ZMP

si:dkeyp-115d2.5

Ensembl ID:

ENSDARG00000075393

ZFIN ID:

ZDB-GENE-090312-170

Description:

Novel protein similar to H.sapiens SPOCK2, sparc/osteonectin, cwcv and kazal-like domains proteoglyc

Human Orthologue:

SPOCK2

Human Description:

sparc/osteonectin, cwcv and kazal-like domains proteoglycan (testican) 2 [Source:HGNC Symbol;Acc:135

Mouse Orthologue:

Spock2

Mouse Description:

sparc/osteonectin, cwcv and kazal-like domains proteoglycan 2 Gene [Source:MGI Symbol;Acc:MGI:189135

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa22325	Essential Splice Site	Available for shipment	Available now
sa45488	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa22325

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC

Mutation:

A > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000110061	Essential Splice Site	64	419	None	10
ENSDART00000132027	Essential Splice Site	67	364	None	11
ENSDART00000143581	Essential Splice Site	64	78	None	2

Genomic Location (Zv9):

Chromosome 13 (position 30306936)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	29952884
GRCz11	13	30083334

KASP Assay ID:

2260-6539.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTCATTCTTTGCAGCTCATTTGACTGTTTGACTTCTTTTTCATTTCTGTC[A/T]GGATGATTACATCAGATCATGGGATGAAAATCAAGGCTCAAATGAAAGTA

Long Flanking Sequence:

CCCAGGAGGCAAATAGATGTTTTCCAGCATTTGTAGCATGTCTTTTTTCTTGATAGTTGCTCCTTGGAGATGCATCGTTCTCCTCTAACTGTCTCCTTCTCTTTTGTCTTTGATTCATCCTTCTCACATTTCACCAGGAAGTGGAGGTCAGTAGTGCTGTATCATGACTTTGCTTGTGTTTGATGTCTCTTTTAAAATGTTTCATCTAATATTCTCTGTCAAAGCCGTAGCCTACTTTTTAATGCAGTCTAAATTGCTTATGCGTCTTTGCTTGACATTTCATTCAAGCGTGTTTCACCTCTCAGAATTTTCCTTCCTTAAAGTTTCATCCCCCCTTTTTTTCCATTAGAGCTTTTCCATGGCTTTTCATAATCTTAGTGTTGTATGTTTAAGTTTTGTTTCACAATAGATGTGACTGTGGTAGAAGTATTATTGACTGAAGATTTCAAGTTCATTCTTTGCAGCTCATTTGACTGTTTGACTTCTTTTTCATTTCTGTC[A/T]GGATGATTACATCAGATCATGGGATGAAAATCAAGGCTCAAATGAAAGTAAGTGATCTTCAATATCACTAATAGTATTATATTATTGCATTCATTCAATAACTTTTAACCAAATGACCAAAATTGCATGAAATACCAAGCAATAGGATTGTTTATTCTTAAATGAAGCTGCTTCTTTTAAGATTAGGAAGAATGTTCAGAATATATATTTGCAATCACAGAGGAATTGATGCCAGCCTTCTAAAGTTTTGTTTTTATGCACATGTCATGACGTTTGCCATGCATCTTCTTTTCTGTCAGATGCATGCAAGAATCAGCACAGTTTCTGTACTTTATCCTAACAAGTCAGGACCAATCGCAATTCAGTATGCAAATAAATTGAGGCGAGAAGACAAATCACAATTAATGATACTAATAAATTGTAAGAAAGAGCACTCAAGGGCTGTGCACATCACTTGCTCTTATCACTGATGTTTAACAAATTATGACTAAACAAAGGCA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa45488

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000110061	None	278	419	7	10
ENSDART00000132027	Nonsense	282	364	8	11
ENSDART00000143581	None	None	78	None	2

Genomic Location (Zv9):

Chromosome 13 (position 30342245)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	29988193
GRCz11	13	30118643

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATCAAGCTGAACTGGCTGCCATTAATCTGGACAAGTATGAAGTGTGTATA[C/A]GGCCCTTCTTCAACTCCTGTGACTCTTACCGCGATGGCAAAGTGTCCACA

Long Flanking Sequence:

GTGATTTATTATCTTATCAGCAAAATTGAACAGCGGTATTGCTTGTACAACAACTTTGATTGCATTTTTTTACAGCTAATCTGATGCAATCAGCTGTTCTGGGAGCGATGGCTTTTGAAAAAAAAGCTCATTAGAATGGGTTATTGTATCTCTGTCCACTGATTATTTGTTCATGTTGGGTGTTTGAAAAGCACTATATAATTAAAAAAATATTATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTGTATTATTATTATTTCTGGGTAATATTTCTCTATTAAAATATACTGCATGATTTTTTTGTGCACAGTTGTGGACCGGACTCTTGTTGCGACCTGTAAGGACTCTATTGGCTGGATGTTCTCCAAGCTGGACACGAACAGTGACCTGTATCTGGATCAAGCTGAACTGGCTGCCATTAATCTGGACAAGTATGAAGTGTGTATA[C/A]GGCCCTTCTTCAACTCCTGTGACTCTTACCGCGATGGCAAAGTGTCCACAGCTGAGTGGTGCCTCTGCTTTTGGAGAGAAAGTGAGTCTTCAATATCTCTACACAATAGTTTTGCTGATAACATAATTAAGTATAATGCATGTGCAGATTTTTTGGAGGACCTGCCTATTGTTTTTCTAATGAATTTCTGATAGATAAAAAAATAGATCTAGCTTTCAACCTAACCTTACAGGAATCTTTTTGAATGTAGTATTTTAAGTATTGAAAATTGTTTTATTTTGTAAATAATAATAATAATAATAATAATAATAATAATAATTCAGTTAAATTTAGTACATTTAAATAAAAATTGATTTTAGTATTTTTTTTAAATAGATTTTTCTTTTGTGGGGCTGCAAAACCTGACACAAACTCACACTATCCTTAAAGTATTTATCACGTTTTATATTTTACTTACAGTAGTAAAATAACTAAACAAGCCTAAGAGATTTTCTTTAATA

Associated Phenotype:

Not determined