Mutagenetix > Incidental Mutation

Incidental Mutation 'R8270:Arhgap44'

639458

Institutional Source

Beutler Lab

Gene Symbol

Arhgap44

Ensembl Gene

ENSMUSG00000033389

Gene Name

Rho GTPase activating protein 44

Synonyms

AU040829

MMRRC Submission

067694-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R8270 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

64892865-65053779 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 64912860 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Methionine to Threonine at position 477 (M477T)

Ref Sequence

ENSEMBL: ENSMUSP00000039139 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000047463] [ENSMUST00000093002]

AlphaFold

Q5SSM3

Predicted Effect

possibly damaging
Transcript: ENSMUST00000047463
AA Change: M477T

PolyPhen 2 Score 0.585 (Sensitivity: 0.88; Specificity: 0.91)

SMART Domains

Protein: ENSMUSP00000039139
Gene: ENSMUSG00000033389
AA Change: M477T

Domain	Start	End	E-Value	Type
BAR	1	242	2.27e-71	SMART
RhoGAP	266	442	1.07e-66	SMART
low complexity region	530	556	N/A	INTRINSIC
low complexity region	561	575	N/A	INTRINSIC
low complexity region	592	606	N/A	INTRINSIC
low complexity region	616	631	N/A	INTRINSIC
low complexity region	664	689	N/A	INTRINSIC
low complexity region	695	707	N/A	INTRINSIC
low complexity region	716	746	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000093002
AA Change: M477T

PolyPhen 2 Score 0.315 (Sensitivity: 0.90; Specificity: 0.89)

SMART Domains

Protein: ENSMUSP00000090681
Gene: ENSMUSG00000033389
AA Change: M477T

Domain	Start	End	E-Value	Type
BAR	1	242	2.27e-71	SMART
RhoGAP	266	442	1.07e-66	SMART
low complexity region	536	562	N/A	INTRINSIC
low complexity region	567	581	N/A	INTRINSIC
low complexity region	598	612	N/A	INTRINSIC
low complexity region	622	637	N/A	INTRINSIC
low complexity region	670	695	N/A	INTRINSIC
low complexity region	701	713	N/A	INTRINSIC
low complexity region	722	752	N/A	INTRINSIC

Predicted Effect

SMART Domains

Protein: ENSMUSP00000115612
Gene: ENSMUSG00000033389
AA Change: M351T

Domain	Start	End	E-Value	Type
Pfam:BAR	1	117	1.1e-29	PFAM
RhoGAP	141	317	1.07e-66	SMART
low complexity region	411	437	N/A	INTRINSIC
low complexity region	442	456	N/A	INTRINSIC
low complexity region	473	487	N/A	INTRINSIC
low complexity region	497	512	N/A	INTRINSIC
low complexity region	545	570	N/A	INTRINSIC
low complexity region	576	588	N/A	INTRINSIC
low complexity region	597	627	N/A	INTRINSIC

Coding Region Coverage

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

Validation Efficiency

98% (52/53)

Allele List at MGI

Other mutations in this stock

Total: 56 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adgrv1	G	A	13: 81,651,163 (GRCm39)	T3044I	probably damaging	Het
Apbb1ip	C	T	2: 22,765,004 (GRCm39)	P562S	unknown	Het
Arhgef12	T	C	9: 42,882,354 (GRCm39)	T1497A	probably benign	Het
Atp5pd	T	C	11: 115,307,698 (GRCm39)	D91G	probably damaging	Het
Atp6v0a4	A	G	6: 38,051,164 (GRCm39)	F405L	probably damaging	Het
Bicc1	T	A	10: 70,767,938 (GRCm39)	T893S	probably damaging	Het
Cacna1i	T	A	15: 80,257,835 (GRCm39)	C1122S	probably damaging	Het
Capn7	A	G	14: 31,080,636 (GRCm39)	E369G	probably damaging	Het
Cass4	T	A	2: 172,269,589 (GRCm39)	L557Q	probably damaging	Het
Cdh5	A	G	8: 104,839,672 (GRCm39)	I48V	probably benign	Het
Crisp3	T	C	17: 40,546,813 (GRCm39)	K35R	probably benign	Het
Csde1	G	A	3: 102,946,071 (GRCm39)	A22T	possibly damaging	Het
Ctse	T	C	1: 131,595,877 (GRCm39)	Y190H	probably damaging	Het
Cyp2d34	T	A	15: 82,504,988 (GRCm39)	D24V	possibly damaging	Het
D630045J12Rik	A	T	6: 38,167,658 (GRCm39)	Y981*	probably null	Het
Dclre1a	G	A	19: 56,533,382 (GRCm39)	T404I	possibly damaging	Het
Dmc1	T	C	15: 79,485,746 (GRCm39)	D23G	probably damaging	Het
Dnah8	C	T	17: 31,059,687 (GRCm39)	T4429M	probably damaging	Het
Esf1	A	T	2: 139,997,033 (GRCm39)		probably benign	Het
Fbxl12	C	A	9: 20,550,160 (GRCm39)	R165L	possibly damaging	Het
Fn3k	A	T	11: 121,330,137 (GRCm39)	M107L	probably benign	Het
Fxyd5	A	G	7: 30,740,854 (GRCm39)	L10P	probably damaging	Het
Gm21958	G	A	3: 54,621,633 (GRCm39)		probably benign	Het
Gm4922	C	T	10: 18,659,760 (GRCm39)	D321N	probably benign	Het
Gtf2h3	A	G	5: 124,734,050 (GRCm39)	*310W	probably null	Het
Hapln2	G	A	3: 87,930,851 (GRCm39)	T180I	possibly damaging	Het
Herc1	T	G	9: 66,395,232 (GRCm39)	V4189G	probably damaging	Het
Iqgap1	A	G	7: 80,379,875 (GRCm39)	V1166A	probably damaging	Het
Kcnk10	T	C	12: 98,401,358 (GRCm39)	N439S		Het
Klhl3	A	T	13: 58,260,968 (GRCm39)	M15K		Het
Klk1b26	A	T	7: 43,665,544 (GRCm39)	T151S	probably benign	Het
Krtap5-1	C	A	7: 141,850,199 (GRCm39)	C176F	unknown	Het
Krtap5-3	T	A	7: 141,755,693 (GRCm39)	C177S	unknown	Het
Lrrc37	T	C	11: 103,434,141 (GRCm39)	I3009M	unknown	Het
Map1a	T	C	2: 121,129,501 (GRCm39)	F180L	probably damaging	Het
Mfap5	T	C	6: 122,498,889 (GRCm39)		probably null	Het
Nckap1	T	A	2: 80,355,008 (GRCm39)	H638L	possibly damaging	Het
Optc	C	T	1: 133,832,810 (GRCm39)	V97M	probably benign	Het
Or5p78	T	A	7: 108,212,150 (GRCm39)	I212N	probably benign	Het
Or8b46	T	G	9: 38,450,644 (GRCm39)	M151R	noncoding transcript	Het
Piezo1	A	G	8: 123,228,298 (GRCm39)	Y330H		Het
Ppp1r12b	G	T	1: 134,803,886 (GRCm39)	N424K	probably benign	Het
Prdm5	T	A	6: 65,913,058 (GRCm39)	F580L	probably damaging	Het
Prr27	A	C	5: 87,994,171 (GRCm39)	K348N	possibly damaging	Het
Prr30	A	G	14: 101,435,822 (GRCm39)	Y247H	possibly damaging	Het
Rbks	A	T	5: 31,807,810 (GRCm39)		probably benign	Het
Sec24d	T	C	3: 123,099,535 (GRCm39)	V336A	possibly damaging	Het
Serac1	A	T	17: 6,101,033 (GRCm39)	L457H	probably damaging	Het
Serpina1f	A	G	12: 103,659,757 (GRCm39)	I175T	probably damaging	Het
Smr2l	T	C	5: 88,430,383 (GRCm39)	V93A	possibly damaging	Het
Sspo	A	T	6: 48,426,897 (GRCm39)	H242L	probably benign	Het
Tcaf2	A	T	6: 42,606,958 (GRCm39)	M332K	probably benign	Het
Tnrc6a	T	A	7: 122,769,294 (GRCm39)	N361K	possibly damaging	Het
Trim43b	G	T	9: 88,967,458 (GRCm39)	H393N	possibly damaging	Het
Ush2a	T	C	1: 188,176,838 (GRCm39)	L1334S	probably benign	Het
Usp35	T	C	7: 96,961,551 (GRCm39)	E625G	probably benign	Het

Other mutations in Arhgap44

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01138:Arhgap44	APN	11	64,932,275 (GRCm39)	missense	probably damaging	0.96
IGL01553:Arhgap44	APN	11	64,943,944 (GRCm39)	missense	probably damaging	1.00
IGL01868:Arhgap44	APN	11	64,902,904 (GRCm39)	missense	probably damaging	1.00
IGL01996:Arhgap44	APN	11	64,896,322 (GRCm39)	utr 3 prime	probably benign
IGL02093:Arhgap44	APN	11	64,965,360 (GRCm39)	missense	probably damaging	1.00
IGL02962:Arhgap44	APN	11	64,957,987 (GRCm39)	splice site	probably benign
IGL02963:Arhgap44	APN	11	64,922,489 (GRCm39)	missense	probably damaging	1.00
IGL03032:Arhgap44	APN	11	64,915,038 (GRCm39)	missense	probably damaging	1.00
R0071:Arhgap44	UTSW	11	64,902,721 (GRCm39)	missense	possibly damaging	0.90
R0152:Arhgap44	UTSW	11	64,902,745 (GRCm39)	missense	probably benign	0.13
R0402:Arhgap44	UTSW	11	64,922,903 (GRCm39)	splice site	probably benign
R1109:Arhgap44	UTSW	11	64,917,642 (GRCm39)	missense	probably benign	0.00
R1694:Arhgap44	UTSW	11	64,944,023 (GRCm39)	missense	probably damaging	1.00
R1946:Arhgap44	UTSW	11	64,902,922 (GRCm39)	missense	probably damaging	0.99
R2036:Arhgap44	UTSW	11	64,932,318 (GRCm39)	missense	possibly damaging	0.83
R2356:Arhgap44	UTSW	11	64,900,851 (GRCm39)	missense	probably damaging	1.00
R4342:Arhgap44	UTSW	11	64,902,887 (GRCm39)	nonsense	probably null
R4657:Arhgap44	UTSW	11	64,896,278 (GRCm39)	critical splice donor site	probably null
R4763:Arhgap44	UTSW	11	64,929,991 (GRCm39)	missense	probably damaging	0.98
R4803:Arhgap44	UTSW	11	64,943,921 (GRCm39)	missense	probably benign	0.00
R5652:Arhgap44	UTSW	11	64,915,064 (GRCm39)	missense	probably damaging	1.00
R5663:Arhgap44	UTSW	11	64,915,117 (GRCm39)	missense	probably damaging	1.00
R5833:Arhgap44	UTSW	11	64,929,503 (GRCm39)	missense	probably damaging	1.00
R6000:Arhgap44	UTSW	11	64,922,910 (GRCm39)	frame shift	probably null
R6001:Arhgap44	UTSW	11	64,922,910 (GRCm39)	frame shift	probably null
R6046:Arhgap44	UTSW	11	64,922,910 (GRCm39)	frame shift	probably null
R6066:Arhgap44	UTSW	11	64,922,910 (GRCm39)	frame shift	probably null
R6160:Arhgap44	UTSW	11	65,053,375 (GRCm39)	unclassified	probably benign
R6661:Arhgap44	UTSW	11	64,900,834 (GRCm39)	missense	probably damaging	0.97
R7062:Arhgap44	UTSW	11	64,902,758 (GRCm39)	missense	probably benign	0.25
R7388:Arhgap44	UTSW	11	64,915,094 (GRCm39)	nonsense	probably null
R7793:Arhgap44	UTSW	11	64,900,750 (GRCm39)	missense	probably damaging	0.99
R8190:Arhgap44	UTSW	11	64,929,479 (GRCm39)	missense	probably damaging	1.00
R8321:Arhgap44	UTSW	11	64,899,053 (GRCm39)	missense	probably benign	0.00
R8369:Arhgap44	UTSW	11	64,950,680 (GRCm39)	missense	probably damaging	1.00
R8876:Arhgap44	UTSW	11	64,898,896 (GRCm39)	missense	possibly damaging	0.93
R9296:Arhgap44	UTSW	11	64,957,933 (GRCm39)	missense	probably damaging	0.99
R9344:Arhgap44	UTSW	11	65,053,463 (GRCm39)	start codon destroyed	probably null	0.04
R9428:Arhgap44	UTSW	11	64,899,168 (GRCm39)	missense	probably damaging	1.00
X0022:Arhgap44	UTSW	11	64,944,038 (GRCm39)	missense	probably damaging	1.00
X0061:Arhgap44	UTSW	11	64,929,471 (GRCm39)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- AATTGCTACAAGCCACCTCAAGTG -3'
(R):5'- TTCTAGAGGCAGCACGTGAG -3'

Sequencing Primer
(F):5'- CAAGTGTCTTAGTAAGTACCGCC -3'
(R):5'- AGCGTCTCTCTGTCTCGGAAG -3'

Posted On

2020-07-28