Mutagenetix > Incidental Mutation

Incidental Mutation 'R2436:Calhm3'

249609

Institutional Source

Beutler Lab

Gene Symbol

Calhm3

Ensembl Gene

ENSMUSG00000094219

Gene Name

calcium homeostasis modulator 3

Synonyms

MMRRC Submission

040397-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.216) question?

Stock #

R2436 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

47140138-47146203 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 47140404 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Alanine at position 230 (T230A)

Ref Sequence

ENSEMBL: ENSMUSP00000136302 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000178630]

AlphaFold

J3QMI4

Predicted Effect

probably damaging
Transcript: ENSMUST00000178630
AA Change: T230A

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000136302
Gene: ENSMUSG00000094219
AA Change: T230A

Domain	Start	End	E-Value	Type
Pfam:Ca_hom_mod	1	252	1.9e-103	PFAM
low complexity region	268	278	N/A	INTRINSIC

Coding Region Coverage

1x: 99.1%
3x: 98.5%
10x: 97.0%
20x: 94.1%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 36 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adgrg7	A	G	16: 56,582,308 (GRCm39)	S277P	possibly damaging	Het
Arl6ip4	T	C	5: 124,254,662 (GRCm39)	S52P	probably benign	Het
Barx2	T	C	9: 31,824,383 (GRCm39)	H2R	probably damaging	Het
Card11	C	T	5: 140,868,117 (GRCm39)	V844M	possibly damaging	Het
Dnah6	C	T	6: 73,126,156 (GRCm39)	R1327Q	probably benign	Het
Dnai4	T	C	4: 102,923,549 (GRCm39)	I427V	probably benign	Het
Ehbp1	C	A	11: 22,039,524 (GRCm39)		probably null	Het
Fgg	T	A	3: 82,921,496 (GRCm39)	I393N	possibly damaging	Het
Foxq1	A	T	13: 31,742,516 (GRCm39)		probably benign	Het
Hmgxb3	T	C	18: 61,280,566 (GRCm39)	T646A	probably benign	Het
Homer3	G	A	8: 70,745,706 (GRCm39)	E324K	possibly damaging	Het
Krt80	A	G	15: 101,257,384 (GRCm39)	F183L	probably damaging	Het
Map3k21	A	T	8: 126,668,354 (GRCm39)	K647*	probably null	Het
Mcm3ap	A	G	10: 76,325,891 (GRCm39)	Y1067C	probably damaging	Het
Myh1	G	T	11: 67,104,097 (GRCm39)	Q921H	probably benign	Het
Nme8	A	G	13: 19,862,029 (GRCm39)	F200S	probably damaging	Het
Nploc4	T	C	11: 120,309,143 (GRCm39)	N153S	possibly damaging	Het
Or14c45	T	C	7: 86,176,591 (GRCm39)	F209L	probably damaging	Het
Or2ak6	T	C	11: 58,592,952 (GRCm39)	C142R	probably damaging	Het
Or4a73	A	G	2: 89,421,117 (GRCm39)	V114A	probably benign	Het
Or5k1	C	T	16: 58,617,607 (GRCm39)	V201I	probably benign	Het
Pipox	T	A	11: 77,782,943 (GRCm39)	L86F	probably damaging	Het
Polr3h	G	T	15: 81,801,406 (GRCm39)	L157I	probably benign	Het
Prex2	G	A	1: 11,336,376 (GRCm39)	V1525M	possibly damaging	Het
Rapgef2	A	T	3: 78,996,079 (GRCm39)	D561E	possibly damaging	Het
Sacs	A	T	14: 61,440,354 (GRCm39)	D800V	possibly damaging	Het
Sbsn	A	T	7: 30,451,655 (GRCm39)	L223F	possibly damaging	Het
Slc16a9	TCCCC	TCCCCC	10: 70,091,911 (GRCm39)		probably null	Het
Srrm3	G	T	5: 135,864,030 (GRCm39)	E43*	probably null	Het
Tcaf3	G	A	6: 42,570,663 (GRCm39)	A363V	probably damaging	Het
Tmem138	A	G	19: 10,552,268 (GRCm39)	F78S	probably damaging	Het
Tnfrsf17	G	A	16: 11,137,676 (GRCm39)	D138N	probably damaging	Het
Tubgcp6	C	T	15: 88,986,568 (GRCm39)	V1344I	probably benign	Het
Usp24	T	A	4: 106,266,842 (GRCm39)	L1875*	probably null	Het
Vmn2r109	C	A	17: 20,774,798 (GRCm39)	G186C	probably damaging	Het
Zfp541	A	G	7: 15,810,373 (GRCm39)	N137D	possibly damaging	Het

Other mutations in Calhm3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
FR4304:Calhm3	UTSW	19	47,140,335 (GRCm39)	frame shift	probably null
R1203:Calhm3	UTSW	19	47,143,839 (GRCm39)	missense	probably damaging	1.00
R1863:Calhm3	UTSW	19	47,140,539 (GRCm39)	missense	probably damaging	1.00
R1911:Calhm3	UTSW	19	47,143,908 (GRCm39)	missense	possibly damaging	0.74
R1951:Calhm3	UTSW	19	47,140,256 (GRCm39)	missense	probably benign	0.00
R2089:Calhm3	UTSW	19	47,140,430 (GRCm39)	missense	probably damaging	1.00
R2091:Calhm3	UTSW	19	47,140,430 (GRCm39)	missense	probably damaging	1.00
R2091:Calhm3	UTSW	19	47,140,430 (GRCm39)	missense	probably damaging	1.00
R2273:Calhm3	UTSW	19	47,145,986 (GRCm39)	missense	probably damaging	0.96
R2274:Calhm3	UTSW	19	47,145,986 (GRCm39)	missense	probably damaging	0.96
R3702:Calhm3	UTSW	19	47,140,187 (GRCm39)	missense	possibly damaging	0.88
R5758:Calhm3	UTSW	19	47,140,190 (GRCm39)	missense	probably damaging	0.99
R5901:Calhm3	UTSW	19	47,146,052 (GRCm39)	missense	probably damaging	1.00
R5938:Calhm3	UTSW	19	47,140,516 (GRCm39)	missense	probably damaging	1.00
R6948:Calhm3	UTSW	19	47,140,344 (GRCm39)	missense	probably damaging	0.99
R9190:Calhm3	UTSW	19	47,146,121 (GRCm39)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- AGGTACTGAGGAGTTGATCCACC -3'
(R):5'- ACATCTCACTAAAGCCTTCTCG -3'

Sequencing Primer
(F):5'- GAGTTGATCCACCTGCTCCCG -3'
(R):5'- AAAGCCTTCTCGTCCTCCAGG -3'

Posted On

2014-11-12