Mutagenetix > Incidental Mutation

Incidental Mutation 'R7965:Tmem161a'

650323

Institutional Source

Beutler Lab

Gene Symbol

Tmem161a

Ensembl Gene

ENSMUSG00000002342

Gene Name

transmembrane protein 161A

Synonyms

MMRRC Submission

046008-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.097) question?

Stock #

R7965 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

70625006-70636331 bp(+) (GRCm39)

Type of Mutation

start gained

DNA Base Change (assembly)

C to T at 70630154 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000138499 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000002413] [ENSMUST00000147656] [ENSMUST00000149105] [ENSMUST00000182365] [ENSMUST00000182715] [ENSMUST00000182980]

AlphaFold

Q8VCA6

Predicted Effect

silent
Transcript: ENSMUST00000002413

SMART Domains

Protein: ENSMUSP00000002413
Gene: ENSMUSG00000002342

Domain	Start	End	E-Value	Type
Pfam:Tmemb_161AB	2	478	6.8e-182	PFAM

Predicted Effect

SMART Domains

Protein: ENSMUSP00000137791
Gene: ENSMUSG00000002342
AA Change: R5C

Domain	Start	End	E-Value	Type
Pfam:Tmemb_161AB	1	119	8.7e-37	PFAM

Predicted Effect

silent
Transcript: ENSMUST00000147656

SMART Domains

Protein: ENSMUSP00000138017
Gene: ENSMUSG00000002342

Domain	Start	End	E-Value	Type
Pfam:Tmemb_161AB	2	270	4.6e-122	PFAM
low complexity region	283	296	N/A	INTRINSIC
low complexity region	309	320	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000149105

SMART Domains

Protein: ENSMUSP00000123084
Gene: ENSMUSG00000002342

Domain	Start	End	E-Value	Type
Pfam:Tmemb_161AB	1	95	5.1e-41	PFAM
Pfam:Tmemb_161AB	93	454	9.5e-148	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000182365

SMART Domains

Protein: ENSMUSP00000138641
Gene: ENSMUSG00000002342

Domain	Start	End	E-Value	Type
Pfam:Tmemb_161AB	2	98	3.7e-42	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000182715

SMART Domains

Protein: ENSMUSP00000138432
Gene: ENSMUSG00000002342

Domain	Start	End	E-Value	Type
Pfam:Tmemb_161AB	2	45	3.3e-15	PFAM
low complexity region	152	165	N/A	INTRINSIC
low complexity region	178	189	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000182980

SMART Domains

Protein: ENSMUSP00000138499
Gene: ENSMUSG00000002342

Domain	Start	End	E-Value	Type
Pfam:Tmemb_161AB	1	328	4.6e-133	PFAM

Coding Region Coverage

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

Validation Efficiency

100% (45/45)

Allele List at MGI

Other mutations in this stock

Total: 49 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ankhd1	A	G	18: 36,791,465 (GRCm39)	T154A		Het
Arhgap21	A	G	2: 20,854,007 (GRCm39)	I1795T	probably damaging	Het
Arhgef4	T	C	1: 34,850,762 (GRCm39)	V436A	probably benign	Het
Bche	A	T	3: 73,609,149 (GRCm39)	N92K	probably damaging	Het
Bmp2	C	T	2: 133,403,105 (GRCm39)	H219Y	probably benign	Het
Cables1	T	G	18: 11,973,269 (GRCm39)	V136G	probably benign	Het
Cacna1d	G	A	14: 29,769,270 (GRCm39)	R1887*	probably null	Het
Chrd	A	G	16: 20,557,903 (GRCm39)	E774G	probably benign	Het
Chrna2	A	G	14: 66,388,525 (GRCm39)	*513W	probably null	Het
Cracr2b	T	C	7: 141,044,161 (GRCm39)	F131S	probably damaging	Het
Ctsf	T	G	19: 4,906,567 (GRCm39)	F165V	probably damaging	Het
Cyfip1	T	A	7: 55,546,523 (GRCm39)	I545N	possibly damaging	Het
Enpp3	T	A	10: 24,654,717 (GRCm39)	T654S	possibly damaging	Het
Glce	A	G	9: 61,968,228 (GRCm39)	S308P	probably damaging	Het
H3c13	C	A	3: 96,176,309 (GRCm39)	Y100*	probably null	Het
Hmmr	A	C	11: 40,606,256 (GRCm39)		probably null	Het
Hoxb9	A	G	11: 96,165,464 (GRCm39)	N178D	probably benign	Het
Igkv10-94	A	T	6: 68,681,595 (GRCm39)	F82I	probably damaging	Het
Igkv1-133	A	T	6: 67,702,578 (GRCm39)	K99*	probably null	Het
Il4i1	A	G	7: 44,489,819 (GRCm39)	Q528R	probably benign	Het
Inhba	G	T	13: 16,201,572 (GRCm39)	G378V	possibly damaging	Het
Katna1	T	C	10: 7,614,623 (GRCm39)	S44P	probably benign	Het
Ldlrad1	G	A	4: 107,066,688 (GRCm39)	A8T	probably benign	Het
Mgat4d	T	C	8: 84,084,722 (GRCm39)	V155A	possibly damaging	Het
Morc2b	C	T	17: 33,354,746 (GRCm39)	E1009K	possibly damaging	Het
Myo9a	T	A	9: 59,695,721 (GRCm39)	L341H	probably damaging	Het
Nell2	C	T	15: 95,129,216 (GRCm39)	D716N	probably damaging	Het
Or1n2	A	G	2: 36,796,953 (GRCm39)		probably benign	Het
Or5t16	A	G	2: 86,818,707 (GRCm39)	V271A	probably benign	Het
Or8g36	C	T	9: 39,422,810 (GRCm39)	V69I	probably benign	Het
Or8k30	A	G	2: 86,338,815 (GRCm39)	H4R	probably benign	Het
Ppp1r37	T	C	7: 19,265,868 (GRCm39)	T633A	probably damaging	Het
Prdm10	A	G	9: 31,258,302 (GRCm39)	K576E	probably damaging	Het
Prl2c5	G	T	13: 13,360,469 (GRCm39)	M45I	probably benign	Het
Rigi	C	A	4: 40,223,824 (GRCm39)	G397*	probably null	Het
Rnf44	A	G	13: 54,830,667 (GRCm39)	S247P	probably benign	Het
Scn3a	A	G	2: 65,336,555 (GRCm39)	F684L	probably damaging	Het
Skint2	T	A	4: 112,502,648 (GRCm39)	M286K	probably benign	Het
Slc39a9	G	A	12: 80,713,450 (GRCm39)	G116D	probably damaging	Het
Smchd1	G	A	17: 71,762,621 (GRCm39)	T206I	possibly damaging	Het
Trpm6	T	A	19: 18,853,474 (GRCm39)	H1831Q	probably damaging	Het
Trpm7	A	T	2: 126,667,614 (GRCm39)	H792Q	probably damaging	Het
Ttc6	A	G	12: 57,720,542 (GRCm39)	Q936R	possibly damaging	Het
Usp53	A	T	3: 122,756,531 (GRCm39)		probably null	Het
Vmn1r236	T	A	17: 21,507,696 (GRCm39)	C271*	probably null	Het
Vmn2r70	T	A	7: 85,211,071 (GRCm39)	M547L	probably damaging	Het
Vwa5b1	G	A	4: 138,332,800 (GRCm39)	T254M	probably damaging	Het
Zc3h4	T	C	7: 16,163,770 (GRCm39)	F655S	unknown	Het
Zfp605	G	A	5: 110,275,316 (GRCm39)	G145S	probably benign	Het

Other mutations in Tmem161a

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02049:Tmem161a	APN	8	70,631,624 (GRCm39)	missense	probably damaging	1.00
IGL02425:Tmem161a	APN	8	70,629,577 (GRCm39)	critical splice donor site	probably null
IGL02597:Tmem161a	APN	8	70,634,693 (GRCm39)	missense	probably damaging	1.00
IGL02622:Tmem161a	APN	8	70,633,887 (GRCm39)	nonsense	probably null
PIT4431001:Tmem161a	UTSW	8	70,634,674 (GRCm39)	missense	probably damaging	0.99
R0498:Tmem161a	UTSW	8	70,633,623 (GRCm39)	missense	probably benign	0.00
R1881:Tmem161a	UTSW	8	70,633,435 (GRCm39)	missense	probably null	1.00
R1970:Tmem161a	UTSW	8	70,629,559 (GRCm39)	missense	probably damaging	1.00
R1971:Tmem161a	UTSW	8	70,629,559 (GRCm39)	missense	probably damaging	1.00
R2027:Tmem161a	UTSW	8	70,630,170 (GRCm39)	missense	probably damaging	1.00
R2384:Tmem161a	UTSW	8	70,630,204 (GRCm39)	missense	probably benign	0.00
R2870:Tmem161a	UTSW	8	70,631,565 (GRCm39)	intron	probably benign
R2872:Tmem161a	UTSW	8	70,631,565 (GRCm39)	intron	probably benign
R4271:Tmem161a	UTSW	8	70,634,162 (GRCm39)	missense	probably damaging	1.00
R4284:Tmem161a	UTSW	8	70,630,076 (GRCm39)	intron	probably benign
R4576:Tmem161a	UTSW	8	70,634,713 (GRCm39)	splice site	probably null
R4677:Tmem161a	UTSW	8	70,633,597 (GRCm39)	splice site	probably null
R6322:Tmem161a	UTSW	8	70,634,764 (GRCm39)	missense	probably damaging	1.00
R6823:Tmem161a	UTSW	8	70,633,849 (GRCm39)	missense	probably damaging	1.00
R7452:Tmem161a	UTSW	8	70,630,138 (GRCm39)	missense	probably damaging	1.00
R8269:Tmem161a	UTSW	8	70,634,608 (GRCm39)	missense	probably benign	0.01
R8695:Tmem161a	UTSW	8	70,627,047 (GRCm39)	missense	probably damaging	0.97
R9261:Tmem161a	UTSW	8	70,631,572 (GRCm39)	missense	probably damaging	0.98
R9355:Tmem161a	UTSW	8	70,633,821 (GRCm39)	missense	probably damaging	0.99
R9657:Tmem161a	UTSW	8	70,630,260 (GRCm39)	critical splice donor site	probably null

Predicted Primers

PCR Primer
(F):5'- TTTCCAGCTGCAGACCTGTC -3'
(R):5'- TGATCCCATAGACAGCAAGTTAG -3'

Sequencing Primer
(F):5'- CTGCTGTGGATGCCCTAGGTAAC -3'
(R):5'- CCCATAGACAGCAAGTTAGAGGGAC -3'

Posted On

2020-09-15