ZMP

si:dkey-218f9.9

Ensembl ID:

ENSDARG00000059154

ZFIN ID:

ZDB-GENE-070705-380

Description:

hypothetical protein LOC100000325 [Source:RefSeq peptide;Acc:NP_001093538]

Human Orthologues:

RRAGC, RRAGD

Human Descriptions:

Ras-related GTP binding C [Source:HGNC Symbol;Acc:19902]
Ras-related GTP binding D [Source:HGNC Symbol;Acc:19903]

Mouse Orthologues:

Rragc, Rragd

Mouse Descriptions:

Ras-related GTP binding C Gene [Source:MGI Symbol;Acc:MGI:1858751]
Ras-related GTP binding D Gene [Source:MGI Symbol;Acc:MGI:1098604]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa36762	Nonsense	Mutation detected in F1 DNA	Not yet available
sa29138	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa36762

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000082187	Nonsense	118	392	2	7

Genomic Location (Zv9):

Chromosome 19 (position 4930265)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	4203826
GRCz11	19	4134652

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCGGACAGGTGGACTTTTTCGACCCTACTTTTGACTACGAGATGATTTTC[A/T]GAGGCACCGGCGCATTGATTTTCGTCATTGATGCTCAGGTAAGTATGTGT

Long Flanking Sequence:

AAGCTTTATATTATAACAAAAATTACACTGATGGTCTGTTGACATAAAGGGAAATGCAAAGAATATTTTCCATATTACTAAGTAGCATTTAATACTGCTTAAATTCCTGAAGTGTGGATTTATTTTTGTGGTTTGTTAAATGTGTTCGGGTGAAATTATATGTTGCCATTTGTGTAAATACTGTGTTAATACTATATAAATACTATAAAGTGACTTTATAATTGTTTATACCTCATCTGTTATTGAAGAAGGAGTGAATGAGATCATGTATTAAATCTCTATAAGTATATTATTTAGCATATTTTTCACCTCTGGTTAAATGTTTTGAATCTCAGGTGGTGTTTCACAAGATGTCTCCCAATGAGACGCTTTTTCTGGAGAGCACCAACAAGATCTACAAGGACGACATCTCTGGCAGCTCCTTCGTCAACTTTCACATATGGGACTTTCCCGGACAGGTGGACTTTTTCGACCCTACTTTTGACTACGAGATGATTTTC[A/T]GAGGCACCGGCGCATTGATTTTCGTCATTGATGCTCAGGTAAGTATGTGTGAAAACATGGCACCAGGGAAATATTCTGAGTGAGGTTGTTGACCTTTCTCTGTGTGTGTTTTTGTGAATACTCATTGCTTGGTTAAAATAGAAATAGCGTCCTTTTCTGGCATAACCTTGCTGTTATTATATTCTATTTTTGTCTTTTATGTTTTTATTTCAGGCAAAATGTATATGTCTCTTTACCTTTTAATCATTTCTAGTCATATTATGCATTATTCATCAGTCCATCTTATTGTGCAAAATAAAAATGCTTCATATTTTTGCGTAATTTCAGTCATGGTCTGCTCACTTAAAGGGAAATGCATTGCAAATACATTATTTTGCATTTGCAAAATAACATTTTATGTTTTATTAATTAAGTAACAATTAACATAAACCTGACAAAGTAGCATAAACCTTGCTGTTATCTTAAGACAATACACCAAATGTTTGTTTCCATGCACCATG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa29138

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000082187	Essential Splice Site	197	392	3	7

Genomic Location (Zv9):

Chromosome 19 (position 4928040)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	4201601
GRCz11	19	4132427

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGAGCCAATGATGATCTTGCTGACGCCAGTCTGGAAAAGCTTCACCTCAG[G/A]TTGGTAAAACTGATTTAAAAACCAGATCAGTCTGCCTTCAAGCTAATGAA

Long Flanking Sequence:

ATGGACGAATTTAGATAAACAACCAATACATAAGATTAATGTCATTTATTACACGTATCACACACTCACCATGAATGTCAGTAGCTACCGATTTCAAACTTTCATCAAAATATCTTTGTTTGTGTTTATTGTGTAAAAAAAATAAATAAATAAATTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATCATTTGGGAATGGTTTGTGGGTCAGCAAATGGTGTGGTATAACAAATGTTGATACTGCCTTTACCATTGTCTTTGTCTCTCTGTAGGATGATTATGTTGAAGCGTTAGGACGGCTTCATCTAACGGTGTCGCGGGCGTTCAGGGTGAACCCGGAGATTAATTTTGAGGTGTTTATACACAAGGTGGACGGTTTATCAGACGATCATAAGATCGAGACGCAGAGAGACATTCATCAGAGAGCCAATGATGATCTTGCTGACGCCAGTCTGGAAAAGCTTCACCTCAG[G/A]TTGGTAAAACTGATTTAAAAACCAGATCAGTCTGCCTTCAAGCTAATGAAAGCATGGATGGAGAGTGTTTGGTGGGATTATGGGGTGTAGTGAAGTGATACCCCAGCAGGTAATTCACTAGATAATAAACAGTGCTATTCCTGAAACGTCTACTAACACTGTAAAAAAAGCTTGACTCAATCTAAAATTAAGGCAACTTGCTGTAGAGCTTTTTGAGTTGACTCAAAGCAATTCAAGTGCAGTACTTGGGTTAAAAGTCAACCCCAAAAAATCTTTGCAGCAAGTTGCAATCAATTTTTAGGTGTCAACTTTTGTTTTTACAGTGAAAACTGCAAAAAGAGCAGTCATTAATTGAATCGAAATACATATATTACATAAGAAATAGAATTGAAATGTTATATTGTTTTGCAGTATTAACATTAAATGAATTTAAAACTGAATAAATGATAGCCTAATGGAAATAAAATATTAAAGTAGATTCAAATATGAATTATAGGATT

Associated Phenotype:

Not determined