Busch Lab

ZMP

rftn2

Ensembl ID:
ENSDARG00000056078
ZFIN ID:
ZDB-GENE-040426-2760
Description:
raftlin-2 [Source:RefSeq peptide;Acc:NP_998585]
Human Orthologue:
RFTN2
Human Description:
raftlin family member 2 [Source:HGNC Symbol;Acc:26402]
Mouse Orthologue:
Rftn2
Mouse Description:
raftlin family member 2 Gene [Source:MGI Symbol;Acc:MGI:1921263]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa16417 Nonsense Available for shipment Available now
sa16706 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa16417
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000078499 Nonsense 73 437 2 9

The following transcripts of ENSDARG00000056078 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 33361881)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 32517827
GRCz11 9 32328573
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTCTATGTGAGCTGCCTCATGCCCTCCAGTCCTACTACACCCAGGGCTA[C/A]GTACTGGCCGCCTTGCATCCCATCATCCTATCTGTGGGACGGACACGCTT
Long Flanking Sequence:
AGTTCATTCCCATTATTGGATGGAAACAGCTTGTGACTGAAGTCATTTATAGTTTTGTGTTTCTCTTCTGAGTTTCTGCTTATTAACAGCAGATGTTCATCATCAGTGCTTAATCATCAACCAATTAATCCTTTAATTTTCTCATTAACTTGCGTAACATTAACTCAATTTAGAAAGGGACCAAATACTATCTAAACTGAGTACATTTTACTCTGAGGATTTAGCTGTGTATATACATCAGATAACCCCTTCCTTTCTAAAAGGGCTGCTCCTGGCCAAAATGAGCTGTTTATGCAAGTCTATGTCTGGGTTTGTCGGAGAACGTGCAGGTTCTTAATGTTGTCATTTATTTTGCTTGTATTGACGGAGCTTTAGAACTATATGGCGGTTTTCAAGGTGTGTATTGTGCTGTATTCCACAGGCAGTCGACCTACTGTGCAGTATCTGTCCTCTCTATGTGAGCTGCCTCATGCCCTCCAGTCCTACTACACCCAGGGCTA[C/A]GTACTGGCCGCCTTGCATCCCATCATCCTATCTGTGGGACGGACACGCTTTCTGCCCTGCAGCCTGCTGTACCGGGCCATACTGGTTCGGCCACGATCCAGGTACATCACCCTTGCACCCTGTATTTTGCACCCTAAAAAGCCAGACCGCCCCCTTCCAAGTAAATAATTAACATTTAATGAGTCGGCATGAATATTTAATGGCAAAGGTCAGACAGTCTAGCTGGAGTGGGAGGGGTCCGAAGTCAGGTTTGGGTGCAGATGTGGTTTGCGTTTAGTTGTAACGAAGCCCTGACAACAGTGTGGTCTTTTAACAACCAATGAGAAACTGCACAGCACGAGTGGAGGAACAAGACAGGCTAGTTTCAGCTGAATAAAATATTGAAAAGTAAAGTCTAGGACAGTTGTCATGTGTTAATAGTATTGTGGCTTGGAAAACACTGAGCTGTGTAATGTCAGCTCCTGTGAATACTTTATGAGTGATGTCTTTATCCAGTGAGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16706
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000078499 Nonsense 271 437 5 9

The following transcripts of ENSDARG00000056078 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 33353538)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 32509484
GRCz11 9 32320230
KASP Assay ID:
2260-2034.1 (used for ordering genotyping assays)
KASP Sequence:
CGCAGCTTATTACCGCAAGGGCTGGTCATTGGTTGATTCCTTTGTATACT[G/A]GGATACCCCTAAAGGTACTTCATGCACACATACAGTAGTCACCATTTGAA
Long Flanking Sequence:
GTAGTCATTGTCGGGTTTAAAATGTATCCTACCCATTTGAAATCAACATAGATTGCTATATTTAACAACGCCTAGAAAGAGTCAGCATTACTATTAGACTCTGGCTGCCATATGCTGCTTTGTGTAGCTGAGAGATAAACAAAAAAGCTATTGGCTACTTTAAGAAAAGGGGAGGAGCTACTCTATATAACACTGCAAGCTTCTCATTTTCTATTGCCTGACTTAATGTTATTACATGTTTTATTATTATTCAGCTCTACATTGGTGATAGATAAATATATGACGATTGTTTTCAGATCTGAGATTGTTGGTGCTGTTCCACTCTTGGGCTCCGGGTTGTGCCCCGCTGGACTCGTTGGCCTGCTGTTACCACCAGGGTGCCCTGTCCATGCGCGTTTCCAGGAAAGGTCAAGTTGTAAGTGCTCTGGAAGCAGATTGGCTGGAACTGACCGCAGCTTATTACCGCAAGGGCTGGTCATTGGTTGATTCCTTTGTATACT[G/A]GGATACCCCTAAAGGTACTTCATGCACACATACAGTAGTCACCATTTGAAGTGGATCATCACCATTCATCAAAGTTGTTGAACAGCACCCATAGGGCAATTTAGAAAAACATTTTTAATTCATTTTGAATGTTGACTACCGTATATAATTTTGATTTCTTTATTTGTTTGTCATTTGAGCATGGTTGTTTGTCGTTTTTGTGTATTTTCTTTAGCTCTTCCCAAGAGATTAAAATGATTGCTCAAGAGGATAAGTCATTTCCATTCTCAGAAGTTGCACTTTTCATCTTCTTCCTTTTAAAGCCCCAGCATCTCTCTATCTTTAACCAAAGCCATGTTTTCTTTCTCCTGTCTCCCACTAGAACTAAATTTAGAGCTCACGTCCCTAACCTCACGACCGTGCTTCCTGTTTCGCACCAGACTAATAGGATCTAAATCAAGTGTGCGTGTGTGCGCGCTAAAGACATCTGGAGCTAGTGAATATTGAACTTGAGAAACGGC
Associated Phenotype:
Not determined