Mutagenetix > Incidental Mutation

Incidental Mutation 'R1896:Pramel23'

211968

Institutional Source

Beutler Lab

Gene Symbol

Pramel23

Ensembl Gene

ENSMUSG00000070617

Gene Name

PRAME like 23

Synonyms

Gm13089

MMRRC Submission

039916-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.063) question?

Stock #

R1896 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

143423070-143429281 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to G at 143424714 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glycine to Alanine at position 243 (G243A)

Ref Sequence

ENSEMBL: ENSMUSP00000073224 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000073532]

AlphaFold

A2AGW7

Predicted Effect

probably benign
Transcript: ENSMUST00000073532
AA Change: G243A

PolyPhen 2 Score 0.106 (Sensitivity: 0.93; Specificity: 0.86)

SMART Domains

Protein: ENSMUSP00000073224
Gene: ENSMUSG00000070617
AA Change: G243A

Domain	Start	End	E-Value	Type
low complexity region	204	216	N/A	INTRINSIC
low complexity region	331	343	N/A	INTRINSIC

Coding Region Coverage

1x: 97.3%
3x: 96.7%
10x: 94.9%
20x: 91.4%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 59 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abo	C	A	2: 26,733,609 (GRCm39)	D199Y	probably damaging	Het
Acvr1c	A	C	2: 58,170,306 (GRCm39)	V277G	probably damaging	Het
Adam23	G	A	1: 63,584,731 (GRCm39)	A380T	probably benign	Het
Art2b	A	G	7: 101,229,236 (GRCm39)	V221A	probably benign	Het
Bcam	A	G	7: 19,500,640 (GRCm39)	S153P	probably damaging	Het
Bltp1	C	T	3: 36,962,380 (GRCm39)	Q494*	probably null	Het
C1qtnf1	G	T	11: 118,334,583 (GRCm39)	G21V	probably damaging	Het
Car13	T	C	3: 14,710,235 (GRCm39)	I59T	probably benign	Het
Cep97	T	C	16: 55,748,107 (GRCm39)	N108D	probably damaging	Het
Cog3	T	A	14: 75,979,784 (GRCm39)	E182D	probably benign	Het
Efcab3	A	G	11: 104,611,514 (GRCm39)	K452R	probably benign	Het
Endou	A	G	15: 97,610,873 (GRCm39)	Y404H	probably damaging	Het
F12	T	C	13: 55,568,540 (GRCm39)	Y373C	probably damaging	Het
Fam221b	T	C	4: 43,660,375 (GRCm39)	T405A	probably damaging	Het
Fetub	A	G	16: 22,751,045 (GRCm39)	R131G	probably damaging	Het
Foxp2	A	T	6: 15,379,767 (GRCm39)		probably benign	Het
Ggt5	T	C	10: 75,440,560 (GRCm39)	V227A	probably damaging	Het
Gipr	A	G	7: 18,897,996 (GRCm39)	S79P	probably benign	Het
Gphn	A	G	12: 78,459,128 (GRCm39)	D72G	possibly damaging	Het
Gzmk	A	G	13: 113,309,427 (GRCm39)	S208P	probably damaging	Het
Itpkc	T	C	7: 26,907,805 (GRCm39)	D633G	probably damaging	Het
Jarid2	T	C	13: 45,038,358 (GRCm39)		probably null	Het
Kif21b	C	A	1: 136,075,583 (GRCm39)	R237S	possibly damaging	Het
Lama1	G	A	17: 68,098,218 (GRCm39)	R1805H	probably benign	Het
Lpin3	C	T	2: 160,747,218 (GRCm39)	P815S	probably damaging	Het
Lrp1	T	A	10: 127,395,867 (GRCm39)	I2468F	possibly damaging	Het
Nav1	T	C	1: 135,388,475 (GRCm39)	N1118S	probably benign	Het
Ncoa3	T	A	2: 165,890,384 (GRCm39)	I90N	probably benign	Het
Notch3	T	C	17: 32,362,402 (GRCm39)	T1408A	probably benign	Het
Nwd2	A	G	5: 63,962,753 (GRCm39)	D779G	probably benign	Het
Obox6	A	T	7: 15,568,770 (GRCm39)	H35Q	possibly damaging	Het
Pkd1l3	C	A	8: 110,350,831 (GRCm39)	P559T	possibly damaging	Het
Pou2af2	A	G	9: 51,203,098 (GRCm39)	S19P	probably damaging	Het
Prex1	T	A	2: 166,428,574 (GRCm39)	I716F	probably benign	Het
Psap	C	T	10: 60,130,826 (GRCm39)	Q219*	probably null	Het
Rab5if	C	T	2: 156,707,252 (GRCm39)	P64S	probably damaging	Het
Shisa5	T	A	9: 108,885,108 (GRCm39)	I126N	probably damaging	Het
Slc11a1	T	C	1: 74,414,931 (GRCm39)	L21P	probably benign	Het
Slc4a4	A	G	5: 89,194,167 (GRCm39)	T172A	probably damaging	Het
Sned1	C	T	1: 93,192,769 (GRCm39)	P352L	probably benign	Het
Sox4	T	C	13: 29,136,127 (GRCm39)	Y293C	probably damaging	Het
Srgap3	T	A	6: 112,715,958 (GRCm39)	H654L	probably benign	Het
Stra6	A	T	9: 58,059,166 (GRCm39)	M510L	probably benign	Het
Syna	C	A	5: 134,588,006 (GRCm39)	M314I	probably benign	Het
Taf5l	A	G	8: 124,730,152 (GRCm39)	L144P	probably damaging	Het
Tll2	A	G	19: 41,101,498 (GRCm39)	F379L	probably benign	Het
Traf3ip3	A	G	1: 192,858,042 (GRCm39)	V492A	probably benign	Het
Uba2	A	G	7: 33,850,455 (GRCm39)	F364S	probably damaging	Het
Unc50	T	A	1: 37,476,323 (GRCm39)	L161Q	probably damaging	Het
Ush2a	T	C	1: 188,282,206 (GRCm39)	V1907A	probably benign	Het
Uso1	A	T	5: 92,348,992 (GRCm39)		probably null	Het
Utf1	C	A	7: 139,524,213 (GRCm39)	L143I	probably damaging	Het
Vmn1r158	C	T	7: 22,490,143 (GRCm39)	C22Y	probably damaging	Het
Vmn1r36	T	A	6: 66,693,756 (GRCm39)	M40L	probably benign	Het
Vmn2r43	A	G	7: 8,258,055 (GRCm39)	V386A	possibly damaging	Het
Vps9d1	C	A	8: 123,973,778 (GRCm39)	R335L	probably damaging	Het
Zbtb26	A	G	2: 37,326,347 (GRCm39)	S230P	possibly damaging	Het
Zfp74	A	T	7: 29,634,569 (GRCm39)	C380S	probably damaging	Het
Zfyve1	A	C	12: 83,602,388 (GRCm39)	V469G	probably damaging	Het

Other mutations in Pramel23

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01720:Pramel23	APN	4	143,423,410 (GRCm39)	utr 3 prime	probably benign
IGL02087:Pramel23	APN	4	143,423,644 (GRCm39)	missense	probably damaging	0.96
IGL02296:Pramel23	APN	4	143,425,051 (GRCm39)	nonsense	probably null
IGL02902:Pramel23	APN	4	143,424,913 (GRCm39)	missense	probably damaging	1.00
IGL02903:Pramel23	APN	4	143,425,736 (GRCm39)	missense	probably benign	0.04
IGL02962:Pramel23	APN	4	143,423,910 (GRCm39)	missense	probably benign	0.28
IGL03351:Pramel23	APN	4	143,423,658 (GRCm39)	missense	possibly damaging	0.80
R0122:Pramel23	UTSW	4	143,424,974 (GRCm39)	missense	probably benign	0.44
R0533:Pramel23	UTSW	4	143,424,590 (GRCm39)	nonsense	probably null
R0609:Pramel23	UTSW	4	143,425,073 (GRCm39)	missense	probably benign	0.00
R0743:Pramel23	UTSW	4	143,425,134 (GRCm39)	missense	probably damaging	0.97
R0744:Pramel23	UTSW	4	143,425,056 (GRCm39)	missense	probably benign	0.19
R0833:Pramel23	UTSW	4	143,425,056 (GRCm39)	missense	probably benign	0.19
R1052:Pramel23	UTSW	4	143,423,477 (GRCm39)	missense	possibly damaging	0.81
R1690:Pramel23	UTSW	4	143,424,693 (GRCm39)	missense	probably benign	0.03
R1764:Pramel23	UTSW	4	143,424,840 (GRCm39)	missense	probably benign	0.14
R2084:Pramel23	UTSW	4	143,425,920 (GRCm39)	missense	probably damaging	1.00
R2178:Pramel23	UTSW	4	143,424,612 (GRCm39)	missense	possibly damaging	0.95
R2888:Pramel23	UTSW	4	143,423,460 (GRCm39)	missense	probably benign	0.00
R3759:Pramel23	UTSW	4	143,423,721 (GRCm39)	missense	probably damaging	1.00
R4193:Pramel23	UTSW	4	143,424,903 (GRCm39)	missense	probably damaging	1.00
R4380:Pramel23	UTSW	4	143,424,856 (GRCm39)	missense	probably benign	0.21
R4385:Pramel23	UTSW	4	143,424,584 (GRCm39)	critical splice donor site	probably null
R4513:Pramel23	UTSW	4	143,424,718 (GRCm39)	missense	probably benign	0.00
R4647:Pramel23	UTSW	4	143,425,914 (GRCm39)	missense	probably benign	0.00
R4920:Pramel23	UTSW	4	143,425,853 (GRCm39)	missense	probably benign	0.05
R4994:Pramel23	UTSW	4	143,424,939 (GRCm39)	missense	possibly damaging	0.94
R5197:Pramel23	UTSW	4	143,424,632 (GRCm39)	missense	possibly damaging	0.86
R6005:Pramel23	UTSW	4	143,425,002 (GRCm39)	missense	probably benign	0.00
R6073:Pramel23	UTSW	4	143,424,838 (GRCm39)	missense	probably damaging	0.99
R6197:Pramel23	UTSW	4	143,423,886 (GRCm39)	missense	possibly damaging	0.90
R6264:Pramel23	UTSW	4	143,425,722 (GRCm39)	missense	possibly damaging	0.50
R6821:Pramel23	UTSW	4	143,425,874 (GRCm39)	nonsense	probably null
R6923:Pramel23	UTSW	4	143,425,676 (GRCm39)	missense	probably benign	0.06
R7034:Pramel23	UTSW	4	143,423,898 (GRCm39)	missense	probably damaging	1.00
R7140:Pramel23	UTSW	4	143,425,002 (GRCm39)	missense	probably benign	0.01
R7298:Pramel23	UTSW	4	143,425,075 (GRCm39)	missense	probably benign	0.23
R7529:Pramel23	UTSW	4	143,429,244 (GRCm39)
R7766:Pramel23	UTSW	4	143,425,809 (GRCm39)	missense	probably damaging	0.98
R7774:Pramel23	UTSW	4	143,423,676 (GRCm39)	missense	possibly damaging	0.89
R7816:Pramel23	UTSW	4	143,424,764 (GRCm39)	missense	probably benign	0.00
R8137:Pramel23	UTSW	4	143,425,835 (GRCm39)	missense	probably damaging	1.00
R8937:Pramel23	UTSW	4	143,423,562 (GRCm39)	missense	probably damaging	1.00
R8982:Pramel23	UTSW	4	143,424,886 (GRCm39)	missense	probably benign	0.01
R9016:Pramel23	UTSW	4	143,423,899 (GRCm39)	missense	possibly damaging	0.76
R9100:Pramel23	UTSW	4	143,425,727 (GRCm39)	missense	probably benign	0.04
R9200:Pramel23	UTSW	4	143,423,856 (GRCm39)	missense	possibly damaging	0.90
R9257:Pramel23	UTSW	4	143,425,685 (GRCm39)	missense	probably damaging	1.00
R9471:Pramel23	UTSW	4	143,423,749 (GRCm39)	missense	probably damaging	1.00
R9517:Pramel23	UTSW	4	143,424,930 (GRCm39)	missense	possibly damaging	0.95
Z1088:Pramel23	UTSW	4	143,424,650 (GRCm39)	missense	probably benign
Z1176:Pramel23	UTSW	4	143,423,515 (GRCm39)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- GTGCTTTCTGTGGTCTACTAGATCC -3'
(R):5'- TACATACTTGTTGCAGTGGGCC -3'

Sequencing Primer
(F):5'- GTGGTCTACTAGATCCCCTCAC -3'
(R):5'- TGAAGATTCAGGGCTCAATCAAC -3'

Posted On

2014-06-30