Busch Lab

ZMP

si:ch1073-55a19.2

Ensembl ID:
ENSDARG00000093125
ZFIN ID:
ZDB-GENE-081104-93
Description:
Novel protein similar to H.sapiens RANBP2-like and GRIP domain containing [Source:UniProtKB/TrEMBL;A
Human Orthologues:
RANBP2, RGPD1, RGPD2, RGPD3, RGPD4, RGPD5, RGPD6, RGPD8
Human Descriptions:
RAN binding protein 2 [Source:HGNC Symbol;Acc:9848]
RANBP2-like and GRIP domain containing 1 [Source:HGNC Symbol;Acc:32414]
RANBP2-like and GRIP domain containing 2 [Source:HGNC Symbol;Acc:32415]
RANBP2-like and GRIP domain containing 3 [Source:HGNC Symbol;Acc:32416]
RANBP2-like and GRIP domain containing 4 [Source:HGNC Symbol;Acc:32417]
RANBP2-like and GRIP domain containing 5 [Source:HGNC Symbol;Acc:32418]
RANBP2-like and GRIP domain containing 6 [Source:HGNC Symbol;Acc:32419]
RANBP2-like and GRIP domain containing 8 [Source:HGNC Symbol;Acc:9849]
Mouse Orthologue:
Ranbp2
Mouse Description:
RAN binding protein 2 Gene [Source:MGI Symbol;Acc:MGI:894323]

Alleles

There is 1 allele of this gene:

Allele Name Consequence Status Availability
sa9097 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa9097
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000135682 None None 604 None 10
ENSDART00000137939 None None 202 None 2
ENSDART00000140596 None None 153 None 5
ENSDART00000140961 Nonsense 230 481 4 4
ENSDART00000145968 None None 199 None 4
Genomic Location (Zv9):
Chromosome 9 (position 412016)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 104348
GRCz11 9 82917
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACACTTTGGGGGCGTCATTGTGGCTCCATCAACATCSACCACTACAACCT[C/A]GACTGCGTTCAAGTTCAACTCCAATTTCAAGTCCAATGATGGCGACTTCA
Long Flanking Sequence:
TACGTGATTGATTGATTACCAGTGTAGAGGGTTGTTTATTGTAATTAGGAAAAGGATCTGAGGACTCACAGTGATTGTTTGTGTTCCTCCGCAGGGTCCGGTGTACGGGATGAACCGTCTTCCTCCACAGCAACACATGTACAGCTACCAGCAGCAAACACATACTCCGCCGCTGCAGTCCACACCGGCCTGCATGTACCCTCAGGAGCAGGTGTTCGGTGCGCCCATTCGCTTTGAGTCTCCAGCCACGTCTCTACTGTCCCCGTACAGCGAAGAGTATTACGCCCACAGCGTTCCTCAGCCTACCGTCAATCCTACATTACCTGAGCCAGGATACTTCACCAAGCCCAACGCTGCAGCGTCTATGCAGCCGTCTAGGAGCAGCGAGAGCAAGACGGAGGCCCGGACCAGCCTCGGGCCGCAGTTCACTCCTGAAGTCTCCAAGGTTCCACACTTTGGGGGCGTCATTGTGGCTCCATCAACATCCACCACTACAACCT[C/A]GACTGCGTTCAAGTTCAACTCCAATTTCAAGTCCAATGATGGCGACTTCACATTCTCCTCCTCCCAGAGGAAAAACAGCGAGAGCCTGCTGGGCCTGCTGACCTCAGATATTCCTCCCAAAACAGATGGACCGTCAGAGCCAAAGCAGAGCCATGAGCAGACCGGAGTCTTCACCTTTGGGAGTAAAAACGCCACAGGATTTTCATTCACTGATGGTTCTCAGAGCAAAATGAATATTTTTGGCAACACTGACCCATTTAGCTTTACAAGTGGAGCCAAACCAGTGCTGGGCGCTGCTGAGGAGAAAAGCGGAGACAGTGATAACGACAGCACACATGTGGAGGAGGACGAGGACGGCCCTCACTTCGAGCCCATCGTGCCTCTGCCTGACAAGGTGGATGTGAAAACCGGCGAAGAGGAGGAAGAGGAAATGTTCTGCAAGAGAGCAAAGCTGTTCCGGTTCGACGCAGACACTAAAGAGTGGAAGGAGAGAGGGATAG
Associated Phenotype:
Not determined