Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03238:Lama5'

414189

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Lama5

Ensembl Gene

ENSMUSG00000015647

Gene Name

laminin, alpha 5

Synonyms

Accession Numbers

Ncbi RefSeq: NM_001081171.2; MGI: 105382

Essential gene?

Essential (E-score: 1.000) question?

Stock #

IGL03238

Quality Score

Status

Chromosome

Chromosomal Location

180176373-180225859 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 180188574 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Threonine at position 1880 (I1880T)

Ref Sequence

ENSEMBL: ENSMUSP00000015791 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000015791]

AlphaFold

no structure available at present

PDB Structure

LAMININ ALPHA5 CHAIN N-TERMINAL FRAGMENT [X-RAY DIFFRACTION]

Predicted Effect

probably benign
Transcript: ENSMUST00000015791
AA Change: I1880T

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000015791
Gene: ENSMUSG00000015647
AA Change: I1880T

Domain	Start	End	E-Value	Type
signal peptide	1	40	N/A	INTRINSIC
LamNT	44	303	1.06e-132	SMART
EGF_Lam	305	361	4.35e-6	SMART
EGF_Lam	364	431	5.78e-11	SMART
EGF_Lam	434	476	1.32e-5	SMART
EGF_Lam	500	544	8.63e-10	SMART
EGF_Lam	547	590	1.16e-10	SMART
EGF_Lam	593	635	4.63e-10	SMART
EGF_Lam	638	680	6.25e-7	SMART
EGF_Lam	683	726	3.1e-11	SMART
EGF_Lam	730	779	2.99e-4	SMART
EGF_Lam	782	831	4.66e-6	SMART
EGF_Lam	834	878	3.48e-5	SMART
low complexity region	1261	1273	N/A	INTRINSIC
EGF_Lam	1443	1486	7.01e-10	SMART
EGF_like	1489	1530	3.64e-1	SMART
EGF_Lam	1533	1579	8.56e-14	SMART
EGF_Lam	1582	1630	1.86e-14	SMART
LamB	1689	1819	5.86e-61	SMART
EGF_like	1818	1862	2.74e0	SMART
EGF_Lam	1865	1912	3.32e-11	SMART
EGF_Lam	1915	1968	1.61e-9	SMART
EGF_Lam	1971	2022	6.39e-13	SMART
EGF_Lam	2025	2069	1.94e-12	SMART
EGF_Lam	2072	2116	1.35e-11	SMART
EGF_like	2103	2145	3.1e1	SMART
EGF_Lam	2119	2166	1.18e-2	SMART
Pfam:Laminin_I	2189	2453	1.7e-65	PFAM
low complexity region	2532	2548	N/A	INTRINSIC
low complexity region	2557	2569	N/A	INTRINSIC
low complexity region	2632	2641	N/A	INTRINSIC
low complexity region	2663	2676	N/A	INTRINSIC
LamG	2760	2912	3.97e-8	SMART
LamG	2966	3103	1.78e-10	SMART
LamG	3149	3274	1.11e-20	SMART
LamG	3359	3497	4.05e-23	SMART
LamG	3539	3670	3e-26	SMART

Coding Region Coverage

Validation Efficiency

MGI Phenotype

Strain: 3624772; 1934917
Lethality: E1-E17
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes one of the vertebrate laminin alpha chains. Laminins, a family of extracellular matrix glycoproteins, are the major noncollagenous constituent of basement membranes. They have been implicated in a wide variety of biological processes including cell adhesion, differentiation, migration, signaling, neurite outgrowth and metastasis. Laminins are composed of 3 non identical chains: laminin alpha, beta and gamma (formerly A, B1, and B2, respectively) and they form a cruciform structure consisting of 3 short arms, each formed by a different chain, and a long arm composed of all 3 chains. Each laminin chain is a multidomain protein encoded by a distinct gene. The protein encoded by this gene is the alpha-5 subunit of of laminin-10 (laminin-511), laminin-11 (laminin-521) and laminin-15 (laminin-523). [provided by RefSeq, Jun 2013]
PHENOTYPE: Homozygotes for a targeted null mutation exhibit disrupted basal laminae leading to exencephaly, syndactyly, placentopathy, kidney defects, abnormal lobar septation with absence of a visceral pleural membrane, and lethality in late gestation. [provided by MGI curators]

Allele List at MGI

All alleles(49) : Targeted(5) Gene trapped(44)

Other mutations in this stock

Total: 40 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aadacl2	A	C	3: 60,024,918 (GRCm38)	T285P	probably benign	Het
Abcf1	T	C	17: 35,963,323 (GRCm38)	K186E	probably damaging	Het
Adam3	T	C	8: 24,687,965 (GRCm38)		probably null	Het
Art1	T	C	7: 102,110,749 (GRCm38)	V85A	possibly damaging	Het
Ccdc110	A	G	8: 45,941,822 (GRCm38)	H250R	probably benign	Het
Cyp3a13	T	A	5: 137,898,889 (GRCm38)	I388F	probably damaging	Het
Dnah11	C	T	12: 118,109,898 (GRCm38)	V1425M	probably damaging	Het
Donson	G	A	16: 91,681,246 (GRCm38)	Q22*	probably null	Het
Eif2b2	A	G	12: 85,223,399 (GRCm38)	T238A	probably benign	Het
Emc2	T	A	15: 43,507,853 (GRCm38)		probably null	Het
Fkbp4	A	T	6: 128,434,757 (GRCm38)	V123E	probably damaging	Het
Frem2	A	T	3: 53,656,261 (GRCm38)	M275K	possibly damaging	Het
Gcat	T	A	15: 79,036,010 (GRCm38)		probably benign	Het
Gemin2	G	A	12: 59,016,962 (GRCm38)		probably benign	Het
Ilf3	T	A	9: 21,392,350 (GRCm38)	V169E	probably damaging	Het
Klra17	T	C	6: 129,868,810 (GRCm38)	H147R	probably benign	Het
Lzts1	T	C	8: 69,138,794 (GRCm38)	D234G	probably damaging	Het
Map3k4	G	A	17: 12,271,158 (GRCm38)	P462L	probably benign	Het
March6	C	A	15: 31,461,941 (GRCm38)		probably benign	Het
Mcm6	A	T	1: 128,355,520 (GRCm38)	F83I	probably benign	Het
Mtpn	A	G	6: 35,522,773 (GRCm38)	L32P	probably damaging	Het
Mybpc3	A	T	2: 91,131,659 (GRCm38)	I841F	probably damaging	Het
Ndst2	G	T	14: 20,728,504 (GRCm38)	H399N	probably damaging	Het
Npat	G	T	9: 53,570,426 (GRCm38)	V1145F	probably damaging	Het
Olfr65	G	A	7: 103,906,510 (GRCm38)	A21T	probably benign	Het
P2ry1	T	A	3: 61,004,495 (GRCm38)	S352T	probably damaging	Het
Plaa	T	C	4: 94,583,896 (GRCm38)	T326A	probably benign	Het
Ppdpf	T	C	2: 181,187,880 (GRCm38)	S43P	probably benign	Het
Prpmp5	T	A	6: 132,312,345 (GRCm38)	Q172L	unknown	Het
Setd1a	C	T	7: 127,785,546 (GRCm38)	T523I	possibly damaging	Het
Sgcz	C	T	8: 37,563,140 (GRCm38)		probably null	Het
Slc12a2	T	C	18: 57,914,234 (GRCm38)	Y740H	possibly damaging	Het
Stab2	A	G	10: 86,855,121 (GRCm38)	C745R	probably damaging	Het
Tmem101	A	T	11: 102,155,785 (GRCm38)	L86Q	probably damaging	Het
Tmtc3	A	C	10: 100,477,840 (GRCm38)	F57V	probably damaging	Het
Vps50	A	G	6: 3,594,771 (GRCm38)	K778R	possibly damaging	Het
Washc5	G	A	15: 59,346,842 (GRCm38)	T692M	probably damaging	Het
Zc3hav1	A	T	6: 38,332,750 (GRCm38)	V379D	probably damaging	Het
Zfp142	G	T	1: 74,576,278 (GRCm38)	R459S	probably benign	Het
Zfp512b	A	G	2: 181,589,760 (GRCm38)	V199A	probably damaging	Het

Other mutations in Lama5

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01067:Lama5	APN	2	180,176,543 (GRCm38)	unclassified	probably benign
IGL01370:Lama5	APN	2	180,197,400 (GRCm38)	missense	possibly damaging	0.87
IGL01474:Lama5	APN	2	180,196,570 (GRCm38)	missense	probably damaging	1.00
IGL01614:Lama5	APN	2	180,180,864 (GRCm38)	missense	probably damaging	1.00
IGL01941:Lama5	APN	2	180,192,392 (GRCm38)	missense	possibly damaging	0.71
IGL01953:Lama5	APN	2	180,190,704 (GRCm38)	missense	probably damaging	0.97
IGL02093:Lama5	APN	2	180,188,587 (GRCm38)	missense	probably damaging	1.00
IGL02197:Lama5	APN	2	180,207,219 (GRCm38)	missense	possibly damaging	0.82
IGL02308:Lama5	APN	2	180,190,327 (GRCm38)	splice site	probably benign
IGL02314:Lama5	APN	2	180,194,482 (GRCm38)	splice site	probably benign
IGL02317:Lama5	APN	2	180,191,319 (GRCm38)	missense	probably damaging	1.00
IGL02354:Lama5	APN	2	180,193,884 (GRCm38)	nonsense	probably null
IGL02361:Lama5	APN	2	180,193,884 (GRCm38)	nonsense	probably null
IGL02557:Lama5	APN	2	180,190,932 (GRCm38)	nonsense	probably null
IGL03026:Lama5	APN	2	180,195,967 (GRCm38)	missense	probably benign	0.34
IGL03160:Lama5	APN	2	180,180,335 (GRCm38)	missense	probably damaging	1.00
IGL03390:Lama5	APN	2	180,207,218 (GRCm38)	missense	probably damaging	1.00
blancmange	UTSW	2	180,180,611 (GRCm38)	missense	probably damaging	0.98
cupcake	UTSW	2	180,185,959 (GRCm38)	missense	probably damaging	1.00
layercake	UTSW	2	180,180,718 (GRCm38)	missense	possibly damaging	0.83
poundcake	UTSW	2	180,195,608 (GRCm38)	missense	probably damaging	1.00
Salty	UTSW	2	180,181,651 (GRCm38)	missense	possibly damaging	0.84
PIT4378001:Lama5	UTSW	2	180,189,445 (GRCm38)	missense	possibly damaging	0.89
R0003:Lama5	UTSW	2	180,178,079 (GRCm38)	splice site	probably null
R0056:Lama5	UTSW	2	180,187,106 (GRCm38)	intron	probably benign
R0147:Lama5	UTSW	2	180,190,406 (GRCm38)	missense	probably benign
R0148:Lama5	UTSW	2	180,190,406 (GRCm38)	missense	probably benign
R0310:Lama5	UTSW	2	180,181,566 (GRCm38)	splice site	probably benign
R0326:Lama5	UTSW	2	180,182,426 (GRCm38)	missense	possibly damaging	0.90
R0368:Lama5	UTSW	2	180,181,230 (GRCm38)	nonsense	probably null
R0479:Lama5	UTSW	2	180,184,457 (GRCm38)	missense	probably benign	0.03
R0490:Lama5	UTSW	2	180,180,169 (GRCm38)	missense	possibly damaging	0.90
R0636:Lama5	UTSW	2	180,189,331 (GRCm38)	critical splice donor site	probably null
R0704:Lama5	UTSW	2	180,179,484 (GRCm38)	missense	possibly damaging	0.84
R0733:Lama5	UTSW	2	180,180,718 (GRCm38)	missense	possibly damaging	0.83
R1017:Lama5	UTSW	2	180,195,420 (GRCm38)	missense	probably damaging	1.00
R1078:Lama5	UTSW	2	180,179,764 (GRCm38)	unclassified	probably benign
R1294:Lama5	UTSW	2	180,190,921 (GRCm38)	missense	probably benign	0.00
R1423:Lama5	UTSW	2	180,195,641 (GRCm38)	missense	probably damaging	1.00
R1438:Lama5	UTSW	2	180,182,800 (GRCm38)	missense	probably benign	0.01
R1447:Lama5	UTSW	2	180,185,878 (GRCm38)	missense	probably damaging	0.99
R1540:Lama5	UTSW	2	180,180,151 (GRCm38)	missense	probably benign
R1601:Lama5	UTSW	2	180,197,745 (GRCm38)	missense	probably damaging	1.00
R1624:Lama5	UTSW	2	180,206,758 (GRCm38)	missense	probably benign	0.02
R1674:Lama5	UTSW	2	180,201,987 (GRCm38)	missense	probably benign	0.00
R1687:Lama5	UTSW	2	180,194,066 (GRCm38)	missense	probably benign	0.00
R1696:Lama5	UTSW	2	180,202,486 (GRCm38)	missense	probably damaging	1.00
R1701:Lama5	UTSW	2	180,221,369 (GRCm38)	missense	probably damaging	1.00
R1778:Lama5	UTSW	2	180,195,481 (GRCm38)	splice site	probably benign
R1936:Lama5	UTSW	2	180,190,921 (GRCm38)	missense	probably benign	0.00
R1939:Lama5	UTSW	2	180,190,921 (GRCm38)	missense	probably benign	0.00
R1940:Lama5	UTSW	2	180,190,921 (GRCm38)	missense	probably benign	0.00
R1953:Lama5	UTSW	2	180,190,747 (GRCm38)	missense	possibly damaging	0.94
R1966:Lama5	UTSW	2	180,188,352 (GRCm38)	missense	probably damaging	1.00
R2024:Lama5	UTSW	2	180,179,130 (GRCm38)	missense	probably benign	0.00
R2079:Lama5	UTSW	2	180,225,508 (GRCm38)	missense	possibly damaging	0.68
R2115:Lama5	UTSW	2	180,186,885 (GRCm38)	missense	probably damaging	1.00
R2173:Lama5	UTSW	2	180,196,242 (GRCm38)	missense	probably benign	0.00
R2272:Lama5	UTSW	2	180,178,603 (GRCm38)	missense	possibly damaging	0.93
R2357:Lama5	UTSW	2	180,180,097 (GRCm38)	missense	probably benign	0.01
R2860:Lama5	UTSW	2	180,187,247 (GRCm38)	missense	probably benign	0.00
R2861:Lama5	UTSW	2	180,187,247 (GRCm38)	missense	probably benign	0.00
R2939:Lama5	UTSW	2	180,198,954 (GRCm38)	missense	probably damaging	1.00
R3053:Lama5	UTSW	2	180,183,067 (GRCm38)	missense	probably damaging	0.99
R3430:Lama5	UTSW	2	180,196,317 (GRCm38)	missense	probably benign	0.00
R3752:Lama5	UTSW	2	180,187,222 (GRCm38)	missense	probably damaging	1.00
R3782:Lama5	UTSW	2	180,194,563 (GRCm38)	missense	possibly damaging	0.57
R3901:Lama5	UTSW	2	180,182,351 (GRCm38)	splice site	probably benign
R4248:Lama5	UTSW	2	180,180,427 (GRCm38)	missense	possibly damaging	0.84
R4626:Lama5	UTSW	2	180,184,460 (GRCm38)	missense	probably damaging	0.98
R4638:Lama5	UTSW	2	180,190,413 (GRCm38)	missense	possibly damaging	0.89
R4669:Lama5	UTSW	2	180,180,637 (GRCm38)	missense	probably damaging	1.00
R4673:Lama5	UTSW	2	180,199,266 (GRCm38)	missense	probably damaging	1.00
R4677:Lama5	UTSW	2	180,179,366 (GRCm38)	missense	possibly damaging	0.69
R4701:Lama5	UTSW	2	180,191,696 (GRCm38)	missense	probably damaging	1.00
R4774:Lama5	UTSW	2	180,185,941 (GRCm38)	missense	probably damaging	1.00
R4880:Lama5	UTSW	2	180,177,068 (GRCm38)	unclassified	probably benign
R4923:Lama5	UTSW	2	180,184,149 (GRCm38)	missense	probably benign	0.18
R4960:Lama5	UTSW	2	180,208,252 (GRCm38)	critical splice donor site	probably null
R4983:Lama5	UTSW	2	180,193,449 (GRCm38)	missense	probably benign	0.13
R5061:Lama5	UTSW	2	180,198,786 (GRCm38)	nonsense	probably null
R5080:Lama5	UTSW	2	180,207,200 (GRCm38)	nonsense	probably null
R5135:Lama5	UTSW	2	180,202,220 (GRCm38)	missense	possibly damaging	0.89
R5206:Lama5	UTSW	2	180,191,304 (GRCm38)	missense	probably damaging	1.00
R5296:Lama5	UTSW	2	180,193,801 (GRCm38)	missense	probably damaging	1.00
R5319:Lama5	UTSW	2	180,181,118 (GRCm38)	missense	probably damaging	1.00
R5355:Lama5	UTSW	2	180,181,651 (GRCm38)	missense	possibly damaging	0.84
R5388:Lama5	UTSW	2	180,190,746 (GRCm38)	missense	possibly damaging	0.83
R5528:Lama5	UTSW	2	180,194,563 (GRCm38)	missense	probably benign	0.21
R5536:Lama5	UTSW	2	180,189,349 (GRCm38)	missense	probably damaging	0.99
R5658:Lama5	UTSW	2	180,208,276 (GRCm38)	nonsense	probably null
R5823:Lama5	UTSW	2	180,192,492 (GRCm38)	missense	probably benign	0.04
R5885:Lama5	UTSW	2	180,201,831 (GRCm38)	missense	probably damaging	1.00
R5889:Lama5	UTSW	2	180,193,674 (GRCm38)	intron	probably benign
R5912:Lama5	UTSW	2	180,195,475 (GRCm38)	missense	probably damaging	1.00
R5955:Lama5	UTSW	2	180,197,474 (GRCm38)	missense	probably damaging	1.00
R6015:Lama5	UTSW	2	180,185,392 (GRCm38)	missense	probably benign	0.36
R6037:Lama5	UTSW	2	180,207,013 (GRCm38)	missense	probably damaging	1.00
R6037:Lama5	UTSW	2	180,207,013 (GRCm38)	missense	probably damaging	1.00
R6191:Lama5	UTSW	2	180,185,959 (GRCm38)	missense	probably damaging	1.00
R6191:Lama5	UTSW	2	180,180,611 (GRCm38)	missense	probably damaging	0.98
R6359:Lama5	UTSW	2	180,195,982 (GRCm38)	missense	probably benign	0.01
R6385:Lama5	UTSW	2	180,196,533 (GRCm38)	missense	probably damaging	1.00
R6406:Lama5	UTSW	2	180,197,464 (GRCm38)	nonsense	probably null
R6552:Lama5	UTSW	2	180,181,154 (GRCm38)	missense	probably damaging	0.98
R6632:Lama5	UTSW	2	180,191,662 (GRCm38)	missense	probably damaging	1.00
R6633:Lama5	UTSW	2	180,191,662 (GRCm38)	missense	probably damaging	1.00
R6645:Lama5	UTSW	2	180,179,670 (GRCm38)	missense	probably damaging	1.00
R6731:Lama5	UTSW	2	180,188,574 (GRCm38)	missense	probably benign	0.09
R6744:Lama5	UTSW	2	180,191,662 (GRCm38)	missense	probably damaging	1.00
R6798:Lama5	UTSW	2	180,191,662 (GRCm38)	missense	probably damaging	1.00
R6799:Lama5	UTSW	2	180,191,662 (GRCm38)	missense	probably damaging	1.00
R6801:Lama5	UTSW	2	180,191,662 (GRCm38)	missense	probably damaging	1.00
R6851:Lama5	UTSW	2	180,191,662 (GRCm38)	missense	probably damaging	1.00
R6869:Lama5	UTSW	2	180,191,662 (GRCm38)	missense	probably damaging	1.00
R6881:Lama5	UTSW	2	180,191,662 (GRCm38)	missense	probably damaging	1.00
R6882:Lama5	UTSW	2	180,191,662 (GRCm38)	missense	probably damaging	1.00
R6884:Lama5	UTSW	2	180,191,662 (GRCm38)	missense	probably damaging	1.00
R7022:Lama5	UTSW	2	180,180,731 (GRCm38)	missense	probably damaging	1.00
R7204:Lama5	UTSW	2	180,202,177 (GRCm38)	missense	probably damaging	1.00
R7207:Lama5	UTSW	2	180,207,084 (GRCm38)	missense	probably damaging	0.98
R7282:Lama5	UTSW	2	180,201,795 (GRCm38)	missense	probably damaging	1.00
R7367:Lama5	UTSW	2	180,192,958 (GRCm38)	missense	probably benign	0.01
R7410:Lama5	UTSW	2	180,202,390 (GRCm38)	critical splice donor site	probably null
R7699:Lama5	UTSW	2	180,180,861 (GRCm38)	missense	probably damaging	1.00
R7849:Lama5	UTSW	2	180,201,812 (GRCm38)	missense	probably damaging	1.00
R7909:Lama5	UTSW	2	180,192,276 (GRCm38)	missense	possibly damaging	0.95
R7948:Lama5	UTSW	2	180,202,201 (GRCm38)	missense	probably damaging	1.00
R8153:Lama5	UTSW	2	180,187,931 (GRCm38)	missense	probably benign	0.37
R8317:Lama5	UTSW	2	180,206,991 (GRCm38)	missense	probably damaging	1.00
R8351:Lama5	UTSW	2	180,195,608 (GRCm38)	missense	probably damaging	1.00
R8370:Lama5	UTSW	2	180,201,487 (GRCm38)	missense	possibly damaging	0.80
R8398:Lama5	UTSW	2	180,197,034 (GRCm38)	critical splice donor site	probably null
R8401:Lama5	UTSW	2	180,198,787 (GRCm38)	missense	probably damaging	1.00
R8404:Lama5	UTSW	2	180,195,222 (GRCm38)	missense	probably damaging	1.00
R8502:Lama5	UTSW	2	180,195,222 (GRCm38)	missense	probably damaging	1.00
R8694:Lama5	UTSW	2	180,180,884 (GRCm38)	missense	probably damaging	0.98
R8705:Lama5	UTSW	2	180,178,561 (GRCm38)	missense	probably damaging	1.00
R8732:Lama5	UTSW	2	180,186,688 (GRCm38)	missense	probably damaging	1.00
R8755:Lama5	UTSW	2	180,190,921 (GRCm38)	missense	probably benign	0.00
R8786:Lama5	UTSW	2	180,196,307 (GRCm38)	missense	probably damaging	1.00
R8926:Lama5	UTSW	2	180,193,990 (GRCm38)	missense	probably benign	0.08
R8928:Lama5	UTSW	2	180,202,039 (GRCm38)	missense	probably damaging	1.00
R8953:Lama5	UTSW	2	180,193,520 (GRCm38)	missense	probably damaging	0.99
R8958:Lama5	UTSW	2	180,193,799 (GRCm38)	missense	probably benign
R9002:Lama5	UTSW	2	180,196,518 (GRCm38)	missense	probably damaging	1.00
R9081:Lama5	UTSW	2	180,192,137 (GRCm38)	nonsense	probably null
R9165:Lama5	UTSW	2	180,179,493 (GRCm38)	missense	probably damaging	0.99
R9233:Lama5	UTSW	2	180,198,709 (GRCm38)	nonsense	probably null
R9264:Lama5	UTSW	2	180,196,478 (GRCm38)	splice site	probably benign
R9311:Lama5	UTSW	2	180,196,482 (GRCm38)	critical splice donor site	probably null
R9443:Lama5	UTSW	2	180,201,729 (GRCm38)	missense	probably benign	0.00
R9488:Lama5	UTSW	2	180,181,441 (GRCm38)	missense	possibly damaging	0.95
R9674:Lama5	UTSW	2	180,198,474 (GRCm38)	critical splice donor site	probably null
R9684:Lama5	UTSW	2	180,207,245 (GRCm38)	missense	probably damaging	1.00
R9749:Lama5	UTSW	2	180,183,640 (GRCm38)	missense	probably benign	0.00
RF020:Lama5	UTSW	2	180,196,178 (GRCm38)	missense	probably benign
X0065:Lama5	UTSW	2	180,181,731 (GRCm38)	missense	probably benign	0.26
Z1177:Lama5	UTSW	2	180,190,714 (GRCm38)	missense	possibly damaging	0.95
Z1177:Lama5	UTSW	2	180,189,419 (GRCm38)	missense	probably damaging	1.00
Z1177:Lama5	UTSW	2	180,183,630 (GRCm38)	missense	probably benign	0.03
Z1177:Lama5	UTSW	2	180,198,810 (GRCm38)	missense	probably damaging	1.00

Posted On

2016-08-02