Mutagenetix > Incidental Mutation

Incidental Mutation 'R2426:Zzef1'

250240

Institutional Source

Beutler Lab

Gene Symbol

Zzef1

Ensembl Gene

ENSMUSG00000055670

Gene Name

zinc finger, ZZ-type with EF hand domain 1

Synonyms

C130099L13Rik, 8430405D05Rik

MMRRC Submission

040388-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R2426 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

72796226-72927120 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 72915265 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Methionine to Valine at position 2647 (M2647V)

Ref Sequence

ENSEMBL: ENSMUSP00000130515 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000069395] [ENSMUST00000172220] [ENSMUST00000207107]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000069395
AA Change: M2647V

PolyPhen 2 Score 0.015 (Sensitivity: 0.96; Specificity: 0.79)

SMART Domains

Protein: ENSMUSP00000068790
Gene: ENSMUSG00000055670
AA Change: M2647V

Domain	Start	End	E-Value	Type
low complexity region	4	20	N/A	INTRINSIC
low complexity region	28	68	N/A	INTRINSIC
low complexity region	78	93	N/A	INTRINSIC
APC10	246	397	2.65e-48	SMART
internal_repeat_1	1122	1192	1.25e-7	PROSPERO
low complexity region	1472	1485	N/A	INTRINSIC
low complexity region	1512	1525	N/A	INTRINSIC
ZnF_ZZ	1775	1823	2.54e-7	SMART
ZnF_ZZ	1824	1868	1.2e-8	SMART
low complexity region	1947	1963	N/A	INTRINSIC
low complexity region	2127	2140	N/A	INTRINSIC
low complexity region	2249	2263	N/A	INTRINSIC
internal_repeat_1	2657	2726	1.25e-7	PROSPERO
low complexity region	2840	2853	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000152063

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000152481

Predicted Effect

probably benign
Transcript: ENSMUST00000172220
AA Change: M2647V

PolyPhen 2 Score 0.015 (Sensitivity: 0.96; Specificity: 0.79)

SMART Domains

Protein: ENSMUSP00000130515
Gene: ENSMUSG00000055670
AA Change: M2647V

Domain	Start	End	E-Value	Type
low complexity region	4	20	N/A	INTRINSIC
low complexity region	28	68	N/A	INTRINSIC
low complexity region	78	93	N/A	INTRINSIC
APC10	246	397	2.65e-48	SMART
internal_repeat_1	1006	1192	1.57e-16	PROSPERO
low complexity region	1472	1485	N/A	INTRINSIC
low complexity region	1512	1525	N/A	INTRINSIC
ZnF_ZZ	1775	1823	2.54e-7	SMART
ZnF_ZZ	1824	1868	1.2e-8	SMART
low complexity region	1947	1963	N/A	INTRINSIC
low complexity region	2127	2140	N/A	INTRINSIC
low complexity region	2249	2263	N/A	INTRINSIC
internal_repeat_1	2583	2759	1.57e-16	PROSPERO
low complexity region	2873	2886	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000207107
AA Change: M2676V

PolyPhen 2 Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)

Coding Region Coverage

1x: 99.1%
3x: 98.5%
10x: 96.9%
20x: 93.8%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 67 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
0610010F05Rik	T	A	11: 23,576,801 (GRCm38)	R190W	probably damaging	Het
Abca14	G	T	7: 120,283,223 (GRCm38)	V1203L	probably benign	Het
Adamtsl1	G	A	4: 86,156,788 (GRCm38)	V131I	probably benign	Het
Adgra3	A	T	5: 50,009,449 (GRCm38)	M187K	possibly damaging	Het
Agbl1	T	C	7: 76,421,902 (GRCm38)	V324A	probably damaging	Het
Ahnak	A	T	19: 9,002,851 (GRCm38)	I500F	possibly damaging	Het
Aldh1l1	A	G	6: 90,598,284 (GRCm38)	D851G	probably damaging	Het
Amot	T	C	X: 145,476,291 (GRCm38)	K460E	probably damaging	Het
Arhgef3	G	T	14: 27,384,181 (GRCm38)	E161*	probably null	Het
Atg9b	A	T	5: 24,386,994 (GRCm38)	I669N	probably damaging	Het
AY761184	T	G	8: 21,702,637 (GRCm38)	K114N	possibly damaging	Het
Ccdc83	A	G	7: 90,228,431 (GRCm38)	Y268H	probably damaging	Het
Cep170	A	G	1: 176,774,635 (GRCm38)	S302P	probably benign	Het
Cyp4a31	T	A	4: 115,571,016 (GRCm38)	M303K	probably damaging	Het
Cyp4v3	T	A	8: 45,317,776 (GRCm38)	Y231F	probably benign	Het
Dock3	A	T	9: 106,914,541 (GRCm38)	L1411Q	possibly damaging	Het
Dsg1a	T	A	18: 20,336,804 (GRCm38)	I629N	probably damaging	Het
Dst	A	T	1: 34,192,812 (GRCm38)	H2837L	probably benign	Het
Fam114a2	G	A	11: 57,493,080 (GRCm38)	P343L	probably benign	Het
Fbrs	A	G	7: 127,487,339 (GRCm38)		probably null	Het
Fbxl13	A	C	5: 21,522,137 (GRCm38)	D620E	probably damaging	Het
Frmd4a	T	A	2: 4,529,862 (GRCm38)	S164T	probably damaging	Het
Gdi2	T	G	13: 3,562,034 (GRCm38)	S330A	probably benign	Het
Gm5878	A	T	6: 85,118,631 (GRCm38)	M70K	probably benign	Het
H2-Q6	G	T	17: 35,424,937 (GRCm38)	A21S	probably benign	Het
Hfm1	A	T	5: 106,847,653 (GRCm38)		probably null	Het
Hnmt	C	T	2: 24,019,155 (GRCm38)	C82Y	probably benign	Het
Il1rl1	C	A	1: 40,446,619 (GRCm38)	A310D	probably damaging	Het
Ints1	A	T	5: 139,771,814 (GRCm38)		probably null	Het
Kcne4	C	A	1: 78,817,971 (GRCm38)	A112E	possibly damaging	Het
Krt32	T	C	11: 100,086,366 (GRCm38)	K236R	possibly damaging	Het
Maml2	T	C	9: 13,706,498 (GRCm38)	L380P	probably damaging	Het
Meis1	A	T	11: 18,988,356 (GRCm38)	D218E	possibly damaging	Het
Mon1b	G	A	8: 113,639,120 (GRCm38)	G360D	probably damaging	Het
Mpp4	A	G	1: 59,130,057 (GRCm38)	S383P	probably damaging	Het
Neb	A	G	2: 52,169,053 (GRCm38)		probably null	Het
Nlgn2	A	T	11: 69,827,086 (GRCm38)	I431N	probably damaging	Het
Nr2e1	A	G	10: 42,563,485 (GRCm38)	L134P	probably damaging	Het
Olfr329-ps	A	T	11: 58,543,094 (GRCm38)	Y127*	probably null	Het
Olfr371	T	C	8: 85,231,064 (GRCm38)	S190P	probably damaging	Het
Olfr777	T	C	10: 129,269,266 (GRCm38)	Q19R	probably benign	Het
Opcml	G	A	9: 28,903,367 (GRCm38)		probably null	Het
Pate2	A	T	9: 35,670,480 (GRCm38)		probably null	Het
Pgr	G	A	9: 8,900,717 (GRCm38)	V84M	probably damaging	Het
Pigu	A	T	2: 155,299,082 (GRCm38)	V296D	probably damaging	Het
Plcb2	G	A	2: 118,715,649 (GRCm38)	T555M	probably damaging	Het
Pld5	T	G	1: 175,963,976 (GRCm38)	D426A	probably benign	Het
Prdm2	G	T	4: 143,111,750 (GRCm38)	C1679*	probably null	Het
Psme2b	A	T	11: 48,946,063 (GRCm38)	V19D	probably benign	Het
Ptpn9	A	T	9: 57,027,428 (GRCm38)	N159Y	possibly damaging	Het
Sdc3	A	T	4: 130,818,803 (GRCm38)	T64S	unknown	Het
Serping1	T	G	2: 84,770,219 (GRCm38)	S260R	probably damaging	Het
Slc20a1	T	C	2: 129,208,230 (GRCm38)	F436S	probably benign	Het
Sntb1	A	T	15: 55,906,179 (GRCm38)	I138N	probably damaging	Het
Sorcs3	A	T	19: 48,722,925 (GRCm38)	Y643F	probably damaging	Het
Spink1	G	T	18: 43,735,222 (GRCm38)	S23*	probably null	Het
Stag1	T	C	9: 100,845,116 (GRCm38)		probably null	Het
Tnfaip8l1	G	A	17: 56,172,030 (GRCm38)	V107I	probably benign	Het
Tnik	A	G	3: 28,646,681 (GRCm38)	S907G	probably damaging	Het
Ttf1	T	A	2: 29,067,185 (GRCm38)	M489K	probably damaging	Het
Ugcg	C	T	4: 59,207,798 (GRCm38)	P46S	probably benign	Het
Usp54	G	A	14: 20,564,940 (GRCm38)	A811V	probably benign	Het
Xirp2	A	G	2: 67,514,471 (GRCm38)	N2352S	probably benign	Het
Zan	T	C	5: 137,388,992 (GRCm38)	Y4933C	unknown	Het
Zbtb8a	A	G	4: 129,360,219 (GRCm38)	S161P	probably benign	Het
Zkscan5	A	T	5: 145,220,940 (GRCm38)	I751L	probably benign	Het
Zscan4d	A	G	7: 11,165,095 (GRCm38)	F85S	probably damaging	Het

Other mutations in Zzef1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00092:Zzef1	APN	11	72,875,126 (GRCm38)	missense	probably benign	0.02
IGL00898:Zzef1	APN	11	72,875,173 (GRCm38)	missense	probably benign	0.00
IGL00970:Zzef1	APN	11	72,915,245 (GRCm38)	missense	probably benign	0.06
IGL01062:Zzef1	APN	11	72,874,969 (GRCm38)	missense	probably benign
IGL01832:Zzef1	APN	11	72,875,066 (GRCm38)	missense	probably damaging	0.99
IGL02005:Zzef1	APN	11	72,888,299 (GRCm38)	missense	probably benign	0.00
IGL02026:Zzef1	APN	11	72,881,338 (GRCm38)	missense	probably benign	0.39
IGL02110:Zzef1	APN	11	72,913,112 (GRCm38)	missense	probably damaging	1.00
IGL02305:Zzef1	APN	11	72,866,597 (GRCm38)	splice site	probably benign
IGL02308:Zzef1	APN	11	72,886,747 (GRCm38)	missense	probably benign	0.04
IGL02315:Zzef1	APN	11	72,875,257 (GRCm38)	nonsense	probably null
IGL02332:Zzef1	APN	11	72,916,509 (GRCm38)	missense	probably benign	0.01
IGL02389:Zzef1	APN	11	72,891,217 (GRCm38)	missense	probably benign
IGL02389:Zzef1	APN	11	72,899,538 (GRCm38)	missense	possibly damaging	0.89
IGL02451:Zzef1	APN	11	72,901,388 (GRCm38)	missense	probably damaging	0.99
IGL02541:Zzef1	APN	11	72,872,649 (GRCm38)	missense	probably damaging	1.00
IGL02950:Zzef1	APN	11	72,917,699 (GRCm38)	splice site	probably benign
IGL02953:Zzef1	APN	11	72,855,398 (GRCm38)	missense	probably benign
IGL03053:Zzef1	APN	11	72,831,539 (GRCm38)	splice site	probably benign
IGL03085:Zzef1	APN	11	72,855,524 (GRCm38)	splice site	probably benign
IGL03152:Zzef1	APN	11	72,923,182 (GRCm38)	critical splice donor site	probably null
IGL03329:Zzef1	APN	11	72,917,273 (GRCm38)	splice site	probably benign
IGL03376:Zzef1	APN	11	72,876,551 (GRCm38)	splice site	probably benign
IGL03394:Zzef1	APN	11	72,886,775 (GRCm38)	splice site	probably null
Dreidel	UTSW	11	72,908,469 (GRCm38)	nonsense	probably null
Hanukkah	UTSW	11	72,893,332 (GRCm38)	missense	probably benign	0.00
Mezuzah	UTSW	11	72,848,733 (GRCm38)	nonsense	probably null
BB005:Zzef1	UTSW	11	72,821,896 (GRCm38)	missense	probably damaging	0.99
BB015:Zzef1	UTSW	11	72,821,896 (GRCm38)	missense	probably damaging	0.99
PIT4508001:Zzef1	UTSW	11	72,895,176 (GRCm38)	missense	probably benign
PIT4581001:Zzef1	UTSW	11	72,899,672 (GRCm38)	missense	probably benign	0.00
PIT4810001:Zzef1	UTSW	11	72,850,745 (GRCm38)	missense	probably damaging	1.00
R0094:Zzef1	UTSW	11	72,817,965 (GRCm38)	missense	probably benign	0.01
R0119:Zzef1	UTSW	11	72,821,851 (GRCm38)	missense	probably benign
R0136:Zzef1	UTSW	11	72,821,851 (GRCm38)	missense	probably benign
R0140:Zzef1	UTSW	11	72,899,551 (GRCm38)	missense	possibly damaging	0.70
R0212:Zzef1	UTSW	11	72,873,910 (GRCm38)	missense	possibly damaging	0.66
R0217:Zzef1	UTSW	11	72,889,068 (GRCm38)	missense	probably damaging	1.00
R0220:Zzef1	UTSW	11	72,865,966 (GRCm38)	missense	probably damaging	1.00
R0304:Zzef1	UTSW	11	72,880,624 (GRCm38)	missense	probably benign	0.10
R0400:Zzef1	UTSW	11	72,895,242 (GRCm38)	missense	probably damaging	1.00
R0422:Zzef1	UTSW	11	72,866,091 (GRCm38)	missense	possibly damaging	0.93
R0471:Zzef1	UTSW	11	72,923,111 (GRCm38)	missense	probably damaging	1.00
R0557:Zzef1	UTSW	11	72,917,730 (GRCm38)	missense	probably damaging	1.00
R0581:Zzef1	UTSW	11	72,851,900 (GRCm38)	missense	probably benign	0.00
R0599:Zzef1	UTSW	11	72,913,178 (GRCm38)	missense	probably damaging	1.00
R0603:Zzef1	UTSW	11	72,818,069 (GRCm38)	missense	probably benign	0.00
R0657:Zzef1	UTSW	11	72,821,851 (GRCm38)	missense	probably benign
R0987:Zzef1	UTSW	11	72,901,333 (GRCm38)	small deletion	probably benign
R1246:Zzef1	UTSW	11	72,874,909 (GRCm38)	missense	probably benign	0.00
R1327:Zzef1	UTSW	11	72,893,414 (GRCm38)	critical splice donor site	probably null
R1438:Zzef1	UTSW	11	72,912,945 (GRCm38)	missense	probably damaging	0.96
R1466:Zzef1	UTSW	11	72,924,679 (GRCm38)	missense	probably damaging	1.00
R1466:Zzef1	UTSW	11	72,924,679 (GRCm38)	missense	probably damaging	1.00
R1485:Zzef1	UTSW	11	72,900,809 (GRCm38)	splice site	probably null
R1556:Zzef1	UTSW	11	72,915,233 (GRCm38)	missense	probably damaging	1.00
R1563:Zzef1	UTSW	11	72,848,733 (GRCm38)	nonsense	probably null
R1584:Zzef1	UTSW	11	72,924,679 (GRCm38)	missense	probably damaging	1.00
R1643:Zzef1	UTSW	11	72,826,202 (GRCm38)	missense	probably damaging	1.00
R1646:Zzef1	UTSW	11	72,864,036 (GRCm38)	critical splice donor site	probably null
R1764:Zzef1	UTSW	11	72,893,332 (GRCm38)	missense	probably benign	0.00
R1777:Zzef1	UTSW	11	72,910,272 (GRCm38)	missense	probably damaging	1.00
R1793:Zzef1	UTSW	11	72,886,709 (GRCm38)	missense	probably damaging	1.00
R1900:Zzef1	UTSW	11	72,848,714 (GRCm38)	missense	probably damaging	0.99
R2096:Zzef1	UTSW	11	72,872,639 (GRCm38)	missense	probably benign	0.02
R2134:Zzef1	UTSW	11	72,880,624 (GRCm38)	missense	probably benign	0.02
R2157:Zzef1	UTSW	11	72,848,634 (GRCm38)	splice site	probably benign
R2183:Zzef1	UTSW	11	72,886,718 (GRCm38)	nonsense	probably null
R2192:Zzef1	UTSW	11	72,910,156 (GRCm38)	splice site	probably null
R2230:Zzef1	UTSW	11	72,884,416 (GRCm38)	missense	probably damaging	0.99
R2259:Zzef1	UTSW	11	72,900,633 (GRCm38)	nonsense	probably null
R2384:Zzef1	UTSW	11	72,858,394 (GRCm38)	missense	probably damaging	0.99
R2915:Zzef1	UTSW	11	72,910,326 (GRCm38)	splice site	probably null
R3700:Zzef1	UTSW	11	72,886,772 (GRCm38)	missense	probably null	1.00
R3875:Zzef1	UTSW	11	72,889,040 (GRCm38)	missense	probably benign	0.22
R3902:Zzef1	UTSW	11	72,908,500 (GRCm38)	missense	probably damaging	1.00
R3927:Zzef1	UTSW	11	72,858,382 (GRCm38)	missense	probably damaging	1.00
R4086:Zzef1	UTSW	11	72,875,053 (GRCm38)	missense	probably benign	0.02
R4301:Zzef1	UTSW	11	72,889,035 (GRCm38)	missense	probably damaging	0.96
R4359:Zzef1	UTSW	11	72,823,508 (GRCm38)	missense	probably damaging	0.98
R4382:Zzef1	UTSW	11	72,875,112 (GRCm38)	missense	probably benign	0.00
R4453:Zzef1	UTSW	11	72,872,639 (GRCm38)	missense	probably benign	0.02
R4466:Zzef1	UTSW	11	72,924,659 (GRCm38)	missense	probably damaging	1.00
R4471:Zzef1	UTSW	11	72,913,331 (GRCm38)	missense	probably damaging	1.00
R4510:Zzef1	UTSW	11	72,888,170 (GRCm38)	missense	probably benign	0.32
R4511:Zzef1	UTSW	11	72,888,170 (GRCm38)	missense	probably benign	0.32
R4714:Zzef1	UTSW	11	72,837,212 (GRCm38)	missense	probably damaging	1.00
R4799:Zzef1	UTSW	11	72,859,623 (GRCm38)	missense	probably benign	0.12
R4906:Zzef1	UTSW	11	72,901,388 (GRCm38)	missense	probably damaging	1.00
R5075:Zzef1	UTSW	11	72,858,344 (GRCm38)	missense	probably damaging	1.00
R5357:Zzef1	UTSW	11	72,843,333 (GRCm38)	nonsense	probably null
R5579:Zzef1	UTSW	11	72,900,637 (GRCm38)	missense	probably damaging	0.98
R5598:Zzef1	UTSW	11	72,916,521 (GRCm38)	missense	probably damaging	1.00
R5725:Zzef1	UTSW	11	72,855,482 (GRCm38)	missense	possibly damaging	0.86
R5765:Zzef1	UTSW	11	72,821,937 (GRCm38)	nonsense	probably null
R5928:Zzef1	UTSW	11	72,912,852 (GRCm38)	missense	probably damaging	1.00
R6003:Zzef1	UTSW	11	72,824,065 (GRCm38)	splice site	probably null
R6047:Zzef1	UTSW	11	72,866,095 (GRCm38)	missense	probably damaging	0.99
R6224:Zzef1	UTSW	11	72,855,383 (GRCm38)	missense	probably damaging	0.99
R6225:Zzef1	UTSW	11	72,869,805 (GRCm38)	missense	possibly damaging	0.62
R6287:Zzef1	UTSW	11	72,923,112 (GRCm38)	missense	probably damaging	1.00
R6361:Zzef1	UTSW	11	72,884,349 (GRCm38)	missense	possibly damaging	0.93
R6451:Zzef1	UTSW	11	72,923,156 (GRCm38)	missense	possibly damaging	0.88
R6467:Zzef1	UTSW	11	72,911,264 (GRCm38)	critical splice donor site	probably null
R6484:Zzef1	UTSW	11	72,895,271 (GRCm38)	missense	probably damaging	1.00
R6493:Zzef1	UTSW	11	72,913,303 (GRCm38)	missense	probably benign	0.06
R6520:Zzef1	UTSW	11	72,826,065 (GRCm38)	missense	probably damaging	1.00
R6527:Zzef1	UTSW	11	72,874,990 (GRCm38)	missense	probably benign	0.00
R6540:Zzef1	UTSW	11	72,913,229 (GRCm38)	missense	probably damaging	1.00
R6608:Zzef1	UTSW	11	72,912,826 (GRCm38)	missense	probably damaging	1.00
R6795:Zzef1	UTSW	11	72,850,659 (GRCm38)	missense	probably benign	0.00
R6927:Zzef1	UTSW	11	72,913,157 (GRCm38)	missense	probably damaging	1.00
R6987:Zzef1	UTSW	11	72,855,514 (GRCm38)	missense	possibly damaging	0.89
R7048:Zzef1	UTSW	11	72,866,699 (GRCm38)	nonsense	probably null
R7076:Zzef1	UTSW	11	72,899,559 (GRCm38)	missense	probably benign	0.00
R7099:Zzef1	UTSW	11	72,872,649 (GRCm38)	missense	possibly damaging	0.92
R7132:Zzef1	UTSW	11	72,917,871 (GRCm38)	critical splice donor site	probably null
R7175:Zzef1	UTSW	11	72,851,901 (GRCm38)	missense	possibly damaging	0.49
R7284:Zzef1	UTSW	11	72,886,690 (GRCm38)	missense	probably damaging	0.99
R7300:Zzef1	UTSW	11	72,875,004 (GRCm38)	missense	probably benign	0.02
R7486:Zzef1	UTSW	11	72,864,786 (GRCm38)	missense	possibly damaging	0.85
R7503:Zzef1	UTSW	11	72,826,067 (GRCm38)	missense	probably damaging	1.00
R7679:Zzef1	UTSW	11	72,893,278 (GRCm38)	missense	probably benign
R7874:Zzef1	UTSW	11	72,859,653 (GRCm38)	missense	probably benign	0.01
R7898:Zzef1	UTSW	11	72,796,547 (GRCm38)	missense	probably damaging	1.00
R7928:Zzef1	UTSW	11	72,821,896 (GRCm38)	missense	probably damaging	0.99
R8021:Zzef1	UTSW	11	72,823,416 (GRCm38)	missense	probably damaging	0.99
R8145:Zzef1	UTSW	11	72,908,469 (GRCm38)	nonsense	probably null
R8255:Zzef1	UTSW	11	72,875,129 (GRCm38)	missense	probably benign	0.00
R8303:Zzef1	UTSW	11	72,917,189 (GRCm38)	missense	probably damaging	1.00
R8492:Zzef1	UTSW	11	72,886,746 (GRCm38)	missense	probably damaging	0.97
R8492:Zzef1	UTSW	11	72,872,604 (GRCm38)	missense	probably damaging	1.00
R8498:Zzef1	UTSW	11	72,853,322 (GRCm38)	missense	probably damaging	1.00
R8547:Zzef1	UTSW	11	72,844,441 (GRCm38)	missense	probably damaging	1.00
R8874:Zzef1	UTSW	11	72,863,989 (GRCm38)	missense	probably benign	0.00
R8885:Zzef1	UTSW	11	72,796,576 (GRCm38)	missense	probably benign	0.00
R8972:Zzef1	UTSW	11	72,900,673 (GRCm38)	missense	probably damaging	1.00
R8979:Zzef1	UTSW	11	72,875,177 (GRCm38)	missense	probably benign	0.00
R9053:Zzef1	UTSW	11	72,922,476 (GRCm38)	missense	probably benign
R9108:Zzef1	UTSW	11	72,899,778 (GRCm38)	missense	probably benign	0.11
R9121:Zzef1	UTSW	11	72,866,120 (GRCm38)	nonsense	probably null
R9253:Zzef1	UTSW	11	72,848,637 (GRCm38)	splice site	probably benign
R9370:Zzef1	UTSW	11	72,853,322 (GRCm38)	missense	probably damaging	1.00
R9408:Zzef1	UTSW	11	72,864,827 (GRCm38)	missense	possibly damaging	0.86
R9467:Zzef1	UTSW	11	72,916,425 (GRCm38)	missense	probably damaging	1.00
R9468:Zzef1	UTSW	11	72,923,183 (GRCm38)	critical splice donor site	probably null
R9563:Zzef1	UTSW	11	72,874,906 (GRCm38)	missense	probably damaging	1.00
R9647:Zzef1	UTSW	11	72,869,825 (GRCm38)	missense	probably benign	0.01
R9667:Zzef1	UTSW	11	72,867,960 (GRCm38)	missense	probably benign
R9742:Zzef1	UTSW	11	72,858,353 (GRCm38)	missense	probably benign
X0028:Zzef1	UTSW	11	72,906,979 (GRCm38)	missense	probably benign	0.29
Z1176:Zzef1	UTSW	11	72,796,528 (GRCm38)	missense	probably damaging	1.00
Z1177:Zzef1	UTSW	11	72,900,631 (GRCm38)	critical splice acceptor site	probably null
Z1177:Zzef1	UTSW	11	72,826,178 (GRCm38)	missense	probably damaging	1.00
Z1177:Zzef1	UTSW	11	72,796,312 (GRCm38)	missense	possibly damaging	0.91
Z1177:Zzef1	UTSW	11	72,915,320 (GRCm38)	missense	probably damaging	1.00
Z1186:Zzef1	UTSW	11	72,889,182 (GRCm38)	missense	probably benign
Z1187:Zzef1	UTSW	11	72,889,182 (GRCm38)	missense	probably benign
Z1188:Zzef1	UTSW	11	72,889,182 (GRCm38)	missense	probably benign
Z1189:Zzef1	UTSW	11	72,889,182 (GRCm38)	missense	probably benign
Z1190:Zzef1	UTSW	11	72,889,182 (GRCm38)	missense	probably benign
Z1191:Zzef1	UTSW	11	72,889,182 (GRCm38)	missense	probably benign
Z1192:Zzef1	UTSW	11	72,889,182 (GRCm38)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- TCTGATTCAGAACAGGGCATG -3'
(R):5'- GCCAGAAGCCCACATTTTCC -3'

Sequencing Primer
(F):5'- CTGGAATTGCATTTGGGGGCAG -3'
(R):5'- CTGATGAACCTCAGTCTGGAG -3'

Posted On

2014-11-12