Gene
kif1b
- ID
- ZDB-GENE-030820-1
- Name
- kinesin family member 1B
- Symbol
- kif1b Nomenclature History
- Previous Names
-
- unm st43
- unm_st43
- wu:fb74c11
- Type
- protein_coding_gene
- Location
- Chr: 23 Mapping Details/Browsers
- Description
- Predicted to enable ATP binding activity; microtubule binding activity; and plus-end-directed microtubule motor activity. Involved in axonal transport and motor neuron axon guidance. Acts upstream of or within several processes, including macrophage differentiation; plasma membrane bounded cell projection organization; and posterior lateral line system development. Predicted to be located in microtubule; synapse; and transport vesicle membrane. Is expressed in central nervous system; nervous system; neurons; spinal cord; and telencephalon. Human ortholog(s) of this gene implicated in Charcot-Marie-Tooth disease type 2A1; hepatocellular carcinoma; multiple sclerosis; neuroblastoma; and ovary epithelial cancer. Orthologous to human KIF1B (kinesin family member 1B).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 3 figures from 3 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- 11 figures from 4 publications
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Allele | Type | Localization | Consequence | Mutagen | Supplier |
---|---|---|---|---|---|
la022637Tg | Transgenic insertion | Unknown | Unknown | DNA | |
sa8450 | Allele with one point mutation | Unknown | Splice Site | ENU | |
sa16498 | Allele with one point mutation | Unknown | Splice Site | ENU | |
sa24361 | Allele with one point mutation | Unknown | Premature Stop | ENU | |
sa37744 | Allele with one point mutation | Unknown | Splice Site | ENU | |
sa44007 | Allele with one point mutation | Unknown | Premature Stop | ENU | |
sa44008 | Allele with one point mutation | Unknown | Splice Site | ENU | |
sa44009 | Allele with one point mutation | Unknown | Premature Stop | ENU | |
st43 | Allele with one point mutation | Unknown | Unknown | not specified | |
uab396 | Allele with one deletion | Unknown | Unknown | CRISPR |
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Targeting Reagent | Created Alleles | Citations |
---|---|---|
CRISPR1-kif1b | LaCoursiere et al., 2024 | |
CRISPR2-kif1b | LaCoursiere et al., 2024 | |
MO1-kif1b | N/A | Lyons et al., 2009 |
MO2-kif1b | N/A | (2) |
MO3-kif1b | N/A | (2) |
MO4-kif1b | N/A | Bielczyk-Maczyńska et al., 2014 |
MO5-kif1b | N/A | Bielczyk-Maczyńska et al., 2014 |
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Human Disease
Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
---|---|---|---|
Charcot-Marie-Tooth disease type 2A1 | Alliance | Charcot-Marie-Tooth disease, type 2A1 | 118210 |
{Neuroblastoma, susceptibility to, 1} | 256700 |
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Domain, Family, and Site Summary
Domain Details Per Protein
Protein | Additional Resources | Length | Forkhead-associated (FHA) domain | Kinesin-associated | Kinesin-like | Kinesin-like KIF1-type | Kinesin-like protein KIF1A/B, pleckstrin homology domain | Kinesin motor domain | Kinesin motor domain, conserved site | Kinesin motor domain superfamily | PH-like domain superfamily | Pleckstrin homology domain | P-loop containing nucleoside triphosphate hydrolase | SMAD/FHA domain superfamily |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
UniProtKB:A0A8M9PKM3 | InterPro | 1795 | ||||||||||||
UniProtKB:A0A8M3AMT9 | InterPro | 1918 | ||||||||||||
UniProtKB:A0A8M3AMV0 | InterPro | 1232 | ||||||||||||
UniProtKB:A0A8M3ANK4 | InterPro | 1848 | ||||||||||||
UniProtKB:A0A8M3AMU4 | InterPro | 1882 |
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Interactions and Pathways
No data available
Plasmids
No data available
No data available
Relationship | Marker Type | Marker | Accession Numbers | Citations |
---|---|---|---|---|
Contained in | BAC | CH211-129O18 | ZFIN Curated Data | |
Contained in | BAC | DKEY-259L18 | ZFIN Curated Data | |
Encodes | EST | 095-d12-2 | ZFIN Curated Data | |
Encodes | EST | fb74c11 |
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Type | Accession # | Sequence | Length (nt/aa) | Analysis |
---|---|---|---|---|
RNA | RefSeq:NM_194382 (1) | 8275 nt | ||
Genomic | GenBank:BX571850 (1) | 236136 nt | ||
Polypeptide | UniProtKB:A0AB32TD35 (1) | 1927 aa |
- LaCoursiere, C.M., Ullmann, J.F.P., Koh, H.Y., Turner, L., Baker, C.M., Robens, B., Shao, W., Rotenberg, A., McGraw, C.M., Poduri, A.H. (2024) Zebrafish models of candidate human epilepsy-associated genes provide evidence of hyperexcitability. iScience. 27:110172110172
- Szenker-Ravi, E., Ott, T., Khatoo, M., de Bellaing, A.M., Goh, W.X., Chong, Y.L., Beckers, A., Kannesan, D., Louvel, G., Anujan, P., Ravi, V., Bonnard, C., Moutton, S., Schoen, P., Fradin, M., Colin, E., Megarbane, A., Daou, L., Chehab, G., Di Filippo, S., Rooryck, C., Deleuze, J.F., Boland, A., Arribard, N., Eker, R., Tohari, S., Ng, A.Y., Rio, M., Lim, C.T., Eisenhaber, B., Eisenhaber, F., Venkatesh, B., Amiel, J., Crollius, H.R., Gordon, C.T., Gossler, A., Roy, S., Attie-Bitach, T., Blum, M., Bouvagnet, P., Reversade, B. (2021) Discovery of a genetic module essential for assigning left-right asymmetry in humans and ancestral vertebrates. Nature Genetics. 54(1):62-72
- Atkins, M., Gasmi, L., Bercier, V., Revenu, C., Del Bene, F., Hazan, J., Fassier, C. (2019) FIGNL1 associates with KIF1Bβ and BICD1 to restrict dynein transport velocity during axon navigation. The Journal of cell biology. 218(10):3290-3306
- Chiquet, B.T., Yuan, Q., Swindell, E.C., Maili, L., Plant, R., Dyke, J., Boyer, R., Teichgraeber, J.F., Greives, M.R., Mulliken, J.B., Letra, A., Blanton, S.H., Hecht, J.T. (2018) Knockdown of Crispld2 in zebrafish identifies a novel network for nonsyndromic cleft lip with or without cleft palate candidate genes. European journal of human genetics : EJHG. 26(10):1441-1450
- Drerup, C.M., Lusk, S., Nechiporuk, A. (2016) Kif1B Interacts with KBP to Promote Axon Elongation by Localizing a Microtubule Regulator to Growth Cones. The Journal of neuroscience : the official journal of the Society for Neuroscience. 36:7014-26
- Diotel, N., Viales, R.R., Armant, O., März, M., Ferg, M., Rastegar, S., Strähle, U. (2015) Comprehensive expression map of transcription regulators in the adult zebrafish telencephalon reveals distinct neurogenic niches. The Journal of comparative neurology. 523(8):1202-21
- Elkon, R., Milon, B., Morrison, L., Shah, M., Vijayakumar, S., Racherla, M., Leitch, C.C., Silipino, L., Hadi, S., Weiss-Gayet, M., Barras, E., Schmid, C.D., Ait-Lounis, A., Barnes, A., Song, Y., Eisenman, D.J., Eliyahu, E., Frolenkov, G.I., Strome, S.E., Durand, B., Zaghloul, N.A., Jones, S.M., Reith, W., Hertzano, R. (2015) RFX transcription factors are essential for hearing in mice. Nature communications. 6:8549
- Bielczyk-Maczyńska, E., Serbanovic-Canic, J., Ferreira, L., Soranzo, N., Stemple, D.L., Ouwehand, W.H., Cvejic, A. (2014) A loss of function screen of identified genome-wide association study Loci reveals new genes controlling hematopoiesis. PLoS Genetics. 10:e1004450
- Campbell, P.D., Shen, K., Sapio, M.R., Glenn, T.D., Talbot, W.S., Marlow, F.L. (2014) Unique Function of Kinesin Kif5A in Localization of Mitochondria in Axons. The Journal of neuroscience : the official journal of the Society for Neuroscience. 34:14717-32
- Zhao, S., Cui, W.Y., Cao, J., Luo, C., Fan, L., and Li, M.D. (2014) Impact of Maternal Nicotine Exposure on Expression of Myelin-Related Genes in Zebrafish Larvae. Zebrafish. 11(1):10-6
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