Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01936:Tmem145'

180664

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Tmem145

Ensembl Gene

ENSMUSG00000043843

Gene Name

transmembrane protein 145

Synonyms

B930076A02Rik

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.102) question?

Stock #

IGL01936

Quality Score

Status

Chromosome

Chromosomal Location

25005531-25015620 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to T at 25010816 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Alanine to Serine at position 383 (A383S)

Ref Sequence

ENSEMBL: ENSMUSP00000104046 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000108409] [ENSMUST00000119703]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000108409
AA Change: A383S

PolyPhen 2 Score 0.974 (Sensitivity: 0.76; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000104046
Gene: ENSMUSG00000043843
AA Change: A383S

Domain	Start	End	E-Value	Type
signal peptide	1	29	N/A	INTRINSIC
Pfam:GpcrRhopsn4	157	411	7.5e-81	PFAM
low complexity region	486	503	N/A	INTRINSIC
low complexity region	505	516	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000119703
AA Change: A369S

PolyPhen 2 Score 0.888 (Sensitivity: 0.82; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000112676
Gene: ENSMUSG00000043843
AA Change: A369S

Domain	Start	End	E-Value	Type
signal peptide	1	29	N/A	INTRINSIC
Pfam:GpcrRhopsn4	143	397	4.3e-81	PFAM
low complexity region	478	493	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000140016

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000205639

Coding Region Coverage

Validation Efficiency

MGI Phenotype

PHENOTYPE: Mice homozygous for an ENU-induced mutation exhibit progressive hearing impairment. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 68 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adamts3	T	A	5: 90,009,282 (GRCm39)	H127L	probably benign	Het
Adamtsl3	T	C	7: 82,244,579 (GRCm39)	V419A	possibly damaging	Het
Arhgap31	T	A	16: 38,423,287 (GRCm39)	L926F	probably damaging	Het
Asgr2	A	T	11: 69,988,877 (GRCm39)		probably null	Het
C3ar1	T	A	6: 122,828,194 (GRCm39)	T8S	probably benign	Het
Caskin2	T	C	11: 115,695,543 (GRCm39)	I273V	probably damaging	Het
Ccnl2	T	A	4: 155,904,856 (GRCm39)	C242S	probably damaging	Het
Cdkn2a	A	T	4: 89,212,569 (GRCm39)		probably null	Het
Cfap45	T	G	1: 172,361,616 (GRCm39)	M231R	probably damaging	Het
Clcn7	A	C	17: 25,374,350 (GRCm39)	N464H	probably benign	Het
Col20a1	T	A	2: 180,651,161 (GRCm39)		probably benign	Het
Col7a1	T	A	9: 108,797,067 (GRCm39)		probably benign	Het
Cops7a	T	C	6: 124,939,379 (GRCm39)	D90G	probably benign	Het
Ctcf	T	C	8: 106,396,864 (GRCm39)	V363A	probably benign	Het
Cyp2j12	A	G	4: 96,021,306 (GRCm39)	V100A	probably benign	Het
Dcaf1	T	A	9: 106,736,800 (GRCm39)	F1085Y	possibly damaging	Het
Drc7	T	A	8: 95,800,760 (GRCm39)	F594Y	possibly damaging	Het
Ehbp1l1	C	A	19: 5,768,277 (GRCm39)	E1009*	probably null	Het
Epg5	C	A	18: 78,028,316 (GRCm39)	R1286S	probably damaging	Het
Etv1	T	C	12: 38,885,060 (GRCm39)		probably benign	Het
Exosc7	T	C	9: 122,964,956 (GRCm39)		probably benign	Het
Fam227a	T	C	15: 79,496,747 (GRCm39)	D610G	possibly damaging	Het
Fat4	T	A	3: 39,033,923 (GRCm39)	M2525K	probably benign	Het
Gimap5	G	T	6: 48,729,999 (GRCm39)	A190S	probably damaging	Het
Glcci1	T	A	6: 8,579,596 (GRCm39)	S79T	probably damaging	Het
Gpnmb	C	T	6: 49,024,384 (GRCm39)	T233I	probably null	Het
Hdac1-ps	T	C	17: 78,799,558 (GRCm39)	V183A	probably damaging	Het
Hyls1	T	C	9: 35,473,363 (GRCm39)	I18V	probably benign	Het
Ighv1-63	C	T	12: 115,459,274 (GRCm39)	E108K	probably damaging	Het
Ighv5-12	C	A	12: 113,665,927 (GRCm39)	R57L	probably damaging	Het
Igkv5-37	T	C	6: 69,940,323 (GRCm39)	Y107C	probably damaging	Het
Il20ra	T	A	10: 19,631,591 (GRCm39)	V264D	probably damaging	Het
Jph1	A	T	1: 17,167,608 (GRCm39)	V74E	probably damaging	Het
Kcnab1	C	T	3: 65,265,695 (GRCm39)	L280F	probably damaging	Het
Kcnk1	T	C	8: 126,751,826 (GRCm39)	F144S	probably damaging	Het
Kcnq1	G	A	7: 142,738,241 (GRCm39)	E294K	possibly damaging	Het
Kdm4b	T	A	17: 56,704,355 (GRCm39)	V813E	probably damaging	Het
Kntc1	T	A	5: 123,949,439 (GRCm39)	F1937I	probably damaging	Het
Ldb2	G	A	5: 44,637,586 (GRCm39)	R241W	probably damaging	Het
Lgr5	T	C	10: 115,288,319 (GRCm39)	N703S	probably damaging	Het
Map4k1	A	T	7: 28,688,032 (GRCm39)	M227L	possibly damaging	Het
Mbnl1	T	A	3: 60,520,940 (GRCm39)	M268K	possibly damaging	Het
Mcm2	C	A	6: 88,868,708 (GRCm39)	G350C	probably damaging	Het
Myh2	A	T	11: 67,082,599 (GRCm39)	T1390S	possibly damaging	Het
Npat	T	A	9: 53,469,526 (GRCm39)		probably benign	Het
Nr2e1	T	A	10: 42,443,969 (GRCm39)	D251V	possibly damaging	Het
Or1x2	A	G	11: 50,918,162 (GRCm39)	N111S	probably benign	Het
Or4d10	C	T	19: 12,051,421 (GRCm39)	V192I	probably benign	Het
Or5b107	C	A	19: 13,142,767 (GRCm39)	P130T	probably damaging	Het
Plekha5	T	A	6: 140,470,621 (GRCm39)	H87Q	probably damaging	Het
Polr3a	A	G	14: 24,529,256 (GRCm39)	V368A	probably damaging	Het
Psmb8	T	A	17: 34,419,168 (GRCm39)	L154Q	probably damaging	Het
Rab40c	A	C	17: 26,103,644 (GRCm39)	C140G	probably damaging	Het
Ranbp17	G	A	11: 33,437,689 (GRCm39)	T183I	probably benign	Het
Ruvbl2	T	C	7: 45,078,122 (GRCm39)	E117G	probably damaging	Het
Serpinb3b	T	A	1: 107,082,368 (GRCm39)	M299L	probably benign	Het
Smpdl3a	A	G	10: 57,678,530 (GRCm39)	H111R	probably damaging	Het
Sspo	C	A	6: 48,452,821 (GRCm39)	P2843H	probably damaging	Het
Stk39	T	C	2: 68,144,908 (GRCm39)	T389A	probably benign	Het
Synrg	T	A	11: 83,910,531 (GRCm39)	F1000Y	probably benign	Het
Thbs2	C	T	17: 14,908,076 (GRCm39)	S229N	probably benign	Het
Thsd1	G	A	8: 22,742,247 (GRCm39)	C305Y	probably damaging	Het
Ticrr	C	A	7: 79,344,297 (GRCm39)	D1387E	probably benign	Het
Tmprss4	A	G	9: 45,090,718 (GRCm39)	V187A	probably damaging	Het
Unc13c	T	A	9: 73,600,524 (GRCm39)	M1407L	probably benign	Het
Vps39	C	T	2: 120,153,609 (GRCm39)	G655D	probably benign	Het
Wwtr1	T	C	3: 57,482,241 (GRCm39)		probably benign	Het
Xrn1	T	C	9: 95,930,397 (GRCm39)	S1535P	probably damaging	Het

Other mutations in Tmem145

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00926:Tmem145	APN	7	25,014,155 (GRCm39)	missense	possibly damaging	0.88
IGL00958:Tmem145	APN	7	25,006,782 (GRCm39)	critical splice donor site	probably null
IGL01347:Tmem145	APN	7	25,014,260 (GRCm39)	missense	probably damaging	0.97
IGL02526:Tmem145	APN	7	25,007,657 (GRCm39)	missense	probably benign	0.20
IGL02686:Tmem145	APN	7	25,014,150 (GRCm39)	missense	probably damaging	1.00
IGL03182:Tmem145	APN	7	25,014,304 (GRCm39)	missense	probably damaging	1.00
R0087:Tmem145	UTSW	7	25,007,268 (GRCm39)	missense	probably damaging	1.00
R0180:Tmem145	UTSW	7	25,014,124 (GRCm39)	missense	probably benign	0.05
R0329:Tmem145	UTSW	7	25,008,099 (GRCm39)	splice site	probably benign
R0504:Tmem145	UTSW	7	25,010,787 (GRCm39)	missense	probably damaging	1.00
R1488:Tmem145	UTSW	7	25,006,860 (GRCm39)	splice site	probably null
R1681:Tmem145	UTSW	7	25,014,159 (GRCm39)	missense	possibly damaging	0.95
R2352:Tmem145	UTSW	7	25,005,598 (GRCm39)	missense	probably benign
R3834:Tmem145	UTSW	7	25,010,786 (GRCm39)	missense	probably damaging	1.00
R4175:Tmem145	UTSW	7	25,008,218 (GRCm39)	missense	probably benign	0.04
R4414:Tmem145	UTSW	7	25,006,554 (GRCm39)	missense	probably damaging	1.00
R4485:Tmem145	UTSW	7	25,006,587 (GRCm39)	missense	possibly damaging	0.76
R4631:Tmem145	UTSW	7	25,007,250 (GRCm39)	missense	probably benign	0.00
R4983:Tmem145	UTSW	7	25,008,027 (GRCm39)	missense	probably benign	0.03
R4999:Tmem145	UTSW	7	25,008,459 (GRCm39)	missense	probably benign	0.04
R5772:Tmem145	UTSW	7	25,015,039 (GRCm39)	missense	probably benign	0.21
R5821:Tmem145	UTSW	7	25,014,946 (GRCm39)	missense	probably benign	0.30
R5909:Tmem145	UTSW	7	25,007,618 (GRCm39)	missense	possibly damaging	0.89
R6021:Tmem145	UTSW	7	25,008,270 (GRCm39)	splice site	probably null
R6430:Tmem145	UTSW	7	25,008,463 (GRCm39)	missense	possibly damaging	0.84
R6768:Tmem145	UTSW	7	25,008,061 (GRCm39)	missense	probably damaging	1.00
R6778:Tmem145	UTSW	7	25,010,801 (GRCm39)	missense	probably benign	0.04
R7428:Tmem145	UTSW	7	25,006,590 (GRCm39)	critical splice donor site	probably null
R7536:Tmem145	UTSW	7	25,007,294 (GRCm39)	missense	probably damaging	1.00
R7748:Tmem145	UTSW	7	25,006,753 (GRCm39)	nonsense	probably null
R7826:Tmem145	UTSW	7	25,006,939 (GRCm39)	missense	probably damaging	1.00
R8253:Tmem145	UTSW	7	25,006,939 (GRCm39)	missense	probably damaging	1.00
R8441:Tmem145	UTSW	7	25,008,200 (GRCm39)	missense	possibly damaging	0.62
R9129:Tmem145	UTSW	7	25,014,265 (GRCm39)	missense	possibly damaging	0.59
R9277:Tmem145	UTSW	7	25,009,165 (GRCm39)	missense	probably benign	0.14
R9297:Tmem145	UTSW	7	25,008,257 (GRCm39)	missense	probably damaging	1.00
Z1177:Tmem145	UTSW	7	25,009,071 (GRCm39)	missense	probably damaging	1.00

Posted On

2014-05-07