Mutagenetix > Incidental Mutation

Incidental Mutation 'R5995:Zfp980'

481053

Institutional Source

Beutler Lab

Gene Symbol

Zfp980

Ensembl Gene

ENSMUSG00000058186

Gene Name

zinc finger protein 980

Synonyms

Gm13242

MMRRC Submission

044174-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.300) question?

Stock #

R5995 (G1)

Quality Score

144.008

Status

Validated

Chromosome

Chromosomal Location

145397267-145431007 bp(+) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

A to T at 145428479 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Lysine to Stop codon at position 403 (K403*)

Ref Sequence

ENSEMBL: ENSMUSP00000137589 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000105738] [ENSMUST00000180014]

AlphaFold

A2A9J5

Predicted Effect

probably null
Transcript: ENSMUST00000105738
AA Change: K403*

SMART Domains

Protein: ENSMUSP00000101364
Gene: ENSMUSG00000058186
AA Change: K403*

Domain	Start	End	E-Value	Type
KRAB	28	90	1.46e-16	SMART
low complexity region	235	246	N/A	INTRINSIC
ZnF_C2H2	251	273	1.84e-4	SMART
ZnF_C2H2	279	301	3.49e-5	SMART
ZnF_C2H2	307	329	1.95e-3	SMART
ZnF_C2H2	335	357	5.67e-5	SMART
ZnF_C2H2	363	385	1.98e-4	SMART
ZnF_C2H2	391	413	1.98e-4	SMART
ZnF_C2H2	419	441	2.4e-3	SMART
ZnF_C2H2	447	469	1.22e-4	SMART
ZnF_C2H2	475	497	5.67e-5	SMART
ZnF_C2H2	503	525	1.98e-4	SMART
ZnF_C2H2	531	553	6.88e-4	SMART
ZnF_C2H2	559	581	1.58e-3	SMART
ZnF_C2H2	587	609	1.22e-4	SMART
ZnF_C2H2	615	635	1.26e1	SMART

Predicted Effect

probably null
Transcript: ENSMUST00000180014
AA Change: K403*

SMART Domains

Protein: ENSMUSP00000137589
Gene: ENSMUSG00000058186
AA Change: K403*

Domain	Start	End	E-Value	Type
KRAB	28	90	1.46e-16	SMART
low complexity region	235	246	N/A	INTRINSIC
ZnF_C2H2	251	273	1.84e-4	SMART
ZnF_C2H2	279	301	3.49e-5	SMART
ZnF_C2H2	307	329	1.95e-3	SMART
ZnF_C2H2	335	357	5.67e-5	SMART
ZnF_C2H2	363	385	1.98e-4	SMART
ZnF_C2H2	391	413	1.98e-4	SMART
ZnF_C2H2	419	441	2.4e-3	SMART
ZnF_C2H2	447	469	1.22e-4	SMART
ZnF_C2H2	475	497	5.67e-5	SMART
ZnF_C2H2	503	525	1.98e-4	SMART
ZnF_C2H2	531	553	6.88e-4	SMART
ZnF_C2H2	559	581	1.58e-3	SMART
ZnF_C2H2	587	609	1.22e-4	SMART
ZnF_C2H2	615	635	1.26e1	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000180968

Meta Mutation Damage Score

0.9755

Coding Region Coverage

1x: 99.9%
3x: 99.5%
10x: 97.4%
20x: 91.7%

Validation Efficiency

100% (56/56)

Allele List at MGI

Other mutations in this stock

Total: 55 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcb8	C	T	5: 24,605,137 (GRCm39)	R108C	possibly damaging	Het
Adgrb2	C	A	4: 129,910,896 (GRCm39)	A1104E	probably damaging	Het
Adgrv1	A	G	13: 81,614,378 (GRCm39)	V4005A	probably benign	Het
Bend6	T	C	1: 33,917,520 (GRCm39)		probably null	Het
Brwd1	A	T	16: 95,865,987 (GRCm39)	V265E	probably damaging	Het
Ccdc96	A	G	5: 36,643,718 (GRCm39)	I575V	probably damaging	Het
Cd109	A	T	9: 78,607,561 (GRCm39)	I1094L	probably benign	Het
Cd44	A	G	2: 102,692,015 (GRCm39)	V91A	probably damaging	Het
Cdv3	C	G	9: 103,241,202 (GRCm39)	G122R	probably damaging	Het
Ces2c	T	A	8: 105,577,533 (GRCm39)	V272D	possibly damaging	Het
Colgalt1	T	A	8: 72,075,754 (GRCm39)	M467K	probably damaging	Het
Crtam	G	A	9: 40,905,836 (GRCm39)	T31M	possibly damaging	Het
Cyp7a1	C	T	4: 6,272,371 (GRCm39)	V281M	possibly damaging	Het
Dnah7a	A	T	1: 53,659,829 (GRCm39)	N726K	probably benign	Het
Dok6	T	C	18: 89,439,142 (GRCm39)	E232G	possibly damaging	Het
Gm12185	T	C	11: 48,806,540 (GRCm39)	E217G	probably benign	Het
Gm7247	C	T	14: 51,601,805 (GRCm39)	S26F	probably benign	Het
Gria1	A	T	11: 57,180,111 (GRCm39)	Y618F	probably damaging	Het
H2-T22	A	G	17: 36,352,377 (GRCm39)	Y183H	probably benign	Het
Hace1	A	T	10: 45,546,487 (GRCm39)	I374L	probably benign	Het
Hif3a	T	A	7: 16,787,694 (GRCm39)	T132S	probably benign	Het
Hoxa3	T	A	6: 52,147,263 (GRCm39)		probably benign	Het
Il27	A	C	7: 126,188,535 (GRCm39)		probably benign	Het
Klhdc1	T	C	12: 69,297,548 (GRCm39)	Y40H	probably damaging	Het
Klhl33	T	G	14: 51,130,108 (GRCm39)	E462A	possibly damaging	Het
Myh10	T	C	11: 68,705,809 (GRCm39)	I1979T	probably benign	Het
Nfkbil1	G	T	17: 35,439,774 (GRCm39)	F246L	probably benign	Het
Nlrp1b	A	T	11: 71,072,572 (GRCm39)	F424I	probably damaging	Het
Nod1	A	G	6: 54,921,539 (GRCm39)	Y260H	probably damaging	Het
Ofcc1	A	G	13: 40,433,898 (GRCm39)	L69P	probably damaging	Het
Onecut2	G	T	18: 64,474,619 (GRCm39)	R390L	probably damaging	Het
Oprm1	A	C	10: 6,782,520 (GRCm39)	M388L	probably benign	Het
Or10q3	A	T	19: 11,848,226 (GRCm39)	I118N	possibly damaging	Het
Or1e26	T	C	11: 73,480,076 (GRCm39)	I163V	probably benign	Het
Or1o3	C	A	17: 37,574,539 (GRCm39)	Q5H	probably benign	Het
Or5aq1	T	C	2: 86,966,200 (GRCm39)	N155S	probably damaging	Het
Or5b96	A	C	19: 12,867,961 (GRCm39)		probably null	Het
Or8g53	A	G	9: 39,683,988 (GRCm39)	V36A	probably benign	Het
Pcdhgc5	T	A	18: 37,954,113 (GRCm39)	Y462*	probably null	Het
Pex1	T	A	5: 3,657,704 (GRCm39)	M425K	possibly damaging	Het
Plec	A	T	15: 76,070,105 (GRCm39)	Y1001N	probably damaging	Het
Poglut3	T	C	9: 53,307,195 (GRCm39)	Y380H	probably damaging	Het
Pou2f2	T	G	7: 24,796,869 (GRCm39)	K236Q	probably damaging	Het
Rbm20	G	A	19: 53,839,698 (GRCm39)	E896K	possibly damaging	Het
Sh3tc2	T	A	18: 62,123,081 (GRCm39)	L614Q	probably damaging	Het
Skint5	T	A	4: 113,751,029 (GRCm39)	I339F	unknown	Het
Slc2a7	T	C	4: 150,252,797 (GRCm39)	I479T	probably damaging	Het
Snrk	A	G	9: 121,986,288 (GRCm39)	N219S	probably damaging	Het
Supt20	T	C	3: 54,616,474 (GRCm39)	S245P	probably damaging	Het
Ttn	A	G	2: 76,591,636 (GRCm39)	I21011T	probably damaging	Het
Vmn2r11	T	A	5: 109,194,921 (GRCm39)	I802F	probably damaging	Het
Vmn2r92	T	C	17: 18,389,213 (GRCm39)		probably null	Het
Ythdc2	T	A	18: 45,019,320 (GRCm39)	M1363K	probably damaging	Het
Zan	T	C	5: 137,377,071 (GRCm39)		probably benign	Het
Zfp521	C	A	18: 13,850,681 (GRCm39)	C1261F	probably damaging	Het

Other mutations in Zfp980

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00828:Zfp980	APN	4	145,428,561 (GRCm39)	missense	probably benign	0.00
R0164:Zfp980	UTSW	4	145,428,567 (GRCm39)	missense	probably benign
R0164:Zfp980	UTSW	4	145,428,567 (GRCm39)	missense	probably benign
R1186:Zfp980	UTSW	4	145,428,653 (GRCm39)	missense	probably benign
R1761:Zfp980	UTSW	4	145,428,612 (GRCm39)	missense	probably damaging	1.00
R3726:Zfp980	UTSW	4	145,428,653 (GRCm39)	missense	probably benign
R4049:Zfp980	UTSW	4	145,429,170 (GRCm39)	missense	probably damaging	1.00
R4467:Zfp980	UTSW	4	145,428,653 (GRCm39)	missense	probably benign
R4610:Zfp980	UTSW	4	145,428,653 (GRCm39)	missense	probably benign
R4622:Zfp980	UTSW	4	145,428,627 (GRCm39)	missense	probably damaging	1.00
R4873:Zfp980	UTSW	4	145,428,653 (GRCm39)	missense	probably benign
R5008:Zfp980	UTSW	4	145,428,653 (GRCm39)	missense	probably benign
R5027:Zfp980	UTSW	4	145,428,653 (GRCm39)	missense	probably benign
R5497:Zfp980	UTSW	4	145,428,017 (GRCm39)	missense	probably damaging	1.00
R6125:Zfp980	UTSW	4	145,429,208 (GRCm39)	makesense	probably null
R7353:Zfp980	UTSW	4	145,428,714 (GRCm39)	missense	probably benign	0.06
R7675:Zfp980	UTSW	4	145,428,164 (GRCm39)	nonsense	probably null
R7939:Zfp980	UTSW	4	145,428,582 (GRCm39)	missense	probably damaging	1.00
R8833:Zfp980	UTSW	4	145,427,596 (GRCm39)	missense	probably benign	0.00
R9122:Zfp980	UTSW	4	145,428,834 (GRCm39)	missense	probably damaging	1.00
R9165:Zfp980	UTSW	4	145,428,024 (GRCm39)	missense	possibly damaging	0.95
R9361:Zfp980	UTSW	4	145,427,999 (GRCm39)	missense	probably benign	0.08
R9469:Zfp980	UTSW	4	145,427,687 (GRCm39)	missense	probably benign	0.14

Predicted Primers

PCR Primer
(F):5'- GTGACAAATGCTTTACTGACAAAGG -3'
(R):5'- AGCATTTGTCACATTCACTGCAT -3'

Sequencing Primer
(F):5'- GCTTTACTGACAAAGGCAGTCTG -3'
(R):5'- CTCAGACCGTTTTTCTCAGTAAAAC -3'

Posted On

2017-06-26