Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02506:Fmn1'

296333

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Fmn1

Ensembl Gene

ENSMUSG00000044042

Gene Name

formin 1

Synonyms

Fmn, formin-1

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.266) question?

Stock #

IGL02506

Quality Score

Status

Chromosome

Chromosomal Location

113327736-113716767 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 113525295 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Serine at position 694 (T694S)

Ref Sequence

ENSEMBL: ENSMUSP00000125052 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000081349] [ENSMUST00000099576] [ENSMUST00000102547] [ENSMUST00000161731]

AlphaFold

Q05860

Predicted Effect

unknown
Transcript: ENSMUST00000081349
AA Change: T566S

SMART Domains

Protein: ENSMUSP00000080093
Gene: ENSMUSG00000044042
AA Change: T566S

Domain	Start	End	E-Value	Type
Blast:FH2	25	641	N/A	BLAST
SCOP:d1jvr__	668	699	2e-3	SMART
FH2	757	1162	1.16e-137	SMART

Predicted Effect

unknown
Transcript: ENSMUST00000099576
AA Change: T792S

SMART Domains

Protein: ENSMUSP00000097171
Gene: ENSMUSG00000044042
AA Change: T792S

Domain	Start	End	E-Value	Type
low complexity region	159	173	N/A	INTRINSIC
Blast:FH2	352	861	N/A	BLAST
SCOP:d1jvr__	894	925	2e-3	SMART
FH2	983	1388	1.16e-137	SMART

Predicted Effect

unknown
Transcript: ENSMUST00000102547
AA Change: T792S

SMART Domains

Protein: ENSMUSP00000099606
Gene: ENSMUSG00000044042
AA Change: T792S

Domain	Start	End	E-Value	Type
low complexity region	159	173	N/A	INTRINSIC
Blast:FH2	352	861	N/A	BLAST
SCOP:d1jvr__	894	925	2e-3	SMART
FH2	983	1424	1.03e-134	SMART

Predicted Effect

unknown
Transcript: ENSMUST00000161731
AA Change: T694S

SMART Domains

Protein: ENSMUSP00000125052
Gene: ENSMUSG00000044042
AA Change: T694S

Domain	Start	End	E-Value	Type
low complexity region	159	173	N/A	INTRINSIC
Blast:FH2	352	619	1e-62	BLAST
Blast:FH2	625	765	3e-53	BLAST
SCOP:d1jvr__	796	827	2e-3	SMART
FH2	885	1290	1.16e-137	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000185668
AA Change: T641S

Coding Region Coverage

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene belongs to the formin homology family and encodes a protein that has a role in the formation of adherens junction and the polymerization of linear actin cables. The homologous gene in mouse is associated with limb deformity. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2015]
PHENOTYPE: Homozygotes for spontaneous, irradiation-induced, and transgene-insertional mutations show severe syndactyly and oligodactyly of the feet, abnormal long bones (including radius-ulna fusions), and reduced or absent kidneys. Many mutants survive and breed. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 57 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcg8	A	G	17: 84,692,488 (GRCm38)	E189G	possibly damaging	Het
Acad11	T	C	9: 104,091,732 (GRCm38)		probably null	Het
Adcy7	G	T	8: 88,317,943 (GRCm38)	R488L	probably damaging	Het
Akt1	C	T	12: 112,659,280 (GRCm38)		probably benign	Het
Ano9	C	T	7: 141,102,254 (GRCm38)		probably benign	Het
Arhgap15	A	G	2: 44,063,808 (GRCm38)	D182G	possibly damaging	Het
Asxl3	T	A	18: 22,452,399 (GRCm38)	V127D	probably benign	Het
Cacna1g	A	G	11: 94,429,129 (GRCm38)	M1407T	probably damaging	Het
Card9	A	C	2: 26,354,415 (GRCm38)		probably benign	Het
Cdh5	A	G	8: 104,137,822 (GRCm38)	N472D	probably damaging	Het
Ceacam2	T	A	7: 25,527,954 (GRCm38)	T343S	probably benign	Het
Cic	T	A	7: 25,290,857 (GRCm38)	C1928S	probably benign	Het
Clk3	C	T	9: 57,754,644 (GRCm38)	W31*	probably null	Het
Cntn4	A	G	6: 106,618,388 (GRCm38)	T489A	probably benign	Het
Crispld1	G	A	1: 17,756,305 (GRCm38)	R431H	probably damaging	Het
Crmp1	T	A	5: 37,278,855 (GRCm38)		probably benign	Het
Cyld	A	G	8: 88,729,590 (GRCm38)	T423A	possibly damaging	Het
Cyp3a44	A	T	5: 145,799,388 (GRCm38)	I84N	probably damaging	Het
D2hgdh	A	G	1: 93,829,785 (GRCm38)	N141D	probably damaging	Het
Dip2b	T	A	15: 100,157,281 (GRCm38)	L341Q	probably damaging	Het
F3	C	T	3: 121,731,674 (GRCm38)	T53I	possibly damaging	Het
Fam227b	T	A	2: 126,003,911 (GRCm38)	Y386F	probably benign	Het
Gcnt2	T	A	13: 40,887,380 (GRCm38)	V5E	probably benign	Het
Herpud1	G	T	8: 94,394,642 (GRCm38)	E355*	probably null	Het
Igf1r	T	C	7: 68,193,396 (GRCm38)	S752P	probably benign	Het
Iqsec1	T	C	6: 90,672,075 (GRCm38)	I687V	possibly damaging	Het
Kdm5a	T	C	6: 120,432,149 (GRCm38)	S1598P	probably damaging	Het
Klk9	A	G	7: 43,795,639 (GRCm38)	E185G	probably benign	Het
Myo16	G	T	8: 10,390,217 (GRCm38)	R423L	probably damaging	Het
Myo7b	T	C	18: 31,967,154 (GRCm38)	E1609G	probably damaging	Het
Nom1	T	A	5: 29,439,816 (GRCm38)		probably benign	Het
Nomo1	A	G	7: 46,078,056 (GRCm38)	I1040V	possibly damaging	Het
Or8b39	G	A	9: 38,085,445 (GRCm38)	G203D	probably damaging	Het
Paqr9	T	C	9: 95,560,695 (GRCm38)	V246A	probably benign	Het
Pfkfb4	A	T	9: 109,030,336 (GRCm38)	D437V	probably benign	Het
Phldb1	G	T	9: 44,710,926 (GRCm38)	D797E	probably benign	Het
Pkd1l3	A	G	8: 109,647,500 (GRCm38)	E1399G	probably damaging	Het
Plekhs1	G	A	19: 56,471,766 (GRCm38)	C97Y	probably damaging	Het
Plscr4	A	T	9: 92,489,991 (GRCm38)	I272L	possibly damaging	Het
Prlhr	A	C	19: 60,467,928 (GRCm38)	Y67D	probably damaging	Het
Rab3gap2	A	G	1: 185,252,024 (GRCm38)		probably benign	Het
Rad23b	T	C	4: 55,382,511 (GRCm38)	V238A	probably benign	Het
Sel1l2	T	C	2: 140,275,460 (GRCm38)	T164A	possibly damaging	Het
Serpinh1	T	A	7: 99,346,992 (GRCm38)	K295M	probably damaging	Het
Slc45a4	T	C	15: 73,581,838 (GRCm38)	E770G	probably benign	Het
Spag4	T	C	2: 156,069,222 (GRCm38)	L390P	probably damaging	Het
Stip1	A	G	19: 7,035,489 (GRCm38)		probably benign	Het
Tacr1	A	G	6: 82,403,758 (GRCm38)	N50S	probably damaging	Het
Tg	T	C	15: 66,741,594 (GRCm38)	V433A	possibly damaging	Het
Ubap1l	T	A	9: 65,369,211 (GRCm38)		probably benign	Het
Usp40	A	T	1: 87,982,016 (GRCm38)	I572K	probably damaging	Het
Vps13b	G	T	15: 35,917,162 (GRCm38)	E3717D	probably damaging	Het
Wdr81	T	C	11: 75,444,406 (GRCm38)	N1778S	probably benign	Het
Ylpm1	T	A	12: 85,049,191 (GRCm38)	F1162Y	probably damaging	Het
Zbtb10	T	A	3: 9,265,237 (GRCm38)	F552I	probably damaging	Het
Zfp507	T	C	7: 35,776,466 (GRCm38)	I811V	probably damaging	Het
Zfp663	A	T	2: 165,353,951 (GRCm38)	V116D	probably benign	Het

Other mutations in Fmn1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00495:Fmn1	APN	2	113,444,467 (GRCm38)	intron	probably benign
IGL01520:Fmn1	APN	2	113,444,368 (GRCm38)	intron	probably benign
IGL02039:Fmn1	APN	2	113,365,080 (GRCm38)	missense	unknown
IGL02222:Fmn1	APN	2	113,593,109 (GRCm38)	missense	probably damaging	1.00
IGL02238:Fmn1	APN	2	113,582,125 (GRCm38)	missense	possibly damaging	0.90
IGL02373:Fmn1	APN	2	113,364,126 (GRCm38)	missense	unknown
IGL02490:Fmn1	APN	2	113,529,472 (GRCm38)	splice site	probably benign
IGL02684:Fmn1	APN	2	113,525,277 (GRCm38)	missense	unknown
IGL03008:Fmn1	APN	2	113,365,100 (GRCm38)	missense	unknown
IGL03058:Fmn1	APN	2	113,441,814 (GRCm38)	intron	probably benign
IGL03076:Fmn1	APN	2	113,584,092 (GRCm38)	missense	probably damaging	0.99
FR4304:Fmn1	UTSW	2	113,525,783 (GRCm38)	small insertion	probably benign
FR4304:Fmn1	UTSW	2	113,525,774 (GRCm38)	small insertion	probably benign
FR4342:Fmn1	UTSW	2	113,525,783 (GRCm38)	small insertion	probably benign
FR4589:Fmn1	UTSW	2	113,525,774 (GRCm38)	small insertion	probably benign
FR4589:Fmn1	UTSW	2	113,525,773 (GRCm38)	small insertion	probably benign
FR4737:Fmn1	UTSW	2	113,525,784 (GRCm38)	small insertion	probably benign
FR4737:Fmn1	UTSW	2	113,525,781 (GRCm38)	small insertion	probably benign
FR4737:Fmn1	UTSW	2	113,525,778 (GRCm38)	small insertion	probably benign
R0349:Fmn1	UTSW	2	113,365,796 (GRCm38)	missense	unknown
R0452:Fmn1	UTSW	2	113,636,779 (GRCm38)	missense	possibly damaging	0.46
R0529:Fmn1	UTSW	2	113,707,853 (GRCm38)	splice site	probably benign
R1215:Fmn1	UTSW	2	113,693,030 (GRCm38)	nonsense	probably null
R1471:Fmn1	UTSW	2	113,693,094 (GRCm38)	missense	possibly damaging	0.95
R1489:Fmn1	UTSW	2	113,365,212 (GRCm38)	missense	unknown
R1491:Fmn1	UTSW	2	113,596,369 (GRCm38)	missense	probably damaging	1.00
R1551:Fmn1	UTSW	2	113,525,862 (GRCm38)	missense	possibly damaging	0.70
R1558:Fmn1	UTSW	2	113,693,118 (GRCm38)	missense	possibly damaging	0.46
R1588:Fmn1	UTSW	2	113,365,698 (GRCm38)	missense	unknown
R1602:Fmn1	UTSW	2	113,525,623 (GRCm38)	missense	unknown
R1690:Fmn1	UTSW	2	113,525,482 (GRCm38)	missense	unknown
R1772:Fmn1	UTSW	2	113,365,355 (GRCm38)	missense	unknown
R1867:Fmn1	UTSW	2	113,709,438 (GRCm38)	missense	probably damaging	1.00
R1923:Fmn1	UTSW	2	113,429,721 (GRCm38)	intron	probably benign
R1941:Fmn1	UTSW	2	113,365,143 (GRCm38)	missense	unknown
R2019:Fmn1	UTSW	2	113,364,480 (GRCm38)	missense	unknown
R2140:Fmn1	UTSW	2	113,595,048 (GRCm38)	missense	probably benign	0.45
R2164:Fmn1	UTSW	2	113,365,617 (GRCm38)	missense	unknown
R2395:Fmn1	UTSW	2	113,365,181 (GRCm38)	missense	unknown
R2999:Fmn1	UTSW	2	113,365,094 (GRCm38)	missense	unknown
R3405:Fmn1	UTSW	2	113,364,348 (GRCm38)	missense	unknown
R3407:Fmn1	UTSW	2	113,365,055 (GRCm38)	missense	unknown
R3771:Fmn1	UTSW	2	113,582,118 (GRCm38)	missense	probably damaging	1.00
R3772:Fmn1	UTSW	2	113,582,118 (GRCm38)	missense	probably damaging	1.00
R3773:Fmn1	UTSW	2	113,582,118 (GRCm38)	missense	probably damaging	1.00
R3777:Fmn1	UTSW	2	113,365,122 (GRCm38)	missense	unknown
R4166:Fmn1	UTSW	2	113,636,735 (GRCm38)	missense	probably benign	0.33
R4477:Fmn1	UTSW	2	113,444,399 (GRCm38)	intron	probably benign
R4614:Fmn1	UTSW	2	113,365,149 (GRCm38)	missense	unknown
R4701:Fmn1	UTSW	2	113,584,071 (GRCm38)	missense	possibly damaging	0.76
R4867:Fmn1	UTSW	2	113,584,120 (GRCm38)	critical splice donor site	probably null
R5063:Fmn1	UTSW	2	113,364,921 (GRCm38)	missense	unknown
R5224:Fmn1	UTSW	2	113,365,125 (GRCm38)	missense	unknown
R5510:Fmn1	UTSW	2	113,596,369 (GRCm38)	missense	probably damaging	1.00
R6083:Fmn1	UTSW	2	113,364,303 (GRCm38)	missense	unknown
R6234:Fmn1	UTSW	2	113,365,655 (GRCm38)	missense	unknown
R6266:Fmn1	UTSW	2	113,596,338 (GRCm38)	missense	probably damaging	1.00
R6764:Fmn1	UTSW	2	113,525,215 (GRCm38)	missense	unknown
R7054:Fmn1	UTSW	2	113,365,008 (GRCm38)	missense	unknown
R7311:Fmn1	UTSW	2	113,525,680 (GRCm38)	missense	unknown
R7439:Fmn1	UTSW	2	113,441,611 (GRCm38)	missense	unknown
R7440:Fmn1	UTSW	2	113,441,611 (GRCm38)	missense	unknown
R7441:Fmn1	UTSW	2	113,441,611 (GRCm38)	missense	unknown
R7444:Fmn1	UTSW	2	113,441,611 (GRCm38)	missense	unknown
R7461:Fmn1	UTSW	2	113,364,071 (GRCm38)	missense	unknown
R7526:Fmn1	UTSW	2	113,688,134 (GRCm38)	missense	probably damaging	0.99
R7540:Fmn1	UTSW	2	113,529,310 (GRCm38)	splice site	probably null
R7576:Fmn1	UTSW	2	113,365,008 (GRCm38)	missense	unknown
R7657:Fmn1	UTSW	2	113,525,193 (GRCm38)	missense	unknown
R7669:Fmn1	UTSW	2	113,365,477 (GRCm38)	missense	unknown
R7713:Fmn1	UTSW	2	113,525,814 (GRCm38)	missense	unknown
R7841:Fmn1	UTSW	2	113,529,465 (GRCm38)	critical splice donor site	probably null
R7953:Fmn1	UTSW	2	113,596,344 (GRCm38)	missense	probably benign	0.03
R7959:Fmn1	UTSW	2	113,365,622 (GRCm38)	missense	unknown
R8041:Fmn1	UTSW	2	113,364,594 (GRCm38)	missense	unknown
R8152:Fmn1	UTSW	2	113,365,692 (GRCm38)	missense	unknown
R8203:Fmn1	UTSW	2	113,525,275 (GRCm38)	missense	unknown
R8318:Fmn1	UTSW	2	113,365,157 (GRCm38)	missense	unknown
R8356:Fmn1	UTSW	2	113,365,040 (GRCm38)	missense	unknown
R8456:Fmn1	UTSW	2	113,365,040 (GRCm38)	missense	unknown
R8698:Fmn1	UTSW	2	113,429,807 (GRCm38)	missense	unknown
R8861:Fmn1	UTSW	2	113,364,804 (GRCm38)	missense	unknown
R8907:Fmn1	UTSW	2	113,525,569 (GRCm38)	missense	unknown
R9147:Fmn1	UTSW	2	113,441,628 (GRCm38)	missense	unknown
R9148:Fmn1	UTSW	2	113,441,628 (GRCm38)	missense	unknown
R9536:Fmn1	UTSW	2	113,478,917 (GRCm38)	missense	unknown
R9574:Fmn1	UTSW	2	113,595,057 (GRCm38)	missense	probably damaging	1.00
R9577:Fmn1	UTSW	2	113,364,125 (GRCm38)	missense	unknown
RF003:Fmn1	UTSW	2	113,525,786 (GRCm38)	small insertion	probably benign
Z1088:Fmn1	UTSW	2	113,441,925 (GRCm38)	intron	probably benign

Posted On

2015-04-16