Mutagenetix > Incidental Mutation

Incidental Mutation 'R9251:Igfn1'

723619

Institutional Source

Beutler Lab

Gene Symbol

Igfn1

Ensembl Gene

ENSMUSG00000051985

Gene Name

immunoglobulin-like and fibronectin type III domain containing 1

Synonyms

9830123M21Rik

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.076) question?

Stock #

R9251 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

135881316-135934080 bp(-) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

C to T at 135894409 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000129680 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000166193]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000124134

SMART Domains

Protein: ENSMUSP00000119230
Gene: ENSMUSG00000051985

Domain	Start	End	E-Value	Type
IG	73	159	1.29e-6	SMART
IG_like	258	344	5.45e1	SMART
IG	354	435	1.79e0	SMART
IG	445	524	3.54e-4	SMART
IG	538	624	4.86e-2	SMART
FN3	627	711	3.99e-10	SMART
FN3	727	810	9.1e-14	SMART
FN3	828	911	1.5e-14	SMART
IG	938	1021	6.41e-2	SMART
FN3	1024	1106	3.2e-9	SMART
IGc2	1152	1219	4.89e-7	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000140703

Predicted Effect

probably benign
Transcript: ENSMUST00000166193

SMART Domains

Protein: ENSMUSP00000129680
Gene: ENSMUSG00000051985

Domain	Start	End	E-Value	Type
low complexity region	90	101	N/A	INTRINSIC
IG	193	279	1.29e-6	SMART
PDB:2LHU\|A	302	365	8e-7	PDB
IG_like	378	464	5.45e1	SMART
IG	474	555	1.79e0	SMART
low complexity region	724	739	N/A	INTRINSIC
internal_repeat_2	838	1006	9.98e-5	PROSPERO
low complexity region	1067	1084	N/A	INTRINSIC
internal_repeat_2	1812	1967	9.98e-5	PROSPERO
Pfam:I-set	2054	2139	6.2e-8	PFAM
IG	2153	2239	4.86e-2	SMART
FN3	2242	2326	3.99e-10	SMART
FN3	2342	2425	9.1e-14	SMART
FN3	2443	2526	1.5e-14	SMART
IG	2553	2636	6.41e-2	SMART
FN3	2639	2721	3.2e-9	SMART
IGc2	2767	2834	4.89e-7	SMART

Coding Region Coverage

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

Validation Efficiency

100% (59/59)

Allele List at MGI

Other mutations in this stock

Total: 59 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Arhgap31	G	T	16: 38,423,218 (GRCm39)	N949K	probably benign	Het
Arv1	T	A	8: 125,452,062 (GRCm39)	I76N	probably damaging	Het
Cfap44	G	A	16: 44,229,276 (GRCm39)	A189T	probably damaging	Het
Ch25h	T	C	19: 34,451,769 (GRCm39)	Y253C	probably damaging	Het
Cnot11	T	C	1: 39,581,587 (GRCm39)	M376T	probably damaging	Het
Cnot7	T	C	8: 40,964,622 (GRCm39)		probably benign	Het
Dnah17	G	A	11: 118,012,618 (GRCm39)	S481F	probably benign	Het
Dnah2	C	T	11: 69,406,619 (GRCm39)	R541Q	probably damaging	Het
Dnah7a	C	T	1: 53,621,671 (GRCm39)	M1151I	probably damaging	Het
Dpf2	T	C	19: 5,957,166 (GRCm39)	D19G	probably damaging	Het
Eefsec	A	T	6: 88,332,574 (GRCm39)	M212K	probably damaging	Het
Elp6	G	A	9: 110,134,666 (GRCm39)	V12I	unknown	Het
Enox1	G	A	14: 77,852,997 (GRCm39)		probably null	Het
Epha1	G	T	6: 42,341,777 (GRCm39)	N424K	probably damaging	Het
Fam171a1	T	C	2: 3,226,525 (GRCm39)	S553P	probably benign	Het
Fbxw21	A	G	9: 108,974,687 (GRCm39)	S278P	probably damaging	Het
Gm45861	T	C	8: 28,032,589 (GRCm39)		probably null	Het
Gm4846	T	A	1: 166,311,307 (GRCm39)	R517S	probably benign	Het
Gnrhr	A	G	5: 86,345,221 (GRCm39)	L155P	possibly damaging	Het
Ik	T	A	18: 36,880,495 (GRCm39)		probably null	Het
Insrr	A	T	3: 87,717,391 (GRCm39)	Q763L	probably benign	Het
Klf5	G	T	14: 99,538,824 (GRCm39)	C79F	possibly damaging	Het
Lrrcc1	A	T	3: 14,623,454 (GRCm39)	R760S	probably damaging	Het
Map3k7	T	A	4: 32,002,080 (GRCm39)		probably benign	Het
Mapkbp1	C	T	2: 119,853,671 (GRCm39)	A1159V	probably benign	Het
Mgst3	C	T	1: 167,205,860 (GRCm39)		probably null	Het
Mtch2	T	A	2: 90,679,980 (GRCm39)	F71I	probably damaging	Het
Myo1e	A	G	9: 70,276,076 (GRCm39)	I764V	probably benign	Het
Myo3b	T	A	2: 70,088,425 (GRCm39)	L896*	probably null	Het
Ndufs5	T	G	4: 123,606,628 (GRCm39)	E103A	probably benign	Het
Nfe2l1	G	A	11: 96,710,421 (GRCm39)	P603S	probably damaging	Het
Or6c211	T	A	10: 129,505,980 (GRCm39)	N136I	possibly damaging	Het
Or8g34	A	T	9: 39,373,668 (GRCm39)	M311L	probably benign	Het
Piezo1	T	C	8: 123,219,354 (GRCm39)	N1093S		Het
Pitpnb	G	A	5: 111,533,390 (GRCm39)	R258H	probably benign	Het
Pla2g4d	T	C	2: 120,099,378 (GRCm39)	E708G	possibly damaging	Het
Plppr4	T	A	3: 117,115,608 (GRCm39)	T750S	probably benign	Het
Prrg4	T	G	2: 104,675,399 (GRCm39)	E68A	probably damaging	Het
Rcan2	C	T	17: 44,328,701 (GRCm39)	T90M	possibly damaging	Het
Rlbp1	T	C	7: 79,027,093 (GRCm39)	E189G	probably damaging	Het
Satb1	A	G	17: 52,112,293 (GRCm39)	F107S	probably damaging	Het
Sdc3	A	T	4: 130,548,513 (GRCm39)		probably benign	Het
Slc22a3	A	T	17: 12,726,093 (GRCm39)	V40D	probably damaging	Het
Slc35d1	A	G	4: 103,048,027 (GRCm39)		probably null	Het
Slfn1	T	C	11: 83,012,121 (GRCm39)	F79S	probably damaging	Het
Snrpg	G	T	6: 86,353,557 (GRCm39)	V46L	probably benign	Het
Tbl1xr1	G	A	3: 22,264,569 (GRCm39)	C508Y	probably benign	Het
Thada	A	T	17: 84,538,564 (GRCm39)	D1481E	probably benign	Het
Tnfsf8	A	G	4: 63,779,217 (GRCm39)	V27A	probably benign	Het
Tns1	T	C	1: 74,030,855 (GRCm39)	H300R	probably damaging	Het
Ttc13	C	A	8: 125,401,992 (GRCm39)	G589V	probably benign	Het
Ttc28	A	G	5: 111,040,698 (GRCm39)	I29V	possibly damaging	Het
Tubb4a	T	A	17: 57,387,778 (GRCm39)	N416I	possibly damaging	Het
Ubr4	T	A	4: 139,177,636 (GRCm39)	I1884N		Het
Usp16	A	G	16: 87,266,640 (GRCm39)	K175E	probably benign	Het
Usp24	A	G	4: 106,217,715 (GRCm39)	I479M	probably benign	Het
Utrn	T	C	10: 12,512,531 (GRCm39)	T2313A	probably benign	Het
Ythdc2	T	C	18: 44,974,442 (GRCm39)	V368A	probably benign	Het
Zfp628	T	C	7: 4,923,880 (GRCm39)	S701P	probably damaging	Het

Other mutations in Igfn1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00753:Igfn1	APN	1	135,894,464 (GRCm39)	missense	probably damaging	1.00
IGL02299:Igfn1	APN	1	135,881,755 (GRCm39)	utr 3 prime	probably benign
Bounty	UTSW	1	135,904,655 (GRCm39)	critical splice donor site	probably null
R2276_Igfn1_773	UTSW	1	135,892,479 (GRCm39)	missense	probably damaging	0.98
R4058_Igfn1_315	UTSW	1	135,897,494 (GRCm39)	missense	probably benign	0.07
R0144:Igfn1	UTSW	1	135,889,751 (GRCm39)	missense	probably damaging	0.99
R0190:Igfn1	UTSW	1	135,889,790 (GRCm39)	missense	probably damaging	1.00
R0350:Igfn1	UTSW	1	135,884,505 (GRCm39)	nonsense	probably null
R0413:Igfn1	UTSW	1	135,895,334 (GRCm39)	missense	probably benign	0.23
R0504:Igfn1	UTSW	1	135,896,267 (GRCm39)	missense	probably benign	0.00
R0606:Igfn1	UTSW	1	135,887,639 (GRCm39)	missense	probably damaging	1.00
R0681:Igfn1	UTSW	1	135,891,591 (GRCm39)	missense	possibly damaging	0.88
R0825:Igfn1	UTSW	1	135,890,864 (GRCm39)	missense	probably damaging	1.00
R0839:Igfn1	UTSW	1	135,882,418 (GRCm39)	missense	probably damaging	1.00
R1066:Igfn1	UTSW	1	135,898,463 (GRCm39)	missense	probably benign
R1078:Igfn1	UTSW	1	135,902,585 (GRCm39)	missense	probably damaging	1.00
R1224:Igfn1	UTSW	1	135,897,494 (GRCm39)	missense	probably benign	0.07
R1569:Igfn1	UTSW	1	135,896,771 (GRCm39)	missense	probably benign
R1626:Igfn1	UTSW	1	135,896,705 (GRCm39)	missense	probably benign	0.29
R1663:Igfn1	UTSW	1	135,896,046 (GRCm39)	missense	probably benign	0.15
R1677:Igfn1	UTSW	1	135,898,839 (GRCm39)	missense	probably damaging	0.99
R1709:Igfn1	UTSW	1	135,883,311 (GRCm39)	missense	probably benign	0.24
R1728:Igfn1	UTSW	1	135,926,421 (GRCm39)	missense	unknown
R1728:Igfn1	UTSW	1	135,926,363 (GRCm39)	missense	probably benign
R1728:Igfn1	UTSW	1	135,910,213 (GRCm39)	missense	probably benign
R1728:Igfn1	UTSW	1	135,907,653 (GRCm39)	missense	probably benign	0.00
R1728:Igfn1	UTSW	1	135,899,865 (GRCm39)	missense	probably benign
R1728:Igfn1	UTSW	1	135,898,149 (GRCm39)	missense	probably benign
R1728:Igfn1	UTSW	1	135,895,937 (GRCm39)	missense	probably benign
R1728:Igfn1	UTSW	1	135,887,666 (GRCm39)	missense	probably damaging	1.00
R1729:Igfn1	UTSW	1	135,910,213 (GRCm39)	missense	probably benign
R1729:Igfn1	UTSW	1	135,907,653 (GRCm39)	missense	probably benign	0.00
R1729:Igfn1	UTSW	1	135,899,865 (GRCm39)	missense	probably benign
R1729:Igfn1	UTSW	1	135,898,149 (GRCm39)	missense	probably benign
R1729:Igfn1	UTSW	1	135,895,937 (GRCm39)	missense	probably benign
R1729:Igfn1	UTSW	1	135,887,666 (GRCm39)	missense	probably damaging	1.00
R1729:Igfn1	UTSW	1	135,926,421 (GRCm39)	missense	unknown
R1729:Igfn1	UTSW	1	135,926,363 (GRCm39)	missense	probably benign
R1730:Igfn1	UTSW	1	135,887,666 (GRCm39)	missense	probably damaging	1.00
R1730:Igfn1	UTSW	1	135,895,937 (GRCm39)	missense	probably benign
R1730:Igfn1	UTSW	1	135,898,149 (GRCm39)	missense	probably benign
R1730:Igfn1	UTSW	1	135,899,865 (GRCm39)	missense	probably benign
R1730:Igfn1	UTSW	1	135,907,653 (GRCm39)	missense	probably benign	0.00
R1730:Igfn1	UTSW	1	135,910,213 (GRCm39)	missense	probably benign
R1730:Igfn1	UTSW	1	135,926,363 (GRCm39)	missense	probably benign
R1730:Igfn1	UTSW	1	135,926,421 (GRCm39)	missense	unknown
R1739:Igfn1	UTSW	1	135,899,865 (GRCm39)	missense	probably benign
R1739:Igfn1	UTSW	1	135,907,653 (GRCm39)	missense	probably benign	0.00
R1739:Igfn1	UTSW	1	135,910,213 (GRCm39)	missense	probably benign
R1739:Igfn1	UTSW	1	135,926,363 (GRCm39)	missense	probably benign
R1739:Igfn1	UTSW	1	135,898,149 (GRCm39)	missense	probably benign
R1739:Igfn1	UTSW	1	135,895,937 (GRCm39)	missense	probably benign
R1739:Igfn1	UTSW	1	135,887,666 (GRCm39)	missense	probably damaging	1.00
R1739:Igfn1	UTSW	1	135,926,421 (GRCm39)	missense	unknown
R1746:Igfn1	UTSW	1	135,897,561 (GRCm39)	missense	possibly damaging	0.88
R1762:Igfn1	UTSW	1	135,926,363 (GRCm39)	missense	probably benign
R1762:Igfn1	UTSW	1	135,910,213 (GRCm39)	missense	probably benign
R1762:Igfn1	UTSW	1	135,907,653 (GRCm39)	missense	probably benign	0.00
R1762:Igfn1	UTSW	1	135,899,865 (GRCm39)	missense	probably benign
R1762:Igfn1	UTSW	1	135,898,149 (GRCm39)	missense	probably benign
R1762:Igfn1	UTSW	1	135,895,937 (GRCm39)	missense	probably benign
R1762:Igfn1	UTSW	1	135,887,666 (GRCm39)	missense	probably damaging	1.00
R1762:Igfn1	UTSW	1	135,926,421 (GRCm39)	missense	unknown
R1783:Igfn1	UTSW	1	135,910,213 (GRCm39)	missense	probably benign
R1783:Igfn1	UTSW	1	135,907,653 (GRCm39)	missense	probably benign	0.00
R1783:Igfn1	UTSW	1	135,899,865 (GRCm39)	missense	probably benign
R1783:Igfn1	UTSW	1	135,898,149 (GRCm39)	missense	probably benign
R1783:Igfn1	UTSW	1	135,895,937 (GRCm39)	missense	probably benign
R1783:Igfn1	UTSW	1	135,887,666 (GRCm39)	missense	probably damaging	1.00
R1783:Igfn1	UTSW	1	135,926,421 (GRCm39)	missense	unknown
R1783:Igfn1	UTSW	1	135,926,363 (GRCm39)	missense	probably benign
R1784:Igfn1	UTSW	1	135,926,421 (GRCm39)	missense	unknown
R1784:Igfn1	UTSW	1	135,926,363 (GRCm39)	missense	probably benign
R1784:Igfn1	UTSW	1	135,910,213 (GRCm39)	missense	probably benign
R1784:Igfn1	UTSW	1	135,907,653 (GRCm39)	missense	probably benign	0.00
R1784:Igfn1	UTSW	1	135,899,865 (GRCm39)	missense	probably benign
R1784:Igfn1	UTSW	1	135,898,149 (GRCm39)	missense	probably benign
R1784:Igfn1	UTSW	1	135,895,937 (GRCm39)	missense	probably benign
R1784:Igfn1	UTSW	1	135,887,666 (GRCm39)	missense	probably damaging	1.00
R1785:Igfn1	UTSW	1	135,926,421 (GRCm39)	missense	unknown
R1785:Igfn1	UTSW	1	135,926,363 (GRCm39)	missense	probably benign
R1785:Igfn1	UTSW	1	135,910,213 (GRCm39)	missense	probably benign
R1785:Igfn1	UTSW	1	135,907,653 (GRCm39)	missense	probably benign	0.00
R1785:Igfn1	UTSW	1	135,899,865 (GRCm39)	missense	probably benign
R1785:Igfn1	UTSW	1	135,898,149 (GRCm39)	missense	probably benign
R1785:Igfn1	UTSW	1	135,895,937 (GRCm39)	missense	probably benign
R1785:Igfn1	UTSW	1	135,887,666 (GRCm39)	missense	probably damaging	1.00
R1847:Igfn1	UTSW	1	135,897,126 (GRCm39)	missense	probably benign
R1866:Igfn1	UTSW	1	135,902,606 (GRCm39)	splice site	probably null
R1921:Igfn1	UTSW	1	135,893,801 (GRCm39)	critical splice donor site	probably null
R1984:Igfn1	UTSW	1	135,889,782 (GRCm39)	missense	probably benign	0.39
R2049:Igfn1	UTSW	1	135,902,590 (GRCm39)	splice site	probably benign
R2049:Igfn1	UTSW	1	135,898,376 (GRCm39)	missense	probably benign
R2098:Igfn1	UTSW	1	135,906,043 (GRCm39)	missense	probably damaging	1.00
R2130:Igfn1	UTSW	1	135,902,590 (GRCm39)	splice site	probably benign
R2141:Igfn1	UTSW	1	135,902,590 (GRCm39)	splice site	probably benign
R2276:Igfn1	UTSW	1	135,892,479 (GRCm39)	missense	probably damaging	0.98
R2425:Igfn1	UTSW	1	135,890,840 (GRCm39)	missense	probably damaging	1.00
R2483:Igfn1	UTSW	1	135,897,275 (GRCm39)	missense	probably benign
R2504:Igfn1	UTSW	1	135,897,054 (GRCm39)	missense	probably benign	0.07
R3109:Igfn1	UTSW	1	135,925,586 (GRCm39)	missense	probably benign	0.12
R3421:Igfn1	UTSW	1	135,904,655 (GRCm39)	critical splice donor site	probably null
R3423:Igfn1	UTSW	1	135,926,379 (GRCm39)	missense	probably benign	0.01
R3705:Igfn1	UTSW	1	135,896,147 (GRCm39)	missense	probably benign
R3871:Igfn1	UTSW	1	135,896,574 (GRCm39)	missense	probably benign	0.03
R3875:Igfn1	UTSW	1	135,882,352 (GRCm39)	missense	probably damaging	1.00
R3953:Igfn1	UTSW	1	135,894,918 (GRCm39)	missense	possibly damaging	0.61
R3955:Igfn1	UTSW	1	135,894,918 (GRCm39)	missense	possibly damaging	0.61
R3957:Igfn1	UTSW	1	135,894,918 (GRCm39)	missense	possibly damaging	0.61
R3965:Igfn1	UTSW	1	135,895,557 (GRCm39)	missense	probably benign
R4006:Igfn1	UTSW	1	135,910,100 (GRCm39)	splice site	probably null
R4058:Igfn1	UTSW	1	135,897,494 (GRCm39)	missense	probably benign	0.07
R4059:Igfn1	UTSW	1	135,897,494 (GRCm39)	missense	probably benign	0.07
R4370:Igfn1	UTSW	1	135,895,844 (GRCm39)	missense	probably benign	0.00
R4380:Igfn1	UTSW	1	135,895,509 (GRCm39)	missense	probably benign	0.00
R4495:Igfn1	UTSW	1	135,897,416 (GRCm39)	missense	possibly damaging	0.79
R4628:Igfn1	UTSW	1	135,887,468 (GRCm39)	missense	possibly damaging	0.47
R4672:Igfn1	UTSW	1	135,893,107 (GRCm39)	missense	possibly damaging	0.72
R4682:Igfn1	UTSW	1	135,926,363 (GRCm39)	missense	probably benign
R4702:Igfn1	UTSW	1	135,894,947 (GRCm39)	missense	possibly damaging	0.71
R4744:Igfn1	UTSW	1	135,910,196 (GRCm39)	missense	probably benign	0.07
R4777:Igfn1	UTSW	1	135,882,600 (GRCm39)	missense	probably benign
R4806:Igfn1	UTSW	1	135,895,095 (GRCm39)	missense	probably benign	0.01
R4840:Igfn1	UTSW	1	135,895,778 (GRCm39)	missense	probably benign	0.00
R4894:Igfn1	UTSW	1	135,882,520 (GRCm39)	missense	probably damaging	1.00
R4998:Igfn1	UTSW	1	135,882,404 (GRCm39)	missense	probably damaging	1.00
R5092:Igfn1	UTSW	1	135,892,564 (GRCm39)	missense	probably benign
R5108:Igfn1	UTSW	1	135,910,179 (GRCm39)	missense	probably benign
R5120:Igfn1	UTSW	1	135,901,240 (GRCm39)	missense	possibly damaging	0.93
R5127:Igfn1	UTSW	1	135,887,634 (GRCm39)	missense	probably damaging	1.00
R5231:Igfn1	UTSW	1	135,894,474 (GRCm39)	missense	probably benign	0.26
R5286:Igfn1	UTSW	1	135,895,599 (GRCm39)	missense	probably benign	0.10
R5307:Igfn1	UTSW	1	135,892,676 (GRCm39)	missense	probably damaging	1.00
R5380:Igfn1	UTSW	1	135,893,825 (GRCm39)	missense	probably damaging	1.00
R5553:Igfn1	UTSW	1	135,895,622 (GRCm39)	missense	probably damaging	1.00
R5660:Igfn1	UTSW	1	135,898,152 (GRCm39)	missense	probably benign	0.01
R5779:Igfn1	UTSW	1	135,894,578 (GRCm39)	missense	probably benign	0.16
R5818:Igfn1	UTSW	1	135,893,864 (GRCm39)	missense	possibly damaging	0.72
R5832:Igfn1	UTSW	1	135,902,533 (GRCm39)	missense	probably damaging	0.96
R5933:Igfn1	UTSW	1	135,898,341 (GRCm39)	nonsense	probably null
R5966:Igfn1	UTSW	1	135,893,152 (GRCm39)	missense	probably damaging	1.00
R6116:Igfn1	UTSW	1	135,898,205 (GRCm39)	missense	probably benign	0.00
R6297:Igfn1	UTSW	1	135,892,399 (GRCm39)	critical splice donor site	probably null
R6652:Igfn1	UTSW	1	135,891,609 (GRCm39)	missense	probably damaging	1.00
R6737:Igfn1	UTSW	1	135,897,605 (GRCm39)	missense	probably benign
R6816:Igfn1	UTSW	1	135,887,466 (GRCm39)	missense	probably benign	0.02
R6886:Igfn1	UTSW	1	135,901,198 (GRCm39)	missense	probably damaging	1.00
R6888:Igfn1	UTSW	1	135,910,218 (GRCm39)	missense	probably benign	0.33
R6975:Igfn1	UTSW	1	135,896,183 (GRCm39)	missense	probably damaging	0.96
R7105:Igfn1	UTSW	1	135,911,956 (GRCm39)	missense	probably benign	0.11
R7114:Igfn1	UTSW	1	135,894,519 (GRCm39)	missense	probably benign	0.01
R7233:Igfn1	UTSW	1	135,897,873 (GRCm39)	missense	probably benign	0.41
R7276:Igfn1	UTSW	1	135,926,376 (GRCm39)	missense	possibly damaging	0.85
R7354:Igfn1	UTSW	1	135,903,770 (GRCm39)	missense	possibly damaging	0.72
R7358:Igfn1	UTSW	1	135,891,738 (GRCm39)	missense	probably damaging	1.00
R7380:Igfn1	UTSW	1	135,889,746 (GRCm39)	missense	probably damaging	1.00
R7389:Igfn1	UTSW	1	135,894,785 (GRCm39)	missense	probably benign	0.00
R7513:Igfn1	UTSW	1	135,887,705 (GRCm39)	missense	probably damaging	1.00
R7718:Igfn1	UTSW	1	135,896,774 (GRCm39)	missense	probably benign
R7769:Igfn1	UTSW	1	135,910,143 (GRCm39)	missense	possibly damaging	0.85
R7810:Igfn1	UTSW	1	135,902,527 (GRCm39)	missense	probably damaging	0.98
R7917:Igfn1	UTSW	1	135,899,706 (GRCm39)	missense	probably damaging	0.99
R7952:Igfn1	UTSW	1	135,891,693 (GRCm39)	missense	probably damaging	0.99
R8041:Igfn1	UTSW	1	135,895,797 (GRCm39)	nonsense	probably null
R8233:Igfn1	UTSW	1	135,895,782 (GRCm39)	missense	probably benign	0.00
R8354:Igfn1	UTSW	1	135,887,619 (GRCm39)	missense	possibly damaging	0.61
R8363:Igfn1	UTSW	1	135,891,625 (GRCm39)	missense	probably benign	0.01
R8428:Igfn1	UTSW	1	135,895,520 (GRCm39)	missense	probably damaging	1.00
R8731:Igfn1	UTSW	1	135,925,574 (GRCm39)	missense	probably benign	0.02
R8756:Igfn1	UTSW	1	135,895,698 (GRCm39)	missense	probably benign	0.10
R8797:Igfn1	UTSW	1	135,902,573 (GRCm39)	missense	possibly damaging	0.93
R8913:Igfn1	UTSW	1	135,891,579 (GRCm39)	missense	possibly damaging	0.90
R8927:Igfn1	UTSW	1	135,905,984 (GRCm39)	missense	probably damaging	1.00
R8928:Igfn1	UTSW	1	135,905,984 (GRCm39)	missense	probably damaging	1.00
R9087:Igfn1	UTSW	1	135,902,606 (GRCm39)	splice site	probably null
R9109:Igfn1	UTSW	1	135,926,327 (GRCm39)	missense	probably benign	0.26
R9113:Igfn1	UTSW	1	135,883,328 (GRCm39)	missense	probably damaging	1.00
R9117:Igfn1	UTSW	1	135,902,528 (GRCm39)	missense	probably benign	0.03
R9205:Igfn1	UTSW	1	135,903,695 (GRCm39)	missense	probably damaging	0.96
R9260:Igfn1	UTSW	1	135,907,694 (GRCm39)	missense	probably benign	0.45
R9275:Igfn1	UTSW	1	135,901,185 (GRCm39)	missense	probably damaging	0.96
R9277:Igfn1	UTSW	1	135,887,520 (GRCm39)	missense	probably damaging	0.98
R9278:Igfn1	UTSW	1	135,901,185 (GRCm39)	missense	probably damaging	0.96
R9287:Igfn1	UTSW	1	135,925,544 (GRCm39)	missense	probably benign	0.33
R9298:Igfn1	UTSW	1	135,926,327 (GRCm39)	missense	probably benign	0.26
R9356:Igfn1	UTSW	1	135,899,825 (GRCm39)	nonsense	probably null
R9371:Igfn1	UTSW	1	135,906,001 (GRCm39)	missense	probably damaging	1.00
R9532:Igfn1	UTSW	1	135,897,229 (GRCm39)	missense	possibly damaging	0.61
R9653:Igfn1	UTSW	1	135,883,323 (GRCm39)	nonsense	probably null
R9666:Igfn1	UTSW	1	135,897,692 (GRCm39)	missense	possibly damaging	0.65
R9741:Igfn1	UTSW	1	135,895,383 (GRCm39)	missense	probably benign	0.00
R9748:Igfn1	UTSW	1	135,926,336 (GRCm39)	missense	possibly damaging	0.89
R9796:Igfn1	UTSW	1	135,897,611 (GRCm39)	missense	probably benign	0.26
Z1176:Igfn1	UTSW	1	135,899,738 (GRCm39)	missense	probably damaging	0.99
Z1177:Igfn1	UTSW	1	135,897,305 (GRCm39)	missense	probably benign	0.26
Z1177:Igfn1	UTSW	1	135,883,547 (GRCm39)	missense	probably damaging	1.00
Z1177:Igfn1	UTSW	1	135,910,164 (GRCm39)	missense	possibly damaging	0.73

Predicted Primers

PCR Primer
(F):5'- CCAAGCAGACCTTTGAGTTTC -3'
(R):5'- TCTCTGAGAGAACCTTGGAGTG -3'

Sequencing Primer
(F):5'- GCAGACCTTTGAGTTTCACATAGC -3'
(R):5'- CTCTGAGAGAACCTTGGAGTGAAGAC -3'

Posted On

2022-09-08