Mutagenetix > Incidental Mutation

Incidental Mutation 'R0070:Cmip'

64461

Institutional Source

Beutler Lab

Gene Symbol

Cmip

Ensembl Gene

ENSMUSG00000034390

Gene Name

c-Maf inducing protein

Synonyms

5830471E12Rik, 4933407C03Rik

MMRRC Submission

038361-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R0070 (G1)

Quality Score

113

Status

Not validated

Chromosome

Chromosomal Location

117983803-118186169 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 118153293 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Asparagine at position 270 (I270N)

Ref Sequence

ENSEMBL: ENSMUSP00000130264 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000095172] [ENSMUST00000166750]

AlphaFold

Q9D486

Predicted Effect

possibly damaging
Transcript: ENSMUST00000095172
AA Change: I182N

PolyPhen 2 Score 0.951 (Sensitivity: 0.79; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000092795
Gene: ENSMUSG00000034390
AA Change: I182N

Domain	Start	End	E-Value	Type
Blast:PH	13	70	5e-33	BLAST
low complexity region	71	79	N/A	INTRINSIC
low complexity region	306	319	N/A	INTRINSIC
SCOP:d1a9na_	564	681	6e-7	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000166750
AA Change: I270N

PolyPhen 2 Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000130264
Gene: ENSMUSG00000034390
AA Change: I270N

Domain	Start	End	E-Value	Type
PH	54	163	2.71e-1	SMART
low complexity region	394	407	N/A	INTRINSIC
SCOP:d1a9na_	652	769	6e-7	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000211913

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000212884

Coding Region Coverage

1x: 99.3%
3x: 98.9%
10x: 97.7%
20x: 96.1%

Validation Efficiency

97% (68/70)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a c-Maf inducing protein that plays a role in T-cell signaling pathway. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2011]

Allele List at MGI

Other mutations in this stock

Total: 59 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adgre4	T	C	17: 56,109,154 (GRCm39)	I387T	probably damaging	Het
Alpi	A	G	1: 87,028,881 (GRCm39)		probably benign	Het
Ankfn1	A	T	11: 89,283,128 (GRCm39)	L173Q	probably damaging	Het
Atp2a1	T	C	7: 126,046,624 (GRCm39)	E892G	probably benign	Het
AU018091	T	C	7: 3,208,738 (GRCm39)		probably null	Het
Capn12	T	C	7: 28,588,551 (GRCm39)		probably benign	Het
Capn2	C	A	1: 182,301,434 (GRCm39)		probably benign	Het
Cd79b	A	G	11: 106,202,744 (GRCm39)		probably benign	Het
Cdh20	C	T	1: 110,026,102 (GRCm39)	A446V	probably benign	Het
Ciapin1	T	C	8: 95,551,847 (GRCm39)	N246S	possibly damaging	Het
Cyp2d40	A	G	15: 82,644,975 (GRCm39)	V225A	unknown	Het
Dnah9	A	G	11: 66,050,866 (GRCm39)	V142A	probably benign	Het
Dnai4	A	T	4: 102,917,131 (GRCm39)	I571K	probably damaging	Het
Flt3	A	G	5: 147,309,536 (GRCm39)		probably benign	Het
Gm10238	A	G	15: 75,109,434 (GRCm39)		noncoding transcript	Het
Gm4787	T	A	12: 81,425,840 (GRCm39)	D106V	probably damaging	Het
Hipk2	G	A	6: 38,795,919 (GRCm39)	R117*	probably null	Het
Hycc1	T	C	5: 24,169,997 (GRCm39)	S451G	probably damaging	Het
Ifna11	A	G	4: 88,738,512 (GRCm39)	D106G	possibly damaging	Het
Igkv1-115	G	A	6: 68,138,402 (GRCm39)	V2I	probably benign	Het
Itga6	T	C	2: 71,657,060 (GRCm39)		probably benign	Het
Kcnj6	C	A	16: 94,742,056 (GRCm39)	K5N	probably benign	Het
Kcnt1	T	C	2: 25,782,374 (GRCm39)	V191A	probably benign	Het
Lcorl	G	A	5: 45,891,043 (GRCm39)	R437C	probably damaging	Het
Man2a1	G	A	17: 64,966,074 (GRCm39)		probably null	Het
Map3k14	T	A	11: 103,130,380 (GRCm39)		probably null	Het
Mtch1	T	A	17: 29,559,033 (GRCm39)		probably benign	Het
Myo1c	A	G	11: 75,551,076 (GRCm39)	N217S	probably benign	Het
Or2h15	A	G	17: 38,441,780 (GRCm39)	L101P	probably damaging	Het
Or2w4	T	C	13: 21,795,431 (GRCm39)	K236R	possibly damaging	Het
Orm3	A	G	4: 63,274,883 (GRCm39)	T64A	probably benign	Het
Phf20l1	T	G	15: 66,511,840 (GRCm39)	W940G	probably damaging	Het
Phldb1	C	T	9: 44,619,201 (GRCm39)	R844H	probably damaging	Het
Piezo2	T	C	18: 63,235,155 (GRCm39)	D814G	probably damaging	Het
Pkd2	T	C	5: 104,614,856 (GRCm39)	C233R	probably damaging	Het
Prkd3	A	G	17: 79,261,939 (GRCm39)	Y792H	probably damaging	Het
Pth1r	A	T	9: 110,556,618 (GRCm39)		probably null	Het
Pxdn	T	C	12: 30,032,726 (GRCm39)	L146S	probably damaging	Het
Rnf32	A	G	5: 29,430,125 (GRCm39)	T315A	probably benign	Het
Rpl5	T	C	5: 108,049,766 (GRCm39)	Y12H	probably benign	Het
Serpinh1	A	T	7: 98,998,521 (GRCm39)	S36R	probably damaging	Het
Setx	A	T	2: 29,051,537 (GRCm39)	T2030S	probably benign	Het
Sf3a3	G	A	4: 124,608,748 (GRCm39)	V21I	probably benign	Het
Sin3b	T	A	8: 73,452,210 (GRCm39)	H105Q	probably damaging	Het
Slitrk1	T	C	14: 109,150,749 (GRCm39)		probably benign	Het
Slx4	A	T	16: 3,805,880 (GRCm39)	D557E	possibly damaging	Het
Sprr3	C	T	3: 92,364,609 (GRCm39)	M78I	probably benign	Het
Ssmem1	A	G	6: 30,519,420 (GRCm39)	E35G	possibly damaging	Het
Stag1	C	T	9: 100,838,461 (GRCm39)	P1238S	probably null	Het
Stra6	C	T	9: 58,059,898 (GRCm39)		probably benign	Het
Tmem127	T	C	2: 127,098,979 (GRCm39)	V171A	probably damaging	Het
Tmem150a	A	G	6: 72,335,742 (GRCm39)		probably null	Het
Top2a	C	G	11: 98,905,886 (GRCm39)		probably null	Het
Ttn	T	C	2: 76,644,771 (GRCm39)		probably null	Het
Tusc3	G	A	8: 39,530,421 (GRCm39)	G129R	possibly damaging	Het
Uspl1	A	G	5: 149,146,515 (GRCm39)	Y422C	probably damaging	Het
Vmn2r88	A	T	14: 51,651,597 (GRCm39)	T312S	probably benign	Het
Zc3hav1l	A	T	6: 38,272,125 (GRCm39)	S215T	probably damaging	Het
Zfp947	T	A	17: 22,365,165 (GRCm39)	T170S	probably benign	Het

Other mutations in Cmip

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02043:Cmip	APN	8	118,172,067 (GRCm39)	missense	probably benign	0.29
IGL02126:Cmip	APN	8	118,175,770 (GRCm39)	missense	probably damaging	0.99
IGL02205:Cmip	APN	8	118,181,714 (GRCm39)	missense	probably damaging	1.00
IGL02352:Cmip	APN	8	118,137,994 (GRCm39)	splice site	probably benign
IGL02359:Cmip	APN	8	118,137,994 (GRCm39)	splice site	probably benign
IGL02558:Cmip	APN	8	118,175,827 (GRCm39)	missense	probably damaging	0.99
R0335:Cmip	UTSW	8	118,172,105 (GRCm39)	missense	probably damaging	0.99
R1225:Cmip	UTSW	8	118,172,110 (GRCm39)	missense	probably damaging	0.98
R1561:Cmip	UTSW	8	118,180,589 (GRCm39)	missense	probably benign	0.41
R2508:Cmip	UTSW	8	118,163,432 (GRCm39)	missense	probably benign
R2885:Cmip	UTSW	8	118,111,704 (GRCm39)	missense	probably benign	0.01
R3415:Cmip	UTSW	8	118,076,116 (GRCm39)	critical splice donor site	probably null
R4024:Cmip	UTSW	8	118,174,155 (GRCm39)	missense	possibly damaging	0.79
R4168:Cmip	UTSW	8	118,183,656 (GRCm39)	missense	probably damaging	1.00
R4169:Cmip	UTSW	8	118,183,656 (GRCm39)	missense	probably damaging	1.00
R4632:Cmip	UTSW	8	118,174,150 (GRCm39)	missense	possibly damaging	0.88
R4706:Cmip	UTSW	8	118,103,893 (GRCm39)	missense	probably damaging	0.99
R4924:Cmip	UTSW	8	117,983,994 (GRCm39)	missense	probably benign	0.00
R5380:Cmip	UTSW	8	118,149,629 (GRCm39)	missense	probably damaging	0.99
R5927:Cmip	UTSW	8	117,984,048 (GRCm39)	missense	possibly damaging	0.85
R6212:Cmip	UTSW	8	118,103,895 (GRCm39)	missense	probably damaging	1.00
R6310:Cmip	UTSW	8	118,156,549 (GRCm39)	missense	possibly damaging	0.63
R6747:Cmip	UTSW	8	118,163,618 (GRCm39)	missense	probably benign	0.02
R6881:Cmip	UTSW	8	118,163,334 (GRCm39)	missense	possibly damaging	0.77
R6968:Cmip	UTSW	8	118,103,895 (GRCm39)	missense	probably damaging	1.00
R7003:Cmip	UTSW	8	118,111,727 (GRCm39)	missense	probably benign	0.13
R7400:Cmip	UTSW	8	117,984,144 (GRCm39)	splice site	probably null
R7583:Cmip	UTSW	8	118,181,691 (GRCm39)	missense	probably damaging	0.96
R8367:Cmip	UTSW	8	118,163,610 (GRCm39)	missense	probably benign	0.05
R8720:Cmip	UTSW	8	118,138,010 (GRCm39)	missense	probably damaging	1.00
R8807:Cmip	UTSW	8	118,138,094 (GRCm39)	missense	probably benign	0.23
R8873:Cmip	UTSW	8	118,103,929 (GRCm39)	missense	probably damaging	0.96
R8902:Cmip	UTSW	8	118,103,925 (GRCm39)	missense	probably damaging	0.98
R8959:Cmip	UTSW	8	118,138,054 (GRCm39)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- AAGCCTGCTCTAAAGCCTGAGGTC -3'
(R):5'- AATGGAAGCCGTGTCCCCAGTAAC -3'

Sequencing Primer
(F):5'- TAAAGCCTGAGGTCTTCCTAAGC -3'
(R):5'- GTGTCCCCAGTAACAACATTTATTC -3'

Posted On

2013-08-06