Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03032:Col24a1'

408505

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Col24a1

Ensembl Gene

ENSMUSG00000028197

Gene Name

collagen, type XXIV, alpha 1

Synonyms

5430404K19Rik

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

IGL03032

Quality Score

Status

Chromosome

Chromosomal Location

145292472-145552011 bp(+) (GRCm38)

Type of Mutation

critical splice donor site (2 bp from exon)

DNA Base Change (assembly)

T to C at 145538703 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000029848 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000029848]

AlphaFold

Q30D77

Predicted Effect

probably null
Transcript: ENSMUST00000029848

SMART Domains

Protein: ENSMUSP00000029848
Gene: ENSMUSG00000028197

Domain	Start	End	E-Value	Type
transmembrane domain	21	40	N/A	INTRINSIC
TSPN	41	230	2.7e-3	SMART
LamG	106	229	8.07e-2	SMART
Pfam:Collagen	506	565	9.6e-10	PFAM
Pfam:Collagen	561	623	3.4e-10	PFAM
Pfam:Collagen	604	678	2.3e-9	PFAM
low complexity region	682	724	N/A	INTRINSIC
Pfam:Collagen	772	837	1.3e-10	PFAM
Pfam:Collagen	865	938	6e-9	PFAM
Pfam:Collagen	967	1042	3.1e-8	PFAM
low complexity region	1056	1075	N/A	INTRINSIC
Pfam:Collagen	1107	1180	8e-9	PFAM
Pfam:Collagen	1159	1218	4.2e-10	PFAM
Pfam:Collagen	1218	1279	1.8e-10	PFAM
Pfam:Collagen	1270	1334	3.1e-9	PFAM
Pfam:Collagen	1378	1443	1.3e-9	PFAM
Pfam:Collagen	1439	1500	1.8e-9	PFAM
COLFI	1533	1733	9.34e-34	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000127379

Coding Region Coverage

Validation Efficiency

MGI Phenotype

FUNCTION: This gene encodes the alpha-1 subunit of type XXIV collagen, one of the low abundance fibril-forming collagens found in cartilage. The encoded protein has structural features of invertebrate fibrillar collagens and is expressed predominantly in bone tissue. Alternate splicing of this gene results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]

Allele List at MGI

Other mutations in this stock

Total: 37 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2310003L06Rik	A	T	5: 87,971,915 (GRCm38)	Y177F	possibly damaging	Het
Als2	C	A	1: 59,216,030 (GRCm38)		probably benign	Het
Arhgap44	A	G	11: 65,024,212 (GRCm38)	L410P	probably damaging	Het
Atp13a2	C	T	4: 141,000,355 (GRCm38)	A481V	possibly damaging	Het
Bod1l	C	A	5: 41,831,584 (GRCm38)	L393F	probably benign	Het
Cflar	T	A	1: 58,741,020 (GRCm38)	I258N	probably damaging	Het
Csmd2	A	T	4: 128,519,041 (GRCm38)	N2542I	probably benign	Het
Cyp2b9	T	C	7: 26,198,600 (GRCm38)		probably benign	Het
Dip2c	A	T	13: 9,551,778 (GRCm38)	I258F	probably damaging	Het
Dock7	A	G	4: 98,966,348 (GRCm38)	S1560P	probably benign	Het
Drc7	C	T	8: 95,076,247 (GRCm38)		probably benign	Het
Gm3667	T	A	14: 6,872,191 (GRCm38)	S203C	probably null	Het
Gramd2a	A	G	9: 59,712,127 (GRCm38)	E190G	probably benign	Het
Gstm4	T	C	3: 108,043,947 (GRCm38)	D8G	probably damaging	Het
Heatr5b	A	T	17: 78,760,499 (GRCm38)	M1820K	probably benign	Het
Irs4	A	G	X: 141,722,798 (GRCm38)	Y801H	unknown	Het
Loxhd1	C	T	18: 77,286,473 (GRCm38)	T80I	possibly damaging	Het
Lrrc40	G	A	3: 158,041,665 (GRCm38)		probably benign	Het
Mapk8ip1	T	G	2: 92,386,613 (GRCm38)	K446Q	probably damaging	Het
Mettl21e	C	A	1: 44,210,159 (GRCm38)		probably null	Het
Mmp8	T	A	9: 7,558,529 (GRCm38)		probably benign	Het
Muc19	A	T	15: 91,910,539 (GRCm38)		noncoding transcript	Het
Nipsnap3b	T	A	4: 53,015,016 (GRCm38)	V21E	possibly damaging	Het
Or1j15	C	A	2: 36,568,704 (GRCm38)	Y35*	probably null	Het
Or5al6	A	G	2: 86,146,699 (GRCm38)	F12L	probably damaging	Het
Or7a38	A	T	10: 78,917,637 (GRCm38)	I266F	probably benign	Het
Parp12	G	A	6: 39,087,586 (GRCm38)		probably null	Het
Pramel14	C	A	4: 143,993,245 (GRCm38)	L183F	probably damaging	Het
Rgsl1	T	A	1: 153,826,202 (GRCm38)	T169S	possibly damaging	Het
Rnf38	T	C	4: 44,152,529 (GRCm38)	R12G	probably damaging	Het
Slc9c1	T	C	16: 45,543,261 (GRCm38)		probably benign	Het
Slpi	T	C	2: 164,355,447 (GRCm38)		probably benign	Het
Snx17	G	A	5: 31,196,011 (GRCm38)	V165I	probably benign	Het
Tnfaip3	A	G	10: 19,004,609 (GRCm38)	V570A	probably benign	Het
Vmn1r63	A	G	7: 5,803,351 (GRCm38)	M94T	probably benign	Het
Vmn2r95	A	G	17: 18,452,313 (GRCm38)	I771V	probably benign	Het
Wiz	A	G	17: 32,356,558 (GRCm38)	V868A	probably benign	Het

Other mutations in Col24a1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00841:Col24a1	APN	3	145,362,309 (GRCm38)	missense	probably damaging	1.00
IGL00931:Col24a1	APN	3	145,461,470 (GRCm38)	missense	probably benign	0.00
IGL01160:Col24a1	APN	3	145,507,713 (GRCm38)	missense	probably damaging	1.00
IGL01355:Col24a1	APN	3	145,314,876 (GRCm38)	missense	probably benign	0.07
IGL01409:Col24a1	APN	3	145,538,564 (GRCm38)	missense	probably benign	0.19
IGL01587:Col24a1	APN	3	145,433,355 (GRCm38)	splice site	probably null
IGL01666:Col24a1	APN	3	145,344,686 (GRCm38)	missense	possibly damaging	0.93
IGL01717:Col24a1	APN	3	145,524,263 (GRCm38)	splice site	probably benign
IGL01721:Col24a1	APN	3	145,538,567 (GRCm38)	missense	probably benign	0.26
IGL01939:Col24a1	APN	3	145,315,244 (GRCm38)	missense	probably damaging	1.00
IGL01988:Col24a1	APN	3	145,524,167 (GRCm38)	splice site	probably null
IGL02002:Col24a1	APN	3	145,356,944 (GRCm38)	missense	possibly damaging	0.81
IGL02172:Col24a1	APN	3	145,314,962 (GRCm38)	missense	probably benign	0.34
IGL02552:Col24a1	APN	3	145,474,207 (GRCm38)	missense	possibly damaging	0.88
IGL02559:Col24a1	APN	3	145,314,173 (GRCm38)	missense	probably benign
IGL02582:Col24a1	APN	3	145,314,486 (GRCm38)	missense	probably damaging	1.00
IGL02652:Col24a1	APN	3	145,492,301 (GRCm38)	nonsense	probably null
IGL02942:Col24a1	APN	3	145,541,665 (GRCm38)	missense	probably damaging	1.00
IGL03108:Col24a1	APN	3	145,323,401 (GRCm38)	missense	probably damaging	1.00
IGL03310:Col24a1	APN	3	145,313,983 (GRCm38)	splice site	probably benign
IGL03405:Col24a1	APN	3	145,315,157 (GRCm38)	missense	possibly damaging	0.73
R0066:Col24a1	UTSW	3	145,545,144 (GRCm38)	missense	probably damaging	1.00
R0066:Col24a1	UTSW	3	145,545,144 (GRCm38)	missense	probably damaging	1.00
R0379:Col24a1	UTSW	3	145,524,142 (GRCm38)	missense	possibly damaging	0.94
R0502:Col24a1	UTSW	3	145,545,316 (GRCm38)	splice site	probably benign
R0556:Col24a1	UTSW	3	145,314,728 (GRCm38)	missense	possibly damaging	0.53
R0587:Col24a1	UTSW	3	145,293,145 (GRCm38)	missense	possibly damaging	0.50
R0617:Col24a1	UTSW	3	145,314,120 (GRCm38)	missense	probably damaging	1.00
R0831:Col24a1	UTSW	3	145,328,759 (GRCm38)	missense	probably damaging	1.00
R1455:Col24a1	UTSW	3	145,460,838 (GRCm38)	missense	probably damaging	1.00
R1664:Col24a1	UTSW	3	145,389,600 (GRCm38)	critical splice donor site	probably null
R1713:Col24a1	UTSW	3	145,366,869 (GRCm38)	nonsense	probably null
R1854:Col24a1	UTSW	3	145,459,140 (GRCm38)	missense	probably damaging	1.00
R1855:Col24a1	UTSW	3	145,459,140 (GRCm38)	missense	probably damaging	1.00
R1861:Col24a1	UTSW	3	145,537,267 (GRCm38)	critical splice donor site	probably null
R1969:Col24a1	UTSW	3	145,314,930 (GRCm38)	missense	probably benign	0.03
R2216:Col24a1	UTSW	3	145,314,981 (GRCm38)	missense	probably benign	0.34
R2290:Col24a1	UTSW	3	145,513,195 (GRCm38)	missense	probably damaging	1.00
R3702:Col24a1	UTSW	3	145,337,860 (GRCm38)	missense	probably benign	0.01
R3772:Col24a1	UTSW	3	145,545,286 (GRCm38)	missense	probably damaging	1.00
R4086:Col24a1	UTSW	3	145,461,437 (GRCm38)	missense	probably damaging	1.00
R4236:Col24a1	UTSW	3	145,524,282 (GRCm38)	nonsense	probably null
R4433:Col24a1	UTSW	3	145,314,383 (GRCm38)	missense	possibly damaging	0.95
R4688:Col24a1	UTSW	3	145,314,383 (GRCm38)	missense	probably benign	0.00
R4972:Col24a1	UTSW	3	145,509,684 (GRCm38)	missense	probably benign	0.42
R5157:Col24a1	UTSW	3	145,345,951 (GRCm38)	nonsense	probably null
R5216:Col24a1	UTSW	3	145,315,310 (GRCm38)	missense	possibly damaging	0.85
R5274:Col24a1	UTSW	3	145,484,678 (GRCm38)	missense	probably benign	0.03
R5334:Col24a1	UTSW	3	145,461,525 (GRCm38)	missense	possibly damaging	0.91
R5416:Col24a1	UTSW	3	145,315,025 (GRCm38)	nonsense	probably null
R5473:Col24a1	UTSW	3	145,537,261 (GRCm38)	missense	probably benign	0.41
R5538:Col24a1	UTSW	3	145,293,121 (GRCm38)	missense	probably damaging	0.99
R5561:Col24a1	UTSW	3	145,298,827 (GRCm38)	missense	probably benign	0.26
R5648:Col24a1	UTSW	3	145,358,566 (GRCm38)	missense	probably benign	0.00
R5920:Col24a1	UTSW	3	145,428,230 (GRCm38)	missense	probably damaging	1.00
R6111:Col24a1	UTSW	3	145,314,054 (GRCm38)	missense	probably damaging	0.99
R6151:Col24a1	UTSW	3	145,314,054 (GRCm38)	missense	probably damaging	0.99
R6701:Col24a1	UTSW	3	145,314,380 (GRCm38)	missense	probably benign	0.00
R6728:Col24a1	UTSW	3	145,315,196 (GRCm38)	missense	probably benign
R6734:Col24a1	UTSW	3	145,508,674 (GRCm38)	missense	probably benign	0.06
R6861:Col24a1	UTSW	3	145,460,834 (GRCm38)	missense	probably damaging	1.00
R6982:Col24a1	UTSW	3	145,315,046 (GRCm38)	nonsense	probably null
R7001:Col24a1	UTSW	3	145,298,866 (GRCm38)	missense	probably benign	0.28
R7148:Col24a1	UTSW	3	145,315,299 (GRCm38)	missense	probably damaging	1.00
R7293:Col24a1	UTSW	3	145,486,304 (GRCm38)	nonsense	probably null
R7315:Col24a1	UTSW	3	145,431,870 (GRCm38)	missense	possibly damaging	0.82
R7358:Col24a1	UTSW	3	145,293,165 (GRCm38)	critical splice donor site	probably null
R7371:Col24a1	UTSW	3	145,343,698 (GRCm38)	missense	probably benign	0.06
R7383:Col24a1	UTSW	3	145,298,838 (GRCm38)	missense	probably benign
R7605:Col24a1	UTSW	3	145,538,687 (GRCm38)	missense	possibly damaging	0.67
R7650:Col24a1	UTSW	3	145,314,453 (GRCm38)	missense	probably benign	0.00
R7679:Col24a1	UTSW	3	145,399,355 (GRCm38)	missense	possibly damaging	0.81
R7701:Col24a1	UTSW	3	145,366,901 (GRCm38)	splice site	probably null
R7701:Col24a1	UTSW	3	145,315,011 (GRCm38)	missense	probably benign
R7805:Col24a1	UTSW	3	145,314,140 (GRCm38)	missense	probably benign	0.02
R7913:Col24a1	UTSW	3	145,431,866 (GRCm38)	nonsense	probably null
R7921:Col24a1	UTSW	3	145,474,238 (GRCm38)	missense	probably damaging	1.00
R8056:Col24a1	UTSW	3	145,314,164 (GRCm38)	missense	possibly damaging	0.73
R8240:Col24a1	UTSW	3	145,507,702 (GRCm38)	missense	probably benign	0.31
R8294:Col24a1	UTSW	3	145,481,089 (GRCm38)	missense	probably null	1.00
R8305:Col24a1	UTSW	3	145,474,182 (GRCm38)	missense	probably benign	0.00
R8430:Col24a1	UTSW	3	145,315,299 (GRCm38)	missense	probably damaging	1.00
R8708:Col24a1	UTSW	3	145,545,265 (GRCm38)	missense	probably damaging	0.99
R8880:Col24a1	UTSW	3	145,314,037 (GRCm38)	missense	probably null
R9056:Col24a1	UTSW	3	145,315,248 (GRCm38)	missense	probably damaging	0.96
R9461:Col24a1	UTSW	3	145,481,124 (GRCm38)	nonsense	probably null
R9612:Col24a1	UTSW	3	145,545,205 (GRCm38)	missense	probably benign	0.32
R9777:Col24a1	UTSW	3	145,315,342 (GRCm38)	nonsense	probably null
Z1176:Col24a1	UTSW	3	145,342,498 (GRCm38)	missense	probably damaging	1.00
Z1177:Col24a1	UTSW	3	145,342,499 (GRCm38)	missense	probably damaging	1.00

Posted On

2016-08-02