Mutagenetix > Incidental Mutation

Incidental Mutation 'R6852:Lhx9'

534995

Institutional Source

Beutler Lab

Gene Symbol

Lhx9

Ensembl Gene

ENSMUSG00000019230

Gene Name

LIM homeobox protein 9

Synonyms

3110009O07Rik, Lhx9 alpha, LH2B

MMRRC Submission

045023-MU

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.743) question?

Stock #

R6852 (G1)

Quality Score

217.468

Status

Not validated

Chromosome

Chromosomal Location

138825186-138848577 bp(-) (GRCm38)

Type of Mutation

frame shift

DNA Base Change (assembly)

ACC to ACCC at 138841806 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000142268 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000019374] [ENSMUST00000046870] [ENSMUST00000093486] [ENSMUST00000112026] [ENSMUST00000112030] [ENSMUST00000194557]

AlphaFold

Q9WUH2

Predicted Effect

probably null
Transcript: ENSMUST00000019374

SMART Domains

Protein: ENSMUSP00000019374
Gene: ENSMUSG00000019230

Domain	Start	End	E-Value	Type
LIM	70	123	4.48e-17	SMART
LIM	132	186	8.04e-19	SMART
HOX	267	319	1.89e-4	SMART

Predicted Effect

probably null
Transcript: ENSMUST00000046870

SMART Domains

Protein: ENSMUSP00000036480
Gene: ENSMUSG00000019230

Domain	Start	End	E-Value	Type
LIM	61	114	4.48e-17	SMART
LIM	123	177	8.04e-19	SMART
HOX	258	320	8.07e-22	SMART
low complexity region	344	368	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000093486

SMART Domains

Protein: ENSMUSP00000091198
Gene: ENSMUSG00000019230

Domain	Start	End	E-Value	Type
LIM	61	114	4.48e-17	SMART
LIM	123	177	8.04e-19	SMART
HOX	258	310	1.89e-4	SMART

Predicted Effect

probably null
Transcript: ENSMUST00000112026

SMART Domains

Protein: ENSMUSP00000107657
Gene: ENSMUSG00000019230

Domain	Start	End	E-Value	Type
LIM	70	123	4.48e-17	SMART
LIM	132	186	8.04e-19	SMART
HOX	267	329	8.07e-22	SMART
low complexity region	353	377	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000112030

SMART Domains

Protein: ENSMUSP00000107661
Gene: ENSMUSG00000019230

Domain	Start	End	E-Value	Type
LIM	61	114	4.48e-17	SMART
LIM	123	177	8.04e-19	SMART
HOX	258	310	1.89e-4	SMART

Predicted Effect

probably null
Transcript: ENSMUST00000194557

Meta Mutation Damage Score

0.9755

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.7%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the LIM homeobox gene family of developmentally expressed transcription factors. The encoded protein contains a homeodomain and two cysteine-rich zinc-binding LIM domains involved in protein-protein interactions. The protein is highly similar to a mouse protein that causes gonadal agenesis when inactivated, suggesting a role in gonadal development. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygotes for a targeted null mutation exhibit failed proliferation of the somatic cells of the genital ridge resulting in lack of discrete gonad formation, infertility in both sexes, and female-like genitalia in genetically male mice. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 72 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1110002E22Rik	C	T	3: 138,065,169 (GRCm38)	Q40*	probably null	Het
1700034E13Rik	T	C	18: 52,663,633 (GRCm38)	V81A	probably damaging	Het
A630089N07Rik	A	G	16: 98,065,655 (GRCm38)	I369T	probably benign	Het
Aatk	T	A	11: 120,010,468 (GRCm38)	Q977L	probably benign	Het
Abca4	A	T	3: 122,135,195 (GRCm38)	Q144H	probably damaging	Het
Ampd3	T	C	7: 110,802,546 (GRCm38)	F416L	probably benign	Het
Anks1b	A	G	10: 90,260,654 (GRCm38)	E425G	probably damaging	Het
Atm	A	G	9: 53,482,430 (GRCm38)	S1737P	possibly damaging	Het
Bsph1	T	A	7: 13,470,330 (GRCm38)		probably null	Het
Cabyr	C	T	18: 12,754,097 (GRCm38)	P262S	probably benign	Het
Cdc14a	G	A	3: 116,328,676 (GRCm38)	P214L	possibly damaging	Het
Cep128	C	A	12: 91,366,342 (GRCm38)		probably null	Het
Cfh	T	A	1: 140,147,749 (GRCm38)	R250S	probably damaging	Het
Ddx39a	T	C	8: 83,723,017 (GRCm38)	I417T	probably benign	Het
Dgka	T	A	10: 128,722,539 (GRCm38)	K548M	probably damaging	Het
Efr3a	G	A	15: 65,829,830 (GRCm38)	V198I	probably benign	Het
Elapor1	T	C	3: 108,482,338 (GRCm38)	E203G	probably damaging	Het
Epg5	C	T	18: 78,012,891 (GRCm38)	T1760I	probably damaging	Het
Fat1	T	C	8: 45,035,598 (GRCm38)	V3472A	possibly damaging	Het
Fbxo48	T	A	11: 16,953,402 (GRCm38)	N9K	probably benign	Het
Fcgbpl1	T	A	7: 28,147,135 (GRCm38)	I1084N	probably damaging	Het
Fer1l6	A	T	15: 58,594,878 (GRCm38)	H833L	probably damaging	Het
Foxn1	G	T	11: 78,360,960 (GRCm38)	Q482K	probably benign	Het
Fstl5	A	G	3: 76,707,855 (GRCm38)	D741G	probably damaging	Het
Gm8909	T	C	17: 36,168,073 (GRCm38)	N95D	possibly damaging	Het
Gmip	C	T	8: 69,817,991 (GRCm38)	Q55*	probably null	Het
Hapln2	G	A	3: 88,022,651 (GRCm38)	T306M	possibly damaging	Het
Kat6a	T	A	8: 22,938,660 (GRCm38)	S1344T	probably benign	Het
Kctd1	C	T	18: 14,986,344 (GRCm38)	D705N	possibly damaging	Het
Micall2	G	T	5: 139,715,793 (GRCm38)	A482D	possibly damaging	Het
Mindy3	T	A	2: 12,419,252 (GRCm38)	M1L	possibly damaging	Het
Mtdh	A	G	15: 34,136,721 (GRCm38)	E352G	probably damaging	Het
Muc5ac	G	A	7: 141,816,907 (GRCm38)	V3219I	probably benign	Het
Myh4	A	G	11: 67,252,968 (GRCm38)		probably null	Het
Ncor1	A	G	11: 62,343,245 (GRCm38)	I377T	probably damaging	Het
Oog4	C	A	4: 143,439,109 (GRCm38)	C156F	possibly damaging	Het
Or5m9	A	T	2: 86,046,604 (GRCm38)	I41F	probably benign	Het
Pcyt1a	T	C	16: 32,470,120 (GRCm38)	S260P	probably damaging	Het
Phf3	A	T	1: 30,804,630 (GRCm38)	F1749L	probably damaging	Het
Prickle2	T	C	6: 92,376,544 (GRCm38)	D647G	probably benign	Het
Raver2	T	C	4: 101,133,590 (GRCm38)	S387P	probably benign	Het
Relch	T	C	1: 105,753,595 (GRCm38)	L1184P	probably damaging	Het
Rgs19	A	G	2: 181,689,148 (GRCm38)	S231P	possibly damaging	Het
Rpl8	G	T	15: 76,905,949 (GRCm38)	R198L	probably benign	Het
Sacs	T	A	14: 61,179,288 (GRCm38)	S77T	possibly damaging	Het
Samd14	G	A	11: 95,021,454 (GRCm38)	G219D	probably damaging	Het
Sec16a	C	T	2: 26,441,419 (GRCm38)	V195M	probably damaging	Het
Sesn2	C	T	4: 132,493,802 (GRCm38)	V453I	possibly damaging	Het
Slc46a3	A	T	5: 147,886,160 (GRCm38)	C291S	probably damaging	Het
Smarcal1	A	G	1: 72,591,173 (GRCm38)	T129A	possibly damaging	Het
Sorl1	T	A	9: 42,024,398 (GRCm38)	R1041W	possibly damaging	Het
Sptlc3	T	C	2: 139,566,586 (GRCm38)	I207T	probably benign	Het
Srgap3	T	C	6: 112,816,661 (GRCm38)	D118G	probably damaging	Het
Tas2r117	T	A	6: 132,802,929 (GRCm38)	V10D	probably benign	Het
Tbcd	A	G	11: 121,609,380 (GRCm38)	K1111E	probably benign	Het
Tor1aip1	A	T	1: 156,035,820 (GRCm38)	L139Q	probably damaging	Het
Trbv23	T	C	6: 41,216,247 (GRCm38)	V23A	probably damaging	Het
Ttll3	AAGTA	AAGTATAGTA	6: 113,399,159 (GRCm38)		probably null	Het
Ttll3	CAAAGTAA	CAAAGTAAAGTAA	6: 113,399,157 (GRCm38)		probably null	Het
Ttll3	GGCAAAG	GGCAAAGCAAAG	6: 113,399,155 (GRCm38)		probably null	Het
Vmn1r42	T	G	6: 89,844,787 (GRCm38)	T267P	possibly damaging	Het
Vmn2r53	C	A	7: 12,606,514 (GRCm38)	V11F	probably damaging	Het
Vmn2r67	T	C	7: 85,152,153 (GRCm38)	M192V	probably damaging	Het
Vmn2r78	T	C	7: 86,954,603 (GRCm38)	V663A	probably damaging	Het
Zdhhc1	C	T	8: 105,477,072 (GRCm38)	G156S	possibly damaging	Het
Zfp318	GAAGAA	GAAGAAAAAGAA	17: 46,412,533 (GRCm38)		probably benign	Het
Zfp318	AAGAAG	AAGAAGTAGAAG	17: 46,412,534 (GRCm38)		probably benign	Het
Zfp318	AGAAG	AGAAGAGGAAG	17: 46,412,538 (GRCm38)		probably benign	Het
Zfp560	A	G	9: 20,348,043 (GRCm38)	C508R	probably damaging	Het
Zfp654	G	A	16: 64,786,598 (GRCm38)	L414F	probably damaging	Het
Zfp872	A	T	9: 22,200,059 (GRCm38)	Y278F	probably damaging	Het
Zscan20	T	C	4: 128,589,722 (GRCm38)	S385G	probably damaging	Het

Other mutations in Lhx9

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00955:Lhx9	APN	1	138,828,680 (GRCm38)	missense	possibly damaging	0.74
IGL01624:Lhx9	APN	1	138,832,783 (GRCm38)	nonsense	probably null
IGL02149:Lhx9	APN	1	138,831,434 (GRCm38)	missense	probably damaging	1.00
IGL02452:Lhx9	APN	1	138,841,842 (GRCm38)	missense	probably damaging	1.00
IGL02982:Lhx9	APN	1	138,838,611 (GRCm38)	missense	probably damaging	1.00
R0123:Lhx9	UTSW	1	138,838,679 (GRCm38)	missense	probably damaging	1.00
R0134:Lhx9	UTSW	1	138,838,679 (GRCm38)	missense	probably damaging	1.00
R0141:Lhx9	UTSW	1	138,840,006 (GRCm38)	missense	possibly damaging	0.86
R0225:Lhx9	UTSW	1	138,838,679 (GRCm38)	missense	probably damaging	1.00
R0281:Lhx9	UTSW	1	138,832,904 (GRCm38)	missense	probably benign	0.00
R1460:Lhx9	UTSW	1	138,838,709 (GRCm38)	splice site	probably benign
R1932:Lhx9	UTSW	1	138,842,009 (GRCm38)	start gained	probably benign
R4738:Lhx9	UTSW	1	138,832,748 (GRCm38)	missense	probably damaging	1.00
R4792:Lhx9	UTSW	1	138,838,351 (GRCm38)	missense	possibly damaging	0.87
R4820:Lhx9	UTSW	1	138,838,367 (GRCm38)	missense	probably benign	0.00
R4877:Lhx9	UTSW	1	138,838,354 (GRCm38)	missense	probably benign	0.04
R6035:Lhx9	UTSW	1	138,838,543 (GRCm38)	missense	possibly damaging	0.67
R6035:Lhx9	UTSW	1	138,838,543 (GRCm38)	missense	possibly damaging	0.67
R6825:Lhx9	UTSW	1	138,841,806 (GRCm38)	frame shift	probably null
R6853:Lhx9	UTSW	1	138,841,806 (GRCm38)	frame shift	probably null
R7264:Lhx9	UTSW	1	138,832,751 (GRCm38)	missense	probably damaging	0.98
R8097:Lhx9	UTSW	1	138,838,351 (GRCm38)	missense	probably damaging	0.97
R8164:Lhx9	UTSW	1	138,832,780 (GRCm38)	missense	probably damaging	1.00
R8245:Lhx9	UTSW	1	138,838,441 (GRCm38)	missense	probably benign	0.24
R8278:Lhx9	UTSW	1	138,838,586 (GRCm38)	missense	probably damaging	0.98
R8951:Lhx9	UTSW	1	138,841,966 (GRCm38)	missense	probably damaging	1.00
R9761:Lhx9	UTSW	1	138,847,196 (GRCm38)	missense	probably benign	0.09
Z1177:Lhx9	UTSW	1	138,831,498 (GRCm38)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- AGACTGGAGAGCTCAGGACTAC -3'
(R):5'- TCACTCGAATGAACTGAGAGC -3'

Sequencing Primer
(F):5'- GAGAGCTCAGGACTACAACATCTTAG -3'
(R):5'- TCGAATGAACTGAGAGCCCCAG -3'

Posted On

2018-09-12