ZMP

NP_998135.1

Ensembl ID:

ENSDARG00000008637

Description:

microsomal triglyceride transfer protein large subunit [Source:RefSeq peptide;Acc:NP_998135]

Human Orthologue:

MTTP

Human Description:

microsomal triglyceride transfer protein [Source:HGNC Symbol;Acc:7467]

Mouse Orthologue:

Mttp

Mouse Description:

microsomal triglyceride transfer protein Gene [Source:MGI Symbol;Acc:MGI:106926]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa32615	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa11757	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa32615

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000015251	Essential Splice Site	21	738	2	15

Genomic Location (Zv9):

Chromosome 1 (position 11420962)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	11437791
GRCz11	1	12124591

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGATCAGAAGATCCAGAAAGTGTCACAGCATGACATTTGTGTGTTTTCTC[A/T]GGTGCTGGACCTCGGCTGGATAACGGCAAACTCTACAGATACAGCTACAG

Long Flanking Sequence:

TCCCACAAATGTAACTTCAAACACATCACAGACTCTACTGTCTGAATCTTTTTAAGACTCAAGGTTAAGTTGTTCACATCATAAACAACTTATGATGTTTCATCATAAGAAGCTAAAAAAAATATGATCTATGTATATATGATGATTACAGATAACTGAGGATTAATAGCTCATAGTACACCGTTATCTGAGACCCACCTACAATTACAGATAGGACAACATTCTTTCCCTTCTGTTTTTACTTCTGTGAAAGGCTGTGGACTTACTCTGAATTGCTTTGCTCGCTCTCTTGATCAAATTATACGAGTTTGAATGCAAAACCCTGTGGATTAAAACAGAGAGAGGATTGAATTTAGGGTTAAAGTCTGTGCTTTGAGATGTTTCCTGTCTGTCTTCTCTCACATTCCTCTCTTGCTGTAGTCCAGCTGTGTCTTACATGCCACTGACCTGAGATCAGAAGATCCAGAAAGTGTCACAGCATGACATTTGTGTGTTTTCTC[A/T]GGTGCTGGACCTCGGCTGGATAACGGCAAACTCTACAGATACAGCTACAGCACTGAGGTCGGGCTGAACCGGCCGACGGGATCCCCTGGAGGCAATGTTGGATTCAGGATTAGCAGTGATGTGGACATCAACCTGGCCTGGAGGAACCCTGAGATCCAGGACGAGCAGCTGCTGCAAGTAAAGGTAAAGGGACAAGAGGGATAACAAAAAAAGGCCACTTTACACACTTCAAGATGCCTTAAGTAAATTTTGCCAAACAATGTTGGCATTTGAAAGCACCAAAACAAACACACATCCAACAAGACCTTGCCTCTTATTTACAGTTTAAGTCAGAACTGTTAGCCCTCCTGTTAGTATTTTTCTTTTTTCAAATATTTCCCAAATAATGTTTAACAGAGCAAGGAAATGTTCACAGTATGTCTGATAATATTTATTCTTCTGGAAAAAGTCTTATTTGTTTTATTTTGGCTACAATAAAAGTAGTTTTTAATTTTTTAAAC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa11757

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000015251	Nonsense	176	738	5	15

Genomic Location (Zv9):

Chromosome 1 (position 11418659)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	11435488
GRCz11	1	12122288

KASP Assay ID:

2259-0303.1 (used for ordering genotyping assays)

KASP Sequence:

TTCTTTTGTAATCYATAGGCTGATGCTTCAGGGAAATGTYTGGTWGAGTA[C/A]AAAGTTARCAAACWTCAGGTGATCCGCACAAAACACTTGGAAACTTGCAA

Long Flanking Sequence:

CAAAATATCCCTGGTGTAAATCACATCCCACTGTCCTGTTCTCAGATTTCAAATATTCAAGTTGAAAGTGCTGGAAAGCACTCCCGCAAAAACAACATCTTCCATGGCAGCTCAGCAGAAAGCATTCTGGGTAAAGTCAGGCTTGAGGCACTTCAGAGGCCCTTCTTGGTGCTGTGGAAGATGGGCAAGGTAAGAAACACTGTTTTTTTATCAGTTAAGTTTGTAACTTTTAAATGTTTTCCATGGTGATTTGACTTTTGTGTTCTTTTGCTTGTCATTTAGATCAGAAGCCTCTATGCCCAAAAAGCGGAGCCTGCTACTGTCAAAAACCTGAAGAGGGGTGTGGCCAGTATGCTAATGATGCAGCTTAAGTCCGGAAAGATGTCAGAGGTAAAGACCAGCAATTGAAATTCTCCTCTGAAGTTTGATTTTCTACTGTACGCTAAATACTTCTTTTGTAATCTATAGGCTGATGCTTCAGGGAAATGTCTGGTTGAGTA[C/A]AAAGTTAACAAACATCAGGTGATCCGCACAAAACACTTGGAAACTTGCAAATCTCAAGAGACGGGATTCACTACTCACAGTCCAGTAAGACCAAAACAAATGTTCTCATCTCACCTCACCCAGCAGGCACAGGACGTCAATATGATGTCAGATTGATGTTGTTCCCCAACATTGTGCGAGCGTTGTATTTTGTTTGGAAATGAAAATCGGGTTGACATCAGACAGATGTCAGTGTCCAACATCCAACCTAAAAATCCACCAAATATTGACGTCTAATGATGTTACAGCTTGACGTTGTGTGGACGTTACAACTATGATGTCTATCAGACGCTGGATTTTGGTTGCCATACCTGACGAAAAACATCAGTATTTGACATCAGTATGATGCTGGTTTAAGAAGTTGCTTCGACTTTGGATTTTGGTCACTTTTCAACAACCTAAAATCAACCAAATATCAAAATCATTTGATGTCGTTATTGAAGATCAAAATAATGTTGTCA

Associated Phenotype:

Not determined