ZMP
si:ch1073-154c4.1
Ensembl ID:
ZFIN ID:
Human Orthologue:
FNDC7
Human Description:
fibronectin type III domain containing 7 [Source:HGNC Symbol;Acc:26668]
Mouse Orthologue:
Fndc7
Mouse Description:
fibronectin type III domain containing 7 Gene [Source:MGI Symbol;Acc:MGI:2443535]
Alleles
There are 26 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10770 | Nonsense | Available for shipment | Available now |
sa10526 | Essential Splice Site | Available for shipment | Available now |
sa24238 | Essential Splice Site | Available for shipment | Available now |
sa12031 | Essential Splice Site | Available for shipment | Available now |
sa24237 | Essential Splice Site | Available for shipment | Available now |
sa37588 | Nonsense | Available for shipment | Available now |
sa15780 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10770
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000115259 | Nonsense | 160 | 4636 | 3 | 55 |
ENSDART00000136037 | None | None | 213 | None | 4 |
ENSDART00000143841 | None | None | 310 | None | 5 |
Genomic Location (Zv9):
Chromosome 23 (position 1653002)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 1621277 |
GRCz11 | 23 | 1630386 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGCWACCTGTGGACAAGGYTCTAGTCTACAACCTTACCATCAAAAACTG[G/A]AATTCGATAAACACTACACTATATTCRAGCACTGTGTTCAACAACACACT
Long Flanking Sequence:
GCGGCATGGTGGCTTAGTGGTTAGCACTGTCGCCTCACAGCAATAAGGGCACTAGTTCAAGTCCCGGCTGGGTCAGTTGGTGTTTCTGTGTGGAGTTTGCATGTTCTCCCTGTGTTGGCATGGGTATCCTCCAAGTGCTCCTGTTCCCCCACAGTCCAAACACAAGCACTATAGGTGAATTGGATTAAAATGGCCAATTGAGTGTGAATGTGAAAGTGTATGGGTGTTTCCCAGTACTGGGTTGCAGCTGGAAGGGCACTGTGTAAAACATATGCTGGAATAGTTGGTGGTTCAGTGACAGTTTTTGTGTAGGGTGTCCAGGTTTTTACATGAATGTAACTGTTATCTTCAAATGTTAACCCCCATTGTTTAATGTCTTGACTCTCAGTGATCCAGCCTCCAGCCGTGGTCACAGTGCTACAGACGGGCCCCCAGTCTGCCCGCATCAGCTGGCAACCTGTGGACAAGGTTCTAGTCTACAACCTTACCATCAAAAACTG[G/A]AATTCGATAAACACTACACTATATTCAAGCACTGTGTTCAACAACACACTAGAGATGACCAGTATGTCACCTTGCTCTTCATACCTAATCTCAGTGTCATCAATTAATGCCCTCATGGAAGTTGGAGAACCCAGGCAGATCAACTATACAACAAGCAGTAAGCCATATCTTTTCAAATATATTTGCAGATTTTCTACTTTTGACCACTTTCAGAAGGAGTTTAAAACATGTTGAAAAAGAATACTTTAGGAATAGACTATGGAGTTTTTTTTTTTAAGTCAAATTAAGTTAATCATATGAGTATTTTGTTTTATTGTTTTGTTTTGTTGTTTTTTTGCCTTTATTTTGATAGAAGAGTATAGGAGCTGTTTTAGAGGTAGGGGTAAGGGTATTGGGAAGTACTGGGTAGTTTTAGCAAGGGTACATAAGCTAGTGCTCGATGATGAAGTTCAAAATGTTAAACTTTTAATACACTTGTAATATACATTTTTGGGGCATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10526
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 |
---|---|---|---|---|---|
ENSDART00000115259 | Essential Splice Site | 1265 | 4636 | 15 | 55 |
ENSDART00000136037 | None | None | 213 | None | 4 |
ENSDART00000143841 | None | None | 310 | None | 5 |
Genomic Location (Zv9):
Chromosome 23 (position 1636441)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 1604816 |
GRCz11 | 23 | 1613923 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGGMCCGCAGTGCTGGAGTWCACCCAGTGCTCCRTTCAGTGTTATCACAG[G/A]TACGTSCACCACACATTCAAAGTTCAGCATCTAGTGATGTGCATTTTTAT
Long Flanking Sequence:
AGCCTAATGTGGCCCAGAGAAGATATAGCAAATGTGGCCCAGCTATCTTAACACATATGTGAACCACATAGACTAAAGTGTTTAGCATGTTCAGGTGTGTTCGATTAATGTTGAAACAAAACTCTGCAGGACACCGGTCCTCCCGGGTCGAGTTTGCCCTGGTTAAGTTCGTATTACTTCAGTCTGGATTGATTGAGCTTTAGCATAATCTTCCTTAACTTGTCTGTGTGATGTCCCAGCACCGTGTCCTCCAACAATGAGGTCTCCTTCACTGAACTGCAGCACTAATGTGGCCCTGGTTTCCTGGGTGAAGGACCCAGATGCATTGTGGGTAAAGGCCAATGCCACGTCTGTCCTGGGACCCACGGCCTCCTGCAACTCCTCTGGCATCAGCTGTTCCCTGGACTCTTTGCAGTGTGGTCAGACCTACAGTGTGTACGGTGTAGCCCAGGGCCCGCAGTGCTGGAGTTCACCCAGTGCTCCATTCAGTGTTATCACAG[G/A]TACGTCCACCACACATTCAAAGTTCAGCATCTAGTGATGTGCATTTTTATTCAATGTGTGACGTGATCTCAACAAAACATGAAGGCATAGGCATAGCCCTGCCCCTTTTATAAAAGCAGCCAATAGCGTTTCGTTTTATCACCGCTCTGTCTGTGGGAGTGGTTGAACTCTTGTGAAGCCTCCTGATGGGGGCGGGGCATGTCAGATACTAGCATTTGATTGGTCATAATTTAATAAGAAATTCTAAGAAGTTATAAGTTTATATCTGTTTCATATCTTCTAAAGCATCTTCACTGTTTTGGCGTACTAGCTTATAGAGATCCTAAAAACTAGCAATACTACTACTAACATCTAAAAACTTTATTTTAATTAACGGGATCTTTAAGAACACATATTTACTATGGAAATAAAGGCTATACATACTTCATAGTCTCGAAATAAAACTTTCCTCTGTTGCTGTTTTCCAGCCCCATGCACCCCTGCAGCAGTGAGCTCTAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24238
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 |
---|---|---|---|---|---|
ENSDART00000115259 | Essential Splice Site | 2571 | 4636 | 31 | 55 |
ENSDART00000136037 | None | None | 213 | None | 4 |
ENSDART00000143841 | None | None | 310 | None | 5 |
Genomic Location (Zv9):
Chromosome 23 (position 1621471)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 1589846 |
GRCz11 | 23 | 1598953 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTTTTCCTAATCGCTTGATCTTGATTTGATTCACTTTCTTTATGTCTA[G/A]TACCTTGTGTGCCGGATTTTGTGACTGCTAATGTGATATGCCAATCGAAC
Long Flanking Sequence:
TAATTACATTGCCATGTGCTTCATAGAAGCTGCCGTGAAGAAACAGGATATTATTACATACAATAAACTCTTACGGTGCGTCCCAATTCGCATACTATCCATCCTAAATAGTATTCGAAATTGGCGATTACATACAGATTACACAGACTTGAACCAGTCTGATCTCACAAGGAAACAAAATTATGTTATGTTTTGTTAGTTTAGTGGCTAATTCGTATGAGTTCAGTCGATTTTAAAATGGAGGTGTGGCACCTAACCCCACCCCTAACCCCAACCGCCATTGGGTGATGAACAAATCGTACTAAATTGTACAAATTAGACTGTATGAATTCATACGAATTAGCCACTAAATCAAAAAGTTACGAATTGCCGTGAGATTGCGTTGATTGAACAGATTAACCTGCTGCTGCTGGACCGTAGTATACATATGCAAATTGGGATGTAGCATTAAACTTTTCCTAATCGCTTGATCTTGATTTGATTCACTTTCTTTATGTCTA[G/A]TACCTTGTGTGCCGGATTTTGTGACTGCTAATGTGATATGCCAATCGAACAGCCTGTTGGTGTCCTGGAAGAAAAGCATTGGAGCAGATTTATATACGGCTATGCTTGAGGACAGCAGCGGCCACTTTACTAGCTGTCAGAGCATGAACAACACCTCCTGTACAATTAATGGACTTCCCTGCGGTCAGACCTACCATATCAGTGTGATAGCATCTGACGGATACTGCGATAGTTTGCCTAGTGCTGTCATTGACACACATTCAGGTAGAAAGCAATGCGAACAGATCTACACAGACATACACCAAATTTATCGAATGTGATGAAGCAGTATGACAAGAACCAAAAAATGACAAACTGAAATGTATTTAATTTAACCCATCTCTTTATACATGTAGAATGGCACACATTACCATTTGGTATTTTTAAGAATACCCTTACAAAGTCCAAAAACTGACACTACATTCTGGGTTCTTTAACACAAATTTGGGTAAAATATGGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12031
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 |
---|---|---|---|---|---|
ENSDART00000115259 | Essential Splice Site | 3182 | 4636 | 38 | 55 |
ENSDART00000136037 | None | None | 213 | None | 4 |
ENSDART00000143841 | None | None | 310 | None | 5 |
Genomic Location (Zv9):
Chromosome 23 (position 1614571)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 1582946 |
GRCz11 | 23 | 1592053 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGTGTTACTGGRTTGTGTATCTATTGTGTGTKTGTTTKTTTTYTCTATA[G/A]CCCCATGTGTGCCGTACAACACCAATACCTTTGTGGAATGCCARAATACC
Long Flanking Sequence:
TGACAGCAACACAAGTTTGTAGGAAACTTTCCAAAAAGTACAGCACTCTTTGTGTAGTTAAGAAACGCAGTTTGTGTATTCAAAGAAATGAAAACCTCTTCTTTCTCCATTTCTTCAGAACCTTGTCAGCCAGCCCAGCTGACAGCTACAGGATCATGTGACAATAACACTGTTCATCTGAACTGGAACAACAGCAGAGGTGCATCGAGATACACCGTGCTTATCACAAGCAATCTAGGATACACAGAATCCCTCCAAACATCTGTACCTATGCTAACAGTGGATCTCCTCTGTGGACAAACCTACACCTTTAAAACAGTAGGGGAAAATGATATATGTGACAGCCTACCAAGCGCCCCTGCCAATTTTAGGACTGGTATGAACCAACACTCATAATGGCTGTAATAACAAGTGACAATTTCTGACTTGTTTTCTCATACTATTTTTGAGCTGTGTTACTGGGTTGTGTATCTATTGTGTGTTTGTTTTTTTTCTCTATA[G/A]CCCCATGTGTGCCGTACAACACCAATACCTTTGTGGAATGCCAGAATACCCTTGGTGCTGTCAGCTGGGCTGCCAGTGAAGGCGCAGAAATGTACACCGCCATTGCCACTGGACAGGATGGCCACACAAACATTTGCATAACGAATACAACGTCCTGCACCTGGGAGGACCTGCACTGCGGAGAAACGTATGTTGTCCAAATCATCGCCAGTGCTCAAATCTGCAGCAGTAAGCCAAGTGTAGGAACAAACATCCACATGGGTGAGTTGCTAAGAAATAAATAAGAGTAGAATTTCATGCAAAAACCCATTCCCTGTTCTGTAGATTTAGATCTAGATTGACTGTGTGCTTACACAATTGTTGGTTGTTAATCTACCAAGAGCTATTTTGTATTGTTTACAGCTCCATGCGTCCCTCACAAACTGGTGCCCTCGTATGATTGTGCCATGAAAGTAGCTTCCCTCAGCTGGGCCGCAAGTGAAAGTGCTCAGATGTACATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24237
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000115259 | Essential Splice Site | 3356 | 4636 | 39 | 55 |
ENSDART00000136037 | None | None | 213 | None | 4 |
ENSDART00000143841 | None | None | 310 | None | 5 |
Genomic Location (Zv9):
Chromosome 23 (position 1613906)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 1582281 |
GRCz11 | 23 | 1591388 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGACATATATGCTGGAGCACAGCCAGCAATGTTTCAGTGCTGCAGACAGG[T/C]TAGGATCCTCTCACACACATGCACAGACACGGTGTCAAAACATGTAGGCA
Long Flanking Sequence:
GAGGACCTGCACTGCGGAGAAACGTATGTTGTCCAAATCATCGCCAGTGCTCAAATCTGCAGCAGTAAGCCAAGTGTAGGAACAAACATCCACATGGGTGAGTTGCTAAGAAATAAATAAGAGTAGAATTTCATGCAAAAACCCATTCCCTGTTCTGTAGATTTAGATCTAGATTGACTGTGTGCTTACACAATTGTTGGTTGTTAATCTACCAAGAGCTATTTTGTATTGTTTACAGCTCCATGCGTCCCTCACAAACTGGTGCCCTCGTATGATTGTGCCATGAAAGTAGCTTCCCTCAGCTGGGCCGCAAGTGAAAGTGCTCAGATGTACATGGTGTCTGCAGAATCAAACACCGGTCACCAGGTGGAACTCTCTACCAATGACACAAGTGCACAGATCTCTGAGTTCAAGTGTGGTCAGTCATACTCAATGACTGTGCAAGCTGTTGGACATATATGCTGGAGCACAGCCAGCAATGTTTCAGTGCTGCAGACAGG[T/C]TAGGATCCTCTCACACACATGCACAGACACGGTGTCAAAACATGTAGGCAACTTTTGGTTTCCTAAGGACAAAATTAGTTTGACCCACTTGTTGAATGACTTGGATTATGTTTGCAGAACCTTGCTCTCCGACATCTGTCACTGGGTTTACGGATTGCATCTCCAACATTGCTACAATATCATGGGACTCAGCTGATGGTGCCGAATATTACACGGCAACAGTGCAAGGCCCAACTGGGCTTTTGGGAACATGCATGTCGTGGTCAGCGAGCTGTGGCATGACTAAACTGTCCTGTGGTGTAACATACAATGTTAGTGTAGTTGCTTCCAATCGTCAGTGTAACTCAACACCCAGTGCCTTGTCTGCTCTAAACACAGGTAATGCATGCAAAGTAGCCTCGATATACATTTTACACACAATTAACCAGATTTCAGACACAACCTCAACATTTGTATTTAGCTAACACTAATGGAGTCTAGCTAATGAGCTTTACAGCTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37588
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 |
---|---|---|---|---|---|
ENSDART00000115259 | Nonsense | 3474 | 4636 | 41 | 55 |
ENSDART00000136037 | None | None | 213 | None | 4 |
ENSDART00000143841 | None | None | 310 | None | 5 |
Genomic Location (Zv9):
Chromosome 23 (position 1612653)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 1581028 |
GRCz11 | 23 | 1590135 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGCGGAAGCTCATGTGTCCTGGAATGCAAGCATGGGGGCGATGTACTA[C/A]ACTGTGTACGCCTGGAGCACAACATTCAATTTCATATCCTGTGATAGCTC
Long Flanking Sequence:
CCTTGCTTTATTATCAGCGTGATTGCTTCAGGATTTACCAGGTCATGAAATCATATCATATATCACTGCTTAAGAACTGCATGGACATCTTTCGACCATCAGAATTTGCACCTTTTATGTCCGACGTTACTACTCTGATATATAAAAGCACATTGGAGACAGAAACCAGAGGCTTTGGTTTTTAGTGTAATTGTTAGAGAACTTGCCTCCCATGTCAGATCCTATTGACAATCAAAAACTGGCAAGTGTAGAACTGGAATCCATTGGTGCAGTGACCCTAATGTGTGTGTGGTTTAAAAAAATGGTTACTATGACCTTCATCTGCATTTCAAGGTATAAATGTTATGCTATCAATAGCTATTTTTTTTGTGAATTTACCTAACTTTCTCTATTTTTCTCTCTCTAGTACCCTGTGTTCCTACAGGTGTGTCTGTGGTGATGGACTGTGCAACTGCGGAAGCTCATGTGTCCTGGAATGCAAGCATGGGGGCGATGTACTA[C/A]ACTGTGTACGCCTGGAGCACAACATTCAATTTCATATCCTGTGATAGCTCTGGACCTGATACACACTGCATTCTTAGTGATCTGATCTGTGGAGATAATTACACTGTTCAGGTGATTGCTGTTGGAGATCAATGCTCCAGCTTGCCCAGTCAGACGGAACGCTTCCGAACAGGTATGGTAATGGTTTGGTTTGTTGTTCTTGATCAGGTGTGTCTAAACTTGTTACTGGAGGATCACTGCCCTGTAAATTTTAGAACAGGCTTAAATTAAACACATCTAAATGAGCTATTCAAGGTTTTCTGACTCATTTGAGGTCCTATACTAAGTGGCATTCTTTAATGATGTAATGCTGCTTTGACCAAGTATATAGCCCTGCAACCCAAAGAGCTCCAAGAGGGAGGTACTTATGCCAAAAGTAGGTCGGGAGATCTCCTTATGTGTGGTACCTTTACTACAAGTAGGTTAGCAGGTCTCCATGTGAGAGAGGCTTACTCCACAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15780
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 |
---|---|---|---|---|---|
ENSDART00000115259 | Nonsense | 3624 | 4636 | 43 | 55 |
ENSDART00000136037 | Nonsense | 40 | 213 | 2 | 4 |
ENSDART00000143841 | None | None | 310 | None | 5 |
Genomic Location (Zv9):
Chromosome 23 (position 1609534)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 1577909 |
GRCz11 | 23 | 1587016 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCTCGCTCTCTCTTTTCYTCTCTCSCTGTGAACAGTACCCTGTCCACCC[C/T]AGAATGTGCTTTCAAATATGCTCTGCTCTTTAAGTTCTGCCAATGTGCAG
Long Flanking Sequence:
CTGCCGTTCTGATGCAGTTAGGGAGTTCATTCCACCAACTAGGCAGATTGAAGGAGAGCGCAACGCAAGTCACAGAACACAAGTTTCTGGAGGGCACATACATCTGCAGAAGTGAGAGCAGATAAGAAGGAGCAATGCCAGAAGTCGCTTTGTAGGCAAACATCAGAGCTTTGAATTTGATGCGAGCAGCAACTGGCAGCCAGTGCAAACGGATGAGCAACGGAGTGACATGTGCTCTTTTAGGTTCATTGAAGACCACGTGTGCTGCTGTGTTCTGGTGCAGCAGGAGCACATGTCGCTTCCACTTTGTAAACCTACTTTTTTAAAAGCAAATTCACAGGAATGCAGGCATATGATGTTCTTTACTTTGTTTTTCCAAAAAAAAAAAAAAGTAATCTATTGAAATAATTTAAACATTTTCTTAACAATGGCTCTTTAACATGCTTTATTCTCTCGCTCTCTCTTTTCTTCTCTCCCTGTGAACAGTACCCTGTCCACCC[C/T]AGAATGTGCTTTCAAATATGCTCTGCTCTTTAAGTTCTGCCAATGTGCAGTGGAGTCCAGCTATGGGAGCAGAATCCTATGAGGTGCATGCTATTAGTGCAAATGGCCTAACAAATGGATGCAACAGCACAAACACTTCCTGTGTTATGCCTAATCTTCATTGTGGCTCCGTTTACAACATCAGTGTGCTTGCCCTTGGTCATCACTGTAATGTGTCCAAGAGTGCAATCACAACACTGCATTCAGGTAGGCAACTGCACAATACATTGCATCTTTACCATAGTGAGTGTGAGAAACTCTCAAATGCAATTTCAGAATACAATCCTAGGCATAATCTTCCATTTTTCCACAGTGCCATGTGTTCCCAGTCAAATTCATGCAAACCTGAGCTGTGGATCTGGTATGGTTGATGTGTCCTGGCAGCCTAGCCTGGGAGCTTCGTCTTACAACGCTGTCGCTCAGGGCAAAGGGGGCTTTGCATCATCCTGTAACAGCAGTGG
Associated Phenotype:
Not determined