ZMP

si:ch211-67n3.1

Ensembl ID:

ENSDARG00000013245

ZFIN ID:

ZDB-GENE-030131-1961

Description:

hypothetical protein LOC555492 [Source:RefSeq peptide;Acc:NP_001037798]

Human Orthologue:

C10orf26

Human Description:

chromosome 10 open reading frame 26 [Source:HGNC Symbol;Acc:23510]

Mouse Orthologue:

D19Wsu162e

Mouse Description:

DNA segment, Chr 19, Wayne State University 162, expressed Gene [Source:MGI Symbol;Acc:MGI:107577]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa35504	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa24935	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa35504

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:

T > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000007211	Essential Splice Site	139	375	3	4

Genomic Location (Zv9):

Chromosome 13 (position 28816242)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	28462190
GRCz11	13	28592640

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATCGCCTACAGAGAAGCCCATAACTACTCCTCTCTGCCCTTCTACTTCAG[T/G]CAGTACCTGCTTCCCTCATTCTTAATACAATCTCAAAACAATAAAAGAAT

Long Flanking Sequence:

TGTAAAGTTAATGCTTAACAGATAATGAATTCACTATATGCTATTGCTTAACAAAGGGTTAATAGTGTGTATTTATTATAATGTGTTGCCGATATTTTTACATTACTGAGTCAAACCAGTCAATACATTGCATTAATGAAATTTCACTGTGGCTGGAGCTAACGGACAATGGAAATAGAAACTGAGCAAGTAACAAAGCATTTATCATCACAGCACTGTTGACAACAGCTCAGCTTAAAATGGAAGAGTAGTGATTCATGTCGTGCTGGTTGGATCGGACGTGATGTTCTCTTCGCTCATTAACAAAACAGTGTTATGTGTATGCTCTTTTCATCAGGGTTTTGGTTGGTCCTGACACTTATCGTCATTCTGGGCTGCTGCTGTGTTTGTCATCACCGTAGAGCCAAACACAGACTGCAACAACAGCAGCGGCAGCACGAGATCAACCTCATCGCCTACAGAGAAGCCCATAACTACTCCTCTCTGCCCTTCTACTTCAG[T/G]CAGTACCTGCTTCCCTCATTCTTAATACAATCTCAAAACAATAAAAGAATTTAATTTTGGCCATTGAGATTGAATCATGTAAATAGAAATGTAGAGGTAAAGAAATAGAGTGATTGTGAGTATAGTTATGTGTAATGTAATTGGGTGTCTTCTATAATAAACATCAGTATACGTACACTTACCGGCCACTTTATTAGGTACACCTTACTAGTACTGGGTTGGACCCTCTTTTGTCTTCAGAACTGCCTTAACCCTTCGTGGCATAGATTCAACAAGGTACTGAAAATATTCATCAGAGATGGGACATGATGGCATCAAGCAGTTGCTGCAGTTTTGTCCGTTGCATATCCGTGATGCGAATCTCTTCCGTTCCACCACATCCCAAAGGTGCTCTATTGGGTTGAGATCTGGTGACTGTGAAGGCCATTTGAGTACAGTGAACTCATTGTCATGTTCAAGAAAACAGTCTGAGATGATTCACGCTTTATAACATGGCCTAC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa24935

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:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000007211	Nonsense	149	375	4	4

Genomic Location (Zv9):

Chromosome 13 (position 28819686)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	28465634
GRCz11	13	28596084

KASP Assay ID:

554-7413.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TAACTCTTCTCTTCTTCAGGGTTTCTACCTGGCTACCTCTTACCAGCCTA[T/A]GAGGAAGTAGAGAACAGACCTCCAACACCCCCTCCTCCATACAGTGCCTC

Long Flanking Sequence:

TTTCTAGGCATTCAAAACACTTTACACATAGGGGGGAAATCTCCTCATCCACCACCAGTGTTAAATCGAGTTTGAAACCCCTGCATTAGAAGTAACATGCCCTCAAACCAATATTAATAGATGCCATAAAATTGTTAGTTCACCCAAAAAATTAAAATTATTTTAATAATTACTCTTTTGTTCCAAACCCCGGGGAGCTTTGTTTTCATCTTTGGAAAACAAATGAAGATATTTTAGTTGAAATCTAAGAGCTCTCTGACACCAAGTTTGCCGACTCAAAAGTCTAGAAAGGTACCAAAAACATCCTCAAAACAGAACATCTACAATGATTAAATCGAAATATCAACAGGCAAGGAGAATACTTTGTATGCACATAAAACAAAAATAACATTATTCCACAGTTTCTTCTCCTCAGTGTCAGTATATAACACACGTCATGTAAAACTAACTTAACTCTTCTCTTCTTCAGGGTTTCTACCTGGCTACCTCTTACCAGCCTA[T/A]GAGGAAGTAGAGAACAGACCTCCAACACCCCCTCCTCCATACAGTGCCTCTCAGCCGGGCCACTCCACCAGCTCTGACCCCTTGTGCTCCGAACAACCGGACGAGCTCTGCCCTCCACTGCAGTCCAGCCCCGTCACCCCGTCTGCATCCGAAAACCACTCTCCAGAGCCCTGCACAGAGCAGCCACAGACTCCCACCACACACCACCCTGCCAAACCACAGTACCTCAGCCTAGAGGAGGACGGGCGACTCCAGCAGGTGGCATGCGCGACCTCACACAGCCTGCTCAAACAGGACAGCTCGGGCGAAGACCTGAGCCAACCTGGAGACTGTTCTCCTGACAGCAAAGATAAGACTCCCGGTCGGCACCGGCGCTTCACTGGTGATTCCGGCATCGAGGTGTGTGTGTGCAACCAGGGGCCTGGGGATGGGGAGGAAGAAGAGGAGATGAAAGAGCTTGTAGGGCATATGGATGCAAGGGGGCTGGAGGAGCAGGACTT

Associated Phenotype:

Not determined