945,120 (GRCm39)	M998K	probably benign	Het
Cpne6	T	C	14: 55,750,516 (GRCm39)	V119A	probably benign	Het
Ddx54	G	T	5: 120,761,645 (GRCm39)	A474S	probably benign	Het
Dmbx1	G	T	4: 115,775,373 (GRCm39)	N302K	probably damaging	Het
Dnah8	A	G	17: 30,882,279 (GRCm39)	E617G	probably benign	Het
Ei24	A	G	9: 36,704,603 (GRCm39)	V10A	probably benign	Het
Elp3	A	G	14: 65,768,989 (GRCm39)	V543A	probably benign	Het
Frmd3	T	C	4: 74,088,928 (GRCm39)	I375T	possibly damaging	Het
Gm6408	A	G	5: 146,421,067 (GRCm39)	D232G	possibly damaging	Het
Inmt	A	T	6: 55,151,933 (GRCm39)	Y12*	probably null	Het
Inpp5k	G	T	11: 75,523,926 (GRCm39)	A44S	probably damaging	Het
Kalrn	T	A	16: 34,177,713 (GRCm39)	T169S	probably damaging	Het
Kif28	A	T	1: 179,523,355 (GRCm39)	F992I	probably damaging	Het
Kmt2c	A	T	5: 25,489,203 (GRCm39)	Y1199N	probably damaging	Het
Large2	C	T	2: 92,196,403 (GRCm39)	E475K	probably benign	Het
Mroh2b	T	A	15: 4,942,366 (GRCm39)		probably null	Het
Mrpl42	T	C	10: 95,336,341 (GRCm39)		probably benign	Het
Muc5b	A	T	7: 141,411,116 (GRCm39)	H1354L	unknown	Het
Myof	C	A	19: 37,928,304 (GRCm39)	E1095*	probably null	Het
Ncor2	A	G	5: 125,110,505 (GRCm39)	V1385A	probably damaging	Het
Nr5a2	T	C	1: 136,773,280 (GRCm39)	Y474C	probably damaging	Het
Or1j10	A	G	2: 36,267,322 (GRCm39)	D178G	probably damaging	Het
Or5a21	C	T	19: 12,311,008 (GRCm39)	D71N	probably damaging	Het
Or5l13	A	T	2: 87,780,145 (GRCm39)		probably null	Het
Pogz	A	G	3: 94,763,428 (GRCm39)	T67A	possibly damaging	Het
Prep	T	A	10: 44,948,225 (GRCm39)		probably null	Het
Prf1	A	G	10: 61,138,807 (GRCm39)	D255G	probably damaging	Het
Psme2	A	G	14: 55,827,539 (GRCm39)	L24P	probably damaging	Het
Scmh1	T	A	4: 120,362,712 (GRCm39)		probably null	Het
Scpep1	A	G	11: 88,820,139 (GRCm39)	V383A	possibly damaging	Het
Slc4a10	A	T	2: 62,073,775 (GRCm39)	N279I	probably benign	Het
Sphkap	T	C	1: 83,245,126 (GRCm39)	S1498G	probably benign	Het
Spinkl	C	A	18: 44,301,206 (GRCm39)	S44I	probably damaging	Het
Tanc2	G	A	11: 105,758,543 (GRCm39)	R768Q	probably damaging	Het
Tle5	T	C	10: 81,397,098 (GRCm39)	S25P	probably damaging	Het
Tmem213	A	G	6: 38,086,386 (GRCm39)	Q14R	probably benign	Het
Tns1	A	T	1: 73,967,256 (GRCm39)	Y1172*	probably null	Het
Ugt2b37	A	C	5: 87,402,036 (GRCm39)	I198M	probably benign	Het
Usp17lb	A	C	7: 104,489,552 (GRCm39)	I457M	probably damaging	Het
Usp6nl	G	T	2: 6,446,150 (GRCm39)	R709L	probably damaging	Het
Zer1	A	G	2: 29,995,009 (GRCm39)	L462P	probably damaging	Het

Other mutations in Zfhx2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00091:Zfhx2	APN	14	55,304,022 (GRCm39)	missense	possibly damaging	0.93
IGL00164:Zfhx2	APN	14	55,302,483 (GRCm39)	missense	possibly damaging	0.73
IGL00235:Zfhx2	APN	14	55,300,714 (GRCm39)	missense	probably benign	0.11
IGL00925:Zfhx2	APN	14	55,310,518 (GRCm39)	missense	probably benign	0.06
IGL01025:Zfhx2	APN	14	55,301,717 (GRCm39)	missense	probably damaging	1.00
IGL01061:Zfhx2	APN	14	55,311,339 (GRCm39)	missense	possibly damaging	0.96
IGL01486:Zfhx2	APN	14	55,304,547 (GRCm39)	missense	probably damaging	1.00
IGL01875:Zfhx2	APN	14	55,301,372 (GRCm39)	missense	unknown
IGL01990:Zfhx2	APN	14	55,311,047 (GRCm39)	missense	probably damaging	0.99
IGL02097:Zfhx2	APN	14	55,300,351 (GRCm39)	missense	probably damaging	1.00
IGL02269:Zfhx2	APN	14	55,309,393 (GRCm39)	missense	probably benign	0.00
IGL02488:Zfhx2	APN	14	55,302,560 (GRCm39)	missense	possibly damaging	0.72
IGL02624:Zfhx2	APN	14	55,304,085 (GRCm39)	missense	probably benign	0.06
IGL03087:Zfhx2	APN	14	55,310,302 (GRCm39)	missense	possibly damaging	0.85
G1patch:Zfhx2	UTSW	14	55,301,539 (GRCm39)	nonsense	probably null
PIT4403001:Zfhx2	UTSW	14	55,312,437 (GRCm39)	missense	probably benign
R0148:Zfhx2	UTSW	14	55,310,354 (GRCm39)	missense	possibly damaging	0.86
R0323:Zfhx2	UTSW	14	55,303,436 (GRCm39)	missense	possibly damaging	0.73
R0328:Zfhx2	UTSW	14	55,309,445 (GRCm39)	missense	probably benign
R0348:Zfhx2	UTSW	14	55,300,965 (GRCm39)	missense	probably damaging	0.99
R0442:Zfhx2	UTSW	14	55,304,357 (GRCm39)	missense	possibly damaging	0.53
R0533:Zfhx2	UTSW	14	55,301,547 (GRCm39)	missense	probably benign	0.23
R0561:Zfhx2	UTSW	14	55,303,346 (GRCm39)	missense	probably benign	0.01
R0627:Zfhx2	UTSW	14	55,302,784 (GRCm39)	missense	probably benign
R0659:Zfhx2	UTSW	14	55,311,258 (GRCm39)	missense	possibly damaging	0.73
R0675:Zfhx2	UTSW	14	55,300,620 (GRCm39)	missense	probably damaging	0.99
R1301:Zfhx2	UTSW	14	55,300,854 (GRCm39)	missense	probably benign	0.32
R1563:Zfhx2	UTSW	14	55,302,545 (GRCm39)	missense	probably benign	0.33
R1607:Zfhx2	UTSW	14	55,300,442 (GRCm39)	missense	probably damaging	1.00
R1694:Zfhx2	UTSW	14	55,311,401 (GRCm39)	missense	possibly damaging	0.91
R1710:Zfhx2	UTSW	14	55,303,455 (GRCm39)	missense	possibly damaging	0.70
R1773:Zfhx2	UTSW	14	55,310,348 (GRCm39)	missense	possibly damaging	0.53
R1879:Zfhx2	UTSW	14	55,310,206 (GRCm39)	missense	possibly damaging	0.96
R1879:Zfhx2	UTSW	14	55,303,074 (GRCm39)	missense	probably benign	0.32
R1933:Zfhx2	UTSW	14	55,312,695 (GRCm39)	start gained	probably benign
R1944:Zfhx2	UTSW	14	55,312,189 (GRCm39)	missense	probably benign	0.18
R2888:Zfhx2	UTSW	14	55,302,260 (GRCm39)	missense	possibly damaging	0.71
R2889:Zfhx2	UTSW	14	55,302,260 (GRCm39)	missense	possibly damaging	0.71
R2915:Zfhx2	UTSW	14	55,302,014 (GRCm39)	missense	probably damaging	0.98
R3971:Zfhx2	UTSW	14	55,311,932 (GRCm39)	missense	probably benign	0.33
R4082:Zfhx2	UTSW	14	55,302,662 (GRCm39)	missense	probably benign
R4134:Zfhx2	UTSW	14	55,302,600 (GRCm39)	missense	possibly damaging	0.93
R4231:Zfhx2	UTSW	14	55,310,991 (GRCm39)	missense	possibly damaging	0.73
R4675:Zfhx2	UTSW	14	55,304,678 (GRCm39)	missense	probably benign	0.03
R4764:Zfhx2	UTSW	14	55,304,372 (GRCm39)	missense	possibly damaging	0.96
R4866:Zfhx2	UTSW	14	55,302,993 (GRCm39)	missense	possibly damaging	0.73
R4940:Zfhx2	UTSW	14	55,303,891 (GRCm39)	missense	possibly damaging	0.53
R5125:Zfhx2	UTSW	14	55,312,232 (GRCm39)	missense	probably benign	0.00
R5178:Zfhx2	UTSW	14	55,312,232 (GRCm39)	missense	probably benign	0.00
R5554:Zfhx2	UTSW	14	55,301,774 (GRCm39)	missense	probably damaging	1.00
R5689:Zfhx2	UTSW	14	55,311,360 (GRCm39)	missense	possibly damaging	0.53
R5768:Zfhx2	UTSW	14	55,311,822 (GRCm39)	missense	probably benign
R5792:Zfhx2	UTSW	14	55,304,303 (GRCm39)	missense	possibly damaging	0.72
R5834:Zfhx2	UTSW	14	55,310,787 (GRCm39)	nonsense	probably null
R5895:Zfhx2	UTSW	14	55,303,348 (GRCm39)	missense	probably benign
R6025:Zfhx2	UTSW	14	55,302,665 (GRCm39)	missense	probably benign	0.00
R6106:Zfhx2	UTSW	14	55,305,767 (GRCm39)	critical splice acceptor site	probably null
R6135:Zfhx2	UTSW	14	55,311,653 (GRCm39)	missense	possibly damaging	0.85
R6186:Zfhx2	UTSW	14	55,300,617 (GRCm39)	missense	probably damaging	0.99
R6379:Zfhx2	UTSW	14	55,311,795 (GRCm39)	missense	probably benign
R6725:Zfhx2	UTSW	14	55,301,539 (GRCm39)	nonsense	probably null
R7089:Zfhx2	UTSW	14	55,303,229 (GRCm39)	missense	probably benign	0.33
R7383:Zfhx2	UTSW	14	55,305,710 (GRCm39)	missense	probably benign	0.00
R7470:Zfhx2	UTSW	14	55,304,207 (GRCm39)	missense	possibly damaging	0.52
R7606:Zfhx2	UTSW	14	55,304,120 (GRCm39)	missense	probably benign	0.12
R7607:Zfhx2	UTSW	14	55,303,688 (GRCm39)	missense	possibly damaging	0.86
R7698:Zfhx2	UTSW	14	55,300,306 (GRCm39)	missense	probably benign	0.00
R7730:Zfhx2	UTSW	14	55,304,357 (GRCm39)	missense	possibly damaging	0.53
R8142:Zfhx2	UTSW	14	55,310,895 (GRCm39)	missense	possibly damaging	0.86
R8188:Zfhx2	UTSW	14	55,301,898 (GRCm39)	missense	probably benign	0.18
R8212:Zfhx2	UTSW	14	55,310,373 (GRCm39)	missense	possibly damaging	0.70
R8264:Zfhx2	UTSW	14	55,302,969 (GRCm39)	missense	possibly damaging	0.53
R8331:Zfhx2	UTSW	14	55,309,444 (GRCm39)	missense	probably benign	0.00
R8369:Zfhx2	UTSW	14	55,304,201 (GRCm39)	missense	probably benign	0.05
R8371:Zfhx2	UTSW	14	55,301,549 (GRCm39)	missense	probably damaging	0.99
R8383:Zfhx2	UTSW	14	55,311,528 (GRCm39)	missense	possibly damaging	0.73
R8415:Zfhx2	UTSW	14	55,308,079 (GRCm39)	missense	probably benign
R8441:Zfhx2	UTSW	14	55,303,985 (GRCm39)	missense	possibly damaging	0.96
R8466:Zfhx2	UTSW	14	55,310,353 (GRCm39)	missense	possibly damaging	0.53
R8504:Zfhx2	UTSW	14	55,303,243 (GRCm39)	missense	probably benign	0.00
R8708:Zfhx2	UTSW	14	55,312,509 (GRCm39)	missense	probably benign
R8804:Zfhx2	UTSW	14	55,312,191 (GRCm39)	missense	probably benign	0.18
R8913:Zfhx2	UTSW	14	55,309,543 (GRCm39)	missense	probably benign	0.02
R8952:Zfhx2	UTSW	14	55,310,207 (GRCm39)	missense	possibly damaging	0.86
R9057:Zfhx2	UTSW	14	55,310,027 (GRCm39)	missense	possibly damaging	0.53
R9060:Zfhx2	UTSW	14	55,311,803 (GRCm39)	missense	probably benign	0.00
R9197:Zfhx2	UTSW	14	55,312,179 (GRCm39)	nonsense	probably null
R9622:Zfhx2	UTSW	14	55,303,483 (GRCm39)	missense	probably benign	0.18
R9623:Zfhx2	UTSW	14	55,302,191 (GRCm39)	missense	probably damaging	0.98
R9775:Zfhx2	UTSW	14	55,304,562 (GRCm39)	missense	probably benign	0.01
R9780:Zfhx2	UTSW	14	55,312,494 (GRCm39)	missense	probably benign	0.02
X0065:Zfhx2	UTSW	14	55,304,417 (GRCm39)	missense	probably benign	0.33
Z1088:Zfhx2	UTSW	14	55,311,637 (GRCm39)	missense	possibly damaging	0.73
Z1177:Zfhx2	UTSW	14	55,304,439 (GRCm39)	missense	possibly damaging	0.70
Z1177:Zfhx2	UTSW	14	55,303,377 (GRCm39)	missense	probably benign	0.40

Predicted Primers

PCR Primer
(F):5'- TAGCCGCAGTTGTAGCTCTC -3'
(R):5'- AAGATTCGCCAGTACCAAGAG -3'

Sequencing Primer
(F):5'- CTACAGTAGCTGCAGTGGCTG -3'
(R):5'- CCAGTACCAAGAGGCGAGGC -3'

Posted On

2017-06-26