ZMP
elfn2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens ELFN2, extracellular leucine-rich repeat and fibronectin type III
Human Orthologue:
ELFN2
Human Description:
extracellular leucine-rich repeat and fibronectin type III domain containing 2 [Source:HGNC Symbol;A
Mouse Orthologue:
Elfn2
Mouse Description:
leucine rich repeat and fibronectin type III, extracellular 2 Gene [Source:MGI Symbol;Acc:MGI:360841
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15928 | Nonsense | Available for shipment | Available now |
sa10305 | Nonsense | Available for shipment | Available now |
sa14520 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15928
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109769 | Nonsense | 100 | 844 | 1 | 5 |
ENSDART00000139892 | Nonsense | 114 | 403 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 22 (position 15154914)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 14985462 |
GRCz11 | 22 | 15010037 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCTCACCAAGAATGAAATCTCCTACATTGAGGACGGTGCCTTTGCAGGA[C/T]AGGCCAATCTACAGGTCTTGCAGCTGGGATATAACAAGCTTACCAATCTC
Long Flanking Sequence:
TTCCTGAAGAGCTGTAACTGCCCTCAAGACCATTTCCCCCCAGTGTCTTTGTAATCCTATTGGCTGTCCATCTCCTGTGATCATTTTTTCTCATTTTATGCCCTAACCTTTTTTTTTGTTTCCCTCCTTGATCAAAACAAATCCAGTTTTTTGCTCCAAAAATGGCCTGCGGGATCAGCTTACCTTGTACTGTTCCAACCTCCTTTCTCATCCTCTCTCTCCCTATTTTTCTCCTCTTCCATGCACCTTCTTTCGTGAGGGGTGACTGCTGGCTAATTGAAGGGGACAAAGGCTACGTGTGGCTGGCAATCTGCAGTCAAAACCAGCCTCCATATGAGACAATCCCACAGCACATTAACAACACCGTCCATGACTTACGGCTGAATGAGAACAAGCTCAAGGCAATTTTCTTCAGCTCCCTCAGCCGATTCACCAACCTTACCGACCTCAACCTCACCAAGAATGAAATCTCCTACATTGAGGACGGTGCCTTTGCAGGA[C/T]AGGCCAATCTACAGGTCTTGCAGCTGGGATATAACAAGCTTACCAATCTCACAGAAGGGATGTTGCGAGGGTTGGGACGAATGCAGTGCCTATATCTGCAGCATAACCTCATAGAGGTAATTGCAACCAATGCCTTCTGGGAGTGCCCAAGCCTTAGCAGTCTCGATCTTTCCTCCAACAAATTAGCAAAGCTGGATGCATCCACCTTTACTGTGTTAGGTGGCCGGCTAATAGTATGCGAACTAGCTGGAAATCCTTTCCACTGTGGCTGTGACTTGTACACCTTTCTTATTTGGCTAGAGGCATTTGACAATGTCACTCACACATACGACAGGCTCCTATGTGAGACCCCAAAGGAACTTTTTGGTTACCCTCTTGTGAGCCCTAGAGGTAATCATGGAAGAAATGCTCGTTCCATTCTGTCATCTATGTGTAAAGACGGTGTGATTGTTGGTGGTATAACTGCCCTGCCTCCAGACTTAGATTCTTCAGGGATGGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10305
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109769 | Nonsense | 193 | 844 | 1 | 5 |
ENSDART00000139892 | Nonsense | 207 | 403 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 22 (position 15154633)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 14985181 |
GRCz11 | 22 | 15009756 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATAGTATGCGAACTAGCTGGAAATCCTTTCCACTGTGGCTGTGACTTGTA[C/A]ACCTTTCTTATTTGGCTAGAGGCATTTGACAATGTCACTCACACATACGA
Long Flanking Sequence:
GGGGACAAAGGCTACGTGTGGCTGGCAATCTGCAGTCAAAACCAGCCTCCATATGAGACAATCCCACAGCACATTAACAACACCGTCCATGACTTACGGCTGAATGAGAACAAGCTCAAGGCAATTTTCTTCAGCTCCCTCAGCCGATTCACCAACCTTACCGACCTCAACCTCACCAAGAATGAAATCTCCTACATTGAGGACGGTGCCTTTGCAGGACAGGCCAATCTACAGGTCTTGCAGCTGGGATATAACAAGCTTACCAATCTCACAGAAGGGATGTTGCGAGGGTTGGGACGAATGCAGTGCCTATATCTGCAGCATAACCTCATAGAGGTAATTGCAACCAATGCCTTCTGGGAGTGCCCAAGCCTTAGCAGTCTCGATCTTTCCTCCAACAAATTAGCAAAGCTGGATGCATCCACCTTTACTGTGTTAGGTGGCCGGCTAATAGTATGCGAACTAGCTGGAAATCCTTTCCACTGTGGCTGTGACTTGTA[C/A]ACCTTTCTTATTTGGCTAGAGGCATTTGACAATGTCACTCACACATACGACAGGCTCCTATGTGAGACCCCAAAGGAACTTTTTGGTTACCCTCTTGTGAGCCCTAGAGGTAATCATGGAAGAAATGCTCGTTCCATTCTGTCATCTATGTGTAAAGACGGTGTGATTGTTGGTGGTATAACTGCCCTGCCTCCAGACTTAGATTCTTCAGGGATGGAGATAGATTTTTATGATCAGATGGGGCCACATATGCAGCCCACAGCTTCATCTACTACAGACCCAACTTATAGTCCAAACATTAGGTTGCAAACTGTCTCCTTCTCAACAGCATCACTCTTGGTTCAGATACCCAAGCCCTACAGTAAGATGTACATTTTAGTGCAGTACAACCACACCTATGTGTCTGATGTCATAAACCTAAAGAACAAGAAACAGACTGTCACATTAAATGACCTAAAGCCCCATACTAATTACACCTTTTGTGTGGCCTCCATTCGCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14520
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109769 | Nonsense | 809 | 844 | 5 | 5 |
ENSDART00000139892 | None | None | 403 | None | 1 |
Genomic Location (Zv9):
Chromosome 22 (position 15152560)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 14983108 |
GRCz11 | 22 | 15007683 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATMTGGGAGCGCTTCCGACCMTRCAAAAAAAGCCCCCGTGAGGAGGCATA[C/A]ATAGCCGCTGGTCATGCTCTTCGRAAGAAAGTGCAGTTTGCAAAGGATGA
Long Flanking Sequence:
CCCGACCCTCGAAGCCCTGAACAATGCAAGAGCAAGTACCCTGAGAAAGGCAGCCCTGTTCGGTGCGGGGAGCCATTAGAGAGGTTGCCCTTAATAGGGGTTCAGGGAGTCAGTAATGGCAGAGGAGATGGTGGCAGCGGGGGTGGAAGGGGAGCCGGTGGTGGCAGTGGTGGTTCGGGTGGGTGTGGTGTTGTGGTTGGTGGTGGGAGCAGCACAGCTCAGCAGCACCACTTGGAGGTGCACCCAGACTACCACTGCTCAGAGCACCGACACTCCTTCCCCGCTCTCTACTATGAGGGTGCCACTGACTCCCCTGCCCAGAAAGTCTCCTTTTTAAAGCCTCTCACTCGCACCAAGAAGGACACTGCCTACTCTCAGCTTTCTCCCCGCCACCACAATTACTCAGGCTACTCTTCCAGCCCTGAGTACTCCTCCGAGAGCACTCTTAAAATATGGGAGCGCTTCCGACCCTACAAAAAAAGCCCCCGTGAGGAGGCATA[C/A]ATAGCCGCTGGTCATGCTCTTCGAAAGAAAGTGCAGTTTGCAAAGGATGAGGATCTCCATGACATTCTGGACTACTGGAAAGGGGTGTCAGCACAGCAGAAACTGTGATGCTTGTGAGAACCACAACAAAGTGAGGAGAAATTGTTGAGAAAAGGACTGATGGCTTTTGAGACAGCTCGGCAGACTCCATCAGCAGGTGCTTTGGTCCCCACAGGCCACCACAGAGACAAGTGTTCTGAAAGGGACAGAATTAAGCAGGTGTTCCAAACTCATTAAGGCATAGGTGTAAGGCAAGCAACCATAAATGCGCAGGAAGTGTGGCACTTAAAAAGGCATCCAGTTTCAGTTGAAAATATTTACCTTGTGTACCACCTGTGCACTTTTGCACTGTAGTTTGGTAAATTAATAGTTTTAAAAAATGAGGATTTAGTGGTATTAATTTAACAAATGTATGAATATAGTCTGAAGACAAGGTGATACCTAATGCTTTGTCAGGATGA
Associated Phenotype:
Not determined