Mutagenetix > Incidental Mutation

Incidental Mutation 'R5742:Zranb2'

445601

Institutional Source

Beutler Lab

Gene Symbol

Zranb2

Ensembl Gene

ENSMUSG00000028180

Gene Name

zinc finger, RAN-binding domain containing 2

Synonyms

Zfp265, Zis, Znf265

MMRRC Submission

043352-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R5742 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

157239797-157254047 bp(+) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

T to A at 157246340 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Stop codon at position 17 (Y17*)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000029831] [ENSMUST00000106057] [ENSMUST00000106058] [ENSMUST00000184802] [ENSMUST00000198915]

AlphaFold

Q9R020

Predicted Effect

probably null
Transcript: ENSMUST00000029831
AA Change: Y87*

SMART Domains

Protein: ENSMUSP00000029831
Gene: ENSMUSG00000028180
AA Change: Y87*

Domain	Start	End	E-Value	Type
ZnF_RBZ	11	35	1.02e-2	SMART
ZnF_RBZ	36	54	2.09e-1	SMART
low complexity region	70	82	N/A	INTRINSIC
low complexity region	108	145	N/A	INTRINSIC
low complexity region	156	293	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000083497

Predicted Effect

probably null
Transcript: ENSMUST00000106057
AA Change: Y124*

SMART Domains

Protein: ENSMUSP00000101672
Gene: ENSMUSG00000028180
AA Change: Y124*

Domain	Start	End	E-Value	Type
ZnF_RBZ	11	37	1.24e-6	SMART
ZnF_RBZ	77	101	3.11e-7	SMART
low complexity region	117	129	N/A	INTRINSIC
low complexity region	155	192	N/A	INTRINSIC
low complexity region	203	312	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000106058
AA Change: Y124*

SMART Domains

Protein: ENSMUSP00000101673
Gene: ENSMUSG00000028180
AA Change: Y124*

Domain	Start	End	E-Value	Type
ZnF_RBZ	11	37	1.24e-6	SMART
ZnF_RBZ	77	101	3.11e-7	SMART
low complexity region	117	129	N/A	INTRINSIC
low complexity region	155	192	N/A	INTRINSIC
low complexity region	203	340	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000106063
AA Change: Y17*

SMART Domains

Protein: ENSMUSP00000101678
Gene: ENSMUSG00000028180
AA Change: Y17*

Domain	Start	End	E-Value	Type
ZnF_RBZ	11	37	8.79e-7	SMART
ZnF_RBZ	67	91	3.11e-7	SMART
low complexity region	107	119	N/A	INTRINSIC
low complexity region	145	182	N/A	INTRINSIC
low complexity region	193	330	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000152882

Predicted Effect

probably benign
Transcript: ENSMUST00000184802

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000196900

Predicted Effect

probably benign
Transcript: ENSMUST00000198915

Coding Region Coverage

1x: 99.3%
3x: 98.8%
10x: 97.5%
20x: 95.8%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 48 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4933427D14Rik	C	T	11: 72,056,379 (GRCm39)	A794T	possibly damaging	Het
Abca9	T	G	11: 110,051,243 (GRCm39)	E151A	probably damaging	Het
Abcb5	A	G	12: 118,881,992 (GRCm39)	V579A	probably damaging	Het
Apob	T	A	12: 8,057,191 (GRCm39)	L1858Q	probably damaging	Het
Cerk	C	T	15: 86,025,773 (GRCm39)	E223K	probably damaging	Het
Cntnap2	T	A	6: 45,897,860 (GRCm39)	Y179*	probably null	Het
Ddx60	A	T	8: 62,401,955 (GRCm39)	Y277F	probably benign	Het
Dlgap1	T	G	17: 71,025,194 (GRCm39)	V538G	probably benign	Het
Duox2	A	G	2: 122,115,402 (GRCm39)	I1050T	probably benign	Het
Dusp10	A	G	1: 183,769,853 (GRCm39)		probably null	Het
Dync2h1	T	A	9: 7,165,762 (GRCm39)	I500F	possibly damaging	Het
Erich3	T	A	3: 154,438,960 (GRCm39)	C398S	probably damaging	Het
Fez1	G	A	9: 36,761,743 (GRCm39)		probably null	Het
Fkbp3	A	C	12: 65,116,812 (GRCm39)	H41Q	probably benign	Het
Fras1	C	G	5: 96,916,240 (GRCm39)	Q3425E	possibly damaging	Het
Fuca1	T	C	4: 135,650,286 (GRCm39)	V119A	probably damaging	Het
Grhl2	A	G	15: 37,328,616 (GRCm39)	K414R	probably damaging	Het
Heatr5a	A	T	12: 52,002,335 (GRCm39)	C200*	probably null	Het
Hmgcs2	A	G	3: 98,204,832 (GRCm39)	N330S	probably benign	Het
Hspd1	A	G	1: 55,123,766 (GRCm39)	V118A	probably benign	Het
Jmjd1c	A	G	10: 67,056,112 (GRCm39)	T511A	probably benign	Het
Kat6b	T	C	14: 21,718,503 (GRCm39)	S1061P	probably damaging	Het
Kcnh6	T	C	11: 105,899,968 (GRCm39)	V79A	probably benign	Het
Kel	C	T	6: 41,675,961 (GRCm39)	G243E	probably damaging	Het
Klc4	C	T	17: 46,953,197 (GRCm39)	R111Q	probably damaging	Het
Lrp1	T	C	10: 127,384,216 (GRCm39)	D3641G	probably damaging	Het
Map2k1	A	T	9: 64,101,053 (GRCm39)	D208E	probably damaging	Het
Masp1	T	A	16: 23,273,675 (GRCm39)	M588L	probably benign	Het
Mgl2	T	A	11: 70,027,510 (GRCm39)	N239K	probably benign	Het
Mki67	G	A	7: 135,306,102 (GRCm39)	T625M	probably benign	Het
Ndufb5	T	C	3: 32,801,930 (GRCm39)	Y112H	probably damaging	Het
Npr3	A	G	15: 11,883,494 (GRCm39)	S312P	probably damaging	Het
Nuf2	A	T	1: 169,344,191 (GRCm39)	I125N	probably damaging	Het
Obox1	G	A	7: 15,289,430 (GRCm39)	G73D	possibly damaging	Het
Odad4	G	A	11: 100,436,699 (GRCm39)	G25R	possibly damaging	Het
Or51a43	G	T	7: 103,717,412 (GRCm39)	H275Q	probably damaging	Het
Or8g19	T	A	9: 39,055,974 (GRCm39)	F193I	probably benign	Het
Pcdhb15	T	C	18: 37,607,820 (GRCm39)	S351P	probably damaging	Het
Phc2	G	T	4: 128,639,661 (GRCm39)	R121L	probably damaging	Het
Pla2g2a	A	G	4: 138,560,653 (GRCm39)	K87E	probably benign	Het
Plekhh2	T	A	17: 84,905,408 (GRCm39)	S1101T	probably damaging	Het
Ppp4r1	T	C	17: 66,144,741 (GRCm39)	I786T	probably damaging	Het
Prxl2a	T	C	14: 40,724,460 (GRCm39)	E57G	possibly damaging	Het
Ros1	A	T	10: 52,018,234 (GRCm39)		probably null	Het
Styxl2	A	T	1: 165,927,023 (GRCm39)	V863E	probably benign	Het
Trnt1	T	A	6: 106,755,878 (GRCm39)	L311*	probably null	Het
Vmn1r47	T	A	6: 89,999,500 (GRCm39)	L211M	probably damaging	Het
Zfp12	A	G	5: 143,230,945 (GRCm39)	E424G	probably damaging	Het

Other mutations in Zranb2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01115:Zranb2	APN	3	157,252,328 (GRCm39)	unclassified	probably benign
IGL01528:Zranb2	APN	3	157,250,602 (GRCm39)	unclassified	probably benign
IGL03008:Zranb2	APN	3	157,252,302 (GRCm39)	splice site	probably null
R0528:Zranb2	UTSW	3	157,240,096 (GRCm39)	missense	probably benign	0.26
R0659:Zranb2	UTSW	3	157,247,400 (GRCm39)	missense	probably benign	0.23
R1170:Zranb2	UTSW	3	157,247,502 (GRCm39)	utr 3 prime	probably benign
R1673:Zranb2	UTSW	3	157,243,277 (GRCm39)	missense	probably damaging	1.00
R1885:Zranb2	UTSW	3	157,248,793 (GRCm39)	critical splice acceptor site	probably null
R4127:Zranb2	UTSW	3	157,243,227 (GRCm39)	nonsense	probably null
R4610:Zranb2	UTSW	3	157,247,521 (GRCm39)	splice site	probably benign
R4981:Zranb2	UTSW	3	157,252,378 (GRCm39)	unclassified	probably benign
R5053:Zranb2	UTSW	3	157,246,796 (GRCm39)	missense	probably damaging	0.96
R5873:Zranb2	UTSW	3	157,242,020 (GRCm39)	nonsense	probably null
R6086:Zranb2	UTSW	3	157,248,883 (GRCm39)	critical splice donor site	probably null
R7015:Zranb2	UTSW	3	157,242,370 (GRCm39)	critical splice acceptor site	probably null
R7547:Zranb2	UTSW	3	157,246,806 (GRCm39)	missense	possibly damaging	0.93
R7579:Zranb2	UTSW	3	157,246,309 (GRCm39)	missense	probably damaging	1.00
R8119:Zranb2	UTSW	3	157,241,969 (GRCm39)	critical splice acceptor site	probably null
R8237:Zranb2	UTSW	3	157,250,677 (GRCm39)	missense	probably null
R8296:Zranb2	UTSW	3	157,247,412 (GRCm39)	missense	unknown
R8345:Zranb2	UTSW	3	157,251,731 (GRCm39)	missense	unknown
R8414:Zranb2	UTSW	3	157,252,312 (GRCm39)	missense	unknown
R8478:Zranb2	UTSW	3	157,251,745 (GRCm39)	makesense	probably null
R8768:Zranb2	UTSW	3	157,247,327 (GRCm39)	splice site	probably benign
R9021:Zranb2	UTSW	3	157,250,720 (GRCm39)	missense	unknown

Predicted Primers

PCR Primer
(F):5'- GTAATTAGTTACGTGAATGACCACC -3'
(R):5'- AGATGGAGGATTTTCCCACTG -3'

Sequencing Primer
(F):5'- CGTGAATGACCACCATTTATTAGATC -3'
(R):5'- CCAGCCAATGGTTGAATTATAGGCTC -3'

Posted On

2016-11-21