ZMP

si:ch211-235o23.2

Ensembl ID:

ENSDARG00000076838

ZFIN IDs:

ZDB-GENE-010605-5, ZDB-GENE-010605-5, ZDB-GENE-010605-5, ZDB-GENE-010605-5, ZDB-GENE-070912-224

Description:

Novel protein [Source:UniProtKB/TrEMBL;Acc:B0S725]

Human Orthologue:

APOM

Human Description:

apolipoprotein M [Source:HGNC Symbol;Acc:13916]

Mouse Orthologue:

Apom

Mouse Description:

apolipoprotein M Gene [Source:MGI Symbol;Acc:MGI:1930124]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa32997	Nonsense	Available for shipment	Available now
sa39906	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa32997

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000114951	Nonsense	82	191	2	7
ENSDART00000132617	Nonsense	80	189	2	6
ENSDART00000136690	Nonsense	94	203	2	7
ENSDART00000141358	Nonsense	106	215	2	7

Genomic Location (Zv9):

Chromosome 2 (position 42333610)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	42383074
GRCz11	2	42232492

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCACAGACAGCATAGTTCTTCAGATCCAGAAAAACAGCGACTCCACCCTG[A/T]AGGTCACTGAAACCATGCGCATGTGAGTGGAGAACACTGCACACAGGCAC

Long Flanking Sequence:

AATCTACATTATAAAAGCGTTATAAAGATTAATTGAATCGAATATTTGGTGAAAAACCCTGATTTTTTTGACAAAACAAATGAAAATATTGTTATTCTGGTCAATCTTTTGTAAAAATGCTTTTAGACCTTAAATACTGGTGAAAATATGCAAATGTAAAATATACATTGTTTTCTGTATATTAGGTGTAATTTCCCTAGTTTGCTAAATAGATATTTAAGCAAACATGAAATATTGAATATCATCTATTGCCAGTGTCTGACGATAGTTCGCACATTCTTGGATTAGATCAAATTCTATGCAATATATGGCTATTATTGAATAAATTCTGTATTTCCAGTATTCCAGTATAAATATTGATATATGTAAATACTTGTGTACAGTATACCGGCACTTGGTATTTTGTGGCAGCAGCTGTGTGGGATGAAGATGATCTGAAGACTCTCCAGACCACAGACAGCATAGTTCTTCAGATCCAGAAAAACAGCGACTCCACCCTG[A/T]AGGTCACTGAAACCATGCGCATGTGAGTGGAGAACACTGCACACAGGCACACACAAGAACTCTTCTATTGTTTGCTATGAGAGTGATGCTTTAAGTATTAAATTCATATTGTTTGTGACTTCACAGTGGAGATGCGTGTCTAAAAAATGTTACGAACTACTATGCATTGCCTGCGACAAGCCCTTTCCTGTTCAGAGAAGGTAAGAAACACTGCAATTATTTAGCTAATTTTAAATGTCCCCTAAAGTTAAACAGTTGAGTTCATTTTTAGCTTAGCTTAGCATAGATCTTTGAATTGGATTAGACCAGTAGTATCGCTCAGAAATGTCAACAAAAAAAAGCTTCTGTGGGTACTTCATGAACTAAGACTGAAAGGAAATAAAAAGTTGATATTTCTTATCATTATTATCTCCTATTCTTGCATAATGATCATGGAACTTTACTTTCCCTACTGAAAAAAACTGCTTAAACCAGCCTAGGCTGGTTGGCTGGTTTTAGCT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa39906

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000114951	Essential Splice Site	114	191	3	7
ENSDART00000132617	Essential Splice Site	112	189	3	6
ENSDART00000136690	Essential Splice Site	126	203	3	7
ENSDART00000141358	Essential Splice Site	138	215	3	7

Genomic Location (Zv9):

Chromosome 2 (position 42333408)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	42382872
GRCz11	2	42232290

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ACGAACTACTATGCATTGCCTGCGACAAGCCCTTTCCTGTTCAGAGAAGG[T/A]AAGAAACACTGCAATTATTTAGCTAATTTTAAATGTCCCCTAAAGTTAAA

Long Flanking Sequence:

TGCTAAATAGATATTTAAGCAAACATGAAATATTGAATATCATCTATTGCCAGTGTCTGACGATAGTTCGCACATTCTTGGATTAGATCAAATTCTATGCAATATATGGCTATTATTGAATAAATTCTGTATTTCCAGTATTCCAGTATAAATATTGATATATGTAAATACTTGTGTACAGTATACCGGCACTTGGTATTTTGTGGCAGCAGCTGTGTGGGATGAAGATGATCTGAAGACTCTCCAGACCACAGACAGCATAGTTCTTCAGATCCAGAAAAACAGCGACTCCACCCTGAAGGTCACTGAAACCATGCGCATGTGAGTGGAGAACACTGCACACAGGCACACACAAGAACTCTTCTATTGTTTGCTATGAGAGTGATGCTTTAAGTATTAAATTCATATTGTTTGTGACTTCACAGTGGAGATGCGTGTCTAAAAAATGTTACGAACTACTATGCATTGCCTGCGACAAGCCCTTTCCTGTTCAGAGAAGG[T/A]AAGAAACACTGCAATTATTTAGCTAATTTTAAATGTCCCCTAAAGTTAAACAGTTGAGTTCATTTTTAGCTTAGCTTAGCATAGATCTTTGAATTGGATTAGACCAGTAGTATCGCTCAGAAATGTCAACAAAAAAAAGCTTCTGTGGGTACTTCATGAACTAAGACTGAAAGGAAATAAAAAGTTGATATTTCTTATCATTATTATCTCCTATTCTTGCATAATGATCATGGAACTTTACTTTCCCTACTGAAAAAAACTGCTTAAACCAGCCTAGGCTGGTTGGCTGGTTTTAGCTGGTAGACCAGGCTGGTTTTAGAGGGGTTTTGGCCACTTCCAGGCTGGTTTTAGCTGGTCAGGCTGGGAGATGACCAGCTAAAACCAGCTTGACCAGCCTAGCTAAGCTGGGAGTAGCTGGATTTGGCTGGTCATTTTCCAGCCTGACCAGCTAAGACCAGGCTGGAAAGGGTTGGAAACCAGCCTGGAAATGGCCAAAACCT

Associated Phenotype:

Not determined