Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL00901:Tnks'

27986

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Tnks

Ensembl Gene

ENSMUSG00000031529

Gene Name

tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase

Synonyms

mTNKS1, 4930554K12Rik, D130072O21Rik, TANK1, tankyrase 1

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

IGL00901

Quality Score

Status

Chromosome

Chromosomal Location

34826460-34965690 bp(-) (GRCm38)

Type of Mutation

nonsense

DNA Base Change (assembly)

A to T at 34838395 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Stop codon at position 92 (Y92*)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000033929]

AlphaFold

Q6PFX9

Predicted Effect

probably null
Transcript: ENSMUST00000033929
AA Change: Y1236*

SMART Domains

Protein: ENSMUSP00000033929
Gene: ENSMUSG00000031529
AA Change: Y1236*

Domain	Start	End	E-Value	Type
low complexity region	8	17	N/A	INTRINSIC
low complexity region	20	55	N/A	INTRINSIC
low complexity region	68	86	N/A	INTRINSIC
low complexity region	91	175	N/A	INTRINSIC
ANK	208	237	4.26e-4	SMART
ANK	241	270	3.23e-4	SMART
ANK	274	303	3.28e-5	SMART
ANK	327	355	2.66e3	SMART
ANK	361	390	7.64e-6	SMART
ANK	394	423	2.62e-4	SMART
ANK	427	456	1.99e-4	SMART
ANK	514	546	3.18e-3	SMART
ANK	550	579	1.51e-4	SMART
ANK	583	612	4.26e-4	SMART
ANK	642	670	2.21e3	SMART
ANK	676	705	4.03e-5	SMART
ANK	709	738	2.48e-5	SMART
ANK	742	771	1.64e-5	SMART
low complexity region	792	810	N/A	INTRINSIC
ANK	829	858	1.47e-7	SMART
ANK	862	891	2.21e-2	SMART
ANK	895	924	3.13e-2	SMART
low complexity region	996	1010	N/A	INTRINSIC
SAM	1017	1082	1.14e-12	SMART
Pfam:PARP	1098	1303	1.5e-28	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000209632
AA Change: Y42*

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000209904

Predicted Effect

probably null
Transcript: ENSMUST00000210014
AA Change: Y92*

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000210870

Coding Region Coverage

Validation Efficiency

MGI Phenotype

PHENOTYPE: Mice homozygous for a null allele fail to exhibit any abonormalities. Male mice homozygous for a gene trapped allele exhibit decreased fat pad weight, increased metabolism, hyperinsulinemia, and hypoglycemia. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 31 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930432K21Rik	A	G	8: 84,166,771 (GRCm38)	D189G	probably damaging	Het
Acot6	A	G	12: 84,106,476 (GRCm38)	Y164C	probably benign	Het
Anpep	A	G	7: 79,839,423 (GRCm38)	S334P	probably benign	Het
Arhgef1	A	G	7: 24,912,693 (GRCm38)	E129G	probably damaging	Het
Bmt2	G	T	6: 13,628,749 (GRCm38)	H312N	probably damaging	Het
Ces2g	A	G	8: 104,965,129 (GRCm38)	Y272C	probably benign	Het
Cfap69	T	A	5: 5,619,162 (GRCm38)		probably benign	Het
Cftr	T	C	6: 18,268,430 (GRCm38)		probably null	Het
Clec2g	A	G	6: 128,948,692 (GRCm38)		probably benign	Het
Cyp2b9	A	T	7: 26,198,505 (GRCm38)	I245F	probably damaging	Het
Fbxo6	T	A	4: 148,146,143 (GRCm38)	I221F	probably damaging	Het
Fbxw21	A	C	9: 109,156,399 (GRCm38)	C104G	probably benign	Het
Flna	A	G	X: 74,229,928 (GRCm38)	S101P	probably damaging	Het
Hnrnpm	C	A	17: 33,649,902 (GRCm38)	R517L	probably damaging	Het
Ift88	T	A	14: 57,444,445 (GRCm38)	F229I	probably damaging	Het
Map2k3	T	C	11: 60,941,921 (GRCm38)	S31P	probably benign	Het
Mia2	A	G	12: 59,108,029 (GRCm38)	D176G	probably damaging	Het
Olfr102	T	G	17: 37,313,707 (GRCm38)	K226Q	possibly damaging	Het
Olfr1145	A	G	2: 87,810,648 (GRCm38)	Y276C	probably damaging	Het
Olfr127	T	A	17: 37,904,257 (GRCm38)	V237D	probably damaging	Het
Pde7b	C	T	10: 20,619,129 (GRCm38)		probably null	Het
Polr3b	T	C	10: 84,631,796 (GRCm38)	I80T	possibly damaging	Het
Prpf4b	T	A	13: 34,894,482 (GRCm38)	Y692N	probably damaging	Het
Rabl2	T	C	15: 89,590,270 (GRCm38)		probably benign	Het
Rasgrp1	T	C	2: 117,285,130 (GRCm38)	K659R	probably damaging	Het
Ryr3	A	T	2: 112,886,589 (GRCm38)	S774T	probably damaging	Het
Sema5b	C	T	16: 35,651,315 (GRCm38)	T426M	probably damaging	Het
Serpinb10	A	G	1: 107,540,996 (GRCm38)	K123R	probably benign	Het
Slc33a1	T	C	3: 63,964,012 (GRCm38)	D60G	probably benign	Het
Tvp23b	T	A	11: 62,883,780 (GRCm38)		probably benign	Het
Wnk1	T	A	6: 119,960,708 (GRCm38)	Q1218L	probably damaging	Het

Other mutations in Tnks

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00498:Tnks	APN	8	34,861,689 (GRCm38)	splice site	probably benign
IGL01448:Tnks	APN	8	34,839,982 (GRCm38)	missense	probably damaging	1.00
IGL01455:Tnks	APN	8	34,940,900 (GRCm38)	missense	probably damaging	0.99
IGL01962:Tnks	APN	8	34,869,524 (GRCm38)	missense	probably damaging	1.00
IGL02088:Tnks	APN	8	34,839,994 (GRCm38)	missense	possibly damaging	0.50
IGL02260:Tnks	APN	8	34,842,983 (GRCm38)	missense	probably damaging	0.99
IGL02454:Tnks	APN	8	34,831,728 (GRCm38)	unclassified	probably benign
IGL02486:Tnks	APN	8	34,851,198 (GRCm38)	missense	probably damaging	1.00
IGL02612:Tnks	APN	8	34,849,299 (GRCm38)	missense	possibly damaging	0.48
IGL03179:Tnks	APN	8	34,848,670 (GRCm38)	missense	probably benign	0.38
IGL03404:Tnks	APN	8	34,940,704 (GRCm38)	missense	probably damaging	1.00
R0256:Tnks	UTSW	8	34,861,547 (GRCm38)	missense	probably benign	0.07
R0265:Tnks	UTSW	8	34,839,970 (GRCm38)	nonsense	probably null
R0334:Tnks	UTSW	8	34,853,259 (GRCm38)	nonsense	probably null
R0414:Tnks	UTSW	8	34,853,309 (GRCm38)	missense	probably damaging	1.00
R0526:Tnks	UTSW	8	34,853,303 (GRCm38)	missense	probably benign	0.23
R0622:Tnks	UTSW	8	34,940,822 (GRCm38)	missense	probably damaging	1.00
R1445:Tnks	UTSW	8	34,834,603 (GRCm38)	splice site	probably benign
R1618:Tnks	UTSW	8	34,875,276 (GRCm38)	missense	probably damaging	1.00
R1779:Tnks	UTSW	8	34,857,518 (GRCm38)	missense	probably benign	0.18
R1919:Tnks	UTSW	8	34,875,232 (GRCm38)	missense	probably damaging	1.00
R1938:Tnks	UTSW	8	34,838,530 (GRCm38)	missense	probably damaging	1.00
R2018:Tnks	UTSW	8	34,851,106 (GRCm38)	missense	probably damaging	1.00
R2198:Tnks	UTSW	8	34,873,067 (GRCm38)	missense	probably benign	0.29
R2198:Tnks	UTSW	8	34,848,649 (GRCm38)	missense	probably benign
R2925:Tnks	UTSW	8	34,965,661 (GRCm38)	missense	unknown
R3828:Tnks	UTSW	8	34,873,178 (GRCm38)	missense	probably damaging	1.00
R3913:Tnks	UTSW	8	34,873,074 (GRCm38)	missense	probably damaging	0.99
R3916:Tnks	UTSW	8	34,853,361 (GRCm38)	missense	probably damaging	1.00
R3917:Tnks	UTSW	8	34,853,361 (GRCm38)	missense	probably damaging	1.00
R3930:Tnks	UTSW	8	34,940,812 (GRCm38)	missense	probably damaging	1.00
R4659:Tnks	UTSW	8	34,849,311 (GRCm38)	missense	possibly damaging	0.53
R4760:Tnks	UTSW	8	34,851,783 (GRCm38)	missense	probably benign	0.38
R5091:Tnks	UTSW	8	34,841,809 (GRCm38)	missense	probably benign	0.40
R5419:Tnks	UTSW	8	34,965,566 (GRCm38)	missense	unknown
R5558:Tnks	UTSW	8	34,965,665 (GRCm38)	start codon destroyed	probably null
R5582:Tnks	UTSW	8	34,940,861 (GRCm38)	missense	probably benign	0.14
R6035:Tnks	UTSW	8	34,918,461 (GRCm38)	missense	possibly damaging	0.93
R6035:Tnks	UTSW	8	34,918,461 (GRCm38)	missense	possibly damaging	0.93
R6495:Tnks	UTSW	8	34,839,966 (GRCm38)	critical splice donor site	probably null
R6527:Tnks	UTSW	8	34,873,093 (GRCm38)	missense	probably benign	0.36
R6991:Tnks	UTSW	8	34,834,493 (GRCm38)	missense	probably damaging	1.00
R7015:Tnks	UTSW	8	34,838,547 (GRCm38)	missense	probably benign	0.04
R7038:Tnks	UTSW	8	34,851,636 (GRCm38)	missense	probably damaging	0.99
R7057:Tnks	UTSW	8	34,840,014 (GRCm38)	missense	probably damaging	1.00
R7167:Tnks	UTSW	8	34,849,304 (GRCm38)	missense	probably damaging	0.98
R7250:Tnks	UTSW	8	34,851,758 (GRCm38)	missense	probably damaging	0.98
R7475:Tnks	UTSW	8	34,831,712 (GRCm38)	missense	probably damaging	1.00
R7790:Tnks	UTSW	8	34,861,540 (GRCm38)	missense	probably benign	0.01
R7818:Tnks	UTSW	8	34,873,028 (GRCm38)	missense	probably benign	0.03
R7909:Tnks	UTSW	8	34,940,704 (GRCm38)	missense	probably damaging	1.00
R7970:Tnks	UTSW	8	34,855,926 (GRCm38)	critical splice donor site	probably null
R8341:Tnks	UTSW	8	34,873,045 (GRCm38)	missense	probably damaging	1.00
R8343:Tnks	UTSW	8	34,834,584 (GRCm38)	missense	probably benign	0.03
R8870:Tnks	UTSW	8	34,847,279 (GRCm38)	critical splice donor site	probably null
R8936:Tnks	UTSW	8	34,853,347 (GRCm38)	nonsense	probably null
R9049:Tnks	UTSW	8	34,841,778 (GRCm38)	missense	probably damaging	0.96
R9080:Tnks	UTSW	8	34,965,312 (GRCm38)	small deletion	probably benign
R9182:Tnks	UTSW	8	34,841,751 (GRCm38)	critical splice donor site	probably null
R9211:Tnks	UTSW	8	34,849,335 (GRCm38)	missense	probably damaging	1.00
R9425:Tnks	UTSW	8	34,873,665 (GRCm38)	missense	probably damaging	1.00
R9649:Tnks	UTSW	8	34,838,935 (GRCm38)	missense	probably damaging	0.96
Z1177:Tnks	UTSW	8	34,965,145 (GRCm38)	missense	probably benign	0.04

Posted On

2013-04-17