ZMP

elovl2

Ensembl ID:

ENSDARG00000045414

ZFIN ID:

ZDB-GENE-060421-5612

Description:

elongation of very long chain fatty acids protein 2 [Source:RefSeq peptide;Acc:NP_001035452]

Human Orthologue:

ELOVL2

Human Description:

elongation of very long chain fatty acids (FEN1/Elo2, SUR4/Elo3, yeast)-like 2 [Source:HGNC Symbol;A

Mouse Orthologue:

Elovl2

Mouse Description:

elongation of very long chain fatty acids (FEN1/Elo2, SUR4/Elo3, yeast)-like 2 Gene [Source:MGI Symb

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa44089	Nonsense	Mutation detected in F1 DNA	Not yet available
sa37827	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa44089

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
ENSDART00000066781	Nonsense	141	295	5	8

Genomic Location (Zv9):

Chromosome 24 (position 8666445)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	8725824
GRCz11	24	8866210

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGATTGAATTCCTGGACACTATCTTCATTGTGCTGAGGAAGAAAAACAGC[C/T]AAATTAGTTTCCTGCATGTGTATCATCATGCCTCTATGTTTAACATCTGG

Long Flanking Sequence:

CAGGATAGGGTAATTAGGCAAGTAATTGTATATCGATGGTTTGTTTTGTAGACAATTGAAAAAATATAGCTTAAAGGGGCTAATAATTTTGGCCTTAAAATGGTTTTGAAAAAATTTAAAACTGCTTTTATTCTAGCCAAAATAAAACAACTAAGATTTTCTCCAGAAGAAAAAATATTATCAGACATACTGTGAAAATTTCCTTGCTCTGTTAAACATCATTTGGAAAATATTTAAAAAAGAAAAAGAAAATTCAAAAGTGGGGCTAATAATTCTGACTTCAACTGTATGTTCAAAGATAGTGTTTTATAAACTAAAACGCTTTATGCTTCATCAGTCAGGGGGAAAACCAGAAATATATTAATCAGTGCACTTAATTTTTATTTGGCATTTCTTTTGTTTTACATGTATAGGTAGCAAAAGTACTATGGTGGTACTATTTCTCGAAGCTGATTGAATTCCTGGACACTATCTTCATTGTGCTGAGGAAGAAAAACAGC[C/T]AAATTAGTTTCCTGCATGTGTATCATCATGCCTCTATGTTTAACATCTGGTGGTGTGTCCTCAACTGGATACCATGTGGACAGAGTAAGTGAGCCAGGAGGACAACATGTGTGTCAGCTATTGTATCAAGCAATTTTTCATTAGATTTAACATTAAAATTAGTAATATTTTTTACATTTCTGGAAATGCTTAATTGAGACAAAATTGTGCACATGGTCAAGTGCAATAATGGTGCAGTTCAAGCTAAATTTTGCAACATCTTTCTCCAGGTTTCTTTGGGCCAACTCTAAACAGTTTCATCCATGTCCTCATGTATTCTTACTATGGTCTGGCAACCATCCCATCTATGCACAAATATCTGTGGTGGAAACGTTACCTCACCCAGGCTCAGCTGGTCAGTAAGCACACTAGCATACTGTGCTCTTATCCCATTTCCTTTTCTATTTTCTTTCGTCCAGACATGCCTGCCTGCCATTTTAATATGTTATGTTCACTTCTTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa37827

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
ENSDART00000066781	Nonsense	168	295	5	8

Genomic Location (Zv9):

Chromosome 24 (position 8666364)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	8725743
GRCz11	24	8866129

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCTCTATGTTTAACATCTGGTGGTGTGTCCTCAACTGGATACCATGTGGA[C/T]AGAGTAAGTGAGCCAGGAGGACAACATGTGTGTCAGCTATTGTATCAAGC

Long Flanking Sequence:

AATAATTTTGGCCTTAAAATGGTTTTGAAAAAATTTAAAACTGCTTTTATTCTAGCCAAAATAAAACAACTAAGATTTTCTCCAGAAGAAAAAATATTATCAGACATACTGTGAAAATTTCCTTGCTCTGTTAAACATCATTTGGAAAATATTTAAAAAAGAAAAAGAAAATTCAAAAGTGGGGCTAATAATTCTGACTTCAACTGTATGTTCAAAGATAGTGTTTTATAAACTAAAACGCTTTATGCTTCATCAGTCAGGGGGAAAACCAGAAATATATTAATCAGTGCACTTAATTTTTATTTGGCATTTCTTTTGTTTTACATGTATAGGTAGCAAAAGTACTATGGTGGTACTATTTCTCGAAGCTGATTGAATTCCTGGACACTATCTTCATTGTGCTGAGGAAGAAAAACAGCCAAATTAGTTTCCTGCATGTGTATCATCATGCCTCTATGTTTAACATCTGGTGGTGTGTCCTCAACTGGATACCATGTGGA[C/T]AGAGTAAGTGAGCCAGGAGGACAACATGTGTGTCAGCTATTGTATCAAGCAATTTTTCATTAGATTTAACATTAAAATTAGTAATATTTTTTACATTTCTGGAAATGCTTAATTGAGACAAAATTGTGCACATGGTCAAGTGCAATAATGGTGCAGTTCAAGCTAAATTTTGCAACATCTTTCTCCAGGTTTCTTTGGGCCAACTCTAAACAGTTTCATCCATGTCCTCATGTATTCTTACTATGGTCTGGCAACCATCCCATCTATGCACAAATATCTGTGGTGGAAACGTTACCTCACCCAGGCTCAGCTGGTCAGTAAGCACACTAGCATACTGTGCTCTTATCCCATTTCCTTTTCTATTTTCTTTCGTCCAGACATGCCTGCCTGCCATTTTAATATGTTATGTTCACTTCTTTTTATTCCATGCGTTTCCATAACTTTCCTCTTTTTGTCTCAGGTTCAGTTTGTACTGACTATAACACACACAGTAAGCGCAT

Associated Phenotype:

Not determined