Mutagenetix > Incidental Mutation

Incidental Mutation 'R7773:Prl6a1'

598724

Institutional Source

Beutler Lab

Gene Symbol

Prl6a1

Ensembl Gene

ENSMUSG00000069259

Gene Name

prolactin family 6, subfamily a, member 1

Synonyms

PLP-B, Prlpb

MMRRC Submission

045829-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.065) question?

Stock #

R7773 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

27496610-27503235 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 27502125 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Threonine at position 164 (I164T)

Ref Sequence

ENSEMBL: ENSMUSP00000089269 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000091679] [ENSMUST00000091680]

AlphaFold

O35257

Predicted Effect

probably damaging
Transcript: ENSMUST00000091679
AA Change: I169T

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000089268
Gene: ENSMUSG00000069259
AA Change: I169T

Domain	Start	End	E-Value	Type
low complexity region	4	15	N/A	INTRINSIC
Pfam:Hormone_1	21	235	8e-65	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000091680
AA Change: I164T

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000089269
Gene: ENSMUSG00000069259
AA Change: I164T

Domain	Start	End	E-Value	Type
Pfam:Hormone_1	16	230	1.1e-61	PFAM

Meta Mutation Damage Score

0.6467

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.3%

Validation Efficiency

98% (55/56)

Allele List at MGI

Other mutations in this stock

Total: 59 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700006A11Rik	A	G	3: 124,206,180 (GRCm39)	I336T	probably benign	Het
4930519P11Rik	T	C	2: 154,455,107 (GRCm39)	Y84C	unknown	Het
4930568D16Rik	C	T	2: 35,244,606 (GRCm39)	G249S	probably damaging	Het
AAdacl4fm3	A	T	4: 144,430,047 (GRCm39)	L314Q	probably damaging	Het
Adprhl1	C	T	8: 13,298,682 (GRCm39)	V83I	probably damaging	Het
Agbl1	T	A	7: 76,348,585 (GRCm39)	V894E	unknown	Het
Amigo3	T	C	9: 107,931,867 (GRCm39)	L430P	probably benign	Het
Aoc1	A	G	6: 48,883,146 (GRCm39)	I341V	probably benign	Het
Bod1l	A	G	5: 41,990,055 (GRCm39)	S223P	probably benign	Het
Cacnb3	T	C	15: 98,537,819 (GRCm39)		probably null	Het
Ccdc63	G	T	5: 122,247,335 (GRCm39)	N503K	probably damaging	Het
Ccdc83	T	A	7: 89,879,120 (GRCm39)	I225F	probably damaging	Het
Cd200r1	A	G	16: 44,610,050 (GRCm39)	T90A	possibly damaging	Het
Cd8a	A	G	6: 71,350,799 (GRCm39)	N88S	probably benign	Het
Cep170	A	G	1: 176,567,642 (GRCm39)	V152A		Het
Chid1	T	C	7: 141,109,518 (GRCm39)	M123V	probably benign	Het
Cnnm4	T	C	1: 36,538,603 (GRCm39)	V595A	probably benign	Het
Coro7	A	G	16: 4,449,870 (GRCm39)	L630P	probably damaging	Het
Cpvl	A	G	6: 53,908,890 (GRCm39)		probably null	Het
Edem3	A	T	1: 151,687,347 (GRCm39)	K762*	probably null	Het
Elp6	T	A	9: 110,141,627 (GRCm39)		probably null	Het
Emilin3	A	T	2: 160,752,718 (GRCm39)	Y77*	probably null	Het
Fam234b	T	A	6: 135,220,912 (GRCm39)	I641N	probably benign	Het
Farsa	T	C	8: 85,590,781 (GRCm39)		probably null	Het
Foxf2	T	C	13: 31,811,182 (GRCm39)	S374P	probably benign	Het
Gm11596	A	T	11: 99,683,667 (GRCm39)	I151N	unknown	Het
Gm9817	C	T	13: 45,232,427 (GRCm39)	Q77*	probably null	Het
Gon4l	A	G	3: 88,803,102 (GRCm39)	K1238E	probably benign	Het
H13	A	G	2: 152,537,431 (GRCm39)	Y292C	probably damaging	Het
Hip1r	A	G	5: 124,139,504 (GRCm39)	N928S	probably benign	Het
Iqcf4	T	C	9: 106,445,812 (GRCm39)	N112D	probably benign	Het
Jak3	A	C	8: 72,131,686 (GRCm39)	T125P	probably benign	Het
Krt7	A	C	15: 101,311,913 (GRCm39)	K124Q	possibly damaging	Het
Ldc1	T	C	4: 130,114,169 (GRCm39)	N83D	probably damaging	Het
Lrrc66	G	A	5: 73,764,664 (GRCm39)	S793F	probably damaging	Het
Mycbp2	C	T	14: 103,485,840 (GRCm39)	V1074I	probably damaging	Het
Nckap5	T	C	1: 125,954,581 (GRCm39)	D657G	probably benign	Het
Nt5el	A	G	13: 105,218,793 (GRCm39)	I42M	probably damaging	Het
Or5b113	T	A	19: 13,342,598 (GRCm39)	V202E	probably benign	Het
Or8k21	T	C	2: 86,145,034 (GRCm39)	I199V	probably benign	Het
Osbpl7	A	G	11: 96,941,548 (GRCm39)	S24G	probably benign	Het
Pcm1	G	T	8: 41,762,610 (GRCm39)	E1385*	probably null	Het
Poc5	A	G	13: 96,547,143 (GRCm39)	T469A	probably damaging	Het
Ppp3ca	A	G	3: 136,596,222 (GRCm39)	T296A	probably benign	Het
Psmd6	GCAGAGCGGGCAGGGCATCTCACTGACCCTGTCACCTACCCAGAGCGGGCAGGGCATCTCACTGACCCTGTCACCTACCCAGAGCGGGCAGGGCATCTCACTGACC	GCAGAGCGGGCAGGGCATCTCACTGACCCTGTCACCTACCCAGAGCGGGCAGGGCATCTCACTGACC	14: 14,119,882 (GRCm38)		probably null	Het
Rnf149	A	C	1: 39,604,299 (GRCm39)	M188R	possibly damaging	Het
Rpl10l	T	C	12: 66,331,041 (GRCm39)	I31V	probably benign	Het
Serinc5	T	C	13: 92,797,592 (GRCm39)	S32P	probably damaging	Het
Sirt1	T	A	10: 63,162,562 (GRCm39)	K137M	possibly damaging	Het
Smc4	A	G	3: 68,923,496 (GRCm39)	Y251C	probably damaging	Het
Sod3	A	C	5: 52,525,643 (GRCm39)	E114A	possibly damaging	Het
Tgfbr3	A	G	5: 107,288,368 (GRCm39)	V431A	probably benign	Het
Tlr4	T	C	4: 66,757,836 (GRCm39)	S210P	probably damaging	Het
Trub2	G	T	2: 29,676,520 (GRCm39)	T70N	probably benign	Het
Tsga10	A	T	1: 37,874,323 (GRCm39)	C159S	unknown	Het
Vmn1r15	A	T	6: 57,235,644 (GRCm39)	I171F	probably benign	Het
Vmn2r50	T	A	7: 9,771,562 (GRCm39)	H713L	possibly damaging	Het
Zcchc14	T	C	8: 122,378,514 (GRCm39)	S43G	unknown	Het
Zfp638	T	C	6: 83,956,196 (GRCm39)	I1601T	probably damaging	Het

Other mutations in Prl6a1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01124:Prl6a1	APN	13	27,500,347 (GRCm39)	missense	possibly damaging	0.72
IGL01688:Prl6a1	APN	13	27,501,969 (GRCm39)	missense	probably damaging	1.00
IGL01922:Prl6a1	APN	13	27,499,343 (GRCm39)	missense	possibly damaging	0.57
IGL02059:Prl6a1	APN	13	27,499,348 (GRCm39)	missense	probably benign	0.02
IGL03170:Prl6a1	APN	13	27,499,406 (GRCm39)	missense	possibly damaging	0.95
R0027:Prl6a1	UTSW	13	27,502,011 (GRCm39)	missense	probably damaging	1.00
R0027:Prl6a1	UTSW	13	27,502,011 (GRCm39)	missense	probably damaging	1.00
R0049:Prl6a1	UTSW	13	27,501,980 (GRCm39)	missense	probably damaging	0.99
R0606:Prl6a1	UTSW	13	27,498,177 (GRCm39)	intron	probably benign
R0944:Prl6a1	UTSW	13	27,502,149 (GRCm39)	splice site	probably benign
R1518:Prl6a1	UTSW	13	27,502,911 (GRCm39)	missense	probably null	0.19
R1518:Prl6a1	UTSW	13	27,502,910 (GRCm39)	missense	possibly damaging	0.72
R1566:Prl6a1	UTSW	13	27,499,410 (GRCm39)	missense	possibly damaging	0.84
R1621:Prl6a1	UTSW	13	27,501,993 (GRCm39)	missense	probably benign	0.01
R2011:Prl6a1	UTSW	13	27,499,352 (GRCm39)	missense	probably benign	0.00
R2058:Prl6a1	UTSW	13	27,503,081 (GRCm39)	missense	probably benign	0.05
R2937:Prl6a1	UTSW	13	27,499,303 (GRCm39)	missense	probably damaging	0.98
R3079:Prl6a1	UTSW	13	27,502,983 (GRCm39)	missense	possibly damaging	0.71
R4685:Prl6a1	UTSW	13	27,500,307 (GRCm39)	missense	probably benign	0.00
R4856:Prl6a1	UTSW	13	27,502,983 (GRCm39)	missense	probably damaging	0.98
R4886:Prl6a1	UTSW	13	27,502,983 (GRCm39)	missense	probably damaging	0.98
R5495:Prl6a1	UTSW	13	27,496,654 (GRCm39)	missense	possibly damaging	0.95
R5923:Prl6a1	UTSW	13	27,500,346 (GRCm39)	missense	probably benign	0.08
R6772:Prl6a1	UTSW	13	27,503,031 (GRCm39)	missense	probably damaging	1.00
R7411:Prl6a1	UTSW	13	27,502,125 (GRCm39)	missense	probably damaging	1.00
R7501:Prl6a1	UTSW	13	27,500,282 (GRCm39)	missense	possibly damaging	0.69
R7549:Prl6a1	UTSW	13	27,502,954 (GRCm39)	missense	probably damaging	0.96
R7563:Prl6a1	UTSW	13	27,498,221 (GRCm39)	critical splice donor site	probably null
R8024:Prl6a1	UTSW	13	27,502,678 (GRCm39)	intron	probably benign
R8994:Prl6a1	UTSW	13	27,499,417 (GRCm39)	missense	probably benign	0.01
R9129:Prl6a1	UTSW	13	27,502,064 (GRCm39)	missense
R9395:Prl6a1	UTSW	13	27,499,400 (GRCm39)	missense	possibly damaging	0.71
Z1177:Prl6a1	UTSW	13	27,499,304 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TACCACATGGGCTAACTCTGTC -3'
(R):5'- CATTTAGATGGATTAAAGTGCCAGGG -3'

Sequencing Primer
(F):5'- ACATGGGCTAACTCTGTCATATTTC -3'
(R):5'- ATTAAAGTGCCAGGGAAGGTTTATTG -3'

Posted On

2019-11-26