Mutagenetix > Incidental Mutation

Incidental Mutation 'R0207:Zranb1'

33397

Institutional Source

Beutler Lab

Gene Symbol

Zranb1

Ensembl Gene

ENSMUSG00000030967

Gene Name

zinc finger, RAN-binding domain containing 1

Synonyms

9330160G10Rik, D7Wsu87e

MMRRC Submission

038460-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.914) question?

Stock #

R0207 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

132532905-132588127 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 132552114 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Threonine at position 255 (I255T)

Ref Sequence

ENSEMBL: ENSMUSP00000101763 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000033265] [ENSMUST00000106157] [ENSMUST00000124096] [ENSMUST00000210507] [ENSMUST00000215716]

AlphaFold

Q7M760

Predicted Effect

probably damaging
Transcript: ENSMUST00000033265
AA Change: I255T

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000033265
Gene: ENSMUSG00000030967
AA Change: I255T

Domain	Start	End	E-Value	Type
ZnF_RBZ	6	30	9.14e-5	SMART
ZnF_RBZ	86	110	6.56e-6	SMART
ZnF_RBZ	151	175	1.69e-8	SMART
low complexity region	180	195	N/A	INTRINSIC
Pfam:OTU	438	586	9.8e-35	PFAM
low complexity region	698	708	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000106157
AA Change: I255T

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000101763
Gene: ENSMUSG00000030967
AA Change: I255T

Domain	Start	End	E-Value	Type
ZnF_RBZ	6	30	9.14e-5	SMART
ZnF_RBZ	86	110	6.56e-6	SMART
ZnF_RBZ	151	175	1.69e-8	SMART
low complexity region	180	195	N/A	INTRINSIC
Pfam:OTU	438	586	1.5e-40	PFAM
low complexity region	698	708	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000124096

SMART Domains

Protein: ENSMUSP00000130971
Gene: ENSMUSG00000030849

Domain	Start	End	E-Value	Type
Pfam:Pkinase	1	118	4.8e-19	PFAM
Pfam:Pkinase_Tyr	1	118	1.7e-50	PFAM
low complexity region	146	160	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000210507
AA Change: I255T

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)

Predicted Effect

probably damaging
Transcript: ENSMUST00000215716
AA Change: I281T

PolyPhen 2 Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.2%
20x: 95.5%

Validation Efficiency

95% (76/80)

MGI Phenotype

PHENOTYPE: Mice homozygous for a knock-out allele exhibit decreased CD4+ T cells and decreased susceptibility to experimental autoimmune encephalomyelitis. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 82 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca1	A	G	4: 53,086,039 (GRCm39)	F488S	probably damaging	Het
Acap3	C	T	4: 155,983,881 (GRCm39)	R116W	probably damaging	Het
Adamts10	C	A	17: 33,764,364 (GRCm39)	P663T	possibly damaging	Het
Akap12	G	A	10: 4,303,333 (GRCm39)	G48S	probably damaging	Het
Ankrd7	T	A	6: 18,870,030 (GRCm39)	M261K	probably benign	Het
Ankzf1	C	A	1: 75,174,948 (GRCm39)	D599E	possibly damaging	Het
Aox1	T	C	1: 58,144,173 (GRCm39)	I1278T	possibly damaging	Het
Apcdd1	T	C	18: 63,083,150 (GRCm39)	Y327H	probably benign	Het
Asxl3	T	A	18: 22,544,553 (GRCm39)		probably benign	Het
Birc6	C	A	17: 74,969,827 (GRCm39)		probably benign	Het
Btaf1	T	A	19: 36,987,048 (GRCm39)	L1714*	probably null	Het
Cacng6	T	A	7: 3,473,520 (GRCm39)		probably benign	Het
Cdc20b	A	G	13: 113,215,146 (GRCm39)	D238G	probably damaging	Het
Celf5	T	A	10: 81,306,532 (GRCm39)	R113W	probably null	Het
Cfap251	T	C	5: 123,421,510 (GRCm39)	V182A	probably damaging	Het
Cfap70	C	A	14: 20,462,415 (GRCm39)	E659D	probably damaging	Het
Clspn	T	A	4: 126,484,391 (GRCm39)	M1183K	possibly damaging	Het
Dpy19l1	G	A	9: 24,365,187 (GRCm39)	R275C	probably damaging	Het
Dst	C	T	1: 34,226,016 (GRCm39)	S1721L	probably benign	Het
Faap100	T	C	11: 120,265,191 (GRCm39)	T562A	probably damaging	Het
Fam168b	T	C	1: 34,858,769 (GRCm39)	M133V	probably damaging	Het
Farp2	T	C	1: 93,496,809 (GRCm39)	I172T	probably damaging	Het
Fer	T	G	17: 64,203,273 (GRCm39)	S68A	probably damaging	Het
Fmo5	A	G	3: 97,552,997 (GRCm39)	E315G	probably damaging	Het
Gpr89	A	T	3: 96,778,796 (GRCm39)	F426I	probably damaging	Het
Hinfp	T	C	9: 44,207,624 (GRCm39)	I461V	possibly damaging	Het
Hsd11b1	A	T	1: 192,922,556 (GRCm39)	V167D	probably damaging	Het
Htt	A	G	5: 35,054,252 (GRCm39)	K2574E	probably benign	Het
I830077J02Rik	A	G	3: 105,833,821 (GRCm39)	S112P	probably benign	Het
Igf2bp3	T	A	6: 49,082,551 (GRCm39)	M344L	probably benign	Het
Itch	A	T	2: 155,044,177 (GRCm39)	Q494L	probably benign	Het
Itga9	T	C	9: 118,598,321 (GRCm39)		probably benign	Het
Jaml	T	A	9: 45,005,065 (GRCm39)	D152E	probably benign	Het
Kif22	A	C	7: 126,641,572 (GRCm39)	M1R	probably null	Het
Kifap3	T	C	1: 163,710,955 (GRCm39)	Y663H	probably benign	Het
Letm2	T	A	8: 26,068,786 (GRCm39)	N472I	probably damaging	Het
Mthfr	T	G	4: 148,136,681 (GRCm39)	V446G	probably damaging	Het
Myh11	T	C	16: 14,029,124 (GRCm39)	E1206G	possibly damaging	Het
Myo6	G	A	9: 80,195,338 (GRCm39)	V903I	probably damaging	Het
Myo9b	C	T	8: 71,807,869 (GRCm39)		probably benign	Het
Nr2f2	G	C	7: 70,009,923 (GRCm39)	P52R	probably damaging	Het
Nsd3	A	G	8: 26,173,273 (GRCm39)	N859S	probably benign	Het
Nucb2	C	A	7: 116,135,245 (GRCm39)	A384E	probably damaging	Het
Ogdhl	C	A	14: 32,063,994 (GRCm39)		probably null	Het
Or10al3	C	A	17: 38,011,949 (GRCm39)	C129*	probably null	Het
Or1e22	A	T	11: 73,377,401 (GRCm39)	L83Q	probably benign	Het
Or1i2	T	C	10: 78,447,705 (GRCm39)	T257A	probably benign	Het
Or4a74	G	A	2: 89,440,207 (GRCm39)	L80F	probably damaging	Het
Or5b105	G	A	19: 13,080,642 (GRCm39)	R3C	possibly damaging	Het
Parp10	C	T	15: 76,126,833 (GRCm39)	S145N	probably benign	Het
Pigh	A	G	12: 79,130,483 (GRCm39)		probably benign	Het
Pigo	A	G	4: 43,023,824 (GRCm39)		probably benign	Het
Pkp4	T	A	2: 59,135,832 (GRCm39)	V199D	possibly damaging	Het
Polr1e	C	A	4: 45,025,143 (GRCm39)		probably null	Het
Ppfia3	C	A	7: 44,997,958 (GRCm39)	R723L	probably damaging	Het
Prex1	C	A	2: 166,427,818 (GRCm39)	A945S	possibly damaging	Het
Prrt3	A	T	6: 113,472,801 (GRCm39)	V457E	probably damaging	Het
Rab39	A	G	9: 53,617,271 (GRCm39)	F49L	possibly damaging	Het
Rrs1	C	A	1: 9,615,987 (GRCm39)		probably null	Het
Rrs1	G	A	1: 9,615,992 (GRCm39)	E82K	probably damaging	Het
Serpinb3c	T	C	1: 107,204,722 (GRCm39)	D8G	probably benign	Het
Slc17a6	A	G	7: 51,295,928 (GRCm39)		probably benign	Het
Slc24a4	T	A	12: 102,195,210 (GRCm39)		probably null	Het
Smc1b	C	T	15: 85,007,960 (GRCm39)	M272I	probably benign	Het
Smc6	T	C	12: 11,333,179 (GRCm39)		probably benign	Het
Tcf20	T	C	15: 82,739,286 (GRCm39)	T722A	probably benign	Het
Tesmin	A	T	19: 3,454,088 (GRCm39)	M141L	probably benign	Het
Tmprss5	T	A	9: 49,024,460 (GRCm39)	H274Q	possibly damaging	Het
Tns1	C	T	1: 73,976,477 (GRCm39)		probably null	Het
Tpr	T	C	1: 150,293,178 (GRCm39)	S868P	possibly damaging	Het
Trank1	C	T	9: 111,195,321 (GRCm39)	T1115I	probably damaging	Het
Trmt44	A	T	5: 35,730,261 (GRCm39)	I203K	possibly damaging	Het
Ulk2	A	T	11: 61,668,611 (GRCm39)	V1037E	probably benign	Het
Usp43	A	G	11: 67,767,325 (GRCm39)	Y682H	probably damaging	Het
Vipr2	A	T	12: 116,106,502 (GRCm39)	Q366L	probably damaging	Het
Vmn1r185	C	A	7: 26,311,014 (GRCm39)	V164L	possibly damaging	Het
Vmn2r120	C	T	17: 57,832,052 (GRCm39)	V246I	probably benign	Het
Wiz	C	T	17: 32,576,007 (GRCm39)	G790R	probably damaging	Het
Wnk1	A	T	6: 119,929,694 (GRCm39)	S1016R	probably damaging	Het
Zc3hav1	A	G	6: 38,288,109 (GRCm39)	L909S	probably benign	Het
Zfp236	T	A	18: 82,658,352 (GRCm39)	I637F	probably damaging	Het
Zfp788	G	A	7: 41,299,020 (GRCm39)	G532D	probably damaging	Het

Other mutations in Zranb1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00499:Zranb1	APN	7	132,584,233 (GRCm39)	splice site	probably benign
IGL00843:Zranb1	APN	7	132,551,622 (GRCm39)	missense	probably benign	0.26
IGL01727:Zranb1	APN	7	132,568,349 (GRCm39)	missense	probably damaging	1.00
IGL02087:Zranb1	APN	7	132,575,146 (GRCm39)	splice site	probably benign
IGL02676:Zranb1	APN	7	132,568,410 (GRCm39)	missense	probably benign	0.16
IGL03081:Zranb1	APN	7	132,552,126 (GRCm39)	missense	probably damaging	0.99
IGL03095:Zranb1	APN	7	132,551,635 (GRCm39)	nonsense	probably null
IGL03186:Zranb1	APN	7	132,551,932 (GRCm39)	missense	possibly damaging	0.68
PIT4151001:Zranb1	UTSW	7	132,551,723 (GRCm39)	missense	probably benign
R0470:Zranb1	UTSW	7	132,584,500 (GRCm39)	missense	probably damaging	1.00
R0854:Zranb1	UTSW	7	132,551,577 (GRCm39)	missense	possibly damaging	0.78
R1318:Zranb1	UTSW	7	132,568,281 (GRCm39)	nonsense	probably null
R1389:Zranb1	UTSW	7	132,573,062 (GRCm39)	missense	probably damaging	1.00
R1480:Zranb1	UTSW	7	132,551,745 (GRCm39)	missense	probably benign	0.39
R1656:Zranb1	UTSW	7	132,551,496 (GRCm39)	missense	probably benign	0.31
R1956:Zranb1	UTSW	7	132,584,458 (GRCm39)	missense	probably damaging	1.00
R1958:Zranb1	UTSW	7	132,584,458 (GRCm39)	missense	probably damaging	1.00
R2010:Zranb1	UTSW	7	132,568,425 (GRCm39)	critical splice donor site	probably null
R2289:Zranb1	UTSW	7	132,551,768 (GRCm39)	missense	probably damaging	1.00
R3831:Zranb1	UTSW	7	132,584,505 (GRCm39)	missense	probably damaging	0.98
R4128:Zranb1	UTSW	7	132,568,281 (GRCm39)	nonsense	probably null
R4745:Zranb1	UTSW	7	132,574,443 (GRCm39)	missense	probably damaging	0.97
R5121:Zranb1	UTSW	7	132,551,916 (GRCm39)	missense	probably benign	0.06
R5262:Zranb1	UTSW	7	132,584,556 (GRCm39)	small insertion	probably benign
R5263:Zranb1	UTSW	7	132,584,556 (GRCm39)	small insertion	probably benign
R5264:Zranb1	UTSW	7	132,584,556 (GRCm39)	small insertion	probably benign
R5522:Zranb1	UTSW	7	132,585,678 (GRCm39)	makesense	probably null
R6252:Zranb1	UTSW	7	132,585,633 (GRCm39)	missense	probably benign	0.00
R6519:Zranb1	UTSW	7	132,551,857 (GRCm39)	nonsense	probably null
R6671:Zranb1	UTSW	7	132,573,042 (GRCm39)	missense	probably damaging	1.00
R6827:Zranb1	UTSW	7	132,551,474 (GRCm39)	missense	probably benign	0.17
R6928:Zranb1	UTSW	7	132,568,323 (GRCm39)	missense	possibly damaging	0.65
R7313:Zranb1	UTSW	7	132,584,481 (GRCm39)	missense	probably damaging	1.00
R7583:Zranb1	UTSW	7	132,585,625 (GRCm39)	missense	probably benign	0.00
R8181:Zranb1	UTSW	7	132,585,508 (GRCm39)	missense	probably damaging	1.00
R8236:Zranb1	UTSW	7	132,551,393 (GRCm39)	missense	probably damaging	0.99
R8463:Zranb1	UTSW	7	132,551,810 (GRCm39)	missense	possibly damaging	0.68
R9006:Zranb1	UTSW	7	132,572,909 (GRCm39)	splice site	probably benign
R9103:Zranb1	UTSW	7	132,584,167 (GRCm39)	missense	probably damaging	0.96
R9134:Zranb1	UTSW	7	132,551,886 (GRCm39)	missense	probably benign	0.00
R9229:Zranb1	UTSW	7	132,583,117 (GRCm39)	missense	probably damaging	0.98
R9244:Zranb1	UTSW	7	132,585,640 (GRCm39)	missense	probably damaging	1.00
R9417:Zranb1	UTSW	7	132,585,466 (GRCm39)	missense	probably damaging	1.00
R9596:Zranb1	UTSW	7	132,552,146 (GRCm39)	missense	probably benign	0.32
R9708:Zranb1	UTSW	7	132,584,600 (GRCm39)	nonsense	probably null

Predicted Primers

PCR Primer
(F):5'- TGAATACAAGGACCCAGCATTGGAC -3'
(R):5'- TTGGTACAAGGCAGACAAGGTCAC -3'

Sequencing Primer
(F):5'- GTTTGCACATATGAAAACTGGGC -3'
(R):5'- GGTCACAGATACAGAACTTTATGC -3'

Posted On

2013-05-09