ZMP
elna
Ensembl ID:
ZFIN ID:
Description:
elastin a [Source:RefSeq peptide;Acc:NP_001073532]
Human Orthologue:
ELN
Human Description:
elastin [Source:HGNC Symbol;Acc:3327]
Mouse Orthologue:
Eln
Mouse Description:
elastin Gene [Source:MGI Symbol;Acc:MGI:95317]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12235 | Nonsense | Available for shipment | Available now |
sa17177 | Nonsense | Available for shipment | Available now |
sa42459 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa42460 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa11039 | Essential Splice Site | Available for shipment | Available now |
sa42461 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa32006 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12235
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102316 | Nonsense | 3 | 1079 | 1 | 52 |
Genomic Location (Zv9):
Chromosome 15 (position 163469)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 386803 |
GRCz11 | 15 | 296244 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGANTTTTCTTTGAATCTGTTGCTACATATCTCTCTGGCTGTAGGTGGATA[T/A]GGGGGTTATGGTGGATATGGTGGTGCTGGAAGATTCTACCCAATGGCTGG
Long Flanking Sequence:
CTAATTAAATGATCTGTTGTTCAAGATTATCAGCAAGATTATTAATTGTATTAGACAAAAATCTCATATCTGTGTGTCAGAATATCAGGATTCTTGAATCTTTAAATCTACAGTGCTCTTAGATTTCTATTGGCAACAAGGCAAAAGAAAGATTGACAAGCAAAGCATTTACTGCACATCCTTTCCATTCCTGTGTTCCTCCCTCCGCTATAAAATAGGAATGCAAGCTTTGCAACCTCATTTGTTTAGCGTTTCCATGTCGAAGGAGGACGCGATGTAGCAATAATTCTCAATGGAGCCTAACTCCTCATTTGCTCAGCCAAAAAGATTCACCGTTAGCCTCGTTCTCTTTCAACTTTCTTTTCTTTTGTTTTCTCATTCCTTCCCTCCCTGTCCTGTTGCTAAATCAGCCCTTAGCATTGACAGTCTAAGTCATTCGAGGGCGGAGGTAGATTTTCTTTGAATCTGTTGCTACATATCTCTCTGGCTGTAGGTGGATA[T/A]GGGGGTTATGGTGGATATGGTGGTGCTGGAAGATTCTACCCAATGGCTGGAGGTCTGAAACCAGCTAAATCAGGTGCTCATTCCATGAACAGTCAGCAAAGTTTATATGGAAAATAGTAATTGAGCATTAATATGAGCATTCATGTTTCCCTCTAGGAGCTGGGCTACCAGGAGGAGTTCTGCCAGGAGGAGTTCTGCCTGGAGGAGTTCTGCCTGGAGGAGTTCTGCCTGGAGGAGTTCTGCCTGGAGGTGGTCTTCCTGGAGGTGCCATTCTGCTGACATTTTCGGTTTTCTTAGTGTCTAAGTAACAAAAGCTGCACAAATGTTTTCTAAATCGGATTCTCTTGTTTCAGGTGCTGGTGGAAAGCCCCCCAAAGGTGGTAATATATGTCCATTGTCTCCAACTCTTTCTAAATGAAACATAGTTCAGAGAAAAACATTTAGAGGGGAATTGGATAGGAAGAAGTTGATCTCTGTTTATTCATGAAGTAAAAACACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17177
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102316 | Nonsense | 13 | 1079 | 1 | 52 |
Genomic Location (Zv9):
Chromosome 15 (position 163497)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 386775 |
GRCz11 | 15 | 296216 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTCTCTGGCTGTAGGTGGATAWGGGGGTTATGGTGGATATGGTGGTGCT[G/T]GAAGATTCTACCCAATGGCTGGAGGTCTGAAACCAGCTAAATCAGGTGCT
Long Flanking Sequence:
ATCAGCAAGATTATTAATTGTATTAGACAAAAATCTCATATCTGTGTGTCAGAATATCAGGATTCTTGAATCTTTAAATCTACAGTGCTCTTAGATTTCTATTGGCAACAAGGCAAAAGAAAGATTGACAAGCAAAGCATTTACTGCACATCCTTTCCATTCCTGTGTTCCTCCCTCCGCTATAAAATAGGAATGCAAGCTTTGCAACCTCATTTGTTTAGCGTTTCCATGTCGAAGGAGGACGCGATGTAGCAATAATTCTCAATGGAGCCTAACTCCTCATTTGCTCAGCCAAAAAGATTCACCGTTAGCCTCGTTCTCTTTCAACTTTCTTTTCTTTTGTTTTCTCATTCCTTCCCTCCCTGTCCTGTTGCTAAATCAGCCCTTAGCATTGACAGTCTAAGTCATTCGAGGGCGGAGGTAGATTTTCTTTGAATCTGTTGCTACATATCTCTCTGGCTGTAGGTGGATATGGGGGTTATGGTGGATATGGTGGTGCT[G/T]GAAGATTCTACCCAATGGCTGGAGGTCTGAAACCAGCTAAATCAGGTGCTCATTCCATGAACAGTCAGCAAAGTTTATATGGAAAATAGTAATTGAGCATTAATATGAGCATTCATGTTTCCCTCTAGGAGCTGGGCTACCAGGAGGAGTTCTGCCAGGAGGAGTTCTGCCTGGAGGAGTTCTGCCTGGAGGAGTTCTGCCTGGAGGAGTTCTGCCTGGAGGTGGTCTTCCTGGAGGTGCCATTCTGCTGACATTTTCGGTTTTCTTAGTGTCTAAGTAACAAAAGCTGCACAAATGTTTTCTAAATCGGATTCTCTTGTTTCAGGTGCTGGTGGAAAGCCCCCCAAAGGTGGTAATATATGTCCATTGTCTCCAACTCTTTCTAAATGAAACATAGTTCAGAGAAAAACATTTAGAGGGGAATTGGATAGGAAGAAGTTGATCTCTGTTTATTCATGAAGTAAAAACACACATGTTCGTTTTTAACACCTTTTACAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42459
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102316 | Essential Splice Site | 558 | 1079 | 24 | 52 |
Genomic Location (Zv9):
Chromosome 15 (position 173902)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 376370 |
GRCz11 | 15 | 285811 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGGTGCTGGTGCACTCTCCCCTGCTCAGGCAAAAGCTGCTAAATATGG[T/A]AAGCATGCATATTAACTGATGTACCAGTGTTAATTAATTATGACCAAAGT
Long Flanking Sequence:
AACCATAATCAAACACACCTGTTGAAAGCTTTCTAATGATCTTGAAGACATTGATTAGCATCTTCGAGTGTGTTTGATTAGTGTTTGAACAAAACTCTGCAGCACAGCAGTCTTCAAGGACCAAGTTTGCCCATCCCTGGTTTAAAGAGATATTTGGAACATCATGAGATCAAGTCTTAGTATTGTTGTACATTTTCAATCTTTGAGGTTTACTTCAGAGTCTATATTTGTATTGGTCCTGGAACATCTGTTCTATCGAGACAGCATTGTTCTAACCCTTCTGCAACCTCAATTCTAACCTCACCATCTCACTGTCTGACATAAATAATTTACCAGGAGCAAAGTTGTCTTGCAAAAAATATGTTCCCCTTTTGTGATGCTTTAGACTTGACTGTCAGTTTATTAGAATGATCTAATAGTCATCTTTTTTGTTGTTGTTTACCTGTGTGTGAAGGTGCTGGTGCACTCTCCCCTGCTCAGGCAAAAGCTGCTAAATATGG[T/A]AAGCATGCATATTAACTGATGTACCAGTGTTAATTAATTATGACCAAAGTCAAACTCATTCAAAGAAGTCAATCAGTGTCTTTAGAATAAGTAGAAATGAACAGGCTGAAGTTTAACATTAGATCTAGACTCTGTAGAACAGAGATGCTCAACCTGTTCCTGGAGATCCACCTTCCCGCAGAGTTCAGCTCCAACCACAATTAAACCCAACTAAACCAACTGAGACGAATCCGAAGGAACACTTGGTAATTAAAGACAGGTGCGTTTGATCAAGGTGGTAGCTAAACTGTTGAGGAAGGTAGATCTCCAAGAACAGGTTTGGACACCCCTGCTGTAAAGTAGCAGTCTTCTTCCAGCACTGAAGACACCTGAAATATTAAATTGGGAATTTCACATTGAGTGTTCATTGCCCTGCCTTGATCCAGGAGCAGTTCCTGGTGGTGCCGGGATTCTTCCTGGTGGTGCTGGGATTTTGCCAGGAGCTGGAGGAGTTTACCCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42460
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102316 | Essential Splice Site | 710 | 1079 | 31 | 52 |
Genomic Location (Zv9):
Chromosome 15 (position 176873)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 373399 |
GRCz11 | 15 | 282840 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTTGAATGCTTTCAGGGCTAGCAGCTGGAGCCAAACCTCCTAAATATG[G/A]TAAGGGCTTGACTCTTTTCTGTTTCAGCTGTCTTGGCAGTGTTATTCAGC
Long Flanking Sequence:
TAACCAGGCTGGGAGCCCAGCCAAAACCAGCTGTGTCCAGCTTAAACCAGGCTGGTTTTAGCTGGTCATTTTCCAGCTTGACCAGCTAAGACCAGGCTGGAAATGGCTGGAAACCAGCCTGGAAATGAAAAAAAAAAAAAACCCTATAAAACCAGGCTGGTAAACCAACTAAAACCAGCCAACCAGCTTAGGCTGGTTTAAGCTGGATTTTTCAGCAGGGATAGCATATTCACAGCACTTTCACCAGACTATAGTAAGTACTGCATGAATAAATGAGCTGCTCACTGTGTGTAGGAGCTGGAGTTGCCCCAGGCTATGGTTCTGTGGCTGGGCTTGGAGGACAGCTTGGGGCTGGAGGTACCGTACATGTTTGAATGTCCCCATTTCTCACAATGGATGTTTGTCAGTTAAGCTAATTTTGTTTTTAGCATTGGAGAACATTTAGTCACAGTGTTGAATGCTTTCAGGGCTAGCAGCTGGAGCCAAACCTCCTAAATATG[G/A]TAAGGGCTTGACTCTTTTCTGTTTCAGCTGTCTTGGCAGTGTTATTCAGCTGTTTGTACATGTGTTGCTCTACAGTTTGTGTTTGAATGTTGTTTGTAATAGAAAATAGTTGTGCTGAGATCATAAAAACTGGTCCACTGACTGAGTGTGAATCGAGTATTGATCGGTCAGATATTATGCTTTGTGGCCGCAGGAGTGCCTGGAGGAACAGGTTTTGGAGTACCCGGAGGAGTCCCTGGAGGAATACCAATAACTGGACCAGGAGGTATGGCTGCTGCTTTCTGGAAAGCACAATGATATGAGAAGCTGAGTTTTATATCTAATTTTTAAACGTGTTTCTGAGGTTTTGAGGATTGTATTATGTTTCAATCTCTTCTTATTTCTATTTTTAAGGATACCCTGCTGGAGCCAAGGCTCTTAAATATGGTATTTATAATAGCTGATTAATTCTGTATTAACTAGTGTGTAGGCACATTAATCTCTCTGGCTAAATGTAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11039
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102316 | Essential Splice Site | 992 | 1079 | 46 | 52 |
Genomic Location (Zv9):
Chromosome 15 (position 185411)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 364861 |
GRCz11 | 15 | 274302 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGAGGAGCGGGTGGTGTTGGMRGTGTTGGAGGACTSTATCCWGGAGCAG[G/A]TGAGACTTCATGCTAAACATCAGCACTTCACATATAATGTTGTGCATRGT
Long Flanking Sequence:
TTTCCTCATTCATTATTAAGGCCAATATTACGGTAGCGCTGGACCGTCTGGAGTCGGGACTGGTGTTTTACCTGGAGCCAAACCGCTGAAAGCCCCTGGTAAGATCACAGTATTTCACCTTCAGAGTTCTCCAGCAAGACTAGCAGTGCTCATGTGAACACAGGTGTTGAGTTTGACATCCAGGCTGCAGAAGAATCCAGAGGCCACATTAGCCTGCATTAGGTGCAGTTCTGGATGAATGTAAATGCAGTCAGATCCTCTGTAACTGGACATGCAAATATTAGTTTCACAGGAATATCTGCTCCACATGTAAATGTCTATGCTTGGAATCATGTCTTGACCTTACATTCATATTCCCGCACACAAATACAGTGCTCAACATTACTGAACACACACCCGCACTGTAGTCTTCTCTCAGTCTGCCTCTGCTTGACTCTGTGCATCAGGTGTTGGAGGAGCGGGTGGTGTTGGCGGTGTTGGAGGACTGTATCCTGGAGCAG[G/A]TGAGACTTCATGCTAAACATCAGCACTTCACATATAATGTTGTGCATGGTGCCAATAATACTGCACGGTAAAGAGAAAAGTGCAAAACCTGAAGCTTTATTCCTGCCCTGTTCACAAGATCTGAACCCAAATCTAAGTGGCCGTCACAGGGCGATGTGGAGAAAACCGTGACACACTTGTGGACCATGTAAACTGAGATCAGTGCACTGCAGCTGGACTGTGATCATACCTGCTCATGACTCTTCTCAGGAGTCTCCTGTATTCACACCAATCGTTCGCCACCCTCCCGCTGTGTTATTTCACCCAGAAAACTCATTATTGGCCTCATCAGCCTTCTCAACATCCCCCCTACCTGTCTTTAACTTTGGTACGGTCTCCCCCACCTAGCATTGAACCCTAAGCTAAGAGGCAGAACTCACCAGAACTCATTAGAATTGCCTTCAATACTCCTTTGTAAACACATTATAATGTAACACTGTTGGCAGACGAATAATACTGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42461
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102316 | Essential Splice Site | 1034 | 1079 | 49 | 52 |
Genomic Location (Zv9):
Chromosome 15 (position 188977)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 361295 |
GRCz11 | 15 | 270736 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCTTCTCTGCAGGCGGTGTAGCTGCTGGAGGATACGGAGCTTATCCAG[G/A]TAATGCTTTAGTGAAATAATAATACAACATATAACACAGTGTCTTCTGAT
Long Flanking Sequence:
TGTGAAGGATGCGTTCTCATAGTCATAGTCAATCCAGGAAATCAGCACAAATTCGAGAATCATTTCTGACGTTCTCAGCTGCTCTCAATGCCTTTCTGTGCTGTGTTCACTCCCATAATGCACTGCATGAGTGCTCAACTTCCATATGAATGAACTGAAAACACACACTACACACTTTCATATCAGTTAAAGGGTCAGTTCACACACACACACACACACACACACACACACACACACACACATGAAAATTTACTCATTATTTACTCTCCTCAAGTGCTTCCTAACCTTTACGAGTTTCTTTATTCTGTTTAACCCTAATCAAGATTTAAAATAATGAATTAATTTTTAATCTTTCTTCAGAAAATCCTAATTTGTGTTTGACATAAGAAAGAAACTGGTAAAGAAATGCAGGAGTGAGTGATCTCCTGTTCATGTGTAAATCTCCATCTCTCTCTTCTCTGCAGGCGGTGTAGCTGCTGGAGGATACGGAGCTTATCCAG[G/A]TAATGCTTTAGTGAAATAATAATACAACATATAACACAGTGTCTTCTGATGGAGTTCAGCTTGTTCTAGTGCAGGGCTATTCAATTAGACTATCATGGGGGCCAGTTCATGTAAAGCATGCTAACTGAGGGGCCGGAGAGAGATGACTTGCAATATGAGTGATGACACAACTGCATATACTGTATGAGCCCATATGCTGTGCTTTTCTCCTTAAGACACCCATGCTGGCTTTGTCTACATTTATATATTAATATGCTGAACTTTATAACTAAATCTAGTTTTGATATCATCGGTGCACTGTCTGGAGGGCCGGAACAGATTGCCTCTGAATTGAATAGCCCTGTTCGGTGGTCTTCAGGGTCATTTATACACTGCAGACATGCTTTTCGGTCTTACCACGAGTCCAAATATCCACCAACTCCTAAATCAAGAAGCATTTTCTAGACAAGAACATAATATTGTGTTGTTTTCAGAAATAATGAGTCAAAACTAATCGAGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32006
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102316 | Nonsense | 1038 | 1079 | 50 | 52 |
Genomic Location (Zv9):
Chromosome 15 (position 190497)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 359775 |
GRCz11 | 15 | 269216 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGAGTTAGACTCATCTCTCTCCTCTGTTTCTGTGTTTCAGGAGGATAT[G/T]GAGCAGGACTATCCCCACAGCAGGGTACGACCTCTACATAACGCACCTTC
Long Flanking Sequence:
TTATTATTAGTATTATTATTATTAGTATTATTATTAGTATCATTATTTTATTGTTATTATTATTAACATTAGTAGTATTATTATTAGTATAATTATAATATTAATTATTATTATTCTTATTATTATTATTACAGATGCTGTTGGTCACAGTTGGCCATTAATCTCCTCGCTTAAAATGCTTTTCTTACTCAGAGTTTTTGTCTTGCTTTCAGAAATAAAAAGTCAAAATTAAGTGCTGAACTTCCCTCATTGTCAGATTATCCTGCCTGTTTTAAAGAGAAACTCTCTTCATTTTGACTCATTATTTCTTGAAACAAGACCATATGCTGTGCTTGTCAAGACAATGCTTCTTGATTTAGCAGTTTGTAGATGTTTGGACTAGAACCAAGACAAACTCAGAGTCAGACAGCTTGTTCTGCTTTTGTTTCACTGATATTCTTTGTTTAATTTGCAGAGTTAGACTCATCTCTCTCCTCTGTTTCTGTGTTTCAGGAGGATAT[G/T]GAGCAGGACTATCCCCACAGCAGGGTACGACCTCTACATAACGCACCTTCAGCTTGACATGGTCTTCTCACCTCTGCATGCACTCTTTGAACACAGGCTAATACCAGGTTGTCTGTAGATATATAATGATCTTTCACCTATTCTTCTTTCCTCAGCCAAAGCAGCTAAATACGGTGGTGGACTGACAGGGTTCCTGGGAGGAGGGTATCGAGGTACGACAGAATTAATCCCTGCTGCCTCATGATCACTGATTCCTCATGATCACTGCGGTGTTTCTGACGGACGTCCCAGACTATACGCTCTGATCACGGCAGACACTGCATGGCCTTCTGCTGCTGACCATTACTACAATATACACACATACATGAGTAACTGAAGAAGAGCGATTCCACATCGAACAGACACATTCCTGGCCGTGTAAAATCTGTGGAAATCTGTCAGCACTTTGTTCCAAACCCACTCCGTTTGGCACAACCGCACATGAAAAACTGCAGTCATTT
Associated Phenotype:
Not determined