ZMP

C10orf90

Ensembl ID:

ENSDARG00000089024

Description:

chromosome 10 open reading frame 90 [Source:HGNC Symbol;Acc:26563]

Human Orthologue:

C10orf90

Human Description:

chromosome 10 open reading frame 90 [Source:HGNC Symbol;Acc:26563]

Mouse Orthologue:

D7Ertd443e

Mouse Description:

DNA segment, Chr 7, ERATO Doi 443, expressed Gene [Source:MGI Symbol;Acc:MGI:1196431]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa10450	Nonsense	Available for shipment	Available now
sa35373	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa10450

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000126327	Nonsense	180	714	1	11

Genomic Location (Zv9):

Chromosome 12 (position 45515100)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	43686389
GRCz11	12	44849921

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GGCTGCCCAKACAAAGACATGTGATTCTGACRGACGTMCCCAACAAYCGA[C/T]ARGACAACAGCAGGGGTCAGCAGGTGAGAAAGTGCAAAAGAGACTAATTG

Long Flanking Sequence:

TTCAGCCCCATGATGCAGCTGGCAAAAACAGCATGAGCTTCCTCCGCAGGTCCTCATCATGGAGGAGGCCTGGAGAGCGAGGTTATTATGAGGGCCCCATGGCGCAGGTGAATGAGCCCCCTCGCGGAGCTCGTCCTCAGAGCTGCATTGAAGGTGGCAGAATGGACAAATGGCTTCAAACCCTGGAGAGACTTCAATCCCGTCGGCTTCAGAAACAAGTACCTGAGTTTTCCGACTGGACCGTGTCAATGCCGGCTCTCCCAAACGAGACGATGGGAAGTAACCCACATTGTCTTGATCTGAACTCTCTCCACAGAAGGAATCAGACTCCTAGTGCCTGTTCAAGTGTTTGTGAAAGCTCCCCGAGCAGCATGGAGTCTGTTCACATTAAGCCTGTTCCCAGTGCTGAAAAAGCAAATTTCTGTGCTCTCGCTCCTGTTCGATTTGGCTGGCTGCCCATACAAAGACATGTGATTCTGACAGACGTCCCCAACAACCGA[C/T]AAGACAACAGCAGGGGTCAGCAGGTGAGAAAGTGCAAAAGAGACTAATTGGAGATGCAGGCTACATTTTGAAATTATTTTTTTGAAATAGACGAGGAAACATGCATGACTGTGCTTTAACATAGTTTACTAATAGAAAGAACAGCCAGAAAGGGAAAACTGATGGATTTGTGAAGAATATTAGCATCACTGACCATAACAATGTACCGTAAGTTACCTATTACTGTCAGCATGTTTGTGTGCTCTTTATAAATTACTGAAAAACAGCTGGGGGTAAAGTATATTGATCGCAAGTGCTCATTTTGTGATCATATCTCGGTTTTGTTCTGTTGATTTGTAGTTTCAAATATTCGTAGCGTGAAACAGATGGAAATATGAAGTTTAGTAAAGTTAGCAACAGATTCATATTTTCCGGATCAATAACTCATGACCTATTCGCTATTAGTAAAGGCTTAATAATGATAACAATAATAGTTTTTATTTATATAGCCCCTTTCCAGA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa35373

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 > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000126327	Essential Splice Site	640	714	9	11

Genomic Location (Zv9):

Chromosome 12 (position 45477667)

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTGTTCTGCA[G/T]AAAGCCTTTTGAAATCTAAAGACAGAAGCATCATGGAAAAGGGGCCACAG

Long Flanking Sequence:

GTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTGTGTGTGTGCGTGCGTGCGTACGTGCGTGCGTGCGTGCGTGCGTGTGTGTGTATGTATGTATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTACGTGTTTTTGTGACATATCAGGACACAAATCTGCATAATGACATGGGTATGACACAGGTATTACAAAAAGGAGGTGAAATATGAGGACATTGGTGACGTCCTCATTTCTCAAAATGCTTATAAATCACACAGAATGAGTTTAATCAGAGAGTAAAGCTGCACACAGTCTCCTGTGATGGTTGGGTTCAGGGGTGGGGTGAGGGCAATACAATATACAGTTTGGACAGTATAAAATAAAATGGAAACCTAGGTAATGTCCCCACTTTTCACAAAAACAAATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTGTTCTGCA[G/T]AAAGCCTTTTGAAATCTAAAGACAGAAGCATCATGGAAAAGGGGCCACAGATGCGGTCCAGGAGGTAAAAAAAAGAGCATGCCAGCTCTTGTTTTGATAAACACCTATTCTGCTTTATTACTTTTTAACACACACACACGCACACACACACACTCACACACACACTCACAGGTGTATCAGTTCTATCTGATTTAAAGGTGTTGTGTCTGTGTGTGCGGCTGCAGGGTTTTGCTGCCCTGATTGTGCTTTTCACAGCTTGTTTGTTTTCCTGCCGCTGAATAAAAGCTCATCCGATTAGATCTGGTCTCACTGTGATTCAGAATTAAACCTCCCTGATGCACGGCTGGATGGATTCTGCACGAATGAGTGGCCATGTTCAGAAGTTTGATTTAGGCTGTGGATATGGTGTGTGACTGAATAAACGGACAGTTATGTCAGATAACAGTGTAAATACGCACTGTTTATTTATTAACTCTGATATAGTATGATGAGAATAGATC

Associated Phenotype:

Not determined