ZMP
efna3b
Ensembl ID:
ZFIN ID:
Description:
ephrin A3b [Source:RefSeq peptide;Acc:NP_571929]
Human Orthologues:
EFNA3, RP11-540D14.8
Human Descriptions:
cDNA FLJ57652, highly similar to Ephrin-A3 [Source:UniProtKB/TrEMBL;Acc:B4DXG7]
ephrin-A3 [Source:HGNC Symbol;Acc:3223]
ephrin-A3 [Source:HGNC Symbol;Acc:3223]
Mouse Orthologue:
Efna3
Mouse Description:
ephrin A3 Gene [Source:MGI Symbol;Acc:MGI:106644]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22828 | Nonsense | Available for shipment | Available now |
sa10600 | Nonsense | Available for shipment | Available now |
sa14686 | Nonsense | Available for shipment | Available now |
sa2851 | Nonsense | F2 line generated | Not yet available |
sa25013 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa22828
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:
C > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103229 | Nonsense | 8 | 195 | 1 | 6 |
ENSDART00000121607 | None | None | 219 | None | 5 |
ENSDART00000146159 | None | None | 64 | None | 3 |
Genomic Location (Zv9):
Chromosome 16 (position 25409935)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 23255610 |
GRCz11 | 16 | 23170642 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTTGATTTTCACAAATTCTCAGAAACAAGCATAGCTTACATTGGCAAT[C/G]AATCCACCAGTAAGCCTTTGTCCTTAATTGACCTACAGTATGTTTTCATT
Long Flanking Sequence:
TTTGAAACATAAATTCACAGTTATGAGAAGAAAAAAAAATAAACAGAAGTGCTAGATATCGACCTTATTCTTCACACAAGAGCGAGCCCAGTCATTGGAACTTTATCGGCTTGGAGATTTCTAGTGTCACTCATTTCCATAGATTTTTTTAGCCATTAGAAAGCTTGTTATGCCGCTTGATATTGTAAACTGGTATTCTCTTATTGTCTTATTATATTTTTATTATTATTTATTTATTATTATTATTATTATTTCTTATTATTTTTAGTCATTAAATATGTTTGTAGAACAAATAGTTTGACTGTTTACAAGTAATTTCTATTCCTAGTTATTTCCCCATAGGCAAATGAATCAGAAGTGAATTGAAAGAGCTTACTTACTTATCTAGCAATTCAAAGCTGCATGTTCTAGTTCGATTTATTTAAACGCTTTTGTCCAGACAAAAAAATTATGTTGATTTTCACAAATTCTCAGAAACAAGCATAGCTTACATTGGCAAT[C/G]AATCCACCAGTAAGCCTTTGTCCTTAATTGACCTACAGTATGTTTTCATTTGGATGACAGGATGTGCAAATGAAAAAACAAAACAACACAGACGCAATGAGCGCACAAAGCTCATGAGTAAAATCCAGGACCATAAACTGAGCAGTGTTTTAGCATCGGGCAAATTTAGACTGTTGTTTTGGGTAGTTGTTTAGTCTCTGGGCTCAACCAAGGTCATCACCCTGCCATGCACCAGTACATGTTCCAGTCGAGGGAGATCGTACTCAACCCCACAAGAGTTGTGAGGGGAAAAAAGTAGAGCTAAAAAGTCACAATTACTTTTTATTTATTTATTTATTTATTTTCGTGCTGTGGCGGAAATGGGCTTCTATACAATACAACTGTGCATTGGAGCGGTTTAACAATATATTACTTGGGTCCCAACACAGCCATCAGTCGTCTCTCCTCCTTCACGCTCACCTTCAGTCAGTCCCTCAGGCCCGAGGGAGTTTCCTCCAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10600
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 |
---|---|---|---|---|---|
ENSDART00000103229 | Nonsense | 27 | 195 | 3 | 6 |
ENSDART00000121607 | Nonsense | 51 | 219 | 2 | 5 |
ENSDART00000146159 | None | None | 64 | None | 3 |
ENSDART00000103229 | Nonsense | 27 | 195 | 3 | 6 |
ENSDART00000121607 | Nonsense | 51 | 219 | 2 | 5 |
ENSDART00000146159 | None | None | 64 | None | 3 |
Genomic Location (Zv9):
Chromosome 16 (position 25411783)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 23257458 |
GRCz11 | 16 | 23172490 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCAGACTTCGTAAGGAGGGCTACACGTTGCAGGTGAATGTCAACGACTA[T/A]CTGGACATCTACTGTCCTCACTACAACAGCAGTCAGAGGGGCATCGCGGA
Long Flanking Sequence:
GAAGAAAGCAAGAATGTAATTTTATTTATTTTTTATTAATAAAATTGTAATTATTAATAAAAGGTGTATAAATTATACATTTTATTTATTAATTGGGAATTAATAAATTACAATCCAGTTATACTTTATCCGATCCATTTTATGAGAAACTGCATTAAATGTTTACACTTTAAAAAATTAGTATATAATTTGTAGTAAAATAATTGCAGATAACTTTGAAGATTGTTGACTAGTTGTTACAGAGATACCAGAAATACACTTTATTAATATGTCATGCATCTGTCAAACATTTGTGTATTAATTTTCAAGTTACTGTAGTTAGGTGAAGGTGTGTATTTATTCTTAGCTTATTTAATAATAATAATAATAATAATAAATAATAACAACAACAACAACAACAATAATAATAATAATGATAATGACAATAATGTTTGTGTATTTTTCTCTGTCATCAGACTTCGTAAGGAGGGCTACACGTTGCAGGTGAATGTCAACGACTA[T/A]CTGGACATCTACTGTCCTCACTACAACAGCAGTCAGAGGGGCATCGCGGAACAGTATGTGCTCTACATGGTCAGTTATCGCGGTTACCGGACCTGTGATCCACAGCTAGGCTTCAAGCGCTGGGAGTGTAACCGTCCTCACGCCCCTCATGCTCCCATCAAATTCTCAGAGAAGTTCCAGCGCTACAGCGCCTTCTCGCTCGGCTACGAGTTTCACGTTGGCCAGGAGTATTATTATATCTGTGAGTATATACACTCTGCTGCAAATAAACTGTATCACAGCTATTGTGAATTATTGCATTCAAGAAGGTCAACTTATAAAGGATAAATTTGTATAAAAATAATAGAATAATATTTTCTGCTTCTGATTTTTTTTATTGTGTTCACTACATTATCATGAGCAGTTATATGCTTCCGAGTTTCATAATGCAAAAATATTATTTCTATGTATAATCTTCCACTAATGATGTGTATATTTTTGTCTAATTTGACTATAATGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14686
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 |
---|---|---|---|---|---|
ENSDART00000103229 | Nonsense | 27 | 195 | 3 | 6 |
ENSDART00000121607 | Nonsense | 51 | 219 | 2 | 5 |
ENSDART00000146159 | None | None | 64 | None | 3 |
ENSDART00000103229 | Nonsense | 27 | 195 | 3 | 6 |
ENSDART00000121607 | Nonsense | 51 | 219 | 2 | 5 |
ENSDART00000146159 | None | None | 64 | None | 3 |
Genomic Location (Zv9):
Chromosome 16 (position 25411783)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 23257458 |
GRCz11 | 16 | 23172490 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCAGACTTCGTAAGGAGGGCTACACGTTGCAGGTGAATGTCAACGACTA[T/G]CTGGACATCTACTGTCCTCACTACAACAGCAGTCAGAGGGGCATCGCGGA
Long Flanking Sequence:
GAAGAAAGCAAGAATGTAATTTTATTTATTTTTTATTAATAAAATTGTAATTATTAATAAAAGGTGTATAAATTATACATTTTATTTATTAATTGGGAATTAATAAATTACAATCCAGTTATACTTTATCCGATCCATTTTATGAGAAACTGCATTAAATGTTTACACTTTAAAAAATTAGTATATAATTTGTAGTAAAATAATTGCAGATAACTTTGAAGATTGTTGACTAGTTGTTACAGAGATACCAGAAATACACTTTATTAATATGTCATGCATCTGTCAAACATTTGTGTATTAATTTTCAAGTTACTGTAGTTAGGTGAAGGTGTGTATTTATTCTTAGCTTATTTAATAATAATAATAATAATAATAAATAATAACAACAACAACAACAACAATAATAATAATAATGATAATGACAATAATGTTTGTGTATTTTTCTCTGTCATCAGACTTCGTAAGGAGGGCTACACGTTGCAGGTGAATGTCAACGACTA[T/G]CTGGACATCTACTGTCCTCACTACAACAGCAGTCAGAGGGGCATCGCGGAACAGTATGTGCTCTACATGGTCAGTTATCGCGGTTACCGGACCTGTGATCCACAGCTAGGCTTCAAGCGCTGGGAGTGTAACCGTCCTCACGCCCCTCATGCTCCCATCAAATTCTCAGAGAAGTTCCAGCGCTACAGCGCCTTCTCGCTCGGCTACGAGTTTCACGTTGGCCAGGAGTATTATTATATCTGTGAGTATATACACTCTGCTGCAAATAAACTGTATCACAGCTATTGTGAATTATTGCATTCAAGAAGGTCAACTTATAAAGGATAAATTTGTATAAAAATAATAGAATAATATTTTCTGCTTCTGATTTTTTTTATTGTGTTCACTACATTATCATGAGCAGTTATATGCTTCCGAGTTTCATAATGCAAAAATATTATTTCTATGTATAATCTTCCACTAATGATGTGTATATTTTTGTCTAATTTGACTATAATGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2851
Status:
F2 line generated
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103229 | Nonsense | 46 | 195 | 3 | 6 |
ENSDART00000121607 | Nonsense | 70 | 219 | 2 | 5 |
ENSDART00000146159 | None | None | 64 | None | 3 |
Genomic Location (Zv9):
Chromosome 16 (position 25411840)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 23257515 |
GRCz11 | 16 | 23172547 |
KASP Assay ID:
554-2893.1 (used for ordering genotyping assays)
KASP Sequence:
ATCTACTGTCCTCACTACAACAGCAGTCAGAGGGGCATCGCGGAACAGTA[T/A]GTGCTCTACATGGTCAGTTATCGCGGTTACCGGACCTGTGATCCACAGCT
Long Flanking Sequence:
TAAAAGGTGTATAAATTATACATTTTATTTATTAATTGGGAATTAATAAATTACAATCCAGTTATACTTTATCCGATCCATTTTATGAGAAACTGCATTAAATGTTTACACTTTAAAAAATTAGTATATAATTTGTAGTAAAATAATTGCAGATAACTTTGAAGATTGTTGACTAGTTGTTACAGAGATACCAGAAATACACTTTATTAATATGTCATGCATCTGTCAAACATTTGTGTATTAATTTTCAAGTTACTGTAGTTAGGTGAAGGTGTGTATTTATTCTTAGCTTATTTAATAATAATAATAATAATAATAAATAATAACAACAACAACAACAACAATAATAATAATAATGATAATGACAATAATGTTTGTGTATTTTTCTCTGTCATCAGACTTCGTAAGGAGGGCTACACGTTGCAGGTGAATGTCAACGACTATCTGGACATCTACTGTCCTCACTACAACAGCAGTCAGAGGGGCATCGCGGAACAGTA[T/A]GTGCTCTACATGGTCAGTTATCGCGGTTACCGGACCTGTGATCCACAGCTAGGCTTCAAGCGCTGGGAGTGTAACCGTCCTCACGCCCCTCATGCTCCCATCAAATTCTCAGAGAAGTTCCAGCGCTACAGCGCCTTCTCGCTCGGCTACGAGTTTCACGTTGGCCAGGAGTATTATTATATCTGTGAGTATATACACTCTGCTGCAAATAAACTGTATCACAGCTATTGTGAATTATTGCATTCAAGAAGGTCAACTTATAAAGGATAAATTTGTATAAAAATAATAGAATAATATTTTCTGCTTCTGATTTTTTTTATTGTGTTCACTACATTATCATGAGCAGTTATATGCTTCCGAGTTTCATAATGCAAAAATATTATTTCTATGTATAATCTTCCACTAATGATGTGTATATTTTTGTCTAATTTGACTATAATGAATATATATATATATATATATATATATATATATATATATATATATATATATATATATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25013
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103229 | Nonsense | 70 | 195 | 3 | 6 |
ENSDART00000121607 | Nonsense | 94 | 219 | 2 | 5 |
ENSDART00000146159 | None | None | 64 | None | 3 |
Genomic Location (Zv9):
Chromosome 16 (position 25411912)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 23257587 |
GRCz11 | 16 | 23172619 |
KASP Assay ID:
554-7555.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCGGTTACCGGACCTGTGATCCACAGCTAGGCTTCAAGCGCTGGGAGTG[T/A]AACCGTCCTCACGCCCCTCATGCTCCCATCAAATTCTCAGAGAAGTTCCA
Long Flanking Sequence:
CCGATCCATTTTATGAGAAACTGCATTAAATGTTTACACTTTAAAAAATTAGTATATAATTTGTAGTAAAATAATTGCAGATAACTTTGAAGATTGTTGACTAGTTGTTACAGAGATACCAGAAATACACTTTATTAATATGTCATGCATCTGTCAAACATTTGTGTATTAATTTTCAAGTTACTGTAGTTAGGTGAAGGTGTGTATTTATTCTTAGCTTATTTAATAATAATAATAATAATAATAAATAATAACAACAACAACAACAACAATAATAATAATAATGATAATGACAATAATGTTTGTGTATTTTTCTCTGTCATCAGACTTCGTAAGGAGGGCTACACGTTGCAGGTGAATGTCAACGACTATCTGGACATCTACTGTCCTCACTACAACAGCAGTCAGAGGGGCATCGCGGAACAGTATGTGCTCTACATGGTCAGTTATCGCGGTTACCGGACCTGTGATCCACAGCTAGGCTTCAAGCGCTGGGAGTG[T/A]AACCGTCCTCACGCCCCTCATGCTCCCATCAAATTCTCAGAGAAGTTCCAGCGCTACAGCGCCTTCTCGCTCGGCTACGAGTTTCACGTTGGCCAGGAGTATTATTATATCTGTGAGTATATACACTCTGCTGCAAATAAACTGTATCACAGCTATTGTGAATTATTGCATTCAAGAAGGTCAACTTATAAAGGATAAATTTGTATAAAAATAATAGAATAATATTTTCTGCTTCTGATTTTTTTTATTGTGTTCACTACATTATCATGAGCAGTTATATGCTTCCGAGTTTCATAATGCAAAAATATTATTTCTATGTATAATCTTCCACTAATGATGTGTATATTTTTGTCTAATTTGACTATAATGAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATCACTGAAAAAAAGTGTTGCATGCAGAACTGTTGCAAACAATTTATTTGTG
Associated Phenotype:
Not determined