ZMP

ENSDARG00000087426

Ensembl ID:

Human Orthologues:

AC106886.1, C20orf27

Human Descriptions:

Uncharacterized protein [Source:UniProtKB/TrEMBL;Acc:A6NC64]
chromosome 20 open reading frame 27 [Source:HGNC Symbol;Acc:15873]

Mouse Orthologue:

1700037H04Rik

Mouse Description:

RIKEN cDNA 1700037H04 gene Gene [Source:MGI Symbol;Acc:MGI:1914576]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa39671	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa39672	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa39671

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
ENSDART00000129819	Essential Splice Site	6	166	1	5

Genomic Location (Zv9):

Chromosome 1 (position 45540784)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	44384003
GRCz11	1	45085306

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CATCCCTGGATTTCCCTGGCCTTATGTCGACATGGCAACAGGAAGGAAAA[G/A]TCAGTGTGTTTTCTGTTCATAATGTGTGAATATATCAGTACATGCACTCT

Long Flanking Sequence:

TATACTGCAAAGTCAATGAAATGCAAATCAACCGTGCTTATGGGCTGCGCAATTAATAATTTAGATCTTGGGGAAATAACATGCATGAATTTAAAGTCTTCAATAAAATTAGTGTTGCACCTGATTGCAATGGAATGTTAGAACGAGCTACAAAAATGACCAAGAAACATGTTTTAGTAGGCATTTGCAGCATTTCATTTGGTTTTTATTAATATCTAAATGCCATTTACATACTATTTTACACATATCTTTACATCCTTAGAAGAACTGTTATCAAAAGGAAACCAAACACTCAGTAGTTTATTTTGTCTTTGTTTTCATATCTAAAACATCACGATTAAATAAATAAGAGTGTTATATTTCACAGGCATCTTCTCTGTCTCTGCAGGGGTCGTTCTCTGTGACTCGGTGTCTGTTCTTTAGAGATGAAAACACTTCGGTGCCAATAATCATCCCTGGATTTCCCTGGCCTTATGTCGACATGGCAACAGGAAGGAAAA[G/A]TCAGTGTGTTTTCTGTTCATAATGTGTGAATATATCAGTACATGCACTCTCAGAAATAAAGGTACGCAAGCTGTCACTGGGGTAGTAGCTTTTTAAAGGGTACAAATTTTGACTTAAAAGGTCCATATTAATACTTCAAGGGGACATATTAGCACCTTAAAAGTACAAAAGTGTTCCTCTTAAAGTTTTTAGGTACCAATATATATATATTTGAAGTACCAATATGTACTCTTTAAGAAACATGTACCTTCTGAACAGGTATCACCTCAGTGACAGCTCATGTACCGTTATTTCTGAGAGTGCGCAAGTCAAAATTATTAGCCTTCCTGTAAAATTTTAATTCCTAGACATTTTTTTGGACACATTTTTAAACATAATAGCTTTAATAACTAATTTCTAATAACTTATTTATTTTGTCTTTGTCATGACGAGAGGTAATAATATTTTACCAGATATTTTACAAAATACTATTTAGCTTAAAGTGCAATTTAAAGGCTTAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa39672

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
ENSDART00000129819	Nonsense	60	166	3	5

Genomic Location (Zv9):

Chromosome 1 (position 45543166)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	44386385
GRCz11	1	45087688

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CACTGACTGCTGCATTCTCTGTTTAGGCCGGATTTTTAAGGAGTCATCAC[A/T]AATATGAAATCGTCTTCTCTTTGCCGCAAGTCCCAACGTTGGGCAAAGAT

Long Flanking Sequence:

ACTACAGTCAGAGCTCAGTGATATGACACGATGCATGAACATGAGTGAAACATTATACTCAGCAGTGTACATGTGTTTGGAGCCTCAAAACAAACATTTGGGGCATATTTTACAATATACACGTTAAACTAACAAAAGATAGAGTTTAACAGACCCACAGAAATGCTAAATACATTAAGAATCTTGATTAATGATATGTGTGGATCATCAGAGTCTTTGTTCTAATTGTTTTCCACCATGATTTTACACTCAAAAATAAGTGTTTGAGGCTCACGGTATGCCATTTCCATGTACTGAACTCTTATTATTGAGCTATTTCTGGGTATATCCATGATTTTATTCTATGGGAGCTTTAAACAAGCACAGCAAATAATGAATTTCCTTTTAAATAGTTTATTTTAATTTGACAAAAATTGCATTGCCAGTGCAAGATGTGTTGTAAGCTGAAATCACTGACTGCTGCATTCTCTGTTTAGGCCGGATTTTTAAGGAGTCATCAC[A/T]AATATGAAATCGTCTTCTCTTTGCCGCAAGTCCCAACGTTGGGCAAAGATGTCACCCTTTCCCCTGCACTCCGTGCCACGGCCAAACCACGGCTACGTGCAACACGCATCACACCACGGGCAGAGGGTATGCTTTTTGTGGTGGTATTATGATGCATCAAATTAAGCCAGAAAGATTGAGTTTACAAACTGGGTCCTGAGTTTCTGAGTTGGGGAATGTCAGCAAAAAAAAATAAATAAATAAATAAAAATTTTAGGCAACATCTACACTAATCCAGATGCATTTGTAAATAGTGTATTTATGTAAAAGTGCCCTCTGTTCACAATATCAAGTTAAAGCTTTATACAAACTTTTCTCATTCACACTAAAACATTGGAAAACACTAAACACCTCTATGCTACGTACAAGTAAATCTATCCTTGCGTGGCACTGCCTTACAACAACTGCAAGAAAGCATTTTGAAGTATTCAAGAATATTCAAATGCCCTTGAAAAAAGGCA

Associated Phenotype:

Not determined