Mutagenetix > Incidental Mutation

Incidental Mutation 'R9295:Krt80'

704575

Institutional Source

Beutler Lab

Gene Symbol

Krt80

Ensembl Gene

ENSMUSG00000037185

Gene Name

keratin 80

Synonyms

2310041I20Rik, Kb20, 1200016G03Rik

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R9295 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

101246196-101268043 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 101249652 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glutamic Acid to Glycine at position 287 (E287G)

Ref Sequence

ENSEMBL: ENSMUSP00000076437 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000077196] [ENSMUST00000230831] [ENSMUST00000230909]

AlphaFold

Q0VBK2

Predicted Effect

probably benign
Transcript: ENSMUST00000077196
AA Change: E287G

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000076437
Gene: ENSMUSG00000037185
AA Change: E287G

Domain	Start	End	E-Value	Type
Pfam:Keratin_2_head	2	79	2.5e-12	PFAM
Filament	82	393	2.18e-113	SMART
low complexity region	419	430	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000230831
AA Change: E72G

PolyPhen 2 Score 0.016 (Sensitivity: 0.95; Specificity: 0.79)

Predicted Effect

probably benign
Transcript: ENSMUST00000230909
AA Change: E234G

PolyPhen 2 Score 0.016 (Sensitivity: 0.95; Specificity: 0.79)

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.] Keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into epithelial keratins and hair keratins. This gene's expression profile shows that it encodes a type II epithelial keratin, although structurally the encoded protein is more like a type II hair keratin. This protein is involved in cell differentiation, localizing near desmosomal plaques in earlier stages of differentiation but then dispersing throughout the cytoplasm in terminally differentiating cells. The type II keratins are clustered in a region of chromosome 12q13. Two transcript variants encoding two different fully functional isoforms have been found for this gene.[provided by RefSeq, Oct 2010]

Allele List at MGI

Other mutations in this stock

Total: 67 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2410002F23Rik	T	A	7: 43,900,116 (GRCm39)	V7E	probably benign	Het
Adam17	A	G	12: 21,399,938 (GRCm39)	V156A	probably benign	Het
Ankrd6	A	T	4: 32,822,160 (GRCm39)	V236E	probably damaging	Het
Apcdd1	C	T	18: 63,055,731 (GRCm39)		probably benign	Het
C2cd3	C	A	7: 100,081,734 (GRCm39)	D1125E		Het
Cacna2d2	A	G	9: 107,386,419 (GRCm39)	E182G	probably benign	Het
Cct3	A	G	3: 88,212,430 (GRCm39)	K139E	probably benign	Het
Cd96	G	T	16: 45,938,244 (GRCm39)	Q74K	probably benign	Het
Cdk5rap1	A	T	2: 154,194,186 (GRCm39)	I373N	probably damaging	Het
Cep350	A	T	1: 155,738,051 (GRCm39)	Y2597*	probably null	Het
Chst13	G	A	6: 90,286,506 (GRCm39)	P152L	probably damaging	Het
Clcn1	G	A	6: 42,290,883 (GRCm39)	G919E	probably benign	Het
Col6a4	G	A	9: 105,957,734 (GRCm39)	A30V	probably damaging	Het
Copa	T	C	1: 171,939,823 (GRCm39)	C655R	probably damaging	Het
Cpt1a	T	A	19: 3,428,441 (GRCm39)	V605E	probably damaging	Het
Ddx46	T	C	13: 55,811,599 (GRCm39)	I600T	possibly damaging	Het
Dhx9	C	A	1: 153,340,673 (GRCm39)	V656L	probably damaging	Het
Dnhd1	T	A	7: 105,363,348 (GRCm39)	M3970K	probably benign	Het
Ercc5	G	T	1: 44,198,017 (GRCm39)	V145F	probably damaging	Het
Erv3	T	C	2: 131,697,979 (GRCm39)	T127A	possibly damaging	Het
Fcer1a	T	C	1: 173,050,174 (GRCm39)	Y172C	probably damaging	Het
Gabra1	A	G	11: 42,044,217 (GRCm39)	M167T	probably damaging	Het
Ggt1	A	G	10: 75,421,743 (GRCm39)	H530R	probably benign	Het
Gli2	C	A	1: 118,764,996 (GRCm39)	V1052L	probably damaging	Het
Gm4491	A	C	14: 57,351,140 (GRCm39)	F84C	unknown	Het
Irf2bp1	C	T	7: 18,739,740 (GRCm39)	T460I	probably benign	Het
Klf3	A	G	5: 64,980,240 (GRCm39)	Y187C	possibly damaging	Het
Lama4	G	T	10: 38,948,747 (GRCm39)	V837F	probably damaging	Het
Lrig3	G	T	10: 125,850,722 (GRCm39)	C1096F	probably benign	Het
Mtrr	T	C	13: 68,719,258 (GRCm39)	R328G	possibly damaging	Het
Nln	TGGTCCAGGTAAAACTGCCCCAGCCAATCAGGTACCTTGGATAGAGGTCCAGGTAAAACTGCCCCAGCCAATCAGGTACCTTGGATAGAGGTCCAGGTAGAACTGCCCCAGC	TGGTCCAGGTAAAACTGCCCCAGCCAATCAGGTACCTTGGATAGAGGTCCAGGTAGAACTGCCCCAGC	13: 104,186,924 (GRCm39)		probably null	Het
Obsl1	A	T	1: 75,476,721 (GRCm39)	D744E	probably damaging	Het
Or2n1d	A	T	17: 38,646,320 (GRCm39)	T91S	possibly damaging	Het
Or4x13	G	A	2: 90,231,441 (GRCm39)	M145I	probably benign	Het
Pde4b	A	G	4: 102,112,478 (GRCm39)	T21A	probably damaging	Het
Phf20l1	G	A	15: 66,513,752 (GRCm39)	G1003D	probably damaging	Het
Phtf1	A	G	3: 103,904,893 (GRCm39)	T514A	probably benign	Het
Phykpl	A	G	11: 51,482,231 (GRCm39)	E115G	possibly damaging	Het
Pramel20	A	G	4: 143,298,704 (GRCm39)	T216A	possibly damaging	Het
Pxmp2	C	A	5: 110,433,944 (GRCm39)		probably benign	Het
Reln	A	G	5: 22,209,209 (GRCm39)	L1123P	possibly damaging	Het
Rusc2	T	C	4: 43,416,382 (GRCm39)	S563P	probably damaging	Het
Secisbp2	T	G	13: 51,808,483 (GRCm39)	S83A	probably damaging	Het
Sema3c	T	A	5: 17,932,495 (GRCm39)	M666K	probably benign	Het
Serbp1	G	T	6: 67,248,208 (GRCm39)	D114Y	probably damaging	Het
Sh3d21	T	A	4: 126,045,276 (GRCm39)	T468S	possibly damaging	Het
Shroom3	T	A	5: 93,098,478 (GRCm39)	D1319E	probably benign	Het
Skida1	T	C	2: 18,051,386 (GRCm39)	R502G	unknown	Het
Slc25a12	C	A	2: 71,128,986 (GRCm39)	G314C	possibly damaging	Het
Smg8	A	G	11: 86,968,789 (GRCm39)	V989A	probably benign	Het
Spon2	G	A	5: 33,373,844 (GRCm39)	P156S	probably damaging	Het
Stx1a	A	G	5: 135,066,370 (GRCm39)	N50S	probably benign	Het
Tmem151b	C	A	17: 45,857,806 (GRCm39)	V147L	probably benign	Het
Trim12c	C	T	7: 103,990,391 (GRCm39)	G362D	unknown	Het
Tsr1	T	C	11: 74,799,135 (GRCm39)	V772A	probably damaging	Het
Tti2	A	T	8: 31,643,550 (GRCm39)	K222*	probably null	Het
Usp48	G	A	4: 137,340,996 (GRCm39)	G332E	probably benign	Het
Vmn1r60	A	G	7: 5,547,218 (GRCm39)	M294T	probably null	Het
Vmn2r6	T	C	3: 64,463,484 (GRCm39)	E450G	probably benign	Het
Vmn2r60	T	A	7: 41,785,955 (GRCm39)	F253I	probably benign	Het
Wnk4	A	T	11: 101,160,078 (GRCm39)	D649V	probably damaging	Het
Zfhx4	T	C	3: 5,394,525 (GRCm39)	S1040P	probably benign	Het
Zfp112	C	T	7: 23,824,805 (GRCm39)	R262C	probably benign	Het
Zfp287	T	A	11: 62,606,115 (GRCm39)	D264V	probably benign	Het
Zfp46	T	C	4: 136,017,876 (GRCm39)	C237R	probably damaging	Het
Zfp773	C	T	7: 7,135,694 (GRCm39)	E301K	probably benign	Het
Zswim2	A	C	2: 83,748,304 (GRCm39)	V292G	probably benign	Het

Other mutations in Krt80

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00980:Krt80	APN	15	101,247,879 (GRCm39)	missense	possibly damaging	0.64
IGL03184:Krt80	APN	15	101,250,135 (GRCm39)	missense	probably damaging	1.00
1mM(1):Krt80	UTSW	15	101,262,089 (GRCm39)	critical splice donor site	probably null
R0394:Krt80	UTSW	15	101,250,180 (GRCm39)	missense	probably damaging	0.97
R0520:Krt80	UTSW	15	101,267,898 (GRCm39)	missense	probably benign	0.00
R1654:Krt80	UTSW	15	101,249,590 (GRCm39)	missense	probably damaging	0.96
R2436:Krt80	UTSW	15	101,257,384 (GRCm39)	missense	probably damaging	0.98
R4326:Krt80	UTSW	15	101,250,189 (GRCm39)	missense	possibly damaging	0.52
R5292:Krt80	UTSW	15	101,250,066 (GRCm39)	missense	probably damaging	1.00
R5783:Krt80	UTSW	15	101,257,360 (GRCm39)	critical splice donor site	probably null
R5927:Krt80	UTSW	15	101,262,089 (GRCm39)	critical splice donor site	probably benign
R6847:Krt80	UTSW	15	101,256,610 (GRCm39)	missense	probably benign	0.03
R8218:Krt80	UTSW	15	101,267,884 (GRCm39)	missense	probably benign
R9376:Krt80	UTSW	15	101,247,978 (GRCm39)	missense	unknown
R9686:Krt80	UTSW	15	101,262,281 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- ATCTTCTGTATGACTGACTGGGC -3'
(R):5'- TTGCAGCATCCAGTCCACAG -3'

Sequencing Primer
(F):5'- CAGTAGCTCTGGGCACTTTACAG -3'
(R):5'- AAGCTGTATGGGGCCTTCC -3'

Posted On

2022-03-25