ZMP
IGFN1 (3 of 3)
Ensembl ID:
Description:
immunoglobulin-like and fibronectin type III domain containing 1 [Source:HGNC Symbol;Acc:24607]
Human Orthologue:
IGFN1
Human Description:
immunoglobulin-like and fibronectin type III domain containing 1 [Source:HGNC Symbol;Acc:24607]
Mouse Orthologue:
Igfn1
Mouse Description:
immunoglobulin-like and fibronectin type III domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:304
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa7047 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa26821 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa11197 | Nonsense | Available for shipment | Available now |
sa33956 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa14197 | Nonsense | Available for shipment | Available now |
sa20805 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa7047
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000123576 | Essential Splice Site | 134 | 1230 | 5 | 22 |
Genomic Location (Zv9):
Chromosome 6 (position 46719702)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 46780636 |
GRCz11 | 6 | 46782518 |
KASP Assay ID:
554-5424.1 (used for ordering genotyping assays)
KASP Sequence:
AAAGGCAATTAGATCTGKCATGTAAATGGTCATTATTTCTTCCATCTTTC[A/T]GTTGGATTCAAGAAAAAGCAAACTGAYGCATCCTCAAATAAAGGTGAATA
Long Flanking Sequence:
TGCTTTTTTTCAACTCAAGGCAAAGTGGCCCTTTTCAAAGCGGTTGTGAATGGAGATCCAGCACCGACTGTAACATGGACTCGCAACAAGGGTGACACTACTGATCCAGAACAATATAAGCCACGTTATGACGAAAGGAACAGGGAACATGTTTTAGAAGTAAAATATATTAATAATTTAGATCTGAAATTACAAGATCATACATTGAAATAAGTTGTGGTGGTAGATACCAATAAATTCTTGTTTAATTTGTTGTTTTGAAAACAACAGATGCCAAATGTGCAAGTAAATCAGGCAGATACGTACAAATGCTTCGCTACAAATACATTTGGACAAGCAGTGTGCACTGCTACGCTGAGCGTATTCTCAGGTAGGCAACATATTCATTTGGCAAAGTGCAATATTCAAGGACATTTAACTCTTTCCAACATATTCATTTAATTTGAAGAAAAAGGCAATTAGATCTGTCATGTAAATGGTCATTATTTCTTCCATCTTTC[A/T]GTTGGATTCAAGAAAAAGCAAACTGATGCATCCTCAAATAAAGGTGAATATACTGTAATCATCCTGAAATAAAATGCAAAGAGAAGTGCTTTATATATTTACGTTGTATTGATATTGTACAATATTTCCTTTTTTGAAGATGGTGAAGCCAATGATCCTGAGGATTTCAGAAAAATGCTTAAAAAGACCAAGTAATTGTTTTCCTTCAAAGAGTCAAGTGTCTCCTACAAATAAATGTTACTTTTTCGCTTATCTTGGAAATCTCTTCATTTAGAATTGTCAAGAAGAGAAAAGAAGAACCCAAGAAAGAGGGAGAGATTGATCCAAAGTTCTGGGATGTGATGCTAAATGCCAAAAAATCTGATTATGAGCGAATCTGTCATGAATTTGGAATCACTGACTATCGGTGGATGCTGAAACAGCTTAACCTAAAGAAAAAGGAGAAGGAGGATGAACAAGCAAAGGTACTTTCAAGGATTTAGAAAATTTGATCTCACTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26821
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 |
---|---|---|---|---|---|
ENSDART00000123576 | Essential Splice Site | 148 | 1230 | 6 | 22 |
Genomic Location (Zv9):
Chromosome 6 (position 46719563)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 46780497 |
GRCz11 | 6 | 46782379 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTATATATTTACGTTGTATTGATATTGTACAATATTTCCTTTTTTGAA[G/A]ATGGTGAAGCCAATGATCCTGAGGATTTCAGAAAAATGCTTAAAAAGACC
Long Flanking Sequence:
ACAGGGAACATGTTTTAGAAGTAAAATATATTAATAATTTAGATCTGAAATTACAAGATCATACATTGAAATAAGTTGTGGTGGTAGATACCAATAAATTCTTGTTTAATTTGTTGTTTTGAAAACAACAGATGCCAAATGTGCAAGTAAATCAGGCAGATACGTACAAATGCTTCGCTACAAATACATTTGGACAAGCAGTGTGCACTGCTACGCTGAGCGTATTCTCAGGTAGGCAACATATTCATTTGGCAAAGTGCAATATTCAAGGACATTTAACTCTTTCCAACATATTCATTTAATTTGAAGAAAAAGGCAATTAGATCTGTCATGTAAATGGTCATTATTTCTTCCATCTTTCAGTTGGATTCAAGAAAAAGCAAACTGATGCATCCTCAAATAAAGGTGAATATACTGTAATCATCCTGAAATAAAATGCAAAGAGAAGTGCTTTATATATTTACGTTGTATTGATATTGTACAATATTTCCTTTTTTGAA[G/A]ATGGTGAAGCCAATGATCCTGAGGATTTCAGAAAAATGCTTAAAAAGACCAAGTAATTGTTTTCCTTCAAAGAGTCAAGTGTCTCCTACAAATAAATGTTACTTTTTCGCTTATCTTGGAAATCTCTTCATTTAGAATTGTCAAGAAGAGAAAAGAAGAACCCAAGAAAGAGGGAGAGATTGATCCAAAGTTCTGGGATGTGATGCTAAATGCCAAAAAATCTGATTATGAGCGAATCTGTCATGAATTTGGAATCACTGACTATCGGTGGATGCTGAAACAGCTTAACCTAAAGAAAAAGGAGAAGGAGGATGAACAAGCAAAGGTACTTTCAAGGATTTAGAAAATTTGATCTCACTGTCTCCCATTGGACTATCTAGTTTTTTATCTAGTCATATTGCTTTAGTGATATTCCGTGTTTATTTTTATTCTAATAGAATAACATTAAAATACAGAATTTTCCTAAATTATATTCATTTTATATCTTACAGGTGGTTGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11197
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000123576 | Nonsense | 556 | 1230 | 12 | 22 |
Genomic Location (Zv9):
Chromosome 6 (position 46717278)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 46778212 |
GRCz11 | 6 | 46780094 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATACATCCATTTCAGMTGATAAATTGCACTTYGCAAGTGGGTTAACAGAC[A/T]AAAATGCCCTCCGTGGMAAACCAGCAGAGTTGGTGTGCAAACTTAGTACT
Long Flanking Sequence:
GGTCGAGATGGTGCAGGGGATGGAGCAGATGATTTTGCAAGATGTCTGGCAGATGAACAGGCCAGACTGCAGAGAGAAAAAGACGAAGCAGCCAGAAGAGGCAAGGGTGCAGATGGCAGAGGTGACGGAGCGGATGGCCATGATGGAAAGCATGGTCATGGTGATTTAACAGATAGCCGTGGTGATGGAGCGGATGGGTGTAGAGGACTTGGCTTGGGAGACAATAGAGATGCGTCAGCAAAGTATGGACAAGGAGAAGACATTACAGTTGTAAGTGGTAAAAATGGAAAGAGTTCTGGAATGGGTTTCGGAGGAGATGGATTGAGTAGCCAATCAGCTGTGGTTGGATCTGGTGGAGATGGTGCAGGTACTATATACAGTATATTTTCTTAAATGCACATTTATTTTTTAAATATATAATAACACGTCAAGTTAATTTAGAGCATTCAAATACATCCATTTCAGATGATAAATTGCACTTCGCAAGTGGGTTAACAGAC[A/T]AAAATGCCCTCCGTGGCAAACCAGCAGAGTTGGTGTGCAAACTTAGTACTGACAAAATTAATGGAGTGTGGTATAAAGATGGAAACAAGGTATGTTTATGTATTATTACAACAATATTACCAACTGTTAAGCCTGAGTTTGACATTCGTTTATCTTTTTTCCCAATCAGTTGACTTCCAAAGATGGAGTGGTGATCTCGAAGGATGGTTGCACACATAAGCTCGTTGTCCAGAATTGCAAAGATTCTGATGCAGGTCTATATCATTTTGAGGTAAATGGTTGCAAGACAGAGGCGATGGTCCGAGTTGGAGGTAATTACATACAATTTTCTTTTTCTTTTATTTGTCTAAACCAGGGCTGTCAAACTCAATTCCTGGAGGGCCGAAGCCCTGCACAGTTTAGTTCCAACCCTGCTCCAACACACTTACCTGTAGGTTTCAAACAAGCCTGAAGGACTCAATTAGTTTGATCAGGTGTGTTTAATTATTGTTGGAACTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33956
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 |
---|---|---|---|---|---|
ENSDART00000123576 | Essential Splice Site | 831 | 1230 | 16 | 22 |
Genomic Location (Zv9):
Chromosome 6 (position 46715889)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 46776823 |
GRCz11 | 6 | 46778705 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATACTGAGCGGTACTTATATCATGCAATATTTTTATTTATGTTGTTGGTA[G/A]TGTTCCCTGGTCCACCAACTCAGCCAAAGGTGGTCAGTGCTTTCAAAAAC
Long Flanking Sequence:
ATTGAAGCTTTATCAAGTCTTACAGTACAAGGTGAATATAAAACATACCATTTAACTGCTATAAAAATAAACAGCCTACAATGTTTTAAAAGACATGCATCTGTGCCTTTAACAGACAAGCCAGGTCCGCCTCAAGGCCCAGTAGAAGTGAATGAAACCACATCATCAGTCCTTGAACTGAAATGGAATCCTCCGAAGGATGAAGGTGGCTCAGCAGTGACCAACTATATAATTGAGCAGCTACAGGTTGGACAGAATACCTGGCAAAAGGTTGGGGATATTCCAGCTAACCATCTTAACTTCAGAGATAGAAGTGTGTCCCTTGGCAAGAGGTACATCTATCGCATCTATGCTGAGAATCCCGAGGGCATCAGTGAGGCTCTGGAGACTGAAAAAATCATGGCTGGCTCTTTAAGTAATCTCTTTAAGTTTTTACAAGATGGATTTTTCATACTGAGCGGTACTTATATCATGCAATATTTTTATTTATGTTGTTGGTA[G/A]TGTTCCCTGGTCCACCAACTCAGCCAAAGGTGGTCAGTGCTTTCAAAAACTGTATTAACCTATCATGGACTCCACCAGAGAAAGATGGAGGGAATAAAATATTGGGGTACCAGATAGAAAAACGCAAGAAAGATACAAACCAGTGGGTGACTCTAAACTCAGTTAAGGATCCTATCAAAGGTAATCCAAACTGAATGAAAGGATATCATTTTAAGTCTATACTGTAAAACAATGTTGAGTCCTAATAACAACTGCTAGGATGCATCAATCAATGACCACTATCTCAAATTCTTACAGGACTGAAGTATGGAGTGAAGGATGTGTCTGAAGGGTCAGAGTATGAGTTCAGAGTAATTGCCATTAATTCATCTGGAGCTGGGGAACCCAGCACTCCCTCTGAAATGGTCTGCGCTAAAAACCCCAACAGTAAGAACAATGCGAAATAAACATAATATCTGAAATGAGGTCAAACACATTTTCTGATTTTAAACTATTTCCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14197
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 |
---|---|---|---|---|---|
ENSDART00000123576 | Nonsense | 1224 | 1230 | 21 | 22 |
Genomic Location (Zv9):
Chromosome 6 (position 46711331)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 46772265 |
GRCz11 | 6 | 46774147 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGAGTACAAAGTGGTGGCSGTCAACTCACTTGGCAGAGCAGAGYGTTCTT[C/A]GACATTAAAAGTGAAAGGTATGACAGCTGCGGTGATCGTTTCTAGGCTTG
Long Flanking Sequence:
CACAACCACCGTACAACCAGGTCAAGAATACCACTTCAGAATCTATGCAAAAAATGACATGGGACTTTCTGATCCTTCGGATTCACCAACGTGGGGTGTCAACAGCAATAAAGGTGAATCGCAAGATTGCTACCATTAGGCTGCCGTATTACACAACAAGAAATATTTACATCCCTTTTTTTCTTCCTGCCTACTAGTTCTAGCACCCTCAACTGTGCCAACCATGGTAAATTTAGAAAAGCCACCATCAATCCTGGTTCCACTAAAACTCCACTCTCCGCCAAAAGGATACCAGTGCTACATGACCTGTGCTGTACGTGGTTTGCCCAGCCCATATATTGCATGGTACCATAATGGGATTTGCATCAACTCCGACAACAACTACTACATCACAAATGCATTTGGCGTCTGCTCAATGTACATCCTCAGAGTCCGGCCTGAAGACAGTGGCGAGTACAAAGTGGTGGCGGTCAACTCACTTGGCAGAGCAGAGTGTTCTT[C/A]GACATTAAAAGTGAAAGGTATGACAGCTGCGGTGATCGTTTCTAGGCTTGAAAAACATTTACCACAGTCACCTGATTTGCATGCTGGTTTGTCCTTTGTAAATGAGTCACGTTGCTAATAATTTGGAACATGATTACGTAATGCAAATGGCTAGATTGGTCTACAGTCCGTGCCAGAGCCTGTCAAAAAGTGACCCGGAGGGCAAATATGGACCGTCAATCATTTTTATGCAGTCACAGATTGATTTAGACAAATTAGCTGCACCGCTTGATGCATTAGAGCGCTTTCTGTACAAATCTCTATGGTGAGTTCAGAAGCACTCAGCAGTCTGCAATTAAAAATAGAGAACTAAAACTAATTGAAGAAGACATATATTAAACTACTGTCTGCTGTATGCACCTTTTAATTAAGCTAAGAATGCTGTGTACTGTATGTGTGCATTCACTGCGACTTTCTGTGTCTTTTTTTTTTTTAAATGAAGCAACACAAAATTATGCTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20805
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000123576 | Essential Splice Site | 1230 | 1230 | 21 | 22 |
Genomic Location (Zv9):
Chromosome 6 (position 46711312)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 46772246 |
GRCz11 | 6 | 46774128 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCAACTCACTTGGCAGAGCAGAGTGTTCTTCGACATTAAAAGTGAAAGG[T/G]ATGACAGCTGCGGTGATCGTTTCTAGGCTTGAAAAACATTTACCACAGTC
Long Flanking Sequence:
GGTCAAGAATACCACTTCAGAATCTATGCAAAAAATGACATGGGACTTTCTGATCCTTCGGATTCACCAACGTGGGGTGTCAACAGCAATAAAGGTGAATCGCAAGATTGCTACCATTAGGCTGCCGTATTACACAACAAGAAATATTTACATCCCTTTTTTTCTTCCTGCCTACTAGTTCTAGCACCCTCAACTGTGCCAACCATGGTAAATTTAGAAAAGCCACCATCAATCCTGGTTCCACTAAAACTCCACTCTCCGCCAAAAGGATACCAGTGCTACATGACCTGTGCTGTACGTGGTTTGCCCAGCCCATATATTGCATGGTACCATAATGGGATTTGCATCAACTCCGACAACAACTACTACATCACAAATGCATTTGGCGTCTGCTCAATGTACATCCTCAGAGTCCGGCCTGAAGACAGTGGCGAGTACAAAGTGGTGGCGGTCAACTCACTTGGCAGAGCAGAGTGTTCTTCGACATTAAAAGTGAAAGG[T/G]ATGACAGCTGCGGTGATCGTTTCTAGGCTTGAAAAACATTTACCACAGTCACCTGATTTGCATGCTGGTTTGTCCTTTGTAAATGAGTCACGTTGCTAATAATTTGGAACATGATTACGTAATGCAAATGGCTAGATTGGTCTACAGTCCGTGCCAGAGCCTGTCAAAAAGTGACCCGGAGGGCAAATATGGACCGTCAATCATTTTTATGCAGTCACAGATTGATTTAGACAAATTAGCTGCACCGCTTGATGCATTAGAGCGCTTTCTGTACAAATCTCTATGGTGAGTTCAGAAGCACTCAGCAGTCTGCAATTAAAAATAGAGAACTAAAACTAATTGAAGAAGACATATATTAAACTACTGTCTGCTGTATGCACCTTTTAATTAAGCTAAGAATGCTGTGTACTGTATGTGTGCATTCACTGCGACTTTCTGTGTCTTTTTTTTTTTTAAATGAAGCAACACAAAATTATGCTTGAGTACATTGAAACTTGTGT
Associated Phenotype:
Not determined