Mutagenetix > Incidental Mutation

Incidental Mutation 'R7030:Whrn'

568409

Institutional Source

Beutler Lab

Gene Symbol

Whrn

Ensembl Gene

ENSMUSG00000039137

Gene Name

whirlin

Synonyms

C430046P22Rik, Dfnb31, wi, 1110035G07Rik

MMRRC Submission

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7030 (G1)

Quality Score

78.0075

Status

Validated

Chromosome

Chromosomal Location

63414910-63495991 bp(-) (GRCm38)

Type of Mutation

unclassified

DNA Base Change (assembly)

G to T at 63495131 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000119280 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000063650] [ENSMUST00000063672] [ENSMUST00000084510] [ENSMUST00000095037] [ENSMUST00000095038] [ENSMUST00000102867] [ENSMUST00000107393] [ENSMUST00000119294] [ENSMUST00000133425]

AlphaFold

Q80VW5

Predicted Effect

unknown
Transcript: ENSMUST00000063650
AA Change: L35M

SMART Domains

Protein: ENSMUSP00000069664
Gene: ENSMUSG00000039137
AA Change: L35M

Domain	Start	End	E-Value	Type
low complexity region	3	38	N/A	INTRINSIC
low complexity region	126	137	N/A	INTRINSIC
PDZ	151	223	3.62e-21	SMART
PDZ	289	361	3.77e-19	SMART
low complexity region	522	541	N/A	INTRINSIC
low complexity region	629	642	N/A	INTRINSIC
PDZ	824	904	2.63e-9	SMART

Predicted Effect

unknown
Transcript: ENSMUST00000063672
AA Change: L35M

SMART Domains

Protein: ENSMUSP00000065838
Gene: ENSMUSG00000039137
AA Change: L35M

Domain	Start	End	E-Value	Type
low complexity region	3	38	N/A	INTRINSIC
low complexity region	126	137	N/A	INTRINSIC
PDZ	151	223	3.62e-21	SMART
PDZ	289	361	3.77e-19	SMART
low complexity region	522	541	N/A	INTRINSIC

Predicted Effect

unknown
Transcript: ENSMUST00000084510
AA Change: L35M

SMART Domains

Protein: ENSMUSP00000081557
Gene: ENSMUSG00000039137
AA Change: L35M

Domain	Start	End	E-Value	Type
low complexity region	3	38	N/A	INTRINSIC
low complexity region	126	137	N/A	INTRINSIC
PDZ	151	223	3.62e-21	SMART
PDZ	289	361	3.77e-19	SMART
low complexity region	522	541	N/A	INTRINSIC
low complexity region	640	653	N/A	INTRINSIC
PDZ	835	915	2.63e-9	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000095037

SMART Domains

Protein: ENSMUSP00000092647
Gene: ENSMUSG00000039137

Domain	Start	End	E-Value	Type
low complexity region	19	38	N/A	INTRINSIC
low complexity region	126	139	N/A	INTRINSIC
PDZ	321	401	2.63e-9	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000095038

SMART Domains

Protein: ENSMUSP00000092648
Gene: ENSMUSG00000039137

Domain	Start	End	E-Value	Type
low complexity region	80	99	N/A	INTRINSIC
low complexity region	198	211	N/A	INTRINSIC
PDZ	393	473	2.63e-9	SMART

Predicted Effect

unknown
Transcript: ENSMUST00000102867
AA Change: L35M

SMART Domains

Protein: ENSMUSP00000099931
Gene: ENSMUSG00000039137
AA Change: L35M

Domain	Start	End	E-Value	Type
low complexity region	3	38	N/A	INTRINSIC
low complexity region	126	137	N/A	INTRINSIC
PDZ	151	223	3.62e-21	SMART
PDZ	289	361	3.77e-19	SMART
low complexity region	522	541	N/A	INTRINSIC
low complexity region	629	642	N/A	INTRINSIC
PDZ	823	903	2.63e-9	SMART

Predicted Effect

unknown
Transcript: ENSMUST00000107393
AA Change: L35M

SMART Domains

Protein: ENSMUSP00000103016
Gene: ENSMUSG00000039137
AA Change: L35M

Domain	Start	End	E-Value	Type
low complexity region	3	38	N/A	INTRINSIC
low complexity region	126	137	N/A	INTRINSIC
PDZ	151	223	1.7e-23	SMART
PDZ	289	361	1.8e-21	SMART
low complexity region	526	545	N/A	INTRINSIC
low complexity region	633	646	N/A	INTRINSIC
PDZ	828	908	1.3e-11	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000119294

SMART Domains

Protein: ENSMUSP00000114030
Gene: ENSMUSG00000039137

Domain	Start	End	E-Value	Type
low complexity region	80	99	N/A	INTRINSIC
low complexity region	187	200	N/A	INTRINSIC
PDZ	382	462	2.63e-9	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000133425

SMART Domains

Protein: ENSMUSP00000119280
Gene: ENSMUSG00000039137

Domain	Start	End	E-Value	Type
PDZ	1	65	6.42e-13	SMART
internal_repeat_1	139	164	3.88e-7	PROSPERO

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 98.9%

Validation Efficiency

98% (92/94)

MGI Phenotype

FUNCTION: This gene encodes a protein required for elongation and actin polymerization in the hair cell stereocilia. The encoded protein is localized to the cytoplasm and co-localizes with the growing end of actin filaments. Mutations in this gene have been linked to deafness. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2013]
PHENOTYPE: Spontaneous mutants lacking both isoforms show short stereocilia, severe deafness and vestibular deficits. Targeted homozygotes lacking the long form show altered OHC stereocilia bundles but a milder phenotype with normal stereocilia in IHCs and a subset of vestibular HCs and no vestibular deficits. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 93 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abr	A	T	11: 76,459,212	I347N	probably damaging	Het
Acbd4	T	A	11: 103,104,159	L50Q	probably damaging	Het
Acsl5	T	G	19: 55,272,819	Y69*	probably null	Het
Agtpbp1	G	A	13: 59,504,294	T401I	probably damaging	Het
Ap3m2	C	T	8: 22,799,791	E99K	probably damaging	Het
Arhgef28	A	T	13: 97,988,261	S504R	possibly damaging	Het
Arsj	T	A	3: 126,439,103	D499E	probably damaging	Het
Bach1	G	A	16: 87,719,291	R240Q	probably benign	Het
Camk2b	T	C	11: 5,989,575	D232G	probably damaging	Het
Casc3	C	T	11: 98,822,533	P258S	possibly damaging	Het
Catspere2	T	A	1: 178,017,714	I100N	probably damaging	Het
Ccdc80	T	A	16: 45,122,889	N787K	possibly damaging	Het
Celsr1	C	A	15: 85,905,478	C2653F	probably damaging	Het
Cep170	T	C	1: 176,756,485	E11G	probably damaging	Het
Chia1	A	C	3: 106,115,325	N12H	probably damaging	Het
Chrna4	T	C	2: 181,029,541	T141A	probably damaging	Het
Col25a1	T	C	3: 130,479,022		probably null	Het
Dcstamp	A	T	15: 39,759,533	I417F	probably damaging	Het
Dnah5	A	G	15: 28,238,592	I427V	probably benign	Het
Dnah5	A	G	15: 28,333,062	E2203G	probably benign	Het
Dnmt3c	A	T	2: 153,717,425	S409C	probably damaging	Het
Dock6	A	T	9: 21,813,079	M1541K	probably damaging	Het
Dzip1l	C	T	9: 99,665,835	T714I	probably benign	Het
Exoc6b	T	C	6: 84,848,825	R535G	probably damaging	Het
Fam196b	T	A	11: 34,402,030	V24E	probably damaging	Het
Fam83h	A	G	15: 76,004,739	S250P	probably benign	Het
Fat4	C	T	3: 38,981,958	T3253I	probably damaging	Het
Fer1l6	T	A	15: 58,629,378	F1302I	probably damaging	Het
Fmnl1	T	G	11: 103,194,774		probably benign	Het
Gckr	C	A	5: 31,302,210	F201L	possibly damaging	Het
Gm10036	A	G	18: 15,833,235	T148A	probably benign	Het
Gm13178	G	T	4: 144,703,603	A272D	possibly damaging	Het
Gm5142	G	A	14: 59,178,460	S83F	probably benign	Het
Gm8765	G	T	13: 50,702,983	V886L	possibly damaging	Het
Gpr37	A	T	6: 25,689,005	V31D	possibly damaging	Het
Gramd3	A	T	18: 56,485,249	Y207F	probably damaging	Het
Hr	T	C	14: 70,563,684		probably null	Het
Igf2r	A	G	17: 12,733,866	L231P	probably damaging	Het
Ighv1-66	A	T	12: 115,593,537	W3R	probably damaging	Het
Kcnu1	T	C	8: 25,918,463	S101P	probably benign	Het
Klhl23	T	G	2: 69,833,966	V553G	probably damaging	Het
Lrp1	T	C	10: 127,552,876	I3235V	probably damaging	Het
Mb	A	T	15: 77,016,056	I57N	probably damaging	Het
Micu1	T	C	10: 59,789,021	I295T	possibly damaging	Het
Mink1	G	A	11: 70,607,775	V589I	possibly damaging	Het
Mndal	T	C	1: 173,875,594	K82E	probably damaging	Het
Mroh1	A	C	15: 76,437,317	K1066T	probably benign	Het
Muc5b	T	A	7: 141,842,455	N149K	unknown	Het
Myo7b	G	T	18: 31,971,573	L1404I	probably damaging	Het
Nlrc4	A	G	17: 74,446,006	S461P	probably damaging	Het
Nudt12	A	T	17: 59,003,353	D418E	probably benign	Het
Olfr130	T	A	17: 38,068,057	D295E	probably benign	Het
Olfr996	G	T	2: 85,579,402	R54S	possibly damaging	Het
Pcdha1	A	G	18: 37,159,273	H817R	probably damaging	Het
Pcdha4	A	G	18: 36,954,027	Y421C	probably damaging	Het
Pcf11	T	C	7: 92,657,678	D1094G	probably benign	Het
Pck2	A	T	14: 55,547,766	D427V	probably damaging	Het
Pclo	A	G	5: 14,676,407	T1760A	probably benign	Het
Pdzk1ip1	T	A	4: 115,092,991	Y83N	probably damaging	Het
Pgs1	T	C	11: 118,002,486	I213T	probably damaging	Het
Plin4	T	A	17: 56,103,969	T1021S	probably damaging	Het
Plxnb1	T	A	9: 109,112,307	I1677N	probably damaging	Het
Pm20d2	T	C	4: 33,174,752	E378G	possibly damaging	Het
Prkcq	T	G	2: 11,226,850		probably null	Het
Psmd2	C	T	16: 20,662,133	P780L	probably damaging	Het
Pvr	A	G	7: 19,905,180	S392P	possibly damaging	Het
Rad51ap2	G	C	12: 11,457,431	L451F	possibly damaging	Het
Rbm20	A	G	19: 53,834,766	E598G	probably damaging	Het
Rho	A	T	6: 115,935,543	N123Y	possibly damaging	Het
Rictor	T	C	15: 6,708,453		probably null	Het
Rilpl2	T	G	5: 124,468,593	K186T	probably damaging	Het
Rps6ka4	A	C	19: 6,839,624	L61R	probably damaging	Het
Sds	C	A	5: 120,480,825	Q118K	probably benign	Het
Sept1	C	T	7: 127,216,985	R91K	probably benign	Het
Sf3a3	A	G	4: 124,722,880	Y185C	probably damaging	Het
Shtn1	T	C	19: 59,009,834	M376V	possibly damaging	Het
Slc6a9	A	G	4: 117,857,436	T189A	possibly damaging	Het
Slc7a6	T	G	8: 106,195,974	V464G	possibly damaging	Het
Smg8	T	A	11: 87,085,093	D554V	probably damaging	Het
Sox8	A	G	17: 25,570,108		probably null	Het
Spats2l	T	A	1: 57,879,530	V41D	probably damaging	Het
Sult2a3	A	T	7: 14,067,568	F282Y	probably damaging	Het
Svs3a	T	G	2: 164,290,171	Y220D	probably damaging	Het
Teddm1a	T	A	1: 153,892,623	Y278N	probably damaging	Het
Tlk1	T	C	2: 70,721,928	Y526C	probably damaging	Het
Tmc3	T	A	7: 83,616,817		probably null	Het
Ttn	T	A	2: 76,766,239	E20110V	probably damaging	Het
Tulp4	A	G	17: 6,214,666	D235G	probably damaging	Het
Usp50	T	C	2: 126,780,475	Y55C	possibly damaging	Het
Vmn1r224	T	C	17: 20,419,527	L122P	probably benign	Het
Vmn2r62	A	G	7: 42,789,049	L121P	possibly damaging	Het
Zer1	G	T	2: 30,111,021	H129Q	probably benign	Het
Zfand4	G	A	6: 116,305,657	A64T	probably benign	Het

Other mutations in Whrn

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01588:Whrn	APN	4	63472778	missense	probably damaging	1.00
IGL01643:Whrn	APN	4	63416435	missense	possibly damaging	0.79
IGL02065:Whrn	APN	4	63418585	missense	possibly damaging	0.52
IGL02119:Whrn	APN	4	63435487	missense	probably damaging	0.99
IGL02589:Whrn	APN	4	63418097	nonsense	probably null
IGL02638:Whrn	APN	4	63419472	missense	possibly damaging	0.47
IGL02865:Whrn	APN	4	63415492	missense	probably benign	0.08
IGL02934:Whrn	APN	4	63416105	missense	probably damaging	1.00
IGL03372:Whrn	APN	4	63418618	missense	probably damaging	0.96
R0090:Whrn	UTSW	4	63432732	missense	possibly damaging	0.79
R0592:Whrn	UTSW	4	63415567	missense	probably damaging	1.00
R0631:Whrn	UTSW	4	63419489	missense	probably damaging	1.00
R1916:Whrn	UTSW	4	63494732	missense	probably damaging	1.00
R1933:Whrn	UTSW	4	63415639	nonsense	probably null
R1958:Whrn	UTSW	4	63435429	missense	possibly damaging	0.62
R2255:Whrn	UTSW	4	63418148	missense	possibly damaging	0.92
R2513:Whrn	UTSW	4	63435412	missense	probably benign	0.22
R3699:Whrn	UTSW	4	63461412	splice site	probably benign
R3919:Whrn	UTSW	4	63495184	nonsense	probably null
R4016:Whrn	UTSW	4	63415639	nonsense	probably null
R4241:Whrn	UTSW	4	63432973	unclassified	probably benign
R4517:Whrn	UTSW	4	63461280	critical splice donor site	probably null
R4739:Whrn	UTSW	4	63418165	missense	probably damaging	1.00
R5207:Whrn	UTSW	4	63432714	missense	probably damaging	1.00
R5281:Whrn	UTSW	4	63418427	missense	probably benign	0.04
R5307:Whrn	UTSW	4	63431843	missense	probably benign	0.01
R5463:Whrn	UTSW	4	63432816	missense	probably benign	0.08
R5663:Whrn	UTSW	4	63418448	missense	probably damaging	0.98
R5754:Whrn	UTSW	4	63416588	missense	probably damaging	0.98
R5933:Whrn	UTSW	4	63494708	missense	probably damaging	1.00
R6212:Whrn	UTSW	4	63494686	nonsense	probably null
R6380:Whrn	UTSW	4	63418592	missense	possibly damaging	0.90
R6381:Whrn	UTSW	4	63472684	missense	probably benign	0.00
R7350:Whrn	UTSW	4	63431959	missense	possibly damaging	0.71
R7382:Whrn	UTSW	4	63418336	missense	probably benign
R7419:Whrn	UTSW	4	63416093	missense	possibly damaging	0.94
R8334:Whrn	UTSW	4	63494810	missense	probably damaging	1.00
R9378:Whrn	UTSW	4	63431842	missense	probably benign	0.00
X0009:Whrn	UTSW	4	63431911	missense	probably benign	0.00
Z1176:Whrn	UTSW	4	63415566	missense	probably damaging	1.00
Z1177:Whrn	UTSW	4	63418499	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- ATGACCAGACGCAGCATG -3'
(R):5'- TAGACTGCAGCCGGTGACTC -3'

Sequencing Primer
(F):5'- CAGCATGGGCAGCAGAC -3'
(R):5'- AGACTCCAGCCGTGACCTC -3'

Posted On

2019-07-17