Mutagenetix > Incidental Mutation

Incidental Mutation 'R1681:Tmem145'

188502

Institutional Source

Beutler Lab

Gene Symbol

Tmem145

Ensembl Gene

ENSMUSG00000043843

Gene Name

transmembrane protein 145

Synonyms

MMRRC Submission

039717-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.112) question?

Stock #

R1681 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

25306106-25316195 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 25314734 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Leucine at position 424 (F424L)

Ref Sequence

ENSEMBL: ENSMUSP00000104046 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000108409] [ENSMUST00000119703] [ENSMUST00000128119]

AlphaFold

no structure available at present

Predicted Effect

possibly damaging
Transcript: ENSMUST00000108409
AA Change: F424L

PolyPhen 2 Score 0.947 (Sensitivity: 0.79; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000104046
Gene: ENSMUSG00000043843
AA Change: F424L

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: F410L

PolyPhen 2 Score 0.499 (Sensitivity: 0.88; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000112676
Gene: ENSMUSG00000043843
AA Change: F410L

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

probably benign
Transcript: ENSMUST00000128119

SMART Domains

Protein: ENSMUSP00000122192
Gene: ENSMUSG00000045039

Domain	Start	End	E-Value	Type
signal peptide	1	27	N/A	INTRINSIC
CUB	33	140	1.24e-15	SMART
EGF	141	170	4.26e0	SMART
EGF	173	203	2.43e1	SMART
Pfam:Kelch_4	227	277	1.3e-11	PFAM
Pfam:Kelch_3	240	287	1.6e-7	PFAM
low complexity region	320	341	N/A	INTRINSIC
low complexity region	517	531	N/A	INTRINSIC
low complexity region	728	738	N/A	INTRINSIC
PSI	847	899	1.37e0	SMART
low complexity region	932	938	N/A	INTRINSIC
PSI	949	991	2.11e-2	SMART
PSI	1005	1073	7.82e-1	SMART
EGF_CA	1074	1115	2.62e-9	SMART
EGF	1117	1160	5.4e-2	SMART
EGF_like	1163	1208	4e-1	SMART
EGF_Lam	1211	1259	1.03e-7	SMART
Blast:CUB	1263	1401	1e-30	BLAST
EGF_like	1406	1445	3.29e1	SMART
Pfam:Kelch_4	1509	1564	6.5e-12	PFAM
Pfam:Kelch_3	1520	1574	1.2e-10	PFAM
PSI	1868	1923	2.75e-1	SMART
PSI	2004	2062	1.6e0	SMART
PSI	2064	2121	1.68e-5	SMART
EGF	2125	2164	1.08e-1	SMART
EGF	2166	2194	4.26e0	SMART
EGF	2204	2244	2.2e1	SMART
EGF_like	2248	2321	6.37e-1	SMART
low complexity region	2493	2504	N/A	INTRINSIC
low complexity region	2530	2541	N/A	INTRINSIC
transmembrane domain	2592	2614	N/A	INTRINSIC
low complexity region	2649	2668	N/A	INTRINSIC
low complexity region	2674	2702	N/A	INTRINSIC
low complexity region	2759	2774	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000205639

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.6%
20x: 93.6%

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: 87 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acaca	T	A	11: 84,226,185 (GRCm38)	I247N	probably damaging	Het
Ankle1	G	T	8: 71,407,618 (GRCm38)	S260I	probably benign	Het
Aoc2	T	C	11: 101,325,192 (GRCm38)	S34P	probably benign	Het
Ap1m1	A	C	8: 72,256,122 (GRCm38)	I397L	possibly damaging	Het
Apba1	C	A	19: 23,936,561 (GRCm38)	D649E	probably damaging	Het
Aptx	C	T	4: 40,697,274 (GRCm38)	V25M	probably benign	Het
Arhgef18	G	A	8: 3,439,645 (GRCm38)	G326R	probably damaging	Het
Atm	A	C	9: 53,522,155 (GRCm38)	I265S	possibly damaging	Het
B3galt4	A	T	17: 33,951,213 (GRCm38)	V17E	probably benign	Het
Bcl7a	T	A	5: 123,356,023 (GRCm38)	M86K	possibly damaging	Het
Cela3a	T	A	4: 137,402,684 (GRCm38)		probably null	Het
Cep85	T	A	4: 134,148,728 (GRCm38)	K456*	probably null	Het
Ces1f	C	A	8: 93,275,414 (GRCm38)	A29S	probably benign	Het
Chd9	A	T	8: 90,973,135 (GRCm38)	I598F	probably damaging	Het
Cntln	T	C	4: 84,947,635 (GRCm38)	L176S	probably damaging	Het
Cntn3	A	T	6: 102,170,668 (GRCm38)	N909K	probably damaging	Het
Cntnap5b	T	C	1: 100,076,107 (GRCm38)	S271P	probably damaging	Het
Col6a3	T	A	1: 90,773,502 (GRCm38)	H2564L	unknown	Het
Cyp2b19	C	A	7: 26,763,340 (GRCm38)		probably null	Het
Dapk1	G	T	13: 60,718,464 (GRCm38)		probably null	Het
Dnah7b	T	A	1: 46,324,712 (GRCm38)	Y3497*	probably null	Het
Duoxa2	T	C	2: 122,299,162 (GRCm38)		probably null	Het
Eny2	T	C	15: 44,432,478 (GRCm38)	W42R	probably damaging	Het
Epha3	A	G	16: 63,595,728 (GRCm38)	V635A	probably damaging	Het
Fam167b	G	C	4: 129,578,276 (GRCm38)	Q34E	probably benign	Het
Fam26f	A	G	10: 34,127,900 (GRCm38)	F4L	probably benign	Het
Fancm	T	C	12: 65,105,656 (GRCm38)	M962T	probably benign	Het
Gimap8	T	A	6: 48,656,411 (GRCm38)	I388N	probably benign	Het
Gpaa1	A	G	15: 76,331,453 (GRCm38)	T22A	probably benign	Het
Hoxc11	T	C	15: 102,955,156 (GRCm38)	S211P	possibly damaging	Het
Hsd17b12	T	C	2: 94,033,561 (GRCm38)	N312S	unknown	Het
Idh2	T	G	7: 80,099,158 (GRCm38)	E125A	probably damaging	Het
Igdcc4	A	G	9: 65,128,795 (GRCm38)	Y712C	probably damaging	Het
Kank1	T	C	19: 25,410,304 (GRCm38)	V447A	possibly damaging	Het
Kif1b	T	A	4: 149,195,501 (GRCm38)		probably null	Het
Klc4	A	T	17: 46,636,770 (GRCm38)	D335E	probably damaging	Het
Klhl33	T	A	14: 50,893,077 (GRCm38)	D320V	probably benign	Het
Krt73	A	T	15: 101,802,047 (GRCm38)	M84K	possibly damaging	Het
Kti12	T	A	4: 108,848,858 (GRCm38)	I323N	probably damaging	Het
Kynu	T	C	2: 43,679,825 (GRCm38)	L373P	probably damaging	Het
Lats1	T	C	10: 7,705,914 (GRCm38)	M821T	probably damaging	Het
Lnx1	A	T	5: 74,685,410 (GRCm38)	H126Q	probably benign	Het
Lonrf2	G	A	1: 38,813,276 (GRCm38)	P165S	probably benign	Het
Lrrc4b	T	A	7: 44,461,177 (GRCm38)	Y158N	probably damaging	Het
Lrrc74b	C	A	16: 17,559,753 (GRCm38)	R87L	probably damaging	Het
Meig1	T	C	2: 3,409,274 (GRCm38)	D63G	probably damaging	Het
Mrpl38	G	A	11: 116,138,429 (GRCm38)		probably benign	Het
Naip2	C	T	13: 100,161,860 (GRCm38)	G556D	probably benign	Het
Naip2	T	C	13: 100,161,854 (GRCm38)	E558G	probably benign	Het
Nlrp1a	T	A	11: 71,142,358 (GRCm38)	E3D	unknown	Het
Nphs2	T	A	1: 156,320,898 (GRCm38)	D110E	probably damaging	Het
Nxn	T	A	11: 76,272,464 (GRCm38)	K244N	probably benign	Het
Oas3	A	T	5: 120,769,908 (GRCm38)	F322L	probably benign	Het
Obscn	T	A	11: 59,103,325 (GRCm38)	Y1577F	probably damaging	Het
Olfr1122	G	A	2: 87,388,620 (GRCm38)	R305K	possibly damaging	Het
Olfr911-ps1	T	A	9: 38,524,117 (GRCm38)	N128K	probably benign	Het
Olfr914	G	A	9: 38,606,948 (GRCm38)	G161D	probably damaging	Het
Olfr917	A	G	9: 38,665,320 (GRCm38)	Y175H	probably benign	Het
Olfr924	T	C	9: 38,848,513 (GRCm38)	M133T	probably damaging	Het
Panx1	T	C	9: 15,007,783 (GRCm38)	D260G	probably benign	Het
Pcdhb15	T	C	18: 37,473,813 (GRCm38)	Y33H	probably damaging	Het
Pik3ap1	C	A	19: 41,308,529 (GRCm38)	V461F	probably damaging	Het
Plpp3	G	A	4: 105,208,805 (GRCm38)		probably null	Het
Prtn3	A	T	10: 79,880,541 (GRCm38)	T61S	probably benign	Het
Psen1	T	A	12: 83,724,620 (GRCm38)	Y225N	probably damaging	Het
Rab44	T	A	17: 29,140,124 (GRCm38)	S429T	possibly damaging	Het
Ralgapa1	T	C	12: 55,762,603 (GRCm38)	I462M	probably benign	Het
Rbfox3	T	C	11: 118,505,669 (GRCm38)	N105S	probably damaging	Het
Rbm7	A	C	9: 48,489,721 (GRCm38)	Y236D	possibly damaging	Het
Samhd1	T	C	2: 157,101,732 (GRCm38)	T621A	probably benign	Het
Samt3	C	A	X: 86,046,650 (GRCm38)	D49E	probably benign	Het
Sass6	T	C	3: 116,603,473 (GRCm38)	V26A	possibly damaging	Het
Scn11a	C	T	9: 119,804,412 (GRCm38)	M418I	possibly damaging	Het
Scrib	T	C	15: 76,064,567 (GRCm38)	E480G	probably damaging	Het
Sec24a	T	G	11: 51,695,189 (GRCm38)	T1071P	probably damaging	Het
Siglecg	A	C	7: 43,408,941 (GRCm38)	E84A	probably benign	Het
Slc6a17	C	T	3: 107,474,386 (GRCm38)	V419I	probably damaging	Het
Soga1	T	C	2: 157,030,530 (GRCm38)	T966A	possibly damaging	Het
Ssr2	T	C	3: 88,581,042 (GRCm38)	M75T	possibly damaging	Het
Tbc1d22b	A	G	17: 29,575,177 (GRCm38)	T275A	possibly damaging	Het
Tbx15	T	A	3: 99,351,824 (GRCm38)		probably null	Het
Tll1	A	C	8: 64,085,551 (GRCm38)	L353R	possibly damaging	Het
Tlr4	C	T	4: 66,841,105 (GRCm38)	P712S	probably damaging	Het
Tnrc18	T	C	5: 142,773,817 (GRCm38)	K755E	unknown	Het
Trmt44	A	G	5: 35,569,977 (GRCm38)	I298T	probably benign	Het
Vmn1r69	A	G	7: 10,580,252 (GRCm38)	V184A	probably benign	Het
Zfp84	T	C	7: 29,777,400 (GRCm38)	C506R	probably damaging	Het

Other mutations in Tmem145

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00926:Tmem145	APN	7	25,314,730 (GRCm38)	missense	possibly damaging	0.88
IGL00958:Tmem145	APN	7	25,307,357 (GRCm38)	critical splice donor site	probably null
IGL01347:Tmem145	APN	7	25,314,835 (GRCm38)	missense	probably damaging	0.97
IGL01936:Tmem145	APN	7	25,311,391 (GRCm38)	missense	probably damaging	0.97
IGL02526:Tmem145	APN	7	25,308,232 (GRCm38)	missense	probably benign	0.20
IGL02686:Tmem145	APN	7	25,314,725 (GRCm38)	missense	probably damaging	1.00
IGL03182:Tmem145	APN	7	25,314,879 (GRCm38)	missense	probably damaging	1.00
R0087:Tmem145	UTSW	7	25,307,843 (GRCm38)	missense	probably damaging	1.00
R0180:Tmem145	UTSW	7	25,314,699 (GRCm38)	missense	probably benign	0.05
R0329:Tmem145	UTSW	7	25,308,674 (GRCm38)	splice site	probably benign
R0504:Tmem145	UTSW	7	25,311,362 (GRCm38)	missense	probably damaging	1.00
R1488:Tmem145	UTSW	7	25,307,435 (GRCm38)	splice site	probably null
R2352:Tmem145	UTSW	7	25,306,173 (GRCm38)	missense	probably benign
R3834:Tmem145	UTSW	7	25,311,361 (GRCm38)	missense	probably damaging	1.00
R4175:Tmem145	UTSW	7	25,308,793 (GRCm38)	missense	probably benign	0.04
R4414:Tmem145	UTSW	7	25,307,129 (GRCm38)	missense	probably damaging	1.00
R4485:Tmem145	UTSW	7	25,307,162 (GRCm38)	missense	possibly damaging	0.76
R4631:Tmem145	UTSW	7	25,307,825 (GRCm38)	missense	probably benign	0.00
R4983:Tmem145	UTSW	7	25,308,602 (GRCm38)	missense	probably benign	0.03
R4999:Tmem145	UTSW	7	25,309,034 (GRCm38)	missense	probably benign	0.04
R5772:Tmem145	UTSW	7	25,315,614 (GRCm38)	missense	probably benign	0.21
R5821:Tmem145	UTSW	7	25,315,521 (GRCm38)	missense	probably benign	0.30
R5909:Tmem145	UTSW	7	25,308,193 (GRCm38)	missense	possibly damaging	0.89
R6021:Tmem145	UTSW	7	25,308,845 (GRCm38)	splice site	probably null
R6430:Tmem145	UTSW	7	25,309,038 (GRCm38)	missense	possibly damaging	0.84
R6768:Tmem145	UTSW	7	25,308,636 (GRCm38)	missense	probably damaging	1.00
R6778:Tmem145	UTSW	7	25,311,376 (GRCm38)	missense	probably benign	0.04
R7428:Tmem145	UTSW	7	25,307,165 (GRCm38)	critical splice donor site	probably null
R7536:Tmem145	UTSW	7	25,307,869 (GRCm38)	missense	probably damaging	1.00
R7748:Tmem145	UTSW	7	25,307,328 (GRCm38)	nonsense	probably null
R7826:Tmem145	UTSW	7	25,307,514 (GRCm38)	missense	probably damaging	1.00
R8253:Tmem145	UTSW	7	25,307,514 (GRCm38)	missense	probably damaging	1.00
R8441:Tmem145	UTSW	7	25,308,775 (GRCm38)	missense	possibly damaging	0.62
R9129:Tmem145	UTSW	7	25,314,840 (GRCm38)	missense	possibly damaging	0.59
R9277:Tmem145	UTSW	7	25,309,740 (GRCm38)	missense	probably benign	0.14
R9297:Tmem145	UTSW	7	25,308,832 (GRCm38)	missense	probably damaging	1.00
Z1177:Tmem145	UTSW	7	25,309,646 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CTGGTGTCCAAGGCAGTCTGAATG -3'
(R):5'- CACTTGTCAATCAGGGAAGGAGTGG -3'

Sequencing Primer
(F):5'- TCTGAATGGTTCAAAGGCAATG -3'
(R):5'- TCAGACGCCAATGAGCAG -3'

Posted On

2014-05-09