ZMP

si:ch211-194c3.5

Ensembl ID:

ENSDARG00000079056

ZFIN ID:

ZDB-GENE-090313-63

Description:

hypothetical protein LOC556058 [Source:RefSeq peptide;Acc:NP_001139034]

Human Orthologue:

C20orf194

Human Description:

chromosome 20 open reading frame 194 [Source:HGNC Symbol;Acc:17721]

Mouse Orthologue:

4930402H24Rik

Mouse Description:

RIKEN cDNA 4930402H24 gene Gene [Source:MGI Symbol;Acc:MGI:1923029]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa35443	Nonsense	Mutation detected in F1 DNA	Not yet available
sa22248	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa35443

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
ENSDART00000110509	Nonsense	484	1157	17	37

Genomic Location (Zv9):

Chromosome 13 (position 13569788)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	13577783
GRCz11	13	13708775

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AACCTAGGATCAGTAGTTTTCTCTGAATCCTTTCTAGAGTCCAGTGTTTA[C/A]ATTCAGCAGAGAGGTAAAAATAACATAAAATATATATTTTTTATTCAAAT

Long Flanking Sequence:

AGCATGTAGACTCCTTGTTGGCCTTGGCTGCACGATATTTGTTTTTGGAAGAAATATCATATGTCCTATTATATGTCTCATTGGATCAAACATTTCCTGTTTGCGTTGTTAATTGAGAGTCTATTTTGTTTGTTTATTTTAGGTCCAAAGCTGTGTTCAGCATACAGGCTGTCAACAACAAGGGGTCGTGAGTTTCTCTACACTAACATGCAACTTCATTGCACGTTTTTCATTATCTTTTAATTGCTTTATTTCATTTTTTCACAATTTCCTTACGCAGAATCGTTCCCCTTAGTGATGAGGACAGCCACTTTCTGGTAAAAACAGTGAGTATACATCTTTCCTGCCCAGCTGCTGCTTTTTAACTGTATAGCAACTTCCAATAAATGTCTGACTCCTTCACAGGCGTCCATGATGGTGTACGATATCCCAGATCTCCAGTGTGGAGGAAACCTAGGATCAGTAGTTTTCTCTGAATCCTTTCTAGAGTCCAGTGTTTA[C/A]ATTCAGCAGAGAGGTAAAAATAACATAAAATATATATTTTTTATTCAAATGGCTGTTACTTTAATAATCCTCAGGCCATTCAAGATGTTAAAATGTCAGAGTTTTTTTCTCCAGTAAAACATTATACAATATTTTTAGCTGAAGCCGTAGTTTTTGGTGGTTCATCAAATGCAAGTCAAAAGTGAGTGGCACGCTGGATGTACTGCTCTGCGGGCACTGTCTTTAGATTGTTCTCCATACAGCGCTAAGCAAGACAAACAGATGCTGAAGGTTTACATTTCTAAGACATGATGGCACTTTGAGAGTCAATAAATAAATTAATAAGCATAGAGGCAACATCAAATTATTAACCAAGGCTCCTGATGATACATTAACACTGGAACTACCGGAATTGTAGCGTTTGTTGGAATTGTAGTCATTCTGACTGTTCAAGGCGTCATTCATTCATTCATTTTCTTGTGGGCTTAGTCCCTATATTAATCCGGGGTTGCCACAGCGGA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa22248

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000110509	Essential Splice Site	821	1157	27	37

Genomic Location (Zv9):

Chromosome 13 (position 13579195)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	13587190
GRCz11	13	13718182

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CAGAGAGAGACAGATATGAACTCATTCAGAGTTGTCCTGCTTATACCAGG[G/A]TATGACAGACACAAACAGTGTGTCCTCAATATACTTAGAGAAAAGTTCTT

Long Flanking Sequence:

AATAACATAAAGCAGTGGATGTAGGAGCTTCCTAGTGATATTTCTGACTAAAATGTTTTGCTGTACTTCTTCAAGAACAGTGTTTCTCAACCACTTTCCTGGTGGACCACTAACACTGCATGCTTTGGTTGTCTCTTTTGACTGACAAACCCATTACAGGTCTTTTAGTCTCTGCTAATTAGCTGATGATCTGAATCAGGTTTGGTTAAGGAGACCTGATAAATATGAGCTAGTGGTGCTTCAGGAACGTGGTTGAAAAACACTAAACTAGAATATGGTAAGTGGATAGTGTCTTGGATGATGATGATGTATAAATTACCATCTTCCTTATATTCCAATACTGATGACTCTTTGATTGACAGGTGGGAGGTGTTTTGCCCTGCTCTGGAAGGCTCTGGGGAATTCAGCGCATCACACCTCCAGCGGTTCCTGAGCAGCCTTCTGGCCAAACAGAGAGAGACAGATATGAACTCATTCAGAGTTGTCCTGCTTATACCAGG[G/A]TATGACAGACACAAACAGTGTGTCCTCAATATACTTAGAGAAAAGTTCTTTCTCATTGTTTGCTGAGAAGCAAAAAGACGTTGAAATCACATATGCAGTGATATACTGATAAACGTTCTGACACCACTGTGCTGTGAGCAATGTTTAGGAGATTATTTAATATATGTGCCATGCCTCTTAATGGCAAAACACAACAATAATGCCAAAAGTGAAAGAACAGCAGTTAGTAGGGATGTAACGGTATCAGAATGTCACGGTACGGTAATACCTCGGTATGAATGTCACGGTACGGTATTTATTGAATCATTTACAGGAAAAAAAAAAACTTTTGAAAATACTCCAAAAAAGTGCCAAAAGTGTCAACGACATACAAATTAGCCATCTATCTGTAAGCTTTGAAACAGGAACTTCAATTTTAATAACAAAAAATTATTAAACCATGTAAAAAAAATAAAGTTTCAATTTAGTAGTGTTAAAAACTCATCACATTTAACATTTAA

Associated Phenotype:

Not determined