ZMP

LOC100334565

Ensembl ID:

ENSDARG00000073784

Human Orthologue:

FEZ2

Human Description:

fasciculation and elongation protein zeta 2 (zygin II) [Source:HGNC Symbol;Acc:3660]

Mouse Orthologue:

Fez2

Mouse Description:

fasciculation and elongation protein zeta 2 (zygin II) Gene [Source:MGI Symbol;Acc:MGI:2675856]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa36016	Nonsense	Mutation detected in F1 DNA	Not yet available
sa39075	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa36016

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000092299	Nonsense	131	376	2	9

Genomic Location (Zv9):

Chromosome 16 (position 3426518)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	16	2584894
GRCz11	16	2822560

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTCAGTCTCGAGTGCGGTCTCTTCACCTGTCAACACTGAGTCTGGATGAC[C/T]GAGCGGTGAGTTTTCAACTTGTCAGTGCTAGGCATAAGATGCGGTTAGGA

Long Flanking Sequence:

TAGGTGATGACCGAAAGGACAAGATCTCGGATACAATCGGATGAAATGAGTTTCTTTCGAAGGGTGGCAGGGTGCAGTCTTATGGATAGGGGGAGGAGCTCTGACACTTGGGAGGAGCTTGGAGTAGAGCCGCTGCTCCTTCACATCCAGAGAAGTCAGCTGAGGTGGCTCAGGCATCTGTTTCGGATGCCTTCTGGATGCCTACCTTGGGAGGTGTTCCAGGCATGTCCCACCGGGAGGAGGCCTCGGGGAATATGAACATTAATGTTGCGCTGGACTGAAAATAGCAACAGTTCACGCAAAACAAGTCTTGCACTTGGGTGTATGATATGGCCCTATTAATTTGGGGGGTGGGTCAGCATTGCTGTTTTGGTTTTAGACTCCGTTTCTTCTGCAGGATCTGGAGCGCTCTGACCGATAATTATGGCCACGTTATGCCGGTGGACTGGAGTCAGTCTCGAGTGCGGTCTCTTCACCTGTCAACACTGAGTCTGGATGAC[C/T]GAGCGGTGAGTTTTCAACTTGTCAGTGCTAGGCATAAGATGCGGTTAGGAAAAGTCGTGGTTTTAAAATAGTCTATTAGTTTATTTAGTTTTTTTAAGGCTACAGTTTCTCCAACAGGAAAAGACCCTCCACATCAAAAGCTAATATGATTCAGGAAACATCTGTGAAACAAATCACTTATACACCAACATTCAAGCATGTTATGTTACTTCATATCCAAAGGAAAGAAAGATTTTCCTAATCAGGGTTTTTTAAACTAATAAAGAGAGTAGAAGTGAATGATTCATGTTAATTATTTAGCCTGACATGTTTACTGCTGTAAAATATTTAAAATGTTTCTTAAAATAAAATATATTGTGTTCAATAGGGTAGGGATGCACGATATATCGGCGGCCATATCGTTATCGGCCGATAAATGCTATTTTTAAGATTATCGTTATCGATCCGATGTCTAAATTAGGCCGATATCTTTAAGCCGATAAATTACGTAATTGTACAGA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa39075

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000092299	Nonsense	276	376	5	9

Genomic Location (Zv9):

Chromosome 16 (position 3429892)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	16	2588268
GRCz11	16	2825934

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ACAGCTTCATCTCGGTGCTCATCGACGTACAGAACCGGCAGAAGCTGCAG[C/T]GAGAGATGCTGAAGAAGAAGAGGAAAGTGAGGAGCACGTCAGGATCAGAG

Long Flanking Sequence:

TATATATATATGTGTATATATATATATATATATATATATATATATATATATATGTATATGTATATATATATACATATAGTGGAGCCATAAATGTGTATTGAAGCCTTGTTTGTACTGTAGGTTATCGAGGAGATCGAGGAGCTCATGCAGGAGTCACCAGAGGTGGAATCAGAGCAAAACGTTTCACACTCAGGCGTCTCCTTCATCTCTCAGAAAAGATCTCACAGCAGCCAGATCTACGAGGACCGTGAGTACGTCCTCCTTAATCACATTCAGTGCTGGTGAAGAGCGTTTGACTGTGAGCTCTTTCTGCAGGAGTGAGGCTGATGTCCGTGCTGGAGCTGAACGATGAGCTGGAGGACGTGGAGACGGCCATTCGAGGATATTCAGAGGAGCTCATCCACCATCTGGCCACCAGGGACGAGCTGGAGTTTGAAAAGGAGGTGAAAAACAGCTTCATCTCGGTGCTCATCGACGTACAGAACCGGCAGAAGCTGCAG[C/T]GAGAGATGCTGAAGAAGAAGAGGAAAGTGAGGAGCACGTCAGGATCAGAGAGACTGCCGTCTTCTGTGAGTAGCAAAACACAATTATTTTCACATTTCTGGGTTTCTCAGAAGTCGCCATATTTGGTAATCTTAGAGCGCAGTGAATGGGAGAGTACAACAAATAATTTTTTACAATTGCAAGAGAGAGGTGGAATGTTCGCGCGTGCGAGATAGAGGCGGAATGTTGGCGCGTGCGAGAGAGAGGTGGAATGTTCGCGCGTGCGAGAGAGAGGCGAAATGTTCGCGCATGCAAGAGAGAGGTGGAATGTTGGCGCGTGTGAGAGAGGCGGAATGTTCGCGCGTGCGAGAGAGGTGGAATGTTCGCGCGTGCGAGAGAGGTGGAATGTTCGCGCGTGCGAGAGAGGTGGAATGTTCGCGCGTGCGAGAGAGGTGGAATGTTCGCGCGTGCGAGAGAGAGAGGCGGAATGTTGGCGCGTGTGAGAGAGGCGGAATGTTCGC

Associated Phenotype:

Not determined