ZMP

LOC558432

Ensembl ID:

ENSDARG00000052435

Human Orthologue:

SPRED2

Human Description:

sprouty-related, EVH1 domain containing 2 [Source:HGNC Symbol;Acc:17722]

Mouse Orthologue:

Spred2

Mouse Description:

sprouty-related, EVH1 domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:2150019]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa8946	Nonsense	Mutation detected in F1 DNA	Not yet available
sa17627	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa8946

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
ENSDART00000074284	Nonsense	268	427	6	6

Genomic Location (Zv9):

Chromosome 1 (position 51958972)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	50806333
GRCz11	1	51450132

KASP Assay ID:

2259-1138.1 (used for ordering genotyping assays)

KASP Sequence:

ACRGACGCTTACGTCCACCTCGCTAAGAGCGAACCTCCCAAACACGACTA[C/A]ACTTACTCTTACCCACTCAGTGGGGACGGACACGTATCCCGTRATGGTAA

Long Flanking Sequence:

GTTTATCTTGTAGACACTAGAGGCAGATTGCTGCTAATAATTGTGACTGTATATACCAGGGATGTCTAAACTCTGTCCTGGAGGTCTGGTGTCCAGTAGATTTATCTCCAACTTGTCTCAACACACCTGGATGTTTCTAGAAAGCCTAGTAAGAGCTTGATTAGCTAGTCCTGGTGTGTCTGATTGCGGAACTAAGCTTTGCAGGACGCTGGCAACTCCAGGAACAAGTTTGGGCACCCCTGGTCTATACTGTATAAACATATTAACACATTTTTTTCATCTCTTCAACAGACGGTGCCCATGTTCCAGTGTTCACGTCACGTCAGGTTTCATGAGGAGGAGGAAGAGATTGTGCGGATAAACCCACGCGAGCGATCTTGGCTAACAGGCTATGAGGACTATCGTCACGCCACCACCGCGACCCGCACCAAACCCCTGCGGCCTGACGTCACGGACGCTTACGTCCACCTCGCTAAGAGCGAACCTCCCAAACACGACTA[C/A]ACTTACTCTTACCCACTCAGTGGGGACGGACACGTATCCCGTGATGGTAAAACGGGCATTGGTGGCGGCGTGGTCACCGGTCAGCCACGGGCGCTAACAGCTAAATGGCTGCCGCGGCGCGTGGAAGACAGCAGAGAGCGCTTACGCTGTGTGTACTGTCAGAATATGTTCAGTCCGTCTGAAAACGGGCGTGGGCGCTGTCAGGAGGCCCCGGACCCCGTGCAGACATGTATACGACGGGTCAGCTTTATGTGGTGTGCGGACAGCCTGCTGTACCACTGCATGTCGGACCCTGAGGGCGATTATTCGGACCCGTGCTCTTGCGACGCCAGCGAAGAGCGCTTCTGTCTGCGCTGGCTAGCACTTCTGGGACTGTCGCTGCTAGCACCGTGCATGTGCTGCTACGTGCCGCTGCGAGCGTGTTACCACTGTGGCGTCGCGTGCCACTGCTGCGGTGGCAAACACAAGGCTACGGGCTGAGCGGGAGAAACACGAGCACA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa17627

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
Order Allele From EZRC

Mutation:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000074284	Nonsense	364	427	6	6

Genomic Location (Zv9):

Chromosome 1 (position 51958685)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	50806046
GRCz11	1	51449845

KASP Assay ID:

2259-1137.1 (used for ordering genotyping assays)

KASP Sequence:

RCGGGTCAGCTTTATGTGGTGTGCGGACAGCCTGCTGTACCACTGCATGT[C/A]GGACCCTGAGGGCGATTRTTCGGACCCGTGCTCTTGCGACGCCAGCGAAG

Long Flanking Sequence:

ACAGACGGTGCCCATGTTCCAGTGTTCACGTCACGTCAGGTTTCATGAGGAGGAGGAAGAGATTGTGCGGATAAACCCACGCGAGCGATCTTGGCTAACAGGCTATGAGGACTATCGTCACGCCACCACCGCGACCCGCACCAAACCCCTGCGGCCTGACGTCACGGACGCTTACGTCCACCTCGCTAAGAGCGAACCTCCCAAACACGACTACACTTACTCTTACCCACTCAGTGGGGACGGACACGTATCCCGTGATGGTAAAACGGGCATTGGTGGCGGCGTGGTCACCGGTCAGCCACGGGCGCTAACAGCTAAATGGCTGCCGCGGCGCGTGGAAGACAGCAGAGAGCGCTTACGCTGTGTGTACTGTCAGAATATGTTCAGTCCGTCTGAAAACGGGCGTGGGCGCTGTCAGGAGGCCCCGGACCCCGTGCAGACATGTATACGACGGGTCAGCTTTATGTGGTGTGCGGACAGCCTGCTGTACCACTGCATGT[C/A]GGACCCTGAGGGCGATTATTCGGACCCGTGCTCTTGCGACGCCAGCGAAGAGCGCTTCTGTCTGCGCTGGCTAGCACTTCTGGGACTGTCGCTGCTAGCACCGTGCATGTGCTGCTACGTGCCGCTGCGAGCGTGTTACCACTGTGGCGTCGCGTGCCACTGCTGCGGTGGCAAACACAAGGCTACGGGCTGAGCGGGAGAAACACGAGCACACCAGCAGCAAAACAACGGCGTGGATGCAAATGAACAGCGGAGGAATGAACTTGTGGCTGCATTTGTGTTTTGCTTCGTTTTTTATTTTCTCCCTGTCCTTCCCGCTGGTGTTTCAGAGGGTTGGTCCATTTTGGGTTTAATTTTCTCAATCTACATTATAATGGACAGCTGTCCTCTTTTTGTGCTGGGCAAAGATTAATCACGATTAATTGCATCCAAAATTATTTGTTTTTACATTATATATATATATAATTATATAAACACATTACAGATAATTCAACAGATAA

Associated Phenotype:

Not determined