ZMP
zgc:153394
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC767653 [Source:RefSeq peptide;Acc:NP_001070061]
Human Orthologues:
ELOVL2, ELOVL4, ELOVL5
Human Descriptions:
ELOVL family member 5, elongation of long chain fatty acids (FEN1/Elo2, SUR4/Elo3-like, yeast) [Sour
elongation of very long chain fatty acids (FEN1/Elo2, SUR4/Elo3, yeast)-like 2 [Source:HGNC Symbol;A
elongation of very long chain fatty acids (FEN1/Elo2, SUR4/Elo3, yeast)-like 4 [Source:HGNC Symbol;A
elongation of very long chain fatty acids (FEN1/Elo2, SUR4/Elo3, yeast)-like 2 [Source:HGNC Symbol;A
elongation of very long chain fatty acids (FEN1/Elo2, SUR4/Elo3, yeast)-like 4 [Source:HGNC Symbol;A
Mouse Orthologues:
Elovl2, Elovl4, Elovl5
Mouse Descriptions:
ELOVL family member 5, elongation of long chain fatty acids (yeast) Gene [Source:MGI Symbol;Acc:MGI:
elongation of very long chain fatty acids (FEN1/Elo2, SUR4/Elo3, yeast)-like 2 Gene [Source:MGI Symb
elongation of very long chain fatty acids (FEN1/Elo2, SUR4/Elo3, yeast)-like 4 Gene [Source:MGI Symb
elongation of very long chain fatty acids (FEN1/Elo2, SUR4/Elo3, yeast)-like 2 Gene [Source:MGI Symb
elongation of very long chain fatty acids (FEN1/Elo2, SUR4/Elo3, yeast)-like 4 Gene [Source:MGI Symb
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39844 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19776 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa39844
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099180 | Nonsense | 96 | 268 | 4 | 8 |
The following transcripts of ENSDARG00000068551 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 27552372)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 27748568 |
GRCz11 | 2 | 27404202 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATTCATGTTTTGCTTTCAGTTCACAGCCTCCTCTTGGTTGGCAAGTTA[C/A]AGTTTGCTCTGTCAGCCTGTGGACTACACTGAAAACCCTCTGCCAATGCG
Long Flanking Sequence:
TACGAGAGGATCTTAGAAAACGGAGGTCTGAATTGCTTTCTTCACACCTAGTAGGCCTATAACATGCATATGCTTATATGTAGATTACTGGTTTAGATTCACTGATTATTATCTTTGACAAATTGGTCCTCACTGGATGTTTTATAAATGGCTTTCTGTTAGAGTAGTTTGACGAGCTGATGAAGTAGAGTTGGTTTATTTCCACAGACAAGAGGACAGATGGATGGCTGCTGGTTTATTCTCCGCTGCCTGTCGGCGGAATCTTCCTCTGTTATCTTGTCATGGTATGGTTTGGACCCAAATTGATGGTTCACAGAGAACCAGTCAACATCCAAGCTCTACTTATTATTTACAATTTTTCCATGGTGTGCCTTTCTGCTTATATGTTTTATGAGGTATGGACCATAGACAAATAAAAACATTCATTCATTCATTCATTCATTCATTCATTCATTCATGTTTTGCTTTCAGTTCACAGCCTCCTCTTGGTTGGCAAGTTA[C/A]AGTTTGCTCTGTCAGCCTGTGGACTACACTGAAAACCCTCTGCCAATGCGGGTGAGCAAGTTAACTTTGTATTGATTTTTTATTTATTTTTTTTGTACAATTATTAAATGATGTTAATATTTTTATTGATTTATGATTCACAATAAGTGGAACAAAACAAGCTGAAAAAATAAGGACAAATATAATGTTTTTATTTTGCATGTGATCTGATCTAACCTCTCATATTGTCTCTTTAAAGAACATGCATCCATCACTTATTTTCAACACCATCATACACATTAAACATCAATCAAGATGTTTTTAACATTTTCAAATACATTCTCATTTGAGCTGCACAATATATCCTTTCAGCATTGATATCGCAATGTGTGCATCCGCACTAGTCACATTGCAAGATATGCAATGTTGAGTTTGTGTGTATATATATATATACATATATATATATAGATGGCCAGAAACCACAAGTCCAAACTCATAAGATATGTAGAGACACTGCATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19776
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099180 | Nonsense | 202 | 268 | 7 | 8 |
The following transcripts of ENSDARG00000068551 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 27557339)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 27753535 |
GRCz11 | 2 | 27409169 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTATATGTATTATGGCCTGGCAGCGCTGGGCCCTCAGATGCAGAAATACT[T/G]ATGGTGGAAACGCTACCTCACTTCCCTCCAGCTGGTAAAACTCTTATTAT
Long Flanking Sequence:
GTCATTGTTTTAATAGTGAAAAGTGTGTTGAGTGAAGCCTTTGATATGAAAAATAAGCATATATTAGAGCTCTGGTTGTTTTAGTGCATTTTAATGTACTAGATGTTGGTAAGAATAACTATAATAATATTTTATGACCTAAATATTAAGAAACAAAGAAAAATGTGTTAAAAATGTATCTACATACTGTTGCAGTAGCACACAGACACCACTAGGTGCTATATTGCTCCAGAAATAGCCAATGAATCTGCTCAGCAATGCATGCTATATTGGCTTAATTTTAGGCAGCTAATAAAAATGCCAAAAATCTCATTGAAGTCCACCGTCGTTTCGGATGCCATATGTTGTAAATTGCCAATATAGAAACAGATTTACTAAAGATGTTCTCTCTCTCTCTCCCCCCTCAGCTTTCCTTATTGGCCTCATAAACTCTTTTGTTCATGTGGTGATGTATATGTATTATGGCCTGGCAGCGCTGGGCCCTCAGATGCAGAAATACT[T/G]ATGGTGGAAACGCTACCTCACTTCCCTCCAGCTGGTAAAACTCTTATTATGAATAATACCTTAATATAAAGGATCAGTCACATTTGTGTCACGGTCATCTTTTTTTCTCCCCCTCAGCTCCAGTTCTTTATTGTGACCATTCACACTGCGTTCAACCTCTATGCTGACTGTGACTTCCCTGACTCCATGAATATGGTGGTGCTCGGATACGCCCTCAGCCTAATCGCTTTGTTTAGTAACTTTTACTACCAGAGTTACCTCTCCAAGAAGACCAAGCTAGCCTAATAGCATCGATGCATATATTTATTGATAGGTTACTTGAATACAAACGTGTCATCATTGGTCCTTCACACTGAGAGTATCTTGAGGACTCTTGTTTAATCCGCTATTTCAGATTCATTTGTCTGTGTTTTCTCCCCTCCTCCAAACGGAGTCCACACAATCTTTGCACCCCCATCCCCCTCTGGTCATTAGGGATTGAGACCCTGCAACGCTCTAGC
Associated Phenotype:
Not determined